| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs180884897 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203417479 | AAACTTTCTTCCACA[A/G]AATAATGGTTTCTCA | 10152 |
| rs180890519 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203388426 | GGTGGCTCATGCCTG[C/T]AATCCCAGCGCTTTG | 10152 |
| rs180897096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203426494 | CAATGAAAATCACAG[C/G]AGGGCTTATAGGTAT | 10152 |
| rs180904071 | snp | A/C | | | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432497 | TTCAACAGACAAACA[A/C]TGAAGATGGGTGTTG | 10152 |
| rs180905657 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203338070 | GTGTGTTACTGGCAT[A/G]AAAGACATGTAGACT | 10152 |
| rs180916536 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203379931 | AAGGTTTTTTTTGGT[G/T]GTTCTTTTCTCCAAA | 10152 |
| rs180918039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203364698 | AATACTTAAAGTTTC[C/T]ATTCTTTTATATTAA | 10152 |
| rs180928781 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406084 | ATGAAATAGGAATAC[C/G]AATTTATCATTAATC | 10152 |
| rs180938183 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203353208 | AATTTTTTTTCAGAT[G/T]ACAATTATCATATAA | 10152 |
| rs180940841 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203347089 | ATTATGATGATTGCC[C/T]TAACATGTGCATCAG | 10152 |
| rs180974872 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203372245 | AGCACAGGGTTGGGG[C/G]TAAGGTCACCGATCA | 10152 |
| rs181091449 | snp | G/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430192 | ATTTTTTGTTTTATT[G/T]TAAGTTTCCCTCTTT | 10152 |
| rs181164537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203403110 | AATTTAGAAGTGGCA[A/G]AGGAAAAGAGAACAT | 10152 |
| rs181175140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203384641 | TAAAAAGAATTTTAA[A/G]ACCCTGTTACTGAGG | 10152 |
| rs181188016 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203422492 | AGGACTTGGGGATGT[C/T]GGGGAAGGTGAGTGA | 10152 |
| rs181274774 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203393151 | GGCAATTCTCTTGCC[C/T]CCAGGCGATTCTCCT | 10152 |
| rs181282794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203375351 | CATTTTTTACTTGCC[A/G]CAGGTGAGTGCTGTT | 10152 |
| rs181291733 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203410957 | AAGATCAATTATATA[G/T]AATATATATATAAAA | 10152 |
| rs181302042 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357891 | CTCCTGCCTCAGCCT[C/G]CCAAGTAGCTGGGAC | 10152 |
| rs181305226 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203335136 | TAAAAATTTCTATAT[A/T]TTCCCATTAGCCGTA | 10152 |
| rs181313966 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203341573 | CAAAAAAATTTCTCC[A/G]GGCTTGTTGGTGTGC | 10152 |
| rs181396272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203368968 | TGGGACTACAGGCAC[A/G]TGCCATGCTTGGCTG | 10152 |
| rs181472311 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203345575 | GCCACCATGCCAGCT[A/G]ATTTGGTATTTTTAG | 10152 |
| rs181481266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203426845 | CTCAAATGAAGAAAC[A/G]GCCATCTTTCTTGAT | 10152 |
| rs181503960 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ABI2 | GRCh38.p7 | 2:203388554 | TGGGCGTGGTGGTGC[A/G]CCTGTAATCCCAGCT | 10152 |
| rs181521290 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ABI2 | GRCh38.p7 | 2:203350003 | AGTTGCACTATTTTC[C/T]ATTTCCACCATCAGT | 10152 |
| rs181539654 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203407337 | ATAAGCATCTCAACT[C/T]GCATGGGCTATATAA | 10152 |
| rs181541957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203354100 | CCCAGGTTGGAGTGC[A/G]GTGGCGCAATCTCAG | 10152 |
| rs181548087 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | ABI2 | GRCh38.p7 | 2:203373498 | TGGGGAGAGGGAGAG[A/G]GAGAGGGAGCGGGAG | 10152 |
| rs181552114 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | ABI2 | GRCh38.p7 | 2:203338453 | CCTTTAGTGATAAGT[C/G]AGTTCTTGCTTGGTT | 10152 |
| rs181554305 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430477 | TATTAATGAAAGTAC[A/T]CTTTATTGTTGCCTT | 10152 |
| rs181619126 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327519 | ACAGCCCTGTGAAGA[A/C]GGCAATTACTACTAG | 10152 |
| rs181642483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203367819 | ACCAGCCTGGGCAGC[A/G]TAGCAAAACCCTGTT | 10152 |
| rs181652180 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203401770 | TTGATTTGGAATTAC[A/G]TCATTTAACCTTTTG | 10152 |
| rs181656848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | ABI2 | GRCh38.p7 | 2:203383271 | GAAGAGCCCAGGCAT[A/G]TGGACACCTGTATTA | 10152 |
| rs181660216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203333670 | AGATTTTCAGTGACA[A/C]ATCAGTCATCTTCAA | 10152 |
| rs181669791 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203348904 | CTGAACCTTGCTGAA[A/G]GTGTTTTTTTTTGTT | 10152 |
| rs181706860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203378701 | TCTTTTAGAAAGGGG[A/T]AATTGAAGTAGGACA | 10152 |
| rs181765674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203393693 | AAGGAACTCTGGGAT[C/T]CATACATAAGTCAGT | 10152 |
| rs181786784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203359129 | ATTTCCTTAGTGTAG[A/G]TCAGACTGTGGGGTG | 10152 |
| rs181865329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203363645 | GCGATCTTTCTGTGC[C/T]TGGCTTGTTTCACTT | 10152 |
| rs181873209 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329585 | TTTTATGGTTATTTT[G/T]AATTATGGGTTCTGC | 10152 |
| rs181875960 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398204 | CTTTTAAAGAAAAGC[G/T]TTCTGCAGTAGATAA | 10152 |
| rs181881184 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359846 | AACATGTACATTTTT[G/T]GGGGGGGGACACAAA | 10152 |
| rs181999017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203375638 | GTTACAGGAGCTTTC[C/G]TAAATTTCTTTTACA | 10152 |
| rs182013640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203364043 | TGCTGGAATTATAGG[C/T]GTGAGCCATGGTACC | 10152 |
| rs182014657 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203411764 | TTCCAGATATCAGAA[G/T]GGCCTTTTATGGTAG | 10152 |
| rs182018995 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203379140 | CTCGTATGTCTTATG[A/T]GAGCATTTAATAAAT | 10152 |
| rs182026743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203346509 | ACTGGTCTGTGTTTT[A/G]GGTTTATCCATTACT | 10152 |
| rs182028044 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342964 | TTAACATGCATAATT[A/G]TGAATTTTATTCATG | 10152 |
| rs182038129 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | ABI2 | GRCh38.p7 | 2:203375598 | TGTAGGAAAAATATA[G/T]TAGCCATATTTTATT | 10152 |
| rs182038774 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203327982 | CGAGAAGTTCCCTAG[A/G]CCGATGACCTCCATG | 10152 |
| rs182124073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203423945 | AATGTATTTTTACTT[C/T]AGCAGAAACATTTAG | 10152 |
| rs182150953 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203403987 | TAAACTCCTGACCTT[A/G]AGTGATTCACCCACC | 10152 |
| rs182228442 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399108 | TAAATTTTTAACGTC[A/G]TAAGAAACTGCCAAG | 10152 |
| rs182251010 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203375857 | TGAAATAGATTTAGT[A/G]CTCTCTGTCAAATTA | 10152 |
| rs182266443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203359486 | TGTTGTAGTTAGACA[A/G]TATACAGGTTATATT | 10152 |
| rs182273619 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203416835 | TTTATATTCCATGAA[C/T]CCAGAAGCTTGGATA | 10152 |
| rs182282527 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203343327 | TGAGATTGCGGCACT[C/G]CACTCTAGCCTGGAC | 10152 |
| rs182300740 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337644 | AGAAAAACCCTAAAA[C/T]TCATAGGAAACCACA | 10152 |
| rs182308316 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ABI2 | GRCh38.p7 | 2:203355470 | TGAGCTGTCATTGCA[C/T]CACTGCACTCTAGCC | 10152 |
| rs182328437 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203339298 | TGAAAAACTGGTTCC[A/G]GCCGGGTGTGGTGGC | 10152 |
| rs182498206 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | ABI2 | GRCh38.p7 | 2:203385288 | AGGCGCCCGCCACCT[C/T]GCCCAGCTAATTTTT | 10152 |
| rs182532723 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203350698 | GTGCCCGCCACTGTG[C/T]GCAGCTAATTTTTAT | 10152 |
| rs182538771 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203413031 | ATGGTAGTCACTTGA[A/C]TAATACCCTGGGAGT | 10152 |
| rs182540404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203352531 | TGTAGGGTTAGGCTA[A/C]TACGTCTGTGTCTCG | 10152 |
| rs182561721 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203431976 | CTCCCAGAGGGAGAG[C/T]TGGTGGTATTATGAG | 10152 |
| rs182578948 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360382 | GCTTTAAACAAAAGG[C/T]GAAGTGTTGGGTGGA | 10152 |
| rs182579132 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | ABI2 | GRCh38.p7 | 2:203376339 | TGCCCACAACAAAGA[A/C]TTATCAAGCCCAAAA | 10152 |
| rs182597108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203390366 | GCCGGGTGCAGTGGC[C/T]CACGCCTGTAATCCT | 10152 |
| rs182625459 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329957 | GACCAGACTGGTCTC[C/G]AACTCCTGACTTCAA | 10152 |
| rs182748293 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428330 | TACTTTGGAAGAGAA[C/T]AGTAGTTATTTTCAA | 10152 |
| rs182767916 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203370451 | AGACAGTTTAATTAC[A/G]TTTTCTTTTCTTTTT | 10152 |
| rs182812253 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203394199 | TCTGTATATTTGGTA[A/T]ATAGAAAGGGAAATG | 10152 |
| rs182817602 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203336054 | TTATGTAGTATATAG[A/C]CTTTTGTGTTTGACT | 10152 |
| rs182834222 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203404143 | TTTTGGAGGGGAAGG[C/T]GGATGAAAAGATGTG | 10152 |
| rs182855549 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ABI2 | GRCh38.p7 | 2:203373992 | GGCAAAATTCCATCT[C/T]TCCAAAAAATGCAAA | 10152 |
| rs182887833 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203367337 | CCTTTTTTTTTTTTT[A/T]AAACAAATTTCATAC | 10152 |
| rs182892286 | snp | A/G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384921 | CTCACTGCAACCTCC[A/G/T]CCTCCCGGGTTCAGG | 10152 |
| rs182901845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203423527 | GCCTCCCAGGTTCAC[A/G]CCATTCTCCTGCCTC | 10152 |
| rs182902730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203403571 | CAACATAAACACTTA[A/G]TTTAAATAATGTTTT | 10152 |
| rs182908262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203350064 | GTCAGCATTTGTGGA[A/C]TGTCTCTTTATTTAA | 10152 |
| rs182909733 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403644 | ATTGGTGATCATTTT[C/T]TTATATCTTATAGGT | 10152 |
| rs182918071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203369367 | GAGTAGGAGAGATTA[C/T]GTGGGTAAATGATGA | 10152 |
| rs182922095 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203335592 | AAGTAGGATATAATT[A/C]CATGTAAATTTACCT | 10152 |
| rs182955094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203409564 | CCATCTTCATAGTTA[C/T]GAAGGGTAAAAATCT | 10152 |
| rs182963881 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428397 | ATGTGCTCTCTGGAC[A/G]TTATTAATGGCCAGT | 10152 |
| rs182980568 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203391356 | CTAGTGAATTTTAAA[A/T]TTGAGGTAAAATCCT | 10152 |
| rs182983580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203355936 | AATTATAGATTGGAA[A/G]TAATTTTTTCCCCAG | 10152 |
| rs182989732 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203374159 | GTGAGACACTGTCTC[A/T]ACAACCCAAAACACA | 10152 |
| rs182998013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203339935 | TGAAAAGTCATCTGT[C/T]CCATCTGTATATGTG | 10152 |
| rs183029324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203408487 | CTTCTTAAAACCACT[A/G]TGGCTTCAGATTTTC | 10152 |
| rs183092886 | snp | G/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203424167 | AAAATCTAGACAGAT[G/T]TTACATTTCTCAACA | 10152 |
| rs183104406 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203400706 | TCCTTATATGACTCC[A/G]TATGAATCTAAGCTT | 10152 |
| rs183109400 | snp | G/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203382220 | AGGTAAGAGATTCCA[G/T]GGCTGGATTTCCATT | 10152 |
| rs183115363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203343905 | GAGGCTGAGGTGGGA[G/T]GATTGCTTGAGCCCA | 10152 |
| rs183143730 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203408314 | GTTACAGGCACCTGC[C/T]ACCACACCTGGCTAA | 10152 |
| rs183146068 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203386261 | CCTACACACACTTCC[A/C]CTCTTCTATTTGTGT | 10152 |
| rs183146992 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203332301 | TTTTTTTTGAGATAC[A/G]TGTAAGACCTGCGTT | 10152 |
| rs183150188 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365662 | TGAGACGGAGTCTCA[C/T]TCTGTTGCCCAGGCT | 10152 |
| rs183153286 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203347924 | GATTTGATCATTAAC[C/G]AGGTGATAATATAAG | 10152 |
| rs183375747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203418397 | AGGTATCAGCTGAGG[C/T]TGCAGTGATCTCAGG | 10152 |
| rs183401708 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203347524 | AAATGTGCAGTGGAA[A/T]CTCATGGTTCAATTT | 10152 |
| rs183424475 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403742 | ATGTTCTTTCTTTCT[G/T]TTTTTTTTTTTTTTT | 10152 |
| rs183457291 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203360882 | ACTCTTATGCTGTTG[A/C]TAATATCATTTATGA | 10152 |
| rs183542945 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203397264 | TCTATACAGTTTTTG[C/G]AAATTATCATTAGAA | 10152 |
| rs183559584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203377341 | ATTTATAGTATGCAG[A/G]TGTGAAATAGAAGCT | 10152 |
| rs183571498 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | ABI2 | GRCh38.p7 | 2:203361947 | CCCTTGTGATCCTTC[A/C]TGAATCCTTAGGAGA | 10152 |
| rs183581828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203345254 | CACGCCATTTTGAGA[A/G]CTGTAACGCTCACTG | 10152 |
| rs183591258 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326680 | AGTTGGACTAGACCA[A/G]CATTTTCAATATCCT | 10152 |
| rs183592613 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ABI2 | GRCh38.p7 | 2:203399999 | AGTTTCAGGTTTTAT[C/T]GCTAGGTTTATGATA | 10152 |
| rs183611372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365035 | TGCCACGCCTGGCCA[G/T]CGTTATGCTTTACTC | 10152 |
| rs183624141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203395992 | TTTGGTGATGTGGCT[C/G]AGTTGCTGCTTTGAG | 10152 |
| rs183630275 | snp | C/T | | | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432476 | GTTAATGTACAGTTT[C/T]TTTAATTCAACAGAC | 10152 |
| rs183661155 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203330865 | TAAGGATTATTAAAG[A/C]TGAAAGGTTAAAGGC | 10152 |
| rs183697271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203376836 | ATGTAAATGTCCCCA[A/G]TCCCTAGACCAAGTC | 10152 |
| rs183697678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203343963 | GACGAGAGAGACCCC[A/G]TCTCTACAAAAATTA | 10152 |
| rs183726359 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203373753 | TAACAATTAAAGGAG[C/G]TGGAAAATAATTATC | 10152 |
| rs183760001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203420344 | TAGAAGTATAAATGA[C/T]ATATAGGAATTGTCA | 10152 |
| rs183773722 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357702 | AAAGGAACAATTTAA[A/G]GAATTTTAGGATTCT | 10152 |
| rs183775604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203382437 | TAGAACAGTACCTGA[C/T]ACACATTAGGTGCTT | 10152 |
| rs183794834 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203374728 | AATTTAAATGTTTAT[G/T]TGAAACATTAGCTTA | 10152 |
| rs183796245 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203341201 | ACTTATCCTTCCATG[A/C]TTTTTTTACGCCTAC | 10152 |
| rs183799598 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203400906 | GAAATATGAAGCCTG[A/G]AAGAGGATATGACTG | 10152 |
| rs183829761 | snp | C/G | 0.00518236 | 0.0507004 | intron-variant | ABI2 | GRCh38.p7 | 2:203378333 | AGCCAGGATGGTCTC[C/G]ATCTCCGGACTTTGT | 10152 |
| rs183838629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203414869 | CCTCCCAATATAAAG[A/G]TGAAATGAAATAATG | 10152 |
| rs183846208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203397799 | TAAGGCAGAGGGGAA[A/G]CACACTGGTCACGTG | 10152 |
| rs183855901 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413504 | TTTTAAAAAGTCATT[C/G]CCTAATTTGACCACC | 10152 |
| rs183914637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203419870 | ATGCATGCCTGTAAT[C/T]CCAACTACTCGGGAG | 10152 |
| rs183951796 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203389024 | TTAAGGTTGAGCTTA[A/C]AGGACTTTGGTTACC | 10152 |
| rs184018926 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203339125 | TGTGAAAATGTGCTC[A/C]ACATCACTAATCATT | 10152 |
| rs184042902 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430327 | TCTGACCAATAAAGC[A/C]ACCATTTTATCAAGA | 10152 |
| rs184043926 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203336545 | CCTCCTAGTTCCCAT[C/G/T]AGATGAGGCTCTCTA | 10152 |
| rs184048806 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203351120 | GCCTTTTCTTTCCCT[C/T]GTTAAATTGTTTTGG | 10152 |
| rs184068917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203411103 | AAAACTTACTAAAAA[C/T]TCCCCCAGTACTTTG | 10152 |
| rs184084228 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376169 | CCTTCCTCTATAGAT[C/T]TTTGGTTCTCAACCA | 10152 |
| rs184160742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203354648 | ACAATAATAGCCAGC[A/G]TATTAGCATTTTCTT | 10152 |
| rs184197398 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | ABI2 | GRCh38.p7 | 2:203348907 | AACCTTGCTGAAGGT[G/T]TTTTTTTTTGTTTTT | 10152 |
| rs184219396 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423046 | TTTTTCCAGTGGCTT[G/T]CTAGTTTAGGGTACT | 10152 |
| rs184230418 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203387918 | TGCTACTTGTCAGGA[A/T]ATGTTTTCTCTCTTA | 10152 |
| rs184235740 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203352673 | TTATGAGGTAAAAAT[G/T]ACAGTAAAGGTTAAT | 10152 |
| rs184243360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203413533 | CCCTATCACAGTTGA[C/T]TGCCTTTTGGATTGG | 10152 |
| rs184263814 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399198 | TTGCATCCTTGTCAG[C/G]CCTTGGTGTTGCCTT | 10152 |
| rs184363775 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366212 | TAATCCCGGCACTTC[A/G]GGAGGCTGAGGCAGG | 10152 |
| rs184371350 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ABI2 | GRCh38.p7 | 2:203332557 | TTGAACCTGGGAAGC[A/G]GAGGTTGCAGTGAGC | 10152 |
| rs184389157 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203371783 | GTAACATTATTATAA[A/G]GATGAATGTTGCTTA | 10152 |
| rs184404630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203337735 | CTGATTTCAAACTAT[A/G]TTACAAAGCTATAGG | 10152 |
| rs184478287 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203348286 | GTAATAAAGGTTAAG[C/G]TTAGTATTTTAAAGT | 10152 |
| rs184502921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203392955 | TAGTCACCACATTTT[A/G]TTCCTTTGCTCCTTT | 10152 |
| rs184517881 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430023 | ACAGTACCTTTTGGG[C/T]TTTCTGCATATTTTA | 10152 |
| rs184542881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203337342 | ATCTGTTGTGTTTCT[A/G]CATATTAACTACAAA | 10152 |
| rs184599035 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203345461 | CCCACCGGAAGGAAC[A/C]AATTCCGGACACAAT | 10152 |
| rs184603410 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203370759 | GAAGATTGAGTTGAA[G/T]GAATGGAGGGTTCAG | 10152 |
| rs184655819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203410503 | GACAGTTTATTAGTT[C/G]TAGGCACTGTGCCAG | 10152 |
| rs184691148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203404533 | AGCACGGGATTACAG[A/G]TACCTGCCACCACGC | 10152 |
| rs184699880 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203425499 | AAGCTACCGCACCTG[A/G]CTGGATTTGCATTTC | 10152 |
| rs184704492 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203370931 | CCTGGGTAAGAACTT[C/T]ACCACCTTTCAGCCT | 10152 |
| rs184715846 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | ABI2 | GRCh38.p7 | 2:203351755 | TGCTCAGGCTGGTCC[C/G]AAACTCCTGGCCTCA | 10152 |
| rs184727558 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | ABI2 | GRCh38.p7 | 2:203421603 | AAGGATATAAAAACT[G/T]TTATGACTGCTTGAC | 10152 |
| rs184733398 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203402179 | AGCTGGAATTACAGG[C/T]GCACGCCACCATACC | 10152 |
| rs184742879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203363402 | GTCTTACTCATTCTT[C/T]TCTATTTTTCGTATC | 10152 |
| rs184746484 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203367838 | CAAAACCCTGTTCTC[C/T]ACCAAAAATACAAAA | 10152 |
| rs184750957 | snp | C/T | 0.0103295 | 0.0711199 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327033 | CAGGATGGTCTCGAT[C/T]TCCTGACCTCGTGAT | 10152 |
| rs184754982 | snp | C/G | 0.00795532 | 0.062565 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429380 | AACTGTTTTAAATTA[C/G]ATGTTCCCATTATTT | 10152 |
| rs184760695 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400079 | TAGTGTGAATAGTGT[C/T]TTTTTTTTTTTTTTT | 10152 |
| rs184762114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203383468 | GATGTGTTAACCTCC[A/G]AAGTGATAGAAATAC | 10152 |
| rs184861775 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203421152 | TATGTAACTTTTTTT[C/G]GAGATACCTGATAAT | 10152 |
| rs185011086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203426379 | CTGTTGAAATTGATA[C/T]AATACTTGGGAACCA | 10152 |
| rs185095553 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382868 | AAGGTGAATATAATT[A/G]TATGCAAAACATCAA | 10152 |
| rs185104206 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203348862 | ATTTTTAATTAAAAA[A/T]TTTTTTAAAAAATAG | 10152 |
| rs185191840 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203367340 | TTTTTTTTTTTTAAA[A/G]CAAATTTCATACTTC | 10152 |
| rs185202496 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203401228 | ACTTATCTCCTCCTT[C/T]TCTCCCTTTCTCTTT | 10152 |
| rs185216205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203329659 | ATGGAAATGGAAGCA[A/G]TATGTTAAACTGTTT | 10152 |
| rs185224533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203346893 | GTAGACCTTAAACCT[A/G]GGCCCTTGTTTGTGC | 10152 |
| rs185255350 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376754 | TTTTTTTTTTTTTTA[C/T]TGTTATGGTCTATGG | 10152 |
| rs185310405 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | ABI2 | GRCh38.p7 | 2:203372865 | CTCATATCCCAGACG[A/G]GGCGGCGGGGCAGAG | 10152 |
| rs185318766 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203353492 | TTATGTATTTATTTA[A/T]TTTTTGAGACAGAAT | 10152 |
| rs185394627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203409889 | GCTGAGTGACCTGAA[A/G]ATCCAACCTCTTTCC | 10152 |
| rs185417716 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203415611 | GATAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 10152 |
| rs185427546 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374393 | TAATCCCAGCTACTC[G/T]GGAGGCTGAGGTAGG | 10152 |
| rs185440533 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203378824 | GTGAAGTGATTTTTC[A/C]AACTCTTTTGACTGC | 10152 |
| rs185452459 | snp | C/G/T | 0.0123082 | 0.0775209 | intron-variant | ABI2 | GRCh38.p7 | 2:203360013 | AACATGGTAAAACCC[C/G/T]GTGCCTGCTAAAAGT | 10152 |
| rs185454274 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203394562 | TACATTAGTAAAGAC[A/T]GAAATTGGTAGCTGG | 10152 |
| rs185456208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203421819 | AAGTTCAAAAATTAG[C/T]TGGGTGTGGTGGTGC | 10152 |
| rs185458652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ABI2 | GRCh38.p7 | 2:203376004 | GTTGTTAGATTACCT[C/T]TATTATTATAGATGT | 10152 |
| rs185466753 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203343580 | GACATCCTCCTGCTT[C/G]GGCCTCCCAAAGTGT | 10152 |
| rs185510225 | snp | A/C | | | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432501 | ACAGACAAACACTGA[A/C]GATGGGTGTTGACTA | 10152 |
| rs185525418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203391701 | TGGCATGCACCTGTA[A/G]TCCCAGCTACTTGCG | 10152 |
| rs185548764 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203393422 | GAGAAATTAATGTTT[C/G]CCATTTTATTGTTTA | 10152 |
| rs185555048 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203375530 | ATTTAACATTGTAAT[A/G]TCAAAGAATATCATG | 10152 |
| rs185560050 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | ABI2 | GRCh38.p7 | 2:203357476 | TGTTCTGAATCTCAC[A/G]AAGATTAACCTCTGA | 10152 |
| rs185561045 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203335307 | TCTGTCACTCAGGCT[G/T]GAGTGTAGTAGCACG | 10152 |
| rs185569880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203350009 | ACTATTTTCCATTTC[C/T]ACCATCAGTGTGTGA | 10152 |
| rs185583470 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419106 | TCCTAAATTAAAGAT[C/T]TTTTTTTTTTTTTTT | 10152 |
| rs185685195 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203399890 | TGTTATTTTTCAAAA[A/T]TTTTTTAAATGAATC | 10152 |
| rs185699402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203418237 | TATTTCCACGTTTGA[C/T]GAAAACTATATTAGT | 10152 |
| rs185775528 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203358017 | CTGTGATCCATCCGC[C/T]TCAGCCTCCTGAAGT | 10152 |
| rs185804755 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203359913 | CAGTTTTGGCCAGGT[A/T]TGGTGGTTCATGCCT | 10152 |
| rs185971613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203426915 | AGGCTCTTAAAAGGT[C/T]ATCAAAAGCACATTT | 10152 |
| rs185989629 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | ABI2 | GRCh38.p7 | 2:203388693 | CTTAAAAAATAATAA[A/T]AATAATAATAAATGT | 10152 |
| rs185999290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203373603 | ACTTATCCATGTTCA[A/G]GTTTGTCATGGCTTA | 10152 |
| rs186009812 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203408007 | CCTTATTAAAGGTTT[G/T]TCCTGGAGAAAAGTA | 10152 |
| rs186015919 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | ABI2 | GRCh38.p7 | 2:203354251 | GTTTCGCCATGTTGC[C/G]CAGGCTGGTCTCAAA | 10152 |
| rs186073867 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203431793 | TAAGAAAAAAGAAAA[A/G]CCAACAAAAAAAGCT | 10152 |
| rs186127100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203368727 | AGTTAAAAAAAAATT[A/G]GTGCGTTTTAATGAG | 10152 |
| rs186134130 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203334971 | GGCCTAGTTGTAGAC[G/T]TTTGATAGCTTATGG | 10152 |
| rs186166759 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | ABI2 | GRCh38.p7 | 2:203347235 | AAGTGAGTTGAGTAA[G/T]TCATTTTTGCTCTAT | 10152 |
| rs186170803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203380020 | CAGATTTGGCCTGTG[A/G]GCCATGGTTTACCAG | 10152 |
| rs186172980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203406821 | GGTGTGTGCCACCAC[A/G]CCTGGCTCTTTTTTT | 10152 |
| rs186195863 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203412653 | TTATGCTATTGGGGC[C/T]GACTCTTCTTTAGCT | 10152 |
| rs186248195 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203384477 | ATGCCTGGCTATTTT[C/T]TAACAAATTTTTTGT | 10152 |
| rs186248919 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203423711 | CAGGCGTGAGCCACC[A/G]CGCCCAGCCCAATCT | 10152 |
| rs186256444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203403716 | ACTTAGGTTTTCTGA[C/T]TCTAAGTTCCATGTT | 10152 |
| rs186282997 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327583 | CATGAATAGGAAAAA[A/G]GACAGCGAAGTTGAT | 10152 |
| rs186304289 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203388464 | AAGGTGGGTGGATCA[C/T]CTGAGGTCAGGAGTT | 10152 |
| rs186317489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203426598 | AAAAAATATATGTAG[C/G]GGACTCCCATCATTC | 10152 |
| rs186325865 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203364980 | TTTAAGCAATGCTCC[C/T]GCCTCAGCCTCCTAA | 10152 |
| rs186333774 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408833 | GCTACCTTCTCCTTT[C/T]TTTTTTTTTTTTTTT | 10152 |
| rs186337584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203330065 | AAAGCATTTTCATGT[C/G]TTAGTGTAAATTTTA | 10152 |
| rs186403996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203384875 | AGTCTTGCTCCGTCA[C/T]CCAGGCTGGAGTGCA | 10152 |
| rs186406901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203423062 | CTAGTTTAGGGTACT[G/T]AATTGTTAGGTGTGG | 10152 |
| rs186507590 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203399294 | ATTTTCTTAATGACT[A/G]ATGATATTGAACATT | 10152 |
| rs186510274 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203364325 | TCTTGAATTCCTGAC[C/T]TCAAATGATCTGCCC | 10152 |
| rs186515428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203379478 | TCCTGGGATCAAGCA[A/G]TCTGCCCACCTTGGC | 10152 |
| rs186554437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203397280 | AAATTATCATTAGAA[A/G]TATTTTCATTATAGG | 10152 |
| rs186560538 | snp | A/G | 0.117886 | 0.21224 | intron-variant | ABI2 | GRCh38.p7 | 2:203378207 | AAGCTCTGCCTCCTG[A/G]GTTCACGCCATTCTC | 10152 |
| rs186563750 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203414577 | AAAGCACACACTACA[C/G]TCAATTGTAAATGAA | 10152 |
| rs186611477 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ABI2 | GRCh38.p7 | 2:203403247 | TTACACTAAATAATC[A/G]GTTGTATCATGCATG | 10152 |
| rs186657229 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203369150 | TGAACTTGGTTTTCT[A/G]TAGAAGGAGGGAGGT | 10152 |
| rs186888430 | snp | A/C | 0.000162377 | 0.00900901 | intron-variant | ABI2 | GRCh38.p7 | 2:203342255 | TCATGGACCAAGTCC[A/C]GTTCTGTTACCATTT | 10152 |
| rs186943106 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203420810 | AATTCCTAGAAAGCT[G/T]CTCAGAGAACATGGC | 10152 |
| rs186949296 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203338620 | GAGCCGATTAAACCT[C/T]TTTTCTTTATAAATT | 10152 |
| rs186984867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203375661 | CTTTTACAACTGACA[A/G]TTGTCTACGAATTTA | 10152 |
| rs186985842 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | ABI2 | GRCh38.p7 | 2:203339567 | GCCTGGGCAACAGAG[C/G]AAGACTCCGTCTCAA | 10152 |
| rs187003241 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203343102 | TGGAGCCTCCAGCCA[A/C]AACTAAAAGCAAGCA | 10152 |
| rs187133702 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203373993 | GCAAAATTCCATCTC[C/T]CCAAAAAATGCAAAA | 10152 |
| rs187145048 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203355701 | GCAGGCATGGTGGCG[A/C]ACGCCTGTAATCCCA | 10152 |
| rs187152504 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346028 | CTACTAAAAATACAC[A/C]CGCGCACACACACAC | 10152 |
| rs187168917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203412034 | GCAGTCTTTGCGAGG[A/G]CCACATCACAATAAT | 10152 |
| rs187170691 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390369 | GGGTGCAGTGGCTCA[C/T]GCCTGTAATCCTAGC | 10152 |
| rs187198211 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | ABI2 | GRCh38.p7 | 2:203370769 | TTGAAGGAATGGAGG[G/T]TTCAGTCAGGTCAAA | 10152 |
| rs187198412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203413466 | GATGACTGCAAAACA[G/T]TATTATAGCAGCACT | 10152 |
| rs187201827 | snp | A/G | 0.00636936 | 0.0560724 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427861 | TTAACCATTTTTACA[A/G]TTATTTCAGATGGCT | 10152 |
| rs187202879 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203395640 | ACTCATGTTTTGGTG[A/G]CTCTTATTTCTTTAG | 10152 |
| rs187204706 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432204 | TATTTATATAAATAA[C/T]CTCTTTTTCTAAGGT | 10152 |
| rs187207038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203393946 | TCCTCTTTACGAGGA[A/T]ATTTTGGGAAAAGGC | 10152 |
| rs187224945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203424064 | TTATCAGTTCCCCAT[A/G]TGATTTTGATACTAT | 10152 |
| rs187227779 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203336730 | TCCTTCTGCCCTCCA[G/T]GTAAATGGTAGGCTT | 10152 |
| rs187232273 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203351211 | GATCTATATGTCTAT[C/G]TGTATGCCAGTACTT | 10152 |
| rs187238195 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203376620 | GTAACTCATTATGTT[G/T]CTATTTTGCCTTCTC | 10152 |
| rs187277576 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203389324 | TCACTTTAAAATATT[A/G]ACATTTCAAAGGTAT | 10152 |
| rs187300686 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203354913 | GGTAGTCAGTACCTC[C/T]GCTCACATGAGTGCA | 10152 |
| rs187367097 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430817 | CCGTGATGTCTGGAC[C/T]GTACCTGTGCTCCTT | 10152 |
| rs187410429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203409565 | CATCTTCATAGTTAC[A/G]AAGGGTAAAAATCTA | 10152 |
| rs187428915 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428846 | AGAATAGAGCTTTGC[C/T]AGGTAACTGCCCTGT | 10152 |
| rs187460278 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203373881 | TAAAAACTTTAGGCT[A/G]GGTGTGGTGGCTCAT | 10152 |
| rs187470631 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203408412 | AGGTGATGCGCCCCC[A/C/T]TCGGCCTTCCAAAGT | 10152 |
| rs187491839 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203347600 | CAGCTGAGAGAAGAG[A/G]TAACAAAATAGTTTC | 10152 |
| rs187501565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203339126 | GTGAAAATGTGCTCA[A/G]CATCACTAATCATTA | 10152 |
| rs187504736 | snp | A/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365620 | TTTTCTGGGGCTGTT[A/T]TCTTTTTTTTTTTTT | 10152 |
| rs187511382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203331780 | AAAATCTGTTTATCA[C/T]GTGTAATAAGTGTTT | 10152 |
| rs187541264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203350503 | TAGAGGTAGACACTA[C/T]CACATGTGGTTACTA | 10152 |
| rs187543312 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203349311 | TTTCCTGATTAATCA[A/C]AAAATAGTCATAACA | 10152 |
| rs187544218 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403645 | TTGGTGATCATTTTC[A/T]TATATCTTATAGGTA | 10152 |
| rs187547512 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326120 | CTGATCCACCTGTGT[C/G]GGCCTCCCAAAGTGC | 10152 |
| rs187548990 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203369385 | GGGTAAATGATGACA[A/G]CAAGCAAATAGCAAT | 10152 |
| rs187550612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203335771 | AACAGCTTTGTTTTG[A/G]ATCATTTACAACATG | 10152 |
| rs187612495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203391468 | TACAGTTTAACTCCA[A/C]CTATCCTTTTTAAGC | 10152 |
| rs187618238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203374317 | CCAGCCTGGCCAACA[C/T]AGTGAAACCCTGTCG | 10152 |
| rs187686906 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203370466 | GTTTTCTTTTCTTTT[G/T]TGTGTGTGTATTTTT | 10152 |
| rs187690038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203404031 | GTGCTGGGATTACAG[A/G]CGTGAGTCACCGTGC | 10152 |
| rs187722346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203336509 | GCCGAGGAGGCTGTA[C/T]GTGATAACAGTGCCT | 10152 |
| rs187740640 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203385032 | TAGAGACAGGGTTTC[A/G]CCATGTTGGCCAGGT | 10152 |
| rs187758460 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203424121 | AAGTGACTTTCTTCC[C/T]TATTGCCAAAACCAG | 10152 |
| rs187769578 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396167 | TAAATTTAGTGGCTG[G/T]ATTGGAATTTAGTAG | 10152 |
| rs187787323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203382263 | GTAGAATATTACATA[C/T]GGGGAGTTAAAGAGA | 10152 |
| rs187798229 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203419973 | AGCCTGGGCAACAAG[A/G]GCGAAACTCCATCTC | 10152 |
| rs187804679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203400772 | ATATAAAACCATTTT[A/G]TAATCATAGACAAGA | 10152 |
| rs187810751 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203394398 | CAACTCTTCTAAGAA[A/G]AGGTAGGGTCTGGGA | 10152 |
| rs187822044 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365928 | GCCACCGTGCCCGGC[A/C]GGGGCTGTTATCTTA | 10152 |
| rs187822414 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203332364 | GGGCACGGTGGCCCA[C/T]GCCTGTAATCCCAGC | 10152 |
| rs187828384 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203348045 | CAGGAGTTCGAGACC[A/T]TCTTGGCCAACGTGG | 10152 |
| rs187932754 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382796 | GTAGAAAAATTATTC[C/T]TTTTTCCAAATAGCT | 10152 |
| rs187938603 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203408658 | AGAGAAACAGTGACT[A/G]AAGTGGGAAATTTCC | 10152 |
| rs187958751 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203348757 | CCCATCACGTATGTA[C/T]AGCCGCCTCCATTAT | 10152 |
| rs187969896 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203385460 | TAATGAGCAGGGCTT[A/T]AGAGTTTTACAGCCA | 10152 |
| rs187980867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203424823 | CAGCTCTCTACCATT[A/G]TAAACAGTCTCTGGA | 10152 |
| rs187997585 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350861 | GTTTTTGTTGTGTGT[G/T]TTGTGTGTGTGTGTG | 10152 |
| rs188025509 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203386361 | GCATGATAGCTCACT[C/G]TATCCTTGGGCTCAA | 10152 |
| rs188051814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203360494 | GATAGAACAGTTGAG[A/G]CACTGTAAACATGAG | 10152 |
| rs188219364 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428332 | CTTTGGAAGAGAATA[A/G]TAGTTATTTTCAAGT | 10152 |
| rs188235189 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203401093 | ATCTGTTCCTCCAGT[C/G]CCCCCTCCTCTACTC | 10152 |
| rs188257149 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203362360 | TTCTTTTAATAACTT[A/C]TAATATAGCAGTATA | 10152 |
| rs188258242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332817 | TGAAAAGCCAACTTG[C/T]TGATATGTACGTTTT | 10152 |
| rs188265387 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326692 | CCAACATTTTCAATA[A/T]CCTTTAATTTAGGTT | 10152 |
| rs188272412 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203404144 | TTTGGAGGGGAAGGC[A/G]GATGAAAAGATGTGA | 10152 |
| rs188274970 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203345413 | CACGGCGAGGGTCCA[C/T]GGGTTCATTCTTGAA | 10152 |
| rs188319422 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355853 | AAAAAAAAAAAAAAC[A/C]CCCCACCAAGAAACC | 10152 |
| rs188326505 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343932 | CCCAGGAGTTTGAGA[C/G]TAGCCTTGGCAAAAA | 10152 |
| rs188476048 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203393033 | TCTCAATTATCAAAT[A/T]ATTTTTACTTGGATG | 10152 |
| rs188483289 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203400605 | TTCTCAGTTGATAGT[A/G]GATTATGTTTAAGCT | 10152 |
| rs188483828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203374916 | AATGACAATGCATGG[A/G]TAATCCTAAAACAAA | 10152 |
| rs188494324 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203410532 | AGGTGATTGAGGTGC[A/G]GGGAAATACACCTTG | 10152 |
| rs188500249 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203357720 | ATTTTAGGATTCTTT[G/T]GTCTCAAGTGACAGA | 10152 |
| rs188505776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365242 | GAATTATGATGATTA[C/T]GTTCAAGATGCTTTG | 10152 |
| rs188514057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203340128 | GCCAGGCACAGAAAG[A/G]CAAATACCGTATGAT | 10152 |
| rs188516920 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | ABI2 | GRCh38.p7 | 2:203341443 | TTTTGGGCCAGGCTC[A/G]GTGGCTCACTCCTAT | 10152 |
| rs188547263 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353826 | AACTCTTATCTGTTT[A/C]TTCTGGTACTTGTCT | 10152 |
| rs188561113 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203373432 | AGTCCAGCTTCTGCT[C/T]GGCATCAGAGGGAGA | 10152 |
| rs188561446 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | ABI2 | GRCh38.p7 | 2:203415345 | TTAATTCACCGGGCG[C/T]GGTGGCTCACGCCTG | 10152 |
| rs188565174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203398196 | CTATATGACTTTTAA[A/G]GAAAAGCTTTCTGCA | 10152 |
| rs188586856 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392339 | CAACAACAACAACAA[A/C]AACAAAACAACCACA | 10152 |
| rs188605889 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345937 | GTAATCCCAGCACTT[C/T]AGGAGGCCGAGGCGG | 10152 |
| rs188722498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203388481 | TGAGGTCAGGAGTTC[A/G]AGACTAGCCTGGCCA | 10152 |
| rs188736983 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203406883 | GGCCAGGCTGATCTC[C/T]GACTCCTGACCTCAA | 10152 |
| rs188744775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203413519 | CCCTAATTTGACCAC[C/T]CTATCACAGTTGATT | 10152 |
| rs188764400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203376924 | AGTCTCAATTTTTCA[A/G]ACAAGAAATATGTGC | 10152 |
| rs188764824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203344102 | GTGCTTGAAATGTCA[A/G]ATGTTACTATTCATT | 10152 |
| rs188778100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203356213 | TTTTTTTTGAGACAA[C/G]GTCTTGCTCTGTCAC | 10152 |
| rs188780280 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430425 | AAATGAATAGTTGTC[C/T]TTTCTTGTCATATTA | 10152 |
| rs188781925 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ABI2 | GRCh38.p7 | 2:203419230 | TTCTTCTGCCTCAGC[C/T]TCCCGAGTAGCTGGG | 10152 |
| rs188790067 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429834 | AACAGAGTTAGTGGC[A/G]GTCAGCAGGAATGCA | 10152 |
| rs188797733 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203381351 | GCACAATCATAGCTC[A/G]CTCCAACCTTGTACT | 10152 |
| rs188810576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203411199 | GTAGTTTCCCTCCTT[C/T]ATGTGTTTATTTTAT | 10152 |
| rs188813971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203393593 | TTATGTAAGGAGACT[C/T]TGAAGGGTAGTAGAG | 10152 |
| rs188954729 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203367551 | CTTGTAAAAGTTTTT[A/T]AAAAAATGTTAATCT | 10152 |
| rs189009189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203396118 | CATATTAGTAACAAA[A/G]GATTGGGCAGATATA | 10152 |
| rs189028861 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203405489 | TAGGAGATGGAAGTT[G/T]CAGTGAGCCGAGATT | 10152 |
| rs189033184 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203361009 | AAGCGTGGCCTCAGC[A/T]TGAGCACTAGCTCCA | 10152 |
| rs189062784 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203337941 | AGGCTGAGTTGGGAG[A/G]ATCGCTTGAACCCAG | 10152 |
| rs189064892 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360208 | AAAAAAAAAAAAAAA[A/G]AAGCAGTTGTACCCT | 10152 |
| rs189067227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203372244 | GAGCACAGGGTTGGG[A/G]CTAAGGTCACCGATC | 10152 |
| rs189171065 | snp | A/G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203333449 | TTATATTTATAGGTC[A/G/T]AGTTCTGTATGTTCT | 10152 |
| rs189179640 | snp | A/T | 0.00479326 | 0.0487202 | intron-variant | ABI2 | GRCh38.p7 | 2:203348868 | AATTAAAAATTTTTT[A/T]AAAAAATAGTACAAA | 10152 |
| rs189235203 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ABI2 | GRCh38.p7 | 2:203359162 | GGATGGAGAGAAGGC[A/G]TTTTGTTTTCCTTTT | 10152 |
| rs189317773 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203387957 | CCTCAAAATAGTTTT[C/T]TTAGGATCAATCATG | 10152 |
| rs189320276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203426493 | GCAATGAAAATCACA[G/T]GAGGGCTTATAGGTA | 10152 |
| rs189352673 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203352934 | ACCATTATGTTAAAA[C/G]TCTCTATAGTATTCC | 10152 |
| rs189402393 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203404583 | TTTTGTTTTGAGACA[A/G]AGTCTTGCTCTGTCA | 10152 |
| rs189414438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203425832 | TTCAAGACCAGCTTG[A/G]CCAACATGGCAAAAC | 10152 |
| rs189425441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203346402 | GGAATATATGGGACT[A/G]ATAGGCATGTGTATC | 10152 |
| rs189432820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203352067 | TTATAGAAGAGCAAA[A/G]GCAGAAGACACACAC | 10152 |
| rs189433193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203387500 | TTGAGCTGTGGCCAT[A/G]CATTAACCTTCATCA | 10152 |
| rs189439296 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203327925 | AGAGTGGAGGCTGTG[C/T]CCTCCTTCGGCCTCC | 10152 |
| rs189441168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203371264 | GTAACTGAACTGTTT[C/G]CCAAATTACTCTGAA | 10152 |
| rs189468761 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203368016 | CTCCAAAAAAAAATA[A/G]AAAAAAGTAGCCAGG | 10152 |
| rs189482371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203348988 | TCTAGGCTGGAGTGC[A/G]ATGGTGTGATCTCGG | 10152 |
| rs189482651 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203383586 | ATGCTTGTTTTCTCT[A/G]AGCCCCAGTATGATT | 10152 |
| rs189495582 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203421948 | TCCAGCCTGGCAACA[C/G]AGTGAGACTCTGTCT | 10152 |
| rs189609073 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363533 | ACCTCCCCACTTTCC[C/T]CCTACCCTTCCCATC | 10152 |
| rs189612244 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327516 | GTAACAGCCCTGTGA[A/G]GAAGGCAATTACTAC | 10152 |
| rs189630027 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203421705 | GGCATGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 10152 |
| rs189638187 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402349 | CCTAATTAGTAAACT[A/G]TTTAGACATAACTTT | 10152 |
| rs189681030 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ABI2 | GRCh38.p7 | 2:203417307 | ATATTGTTCCTATTG[A/G]ACATGCTTTTTATGA | 10152 |
| rs189685671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203399579 | GGAGTGCAATGGCAG[C/G]ATCTCAGCTCACTGC | 10152 |
| rs189702499 | snp | A/G | | | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432489 | TTTTTTAATTCAACA[A/G]ACAAACACTGAAGAT | 10152 |
| rs189721614 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | ABI2 | GRCh38.p7 | 2:203364401 | GGCTGGCAGGGAAAG[A/C]TACTTGTACATGGGT | 10152 |
| rs189721925 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203379894 | GGAAAAGCAAATTTG[A/G]ATTTTATATAATTTT | 10152 |
| rs189731365 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203329839 | CCTCCTAGGTTTGAG[C/G]AATTCTCATGCTTCA | 10152 |
| rs189731515 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330207 | TTGTATTTGAGAATG[A/G]CCCGAACCACTGTAT | 10152 |
| rs189735212 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203346940 | CTATAGTGCATTTTA[A/T]AATTTATTCAGCCAT | 10152 |
| rs189753033 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430144 | ATGTAATATTTCATA[C/G]ATTGCATGCTATTAA | 10152 |
| rs189786837 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203426677 | GCATAGGCTCCAGAG[A/T]GAGTGAGAAAGGAGA | 10152 |
| rs189847509 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203375580 | CTGATACTGTGAATT[C/T]GATGTAGGAAAAATA | 10152 |
| rs189850012 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203378334 | GCCAGGATGGTCTCG[A/C/G]TCTCCGGACTTTGTG | 10152 |
| rs189869810 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345468 | GAAGGAACCAATTCC[G/T]GACACAATCTTAGCT | 10152 |
| rs189879364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203401551 | AGTTGACATTAGCTG[G/T]GGAAGAACTCTCAAG | 10152 |
| rs189888337 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203342830 | TTGCCTGGCTTGATA[C/T]AATGTCTATACACAC | 10152 |
| rs189925082 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203413000 | CACAAATCCGGTTTA[A/C]TCACAATGATTAATG | 10152 |
| rs189946900 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203431973 | TAGCTCCCAGAGGGA[C/G]AGTTGGTGGTATTAT | 10152 |
| rs190095392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203421420 | GTCTTTCTTAAATTT[C/T]GTTGAAAGCAAAGGA | 10152 |
| rs190121700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203338104 | GGAACAGAATGGAGC[C/T]CGGAAATGTAGCCAC | 10152 |
| rs190127347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203358579 | GTGTCTCGTTTCTGC[C/T]TCTTTATGCATGTTG | 10152 |
| rs190140310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203383026 | GCCTGCCTAAAATAC[A/G]AGGTTACTACAATTA | 10152 |
| rs190160113 | snp | A/G | 4.99355e-05 | 0.00499652 | intron-variant | ABI2 | GRCh38.p7 | 2:203394876 | TCAGTGCAAAATGTG[A/G]TGGTCATAGTACCAT | 10152 |
| rs190166019 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203360126 | GGAGGTGGAGGTTGC[A/G]GGGAGCTAAGATTGC | 10152 |
| rs190168378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203376203 | AAGTTTTGCCCCCAA[A/G]GGGACATTTGGCAAT | 10152 |
| rs190176798 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425247 | TTCTTTTTTGAGACA[A/G]GAGTCTCACTCTGTC | 10152 |
| rs190182610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203343737 | TGCATATAGGCTCTT[C/G]TGACAAAAATATGTT | 10152 |
| rs190297664 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203416356 | CCCAGGCTGGAGTGG[C/T]GTGATCTCGACTCAC | 10152 |
| rs190311818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203378871 | TTTTTTTTACGTTGT[A/G]TTCAGCACATAATTC | 10152 |
| rs190333968 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384920 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAG | 10152 |
| rs190364148 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203335502 | ACCTGGGCTCAAGCA[A/G]TTCTCCTGCCTTGGC | 10152 |
| rs190368787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203369249 | TGAAGCATTAGCAAA[A/G]GATGTTAAAAAGAAA | 10152 |
| rs190390934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203392544 | CTGCTTAGAGAGAGA[A/G]AAAATCTAGTGGATC | 10152 |
| rs190393684 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329315 | TGTTTCTTAGAGAGA[A/G]TTGGGAAGATGAACC | 10152 |
| rs190414252 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203334465 | CAGTTTCAGGGTGTG[A/T]AAGGTAATCTTTTGG | 10152 |
| rs190436137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203357602 | TTCCAGTTTGTCTAT[A/G]CATATGTTGTCTAGG | 10152 |
| rs190446606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203413473 | GCAAAACATTATTAT[A/G]GCAGCACTACCTATA | 10152 |
| rs190458826 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432235 | GGTATCTTGAGTTTA[C/T]GTGTTAGGGATAATC | 10152 |
| rs190577872 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203363859 | AACCTCTGCCTCCTG[A/G]GTTCAAGCAATTCTC | 10152 |
| rs190578203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203398799 | AACATAAATGAAAGC[A/G]TATAGTATGTAGCTT | 10152 |
| rs190582792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203382013 | GAGAAACTTCTGTTC[A/G]TGACACATTCTGCTT | 10152 |
| rs190615175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203373973 | AGACCAGCCTAGCCA[A/G]CATGGCAAAATTCCA | 10152 |
| rs190619225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203337434 | AATAAATGTAATCAA[A/G]GAGGTGAAAGGTCTG | 10152 |
| rs190625609 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408463 | CCACCGTGCCTGGCT[A/G]CTGGTGTACTTCTTA | 10152 |
| rs190633512 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ABI2 | GRCh38.p7 | 2:203339233 | TGGCAAGCAGGTGGA[A/G]AAAAGAGAATCCTTG | 10152 |
| rs190658598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203409998 | TTCTCTTTGGGTATC[C/T]TTTCCTAGCCATATG | 10152 |
| rs190674666 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203340591 | TCGAACTCCTGGGCT[A/C/G]TACCCATCCACCCAC | 10152 |
| rs190678718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203374486 | CCTGGGTGGCAAAGC[C/G]AGACTCTGTCTCAAA | 10152 |
| rs190797155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203388814 | ATTTAAACAAAAACA[C/T]CTTGCATACCAAAAC | 10152 |
| rs190799382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365527 | GAAGCCCTTGAGGTG[C/T]TGGTATTTTTTTTAT | 10152 |
| rs190803495 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203373701 | TCCCAAGGGCTGAGT[A/C]GGACTTACTGGGCCA | 10152 |
| rs190807240 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203408273 | GTTCAAGCGATTCTC[C/T]TGGTTCAGCCTCCCG | 10152 |
| rs190809119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332176 | CTAGAAAATGGGATA[C/G]TCAATATTTTTTCTA | 10152 |
| rs190813421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203347837 | CAGTTGTTTGAGGAA[C/T]ATTTACATATAGGAT | 10152 |
| rs190838780 | snp | A/T | 0.00636936 | 0.0560724 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427907 | ACTGTAAATTCTGCA[A/T]TCTCTCAGCACTTGA | 10152 |
| rs190875807 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403651 | ATCATTTTCTTATAT[A/C]TTATAGGTAAGGAAA | 10152 |
| rs190878530 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203412618 | TCACATATAATTAGG[G/T]TGATTTCATATGTTT | 10152 |
| rs190880866 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203389403 | GGCTATTCATTTGAA[G/T]AATTTGTTTCTTGAG | 10152 |
| rs190896553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203355024 | TTCTCCAATCTGGAT[C/T]GTCTGGATTGTTAAC | 10152 |
| rs191020218 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423712 | AGGCGTGAGCCACCG[C/T]GCCCAGCCCAATCTG | 10152 |
| rs191039143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203343278 | TTGAAGCAGGAGAAT[C/T]GCATGAACTCGGGAA | 10152 |
| rs191040228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203385265 | ACCTCCTGAGTAGCT[A/G]GGACTACAGGCGCCC | 10152 |
| rs191048128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203369823 | GATAAAGGATCAAGT[C/G]TGAGAAATAGGCTGA | 10152 |
| rs191058937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203403939 | GTATTTTATTGTAGA[A/G]ACAGGGTTTCACTAT | 10152 |
| rs191086646 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203357669 | TGAGAACTGAAGCCA[G/T]TATATGTTAAATGAT | 10152 |
| rs191090792 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203382351 | TTTGTCATGCAACTT[G/T]GTGGTGTGTCTTCAT | 10152 |
| rs191102662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203420304 | TATTCTTTTGTTCTT[C/T]TGGCTCAGTGATACA | 10152 |
| rs191104824 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203340781 | CATCATGTTGTACAC[C/T]TTAAATATATACAGT | 10152 |
| rs191111156 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203400864 | GTCTCATATTAAGGT[A/G]GAATAAAGATGGTAA | 10152 |
| rs191111337 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203348229 | CTGGGGGACAGAGCG[A/T]AACTTTGTCTCAAAA | 10152 |
| rs191119235 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203394400 | ACTCTTCTAAGAAGA[A/G]GTAGGGTCTGGGAAA | 10152 |
| rs191120588 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203384619 | CTGGCCAGTACTCTT[A/T]TAGTAGTAAAAAGAA | 10152 |
| rs191124810 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203349729 | TTTTTTTTTTTTTAC[A/G/T]GCTGAATAATATTCT | 10152 |
| rs191127287 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366081 | TCTTAGACATCATTA[A/G]TGGATAGAAATCTTA | 10152 |
| rs191135510 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203335883 | AAGGTTTATGAATTA[A/C]AATAAACTTACATAG | 10152 |
| rs191172229 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331808 | TTTTTGCTCAGTGTT[C/T]TTTTTTTTTTTTTTT | 10152 |
| rs191188366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203330759 | AATAAAAAATAAACA[C/G]ATTTCTCTCTCTTTT | 10152 |
| rs191328414 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402985 | TTTGAATATTTTAGT[G/T]GTTATTTGCTTTTTA | 10152 |
| rs191338980 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203378236 | TCCTGCCTCAGCCCC[A/C]CAAGTAGCTGGGACT | 10152 |
| rs191342198 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203399903 | AATTTTTTTAAATGA[A/C]TCGTGCTTTGATGGC | 10152 |
| rs191343126 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203414627 | TCATGACTTTTGCCT[A/G]CTGCCCTTTTCTCAA | 10152 |
| rs191353066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203397604 | CTGCTATAAAATGTA[C/T]GTGTTTGGACATATA | 10152 |
| rs191358040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365025 | AGACATGAACTGCCA[C/T]GCCTGGCCAGCGTTA | 10152 |
| rs191361843 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384278 | CTGTTCCATACTCTT[G/T]TTTTTGTTTTTGTTT | 10152 |
| rs191362203 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203362900 | GCAGTGACCTGATCT[C/G]AGCTCACTGCAGCCT | 10152 |
| rs191370475 | snp | C/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203368755 | GAGTGTAAGGTAAAT[C/T]TCAGTTGGGAAAGGC | 10152 |
| rs191378674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345420 | AGGGTCCACGGGTTC[A/G]TTCTTGAAGTCAGCC | 10152 |
| rs191382650 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203335093 | TTTCCTTCCAGATAC[A/G]AAGCTCCTAGAAGAT | 10152 |
| rs191419383 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203389633 | TATAATTTGACTACT[C/T]TAGCCATATTATTTT | 10152 |
| rs191427814 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403317 | TTGTTTACTCCCCAG[A/G]GAGGGCAAGAACAAA | 10152 |
| rs191591864 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203418308 | GCTTAAACAAAACAT[C/G]CATTATCTCCCAGTT | 10152 |
| rs191614669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203347419 | GTTCTGAAGATACTT[C/T]TAGCCTTGTAATCCC | 10152 |
| rs191616875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203380994 | ACTTAATGATTCAGA[A/G]CTTTAGCTGAGTATT | 10152 |
| rs191639624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203395854 | GATTTAATTATGGTG[A/G]GCTTTCTTCGTAATC | 10152 |
| rs191669261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203423397 | CTCCTCTTTGTTTCA[A/G]TTTACTATTTTAGGA | 10152 |
| rs191679745 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203419801 | GGAGACCAGCCTGAC[C/T]AACATGGAGAAACCC | 10152 |
| rs191823012 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354317 | CCAAAGTGCTGGGAT[C/T]ACAGGTGTGAGCCAC | 10152 |
| rs191890691 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203409235 | AGTGGGAAGCAGACA[A/C/G]GCAAGTCAAGGATTT | 10152 |
| rs191896687 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428360 | AGTCTCCTGACAGTC[A/T]CTGGGAGTACAAGGT | 10152 |
| rs191900747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203374067 | AGGAGGCTGAGGCGG[C/G]AGTATCACTTGAGCC | 10152 |
| rs191907822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203354635 | CTTTATTACAGCAAC[A/G]ATAATAGCCAGCATA | 10152 |
| rs191918403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203355891 | TGCTGAAAATCTTCA[A/G]CTTTCACTAGATGGT | 10152 |
| rs191920565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203390618 | GCCTGGGTAACAAAG[C/T]GAGACTCTGTCTCAG | 10152 |
| rs191934561 | snp | A/G | 0.0944967 | 0.195752 | intron-variant | ABI2 | GRCh38.p7 | 2:203339592 | TCTCAAAAAAAAAAA[A/G]AAAAAGAAAAAGAAA | 10152 |
| rs191954799 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400673 | AAATGTTATAACAAG[C/T]CTTGAGTGCTCTTAT | 10152 |
| rs191955425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203370841 | AGTTGTAAGGGTAGA[A/G]TTGTTTAGGACTAGT | 10152 |
| rs191966547 | snp | A/G | 0.00084674 | 0.0205585 | intron-variant | ABI2 | GRCh38.p7 | 2:203351683 | TGGGACTACAGGTGC[A/G]TGCTACTGTGCCCGG | 10152 |
| rs191975801 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203386503 | CTGGAATCCTGTTCT[G/T]TTAAAACTTAACAAG | 10152 |
| rs191985690 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203336883 | CAAACTCTTTTCCAA[A/C]AACGATGGTACCGTT | 10152 |
| rs192123859 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203359221 | ATCTGCTATGACAGA[G/T]TAAGGTTTTTTTAAA | 10152 |
| rs192130710 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203335938 | TTTTCCTTGTACCCT[C/G]TGTAGTCAGTCCTGT | 10152 |
| rs192131919 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203394058 | TCATTCCCTTCCCCC[C/G/T]ACCTTTGTAAATGTT | 10152 |
| rs192139252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203404373 | CTGCCTTAATTGATA[C/T]ATACTTCCCTTCTAT | 10152 |
| rs192151259 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203374567 | GAAGGTTATCAATAC[A/G]TAATTATGCATAGAA | 10152 |
| rs192210946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203409674 | TAAAGTTCTCTCCTT[C/T]TCTAGAAACTGCTTT | 10152 |
| rs192233991 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429352 | TCTTCGTGTACTGGT[C/T]TATAATTAGAAAAAC | 10152 |
| rs192236174 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | ABI2 | GRCh38.p7 | 2:203339095 | CAAAGAAGACACACA[A/G]GCGTCCAACAGGTAT | 10152 |
| rs192312663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203410134 | TGGCAGGTTCCCTTC[C/T]TCAAGTCCCTGCTGA | 10152 |
| rs192380121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203424123 | GTGACTTTCTTCCCT[A/G]TTGCCAAAACCAGTT | 10152 |
| rs192405150 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327012 | ACGGGTTTTCACTGT[C/G]TTAGCCAGGATGGTC | 10152 |
| rs192418294 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203386247 | ACATACAGACACAAC[A/C]TACACACACTTCCCC | 10152 |
| rs192465140 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203412308 | CCAGCACTTGGAAAA[C/G]CATCTGACACATAGC | 10152 |
| rs192487763 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203375776 | AAGCTATAAAAAAAT[A/T]GAAGCAGATGATTGC | 10152 |
| rs192489878 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203350662 | CTCCTGTCTCAGCCT[C/T]CCAAGTAGCAGGGAT | 10152 |
| rs192561934 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203332378 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCG | 10152 |
| rs192597116 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203404675 | GCGATTCTCCTGCCT[A/C]AGCCTCCCAAGTAGC | 10152 |
| rs192613007 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425987 | GATAGTGCCACTGCA[C/T]TCCAGCCTGGGCGAT | 10152 |
| rs192624257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203387521 | ACCTTCATCACCTAA[A/G]TGAAATATTTCTTCT | 10152 |
| rs192635210 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203350905 | GTGCGCGCGCGCATA[A/C]TTTTAGGTGTTATAT | 10152 |
| rs192653386 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203361015 | GGCCTCAGCATGAGC[A/C/G]CTAGCTCCACAGGTG | 10152 |
| rs192672131 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203344984 | TCTGTAAAATGGACC[A/C]ATCAGTAGGACGTGG | 10152 |
| rs192685180 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326525 | TCATTTAAATAACTA[C/T]TCATTTCCATCACTC | 10152 |
| rs192706302 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392811 | CAAGTTTTGAAGATT[G/T]GCTCATATACCAATG | 10152 |
| rs192710243 | snp | A/C | 0.00835141 | 0.0640778 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429870 | TCTTTTGGACCCCTA[A/C]GGGATGGGGGCAGTG | 10152 |
| rs192756973 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203370704 | AGACCAGATTTTTGT[G/T]CAACTTGGGCAAAAA | 10152 |
| rs192762119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203404032 | TGCTGGGATTACAGG[C/T]GTGAGTCACCGTGCC | 10152 |
| rs192771979 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203367335 | CGCCTTTTTTTTTTT[C/T]TAAAACAAATTTCAT | 10152 |
| rs192775244 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203401095 | CTGTTCCTCCAGTCC[C/T]CCCTCCTCTACTCTC | 10152 |
| rs192791418 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203332888 | AGTTCACATAGATGC[A/C]TAGTAAAATCTTATT | 10152 |
| rs192822829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203343958 | AAAAAGACGAGAGAG[A/G]CCCCGTCTCTACAAA | 10152 |
| rs192825025 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203376653 | CCTGGAGGCTTAGTG[C/T]CAATTTTTTTGCTCT | 10152 |
| rs192874998 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203336537 | CCTCATCACCTCCTA[G/T]TTCCCATGAGATGAG | 10152 |
| rs192915639 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203421501 | CTTTTAATATGAGCA[C/G]CATTATTTTGAATGG | 10152 |
| rs192933075 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203391533 | AATATTGAGCTTCAG[G/T]CCAGGTGTGTTGGCT | 10152 |
| rs192950371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203356399 | TTTGAGACAGAGTCT[C/T]GCTCTGTTGCCCAGG | 10152 |
| rs192968082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203420963 | CCAGTGCATGAGGGT[A/G]GGGGTGGGTTGTAGG | 10152 |
| rs192975061 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382803 | AATTATTCTTTTTTC[C/G]AAATAGCTGTATAAA | 10152 |
| rs192990666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203348762 | CACGTATGTACAGCC[A/G]CCTCCATTATTAATA | 10152 |
| rs193034971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203360841 | TCAACACAAGGTTAA[A/G]TGGGACTCTTGTTTA | 10152 |
| rs193122680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203425322 | ATTCTCTTGCCTCAG[A/C]CTCCCAAGTAGCTGG | 10152 |
| rs193133361 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203396463 | TTAGTGTATTATGTT[A/C]GTTTTGTATACTATA | 10152 |
| rs193137799 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203371288 | CTCTGAATTGTAATC[C/G/T]GAGGATGGGAATTCC | 10152 |
| rs193178456 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203374373 | GGTGTGGTAGTGGGC[A/T]CCTGTAATCCCAGCT | 10152 |
| rs193231552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203340158 | TTTCACTTATATGAG[C/G]AATCTAAAAAGATGA | 10152 |
| rs193290485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203413522 | TAATTTGACCACCCT[A/G]TCACAGTTGATTGCC | 10152 |
| rs193293710 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377110 | ATTGTTTGAGGTCAG[A/G]AGTTCAAGACCATCC | 10152 |
| rs199497527 | snp | C/T | 0.000347584 | 0.0131784 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203391072 | GAACATGAAGATGGG[C/T]GGGCTGCCGCGTACA | 10152 |
| rs199526080 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354296 | TGATCTTCTCGCCTC[A/C]GCCTCCCAAAGTGCT | 10152 |
| rs199558891 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344361 | TTTAAATTTTTTTTT[-/T]CCTTTTTTTTTGAGA | 10152 |
| rs199618516 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203373630 | CTTAGAAAAAAAGAT[A/T]AAGCAAGGTCAAAAG | 10152 |
| rs199624030 | snp | C/T | 0.000633217 | 0.0177822 | intron-variant | ABI2 | GRCh38.p7 | 2:203395801 | ACATTCATGGTGCCT[C/T]GTCTTCACTTTTCCT | 10152 |
| rs199626636 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203395454 | ATATATATATACACA[C/T]ACACACACACACACA | 10152 |
| rs199664704 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427185 | CTCCTAGTTGTGGCA[A/G]TTTATGACTATACAA | 10152 |
| rs199677417 | in-del | -/AAGTT | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428996 | TGGTGTCGGATGCAG[-/AAGTT]AATATTCCACTTAAT | 10152 |
| rs199695236 | in-del | -/AGG | 0.0228947 | 0.104514 | intron-variant | ABI2 | GRCh38.p7 | 2:203374406 | TCTGGAGGCTGAGGT[-/AGG]AGAATTGCTTGAACC | 10152 |
| rs199774577 | snp | C/T | 0.000181493 | 0.00952436 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416951 | TGTGGAAGAACCAGT[C/T]TTTGATGAGTCTCCC | 10152 |
| rs199806802 | snp | G/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366644 | ATAATGGCTTTAGGG[G/T]TTTATTTGCATCTGT | 10152 |
| rs199823599 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203405722 | TTTTTTTTGGGGGGG[-/G]TAATTGGAGTCTTGC | 10152 |
| rs199840649 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378905 | TATATATTTATATAT[A/G]TAATAAACAGACTTT | 10152 |
| rs199841247 | snp | A/G | 0.00199806 | 0.0315443 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427339 | TTGAGTCTATCATGC[A/G]TTATTCTGAGTAAAG | 10152 |
| rs199851714 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344372 | TAAATTTTTTTTTCC[-/T]TTTTTTTTTGAGACA | 10152 |
| rs199864348 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203352580 | TAAAGAAAAAAAAAA[-/T]AGAGAAAAGAGAAAA | 10152 |
| rs199948488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203391016 | TTTATTTCACTGCAT[A/G]CAAGTTGAGTTTTCC | 10152 |
| rs199992443 | snp | A/G | 7.03631e-05 | 0.00593099 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203391061 | GTGAGTACCCAGAAC[A/G]TGAAGATGGGTGGGC | 10152 |
| rs200166293 | in-del | -/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203333946 | CTTTTTTCTTTCTTT[-/C]TTTTTTTTTTTTGAG | 10152 |
| rs200198424 | in-del | -/TG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350863 | TTTTGTTGTGTGTTT[-/TG]TGTGTGTGTGTGTGT | 10152 |
| rs200220880 | snp | A/T | 0.000510906 | 0.0159747 | intron-variant, missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203411308 | GCTCCTCCTCCTCCC[A/T]CCATCCTACAGGTAA | 10152 |
| rs200342172 | in-del | -/TTTTG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384286 | TACTCTTGTTTTTGT[-/TTTTG]TTTTTTTTTTTTTTT | 10152 |
| rs200363290 | in-del | -/T | 0.0146672 | 0.084371 | intron-variant | ABI2 | GRCh38.p7 | 2:203343449 | GCATTATATTCCAGG[-/T]TTTTTTTTTCCTTCT | 10152 |
| rs200380182 | in-del | -/C | 0.0178098 | 0.0926698 | intron-variant | ABI2 | GRCh38.p7 | 2:203370376 | TACAGGCATGAGCCA[-/C]CATGCCCAGCAAAGA | 10152 |
| rs200392800 | in-del | -/AA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203426786 | GTAAAGAAAAGCTTT[-/AA]AAAAAAAAAAAAAAA | 10152 |
| rs200393851 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350864 | TTTGTTGTGTGTTTT[G/T]TGTGTGTGTGTGTGT | 10152 |
| rs200399814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203390183 | AGATACTAACTAAAT[C/T]TGACTTATAAGGCTG | 10152 |
| rs200410889 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203391883 | GAGTTGGGCTCTAGA[-/T]TTGACTTTTGGCAAA | 10152 |
| rs200518146 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329314 | CTGTTTCTTAGAGAG[-/A]ATTGGGAAGATGAAC | 10152 |
| rs200523699 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376725 | TCTATTTACTGTATT[A/G]GTCTTCCCTTTTTTT | 10152 |
| rs200585534 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350895 | GTGTGTGTGTGTGCG[C/T]GCGCGCATACTTTTA | 10152 |
| rs200611334 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422265 | ATTGCACCACTGCCT[-/G]GGGGACAGTAAGACT | 10152 |
| rs200705875 | in-del | -/AGGTGGTTAGC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402826 | CAAATAGTGCATGGT[-/AGGTGGTTAGC]ACCATTTGTTGAATG | 10152 |
| rs200768274 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422426 | CGGTGACTATGATGA[C/T]GGAGAGAAGTCGAGT | 10152 |
| rs200782263 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368983 | TGCCATGCTTGGCTG[-/A]ATTTTTTTTTTTTTT | 10152 |
| rs200840835 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368004 | TGAAACCCTGTCTCC[-/A]AAAAAAAAATAAAAA | 10152 |
| rs200842272 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203349110 | GTAATTTTTTTTTTT[-/T]GTATTTTTTTTTTTA | 10152 |
| rs200847223 | snp | C/T | 0.000363155 | 0.0134702 | intron-variant | ABI2 | GRCh38.p7 | 2:203427147 | AATATTACTGTCTTT[C/T]ACATCCTGTTTTGTT | 10152 |
| rs200958880 | snp | A/G | 6.91551e-05 | 0.00587986 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203391081 | GATGGGTGGGCTGCC[A/G]CGTACAACACCTCCA | 10152 |
| rs200999049 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406671 | GCAGGAGCAGGAAGA[-/T]TTTTTTTTTCTCCCC | 10152 |
| rs201003347 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400779 | ACCATTTTATAATCA[C/T]AGACAAGATGAAAAA | 10152 |
| rs201078076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203395792 | CCAGGTAAAACATTC[A/G]TGGTGCCTCGTCTTC | 10152 |
| rs201078257 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408179 | CTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTTGC | 10152 |
| rs201137565 | snp | A/G | 0.00310378 | 0.0392716 | intron-variant | ABI2 | GRCh38.p7 | 2:203367088 | TATGAGGAACCCTTA[A/G]TAATAAACACAGGCT | 10152 |
| rs201209202 | in-del | -/TTTTTTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331349 | ATGGTCAATTTAGCC[-/TTTTTTTT]TTTTTTTTTTTTCTG | 10152 |
| rs201288870 | in-del | -/TTTA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342553 | TCTCCCTCAAAACCT[-/TTTA]TTTATTTATTTATTT | 10152 |
| rs201293538 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203388748 | GTTTATTTTATGCTA[-/T]TTTTTTTGGTGGGGG | 10152 |
| rs201318028 | snp | A/G | 0.0029954 | 0.038584 | intron-variant | ABI2 | GRCh38.p7 | 2:203382255 | GTTCTTATGTAGAAT[A/G]TTACATATGGGGAGT | 10152 |
| rs201338926 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203340869 | AAACAATATTGCCTG[G/T]AAGCCACAAACAATC | 10152 |
| rs201368474 | snp | G/T | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326106 | ACTCCTGACCTCAGC[G/T]GATCCACCTGTGTCG | 10152 |
| rs201411546 | in-del | -/GGGAGAGGGAGC | 0.0850919 | 0.187897 | intron-variant | ABI2 | GRCh38.p7 | 2:203373497 | GTGGGGAGAGGGAGA[-/GGGAGAGGGAGC]GGGAGAGGGAGAGGG | 10152 |
| rs201469518 | snp | G/T | 0.00199792 | 0.0315431 | intron-variant | ABI2 | GRCh38.p7 | 2:203395797 | TAAAACATTCATGGT[G/T]CCTCGTCTTCACTTT | 10152 |
| rs201487046 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424199 | CGGTATTTTGAATAT[C/T]GGTGAAAACACAGAT | 10152 |
| rs201494250 | snp | C/G/T | 0.000137147 | 0.00827987 | intron-variant | ABI2 | GRCh38.p7 | 2:203416899 | GTTGTCAGCCTGATA[C/G/T]GTTCTTAGTTTCAGA | 10152 |
| rs201694906 | in-del | -/G | 0.00914312 | 0.0669923 | intron-variant | ABI2 | GRCh38.p7 | 2:203370276 | TTTTGGTTGGGGGAT[-/G]GGGGTCTCATGATGT | 10152 |
| rs201700434 | snp | A/G | 0.000360588 | 0.0134225 | intron-variant | ABI2 | GRCh38.p7 | 2:203402769 | TGCATTCTATAGAAT[A/G]TATTTAATTAAAAAC | 10152 |
| rs201742441 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343369 | TATGTCTCAAAAAAC[A/G]TAAAAAAATTTAATG | 10152 |
| rs201742774 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355753 | GGAGAATCGCTTGAA[C/T]CTGGGAGGCAGAGGT | 10152 |
| rs201791040 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342009 | CATATTAGATGAGAC[A/T]ACTCAAGTTTACCTC | 10152 |
| rs201864332 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384308 | TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 10152 |
| rs201902267 | in-del | -/TC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203333945 | TCTTTTTTCTTTCTT[-/TC]TTTTTTTTTTTTTGA | 10152 |
| rs201903160 | in-del | -/GA | 0.00874735 | 0.0655527 | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432023 | CAGGGGAACTTGAGG[-/GA]GCAGTCTGTTGCCAG | 10152 |
| rs201919959 | snp | C/T | 4.94376e-05 | 0.00497156 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427247 | AGGAGCCATTATTTA[C/T]GTCATCAAGAAGAAT | 10152 |
| rs201925152 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431709 | ATTAAAAAAAAAAAA[-/C]AATTAAAACGAAACG | 10152 |
| rs202078297 | in-del | -/TGTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346339 | AACCACAAAAGACTA[-/TGTT]TGTTTGTTTGTTTGT | 10152 |
| rs202229869 | in-del | -/AA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330393 | GTGAGACTACATATC[-/AA]AAAAAAAAAAAAAAA | 10152 |
| rs202238107 | snp | C/T | 1.65765e-05 | 0.00287888 | intron-variant | ABI2 | GRCh38.p7 | 2:203395627 | ACTGTTTATAAATAC[C/T]CATGTTTTGGTGGCT | 10152 |
| rs367545073 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420113 | GTGTTAGAATTGGGA[G/T]TTGACTGGGTGGTAT | 10152 |
| rs367549964 | snp | C/G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398567 | CCAAGGTATAACTTA[C/G/T]GTACAGTAAAATTCA | 10152 |
| rs367569476 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203409266 | ACTGCCAAGAATTAT[A/C/G]ACTTTAGGGAAAAAC | 10152 |
| rs367571359 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379091 | ATTCACCCTCTGTTA[A/G]CAAATAGAAGATTGT | 10152 |
| rs367582312 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ABI2 | GRCh38.p7 | 2:203350232 | TGGGTGTGCATTACT[A/G]TGCCCGGCTAATTCT | 10152 |
| rs367660149 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203373766 | AGCTGGAAAATAATT[A/T]TCATAAAATAATATA | 10152 |
| rs367717573 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430655 | TATCTCCCTCAGAGG[C/T]GCCTGCTGTTCCCAT | 10152 |
| rs367813885 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357573 | TGAATATCAAGTTAA[C/T]CTGCCTCAGTTATTT | 10152 |
| rs367826242 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402067 | TGAGACAGAGTCTCA[C/G]TCTGTCACCCAGGCT | 10152 |
| rs367827834 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429163 | TCCCAGCACTTTGTA[A/T]TTATTAGCTTTCATT | 10152 |
| rs367829312 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203406791 | GCCTCAGCCTCCCGA[A/G]TAGTTGGAACTACAG | 10152 |
| rs367846844 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344813 | AGCTAAAGGTTTGCA[A/G]GCGCACCAATCTGCA | 10152 |
| rs367846935 | snp | A/C | 1.67256e-05 | 0.0028918 | intron-variant | ABI2 | GRCh38.p7 | 2:203394675 | CTTGCTTAATCATAC[A/C]ATACATACGCTCTTC | 10152 |
| rs367897620 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203414165 | GGAGTACAGTGGTGC[A/C]ATCTTGGCTCTCTGC | 10152 |
| rs367964628 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203409799 | TGTTTTCATATCACA[C/T]TTATGGAATAGGCCT | 10152 |
| rs368052468 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203357686 | ATATGTTAAATGATT[-/A]AAAGGAACAATTTAA | 10152 |
| rs368083178 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419146 | CGGAGTTTCGCTCTT[A/G]TTGCCCAGGCTGGAG | 10152 |
| rs368085697 | snp | C/T | 0.000461893 | 0.0151899 | intron-variant | ABI2 | GRCh38.p7 | 2:203411246 | TTTAATGTAACTCGC[C/T]CTTATCCCTTATCCT | 10152 |
| rs368092244 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330053 | TAGCTATATAGGAAA[G/T]CATTTTCATGTCTTA | 10152 |
| rs368098891 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203336455 | ATTATGGAAGTTTGC[A/G]AGGACCTTATGTGAA | 10152 |
| rs368194378 | snp | G/T | 0.000242911 | 0.011018 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427385 | CTTGCCTCACAGGAA[G/T]AGTCAGGTCTTCCCA | 10152 |
| rs368216381 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359358 | CACTTGAGTTCTTAT[C/G]AGTGATGTCTTAATT | 10152 |
| rs368302926 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346525 | GGTTTATCCATTACT[A/G]GAGTTGCACGTTTTC | 10152 |
| rs368323833 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400825 | TTTCCTCTAATACTT[G/T]TAATTAAAATTACCA | 10152 |
| rs368336155 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342794 | CTAGAAGAGCAGGCT[A/G]GGTTGACAAAAATAT | 10152 |
| rs368354540 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203349624 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 10152 |
| rs368413280 | snp | C/G | 3.5825e-05 | 0.00423216 | intron-variant | ABI2 | GRCh38.p7 | 2:203402765 | TTTTTGCATTCTATA[C/G]AATGTATTTAATTAA | 10152 |
| rs368490570 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345403 | CTGTAACATTCACGG[C/T]GAGGGTCCACGGGTT | 10152 |
| rs368503449 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419804 | GACCAGCCTGACCAA[C/T]ATGGAGAAACCCCGT | 10152 |
| rs368505246 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408887 | CCCAGGTCGGACTGC[A/G]GACTGCAGTGGCGCA | 10152 |
| rs368542310 | snp | G/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365617 | GTGTTTTCTGGGGCT[G/T]TTATCTTTTTTTTTT | 10152 |
| rs368719356 | snp | C/T | 0.000157996 | 0.00888668 | intron-variant | ABI2 | GRCh38.p7 | 2:203416866 | GGAAATACTGAACTT[C/T]GCATAACATATAGTT | 10152 |
| rs368735879 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379648 | AACTAGATTAATTTC[A/G]GGGGCTTTCTTAATC | 10152 |
| rs368740855 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331304 | GGACCCTGCAGTAGA[C/T]GAAAGTTAATTCACA | 10152 |
| rs368862926 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410949 | TATGAAAAAAGATCA[A/G]TTATATATAATATAT | 10152 |
| rs368978443 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203333376 | AAGAACCTTTTAAGG[A/T]TGCTGGGCTTGACTT | 10152 |
| rs368989918 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203334188 | TCAAGTGATCCACCC[A/G]CCTTGGCCTTCCACA | 10152 |
| rs369100486 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203416325 | GTTGTTTTTGAGATG[C/T]GGTCTTGCCCTATGG | 10152 |
| rs369125262 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203409370 | TTCAAGATTATCTGC[C/T]TAACTCTTGTCTGTG | 10152 |
| rs369147794 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203372489 | AGAGGGGCTCCTCAC[A/T]TCCCAGTAGGGGCGG | 10152 |
| rs369229903 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384809 | ATTTCAGTTGAACAT[C/T]GCCCAAGCAGATTCT | 10152 |
| rs369285631 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203391615 | CACTTGAGCCCAGGA[G/T]TTTAAGACCAGCCTG | 10152 |
| rs369304387 | snp | C/T | 8.60385e-05 | 0.00655834 | intron-variant | ABI2 | GRCh38.p7 | 2:203417126 | GGGAAGAAACCTCTA[C/T]ATAGAAATGAAATTT | 10152 |
| rs369306670 | snp | A/T | 1.65386e-05 | 0.00287559 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203380259 | GAAATTGGTATTTTG[A/T]CTACCAATAAAAACA | 10152 |
| rs369399914 | in-del | -/TTCATTTCTGAA | 0.0154538 | 0.0865337 | intron-variant | ABI2 | GRCh38.p7 | 2:203377405 | TTACACTCTTATAGT[-/TTCATTTCTGAA]TAAGTTAAGTACATT | 10152 |
| rs369452076 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345423 | GTCCACGGGTTCATT[C/G]TTGAAGTCAGCCAGA | 10152 |
| rs369482737 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203392529 | GTGGACAAAATAATT[C/G]TGCTTAGAGAGAGAG | 10152 |
| rs369489569 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203362942 | TTCAAGTGATTCTCC[C/T]GCCTCAGCCTCCTGA | 10152 |
| rs369515755 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203406977 | CTTTAACAAGGTGGT[C/T]GAAATTAATTCAGAT | 10152 |
| rs369571277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203349053 | TTCTCCTGCCTCAGC[C/T]TCCTGAGTAGCTGGG | 10152 |
| rs369582369 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203391657 | GAAACCCTGTCTCTA[C/T]GAAAAATACAAAAAT | 10152 |
| rs369623945 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376191 | TCTCAACCAGGGAAG[G/T]TTTGCCCCCAAGGGG | 10152 |
| rs369625466 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422437 | ATGATGGAGAGAAGT[C/T]GAGTGTTGGTATTTG | 10152 |
| rs369656211 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410461 | TACCTGGCTTATTAG[C/T]GCAATTATATATGTT | 10152 |
| rs369669757 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382473 | ATATTTGTTGAATGA[A/G]TGGTTATTTTGTAAT | 10152 |
| rs369688227 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431194 | TTGAGCTAGATGAAA[G/T]TTTTAAAATTTCTGG | 10152 |
| rs369713376 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203364853 | ATCCTCCCACCTCAA[C/T]CTCTCTAGTAGATAG | 10152 |
| rs369718474 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203372840 | CCAGACGGGGTCGCG[A/G]CTGGGCGCCCTCATA | 10152 |
| rs369744130 | snp | C/T | 1.68187e-05 | 0.00289984 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416915 | GTTCTTAGTTTCAGA[C/T]ACACCACCTCCACCG | 10152 |
| rs369794754 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347166 | CTAACAGGGTAAGGA[A/G]TGATCATATAGAAAG | 10152 |
| rs369806628 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203383566 | CTTGCCCAAGCTACT[A/G]TCTCATGCTTGTTTT | 10152 |
| rs369858216 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390236 | ATTTTCTGTATATAT[C/T]ACATGATTTATCTTT | 10152 |
| rs369904481 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203401402 | GTCTGCTATTGTGCT[C/G]TCTCATGGGTGCTGT | 10152 |
| rs369915847 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203340477 | GCTCAAGTGATGCTC[C/T]CACCTTAGCCTTCCG | 10152 |
| rs369937232 | snp | A/T | 1.78194e-05 | 0.00298486 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203391112 | ACTCAGAAGCCCCCT[A/T]GTCCCCCTATGTCAG | 10152 |
| rs370055393 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203373086 | CAGAGGCTGCAATCT[C/T]GGCACTTTGGGAGGC | 10152 |
| rs370063566 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203340996 | GGCATACTTCTGCCT[C/T]AGGGCCTTTTTGCTT | 10152 |
| rs370078140 | snp | C/G | 6.99362e-05 | 0.00591297 | intron-variant | ABI2 | GRCh38.p7 | 2:203427131 | GTTCTGTCTTTCTAG[C/G]AATATTACTGTCTTT | 10152 |
| rs370112375 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355639 | GTTCCAGACCAGCCT[C/G]ATCAACATGGAGAAA | 10152 |
| rs370112507 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396573 | TTTGTTTTTAATGAA[C/T]TGAAAAAATCTGCAC | 10152 |
| rs370126313 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360057 | GGGCGTGGTGGTGCA[C/T]GCCTGTAGTCCCAGC | 10152 |
| rs370162988 | snp | A/C | | | synonymous-codon, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394701 | TCTTCTTTTTGTAGG[A/C]GGCACTCCCCCTATC | 10152 |
| rs370180869 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344663 | TGGGCTTCTGGGTCC[A/G]GTGGGGACTTGGAGA | 10152 |
| rs370218524 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418986 | AAGATAAGAATGACT[A/G]CATGGTTCTCATCAA | 10152 |
| rs370240381 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377896 | GGGCGACAGAGTGAG[A/T]TACTGTCTCATAAAA | 10152 |
| rs370254027 | snp | C/T | 0.167158 | 0.235875 | intron-variant | ABI2 | GRCh38.p7 | 2:203331348 | AATGGTCAATTTAGC[C/T]TTTTTTTTTTTTTTT | 10152 |
| rs370267709 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385333 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 10152 |
| rs370282443 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203386939 | GCCACCATGCCCAGC[C/T]AGACATTGCTTTTTA | 10152 |
| rs370295013 | in-del | -/T/TT/TTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376733 | TGTATTGGTCTTCCC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 10152 |
| rs370295075 | snp | C/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328598 | CACAAATCTGGAACG[C/G]GTGGCCGATTACTGC | 10152 |
| rs370439901 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342292 | CTATGAAGAATCTTC[A/G]TTGTAAATTTTGAAT | 10152 |
| rs370440226 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425851 | ACATGGCAAAACCCC[A/G]TCTCTACTAAAAATA | 10152 |
| rs370444386 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404525 | TGTTCAGGAGCACGG[A/G]ATTACAGGTACCTGC | 10152 |
| rs370539214 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203395759 | GCTGTTCCTACTCCA[C/T]CTCCTCCCAGTGTCT | 10152 |
| rs370635108 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430302 | TATAACAGACGATCC[A/G]AGTCCAAAATCTGAC | 10152 |
| rs370704799 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203349033 | TACCTCGTGGGTTCA[A/G]GTGATTCTCCTGCCT | 10152 |
| rs370781655 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406786 | CTCCTGCCTCAGCCT[C/T]CCGAGTAGTTGGAAC | 10152 |
| rs370812418 | snp | A/G | 0.000155988 | 0.00883004 | intron-variant | ABI2 | GRCh38.p7 | 2:203380157 | TATTTTGATTTTTGT[A/G]GATATTAGAACTATA | 10152 |
| rs370873205 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398129 | TCTTTACATGTTTTA[A/C]AAGACACTTTTAGCC | 10152 |
| rs370903667 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355863 | AAAACACCCCACCAA[A/G]AAACCCCTGGTGTGC | 10152 |
| rs370907556 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427265 | CATCAAGAAGAATGA[C/T]GATGGTTGGTATGAG | 10152 |
| rs370923890 | snp | A/C | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394712 | TAGGCGGCACTCCCC[A/C]TATCGCACACTGGAG | 10152 |
| rs370999877 | snp | A/G | 7.15986e-05 | 0.00598282 | intron-variant | ABI2 | GRCh38.p7 | 2:203380421 | CTTTTAAAAGTAGTA[A/G]CCCATAATGAAACCA | 10152 |
| rs371002169 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203410125 | TGTCAGCTTGGCAGG[-/T]TTCCCTTCTTCAAGT | 10152 |
| rs371015746 | in-del | -/CT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203332618 | CGACAGAGCAAGACT[-/CT]GTCTCAAAAAAACAA | 10152 |
| rs371022915 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203393704 | GGATCCATACATAAG[G/T]CAGTAGAGCAACATC | 10152 |
| rs371068670 | snp | A/G | 3.80438e-05 | 0.00436124 | intron-variant | ABI2 | GRCh38.p7 | 2:203402550 | TTTTCTTTTAATGAC[A/G]TATGTATGTTCTATC | 10152 |
| rs371197557 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369061 | GGCTGGTCCTGAAAT[C/T]CTGGGCTCAAGCAGT | 10152 |
| rs371221385 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342969 | ATGCATAATTATGAA[G/T]TTTATTCATGTGTAA | 10152 |
| rs371242683 | in-del | -/G | 0.000847286 | 0.0205651 | intron-variant | ABI2 | GRCh38.p7 | 2:203380185 | ATACATTTTTGTGTT[-/G]TTTTTTACATTATAT | 10152 |
| rs371251656 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378325 | ACCGTGTTAGCCAGG[A/C]TGGTCTCGATCTCCG | 10152 |
| rs371257211 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203349700 | GTGAGCCACTGTGCC[C/T]GGCTGTGTTCATTTT | 10152 |
| rs371263753 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415561 | GGCAGAGCTTGCAAT[A/G]AGCCGAGATCACACC | 10152 |
| rs371313997 | in-del | -/AAAA | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203355535 | AAAACAACAAAAAAC[-/AAAA]AACCCAAGAGGCCAG | 10152 |
| rs371440191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203364846 | TCAAGTCATCCTCCC[A/G]CCTCAACCTCTCTAG | 10152 |
| rs371453323 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430752 | CATCCCCTCCTTTTT[C/T]CTACTGCTGGTGTTT | 10152 |
| rs371453527 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388544 | AAAAAGTAGCTGGGC[A/G]TGGTGGTGCGCCTGT | 10152 |
| rs371501537 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418157 | TCAGATAGTCTTTAT[A/G]TATGTGTAATTGGAG | 10152 |
| rs371616640 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357888 | ATTCTCCTGCCTCAG[A/C]CTCCCAAGTAGCTGG | 10152 |
| rs371621701 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329574 | TTTGCTTTTTTTTTT[A/G]TGGTTATTTTGAATT | 10152 |
| rs371645171 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338424 | AGATCCCTCATGAAT[A/G]ATGTAGCACCATCCC | 10152 |
| rs371687933 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388234 | TCTTTTAATAGAAAG[A/G]TAATGAAATATTAGG | 10152 |
| rs371727199 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420201 | GACCTAGGATTGAGT[A/C]TTGGCTTTACAGTTT | 10152 |
| rs371802664 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203386457 | TTTTTTTTTTTTTTT[G/T]GAGAGACGTGGTCTT | 10152 |
| rs371803545 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203409274 | GAATTATGACTTTAG[G/T]GAAAAACCTAACCAA | 10152 |
| rs371908177 | in-del | -/GGAGACAGAAA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203426688 | AGAGAGAGTGAGAAA[-/GGAGACAGAAA]TCTGCTGTTCCATTA | 10152 |
| rs371923641 | in-del | -/TCCTGACCTCAGGTGAT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399739 | AGGTTGGTCTTGAAC[-/TCCTGACCTCAGGTGAT]CCGCCCGCCTCAGCC | 10152 |
| rs371941606 | snp | A/C | 3.31263e-05 | 0.00406965 | intron-variant | ABI2 | GRCh38.p7 | 2:203411267 | CCCTTATCCTCCACA[A/C]CTTTTTTGTTTTTGC | 10152 |
| rs371992840 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415865 | CTGAGTTTGAAGATA[A/G]TCTTTTTGATGTTAC | 10152 |
| rs371992967 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388566 | TGCGCCTGTAATCCC[A/T]GCTACTCGGGAGGCT | 10152 |
| rs372018769 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406844 | CTTTTTTTTTCTTTA[A/G]TAGAGACAAGCTTTC | 10152 |
| rs372038723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332205 | TAAAATATGATAAAC[A/G]GGTATAACTACAGTT | 10152 |
| rs372069336 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203375154 | AGCTTGGCAATATCA[A/G]TGAGAAGGATGGGGA | 10152 |
| rs372111114 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203383966 | AGAGAAAGTCATCAT[A/G]CTTTAGGACCAGACA | 10152 |
| rs372187838 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404704 | GCAGGGATTACAGGC[A/C]CCTGCCACTACACCC | 10152 |
| rs372196083 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351062 | TTCATATTTACTCTT[C/T]TGCATGTCACTATCC | 10152 |
| rs372210097 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382259 | TTATGTAGAATATTA[C/T]ATATGGGGAGTTAAA | 10152 |
| rs372227424 | snp | A/G | 0.000216117 | 0.0103929 | intron-variant | ABI2 | GRCh38.p7 | 2:203391179 | TGAAAACCATTTCAT[A/G]TAGTATTGTTTAAAA | 10152 |
| rs372273472 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398441 | ATGTGAGGGGATAAT[A/T]AACTGTGGTTTTTAA | 10152 |
| rs372285056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203336879 | TTGCCAAACTCTTTT[C/T]CAAAAACGATGGTAC | 10152 |
| rs372390320 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374275 | AGGCTAAGGGTGGCC[A/G]GATCACCTGAGGTCA | 10152 |
| rs372395964 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360446 | GAAAGGAGAAATGGG[A/G]TATGATGAAGGGAAA | 10152 |
| rs372464516 | in-del | -/TT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413051 | CCCTGGGAGTTTTTT[-/TT]CTGTTTTTACTATTG | 10152 |
| rs372540709 | snp | G/T | 0.000153988 | 0.00877327 | intron-variant | ABI2 | GRCh38.p7 | 2:203380184 | TATACATTTTTGTGT[G/T]GTTTTTTACATTATA | 10152 |
| rs372561290 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203373191 | GAGCACTGAGTGAAC[C/G]AGACTCTGTCTGCAA | 10152 |
| rs372567873 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342156 | ACTCACACCATTTAT[G/T]TTATTATATGTTTTT | 10152 |
| rs372581889 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | ABI2 | GRCh38.p7 | 2:203344906 | AGCACTCTGTAAAAA[C/T]GAACCAATCAGCGCT | 10152 |
| rs372760456 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419818 | ACATGGAGAAACCCC[A/G]TCTCTACTAAAAGTA | 10152 |
| rs372804456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203392950 | TTGCCTAGTCACCAC[A/G]TTTTGTTCCTTTGCT | 10152 |
| rs372878946 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203391264 | CTTTGTAGGATTGTT[G/T]TTTGTGTGTATAACT | 10152 |
| rs372881184 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374332 | TAGTGAAACCCTGTC[A/G]CTACTAAAAATACAA | 10152 |
| rs372891406 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ABI2 | GRCh38.p7 | 2:203417124 | ATGGGAAGAAACCTC[C/T]ACATAGAAATGAAAT | 10152 |
| rs372924283 | in-del | -/TATATATA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203395449 | atatatatatatata[-/TATATATA]cacacacacacacac | 10152 |
| rs372947714 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203372584 | ACCTCCCTCCCGGAC[A/G]GGGCGGGTGGCTGGG | 10152 |
| rs372974083 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203391359 | GTGAATTTTAAATTT[A/G]AGGTAAAATCCTAGC | 10152 |
| rs372984917 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385167 | TGAGACAGTCTTGCC[A/G]TTGCCCAGGCTGGAG | 10152 |
| rs372995538 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203412508 | AAATAGTCTATTTTA[C/G]TTACTTTTGTTTATT | 10152 |
| rs373064167 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424635 | AACTCATGGCCTCAA[C/G]TGATTCTCCTGCCTC | 10152 |
| rs373109983 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203411053 | ATATATTTAACATAT[C/G]TGTGTATGATAAATG | 10152 |
| rs373128083 | in-del | -/AA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392319 | accaccaccaccaAC[-/AA]caacaacaacaacaa | 10152 |
| rs373187732 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203431821 | GCTTATTTTCACATT[A/G]AAATGAAACCTCTTT | 10152 |
| rs373196772 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203334941 | GCTGGGATTACAGCG[C/T]AAGCCACCGTGCCTG | 10152 |
| rs373275645 | snp | A/G | 0.000137931 | 0.0083034 | intron-variant | ABI2 | GRCh38.p7 | 2:203417130 | AGAAACCTCTACATA[A/G]AAATGAAATTTGCGG | 10152 |
| rs373302782 | snp | A/G | 3.51809e-05 | 0.00419395 | intron-variant | ABI2 | GRCh38.p7 | 2:203402755 | TTTTTTTGTTTTTTT[A/G]CATTCTATAGAATGT | 10152 |
| rs373314253 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355436 | AGGATTGCTTGAGCC[G/T]GAGAGTTTGAAGCTG | 10152 |
| rs373315374 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203340654 | TGAGCTACCATTTGC[C/T]TGGCTGAGAGTAGAT | 10152 |
| rs373371654 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406166 | TAACAGTCTCTACTT[G/T]AAATGTAAATATGAA | 10152 |
| rs373434908 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203339817 | TGTACTGCATGCACA[C/G]TTCTCCTTCAGTCTA | 10152 |
| rs373464429 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404091 | TCCTACCTACATATT[A/T]AAAAAATTTTTCTCT | 10152 |
| rs373530390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203377487 | GTGTTATCTGATGAA[C/T]CTTTTATTGATCTGA | 10152 |
| rs373538806 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418613 | TGAACAAGCAAGAAG[C/T]GCCAAAAAGAGAATG | 10152 |
| rs373588969 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203417902 | TACTATAAATACCAC[-/AT]GTGATCAAGAAAGTA | 10152 |
| rs373622693 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203349861 | CGTTATAAATATTCA[C/T]GTACAAGTTTTTGTG | 10152 |
| rs373642791 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387453 | CTCCGGTGGTATTTG[C/T]ATTCCTTCATCATAG | 10152 |
| rs373653545 | snp | C/G | 5.25942e-05 | 0.0051278 | intron-variant | ABI2 | GRCh38.p7 | 2:203328655 | CATCCCCAGCTGGGC[C/G]GCGTCGGGGACCCCC | 10152 |
| rs373673663 | in-del | -/TCTCTCTCTC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370187 | GTGTCATTCTCCTAT[-/TCTCTCTCTC]TCTCTCTCTCTCTCT | 10152 |
| rs373741015 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342069 | GAGGAATTATGTTCA[-/T]TTTTTTTTTTGCCTG | 10152 |
| rs373757568 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365609 | CAGGCTACGTGTTTT[C/T]TGGGGCTGTTATCTT | 10152 |
| rs373780148 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423495 | CAGTGGTGCAATCTC[C/G]GCTCACTGCAACCTC | 10152 |
| rs373789015 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365196 | TTTTTGGACTTTTTT[-/TT]GTGCTTGTATTTACA | 10152 |
| rs373806678 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203416451 | CGGGCGCCCACGACC[A/G]TGTGCGACTAATTTT | 10152 |
| rs373880521 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | ABI2 | GRCh38.p7 | 2:203409752 | CTTTTTTTAATCTTT[C/G]CAGCCACTATTGGAA | 10152 |
| rs373881221 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369265 | GATGTTAAAAAGAAA[C/T]GTTAAAAAAAAGAAC | 10152 |
| rs373891546 | snp | C/G | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327239 | TCTAACTACACAAGT[C/G]TAAGATGGTACTGCC | 10152 |
| rs373915531 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344358 | GAACAATATAATTTT[A/T]AAATTTTTTTTTCCT | 10152 |
| rs373939468 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419140 | TTGAGACGGAGTTTC[A/G]CTCTTGTTGCCCAGG | 10152 |
| rs373941580 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203394918 | ATTACTTCAGGTAAA[G/T]CTCTCATTTTCCAAG | 10152 |
| rs373945400 | in-del | -/TT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396260 | ATACACACTTAAAAC[-/TT]AGTTTTGAAAACGTG | 10152 |
| rs373974797 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385680 | TTAAAAATTTATCCG[A/G]CACAGCACCTGGAGG | 10152 |
| rs373977202 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203421376 | AATAACGTATCTTCA[A/G]AAATCATGTTTGATG | 10152 |
| rs373998154 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203386900 | CCACCCTGGCCTCCC[A/G]GAGTGCTGGGATTAC | 10152 |
| rs374024818 | snp | A/C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203412249 | TAGAATGTAAGCTCT[A/C/G]TAAGAGCAAGGAGTT | 10152 |
| rs374104326 | in-del | -/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350540 | CTTTTTCTTTCTTTT[-/C]TTTTTTTTTTTTTTT | 10152 |
| rs374107326 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388454 | TTGGGAGGCCAAGGT[A/G]GGTGGATCACCTGAG | 10152 |
| rs374109025 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203359211 | GACAAATGTGATCTG[C/T]TATGACAGATTAAGG | 10152 |
| rs374109398 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203417513 | TCTTTGCCAAGTAAT[A/C]TTGGGCATTTCTTTT | 10152 |
| rs374111967 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427323 | TTTCCTGGGAATTAC[A/G]TTGAGTCTATCATGC | 10152 |
| rs374180821 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359824 | ATCAACATCAGTGTT[A/G]GGTTCCAACATGTAC | 10152 |
| rs374189699 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346141 | GTGACAAGAGTGAAA[C/T]TCCATCTCAAAAAAA | 10152 |
| rs374192145 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363089 | GCCTGCCTCGGCCTT[G/T]CAAACTTTTGGGATT | 10152 |
| rs374218958 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419657 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC | 10152 |
| rs374224660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203397128 | CCAAAGATTAGCATT[G/T]CCTGAGAAAATTGAG | 10152 |
| rs374231077 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203336763 | TGAACCTAACAAGCA[A/G]TTGGGCAGGTCTATC | 10152 |
| rs374258193 | in-del | -/TCTC | 0.00557542 | 0.0525036 | intron-variant | ABI2 | GRCh38.p7 | 2:203387843 | ATGGTATATGTTCTG[-/TCTC]TCTCTCTGTCGCTGT | 10152 |
| rs374365036 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428966 | CAAGTGTAGTAGTGT[G/T]TGAGAAAATTCAGAT | 10152 |
| rs374374902 | snp | A/G | 4.2526e-05 | 0.00461099 | intron-variant | ABI2 | GRCh38.p7 | 2:203391146 | AAGGGACACTTGGGT[A/G]AGTATATAAGTAGTA | 10152 |
| rs374380960 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379845 | AGATAAGCAAGTGAG[C/T]GGCATGGCTGTATTC | 10152 |
| rs374382970 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413890 | ATTTGGAACCAGTTA[G/T]AGTGACCCAGTTATA | 10152 |
| rs374502666 | snp | A/C | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402652 | AGGGGGCTCGTTGCC[A/C]TATAGACGCCCTCCT | 10152 |
| rs374589375 | in-del | -/CA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385158 | TTTTTTTTTGAGACA[-/CA]GTCTTGCCGTTGCCC | 10152 |
| rs374632967 | snp | A/C | 0.00017353 | 0.00931315 | intron-variant | ABI2 | GRCh38.p7 | 2:203427143 | TAGGAATATTACTGT[A/C]TTTCACATCCTGTTT | 10152 |
| rs374714475 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329341 | GAACCTCCTGGTTTA[A/T]TTTTTTTTTTTTTTT | 10152 |
| rs374753562 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351061 | GTTCATATTTACTCT[C/T]TTGCATGTCACTATC | 10152 |
| rs374781182 | in-del | -/TG | 0.497151 | 0.037632 | intron-variant | ABI2 | GRCh38.p7 | 2:203358072 | TGTGCCTGGCCTGTT[-/TG]TGTGTGTGTGTGTGT | 10152 |
| rs374861995 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404223 | CATCCTGGAATATTG[C/T]TCAGGAACTGTTTGT | 10152 |
| rs374916082 | snp | A/G/T | 3.36447e-05 | 0.00410139 | intron-variant | ABI2 | GRCh38.p7 | 2:203394651 | CTCTTTGAATTTATT[A/G/T]TGCCGAAACTTGCTT | 10152 |
| rs374929024 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203391486 | ATCCTTTTTAAGCTG[A/T]GTAGATTATAAAATT | 10152 |
| rs374929461 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203333011 | TTGAACAATAGGAGA[C/T]ATATTAGTAGCTTTC | 10152 |
| rs374957389 | snp | A/T | 3.37638e-05 | 0.00410862 | intron-variant | ABI2 | GRCh38.p7 | 2:203411240 | TTTCCTTTTAATGTA[A/T]CTCGCCCTTATCCCT | 10152 |
| rs375003244 | snp | A/G | 0.000307953 | 0.0124049 | intron-variant, missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203411320 | CCCTCCATCCTACAG[A/G]TAACTCCTCAGTTAC | 10152 |
| rs375034340 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376975 | GTGTTAGTGTAAATA[A/C]TAAGTGGAAGATTAC | 10152 |
| rs375056626 | in-del | -/TT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376751 | TTTTTTTTTTTTTTT[-/TT]ACTGTTATGGTCTAT | 10152 |
| rs375104091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203370730 | AAAAATACTAGATTC[C/T]GAGAGTTTGTAGAGA | 10152 |
| rs375111093 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408537 | AAATAAGCATATTCA[C/T]CTTAAAAAAAAAAAC | 10152 |
| rs375190652 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350296 | TGGCCTGGCTGGCCT[C/T]GAACTCTTGACCTCA | 10152 |
| rs375216747 | in-del | -/TTTGTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203358114 | GTGTGTGTGTGTGTG[-/TTTGTT]TGTTTGTTTGTTTTT | 10152 |
| rs375231333 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415383 | AGCACTTTGGGAGGC[C/G]GAGGTGGGCGGATCA | 10152 |
| rs375252010 | snp | G/T | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327590 | AGGAAAAAGGACAGC[G/T]AAGTTGATAGCATTA | 10152 |
| rs375273891 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430533 | CAGAAACAAAAATAG[C/T]GCCAATGTGTCAAAA | 10152 |
| rs375288845 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203375859 | AAATAGATTTAGTGC[C/T]CTCTGTCAAATTATT | 10152 |
| rs375291230 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203336108 | CATTTGAAAATCATC[A/G]GTGTTATTGTGTTTT | 10152 |
| rs375300726 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392911 | TGCTAGTTGATGGCT[A/G]TAACCTGTTTTTCCA | 10152 |
| rs375397835 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328108 | TGGGGGCTTCTCCAG[A/C]CGCTCCAGCGGCGGG | 10152 |
| rs375434697 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410668 | CCGATTCTCAGAGGA[C/T]GGTTTTGATACTGTT | 10152 |
| rs375436946 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203384244 | CCATATAAAAGTGGA[A/G]TGTACCTTGAACTGG | 10152 |
| rs375443755 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374195 | TTTATATAGATAGCC[G/T]TGCTTAAGAATTTCT | 10152 |
| rs375446293 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351416 | ATTGAATCTGTAGAT[A/G]AACTTGGGGAGCCAT | 10152 |
| rs375502280 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429753 | AGAGCGAGACTCCAT[A/C]AAAAAAAAAAAAAAA | 10152 |
| rs375524226 | in-del | -/G | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327354 | TTACATTGTGTGGGG[-/G]TAGTCTGATTTAGGA | 10152 |
| rs375653225 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203386095 | GTAGGAACATACATC[C/T]TCTGAAGAGAGGGAT | 10152 |
| rs375660963 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203407413 | GTAGTTTTTAGAGCG[C/T]TTATTTTGTCTAATA | 10152 |
| rs375704389 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203349281 | TTAGTGTGTTTTTTC[C/T]ACAAACAAGAATGTT | 10152 |
| rs375772003 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ABI2 | GRCh38.p7 | 2:203359970 | GGCGGGTGGATCATG[A/T]GGTCAAGAGATTGAG | 10152 |
| rs375851752 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361238 | CTTTTGGCAGGCTTG[C/G]GTCATGTGTCCCTTC | 10152 |
| rs375893873 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ABI2 | GRCh38.p7 | 2:203371747 | CTTGTACAGGTACAC[A/G]TACCTTTAAGTCAGT | 10152 |
| rs375911001 | in-del | -/AT/ATATAT/ATATATAT/ATATATATAT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203395432 | TTTATTAATAAGTAA[lengthTooLong]ATATATATATATATA | 10152 |
| rs375918533 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203341043 | TCTGCCAGGAGTACT[C/T]TACTCCAAGATAGTT | 10152 |
| rs375921047 | snp | A/C | | | intron-variant, synonymous-codon | ABI2 | GRCh38.p7 | 2:203383279 | CAGGCATATGGACAC[A/C]TGTATTATTGATTGG | 10152 |
| rs375941670 | in-del | -/TCTTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400078 | ATAGTGTGAATAGTG[-/TCTTTT]TTTTTTTTTTTTTTT | 10152 |
| rs375947285 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203388667 | GCCTGGGTGACAGAG[C/T]GAGACTCTGTCTTAA | 10152 |
| rs375970505 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422703 | AAGGCCAGTTTTTTT[-/T]CAAGTGAATAGTTTC | 10152 |
| rs375991080 | in-del | -/ATC | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365620 | TTTTCTGGGGCTGTT[-/ATC]TTTTTTTTTTTTTTT | 10152 |
| rs376044526 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403504 | TTGTCTCTGTGGCTG[G/T]GACCTATAGTGATAT | 10152 |
| rs376089389 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382096 | TTAACTTGTTTTTTC[C/T]TTTTTTCCTTTCTCT | 10152 |
| rs376133193 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203394444 | GGTAGAGAACCTTTG[C/T]GCTCTTTGAGAATAA | 10152 |
| rs376154912 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406919 | CCAGTTCCATCTGGC[A/G]TAACAAAGGTCATCC | 10152 |
| rs376214616 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203355396 | GCGTGCTTCTAGTCC[A/G]GACTACTTGGGAGGC | 10152 |
| rs376295031 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203409085 | CCTCATGATCCACCC[A/G]CCTCGGCCTCCCAAA | 10152 |
| rs376314444 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350141 | GAGTGCAGTGGTGCT[A/G]TCTTGGCTCACTGTA | 10152 |
| rs376334706 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425999 | GCACTCCAGCCTGGG[C/T]GATAAGAGTGAGACT | 10152 |
| rs376348180 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | ABI2 | GRCh38.p7 | 2:203416538 | TGACCTCAGGTGATC[C/T]GCCTGCTTCGGCCTC | 10152 |
| rs376378292 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | ABI2 | GRCh38.p7 | 2:203411252 | GTAACTCGCCCTTAT[C/T]CCTTATCCTCCACAC | 10152 |
| rs376382826 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203352238 | CCCGAGATGGAAGGA[C/T]GGCTTGAGTTCAGAA | 10152 |
| rs376386538 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366834 | GTTTGCTAGAAATGG[C/G]TTATTTTTGAATTAA | 10152 |
| rs376415031 | in-del | -/C | | | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432071 | CCATTAAACCACCTC[-/C]AGATGAGTGGAGGAA | 10152 |
| rs376443628 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203340700 | CTCCCCGCTCCCACC[A/G]AAGATAATCAAGAAA | 10152 |
| rs376492783 | snp | A/G | 1.66524e-05 | 0.00288547 | intron-variant | ABI2 | GRCh38.p7 | 2:203394879 | GTGCAAAATGTGATG[A/G]TCATAGTACCATAAT | 10152 |
| rs376494388 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344121 | TTACTATTCATTTAT[A/G]TATTTCCATTTGGTT | 10152 |
| rs376559462 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403765 | TTTTTTTTTTTTTTT[A/T]AATTGAGATGGAGTC | 10152 |
| rs376569776 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428665 | AATTCAGTGGAGTCT[G/T]TAGGGCAGATAACTT | 10152 |
| rs376580185 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203332267 | TGCCTATACAAAGGA[C/T]TTAGTAGTTGGTAGA | 10152 |
| rs376601718 | in-del | -/CCTGACCTCAAATGATCTGCCCG | 0.00914312 | 0.0669923 | intron-variant | ABI2 | GRCh38.p7 | 2:203364319 | GGCTACTCTTGAATT[-/CCTGACCTCAAATGATCTGCCCG]CCTCAGCCTCCCAAA | 10152 |
| rs376662974 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331934 | CCTGCCTCAGCCTCC[A/C]GAGTAGCTGGGATTA | 10152 |
| rs376672899 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203420610 | ATGTTAGCCAGGATG[G/T]TCTCAATCTCCTGAC | 10152 |
| rs376725319 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374304 | CAGGAGTTTGAGACC[A/G]GCCTGGCCAACATAG | 10152 |
| rs376751476 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203399182 | ATGTGTGAGTTTCCA[A/G/T]TTGCATCCTTGTCAG | 10152 |
| rs376753621 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398510 | TCAGGATAGTCTGTT[C/T]TATACAGTACCTGAG | 10152 |
| rs376762566 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415816 | GTTCAGTTGTGCTCA[C/T]GTATTTACCAACCAT | 10152 |
| rs376817916 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363286 | CACCTCAAACATTTA[A/C]CCTTTGTATTATAAA | 10152 |
| rs376823234 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337894 | AAATTATAGGGCATG[C/G]TGGCACACGCCTGTA | 10152 |
| rs376863891 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203341716 | CTCCATCTCAAAAAA[A/C]AACAAAAGAAATTAG | 10152 |
| rs376881398 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418832 | TATAAACTCACAGAT[C/G]CAAGAAGTTCAATAA | 10152 |
| rs376959255 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203367985 | CTTCAGCCTGGGAGA[A/C]AGAGTGAAACCCTGT | 10152 |
| rs376959513 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328376 | CTCCCCTGTCGCGCG[C/T]TGGGGCTGTTTCTCG | 10152 |
| rs376964095 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203372863 | CCCTCATATCCCAGA[C/T]GGGGCGGCGGGGCAG | 10152 |
| rs377011813 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423717 | TGAGCCACCGCGCCC[A/G]GCCCAATCTGGGTCC | 10152 |
| rs377067706 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384757 | AAGCATATTAGTTTA[A/G]TCAAAAGTAATAAAA | 10152 |
| rs377097361 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385330 | TAGAGACGGGGTTTC[A/G]CCGTGTTAGCCAGGA | 10152 |
| rs377174081 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424094 | TGCGTGATATACATG[C/T]ATAATTGGAAAAAGT | 10152 |
| rs377178598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203349013 | TCTCGGCTCACTGCA[A/G]CCTCTACCTCGTGGG | 10152 |
| rs377208274 | snp | A/C/G | 0.000495603 | 0.0157343 | intron-variant | ABI2 | GRCh38.p7 | 2:203416900 | TTGTCAGCCTGATAC[A/C/G]TTCTTAGTTTCAGAT | 10152 |
| rs377209507 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203408021 | TGTCCTGGAGAAAAG[C/T]AGAATTTGGGATGAC | 10152 |
| rs377273409 | snp | C/T | 3.29571e-05 | 0.00405924 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416978 | TCCCCCACCTCCTCC[C/T]CCTCCAGAAGATTAC | 10152 |
| rs377273662 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347965 | ATGATTTGGGCTGGG[C/T]GCAGGTGGCTCATGC | 10152 |
| rs377313451 | in-del | -/GATAT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402410 | CTGCTTTTGTACTCT[-/GATAT]AATATCAGCGAACAA | 10152 |
| rs377359440 | in-del | -/TTTGTTTG | 0.0036261 | 0.0424252 | intron-variant | ABI2 | GRCh38.p7 | 2:203348921 | TGTTTTTTTTTGTTT[-/TTTGTTTG]TTTGTTTGTTTGTTT | 10152 |
| rs377388430 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203393304 | AAGTGCTCTGCCTGC[C/T]CCGGCCTCCCGAAGT | 10152 |
| rs377536138 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203401921 | CTTGTCGATTTTAGT[C/T]TTCAGTGTTCAGTGG | 10152 |
| rs377557602 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203416689 | ACTTTATTCAGTGTC[C/T]ATTAGCATTAATCCA | 10152 |
| rs377567877 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203334591 | GGGAAAAAAACAATA[C/G]AGAAGACAAAGCCAG | 10152 |
| rs377581844 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378196 | CGGCTCATTGCAAGC[A/T]CTGCCTCCTGGGTTC | 10152 |
| rs377640623 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203385881 | ACCTGTTTCTCTTTC[C/T]TCTTACTCCTAATCT | 10152 |
| rs377642013 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355512 | GCAGGACCCTGTCTC[A/G]ACAAAAGAAAACAAC | 10152 |
| rs377657499 | snp | A/G | 5.03461e-05 | 0.00501702 | intron-variant | ABI2 | GRCh38.p7 | 2:203391172 | TAGTAATTGAAAACC[A/G]TTTCATGTAGTATTG | 10152 |
| rs386654280 | multinucleotide-polymorphism | CC/GT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408828 | TCTATGCTACCTTCT[CC/GT]TTTCTTTTTTTTTTT | 10152 |
| rs386654281 | multinucleotide-polymorphism | AG/GC | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429885 | CGGGATGGGGGCAGT[AG/GC]AGAAGACACTGGTGA | 10152 |
| rs397725950 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203412619 | CACATATAATTAGGT[-/T]GATTTCATATGTTTT | 10152 |
| rs397798753 | in-del | -/C/T/TC | 0.00150899 | 0.02743 | intron-variant | ABI2 | GRCh38.p7 | 2:203351547 | TTTTTTTTTTTTTTT[-/C/T/TC]CCTTTAGAGATGGGG | 10152 |
| rs397804135 | in-del | -/A/T | 0.00835517 | 0.064092 | intron-variant | ABI2 | GRCh38.p7 | 2:203392977 | GCTCCTTTTTTTTTT[-/A/T]AAAAAAAATCTTATT | 10152 |
| rs397871759 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400105 | TTTTTTTTTTTTTTT[-/T]TTGAGACAGAGTCTC | 10152 |
| rs397871910 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400106 | TTTTTTTTTTTTTTT[-/T]TGAGACAGAGTCTCA | 10152 |
| rs397987414 | in-del | -/G | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203359854 | CATTTTTGGGGGGGG[-/G]ACACAAAAATTCAGA | 10152 |
| rs397987415 | in-del | -/A | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203363161 | TTACATTAAAAAAAA[-/A]TTTTTCGTGAGTATA | 10152 |
| rs397987418 | in-del | -/T | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203369925 | GAAATTTTTTTTTTT[-/T]ACTTGTGTTTACAGG | 10152 |
| rs397987421 | in-del | -/A | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431708 | TATTAAAAAAAAAAA[-/A]CAATTAAAACGAAAC | 10152 |
| rs398040288 | in-del | -/TTTTTT | 0.5 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203331368 | TTTTTTTTTTTTTTT[-/TTTTTT]CTGAGACAGAGTCTC | 10152 |
| rs398071479 | in-del | -/CAG/CAGC/CAT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413900 | GTTATAGTGACCCAG[-/CAG/CAGC/CAT]TTATACTGGGGTAAG | 10152 |
| rs527258723 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203329174 | GTAGAAGAGCAGCAG[-/T]TTCTTGTTGGAAGTT | 10152 |
| rs527264780 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203331707 | CACTAGCTCGAGTTA[A/C]CTAACCCAACACTCA | 10152 |
| rs527300957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203339216 | AAAAGAGAGATAAGT[A/G]TTGGCAAGCAGGTGG | 10152 |
| rs527354612 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203371703 | CTAAATATATACTTA[C/T]CAGAGCAAACATGTA | 10152 |
| rs527371041 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345040 | CTGGCTGCCGGAGCC[C/T]GCAGTGGCAACCCGC | 10152 |
| rs527375660 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342776 | AAACCTTTTATTCTG[A/G]ATCTAGAAGAGCAGG | 10152 |
| rs527396930 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429626 | GCTGGGCGTGGTGGC[A/G]CACACCTGTAGTCCC | 10152 |
| rs527424327 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364340 | CTCAAATGATCTGCC[C/T]GCCTCAGCCTCCCAA | 10152 |
| rs527436964 | snp | C/G | 0.000141233 | 0.00840217 | intron-variant, missense | ABI2 | GRCh38.p7 | 2:203376057 | AATATCTATACTTAG[C/G]CAAATTAGAGGCGTT | 10152 |
| rs527492786 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337657 | AATTCATAGGAAACC[A/G]CAAAATACTTTGAAT | 10152 |
| rs527506409 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203367707 | TTTTCCTGTAAGTAG[-/T]TTTTTTTTAAATGTA | 10152 |
| rs527518388 | snp | A/G | 0.000397772 | 0.0140971 | intron-variant | ABI2 | GRCh38.p7 | 2:203351508 | AAATTTCTTTCAATG[A/G]TGTTTTGTAGTTTTC | 10152 |
| rs527538907 | in-del | -/TCTT | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430203 | TATTGTAAGTTTCCC[-/TCTT]TTTTTATAAATTAAA | 10152 |
| rs527580151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345971 | AATCACCTGAGATCA[A/G]GAGTTTAAGACTAGC | 10152 |
| rs527610014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203399717 | ACGGGGTTTCACCAC[A/G]TTGGCCAGGTTGGTC | 10152 |
| rs527610093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203390191 | ACTAAATCTGACTTA[C/T]AAGGCTGGCCCACAA | 10152 |
| rs527618478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345548 | CCTGAGTAGCTGGGA[C/G]AACAGGTGCCCGCCA | 10152 |
| rs527666740 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203401362 | TCTCCGCCTCCTCTT[C/T]TCTCTTGCCCTCCCC | 10152 |
| rs527679225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203400977 | TCAAATTCCATATTA[C/T]ATAAGTCTTATCTCA | 10152 |
| rs527737227 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203417524 | AATATTGGGCATTTC[-/T]TTTTAGTGAAAAGCT | 10152 |
| rs527784071 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203340761 | AGTTTATGTGTGTAT[C/G]ATGTCATCATGTTGT | 10152 |
| rs527807890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203393350 | ATGAGCCACTGCACC[C/T]GGCTGCAACAAAACA | 10152 |
| rs527821130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203347566 | TATCAATCTCCACCA[C/T]GTGCCAAGCCTTTCT | 10152 |
| rs527845603 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203359981 | CATGAGGTCAAGAGA[C/T]TGAGACCATCCTGGC | 10152 |
| rs527868899 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203415645 | AAAAAAAAAAAAAAT[C/G]CATTTAATTCAATTC | 10152 |
| rs527883807 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345057 | CAGTGGCAACCCGCC[A/G]GGGTCCTCTTCCATG | 10152 |
| rs527886937 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374255 | TGTAATCCCAGCACT[G/T]TGAGAGGCTAAGGGT | 10152 |
| rs527898403 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203341667 | GTGAGCCTAGATTGC[A/G]CCACTGCACTCCAGC | 10152 |
| rs527924099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203415029 | TCAAGGTTATTGTTT[C/T]GAAAGTTCCTTTGGA | 10152 |
| rs527937566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203423124 | TCTTTTTAGTTCAGA[C/T]CAGTCACTTCTATGT | 10152 |
| rs527980486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203360615 | TGGAGAATTTAGATA[C/T]CAGGAATGACCTGAT | 10152 |
| rs528066296 | snp | C/T | 0.00122324 | 0.0247007 | synonymous-codon, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203396885 | CTCCACTGCCCCAGA[C/T]GCTGCTGCTGGGGGT | 10152 |
| rs528077311 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203412337 | GCAGGCACTTTTGGT[C/G]CCTGCTTTTTTCTGC | 10152 |
| rs528144098 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203344712 | AGGATTGTAAACACA[C/G]CAAACAGTGCTCTGT | 10152 |
| rs528200050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203387896 | AGCACATAGAGATCT[C/T]ATGTTTTGCTACTTG | 10152 |
| rs528232682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203344074 | GGGTTGGAGGCTGCA[A/G]TGACCCTTGATAGTG | 10152 |
| rs528235675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203373147 | AGCGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 10152 |
| rs528236006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203363952 | TATTTTTAGTAGAGA[C/T]GGGGTTTTACCATGT | 10152 |
| rs528250433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203410394 | TAAAGGAAACTGTAA[C/T]TGTAGAGTAATCTTT | 10152 |
| rs528273885 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203419171 | CTGGAGTGCAATGGC[A/G]TGATCTCAGCTCACA | 10152 |
| rs528274843 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327572 | AATACTGAATCCATG[A/C]ATAGGAAAAAGGACA | 10152 |
| rs528304797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203353390 | TTTGATTATTTTCAA[C/T]GTTGCAGTTTTATTA | 10152 |
| rs528341933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203426042 | AAAAAAAAAAATTCT[G/T]GTGTTCCTACAATAT | 10152 |
| rs528368645 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203402801 | TTCAACTACAAAAAA[A/C]CCTTAATTACAAATA | 10152 |
| rs528375746 | snp | A/G | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203356430 | CTGGAGTGCATTGGC[A/G]TGATCTTGGCTCACT | 10152 |
| rs528388297 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203364684 | GTTGACTAGGATAGA[A/G]TACTTAAAGTTTCTA | 10152 |
| rs528417429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203422487 | TTAACAGGACTTGGG[A/G]ATGTCGGGGAAGGTG | 10152 |
| rs528433592 | in-del | -/GTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384290 | CTTGTTTTTGTTTTT[-/GTTT]TTTTTTTTTTTTTTT | 10152 |
| rs528454061 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203421592 | AGAAGGACAAAAAGG[A/T]TATAAAAACTTTTAT | 10152 |
| rs528461789 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203333728 | CTAATTTATATTTGA[A/G]CCCCTTGCTCTTTTA | 10152 |
| rs528478327 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351727 | TTTTTGTAGAGCCAG[C/T]ATCTCACTTCATTGC | 10152 |
| rs528493202 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363359 | ATTATTTTTTATGAA[A/G]TCACCCTGTTGTGCT | 10152 |
| rs528547024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203350921 | TTTTAGGTGTTATAT[A/G]TAAGAAACTATTGCC | 10152 |
| rs528596493 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203336708 | GGGCTGTATCTTTTA[C/T]TACTATTCCTTCTGC | 10152 |
| rs528637435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203380128 | AGTAGCAATATTAAA[C/T]CTCTAGGCATATATA | 10152 |
| rs528665645 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203394573 | AGACTGAAATTGGTA[C/G]CTGGGTTATGTTAAA | 10152 |
| rs528699286 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203336556 | CCATGAGATGAGGCT[C/G]TCTATTGTACCCTTT | 10152 |
| rs528703405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203388503 | GCCTGGCCAACATGA[C/T]GAAACCCCATCTCTA | 10152 |
| rs528728937 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423289 | AGTATCCAAAAAGCT[A/G]GGCCTTGTGTTAGGC | 10152 |
| rs528743201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203420074 | AGGAAAGTTAAGTAT[A/G]TACTGTAAACTATTA | 10152 |
| rs528769997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203329434 | GAGGCGGGGGATACC[A/G]GATGGTATGAGATCC | 10152 |
| rs528821228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203381128 | TTTTCTAATATAAAC[A/G]TACTTAAAAAACACT | 10152 |
| rs528823727 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382373 | TGTCTTCATGTTCCT[C/T]GAGGGCAGATATTTT | 10152 |
| rs528832949 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203373933 | GGAGGCTGAGGCAGG[C/T]GGATCCCTTGAGGTC | 10152 |
| rs528962355 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203408594 | GTAGGTTAAGCACCT[A/C]ATCATTCTTTTTTAG | 10152 |
| rs528969917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203362762 | GAACTCCTGACCTCA[A/G]GTGATCCACCTGGCT | 10152 |
| rs528982258 | in-del | -/TTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203349416 | TGATATCCTTTCTTC[-/TTTT]TTGAGGCGGAGTTTT | 10152 |
| rs529010856 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203383073 | GCATTTCTTCTTTGA[-/T]TTTTTTTTTGTAGGT | 10152 |
| rs529091896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203340136 | CAGAAAGACAAATAC[C/T]GTATGATTTCACTTA | 10152 |
| rs529110355 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430984 | ACTACCTTTTCTTTT[C/G]TCCTTTGTGGAGACA | 10152 |
| rs529141030 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408464 | CACCGTGCCTGGCTG[C/T]TGGTGTACTTCTTAA | 10152 |
| rs529147930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203423413 | TTTACTATTTTAGGA[A/G]AGAAAAAATCATCTG | 10152 |
| rs529173383 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430399 | GTTTGTGTGTCCAGT[C/T]CCCTTAAAAAAAATG | 10152 |
| rs529180058 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203333076 | AGTTCACTAAAAACT[A/T]CATGAGAGGTTTACA | 10152 |
| rs529180071 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203369889 | AAATTTATGTATTTT[C/G]TAGCATTTGCCTCAA | 10152 |
| rs529199265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332396 | CTTTGGGAGGCCGAG[A/G]CAGGCACATCACGAG | 10152 |
| rs529201750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203378320 | GTTTCACCGTGTTAG[C/T]CAGGATGGTCTCGAT | 10152 |
| rs529245488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203377067 | TCATGCCTATAATCC[C/T]AGCACTTTGGGAGAC | 10152 |
| rs529272239 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | ABI2 | GRCh38.p7 | 2:203378417 | GCCTGGCTGAGATTG[-/T]TTTTTTTCTTGAATA | 10152 |
| rs529288498 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203385906 | TAATCTTATGTTCCC[G/T]TATTCTCTGTGTTTT | 10152 |
| rs529304093 | snp | C/T | 0.00026541 | 0.0115167 | intron-variant | ABI2 | GRCh38.p7 | 2:203395611 | GTGCTGATGATCTCT[C/T]ACTGTTTATAAATAC | 10152 |
| rs529325762 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | ABI2 | GRCh38.p7 | 2:203372385 | TCCCCACCTTTCCCC[C/G]CTTTCTATTCCACAA | 10152 |
| rs529325908 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203379336 | CACTGCAGCTTTGAC[C/T]TCCTGGACTCAAGCA | 10152 |
| rs529340328 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432304 | ATTACTGAAGAAGTC[A/G]TCTTTTTAAATTTTC | 10152 |
| rs529340598 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385383 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 10152 |
| rs529376720 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326905 | TTCTCCCAGGATGAC[C/G]CCATTCTTCTGCCTC | 10152 |
| rs529386222 | snp | A/G/T | 0.00199529 | 0.0315338 | intron-variant | ABI2 | GRCh38.p7 | 2:203378494 | TCCATTTATACATTC[A/G/T]TTAGCTCTGGAACAT | 10152 |
| rs529414077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203335148 | TATTTTCCCATTAGC[C/T]GTAGGATGTTCTCCA | 10152 |
| rs529514586 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203401665 | TTATATCTTAATTTT[A/T]TTCATGATTGTAAAT | 10152 |
| rs529590196 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203394377 | AATATGATACTAAAA[G/T]AATTCCAACTCTTCT | 10152 |
| rs529652618 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203390047 | GAACTAGGACATTGC[A/C]TGTGGCCCTTGTGCT | 10152 |
| rs529657057 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345466 | CGGAAGGAACCAATT[C/G]CGGACACAATCTTAG | 10152 |
| rs529695553 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203426667 | TAGCGAAGAGGCATA[C/G]GCTCCAGAGAGAGTG | 10152 |
| rs529702314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203389308 | ATTACAGATAAATGC[A/T]TCACTTTAAAATATT | 10152 |
| rs529710576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203337673 | CAAAATACTTTGAAT[A/G]GCCAAAGCAGTTTTG | 10152 |
| rs529730887 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379601 | ATGTTTAAACATGAA[G/T]AGAAATTATACTAAT | 10152 |
| rs529759975 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203401480 | TGCAGTCAAGGTAAA[G/T]TTTAGGGAGTGGATT | 10152 |
| rs529781503 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203338232 | AAAGAATGAAATTTG[A/G]TTGTTATATCACACA | 10152 |
| rs529790170 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368575 | TATTTTTGAAAATTT[G/T]TCAGACCAATTTAGA | 10152 |
| rs529794533 | in-del | -/C/CC | 0.00726745 | 0.0598424 | intron-variant | ABI2 | GRCh38.p7 | 2:203328665 | GGGCCGCGTCGGGGA[-/C/CC]CCCCCCCGCCGGGGG | 10152 |
| rs529818359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203350395 | TCTCTGTCGCCCAGG[C/T]TGGAGTACAGCGGCA | 10152 |
| rs529898088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203405383 | ACTTTTATTTTATAT[C/T]CATTAGAATATTATT | 10152 |
| rs529958764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203413098 | TAGAGAATTCTGCCA[A/G]TCAATTGCTACTGCA | 10152 |
| rs529972212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203398511 | CAGGATAGTCTGTTT[C/T]ATACAGTACCTGAGT | 10152 |
| rs530030651 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203407663 | TAAACATTCTTGTAT[A/T]TTGTGAAAATTACAT | 10152 |
| rs530041070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203406903 | CCTGACCTCAAGTGA[C/T]CCAGTTCCATCTGGC | 10152 |
| rs530048985 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant | ABI2 | GRCh38.p7 | 2:203367511 | TATTATATATAATTT[-/A]AAAAAAAGTGTATTA | 10152 |
| rs530093592 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203352434 | GGAGATGACAGTTCC[A/G]TAAGTGTTATTGCCT | 10152 |
| rs530194989 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | ABI2 | GRCh38.p7 | 2:203375985 | CAAGAATGCAAATTA[C/T]ACCGTTGTTAGATTA | 10152 |
| rs530214138 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203422268 | TGCACCACTGCCTGG[C/G]GACAGTAAGACTCTG | 10152 |
| rs530223581 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337887 | AATACAAAAATTATA[C/G]GGCATGCTGGCACAC | 10152 |
| rs530232112 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403178 | TATACAATTCTCATA[A/C]CAAACCCATGGTGGA | 10152 |
| rs530240719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203391285 | GTGTATAACTTCCTC[G/T]TCTCTTGGGAAACAC | 10152 |
| rs530299634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203414765 | TTAAGATAATAGGCA[C/T]TGGAGTTCAGGTGCT | 10152 |
| rs530314557 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203359957 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCATGAGG | 10152 |
| rs530322803 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368665 | TTCACATTTTATACA[A/G]ACTTCTGCAGACATA | 10152 |
| rs530352479 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203336531 | ACAGTGCCTCATCAC[C/T]TCCTAGTTCCCATGA | 10152 |
| rs530364293 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429518 | AATCCCAGCACTTTC[A/G]GAGGCCGAGGTGGGT | 10152 |
| rs530407943 | snp | A/G | 0.000168902 | 0.00918816 | intron-variant | ABI2 | GRCh38.p7 | 2:203411244 | CTTTTAATGTAACTC[A/G]CCCTTATCCCTTATC | 10152 |
| rs530469341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203410232 | GGGTTAAGATTATCA[C/T]GTATTCTTCTGTTTC | 10152 |
| rs530474101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203359223 | CTGCTATGACAGATT[A/C]AGGTTTTTTTAAATA | 10152 |
| rs530478217 | snp | A/G | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326121 | TGATCCACCTGTGTC[A/G]GCCTCCCAAAGTGCT | 10152 |
| rs530576154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203378402 | AGGCGTGAGCCACCA[C/T]GCCTGGCTGAGATTG | 10152 |
| rs530576635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203349647 | TGACCTCAGGTGATC[C/T]GCCTGCCTTGGCCTC | 10152 |
| rs530577837 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203371596 | CTTTGTTGCTGTTAT[A/C]CTATTCATTCTTTGG | 10152 |
| rs530647993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203424769 | AATAGTGAATACTAA[C/T]TTTGGCAAAAGAAAA | 10152 |
| rs530672357 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203418232 | CAAAATATTTCCACG[G/T]TTGATGAAAACTATA | 10152 |
| rs530696215 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326880 | CACGATCTCCGCTCA[C/T]TGCAAGCTCTTCTCC | 10152 |
| rs530731988 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415407 | CGGATCACAGGGTCA[A/G]GAGATCTAGACGATC | 10152 |
| rs530733017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203417282 | GATTTTAAAAAACTG[A/T]TGGTTATCTATATTG | 10152 |
| rs530734349 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326046 | GCTAATTTTTGTATT[C/T]TTAGTAGAGACGGGG | 10152 |
| rs530739045 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203352800 | CCCTCCTATTACCCA[A/G]ACATGTTCTAGTCCT | 10152 |
| rs530807501 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359958 | TTGGGAGGCTGAGGC[A/G]GGTGGATCATGAGGT | 10152 |
| rs530815372 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203394002 | GTCTGGTTTGTATTT[C/T]ACAGTTCAAAGTAAA | 10152 |
| rs530817671 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328413 | CCGAGTTACCGCCGC[C/T]GTCGCCGCCGCTCCT | 10152 |
| rs530834601 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203373328 | ACCAGTCAGGCGTGG[C/T]GGCGCGCGCCTGTAA | 10152 |
| rs530851932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203425259 | ACAAGAGTCTCACTC[C/T]GTCACCAAGGCTGGA | 10152 |
| rs530865853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203420819 | AAAGCTTCTCAGAGA[A/C]CATGGCGTTCTTGGT | 10152 |
| rs530887961 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425391 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 10152 |
| rs530892616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366392 | ATCATATTATTTATA[A/G]TTTTTTTCTTAAAAT | 10152 |
| rs530895772 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203373827 | GTATTGAAAGGCAGT[G/T]GCCTTAAGAACTCAA | 10152 |
| rs530916077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203419942 | GGGGAGAGCTGAGAT[C/T]GCCCCATTGCACTCC | 10152 |
| rs530939083 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330916 | ATATTTTATACATTT[C/T]CTTCAGTTGAAAAGA | 10152 |
| rs530943532 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363116 | GATTACAGGTGTGGC[C/G]CAGTGCACCTGGCAG | 10152 |
| rs530988221 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420693 | CCACCACGCCCAGCC[A/G]ACAGTCCCTTATCTG | 10152 |
| rs530995236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203412651 | AATTATGCTATTGGG[A/G]CCGACTCTTCTTTAG | 10152 |
| rs531048646 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ABI2 | GRCh38.p7 | 2:203406962 | TTCTCCACGGCAAAC[C/T]TTTAACAAGGTGGTC | 10152 |
| rs531074039 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388899 | ATAGAATAAAATTCT[C/G]TCTTAAATTCCTGCT | 10152 |
| rs531122904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203387763 | GTAACTTTAAAAAGT[A/G]TTTCAAGTGAAATTA | 10152 |
| rs531140928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203388432 | TCATGCCTGTAATCC[C/T]AGCGCTTTGGGAGGC | 10152 |
| rs531197080 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374430 | GCTTGAACCTGGGAG[C/T]GGAGGTTGCAGTGAG | 10152 |
| rs531211659 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203405888 | GTTTGAAAAAGGGCA[A/G]TTATAACATAGGAGT | 10152 |
| rs531238781 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430221 | TTTTTTATAAATTAA[A/G]AGATGGTTGGTATTA | 10152 |
| rs531264710 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203335963 | TCCTGTCCCTCCACT[A/T]CTAGCCTTTGGTAAA | 10152 |
| rs531286130 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203334524 | TGCTGTGATTTGCTT[-/A]CACCCACCCCAAATC | 10152 |
| rs531288168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203360814 | GGAAACTTCTGAGTT[C/T]AGAACATTGACTCAA | 10152 |
| rs531293895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203339320 | TGTGGTGGCTCATGC[C/T]TGTAATCCCAGCACT | 10152 |
| rs531352919 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203369774 | CAATTCTCAGTGGCT[G/T]TTAAGTTTATACAGA | 10152 |
| rs531356282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203384217 | TGGAGGTGTTTTCAT[A/G]TATACCTAAGGCCAT | 10152 |
| rs531388586 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203415817 | TTCAGTTGTGCTCAC[A/G]TATTTACCAACCATT | 10152 |
| rs531390738 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203423687 | TGGCCTTCCAAAGTG[C/G]TGGGATTACAGGCGT | 10152 |
| rs531419498 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203370727 | GGCAAAAATACTAGA[A/T]TCCGAGAGTTTGTAG | 10152 |
| rs531425916 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203346031 | CTAAAAATACACACG[C/T]GCACACACACACACA | 10152 |
| rs531463384 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345294 | GTGGCTTCACCCTGA[A/G]GTCAAGCGAAACCAG | 10152 |
| rs531532796 | in-del | -/TGA | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203329303 | CAGACTATGACTGTT[-/TGA]TCTTAGAGAGAATTG | 10152 |
| rs531533750 | snp | A/G | 3.45447e-05 | 0.00415586 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203391083 | TGGGTGGGCTGCCGC[A/G]TACAACACCTCCAAC | 10152 |
| rs531576389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203382978 | GGTATCGTGGAGGAT[C/T]CGTGATAAAAGAAAT | 10152 |
| rs531616678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203393430 | AATGTTTCCCATTTT[A/G]TTGTTTAATATTTGC | 10152 |
| rs531626280 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429668 | AGGCTGAGGCAGGAG[A/G]ATCACTGGAACCTGG | 10152 |
| rs531630712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203340108 | ACATTAGGTAAGTGA[A/G]ATAAGCCAGGCACAG | 10152 |
| rs531673522 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203392137 | TATAAATTTTTCAAG[G/T]TCACTGTACCACAAA | 10152 |
| rs531704179 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432216 | TAACCTCTTTTTCTA[A/G]GGTGGTATCTTGAGT | 10152 |
| rs531718926 | in-del | -/A | 0.0138799 | 0.0821421 | intron-variant | ABI2 | GRCh38.p7 | 2:203421065 | CGAAGGTGTTGGATT[-/A]AAAAAAAAATCTGGT | 10152 |
| rs531728653 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203385874 | TTTCTTTACCTGTTT[C/G]TCTTTCCTCTTACTC | 10152 |
| rs531758435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203361538 | CAGGGGACAGTTTGC[C/T]GCACTGAATTTTCTC | 10152 |
| rs531838804 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203334280 | GGTATGGGTAATGTG[A/G]GAATGTATGATAGGT | 10152 |
| rs531865655 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203341676 | GATTGCACCACTGCA[C/G]TCCAGCCTGGGCAAC | 10152 |
| rs531867068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203347751 | GTTTCTAACTGGGAA[A/G]TTGTAGGTGCTTGTT | 10152 |
| rs531882813 | snp | A/G | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203401498 | TAGGGAGTGGATTAT[A/G]TTATTAGGAAACTGA | 10152 |
| rs531890515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203354099 | GCCCAGGTTGGAGTG[C/T]GGTGGCGCAATCTCA | 10152 |
| rs531925462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203408358 | AGTAGAGATGGGGTT[C/T]CACCATGTTGGCCAG | 10152 |
| rs531979470 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203388622 | GGAGGTGGAGGTTGT[A/G]GTGAGCCGAGATCAG | 10152 |
| rs531983324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203416417 | TCTTGTGCCTTGGCC[C/T]CCTGAGTAGCTGGGA | 10152 |
| rs532010024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203398334 | GCATCAGAAAGGACA[A/G]ATCACCCCCAACTGA | 10152 |
| rs532111899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203389189 | ATTTTAAGATACAAG[C/T]AGTATACCCTCCGCT | 10152 |
| rs532124541 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423573 | TGGGACTACAGGCGC[C/T]GGCCACCATGCCTGC | 10152 |
| rs532132020 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399181 | AATGTGTGAGTTTCC[A/G]GTTGCATCCTTGTCA | 10152 |
| rs532141728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203345056 | GCAGTGGCAACCCGC[C/T]GGGGTCCTCTTCCAT | 10152 |
| rs532254933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203411783 | CTTTTATGGTAGGGC[C/T]CAGAGGACCAGGCTG | 10152 |
| rs532277347 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203336601 | AGGCTGTAAGACTTT[A/G]GTTGCAGCATGGCAT | 10152 |
| rs532279828 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203357287 | GACTCCTTGGGAGTA[A/T]AAATTAATTATTTAA | 10152 |
| rs532284782 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203348074 | GGTGAACCCTCGTGT[C/T]TCCTAAAAATACAAA | 10152 |
| rs532293651 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, missense | ABI2 | GRCh38.p7 | 2:203383273 | AGAGCCCAGGCATAT[A/G]GACACCTGTATTATT | 10152 |
| rs532331711 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203412567 | TTTACCACACCGTGA[A/C]TTCATAAGATGTTTT | 10152 |
| rs532344263 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330113 | TTTTATAGGTTCATA[A/C]ATTTTGTAATGGCCA | 10152 |
| rs532346048 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359650 | CGTCAGCAGATTTGG[G/T]GTCTGTTGATGACCT | 10152 |
| rs532357180 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327010 | AGACGGGTTTTCACT[A/G]TGTTAGCCAGGATGG | 10152 |
| rs532387415 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203419857 | GCTGGGCATGGTGAT[G/T]CATGCCTGTAATCCC | 10152 |
| rs532400475 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339722 | GACATCTGCACACCC[A/G]TGTTCATTTCAGCAT | 10152 |
| rs532417519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203413984 | GGCTCTTTGGATAGA[A/G]TCCAAACTGCTGTAA | 10152 |
| rs532451866 | in-del | -/GTTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384290 | CTTGTTTTTGTTTTT[-/GTTTT]TTTTTTTTTTTTTTT | 10152 |
| rs532523179 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203406379 | ATAAAGTGAATGTTG[C/G]TTCCAAGAGATGTGT | 10152 |
| rs532553383 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337179 | AAAAATAAACAAAAG[A/G]CATCAAAATTGGAAG | 10152 |
| rs532576943 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203356161 | GAGTGCAGTTAGTGG[-/A]AGACATACTTTTCAG | 10152 |
| rs532587299 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363905 | AAGTAGCTGGGATTA[C/T]AGGCATGTGCCACCA | 10152 |
| rs532596134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203345620 | CACCGTCTTGGCCAG[C/T]CTGGTCTCGAACTCC | 10152 |
| rs532607701 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203352256 | CTTGAGTTCAGAAGT[A/T]CAAGGTTACAGTGAT | 10152 |
| rs532684035 | snp | C/T | 0.00039976 | 0.0141322 | intron-variant | ABI2 | GRCh38.p7 | 2:203351682 | CTGGGACTACAGGTG[C/T]GTGCTACTGTGCCCG | 10152 |
| rs532711773 | snp | C/G | 0 | 0 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428702 | TCACTACTGTAGTCA[C/G]TATAAGAAATGCTGA | 10152 |
| rs532721277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203330545 | TAGTTAATTTATACT[C/T]TGTAGTGCACTGCTG | 10152 |
| rs532739836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203375338 | TGCTAGCAGAACACA[A/T]TTTTTACTTGCCACA | 10152 |
| rs532741206 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203417868 | GAGAGAAGGAAATTA[A/T]TTTTTTTCTTTATGT | 10152 |
| rs532756542 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428661 | TTCAAATTCAGTGGA[A/G]TCTGTAGGGCAGATA | 10152 |
| rs532762050 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203381260 | TTTGATGCAAGCACT[A/G]TTATCTGGAATATGA | 10152 |
| rs532770487 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428171 | GACACGAAGGTCCCT[A/G]AGGTTCTGAAGAGAC | 10152 |
| rs532777657 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203409589 | AAATCTAAGAATGAC[C/T]TTCAGCTTGTTGCTG | 10152 |
| rs532801814 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203349892 | TGGGCATATGTGCTC[A/G]TTTCTTTGGGGTATA | 10152 |
| rs532802392 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203417222 | TACTGAGTTTACAAG[A/G]TTCATGATTTTGAAA | 10152 |
| rs532844909 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423556 | TCAGCCCCACGAGTA[C/G]CTGGGACTACAGGCG | 10152 |
| rs532862354 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203402444 | ATAACTCACCTTGCA[C/T]TGTATATTTCAGATA | 10152 |
| rs532901337 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366682 | TGTGTCTATTCAACA[C/T]GAAAACATTAGTGAG | 10152 |
| rs532922308 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203363002 | CGCCCGGCTATTTTT[C/T]GTATTTTTAGTAGAG | 10152 |
| rs532938580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203377976 | ATTAAGTGAATTCCA[A/G]TATCATCACTAATAT | 10152 |
| rs533009199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203424546 | ACCACAGACGTGCAC[C/T]ACCATGCCTGGCTAA | 10152 |
| rs533037363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203355637 | GAGTTCCAGACCAGC[C/G]TGATCAACATGGAGA | 10152 |
| rs533052522 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379747 | TTTTCTGTAAAGGAG[C/T]CAGCTAATATATACT | 10152 |
| rs533064777 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203363738 | GGCCGAATAGTACTC[A/C]ATTGGGCATATGTAC | 10152 |
| rs533098892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203385729 | TCAACCTTTGAGAGA[C/T]CCATCTGTTTTTGCC | 10152 |
| rs533132808 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203334190 | AAGTGATCCACCCGC[C/G]TTGGCCTTCCACAGT | 10152 |
| rs533164681 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203335077 | TTCATTTACTTTGTG[-/T]TTTCCTTCCAGATAC | 10152 |
| rs533165838 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203335907 | TACATAGTCATGTAA[C/G]CACCACAATGTAAAA | 10152 |
| rs533173403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203333249 | ATGGAAAATTGCCCG[A/G]TCATCTTGAATATAT | 10152 |
| rs533199362 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420019 | TTGAAATGTTAGCTC[C/T]ATTGTAATTCCCATT | 10152 |
| rs533240308 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203356835 | TATTTCTGAAAGTTT[A/T]TGGTTTTACACAATT | 10152 |
| rs533252327 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428396 | AATGTGCTCTCTGGA[C/T]GTTATTAATGGCCAG | 10152 |
| rs533296407 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392968 | TGTTCCTTTGCTCCT[-/T]TTTTTTTTTAAAAAA | 10152 |
| rs533313056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203379428 | ACTTTTTGTAGAGAC[A/G]GGGTTTCGCCATGTT | 10152 |
| rs533371800 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203359198 | AAGATGCTTCTGAGA[A/C]AAATGTGATCTGCTA | 10152 |
| rs533398896 | in-del | -/AATT | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428589 | AATCACATTGATAAA[-/AATT]AATATAACTGACACA | 10152 |
| rs533399245 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203379353 | CCTGGACTCAAGCAG[-/T]TCTCTTATTTCAGCC | 10152 |
| rs533412183 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203386040 | TGATTTTCCTCAGAG[C/G]ATCTTTTGGTCCTTT | 10152 |
| rs533498296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203367128 | GCTGGCAGCTTTTAT[C/T]ATGTAAGTTAACTCA | 10152 |
| rs533502135 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | ABI2 | GRCh38.p7 | 2:203375597 | ATGTAGGAAAAATAT[A/T]GTAGCCATATTTTAT | 10152 |
| rs533509147 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203373247 | TGGCGGATCACTCGC[A/G]GTTAGGAGCTGGAGA | 10152 |
| rs533539899 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369187 | ATTGCTAATGTGATA[C/T]AGAATTTCAAGATCT | 10152 |
| rs533613450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203414181 | ATCTTGGCTCTCTGC[C/T]ACCTTCCCCTCCTGG | 10152 |
| rs533629710 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203359323 | TCCCAAGTTGATAGA[A/C]TTTTCACTGATTACA | 10152 |
| rs533682128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203367991 | CCTGGGAGACAGAGT[A/G]AAACCCTGTCTCCAA | 10152 |
| rs533695341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203396490 | TATATACAGAATGTT[A/G]TGCTAAAAATAACAA | 10152 |
| rs533702836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203386723 | GCTCACTGCAACCCC[C/T]GCCTCCTGGGTTCAA | 10152 |
| rs533736804 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203389391 | ACTTGTTCACTGGGC[A/T]ATTCATTTGAAGAAT | 10152 |
| rs533757863 | in-del | -/CATC | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203336189 | GAATCATAATTTGTT[-/CATC]CATTCACCAACTGAT | 10152 |
| rs533761191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203345253 | ACACGCCATTTTGAG[A/G]GCTGTAACGCTCACT | 10152 |
| rs533771806 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203424047 | TTTTTCTTACATGTG[C/T]TTTATCAGTTCCCCA | 10152 |
| rs533797910 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429087 | CTTATCAAGACTTTT[C/T]GGTTTTAAAGTTGTT | 10152 |
| rs533833797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203364913 | TGATTTTCTAAACTT[C/T]TGTGGAGTTGAGGTC | 10152 |
| rs533863818 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396284 | AAAACGTGACACAAA[A/G]TACATTAATAGAATG | 10152 |
| rs533869399 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203337870 | ACCTCATCTCTACTA[A/C]AAATACAAAAATTAT | 10152 |
| rs533873220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203381417 | TGGGACTACAGGCAC[A/G]TGCCACCATGCTGAG | 10152 |
| rs533929471 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203358580 | TGTCTCGTTTCTGCT[G/T]CTTTATGCATGTTGG | 10152 |
| rs533931150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203383836 | AATTTAAAACCTATT[C/T]AAGACCTAGTCGTTT | 10152 |
| rs533933845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203391362 | AATTTTAAATTTGAG[A/G]TAAAATCCTAGCCCA | 10152 |
| rs533979591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203398584 | TACAGTAAAATTCAC[C/G]CTTTATACCATATAT | 10152 |
| rs533980860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203380886 | TTAATATTGCCACTG[C/G]TTTTGAGTGTGTAGC | 10152 |
| rs534017631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203422552 | TGGCTCCACAGAAGC[A/G]TAGTAATCAGATAAC | 10152 |
| rs534029310 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429863 | CAGCTGGTCTTTTGG[A/T]CCCCTACGGGATGGG | 10152 |
| rs534062028 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203376596 | CCTGATGAATTGATA[A/T]ATTTCCTCGTAACTC | 10152 |
| rs534070122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332161 | TCATTATTCTAACCT[C/T]TAGAAAATGGGATAG | 10152 |
| rs534083643 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427688 | CTTTCTCAGGAATAC[C/T]GTATACCCTTGGGAT | 10152 |
| rs534112791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203399447 | AAATATATGTCCTTT[A/G]TAGATTATGAGTTAC | 10152 |
| rs534132273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203328925 | CTCCGCGCCGGTCAG[C/G]GTTCCGGATGGCGGA | 10152 |
| rs534140305 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430272 | AAAATCTTACATGCT[G/T]TGTACTATTAATATT | 10152 |
| rs534175968 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203406504 | AAAGCGACTAAAAAA[A/T]TAGGAAACAATGTTG | 10152 |
| rs534187012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203400040 | TATATTTTTAAAACC[C/T]CAAATGGTAAATCGA | 10152 |
| rs534209783 | in-del | -/TCTTTTTTCTT | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203410405 | GTAACTGTAGAGTAA[-/TCTTTTTTCTT]TCTTTTTTTTGCCGC | 10152 |
| rs534242993 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406862 | GAGACAAGCTTTCAC[C/T]GGGTTGGCCAGGCTG | 10152 |
| rs534248651 | in-del | -/AGGCTCCTGAGT | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203364210 | TGATTCTCCTGCCTC[-/AGGCTCCTGAGT]AGGCTCCTGAGTAGC | 10152 |
| rs534285916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332486 | AAAAATTAGCTGGCT[A/C]TGGTGGCGTGTGCCT | 10152 |
| rs534289042 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430501 | TTGCCTTTGAACTTA[C/T]GGCCAAGGCAATAAA | 10152 |
| rs534318117 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203395885 | AGGATTTTTTTTCTT[C/T]AGGAATCATAAATAT | 10152 |
| rs534344081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203334903 | TGACCTTAGGTGATC[C/T]GCCCGCCTCGGCCTC | 10152 |
| rs534383167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203386799 | ATCTGCCACCATGCC[C/T]GGCTAATTTTTGTAT | 10152 |
| rs534401879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203425798 | AGGCCGAGGCAAGTG[A/G]ATCACCTGAGGTCAG | 10152 |
| rs534438456 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203417143 | TAGAAATGAAATTTG[C/T]GGTACTGAAGAGAAT | 10152 |
| rs534449555 | in-del | -/AATT | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431710 | TTAAAAAAAAAAAAC[-/AATT]AAAACGAAACGGCGG | 10152 |
| rs534451757 | snp | A/C | 0 | 0 | intron-variant | ABI2 | GRCh38.p7 | 2:203338756 | TTTATAAATATGACA[A/C]CAAAAGCACAGGCAA | 10152 |
| rs534506187 | in-del | -/AAA | 0.0154538 | 0.0865337 | intron-variant | ABI2 | GRCh38.p7 | 2:203396369 | AAAGATTTGTGTTTT[-/AAA]AAAAATTTTTAATCT | 10152 |
| rs534544240 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345683 | CAGAGAGCTGGGATT[A/T]CAGGCCTGAGCCACC | 10152 |
| rs534556223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203352534 | AGGGTTAGGCTAATA[C/T]GTCTGTGTCTCGGTT | 10152 |
| rs534567946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203394984 | CTCATCTGATTTCAC[C/T]TCTCTCTCCTCATGT | 10152 |
| rs534569491 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203403381 | GTCAACTTACTGCTT[G/T]TTTCTGTATTTTTGC | 10152 |
| rs534599000 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203386888 | CAGGCGATCTGCCCA[C/T]CCTGGCCTCCCAGAG | 10152 |
| rs534627904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203343304 | GGGAAGCGGAGGTTG[C/T]AGTTAGCTGAGATTG | 10152 |
| rs534671108 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420897 | AAGGGCCTTCCAAGC[A/T]GAGGGAATCACGTGA | 10152 |
| rs534703446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203331180 | GGATGATAGCTCTTA[C/T]ATGATTTGTTGATTT | 10152 |
| rs534712602 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327154 | CCTCATCATCTGAAT[A/G]AAAAAAATTCACTGT | 10152 |
| rs534746232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203412690 | TGACCCACACTGGCT[C/T]GAGGAGAAAACTGCC | 10152 |
| rs534754644 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203344937 | CTGTAAAATGGACCA[A/G]CCAGTGCTCTGTAAA | 10152 |
| rs534779531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203355068 | TTCTCAGCTGCATCT[C/T]AGAAGTTTCCTTTGC | 10152 |
| rs534821269 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203371727 | ACATGTAATTTTACT[C/G]AATACTTGTACAGGT | 10152 |
| rs534857609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203409700 | GCTTTGATTTATTAC[A/G]TGCCAGCCACTGGGT | 10152 |
| rs534875811 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357215 | AAAAGAATCATGACA[-/T]TTTATAGCTGAAAAG | 10152 |
| rs534877279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203349131 | TTTTTTTTTAGAGGT[A/G]GGCTTTTGCCTTGTT | 10152 |
| rs534914969 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203327984 | AGAAGTTCCCTAGGC[C/G]GATGACCTCCATGGG | 10152 |
| rs534923906 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203426483 | AGTGATTTAAGCAAT[C/G]AAAATCACAGGAGGG | 10152 |
| rs534924947 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203379564 | CATTATATTTCAGCC[C/G]TCTTTCTTTTTAAAT | 10152 |
| rs534931219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203418701 | TGCCATTTTCTGTTC[A/G]TTAAAGCAAGTTAAT | 10152 |
| rs534935624 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354952 | TGGAAAATTGTCTTC[G/T]AATATCAGTTTCATC | 10152 |
| rs534955837 | snp | C/G | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327736 | AGAACAGCGTTAGTG[C/G]GGAAGTGCAAAGAGG | 10152 |
| rs534972514 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388319 | TATGTTAGTCATCCA[A/T]TCCCATTAACCAAAC | 10152 |
| rs535025906 | in-del | -/ATATATATATATATAAATATATATATATATATATAA | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203338948 | TGTATATATATATAT[lengthTooLong]ATATATATATATATA | 10152 |
| rs535069616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203352825 | AGTCCTGTAAGCTGC[A/G]TTGATGGTAAGTGCC | 10152 |
| rs535086379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203398030 | TCAAAGCATATCAAT[C/T]ACCGTAGTGTTCCAC | 10152 |
| rs535093903 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203349843 | TAATTTCATAACATA[C/T]AACGTTATAAATATT | 10152 |
| rs535154917 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378493 | TTCCATTTATACATT[C/T]GTTAGCTCTGGAACA | 10152 |
| rs535176771 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203373367 | ACTCGGCAGGCTGAG[G/T]CAGGAGAATCAGGCA | 10152 |
| rs535181699 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203364294 | AGACGGGGTTTCACC[A/C]TGTTGGTCAGGCTAC | 10152 |
| rs535254612 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203373610 | CATGTTCAAGTTTGT[C/G]ATGGCTTAGAAAAAA | 10152 |
| rs535265296 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390055 | ACATTGCCTGTGGCC[C/T]TTGTGCTGCTCCCAG | 10152 |
| rs535272990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203412152 | CTCATAACAAGGATG[A/G]ATGACTTCACTGGTG | 10152 |
| rs535302602 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429795 | GCTCACCACTACAGA[A/G]GCAGGGAAGACAACT | 10152 |
| rs535310490 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369898 | TATTTTCTAGCATTT[C/G]CCTCAAGGATTGAAA | 10152 |
| rs535348596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203415339 | ATCCATTTAATTCAC[C/T]GGGCGCGGTGGCTCA | 10152 |
| rs535351739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203419412 | CTCGCTCTGTCGCCC[A/G]GGCTGGAGTGCAGTG | 10152 |
| rs535362013 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203360039 | AAAGTACAGAAATTA[G/T]CTGGGCGTGGTGGTG | 10152 |
| rs535379388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203364974 | CCTGTCTTTAAGCAA[C/T]GCTCCCGCCTCAGCC | 10152 |
| rs535393455 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203360864 | CTTGTTTAGTCTCCT[G/T]TGACTCTTATGCTGT | 10152 |
| rs535409140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203371163 | CTCACAAATGAGCTT[A/G]ATTTTATTTGCTTCC | 10152 |
| rs535507017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203401154 | GAAATGTTTCAGTGG[A/T]TTCTTTTGCCCTCTG | 10152 |
| rs535536150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203353625 | GCTAGGACTACAGGC[A/G]TGTGCCACCACGCCT | 10152 |
| rs535591242 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203371709 | ATATACTTATCAGAG[C/G]AAACATGTAATTTTA | 10152 |
| rs535600010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203416826 | AAGTCTAGGTTTATA[C/T]TCCATGAACCCAGAA | 10152 |
| rs535615512 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203361961 | CATGAATCCTTAGGA[G/T]ATTTAGCTAAAAATA | 10152 |
| rs535650017 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203340425 | AGGCTGGAGTACAGT[A/G]GCATGATCACGGCTC | 10152 |
| rs535652280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332046 | AACTCCTGACCCCAG[A/G]TGACCCACCCACCTC | 10152 |
| rs535665496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203384599 | ACAGTTGTGAGCCAC[C/T]GTGCCTGGCCAGTAC | 10152 |
| rs535668828 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415625 | CGTCTCAAAAAAAAA[-/A]AAAAAAAAAAAAAAA | 10152 |
| rs535751793 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203414063 | TTTGGACAGTTCTTT[C/G]AAAGTTTCTTGCTTT | 10152 |
| rs535824633 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203381868 | ATTCTTATAATCCTC[A/G]AAGTAAAATGTTTTT | 10152 |
| rs535859829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203380607 | GAATGAATTATATTT[C/G]CTTGGTTATGATAAT | 10152 |
| rs535922815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203350784 | ACCTCATGATCCACC[C/T]GCCTCGGCCTCCCAA | 10152 |
| rs535926161 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203421134 | TGATAATATCCATCT[A/T]CTTATGTAACTTTTT | 10152 |
| rs535986107 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428232 | CCCGAACCCCTGCTT[C/T]GGTGCTGTTTTGAGG | 10152 |
| rs536108539 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203336727 | TATTCCTTCTGCCCT[C/G]CATGTAAATGGTAGG | 10152 |
| rs536159106 | snp | C/T | 0.00993419 | 0.0697739 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430964 | AAGAACTGTTTTTAT[C/T]TTTTACTACCTTTTC | 10152 |
| rs536166328 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430792 | CTAGACAATATTTTA[C/T]GCATATTTACCGTGA | 10152 |
| rs536168803 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203379913 | TTATATAATTTTCAC[G/T]TGAAGGTTTTTTTTG | 10152 |
| rs536171287 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408052 | CTTTGTAACCCCAGA[C/T]GGAACTGAATTTTTG | 10152 |
| rs536177358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203385332 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 10152 |
| rs536178058 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347718 | TGTATTATACGACAC[A/G]TAACTTATGACACTT | 10152 |
| rs536192841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203344897 | GCACCAATAAGCACT[C/T]TGTAAAAACGAACCA | 10152 |
| rs536232021 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398924 | GTATTGTATGGGGAT[A/G]TACCACAATTTGTTT | 10152 |
| rs536242072 | in-del | -/G | 0.00478944 | 0.0487009 | intron-variant | ABI2 | GRCh38.p7 | 2:203405715 | ATGAGCTTTTTTTTT[-/G]GGGGGGGTAATTGGA | 10152 |
| rs536257453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203399380 | AATGTTTTGTTCCTT[C/T]TCACCTTTTTAATAG | 10152 |
| rs536266427 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203328753 | CCCGATGGGGGTGGG[C/G]AGCTGGGTGAGGGCT | 10152 |
| rs536281475 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427460 | GAAGGATACAAATGA[C/T]AAAAATTACACTTTT | 10152 |
| rs536299272 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203395619 | GATCTCTTACTGTTT[A/G]TAAATACTCATGTTT | 10152 |
| rs536299616 | in-del | -/TTTG | 0.00716266 | 0.059414 | intron-variant | ABI2 | GRCh38.p7 | 2:203357759 | TGGTTTTTGGGGTTT[-/TTTG]TTTGTTTGTTTGTTT | 10152 |
| rs536300837 | snp | G/T | 0.167158 | 0.235875 | intron-variant | ABI2 | GRCh38.p7 | 2:203331346 | CAAATGGTCAATTTA[G/T]CCTTTTTTTTTTTTT | 10152 |
| rs536346641 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429264 | TCCTGCAGTGTAATG[A/G]CCCTGAATGTCCTCT | 10152 |
| rs536387285 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203338575 | AAGTACGTGCCAGCA[C/G]TGTGCTTTGTGTAAA | 10152 |
| rs536407921 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203358510 | GTTATTAATTAAACC[A/G/T]TGTGAAGGAACAGGA | 10152 |
| rs536425065 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | ABI2 | GRCh38.p7 | 2:203344361 | CAATATAATTTTTAA[A/T]TTTTTTTTTCCTTTT | 10152 |
| rs536427818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203405686 | TTAACAAAAATGATC[C/T]GAAGTGTGTGTTTTA | 10152 |
| rs536438935 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203388063 | ATATAGATTTTACCT[A/G]TTATAAAAATTGTTT | 10152 |
| rs536451138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203397168 | CTCATACATTTTTCC[A/G]ATAGGGTAGCATAAA | 10152 |
| rs536618619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203341449 | GCCAGGCTCAGTGGC[C/T]CACTCCTATAATCCT | 10152 |
| rs536623695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203345649 | CCTGACTTCAGGTGA[C/T]CCACCCACCTCGGCC | 10152 |
| rs536701031 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413668 | CTTAAACATTAGTCA[A/G]ATAATAAACATTATT | 10152 |
| rs536712032 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402401 | TTTGCTTTTCTGCTT[C/T]TGTACTCTGATATAA | 10152 |
| rs536769415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203382747 | AAATATTCAGTGACA[C/T]GGGTTTTTTTTTTAA | 10152 |
| rs536776738 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431389 | GTTTTCAGGAATATA[A/C]GTGAAAAGACATGCC | 10152 |
| rs536889362 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203416788 | GCTCATTGATTTTTT[A/G]AAGGAATATTACATT | 10152 |
| rs536903292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203409638 | AATCATTAATTGCCA[A/G]CTACTCTCTTCCCAC | 10152 |
| rs536909994 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203345372 | GAACAAACTCCGGAC[A/G]CACCATCTTTAAGAA | 10152 |
| rs536910224 | snp | C/T | 0.000739918 | 0.0192201 | intron-variant | ABI2 | GRCh38.p7 | 2:203351696 | GCGTGCTACTGTGCC[C/T]GGCTGATTTTCGTAT | 10152 |
| rs536913176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203348088 | TCTCCTAAAAATACA[A/C]AAGTTAGCTGGGCAT | 10152 |
| rs536915353 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203401967 | GGAGTAGATAAATTT[C/T]AATTAATTGTGATGA | 10152 |
| rs536946447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203351121 | CCTTTTCTTTCCCTC[A/G]TTAAATTGTTTTGGC | 10152 |
| rs537052799 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356997 | TGAGTAAAAAGAAAA[C/G]TAAAAAACGATTACT | 10152 |
| rs537104847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203334724 | GGAGTACAGTGGTGC[A/G]ATCTCAGCTTACTGC | 10152 |
| rs537149372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203349446 | TTTTGCTCTTGTTGC[C/T]CAGGCTGGAGTGCAA | 10152 |
| rs537166822 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203411186 | ATGTTTGTGAATAGT[A/G]GTTTCCCTCCTTTAT | 10152 |
| rs537210306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203361902 | GATTGTACTATATTA[A/G]TGAGGAAGGCTAGTG | 10152 |
| rs537240194 | in-del | -/T | 0.312837 | 0.241974 | intron-variant | ABI2 | GRCh38.p7 | 2:203386641 | ATCTGTAGACATTGC[-/T]TTTTTTTTTTTTTTT | 10152 |
| rs537264958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203360944 | TAATTGTTACCCTTT[C/T]AAGGATGACGTATGC | 10152 |
| rs537265394 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326386 | TTAACTCACCTGATG[A/C]GCTTCTTCAACATTA | 10152 |
| rs537274671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203371049 | GCTGACTTGTGTGAC[A/G]TTTGACTTCTTTGAA | 10152 |
| rs537279726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203424912 | AGTCTCACTCTGTTA[A/C]CCAGGCTAGAGTGCA | 10152 |
| rs537285254 | in-del | -/TTC | 0.00318978 | 0.0398085 | cds-indel, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431238 | CTGATGAGGTGAGTT[-/TTC]TTCTTCATATGAACA | 10152 |
| rs537326390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203355008 | TGTGTCCCCTTTGCC[A/G]TTCTCCAATCTGGAT | 10152 |
| rs537361829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203398134 | ACATGTTTTAAAAGA[C/T]ACTTTTAGCCAAAAT | 10152 |
| rs537378628 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327059 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 10152 |
| rs537389767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203354345 | CACTGCACCCAGCCA[A/G]TTAGACTTCTTAAAT | 10152 |
| rs537423135 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203411976 | TGCTGTCACAGAGAC[C/G]AGTGAACATAGACTG | 10152 |
| rs537430592 | in-del | -/CT | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203342028 | CAAGTTTACCTCTGA[-/CT]CTGCTAAACTAAAAT | 10152 |
| rs537477443 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203420316 | TTCTGGCTCAGTGAT[-/A]ACAGCTTTTAGCTAG | 10152 |
| rs537477847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203364185 | TGCAACCCCCGCCTC[C/T]TGGGTTCAAGTGATT | 10152 |
| rs537484495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203410918 | TGCTTTCCTTGAGAA[A/G]GCATGATGTTAATGA | 10152 |
| rs537511615 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203404109 | AAAATTTTTCTCTTA[C/T]CCTCCCAAGTCTTCT | 10152 |
| rs537530062 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390672 | TAAAAATAAGGAATT[A/G]CTTAAAAGCATTATT | 10152 |
| rs537594588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203360010 | GCCAACATGGTAAAA[C/T]CCCGTGCCTGCTAAA | 10152 |
| rs537597674 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379337 | ACTGCAGCTTTGACC[G/T]CCTGGACTCAAGCAG | 10152 |
| rs537666426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203330049 | ACATTAGCTATATAG[A/G]AAAGCATTTTCATGT | 10152 |
| rs537670469 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203338454 | CTTTAGTGATAAGTG[A/T]GTTCTTGCTTGGTTC | 10152 |
| rs537687024 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203399618 | CCTCGCGGGTTCAAG[C/T]GATTCTCCTGCCCAG | 10152 |
| rs537690587 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203375179 | TGGGGAAGCTAATTA[A/G]TAAGGAACTGTGGGA | 10152 |
| rs537692358 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431048 | GAAAAAGGTTTGATG[G/T]AGGAATTCACAGGTG | 10152 |
| rs537782661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203372839 | CCCAGACGGGGTCGC[A/G]GCTGGGCGCCCTCAT | 10152 |
| rs537807102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203369098 | CCTTAGTCTCCCAAG[A/G]TGTTGGGATTACAGG | 10152 |
| rs537849688 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203338840 | GCAAAGGACACAAAA[A/T]GAAAAGGCAATTTAT | 10152 |
| rs537856591 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203384509 | GAGATGGGGTCTCAC[C/T]GTGTTGGCCTGGCTG | 10152 |
| rs537872056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203414299 | TAGAGACGGGGTTTC[A/G]CCATATTGGCCAGGC | 10152 |
| rs537885877 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430594 | GGAATAAATATGAAT[A/C]TTCTAAGCTATCTTG | 10152 |
| rs537925385 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203333014 | AACAATAGGAGACAT[A/G]TTAGTAGCTTTCCTT | 10152 |
| rs537957592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203415174 | TTATTAATAAAAACT[A/G]TTAGGATGAAAGACA | 10152 |
| rs537966320 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ABI2 | GRCh38.p7 | 2:203406573 | TTCTCTAAATGATTT[C/G]TGAAGTTACAGCATC | 10152 |
| rs537972997 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203423477 | GTCGCTCAGGCTAGA[G/T]TGCAGTGGTGCAATC | 10152 |
| rs537991412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203370295 | GTCTCATGATGTTGC[C/T]CAGGGTGGTCTTGAA | 10152 |
| rs538032886 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203382495 | TTTTGTAATGTTAAT[A/G]TATTTTGTGAAACTG | 10152 |
| rs538034306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203346473 | ATCAGCTGTAAGAAG[A/G]AAGGTGAGAATTTGA | 10152 |
| rs538051111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203381568 | CATCGTGCCTGCCCA[A/G]TATTTAATTTTATAG | 10152 |
| rs538100601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203400159 | CAGTGGCAATCTCGG[C/T]CCACTGCAATCTCCG | 10152 |
| rs538107769 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369504 | GCCACCCTAGATTTT[G/T]AGTATATGTATTAAT | 10152 |
| rs538126551 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377060 | TAGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 10152 |
| rs538130848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203421837 | GGTGTGGTGGTGCAC[A/G]CCTGTAGTCCCAGCA | 10152 |
| rs538217843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203409084 | ACCTCATGATCCACC[C/T]GCCTCGGCCTCCCAA | 10152 |
| rs538258983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332510 | TGTGCCTGTAGTCCC[A/G]GCTACTTGGGAGGCT | 10152 |
| rs538259025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203387967 | GTTTTTTTAGGATCA[A/G]TCATGATGGCTGTCT | 10152 |
| rs538264759 | in-del | -/A | 0.0134861 | 0.0810011 | intron-variant | ABI2 | GRCh38.p7 | 2:203399057 | TTATATCAGGTAAAT[-/A]ACCTAGGGAATAGAA | 10152 |
| rs538289309 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423906 | TTGAAATGCTAAATA[C/T]GAACAATGTACTTTG | 10152 |
| rs538305439 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346784 | GGACAAAATAATAAC[C/G]TGTGGCCAAAAGGAG | 10152 |
| rs538310016 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378214 | GCCTCCTGGGTTCAC[A/G]CCATTCTCCTGCCTC | 10152 |
| rs538339163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203419530 | CCTGCCACCATGCCT[C/G]GGTAATTTTTTGTAT | 10152 |
| rs538358191 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431522 | TATAAACACTTTCCC[A/G]TAAGGTGTGTGCAGT | 10152 |
| rs538432891 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203395990 | CCTTTGGTGATGTGG[C/G]TCAGTTGCTGCTTTG | 10152 |
| rs538500448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203392867 | GGTTCTGCAAGATCC[C/T]TGGGGACCAGAGTTG | 10152 |
| rs538513857 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203344172 | AGCGCTTCAACTGTT[A/T]AGAGACAGTCTTATT | 10152 |
| rs538530376 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203369233 | AAAATTTTTCCATGT[G/T]TGAAGCATTAGCAAA | 10152 |
| rs538572692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203347157 | TTGCATGTCCTAACA[A/G]GGTAAGGAGTGATCA | 10152 |
| rs538601140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203349755 | ATTCTAGTACATGGA[C/T]AATACCACATTTTGT | 10152 |
| rs538618538 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390420 | GTGGATTGCCTAAGC[C/T]CAGGAGTTTGAGATC | 10152 |
| rs538623062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203379724 | TTTAACCCAGGGGTT[A/G]GCAAACCTTTTCTGT | 10152 |
| rs538636553 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203350999 | GCTCTTACATTTAGA[A/T]CTTTGATCCATTTTG | 10152 |
| rs538659585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203336161 | TTACTGAGTAATATT[C/T]TAGAGTATGAAAGAA | 10152 |
| rs538694444 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203348749 | TTCTTCCTCCCATCA[C/T]GTATGTACAGCCGCC | 10152 |
| rs538703267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203405534 | CAGCCTGGGCAACAG[A/G]GTGAGACCCTGTCTC | 10152 |
| rs538732114 | snp | C/T | 3.67087e-05 | 0.00428404 | intron-variant | ABI2 | GRCh38.p7 | 2:203328669 | CCGCGTCGGGGACCC[C/T]CCCGCCGGGGGCCGC | 10152 |
| rs538758814 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203373508 | GAGAGGGAGAGGGAG[A/C/T]GGGAGAGGGAGAGGG | 10152 |
| rs538771860 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328092 | AAAGGCCGCCGGGAG[A/G]TGGGGGCTTCTCCAG | 10152 |
| rs538798821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345338 | GGAAGAAACTCCGGA[C/T]AGATCTGAACATCTG | 10152 |
| rs538857311 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328000 | GATGACCTCCATGGG[G/T]ACGGAGCCGAGATGA | 10152 |
| rs538874772 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203403510 | CTGTGGCTGTGACCT[A/G]TAGTGATATTCTTTG | 10152 |
| rs538904834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203413431 | GACTATCACTTTAAG[A/G]CTTAGGAATGTCTTA | 10152 |
| rs538968867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203343355 | GACGACAGCGAGACT[A/G]TGTCTCAAAAAACAT | 10152 |
| rs538995445 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396503 | TTATGCTAAAAATAA[C/T]AATACGAAGGGAACA | 10152 |
| rs539003994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203344962 | TGTAAAATGGACCAA[C/T]CAGTGCTCTGTAAAA | 10152 |
| rs539032144 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203344362 | AATATAATTTTTAAA[A/T]TTTTTTTTCCTTTTT | 10152 |
| rs539105111 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203341370 | ATTCGCTAAATGAGC[A/G]AATTAGATCTTTTCT | 10152 |
| rs539105263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203389651 | GCCATATTATTTTTA[A/G]AAAAGTTGAGGTCCT | 10152 |
| rs539192626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365950 | GTTATCTTAATGCTT[A/G]CAGGACTTTATTTGT | 10152 |
| rs539212940 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331484 | CTGCCTCAGCCTTCC[A/G]AGTAGCTGGGACTAC | 10152 |
| rs539224983 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360888 | ATGCTGTTGCTAATA[C/T]CATTTATGAAATCAG | 10152 |
| rs539234551 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346117 | ATCATGCCATTCACT[C/G]CAGTCTGGGTGACAA | 10152 |
| rs539258552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365080 | AGTAATACATGCCCA[A/G]GTTAAAAAAAAATTA | 10152 |
| rs539277017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203423441 | CTGGGTCCTTTTTTT[C/T]CTGAGACGGAGTCTC | 10152 |
| rs539279507 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203404774 | ATATCGGCCAAGCTG[C/G]TCTTGAACTCCTGAC | 10152 |
| rs539287761 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203350558 | TTTTTTTTTTTTTTA[A/C]AGTTGAAGTCTTAAT | 10152 |
| rs539299257 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203416748 | GGAGCTCTAGAACGT[C/T]ATAGTTGGTGGGAAG | 10152 |
| rs539333812 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203353698 | AGATGGGGTTTTACC[A/C]TGTTGGCCAGGCTGG | 10152 |
| rs539362580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203416049 | AGTAACCCAAGTTTG[C/T]TGATGATTTTTTTCC | 10152 |
| rs539405068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203372564 | GGCGGGGGGCTGACC[C/T]CCCCACCTCCCTCCC | 10152 |
| rs539467967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203408719 | CATGCCAACAGAAGA[C/G]GAGCATTTCATCTTG | 10152 |
| rs539512820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203393715 | TAAGTCAGTAGAGCA[A/G]CATCATTTCAGGAAA | 10152 |
| rs539566333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203348012 | TTGGGAGGGTGAGGT[A/G]GGTGGATCACTTGAG | 10152 |
| rs539587429 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203364025 | CACCTTGGCCTCCCA[A/G]AGTGCTGGAATTATA | 10152 |
| rs539589218 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203355205 | CCTGACAAAGAATAC[A/G]TGGAAAGTTAAAAAA | 10152 |
| rs539595971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203370018 | ATATTATTCTCTAGT[A/G]TAGAAGAAAACATTT | 10152 |
| rs539623378 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413179 | CTTCTGGAGTAAAGG[C/G]CAGATTTTGAAACTG | 10152 |
| rs539640141 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203378188 | CACAATCTCGGCTCA[C/T]TGCAAGCTCTGCCTC | 10152 |
| rs539641483 | in-del | -/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428383 | ACAAGGTTTGCTAAT[-/G]GTGCTCTCTGGACGT | 10152 |
| rs539665223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203341924 | TACTCAATAGTGGAA[A/G]CTCATCAAATGTCTG | 10152 |
| rs539705242 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203380651 | TGAGTAAATAAGTGT[-/C]GTGTAATCTTTCCAA | 10152 |
| rs539710755 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203383178 | AAGTGATGACAAGAT[A/G]ACTGAGCTCTGAATC | 10152 |
| rs539727179 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203349602 | TAAAGACAGGGTTTC[A/G/T]CCACGTTGGTCAGGC | 10152 |
| rs539786843 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203360877 | CTTTGACTCTTATGC[A/T]GTTGCTAATATCATT | 10152 |
| rs539800323 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203357873 | TCCTGGCTTCAAACG[A/T]TTCTCCTGCCTCAGC | 10152 |
| rs539839995 | in-del | -/TT | 0.497959 | 0.0318836 | intron-variant | ABI2 | GRCh38.p7 | 2:203414102 | TGTACTTGCATTGTC[-/TT]TTTTTTTTTTTTTTT | 10152 |
| rs539860341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366140 | TAACTGCATGTGTCA[A/G]CTTAATTTATTTTAA | 10152 |
| rs539868801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203425492 | CAGGCGTAAGCTACC[A/G]CACCTGGCTGGATTT | 10152 |
| rs539870829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203417375 | TCAGGAAGATTATTT[C/T]TCCACATTATTATTC | 10152 |
| rs539883602 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203412973 | CATTACAGTAAAATA[A/T]TTTTTTTCCATCACA | 10152 |
| rs539904430 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203398230 | GATAAATGTAAACAT[A/G]GGGTGTTTTTTGATC | 10152 |
| rs539955140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203418378 | CTTCACACGGCTGCA[A/G]TCAAGGTATCAGCTG | 10152 |
| rs539959899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203350704 | GCCACTGTGCGCAGC[C/T]AATTTTTATATTTTT | 10152 |
| rs539975788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203404985 | ATAATACATACTTCA[A/G]TAGTTTCTTTGTAAA | 10152 |
| rs540035216 | in-del | -/C | 0.0023933 | 0.0345097 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327052 | TGACCTCGTGATCCG[-/C]CCGCCTCGGCCTCCC | 10152 |
| rs540036331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203386027 | CTGGTTTCAGCTTTG[A/G]TTTTCCTCAGAGGAT | 10152 |
| rs540048888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203385426 | GTGAGCCACCGTGCC[C/T]GGCCAGATTCTTAAT | 10152 |
| rs540048892 | snp | C/T | 3.3653e-05 | 0.00410188 | intron-variant | ABI2 | GRCh38.p7 | 2:203394655 | TTGAATTTATTGTGC[C/T]GAAACTTGCTTAATC | 10152 |
| rs540070326 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | ABI2 | GRCh38.p7 | 2:203411216 | TGTGTTTATTTTATT[C/G]TATTATCCTTTCCTT | 10152 |
| rs540079245 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328318 | CGTCGCCGCGGTGAC[C/G]GTCCTCGGAGTCCGT | 10152 |
| rs540115378 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203362177 | GTTGTGGCAAAAACT[C/T]TTGTACTGAAACAAG | 10152 |
| rs540120207 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326207 | GAAACTAGGTCCAAA[A/G]AGATTGTCACTAATT | 10152 |
| rs540152725 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203393876 | TAATTTAATAAACAC[A/T]AATTTCCCCATGTGC | 10152 |
| rs540156871 | in-del | -/TT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420398 | ACTGTGACAGTCCCT[-/TT]TTTTTTTTTTTTGAG | 10152 |
| rs540165937 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365416 | AATGAGTTCATGAAC[A/G]TGAATATTCTTGTCT | 10152 |
| rs540218359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203350233 | GGGTGTGCATTACTA[C/T]GCCCGGCTAATTCTC | 10152 |
| rs540242247 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203357128 | AAATAGATATAAAAT[A/T]TGTGATTTGTTACTT | 10152 |
| rs540278663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332556 | CTTGAACCTGGGAAG[C/T]GGAGGTTGCAGTGAG | 10152 |
| rs540300965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345047 | CCGGAGCCCGCAGTG[A/G]CAACCCGCCGGGGTC | 10152 |
| rs540362416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203414494 | CTTACTCTTCCTTCA[A/G]GTTTCAGGAAGCCTT | 10152 |
| rs540472831 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203398867 | TTACCCATGTTGTTG[C/T]ATGTTTAAGTATTTC | 10152 |
| rs540527271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203330315 | CAAATGTCCACTTGT[A/G]ATGTACTTTGCTGAT | 10152 |
| rs540542912 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359210 | AGACAAATGTGATCT[A/G]CTATGACAGATTAAG | 10152 |
| rs540589363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203424503 | GGGCTCAAGCGATCC[C/T]CCTGCTTCAGCCTCC | 10152 |
| rs540617489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203375892 | AACTCCAAATAGAAC[C/T]GTAGCCATTTTCTAA | 10152 |
| rs540625364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203367769 | GCACTTTGGGAGGCT[A/G]AGGTGGGAGGATCGC | 10152 |
| rs540631579 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203382912 | TGTTTAACAGAATAT[C/G]AGTTAAGAATTAGAG | 10152 |
| rs540641957 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203331384 | CTGAGACAGAGTCTC[A/G]CTCTGTCGCCCAGGC | 10152 |
| rs540652123 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | ABI2 | GRCh38.p7 | 2:203357911 | GTAGCTGGGACTACA[-/G]GTGTGGACCACCACA | 10152 |
| rs540662297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203367743 | GGGCTGGGCACACAT[C/T]TGTAATCCCAGCACT | 10152 |
| rs540662950 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203378358 | CTTTGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA | 10152 |
| rs540705962 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379610 | CATGAATAGAAATTA[C/T]ACTAATAGGTCATTA | 10152 |
| rs540763135 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203368361 | TTTGAATGATTATTA[C/T]TCAACACTCTTTTTA | 10152 |
| rs540770537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203417144 | AGAAATGAAATTTGC[A/G]GTACTGAAGAGAATC | 10152 |
| rs540770556 | snp | C/G/T | 0.00755907 | 0.0610114 | intron-variant | ABI2 | GRCh38.p7 | 2:203378332 | TAGCCAGGATGGTCT[C/G/T]GATCTCCGGACTTTG | 10152 |
| rs540814189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345416 | GGCGAGGGTCCACGG[A/G]TTCATTCTTGAAGTC | 10152 |
| rs540875954 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400943 | TTGATCATGAAGATT[G/T]CAACAAATCAAGCAT | 10152 |
| rs540901742 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203431970 | TTTTAGCTCCCAGAG[A/G]GAGAGTTGGTGGTAT | 10152 |
| rs540943215 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428379 | GGAGTACAAGGTTTG[C/T]TAATGTGCTCTCTGG | 10152 |
| rs540962685 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203411669 | CTCTGGGTTGCTCAG[A/G]TAAGTGGTAGTCTAG | 10152 |
| rs541015606 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203333145 | CAAAATGATACAAAG[A/T]TTTAAAATTTTTATT | 10152 |
| rs541018643 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203371376 | TCTTTCTAAATGTCA[A/G]ATGTTTTCAAAAACA | 10152 |
| rs541060247 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396285 | AAACGTGACACAAAA[A/T]ACATTAATAGAATGT | 10152 |
| rs541122545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203421880 | GAGGCAGGAGAATCA[C/T]TTGAACCCAGGAGGT | 10152 |
| rs541141122 | snp | A/C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346780 | GCAGGGACAAAATAA[A/C/T]AACCTGTGGCCAAAA | 10152 |
| rs541143141 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402928 | ATCAGTATGTGATTT[C/G]CACGTAAAGTCATAC | 10152 |
| rs541143973 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384422 | AGTGGTTCTCCTGCC[G/T]CAGCTTCCTGAGTAG | 10152 |
| rs541183211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203419487 | CATTCTCCTGCCTCA[A/G]CCTGCTGAGTAGCTG | 10152 |
| rs541212849 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203340699 | ACTCCCCGCTCCCAC[A/C]AAAGATAATCAAGAA | 10152 |
| rs541212905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203348129 | GTCTGTAATCCCAGC[C/T]ACTTGGGAGGCTCAG | 10152 |
| rs541296777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203343041 | TGGAAGAAGAAAAAG[A/G]AGAACTTTATTTCCT | 10152 |
| rs541303267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203335149 | ATTTTCCCATTAGCC[A/G]TAGGATGTTCTCCAT | 10152 |
| rs541333566 | snp | G/T | 0.000808081 | 0.0200845 | intron-variant | ABI2 | GRCh38.p7 | 2:203348920 | GTGTTTTTTTTTGTT[G/T]TTTGTTTGTTTGTTT | 10152 |
| rs541341433 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385532 | TCTTGAAGATCCATC[A/T]TTTAGCCCCATGTTT | 10152 |
| rs541385074 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203410963 | AATTATATATAATAT[A/G]TATATAAAACATGAT | 10152 |
| rs541385342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203341536 | CTTGGCCAAGATGGC[A/G]AAACCCCATCTCTAC | 10152 |
| rs541412442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345961 | GAGGCGGGCAAATCA[C/T]CTGAGATCAGGAGTT | 10152 |
| rs541437930 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203390967 | TCCCCTCCTTTGTTA[C/T]GTAGTGTAGCATATT | 10152 |
| rs541485788 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203396376 | TGTGTTTTAAAAAAA[A/T]TTTTTAATCTGATAA | 10152 |
| rs541486685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203379388 | AGTTAGCTGGGATTA[C/T]AGGCATGTGCTGTCA | 10152 |
| rs541517392 | in-del | -/TC | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203382794 | TTGTAGAAAAATTAT[-/TC]TTTTTTCCAAATAGC | 10152 |
| rs541518170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203426237 | CAGTGTGTTTGTCTT[A/G]GAACAATGGATAGGT | 10152 |
| rs541521755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203331699 | GTCTTAGCCACTAGC[C/T]CGAGTTAACTAACCC | 10152 |
| rs541608767 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339470 | TCTGCAGTCCTAGCT[A/C]CTCCAGAGGCTGAAG | 10152 |
| rs541611930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203358905 | TAATCTTAGCTGCTC[C/T]GGAGACTGAGGCACA | 10152 |
| rs541627819 | in-del | -/AA | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203330976 | TTAGCAATGGGACTC[-/AA]AATTTAGTGTGGTGA | 10152 |
| rs541629108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203363631 | ATAAGTGAGAACATG[C/T]GATCTTTCTGTGCCT | 10152 |
| rs541673422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203367700 | GTAATCCTTTTTCCT[A/G]TAAGTAGTTTTTTTT | 10152 |
| rs541684891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203413612 | GTATAAAAAAATTGT[A/G]TATGAGGTGTGCTGT | 10152 |
| rs541695516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203352109 | AAAACTATGAAAGTA[C/T]AATAATAAAGACACT | 10152 |
| rs541730135 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ABI2 | GRCh38.p7 | 2:203422554 | GCTCCACAGAAGCGT[A/G]GTAATCAGATAACTG | 10152 |
| rs541732524 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203351459 | AACTTTTCTGATCCA[G/T]GAACATGGATGTCTT | 10152 |
| rs541770356 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203402998 | GTGGTTATTTGCTTT[G/T]TAAAATAACATTGTG | 10152 |
| rs541834852 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203370393 | ATGCCCAGCAAAGAG[A/G]GATGACATTGCATGT | 10152 |
| rs541851182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203356607 | ACTCCTGAGCTCAGG[C/T]GATCCACCCACCTTG | 10152 |
| rs541854693 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203353164 | ATTCCTAAATATTTT[A/T]TTCTTTTTCTGTTGT | 10152 |
| rs541871698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203401342 | TTCTTCTCCACCTGC[C/T]TATTTCTCCGCCTCC | 10152 |
| rs541902919 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ABI2 | GRCh38.p7 | 2:203403359 | ATGGCTATTGTGGAC[A/G]TGGTATGTCAACTTA | 10152 |
| rs541923829 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429524 | AGCACTTTCGGAGGC[C/T]GAGGTGGGTGGATCA | 10152 |
| rs542070384 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203370872 | AGATACTAGTTATCT[-/A]GGGTATTGAGTTTCT | 10152 |
| rs542099258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203399166 | TACACTCCCAGCAGC[A/G]ATGTGTGAGTTTCCA | 10152 |
| rs542145822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203359635 | AGTCCAAGATCAAGA[C/T]GTCAGCAGATTTGGT | 10152 |
| rs542158350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203361154 | CTGTTAGAAAAGTCC[A/C]AGAGAAGTCTCCTGT | 10152 |
| rs542158597 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203406119 | CAGTGGTAAGGAGGG[A/G]GTCATAGAAACACAT | 10152 |
| rs542159863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203423059 | TTGCTAGTTTAGGGT[A/G]CTTAATTGTTAGGTG | 10152 |
| rs542242564 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203411475 | TGATACTTCAACATT[G/T]CAATATTATGAACAA | 10152 |
| rs542245204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203416342 | GTCTTGCCCTATGGC[C/T]CAGGCTGGAGTGGCG | 10152 |
| rs542249796 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385941 | TTGGACTCTTGACTC[A/G]ATAGGCTTTTTTGTC | 10152 |
| rs542267011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203404398 | TTCTATCTTTTATCA[C/T]GTTTAGTGTTTTTGG | 10152 |
| rs542288782 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346966 | GCCATTCATTTCTTA[C/T]CTTATAAACTTGAAT | 10152 |
| rs542292633 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203419594 | GTGTTAGCCAGGATG[G/T]TCTCGATCTCCTGAC | 10152 |
| rs542328498 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203412312 | CACTTGGAAAAGCAT[A/C]TGACACATAGCAGGC | 10152 |
| rs542349360 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203353819 | TACTTTAAACTCTTA[C/T]CTGTTTCTTCTGGTA | 10152 |
| rs542394990 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203356939 | TCCTGTCTTTTTTGT[C/G]GGGGAGGGAATGACC | 10152 |
| rs542403767 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203379240 | ACTTGGTCTTTTGGG[G/T]TCAAAAAATGGCTTT | 10152 |
| rs542407343 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430064 | ACAGTTTTGAATTCT[A/G]TAGATTGTCTTGGAA | 10152 |
| rs542410393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203383975 | CATCATACTTTAGGA[A/C]CAGACATGTGGGATT | 10152 |
| rs542414403 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203378447 | ACTTAAAATTGTAAG[A/G]TTACTACCATGGTTA | 10152 |
| rs542431105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332258 | TTTATTTCTTGCCTA[G/T]ACAAAGGATTTAGTA | 10152 |
| rs542462115 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203387211 | TTAATGGGAGATTTC[A/G]TAGCAGAGGTGATGT | 10152 |
| rs542554946 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203426671 | GAAGAGGCATAGGCT[A/C]CAGAGAGAGTGAGAA | 10152 |
| rs542596047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203356414 | CGCTCTGTTGCCCAG[A/G]CTGGAGTGCATTGGC | 10152 |
| rs542634217 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203329208 | GCCATTTTTTTCCCT[A/G]TGGAGAAGGATGATG | 10152 |
| rs542670131 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366243 | CCAATGAATCACTTG[A/G]GTCTAGGAGTTCGAG | 10152 |
| rs542779305 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400357 | ACCTCCCATAGTACT[A/G]TGATTAAAGGCCTGA | 10152 |
| rs542832871 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203398169 | TTTGGGTGATGTCTT[A/G/T]TGGGATTCCTTCTAT | 10152 |
| rs542842428 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418148 | GAGACAAGGTCAGAT[A/G]GTCTTTATGTATGTG | 10152 |
| rs542854332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203404860 | CACCGCACCCGGCCT[A/G]TACAGGGATATTTCA | 10152 |
| rs542876017 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384927 | GCAACCTCCGCCTCC[C/T]GGGTTCAGGCGATTC | 10152 |
| rs542902938 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392001 | GGTTGGCATTAGTAT[A/G]GCCCAGAAGCCAGGT | 10152 |
| rs542905713 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203418951 | CAGAGGAAAAATGAC[A/T]TATTACATACAGAGG | 10152 |
| rs542916444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203337341 | AATCTGTTGTGTTTC[C/T]ACATATTAACTACAA | 10152 |
| rs542917921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203426000 | CACTCCAGCCTGGGC[A/G]ATAAGAGTGAGACTG | 10152 |
| rs542936324 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203373100 | TCGGCACTTTGGGAG[A/G]CCAAGGCAGGCGGCT | 10152 |
| rs542966203 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387973 | TTAGGATCAATCATG[A/G]TGGCTGTCTAGTAAA | 10152 |
| rs542991073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332822 | AGCCAACTTGTTGAT[A/G]TGTACGTTTTTCTTT | 10152 |
| rs542998594 | snp | A/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328057 | AGCTGAGCAGGGTGG[A/T]GTGTTCCCGCCGGGC | 10152 |
| rs543024903 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430943 | AGTAGGTGACCTTTC[C/T]GCATTAAGAACTGTT | 10152 |
| rs543043758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203381099 | GATACTGTACAGTTC[A/G]TGTAGTTGATTTTTT | 10152 |
| rs543048532 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408405 | TGACCTCAGGTGATG[C/T]GCCCCCCTCGGCCTT | 10152 |
| rs543066907 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379082 | TGTGGAGAAATTCAC[C/T]CTCTGTTAGCAAATA | 10152 |
| rs543083013 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203398098 | TTGCTGTTATACATG[C/T]TAAACATATATAAGA | 10152 |
| rs543089085 | in-del | -/AGCC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354557 | GGAAGTTAACAGGTT[-/AGCC]AGGGAGTTTTGTAGA | 10152 |
| rs543120218 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203420872 | TTCTCAGGCAGAGAA[C/G]AGAGAAAGGAAGGGC | 10152 |
| rs543121733 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418075 | AACTATCCAAAATAA[A/G]GCACAGAGAAGAAAG | 10152 |
| rs543134704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366431 | CCTGGATGCTCTTAT[A/G]GGGTTAAACATTATT | 10152 |
| rs543146973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203330121 | GTTCATAAATTTTGT[A/G]ATGGCCACATTGTTG | 10152 |
| rs543169923 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354484 | TGAACATACTGAAAC[A/G]TATCAGTAAACTACC | 10152 |
| rs543192998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203344585 | TTTTTTTTTTGAGTC[A/G]GAGGTTTGCTCTTAT | 10152 |
| rs543230900 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203350683 | TAGCAGGGATTACGG[A/G]TGCCCGCCACTGTGC | 10152 |
| rs543231226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203392267 | TGGCTTCCTCAGCAC[A/C]ACCACCATCACCACC | 10152 |
| rs543241755 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203346786 | ACAAAATAATAACCT[A/G]TGGCCAAAAGGAGGG | 10152 |
| rs543244140 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203397540 | TAGACTCAATTGCTA[C/T]GAAATATATTTGTAG | 10152 |
| rs543256582 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203408150 | GCGATTGATCTTTCC[C/G]TGGCTGCTGGTGGAC | 10152 |
| rs543280511 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203407657 | TATATCTAAACATTC[C/T]TGTATATTGTGAAAA | 10152 |
| rs543296480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203400679 | TATAACAAGCCTTGA[C/G]TGCTCTTATAATCCT | 10152 |
| rs543310136 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203387953 | CTTCCCTCAAAATAG[-/T]TTTTTTAGGATCAAT | 10152 |
| rs543352029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203340110 | ATTAGGTAAGTGAAA[C/T]AAGCCAGGCACAGAA | 10152 |
| rs543401302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203348869 | ATTAAAAATTTTTTT[A/G]AAAAATAGTACAAAG | 10152 |
| rs543432712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203385518 | AATTTTGCTTAAGAT[C/G]TTGAAGATCCATCAT | 10152 |
| rs543436064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203355461 | AAGCTGCAGTGAGCT[C/G]TCATTGCACCACTGC | 10152 |
| rs543512184 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203431854 | CAACTTAAGAATTCT[A/G]TGGAAAAGCAGTTTT | 10152 |
| rs543517047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203343417 | GGTACAAACATGTTA[C/T]GTGCATGTAATGACA | 10152 |
| rs543517178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203396122 | TTAGTAACAAAGGAT[C/T]GGGCAGATATAAAAA | 10152 |
| rs543551547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203415445 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 10152 |
| rs543594191 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404202 | TGTCAGTCTTTTATA[C/T]AGTTACATCCTGGAA | 10152 |
| rs543603116 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | ABI2 | GRCh38.p7 | 2:203353752 | GTCTGTCCACCTTGG[C/T]GTTCCAAAGTGTTGG | 10152 |
| rs543668371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203353059 | AGTTTACTCTGTGAT[A/G]TTTGCACAGTGACAG | 10152 |
| rs543676293 | in-del | -/TTTTTTT | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203382096 | TTAACTTGTTTTTTC[-/TTTTTTT]CCTTTCTCTTCACAT | 10152 |
| rs543712948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203402271 | AACTCCTGACCTCAA[A/G]TGATCTGCCTGCCTT | 10152 |
| rs543827964 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203358781 | TTGGGAGGCTGAGGT[G/T]GGCAGATCACTTAAA | 10152 |
| rs543832281 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203350785 | CCTCATGATCCACCC[A/G]CCTCGGCCTCCCAAA | 10152 |
| rs543864711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203335055 | GCAACACATTCTATT[C/T]TGGATTTTTCATTTA | 10152 |
| rs543939582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203338146 | CAACTAAGCTTTGAT[A/G]AAGGCACCAGGTACA | 10152 |
| rs543976296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345452 | GACCAAGAACCCACC[A/G]GAAGGAACCAATTCC | 10152 |
| rs543993181 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203398953 | TTATCCCTTTCTCAG[A/T]GGACATTTAGATTTT | 10152 |
| rs544075237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366257 | GAGTCTAGGAGTTCG[A/C]GACCAGCTTGGGCAA | 10152 |
| rs544099043 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203337334 | ATACAAAAATCTGTT[G/T]TGTTTCTACATATTA | 10152 |
| rs544135559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203358050 | TGGGATTACAGCCAT[A/G]AGCCACTGTGCCTGG | 10152 |
| rs544139385 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203355913 | CTAGATGGTTTGACT[A/G]GATGTAGAATTATAG | 10152 |
| rs544233168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203414602 | AATGAAGATTTGGTC[A/G]TTCATGTCTTCATGA | 10152 |
| rs544238041 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ABI2 | GRCh38.p7 | 2:203419346 | CTCATGATCCGCCCG[C/T]CTAGGCCTCCTAAAG | 10152 |
| rs544253490 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203399520 | TTTTTTTGGCGGGGG[C/G]AGGAGGGGCGGGCGG | 10152 |
| rs544253995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203407641 | AAAGCCTTTTACTGT[G/T]TATATCTAAACATTC | 10152 |
| rs544263287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345770 | AGGCTGGTTTCAAAC[G/T]CCTGACCTCAAGTGA | 10152 |
| rs544284183 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429235 | GTCATTTCTACATCC[C/T]TTATTCCTTGTTTTC | 10152 |
| rs544319806 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203415495 | GGTGGCGGGCGCCTG[C/T]AGTCCCAGCTACTTG | 10152 |
| rs544376247 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203332930 | GAGTAGAATCATCCC[A/G]TAATATGGATTTATT | 10152 |
| rs544385640 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203383121 | TTCAAATATATATTC[C/G]TCCCATCTAATACCC | 10152 |
| rs544437688 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203362932 | ACCTCCTGAGTTCAA[A/G]TGATTCTCCTGCCTC | 10152 |
| rs544449985 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203405171 | TTTTTGTTTTTCTGT[A/T]CTCTGCTCTATTAAG | 10152 |
| rs544450863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203390766 | TGAATGTAATATCAA[A/G]TAATCTAACCAGTGA | 10152 |
| rs544475003 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203413595 | TTTCTCATTTACACA[A/T]CGTATAAAAAAATTG | 10152 |
| rs544549915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | ABI2 | GRCh38.p7 | 2:203375952 | ACTGCAGTTCAACCC[C/T]GTGTGGTAGTATGAT | 10152 |
| rs544575978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203422133 | ATACCCTCGTCTCTA[C/T]AAAAAATTAGAAAAC | 10152 |
| rs544586210 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429435 | AGCTTAGTGGATTAA[C/T]GAGGCAGAGGGTGTT | 10152 |
| rs544616127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203359886 | TATAGCAATGAATAT[G/T]TAGAAATTAAGCAGT | 10152 |
| rs544627838 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203422741 | TGGTAGGGGCAGAAG[A/G]AATATGGCTGTATTA | 10152 |
| rs544639621 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342370 | TTGATGTTATGTGGC[C/T]TTACCCACTTATGTG | 10152 |
| rs544669556 | snp | A/G | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203325908 | GACAGAGCCTCCGTC[A/G]CCCAGGTTGGAGTGC | 10152 |
| rs544672551 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203372962 | CGGCCAGGAAGAGGC[A/G]CTCCTCACTTTCCAG | 10152 |
| rs544684682 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203379184 | TGAAATATTTTACAG[A/G]CATTTTGTCATGATA | 10152 |
| rs544710425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203418844 | GATCCAAGAAGTTCA[A/G]TAAACCCCAAATAGA | 10152 |
| rs544753038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203360377 | GGAATGCTTTAAACA[A/G]AAGGCGAAGTGTTGG | 10152 |
| rs544771678 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | ABI2 | GRCh38.p7 | 2:203339007 | ATATATATATATATA[A/T]AAAGGATTCATACAA | 10152 |
| rs544847659 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203385750 | TGTTTTTGCCTATAA[G/T]TTCCAACCTTAAGCC | 10152 |
| rs544882914 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429886 | GGGATGGGGGCAGTG[C/G]AGAAGACACTGGTGA | 10152 |
| rs544931726 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384748 | TTTTAAAATAAGCAT[A/G]TTAGTTTAATCAAAA | 10152 |
| rs544935572 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403140 | TTTTTGAAGCTACTT[C/T]GTGCTAGGGAATTAT | 10152 |
| rs545028359 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203422088 | ATTGCTTGAGACGAG[C/G]AGTTCAAGACCAGCC | 10152 |
| rs545033994 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346328 | TTTTTGCTAACAACC[A/G]CAAAAGACTATGTTT | 10152 |
| rs545050962 | in-del | -/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396688 | TTGGTTAGTGTTAAG[-/C]ACTGAATATCTAACA | 10152 |
| rs545066061 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ABI2 | GRCh38.p7 | 2:203362967 | TCCTGAGGAGCTGGG[A/G]CTACAGGCATACACC | 10152 |
| rs545107575 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329494 | GTGGATTAAAAAAAT[C/T]CTTCTTTAAAAATTA | 10152 |
| rs545111557 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424956 | GGCTTATTTCAGCCT[C/T]AACTTTGCTGAGCTC | 10152 |
| rs545127253 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359663 | GGTGTCTGTTGATGA[C/T]CTGTTCCTCATAAAT | 10152 |
| rs545138527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203337224 | CTGTTTGCAAATGAC[A/G]TGATTCCTTATGTAT | 10152 |
| rs545140246 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328350 | GGCTCGCGCCCCGCC[A/C]CCGTCGCCCCCTCCC | 10152 |
| rs545230147 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203412221 | CTTATTTGGAAATGG[G/T]CACTGCCAGTACTAG | 10152 |
| rs545262575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203378397 | ATTATAGGCGTGAGC[C/T]ACCATGCCTGGCTGA | 10152 |
| rs545336157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203397392 | CTGTAAGTCTATTTT[C/T]AACAGAATCTGTTGC | 10152 |
| rs545344015 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203344480 | AAGCGATTCTTCTGC[C/G]TTAGCCTCCTGAGTA | 10152 |
| rs545377856 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203340052 | CAGCCATAAAAAGAA[A/G]GAAACCCTGCTATTT | 10152 |
| rs545402657 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203388931 | CTTTTCCTTCCTGTT[A/T]CTCAGCAAATTGATG | 10152 |
| rs545406677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203380003 | AAAATCAGATGATGG[A/G]CCAGATTTGGCCTGT | 10152 |
| rs545464158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203388378 | GATCATAAAATGTAC[C/T]AAGTTATATTCATAG | 10152 |
| rs545468165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203384106 | TGTTTTTCTTCAGTC[A/G]AGTTACAAATTTAAG | 10152 |
| rs545473960 | in-del | -/TTTTT/TTTTTT/TTTTTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331348 | ATGGTCAATTTAGCC[-/TTTTT/TTTTTT/TTTTTTT]TTTTTTTTTTTTTTT | 10152 |
| rs545491218 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203426928 | GTCATCAAAAGCACA[A/T]TTGATTAAATGTGCT | 10152 |
| rs545512721 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203405639 | ACAATGAGAATATTT[A/G]TTGTGCTTTCTCAAG | 10152 |
| rs545537595 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203340497 | TTAGCCTTCCGAATA[G/T]CTGGGACTACATGTG | 10152 |
| rs545541310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332314 | ACATGTAAGACCTGC[A/G]TTTTTCTTCATTTAT | 10152 |
| rs545614302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203403877 | CTGCCTCAGCCTCCT[A/G]AGTAGCTGGGATTAC | 10152 |
| rs545630180 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203384830 | AGCAGATTCTTTTTT[C/T]TTTTTCTTTTTTTCT | 10152 |
| rs545638278 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203356277 | ACTACGAGCTCAGAC[C/T]CCTGGGATCTCATGT | 10152 |
| rs545673757 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203352216 | TATAATCCCAGCTTT[G/T]TGGGAGCCCGAGATG | 10152 |
| rs545712863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203406789 | CTGCCTCAGCCTCCC[A/G]AGTAGTTGGAACTAC | 10152 |
| rs545780251 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203401101 | CTCCAGTCCCCCCTC[C/T]TCTACTCTCCCCTCT | 10152 |
| rs545801849 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203392978 | GCTCCTTTTTTTTTT[A/T]AAAAAAATCTTATTT | 10152 |
| rs545811513 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203362510 | TTGTTTTTTCTACTG[A/G]TATTTTATTTATTTT | 10152 |
| rs545834653 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203374331 | ATAGTGAAACCCTGT[C/G/T]GCTACTAAAAATACA | 10152 |
| rs545848841 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203394134 | GGGAGAAAGTGAGAA[C/T]GGAAGATGAGATTAA | 10152 |
| rs545857328 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203384664 | TACTGAGGTCAGTAT[G/T]ATGTGTTTGTAATGA | 10152 |
| rs545861559 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430866 | TAACTAAAGATTTTT[A/C]TCTTTGGGAGGCATC | 10152 |
| rs545895317 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203423125 | CTTTTTAGTTCAGAT[C/T]AGTCACTTCTATGTA | 10152 |
| rs545898527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203354009 | TCTATATAAGTAATC[A/G]CAGCTGAAGCATAGA | 10152 |
| rs545945626 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203348861 | TATTTTTAATTAAAA[A/T]TTTTTTTAAAAAATA | 10152 |
| rs546006147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203415473 | ATACAAAAAATTAGC[C/T]GGGTGTGGTGGCGGG | 10152 |
| rs546022155 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421846 | GTGCACGCCTGTAGT[C/T]CCAGCAACTCAGGAG | 10152 |
| rs546048914 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203346643 | GGGAGTGTAAACTTG[C/T]GCTGTTCTCTTTCTC | 10152 |
| rs546085657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203352998 | GGAGCAGTAGGCTAT[A/G]CCATATAGCCTAGTG | 10152 |
| rs546100219 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203407506 | CTTTTTGAATTGGAC[A/T]TCTAAAATACAAGCT | 10152 |
| rs546122800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203361368 | GCTTGGTGTGGTAGT[A/G]TGTGCCTCTAGTCCC | 10152 |
| rs546139364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203399794 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGGGTC | 10152 |
| rs546212378 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203409114 | AAGTGCTGGGATTAC[A/C]GGCGTGAGCCACCGC | 10152 |
| rs546224920 | snp | C/G | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203396898 | GACGCTGCTGCTGGG[C/G]GTGCCCAGACCCTTG | 10152 |
| rs546283503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203348274 | GTGAAAATAAATGTA[A/G]TAAAGGTTAAGCTTA | 10152 |
| rs546299834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203402224 | GTTTTTAGTTGAAAC[A/G]GGGTTTCACCACGTT | 10152 |
| rs546314427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203397683 | TAATTTATGCAGAAA[A/G]GAGGTTTAATTGGCT | 10152 |
| rs546339990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203388553 | CTGGGCGTGGTGGTG[C/T]GCCTGTAATCCCAGC | 10152 |
| rs546388517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203423582 | AGGCGCCGGCCACCA[C/T]GCCTGCTAAATTTTG | 10152 |
| rs546396586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203363998 | CAAATGCCTGACCTC[A/G]GGTGATCTGCCCACC | 10152 |
| rs546442753 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203348848 | CCAAAATTTCTTTTA[C/T]TTTTAATTAAAAATT | 10152 |
| rs546444353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203419187 | TGATCTCAGCTCACA[A/G]CAACCTCCACCTCCC | 10152 |
| rs546463924 | in-del | -/CA | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203408674 | AAGTGGGAAATTTCC[-/CA]CTTTTCTGTTACACG | 10152 |
| rs546498543 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203403465 | TCCATTTTTGATAAG[C/G]CTTGAATTTTATGGA | 10152 |
| rs546498983 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203377609 | GATTTAGAATGACTC[A/G]CTAAACTTTATTCAA | 10152 |
| rs546511305 | snp | A/T | 1.6517e-05 | 0.00287372 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416944 | CGCCACCTGTGGAAG[A/T]ACCAGTCTTTGATGA | 10152 |
| rs546523843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203416389 | CAACCTCCACCTCCC[C/T]GGTTCCAGCGATTCT | 10152 |
| rs546587609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203411698 | AGTTTCTTATCACTG[A/G]AGTTTTATGGGTATT | 10152 |
| rs546629592 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203333816 | TCATAATTTCCGTTA[C/T]TGATCCAGGAAATCC | 10152 |
| rs546647180 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328049 | AGGAAGCCAGCTGAG[C/T]AGGGTGGTGTGTTCC | 10152 |
| rs546648669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203413353 | GCAAGCTTTGTAGAA[A/G]CAGCAAAATGTTTCA | 10152 |
| rs546724174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203344744 | TCTAGCTAAAGGTTT[C/G]TAAGCGCACCAATCA | 10152 |
| rs546726111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203336073 | TTGTGTTTGACTTCT[C/T]GGTACTAGAAGTCCT | 10152 |
| rs546744544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203410470 | TATTAGTGCAATTAT[A/G]TATGTTAAACATCTG | 10152 |
| rs546841247 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331240 | GACAGTGGATTTGTG[C/G]TGATCCAGCTGTACA | 10152 |
| rs546856379 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203356740 | TCCTGGGCTCAAGCA[A/G]TCTTCCTGCCTCGAC | 10152 |
| rs546868208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203420926 | GAGTGAGAGGGCATG[A/G]CTGTTTGGGGCAGAG | 10152 |
| rs546912414 | in-del | -/A | 0.00519062 | 0.0506791 | intron-variant | ABI2 | GRCh38.p7 | 2:203348868 | ATTAAAAATTTTTTT[-/A]AAAAAATAGTACAAA | 10152 |
| rs546922774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203380141 | AATCTCTAGGCATAT[A/G]TATTTTGATTTTTGT | 10152 |
| rs546930688 | in-del | -/TTTTC | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203363758 | GGCATATGTACCATA[-/TTTTC]TTTTCTTTTCTTTTT | 10152 |
| rs546981358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203357604 | CCAGTTTGTCTATAC[A/G]TATGTTGTCTAGGCA | 10152 |
| rs546996130 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203397566 | TGTAGAGTTAATGAT[G/T]CTGGCTAGTAACAGG | 10152 |
| rs547082404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203360871 | AGTCTCCTTTGACTC[C/T]TATGCTGTTGCTAAT | 10152 |
| rs547199352 | snp | A/G | 0.0123036 | 0.0774623 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429561 | CAATAAATTGAGACC[A/G]TCCTGGCCAACATGG | 10152 |
| rs547205698 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359519 | AATATGTGCAAGTAT[A/G]TAAATGTATGTGTCT | 10152 |
| rs547254089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203412697 | CACTGGCTCGAGGAG[A/G]AAACTGCCTCTCAGC | 10152 |
| rs547285598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365890 | CGCCTCAGCCTCACA[A/G]AGAGCTGGGATTACA | 10152 |
| rs547285980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203360349 | ATAAAGGTTCTTATT[C/G]GTAAGAGGATGAGGA | 10152 |
| rs547287255 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345831 | GGTTACAGGCGTGAG[A/G]CACTGTGCCCAGCAA | 10152 |
| rs547304408 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406646 | GGGCTTTAGCAAAGT[A/G]TAAATAAAGAGCAGG | 10152 |
| rs547311469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203346481 | TAAGAAGGAAGGTGA[C/G]AATTTGAGAAATACT | 10152 |
| rs547326031 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431043 | CCTTTGAAAAAGGTT[C/T]GATGGAGGAATTCAC | 10152 |
| rs547327840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203423428 | GAGAAAAAATCATCT[A/G]GGTCCTTTTTTTTCT | 10152 |
| rs547353395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203416006 | ATTAGAAGAAATTCT[A/G]TAAGTAAACAAACAT | 10152 |
| rs547363204 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203361723 | TAAAACATGACTGTT[A/C]TATGCAAATACAGGA | 10152 |
| rs547370994 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203371740 | CTGAATACTTGTACA[C/G]GTACACATACCTTTA | 10152 |
| rs547384795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203375401 | AAGTAGGTTTATTGT[C/T]ATATAACTAGTAACT | 10152 |
| rs547442813 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365830 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 10152 |
| rs547456440 | snp | C/T | 0.084728 | 0.187577 | intron-variant | ABI2 | GRCh38.p7 | 2:203372547 | GACGGGGCGGCTGGC[C/T]GGGCGGGGGGCTGAC | 10152 |
| rs547512453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203401748 | TTTGATTAAAAGAAA[C/G]AAATGTTTGATTTGG | 10152 |
| rs547521760 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ABI2 | GRCh38.p7 | 2:203386657 | TTTTTTTTTTTTTTT[C/T]CCACGTGGAGTCTCA | 10152 |
| rs547556919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203332451 | CCAACATGGTGAAAC[C/T]GCGTATCTACTAAAA | 10152 |
| rs547570045 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203386641 | TCTGTAGACATTGCT[-/T]TTTTTTTTTTTTTTT | 10152 |
| rs547579744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203341343 | CTGGCACAAAATAGG[C/T]ACTCCGTAAATATTC | 10152 |
| rs547580134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203348510 | TATATGTTATATGTC[A/G]ACAAGATAATTAAAA | 10152 |
| rs547593712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203377129 | TCAAGACCATCCTGG[A/G]CAACACAGTGACATC | 10152 |
| rs547601060 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203393351 | TGAGCCACTGCACCC[A/G]GCTGCAACAAAACAT | 10152 |
| rs547620516 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326929 | CTGCCTCAGCTTCCC[A/G]AGTAGCTGGGACTAC | 10152 |
| rs547668082 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378108 | TTTCTTTTTCTTTTT[A/C]TTTTCTTTTCTTTTT | 10152 |
| rs547680853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203377853 | CGAGGATGCAGTGAG[C/T]CATGATCGGGCCAGT | 10152 |
| rs547681178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203369892 | TTTATGTATTTTCTA[A/G]CATTTGCCTCAAGGA | 10152 |
| rs547693903 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203341870 | GTGGTTGGTGCTTTA[C/G]GGTTAAGCAGTTTAT | 10152 |
| rs547695744 | in-del | -/A | 0.488726 | 0.0742286 | intron-variant | ABI2 | GRCh38.p7 | 2:203421965 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 10152 |
| rs547715180 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387334 | AGGTAGAGCAGGATA[A/G]GTAGGAGCATTGTAG | 10152 |
| rs547762677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203374806 | GTTAATCCACTGTAA[C/T]TGTTTGATTGCAGAT | 10152 |
| rs547799718 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415892 | TTACTATATATTGGT[A/G]TGCAAGCTGTGGAAG | 10152 |
| rs547822829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203381359 | ATAGCTCGCTCCAAC[C/T]TTGTACTCCTGGGCT | 10152 |
| rs547846830 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203375532 | TTAACATTGTAATGT[C/G]AAAGAATATCATGAG | 10152 |
| rs547847365 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430084 | TTGTCTTGGAAGGAT[A/G]CTGTGTGATGGGTCA | 10152 |
| rs547847735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203418325 | ATTATCTCCCAGTTT[C/T]TCTGCGTGGCTCAGC | 10152 |
| rs547862695 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353491 | TTTATGTATTTATTT[A/T]TTTTTTGAGACAGAA | 10152 |
| rs547884508 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385884 | TGTTTCTCTTTCCTC[G/T]TACTCCTAATCTTAT | 10152 |
| rs547952592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203421805 | CCCACCTCTACTACA[A/G]GTTCAAAAATTAGCT | 10152 |
| rs547953719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203425375 | GCTTGGCTAATTTTT[G/T]TATTTTTAGTAGAGA | 10152 |
| rs547978949 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203350896 | TGTGTGTGTGTGCGC[A/G]CGCGCATACTTTTAG | 10152 |
| rs547988257 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203401563 | CTGTGGAAGAACTCT[A/C]AAGAGAGCAAAATAC | 10152 |
| rs548015899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203350479 | CTTAGTCTCCCTAGT[A/G]GCTAGGACTAGAGGT | 10152 |
| rs548029779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203385919 | CCTTATTCTCTGTGT[C/T]TTATTGTTGGACTCT | 10152 |
| rs548039767 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203334503 | AATATATTTGGTGGA[C/T]GAATATGCTGTGATT | 10152 |
| rs548047502 | in-del | -/AATT | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203374604 | CTTTTTATACTTCCC[-/AATT]AATTTCCTATGTAGT | 10152 |
| rs548089521 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345155 | CTACCTTTATGAGTT[C/G]TAACACTCACATTGA | 10152 |
| rs548131479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203394434 | TGGCTTAAATGGTAG[A/G]GAACCTTTGTGCTCT | 10152 |
| rs548137084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203389315 | ATAAATGCTTCACTT[C/T]AAAATATTGACATTT | 10152 |
| rs548148078 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410553 | ATACACCTTGGGAAG[A/G]AGAGTGGAATGATTT | 10152 |
| rs548205483 | in-del | -/TT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420410 | CCTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTTGC | 10152 |
| rs548214869 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203400025 | TGATAATTAGGTATA[C/T]ATATTTTTAAAACCC | 10152 |
| rs548290888 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203389372 | TGTTTTAACATCACA[C/T]ACAACTTGTTCACTG | 10152 |
| rs548303996 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368915 | TCGAACTCCTGGGCT[A/C]AAGGGATCCTCCTGC | 10152 |
| rs548346204 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428939 | GAAAGTGGAACTTGA[C/T]TGAAAAGTGAACAAG | 10152 |
| rs548363042 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332083 | CCAAAGTGCTAGGAT[G/T]ACAGGCGTGAGCCAC | 10152 |
| rs548365652 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203368879 | TGGAGTATAGTTGTA[C/G]AATCATGGCTCACTG | 10152 |
| rs548381403 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203358192 | TAGTTAGTCATAGCT[C/T]GCTATATCTTCACTG | 10152 |
| rs548416866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203391301 | TCTCTTGGGAAACAC[A/G]TTTTTATACTTCAGA | 10152 |
| rs548431993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203405388 | TATTTTATATTCATT[A/G]GAATATTATTTATGA | 10152 |
| rs548447258 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203426952 | ATGTGCTTTTTCCCC[A/G]TTTGTACTCAATTTA | 10152 |
| rs548471899 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203406933 | CGTAACAAAGGTCAT[C/G]CCAAATTCTACTTTT | 10152 |
| rs548483907 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203406487 | ACCCCTGAATGGTTT[A/T]AAAAGCGACTAAAAA | 10152 |
| rs548488160 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203359302 | TATGAACTGAAGACT[G/T]CTAATTCCCAAGTTG | 10152 |
| rs548596893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203352517 | TGATCCTGACCCTGT[A/G]TAGGGTTAGGCTAAT | 10152 |
| rs548597471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203346394 | GCAGCTTGGGAATAT[A/G]TGGGACTAATAGGCA | 10152 |
| rs548600806 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203404033 | GCTGGGATTACAGGC[A/G]TGAGTCACCGTGCCT | 10152 |
| rs548641559 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203413045 | ATAATACCCTGGGAG[-/TT]TTTTTTCTGTTTTTA | 10152 |
| rs548683829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203403981 | TGGTCTTAAACTCCT[C/G]ACCTTAAGTGATTCA | 10152 |
| rs548725695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203422285 | ACAGTAAGACTCTGT[C/T]TCAATAAAAAGAAAA | 10152 |
| rs548754968 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203396853 | CCTGCTCCTCTTGTT[C/T]CTGCTACTGTCCCTT | 10152 |
| rs548786008 | in-del | -/AT | 0.000227816 | 0.0106703 | intron-variant | ABI2 | GRCh38.p7 | 2:203416873 | TGAACTTTGCATAAC[-/AT]ATATAGTTTTGTTGT | 10152 |
| rs548835680 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338025 | ACAGAGCGAGACTCT[A/G]TCTCAAAAAAAGCTA | 10152 |
| rs548892376 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ABI2 | GRCh38.p7 | 2:203372291 | AGAAGAATTTTTCTT[A/G]GTACAGAACAAAATG | 10152 |
| rs548893647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203359961 | GGAGGCTGAGGCGGG[C/T]GGATCATGAGGTCAA | 10152 |
| rs548902199 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428930 | ACAAGTTCAGAAAGT[C/G]GAACTTGATTGAAAA | 10152 |
| rs548939175 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378699 | GTTCTTTTAGAAAGG[A/G]GAAATTGAAGTAGGA | 10152 |
| rs549000165 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203402208 | CCTGGCTAATTTTTG[-/T]GTTTTTAGTTGAAAC | 10152 |
| rs549013380 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203355843 | TCAAAAAAAAAAAAA[A/C]AAAAAAAACACCCCA | 10152 |
| rs549014271 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203386811 | GCCCGGCTAATTTTT[C/G]TATTTTTAGTAGAGA | 10152 |
| rs549023908 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203333532 | GAGAGTAAGGAGACT[A/G]AGTAGAATTTGGGAG | 10152 |
| rs549034824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203335473 | CACTATGTTGCTCCG[C/G]CTGGTCTTGGAACAC | 10152 |
| rs549035176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203363873 | GGGTTCAAGCAATTC[G/T]CCTGCCTCAGACTCC | 10152 |
| rs549071986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203343257 | TAGTCCCAGCTACTC[A/G]GGAGGTTGAAGCAGG | 10152 |
| rs549077944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203395863 | ATGGTGGGCTTTCTT[C/T]GTAATCAGGATTTTT | 10152 |
| rs549114828 | in-del | -/C | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432070 | GCCATTAAACCACCT[-/C]CAGATGAGTGGAGGA | 10152 |
| rs549151481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203363192 | TAGGAGTAGGTGTAT[A/G]TATTTATGGGTTACC | 10152 |
| rs549161978 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203371680 | TAAATTAACATTAAA[G/T]ATTTCCCCTAAATAT | 10152 |
| rs549224529 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328436 | CCGCTCCTCCTCTCC[C/G]GGTCCTGGGTTTCCT | 10152 |
| rs549230198 | in-del | -/AAT | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203348597 | TTAAAAACATTCAAC[-/AAT]AATGTAATATCACCT | 10152 |
| rs549273279 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203389509 | TTTGATAGCCTCACT[A/T]CTCTGTATACAATTA | 10152 |
| rs549317656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203353073 | TGTTTGCACAGTGAC[A/G]GAATTGTCTAATGAC | 10152 |
| rs549351280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203387803 | AGTGGCTGCAGTATT[G/T]CTTTGTTTTCCTTGT | 10152 |
| rs549355535 | in-del | -/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203384837 | TCTTTTTTTTTTTTC[-/T]TTTTTTCTTTTTTTT | 10152 |
| rs549399528 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203374749 | CATTAGCTTACTAAT[-/A]AAAAAAATTGAGACA | 10152 |
| rs549444254 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203413119 | TGCTACTGCATGTTC[A/T]GTGAGATGTTGTCAT | 10152 |
| rs549514497 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203369143 | CCTGGCCTGAACTTG[A/G]TTTTCTGTAGAAGGA | 10152 |
| rs549561111 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368683 | TTCTGCAGACATATC[A/T]TTTATTGCTTGTTAT | 10152 |
| rs549599768 | snp | A/G | 0.000419873 | 0.0144831 | intron-variant | ABI2 | GRCh38.p7 | 2:203380197 | GTTGTTTTTTACATT[A/G]TATTTTGCAGACAGT | 10152 |
| rs549632920 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345317 | GAAACCAGGAACCCA[C/G]TGGAAGGAAGAAACT | 10152 |
| rs549666408 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203373356 | TAATCGCAGGCACTC[A/G]GCAGGCTGAGGCAGG | 10152 |
| rs549666473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203380095 | AATAAAAATTTAGCA[A/G]GCATAGTTTAGAATA | 10152 |
| rs549667163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203331993 | TTTTGTATTTTTGGT[A/G]GAGATGGGGTTTTGC | 10152 |
| rs549675619 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404027 | CAAAGTGCTGGGATT[A/G]CAGGCGTGAGTCACC | 10152 |
| rs549737627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203338481 | GTTCACGTGAGAACT[A/G]GTTGTTTAAAATTAG | 10152 |
| rs549745090 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203378135 | TTTTTTTTTTTAAGA[C/T]GGAGTCTCGCTCTGT | 10152 |
| rs549760417 | in-del | -/CT | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203332616 | GGCGACAGAGCAAGA[-/CT]CTGTCTCAAAAAAAC | 10152 |
| rs549779351 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342144 | AATGAACTTATGACT[C/T]ACACCATTTATTTTA | 10152 |
| rs549794883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203422463 | ATTTGGGAGATTTAG[A/G]AGGTGGAATTAACAG | 10152 |
| rs549804374 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203377024 | TGGAGATTTATTAAT[A/C]TTTCTAGTATGTGCC | 10152 |
| rs549873248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203360830 | AGAACATTGACTCAA[C/G]ACAAGGTTAAATGGG | 10152 |
| rs549876755 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203409251 | GCAAGTCAAGGATTT[A/C]CTGCCAAGAATTATG | 10152 |
| rs549891971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203407893 | TTTCAGCTCAACTCC[A/C]AGAAAGACAGTATAT | 10152 |
| rs549895434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203341690 | ACTCCAGCCTGGGCA[A/G]CAGAGCGAGACTCCA | 10152 |
| rs549900221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203416440 | AGCTGGGATTACGGG[C/T]GCCCACGACCATGTG | 10152 |
| rs549901598 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387984 | CATGATGGCTGTCTA[A/G]TAAATATATTTTTAT | 10152 |
| rs549938640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203339302 | AAACTGGTTCCGGCC[G/T]GGTGTGGTGGCTCAT | 10152 |
| rs549973422 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203346179 | TGCTTGTAATTCTAT[C/G]TTGATTCCAAATAAG | 10152 |
| rs549976303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203353519 | GAATCTCGCTCTGTC[A/G]CCCAGACTGGAGTGC | 10152 |
| rs549978127 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203383522 | AATACAGAAACACAC[A/G]GATTCTTTACCCTTA | 10152 |
| rs549992078 | snp | A/G | 1.93358e-05 | 0.00310927 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203391135 | TATGTCAGGGAAAGG[A/G]ACACTTGGGTGAGTA | 10152 |
| rs550035926 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430289 | GTACTATTAATATTA[C/T]AACAGACGATCCAAG | 10152 |
| rs550120231 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343411 | GTTTGTGGTACAAAC[A/G]TGTTATGTGCATGTA | 10152 |
| rs550133930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203333333 | TTTTTGTAGAAATGG[A/G]TTTATGTTCTATATT | 10152 |
| rs550134942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203401097 | GTTCCTCCAGTCCCC[C/G]CTCCTCTACTCTCCC | 10152 |
| rs550137591 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203380469 | GCTTTTTATCTGTCT[G/T]TCTTTCCTAGAGGAC | 10152 |
| rs550139454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203389228 | AGAGGGAGAGCAAGG[A/G]TAAGTTAATCTTTAC | 10152 |
| rs550181122 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203395590 | CATCTCAGAAAATGT[C/T]GGGAAGTGCTGATGA | 10152 |
| rs550202947 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203388636 | TAGTGAGCCGAGATC[A/C]GGCCATTGCACTCCA | 10152 |
| rs550227243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203381292 | ATTTAATTTAACTTT[C/T]TTGAGACAGGGTCTC | 10152 |
| rs550263269 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408541 | AAGCATATTCATCTT[-/A]AAAAAAAAAACCTCA | 10152 |
| rs550263329 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326057 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 10152 |
| rs550346310 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432233 | GTGGTATCTTGAGTT[A/T]ACGTGTTAGGGATAA | 10152 |
| rs550358437 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203357302 | TAAATTAATTATTTA[A/C]GAGCAAGTAAGATAG | 10152 |
| rs550372464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203356529 | GCGTGCTGCCACGCC[C/T]GGCTAATTTTTTGTA | 10152 |
| rs550400597 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203393438 | CCATTTTATTGTTTA[A/T]TATTTGCATTATAAT | 10152 |
| rs550423125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203341060 | ACTCCAAGATAGTTG[C/T]ATGATTGGTTCTTTT | 10152 |
| rs550540038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345063 | CAACCCGCCGGGGTC[C/T]TCTTCCATGCTGTGG | 10152 |
| rs550568017 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423639 | CATATTGGCCAGGCT[A/G]GTCTCAAACCTGACC | 10152 |
| rs550584319 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203336648 | GAGTGTCATATCTAT[G/T]TTGTAGTCACCTGGC | 10152 |
| rs550591515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203406391 | TTGGTTCCAAGAGAT[A/G]TGTCTATATATAGTT | 10152 |
| rs550658778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203329727 | CACCTCCATCTCTCC[A/G]GGGATCCTTCTTTTT | 10152 |
| rs550697298 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203328694 | GGCCGCGCGCCTCGG[C/G]GCGTGGGGCCGAGGC | 10152 |
| rs550701105 | in-del | -/CGCTGCGGCCGCCGCTCC | 0.00318978 | 0.0398085 | cds-indel, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328455 | CCTGGGTTTCCTTGG[-/CGCTGCGGCCGCCGCTCC]CTCTGCGACCTGTAT | 10152 |
| rs550702395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203349774 | ACCACATTTTGTTTA[C/G]CCATTTGTCAGTTGA | 10152 |
| rs550734764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203421079 | TAAAAAAAAAATCTG[A/G]TAGTAGAGGGAAATT | 10152 |
| rs550809997 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345623 | CGTCTTGGCCAGTCT[C/G]GTCTCGAACTCCTGA | 10152 |
| rs550813934 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203399365 | TGAAGTATCTGTTCA[A/T]ATGTTTTGTTCCTTC | 10152 |
| rs550815890 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357101 | TACCACACTCAATTT[C/T]TTCCTAATATAAAAT | 10152 |
| rs550883553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366759 | CAATTCTGGTGGATT[A/G]GTTTTTTTACTTTCT | 10152 |
| rs550895972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203374589 | TGCATAGAAAGTAGA[C/T]TTTTTATACTTCCCA | 10152 |
| rs551040266 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431117 | CTGGTCTTTTTGGCC[G/T]GGAACTCCTGATTGG | 10152 |
| rs551050315 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203390387 | CTGTAATCCTAGCAC[A/T]TTGGGAGGCCGAGGC | 10152 |
| rs551062131 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203409383 | GCTTAACTCTTGTCT[G/T]TGCATTTATATGTCC | 10152 |
| rs551099251 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203426737 | TCTCACTTGACTCTC[A/G]TAGTGTATCTCATTG | 10152 |
| rs551109156 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203352325 | TTGTACTTTTTATTT[C/T]AGAGTTTACTCCTAC | 10152 |
| rs551124329 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428712 | AGTCAGTATAAGAAA[A/T]GCTGAAAAAAATCCA | 10152 |
| rs551182696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203403198 | CCCATGGTGGAAAAA[C/G]TAGGAATTGGGTAAA | 10152 |
| rs551188491 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203352080 | AAGGCAGAAGACACA[A/C]ACATCACAATTTTAA | 10152 |
| rs551188780 | in-del | -/TCTTTTTTT | 0.00993419 | 0.0697739 | intron-variant | ABI2 | GRCh38.p7 | 2:203364090 | TTCTTTGTCCATTCA[-/TCTTTTTTT]TTTTTTTAAGTTTTA | 10152 |
| rs551257694 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432113 | AATTTTTTAATTGTA[C/T]TTGGAATTGTTGCCG | 10152 |
| rs551266039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203421707 | CATGGTGGCTCACGC[C/G]TGTAATCCCAGCACT | 10152 |
| rs551270714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203424651 | TGATTCTCCTGCCTC[A/G]GCCTCCCAAAGTTCT | 10152 |
| rs551273988 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203378276 | CGCCACCATGCCCGG[A/C]TAATTTTTGTATTTT | 10152 |
| rs551284220 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | ABI2 | GRCh38.p7 | 2:203383256 | AGGTAGATTTGATTG[A/G]AAGAGCCCAGGCATA | 10152 |
| rs551316783 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378184 | GTGGCACAATCTCGG[C/G]TCATTGCAAGCTCTG | 10152 |
| rs551378304 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203408788 | AGTTGCTGCCTGCTA[C/G]TGTTTCTCAGTTTTA | 10152 |
| rs551389181 | snp | C/G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388785 | AGGTCCAAAGACTTA[C/G/T]AGAAGATACTGCAAT | 10152 |
| rs551393966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203354957 | AATTGTCTTCTAATA[C/T]CAGTTTCATCCATCC | 10152 |
| rs551404771 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347894 | CTGCAGTTTCGATGC[C/T]TTCTAGATATTTAGG | 10152 |
| rs551406419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203354293 | AAGTGATCTTCTCGC[C/T]TCAGCCTCCCAAAGT | 10152 |
| rs551406459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203363003 | GCCCGGCTATTTTTC[A/G]TATTTTTAGTAGAGA | 10152 |
| rs551436306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203364752 | TTTTTTTTTTTTTCA[A/G]GAGACAGGGTCTTGC | 10152 |
| rs551449375 | snp | C/T | 3.29728e-05 | 0.00406021 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394758 | GTGGTACCAAATGAT[C/T]ACGTACCTAGCCCAA | 10152 |
| rs551457845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203426344 | TTGAGGATGTTACAG[A/G]GCATCCCAGTATAAC | 10152 |
| rs551468774 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203348639 | GAAATGAGTTTATTT[A/T]ATCTTATTATTTTTT | 10152 |
| rs551470096 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203373264 | TTAGGAGCTGGAGAC[C/T]AGCCCGGCCAACACA | 10152 |
| rs551506016 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343135 | TGGGGAGGCTGAGGC[A/C]GGTGGATCACGTGAG | 10152 |
| rs551511851 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203348917 | AGGTGTTTTTTTTTG[-/T]TTTTTTGTTTGTTTG | 10152 |
| rs551513293 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354183 | CAAGTAGCTGGGACT[A/G]CAGGCACGCTTCACC | 10152 |
| rs551600661 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203377991 | ATATCATCACTAATA[C/T]GCAAGCTTAACTTTT | 10152 |
| rs551602989 | in-del | -/TG | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427622 | GTATAACAGCATAAC[-/TG]TGTAGCCAAAACAAA | 10152 |
| rs551626997 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203335936 | AATTTTCCTTGTACC[C/G]TCTGTAGTCAGTCCT | 10152 |
| rs551627139 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203383502 | AAAGTTTAATTGAAG[-/A]AAAAAATACAGAAAC | 10152 |
| rs551649289 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420555 | CCTGCCAGCACACCC[A/G]GCTAATTTTTTGTAT | 10152 |
| rs551663091 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203335430 | GCCCAGCTAATTTTT[G/T]TTGTTGTTGTTGTTA | 10152 |
| rs551672043 | in-del | -/TT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379971 | ATGTAAACACCACTC[-/TT]AGCTTGTGGGCTGTA | 10152 |
| rs551673142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203361875 | AAGTTTGCAGGAATC[A/G]AAATTTTGAGTGATT | 10152 |
| rs551715996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203349001 | GCAATGGTGTGATCT[C/T]GGCTCACTGCAGCCT | 10152 |
| rs551805517 | snp | G/T | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327120 | TCCTAAAGTGATTTT[G/T]TTTTGAAAGTATAAG | 10152 |
| rs551825507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203369054 | ATGCTGGGGCTGGTC[C/T]TGAAATCCTGGGCTC | 10152 |
| rs551913264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203419251 | AGTAGCTGGGACTAC[C/T]GGCGCCCACCACCGC | 10152 |
| rs551938006 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203341709 | GCGAGACTCCATCTC[-/A]AAAAAAAAACAAAAG | 10152 |
| rs551945215 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203337897 | TTATAGGGCATGCTG[G/T]CACACGCCTGTAGTC | 10152 |
| rs551977582 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203342079 | TGTTCATTTTTTTTT[G/T]GCCTGTTATGTCCTC | 10152 |
| rs552037664 | snp | C/G | 3.36831e-05 | 0.00410371 | intron-variant | ABI2 | GRCh38.p7 | 2:203395831 | TTTCTGAATTTGATT[C/G]AATTTGTGATTTAAT | 10152 |
| rs552044093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203386081 | CCTTAGGAATTGAAG[C/T]AGGAACATACATCCT | 10152 |
| rs552055489 | in-del | -/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430204 | ATTGTAAGTTTCCCT[-/C]TTTTTTTATAAATTA | 10152 |
| rs552062136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203387681 | ATTATGATTGGTATC[A/G]GCCACCAGAGTATTG | 10152 |
| rs552071466 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203378269 | AGGCACCCGCCACCA[C/T]GCCCGGCTAATTTTT | 10152 |
| rs552106631 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429631 | GCGTGGTGGCGCACA[C/G/T]CTGTAGTCCCAGCTA | 10152 |
| rs552125510 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203386747 | GGTTCAAGTGATTCT[C/T]CCTTCCTCAGACTTC | 10152 |
| rs552171212 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429122 | ATGCATTGCAAGTTA[C/T]AATAGCTATTTTGCT | 10152 |
| rs552194591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203383426 | TGGCCCTTTTACCCT[A/G]AAGTCTGTATTCAAA | 10152 |
| rs552210649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203385166 | TTGAGACAGTCTTGC[C/T]GTTGCCCAGGCTGGA | 10152 |
| rs552272148 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203393383 | TTTATTGCCTGGGAA[A/T]AATTGTCTGAAAATT | 10152 |
| rs552273967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203384483 | GGCTATTTTTTAACA[A/C]ATTTTTTGTAGAGAT | 10152 |
| rs552283079 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203415096 | TTATCTTACAAATGG[A/T]AATAGGATAAATTTC | 10152 |
| rs552314242 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203369761 | GGTAATAGATCTGCA[A/T]TTCTCAGTGGCTGTT | 10152 |
| rs552324271 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203401405 | TGCTATTGTGCTCTC[G/T]CATGGGTGCTGTGGT | 10152 |
| rs552343943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203422353 | CACTGCTTAGAAAAT[C/G]TCAGGTACCCTGAGT | 10152 |
| rs552349604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203360638 | GACCTGATTCAGGCT[A/G]GTAAGTGACGTTTGC | 10152 |
| rs552362006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203359991 | AGAGATTGAGACCAT[C/T]CTGGCCAACATGGTA | 10152 |
| rs552411886 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385226 | GGCTCCACCTCCCAG[A/G]TTTCACGCCATTCTC | 10152 |
| rs552434247 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203399241 | CCATTCCAATACATG[C/T]GTAATGGTTTCTCAT | 10152 |
| rs552434898 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430550 | CCAATGTGTCAAAAT[C/T]GACATCTGAGAGATT | 10152 |
| rs552435789 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203401823 | AACCATACTTTTTTG[C/G]TACCTTACGTTTATT | 10152 |
| rs552464158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203407045 | TCTGACTAGAATGTC[C/T]GTGAGCCAGAATATA | 10152 |
| rs552518735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203390257 | ATTTATCTTTATATT[C/T]TCTAGTTACAGTGGA | 10152 |
| rs552602944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203400050 | AAACCCCAAATGGTA[A/G]ATCGACTCATTAATA | 10152 |
| rs552611434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203346445 | GATACCATATTACTG[C/T]CTGAATGAACACATC | 10152 |
| rs552624194 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431435 | CCATCAGAGTTGTGT[A/G]AAGGCGTGTACTAAG | 10152 |
| rs552632567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203418758 | GGATTACATAAAGGC[A/G]TGAATACTATGAGGC | 10152 |
| rs552648175 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203413817 | TATTTTGAAGATATT[-/C]CTTGGTAGCAAATAC | 10152 |
| rs552670339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203333263 | GATCATCTTGAATAT[A/G]TATCTGGTACTCATA | 10152 |
| rs552692873 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408931 | GCAAGCTCCGCTTCC[C/T]GGGTTCACGCCATTC | 10152 |
| rs552695867 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203425803 | GAGGCAAGTGGATCA[C/T]CTGAGGTCAGGAGTT | 10152 |
| rs552724779 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203416296 | TTTTTATTGTTTATT[C/T]TTTTTTTGCTGTTGT | 10152 |
| rs552725164 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203386947 | GCCCAGCCAGACATT[C/G]CTTTTTATTTTAGGC | 10152 |
| rs552772574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203415661 | CATTTAATTCAATTC[A/G]TAGGCTTAGATTAAA | 10152 |
| rs552775497 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345114 | TCCCCAGTAAATCTT[C/G]CTGCTGCTCACTCTT | 10152 |
| rs552786450 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390123 | ATGTTTAGGAACATG[A/G]CTTGAACTTCTAGCA | 10152 |
| rs552843009 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203407736 | AGTCTTGTCTTATGA[A/G]GAATCATTTTAGCTA | 10152 |
| rs552844505 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203395890 | TTTTTTTCTTTAGGA[A/T]TCATAAATATTGGGA | 10152 |
| rs552851305 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203353407 | TTGCAGTTTTATTAG[A/T]TACCAAATAAAAACA | 10152 |
| rs552854940 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203395105 | CTGGAAAAAAAATTA[G/T]GGACCAAATGTGGGA | 10152 |
| rs552924660 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326682 | TTGGACTAGACCAAC[A/G]TTTTCAATATCCTTT | 10152 |
| rs552941825 | in-del | -/TTTG | 0.0202039 | 0.0984569 | intron-variant | ABI2 | GRCh38.p7 | 2:203348925 | TTTTTTTGTTTTTTG[-/TTTG]TTTGTTTGTTTGTTT | 10152 |
| rs552961299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203334962 | ACCGTGCCTGGCCTA[A/G]TTGTAGACTTTTGAT | 10152 |
| rs552967047 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203417471 | TCCACATGAAACTTT[C/G]TTCCACAGAATAATG | 10152 |
| rs552969366 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203378362 | GTGATCCGCCCACCT[C/T]GGCCTCCCAAAGTGC | 10152 |
| rs553026399 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354972 | TCAGTTTCATCCATC[C/T]TCCCCACAAGAAGAC | 10152 |
| rs553031327 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203392976 | TGCTCCTTTTTTTTT[-/A]TAAAAAAAATCTTAT | 10152 |
| rs553038802 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203386999 | GAATACCTTTAAAGC[A/G]GAGAAATCATTCTAT | 10152 |
| rs553065103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203372901 | CCCCACATCTCAGGC[A/G]ATGGGCGGCTGGGCA | 10152 |
| rs553067787 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203344938 | TGTAAAATGGACCAA[C/T]CAGTGCTCTGTAAAA | 10152 |
| rs553106907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203419423 | GCCCAGGCTGGAGTG[C/T]AGTGGTGTGATCCTG | 10152 |
| rs553281096 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203411469 | ATTTGCTGATACTTC[A/T]ACATTTCAATATTAT | 10152 |
| rs553307215 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203346600 | TTGAGTTGAATTAAC[A/T]CTTTCTCCCCCACCA | 10152 |
| rs553315945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203357648 | ATTTTAAAAGTGTCA[C/T]GTTATTGAGAACTGA | 10152 |
| rs553322447 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203342679 | CTGCCTCCTGGTCTC[A/G]GGCACTCCTTCTGCC | 10152 |
| rs553361562 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203356663 | GCGTTAGCCACCATT[C/T]CAGTCCAAATTTTTA | 10152 |
| rs553373528 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203404273 | TTGTTCATTTTTCCA[A/C]ATCCCTTCACTGTTC | 10152 |
| rs553393862 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203353554 | GCATGGTCTTCTCTC[A/G/T]CAGCAACCTCTGCCT | 10152 |
| rs553434787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203412202 | CTGTGGCTTAGGACT[C/T]CTGCTTATTTGGAAA | 10152 |
| rs553468425 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203339944 | ATCTGTCCCATCTGT[A/C]TATGTGGATGAATAC | 10152 |
| rs553481994 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203353637 | GGCATGTGCCACCAC[A/G]CCTGGCTGGTGGCTC | 10152 |
| rs553499827 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203388832 | TGCATACCAAAACTT[A/C]AAACAAATATAAGCT | 10152 |
| rs553500717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203411025 | ATATATAAAACATAC[A/G]ATTATGTTATATATA | 10152 |
| rs553513945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203398033 | AAGCATATCAATCAC[C/T]GTAGTGTTCCACTTG | 10152 |
| rs553517086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203356228 | GGTCTTGCTCTGTCA[C/T]CCAGGCTGGAGGGCA | 10152 |
| rs553568710 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429833 | AAACAGAGTTAGTGG[C/T]GGTCAGCAGGAATGC | 10152 |
| rs553578878 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339497 | GAAGCAGGAGAATTG[A/C]TTGAACCCGGGAGGC | 10152 |
| rs553590965 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203393877 | AATTTAATAAACACT[A/G]ATTTCCCCATGTGCA | 10152 |
| rs553640336 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203414455 | CTCTGCCATCCTACC[C/T]TCCCCTCTTCCTCCC | 10152 |
| rs553648124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203373450 | CATCAGAGGGAGACC[A/G]TGGAAAGAGAGGGAG | 10152 |
| rs553668821 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203359636 | GTCCAAGATCAAGAC[A/G]TCAGCAGATTTGGTG | 10152 |
| rs553772916 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203400289 | AGACAAAGTTTCACC[A/G]TGTTGGTCAGGCTGG | 10152 |
| rs553774075 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203352885 | ATGCTGTGTTGTTAC[A/T]GTACCTTCTCTATGT | 10152 |
| rs553794052 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203371204 | GTTGGTTCTGCTCTT[C/T]ACCTCAATCTGTGTC | 10152 |
| rs553818775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203363364 | TTTTTATGAAATCAC[C/T]CTGTTGTGCTAGCAA | 10152 |
| rs553829611 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203392965 | ATTTTGTTCCTTTGC[C/T]CCTTTTTTTTTTAAA | 10152 |
| rs553886715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203422493 | GGACTTGGGGATGTC[A/G]GGGAAGGTGAGTGAG | 10152 |
| rs553915704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203401195 | GGGTTTAGCAAAAGT[G/T]TTTTTTTTTTCCTTT | 10152 |
| rs553978278 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203340435 | ACAGTGGCATGATCA[C/T]GGCTCACTGCAGCCT | 10152 |
| rs553991554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203369201 | ATAGAATTTCAAGAT[A/C]TATTCTTGAGAATCC | 10152 |
| rs554015490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203417318 | ATTGGACATGCTTTT[A/T]ATGAATGGTTTCTAT | 10152 |
| rs554041881 | in-del | -/ATGCCTTA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408070 | ACTGAATTTTTGAAC[-/ATGCCTTA]ATGCCTTAGACTAGC | 10152 |
| rs554052914 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203368228 | AAAATAATACTGCAG[G/T]GAAAAACCAATTAAG | 10152 |
| rs554054791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203376546 | AACAACAAATATATT[C/T]TTAAAGAATTTAATC | 10152 |
| rs554063349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203377531 | TATAAAAAAAGTGTC[A/G]TATTTTATTTTTTGA | 10152 |
| rs554074761 | snp | A/G | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327856 | CATTGAAAGCTGCGT[A/G]GAAGTTTTATTCCTG | 10152 |
| rs554092948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203407425 | GCGCTTATTTTGTCT[A/G]ATATTCTCAGAGTAT | 10152 |
| rs554124193 | in-del | -/T | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327115 | CCCGTCCTAAAGTGA[-/T]TTTTTTTTTGAAAGT | 10152 |
| rs554161816 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | ABI2 | GRCh38.p7 | 2:203415148 | GTAAATCACATATCT[A/G]TATCTTTTGTTTATT | 10152 |
| rs554191902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203385353 | AGCCAGGATGGTCTC[A/G]ATCTCCTGATCTCGT | 10152 |
| rs554220420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203420456 | TGGAGTGCAGTGGCA[C/T]GGTCTTGGCTCACTG | 10152 |
| rs554234072 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203348504 | GTCAGTTATATGTTA[C/T]ATGTCGACAAGATAA | 10152 |
| rs554247061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366073 | ATAGTATTTCTTAGA[C/T]ATCATTAATGGATAG | 10152 |
| rs554251128 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | ABI2 | GRCh38.p7 | 2:203397773 | GCCTCAGGAAACTTA[A/C]ACTCATGGCCTAAGG | 10152 |
| rs554322228 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350859 | TTGTTTTTGTTGTGT[A/G]TTTTGTGTGTGTGTG | 10152 |
| rs554336838 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203357840 | GTGGCGCAGTCTTGG[C/G]TCACTGCAGCCTCCG | 10152 |
| rs554340039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332749 | ATTACAATATAGTTG[C/T]CTTAATGTTTTGGTA | 10152 |
| rs554386836 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203416293 | ATTTTTTATTGTTTA[-/T]TTTTTTTTTTGCTGT | 10152 |
| rs554396626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203380666 | CGTGTAATCTTTCCA[A/G]TTTTAATTTAATATG | 10152 |
| rs554502404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203388073 | TACCTATTATAAAAA[C/T]TGTTTTGTTTGGCAT | 10152 |
| rs554534523 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203431760 | AATGATCCTTGCTGA[A/G]TATCTTAAGGTTTTT | 10152 |
| rs554534826 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ABI2 | GRCh38.p7 | 2:203423530 | TCCCAGGTTCACGCC[A/G]TTCTCCTGCCTCAGC | 10152 |
| rs554573876 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328287 | AAGGGAGCGCGCGTG[C/G]GCGCGCCCGGCCGGC | 10152 |
| rs554609243 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345209 | GCCAGCGAGACCACA[A/G]ACTTATCGGGAGGAA | 10152 |
| rs554612992 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423856 | GTTTTTTTCAGTTTT[A/T]CAGACCTTCATAAAA | 10152 |
| rs554617778 | snp | C/T | 3.5317e-05 | 0.00420205 | intron-variant | ABI2 | GRCh38.p7 | 2:203367096 | ACCCTTAATAATAAA[C/T]ACAGGCTATCTGTAA | 10152 |
| rs554618629 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427609 | ATGTATGTCAAAGGT[A/G]TAACAGCATAACTGT | 10152 |
| rs554632734 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431441 | GAGTTGTGTAAAGGC[A/G]TGTACTAAGTGCAAT | 10152 |
| rs554633480 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369954 | GGTAGAATTCTTTAT[G/T]TAAAAAGTCAGTTGA | 10152 |
| rs554661494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203330127 | AAATTTTGTAATGGC[C/T]ACATTGTTGATCGCG | 10152 |
| rs554674494 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429313 | TGGACCCAAACTAGA[C/G]TATACTTGGATAAGT | 10152 |
| rs554698136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203381828 | CATTTTTTTAAAATA[C/T]ATAATTCATAGGTTT | 10152 |
| rs554715176 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364471 | TTCTACCACTGAACC[A/G]CCATTGCGCTGACTT | 10152 |
| rs554715180 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203332461 | GAAACCGCGTATCTA[A/C]TAAAAATACAAAAAT | 10152 |
| rs554715412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203405696 | TGATCTGAAGTGTGT[A/G]TTTTATGAGCTTTTT | 10152 |
| rs554716076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203421756 | CAGATGACAAGGTCA[A/G]GAGATCAAGACCATC | 10152 |
| rs554769874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203402456 | GCATTGTATATTTCA[A/G]ATACCAGTTAAACTA | 10152 |
| rs554822490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203328780 | GGCTGGGGCTGGTGA[A/G]TGGGTGGGAATTCTC | 10152 |
| rs554840083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203399404 | TTAATAGGGTTTTTT[C/T]CCTTATCATTGAGTT | 10152 |
| rs554852715 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392218 | TGGCTTTATGATATA[C/T]GCTAAACAAGTTTTT | 10152 |
| rs554883269 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388950 | AGCAAATTGATGTAG[C/T]TTTAGTGTTTGGTTC | 10152 |
| rs554884223 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203352741 | GCGTAGCATAAATCT[A/G]CAGTGTTTTTAAAGT | 10152 |
| rs554894686 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203358483 | CTTAAACAACAAAAC[A/G]TAAATTTATTAGTTA | 10152 |
| rs554963692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203389737 | ATCACATATGAACCT[A/G]TGTGGTGAACATTAA | 10152 |
| rs554982968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203390492 | AAAAAATTAGCTGGT[C/T]GTGGTGGCATGCACC | 10152 |
| rs555004816 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374165 | CACTGTCTCAACAAC[C/T]CAAAACACAAAAACT | 10152 |
| rs555029884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203383900 | CTTTTTGAGCTCTGT[C/G]TTTGCTGCTCCCATT | 10152 |
| rs555036492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345653 | ACTTCAGGTGATCCA[A/C]CCACCTCGGCCTCCC | 10152 |
| rs555052398 | snp | C/T | 0.167158 | 0.235875 | intron-variant | ABI2 | GRCh38.p7 | 2:203331347 | AAATGGTCAATTTAG[C/T]CTTTTTTTTTTTTTT | 10152 |
| rs555066510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203382795 | TGTAGAAAAATTATT[A/C]TTTTTTCCAAATAGC | 10152 |
| rs555096710 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203394900 | GTACCATAATCTGTT[C/G]AGATTACTTCAGGTA | 10152 |
| rs555106360 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203408934 | AGCTCCGCTTCCCGG[A/G]TTCACGCCATTCTCC | 10152 |
| rs555150208 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203358571 | AGAATTCTGTGTCTC[A/G]TTTCTGCTTCTTTAT | 10152 |
| rs555158837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203351142 | TTGTTTTGGCATCTT[C/T]GTCAAAAATTACCCA | 10152 |
| rs555182509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203334853 | TTTAGTAGAGACGGG[A/G]TTTCACCGTATTGGC | 10152 |
| rs555184744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203386174 | GGGGAACAAAACTGG[A/G]CAGAGAATGAAGGCC | 10152 |
| rs555243538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203402154 | ATTCTTACGCCTCAG[C/T]CTCCCGAGTAGCTGG | 10152 |
| rs555300905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203349461 | CCAGGCTGGAGTGCA[A/G]TGGTAGGATCTTTGC | 10152 |
| rs555320693 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203345375 | CAAACTCCGGACACA[C/T]CATCTTTAAGAACTG | 10152 |
| rs555340623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203334001 | GTTAGAGTGCAGTGG[C/T]GTGATCTTCGCTCAC | 10152 |
| rs555343567 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418559 | CACATAGGCTTCTCC[A/G]TAGGGCAGCTCACAA | 10152 |
| rs555377188 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203341450 | CCAGGCTCAGTGGCT[C/G]ACTCCTATAATCCTA | 10152 |
| rs555438835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203348743 | TGTATTTTCTTCCTC[C/G]CATCACGTATGTACA | 10152 |
| rs555463085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203349916 | GGGTATATACCTAAG[A/G]GTAGAATTGCTGGAT | 10152 |
| rs555484841 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413836 | GGTAGCAAATACTCA[C/T]TCTGCATTAAGTTTG | 10152 |
| rs555514188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203386465 | TTTTTTTGGAGAGAC[A/G]TGGTCTTGCTGTGTT | 10152 |
| rs555526916 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327126 | AGTGATTTTTTTTTG[A/C]AAGTATAAGTTTCCT | 10152 |
| rs555584170 | in-del | -/CTC | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203340906 | TAGCCTTGACATCAT[-/CTC]CTGTTACACTCCTTT | 10152 |
| rs555591834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203354490 | TACTGAAACATATCA[A/G]TAAACTACCAATTGT | 10152 |
| rs555604254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203353775 | AGTGTTGGGATTACA[A/G]GCGTGAGCCACCATG | 10152 |
| rs555631549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203425684 | AGGCATTTGGTTATA[C/T]ATTGAGAAATGCACA | 10152 |
| rs555642581 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423845 | TAAGCTAAGAAGTTT[C/T]TTTCAGTTTTACAGA | 10152 |
| rs555722062 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203348090 | TCCTAAAAATACAAA[A/C]GTTAGCTGGGCATGA | 10152 |
| rs555741995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203359548 | CTTAGTTCATTGGTC[C/G]TTCTAAAACAAAATA | 10152 |
| rs555750007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203364260 | CACCACACCCAGCTA[A/G]TTTTTGTATTTTTAG | 10152 |
| rs555773197 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203403631 | CGTACAAAATAAGAT[G/T]GGTGATCATTTTCTT | 10152 |
| rs555825255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203418596 | AGCTAACTTCATTAG[A/G]ATGAACAAGCAAGAA | 10152 |
| rs555839868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203396207 | ATACTACCCTCTTTT[C/G]TCTGAAACAGAAAAA | 10152 |
| rs555864520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203352696 | AGGTTAATTTATTAT[C/T]GGAGAGAGAAAATTT | 10152 |
| rs555880647 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203417486 | CTTCCACAGAATAAT[A/G]GTTTCTCAGTTTCTT | 10152 |
| rs555908265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203404138 | CTCTTTTTTGGAGGG[G/T]AAGGCGGATGAAAAG | 10152 |
| rs555915585 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402173 | CGAGTAGCTGGAATT[-/A]ACAGGCGCACGCCAC | 10152 |
| rs555930166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203331273 | TGGTTGACCAGCAGG[C/G]GTTTTGATGCTGCCT | 10152 |
| rs555943700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203424940 | GCAGTGGGAAAATCA[A/C]GGCTTATTTCAGCCT | 10152 |
| rs555997808 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | ABI2 | GRCh38.p7 | 2:203348257 | AAATAATAATATTTT[A/T]TGTGAAAATAAATGT | 10152 |
| rs556006972 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203345846 | GCACTGTGCCCAGCA[A/G]TATTTTCTTTTTTAA | 10152 |
| rs556037118 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ABI2 | GRCh38.p7 | 2:203371955 | TATTTTTAATTGATC[A/G]TTCTTGGGTGTTTCT | 10152 |
| rs556039019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203378995 | TGATTTGAAATAATT[A/G]CTGCTTACATACCAC | 10152 |
| rs556047567 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203421443 | GCAAAGGAATAAGAG[A/C]CACCTGATTTGCAAA | 10152 |
| rs556081856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203410941 | GTTAATGATATGAAA[A/C]AAGATCAATTATATA | 10152 |
| rs556123304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203375135 | GCCTGCAGCATGCAA[C/G]ATCAGCTTGGCAATA | 10152 |
| rs556157759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203406596 | ACAGCATCACCATAA[A/G]TGTCTAAAACGTCTA | 10152 |
| rs556168646 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327373 | TCTGATTTAGGAAAA[C/T]AAGACACAGTATCTG | 10152 |
| rs556182878 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203377365 | AGAAGCTATAAGCTT[C/G]TAATTCTGTTATGGC | 10152 |
| rs556284263 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429181 | ATTAGCTTTCATTAA[C/T]TTGCCTCCAGTATAC | 10152 |
| rs556296018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203407358 | GGCTATATAATATAT[A/G]TATCTCCTCTAAATG | 10152 |
| rs556346268 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203371068 | GACTTCTTTGAACTT[A/C]GGTTTTTTCATCTGT | 10152 |
| rs556388521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203368163 | GGCTGCATAATGTTG[C/T]GTGTATATGTTGTAC | 10152 |
| rs556390151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203384529 | TGGCCTGGCTGGTCT[C/T]GAACTCCTGTGCTCA | 10152 |
| rs556393123 | in-del | -/TTATC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346831 | TGAAATGTCATTCCT[-/TTATC]TTATCTTATATTCTT | 10152 |
| rs556394325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203376678 | TGCTCTATTATAACA[A/G]TGACCCTTTATTTTA | 10152 |
| rs556434715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203382501 | AATGTTAATATATTT[G/T]GTGAAACTGAAATGT | 10152 |
| rs556470515 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203421854 | CTGTAGTCCCAGCAA[A/C]TCAGGAGGCTGAGGC | 10152 |
| rs556472394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203423486 | GCTAGAGTGCAGTGG[C/T]GCAATCTCGGCTCAC | 10152 |
| rs556571575 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376538 | TAAAAAGCAACAACA[A/C]ATATATTTTTAAAGA | 10152 |
| rs556577203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203379846 | GATAAGCAAGTGAGC[A/G]GCATGGCTGTATTCC | 10152 |
| rs556591126 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | ABI2 | GRCh38.p7 | 2:203418651 | GACACTAGTCCTTTT[G/T]TCACCTTAACCCAGC | 10152 |
| rs556606732 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429960 | CATGGGTCTGCTGAT[C/T]TTTTTTCCCTATTTA | 10152 |
| rs556615844 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203412258 | AGCTCTATAAGAGCA[A/T]GGAGTTTTGCCTGTT | 10152 |
| rs556623298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203420301 | ATCTATTCTTTTGTT[C/T]TTCTGGCTCAGTGAT | 10152 |
| rs556626155 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338418 | GGGGGCAGATCCCTC[A/G]TGAATGATGTAGCAC | 10152 |
| rs556672840 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203410958 | GATCAATTATATATA[-/AT]ATATATATATAAAAC | 10152 |
| rs556686352 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203419546 | GGTAATTTTTTGTAT[A/T]TTTTTTTTTTTTGGT | 10152 |
| rs556742206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203391547 | GGCCAGGTGTGTTGG[C/T]TCATGCCTGTAATTC | 10152 |
| rs556775917 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361017 | CCTCAGCATGAGCAC[G/T]AGCTCCACAGGTGTG | 10152 |
| rs556788683 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203379222 | AGCAGCTTTGCCCAA[A/G]CAACTTGGTCTTTTG | 10152 |
| rs556792716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203388005 | ATATTTTTATATTTA[C/T]CAGATTATTTTAGTT | 10152 |
| rs556854247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203387178 | GTCTGCCACTGTTCT[A/G]TGGTAGTAGGTCATC | 10152 |
| rs556881696 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374101 | GTGGTCGAGGCTGCA[A/G]TGAGCCATGTTCATG | 10152 |
| rs556906227 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332237 | GCTGATATTTATCAG[A/T]TCAATTTTATTTCTT | 10152 |
| rs556914733 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203349426 | TCTTCTTTTTTGAGG[C/T]GGAGTTTTGCTCTTG | 10152 |
| rs556915975 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368771 | TCAGTTGGGAAAGGC[A/C]TCCTGAAGGAAATAA | 10152 |
| rs556954837 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203373009 | GAGGGGCTCCTCACG[C/T]CCCAGACGATGGGCA | 10152 |
| rs556985205 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328095 | GGCCGCCGGGAGGTG[G/T]GGGCTTCTCCAGCCG | 10152 |
| rs557024107 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203336182 | TATGAAAGAATCATA[A/T]TTTGTTCATCCATTC | 10152 |
| rs557026967 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203357854 | GCTCACTGCAGCCTC[C/T]GCCTCCTGGCTTCAA | 10152 |
| rs557053105 | in-del | -/TG | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203396417 | GTCTATTTTCTGATT[-/TG]TGTAATTCAAAATGG | 10152 |
| rs557066088 | snp | A/G | 1.85803e-05 | 0.00304792 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427382 | GTGCTTGCCTCACAG[A/G]AATAGTCAGGTCTTC | 10152 |
| rs557075785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203337264 | TAAAGACTCCACCAA[A/G]AGACTGTTAGAATTA | 10152 |
| rs557158269 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203342733 | GGGATTACAGGTGCT[C/T]GCCACCATGCCTGGC | 10152 |
| rs557279806 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421534 | CCTTTGGCACCCAGT[C/G]TTTTGTACTTTAAGA | 10152 |
| rs557283523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203340530 | TACCACCACACATGG[C/T]TAATTTTTGTAGTGA | 10152 |
| rs557308269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203335603 | AATTACATGTAAATT[C/T]ACCTTGCAAGTTTTT | 10152 |
| rs557351682 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203398757 | TTGATGTGTTTTTTT[C/T]CTCTAAAGTTGTGCC | 10152 |
| rs557372635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203404829 | CTCCCAAAGTGCTCA[C/G]ATTACAGGTGTGAGC | 10152 |
| rs557416178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203388944 | TTTCTCAGCAAATTG[A/G]TGTAGTTTTAGTGTT | 10152 |
| rs557416843 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410859 | TAAACTTGTAACCTT[C/T]CAAGGTAAAATTCAG | 10152 |
| rs557428419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203351092 | CAGTTGACCCAACAC[C/T]ATTTGTTTAAAAGCC | 10152 |
| rs557442268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203337944 | CTGAGTTGGGAGAAT[C/T]GCTTGAACCCAGGAA | 10152 |
| rs557445430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203341385 | GAATTAGATCTTTTC[C/T]AGTAAGCATTAGAAA | 10152 |
| rs557499025 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203401879 | TGTGTGTCAAACATT[G/T]TTTCTCTTGCTTTCC | 10152 |
| rs557500454 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203416108 | AAAAATTCATTAAGA[C/G]GAAAGTAGTGGGTTA | 10152 |
| rs557508243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203389662 | TTTAGAAAAGTTGAG[A/G]TCCTTTTTCAAAATA | 10152 |
| rs557532000 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365952 | TATCTTAATGCTTAC[A/C]GGACTTTATTTGTAT | 10152 |
| rs557581357 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203376479 | CTTTCTGTATACTTA[G/T]GCTGTTTAAAAAACA | 10152 |
| rs557616085 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392598 | AGAATGTAGATGGCA[C/T]AGTAGTGTATAATGG | 10152 |
| rs557623515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203405575 | AATTATGTAAGTCTC[C/T]TGTATTACTCCCAGT | 10152 |
| rs557631298 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203353025 | AGTGTGTAGTATGCT[C/G]TTTCATCTAGATTTG | 10152 |
| rs557711847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203350632 | GCAATCTCTGCCTCC[C/T]GGGTTCAAGTGATTC | 10152 |
| rs557718459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203355356 | AAAAATAAAATAAAA[A/T]AAAAAATTAGCCAGG | 10152 |
| rs557779841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203363413 | TCTTTTCTATTTTTC[A/G]TATCCATTAACCATT | 10152 |
| rs557822931 | snp | C/T | 0.272511 | 0.248984 | intron-variant | ABI2 | GRCh38.p7 | 2:203395446 | AAATATATATATATA[C/T]ATACACACACACACA | 10152 |
| rs557902277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203393784 | TTCTTTTAGTGACCA[A/G]GATCTCATCTACAAT | 10152 |
| rs557902803 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413535 | CTATCACAGTTGATT[C/G]CCTTTTGGATTGGTC | 10152 |
| rs557954328 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203333918 | TAATAAACTGTTCAT[G/T]TATTTTTTCTTTTCT | 10152 |
| rs557962013 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203403532 | TATTCTTTGAAAGAG[A/T]CTTGCAGAAGAAATT | 10152 |
| rs557974710 | in-del | -/CT | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203374658 | AAAAACTGAAAATTA[-/CT]CTGTTAGTAACTAAT | 10152 |
| rs557993257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203362680 | GACAGGTGTGGGCCA[C/T]CGTGCCTGGCTAATT | 10152 |
| rs558005755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203353699 | GATGGGGTTTTACCA[C/T]GTTGGCCAGGCTGGT | 10152 |
| rs558026706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203401218 | TTTCCTTTTCACTTA[C/T]CTCCTCCTTTTCTCC | 10152 |
| rs558029829 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326324 | GCCATAGTTGAAAAA[A/T]TGCTGGGTGGGAATA | 10152 |
| rs558033256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203360334 | GGTCGGTTATCAATG[A/G]TAAAGGTTCTTATTG | 10152 |
| rs558039872 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203383188 | AAGATGACTGAGCTC[C/T]GAATCATTAACTAGT | 10152 |
| rs558041264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203379519 | GCTTGGATTACGGGC[C/T]TGAGCCACTGTGCCT | 10152 |
| rs558054471 | in-del | -/TG | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203426592 | TTTTGAAAAAATATA[-/TG]TGTAGCGGACTCCCA | 10152 |
| rs558062237 | in-del | -/TCTTT | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203386287 | TGTGTGTTTAAATTC[-/TCTTT]TCTTTTTTTTAAAGA | 10152 |
| rs558115738 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203358690 | CTGACATCAGAAGAC[A/G]AAAGCATTCTCTCTT | 10152 |
| rs558149971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203409875 | ATCAGAGATTTGAGG[A/C]TGAGTGACCTGAAAA | 10152 |
| rs558156002 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203418384 | ACGGCTGCAATCAAG[A/G]TATCAGCTGAGGCTG | 10152 |
| rs558168316 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423967 | AACATTTAGAAGAAC[A/G]ATGTGTAAGTCCTTT | 10152 |
| rs558175483 | in-del | -/TTTG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203348921 | TGTTTTTTTTTGTTT[-/TTTG]TTTGTTTGTTTGTTT | 10152 |
| rs558177158 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203367141 | ATTATGTAAGTTAAC[G/T]CACATGTACGATTTG | 10152 |
| rs558203376 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203359326 | CAAGTTGATAGAATT[G/T]TCACTGATTACATTT | 10152 |
| rs558221998 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203398906 | TTATTGCTTAGTAGT[A/G]TTGTATTGTATGGGG | 10152 |
| rs558286887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203410545 | GCAGGGAAATACACC[C/T]TGGGAAGGAGAGTGG | 10152 |
| rs558375249 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203405783 | GACAATCTTTGGAAG[C/G]TTTCATGTGAATATA | 10152 |
| rs558465238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203328926 | TCCGCGCCGGTCAGC[G/T]TTCCGGATGGCGGAG | 10152 |
| rs558517574 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | ABI2 | GRCh38.p7 | 2:203349173 | TCTCCAACTCCTGAA[C/T]TCAAACAGTCTGCCT | 10152 |
| rs558535701 | snp | C/G | 1.65075e-05 | 0.00287289 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416947 | CACCTGTGGAAGAAC[C/G]AGTCTTTGATGAGTC | 10152 |
| rs558566751 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365202 | GACTTTTTTTTGTGC[C/T]TGTATTTACACACAG | 10152 |
| rs558575648 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399459 | TTTATAGATTATGAG[C/T]TACAAATATTTTCTT | 10152 |
| rs558578896 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329733 | CATCTCTCCAGGGAT[C/T]CTTCTTTTTTCTTTT | 10152 |
| rs558601078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203374179 | CCCAAAACACAAAAA[C/G]TTTATATAGATAGCC | 10152 |
| rs558610348 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203415477 | AAAAAATTAGCTGGG[C/T]GTGGTGGCGGGCGCC | 10152 |
| rs558612922 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203406555 | AAAAAGCCATTTCAC[A/G]TATTCTCTAAATGAT | 10152 |
| rs558616169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203336315 | TTGGGTAAATTTAAG[A/G]GAAAAGATCAACTGT | 10152 |
| rs558625250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203414187 | GCTCTCTGCCACCTT[C/T]CCCTCCTGGGTTCAA | 10152 |
| rs558678795 | snp | A/G/T | 0.00239393 | 0.0345281 | intron-variant | ABI2 | GRCh38.p7 | 2:203344427 | TTGGAGTGCAGGGGC[A/G/T]TGATCATGTCTCACT | 10152 |
| rs558682546 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396406 | ATATGGAATATGTCT[A/G]TTTTCTGATTTGTGT | 10152 |
| rs558703649 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338407 | AATTGGATTATGGGG[A/G]CAGATCCCTCATGAA | 10152 |
| rs558744660 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427773 | GGTTAACCTCATGGC[C/T]CAGTGGGTACCCTAG | 10152 |
| rs558756336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203399488 | TTCCATTTTGTGATT[C/T]GTTTGCTTATTTTCT | 10152 |
| rs558786629 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203373887 | CTTTAGGCTGGGTGT[C/G]GTGGCTCATGCCTGT | 10152 |
| rs558819599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203329988 | GTCATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 10152 |
| rs558837645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203381537 | CTCCCAAAATATTGG[A/G]ATTACAGGTGTAAGC | 10152 |
| rs558840139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203390655 | AAAAAGAAAGTTATC[G/T]CTAAAAATAAGGAAT | 10152 |
| rs558879353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203425012 | CCACAGGCACGCGCT[A/G]CCATGCCAGGCTAAT | 10152 |
| rs558937746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203420684 | AGGTGTGAGCCACCA[C/T]GCCCAGCCGACAGTC | 10152 |
| rs558942616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203424544 | GGACCACAGACGTGC[A/G]CCACCATGCCTGGCT | 10152 |
| rs558958147 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203404622 | GGAGTGCAGTGGTAC[A/T]ATCTCGGCTCACTGC | 10152 |
| rs559001351 | snp | A/G | | | intron-variant, missense | ABI2 | GRCh38.p7 | 2:203376070 | AGGCAAATTAGAGGC[A/G]TTGATCTTGAGTCGA | 10152 |
| rs559011498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203339998 | TATATTGGACCCACA[C/T]AGTTAAAGGGTCAAC | 10152 |
| rs559023091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203331408 | CCCAGGCTAGAGTGT[A/G]GTGGCGCGATCTCGA | 10152 |
| rs559028562 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203352249 | AGGACGGCTTGAGTT[C/T]AGAAGTTCAAGGTTA | 10152 |
| rs559054801 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384663 | TTACTGAGGTCAGTA[C/T]GATGTGTTTGTAATG | 10152 |
| rs559061367 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203345700 | AGGCCTGAGCCACCA[C/G]GCCCAGCCCTAATTT | 10152 |
| rs559117084 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431116 | TCTGGTCTTTTTGGC[C/T]GGGAACTCCTGATTG | 10152 |
| rs559165628 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203410138 | AGGTTCCCTTCTTCA[A/C]GTCCCTGCTGAGAGG | 10152 |
| rs559227927 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203417815 | AATTTTAAAACCCCA[C/T]AAAATAATGGTTTTC | 10152 |
| rs559260123 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203417167 | AGAGAATCTTATTTT[C/G]TACTAAGTGAAGTTC | 10152 |
| rs559269178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203422411 | GTGCACTAACTGGGG[C/T]GGTGACTATGATGAT | 10152 |
| rs559277745 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203335856 | TGGTACAAGTCACCC[A/T]TTTTAGGTGTAAAGG | 10152 |
| rs559278344 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403008 | GCTTTTTAAAATAAC[A/G]TTGTGGTGAATGGTA | 10152 |
| rs559314368 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203406732 | CAGTGGCACAATCTT[-/G]GGCTCACTGCAACCT | 10152 |
| rs559339866 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404600 | GTCTTGCTCTGTCAC[C/G]CAGGCTGGAGTGCAG | 10152 |
| rs559359671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203354882 | AACATTTCTGGAAAA[C/G]ATGGTGTGGAATAAA | 10152 |
| rs559360017 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203335226 | TTGAATATGCAAGAG[A/C]CTATGCACTGAATTA | 10152 |
| rs559363814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203343879 | TCACACCTCTAATCT[C/T]AGCACTTTGGGAGGC | 10152 |
| rs559382053 | in-del | -/GATT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388729 | AGATTTTAATATATA[-/GATT]GTTTATTTTATGCTA | 10152 |
| rs559386145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203378267 | ACAGGCACCCGCCAC[C/T]ATGCCCGGCTAATTT | 10152 |
| rs559404801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203334160 | TGGCCAGGCTGGTCT[C/G]GAATTCCTGACCTCA | 10152 |
| rs559418941 | snp | A/G | 0.084728 | 0.187577 | intron-variant | ABI2 | GRCh38.p7 | 2:203373199 | AGTGAACCAGACTCT[A/G]TCTGCAATCCCGGCA | 10152 |
| rs559459645 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422067 | TTAAGAGGCTGAGGC[C/T]GGCGGATTGCTTGAG | 10152 |
| rs559513969 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203372212 | TAACCCTGAGTGGAC[A/C]CAGCACATGTTTCAG | 10152 |
| rs559542126 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203341540 | GCCAAGATGGCGAAA[A/C]CCCATCTCTACTAAA | 10152 |
| rs559569700 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392876 | AGATCCTTGGGGACC[A/G]GAGTTGCTGAGGCCC | 10152 |
| rs559595922 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203343044 | AAGAAGAAAAAGGAG[A/T]ACTTTATTTCCTATA | 10152 |
| rs559601873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203379420 | ACCCAGCTACTTTTT[A/G]TAGAGACGGGGTTTC | 10152 |
| rs559611675 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327599 | GACAGCGAAGTTGAT[A/G]GCATTAGAGAAATGA | 10152 |
| rs559614903 | in-del | -/AT | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203343369 | TATGTCTCAAAAAAC[-/AT]AAAAAAATTTAATGT | 10152 |
| rs559648954 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203401286 | CTTGCCCTCCTCCAC[C/T]TTCATCTCCTCCTCC | 10152 |
| rs559743270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203355633 | TCTGGAGTTCCAGAC[C/T]AGCCTGATCAACATG | 10152 |
| rs559758308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203338266 | AAATTAGCTAGAAAT[A/G]GATTAAAGACTTAAA | 10152 |
| rs559760097 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203345966 | GGGCAAATCACCTGA[G/T]ATCAGGAGTTTAAGA | 10152 |
| rs559777299 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356821 | TTTTAAAATGCAGTT[A/G]TTTCTGAAAGTTTTT | 10152 |
| rs559794930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203379957 | CCAAACATTAAAAAA[C/T]GTAAACACCACTCTT | 10152 |
| rs559814611 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | ABI2 | GRCh38.p7 | 2:203376039 | TAAAAGTTATTTACT[A/T]AAAATATCTATACTT | 10152 |
| rs559838220 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388435 | TGCCTGTAATCCCAG[C/T]GCTTTGGGAGGCCAA | 10152 |
| rs559919917 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203426277 | ATTGAGTGGTATAAA[A/G]TAGGTACAGAAGATG | 10152 |
| rs559972775 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203371434 | TATCAGACACTTTTT[C/T]GTATTAAAAGGACAA | 10152 |
| rs559975571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203349568 | TGCCACCATGCCTGG[C/G]TAATTTTTGTATTTT | 10152 |
| rs559984608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203384029 | TTAAAAGTTTAACTT[C/T]TACTATTTTATACAG | 10152 |
| rs559986925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203386684 | CTCACTCTGTCACCC[A/G]AGGTGGAGTGCAGTG | 10152 |
| rs559996098 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203345491 | TCTTAGCTCACTGCA[A/G]TCTCCACCTCCTGGG | 10152 |
| rs560028653 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403408 | TTGCCAGGAAGCCAG[G/T]AAGCCTATGTGTGAA | 10152 |
| rs560039589 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203403733 | CTAAGTTCCATGTTC[G/T]TTCTTTCTGTTTTTT | 10152 |
| rs560063469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203390972 | TCCTTTGTTATGTAG[C/T]GTAGCATATTATTTC | 10152 |
| rs560093339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203395629 | TGTTTATAAATACTC[A/G]TGTTTTGGTGGCTCT | 10152 |
| rs560167608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203352151 | ATACAGATACACATA[C/T]AGATGTAGCAGCTGG | 10152 |
| rs560168034 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203405143 | GTAATGTGTGAGTCA[A/G]TTTAGTTGTGCTTTT | 10152 |
| rs560197236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203393314 | CCTGCCCCGGCCTCC[C/T]GAAGTGCTGGGATTA | 10152 |
| rs560208368 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203331701 | CTTAGCCACTAGCTC[A/G]AGTTAACTAACCCAA | 10152 |
| rs560245784 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203408287 | CCTGGTTCAGCCTCC[A/C]GAGTAGCTGGGGTTA | 10152 |
| rs560258262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203401352 | CCTGCTTATTTCTCC[A/G]CCTCCTCTTCTCTCT | 10152 |
| rs560270978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203353914 | TATGAGATATGGTAA[C/T]TTAGCTTTCTTATAT | 10152 |
| rs560316346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203413644 | ACTAATTTTACAGAC[A/G]TGGCAGGACTTAAAC | 10152 |
| rs560340680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203358992 | ACTTCAGCCTGGGTG[A/G]CAGAGTGAGACTCTG | 10152 |
| rs560349420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203368905 | CACTGCAACCTCGAA[C/T]TCCTGGGCTCAAGGG | 10152 |
| rs560351275 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203376833 | AATATGTAAATGTCC[C/G]CAATCCCTAGACCAA | 10152 |
| rs560433213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203369565 | ATCATATAAATTGGC[A/G]TTTAATTAATGTGGT | 10152 |
| rs560461228 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203399667 | TTACAGGCACCCACC[A/G]CCATGCCCAGCTAAT | 10152 |
| rs560477219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203406766 | CCTCCTGGGTTCAAG[A/C]GATTCTCCTGCCTCA | 10152 |
| rs560482100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203347022 | TTATTTAGGAAGGAC[C/T]TTGTGTTCTTACATG | 10152 |
| rs560554211 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203407732 | AAAGAGTCTTGTCTT[A/G]TGAGGAATCATTTTA | 10152 |
| rs560632408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203397541 | AGACTCAATTGCTAC[A/G]AAATATATTTGTAGA | 10152 |
| rs560637741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203341617 | CGGGAGGCTGAGGCA[C/T]GAGAGTTGCTTGAAC | 10152 |
| rs560688410 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203422304 | ATAAAAAGAAAAAAA[A/T]TATCGAGAGTCCCTA | 10152 |
| rs560756070 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347025 | TTTAGGAAGGACTTT[A/G]TGTTCTTACATGAGT | 10152 |
| rs560765869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203356415 | GCTCTGTTGCCCAGG[C/T]TGGAGTGCATTGGCG | 10152 |
| rs560768350 | snp | C/G/T | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203345037 | AAGCTGGCTGCCGGA[C/G/T]CCCGCAGTGGCAACC | 10152 |
| rs560781227 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203379276 | TTTTTGACACAGGGT[C/G]TTGCTCTGTCACCCA | 10152 |
| rs560783038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203372309 | ACAGAACAAAATGAA[A/G]AGTCTCCCATGTCTA | 10152 |
| rs560797735 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203360596 | AAGAAGCAGTTTAGC[A/C]AAATGGAGAATTTAG | 10152 |
| rs560870029 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203373145 | GTAGCGAGCCGAGAT[C/T]ACGCCACTGCACTCC | 10152 |
| rs560871598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203415612 | ATAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 10152 |
| rs560895292 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329049 | CAAATTCTGGATGAT[A/T]TTTAAGGGGTTATCT | 10152 |
| rs560900112 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203412329 | GACACATAGCAGGCA[C/T]TTTTGGTCCCTGCTT | 10152 |
| rs560909268 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203400203 | AGTGATTCTCCTGCC[A/G]TAGCCTCCTGAGGAG | 10152 |
| rs560910820 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363292 | AAACATTTACCCTTT[A/G]TATTATAAACAATCC | 10152 |
| rs560920663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203356962 | GAATGACCGAAAGCA[C/T]TGGGAATGTTAAAGG | 10152 |
| rs560942229 | snp | A/C | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366309 | GGGTTATAACACTTA[A/C]AATGTTTGGGAAGGA | 10152 |
| rs560951956 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427931 | CACTTGAGTGCACCA[A/G]ACGAGTGAATGCTGA | 10152 |
| rs560955399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203419626 | TCGTGATCTGCCCAC[C/T]TCTGCCTCCCAAAGT | 10152 |
| rs560982780 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203364585 | GCCCCAAATAACTTT[A/T]TGACGAGCATGCAAA | 10152 |
| rs560983918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365227 | ACACAGGCACATACA[A/G]AATTATGATGATTAT | 10152 |
| rs561031813 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388071 | TTTACCTATTATAAA[A/C]ATTGTTTTGTTTGGC | 10152 |
| rs561033684 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203336572 | TCTATTGTACCCTTT[C/T]AGGTAGTAGCTGCAG | 10152 |
| rs561048314 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366485 | TATGGCCACATTTCA[C/T]ATATTAGAGTGAAAG | 10152 |
| rs561058311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203419090 | TTAGCAAAAATATCC[C/T]TCCTAAATTAAAGAT | 10152 |
| rs561058817 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327552 | AAATCGTTTTCAAAA[A/T]TTTAAATACTGAATC | 10152 |
| rs561083179 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203379127 | CAATACATTCTTACT[C/T]GTATGTCTTATGTGA | 10152 |
| rs561098887 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326892 | TCACTGCAAGCTCTT[C/T]TCCCAGGATGACGCC | 10152 |
| rs561168354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203335692 | TTTGCATAATTCATG[C/T]AAGGAACATAGTTTT | 10152 |
| rs561169116 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203356510 | AGTAGCTGGGACTAC[A/G]GGCGCGTGCTGCCAC | 10152 |
| rs561183740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203358198 | GTCATAGCTCGCTAT[A/G]TCTTCACTGCAGCTT | 10152 |
| rs561200482 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385791 | TTTTGACAAAAGCCA[C/G]TTGTTAGAATCTGTT | 10152 |
| rs561224933 | snp | A/G | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326485 | GATTATTCATATGTC[A/G]TATTCACTGAAGCAA | 10152 |
| rs561313073 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377619 | GACTCACTAAACTTT[A/C]TTCAAGGCCAGTACA | 10152 |
| rs561326177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203367733 | ATGTAACTGTGGGCT[A/G]GGCACACATCTGTAA | 10152 |
| rs561335606 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203431920 | AATGGCTTACAAAAA[A/G]GAATGTAAACAATTT | 10152 |
| rs561368989 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203329416 | GGTAGGGGCGTGTGT[A/G]TGGAGGCGGGGGATA | 10152 |
| rs561387165 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203375233 | TACAATTGCAGTGAT[A/T]TATCTTGGTGTGTTT | 10152 |
| rs561425405 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345033 | ATAAAAGCTGGCTGC[A/C/G]GGAGCCCGCAGTGGC | 10152 |
| rs561432923 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203349273 | TGAACACTTTAGTGT[G/T]TTTTTTCCACAAACA | 10152 |
| rs561445689 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328487 | CCTCTGCGACCTGTA[G/T]GAGGAGGAGGAGGAG | 10152 |
| rs561450277 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347685 | AATACTTTAGGTTTA[C/T]TCTGCACAGGCAAAC | 10152 |
| rs561463957 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368818 | GACGAAATAGATGAA[-/T]TTTTTTTTTTTTTTA | 10152 |
| rs561515124 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203335467 | GGATCTCACTATGTT[C/G]CTCCGGCTGGTCTTG | 10152 |
| rs561560473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332864 | AAGTTACTGATTTTT[A/G]TGAGTGACAGTTCAC | 10152 |
| rs561574948 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203380107 | GCAAGCATAGTTTAG[A/T]ATATGAGTAGCAATA | 10152 |
| rs561649655 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203393375 | AAAACATTTTTATTG[-/C]CTGGGAAAAATTGTC | 10152 |
| rs561699532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203377768 | GAAATTAGGCCAGCA[C/T]GGTGGAACACGCCTG | 10152 |
| rs561706789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203401289 | GCCCTCCTCCACCTT[C/T]ATCTCCTCCTCCTCT | 10152 |
| rs561777698 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203361645 | AGAGCCTGTTGTGTT[G/T]CATGGCAATAAAACC | 10152 |
| rs561782570 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203378238 | CTGCCTCAGCCCCCC[A/G]AGTAGCTGGGACTAC | 10152 |
| rs561824882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203347540 | CTCATGGTTCAATTT[A/G]ACAAGGCGTTTATCA | 10152 |
| rs561841057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203370751 | TTTGTAGAGAAGATT[A/G]AGTTGAAGGAATGGA | 10152 |
| rs561842044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203378478 | GTTTTTTATTTGATG[C/T]TCCATTTATACATTC | 10152 |
| rs561846270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203393110 | GTACAATATTGGCTC[A/G]CTGCAACCTCTGCCT | 10152 |
| rs561848989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203416509 | CCATGTTGCCCAGGC[C/T]GGTCTTGAACTTCTG | 10152 |
| rs561890511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203342923 | TTTCTAGTTTTTTAA[C/T]CATTCATGCATTTGT | 10152 |
| rs561910456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203346891 | CAGTAGACCTTAAAC[C/T]TAGGCCCTTGTTTGT | 10152 |
| rs561928010 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203354803 | TATTGGTCTGTAAAC[A/C]TGCCTGCCCTTTGCT | 10152 |
| rs562012454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203355464 | CTGCAGTGAGCTGTC[A/G]TTGCACCACTGCACT | 10152 |
| rs562020163 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418808 | TTTAGAAGTTGTCTC[C/T]CACAAAACTATAAAC | 10152 |
| rs562036021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332393 | GCACTTTGGGAGGCC[A/G]AGGCAGGCACATCAC | 10152 |
| rs562081071 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203424831 | TACCATTATAAACAG[A/T]CTCTGGAATCATGTT | 10152 |
| rs562085499 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408686 | TCCCACTTTTCTGTT[A/C]CACGGAAGGTTAGGT | 10152 |
| rs562096737 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413309 | TAAAGCAGGATGTCA[C/T]TGGTTTTCGCCAGTC | 10152 |
| rs562116835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203389253 | CTTTACTCTTACTTG[A/C]TAATGTTTGTTTTTA | 10152 |
| rs562140383 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385352 | TAGCCAGGATGGTCT[C/T]GATCTCCTGATCTCG | 10152 |
| rs562157519 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203341718 | CCATCTCAAAAAAAA[A/C]CAAAAGAAATTAGTT | 10152 |
| rs562159143 | snp | C/G | 1.711e-05 | 0.00292484 | intron-variant | ABI2 | GRCh38.p7 | 2:203417120 | ATAGATGGGAAGAAA[C/G]CTCTACATAGAAATG | 10152 |
| rs562192774 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203351363 | GATCATTTGTTAATT[A/T]CTGCCACAAAGGCAG | 10152 |
| rs562209034 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203387480 | ATAGCCTATTGGGAA[A/C]GTGTTTGAGCTGTGG | 10152 |
| rs562224025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203409236 | GTGGGAAGCAGACAC[A/G]CAAGTCAAGGATTTA | 10152 |
| rs562252721 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415596 | CACTCCAGCCTGGGC[A/G]ATAGAGCGAGACTCC | 10152 |
| rs562322109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203358169 | TTGACCAGGCTGGAG[C/T]GCAGTGGTAGTTAGT | 10152 |
| rs562330599 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390716 | TTACTCTTTATTAAA[A/G]CTAAAATTTTGTAGT | 10152 |
| rs562353831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203402931 | AGTATGTGATTTCCA[C/T]GTAAAGTCATACAAC | 10152 |
| rs562384699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203357376 | ATATCCACAGCATTT[C/G]TAGAAACCTCACTTA | 10152 |
| rs562390262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345069 | GCCGGGGTCCTCTTC[C/T]ATGCTGTGGAAGCTT | 10152 |
| rs562393303 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203394373 | CTTTAATATGATACT[A/G]AAAGAATTCCAACTC | 10152 |
| rs562432702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203390781 | ATAATCTAACCAGTG[A/G]TCTGTTGGTGTGATG | 10152 |
| rs562468998 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203399082 | ATAGAATTGCTGGGT[C/T]ATATTGTAAGTAAAT | 10152 |
| rs562481598 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338922 | TCTGTGTGTGTGTGT[A/G]TGTGTGTATATGTAT | 10152 |
| rs562516614 | in-del | -/AGT | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203333121 | GTCAGTTTCATCAAA[-/AGT]AATTACCAAAATGAT | 10152 |
| rs562556420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203414759 | TAGCTTTTAAGATAA[C/T]AGGCATTGGAGTTCA | 10152 |
| rs562625980 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203398482 | AAGGTAAATGTCTTA[C/T]TAATAATTTATATCA | 10152 |
| rs562626842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203338160 | TAAAGGCACCAGGTA[C/T]ACAATGGGGAAAGGA | 10152 |
| rs562690325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203407660 | ATCTAAACATTCTTG[C/T]ATATTGTGAAAATTA | 10152 |
| rs562695999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203412629 | TAGGTTGATTTCATA[C/T]GTTTTAAATTATGCT | 10152 |
| rs562745262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366313 | TATAACACTTACAAT[A/G]TTTGGGAAGGAAGGA | 10152 |
| rs562748794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203405896 | AAGGGCAATTATAAC[A/G]TAGGAGTTAAAATAT | 10152 |
| rs562753502 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | ABI2 | GRCh38.p7 | 2:203422828 | TTAGAATACATTAAG[C/T]GGTTTAACCAACTCT | 10152 |
| rs562771298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203383126 | ATATATATTCCTCCC[A/G]TCTAATACCCATTAT | 10152 |
| rs562784090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203369357 | CATTAGGGGAGAGTA[A/G]GAGAGATTATGTGGG | 10152 |
| rs562819670 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | ABI2 | GRCh38.p7 | 2:203405197 | TTAAGTTCTGCCTTT[A/C]ATCTCCAGGGATTTG | 10152 |
| rs562942284 | snp | A/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428724 | AAATGCTGAAAAAAA[A/T]CCAGGAGGGCTTGTC | 10152 |
| rs563024516 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203340546 | TAATTTTTGTAGTGA[C/T]GGGGTTTCGCCCTGT | 10152 |
| rs563029423 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403173 | TAGCTTATACAATTC[C/T]CATACCAAACCCATG | 10152 |
| rs563086086 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429511 | TGCCTGTAATCCCAG[C/G]ACTTTCGGAGGCCGA | 10152 |
| rs563096941 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203401436 | GCTCTGTCTGTAAGA[A/G]AAAGTTCTCAGCTTA | 10152 |
| rs563113053 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203330571 | TGCTGGTACCAAGGA[G/T]GACTGGAGGAAGCAA | 10152 |
| rs563118052 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203381763 | AAAGACACTTAGAAT[A/G]TAAAAGATGACATTT | 10152 |
| rs563118596 | snp | A/G | | | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432592 | TTTGTTGCTATGAGA[A/G]CCTAGATTATAAAAG | 10152 |
| rs563156063 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | ABI2 | GRCh38.p7 | 2:203398804 | AAATGAAAGCATATA[A/G]TATGTAGCTTTTTTG | 10152 |
| rs563213740 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203403917 | CGACCACACCCAGCT[A/G]ATATTTGTATTTTAT | 10152 |
| rs563223506 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203371323 | ACTGTACTCTGTATC[A/G]GGGAGAAATACTTCA | 10152 |
| rs563224543 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203422184 | ATGCCTGTAGTTCCA[C/G]CTACTCTGGAGGCTG | 10152 |
| rs563244306 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425486 | GGATTACAGGCGTAA[A/G]CTACCGCACCTGGCT | 10152 |
| rs563246826 | snp | A/G | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203325963 | AACCTACGCCACCCT[A/G]GTTCAAGCGATTCTC | 10152 |
| rs563301064 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203393667 | TGAGTGCCCCAGGAA[A/G]GCAATAGTTAAAGGA | 10152 |
| rs563311245 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203363809 | TGCTTTTGTTACCCA[C/G]GCTGGAGTGCAATGG | 10152 |
| rs563340159 | snp | A/C | 0.00358779 | 0.0422022 | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328405 | CGCTCCTTCCGAGTT[A/C]CCGCCGCCGTCGCCG | 10152 |
| rs563379326 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327843 | TGAAGTCAGGTGGCA[C/T]TGAAAGCTGCGTGGA | 10152 |
| rs563394530 | snp | A/G | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203366900 | TAAGCAGAGAGCCCT[A/G]GAAGAAACCAAAGCC | 10152 |
| rs563426358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203335030 | TTGGATTCATGAGGT[A/G]GCATGTAGGGCAACA | 10152 |
| rs563428790 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363074 | GGCCTCAAGTGATCC[A/G]CCTGCCTCGGCCTTG | 10152 |
| rs563434404 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415382 | CAGCACTTTGGGAGG[A/C]CGAGGTGGGCGGATC | 10152 |
| rs563435382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203403244 | TAATTACACTAAATA[A/G]TCGGTTGTATCATGC | 10152 |
| rs563435995 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203380080 | TCAGTAGTCCAGAAG[A/T]ATAAAAATTTAGCAA | 10152 |
| rs563451127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203329042 | CATCCCCCAAATTCT[A/G]GATGATTTTTAAGGG | 10152 |
| rs563455229 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203350979 | CTAGGAGTTTTATAG[-/T]TTTAGCTCTTACATT | 10152 |
| rs563486415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203424673 | CAAAGTTCTGGGATT[A/G]TAGGTGTGAGCCACA | 10152 |
| rs563509944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203334230 | ACAGGTGTGAGCCAT[C/T]GTGCCCAGCCTCATT | 10152 |
| rs563528760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203378279 | CACCATGCCCGGCTA[A/C]TTTTTGTATTTTTAG | 10152 |
| rs563589770 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326834 | TTTTGAGACGGAGTC[C/T]CGCTCTGTCGCCCAG | 10152 |
| rs563616775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203371572 | ATTTTAAAGAAATTT[C/T]ATCTCTAGCTTTGTT | 10152 |
| rs563617798 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384758 | AGCATATTAGTTTAA[C/T]CAAAAGTAATAAAAA | 10152 |
| rs563650650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203373814 | TCTCAAGAGCTAGGT[A/G]TTGAAAGGCAGTGGC | 10152 |
| rs563663681 | snp | A/C/G | 0.0001812 | 0.0095168 | intron-variant | ABI2 | GRCh38.p7 | 2:203402563 | ACATATGTATGTTCT[A/C/G]TCTCTTTTTCAGGTC | 10152 |
| rs563672762 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420556 | CTGCCAGCACACCCG[C/G]CTAATTTTTTGTATT | 10152 |
| rs563696408 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203396592 | AAAAATCTGCACATT[A/T]CCCTGAGCATCTTGA | 10152 |
| rs563699482 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203405716 | ATGAGCTTTTTTTTT[-/G]GGGGGGTAATTGGAG | 10152 |
| rs563757191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203374251 | CGCCTGTAATCCCAG[A/C]ACTTTGAGAGGCTAA | 10152 |
| rs563775183 | in-del | -/GA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203333797 | CCAAGGAACTTAAGT[-/GA]CCTCATAATTTCCGT | 10152 |
| rs563778630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203340093 | GGATGAACCTGGAGA[A/G]CATTAGGTAAGTGAA | 10152 |
| rs563789944 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330583 | GGAGGACTGGAGGAA[A/G]CAATGCTGTTCTGAG | 10152 |
| rs563791246 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203380997 | TAATGATTCAGAGCT[G/T]TAGCTGAGTATTAAT | 10152 |
| rs563834619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203350049 | TTTCTCCACATTGTT[A/G]TCAGCATTTGTGGAC | 10152 |
| rs563853434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203359741 | CTTGGACCTCTTTTA[C/T]AAGGGCACTAATCCC | 10152 |
| rs563927164 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359747 | CCTCTTTTATAAGGG[C/T]ACTAATCCCATTCAT | 10152 |
| rs563974156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203387748 | AGTTCTGCTATGTTT[A/G]TAACTTTAAAAAGTA | 10152 |
| rs564007620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345144 | TTGGGTCCGCACTAC[C/T]TTTATGAGTTGTAAC | 10152 |
| rs564008259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203397430 | AGCAGCATTGGAAAC[G/T]CATAGACAATGGACT | 10152 |
| rs564016682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203339296 | TATGAAAAACTGGTT[C/G]CGGCCGGGTGTGGTG | 10152 |
| rs564034554 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | ABI2 | GRCh38.p7 | 2:203344512 | CTGTGATTACAGGCA[A/C]CTGCCGCCACACCCG | 10152 |
| rs564064537 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430886 | TGGGAGGCATCAAAA[C/T]GATGGTAGTTTGCTT | 10152 |
| rs564070889 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374409 | GGAGGCTGAGGTAGG[A/G]GAATTGCTTGAACCT | 10152 |
| rs564101002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203384173 | TTTATAGCAAAGGAC[G/T]TACAAGGTCAGTGGA | 10152 |
| rs564105782 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430217 | CTCTTTTTTTATAAA[C/T]TAAAAGATGGTTGGT | 10152 |
| rs564191101 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377253 | TAGGAGTTCAAGACT[A/G]CAGTATGCTATGATT | 10152 |
| rs564199870 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203346745 | GTGAATTAACTACTT[A/T]GAGAGAAATAGGAGA | 10152 |
| rs564206772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203423305 | GGCCTTGTGTTAGGC[A/G]CTAGGGATACACAGA | 10152 |
| rs564226826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203400478 | GTAGGTTTGTATTAG[C/T]TTGCTATAGATTAAT | 10152 |
| rs564227904 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203385850 | TTTATTTCTCTTGTT[G/T]TCTTCTGCTTTCTTT | 10152 |
| rs564271009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203346023 | TGTCTCTACTAAAAA[C/T]ACACACGCGCACACA | 10152 |
| rs564275066 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203399857 | TTCAAATAGCAGAAA[A/T]TCTTCATTTTTATTA | 10152 |
| rs564288081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203402237 | ACGGGGTTTCACCAC[A/G]TTGGCCAGGCTGGTC | 10152 |
| rs564315663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203361428 | CACTTGAGCCCAGGA[A/G]TTGGAGTCTAACCTG | 10152 |
| rs564360351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203383456 | ATTTTGACCATTGAT[A/G]TGTTAACCTCCAAAG | 10152 |
| rs564366330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203392094 | ATTCAGTTTTTTCAT[C/G]TGTAAAAGGGGGGTA | 10152 |
| rs564380302 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203360648 | AGGCTAGTAAGTGAC[A/G]TTTGCCTAGAGATCA | 10152 |
| rs564402661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203354044 | ATTGTGATTAGATTT[C/T]ATTTATTTATTTATT | 10152 |
| rs564447403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203341662 | TTACAGTGAGCCTAG[A/G]TTGCACCACTGCACT | 10152 |
| rs564463732 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365027 | ACATGAACTGCCACG[C/T]CTGGCCAGCGTTATG | 10152 |
| rs564466930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203340860 | ACTGAACCAAAACAA[C/T]ATTGCCTGCAAGCCA | 10152 |
| rs564509134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203397769 | GGAGGCCTCAGGAAA[C/T]TTACACTCATGGCCT | 10152 |
| rs564524973 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413751 | ACATTTCTTTTGGTA[C/T]ATCTTCAAAGATAAT | 10152 |
| rs564554061 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203347601 | AGCTGAGAGAAGAGA[G/T]AACAAAATAGTTTCT | 10152 |
| rs564585641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203357887 | GATTCTCCTGCCTCA[A/G]CCTCCCAAGTAGCTG | 10152 |
| rs564630685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203389184 | TTTTCATTTTAAGAT[A/G]CAAGTAGTATACCCT | 10152 |
| rs564673386 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347466 | CATTACACGAAGAAC[C/T]GTAGCATGTAGTAAA | 10152 |
| rs564691485 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203423633 | TTTCACCATATTGGC[C/T]AGGCTGGTCTCAAAC | 10152 |
| rs564702151 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346381 | GGAAAATATTTCTGC[A/G]GCTTGGGAATATATG | 10152 |
| rs564751818 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | ABI2 | GRCh38.p7 | 2:203378114 | TTTCTTTTTCTTTTC[A/T]TTTCTTTTTTTTTTT | 10152 |
| rs564774044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203364715 | TTCTTTTATATTAAT[A/G]CACATACATATTTTT | 10152 |
| rs564831498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203344749 | CTAAAGGTTTGTAAG[C/T]GCACCAATCAGCACT | 10152 |
| rs564838925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203408343 | AATTTTTGTATTTTT[A/G]GTAGAGATGGGGTTT | 10152 |
| rs564859988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365446 | TGTACCTTTTTCTTA[C/T]TTCATTATTGTATAA | 10152 |
| rs564862399 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203350759 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 10152 |
| rs564866373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203405012 | TAAATCTGATTTTCA[A/G]ATGCTTGAAAGTATA | 10152 |
| rs564882801 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203363165 | ATTAAAAAAAAATTT[C/T]TCGTGAGTATATAGG | 10152 |
| rs564888598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203413834 | TTGGTAGCAAATACT[C/G]ACTCTGCATTAAGTT | 10152 |
| rs564898152 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359330 | TTGATAGAATTTTCA[C/T]TGATTACATTTTCAC | 10152 |
| rs564960546 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ABI2 | GRCh38.p7 | 2:203421618 | TTTATGACTGCTTGA[C/T]TGAAGGTATGATCTC | 10152 |
| rs564971146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345054 | CCGCAGTGGCAACCC[A/G]CCGGGGTCCTCTTCC | 10152 |
| rs564994628 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203357136 | ATAAAATTTGTGATT[A/T]GTTACTTTTTATGTA | 10152 |
| rs565010610 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399617 | GCCTCGCGGGTTCAA[A/G]CGATTCTCCTGCCCA | 10152 |
| rs565011182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203404541 | ATTACAGGTACCTGC[C/T]ACCACGCCTGGCTAA | 10152 |
| rs565074161 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203412516 | TATTTTACTTACTTT[C/T]GTTTATTGGAAGGTA | 10152 |
| rs565083356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203414518 | AAGCCTTTCCTGACC[C/T]ACATAACAAGTGTGG | 10152 |
| rs565097510 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203419223 | CACGCCATTCTTCTG[C/T]CTCAGCCTCCCGAGT | 10152 |
| rs565104824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203336903 | ATGGTACCGTTTTGC[A/G]TTCCCACCAGCAAAG | 10152 |
| rs565118515 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328330 | GACCGTCCTCGGAGT[C/T]CGTCGGCTCGCGCCC | 10152 |
| rs565122194 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203373735 | GTTAAATTAGTTAGC[A/C]GGTAACAATTAAAGG | 10152 |
| rs565164961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203389850 | TTCTGTATAAGTGCT[A/C]ACATACTCCTTTGGT | 10152 |
| rs565172869 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203332564 | TGGGAAGCGGAGGTT[G/T]CAGTGAGCCAAGATC | 10152 |
| rs565248885 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370425 | AGGATAGAGATGTGG[A/G]CAGATTTGAGAGACA | 10152 |
| rs565275724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203406247 | TACATATACTTACAT[A/G]AGCCTTGTTTGTTAA | 10152 |
| rs565276169 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203381191 | AATGGAGATCTAGGT[A/G]AAAAGAAAATATACA | 10152 |
| rs565318065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203367782 | CTGAGGTGGGAGGAT[C/T]GCTTCAGCCCAGGAG | 10152 |
| rs565335068 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428164 | GAAGCTAGACACGAA[A/G]GTCCCTAAGGTTCTG | 10152 |
| rs565340790 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203359848 | CATGTACATTTTTGG[G/T]GGGGGGACACAAAAA | 10152 |
| rs565365573 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203381182 | TCTAAATTTAATGGA[G/T]ATCTAGGTAAAAAGA | 10152 |
| rs565383289 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339695 | TAGGGAATGAAATCA[G/T]TATCTCAAAGAGACA | 10152 |
| rs565402017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203368543 | AAATATAGTCCAGAT[A/G]ATAAAATCAGATATG | 10152 |
| rs565454752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203374566 | TGAAGGTTATCAATA[C/T]GTAATTATGCATAGA | 10152 |
| rs565501712 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425360 | GGCGCCCACCACCAC[A/G]CTTGGCTAATTTTTG | 10152 |
| rs565516059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203337470 | TAAAAACTATAAGAC[A/G]TTTATGAAAGTAATT | 10152 |
| rs565524863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203375300 | TTAATTGTGTATTTG[A/G]ATTAGTTTTGGTCAT | 10152 |
| rs565533620 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203423438 | CATCTGGGTCCTTTT[A/T]TTTCTGAGACGGAGT | 10152 |
| rs565589311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203330361 | AAGATTCAGAGGTTC[A/G]GGCCTGGGCGATAAG | 10152 |
| rs565606640 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428604 | AATTAATATAACTGA[C/G]ACAATAAAACACATT | 10152 |
| rs565617126 | in-del | -/ATAT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347843 | TTGAGGAACATTTAC[-/ATAT]ATATAGGATTAACCT | 10152 |
| rs565661999 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203354206 | GCTTCACCACGCCCT[C/G]CTAATTTTTGTATTT | 10152 |
| rs565705748 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203353679 | GTTTTTATATTTTTA[G/T]TAGAGATGGGGTTTT | 10152 |
| rs565716280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203361827 | GTGTCATTTATTGAG[C/T]GAGGTACCCTTTCTC | 10152 |
| rs565760916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203393708 | CCATACATAAGTCAG[C/T]AGAGCAACATCATTT | 10152 |
| rs565779752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332463 | AACCGCGTATCTACT[A/G]AAAATACAAAAATTA | 10152 |
| rs565786915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203364009 | CCTCAGGTGATCTGC[C/T]CACCTTGGCCTCCCA | 10152 |
| rs565821225 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203375763 | TTTCTACAAGTGAAA[C/G]CTATAAAAAAATTGA | 10152 |
| rs565821838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203401769 | TTTGATTTGGAATTA[C/T]GTCATTTAACCTTTT | 10152 |
| rs565849279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203363377 | ACCCTGTTGTGCTAG[C/G]AAATACTAGGTCTTA | 10152 |
| rs565851195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203372561 | CCGGGCGGGGGGCTG[A/G]CCCCCCCACCTCCCT | 10152 |
| rs565865189 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203401602 | TGATGATAACTATAT[A/T]TGGACTTAGGGATGA | 10152 |
| rs565899483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203333812 | GACCTCATAATTTCC[A/G]TTATTGATCCAGGAA | 10152 |
| rs565901059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203341872 | GGTTGGTGCTTTAGG[A/G]TTAAGCAGTTTATTT | 10152 |
| rs565933057 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410279 | CTTGAGAGCAGAGAC[A/G]TGTTCATCTTTTTAG | 10152 |
| rs565936799 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203418004 | AATATTTCTGGAGAC[-/G]GAAAAACACATGCTG | 10152 |
| rs565948255 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387992 | CTGTCTAGTAAATAT[A/G]TTTTTATATTTACCA | 10152 |
| rs565978064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203360874 | CTCCTTTGACTCTTA[C/T]GCTGTTGCTAATATC | 10152 |
| rs566008087 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203334511 | TGGTGGATGAATATG[C/G]TGTGATTTGCTTACA | 10152 |
| rs566023614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203351193 | TGGACTCTGAATTCC[A/G]TTGATCTATATGTCT | 10152 |
| rs566033823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203371318 | CATTGACTGTACTCT[A/G]TATCGGGGAGAAATA | 10152 |
| rs566078859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203425461 | CCTGCCTTGGCCTCC[C/T]AAAGTGTTGGGATTA | 10152 |
| rs566089248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203424824 | AGCTCTCTACCATTA[C/T]AAACAGTCTCTGGAA | 10152 |
| rs566092874 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203378618 | AGGATAAATGATCAG[G/T]GTTCAGATTTCTTAA | 10152 |
| rs566112958 | snp | A/G | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326005 | TTCTGAGTAGCTGGG[A/G]TTACAGGCACCCGCT | 10152 |
| rs566187844 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376439 | ACAATTAAAAACATC[A/G]TATAGCCAAACTAAA | 10152 |
| rs566212186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203418355 | CTGGGCCCTCTGGTT[C/T]AGGGACTCTTCACAC | 10152 |
| rs566217006 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432455 | CTTTTCTCCAAATCT[A/G]ATTCTGTTAATGTAC | 10152 |
| rs566226904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203367969 | GTGATTATGACATGC[C/T]CTTCAGCCTGGGAGA | 10152 |
| rs566231463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203378329 | TGTTAGCCAGGATGG[C/T]CTCGATCTCCGGACT | 10152 |
| rs566231886 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203385378 | TCTCGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 10152 |
| rs566241233 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203367107 | TAAACACAGGCTATC[G/T]GTAATGCTGGCAGCT | 10152 |
| rs566318652 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203382382 | GTTCCTTGAGGGCAG[A/T]TATTTTTGTCTGTTT | 10152 |
| rs566335433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203344929 | TCAGCGCTCTGTAAA[A/G]TGGACCAACCAGTGC | 10152 |
| rs566403158 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428225 | CAGGCATCCCGAACC[C/G]CTGCTTCGGTGCTGT | 10152 |
| rs566414400 | in-del | -/TGA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203401587 | AAAATACAGTGAAAT[-/TGA]TGATAACTATATATG | 10152 |
| rs566469182 | snp | A/C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429026 | TTAATGTTATCTGAG[A/C/T]ATTAAAAATCATCAG | 10152 |
| rs566484167 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428281 | AGACCAACTATGACT[A/G]TCATTTCCTTCACTA | 10152 |
| rs566507824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203388725 | CACCAGATTTTAATA[C/T]ATAGATTGTTTATTT | 10152 |
| rs566603647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203421817 | ACAAGTTCAAAAATT[A/G]GCTGGGTGTGGTGGT | 10152 |
| rs566629038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203398571 | GGTATAACTTATGTA[C/T]AGTAAAATTCACCCT | 10152 |
| rs566669032 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203392701 | TCATGTGTAGTGCCT[G/T]ATGGATTTTGTTGGG | 10152 |
| rs566681505 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427619 | AAGGTATAACAGCAT[A/G]ACTGTGTAGCCAAAA | 10152 |
| rs566692648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203405455 | CTCAGGAGGCTGAGG[C/T]AGAACGATTGGTTGA | 10152 |
| rs566694621 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203398028 | ATTCAAAGCATATCA[A/G]TCACCGTAGTGTTCC | 10152 |
| rs566803409 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203400034 | GGTATATATATTTTT[A/G]AAACCCCAAATGGTA | 10152 |
| rs566836384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203339575 | AACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA | 10152 |
| rs566864712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203399405 | TAATAGGGTTTTTTT[C/T]CTTATCATTGAGTTC | 10152 |
| rs566887111 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404552 | CTGCCACCACGCCTG[G/T]CTAATTTTTGTTTTG | 10152 |
| rs566933011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332144 | TAAAAATTTAGATAG[C/T]TTCATTATTCTAACC | 10152 |
| rs566945623 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203403364 | TATTGTGGACATGGT[A/T]TGTCAACTTACTGCT | 10152 |
| rs566950584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203340153 | TATGATTTCACTTAT[A/G]TGAGGAATCTAAAAA | 10152 |
| rs566988522 | in-del | -/TA | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203360929 | AATTAGGGTAACAAC[-/TA]ATTGTTACCCTTTCA | 10152 |
| rs567072345 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203414168 | GTACAGTGGTGCAAT[C/T]TTGGCTCTCTGCCAC | 10152 |
| rs567090161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203359305 | GAACTGAAGACTTCT[A/G]ATTCCCAAGTTGATA | 10152 |
| rs567107953 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203395872 | TTTCTTCGTAATCAG[G/T]ATTTTTTTTCTTTAG | 10152 |
| rs567118574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203409699 | TGCTTTGATTTATTA[C/T]GTGCCAGCCACTGGG | 10152 |
| rs567161510 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203345674 | TCGGCCTCCCAGAGA[A/G]CTGGGATTACAGGCC | 10152 |
| rs567180407 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203351798 | ACTGTGGCCTCCCCA[A/T]GTGCTGGTATTACAG | 10152 |
| rs567188240 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203413707 | TAAGTCTTTAAACTC[C/T]TTAAAACATTCACCT | 10152 |
| rs567275940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203349093 | ATGTGCCACTGCACC[C/T]GAGTAATTTTTTTTT | 10152 |
| rs567285825 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330986 | GACTCAAAATTTAGT[A/G]TGGTGACATTTTAAA | 10152 |
| rs567293431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203386877 | ACTCCTGGCCTCAGG[C/T]GATCTGCCCACCCTG | 10152 |
| rs567354220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203417310 | TTGTTCCTATTGGAC[A/G]TGCTTTTTATGAATG | 10152 |
| rs567382862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203363202 | TGTATATATTTATGG[A/G]TTACCTGAGATATTT | 10152 |
| rs567399529 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203396860 | CTCTTGTTCCTGCTA[C/T]TGTCCCTTCCTCCAC | 10152 |
| rs567412910 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203350491 | AGTAGCTAGGACTAG[A/G]GGTAGACACTACCAC | 10152 |
| rs567434243 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203347433 | TCTAGCCTTGTAATC[C/G]CATAATGGACATAAG | 10152 |
| rs567446538 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203418265 | AGTTGTGTATTGCTA[C/T]CTAACAAGTTATTCC | 10152 |
| rs567469182 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203355051 | TAACGTTTTAGTCCT[G/T]CTTCTCAGCTGCATC | 10152 |
| rs567477770 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203344475 | GTTCAAGCGATTCTT[-/A]CTGCCTTAGCCTCCT | 10152 |
| rs567514607 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203426416 | ATCTGGTTGAAATAA[C/G]ATAACAGTTGAAATA | 10152 |
| rs567523364 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387436 | AAAGGAACTGCTTCT[A/G]CCTCCGGTGGTATTT | 10152 |
| rs567586686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203427028 | GTATTACTTAGAAAA[A/G]AAAACATGTAAGTTT | 10152 |
| rs567588066 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203356629 | CCCACCTTGGCCTCC[A/G]AAAGTGCTATGATTG | 10152 |
| rs567594855 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360046 | AGAAATTAGCTGGGC[A/G]TGGTGGTGCATGCCT | 10152 |
| rs567598990 | snp | A/G | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327489 | TTCACAATAAACGTT[A/G]ATTTTATCTATGTAA | 10152 |
| rs567609743 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203338239 | GAAATTTGATTGTTA[C/T]ATCACACATACAAAT | 10152 |
| rs567644864 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203412654 | TATGCTATTGGGGCC[A/G]ACTCTTCTTTAGCTT | 10152 |
| rs567687768 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384149 | TTTTAAAAACACTAT[A/G]GTAATAGTTTTATAG | 10152 |
| rs567777506 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420826 | CTCAGAGAACATGGC[A/G]TTCTTGGTGCCTTGA | 10152 |
| rs567835176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203379536 | GAGCCACTGTGCCTG[A/G]CTTTATTTTTAACAT | 10152 |
| rs567861408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203364934 | AGTTGAGGTCTCACA[A/G]TGTTGCCCAGGCTGG | 10152 |
| rs567866866 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203386609 | CCACATTGATATTTC[-/T]TTTTTTTTTCTATAG | 10152 |
| rs567872052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332020 | TTGCCATGTTGGCCA[A/G]GCTAGTCTCAAACTC | 10152 |
| rs567894833 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429774 | AAAAAAAAAAAAGTT[C/T]CCACAGCTCACCACT | 10152 |
| rs567897011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203419377 | TGCTGGGATTACAGG[C/T]GTGAGCCACGAGGCA | 10152 |
| rs567937123 | in-del | -/CTC | 0.00279162 | 0.0372561 | cds-indel, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427706 | ATACCCTTGGGATTT[-/CTC]CTCCTGCAGAATCTG | 10152 |
| rs567955321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203415921 | AGCAGATCTCCATGT[A/G]AGATATTTTAAATTA | 10152 |
| rs567959990 | snp | A/T | 0.167158 | 0.235875 | intron-variant | ABI2 | GRCh38.p7 | 2:203331345 | TCAAATGGTCAATTT[A/T]GCCTTTTTTTTTTTT | 10152 |
| rs567971431 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203373359 | TCGCAGGCACTCGGC[A/C]GGCTGAGGCAGGAGA | 10152 |
| rs567986092 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360458 | GGGATATGATGAAGG[A/G]AAACAAATTTGGTGG | 10152 |
| rs568053199 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203372882 | GCGGCGGGGCAGAGG[C/T]GCTCCCCACATCTCA | 10152 |
| rs568083638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203378173 | GCTGGAGTGCAGTGG[C/T]ACAATCTCGGCTCAT | 10152 |
| rs568097761 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410965 | TTATATATAATATAT[A/G]TATAAAACATGATTG | 10152 |
| rs568178597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203348732 | GAGATTTCTCATGTA[C/T]TTTCTTCCTCCCATC | 10152 |
| rs568202173 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404236 | TGCTCAGGAACTGTT[C/T]GTTGAATGCCAAATG | 10152 |
| rs568203787 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429191 | ATTAACTTGCCTCCA[C/G]TATACATTCCACTTC | 10152 |
| rs568209147 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203371694 | ATATTTCCCCTAAAT[A/C]TATACTTATCAGAGC | 10152 |
| rs568223086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203371114 | AGATAATTTCTTAAA[C/T]GTTTTCCATCTTGAA | 10152 |
| rs568223141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203378315 | ACGGGGTTTCACCGT[A/G]TTAGCCAGGATGGTC | 10152 |
| rs568230894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203375704 | CTGCATGATAGATGT[C/G]AGGAGGGAGTGTTTA | 10152 |
| rs568232758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203383549 | CTTAAAGTTTAGACT[A/G]GCTTGCCCAAGCTAC | 10152 |
| rs568358422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203377045 | AGTATGTGCCAGGCA[C/T]AGTGGCTCATGCCTA | 10152 |
| rs568415182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203378261 | GGGACTACAGGCACC[C/T]GCCACCATGCCCGGC | 10152 |
| rs568416867 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203385887 | TTCTCTTTCCTCTTA[C/G]TCCTAATCTTATGTT | 10152 |
| rs568430706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203424800 | AGCTGAACAGTTGTT[A/G]AAACTCTCAGCTCTC | 10152 |
| rs568446033 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404906 | TGCTCCAAAATAGTC[C/T]TATGAGAACTCTGTA | 10152 |
| rs568509343 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431666 | TTTGTGCTGACCTTT[G/T]TTCCTGTTTTGAGAA | 10152 |
| rs568571350 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410417 | AATCTTTTTTCTTTC[-/T]TTTTTTTTGCCGCTT | 10152 |
| rs568573748 | snp | A/G | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326868 | GGAGTGCAGTGGCAC[A/G]ATCTCCGCTCACTGC | 10152 |
| rs568606601 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203381792 | TTGTGTTTGCCCAAT[G/T]ACATAAGAAAAAAGT | 10152 |
| rs568607006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203340415 | TCTGTTACCCAGGCT[A/G]GAGTACAGTGGCATG | 10152 |
| rs568613900 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203381303 | CTTTTTTGAGACAGG[A/G]TCTCACTCTGTCACC | 10152 |
| rs568614014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203389733 | TAGAATCACATATGA[A/G]CCTGTGTGGTGAACA | 10152 |
| rs568647708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203385305 | CCCAGCTAATTTTTT[G/T]TATTTTTAGTAGAGA | 10152 |
| rs568659141 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203332522 | CCCAGCTACTTGGGA[A/G]GCTGAGATGGGAGAA | 10152 |
| rs568675736 | in-del | -/G | 0.179284 | 0.23979 | intron-variant | ABI2 | GRCh38.p7 | 2:203359846 | ACATGTACATTTTTG[-/G]GGGGGGGGACACAAA | 10152 |
| rs568682321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203350347 | ACCAACCACGCCTGG[C/T]CAACGGTCTCTGTTT | 10152 |
| rs568709119 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203393532 | CTTTTGACCCAAGAT[G/T]TCATCCAGTGTCCCT | 10152 |
| rs568717417 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203337560 | TGTTAACATGTCCAT[A/G]CTACACAAAGCCATC | 10152 |
| rs568719151 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203349834 | AATTATGAGTAATTT[C/T]ATAACATATAACGTT | 10152 |
| rs568738077 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427439 | TCCACTCCAGTAAAG[C/T]AGAATGAAGGATACA | 10152 |
| rs568818632 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382968 | ATAATGTTTTGGTAT[C/T]GTGGAGGATTCGTGA | 10152 |
| rs568823940 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203395541 | TTTATTTTGAAGTGG[G/T]ACGCTTTTGAATTAC | 10152 |
| rs568827812 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | ABI2 | GRCh38.p7 | 2:203328706 | CGGGGCGTGGGGCCG[A/C]GGCCGCCTCGGGGAC | 10152 |
| rs568879402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203336672 | ACCTGGCTCCTTTTG[C/T]TTTAGTATTGCTTTA | 10152 |
| rs568899100 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428224 | GCAGGCATCCCGAAC[C/T]CCTGCTTCGGTGCTG | 10152 |
| rs568925430 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203374689 | TTTGTTTTATGAATG[A/T]TACATAATTTGAAGC | 10152 |
| rs568930555 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203344251 | CCATTAATAATATTC[A/G]TAGAAAGGAAACAAT | 10152 |
| rs568981291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203404106 | TAAAAAATTTTTCTC[A/T]TATCCTCCCAAGTCT | 10152 |
| rs568996683 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203404554 | GCCACCACGCCTGGC[G/T]AATTTTTGTTTTGTT | 10152 |
| rs568997925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203329776 | CAACCTCGTTCTGTA[A/G]TCCAGGTTGGAGTGC | 10152 |
| rs569007941 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398671 | CAGAACAGTCCTATC[A/T]TCGCAAAAATTTCCT | 10152 |
| rs569014082 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361043 | GTGTGGCTGATGGCT[A/G]TCAGTGCTTTGTAAA | 10152 |
| rs569038525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203336189 | GAATCATAATTTGTT[C/T]ATCCATTCACCAACT | 10152 |
| rs569117275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203344853 | AACGCACCAGTCAGC[A/G]CTCTGTGTCTTGCTA | 10152 |
| rs569166857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345368 | GAAGGAACAAACTCC[A/G]GACACACCATCTTTA | 10152 |
| rs569180441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203397857 | GGGAGGTGCTACACA[C/T]TTTTAAACAACCAGA | 10152 |
| rs569203665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345628 | TGGCCAGTCTGGTCT[C/G]GAACTCCTGACTTCA | 10152 |
| rs569237316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203391199 | ATTGTTTAAAAATGA[A/G]GCACAACATATTTAA | 10152 |
| rs569245760 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203405597 | ACTCCCAGTAGCCCT[C/G]CAATTGTCCCTATTT | 10152 |
| rs569280751 | snp | C/T | 0.00262984 | 0.0361664 | intron-variant | ABI2 | GRCh38.p7 | 2:203351694 | GTGCGTGCTACTGTG[C/T]CCGGCTGATTTTCGT | 10152 |
| rs569283625 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431276 | TTAATAACAGCAGAG[G/T]TCTCACTCAGTGCTC | 10152 |
| rs569314053 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203334843 | TTTTTGTATTTTTAG[G/T]AGAGACGGGGTTTCA | 10152 |
| rs569318729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203338573 | AGAAGTACGTGCCAG[C/T]ACTGTGCTTTGTGTA | 10152 |
| rs569334372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203409613 | GTTGCTGTCCTTGAT[A/G]TGCTAGCTAAATCAT | 10152 |
| rs569356596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203382652 | TAGCCTTTTTATTCT[A/G]TAAATGGTATGCTTT | 10152 |
| rs569358481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203346243 | AAATCTTTGAGGAGT[C/T]TATTGTTGCAGATGT | 10152 |
| rs569436858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203421121 | TTAAAAAGGTTAATG[A/G]TAATATCCATCTACT | 10152 |
| rs569465289 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366792 | TGGACTCAGCAGAAT[C/T]GTTGTGATGAGTTTT | 10152 |
| rs569468505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203367843 | CCCTGTTCTCTACCA[A/G]AAATACAAAAATTAG | 10152 |
| rs569495971 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364187 | CAACCCCCGCCTCCT[A/G]GGTTCAAGTGATTCT | 10152 |
| rs569501471 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203402472 | ATACCAGTTAAACTA[G/T]CTGTTATTTTTAATT | 10152 |
| rs569502493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203416769 | TGGTGGGAAGACTTA[C/T]CTTGCTCATTGATTT | 10152 |
| rs569523598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203348642 | ATGAGTTTATTTTAT[C/G]TTATTATTTTTTTAA | 10152 |
| rs569634751 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203394955 | TTCTTTTCCTCACTC[-/T]TATTCTCCCAAACCT | 10152 |
| rs569636324 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203342185 | TTTTCCTTCCTGGTC[A/G]TTCAAAAATAGTTAT | 10152 |
| rs569639761 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203417272 | GTGAATATTTGATTT[A/T]AAAAAACTGATGGTT | 10152 |
| rs569643143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203348046 | AGGAGTTCGAGACCA[C/T]CTTGGCCAACGTGGT | 10152 |
| rs569654705 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369090 | GTCTCCCACCTTAGT[C/T]TCCCAAGGTGTTGGG | 10152 |
| rs569657640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203401898 | CTCTTGCTTTCCCAA[A/G]CATCATTCTTGTCGA | 10152 |
| rs569708776 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203354976 | TTTCATCCATCCTCC[C/G]CACAAGAAGACATAA | 10152 |
| rs569710193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203395837 | AATTTGATTCAATTT[A/G]TGATTTAATTATGGT | 10152 |
| rs569716031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203348326 | CCTAGGGAGTAATAG[C/T]TCCCACATTAAACAT | 10152 |
| rs569746057 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203386126 | AGAGGTCTCTAGAAA[A/G]CCAAATAATTATGTA | 10152 |
| rs569751638 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203423970 | ATTTAGAAGAACAAT[G/T]TGTAAGTCCTTTTCT | 10152 |
| rs569768654 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203356557 | GTATTTTAGTAGAGA[C/T]GGGAATCTCACCATG | 10152 |
| rs569781297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203370970 | TTTCATCTATTTTAA[C/T]GAAAAAGAACGCTGA | 10152 |
| rs569796661 | in-del | -/GGCT | 0.00358779 | 0.0422022 | intron-variant | ABI2 | GRCh38.p7 | 2:203353708 | TTACCATGTTGGCCA[-/GGCT]GGTCTCGAACTTTTT | 10152 |
| rs569832547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203355996 | CTCCTAGCTTTTGTT[A/G]TTGCCTTTGAAAAGT | 10152 |
| rs569877361 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326329 | AGTTGAAAAAATGCT[A/G]GGTGGGAATAAGTAA | 10152 |
| rs569910745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203356918 | ACAGAGTATACTTCA[C/T]ATTGTTCCTGTCTTT | 10152 |
| rs569919396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203354304 | TCGCCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC | 10152 |
| rs569919449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203363012 | TTTTTCGTATTTTTA[G/T]TAGAGACAGGGTTTT | 10152 |
| rs569964625 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203334699 | AGACAGAGTCTCTGT[C/T]GCCCAGGCTGGAGTA | 10152 |
| rs569981973 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203364179 | GCTCACTGCAACCCC[C/G/T]GCCTCCTGGGTTCAA | 10152 |
| rs570019141 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203333389 | GATGCTGGGCTTGAC[-/T]TTTTTTTTAAATGGA | 10152 |
| rs570035724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203426361 | CATCCCAGTATAACT[A/C]AACTGTTGAAATTGA | 10152 |
| rs570047510 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339405 | GCCAATATGGTGAAA[C/T]CCTGTTTCTCCTAAA | 10152 |
| rs570049097 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203386368 | AGCTCACTGTATCCT[A/T]GGGCTCAAATGATCC | 10152 |
| rs570053806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203419310 | AGAGACGTGGTTTCA[C/T]GGTGGTCTTGATCTC | 10152 |
| rs570054259 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354200 | AGGCACGCTTCACCA[C/T]GCCCTGCTAATTTTT | 10152 |
| rs570060446 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203373281 | GCCCGGCCAACACAG[C/T]GAAACCCCGTCTCCA | 10152 |
| rs570063747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203410860 | AAACTTGTAACCTTC[A/C]AAGGTAAAATTCAGA | 10152 |
| rs570067813 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203418391 | CAATCAAGGTATCAG[C/T]TGAGGCTGCAGTGAT | 10152 |
| rs570100640 | snp | A/G | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327183 | GTAGGAGGGCCAAGA[A/G]ATCACCAGATTAAGA | 10152 |
| rs570137865 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203403986 | TTAAACTCCTGACCT[G/T]AAGTGATTCACCCAC | 10152 |
| rs570140507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203368076 | ATAAAATTTTGGGTT[C/T]TGCTTTTTTAACTTA | 10152 |
| rs570158608 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388183 | TAGAAACATTTTTCA[C/T]ACGGGAAAAGCTGCC | 10152 |
| rs570165553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203360000 | GACCATCCTGGCCAA[C/T]ATGGTAAAACCCCGT | 10152 |
| rs570198975 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203411973 | AATTGCTGTCACAGA[G/T]ACCAGTGAACATAGA | 10152 |
| rs570227560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203386774 | CTTCCAAGCAGCTGG[A/G]ATTACAGGCATCTGC | 10152 |
| rs570237719 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423092 | GTTGCTAATACCCTA[C/T]AATATTTGGTGGTCA | 10152 |
| rs570271907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203329991 | ATCCACCCACCTCGG[C/T]CTCCCAAAGTGCTGG | 10152 |
| rs570278859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203343235 | GGGATGTGGTGGCAC[C/G]CATCTGTAGTCCCAG | 10152 |
| rs570310181 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338422 | GCAGATCCCTCATGA[A/G]TGATGTAGCACCATC | 10152 |
| rs570322427 | in-del | -/CTCT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370224 | TCTCTCTCTCTCTCT[-/CTCT]TTCTGTGTGTATGTG | 10152 |
| rs570361319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203337898 | TATAGGGCATGCTGG[C/T]ACACGCCTGTAGTCC | 10152 |
| rs570363681 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429643 | ACACCTGTAGTCCCA[A/G]CTACTTGGGAGGCTG | 10152 |
| rs570378483 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369339 | GGAACAAGTTTTACT[A/T]GGCATTAGGGGAGAG | 10152 |
| rs570378903 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203376217 | AGGGGACATTTGGCA[A/G]TGTTAGACATTTTTG | 10152 |
| rs570445380 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402115 | TCTTGGCTCACTACA[A/G]CCTCTGCCTCCTGAG | 10152 |
| rs570450509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203414195 | CCACCTTCCCCTCCT[A/G]GGTTCAAGTGATTCT | 10152 |
| rs570467807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203369074 | ATCCTGGGCTCAAGC[A/G]GTCTCCCACCTTAGT | 10152 |
| rs570473437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203421836 | GGGTGTGGTGGTGCA[C/T]GCCTGTAGTCCCAGC | 10152 |
| rs570483824 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203369222 | TTGAGAATCCTAAAA[G/T]TTTTCCATGTTTGAA | 10152 |
| rs570521936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203381542 | AAAATATTGGGATTA[C/T]AGGTGTAAGCCATCG | 10152 |
| rs570571722 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203341902 | TACAGTTACTTAGTG[C/T]AGGACTTACTCAATA | 10152 |
| rs570604450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345596 | GTATTTTTAGTAGAG[A/G]TGGGGTTTCACCGTC | 10152 |
| rs570613183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203385251 | ATTCTCCTGCCTCAA[C/T]CTCCTGAGTAGCTGG | 10152 |
| rs570623974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203390292 | ATGCATAGTTGCATA[C/T]TTTTATTTGGGAAAT | 10152 |
| rs570685229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203353428 | AATAAAAACAAAAAA[A/G]TGAGTACCCCTTTTA | 10152 |
| rs570689928 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429124 | GCATTGCAAGTTACA[A/G]TAGCTATTTTGCTTT | 10152 |
| rs570729906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203382476 | TTTGTTGAATGAATG[A/G]TTATTTTGTAATGTT | 10152 |
| rs570787065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203392815 | TTTTGAAGATTTGCT[C/T]ATATACCAATGTTTG | 10152 |
| rs570820512 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203332494 | GCTGGCTATGGTGGC[C/G]TGTGCCTGTAGTCCC | 10152 |
| rs570822992 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431485 | AATAATCTTCATTTA[C/T]CCCTCCTAAAACTAC | 10152 |
| rs570849775 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203378018 | TTTTCTGTTACAGTT[C/T]TCCCAAGCAGTTGAA | 10152 |
| rs570850233 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203391473 | TTTAACTCCAACTAT[C/T]CTTTTTAAGCTGTGT | 10152 |
| rs570855179 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203407354 | CATGGGCTATATAAT[A/G]TATATATCTCCTCTA | 10152 |
| rs570887306 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203423476 | TGTCGCTCAGGCTAG[A/C]GTGCAGTGGTGCAAT | 10152 |
| rs570917774 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203370200 | ATTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT | 10152 |
| rs570975208 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203400115 | TTTTTTTTGAGACAG[A/T]GTCTCACTCTGTCAC | 10152 |
| rs570989939 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ABI2 | GRCh38.p7 | 2:203408995 | AGGCGCCCGCCACCG[C/T]GCCCGGCTAATTTTT | 10152 |
| rs570997340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203346446 | ATACCATATTACTGC[C/T]TGAATGAACACATCA | 10152 |
| rs570997804 | snp | A/G | 0.00036325 | 0.0134719 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427392 | CACAGGAATAGTCAG[A/G]TCTTCCCAGATTATC | 10152 |
| rs571030490 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392666 | GTTTTTATTTTCCTA[C/T]GTAAACATTTACATT | 10152 |
| rs571034438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203352671 | GTTTATGAGGTAAAA[A/G]TTACAGTAAAGGTTA | 10152 |
| rs571041517 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203347111 | GTGCATCAGGTACTT[C/T]TTTGTTTTGTAGTTG | 10152 |
| rs571066581 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410218 | CTACAAATATTGTTG[A/G]GTTAAGATTATCATG | 10152 |
| rs571146262 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203339751 | ATTATTCATGGTAAC[A/T]AAGATATGGAAACAA | 10152 |
| rs571187738 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203405808 | AATATAAATTCAGTG[C/G]GGTTCTGTGAGGTGT | 10152 |
| rs571188177 | snp | A/C | 0.00164812 | 0.0286591 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203396962 | TTTCTTCCACTCCCC[A/C]TACAGGTAAGTATTT | 10152 |
| rs571210844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203337344 | CTGTTGTGTTTCTAC[A/G]TATTAACTACAAACG | 10152 |
| rs571250756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203395946 | CAAGTGATTTGTAAG[C/T]GTTTGCTCACTTTGC | 10152 |
| rs571262081 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420993 | GGAGAGAGGGTGATA[A/T]GAGCACGCAAAGGGA | 10152 |
| rs571304241 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344213 | AGTTGTACCATCTTA[A/C]AATTATAAGAAAAGA | 10152 |
| rs571328261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203349228 | GTTACAGGCATTAGC[C/T]TCTGAACCCAGCTGG | 10152 |
| rs571342094 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | ABI2 | GRCh38.p7 | 2:203336600 | CAGGCTGTAAGACTT[A/T]AGTTGCAGCATGGCA | 10152 |
| rs571355436 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390354 | AGAAAGTTACTGGCC[G/T]GGTGCAGTGGCTCAC | 10152 |
| rs571374600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203411745 | TCTTCCTCCAGTTTT[A/G]TGATTCCAGATATCA | 10152 |
| rs571390054 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203355931 | TGTAGAATTATAGAT[C/T]GGAAATAATTTTTTC | 10152 |
| rs571402839 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203423474 | TCTGTCGCTCAGGCT[A/G]GAGTGCAGTGGTGCA | 10152 |
| rs571506807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203349746 | CTGAATAATATTCTA[A/G]TACATGGATAATACC | 10152 |
| rs571520061 | snp | A/G | 1.67826e-05 | 0.00289673 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427337 | CGTTGAGTCTATCAT[A/G]CATTATTCTGAGTAA | 10152 |
| rs571562630 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203350535 | TTTTTCTTTTTCTTT[C/G]TTTTCTTTTTTTTTT | 10152 |
| rs571567169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203404773 | CATATCGGCCAAGCT[A/G]GTCTTGAACTCCTGA | 10152 |
| rs571590405 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203350964 | TTTGAAGATTTTCTC[A/C]TAGGAGTTTTATAGT | 10152 |
| rs571592722 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203333915 | AATTAATAAACTGTT[C/T]ATTTATTTTTTCTTT | 10152 |
| rs571627357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203399254 | TGTGTAATGGTTTCT[C/T]ATTACATGTGTGGTT | 10152 |
| rs571630144 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203413370 | AGCAAAATGTTTCAT[A/G]AACCAAACCTAAGAA | 10152 |
| rs571651211 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331435 | TCGATCTCTGCTCAC[C/T]GCAACCTCCGCCTCC | 10152 |
| rs571706707 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360461 | ATATGATGAAGGGAA[A/G]CAAATTTGGTGGTTT | 10152 |
| rs571707364 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203358416 | TCTTCCCAAAGTGCC[A/G]GGATTACAGGTGTGA | 10152 |
| rs571721292 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203346615 | TCTTTCTCCCCCACC[A/T]CATTTAACTCTAGGG | 10152 |
| rs571745090 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203389438 | TATTTCTTGCCTATT[C/G]AAATAACAGGTAGTA | 10152 |
| rs571796589 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203334490 | TTTGGTGGATGAAAT[-/A]ATATTTGGTGGATGA | 10152 |
| rs571798595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203340480 | CAAGTGATGCTCCCA[C/T]CTTAGCCTTCCGAAT | 10152 |
| rs571808249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203398645 | ATGTAATTGCCACCA[C/T]AATCAAGTTACAGAA | 10152 |
| rs571849806 | snp | A/C | 0.104149 | 0.203046 | intron-variant | ABI2 | GRCh38.p7 | 2:203328665 | TGGGCCGCGTCGGGG[A/C]CCCCCCCGCCGGGGG | 10152 |
| rs571872946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203412750 | AGCATGTGCCAAGCA[C/T]ATCCATAGTGTGATC | 10152 |
| rs571920335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366664 | TTTGCATCTGTGCAA[A/G]GATGTGTCTATTCAA | 10152 |
| rs571920441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203357626 | GTCTAGGCAGATGAT[A/G]TAACATATTTTAAAA | 10152 |
| rs571930984 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339530 | AGGTTGCAGTGAGCC[A/G]AGATTGCGCCACTGC | 10152 |
| rs571974528 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378278 | CCACCATGCCCGGCT[A/G]ATTTTTGTATTTTTA | 10152 |
| rs572020163 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203405498 | GAAGTTTCAGTGAGC[C/T]GAGATTGTGCCACTG | 10152 |
| rs572024636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203401205 | AAAGTGTTTTTTTTT[C/T]CCTTTTCACTTATCT | 10152 |
| rs572026476 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203391981 | GTGATTGAGATTTAC[A/G]ATTAGGTTGGCATTA | 10152 |
| rs572088385 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203400369 | ACTGTGATTAAAGGC[C/G]TGAGCCACCATGCCC | 10152 |
| rs572132646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203362394 | TCATGTTGTTTGGAC[A/G]TTCTGGGGGTAGTTG | 10152 |
| rs572149610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203384087 | ATCTGAAATTTGGAT[C/T]AACTGTTTTTCTTCA | 10152 |
| rs572165860 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399681 | CACCATGCCCAGCTA[A/G]TTTTTGTATTTTTAG | 10152 |
| rs572197286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203352996 | TAGGAGCAGTAGGCT[A/G]TACCATATAGCCTAG | 10152 |
| rs572215332 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203414487 | ATTAACTCTTACTCT[A/T]CCTTCAGGTTTCAGG | 10152 |
| rs572231393 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203359661 | TTGGTGTCTGTTGAT[C/G]ACCTGTTCCTCATAA | 10152 |
| rs572234830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203402183 | GGAATTACAGGCGCA[C/T]GCCACCATACCTGGC | 10152 |
| rs572279129 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203407454 | ATTTATAAAGCTGTA[A/G]AAATAAGATGTAAAA | 10152 |
| rs572327437 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388486 | TCAGGAGTTCGAGAC[C/T]AGCCTGGCCAACATG | 10152 |
| rs572339711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203409086 | CTCATGATCCACCCG[C/T]CTCGGCCTCCCAAAG | 10152 |
| rs572396114 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203361350 | TGAACAAGAAAATGT[A/T]TGGCTTGGTGTGGTA | 10152 |
| rs572453478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203355190 | TATCCTCTGGTGCTT[C/T]CTGACAAAGAATACA | 10152 |
| rs572479429 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203349726 | ATTTTTTTTTTTTTT[A/T]ACGGCTGAATAATAT | 10152 |
| rs572499654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332784 | AAATAACTCCCTATT[C/T]GTTACTTCCCTGAAA | 10152 |
| rs572511587 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203377604 | TTAATGATTTAGAAT[C/G]ACTCACTAAACTTTA | 10152 |
| rs572554827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332768 | AATGTTTTGGTAGAT[A/G]AAATAACTCCCTATT | 10152 |
| rs572556910 | in-del | -/TAGTT | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366707 | AGTGAGTTCAGTCAA[-/TAGTT]TGGTTTGGGGTTTAT | 10152 |
| rs572587633 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203431765 | TCCTTGCTGAATATC[G/T]TAAGGTTTTTTGTAA | 10152 |
| rs572595676 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376999 | AGATTACTTCTCCCT[G/T]TTCATTCTCTGGAGA | 10152 |
| rs572632132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203404973 | TAAATGCATTTTATA[A/G]TACATACTTCAATAG | 10152 |
| rs572637102 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203416730 | GGGAGAACGTCATAC[-/T]TTGGAGCTCTAGAAC | 10152 |
| rs572663588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203423566 | GAGTAGCTGGGACTA[C/T]AGGCGCCGGCCACCA | 10152 |
| rs572672795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203416370 | GCGTGATCTCGACTC[A/G]CTGCAACCTCCACCT | 10152 |
| rs572681957 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203378340 | ATGGTCTCGATCTCC[G/T]GACTTTGTGATCCGC | 10152 |
| rs572700791 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203378181 | GCAGTGGCACAATCT[C/T]GGCTCATTGCAAGCT | 10152 |
| rs572719641 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369947 | GTTTACAGGTAGAAT[C/T]CTTTATTTAAAAAGT | 10152 |
| rs572724399 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430818 | CGTGATGTCTGGACC[A/G]TACCTGTGCTCCTTG | 10152 |
| rs572747473 | in-del | -/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329695 | AGTCTTTTTTTTTTT[-/C]CCTTTTTTCTTGCTC | 10152 |
| rs572806219 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203420570 | GGCTAATTTTTTGTA[A/T]TTTTAGTAGAGACAG | 10152 |
| rs572830126 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203332469 | GTATCTACTAAAAAT[A/T]CAAAAATTAGCTGGC | 10152 |
| rs572893327 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329102 | GGCTTCAGTTTTCTG[G/T]TCCTGTGAATGCTTC | 10152 |
| rs572942508 | in-del | -/CACCACCAACAACAA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392309 | CACCACCACCACCAC[-/CACCACCAACAACAA]CAACAACAACAACAA | 10152 |
| rs572948944 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428456 | TTAGCTGTAGAAAGG[C/G]TAATACTCTCCTGAT | 10152 |
| rs572953461 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203379929 | TGAAGGTTTTTTTTG[A/G]TTGTTCTTTTCTCCA | 10152 |
| rs572961804 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328306 | CGCCCGGCCGGCCGT[C/T]GCCGCGGTGACCGTC | 10152 |
| rs572975493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203421963 | GAGTGAGACTCTGTC[C/T]CAAAAAAAAAAAAAA | 10152 |
| rs573026443 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203419672 | GTGAGCCACTGCGCC[C/T]AGCCTGTGCTTTGTA | 10152 |
| rs573034940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203328884 | GTCCCGCCTCCTCGC[C/G]GCTCCCGCCCTCGGC | 10152 |
| rs573054275 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203398864 | GAATTACCCATGTTG[A/T]TGCATGTTTAAGTAT | 10152 |
| rs573117209 | snp | G/T | 0.00359639 | 0.0422524 | intron-variant | ABI2 | GRCh38.p7 | 2:203405715 | TATGAGCTTTTTTTT[G/T]GGGGGGGTAATTGGA | 10152 |
| rs573119175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203398201 | TGACTTTTAAAGAAA[A/G]GCTTTCTGCAGTAGA | 10152 |
| rs573119504 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396093 | CACAGTGGGAACTCA[G/T]TGTGAGAACCATATT | 10152 |
| rs573120553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203382856 | TAAGAGCTTTTAAAG[A/G]TGAATATAATTATAT | 10152 |
| rs573151364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203367320 | CTTCATCCATTCCCC[C/T]GCCTTTTTTTTTTTT | 10152 |
| rs573191234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203330196 | GTAGACAACATTTGT[A/G]TTTGAGAATGACCCG | 10152 |
| rs573199400 | in-del | -/C | 0.0138799 | 0.0821421 | intron-variant | ABI2 | GRCh38.p7 | 2:203355841 | CTCAAAAAAAAAAAA[-/C]AAAAAAAAAACACCC | 10152 |
| rs573203895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203358759 | TCACACCTGTAATTC[C/T]AGCACTTTGGGAGGC | 10152 |
| rs573240545 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203375234 | ACAATTGCAGTGATA[A/T]ATCTTGGTGTGTTTT | 10152 |
| rs573275384 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203338753 | GTTTTTATAAATATG[A/T]CACCAAAAGCACAGG | 10152 |
| rs573321810 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370044 | CATTTTCTGCTTACA[A/C]AACAAATAGTAAATA | 10152 |
| rs573346011 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203431966 | GTACTTTTAGCTCCC[A/G]GAGGGAGAGTTGGTG | 10152 |
| rs573363679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203368334 | AAATGTTCTATTTTA[G/T]CACTCTTGTCATTTG | 10152 |
| rs573372847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203425006 | CTGGGACCACAGGCA[C/T]GCGCTACCATGCCAG | 10152 |
| rs573382159 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326565 | AACTAATGAATCTTA[A/G]TGTGTGTGACCCTGC | 10152 |
| rs573438837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203390531 | CAGCTACTTGGGAGG[C/G]TGAGGCAGGAGAATT | 10152 |
| rs573453472 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203394303 | TGAATATCTTTGGTT[A/G]GGGAGAGAAGGGAGA | 10152 |
| rs573506623 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203408972 | GCCTCCCGAGTAGCT[C/G]GGACTACAGGCGCCC | 10152 |
| rs573522325 | in-del | -/ATT | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203397273 | TTTTTGGAAATTATC[-/ATT]AGAAATATTTTCATT | 10152 |
| rs573522359 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203389816 | TGATTTTTCTTAGCT[G/T]TTTGAGATAGCCAGG | 10152 |
| rs573550410 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428307 | CACTATCTAGAAAAA[C/T]GCTATTCTACTTTGG | 10152 |
| rs573561785 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203334011 | AGTGGCGTGATCTTC[A/G]CTCACTACAACCTCC | 10152 |
| rs573564938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203338078 | CTGGCATAAAAGACA[C/T]GTAGACTAATGGAAC | 10152 |
| rs573566220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203424229 | TACTTTATTACACCG[C/T]TTTAGAGTTACTTTG | 10152 |
| rs573576170 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203385693 | CGACACAGCACCTGG[A/T]GGAAAACCTTTGTAG | 10152 |
| rs573682807 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203342344 | AATATGGGACTGTTT[G/T]TTTGTTTTTCTTGAT | 10152 |
| rs573683539 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203383958 | CAGTCTCCAGAGAAA[A/G]TCATCATACTTTAGG | 10152 |
| rs573712521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203349499 | AACCTCTGCCTCCCA[C/T]GTTCAAGCGATTCTC | 10152 |
| rs573764918 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203371958 | TTTTAATTGATCATT[C/T]TTGGGTGTTTCTCGC | 10152 |
| rs573785524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203344422 | CCAGGTTGGAGTGCA[A/G]GGGCGTGATCATGTC | 10152 |
| rs573824147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203343660 | GAGGTTTAAAAACAT[A/G]TTTTTAGAAGTAGAT | 10152 |
| rs573824270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203349955 | AACTGTATATTTAAC[C/T]ATTTGAGGAACTGCC | 10152 |
| rs573845550 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203341485 | TTTGGGAGGCTGAGG[A/C]AGGCAGACTTCCTGA | 10152 |
| rs573853502 | in-del | -/CA | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203346032 | AAAAATACACACGCG[-/CA]CACACACACACACAA | 10152 |
| rs573885945 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ABI2 | GRCh38.p7 | 2:203393970 | AAAAGGCGGGAAATA[C/T]GTGTTAATAAAATCC | 10152 |
| rs573897012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203347555 | GACAAGGCGTTTATC[A/G]ATCTCCACCATGTGC | 10152 |
| rs573904315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203425741 | TAAAGTATTTTCTGA[C/T]CAGGTGCAGGTGGCT | 10152 |
| rs573912755 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203351942 | ATTATAACAGCTGAA[A/G]AATTCCTAACACCTA | 10152 |
| rs574039364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203335748 | TTTGTAGAAAATTTG[C/G]ATGAGGTAACAGCTT | 10152 |
| rs574052425 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419254 | AGCTGGGACTACCGG[C/T]GCCCACCACCGCGCC | 10152 |
| rs574057531 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | ABI2 | GRCh38.p7 | 2:203416357 | CCAGGCTGGAGTGGC[A/G]TGATCTCGACTCACT | 10152 |
| rs574058310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203388165 | TTATTGTTTTACTTA[A/G]CGTAGAAACATTTTT | 10152 |
| rs574124337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203363616 | TTTTAACTCCCACAA[A/G]TAAGTGAGAACATGC | 10152 |
| rs574220406 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203397951 | ATCCAGTCACCTCCC[C/T]CTAGGCCCCACCTCC | 10152 |
| rs574221820 | snp | A/G | 0.000826431 | 0.0203109 | intron-variant | ABI2 | GRCh38.p7 | 2:203380425 | TAAAAGTAGTAACCC[A/G]TAATGAAACCAACTC | 10152 |
| rs574222189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345874 | TAATCAGATGAGTTT[C/T]GCTTTTGACAAAAAT | 10152 |
| rs574227876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203397237 | ATTTTTAAGTTTAAT[A/G]TGGAGCTACCTTCTA | 10152 |
| rs574244690 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369759 | GGGGTAATAGATCTG[C/T]AATTCTCAGTGGCTG | 10152 |
| rs574276777 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203410129 | CAGCTTGGCAGGTTC[A/C]CTTCTTCAAGTCCCT | 10152 |
| rs574284476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203364269 | CAGCTAATTTTTGTA[C/T]TTTTAGTAGAGACGG | 10152 |
| rs574296350 | in-del | -/TG | 0.00557542 | 0.0525036 | intron-variant | ABI2 | GRCh38.p7 | 2:203333531 | TGAGAGTAAGGAGAC[-/TG]AGTAGAATTTGGGAG | 10152 |
| rs574346899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203351409 | TAATTATATTGAATC[C/T]GTAGATAAACTTGGG | 10152 |
| rs574465315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203339109 | AGGCGTCCAACAGGT[A/G]TGTGAAAATGTGCTC | 10152 |
| rs574481986 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203400202 | AAGTGATTCTCCTGC[C/T]GTAGCCTCCTGAGGA | 10152 |
| rs574498400 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203336525 | GTGATAACAGTGCCT[A/C]ATCACCTCCTAGTTC | 10152 |
| rs574508259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203390819 | GGCAAATAAAGTCTT[C/T]GCATACAAGTTTATA | 10152 |
| rs574618539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203421454 | AGAGCCACCTGATTT[A/G]CAAACGGATTGAGTT | 10152 |
| rs574620008 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354442 | TAATTCATCTCTAAA[C/T]TCTCCTCTGGATGTA | 10152 |
| rs574639640 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203359634 | AAGTCCAAGATCAAG[A/G]CGTCAGCAGATTTGG | 10152 |
| rs574653157 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203368166 | TGCATAATGTTGCGT[A/G]TATATGTTGTACCTT | 10152 |
| rs574684601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203358839 | ACATGGCGAAACCCA[A/G]TCTCTACTAAAACAA | 10152 |
| rs574715959 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203370352 | CTCAGCCTCCCAAAG[G/T]GCTGGGATTACAGGC | 10152 |
| rs574717419 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203345318 | AAACCAGGAACCCAC[C/T]GGAAGGAAGAAACTC | 10152 |
| rs574736220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203416273 | TCTCTGGGTTTTTTT[A/G]TTCTTATTTTTTATT | 10152 |
| rs574748605 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203423512 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCACG | 10152 |
| rs574749020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203360390 | CAAAAGGCGAAGTGT[C/T]GGGTGGAGCAGATTA | 10152 |
| rs574753807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203406065 | TCTTAATCTAATCCA[C/G]CCAATGAAATAGGAA | 10152 |
| rs574782185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203415585 | TCACACCACTGCACT[C/G]CAGCCTGGGCGATAG | 10152 |
| rs574837715 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203384530 | GGCCTGGCTGGTCTC[A/G]AACTCCTGTGCTCAA | 10152 |
| rs574840709 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346896 | GACCTTAAACCTAGG[A/C]CCTTGTTTGTGCTGC | 10152 |
| rs574844267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203416814 | ACATTTATTTTCAAG[G/T]CTAGGTTTATATTCC | 10152 |
| rs574902580 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203332241 | ATATTTATCAGATCA[A/G]TTTTATTTCTTGCCT | 10152 |
| rs574937479 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203339927 | CGTGTATATGAAAAG[A/T]CATCTGTCCCATCTG | 10152 |
| rs574939231 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374426 | AATTGCTTGAACCTG[A/G]GAGCGGAGGTTGCAG | 10152 |
| rs574939816 | snp | C/T | 0.0112622 | 0.0741907 | intron-variant | ABI2 | GRCh38.p7 | 2:203355181 | GACAGTGCATATCCT[C/T]TGGTGCTTCCTGACA | 10152 |
| rs574966176 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | ABI2 | GRCh38.p7 | 2:203404886 | TTTCATGCTTTGTTC[A/G]TGTATGCTCCAAAAT | 10152 |
| rs574980768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203331674 | CAATTTAGCCTTATT[A/G]TAGCATCATGTCTTA | 10152 |
| rs575030679 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388973 | TTTGGTTCACTTCTC[C/T]CTCATCACTTAAAGT | 10152 |
| rs575056431 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203387195 | GGTAGTAGGTCATCT[G/T]TTAATGGGAGATTTC | 10152 |
| rs575060559 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203361342 | ATGGATGCTGAACAA[-/G]AAAATGTTTGGCTTG | 10152 |
| rs575103267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203364490 | TTGCGCTGACTTATC[C/T]GTAGAGCAGATAAAC | 10152 |
| rs575156985 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | ABI2 | GRCh38.p7 | 2:203419571 | TTTGGTAGAGACGGG[C/G]TTTCACCGTGTTAGC | 10152 |
| rs575174707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203418884 | AATCTTGCCAAGGCA[C/T]ATCATAATCAATTTG | 10152 |
| rs575200970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203329133 | AGAAACCCTTTCTTA[A/G]TATTTTATGTTCTAA | 10152 |
| rs575208271 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356013 | TGCCTTTGAAAAGTC[A/C]AGTAGTGTTTTGATT | 10152 |
| rs575221108 | snp | A/C | 0.000330961 | 0.0128597 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203396937 | TTCACTTCTCCAACT[A/C]CCCCTGTTGTTTCTT | 10152 |
| rs575245875 | in-del | -/TTTGTTTATT | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365975 | ATTTGTATTTTTATC[-/TTTGTTTATT]TTTGTTTTTTAAATT | 10152 |
| rs575262530 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203358236 | CTGGGCTCAAGTGAT[C/T]CTCCCTTCTCTGCCT | 10152 |
| rs575276412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203331902 | GCAACCTTCGTCCCC[C/T]GGGTTCAAGTGATTG | 10152 |
| rs575284272 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203328982 | TGACGGAATCCTGCT[A/C]CCCACCTTAGGGTAG | 10152 |
| rs575304722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365134 | AATACAAATCAACTT[C/T]ATTTCCAACATTCAG | 10152 |
| rs575318228 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203330066 | AAGCATTTTCATGTC[A/T]TAGTGTAAATTTTAA | 10152 |
| rs575329515 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203391867 | CTTTATTTTGGTCCT[A/G]GAGTTGGGCTCTAGA | 10152 |
| rs575339003 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418069 | AATAGAAACTATCCA[A/G]AATAAGGCACAGAGA | 10152 |
| rs575355357 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328125 | GCTCCAGCGGCGGGC[A/G]GGCGGCGGAAGGGTT | 10152 |
| rs575367116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203335620 | CCTTGCAAGTTTTTT[C/T]CTATTTGATTTTTTG | 10152 |
| rs575367834 | in-del | -/C | 0.0821764 | 0.185298 | intron-variant | ABI2 | GRCh38.p7 | 2:203355829 | AGAGCAAAACTGTCT[-/C]AAAAAAAAAAAAAAA | 10152 |
| rs575401998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203343397 | ATGTTAGCAGGTTAG[A/T]TTGTGGTACAAACAT | 10152 |
| rs575405359 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203425948 | ATCGCTTGAACCTGG[C/G]ACATGGAGGTTGCAG | 10152 |
| rs575428989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203404854 | GTGAGCCACCGCACC[C/T]GGCCTATACAGGGAT | 10152 |
| rs575430089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203373037 | GCAGCCACGCAGAGA[C/T]GCTCCTCACTTCCCA | 10152 |
| rs575513469 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203389670 | AGTTGAGGTCCTTTT[G/T]CAAAATATGTTTTGA | 10152 |
| rs575521259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203337945 | TGAGTTGGGAGAATC[G/T]CTTGAACCCAGGAAG | 10152 |
| rs575523843 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203421576 | TGTGCTTTTTTTAAG[G/T]AGAAGGACAAAAAGG | 10152 |
| rs575532927 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427896 | TCCTCTGTGACACTG[G/T]AAATTCTGCATTCTC | 10152 |
| rs575551288 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425126 | GAAGAAAATGAATGT[A/G]GATAGAGCTTACTAA | 10152 |
| rs575587220 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427934 | TTGAGTGCACCAAAC[A/G]AGTGAATGCTGAACT | 10152 |
| rs575597259 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203418780 | CTATGAGGCAGAAAT[C/T]ATTGGGAGCTGTTTT | 10152 |
| rs575625384 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408388 | GGCTGGTCTTGAACT[A/C]CTGACCTCAGGTGAT | 10152 |
| rs575671697 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203381094 | ATAATGATACTGTAC[A/C]GTTCATGTAGTTGAT | 10152 |
| rs575714148 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203333921 | TAAACTGTTCATTTA[A/T]TTTTTCTTTTCTTTT | 10152 |
| rs575743650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203397435 | CATTGGAAACTCATA[C/G]ACAATGGACTTTTAA | 10152 |
| rs575791287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203375167 | CAGTGAGAAGGATGG[A/G]GAAGCTAATTAATAA | 10152 |
| rs575833594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203416200 | TATGGTTTTCAGTGT[C/T]AGTATTTCTGATAAC | 10152 |
| rs575852478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203381764 | AAGACACTTAGAATA[C/T]AAAAGATGACATTTG | 10152 |
| rs575852621 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203374316 | ACCAGCCTGGCCAAC[A/G]TAGTGAAACCCTGTC | 10152 |
| rs575879514 | snp | G/T | 0.0858192 | 0.188533 | intron-variant | ABI2 | GRCh38.p7 | 2:203344564 | GTTGTTGTTGTTGTT[G/T]TTGTTTTTTTTTTTT | 10152 |
| rs575905626 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant | ABI2 | GRCh38.p7 | 2:203334578 | TCCAGAGATTCTGGG[-/A]AAAAAAACAATAGAG | 10152 |
| rs575954080 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398659 | ACAATCAAGTTACAG[A/T]ACAGTCCTATCATCG | 10152 |
| rs576002017 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203327974 | AAAAGCCTCGAGAAG[C/T]TCCCTAGGCCGATGA | 10152 |
| rs576009394 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203431847 | TCTTTTGCAACTTAA[A/G]AATTCTATGGAAAAG | 10152 |
| rs576040916 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203378234 | TCTCCTGCCTCAGCC[C/T]CCCAAGTAGCTGGGA | 10152 |
| rs576068499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203384810 | TTTCAGTTGAACATC[A/G]CCCAAGCAGATTCTT | 10152 |
| rs576109755 | in-del | -/TG | 0.00358779 | 0.0422022 | intron-variant | ABI2 | GRCh38.p7 | 2:203344725 | CACCAAACAGTGCTC[-/TG]TGTCTAGCTAAAGGT | 10152 |
| rs576122997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203349427 | CTTCTTTTTTGAGGC[A/G]GAGTTTTGCTCTTGT | 10152 |
| rs576129732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203393095 | CACTGGAGTGCGGTT[A/G]TACAATATTGGCTCA | 10152 |
| rs576131724 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203377668 | CCCAGCACTTTGGGA[C/G]GCCAAGGTGGGTGGA | 10152 |
| rs576156900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203408109 | AAGTCTAACTTGTTA[C/T]CAAGTCATTCTTTTA | 10152 |
| rs576181746 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346358 | TGTTTGTTTGTTTGT[A/G]TATTAGAGGAAAATA | 10152 |
| rs576196333 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203407624 | AGGTTTGGATTGCTT[G/T]GAAAGCCTTTTACTG | 10152 |
| rs576251743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203385501 | AATATAATACTTTTA[A/G]AAATTTTGCTTAAGA | 10152 |
| rs576252787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203347503 | GATGACATTACCACC[C/T]AAGGAAAATGTGCAG | 10152 |
| rs576295545 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203401224 | TTTCACTTATCTCCT[C/T]CTTTTCTCCCTTTCT | 10152 |
| rs576318342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203346754 | CTACTTTGAGAGAAA[C/T]AGGAGAAAGAGCAGG | 10152 |
| rs576322935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203354726 | GAGGCCCAGGTGATA[C/G]TTGTATATGCAAGGG | 10152 |
| rs576324290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203353041 | TTTCATCTAGATTTG[C/T]GAAGTTTACTCTGTG | 10152 |
| rs576334152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203360902 | ATCATTTATGAAATC[A/G]GCAAGGACCAAAATT | 10152 |
| rs576486397 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203335279 | TATTTTATTTTTTGA[A/G]ACAGGGTCTCACTCT | 10152 |
| rs576496789 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203395531 | TCAAGGAAATTTTAT[A/T]TTGAAGTGGTACGCT | 10152 |
| rs576529061 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419667 | CAGGCGTGAGCCACT[A/G]CGCCCAGCCTGTGCT | 10152 |
| rs576531600 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203371322 | GACTGTACTCTGTAT[C/T]GGGGAGAAATACTTC | 10152 |
| rs576532276 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203348989 | CTAGGCTGGAGTGCA[A/G]TGGTGTGATCTCGGC | 10152 |
| rs576596268 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203407776 | AAAACAAGTTTGCTT[C/T]CTGCTCTTCTTTGCC | 10152 |
| rs576622484 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399567 | GGTGTCCAGGCTGGA[G/T]TGCAATGGCAGGATC | 10152 |
| rs576634506 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396584 | TGAATTGAAAAAATC[C/T]GCACATTACCCTGAG | 10152 |
| rs576666537 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203363429 | TATCCATTAACCATT[A/C]TCACTTACCCCTACC | 10152 |
| rs576700119 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351403 | TGACAGTAATTATAT[C/T]GAATCTGTAGATAAA | 10152 |
| rs576770993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203405801 | TCATGTGAATATAAA[C/T]TCAGTGGGGTTCTGT | 10152 |
| rs576804075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203422666 | AACATTAGACAAAGA[A/G]CTGAGAAGAGGCTCA | 10152 |
| rs576863079 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203351971 | TAGTGACATGGTAGC[C/T]GTCCTAATGTTGTAG | 10152 |
| rs576866155 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361354 | CAAGAAAATGTTTGG[C/T]TTGGTGTGGTAGTGT | 10152 |
| rs576868273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203345451 | AGACCAAGAACCCAC[C/T]GGAAGGAACCAATTC | 10152 |
| rs576891705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203406571 | TATTCTCTAAATGAT[C/T]TGTGAAGTTACAGCA | 10152 |
| rs576904849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203351318 | TATTTTGGCTATTCT[A/G]TAGCCCCTGAATTTC | 10152 |
| rs576906759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203398913 | TTAGTAGTGTTGTAT[C/T]GTATGGGGATGTACC | 10152 |
| rs576926549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203413553 | TTTTGGATTGGTCTT[G/T]TTCATCTTTTCCTAC | 10152 |
| rs576938343 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428339 | AGAGAATAGTAGTTA[C/T]TTTCAAGTCTCCTGA | 10152 |
| rs576963480 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ABI2 | GRCh38.p7 | 2:203362750 | CAGGCCGGTCTTGAA[C/T]TCCTGACCTCAGGTG | 10152 |
| rs576976303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203390680 | AGGAATTGCTTAAAA[A/G]CATTATTGTTTTTGA | 10152 |
| rs577046019 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203389907 | TCTTTCCTACACTTG[C/G]ATTTTCAGTTGGGGA | 10152 |
| rs577100207 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203332827 | ACTTGTTGATATGTA[C/T]GTTTTTCTTTTTGTT | 10152 |
| rs577105452 | snp | A/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365274 | AACCAGCTTTTTTTC[A/T]CTTAGTTATATCGTA | 10152 |
| rs577130816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203376623 | ACTCATTATGTTTCT[A/G]TTTTGCCTTCTCTCC | 10152 |
| rs577171874 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203421405 | TGATGTATCATCAAG[G/T]TCTTTCTTAAATTTT | 10152 |
| rs577206095 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429885 | CGGGATGGGGGCAGT[A/G]CAGAAGACACTGGTG | 10152 |
| rs577256325 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203425042 | TTTTTTTTTTTTTTT[G/T]TGTATTTTTTTTTTG | 10152 |
| rs577310492 | in-del | -/TGTTAC | 0.00318978 | 0.0398085 | intron-variant | ABI2 | GRCh38.p7 | 2:203360933 | AGGGTAACAACTAAT[-/TGTTAC]CCTTTCAAGGATGAC | 10152 |
| rs577361269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203332182 | AATGGGATAGTCAAT[A/G]TTTTTTCTAAAATAT | 10152 |
| rs577368309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203395300 | TTAAACTGGAATATA[A/G]AAAGGCAATATTTAT | 10152 |
| rs577377134 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203345743 | TAGAGACGGGGTTTC[A/G]CCACATTGGCCAGGC | 10152 |
| rs577381219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203399515 | TTCTATTTTTTTGGC[A/G]GGGGGAGGAGGGGCG | 10152 |
| rs577460979 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346057 | ACACAAACTGAGGCA[A/G]GAGAATCGCTTGAAC | 10152 |
| rs577487160 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | ABI2 | GRCh38.p7 | 2:203338877 | GGAGAAAATGTGCAA[A/C]CCATACATCTATCTG | 10152 |
| rs577496358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203386962 | GCTTTTTATTTTAGG[C/T]ATGTGAGTCTTATTT | 10152 |
| rs577583966 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403113 | TTAGAAGTGGCAAAG[A/G]AAAAGAGAACATTTT | 10152 |
| rs577599225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203331415 | TAGAGTGTAGTGGCG[C/T]GATCTCGATCTCTGC | 10152 |
| rs577611552 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203360383 | CTTTAAACAAAAGGC[A/G]AAGTGTTGGGTGGAG | 10152 |
| rs577648358 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377337 | GTATATTTATAGTAT[A/G]CAGATGTGAAATAGA | 10152 |
| rs577668294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203372939 | TCCTCACTTCCTAGA[C/T]GGGATGGCGGCCAGG | 10152 |
| rs577679000 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203372217 | CTGAGTGGACACAGC[A/T]CATGTTTCAGAGAGC | 10152 |
| rs577685820 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424859 | GTTAAGTGTAAATTC[G/T]ATCTAATCTAGTTTC | 10152 |
| rs577697534 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355318 | GAAGACTAGCCTGAG[A/C]AACATGGTGAGTTGT | 10152 |
| rs577779725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203348843 | ATCACCCAAAATTTC[C/T]TTTATTTTTAATTAA | 10152 |
| rs577802531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203364341 | TCAAATGATCTGCCC[A/G]CCTCAGCCTCCCAAA | 10152 |
| rs577886226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203342703 | TTCTGCCTCAGCCTC[C/T]TTAGTACTACTGCTG | 10152 |
| rs577933604 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ABI2 | GRCh38.p7 | 2:203344942 | AAATGGACCAACCAG[C/T]GCTCTGTAAAATGGA | 10152 |
| rs577978162 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203344454 | CACTGCAGTCTCTGC[C/T]TCCTGGGTTCAAGCG | 10152 |
| rs578023632 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328343 | GTCCGTCGGCTCGCG[C/T]CCCGCCCCCGTCGCC | 10152 |
| rs578033713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203380950 | TTGGGTGCCTAGAAC[A/G]TGCAAATTTCATTTA | 10152 |
| rs578034822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203398093 | CAGCTTTGCTGTTAT[A/G]CATGTTAAACATATA | 10152 |
| rs578036354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203388210 | TGCCTTGAGGAAATA[C/T]TGAAAAACTCTTTTA | 10152 |
| rs578068246 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ABI2 | GRCh38.p7 | 2:203379982 | ACTCTTAGCTTGTGG[C/G]CTGTAAAAATCAGAT | 10152 |
| rs578068487 | in-del | -/AAT | 0.00119737 | 0.0244387 | intron-variant | ABI2 | GRCh38.p7 | 2:203346775 | AAAGAGCAGGGACAA[-/AAT]AATAACCTGTGGCCA | 10152 |
| rs578115016 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203412210 | TAGGACTCCTGCTTA[A/T]TTGGAAATGGGCACT | 10152 |
| rs578131083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203356252 | GAGGGCAGTGTTGCA[A/G]TCATGGCTCACTACG | 10152 |
| rs578212494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203349570 | CCACCATGCCTGGCT[A/G]ATTTTTGTATTTTTA | 10152 |
| rs578215274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ABI2 | GRCh38.p7 | 2:203404301 | TTCTGGGTCCCTCTC[A/G]TAAATTAAGTGCTGT | 10152 |
| rs745349093 | snp | C/T | 3.48214e-05 | 0.00417247 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366857 | TGAATTAATGATCAC[C/T]GGTTTGTTTTTTTTC | 10152 |
| rs745359563 | in-del | -/T | 8.66709e-05 | 0.0065824 | intron-variant | ABI2 | GRCh38.p7 | 2:203402747 | AGGTTAGTTTTTTTG[-/T]TTTTTTTGCATTCTA | 10152 |
| rs745380354 | in-del | -/ATTAA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203426549 | TGTTATTATAGTTAT[-/ATTAA]ATTGGTGACATAGTG | 10152 |
| rs745384913 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203381231 | TATTTTTAAAATCTC[G/T]TTGTCTTCAGGGTTT | 10152 |
| rs745407943 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203335529 | TGGCTTCCCAAAGTG[C/T]TGGGATTACACCTGT | 10152 |
| rs745421724 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399105 | AAGTAAATTTTTAAC[A/G]TCATAAGAAACTGCC | 10152 |
| rs745427453 | in-del | -/CTATC | 0.000162324 | 0.00900755 | intron-variant | ABI2 | GRCh38.p7 | 2:203374859 | CTAACTGAGGTAGTG[-/CTATC]CAGTACAGTCAACTT | 10152 |
| rs745433549 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421170 | GATACCTGATAATAG[C/T]GTAGAGTGCATTGGA | 10152 |
| rs745486722 | snp | A/G | 1.69266e-05 | 0.00290913 | intron-variant | ABI2 | GRCh38.p7 | 2:203417105 | CAGAAGGATATCTGG[A/G]TAGATGGGAAGAAAC | 10152 |
| rs745514730 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354159 | AAGCCAACCTCCCAC[C/T]TTGGCCTCCAAGTAG | 10152 |
| rs745533687 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203371016 | ATCAGGGCATCTAGG[C/G]TTTACCCTGACTCTT | 10152 |
| rs745580953 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203367467 | ACCTGCAATAATGGA[A/G]AGACTAGCAAACCTT | 10152 |
| rs745596160 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344526 | AACTGCCGCCACACC[C/T]GGCTAATTTTTGCTT | 10152 |
| rs745642610 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392399 | CACTGAATCAGGATA[A/G]GACCAAATGATTTGA | 10152 |
| rs745646231 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428931 | CAAGTTCAGAAAGTG[C/G]AACTTGATTGAAAAG | 10152 |
| rs745709946 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415345 | TAATTCACCGGGCGC[-/A]GGTGGCTCACGCCTG | 10152 |
| rs745710919 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343719 | ATACTATTTGATGTT[A/G]TTTGCATATAGGCTC | 10152 |
| rs745740541 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203416617 | ATCTCTTTGGAAAGA[A/G]GATTTGTGTTAATAT | 10152 |
| rs745743158 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361078 | GTTCTCTTGAAAGGA[C/G]ATCTGAATATATGTG | 10152 |
| rs745797815 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329961 | AGACTGGTCTCGAAC[C/T]CCTGACTTCAAGTCA | 10152 |
| rs745831132 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376542 | AAGCAACAACAAATA[C/T]ATTTTTAAAGAATTT | 10152 |
| rs745868936 | snp | C/T | 1.65515e-05 | 0.00287671 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402636 | ATACTCCCCCAACAA[C/T]AGGGGGCTCGTTGCC | 10152 |
| rs745886780 | snp | A/G | 0.000131053 | 0.00809378 | intron-variant | ABI2 | GRCh38.p7 | 2:203351697 | CGTGCTACTGTGCCC[A/G]GCTGATTTTCGTATT | 10152 |
| rs745899975 | snp | A/C | 1.65029e-05 | 0.00287248 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203380290 | CTTCAAGGACACATA[A/C]GATTATTGCTCCAGC | 10152 |
| rs745931848 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203401745 | TTTTTTGATTAAAAG[A/G]AAGAAATGTTTGATT | 10152 |
| rs745954384 | snp | C/G | 2.33495e-05 | 0.00341675 | intron-variant | ABI2 | GRCh38.p7 | 2:203391000 | TTCCCAAAAGTGCCA[C/G]TTTATTTCACTGCAT | 10152 |
| rs745963979 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203362701 | CTGGCTAATTTTTAT[A/T]TGTTTAGTAGAGATG | 10152 |
| rs746004145 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203332409 | AGGCAGGCACATCAC[A/G]AGATCAGGAGATCCA | 10152 |
| rs746012630 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385962 | CTTTTTTGTCTTTTA[A/G]CCCTTTTTCTAAAAA | 10152 |
| rs746147380 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350276 | GAGACGAGGTTTCAC[C/T]GTGTTGGCCTGGCTG | 10152 |
| rs746147476 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337261 | CCCTAAAGACTCCAC[C/G]AAAAGACTGTTAGAA | 10152 |
| rs746184371 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410270 | TGTGATCTCCTTGAG[A/G]GCAGAGACATGTTCA | 10152 |
| rs746200396 | snp | A/G | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203395687 | GGAGGGAGCCACCCA[A/G]GTAGTCGGAGCAGCA | 10152 |
| rs746234350 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378328 | GTGTTAGCCAGGATG[A/G]TCTCGATCTCCGGAC | 10152 |
| rs746240493 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425228 | ATTTCTTTTTCTTTT[A/C]TTTTTCTTTTTTGAG | 10152 |
| rs746243080 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370579 | GCCTTAGTTTGCCAG[C/T]CCCTGCTCTAAAATA | 10152 |
| rs746253554 | snp | C/T | 1.93343e-05 | 0.00310915 | stop-gained, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328629 | GAGAACAACTACATA[C/T]AGGTGCGAAGCATCC | 10152 |
| rs746276338 | in-del | -/TTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203414102 | TGTACTTGCATTGTC[-/TTT]TTTTTTTTTTTTTTT | 10152 |
| rs746341971 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396722 | AATACTCTAATACCT[C/T]TTCTAATCCTGCCTC | 10152 |
| rs746351261 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357147 | GATTTGTTACTTTTT[A/C]TGTAAGCATATATAG | 10152 |
| rs746360988 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345559 | GGGACAACAGGTGCC[C/T]GCCACCATGCCAGCT | 10152 |
| rs746403114 | snp | A/G | 0.000153331 | 0.00875454 | intron-variant | ABI2 | GRCh38.p7 | 2:203411419 | GATTGTAGGCATAAA[A/G]TGTCATTTATATGTG | 10152 |
| rs746431938 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394777 | TACCTAGCCCAACCC[A/G]TAATATGGCTCCCTC | 10152 |
| rs746472029 | snp | C/T | 3.5706e-05 | 0.00422513 | intron-variant | ABI2 | GRCh38.p7 | 2:203328668 | GCCGCGTCGGGGACC[C/T]CCCCGCCGGGGGCCG | 10152 |
| rs746472326 | snp | C/T | | | intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203407928 | GCTCACAGACGTTCT[C/T]GTCAGATGAAATCTT | 10152 |
| rs746526160 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354407 | TTTTTGACTTGCTTA[C/G]TTACCTGTGAATCTA | 10152 |
| rs746565091 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423361 | GGAGTTTATAGTGTA[G/T]AGAGTTTTATGTTTA | 10152 |
| rs746582008 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203386223 | TTTTTTCCCATCCTC[-/A]ACTATTTCACATACA | 10152 |
| rs746592493 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350591 | GTCGCCCAGGCTAGA[A/G]TGTAGTGGCGTGATC | 10152 |
| rs746601331 | in-del | -/TT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396203 | GAAAATACTACCCTC[-/TT]TTCTCTGAAACAGAA | 10152 |
| rs746694913 | in-del | -/T | 1.65362e-05 | 0.00287538 | intron-variant | ABI2 | GRCh38.p7 | 2:203411276 | TCCACACCTTTTTTG[-/T]TTTTGCAGTATCTCT | 10152 |
| rs746779213 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431697 | TCTCATATAATTATT[A/T]AAAAAAAAAAACAAT | 10152 |
| rs746821209 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377898 | GCGACAGAGTGAGAT[A/G]CTGTCTCATAAAAAT | 10152 |
| rs746842676 | in-del | -/GTGCGC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350890 | TGTGTGTGTGTGTGT[-/GTGCGC]GCGCGCATACTTTTA | 10152 |
| rs746870547 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203336767 | CCTAACAAGCAGTTG[A/G]GCAGGTCTATCACAT | 10152 |
| rs746886279 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366351 | ATTACTTTTAGTTTA[C/T]CATGATTATTATTAC | 10152 |
| rs746904405 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403085 | ATGAAAGTTGTGTGC[A/G]CATGAACAGAATTTA | 10152 |
| rs746927743 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364051 | TTATAGGCGTGAGCC[A/G]TGGTACCTGGCCTGT | 10152 |
| rs746936440 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418347 | TGGCTCAGCTGGGCC[C/T]TCTGGTTCAGGGACT | 10152 |
| rs746946772 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343007 | AGTCTATACCGTTAA[C/T]AAAAGACCATGAGAT | 10152 |
| rs746959165 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402069 | AGACAGAGTCTCACT[C/T]TGTCACCCAGGCTGG | 10152 |
| rs747005348 | snp | A/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203395711 | AGCAGCAGTCGAGAG[A/T]ACAGTGGAAGTGGTA | 10152 |
| rs747093664 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338435 | GAATGATGTAGCACC[A/G]TCCCTTTAGTGATAA | 10152 |
| rs747104985 | snp | A/T | 1.67598e-05 | 0.00289476 | intron-variant | ABI2 | GRCh38.p7 | 2:203411401 | TCTTTATGCTGTAGA[A/T]CAGATTGTAGGCATA | 10152 |
| rs747109407 | in-del | -/AA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421966 | TGAGACTCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 10152 |
| rs747147583 | in-del | -/TTTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400080 | AGTGTGAATAGTGTC[-/TTTTT]TTTTTTTTTTTTTTT | 10152 |
| rs747151037 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203412869 | TACCAAGTAGAAAAG[G/T]ATTTAATTACAGTAC | 10152 |
| rs747182919 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356735 | CGAACTCCTGGGCTC[A/G]AGCAATCTTCCTGCC | 10152 |
| rs747187945 | snp | C/T | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427374 | GCAGGGCTGTGCTTG[C/T]CTCACAGGAATAGTC | 10152 |
| rs747207762 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359553 | TTCATTGGTCCTTCT[A/G]AAACAAAATATCTTA | 10152 |
| rs747240078 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425325 | CTCTTGCCTCAGCCT[C/T]CCAAGTAGCTGGGAT | 10152 |
| rs747241663 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331461 | CCTCCTGGGTTCAAG[C/T]GATTCTTCTGCCTCA | 10152 |
| rs747295483 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370651 | TGTATTATTATTTAA[A/C]ATATTGTGTGTTTCT | 10152 |
| rs747297124 | snp | A/T | 1.65132e-05 | 0.00287339 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203380272 | TGACTACCAATAAAA[A/T]CACTTCAAGGACACA | 10152 |
| rs747300956 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388087 | ATTGTTTTGTTTGGC[A/G]TTTATTTCTGTTCTT | 10152 |
| rs747306354 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203397011 | AGATGCAGTCATCTG[G/T]CTATTCTCTTACTTG | 10152 |
| rs747339200 | snp | A/G | 1.66277e-05 | 0.00288333 | intron-variant | ABI2 | GRCh38.p7 | 2:203394869 | CTCTACCTCAGTGCA[A/G]AATGTGATGGTCATA | 10152 |
| rs747341036 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357317 | AGAGCAAGTAAGATA[C/G]TAGCAGAGCTAGAAC | 10152 |
| rs747350758 | snp | A/G | 3.30066e-05 | 0.00406229 | synonymous-codon, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394721 | CTCCCCCTATCGCAC[A/G]CTGGAGCCAGTGCGT | 10152 |
| rs747360580 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406607 | ATAAATGTCTAAAAC[A/G]TCTAGAAGAATACTG | 10152 |
| rs747433398 | in-del | -/GT | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428111 | GTACCCAGATGTGAA[-/GT]GTGTGGTAGGCTGGT | 10152 |
| rs747487631 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203334484 | GTAATCTTTTGGTGG[A/G]TGAAATATATTTGGT | 10152 |
| rs747487710 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347646 | GGAATAGAAATGATA[C/T]AAGGATTGAGATGAT | 10152 |
| rs747504501 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423415 | ACTATTTTAGGAGAG[-/A]AAAAAATCATCTGGG | 10152 |
| rs747516242 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203348613 | ATAATGTAATATCAC[C/G]TCACCTGGGTGAAAT | 10152 |
| rs747575696 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346839 | CATTCCTTTATCTTA[C/T]CTTATATTCTTGCAG | 10152 |
| rs747586504 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203394425 | GGGAAACATTGGCTT[A/G]AATGGTAGAGAACCT | 10152 |
| rs747611862 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398356 | CCCAACTGAGAGTCT[A/G]TGTTTTAGTAATTAA | 10152 |
| rs747612709 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203395032 | CAGTCAGGAAGTTGA[C/T]AAAGAACAGACATCT | 10152 |
| rs747640939 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430781 | TTATTATCCAGCTAG[A/C]CAATATTTTATGCAT | 10152 |
| rs747772459 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203332598 | CCATTGCACTCCAGC[C/G]TGGGCGACAGAGCAA | 10152 |
| rs747791367 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378346 | TCGATCTCCGGACTT[C/T]GTGATCCGCCCACCT | 10152 |
| rs747798616 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378067 | AATTAGCCTAACATG[C/T]GTAGAAAAGTTTAGA | 10152 |
| rs747812868 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345472 | GAACCAATTCCGGAC[A/G]CAATCTTAGCTCACT | 10152 |
| rs747845264 | snp | C/G | 1.72856e-05 | 0.00293982 | intron-variant | ABI2 | GRCh38.p7 | 2:203367083 | TTGCCTATGAGGAAC[C/G]CTTAATAATAAACAC | 10152 |
| rs747860963 | snp | G/T | 2.55869e-05 | 0.0035767 | intron-variant | ABI2 | GRCh38.p7 | 2:203328651 | GAAGCATCCCCAGCT[G/T]GGCCGCGTCGGGGAC | 10152 |
| rs747884411 | in-del | -/TAA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392720 | GATTTTGTTGGGTTT[-/TAA]GTCAAGATTGTTAGT | 10152 |
| rs747957583 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423029 | TCTTACTAGCATTTT[A/G]ATTTTTCCAGTGGCT | 10152 |
| rs747977271 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203334145 | AGGGTTTCTCCATGT[A/T]GGCCAGGCTGGTCTC | 10152 |
| rs747978075 | snp | A/G | 1.72564e-05 | 0.00293733 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203380217 | TTGCAGACAGTTGAT[A/G]TTCATAAAGAGAAAG | 10152 |
| rs747991596 | in-del | -/TGTGTGTGTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203358106 | GTGTGTGTGTGTGTG[-/TGTGTGTGTT]TGTTTGTTTGTTTGT | 10152 |
| rs748007137 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427789 | CAGTGGGTACCCTAG[C/T]CCCTTCTTTTCTTCC | 10152 |
| rs748027386 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364044 | GCTGGAATTATAGGC[A/G]TGAGCCATGGTACCT | 10152 |
| rs748031296 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330395 | GAGACTACATATCAA[-/A]AAAAAAAAAAAAAAA | 10152 |
| rs748093264 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404502 | AACCATGTTTTCAAA[C/T]TCACATTTGTTCAGG | 10152 |
| rs748257452 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203389869 | TACTCCTTTGGTGAC[C/T]TCCATTATTCCCAGA | 10152 |
| rs748299731 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359365 | GTTCTTATGAGTGAT[A/G]TCTTAATTTAGAGTA | 10152 |
| rs748384787 | snp | A/G | 1.65217e-05 | 0.00287412 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402681 | CTTCCATTACTTCAC[A/G]AACAAGCCTTCAGAA | 10152 |
| rs748446925 | in-del | -/AAAAA | 0.00151911 | 0.0275182 | intron-variant | ABI2 | GRCh38.p7 | 2:203355215 | AATACATGGAAAGTT[-/AAAAA]AAGAAGACTGGGTAC | 10152 |
| rs748451371 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374887 | TCAACTTTCAATTAT[C/T]TGTGGTAATGGGAAA | 10152 |
| rs748456382 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203335658 | TTATGTTCTGTAAAG[C/T]TTTGCAGTACTTTTC | 10152 |
| rs748459612 | snp | A/T | 1.66117e-05 | 0.00288194 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203417070 | GGGCTCCACGTTCTT[A/T]CTTGGAAAAGGGTAA | 10152 |
| rs748474370 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357535 | TTTTTCTAAAGTGCT[C/T]CTCTGACACTTTGGT | 10152 |
| rs748480323 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387056 | CGCAGGCTCCCTTCC[-/T]TTTTTTTTTTTTTTT | 10152 |
| rs748489372 | in-del | -/CACCACCACCAACAA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392306 | CACCACCACCACCAC[-/CACCACCACCAACAA]CAACAACAACAACAA | 10152 |
| rs748533381 | snp | C/T | 2.6274e-05 | 0.0036244 | intron-variant | ABI2 | GRCh38.p7 | 2:203391176 | AATTGAAAACCATTT[C/T]ATGTAGTATTGTTTA | 10152 |
| rs748547453 | snp | A/G | 1.65187e-05 | 0.00287386 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427199 | AATTTATGACTATAC[A/G]AAAGACAAGGAAGAT | 10152 |
| rs748558846 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402945 | ACGTAAAGTCATACA[A/G]CTTAGTTTTTCTGAG | 10152 |
| rs748568159 | in-del | -/TT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203380752 | TATTTATCAGCAGAC[-/TT]TTGGCATTAGTTTTC | 10152 |
| rs748640127 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203367755 | CATCTGTAATCCCAG[C/T]ACTTTGGGAGGCTGA | 10152 |
| rs748672330 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422071 | GAGGCTGAGGCCGGC[A/G]GATTGCTTGAGACGA | 10152 |
| rs748684282 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203334435 | CTTTTAAAATGCAGG[A/G]AATTTAATAGTATGC | 10152 |
| rs748701407 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203375457 | TACTTTTCTTACTTT[A/T]AAAATTCATCCTAAA | 10152 |
| rs748728251 | snp | G/T | 1.64789e-05 | 0.0028704 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427275 | AATGACGATGGTTGG[G/T]ATGAGGGAGTTATGA | 10152 |
| rs748729529 | snp | C/T | 1.65353e-05 | 0.00287531 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394708 | TTTGTAGGCGGCACT[C/T]CCCCTATCGCACACT | 10152 |
| rs748777901 | snp | A/G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346717 | GGGGAATGAATTAAC[A/G/T]TCTTTAAGGGAAGTG | 10152 |
| rs748788810 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419106 | CCTAAATTAAAGATC[-/T]TTTTTTTTTTTTTTT | 10152 |
| rs748790746 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378371 | CCACCTTGGCCTCCC[A/G]AAGTGCTGGGATTAT | 10152 |
| rs748833078 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404096 | CCTACATATTTAAAA[A/C]ATTTTTCTCTTATCC | 10152 |
| rs748841536 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351992 | AATGTTGTAGCACAA[G/T]GCATTACTCTTGTGT | 10152 |
| rs748844880 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432047 | GTTGCCAGTAATGTT[C/T]CTTGTGTGCCATTAA | 10152 |
| rs748845339 | snp | A/G | 0.000162324 | 0.00900755 | intron-variant | ABI2 | GRCh38.p7 | 2:203374882 | TACAGTCAACTTTCA[A/G]TTATCTGTGGTAATG | 10152 |
| rs748863110 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203333042 | CTTTTCTTCTCTTAA[A/T]CAATGTGGATACTCC | 10152 |
| rs748869435 | in-del | -/AGG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339487 | TCCAGAGGCTGAAGC[-/AGG]AGAATTGCTTGAACC | 10152 |
| rs748888357 | in-del | -/TTTTCTTTTTTCTTTCTTTTTTTTTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203333928 | TTCATTTATTTTTTC[-/TTTTCTTTTTTCTTTCTTTTTTTTTTT]TTTTGAGATGGAGTC | 10152 |
| rs748896268 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404561 | CGCCTGGCTAATTTT[C/T]GTTTTGTTTTGTTTT | 10152 |
| rs748918173 | snp | C/G | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365151 | TTTCCAACATTCAGA[C/G]AAAACTTAGGTTATC | 10152 |
| rs749102478 | snp | C/T | 1.66568e-05 | 0.00288585 | missense, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203366881 | TTTTTTCCCAGTCAG[C/T]AGATAAGCAGAGAGC | 10152 |
| rs749113260 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353240 | AATACAGTTGATTTT[C/G]TATATTGATCTTTCA | 10152 |
| rs749130784 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203414615 | TCGTTCATGTCTTCA[C/T]GACTTTTGCCTACTG | 10152 |
| rs749136679 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203375418 | TATAACTAGTAACTT[A/T]AAAAACCCAGAATAA | 10152 |
| rs749164602 | in-del | -/AACAACAA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392319 | ACCACCACCACCAAC[-/AACAACAA]CAACAACAACAACAA | 10152 |
| rs749187484 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392714 | CTTATGGATTTTGTT[A/G]GGTTTTAAGTCAAGA | 10152 |
| rs749189636 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343431 | ATGTGCATGTAATGA[C/G]AAGGCATTATATTCC | 10152 |
| rs749200502 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428656 | ACAGCTTCAAATTCA[A/G]TGGAGTCTGTAGGGC | 10152 |
| rs749216037 | in-del | -/AAGT | | | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432636 | GTATCTGAGGGTAGC[-/AAGT]AAGTAAGTTTGTCTT | 10152 |
| rs749300109 | snp | C/T | 3.41553e-05 | 0.00413237 | intron-variant | ABI2 | GRCh38.p7 | 2:203367071 | ATATTTTCCTATTTG[C/T]CTATGAGGAACCCTT | 10152 |
| rs749337376 | snp | A/G | 2.27544e-05 | 0.00337294 | intron-variant | ABI2 | GRCh38.p7 | 2:203391156 | TGGGTGAGTATATAA[A/G]TAGTAATTGAAAACC | 10152 |
| rs749386435 | in-del | -/TTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331810 | TTTGCTCAGTGTTCT[-/TTT]TTTTTTTTTTTTTTT | 10152 |
| rs749388954 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359536 | AAATGTATGTGTCTT[A/T]GTTCATTGGTCCTTC | 10152 |
| rs749395471 | snp | A/G | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327696 | CACCGCAAACCAGGA[A/G]AGAAAGGGGCTAATC | 10152 |
| rs749397689 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376332 | TCACCCCTGCCCACA[A/G]CAAAGAATTATCAAG | 10152 |
| rs749400356 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203401581 | GAGAGCAAAATACAG[C/T]GAAATTGATGATAAC | 10152 |
| rs749470310 | in-del | -/GTTTGT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203358113 | TGTGTGTGTGTGTGT[-/GTTTGT]TTGTTTGTTTGTTTT | 10152 |
| rs749475110 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382033 | ACATTCTGCTTTAAC[A/C]ACTCTTTCTATGATC | 10152 |
| rs749478520 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203414121 | TTTTTTTTTTTTTTT[-/G]GAGACAGTCTCACTC | 10152 |
| rs749482719 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382376 | CTTCATGTTCCTTGA[A/G]GGCAGATATTTTTGT | 10152 |
| rs749567238 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399833 | TCATTTATTTTTTTG[A/G]TGTTGTATTTCAAAT | 10152 |
| rs749584952 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360935 | GGTAACAACTAATTG[C/T]TACCCTTTCAAGGAT | 10152 |
| rs749606293 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338043 | TCAAAAAAAGCTATA[A/G]TAATCAAAACAGTGT | 10152 |
| rs749619009 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329341 | AACCTCCTGGTTTAA[-/T]TTTTTTTTTTTTTTT | 10152 |
| rs749626492 | snp | C/T | 0.000224442 | 0.0105911 | intron-variant | ABI2 | GRCh38.p7 | 2:203351633 | CTTGAACTCCTGTGC[C/T]CAAGTGATCATCCTG | 10152 |
| rs749630077 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368023 | AAAAAATAAAAAAAA[G/T]TAGCCAGGATTATAA | 10152 |
| rs749644438 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203336917 | CGTTCCCACCAGCAA[A/G]GATCCAGTTGTTCTT | 10152 |
| rs749688383 | snp | A/G | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416959 | AACCAGTCTTTGATG[A/G]GTCTCCCCCACCTCC | 10152 |
| rs749716535 | in-del | -/AT | 3.81454e-05 | 0.00436706 | intron-variant | ABI2 | GRCh38.p7 | 2:203402550 | TTTTCTTTTAATGAC[-/AT]ATGTATGTTCTATCT | 10152 |
| rs749782829 | in-del | -/GA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385570 | GGACTGTTTTCACTT[-/GA]GTACTATTTTTAGCA | 10152 |
| rs749826979 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408097 | TAGCTTTGAAAAAAG[C/T]CTAACTTGTTACCAA | 10152 |
| rs749830902 | snp | C/T | 1.94214e-05 | 0.00311614 | intron-variant | ABI2 | GRCh38.p7 | 2:203391038 | GAGTTTTCCTTAAAA[C/T]TTTTTAGGTGAGTAC | 10152 |
| rs749839606 | in-del | -/C | 1.6897e-05 | 0.00290658 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366871 | TGGTTTGTTTTTTTT[-/C]CCCAGTCAGCAGATA | 10152 |
| rs749870963 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203336711 | CTGTATCTTTTACTA[C/G]TATTCCTTCTGCCCT | 10152 |
| rs749880507 | snp | C/T | 1.65053e-05 | 0.0028727 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203417052 | CTGAAGAGGACCCAC[C/T]GTGGGCTCCACGTTC | 10152 |
| rs749933424 | snp | A/G | 1.71111e-05 | 0.00292494 | intron-variant | ABI2 | GRCh38.p7 | 2:203402738 | GCCAGAATCCAGGTT[A/G]GTTTTTTTGTTTTTT | 10152 |
| rs749953142 | in-del | -/TA | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430702 | GCCTGCTAATTTTGC[-/TA]TGTTCCTAAAAGTTA | 10152 |
| rs749970755 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400960 | AACAAATCAAGCATT[A/C]ATCAAATTCCATATT | 10152 |
| rs749977401 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421373 | TCAAATAACGTATCT[G/T]CAAAAATCATGTTTG | 10152 |
| rs749984907 | snp | C/T | 1.6819e-05 | 0.00289987 | intron-variant | ABI2 | GRCh38.p7 | 2:203367052 | TTTCACAAGTGAGAC[C/T]ACAATATTTTCCTAT | 10152 |
| rs749988231 | snp | C/T | 0.000147373 | 0.00858282 | intron-variant | ABI2 | GRCh38.p7 | 2:203376161 | TAATTAGTCCTTCCT[C/T]TATAGATCTTTGGTT | 10152 |
| rs749988422 | snp | C/T | 1.64893e-05 | 0.0028713 | intron-variant, missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203411297 | CAGTATCTCTTGCTC[C/T]TCCTCCTCCCTCCAT | 10152 |
| rs750080427 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368790 | TGAAGGAAATAATCA[A/G]TGGGATTTTAAATGA | 10152 |
| rs750105435 | in-del | -/GTGTGCGC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350888 | TGTGTGTGTGTGTGT[-/GTGTGCGC]GCGCGCATACTTTTA | 10152 |
| rs750108497 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329877 | GAGTAGCTGGGACTA[C/T]AGGCGCCCGCCACCA | 10152 |
| rs750156965 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382969 | TAATGTTTTGGTATC[A/G]TGGAGGATTCGTGAT | 10152 |
| rs750198647 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203409777 | TTGGAAGTAGGTTGC[A/G]TTACCTTGTTTTCAT | 10152 |
| rs750209173 | in-del | -/CAC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392281 | CACCACCATCACCAC[-/CAC]CACCACCACCACCAC | 10152 |
| rs750274870 | snp | A/G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370353 | TCAGCCTCCCAAAGT[A/G/T]CTGGGATTACAGGCA | 10152 |
| rs750301270 | in-del | -/TT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203414103 | GTACTTGCATTGTCT[-/TT]TTTTTTTTTTTTTTT | 10152 |
| rs750302706 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396146 | ATAAAAAGTAGTTTT[C/G]ACAGTTAAATTTAGT | 10152 |
| rs750311509 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374583 | TAATTATGCATAGAA[A/G]GTAGACTTTTTATAC | 10152 |
| rs750313767 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203407501 | CCAAACTTTTTGAAT[C/T]GGACATCTAAAATAC | 10152 |
| rs750326278 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377812 | TTAGGAAGCTCAGGC[A/G]GGAGAATCATTTCAG | 10152 |
| rs750338296 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431587 | ACAGCACAGCAGCCT[G/T]ATTGGAGAGAGCCTT | 10152 |
| rs750379504 | in-del | -/AC/ATATATATATACAC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203395448 | TATATATATATATAT[-/AC/ATATATATATACAC]ACACACACACACACA | 10152 |
| rs750406142 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347892 | TCCTGCAGTTTCGAT[A/G]CTTTCTAGATATTTA | 10152 |
| rs750427672 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203393806 | ATCTACAATATGTCA[A/G]TTGACTGTTTATCAT | 10152 |
| rs750431344 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203333737 | ATTTGAGCCCCTTGC[G/T]CTTTTAAACATTTTG | 10152 |
| rs750437035 | snp | C/T | 0.000165577 | 0.0090973 | intron-variant | ABI2 | GRCh38.p7 | 2:203355202 | CTTCCTGACAAAGAA[C/T]ACATGGAAAGTTAAA | 10152 |
| rs750443013 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203411443 | ATATGTGATTGACTG[A/G]ATAGTCATTCATTTG | 10152 |
| rs750518565 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346330 | TTTGCTAACAACCAC[A/T]AAAGACTATGTTTGT | 10152 |
| rs750543376 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368713 | ATTGTGTATCTTAAG[-/T]TTAAAAAAAAATTGG | 10152 |
| rs750570376 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203397445 | TCATAGACAATGGAC[G/T]TTTAAAGAATTTCAG | 10152 |
| rs750621064 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365787 | GGCGCCCGCCACCAT[A/G]CCTGGCTAATTTTTT | 10152 |
| rs750644895 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351649 | CAAGTGATCATCCTG[C/T]CTCAGTCTCTCAGTA | 10152 |
| rs750670789 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363749 | ACTCCATTGGGCATA[C/T]GTACCATATTTTCTT | 10152 |
| rs750673748 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369266 | ATGTTAAAAAGAAAC[A/G]TTAAAAAAAAGAACA | 10152 |
| rs750703023 | snp | G/T | 1.74482e-05 | 0.00295361 | intron-variant | ABI2 | GRCh38.p7 | 2:203427134 | CTGTCTTTCTAGGAA[G/T]ATTACTGTCTTTCAC | 10152 |
| rs750752991 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203341434 | ATAAATTAGTTTTGG[G/T]CCAGGCTCAGTGGCT | 10152 |
| rs750786500 | snp | C/T | 0.00028715 | 0.0119788 | intron-variant | ABI2 | GRCh38.p7 | 2:203396773 | CTGCCTCTTACTCCT[C/T]TTTCCCCTCAGCCCC | 10152 |
| rs750825693 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203352518 | GATCCTGACCCTGTG[G/T]AGGGTTAGGCTAATA | 10152 |
| rs750844908 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339907 | GCAGTCACCCTTGTG[A/G]AACGCGTGTATATGA | 10152 |
| rs750848761 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415887 | TGATGTTACTATATA[C/T]TGGTATGCAAGCTGT | 10152 |
| rs750858823 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413709 | AGTCTTTAAACTCTT[C/T]AAAACATTCACCTTG | 10152 |
| rs750893514 | in-del | -/CACCACCAACAACAACAACAA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392309 | CACCACCACCACCAC[-/CACCACCAACAACAACAACAA]CAACAACAACAACAA | 10152 |
| rs750894927 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384882 | CTCCGTCACCCAGGC[C/T]GGAGTGCAGTGGCAC | 10152 |
| rs750899943 | in-del | -/CTTGT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387814 | TATTGCTTTGTTTTC[-/CTTGT]CTTGAGTTTATGGTA | 10152 |
| rs750934420 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388873 | TTTCAAATATTTTAG[C/T]TATCCCATGTATAGA | 10152 |
| rs750936301 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203352772 | CTACAGTACTGTACA[A/G]TAATGTCCTAGGCCC | 10152 |
| rs750955168 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343153 | TGGATCACGTGAGGT[C/T]AGGAGTTTGAGACCA | 10152 |
| rs750982222 | snp | C/G | 1.93048e-05 | 0.00310677 | intron-variant | ABI2 | GRCh38.p7 | 2:203402547 | TAATTTTCTTTTAAT[C/G]ACATATGTATGTTCT | 10152 |
| rs750994074 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203371340 | GGAGAAATACTTCAA[C/T]AAAACAAAGTAATAA | 10152 |
| rs750994582 | snp | A/G | 0.000146424 | 0.00855514 | intron-variant | ABI2 | GRCh38.p7 | 2:203351560 | TTTCCTTTAGAGATG[A/G]GGTCTTGGTATGTCA | 10152 |
| rs751012351 | in-del | -/TTG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344540 | CGGCTAATTTTTGCT[-/TTG]TTGTTGTTGTTGTTG | 10152 |
| rs751080599 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423943 | AGAATGTATTTTTAC[A/T]TTAGCAGAAACATTT | 10152 |
| rs751085479 | snp | A/T | 1.72098e-05 | 0.00293336 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402585 | TTTCAGGTCATCCTG[A/T]ACAGTTCTACAGCAT | 10152 |
| rs751087973 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385544 | ATCATTTAGCCCCAT[C/G]TTTAAAAAATGGACT | 10152 |
| rs751091241 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337878 | TCTACTAAAAATACA[A/T]AAATTATAGGGCATG | 10152 |
| rs751102172 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351101 | CAACACCATTTGTTT[A/C]AAAGCCTTTTCTTTC | 10152 |
| rs751143730 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370847 | AAGGGTAGAGTTGTT[C/T]AGGACTAGTAGATAC | 10152 |
| rs751193483 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203352365 | AAAAGTTAACTGTAA[A/G]GGAGTCTCAGGCAGT | 10152 |
| rs751216466 | in-del | -/TTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420397 | GACTGTGACAGTCCC[-/TTT]TTTTTTTTTTTTGAG | 10152 |
| rs751229231 | snp | A/G | 1.67975e-05 | 0.00289802 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402722 | GGAGGACCTTTTTAT[A/G]GCCAGAATCCAGGTT | 10152 |
| rs751244759 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354767 | GGGAAGAACCTGAAT[C/T]TAGGTAACCTAAATC | 10152 |
| rs751268842 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430125 | AATTGGAGACTTTTA[A/G]TGTATGTAATATTTC | 10152 |
| rs751285843 | snp | C/G | 7.07727e-05 | 0.00594822 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366851 | TATTTTTGAATTAAT[C/G]ATCACTGGTTTGTTT | 10152 |
| rs751288155 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370361 | CCAAAGTGCTGGGAT[G/T]ACAGGCATGAGCCAC | 10152 |
| rs751388301 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413145 | GTCATTCATTTTGAA[C/G]AAAAGTGGTTCTGAG | 10152 |
| rs751422187 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345320 | ACCAGGAACCCACTG[C/G]AAGGAAGAAACTCCG | 10152 |
| rs751424244 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356972 | AAGCATTGGGAATGT[G/T]AAAGGCAAATGAGTA | 10152 |
| rs751443126 | snp | A/G/T | 6.71416e-05 | 0.00579369 | intron-variant | ABI2 | GRCh38.p7 | 2:203394661 | TTATTGTGCCGAAAC[A/G/T]TGCTTAATCATACAA | 10152 |
| rs751471965 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420536 | GTAGGTGGGACTACA[A/G]GCACCTGCCAGCACA | 10152 |
| rs751537733 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203352728 | AGAAATAAATTTAGC[A/G]TAGCATAAATCTACA | 10152 |
| rs751564722 | snp | A/G | 5.00146e-05 | 0.00500048 | intron-variant | ABI2 | GRCh38.p7 | 2:203395802 | CATTCATGGTGCCTC[A/G]TCTTCACTTTTCCTT | 10152 |
| rs751582617 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365929 | CCACCGTGCCCGGCC[A/G]GGGCTGTTATCTTAA | 10152 |
| rs751587341 | in-del | -/CAAAATGTGATGGTCATAGTAC | 1.66233e-05 | 0.00288295 | intron-variant | ABI2 | GRCh38.p7 | 2:203394867 | TTCTCTACCTCAGTG[-/CAAAATGTGATGGTCATAGTAC]CATAATCTGTTCAGA | 10152 |
| rs751625414 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420546 | CTACAGGCACCTGCC[A/T]GCACACCCGGCTAAT | 10152 |
| rs751638695 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203335041 | AGGTAGCATGTAGGG[A/C]AACACATTCTATTTT | 10152 |
| rs751659474 | snp | C/T | 1.7821e-05 | 0.00298499 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328610 | ACGGGTGGCCGATTA[C/T]TGCGAGAACAACTAC | 10152 |
| rs751665881 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404399 | TCTATCTTTTATCAC[A/G]TTTAGTGTTTTTGGC | 10152 |
| rs751674303 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364826 | TGCATCTTTGGCTTC[C/T]GGGCTCAAGTCATCC | 10152 |
| rs751683679 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203394388 | AAAAGAATTCCAACT[C/T]TTCTAAGAAGAGGTA | 10152 |
| rs751738794 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203362987 | AGGCATACACCACCA[C/T]GCCCGGCTATTTTTC | 10152 |
| rs751772175 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203389201 | AAGTAGTATACCCTC[C/T]GCTTATTAATGAGAG | 10152 |
| rs751803590 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353612 | AGCCTCCTGAGTAGC[C/T]AGGACTACAGGCATG | 10152 |
| rs751895933 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203405015 | ATCTGATTTTCAAAT[A/G]CTTGAAAGTATATGT | 10152 |
| rs751932848 | snp | G/T | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327441 | ATTATCTGCCTTGAA[G/T]TTTTGTAGCACTTAA | 10152 |
| rs751960852 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374283 | GGTGGCCGGATCACC[G/T]GAGGTCAGGAGTTTG | 10152 |
| rs751982740 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360632 | AGGAATGACCTGATT[C/G]AGGCTAGTAAGTGAC | 10152 |
| rs751995228 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203416683 | GTCTAAACTTTATTC[A/C]GTGTCCATTAGCATT | 10152 |
| rs752002322 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390729 | AAACTAAAATTTTGT[A/G]GTTATTCTATTTAAT | 10152 |
| rs752057023 | in-del | -/TTCAGAAACAAGTTATTGAAAGGAAAGG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203405975 | TTTTCATGAGATTAT[-/TTCAGAAACAAGTTATTGAAAGGAAAGG]AACCCTTTGATCAGG | 10152 |
| rs752071370 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345597 | ATTTTTAGTAGAGAT[-/G]GGGGTTTCACCGTCT | 10152 |
| rs752083974 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338080 | GGCATAAAAGACATG[G/T]AGACTAATGGAACAG | 10152 |
| rs752120408 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415433 | CGATCCTGGCTAACA[C/T]GGTGAAACCCCATCT | 10152 |
| rs752167025 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359033 | ACAAAAAACAAAAGA[A/C]AAATCCATGGAGGGA | 10152 |
| rs752167228 | snp | G/T | 1.65029e-05 | 0.00287248 | intron-variant | ABI2 | GRCh38.p7 | 2:203395652 | GTGGCTCTTATTTCT[G/T]TAGCAGCAGTGGGAG | 10152 |
| rs752171760 | in-del | -/TTTG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357764 | TTTTGGGGTTTTTTG[-/TTTG]TTTGTTTGTTTGTTT | 10152 |
| rs752206114 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203371151 | ATTTTTGCGATTCTC[A/G]CAAATGAGCTTGATT | 10152 |
| rs752229506 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203412229 | GAAATGGGCACTGCC[A/C]GTACTAGAATGTAAG | 10152 |
| rs752271602 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203411139 | GTTAATGAGTTGTCC[C/T]TCAACAGGGGATCCT | 10152 |
| rs752297680 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203341226 | GCCTACATATTTTCT[C/T]TTAACATACAGTGTT | 10152 |
| rs752300303 | in-del | -/TGTGTATA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338924 | GTGTGTGTGTGTGTG[-/TGTGTATA]TGTGTATATGTATAT | 10152 |
| rs752335694 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398048 | CGTAGTGTTCCACTT[G/T]CCAGTGAAGAACTTC | 10152 |
| rs752363189 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346573 | TAGCTTTTAGCTCTT[C/T]CTCATTGTCTGTTGA | 10152 |
| rs752369214 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379274 | GTTTTTTGACACAGG[G/T]TCTTGCTCTGTCACC | 10152 |
| rs752397095 | in-del | -/AAAA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339032 | ATACAACTTAATAGC[-/AAAA]AACCAAATAACCAGA | 10152 |
| rs752402792 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374119 | AGCCATGTTCATGCC[A/G]CTGGATTCAAGCATG | 10152 |
| rs752405805 | in-del | -/T | 0.0895119 | 0.191686 | intron-variant | ABI2 | GRCh38.p7 | 2:203351533 | GTTTTCAGTGTTTAG[-/T]TTTTTTTTTTTTTTC | 10152 |
| rs752410908 | snp | G/T | 0.000158065 | 0.00888862 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203396850 | GCCCCTGCTCCTCTT[G/T]TTCCTGCTACTGTCC | 10152 |
| rs752444235 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379439 | AGACGGGGTTTCGCC[A/G]TGTTGCCCAGGCTGG | 10152 |
| rs752452908 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347344 | GTTTTCACTCATCTT[G/T]TGTGTGAAATTTCTG | 10152 |
| rs752455709 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374822 | TGTTTGATTGCAGAT[A/G]TTTTCCCACACTGAT | 10152 |
| rs752462227 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413579 | CCTACAATCATATAC[A/G]TTTCTCATTTACACA | 10152 |
| rs752473026 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425336 | GCCTCCCAAGTAGCT[A/G]GGATTACAGGCGCCC | 10152 |
| rs752485907 | snp | A/C | 1.65236e-05 | 0.00287429 | intron-variant, missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203411363 | TTGTGGCCAGAGTCC[A/C]AGAAAATAGTAAGTT | 10152 |
| rs752524306 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203397880 | CAACCAGATCTCATT[A/G]TTGCAAGAACAGCTC | 10152 |
| rs752566574 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398883 | ATGTTTAAGTATTTC[A/G]TTACATTTTATTGCT | 10152 |
| rs752608656 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203405272 | TCAGAGTACTTTTTG[C/T]AAACTAATTTTTTTT | 10152 |
| rs752632496 | snp | C/T | 1.75798e-05 | 0.00296472 | intron-variant | ABI2 | GRCh38.p7 | 2:203380406 | ATAATTTTTTTCAAG[C/T]TTTTAAAAGTAGTAA | 10152 |
| rs752655437 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366203 | TCATGCCTGTAATCC[C/T]GGCACTTCAGGAGGC | 10152 |
| rs752694985 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365060 | TTACTCCTTTTGATA[A/G]TGGAAGTAATACATG | 10152 |
| rs752713441 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343364 | GAGACTATGTCTCAA[A/G]AAACATAAAAAAATT | 10152 |
| rs752715303 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355093 | CTTTGCTGTCAACCT[C/T]GGATTTCCCTTTTCC | 10152 |
| rs752729253 | snp | G/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416991 | CCTCCTCCAGAAGAT[G/T]ACGAAGAGGAGGAAG | 10152 |
| rs752740645 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203407161 | GTTCTAATCCTAGTC[A/C]TTTTGTTACTGCTTT | 10152 |
| rs752801855 | snp | A/G | 1.65586e-05 | 0.00287733 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394839 | AATCAAAGAAATCGA[A/G]CTTACAGGTATTTTC | 10152 |
| rs752803347 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353751 | GGTCTGTCCACCTTG[A/G]CGTTCCAAAGTGTTG | 10152 |
| rs752808453 | in-del | -/CAGGTCTTCC | 1.87947e-05 | 0.00306545 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427389 | CCTCACAGGAATAGT[-/CAGGTCTTCC]CAGATTATCTGAAGG | 10152 |
| rs752812571 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419408 | GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 10152 |
| rs752834872 | in-del | -/TG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347701 | TCTGCACAGGCAAAC[-/TG]TGTATTATACGACAC | 10152 |
| rs752856771 | snp | A/G | 1.65446e-05 | 0.00287612 | intron-variant | ABI2 | GRCh38.p7 | 2:203395637 | AATACTCATGTTTTG[A/G]TGGCTCTTATTTCTT | 10152 |
| rs752859471 | snp | A/G | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327514 | ATGTAACAGCCCTGT[A/G]AAGAAGGCAATTACT | 10152 |
| rs752871688 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428541 | CAGACTAAGAATATA[A/G]TGAATAAGATTAATA | 10152 |
| rs752911345 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344162 | AGTAAAGCTTAGCGC[G/T]TCAACTGTTTAGAGA | 10152 |
| rs752911948 | snp | A/T | 1.76316e-05 | 0.00296909 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328572 | GGCCGCCGGGCCCTC[A/T]TCGACAGCTACACAA | 10152 |
| rs752914048 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203393158 | CTCTTGCCTCCAGGC[A/G]ATTCTCCTGCTTCAG | 10152 |
| rs752949043 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376159 | GCTAATTAGTCCTTC[C/T]TCTATAGATCTTTGG | 10152 |
| rs752966032 | in-del | -/T | 1.67203e-05 | 0.00289134 | intron-variant | ABI2 | GRCh38.p7 | 2:203395810 | GTGCCTCGTCTTCAC[-/T]TTTCCTTTCTGAATT | 10152 |
| rs752975781 | snp | A/G | 1.65897e-05 | 0.00288003 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203367027 | AGGATGGAATCTTCA[A/G]TCAATCATATTTCAC | 10152 |
| rs752983581 | in-del | -/GT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390608 | TGCACTCCAGCCTGG[-/GT]GTAACAAAGCGAGAC | 10152 |
| rs753004161 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203391315 | CATTTTTATACTTCA[A/G]AAAGATTTGTTTAGA | 10152 |
| rs753080554 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203409571 | CATAGTTACGAAGGG[C/T]AAAAATCTAAGAATG | 10152 |
| rs753112382 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377376 | GCTTGTAATTCTGTT[A/C]TGGCTGCTCAGGTTT | 10152 |
| rs753112767 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350169 | GTAACCTCTGTCTCC[C/T]GGATTCAAGCCATTC | 10152 |
| rs753127911 | snp | C/T | 0.00016094 | 0.00896906 | intron-variant, utr-variant-5-prime | ABI2 | GRCh38.p7 | 2:203376013 | TTACCTTTATTATTA[C/T]AGATGTTTTTTAAAA | 10152 |
| rs753133389 | in-del | -/TGTG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350863 | TTTTGTTGTGTGTTT[-/TGTG]TGTGTGTGTGTGTGT | 10152 |
| rs753156430 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329268 | TTAGAATAGGCAGTT[C/T]TCCTGGGGGTGGGAG | 10152 |
| rs753200532 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361653 | TTGTGTTGCATGGCA[A/G]TAAAACCAGATGAAG | 10152 |
| rs753213419 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331038 | TAATATTAATTTAAT[A/G]GAAATGAACTTAGAT | 10152 |
| rs753223095 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330487 | GGGGTGGATGGTACA[C/T]ACCTAGTAGGAGAGG | 10152 |
| rs753236983 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203362206 | AGTGAAGTACAGATA[A/G]TGTGACATCCAGAAT | 10152 |
| rs753269188 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203417963 | GAATATATCTTTAAA[A/G]AGAGAGAGAGAGAGA | 10152 |
| rs753286343 | in-del | -/TTT | | | cds-indel, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431236 | GACTGATGAGGTGAG[-/TTT]TCTTCTTCATATGAA | 10152 |
| rs753289010 | snp | G/T | 1.81721e-05 | 0.00301425 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427373 | AGCAGGGCTGTGCTT[G/T]CCTCACAGGAATAGT | 10152 |
| rs753292159 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203335019 | TGGTTAATAGATTGG[A/G]TTCATGAGGTAGCAT | 10152 |
| rs753331713 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404794 | GAACTCCTGACCTCA[A/G]GTCATCCACTTGCCT | 10152 |
| rs753366835 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415344 | TTTAATTCACCGGGC[A/G]CGGTGGCTCACGCCT | 10152 |
| rs753378893 | snp | C/T | 1.7412e-05 | 0.00295055 | intron-variant | ABI2 | GRCh38.p7 | 2:203416886 | AACATATAGTTTTGT[C/T]GTCAGCCTGATACGT | 10152 |
| rs753426864 | snp | C/T | 1.67139e-05 | 0.00289079 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203380358 | ATTGACTATACAATT[C/T]TAGATGATATTGGAC | 10152 |
| rs753431508 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203348204 | AGAGATCGCGCCACT[G/T]CACTGTAGCCTGGGG | 10152 |
| rs753477438 | snp | C/T | | | intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203407922 | ATTCTGGCTCACAGA[C/T]GTTCTTGTCAGATGA | 10152 |
| rs753490155 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203381067 | GATGTGACTAAATAA[A/G]TATACATGCTTATAA | 10152 |
| rs753520136 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203335439 | ATTTTTTTTGTTGTT[A/G]TTGTTAGAAATGGGA | 10152 |
| rs753521975 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203334809 | GGGATTACAGGTGCA[C/T]GCCACCACGCCTGGC | 10152 |
| rs753579391 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366775 | GTTTTTTTACTTTCT[A/G]GTGGACTCAGCAGAA | 10152 |
| rs753597590 | snp | G/T | 1.78465e-05 | 0.00298712 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328564 | TCCCGGGGGGCCGCC[G/T]GGCCCTCTTCGACAG | 10152 |
| rs753601204 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422808 | AGTGGGTTCTAAAAC[A/G]TTTCTTAGAATACAT | 10152 |
| rs753612759 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399171 | TCCCAGCAGCAATGT[A/G]TGAGTTTCCAGTTGC | 10152 |
| rs753628590 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203336454 | GATTATGGAAGTTTG[C/T]GAGGACCTTATGTGA | 10152 |
| rs753632703 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379092 | TTCACCCTCTGTTAG[C/T]AAATAGAAGATTGTA | 10152 |
| rs753689377 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382869 | AGGTGAATATAATTA[C/T]ATGCAAAACATCAAA | 10152 |
| rs753710994 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203409687 | TTTTCTAGAAACTGC[C/T]TTGATTTATTACGTG | 10152 |
| rs753772305 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360961 | GGATGACGTATGCTC[-/T]TGTTTATTCAAGAGT | 10152 |
| rs753772762 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354095 | TGTCGCCCAGGTTGG[A/G]GTGCGGTGGCGCAAT | 10152 |
| rs753773808 | snp | C/T | 0.000492166 | 0.0156793 | intron-variant | ABI2 | GRCh38.p7 | 2:203355179 | TTGACAGTGCATATC[C/T]TCTGGTGCTTCCTGA | 10152 |
| rs753790334 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203394615 | ATCTCTGATTACAAA[C/T]TGTATCTCAACTGCT | 10152 |
| rs753790373 | in-del | -/TAT | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366381 | CCATTTTATTTATCA[-/TAT]TATTTATAATTTTTT | 10152 |
| rs753831241 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423713 | GGCGTGAGCCACCGC[A/G]CCCAGCCCAATCTGG | 10152 |
| rs753833427 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203407411 | AAGTAGTTTTTAGAG[A/C]GCTTATTTTGTCTAA | 10152 |
| rs753851806 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345159 | CTTTATGAGTTGTAA[C/T]ACTCACATTGAAGGT | 10152 |
| rs753865013 | snp | A/G | 1.65592e-05 | 0.00287738 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394702 | CTTCTTTTTGTAGGC[A/G]GCACTCCCCCTATCG | 10152 |
| rs753868805 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368557 | TAATAAAATCAGATA[C/T]GGTATTTTTGAAAAT | 10152 |
| rs753884266 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203405549 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAATTA | 10152 |
| rs753933400 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344359 | AACAATATAATTTTT[A/T]AATTTTTTTTTCCTT | 10152 |
| rs754005472 | snp | G/T | 1.70406e-05 | 0.0029189 | synonymous-codon, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427346 | TATCATGCATTATTC[G/T]GAGTAAAGCTCAGCA | 10152 |
| rs754042728 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331444 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 10152 |
| rs754053580 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418062 | CCATGACAATAGAAA[C/T]TATCCAAAATAAGGC | 10152 |
| rs754072385 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377530 | TTATAAAAAAAGTGT[A/C]ATATTTTATTTTTTG | 10152 |
| rs754077759 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345239 | ACAAATAACTCCAGA[C/T]ACGCCATTTTGAGAG | 10152 |
| rs754118060 | in-del | -/AGG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203341033 | GTTATGCCCTCTGCC[-/AGG]AGGAGTACTCTACTC | 10152 |
| rs754124075 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203416099 | CTATTTTAGAAAAAT[A/T]CATTAAGAGGAAAGT | 10152 |
| rs754127972 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431284 | AGCAGAGTTCTCACT[C/T]AGTGCTCAGTACTTA | 10152 |
| rs754131664 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419675 | AGCCACTGCGCCCAG[A/C]CTGTGCTTTGTATTT | 10152 |
| rs754142697 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385276 | AGCTGGGACTACAGG[C/T]GCCCGCCACCTCGCC | 10152 |
| rs754231144 | snp | A/T | 1.8039e-05 | 0.00300319 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366836 | TTGCTAGAAATGGGT[A/T]ATTTTTGAATTAATG | 10152 |
| rs754283915 | snp | C/T | 1.6489e-05 | 0.00287128 | synonymous-codon, missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203366972 | CACCTTGGCCAACAA[C/T]GTCCTGCAGATGCTG | 10152 |
| rs754285685 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363638 | AGAACATGCGATCTT[C/T]CTGTGCCTGGCTTGT | 10152 |
| rs754318314 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419239 | CTCAGCCTCCCGAGT[A/G]GCTGGGACTACCGGC | 10152 |
| rs754320309 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388009 | TTTTATATTTACCAG[A/T]TTATTTTAGTTCTGA | 10152 |
| rs754345879 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355659 | ACATGGAGAAACCCC[A/G]TCTTTACTAAAAAAA | 10152 |
| rs754357039 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425145 | AGAGCTTACTAACTT[C/T]CCACTTCTAAGCATC | 10152 |
| rs754371251 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390462 | CACGGTGAAACCCTG[C/T]CTCTACTAAAATACA | 10152 |
| rs754412987 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385732 | ACCTTTGAGAGACCC[A/T]TCTGTTTTTGCCTAT | 10152 |
| rs754425198 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329315 | TGTTTCTTAGAGAGA[-/A]TTGGGAAGATGAACC | 10152 |
| rs754444614 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370370 | TGGGATTACAGGCAT[A/G]AGCCACCATGCCCAG | 10152 |
| rs754458709 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339651 | AAAAATAGGACAAAC[A/G]TACAATCCCACTTCT | 10152 |
| rs754467735 | snp | C/T | 1.68261e-05 | 0.00290048 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203380368 | CAATTCTAGATGATA[C/T]TGGACATGGAGTAAA | 10152 |
| rs754475824 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424931 | GGCTAGAGTGCAGTG[C/G]GAAAATCACGGCTTA | 10152 |
| rs754508687 | in-del | -/GC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350894 | TGTGTGTGTGTGTGC[-/GC]GCGCGCATACTTTTA | 10152 |
| rs754509388 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330726 | TGGAAAAGTGGATTG[C/T]AATTATTACCAGTAA | 10152 |
| rs754528419 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378151 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 10152 |
| rs754545882 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203375126 | ATGGGGAAAGCCTGC[A/G]GCATGCAAGATCAGC | 10152 |
| rs754652339 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203395691 | GGAGCCACCCAAGTA[A/G]TCGGAGCAGCAGTCG | 10152 |
| rs754738603 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378339 | GATGGTCTCGATCTC[C/T]GGACTTTGTGATCCG | 10152 |
| rs754747980 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427736 | CTGTGGCATTGGATG[C/T]TCTTCATTGCCTGTG | 10152 |
| rs754783805 | snp | A/G | 3.56532e-05 | 0.004222 | intron-variant | ABI2 | GRCh38.p7 | 2:203402762 | GTTTTTTTGCATTCT[A/G]TAGAATGTATTTAAT | 10152 |
| rs754806148 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351723 | GTATTTTTTGTAGAG[C/G]CAGCATCTCACTTCA | 10152 |
| rs754811181 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422707 | GCCAGTTTTTTTCAA[C/G]TGAATAGTTTCATTG | 10152 |
| rs754814794 | in-del | -/GACCATCTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203348041 | AGGTCAGGAGTTCGA[-/GACCATCTT]GGCCAACGTGGTGAA | 10152 |
| rs754846492 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364860 | CACCTCAACCTCTCT[A/G]GTAGATAGGACTACA | 10152 |
| rs754864395 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431726 | ATTAAAACGAAACGG[C/T]GGGGCCTAGCTGTGT | 10152 |
| rs754896489 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379368 | TTCTCTTATTTCAGC[C/T]TCTCAGTTAGCTGGG | 10152 |
| rs754909678 | snp | A/G | 1.64982e-05 | 0.00287208 | intron-variant, missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203411350 | CCTTTAATGGGATTT[A/G]TGGCCAGAGTCCAAG | 10152 |
| rs754910313 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203407825 | GATTAGAACTGAATA[-/T]TGCAACAATTCTTTC | 10152 |
| rs754970100 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203395031 | GCAGTCAGGAAGTTG[-/A]TAAAGAACAGACATC | 10152 |
| rs754983755 | snp | A/G | 1.77118e-05 | 0.00297583 | splice-acceptor-variant | ABI2 | GRCh38.p7 | 2:203380206 | TACATTATATTTTGC[A/G]GACAGTTGATATTCA | 10152 |
| rs755024902 | snp | A/C/G | 3.3087e-05 | 0.00406726 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394705 | CTTTTTGTAGGCGGC[A/C/G]CTCCCCCTATCGCAC | 10152 |
| rs755094165 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388129 | AATTTGATGGCAGTA[G/T]TTATATTCTGCATAG | 10152 |
| rs755099577 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374608 | TTATACTTCCCAATT[A/T]ATTTCCTATGTAGTT | 10152 |
| rs755107712 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343339 | ACTGCACTCTAGCCT[A/G]GACGACAGCGAGACT | 10152 |
| rs755110435 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203414166 | GAGTACAGTGGTGCA[A/G]TCTTGGCTCTCTGCC | 10152 |
| rs755172782 | snp | A/C | 1.82917e-05 | 0.00302416 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427378 | GGCTGTGCTTGCCTC[A/C]CAGGAATAGTCAGGT | 10152 |
| rs755186672 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378279 | ACCATGCCCGGCTAA[-/T]TTTTTGTATTTTTAG | 10152 |
| rs755221948 | in-del | -/CAC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392275 | CAGCACCACCACCAT[-/CAC]CACCACCACCACCAC | 10152 |
| rs755245338 | snp | A/G | 3.30524e-05 | 0.00406511 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394825 | GGACAGCTTCTGTGA[A/G]TCAAAGAAATCGAAC | 10152 |
| rs755268731 | snp | G/T | 0.000107049 | 0.00731527 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366847 | GGGTTATTTTTGAAT[G/T]AATGATCACTGGTTT | 10152 |
| rs755275072 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415459 | CATCTCTACTAAAAA[C/T]ACAAAAAATTAGCTG | 10152 |
| rs755314614 | in-del | -/CCACCAACAACAACA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392311 | CCACCACCACCACCA[-/CCACCAACAACAACA]ACAACAACAACAACA | 10152 |
| rs755368526 | snp | A/G | | | intron-variant, utr-variant-5-prime | ABI2 | GRCh38.p7 | 2:203375989 | AATGCAAATTATACC[A/G]TTGTTAGATTACCTT | 10152 |
| rs755415150 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390624 | GTAACAAAGCGAGAC[A/T]CTGTCTCAGAAAAAA | 10152 |
| rs755505116 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203362488 | TTGAGTTTTACTATA[-/T]TTTATTTTGTTTTTT | 10152 |
| rs755537047 | in-del | -/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421321 | GGATTTTTCAAGTGG[-/C]ATTGTAACTGCACTT | 10152 |
| rs755539158 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399424 | ATCATTGAGTTCTTT[C/T]ATATTCTAAATATAT | 10152 |
| rs755561558 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360755 | AGTTTGCTTGGCAAA[C/G]CAGAGATTCTACCAA | 10152 |
| rs755570409 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357122 | AATATAAAATAGATA[C/T]AAAATTTGTGATTTG | 10152 |
| rs755623364 | snp | A/C | 1.68576e-05 | 0.00290319 | intron-variant | ABI2 | GRCh38.p7 | 2:203367054 | TCACAAGTGAGACCA[A/C]AATATTTTCCTATTT | 10152 |
| rs755647670 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203426862 | CCATCTTTCTTGATT[C/G]TAGGATTGTGTACCT | 10152 |
| rs755668517 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396567 | GGAATGTTTGTTTTT[A/C]ATGAATTGAAAAAAT | 10152 |
| rs755747191 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347462 | AGACCATTACACGAA[C/G]AACCGTAGCATGTAG | 10152 |
| rs755768014 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346613 | ACTCTTTCTCCCCCA[A/C]CACATTTAACTCTAG | 10152 |
| rs755794220 | snp | A/C/G | 5.73568e-05 | 0.00535497 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427391 | TCACAGGAATAGTCA[A/C/G]GTCTTCCCAGATTAT | 10152 |
| rs755817692 | snp | A/G | 7.98228e-05 | 0.00631704 | intron-variant | ABI2 | GRCh38.p7 | 2:203380170 | GTGGATATTAGAACT[A/G]TACATTTTTGTGTTG | 10152 |
| rs755831276 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203380996 | TTAATGATTCAGAGC[G/T]TTAGCTGAGTATTAA | 10152 |
| rs755845530 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421739 | TGGGAGGCCAAGGCC[A/G]GCAGATGACAAGGTC | 10152 |
| rs755904816 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365073 | TAATGGAAGTAATAC[A/G]TGCCCAAGTTAAAAA | 10152 |
| rs755912974 | in-del | -/TGG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360468 | GAAGGGAAACAAATT[-/TGG]TGGTTTGGGATAGAA | 10152 |
| rs755969928 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420888 | AGAGAAAGGAAGGGC[C/G]TTCCAAGCTGAGGGA | 10152 |
| rs755978066 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353790 | GGCGTGAGCCACCAT[A/G]CCAGGCCCAGAGGTA | 10152 |
| rs755983532 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203335209 | ATGTAAGAAATACAG[A/T]CTTGAATATGCAAGA | 10152 |
| rs755990859 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379552 | CTTTATTTTTAACAT[A/T]ATATTTCAGCCCTCT | 10152 |
| rs755996178 | in-del | -/AGTTGCACGTTTTC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346527 | TTTATCCATTACTGG[-/AGTTGCACGTTTTC]CCTTGTCATAATTCC | 10152 |
| rs756023939 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366587 | AAGCAATATATACTT[C/T]GCTGCCACTGCTCAA | 10152 |
| rs756089115 | snp | A/C | 1.65436e-05 | 0.00287602 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402643 | CCCAACAATAGGGGG[A/C]TCGTTGCCCTATAGA | 10152 |
| rs756146113 | snp | G/T | 1.7416e-05 | 0.00295088 | intron-variant | ABI2 | GRCh38.p7 | 2:203402748 | AGGTTAGTTTTTTTG[G/T]TTTTTTGCATTCTAT | 10152 |
| rs756148638 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428571 | AGGCCAAAATATGTA[C/T]CTAATCACATTGATA | 10152 |
| rs756210107 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203391444 | GAAAATGTATATAGT[C/G]TTTTATATTACAGTT | 10152 |
| rs756234043 | in-del | -/AAAC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203332629 | GACTCTGTCTCAAAA[-/AAAC]AAAAATTACACATAT | 10152 |
| rs756255462 | snp | C/T | 1.74303e-05 | 0.00295209 | intron-variant | ABI2 | GRCh38.p7 | 2:203427139 | TTTCTAGGAATATTA[C/T]TGTCTTTCACATCCT | 10152 |
| rs756289181 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203349260 | GCCCTATAACTCTTG[A/G]ACACTTTAGTGTGTT | 10152 |
| rs756308781 | snp | A/G | 1.67253e-05 | 0.00289178 | intron-variant | ABI2 | GRCh38.p7 | 2:203394676 | TTGCTTAATCATACA[A/G]TACATACGCTCTTCT | 10152 |
| rs756312581 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430000 | TGTGTGTGATCTTTG[G/T]TTTACAAACAGTACC | 10152 |
| rs756342559 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377448 | CTAAAAACTGAGGAG[A/G]ATAAAAACAATGTCT | 10152 |
| rs756344452 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360925 | CCAAAATTAGGGTAA[C/G]AACTAATTGTTACCC | 10152 |
| rs756352577 | in-del | -/TTTTC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329740 | CCAGGGATCCTTCTT[-/TTTTC]TTTTCTTTTTGAGAC | 10152 |
| rs756359107 | snp | A/G | 1.9726e-05 | 0.00314048 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203391138 | GTCAGGGAAAGGGAC[A/G]CTTGGGTGAGTATAT | 10152 |
| rs756375740 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396713 | TAACATTAAATACTC[-/T]TAATACCTTTTCTAA | 10152 |
| rs756409386 | snp | G/T | 0.000163948 | 0.00905246 | synonymous-codon, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203396822 | TCCTCCCCTTCCTGC[G/T]ACTTCTGCATCTGCC | 10152 |
| rs756419238 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203341696 | GCCTGGGCAACAGAG[C/T]GAGACTCCATCTCAA | 10152 |
| rs756430418 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376259 | TCATGGTGGGGGAGT[A/G]CTACAGTTATCTACC | 10152 |
| rs756436939 | snp | A/G | 1.96007e-05 | 0.00313049 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328631 | GAACAACTACATACA[A/G]GTGCGAAGCATCCCC | 10152 |
| rs756504054 | in-del | -/AGATGAATGTAGCTACAATA | 1.67598e-05 | 0.00289476 | intron-variant | ABI2 | GRCh38.p7 | 2:203395821 | CACTTTTCCTTTCTG[-/AGATGAATGTAGCTACAATA]AATTTGATTCAATTT | 10152 |
| rs756549021 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385248 | CCATTCTCCTGCCTC[-/A]AACCTCCTGAGTAGC | 10152 |
| rs756558806 | in-del | -/T | 0.00015836 | 0.00889691 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366863 | ATGATCACTGGTTTG[-/T]TTTTTTTTCCCAGTC | 10152 |
| rs756572331 | snp | C/T | 0.000142035 | 0.008426 | intron-variant | ABI2 | GRCh38.p7 | 2:203351578 | TCTTGGTATGTCATG[C/T]AGGCTGGAATGCAGT | 10152 |
| rs756602537 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337932 | CTACTCAGGAGGCTG[A/C]GTTGGGAGAATCGCT | 10152 |
| rs756615719 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402520 | GTACATAAAGTATTT[A/C]ATGATCTGAGATAAT | 10152 |
| rs756648398 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203383729 | TTGGAGACCTGTGGA[C/T]TCTAGCAAGTGTCTT | 10152 |
| rs756663897 | snp | C/G | 1.67461e-05 | 0.00289357 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402611 | AGCATGAATAGGCCT[C/G]CCTCTCGCCATACTC | 10152 |
| rs756689002 | snp | C/T | 0.000365831 | 0.0135197 | intron-variant | ABI2 | GRCh38.p7 | 2:203355234 | AAAGAAGACTGGGTA[C/T]GGTGGCTCATTCCTG | 10152 |
| rs756804223 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379686 | TAGTCTAAATCTTAA[C/T]GGAGAGGGAAAAATT | 10152 |
| rs756857928 | snp | A/G | 3.52616e-05 | 0.00419875 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366852 | ATTTTTGAATTAATG[A/G]TCACTGGTTTGTTTT | 10152 |
| rs756869910 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398242 | CATGGGGTGTTTTTT[G/T]ATCCAGATACAACTG | 10152 |
| rs756875606 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366793 | GGACTCAGCAGAATC[A/G]TTGTGATGAGTTTTT | 10152 |
| rs756883022 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421869 | CTCAGGAGGCTGAGG[C/T]AGGAGAATCACTTGA | 10152 |
| rs756930728 | snp | A/G | 1.68932e-05 | 0.00290625 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402726 | GACCTTTTTATAGCC[A/G]GAATCCAGGTTAGTT | 10152 |
| rs756937866 | in-del | -/TG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203358075 | CCTGGCCTGTTTGTG[-/TG]TGTGTGTGTGTGTGT | 10152 |
| rs756981033 | snp | C/T | 1.80439e-05 | 0.0030036 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203391117 | GAAGCCCCCTAGTCC[C/T]CCTATGTCAGGGAAA | 10152 |
| rs756983744 | snp | A/G | 1.66087e-05 | 0.00288168 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203367031 | TGGAATCTTCAATCA[A/G]TCATATTTCACAAGT | 10152 |
| rs757000424 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203381131 | TCTAATATAAACATA[C/T]TTAAAAAACACTGTT | 10152 |
| rs757026947 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398488 | AATGTCTTATTAATA[A/G]TTTATATCAGGATAG | 10152 |
| rs757069827 | snp | A/G | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327046 | ATCTCCTGACCTCGT[A/G]ATCCGCCCGCCTCGG | 10152 |
| rs757094732 | in-del | -/AAT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388687 | TCTGTCTTAAAAAAT[-/AAT]AATAATAATAATAAT | 10152 |
| rs757099162 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344441 | CGTGATCATGTCTCA[A/C]TGCAGTCTCTGCCTC | 10152 |
| rs757111933 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422821 | ACATTTCTTAGAATA[C/T]ATTAAGTGGTTTAAC | 10152 |
| rs757218182 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203409693 | AGAAACTGCTTTGAT[C/T]TATTACGTGCCAGCC | 10152 |
| rs757308237 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422448 | AAGTCGAGTGTTGGT[A/G]TTTGGGAGATTTAGA | 10152 |
| rs757317820 | in-del | -/AAA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421965 | GTGAGACTCTGTCTC[-/AAA]AAAAAAAAAAAAAAA | 10152 |
| rs757323342 | snp | A/G | 0.000191847 | 0.00979216 | intron-variant | ABI2 | GRCh38.p7 | 2:203351553 | TTTTTTTTTTCCTTT[A/G]GAGATGGGGTCTTGG | 10152 |
| rs757346656 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329947 | TCACCATGTTGACCA[C/G]ACTGGTCTCGAACTC | 10152 |
| rs757443806 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418203 | AGAGGAAAAAGAGTT[C/G]AAACAATCATAGACA | 10152 |
| rs757465070 | snp | C/T | 1.67022e-05 | 0.00288978 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416922 | GTTTCAGATACACCA[C/T]CTCCACCGCCACCTG | 10152 |
| rs757477812 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430178 | TCTGTGAGGGTAGTA[G/T]TTTTTGTTTTATTGT | 10152 |
| rs757483197 | snp | C/T | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203417030 | GTTGAGTATAGTGAT[C/T]CTTATGCTGAAGAGG | 10152 |
| rs757486022 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363698 | TCTATGTTGTTGCAA[A/G]TGACTGAATCTCATT | 10152 |
| rs757519335 | in-del | -/ATATATATATATATATAAATATATATATATATATATAA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338946 | TATGTATATATATAT[lengthTooLong]ATATATATATATATA | 10152 |
| rs757568803 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203411834 | CCTCATAGGTTGGCA[A/G]TGAATTTCCCTTGGC | 10152 |
| rs757576248 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361974 | GAGATTTAGCTAAAA[A/G]TAATTTTTTGTTAGA | 10152 |
| rs757585780 | snp | A/G | 1.66335e-05 | 0.00288383 | intron-variant | ABI2 | GRCh38.p7 | 2:203394873 | ACCTCAGTGCAAAAT[A/G]TGATGGTCATAGTAC | 10152 |
| rs757605464 | snp | A/C | | | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402696 | AAACAAGCCTTCAGA[A/C]TCAGATGAATGGAGG | 10152 |
| rs757608558 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385829 | TCAAGCAGGAGTTTG[C/T]CCATCTTTATTTCTC | 10152 |
| rs757703666 | snp | A/G | 3.29685e-05 | 0.00405995 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203395665 | CTTTAGCAGCAGTGG[A/G]AGTAGTGGAGGGAGC | 10152 |
| rs757783544 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422861 | ATTGATAGTGTCCAG[G/T]TTAACTTTGCTCTAC | 10152 |
| rs757788486 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370468 | TTTCTTTTCTTTTTT[G/T]TGTGTGTATTTTTAA | 10152 |
| rs757791775 | in-del | -/TT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387058 | GCAGGCTCCCTTCCT[-/TT]TTTTTTTTTTTTTTT | 10152 |
| rs757811635 | in-del | -/T | 1.72867e-05 | 0.00293991 | intron-variant | ABI2 | GRCh38.p7 | 2:203402739 | CAGAATCCAGGTTAG[-/T]TTTTTTTGTTTTTTT | 10152 |
| rs757818856 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339760 | GGTAACTAAGATATG[G/T]AAACAACCTAAGTGT | 10152 |
| rs757841213 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413643 | GACTAATTTTACAGA[C/T]GTGGCAGGACTTAAA | 10152 |
| rs757893056 | snp | C/G | 1.84892e-05 | 0.00304044 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328619 | CGATTACTGCGAGAA[C/G]AACTACATACAGGTG | 10152 |
| rs757918116 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350329 | TGATCCTCCCGCCTC[A/G]TGACCAACCACGCCT | 10152 |
| rs757919106 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203336764 | GAACCTAACAAGCAG[C/T]TGGGCAGGTCTATCA | 10152 |
| rs757955051 | snp | C/T | 0.000155533 | 0.00881716 | synonymous-codon, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203396870 | TGCTACTGTCCCTTC[C/T]TCCACTGCCCCAGAC | 10152 |
| rs757984431 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203381508 | CTGTACTTAAGTGAT[C/T]TTCCCACCTTGGTCT | 10152 |
| rs758010131 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203407858 | CAAAATTCTGCTTAA[A/G]TTCACTTAAAATGGT | 10152 |
| rs758061015 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355556 | CCCAAGAGGCCAGGC[A/G]CAGTGGCTCATGCCT | 10152 |
| rs758146717 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368792 | AAGGAAATAATCAAT[A/G]GGATTTTAAATGACG | 10152 |
| rs758176802 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203393888 | CACTAATTTCCCCAT[C/G]TGCATCCTGTTCCCT | 10152 |
| rs758210638 | in-del | -/CTACTCTCCCCTCTTCTCCAGTAGGCTGACCTCCATG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203401103 | CCAGTCCCCCCTCCT[lengthTooLong]AAATGTTTCAGTGGA | 10152 |
| rs758211300 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203352097 | CATCACAATTTTAAA[A/C]CTATGAAAGTACAAT | 10152 |
| rs758218590 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203332238 | CTGATATTTATCAGA[A/T]CAATTTTATTTCTTG | 10152 |
| rs758249464 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431633 | TGGAGGCATTGAGCT[C/T]ATTACCTTTAAGTTT | 10152 |
| rs758254229 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203409785 | AGGTTGCATTACCTT[A/G]TTTTCATATCACATT | 10152 |
| rs758254938 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356392 | TATTTATTTTGAGAC[A/G]GAGTCTCGCTCTGTT | 10152 |
| rs758308845 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345306 | TGAAGTCAAGCGAAA[C/G]CAGGAACCCACTGGA | 10152 |
| rs758336392 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396161 | GACAGTTAAATTTAG[A/T]GGCTGTATTGGAATT | 10152 |
| rs758351931 | snp | A/C | 1.76883e-05 | 0.00297386 | intron-variant | ABI2 | GRCh38.p7 | 2:203380411 | TTTTTTCAAGCTTTT[A/C]AAAGTAGTAACCCAT | 10152 |
| rs758362838 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377838 | TTCAGCCTGAGAGGT[C/T]GAGGATGCAGTGAGC | 10152 |
| rs758407221 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345917 | GGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 10152 |
| rs758435924 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388408 | GAAATGTTGGCCAGG[C/T]ATGGTGGCTCATGCC | 10152 |
| rs758486365 | snp | C/T | 4.95716e-05 | 0.00497829 | intron-variant | ABI2 | GRCh38.p7 | 2:203395643 | CATGTTTTGGTGGCT[C/T]TTATTTCTTTAGCAG | 10152 |
| rs758494818 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402863 | AATGAATGGGAGAAT[A/G]AATGAATTGTAGGTT | 10152 |
| rs758496994 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420518 | CCTGCCTCAGCCTCC[A/T]GAGTAGGTGGGACTA | 10152 |
| rs758586244 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203391746 | GGATCACCTGAGCCC[A/G]GGAGGTTGAGGCTGC | 10152 |
| rs758608781 | in-del | -/G | 0.000649375 | 0.0180074 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427391 | TCACAGGAATAGTCA[-/G]GTCTTCCCAGATTAT | 10152 |
| rs758622398 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418258 | CTATATTAGTTGTGT[A/T]TTGCTACCTAACAAG | 10152 |
| rs758626955 | in-del | -/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421964 | AGTGAGACTCTGTCT[-/C]AAAAAAAAAAAAAAA | 10152 |
| rs758648667 | snp | A/T | 1.66568e-05 | 0.00288585 | intron-variant | ABI2 | GRCh38.p7 | 2:203411385 | TAGTAAGTTTATGTC[A/T]TCTTTATGCTGTAGA | 10152 |
| rs758657293 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203340131 | AGGCACAGAAAGACA[A/G]ATACCGTATGATTTC | 10152 |
| rs758681743 | snp | A/G | 1.74958e-05 | 0.00295764 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328597 | ACACAAATCTGGAAC[A/G]GGTGGCCGATTACTG | 10152 |
| rs758723292 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203427106 | GAACAGATAGCTATT[A/C]ACTGGCTTGGTTCTG | 10152 |
| rs758726903 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404292 | CCTTCACTGTTCTGG[A/G]TCCCTCTCGTAAATT | 10152 |
| rs758838525 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203358767 | GTAATTCCAGCACTT[A/T]GGGAGGCTGAGGTGG | 10152 |
| rs758847682 | snp | C/G | 3.29712e-05 | 0.00406011 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427220 | CAAGGAAGATGAGCT[C/G]TCCTTTCAGGAAGGA | 10152 |
| rs758849575 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203341545 | GATGGCGAAACCCCA[C/T]CTCTACTAAAAACAA | 10152 |
| rs758860918 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203394312 | TGGTTAGGGAGAGAA[-/G]GGGAGAGGAGAATAA | 10152 |
| rs758861426 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331144 | TTAGGATGCCTTAGG[C/T]ATATAATTGGTACAC | 10152 |
| rs758911435 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203335395 | CCAAAGTAGCTGGGA[C/G]TACAGGCTTGTGCCA | 10152 |
| rs758926111 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357188 | AATGACCAACTTCCA[A/G]ATGTGTTCCAGAAAA | 10152 |
| rs758941106 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387478 | TCATAGCCTATTGGG[A/G]AAGTGTTTGAGCTGT | 10152 |
| rs758961168 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408275 | TCAAGCGATTCTCCT[A/G]GTTCAGCCTCCCGAG | 10152 |
| rs758971744 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413750 | TACATTTCTTTTGGT[A/G]CATCTTCAAAGATAA | 10152 |
| rs758995517 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343168 | CAGGAGTTTGAGACC[A/G]GCCTGGCCAACATGG | 10152 |
| rs758995568 | snp | C/T | 3.32242e-05 | 0.00407566 | intron-variant | ABI2 | GRCh38.p7 | 2:203394860 | AGGTATTTTCTCTAC[C/T]TCAGTGCAAAATGTG | 10152 |
| rs759005120 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203334849 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTAT | 10152 |
| rs759047068 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387382 | AATAATTGGCTTAAT[G/T]TGTGGTGCCAGTTGT | 10152 |
| rs759047716 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416985 | CCTCCTCCTCCTCCA[A/G]AAGATTACGAAGAGG | 10152 |
| rs759084753 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342838 | CTTGATATAATGTCT[A/G]TACACACACACATCT | 10152 |
| rs759101708 | in-del | -/AGG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361957 | CCTTCATGAATCCTT[-/AGG]AGATTTAGCTAAAAA | 10152 |
| rs759101803 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396561 | TGAAAAGGAATGTTT[C/G]TTTTTAATGAATTGA | 10152 |
| rs759137858 | in-del | -/C | 3.77337e-05 | 0.00434344 | intron-variant | ABI2 | GRCh38.p7 | 2:203328666 | GGGCCGCGTCGGGGA[-/C]CCCCCCGCCGGGGGC | 10152 |
| rs759150569 | snp | C/T | 2.88988e-05 | 0.00380113 | intron-variant | ABI2 | GRCh38.p7 | 2:203391185 | CCATTTCATGTAGTA[C/T]TGTTTAAAAATGAAG | 10152 |
| rs759154776 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364373 | TGTTGGGATTACAGG[C/T]GTGAGCCACTGTGGC | 10152 |
| rs759192196 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337353 | TTCTACATATTAACT[A/G]CAAACGATCTGAAAA | 10152 |
| rs759204265 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388630 | AGGTTGTAGTGAGCC[A/G]AGATCAGGCCATTGC | 10152 |
| rs759215308 | in-del | -/TTAAT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359368 | CTTATGAGTGATGTC[-/TTAAT]TTAGAGTATTCAGCC | 10152 |
| rs759234811 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357983 | CATATTGACCAGGCT[C/G]TCTCGAACTCCTGAC | 10152 |
| rs759244606 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370980 | TTTAACGAAAAAGAA[C/T]GCTGAGTTGGCCTGA | 10152 |
| rs759265140 | snp | A/C/T | 9.70273e-05 | 0.00696463 | intron-variant | ABI2 | GRCh38.p7 | 2:203328672 | CGTCGGGGACCCCCC[A/C/T]GCCGGGGGCCGCGCG | 10152 |
| rs759293008 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203426487 | ATTTAAGCAATGAAA[A/T]TCACAGGAGGGCTTA | 10152 |
| rs759295761 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203383645 | GTTTCCATTGTGAGA[A/G]ACAGGCCAAACAGAG | 10152 |
| rs759334281 | snp | A/G | 1.78115e-05 | 0.0029842 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328565 | CCCGGGGGGCCGCCG[A/G]GCCCTCTTCGACAGC | 10152 |
| rs759370952 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379112 | AGAAGATTGTAATTA[C/T]AATACATTCTTACTC | 10152 |
| rs759398953 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203414784 | AGTTCAGGTGCTTTT[C/G]CACTTACTTGCTGTC | 10152 |
| rs759450190 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413284 | TGAGACTTGAAAGTT[A/G]AATAGGATTTAAAGC | 10152 |
| rs759463740 | in-del | -/CCT | 1.64838e-05 | 0.00287083 | cds-indel, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416970 | GATGAGTCTCCCCCA[-/CCT]CCTCCTCCTCCAGAA | 10152 |
| rs759497093 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203335057 | AACACATTCTATTTT[A/G]GATTTTTCATTTACT | 10152 |
| rs759497243 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347968 | ATTTGGGCTGGGCGC[A/C]GGTGGCTCATGCCTA | 10152 |
| rs759503618 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351772 | AACTCCTGGCCTCAA[A/G]CAGTCCTCCCACTGT | 10152 |
| rs759526625 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354084 | AGGTTTGACTCTGTC[A/G]CCCAGGTTGGAGTGC | 10152 |
| rs759528261 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398688 | CGCAAAAATTTCCTC[C/T]ATGCCCCCTTTATAG | 10152 |
| rs759553241 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359963 | AGGCTGAGGCGGGTG[A/G]ATCATGAGGTCAAGA | 10152 |
| rs759587105 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347150 | GGAGCCATTGCATGT[C/T]CTAACAGGGTAAGGA | 10152 |
| rs759601193 | snp | C/G | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366014 | TTTTTTACTTTTTGT[C/G]TTTTTTTCCATATTG | 10152 |
| rs759609190 | in-del | -/TT | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427796 | TACCCTAGCCCCTTC[-/TT]TTCTTCCACTTGTAT | 10152 |
| rs759612760 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376468 | AATTATTTTGACTTT[C/T]TGTATACTTATGCTG | 10152 |
| rs759642333 | snp | A/C | 5.1856e-05 | 0.00509169 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427353 | CATTATTCTGAGTAA[A/C]GCTCAGCAGGGCTGT | 10152 |
| rs759713368 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354970 | TATCAGTTTCATCCA[A/T]CCTCCCCACAAGAAG | 10152 |
| rs759726423 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203389086 | AAGATATGCAGTTTT[-/A]AAAGCTATTCATTAT | 10152 |
| rs759751504 | snp | A/T | 1.66991e-05 | 0.00288951 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402715 | GATGAATGGAGGACC[A/T]TTTTATAGCCAGAAT | 10152 |
| rs759752661 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408373 | TCACCATGTTGGCCA[A/G]GCTGGTCTTGAACTC | 10152 |
| rs759780552 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390835 | GCATACAAGTTTATA[A/C]TGATTTGAAAATCTC | 10152 |
| rs759787846 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419330 | GTCTTGATCTCCTGA[A/C]CTCATGATCCGCCCG | 10152 |
| rs759801159 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368208 | CCCATATTTTGGGGC[C/T]ATTTAAAATAATACT | 10152 |
| rs759808062 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423574 | GGGACTACAGGCGCC[C/G]GCCACCATGCCTGCT | 10152 |
| rs759916068 | in-del | -/TAAC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203411541 | TTTTCTACTTTTAAA[-/TAAC]TAATAGTAAAGACAT | 10152 |
| rs759945256 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203393065 | AACAGAACTTATTTT[C/T]TTGAGACAGAGTCTC | 10152 |
| rs759954738 | in-del | -/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354154 | GGCTCAAGCCAACCT[-/C]CCACCTTGGCCTCCA | 10152 |
| rs759957417 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344143 | CATTTGGTTCTTACT[C/T]CATAGTAAAGCTTAG | 10152 |
| rs759965427 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422070 | AGAGGCTGAGGCCGG[C/T]GGATTGCTTGAGACG | 10152 |
| rs760051915 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203393376 | AAACATTTTTATTGC[C/T]TGGGAAAAATTGTCT | 10152 |
| rs760064818 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430972 | TTTTTATCTTTTACT[A/G]CCTTTTCTTTTCTCC | 10152 |
| rs760075671 | snp | C/T | 1.65946e-05 | 0.00288046 | intron-variant | ABI2 | GRCh38.p7 | 2:203411262 | CTTATCCCTTATCCT[C/T]CACACCTTTTTTGTT | 10152 |
| rs760077474 | snp | C/T | 0.00159172 | 0.0281661 | intron-variant, utr-variant-5-prime | ABI2 | GRCh38.p7 | 2:203375976 | GTATGATGGCAAGAA[C/T]GCAAATTATACCGTT | 10152 |
| rs760136728 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351635 | TGAACTCCTGTGCTC[A/C]AGTGATCATCCTGCC | 10152 |
| rs760154782 | in-del | -/GGA | | | cds-indel, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432080 | CACCTCCAGATGAGT[-/GGA]GGAACATCACTTTTT | 10152 |
| rs760157430 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329114 | CTGTTCCTGTGAATG[C/G]TTCAGAAACCCTTTC | 10152 |
| rs760174238 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377259 | TTCAAGACTACAGTA[C/T]GCTATGATTGTCCCA | 10152 |
| rs760202490 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390458 | GCAACACGGTGAAAC[C/T]CTGTCTCTACTAAAA | 10152 |
| rs760203626 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360321 | TGTTGTCATGTGAGG[A/T]CGGTTATCAATGATA | 10152 |
| rs760270478 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343013 | TACCGTTAACAAAAG[A/G]CCATGAGATCTGTGG | 10152 |
| rs760273334 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330069 | CATTTTCATGTCTTA[C/G]TGTAAATTTTAAAAA | 10152 |
| rs760277109 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429028 | AATGTTATCTGAGCA[C/T]TAAAAATCATCAGCA | 10152 |
| rs760277937 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203393004 | TATTTGTGTCATTGC[C/T]TTCACTCTGTAGTTC | 10152 |
| rs760330350 | in-del | -/T | 1.92258e-05 | 0.00310041 | intron-variant | ABI2 | GRCh38.p7 | 2:203380185 | TACATTTTTGTGTTG[-/T]TTTTTTACATTATAT | 10152 |
| rs760335160 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361757 | TTTAAAAGGGCCATT[A/T]ACATAGACATTCTCC | 10152 |
| rs760369485 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203375699 | TAAAGCTGCATGATA[A/G]ATGTGAGGAGGGAGT | 10152 |
| rs760376765 | snp | A/G | 3.50816e-05 | 0.00418802 | intron-variant | ABI2 | GRCh38.p7 | 2:203416869 | AATACTGAACTTTGC[A/G]TAACATATAGTTTTG | 10152 |
| rs760426159 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203426020 | GAGTGAGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 10152 |
| rs760429525 | snp | A/G | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326644 | CTACAGAAGATGGTT[A/G]AAGTGCTTAAGAATA | 10152 |
| rs760447848 | snp | C/G | 1.64893e-05 | 0.0028713 | synonymous-codon, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394790 | CCGTAATATGGCTCC[C/G]TCGCAGCAGAGCCCT | 10152 |
| rs760456910 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364423 | ACATGGGTCAGGAAT[-/A]TGAACCCGGGTCTCC | 10152 |
| rs760461168 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384522 | ACTGTGTTGGCCTGG[C/G]TGGTCTCGAACTCCT | 10152 |
| rs760464824 | snp | C/T | 3.29734e-05 | 0.00406025 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416964 | GTCTTTGATGAGTCT[C/T]CCCCACCTCCTCCTC | 10152 |
| rs760478038 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361272 | AGGGGATGGGAGTCA[A/G]TTCTCGGGCTTAAAT | 10152 |
| rs760544564 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400240 | TTACAAGTGTGAGCC[A/G]CCACACCCAGCTAAT | 10152 |
| rs760593021 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368332 | TGAAATGTTCTATTT[G/T]AGCACTCTTGTCATT | 10152 |
| rs760597699 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399013 | GCTATAAACATGTAC[A/C]TACAGGGTTTTTTTT | 10152 |
| rs760623969 | in-del | -/TTA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343637 | CCCAGCACTTCAGAG[-/TTA]TTAATGAGGTTTAAA | 10152 |
| rs760630657 | snp | C/T | 1.64882e-05 | 0.00287121 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203366957 | TGCCTATCTGATAAA[C/T]ACCTTGGCCAACAAT | 10152 |
| rs760641560 | snp | A/G | 2.24027e-05 | 0.00334677 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328523 | TGTGAAGATGGCGGA[A/G]CTGCAGATGCTGCTG | 10152 |
| rs760643861 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337496 | TAATTGAAGAACATG[C/T]AAATAAATGGGAAGA | 10152 |
| rs760725446 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355160 | TCTTTCTAGGCTTTC[C/T]GTTTTGACAGTGCAT | 10152 |
| rs760731183 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424425 | TACTTATCAGGGTCT[C/T]GTTCTGTCACCTGGG | 10152 |
| rs760735167 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203349606 | GACAGGGTTTCACCA[C/T]GTTGGTCAGGCTGGT | 10152 |
| rs760762189 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399906 | TTTTTTAAATGAATC[A/G]TGCTTTGATGGCATA | 10152 |
| rs760815645 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203393190 | CTCCTGAGTAGCTGG[G/T]ATTACAGGTGTGCGC | 10152 |
| rs760847127 | in-del | -/AT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329314 | TGTTTCTTAGAGAGA[-/AT]ATTGGGAAGATGAAC | 10152 |
| rs760904702 | snp | C/G/T | 0.000116157 | 0.00762013 | intron-variant | ABI2 | GRCh38.p7 | 2:203395609 | AAGTGCTGATGATCT[C/G/T]TTACTGTTTATAAAT | 10152 |
| rs760923574 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356160 | ATGAGTGCAGTTAGT[A/G]GAGACATACTTTTCA | 10152 |
| rs760934002 | in-del | -/TGTGCG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350889 | GTGTGTGTGTGTGTG[-/TGTGCG]CGCGCGCATACTTTT | 10152 |
| rs760934093 | snp | C/T | | | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432303 | TATTACTGAAGAAGT[C/T]GTCTTTTTAAATTTT | 10152 |
| rs761027989 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345698 | ACAGGCCTGAGCCAC[C/G]ACGCCCAGCCCTAAT | 10152 |
| rs761033035 | in-del | -/TAT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354466 | GATGTATGAATCTTA[-/TAT]TATGAACATACTGAA | 10152 |
| rs761035115 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347354 | ATCTTTTGTGTGAAA[-/T]TTCTGGTGGCATAGG | 10152 |
| rs761085657 | snp | A/G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203417991 | AGAAAGAGAAACATA[A/G/T]TATTTCTGGAGACGA | 10152 |
| rs761089846 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419271 | CCCACCACCGCGCCC[C/T]GCTAATTTTTTTGTA | 10152 |
| rs761103753 | in-del | -/TCTC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370193 | TTCTCCTATTCTCTC[-/TCTC]TCTCTCTCTCTCTCT | 10152 |
| rs761140880 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431123 | TTTTTGGCCGGGAAC[A/T]CCTGATTGGTGTTAA | 10152 |
| rs761200676 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415650 | AAAAAAAAATCCATT[C/T]AATTCAATTCGTAGG | 10152 |
| rs761201228 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418627 | GCGCCAAAAAGAGAA[G/T]GCAAGCAAGACACTA | 10152 |
| rs761223298 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364534 | GGTCCTTTAAACTTC[A/G]TCTTGAACTTAGAAA | 10152 |
| rs761277403 | in-del | -/TGTGTTTGTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203358110 | GTGTGTGTGTGTGTG[-/TGTGTTTGTT]TGTTTGTTTGTTTTT | 10152 |
| rs761309280 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363596 | GTGAGTTCAATTGTT[G/T]TAATTTTTAACTCCC | 10152 |
| rs761322913 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402328 | GCATGAGTCACTGCA[C/T]CCGGCCCTAATTAGT | 10152 |
| rs761336171 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387762 | TGTAACTTTAAAAAG[C/T]ATTTCAAGTGAAATT | 10152 |
| rs761355003 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429211 | CATTCCACTTCGTGC[C/T]TTTCTTAGGTCATTT | 10152 |
| rs761373853 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377040 | TTTCTAGTATGTGCC[A/T]GGCATAGTGGCTCAT | 10152 |
| rs761412640 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203417540 | TTTTAGTGAAAAGCT[G/T]CTTTGATATTAGCTA | 10152 |
| rs761463637 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203389218 | CTTATTAATGAGAGG[A/G]AGAGCAAGGATAAGT | 10152 |
| rs761493802 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361407 | GGGAGGCAGAGGCAG[A/G]AGGATCACTTGAGCC | 10152 |
| rs761499316 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382894 | ATCAAAAGCTCATGA[C/T]AATGTTTAACAGAAT | 10152 |
| rs761521136 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337599 | TAATGCAATCTCTAT[C/G]AATATTCCAATGGTA | 10152 |
| rs761531304 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400909 | ATATGAAGCCTGGAA[A/G]AGGATATGACTGCAG | 10152 |
| rs761583557 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357246 | GACCTAAAAATCCAG[G/T]CCTTTTAATATAACA | 10152 |
| rs761629843 | snp | C/T | 1.66308e-05 | 0.00288359 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427329 | GGGAATTACGTTGAG[C/T]CTATCATGCATTATT | 10152 |
| rs761644948 | in-del | -/TT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329316 | GTTTCTTAGAGAGAA[-/TT]GGGAAGATGAACCTC | 10152 |
| rs761655337 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382737 | GAGAAGCAGAAAATA[-/T]TCAGTGACACGGGTT | 10152 |
| rs761663285 | in-del | -/AA | 1.71761e-05 | 0.00293049 | intron-variant | ABI2 | GRCh38.p7 | 2:203416897 | TGTTGTCAGCCTGAT[-/AA]ACGTTCTTAGTTTCA | 10152 |
| rs761692979 | in-del | -/TTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400081 | GTGTGAATAGTGTCT[-/TTTT]TTTTTTTTTTTTTTT | 10152 |
| rs761726998 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353212 | TTTTTTCAGATTACA[A/G]TTATCATATAAAAAT | 10152 |
| rs761744534 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203386431 | AGCCACTCCTGGCTG[-/T]TTTTTTTTTTTTTTT | 10152 |
| rs761761705 | in-del | -/GGCCGGGCGCGGTGGCTCACGCCTGTAATCCC | 1.65143e-05 | 0.00287348 | intron-variant | ABI2 | GRCh38.p7 | 2:203380426 | AAAGTAGTAACCCAT[lengthTooLong]AATGAAACCAACTCT | 10152 |
| rs761762688 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402526 | AAAGTATTTAATGAT[C/G]TGAGATAATTTTCTT | 10152 |
| rs761783921 | snp | C/G | 1.64882e-05 | 0.00287121 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394776 | GTACCTAGCCCAACC[C/G]GTAATATGGCTCCCT | 10152 |
| rs761785502 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203407349 | ACTCGCATGGGCTAT[A/G]TAATATATATATCTC | 10152 |
| rs761796222 | snp | A/G | 6.61037e-05 | 0.00574869 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203367010 | AGGCATCCCAGCTAC[A/G]AAGGATGGAATCTTC | 10152 |
| rs761813567 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356781 | GTTGGGATTATAGGC[A/G]TGAACTACCACACTC | 10152 |
| rs761845803 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424547 | CCACAGACGTGCACC[A/C]CCATGCCTGGCTAAT | 10152 |
| rs761869027 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203362446 | ATTGGGAGTGTATTA[C/T]CTTTGGGTCCCACTA | 10152 |
| rs761878242 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203395943 | AAGCAAGTGATTTGT[A/G]AGTGTTTGCTCACTT | 10152 |
| rs761931050 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410798 | AAAAGTATCCATTTA[A/G]AGTGTTGGGATGTAA | 10152 |
| rs761969695 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382471 | AAATATTTGTTGAAT[A/G]AATGGTTATTTTGTA | 10152 |
| rs762009242 | in-del | -/AAC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347602 | GCTGAGAGAAGAGAT[-/AAC]AAAATAGTTTCTGTT | 10152 |
| rs762011989 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346223 | AAGCTATTTCCCAAC[C/T]ATTTAAATCTTTGAG | 10152 |
| rs762075158 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421287 | GATTGTTTACATAAA[A/T]AAGCAGATACAAATA | 10152 |
| rs762133397 | snp | C/G | 1.64977e-05 | 0.00287203 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203366915 | AGAAGAAACCAAAGC[C/G]TACACCACCCAATCC | 10152 |
| rs762199273 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203334768 | TGGGTTCAAGCAATT[A/C]TCCTGTCTCAGCTTC | 10152 |
| rs762223357 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364668 | ATAATTATTCCTTAT[A/G]GTTGACTAGGATAGA | 10152 |
| rs762227710 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404035 | TGGGATTACAGGCGT[A/G]AGTCACCGTGCCTGG | 10152 |
| rs762232494 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404804 | CCTCAAGTCATCCAC[A/T]TGCCTTGGCCTCCCA | 10152 |
| rs762238965 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344382 | TTTTCCTTTTTTTTT[A/G]AGACAGGGTCTCTTG | 10152 |
| rs762260859 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388747 | TGTTTATTTTATGCT[A/G]TTTTTTTTGGTGGGG | 10152 |
| rs762269453 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365522 | ATATTGAAGCCCTTG[A/G]GGTGTTGGTATTTTT | 10152 |
| rs762309226 | in-del | -/TCA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203393928 | CCTTTCTTCCTCTTT[-/TCA]TCCTCTTTACGAGGA | 10152 |
| rs762334019 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406286 | TAATGTAGCATGTAA[C/G]TATTGAAGACTTTAG | 10152 |
| rs762364214 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203341244 | AACATACAGTGTTTC[C/T]TATTTATTTGTGTGT | 10152 |
| rs762435953 | snp | C/T | 1.67259e-05 | 0.00289183 | intron-variant | ABI2 | GRCh38.p7 | 2:203395815 | TCGTCTTCACTTTTC[C/T]TTTCTGAATTTGATT | 10152 |
| rs762469897 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203386938 | AGCCACCATGCCCAG[C/T]CAGACATTGCTTTTT | 10152 |
| rs762483398 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413548 | TTGCCTTTTGGATTG[A/G]TCTTTTTCATCTTTT | 10152 |
| rs762490918 | in-del | -/CCGCGTCGGGGACCC | 1.66161e-05 | 0.00288232 | intron-variant | ABI2 | GRCh38.p7 | 2:203328653 | GCATCCCCAGCTGGG[-/CCGCGTCGGGGACCC]CCGCGTCGGGGACCC | 10152 |
| rs762494055 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203417915 | ACATGTGATCAAGAA[A/C]GTAAAGGAGAACATG | 10152 |
| rs762509478 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363344 | AAAATGTACAATTAA[A/T]TTATTTTTTATGAAA | 10152 |
| rs762522768 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403862 | GTTCAAGAGATTCTC[C/T]TGCCTCAGCCTCCTG | 10152 |
| rs762536786 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415485 | AGCTGGGTGTGGTGG[C/T]GGGCGCCTGTAGTCC | 10152 |
| rs762536882 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384361 | ACCCAGGCTGGAGTG[C/T]ACTGGTGTGATCATG | 10152 |
| rs762539786 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368747 | GTTTTAATGAGTGTA[A/C]GGTAAATTTCAGTTG | 10152 |
| rs762541828 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337727 | CATACTTCCTGATTT[C/T]AAACTATATTACAAA | 10152 |
| rs762558547 | in-del | -/AG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392537 | AATAATTCTGCTTAG[-/AG]AGAGAGAAAATCTAG | 10152 |
| rs762559848 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430203 | TATTGTAAGTTTCCC[-/T]CTTTTTTTATAAATT | 10152 |
| rs762594444 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203340535 | CCACACATGGCTAAT[A/T]TTTGTAGTGACGGGG | 10152 |
| rs762640856 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203411493 | ATATTATGAACAAAT[A/C]ACTGTCTGGCTAGTG | 10152 |
| rs762647751 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203412596 | TTGTTGAGTTTAAGA[-/G]CTATTTTCACATATA | 10152 |
| rs762691511 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385427 | TGAGCCACCGTGCCC[A/G]GCCAGATTCTTAATA | 10152 |
| rs762693986 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424650 | GTGATTCTCCTGCCT[C/T]GGCCTCCCAAAGTTC | 10152 |
| rs762705351 | in-del | -/GGA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329280 | GTTTTCCTGGGGGTG[-/GGA]GGAGGACAGACTATG | 10152 |
| rs762705761 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351066 | TATTTACTCTTTTGC[A/G]TGTCACTATCCAGTT | 10152 |
| rs762710289 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354689 | GGTTCCCAAGGCCCC[A/G]GTTCACATATTGTGA | 10152 |
| rs762715013 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388731 | ATTTTAATATATAGA[-/T]TGTTTATTTTATGCT | 10152 |
| rs762735941 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387130 | AGGAGATTAATATAT[A/T]AGGTGTATACCACAC | 10152 |
| rs762740005 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203340690 | GTGTTGCCCACTCCC[C/T]GCTCCCACCAAAGAT | 10152 |
| rs762790738 | snp | C/T | 0.000167856 | 0.00915967 | intron-variant | ABI2 | GRCh38.p7 | 2:203355143 | TTTCTGGATCCCATG[C/T]TTCTTTCTAGGCTTT | 10152 |
| rs762830663 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370814 | TTTATTGGAATGGCA[A/G]TAAGCCTCAAGAGTT | 10152 |
| rs762846357 | snp | C/T | 6.59044e-05 | 0.00574002 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416993 | TCCTCCAGAAGATTA[C/T]GAAGAGGAGGAAGCT | 10152 |
| rs762848081 | snp | A/G | 1.75268e-05 | 0.00296025 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203391104 | CACCTCCAACTCAGA[A/G]GCCCCCTAGTCCCCC | 10152 |
| rs762898716 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346338 | CAACCACAAAAGACT[A/T]TGTTTGTTTGTTTGT | 10152 |
| rs762926119 | in-del | -/AAG | | | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432604 | GAGCCTAGATTATAA[-/AAG]AAGAATTTTCTAATG | 10152 |
| rs762948116 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347093 | TGATGATTGCCCTAA[C/T]ATGTGCATCAGGTAC | 10152 |
| rs762949758 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203328942 | TTCCGGATGGCGGAG[A/G]GGGCGGAGAGTGGCA | 10152 |
| rs763134412 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364735 | TACATATTTTTTTAA[A/T]TTTTTTTTTTTTTTC | 10152 |
| rs763142849 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203334961 | CACCGTGCCTGGCCT[A/G]GTTGTAGACTTTTGA | 10152 |
| rs763197972 | in-del | -/TAT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203394155 | TGAGATTAAAGTGTG[-/TAT]TATTTTTGTATATAG | 10152 |
| rs763210979 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203336010 | GTCCCTCTAGTTTTT[A/G]CCTTTTCCAGAATGC | 10152 |
| rs763255741 | snp | A/G | 3.32657e-05 | 0.0040782 | intron-variant | ABI2 | GRCh38.p7 | 2:203395795 | GGTAAAACATTCATG[A/G]TGCCTCGTCTTCACT | 10152 |
| rs763302630 | snp | A/T | | | intron-variant, utr-variant-5-prime | ABI2 | GRCh38.p7 | 2:203375947 | GCAATACTGCAGTTC[A/T]ACCCCGTGTGGTAGT | 10152 |
| rs763309408 | snp | A/C | 0.000101662 | 0.00712887 | intron-variant | ABI2 | GRCh38.p7 | 2:203396985 | AAGTATTTGCTTATT[A/C]ATTGGCAGGCAGATG | 10152 |
| rs763339990 | snp | A/C/G | 3.5186e-05 | 0.00419428 | intron-variant | ABI2 | GRCh38.p7 | 2:203416858 | CTTGGATAGGAAATA[A/C/G]TGAACTTTGCATAAC | 10152 |
| rs763382512 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390539 | TGGGAGGCTGAGGCA[A/G]GAGAATTGCTTGAAC | 10152 |
| rs763389915 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353572 | GCAACCTCTGCCTCC[C/T]GGGCTCAAGTGATTC | 10152 |
| rs763393954 | snp | C/T | 3.30606e-05 | 0.00406561 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203380328 | GAACGACCAGTTCGT[C/T]ATATTAGAAAACCTA | 10152 |
| rs763437808 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354533 | AGGGACTGAATTTTT[A/C]CCCTGTCTGGAAGTT | 10152 |
| rs763457033 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422105 | GTTCAAGACCAGCCT[A/G]GGCAACATGGCGATA | 10152 |
| rs763460242 | in-del | -/TTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400082 | TGTGAATAGTGTCTT[-/TTT]TTTTTTTTTTTTTTT | 10152 |
| rs763468068 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415248 | GTATAGAGGGGCACA[A/G]CAGATGGGAAGAATA | 10152 |
| rs763475702 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392877 | GATCCTTGGGGACCA[A/G]AGTTGCTGAGGCCCA | 10152 |
| rs763477187 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428105 | GGCCAGTGTACCCAG[A/G]TGTGAAGTGTGGTAG | 10152 |
| rs763491757 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364814 | ATCATGGCTCACTGC[A/G]TCTTTGGCTTCTGGG | 10152 |
| rs763517308 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427968 | TTGCATCCCTTCATG[A/T]TTCTGTTTGTGGATT | 10152 |
| rs763530027 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413565 | CTTTTTCATCTTTTC[C/G]TACAATCATATACGT | 10152 |
| rs763623937 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343200 | GAAACCTTGTCTCTA[C/T]TAAAAATACAAAAAT | 10152 |
| rs763655407 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347492 | GTAAATGGCATGATG[A/G]CATTACCACCCAAGG | 10152 |
| rs763725857 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384373 | GTGCACTGGTGTGAT[C/T]ATGACTCACTGCAGC | 10152 |
| rs763738295 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360330 | GTGAGGTCGGTTATC[A/C]ATGATAAAGGTTCTT | 10152 |
| rs763743153 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428180 | GTCCCTAAGGTTCTG[A/G]AGAGACTTGAACTGT | 10152 |
| rs763780804 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387456 | CGGTGGTATTTGCAT[G/T]CCTTCATCATAGCCT | 10152 |
| rs763810553 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399035 | GTTTTTTTTGTGCAC[A/G]TGGGTTTTTATATCA | 10152 |
| rs763820521 | snp | A/G | 1.67792e-05 | 0.00289643 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402720 | ATGGAGGACCTTTTT[A/G]TAGCCAGAATCCAGG | 10152 |
| rs763883143 | in-del | -/TAATTTTTTTCAAGCT | 1.7239e-05 | 0.00293585 | intron-variant | ABI2 | GRCh38.p7 | 2:203380392 | GAGTAAAGGTAGGTA[-/TAATTTTTTTCAAGCT]TTTAAAAGTAGTAAC | 10152 |
| rs763939570 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382550 | AATGTTATGAAATAT[A/G]ATTAGCTGGATTTTT | 10152 |
| rs763942603 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416994 | CCTCCAGAAGATTAC[A/G]AAGAGGAGGAAGCTG | 10152 |
| rs763952023 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368438 | GTGCATATTATTATT[A/T]TTTTTAATGTCTTGA | 10152 |
| rs763961244 | snp | C/T | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326952 | GGGACTACAGGCGCC[C/T]GCCACCATGCCCAGC | 10152 |
| rs763964421 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337518 | ATGGGAAGATATCCC[G/T]TGCTCATGAATTGGT | 10152 |
| rs764043362 | snp | C/T | 1.78217e-05 | 0.00298505 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203391110 | CAACTCAGAAGCCCC[C/T]TAGTCCCCCTATGTC | 10152 |
| rs764069334 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422755 | GGAATATGGCTGTAT[C/T]AGTTAAGCAGCATTA | 10152 |
| rs764079229 | in-del | -/TTA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203426536 | GTCACTTTTAGTCTG[-/TTA]TTATAGTTATATTAA | 10152 |
| rs764100372 | in-del | -/TC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387845 | GGTATATGTTCTGTC[-/TC]TCTCTCTGTCGCTGT | 10152 |
| rs764109133 | snp | C/T | | | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432649 | AGCAAGTAAGTTTGT[C/T]TTCACAATACCCAAA | 10152 |
| rs764134993 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344236 | AGAAAAGACTATAGG[A/C]CATTAATAATATTCA | 10152 |
| rs764142918 | snp | A/C | 0.000492166 | 0.0156793 | intron-variant | ABI2 | GRCh38.p7 | 2:203355176 | GTTTTGACAGTGCAT[A/C]TCCTCTGGTGCTTCC | 10152 |
| rs764203896 | snp | A/G | | | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203395769 | CTCCATCTCCTCCCA[A/G]TGTCTTTCCAGGTAA | 10152 |
| rs764209578 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356244 | CCAGGCTGGAGGGCA[A/G]TGTTGCAATCATGGC | 10152 |
| rs764218187 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431124 | TTTTGGCCGGGAACT[A/C]CTGATTGGTGTTAAG | 10152 |
| rs764227275 | in-del | -/AACT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337023 | ATATGACAAGCCTAC[-/AACT]AACTAACATCATACT | 10152 |
| rs764250863 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203409495 | ACTTACCTGTTTACC[A/G]TCCCATTTCTTTCCC | 10152 |
| rs764299652 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369986 | TATCAAAACTATTTG[A/T]TATTCTTCAGACTGG | 10152 |
| rs764326599 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203397114 | CAGAAAGTATGTGAC[C/T]AAAGATTAGCATTTC | 10152 |
| rs764327328 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345149 | TCCGCACTACCTTTA[C/T]GAGTTGTAACACTCA | 10152 |
| rs764383841 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203364947 | CAATGTTGCCCAGGC[C/T]GGTCTTGAACTCCTG | 10152 |
| rs764393175 | snp | G/T | 0.000162536 | 0.0090134 | intron-variant | ABI2 | GRCh38.p7 | 2:203342274 | CTGTTACCATTTTGA[G/T]TTCTATGAAGAATCT | 10152 |
| rs764395390 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377494 | CTGATGAACCTTTTA[C/T]TGATCTGACGAAGAC | 10152 |
| rs764426893 | snp | C/T | 4.95995e-05 | 0.00497969 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203380330 | ACGACCAGTTCGTTA[C/T]ATTAGAAAACCTATT | 10152 |
| rs764471571 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419279 | CGCGCCCCGCTAATT[C/T]TTTTGTATTTTTAGT | 10152 |
| rs764524896 | snp | C/T | 1.65091e-05 | 0.00287303 | intron-variant | ABI2 | GRCh38.p7 | 2:203395647 | TTTTGGTGGCTCTTA[C/T]TTCTTTAGCAGCAGT | 10152 |
| rs764585367 | in-del | -/CACCAC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392276 | CAGCACCACCACCAT[-/CACCAC]CACCACCACCACCAC | 10152 |
| rs764635417 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361455 | CCTGGGCAACGTAGT[A/G]AGACCCTGTCTCAGA | 10152 |
| rs764662009 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337464 | GTACACTAAAAACTA[C/T]AAGACATTTATGAAA | 10152 |
| rs764670017 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203416619 | CTCTTTGGAAAGAGG[A/G]TTTGTGTTAATATAA | 10152 |
| rs764777401 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203412377 | GACCAAATGCCCCCC[-/T]TTTTATCAGCACATT | 10152 |
| rs764793924 | in-del | -/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364749 | TTTTTTTTTTTTTTT[-/C]CAAGAGACAGGGTCT | 10152 |
| rs764856502 | in-del | -/TAA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203411126 | GTACTTTGTTTGTGT[-/TAA]TGAGTTGTCCCTCAA | 10152 |
| rs764865045 | in-del | -/TTTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384285 | ATACTCTTGTTTTTG[-/TTTTT]GTTTTTTTTTTTTTT | 10152 |
| rs764888529 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350264 | GTATTTTTAGTAGAG[A/G]CGAGGTTTCACCGTG | 10152 |
| rs764888742 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337609 | TCTATCAATATTCCA[A/G]TGGTATTTTTCACAA | 10152 |
| rs764894486 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424599 | AGACAGGGTTTTGCT[A/G]TGTTTCCCAGACCAG | 10152 |
| rs764909765 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413317 | GATGTCATTGGTTTT[C/T]GCCAGTCACCAGTGA | 10152 |
| rs764962993 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203409762 | TCTTTGCAGCCACTA[C/T]TGGAAGTAGGTTGCA | 10152 |
| rs764969823 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382946 | TTTCCTGTTAGAATT[C/T]GTTTCAATAATGTTT | 10152 |
| rs765077915 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370336 | CAAGTGATCCTCCCA[C/T]CTCAGCCTCCCAAAG | 10152 |
| rs765087879 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423746 | CCTTTTCTGCTGGCA[C/T]GGTACCATTATTCTT | 10152 |
| rs765095085 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356315 | TCCCAAGTAGCTGGG[A/C]TCACAGGCCTGTGCC | 10152 |
| rs765109777 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416987 | TCCTCCTCCTCCAGA[A/G]GATTACGAAGAGGAG | 10152 |
| rs765143912 | in-del | -/TGATGA | 3.29954e-05 | 0.0040616 | cds-indel, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416954 | GGAAGAACCAGTCTT[-/TGATGA]GTCTCCCCCACCTCC | 10152 |
| rs765198855 | in-del | -/GT | 2.15882e-05 | 0.00328537 | intron-variant | ABI2 | GRCh38.p7 | 2:203391147 | GGGACACTTGGGTGA[-/GT]GTATATAAGTAGTAA | 10152 |
| rs765232686 | snp | C/T | 1.73222e-05 | 0.00294292 | intron-variant | ABI2 | GRCh38.p7 | 2:203380395 | TAAAGGTAGGTATAA[C/T]TTTTTTCAAGCTTTT | 10152 |
| rs765233705 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203397367 | ATTTGATACAACAAA[G/T]GGAAAGCCTCTGTAA | 10152 |
| rs765265541 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203397811 | GAAGCACACTGGTCA[C/T]GTGGCCAGAGTAGGA | 10152 |
| rs765306380 | in-del | -/TTAC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203427016 | GTATATGACTGGGTA[-/TTAC]TTAGAAAAAAAAACA | 10152 |
| rs765317846 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345436 | TTCTTGAAGTCAGCC[A/G]GACCAAGAACCCACC | 10152 |
| rs765358621 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396024 | TTTCAGATCACACTT[C/T]GTTATGAGTACAAGT | 10152 |
| rs765379653 | snp | C/T | 1.77316e-05 | 0.0029775 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328568 | GGGGGGCCGCCGGGC[C/T]CTCTTCGACAGCTAC | 10152 |
| rs765386775 | snp | C/T | 3.4943e-05 | 0.00417975 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427355 | TTATTCTGAGTAAAG[C/T]TCAGCAGGGCTGTGC | 10152 |
| rs765391719 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379081 | ATGTGGAGAAATTCA[A/C]CCTCTGTTAGCAAAT | 10152 |
| rs765416202 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356786 | GATTATAGGCATGAA[C/T]TACCACACTCGGCAG | 10152 |
| rs765441167 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431560 | TTATATTACTCCAAC[A/G]CTGGCAGGAGCACAG | 10152 |
| rs765445473 | snp | C/G | 1.65501e-05 | 0.00287659 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394836 | GTGAATCAAAGAAAT[C/G]GAACTTACAGGTATT | 10152 |
| rs765464921 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203333634 | TTAGTCCCTAACTCT[C/T]AGCAGAGACATTTGG | 10152 |
| rs765505779 | snp | C/T | 1.65767e-05 | 0.00287891 | intron-variant | ABI2 | GRCh38.p7 | 2:203395628 | CTGTTTATAAATACT[C/T]ATGTTTTGGTGGCTC | 10152 |
| rs765508716 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363727 | TTATTTTTTATGGCC[A/G]AATAGTACTCCATTG | 10152 |
| rs765533921 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404234 | ATTGCTCAGGAACTG[C/T]TTGTTGAATGCCAAA | 10152 |
| rs765544023 | in-del | -/CTTGATGACCC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203341109 | CTGATACATCACGTT[-/CTTGATGACCC]CTTCCTGGCTACTCT | 10152 |
| rs765588858 | snp | A/C/G | 3.31632e-05 | 0.00407194 | intron-variant | ABI2 | GRCh38.p7 | 2:203411264 | TATCCCTTATCCTCC[A/C/G]CACCTTTTTTGTTTT | 10152 |
| rs765596697 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404844 | GATTACAGGTGTGAG[C/T]CACCGCACCCGGCCT | 10152 |
| rs765659242 | snp | A/G | 9.9208e-05 | 0.00704231 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203367015 | TCCCAGCTACGAAGG[A/G]TGGAATCTTCAATCA | 10152 |
| rs765705177 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203358339 | TTTTTGTAGAGACAA[A/G]GTCTTTCTCTGTTGC | 10152 |
| rs765708910 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203393507 | CAAAGTCCTGACATT[A/G]CTTTTTCCTCTTTTG | 10152 |
| rs765713258 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421401 | TTGATGATGTATCAT[A/C]AAGGTCTTTCTTAAA | 10152 |
| rs765769395 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385543 | CATCATTTAGCCCCA[C/T]GTTTAAAAAATGGAC | 10152 |
| rs765781807 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351093 | AGTTGACCCAACACC[A/G]TTTGTTTAAAAGCCT | 10152 |
| rs765784466 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343114 | CCAAAACTAAAAGCA[A/G]GCACCTGGGGAGGCT | 10152 |
| rs765786929 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421964 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 10152 |
| rs765806665 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403875 | TCCTGCCTCAGCCTC[C/T]TGAGTAGCTGGGATT | 10152 |
| rs765853407 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337856 | GCCAGCGTGGAGAAA[C/T]CTCATCTCTACTAAA | 10152 |
| rs765863203 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357895 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGACTACA | 10152 |
| rs765880118 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353547 | TGCAGTGGCATGGTC[C/T]TCTCTCACAGCAACC | 10152 |
| rs765880324 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203341310 | TCTCTTACTCATTTC[C/T]AGTACCTGGAACAGT | 10152 |
| rs765908795 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203362070 | ATCAGCATAGTAATA[C/T]ATTTCTAGTTTATTT | 10152 |
| rs765927935 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402429 | TAATATCAGCGAACA[A/G]TAACTCACCTTGCAT | 10152 |
| rs765965011 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370354 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAGGCAT | 10152 |
| rs765970080 | snp | C/T | 6.59381e-05 | 0.00574149 | intron-variant, synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203411310 | TCCTCCTCCTCCCTC[C/T]ATCCTACAGGTAACT | 10152 |
| rs765973622 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350122 | CTCACTGTCACCTAG[A/G]CGGGAGTGCAGTGGT | 10152 |
| rs766003652 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203334472 | AGGGTGTGTAAGGTA[A/G]TCTTTTGGTGGATGA | 10152 |
| rs766050368 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339506 | GAATTGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 10152 |
| rs766057110 | snp | C/T | 5.24544e-05 | 0.00512098 | intron-variant | ABI2 | GRCh38.p7 | 2:203416877 | ACTTTGCATAACATA[C/T]AGTTTTGTTGTCAGC | 10152 |
| rs766066461 | in-del | -/TGCG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350891 | GTGTGTGTGTGTGTG[-/TGCG]CGCGCGCATACTTTT | 10152 |
| rs766074391 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387128 | GTAGGAGATTAATAT[A/G]TAAGGTGTATACCAC | 10152 |
| rs766075623 | snp | A/G | 1.66499e-05 | 0.00288525 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203380350 | GAAAACCTATTGACT[A/G]TACAATTCTAGATGA | 10152 |
| rs766120063 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396360 | AAAAATCATAAAGAT[C/T]TGTGTTTTAAAAAAA | 10152 |
| rs766122478 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424810 | TTGTTAAAACTCTCA[C/G]CTCTCTACCATTATA | 10152 |
| rs766156037 | in-del | -/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410448 | TAGTTTCCACACATA[-/C]CTGGCTTATTAGTGC | 10152 |
| rs766184910 | in-del | -/AACAAAA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355525 | TCAACAAAAGAAAAC[-/AACAAAA]AACAAAAAACCCAAG | 10152 |
| rs766235625 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377440 | TACATTTCTAAAAAC[-/T]TGAGGAGAATAAAAA | 10152 |
| rs766286958 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203426093 | ACAATTTAAGGAAGC[C/T]ATTTAATTTTTATTA | 10152 |
| rs766288933 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378891 | GCACATAATTCATGT[A/C]TATATTTATATATAT | 10152 |
| rs766318050 | snp | G/T | 1.83707e-05 | 0.00303068 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328553 | GGAAGAGGAAATCCC[G/T]GGGGGCCGCCGGGCC | 10152 |
| rs766318119 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427793 | GGGTACCCTAGCCCC[-/T]TCTTTTCTTCCACTT | 10152 |
| rs766325299 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400317 | TGGTCTTGAACTCCT[A/G]ATCTGAAATGATCCA | 10152 |
| rs766344265 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356394 | TTTATTTTGAGACAG[A/C]GTCTCGCTCTGTTGC | 10152 |
| rs766421782 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357855 | CTCACTGCAGCCTCC[A/G]CCTCCTGGCTTCAAA | 10152 |
| rs766452506 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346398 | CTTGGGAATATATGG[C/G]ACTAATAGGCATGTG | 10152 |
| rs766459773 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370166 | AGGTTTTGTGGGCTA[C/T]GTATGGTGTCATTCT | 10152 |
| rs766475115 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422202 | ACTCTGGAGGCTGAG[A/G]TGGGAGCATCACCTG | 10152 |
| rs766487005 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379172 | TAAATAAATTAATGA[A/C]ATATTTTACAGGCAT | 10152 |
| rs766489734 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415617 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 10152 |
| rs766542801 | snp | A/G | 1.7376e-05 | 0.00294749 | intron-variant | ABI2 | GRCh38.p7 | 2:203427141 | TCTAGGAATATTACT[A/G]TCTTTCACATCCTGT | 10152 |
| rs766574102 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420534 | GAGTAGGTGGGACTA[C/T]AGGCACCTGCCAGCA | 10152 |
| rs766585354 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345380 | TCCGGACACACCATC[-/T]TTAAGAACTGTAACA | 10152 |
| rs766596999 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365924 | GTGAGCCACCGTGCC[C/T]GGCCGGGGCTGTTAT | 10152 |
| rs766623089 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347095 | ATGATTGCCCTAACA[G/T]GTGCATCAGGTACTT | 10152 |
| rs766624049 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343230 | TTAGCGGGATGTGGT[A/G]GCACGCATCTGTAGT | 10152 |
| rs766676309 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404928 | AACTCTGTAGGTAGA[A/G]TTTATTTGAAGGCTG | 10152 |
| rs766688017 | in-del | -/TT | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430205 | TTGTAAGTTTCCCTC[-/TT]TTTTTATAAATTAAA | 10152 |
| rs766698309 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390654 | AAAAAAGAAAGTTAT[C/T]TCTAAAAATAAGGAA | 10152 |
| rs766705269 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345128 | TGCTGCTGCTCACTC[C/T]TTGGGTCCGCACTAC | 10152 |
| rs766711863 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203389023 | TTTAAGGTTGAGCTT[A/G]AAGGACTTTGGTTAC | 10152 |
| rs766712220 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353573 | CAACCTCTGCCTCCC[C/G]GGCTCAAGTGATTCT | 10152 |
| rs766766937 | snp | C/T | 1.85541e-05 | 0.00304577 | intron-variant | ABI2 | GRCh38.p7 | 2:203402557 | TTAATGACATATGTA[C/T]GTTCTATCTCTTTTT | 10152 |
| rs766819729 | snp | C/T | 0.000191994 | 0.00979592 | intron-variant | ABI2 | GRCh38.p7 | 2:203355246 | GTACGGTGGCTCATT[C/T]CTGTAATCCTAGCAC | 10152 |
| rs766821803 | snp | A/T | 1.65564e-05 | 0.00287714 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402697 | AACAAGCCTTCAGAA[A/T]CAGATGAATGGAGGA | 10152 |
| rs766875319 | snp | C/T | 1.64876e-05 | 0.00287116 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203366960 | CTATCTGATAAACAC[C/T]TTGGCCAACAATGTC | 10152 |
| rs766893070 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370981 | TTAACGAAAAAGAAC[A/G]CTGAGTTGGCCTGAA | 10152 |
| rs766904977 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353495 | TGTATTTATTTATTT[A/T]TTGAGACAGAATCTC | 10152 |
| rs766908210 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406611 | ATGTCTAAAACGTCT[A/G]GAAGAATACTGATGT | 10152 |
| rs766922373 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428200 | ACTTGAACTGTGGAA[A/G]TGCTCTTAGCAGGCA | 10152 |
| rs766933151 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344046 | GCTGAGGTGGGAGGA[C/T]TGCTTGAGCTCAGGG | 10152 |
| rs766952104 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203389590 | TCTGATTTCAATGGT[A/G]TGATGTCTTGCAATT | 10152 |
| rs766977673 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419202 | GCAACCTCCACCTCC[C/T]GGGTTCACGCCATTC | 10152 |
| rs767014738 | snp | A/C | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327375 | TGATTTAGGAAAACA[A/C]GACACAGTATCTGGA | 10152 |
| rs767014984 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387809 | TGCAGTATTGCTTTG[C/T]TTTCCTTGTCTTGAG | 10152 |
| rs767028309 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354846 | GCTATCTTAGTATCT[C/T]CTAAGACTGTTTTCG | 10152 |
| rs767075547 | snp | A/G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387467 | GCATTCCTTCATCAT[A/G/T]GCCTATTGGGAAAGT | 10152 |
| rs767085964 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203426597 | GAAAAAATATATGTA[G/T]CGGACTCCCATCATT | 10152 |
| rs767087029 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357007 | GAAAACTAAAAAACG[A/G]TTACTTCTTCAAATA | 10152 |
| rs767111046 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339742 | CATTTCAGCATTATT[A/C]ATGGTAACTAAGATA | 10152 |
| rs767181000 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398878 | GTTGCATGTTTAAGT[A/G]TTTCATTACATTTTA | 10152 |
| rs767190257 | in-del | -/AAAG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339601 | AAAAAAAAAAAAGAA[-/AAAG]AAAAAAAGAAAACCC | 10152 |
| rs767190402 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203352204 | TGCCCCCATGCCTAT[A/G]ATCCCAGCTTTTTGG | 10152 |
| rs767207393 | snp | G/T | 0.000426348 | 0.0145943 | intron-variant, missense | ABI2 | GRCh38.p7 | 2:203376126 | TTGCAGTTTGAGATT[G/T]AATGAGGTAAGGGAC | 10152 |
| rs767214339 | snp | A/T | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327303 | AAGGTCATGGCTTCA[A/T]ATCTCAGCAATGGTC | 10152 |
| rs767224760 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357647 | TATTTTAAAAGTGTC[A/G]TGTTATTGAGAACTG | 10152 |
| rs767233160 | snp | A/G | 1.65015e-05 | 0.00287237 | intron-variant, synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203411286 | TTTTGTTTTTGCAGT[A/G]TCTCTTGCTCCTCCT | 10152 |
| rs767243775 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413458 | CTTAAGTAGATGACT[C/G]CAAAACATTATTATA | 10152 |
| rs767254076 | in-del | -/CCCCCGCCGGGGGCCG | 3.58237e-05 | 0.00423209 | intron-variant | ABI2 | GRCh38.p7 | 2:203328668 | GCCGCGTCGGGGACC[-/CCCCCGCCGGGGGCCG]CGCGCCTCGGGGCGT | 10152 |
| rs767284794 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420769 | GATTGTTAAAAAATG[-/A]ATAGTGCCATTAATT | 10152 |
| rs767340451 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203380852 | GCAAGAATAGTGTTA[C/G]GTAAAAGTGATAGGT | 10152 |
| rs767340566 | in-del | -/TTC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387075 | TTTTTTTTTTTTTTT[-/TTC]CCCACATGCCTTTAC | 10152 |
| rs767346323 | in-del | -/TTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400080 | AGTGTGAATAGTGTC[-/TTT]TTTTTTTTTTTTTTT | 10152 |
| rs767348651 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421704 | AGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 10152 |
| rs767371676 | snp | C/T | 1.67438e-05 | 0.00289338 | intron-variant | ABI2 | GRCh38.p7 | 2:203394672 | AAACTTGCTTAATCA[C/T]ACAATACATACGCTC | 10152 |
| rs767381069 | snp | A/G | 1.67108e-05 | 0.00289052 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427332 | AATTACGTTGAGTCT[A/G]TCATGCATTATTCTG | 10152 |
| rs767399321 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398016 | GCAGGGACACAGATT[C/G]AAAGCATATCAATCA | 10152 |
| rs767409494 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357988 | TGACCAGGCTGTCTC[G/T]AACTCCTGACCTCCT | 10152 |
| rs767416627 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427679 | ATCTGGGATCTTTCT[C/T]AGGAATACTGTATAC | 10152 |
| rs767424735 | snp | A/G | 1.64876e-05 | 0.00287116 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394779 | CCTAGCCCAACCCGT[A/G]ATATGGCTCCCTCGC | 10152 |
| rs767435822 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203414855 | AATGAAAAACACCAC[C/T]TCCCAATATAAAGAT | 10152 |
| rs767514176 | in-del | -/TTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331809 | TTTTGCTCAGTGTTC[-/TTTT]TTTTTTTTTTTTTTT | 10152 |
| rs767523057 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425025 | CTACCATGCCAGGCT[A/G]ATTTTTTTTTTTTTT | 10152 |
| rs767534165 | in-del | -/TAA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203340333 | TGTAGTAACTATAGT[-/TAA]TAATATTGTATACTT | 10152 |
| rs767535119 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353745 | TCAAGTGGTCTGTCC[A/G]CCTTGGCGTTCCAAA | 10152 |
| rs767575827 | in-del | -/TCG | 1.66532e-05 | 0.00288554 | intron-variant | ABI2 | GRCh38.p7 | 2:203395800 | AACATTCATGGTGCC[-/TCG]TCTTCACTTTTCCTT | 10152 |
| rs767589658 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406831 | ACCACGCCTGGCTCT[C/T]TTTTTTTCTTTAATA | 10152 |
| rs767591287 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203335130 | ATTTCTTAAAAATTT[C/G]TATATTTTCCCATTA | 10152 |
| rs767664906 | in-del | -/T | 1.648e-05 | 0.0028705 | frameshift-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427243 | AGGAAGGAGCCATTA[-/T]TTATGTCATCAAGAA | 10152 |
| rs767680219 | in-del | -/GGGAGA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203373509 | AGAGGGAGAGGGAGC[-/GGGAGA]GGGAGAGGGAGACTA | 10152 |
| rs767681189 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351484 | TGTCTTTTCATTTAC[A/G]TCATCTTAAAATTTC | 10152 |
| rs767710044 | snp | C/G/T | 3.29588e-05 | 0.00405938 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203417031 | TTGAGTATAGTGATC[C/G/T]TTATGCTGAAGAGGA | 10152 |
| rs767729671 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355034 | TGGATTGTCTGGATT[C/G]TTAACGTTTTAGTCC | 10152 |
| rs767743477 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329206 | ATGCCATTTTTTTCC[C/T]TATGGAGAAGGATGA | 10152 |
| rs767764232 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399659 | AGCTGGGATTACAGG[C/T]ACCCACCACCATGCC | 10152 |
| rs767777928 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203341609 | TAGTGCCTCGGGAGG[C/T]TGAGGCACGAGAGTT | 10152 |
| rs767783691 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343342 | GCACTCTAGCCTGGA[C/T]GACAGCGAGACTATG | 10152 |
| rs767822250 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390971 | CTCCTTTGTTATGTA[G/T]TGTAGCATATTATTT | 10152 |
| rs767822552 | snp | A/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365600 | TCTCTCTCTCAGGCT[A/T]CGTGTTTTCTGGGGC | 10152 |
| rs767828412 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344159 | CATAGTAAAGCTTAG[C/T]GCTTCAACTGTTTAG | 10152 |
| rs767874280 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338321 | CTTTGGTATGGGTCA[C/G]ATGTTTGTTCCCTTC | 10152 |
| rs767880565 | in-del | -/TG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350865 | TTGTTGTGTGTTTTG[-/TG]TGTGTGTGTGTGTGT | 10152 |
| rs767887176 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203401771 | TGATTTGGAATTACG[C/T]CATTTAACCTTTTGT | 10152 |
| rs767888667 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345048 | CGGAGCCCGCAGTGG[C/T]AACCCGCCGGGGTCC | 10152 |
| rs767909336 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413789 | AATTATCTTCAAAGC[-/T]TTCCAGGTATATTAT | 10152 |
| rs767917554 | snp | A/T | 0.000189915 | 0.00974278 | intron-variant | ABI2 | GRCh38.p7 | 2:203351557 | TTTTTTCCTTTAGAG[A/T]TGGGGTCTTGGTATG | 10152 |
| rs767981272 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203417944 | TGAACATGAGAGAGA[C/T]GTGGAATATATCTTT | 10152 |
| rs768030047 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203371421 | TAGGAATATATAGTA[G/T]CAGACACTTTTTTGT | 10152 |
| rs768037070 | snp | G/T | | | intron-variant, missense | ABI2 | GRCh38.p7 | 2:203376090 | TCTTGAGTCGACTTT[G/T]GTGACCAAATTTGGA | 10152 |
| rs768058461 | in-del | -/GTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331063 | TTAGATTTTAAAATA[-/GTTT]ATTTCTTCAGTTTAG | 10152 |
| rs768152672 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330764 | AAAATAAACAGATTT[A/C]TCTCTCTTTTGCAAG | 10152 |
| rs768164887 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430704 | CTGCTAATTTTGCTA[C/T]GTTCCTAAAAGTTAC | 10152 |
| rs768166559 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429128 | TGCAAGTTACAATAG[C/T]TATTTTGCTTTTAGA | 10152 |
| rs768181164 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415566 | AGCTTGCAATGAGCC[A/G]AGATCACACCACTGC | 10152 |
| rs768200359 | snp | C/T | 1.92469e-05 | 0.00310211 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427395 | AGGAATAGTCAGGTC[C/T]TCCCAGATTATCTGA | 10152 |
| rs768218191 | snp | A/C | 3.54843e-05 | 0.00421199 | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328486 | CCCTCTGCGACCTGT[A/C]TGAGGAGGAGGAGGA | 10152 |
| rs768278323 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355657 | CAACATGGAGAAACC[C/G]CGTCTTTACTAAAAA | 10152 |
| rs768278361 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343980 | CTCTACAAAAATTAC[A/G]GAAATTAGCTGGATA | 10152 |
| rs768289509 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421163 | TTTTGGAGATACCTG[A/G]TAATAGTGTAGAGTG | 10152 |
| rs768302263 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376966 | TATTACTGTGTGTTA[C/G]TGTAAATAATAAGTG | 10152 |
| rs768307897 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203349661 | CCGCCTGCCTTGGCC[A/T]CCCAAAGTGGTGGGA | 10152 |
| rs768345558 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419545 | GGGTAATTTTTTGTA[-/T]TTTTTTTTTTTTTGG | 10152 |
| rs768355554 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369884 | TTTAAAAATTTATGT[A/G]TTTTCTAGCATTTGC | 10152 |
| rs768392129 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388901 | AGAATAAAATTCTCT[C/T]TTAAATTCCTGCTCC | 10152 |
| rs768392252 | in-del | -/CTC | 1.64928e-05 | 0.00287161 | intron-variant, cds-indel, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203411294 | TTGCAGTATCTCTTG[-/CTC]CTCCTCCTCCCTCCA | 10152 |
| rs768410491 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203362992 | TACACCACCACGCCC[A/G]GCTATTTTTCGTATT | 10152 |
| rs768445520 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356943 | GTCTTTTTTGTGGGG[C/G]AGGGAATGACCGAAA | 10152 |
| rs768447538 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392715 | TTATGGATTTTGTTG[A/G]GTTTTAAGTCAAGAT | 10152 |
| rs768470452 | in-del | -/AT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392688 | ATTTACATTTATATC[-/AT]GTGTAGTGCCTTATG | 10152 |
| rs768500403 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378013 | TTAACTTTTCTGTTA[C/T]AGTTTTCCCAAGCAG | 10152 |
| rs768516875 | snp | A/T | 1.65559e-05 | 0.00287709 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203366894 | AGCAGATAAGCAGAG[A/T]GCCCTAGAAGAAACC | 10152 |
| rs768575007 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338551 | TCTGCCATGATTACA[C/T]CTCACCAGAAGTACG | 10152 |
| rs768598007 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370740 | GATTCCGAGAGTTTG[C/T]AGAGAAGATTGAGTT | 10152 |
| rs768609353 | snp | C/T | 1.64836e-05 | 0.0028708 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427288 | GGTATGAGGGAGTTA[C/T]GAATGGAGTGACTGG | 10152 |
| rs768616835 | in-del | -/TA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203401651 | TTTTGACCCTCTTTT[-/TA]TATCTTAATTTTTTT | 10152 |
| rs768640262 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360546 | TAAGTAGTGGAGGAC[A/G]GAGATGGTAAGAATA | 10152 |
| rs768680496 | snp | A/G | 3.41933e-05 | 0.00413467 | intron-variant | ABI2 | GRCh38.p7 | 2:203367074 | TTTTCCTATTTGCCT[A/G]TGAGGAACCCTTAAT | 10152 |
| rs768686954 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410702 | CTAGCAGGTGTTTGC[C/T]ACTTACTTAGTATGA | 10152 |
| rs768727482 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384562 | CCATCCTCTCACCTC[A/G]GCCTCCCAAAATGTT | 10152 |
| rs768737716 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403086 | TGAAAGTTGTGTGCA[C/T]ATGAACAGAATTTAG | 10152 |
| rs768737994 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424430 | ATCAGGGTCTCGTTC[G/T]GTCACCTGGGCTGGA | 10152 |
| rs768741304 | snp | A/C | 0.000103686 | 0.00719946 | intron-variant | ABI2 | GRCh38.p7 | 2:203396991 | TTGCTTATTCATTGG[A/C]AGGCAGATGCAGTCA | 10152 |
| rs768809248 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378608 | GCAGTTTAGAAGGAT[A/T]AATGATCAGTGTTCA | 10152 |
| rs768811925 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345834 | TACAGGCGTGAGGCA[C/G]TGTGCCCAGCAATAT | 10152 |
| rs768844600 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203412884 | GATTTAATTACAGTA[C/T]GAGAATTGAAGGACT | 10152 |
| rs768845503 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398379 | GTAATTAAATATTAA[C/T]TGAATAACAGGTGCC | 10152 |
| rs768865627 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357474 | TATGTTCTGAATCTC[A/C]CGAAGATTAACCTCT | 10152 |
| rs768897142 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203386055 | GATCTTTTGGTCCTT[G/T]TCCTGGTGTCCCTTA | 10152 |
| rs768914816 | in-del | -/AG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369629 | GATTAAGTAAAAAAC[-/AG]AAGAATGGATAGAGA | 10152 |
| rs768957658 | snp | A/G | 1.65269e-05 | 0.00287457 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402654 | GGGGCTCGTTGCCCT[A/G]TAGACGCCCTCCTTC | 10152 |
| rs769008194 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346843 | CCTTTATCTTATCTT[A/G]TATTCTTGCAGTGCT | 10152 |
| rs769013230 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421223 | GACCATTTTGGATAA[A/G]CTTTGAAGCAAGGGA | 10152 |
| rs769025104 | in-del | -/GAG | 0.0272057 | 0.113414 | cds-indel, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328488 | CTCTGCGACCTGTAT[-/GAG]GAGGAGGAGGAGGAG | 10152 |
| rs769026395 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431298 | TCAGTGCTCAGTACT[C/T]AATTTTCCACTGCAC | 10152 |
| rs769056552 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385996 | TAACCTCTGTCCTGA[A/G]TTTATACTCTAATTC | 10152 |
| rs769070391 | snp | C/T | 2.48432e-05 | 0.00352434 | intron-variant | ABI2 | GRCh38.p7 | 2:203391170 | AGTAGTAATTGAAAA[C/T]CATTTCATGTAGTAT | 10152 |
| rs769131586 | in-del | -/AACAA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392319 | ACCACCACCACCAAC[-/AACAA]CAACAACAACAACAA | 10152 |
| rs769180413 | snp | C/T | 1.91444e-05 | 0.00309384 | intron-variant | ABI2 | GRCh38.p7 | 2:203391040 | GTTTTCCTTAAAATT[C/T]TTTAGGTGAGTACCC | 10152 |
| rs769251321 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203431988 | GAGTTGGTGGTATTA[C/T]GAGTTGAGTAAAAAC | 10152 |
| rs769272336 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368909 | GCAACCTCGAACTCC[C/T]GGGCTCAAGGGATCC | 10152 |
| rs769276603 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364378 | GGATTACAGGCGTGA[A/G]CCACTGTGGCTGGCA | 10152 |
| rs769279971 | in-del | -/GTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338482 | TTCACGTGAGAACTG[-/GTT]GTTTAAAATTAGTCT | 10152 |
| rs769289822 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364589 | CAAATAACTTTTTGA[C/T]GAGCATGCAAATGTA | 10152 |
| rs769305339 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418623 | AGAAGCGCCAAAAAG[A/T]GAATGCAAGCAAGAC | 10152 |
| rs769317526 | snp | A/T | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427255 | TTATTTATGTCATCA[A/T]GAAGAATGACGATGG | 10152 |
| rs769341470 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345490 | ATCTTAGCTCACTGC[A/T]ATCTCCACCTCCTGG | 10152 |
| rs769362739 | snp | C/T | 3.29881e-05 | 0.00406115 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394734 | ACACTGGAGCCAGTG[C/T]GTCCTCCAGTGGTAC | 10152 |
| rs769380271 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350991 | TAGTTTTAGCTCTTA[C/G]ATTTAGATCTTTGAT | 10152 |
| rs769386616 | snp | C/G | 3.39893e-05 | 0.00412232 | intron-variant | ABI2 | GRCh38.p7 | 2:203417113 | TATCTGGATAGATGG[C/G]AAGAAACCTCTACAT | 10152 |
| rs769424645 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330954 | GTTACTACTATCAAT[C/G]TCTGTTTTAGCAATG | 10152 |
| rs769446560 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343484 | AAATGAGTGATTAAA[A/G]ATAGAATTTCTAGGA | 10152 |
| rs769464448 | snp | A/T | 3.61435e-05 | 0.00425093 | intron-variant | ABI2 | GRCh38.p7 | 2:203391194 | GTAGTATTGTTTAAA[A/T]ATGAAGCACAACATA | 10152 |
| rs769478999 | in-del | -/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387077 | TTTTTTTTTTTTTTT[-/C]CCCACATGCCTTTAC | 10152 |
| rs769519797 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363127 | TGGCCCAGTGCACCT[A/G]GCAGTATTTTAAATA | 10152 |
| rs769542783 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403368 | GTGGACATGGTATGT[C/T]AACTTACTGCTTTTT | 10152 |
| rs769587913 | snp | A/G | 0.000129024 | 0.0080309 | intron-variant | ABI2 | GRCh38.p7 | 2:203351708 | GCCCGGCTGATTTTC[A/G]TATTTTTTGTAGAGC | 10152 |
| rs769595919 | in-del | -/TTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387057 | CGCAGGCTCCCTTCC[-/TTT]TTTTTTTTTTTTTTT | 10152 |
| rs769621171 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203332708 | GTTAACTTGGAATCT[A/T]CGTTTTTACAAATAG | 10152 |
| rs769653754 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203386585 | CTCTATGAAACATTC[C/T]GTAACCTTCCCACAT | 10152 |
| rs769708409 | snp | A/T | 2.32426e-05 | 0.00340892 | intron-variant | ABI2 | GRCh38.p7 | 2:203391002 | CCCAAAAGTGCCACT[A/T]TATTTCACTGCATAC | 10152 |
| rs769758269 | in-del | -/GTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347824 | GTCTAAGGCCTAGCA[-/GTT]GTTTGAGGAACATTT | 10152 |
| rs769771444 | snp | C/T | 0.000237727 | 0.0108999 | intron-variant | ABI2 | GRCh38.p7 | 2:203396977 | CTACAGGTAAGTATT[C/T]GCTTATTCATTGGCA | 10152 |
| rs769797473 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203414544 | TGTGGTTTATGCTGT[A/G]TGCTTCTATAGTATC | 10152 |
| rs769819656 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427711 | CTTGGGATTTCTCCT[C/T]CTGCAGAATCTGTGG | 10152 |
| rs769839523 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388799 | ACAGAAGATACTGCA[A/G]TTTAAACAAAAACAC | 10152 |
| rs769861150 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370797 | AAAGACAAGATCACA[C/T]ATTTATTGGAATGGC | 10152 |
| rs769877930 | snp | A/G | 3.47349e-05 | 0.00416728 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366858 | GAATTAATGATCACT[A/G]GTTTGTTTTTTTTCC | 10152 |
| rs769880133 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406829 | CACCACGCCTGGCTC[-/T]TTTTTTTTTCTTTAA | 10152 |
| rs769888236 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203332444 | ATCCTGGCCAACATG[A/G]TGAAACCGCGTATCT | 10152 |
| rs769908896 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410160 | CTGAGAGGTCATTTC[-/A]ATTGTAGCCCTCCTT | 10152 |
| rs769918101 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203412928 | TCCATTCTACATACT[C/T]CATACAAGGTGGAAA | 10152 |
| rs769932256 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346997 | TTGTTTTAATTTTGT[A/G]TAGTTTTTCTTATTT | 10152 |
| rs770023877 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398570 | AGGTATAACTTATGT[A/C]CAGTAAAATTCACCC | 10152 |
| rs770034713 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203381847 | ATTCATAGGTTTACA[C/T]CCCCCATTCTTATAA | 10152 |
| rs770108006 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203426787 | TAAAGAAAAGCTTTA[-/A]AAAAAAAAAAAAAAA | 10152 |
| rs770115446 | in-del | -/TT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331811 | TTGCTCAGTGTTCTT[-/TT]TTTTTTTTTTTTTTT | 10152 |
| rs770144700 | snp | C/T | 1.64996e-05 | 0.0028722 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203395760 | CTGTTCCTACTCCAT[C/T]TCCTCCCAGTGTCTT | 10152 |
| rs770165171 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359463 | AAAAAATCAATATTT[C/T]TAAAATCTGTTGTAG | 10152 |
| rs770172810 | snp | G/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365531 | CCCTTGAGGTGTTGG[G/T]ATTTTTTTTATTTTA | 10152 |
| rs770180297 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406397 | CCAAGAGATGTGTCT[A/G]TATATAGTTCTATGA | 10152 |
| rs770182587 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203335662 | GTTCTGTAAAGTTTT[A/G]CAGTACTTTTCATAT | 10152 |
| rs770183652 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399619 | CTCGCGGGTTCAAGC[A/G]ATTCTCCTGCCCAGC | 10152 |
| rs770194808 | in-del | -/GAGGAG | 0.000243828 | 0.0110388 | cds-indel, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328488 | CTCTGCGACCTGTAT[-/GAGGAG]GAGGAGGAGGAGGAT | 10152 |
| rs770245720 | in-del | -/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203426805 | AAAAAAAAAAAAAAA[-/C]CACAATATGGTATCT | 10152 |
| rs770313864 | snp | A/G | 3.41495e-05 | 0.00413202 | intron-variant | ABI2 | GRCh38.p7 | 2:203411421 | TTGTAGGCATAAAAT[A/G]TCATTTATATGTGAT | 10152 |
| rs770359669 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421139 | ATATCCATCTACTTA[C/T]GTAACTTTTTTTGGA | 10152 |
| rs770364969 | snp | C/T | 1.65143e-05 | 0.00287348 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203380320 | CCAACCTTGAACGAC[C/T]AGTTCGTTATATTAG | 10152 |
| rs770367287 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354421 | AGTTACCTGTGAATC[C/T]ATCTTTAATTCATCT | 10152 |
| rs770427818 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353296 | TACATTTAAAATTAC[A/C]TTTTGCATTTCCACT | 10152 |
| rs770448546 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364478 | ACTGAACCACCATTG[C/T]GCTGACTTATCCGTA | 10152 |
| rs770449460 | snp | C/G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404367 | TACCAACTGCCTTAA[C/G/T]TGATATATACTTCCC | 10152 |
| rs770456929 | snp | A/G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203334458 | TAGTATGCAGTTTCA[A/G/T]GGTGTGTAAGGTAAT | 10152 |
| rs770459524 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370127 | TATTTTAGGTTTTGT[-/G]GGCCATGTGTTGATA | 10152 |
| rs770484492 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418829 | AACTATAAACTCACA[C/G]ATCCAAGAAGTTCAA | 10152 |
| rs770494178 | in-del | -/TTGGCCAA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425829 | GAGTTCAAGACCAGC[-/TTGGCCAA]CATGGCAAAACCCCG | 10152 |
| rs770512647 | in-del | -/CTTTT | 1.65647e-05 | 0.00287786 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203366892 | CAGCAGATAAGCAGA[-/CTTTT]GAGCCCTAGAAGAAA | 10152 |
| rs770512736 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203340767 | TGTGTGTATCATGTC[A/C]TCATGTTGTACACTT | 10152 |
| rs770514602 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423456 | TCTGAGACGGAGTCT[C/T]GCTCTGTCGCTCAGG | 10152 |
| rs770523535 | snp | C/T | 3.37149e-05 | 0.00410564 | intron-variant | ABI2 | GRCh38.p7 | 2:203417098 | TAAGTTTCAGAAGGA[C/T]ATCTGGATAGATGGG | 10152 |
| rs770561196 | snp | A/C | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416968 | TTGATGAGTCTCCCC[A/C]ACCTCCTCCTCCTCC | 10152 |
| rs770569424 | in-del | -/TG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396439 | TTCAAAATGGAAAAC[-/TG]TTGTTTTTTAGTGTA | 10152 |
| rs770587801 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364216 | TCCTGCCTCAGGCTC[-/A]CTGAGTAGCTGGGAT | 10152 |
| rs770646882 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203352134 | GACACTGTGGTACTG[G/T]CATACAGATACACAT | 10152 |
| rs770650282 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339822 | TGCATGCACAGTTCT[C/T]CTTCAGTCTACATGG | 10152 |
| rs770671214 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364336 | TGACCTCAAATGATC[G/T]GCCCGCCTCAGCCTC | 10152 |
| rs770705051 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342321 | ATTAATGGAGTTGAA[C/T]TGCATATAATATGGG | 10152 |
| rs770705874 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390029 | TGGGTCCAATTCCCA[C/T]TGGAACTAGGACATT | 10152 |
| rs770708704 | snp | C/T | 1.73471e-05 | 0.00294504 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203391076 | ATGAAGATGGGTGGG[C/T]TGCCGCGTACAACAC | 10152 |
| rs770750525 | snp | A/G | 1.64792e-05 | 0.00287042 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203395741 | AGTGTGGGGGTTCCT[A/G]TTGCTGTTCCTACTC | 10152 |
| rs770840415 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382475 | ATTTGTTGAATGAAT[A/G]GTTATTTTGTAATGT | 10152 |
| rs770854737 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399924 | CTTTGATGGCATATC[C/T]AAGAACTCTTTACCT | 10152 |
| rs770875601 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203414673 | CCAGCCATATTAGTT[A/C]ATGTTTGTTGAATAA | 10152 |
| rs770902149 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203375429 | ACTTAAAAAACCCAG[A/G]ATAAATTTGAAATAC | 10152 |
| rs770907223 | snp | C/T | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203325951 | TCGGCTCACTGCAAC[C/T]TACGCCACCCTGGTT | 10152 |
| rs770932826 | snp | A/C | 0.000150071 | 0.00866101 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203396908 | CTGGGGGTGCCCAGA[A/C]CCTTGCTGATGGCTT | 10152 |
| rs770967607 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415135 | ACCCAAGTATATGGT[A/C]AATCACATATCTATA | 10152 |
| rs770968123 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428714 | TCAGTATAAGAAATG[C/T]TGAAAAAAATCCAGG | 10152 |
| rs771054665 | snp | G/T | 0.000162351 | 0.00900828 | intron-variant | ABI2 | GRCh38.p7 | 2:203374860 | TAACTGAGGTAGTGC[G/T]ATCCAGTACAGTCAA | 10152 |
| rs771056688 | snp | A/G | 1.6786e-05 | 0.00289702 | intron-variant | ABI2 | GRCh38.p7 | 2:203411404 | TTATGCTGTAGATCA[A/G]ATTGTAGGCATAAAA | 10152 |
| rs771079599 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203336086 | CTTGGTACTAGAAGT[C/T]CTAATACATTTGAAA | 10152 |
| rs771106761 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398661 | AATCAAGTTACAGAA[C/T]AGTCCTATCATCGCA | 10152 |
| rs771111985 | snp | A/G | 1.65075e-05 | 0.00287289 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203380281 | ATAAAAACACTTCAA[A/G]GACACATAAGATTAT | 10152 |
| rs771116747 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203336941 | TGTTCTTCATCTTTG[C/T]CAGCATTTGGTTTTG | 10152 |
| rs771134584 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424060 | TGCTTTATCAGTTCC[C/G]CATATGATTTTGATA | 10152 |
| rs771150537 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382231 | TCCAGGGCTGGATTT[A/C]CATTCTTTGTTCTTA | 10152 |
| rs771154099 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203328876 | TGTGTCGCGTCCCGC[C/T]TCCTCGCCGCTCCCG | 10152 |
| rs771280260 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408583 | AAAAGACTGCTGTAG[A/G]TTAAGCACCTAATCA | 10152 |
| rs771297033 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354552 | TGTCTGGAAGTTAAC[A/G]GGTTAGCCAGGGAGT | 10152 |
| rs771316531 | in-del | -/GACCC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330205 | TTTGTATTTGAGAAT[-/GACCC]GACCCGAACCACTGT | 10152 |
| rs771346664 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368127 | TCTTGATGTTGTAAG[A/T]TCTTCATAAACATTC | 10152 |
| rs771371754 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355754 | GAGAATCGCTTGAAT[C/G]TGGGAGGCAGAGGTT | 10152 |
| rs771380685 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423352 | TTACCTCCAGGAGTT[G/T]ATAGTGTAGAGAGTT | 10152 |
| rs771449790 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347218 | CTCTGGTCAAACCAT[A/G]GAAGTGAGTTGAGTA | 10152 |
| rs771498738 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203381795 | TGTTTGCCCAATTAC[-/A]TAAGAAAAAAGTAAT | 10152 |
| rs771503136 | in-del | -/TTG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203414119 | TTTTTTTTTTTTTTT[-/TTG]GAGACAGTCTCACTC | 10152 |
| rs771519788 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355829 | GAGCAAAACTGTCTC[-/A]AAAAAAAAAAAAAAA | 10152 |
| rs771544246 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406206 | TGGTCAAGAAGAATA[C/T]ACATATATCTACATG | 10152 |
| rs771562083 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343808 | TTCTCCCTTTCCAAA[A/G]GTAACAGTTTTTGTC | 10152 |
| rs771583589 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410027 | TGGAAACATTTCTGG[C/T]CCTGTGAACTGGTTA | 10152 |
| rs771585397 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392929 | ACCTGTTTTTCCACA[C/T]AGTCTTTGCCTAGTC | 10152 |
| rs771624986 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203395694 | GCCACCCAAGTAGTC[A/G]GAGCAGCAGTCGAGA | 10152 |
| rs771625013 | snp | A/G | 1.65135e-05 | 0.00287341 | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328505 | GGAGGAGGAGGAGGA[A/G]GATGTGAAGATGGCG | 10152 |
| rs771626096 | in-del | -/T | 1.65673e-05 | 0.00287808 | intron-variant | ABI2 | GRCh38.p7 | 2:203411269 | CTTATCCTCCACACC[-/T]TTTTTGTTTTTGCAG | 10152 |
| rs771674901 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421920 | AGTGAGCCAAGATCA[C/T]TCGCCACCGCACTCC | 10152 |
| rs771675300 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353511 | TTGAGACAGAATCTC[A/G]CTCTGTCGCCCAGAC | 10152 |
| rs771693207 | snp | A/G | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326236 | TTAGAGAAAATACTA[A/G]AATCTTTTCTAGGTA | 10152 |
| rs771713104 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425027 | ACCATGCCAGGCTAA[-/T]TTTTTTTTTTTTTTT | 10152 |
| rs771738011 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203395498 | ACATTTTTTTTTAAC[C/T]TGTCACTGACTTGGA | 10152 |
| rs771765247 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365286 | TTCACTTAGTTATAT[C/T]GTAGATATCTTTACA | 10152 |
| rs771805534 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429001 | TCGGATGCAGAAGTT[-/A]ATATTCCACTTAATG | 10152 |
| rs771821945 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392725 | TGTTGGGTTTTAAGT[C/T]AAGATTGTTAGTAAG | 10152 |
| rs771860953 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430537 | AACAAAAATAGTGCC[A/G]ATGTGTCAAAATCGA | 10152 |
| rs771896564 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392487 | TAAAAATAAATTCCA[A/G]CCAGGAATAGGATGA | 10152 |
| rs771909823 | in-del | -/TT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346678 | CATGTTTCTGTTGTC[-/TT]TTAGTTAACATCTTG | 10152 |
| rs771919386 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203375669 | ACTGACAATTGTCTA[C/T]GAATTTATGAATGTT | 10152 |
| rs771985589 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203349285 | TGTGTTTTTTCCACA[A/G]ACAAGAATGTTTTCC | 10152 |
| rs771993455 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384196 | TCAGTGGATAGAATG[A/C]CATATTGGAGGTGTT | 10152 |
| rs771996993 | snp | G/T | 0.000783392 | 0.0197758 | intron-variant | ABI2 | GRCh38.p7 | 2:203395057 | ACATCTCAAAGTGCA[G/T]ACTTCTCTCCAAGTT | 10152 |
| rs772008517 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428987 | AAATTCAGATGGTGT[C/T]GGATGCAGAAGTTAA | 10152 |
| rs772012808 | snp | A/G | | | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402635 | CATACTCCCCCAACA[A/G]TAGGGGGCTCGTTGC | 10152 |
| rs772075747 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361200 | CAGTGCCTTAGCCTG[A/T]CAGTGGCCAACAGGT | 10152 |
| rs772083844 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330018 | CTGGGATTATAGGCG[A/T]GAGGCACCTTTCTTA | 10152 |
| rs772113717 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203401811 | TCATTTTCCTTTAAC[C/T]ATACTTTTTTGCTAC | 10152 |
| rs772158653 | snp | C/T | 4.94817e-05 | 0.00497377 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203366921 | AACCAAAGCCTACAC[C/T]ACCCAATCCTTAGCA | 10152 |
| rs772178472 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410170 | CATTTCATTGTAGCC[C/T]TCCTTACCTCCACCA | 10152 |
| rs772230693 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382374 | GTCTTCATGTTCCTT[C/G]AGGGCAGATATTTTT | 10152 |
| rs772262924 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203412664 | GGGCCGACTCTTCTT[C/T]AGCTTGGGTGTGACC | 10152 |
| rs772264742 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427886 | ATGGCTTTTTTCCTC[A/T]GTGACACTGTAAATT | 10152 |
| rs772270370 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337286 | TTAGAATTAATTAAC[A/G]AATTTAGTAAAGTTG | 10152 |
| rs772302856 | in-del | -/TCAAGA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392711 | GCCTTATGGATTTTG[-/TCAAGA]TTGGGTTTTAAGTCA | 10152 |
| rs772308479 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424354 | TTTCCCTGGAGTGAA[A/G]TAAACTACTGGTGTA | 10152 |
| rs772370930 | in-del | -/AATG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403069 | TTTTAAATAACAAAT[-/AATG]AAAGTTGTGTGCACA | 10152 |
| rs772390993 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356650 | GCTATGATTGCAGGC[A/G]TTAGCCACCATTCCA | 10152 |
| rs772395558 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203333100 | GTTTACAAGGGAATA[C/T]TATCAGTCAGTTTCA | 10152 |
| rs772425921 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432111 | TTAATTTTTTAATTG[C/T]ATTTGGAATTGTTGC | 10152 |
| rs772427492 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406244 | GTGTACATATACTTA[C/T]ATAAGCCTTGTTTGT | 10152 |
| rs772476684 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345619 | TCACCGTCTTGGCCA[A/G]TCTGGTCTCGAACTC | 10152 |
| rs772481773 | in-del | -/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203414488 | TTAACTCTTACTCTT[-/C]CTTCAGGTTTCAGGA | 10152 |
| rs772482568 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356070 | TCTCTCTCTCTGAAA[C/G]CTTATGGAATCATTT | 10152 |
| rs772489879 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203373427 | AGTACAGTCCAGCTT[C/T]TGCTCGGCATCAGAG | 10152 |
| rs772498574 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346718 | GGGAATGAATTAACT[A/T]CTTTAAGGGAAGTGA | 10152 |
| rs772501775 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203394967 | ACTCTATTCTCCCAA[A/C]CCTCATCTGATTTCA | 10152 |
| rs772513302 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203375742 | ATCTAATTTGAATAT[A/G]CTTATTTTCTACAAG | 10152 |
| rs772518444 | snp | C/T | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365036 | GCCACGCCTGGCCAG[C/T]GTTATGCTTTACTCC | 10152 |
| rs772543218 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370602 | CTAAAATACTTTTTC[C/T]AAATGTTTGAGTGTT | 10152 |
| rs772555051 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328281 | GGAGGGAAGGGAGCG[C/T]GCGTGCGCGCGCCCG | 10152 |
| rs772675483 | snp | A/C/G | 3.30323e-05 | 0.0040639 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394714 | GGCGGCACTCCCCCT[A/C/G]TCGCACACTGGAGCC | 10152 |
| rs772692363 | in-del | -/TCTCTC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370191 | CATTCTCCTATTCTC[-/TCTCTC]TCTCTCTCTCTCTCT | 10152 |
| rs772701066 | snp | A/G | 0.000293314 | 0.0121066 | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328506 | GAGGAGGAGGAGGAG[A/G]ATGTGAAGATGGCGG | 10152 |
| rs772705687 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392955 | TAGTCACCACATTTT[-/G]TTCCTTTGCTCCTTT | 10152 |
| rs772727716 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203431993 | GGTGGTATTATGAGT[C/T]GAGTAAAAACCATCC | 10152 |
| rs772754179 | snp | A/C | 7.12581e-05 | 0.00596858 | intron-variant | ABI2 | GRCh38.p7 | 2:203328666 | GGGCCGCGTCGGGGA[A/C]CCCCCCGCCGGGGGC | 10152 |
| rs772762608 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361750 | AGGAAAATTTAAAAG[A/G]GCCATTAACATAGAC | 10152 |
| rs772786064 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203340539 | ACATGGCTAATTTTT[-/G]TAGTGACGGGGTTTC | 10152 |
| rs772802114 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203332881 | GAGTGACAGTTCACA[G/T]AGATGCATAGTAAAA | 10152 |
| rs772804830 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361583 | AGTATAGAAGTTGAC[A/G]GAATGCTAAGGAAAA | 10152 |
| rs772839835 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351028 | TGAGTTAATTTTTGC[A/T]TATGTTGTAAAGTAG | 10152 |
| rs772873316 | snp | G/T | 5.03149e-05 | 0.00501547 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427336 | ACGTTGAGTCTATCA[G/T]GCATTATTCTGAGTA | 10152 |
| rs772890174 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331087 | TTCAGTTTAGCATCT[G/T]AAGTATATTTTACAC | 10152 |
| rs772910093 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364438 | TTGAACCCGGGTCTC[C/T]TGTGTGAAAGGCGAG | 10152 |
| rs772959095 | in-del | -/AA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342749 | CCACCATGCCTGGCT[-/AA]AATCGCCCTCAAAAC | 10152 |
| rs772964560 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203412941 | CTCCATACAAGGTGG[A/G]AAGTCTAAGTAAATG | 10152 |
| rs773031186 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339450 | CTGGGTGTGGTTGGC[A/G]GGTGTCTGCAGTCCT | 10152 |
| rs773061461 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203386869 | GTCTCTGAACTCCTG[A/G]CCTCAGGCGATCTGC | 10152 |
| rs773086881 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370805 | GATCACACATTTATT[G/T]GAATGGCAATAAGCC | 10152 |
| rs773118836 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203336713 | GTATCTTTTACTACT[A/G]TTCCTTCTGCCCTCC | 10152 |
| rs773140787 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427782 | CATGGCCCAGTGGGT[A/T]CCCTAGCCCCTTCTT | 10152 |
| rs773141076 | snp | A/C | 0.000134707 | 0.00820582 | intron-variant | ABI2 | GRCh38.p7 | 2:203395112 | AAAAATTATGGACCA[A/C]ATGTGGGAAATGTCA | 10152 |
| rs773145490 | in-del | -/TTGTTTTTGTTTTTGTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384276 | TCCTGTTCCATACTC[-/TTGTTTTTGTTTTTGTTT]TTTTTTTTTTTTTTT | 10152 |
| rs773212762 | in-del | -/CCT | 1.64838e-05 | 0.00287083 | cds-indel, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416969 | GATGAGTCTCCCCCA[-/CCT]CCTCCTCCTCCTCCA | 10152 |
| rs773240579 | snp | A/C | 1.74943e-05 | 0.00295751 | intron-variant | ABI2 | GRCh38.p7 | 2:203367093 | GGAACCCTTAATAAT[A/C]AACACAGGCTATCTG | 10152 |
| rs773241880 | snp | A/G | 1.6525e-05 | 0.00287441 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402683 | TCCATTACTTCACAA[A/G]CAAGCCTTCAGAATC | 10152 |
| rs773258400 | in-del | GAGACGGAGTCTCACTC/TTTGGGGGTTTCCCCTTTT | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365648 | TTTTTTTTTTTTTTT[lengthTooLong]TGTTGCCCAGGCTAG | 10152 |
| rs773281313 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203373869 | GCTTTTACTGTCTAA[A/G]AACTTTAGGCTGGGT | 10152 |
| rs773281754 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356817 | CATATTTTAAAATGC[A/G]GTTATTTCTGAAAGT | 10152 |
| rs773300888 | snp | C/G/T | 3.37971e-05 | 0.00411067 | intron-variant | ABI2 | GRCh38.p7 | 2:203411243 | CCTTTTAATGTAACT[C/G/T]GCCCTTATCCCTTAT | 10152 |
| rs773316179 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378840 | AACTCTTTTGACTGC[A/G]ACACACAGGAAAAAA | 10152 |
| rs773320943 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347817 | GCAGTTTGTCTAAGG[A/C]CTAGCAGTTGTTTGA | 10152 |
| rs773357068 | in-del | -/TATATC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353990 | ATTCATTGTATCCAT[-/TATATC]TATATAAGTAATCAC | 10152 |
| rs773360186 | snp | G/T | 1.64882e-05 | 0.00287121 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203366942 | ATCCTTAGCAAGTGT[G/T]GCCTATCTGATAAAC | 10152 |
| rs773372340 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203414610 | TTTGGTCGTTCATGT[C/T]TTCATGACTTTTGCC | 10152 |
| rs773386266 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353556 | ATGGTCTTCTCTCAC[A/G]GCAACCTCTGCCTCC | 10152 |
| rs773397612 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399795 | GCTGGGATTACAGGC[A/G]TGAGCCACTGGGTCC | 10152 |
| rs773450728 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403331 | GAGAGGGCAAGAACA[A/C]ATATTAGACACCATG | 10152 |
| rs773481513 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379098 | CTCTGTTAGCAAATA[A/G]AAGATTGTAATTACA | 10152 |
| rs773488724 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203335853 | ATATGGTACAAGTCA[C/T]CCTTTTTAGGTGTAA | 10152 |
| rs773562643 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368015 | TCTCCAAAAAAAAAT[A/T]AAAAAAAGTAGCCAG | 10152 |
| rs773621072 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328325 | GCGGTGACCGTCCTC[C/G]GAGTCCGTCGGCTCG | 10152 |
| rs773704866 | snp | A/G | 2.79685e-05 | 0.00373945 | intron-variant | ABI2 | GRCh38.p7 | 2:203391182 | AAACCATTTCATGTA[A/G]TATTGTTTAAAAATG | 10152 |
| rs773756610 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203390505 | GTCGTGGTGGCATGC[A/G]CCTGTAGTACCAGCT | 10152 |
| rs773756806 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354434 | TCTATCTTTAATTCA[C/T]CTCTAAACTCTCCTC | 10152 |
| rs773816024 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347283 | GGAAGGATGATATCC[C/T]GACTCCCAGTTTATG | 10152 |
| rs773818297 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382750 | ATTCAGTGACACGGG[-/T]TTTTTTTTTTAAGTT | 10152 |
| rs773841332 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408022 | GTCCTGGAGAAAAGT[A/G]GAATTTGGGATGACC | 10152 |
| rs773849369 | snp | A/C | 1.64874e-05 | 0.00287113 | synonymous-codon, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394763 | ACCAAATGATTACGT[A/C]CCTAGCCCAACCCGT | 10152 |
| rs773856098 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418390 | GCAATCAAGGTATCA[A/G]CTGAGGCTGCAGTGA | 10152 |
| rs773871236 | in-del | -/ACTG | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428599 | ATAAAAATTAATATA[-/ACTG]ACACAATAAAACACA | 10152 |
| rs773879810 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403904 | TTACAGGCACCCACG[A/T]CCACACCCAGCTAAT | 10152 |
| rs773894596 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406417 | TAGTTCTATGAGATA[C/T]AGGAGTTTCTGAATG | 10152 |
| rs773902631 | snp | A/G | 1.66643e-05 | 0.0028865 | intron-variant | ABI2 | GRCh38.p7 | 2:203394882 | CAAAATGTGATGGTC[A/G]TAGTACCATAATCTG | 10152 |
| rs773912918 | in-del | -/G | 8.22447e-05 | 0.00641214 | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328505 | GGAGGAGGAGGAGGA[-/G]GATGTGAAGATGGCG | 10152 |
| rs773919906 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387312 | GAAGTATTGAATGTA[C/T]CAAAGAAGGTAGAGC | 10152 |
| rs773954198 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364261 | ACCACACCCAGCTAA[-/T]TTTTGTATTTTTAGT | 10152 |
| rs773956643 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203375542 | AATGTCAAAGAATAT[A/C]ATGAGGGCAAATGCC | 10152 |
| rs773980418 | in-del | -/CC | 1.65548e-05 | 0.002877 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203366896 | CAGATAAGCAGAGAG[-/CC]CTAGAAGAAACCAAA | 10152 |
| rs773991929 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344832 | CACCAATCTGCACTT[C/T]GTAAAAACGCACCAG | 10152 |
| rs774017421 | snp | A/C | 2.82721e-05 | 0.00375969 | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328501 | ATGAGGAGGAGGAGG[A/C]GGAGGATGTGAAGAT | 10152 |
| rs774024477 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388909 | ATTCTCTCTTAAATT[A/C]CTGCTCCTTTTCCTT | 10152 |
| rs774043952 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388574 | TAATCCCAGCTACTC[C/G]GGAGGCTGAGTCAGG | 10152 |
| rs774080173 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203426293 | TAGGTACAGAAGATG[A/G]AGAGGTTGGAGCAAA | 10152 |
| rs774134853 | snp | A/G | 3.44359e-05 | 0.00414931 | intron-variant | ABI2 | GRCh38.p7 | 2:203417127 | GGAAGAAACCTCTAC[A/G]TAGAAATGAAATTTG | 10152 |
| rs774138497 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398673 | GAACAGTCCTATCAT[C/T]GCAAAAATTTCCTCC | 10152 |
| rs774142395 | in-del | -/AAT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388685 | GACTCTGTCTTAAAA[-/AAT]AATAATAATAATAAT | 10152 |
| rs774144219 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339902 | ATCCTGCAGTCACCC[-/T]TGTGGAACGCGTGTA | 10152 |
| rs774156753 | in-del | -/AG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331675 | ATTTAGCCTTATTAT[-/AG]AGCATCATGTCTTAG | 10152 |
| rs774191683 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203414743 | CCATCCCATAATAGT[A/G]TAGCTTTTAAGATAA | 10152 |
| rs774200941 | in-del | -/AC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203395446 | AATATATATATATAT[-/AC]ATACACACACACACA | 10152 |
| rs774204082 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203333056 | ATCAATGTGGATACT[C/G]CCAGAGTTCACTAAA | 10152 |
| rs774222086 | snp | A/G | 1.66214e-05 | 0.00288278 | synonymous-codon, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427328 | TGGGAATTACGTTGA[A/G]TCTATCATGCATTAT | 10152 |
| rs774227777 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357956 | GTATTTTTAGTAGAG[A/T]TGAGGTTTCACCATA | 10152 |
| rs774229334 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374017 | TGCAAAAATTAGCCA[G/T]GTGTGGTGGTGCACA | 10152 |
| rs774239555 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342658 | GATCTCAGCTCACTG[C/T]AGCCTCTGCCTCCTG | 10152 |
| rs774280959 | snp | C/T | 1.65403e-05 | 0.00287574 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203366898 | GATAAGCAGAGAGCC[C/T]TAGAAGAAACCAAAG | 10152 |
| rs774348099 | in-del | -/AGAG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392535 | AAAATAATTCTGCTT[-/AGAG]AGAGAGAAAATCTAG | 10152 |
| rs774361633 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382326 | ATAATTCCTCCTTTT[A/T]GTTTTATTTTTTGTC | 10152 |
| rs774375379 | snp | C/G | 0.000132151 | 0.0081276 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402665 | CCCTATAGACGCCCT[C/G]CTTCCATTACTTCAC | 10152 |
| rs774424187 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347132 | TTTGTAGTTGGTTTT[A/T]TTGGAGCCATTGCAT | 10152 |
| rs774448053 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203336094 | TAGAAGTCCTAATAC[A/C]TTTGAAAATCATCAG | 10152 |
| rs774449659 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203380524 | TGAAGATTCCTTGCT[A/G]CTATAACTGTTTTAC | 10152 |
| rs774490522 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400168 | TCTCGGCCCACTGCA[A/G]TCTCCGCTGCCTGGA | 10152 |
| rs774565452 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427813 | TCTTCCACTTGTATG[-/C]AAGAGGAGGGAACCA | 10152 |
| rs774625169 | in-del | -/TGTG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203358072 | TGTGCCTGGCCTGTT[-/TGTG]TGTGTGTGTGTGTGT | 10152 |
| rs774650965 | snp | C/T | 0.000164082 | 0.00905617 | intron-variant | ABI2 | GRCh38.p7 | 2:203355178 | TTTGACAGTGCATAT[C/T]CTCTGGTGCTTCCTG | 10152 |
| rs774691484 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368931 | AAGGGATCCTCCTGC[C/T]TCAGCCTCTCAAGTA | 10152 |
| rs774709338 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355901 | CTTCAACTTTCACTA[C/G]ATGGTTTGACTAGAT | 10152 |
| rs774715001 | in-del | -/TGTGTGTATA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338922 | CTGTGTGTGTGTGTG[-/TGTGTGTATA]TGTGTGTATATGTAT | 10152 |
| rs774718716 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369316 | TATATTTGAGTTCCT[A/G]AAAAGGAGGAACAAG | 10152 |
| rs774776788 | snp | A/G | 1.65362e-05 | 0.00287538 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203380331 | CGACCAGTTCGTTAT[A/G]TTAGAAAACCTATTG | 10152 |
| rs774826200 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342933 | TTTAATCATTCATGC[A/G]TTTGTTTATAATGCA | 10152 |
| rs774855487 | snp | C/T | 1.64882e-05 | 0.00287121 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416963 | AGTCTTTGATGAGTC[C/T]CCCCCACCTCCTCCT | 10152 |
| rs774940590 | in-del | -/TTTTTGTTTTTTTTTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384285 | ATACTCTTGTTTTTG[-/TTTTTGTTTTTTTTTTT]TTTTTTTTTTTTTTT | 10152 |
| rs774940754 | in-del | -/T | 1.65673e-05 | 0.00287808 | intron-variant | ABI2 | GRCh38.p7 | 2:203411268 | CTTATCCTCCACACC[-/T]TTTTTTGTTTTTGCA | 10152 |
| rs774976458 | snp | C/G | 1.70214e-05 | 0.00291726 | intron-variant | ABI2 | GRCh38.p7 | 2:203417116 | CTGGATAGATGGGAA[C/G]AAACCTCTACATAGA | 10152 |
| rs774990502 | snp | A/C | 1.64895e-05 | 0.00287132 | synonymous-codon, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394742 | GCCAGTGCGTCCTCC[A/C]GTGGTACCAAATGAT | 10152 |
| rs775012472 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203371152 | TTTTGCGATTCTCAC[-/A]AAATGAGCTTGATTT | 10152 |
| rs775014475 | snp | G/T | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203326403 | CTTCTTCAACATTAT[G/T]TTTTGATCTATTGAA | 10152 |
| rs775079485 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361266 | TTCCTGAGGGGATGG[A/G]AGTCAATTCTCGGGC | 10152 |
| rs775086263 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368678 | CAAACTTCTGCAGAC[A/G]TATCATTTATTGCTT | 10152 |
| rs775090958 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203375670 | CTGACAATTGTCTAC[A/G]AATTTATGAATGTTA | 10152 |
| rs775100961 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413420 | GTAAAGTGCATGACT[A/G]TCACTTTAAGACTTA | 10152 |
| rs775142811 | snp | A/G | 6.59707e-05 | 0.00574291 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394735 | CACTGGAGCCAGTGC[A/G]TCCTCCAGTGGTACC | 10152 |
| rs775190810 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353514 | AGACAGAATCTCGCT[C/G]TGTCGCCCAGACTGG | 10152 |
| rs775219246 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203414943 | AAGTAGTAGCTTATT[A/C]AACTGGCAGTTACAA | 10152 |
| rs775224376 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343901 | TTGGGAGGCTGAGGT[A/G]GGAGGATTGCTTGAG | 10152 |
| rs775274261 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203349364 | TTTCCACTGTCTAAT[C/T]CTGAAGTCTCCATTA | 10152 |
| rs775285620 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376865 | TCACATCTCTATAAG[A/G]TCAAATGAACAGATT | 10152 |
| rs775286196 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347977 | GGGCGCAGGTGGCTC[A/G]TGCCTATAATCCCAG | 10152 |
| rs775287796 | in-del | -/TT/TTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403742 | TGTTCTTTCTTTCTG[-/TT/TTT]TTTTTTTTTTTTTTT | 10152 |
| rs775292738 | in-del | -/GAT | | | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432501 | CAGACAAACACTGAA[-/GAT]GATGGGTGTTGACTA | 10152 |
| rs775315122 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356608 | CTCCTGAGCTCAGGC[A/G]ATCCACCCACCTTGG | 10152 |
| rs775324577 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387094 | CCACATGCCTTTACT[C/T]TTGTACCTAGAGGGT | 10152 |
| rs775379479 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203388875 | TCAAATATTTTAGCT[-/A]TCCCATGTATAGAAT | 10152 |
| rs775394258 | in-del | -/TG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203426365 | CCAGTATAACTAAAC[-/TG]TTGAAATTGATATAA | 10152 |
| rs775419215 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203327967 | GAGGGAGAAAAGCCT[C/G]GAGAAGTTCCCTAGG | 10152 |
| rs775422347 | snp | C/T | 0.000257367 | 0.011341 | intron-variant | ABI2 | GRCh38.p7 | 2:203396983 | GTAAGTATTTGCTTA[C/T]TCATTGGCAGGCAGA | 10152 |
| rs775460279 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203368280 | ATATAAAAATGATAA[A/G]GGTTTTGGTCTGCCT | 10152 |
| rs775475305 | snp | A/G | 0.000642219 | 0.017908 | intron-variant | ABI2 | GRCh38.p7 | 2:203351710 | CCGGCTGATTTTCGT[A/G]TTTTTTGTAGAGCCA | 10152 |
| rs775519820 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410403 | CTGTAACTGTAGAGT[A/G]ATCTTTTTTCTTTCT | 10152 |
| rs775556896 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203401932 | TAGTTTTCAGTGTTC[A/G]GTGGCTGTATTTTGG | 10152 |
| rs775580723 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369755 | TGGAGGGGTAATAGA[C/T]CTGCAATTCTCAGTG | 10152 |
| rs775611974 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203400226 | CTGAGGAGCTGGGAT[G/T]ACAAGTGTGAGCCAC | 10152 |
| rs775631405 | snp | A/T | 2.02879e-05 | 0.00318489 | intron-variant | ABI2 | GRCh38.p7 | 2:203391032 | CAAGTTGAGTTTTCC[A/T]TAAAATTTTTTAGGT | 10152 |
| rs775650613 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351189 | TTTCTGGACTCTGAA[A/T]TCCATTGATCTATAT | 10152 |
| rs775680412 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356105 | CTCATGATGATGATC[A/C]TTCCTACGGGTCTTT | 10152 |
| rs775680986 | snp | A/C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331419 | GTGTAGTGGCGCGAT[A/C/G]TCGATCTCTGCTCAC | 10152 |
| rs775742502 | snp | A/G | 1.75804e-05 | 0.00296478 | intron-variant | ABI2 | GRCh38.p7 | 2:203416857 | GCTTGGATAGGAAAT[A/G]CTGAACTTTGCATAA | 10152 |
| rs775748934 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203337409 | CAGCAGAAAGAATAG[A/G]ATACTTAGGAATAAA | 10152 |
| rs775757932 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424417 | TTAAAAATTACTTAT[C/T]AGGGTCTCGTTCTGT | 10152 |
| rs775797737 | snp | C/G | 1.65168e-05 | 0.00287369 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203380322 | AACCTTGAACGACCA[C/G]TTCGTTATATTAGAA | 10152 |
| rs775798093 | snp | C/G | 1.65578e-05 | 0.00287726 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203395777 | CCTCCCAGTGTCTTT[C/G]CAGGTAAAACATTCA | 10152 |
| rs775805257 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203349337 | TAACAATCAGGAAAT[A/G]ATATTGATATATTTC | 10152 |
| rs775878543 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356701 | TGTGGAGATGATGTC[C/T]CACCATGTTGCCCAG | 10152 |
| rs775878653 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345070 | CCGGGGTCCTCTTCC[A/G]TGCTGTGGAAGCTTT | 10152 |
| rs775917096 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203419037 | TTGAGCAAAATCTTC[A/G]AAGTAATGAAGGAAA | 10152 |
| rs775985943 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203429210 | ACATTCCACTTCGTG[C/T]TTTTCTTAGGTCATT | 10152 |
| rs775991724 | in-del | -/AA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203395217 | GTATGATTATTAATT[-/AA]AATTACTCAAATCTG | 10152 |
| rs776008104 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392863 | CAATGGTTCTGCAAG[A/G]TCCTTGGGGACCAGA | 10152 |
| rs776036611 | in-del | -/TGTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203358112 | GTGTGTGTGTGTGTG[-/TGTT]TGTTTGTTTGTTTGT | 10152 |
| rs776052531 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203412231 | AATGGGCACTGCCAG[-/T]ACTAGAATGTAAGCT | 10152 |
| rs776081441 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203333248 | AATGGAAAATTGCCC[C/G]ATCATCTTGAATATA | 10152 |
| rs776095801 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399234 | GCTTTAGCCATTCCA[A/G]TACATGTGTAATGGT | 10152 |
| rs776106872 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378738 | TGGGACTGGGGAGGA[C/G]TTAGCAAAAAATGTG | 10152 |
| rs776130502 | snp | C/G | | | downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203432267 | GACTTTTCTGTTGCT[C/G]TAAACCAGGGAGCTG | 10152 |
| rs776141007 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364360 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 10152 |
| rs776149092 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410519 | TAGGCACTGTGCCAG[C/G]TGATTGAGGTGCAGG | 10152 |
| rs776174355 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364768 | GAGACAGGGTCTTGC[-/T]TTGTTACCCAGGCCA | 10152 |
| rs776214950 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203416527 | TCTTGAACTTCTGAC[C/T]TCAGGTGATCCGCCT | 10152 |
| rs776221809 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396554 | TTTCAATTGAAAAGG[A/T]ATGTTTGTTTTTAAT | 10152 |
| rs776230129 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328202 | GTCGCTAGGAGACGC[C/T]GGAAGTGGGGGAGGG | 10152 |
| rs776232178 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344840 | TGCACTTTGTAAAAA[C/T]GCACCAGTCAGCGCT | 10152 |
| rs776245189 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203382245 | CCATTCTTTGTTCTT[-/A]ATGTAGAATATTACA | 10152 |
| rs776293525 | in-del | -/TTTTG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384285 | TACTCTTGTTTTTGT[-/TTTTG]TTTTGTTTTTTTTTT | 10152 |
| rs776299849 | snp | A/G | 0.000101521 | 0.00712392 | intron-variant | ABI2 | GRCh38.p7 | 2:203417103 | TTCAGAAGGATATCT[A/G]GATAGATGGGAAGAA | 10152 |
| rs776322203 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344010 | ATAGAGGTGTGTGAT[A/G]GTGTCCCAGCTAGTT | 10152 |
| rs776374672 | in-del | -/AT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374764 | AAAAAAAATTGAGAC[-/AT]ATTTAAAAACACCCA | 10152 |
| rs776400193 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370040 | AAAACATTTTCTGCT[A/T]ACAAAACAAATAGTA | 10152 |
| rs776415271 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430762 | TTTTTCCTACTGCTG[C/G]TGTTTATTATCCAGC | 10152 |
| rs776427248 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330849 | TATAAAGGTAAAAGG[A/G]TAAGGATTATTAAAG | 10152 |
| rs776449038 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338565 | ACCTCACCAGAAGTA[C/T]GTGCCAGCACTGTGC | 10152 |
| rs776463030 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203363085 | ATCCGCCTGCCTCGG[A/C]CTTGCAAACTTTTGG | 10152 |
| rs776488458 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424458 | GGAGTGCAGTGGTAC[A/G]TTCAGTGCTTACTGC | 10152 |
| rs776506090 | snp | C/G/T | 3.29686e-05 | 0.00405998 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203395750 | GTTCCTATTGCTGTT[C/G/T]CTACTCCATCTCCTC | 10152 |
| rs776511177 | in-del | -/GCATGCTTTAACCCAGGGGTTGGCAAACCTTTTCTG | 1.76443e-05 | 0.00297016 | intron-variant | ABI2 | GRCh38.p7 | 2:203380409 | TTTTTTTCAAGCTTT[lengthTooLong]TAAAAGTAGTAACCC | 10152 |
| rs776513186 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203328886 | CCCGCCTCCTCGCCG[C/G]TCCCGCCCTCGGCCG | 10152 |
| rs776543370 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203412994 | TTCCATCACAAATCC[A/G]GTTTAATCACAATGA | 10152 |
| rs776563773 | snp | C/T | 7.59013e-05 | 0.00615994 | intron-variant | ABI2 | GRCh38.p7 | 2:203328670 | CGCGTCGGGGACCCC[C/T]CCGCCGGGGGCCGCG | 10152 |
| rs776596309 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203383486 | GTGATAGAAATACAC[A/G]GAAAGTTTAATTGAA | 10152 |
| rs776704366 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203397239 | TTTTAAGTTTAATAT[A/G]GAGCTACCTTCTATA | 10152 |
| rs776704380 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357527 | TAACCTCCTTTTTCT[A/G]AAGTGCTCCTCTGAC | 10152 |
| rs776707397 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356750 | AAGCAATCTTCCTGC[C/G]TCGACCTCCCAGAGT | 10152 |
| rs776714066 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203410713 | TTGCCACTTACTTAG[C/T]ATGAAGTCAGTAAGT | 10152 |
| rs776716196 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425456 | GTCTGCCTGCCTTGG[C/T]CTCCCAAAGTGTTGG | 10152 |
| rs776729253 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351514 | CTTTCAATGATGTTT[G/T]GTAGTTTTCAGTGTT | 10152 |
| rs776742630 | snp | A/G | 1.65072e-05 | 0.00287286 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203380282 | TAAAAACACTTCAAG[A/G]ACACATAAGATTATT | 10152 |
| rs776767859 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384565 | TCCTCTCACCTCGGC[C/T]TCCCAAAATGTTGGG | 10152 |
| rs776824437 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346034 | AAAATACACACGCGC[A/G]CACACACACACAAAC | 10152 |
| rs776879629 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406647 | GGCTTTAGCAAAGTA[C/T]AAATAAAGAGCAGGA | 10152 |
| rs776890593 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378900 | TCATGTATATATTTA[C/T]ATATATAATAAACAG | 10152 |
| rs776910631 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347513 | CCACCCAAGGAAAAT[A/G]TGCAGTGGAAACTCA | 10152 |
| rs776935034 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203334537 | TTACACCCACCCCAA[A/C]TCCATTTTGCAGCAC | 10152 |
| rs776959699 | in-del | -/TTGTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384288 | CTCTTGTTTTTGTTT[-/TTGTTT]TTTTTTTTTTTTTTT | 10152 |
| rs776996207 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379809 | TGGCTCATCTCTGCC[A/G]TTACAGTGTAAAGCC | 10152 |
| rs777010728 | snp | C/G | 0.00011602 | 0.00761554 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402700 | AAGCCTTCAGAATCA[C/G]ATGAATGGAGGACCT | 10152 |
| rs777024920 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346923 | CTGCCCGACTTCATG[C/T]GCTATAGTGCATTTT | 10152 |
| rs777047555 | in-del | -/AACAA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392316 | ACCACCACCACCACC[-/AACAA]CAACAACAACAACAA | 10152 |
| rs777065760 | snp | C/G | 1.66308e-05 | 0.00288359 | intron-variant | ABI2 | GRCh38.p7 | 2:203411259 | GCCCTTATCCCTTAT[C/G]CTCCACACCTTTTTT | 10152 |
| rs777075357 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364602 | GACGAGCATGCAAAT[A/G]TAAAATACACTTCAG | 10152 |
| rs777140296 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203395710 | GAGCAGCAGTCGAGA[A/G]AACAGTGGAAGTGGT | 10152 |
| rs777175812 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203358268 | CAAGTAGCTGGGACT[-/A]ACAGGTGTATGCCAC | 10152 |
| rs777250441 | snp | G/T | 1.79512e-05 | 0.00299588 | intron-variant | ABI2 | GRCh38.p7 | 2:203402566 | TATGTATGTTCTATC[G/T]CTTTTTCAGGTCATC | 10152 |
| rs777261282 | in-del | -/CA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423990 | AGTCCTTTTCTGTTT[-/CA]GTCATAACTGCACAA | 10152 |
| rs777271375 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203352266 | GAAGTTCAAGGTTAC[A/G]GTGATAATAATAAAG | 10152 |
| rs777275411 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365301 | CGTAGATATCTTTAC[A/G]TAGCAGTAATGCATA | 10152 |
| rs777284291 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346659 | GCTGTTCTCTTTCTC[A/G]TTCCATGTTTCTGTT | 10152 |
| rs777293121 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203345635 | CTGGTCTCGAACTCC[-/T]TGACTTCAGGTGATC | 10152 |
| rs777305006 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357129 | AATAGATATAAAATT[A/T]GTGATTTGTTACTTT | 10152 |
| rs777308248 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203393311 | CTGCCTGCCCCGGCC[C/T]CCCGAAGTGCTGGGA | 10152 |
| rs777308401 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423614 | ATTTTTAGTAGAGGC[A/G]GGGTTTCACCATATT | 10152 |
| rs777328983 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392531 | GGACAAAATAATTCT[G/T]CTTAGAGAGAGAGAA | 10152 |
| rs777373992 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398150 | ACTTTTAGCCAAAAT[A/G]GATTTTGGGTGATGT | 10152 |
| rs777390135 | snp | A/G | 0.000153128 | 0.00874874 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203396884 | CCTCCACTGCCCCAG[A/G]CGCTGCTGCTGGGGG | 10152 |
| rs777414061 | snp | A/G | 3.55429e-05 | 0.00421547 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366849 | GTTATTTTTGAATTA[A/G]TGATCACTGGTTTGT | 10152 |
| rs777468584 | snp | A/G | 7.14426e-05 | 0.0059763 | intron-variant | ABI2 | GRCh38.p7 | 2:203380420 | GCTTTTAAAAGTAGT[A/G]ACCCATAATGAAACC | 10152 |
| rs777483494 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203334431 | TTTTCTTTTAAAATG[C/G]AGGGAATTTAATAGT | 10152 |
| rs777503103 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353235 | ATAAAAATACAGTTG[A/C]TTTTGTATATTGATC | 10152 |
| rs777521489 | snp | C/T | 1.69965e-05 | 0.00291513 | intron-variant | ABI2 | GRCh38.p7 | 2:203416905 | AGCCTGATACGTTCT[C/T]AGTTTCAGATACACC | 10152 |
| rs777548696 | in-del | -/T | | | frameshift-variant, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203394713 | AGGCGGCACTCCCCC[-/T]ATCGCACACTGGAGC | 10152 |
| rs777562612 | in-del | -/TG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203358074 | TGCCTGGCCTGTTTG[-/TG]TGTGTGTGTGTGTGT | 10152 |
| rs777579796 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366674 | TGCAAAGATGTGTCT[A/G]TTCAACATGAAAACA | 10152 |
| rs777608395 | snp | A/G | 0.000165196 | 0.00908685 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203380266 | GTATTTTGACTACCA[A/G]TAAAAACACTTCAAG | 10152 |
| rs777656924 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203420512 | CATTCTCCTGCCTCA[G/T]CCTCCTGAGTAGGTG | 10152 |
| rs777663487 | in-del | -/AA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330394 | TGAGACTACATATCA[-/AA]AAAAAAAAAAAAAAA | 10152 |
| rs777695541 | snp | A/G | | | upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203327653 | GCGAATCATAGAAAT[A/G]GCAAACATAAAAAGC | 10152 |
| rs777699107 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342139 | AGTAAAATGAACTTA[C/T]GACTCACACCATTTA | 10152 |
| rs777725551 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339719 | AGAGACATCTGCACA[C/T]CCATGTTCATTTCAG | 10152 |
| rs777730826 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203389915 | ACACTTGCATTTTCA[G/T]TTGGGGATAGAATAG | 10152 |
| rs777732462 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203391554 | TGTGTTGGCTCATGC[C/T]TGTAATTCCCAAAGT | 10152 |
| rs777779743 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203353955 | CTTCTTAACATGTAG[A/G]TTTAGCAACTTTTAG | 10152 |
| rs777791291 | in-del | -/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355433 | AGAGGATTGCTTGAG[-/C]CCTGAGAGTTTGAAG | 10152 |
| rs777902314 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203415969 | GACATTTAGCCTGAA[G/T]AAATTCTGAATTATA | 10152 |
| rs777904024 | snp | A/G | 5.02063e-05 | 0.00501005 | intron-variant | ABI2 | GRCh38.p7 | 2:203411396 | TGTCTTCTTTATGCT[A/G]TAGATCAGATTGTAG | 10152 |
| rs777951265 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374498 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 10152 |
| rs777951390 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350226 | GGATTATGGGTGTGC[A/G]TTACTATGCCCGGCT | 10152 |
| rs777962366 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359472 | ATATTTTTAAAATCT[G/T]TTGTAGTTAGACAAT | 10152 |
| rs777969737 | snp | C/T | 3.29592e-05 | 0.00405938 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427241 | TCAGGAAGGAGCCAT[C/T]ATTTATGTCATCAAG | 10152 |
| rs778006024 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329491 | TCTGTGGATTAAAAA[A/T]ATCCTTCTTTAAAAA | 10152 |
| rs778048658 | snp | C/G | 3.29783e-05 | 0.00406055 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416962 | CAGTCTTTGATGAGT[C/G]TCCCCCACCTCCTCC | 10152 |
| rs778067406 | snp | C/T | 3.54522e-05 | 0.00421009 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328607 | GGAACGGGTGGCCGA[C/T]TACTGCGAGAACAAC | 10152 |
| rs778105888 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430122 | AGTAATTGGAGACTT[C/T]TAATGTATGTAATAT | 10152 |
| rs778124792 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360928 | AAATTAGGGTAACAA[C/T]TAATTGTTACCCTTT | 10152 |
| rs778140160 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392316 | ACCACCACCACCACC[-/A]ACAACAACAACAACA | 10152 |
| rs778192393 | in-del | -/AAAAG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359027 | AAAAAAACAAAAAAC[-/AAAAG]AAAAATCCATGGAGG | 10152 |
| rs778247330 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203331228 | ATAGAACGTGGTGAC[A/G]GTGGATTTGTGCTGA | 10152 |
| rs778300578 | in-del | -/TGAGA | 3.97606e-05 | 0.00445856 | intron-variant | ABI2 | GRCh38.p7 | 2:203402527 | AAGTATTTAATGATC[-/TGAGA]TAATTTTCTTTTAAT | 10152 |
| rs778355722 | in-del | -/T | 0.00015836 | 0.00889691 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366864 | ATGATCACTGGTTTG[-/T]TTTTTTTCCCAGTCA | 10152 |
| rs778360268 | snp | G/T | 1.98281e-05 | 0.0031486 | utr-variant-3-prime, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203427401 | AGTCAGGTCTTCCCA[G/T]ATTATCTGAAGGCCC | 10152 |
| rs778386215 | snp | C/G | 1.66178e-05 | 0.00288247 | intron-variant | ABI2 | GRCh38.p7 | 2:203394864 | ATTTTCTCTACCTCA[C/G]TGCAAAATGTGATGG | 10152 |
| rs778407097 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203424001 | GTTTCAGTCATAACT[A/G]CACAAAAACCAGATG | 10152 |
| rs778417872 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422824 | TTTCTTAGAATACAT[G/T]AAGTGGTTTAACCAA | 10152 |
| rs778461875 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203423183 | TACATTGTTATTTTA[A/G]TATCACCTTAATTTT | 10152 |
| rs778464465 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347622 | AATAGTTTCTGTTTT[A/G]GAGAACAGGGAATAG | 10152 |
| rs778466632 | snp | C/G/T | 3.29545e-05 | 0.00405911 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203395693 | AGCCACCCAAGTAGT[C/G/T]GGAGCAGCAGTCGAG | 10152 |
| rs778488477 | in-del | -/TACT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203381129 | TTTCTAATATAAACA[-/TACT]TAAAAAACACTGTTA | 10152 |
| rs778520211 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343682 | GAAGTAGATTTAAAG[C/T]TCTCTGATTGAGATT | 10152 |
| rs778527953 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203406016 | GGAACCCTTTGATCA[A/G]GGCATAACTGAAATC | 10152 |
| rs778586904 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203379699 | AATGGAGAGGGAAAA[A/G]TTAGCATGCTTTAAC | 10152 |
| rs778620222 | snp | A/G | 3.29989e-05 | 0.00406182 | intron-variant, synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203411352 | TTTAATGGGATTTGT[A/G]GCCAGAGTCCAAGAA | 10152 |
| rs778624184 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392717 | ATGGATTTTGTTGGG[A/T]TTTAAGTCAAGATTG | 10152 |
| rs778663637 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421478 | TTGAGTTACTCAGTG[C/G]AGTAATTCTTTTAAT | 10152 |
| rs778668081 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421877 | GCTGAGGCAGGAGAA[A/T]CACTTGAACCCAGGA | 10152 |
| rs778671701 | snp | C/T | 1.7412e-05 | 0.00295055 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203380212 | ATATTTTGCAGACAG[C/T]TGATATTCATAAAGA | 10152 |
| rs778688227 | in-del | -/TT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346535 | TACTGGAGTTGCACG[-/TT]TTTTCCCTTGTCATA | 10152 |
| rs778694946 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347154 | CCATTGCATGTCCTA[A/G]CAGGGTAAGGAGTGA | 10152 |
| rs778723196 | snp | C/T | | | | | GRCh38.p7 | 2:203355430 | GGCTAGAGGATTGCT[C/T]GAGCCTGAGAGTTTG | 10152 |
| rs778815155 | snp | A/C | 0.000172646 | 0.00928941 | intron-variant | ABI2 | GRCh38.p7 | 2:203367082 | TTTGCCTATGAGGAA[A/C]CCTTAATAATAAACA | 10152 |
| rs778815963 | in-del | -/A | 0.000126056 | 0.00793801 | intron-variant | ABI2 | GRCh38.p7 | 2:203395033 | AGTCAGGAAGTTGAT[-/A]AAGAACAGACATCTC | 10152 |
| rs778818554 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203362202 | AACAAGTGAAGTACA[A/G]ATAATGTGACATCCA | 10152 |
| rs778904832 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376448 | AACATCATATAGCCA[A/G]ACTAAATTATTTTGA | 10152 |
| rs778906688 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377716 | TTCAAGACCTGCCTG[A/G]GCAACATGGAAAAAC | 10152 |
| rs778910158 | in-del | -/AA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361860 | AGCTGTGTCTGTGCT[-/AA]GTTTGCAGGAATCGA | 10152 |
| rs778912113 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203342843 | TATAATGTCTATACA[C/T]ACACACATCTCATTG | 10152 |
| rs778917582 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344517 | ATTACAGGCAACTGC[C/T]GCCACACCCGGCTAA | 10152 |
| rs778988962 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203414263 | TGCACCACCATGTGC[A/G]TCTAATTTTTGTATT | 10152 |
| rs779018442 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329956 | TGACCAGACTGGTCT[C/T]GAACTCCTGACTTCA | 10152 |
| rs779032293 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428902 | GCTGGATATATTTCA[A/G]ATGAGGTTTTGAACA | 10152 |
| rs779071860 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384145 | AGATTTTTAAAAACA[C/G]TATGGTAATAGTTTT | 10152 |
| rs779097447 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203361032 | TAGCTCCACAGGTGT[A/G]GCTGATGGCTGTCAG | 10152 |
| rs779167458 | snp | A/G | 1.65091e-05 | 0.00287303 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203417053 | TGAAGAGGACCCACC[A/G]TGGGCTCCACGTTCT | 10152 |
| rs779178397 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370544 | ATAAAAGCAGGCAGC[A/G]GGCCACATTCTGGCA | 10152 |
| rs779196182 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203402790 | AATTAAAAACCTTCA[A/G]CTACAAAAAACCCTT | 10152 |
| rs779256808 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385999 | CTCTGTCCTGAATTT[-/A]ATACTCTAATTCCTG | 10152 |
| rs779273337 | in-del | -/TT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203386289 | TGTGTTTAAATTCTC[-/TT]TTCTTTTTTTTAAAG | 10152 |
| rs779288016 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350266 | ATTTTTAGTAGAGAC[A/G]AGGTTTCACCGTGTT | 10152 |
| rs779311427 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431486 | ATAATCTTCATTTAC[A/C]CCTCCTAAAACTACA | 10152 |
| rs779328510 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418230 | GACAAAATATTTCCA[C/T]GTTTGATGAAAACTA | 10152 |
| rs779350527 | in-del | -/AAA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330393 | GTGAGACTACATATC[-/AAA]AAAAAAAAAAAAAAA | 10152 |
| rs779351709 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203385911 | TTATGTTCCCTTATT[C/G]TCTGTGTTTTATTGT | 10152 |
| rs779377719 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355788 | GTGAGCCGAGATTAC[A/G]CCATTGCACTCCAGC | 10152 |
| rs779394242 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339827 | GCACAGTTCTCCTTC[A/C]GTCTACATGGGGCAT | 10152 |
| rs779416920 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203405568 | AAAAAAAAATTATGT[A/G]AGTCTCCTGTATTAC | 10152 |
| rs779436109 | snp | C/T | 0.000115951 | 0.00761327 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203417063 | CCACCGTGGGCTCCA[C/T]GTTCTTACTTGGAAA | 10152 |
| rs779483269 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351464 | TTCTGATCCATGAAC[A/G]TGGATGTCTTTTCAT | 10152 |
| rs779523994 | snp | A/G | 1.70749e-05 | 0.00292184 | intron-variant | ABI2 | GRCh38.p7 | 2:203427155 | TGTCTTTCACATCCT[A/G]TTTTGTTTTCTTCCC | 10152 |
| rs779542932 | in-del | -/T | 1.72867e-05 | 0.00293991 | intron-variant | ABI2 | GRCh38.p7 | 2:203402740 | CAGAATCCAGGTTAG[-/T]TTTTTTGTTTTTTTG | 10152 |
| rs779567688 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203409818 | TGGAATAGGCCTGAA[A/G]AAGTTAATTGACTAG | 10152 |
| rs779597221 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203336831 | TAGTGGGATTATTAC[C/T]GTATGGTAAATGTGT | 10152 |
| rs779649497 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422876 | GTTAACTTTGCTCTA[C/T]CTCAGGACAGGTTAT | 10152 |
| rs779675422 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203354290 | CTCAAGTGATCTTCT[C/T]GCCTCAGCCTCCCAA | 10152 |
| rs779689038 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330594 | GGAAGCAATGCTGTT[C/G]TGAGGGATTTCACAA | 10152 |
| rs779736195 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203430548 | TGCCAATGTGTCAAA[A/G]TCGACATCTGAGAGA | 10152 |
| rs779758906 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203377860 | GCAGTGAGCCATGAT[C/T]GGGCCAGTCCACTCC | 10152 |
| rs779783021 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344662 | CTGGGCTTCTGGGTC[C/T]GGTGGGGACTTGGAG | 10152 |
| rs779836869 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203394017 | TACAGTTCAAAGTAA[A/G]TAATATAGAAAGGCT | 10152 |
| rs779870001 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355578 | CTCATGCCTGTAATC[C/G]CAGCACTTTGGGAGG | 10152 |
| rs779952608 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351679 | AGTCTGGGACTACAG[A/G]TGCGTGCTACTGTGC | 10152 |
| rs779955780 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346646 | AGTGTAAACTTGTGC[C/T]GTTCTCTTTCTCATT | 10152 |
| rs779971202 | snp | C/T | 1.65061e-05 | 0.00287277 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203417051 | GCTGAAGAGGACCCA[C/T]CGTGGGCTCCACGTT | 10152 |
| rs779989731 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392713 | CCTTATGGATTTTGT[C/T]GGGTTTTAAGTCAAG | 10152 |
| rs780007034 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347903 | CGATGCTTTCTAGAT[A/G]TTTAGGATTTGATCA | 10152 |
| rs780009934 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203338912 | GGGGTTTATATCTGT[C/G]TGTGTGTGTGTGTGT | 10152 |
| rs780045827 | snp | A/G/T | 6.61489e-05 | 0.00575071 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402646 | AACAATAGGGGGCTC[A/G/T]TTGCCCTATAGACGC | 10152 |
| rs780067741 | snp | A/G | | | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203365846 | GTGTTAGCCAGGATG[A/G]TCTCAATCTCCTGAC | 10152 |
| rs780070675 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203332354 | CACCTAGGCCGGGCA[C/T]GGTGGCCCACGCCTG | 10152 |
| rs780103431 | snp | G/T | 1.7402e-05 | 0.0029497 | intron-variant | ABI2 | GRCh38.p7 | 2:203402749 | GGTTAGTTTTTTTGT[G/T]TTTTTGCATTCTATA | 10152 |
| rs780103534 | snp | C/T | 1.6897e-05 | 0.00290658 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366871 | CTGGTTTGTTTTTTT[C/T]CCCAGTCAGCAGATA | 10152 |
| rs780129957 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418327 | TATCTCCCAGTTTCT[C/G]TGCGTGGCTCAGCTG | 10152 |
| rs780135439 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203370605 | AAATACTTTTTCCAA[A/G]TGTTTGAGTGTTAAA | 10152 |
| rs780140464 | in-del | -/G | 0.000196367 | 0.00990682 | intron-variant | ABI2 | GRCh38.p7 | 2:203351535 | TTCAGTGTTTAGTTT[-/G]TTTTTTTTTTTTCCT | 10152 |
| rs780156520 | snp | A/G | 1.69913e-05 | 0.00291468 | intron-variant | ABI2 | GRCh38.p7 | 2:203367066 | CCACAATATTTTCCT[A/G]TTTGCCTATGAGGAA | 10152 |
| rs780181026 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203417148 | ATGAAATTTGCGGTA[C/T]TGAAGAGAATCTTAT | 10152 |
| rs780200103 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203369310 | ACTAGTATATTTGAG[-/T]TTCCTAAAAAGGAGG | 10152 |
| rs780225054 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350478 | CCTTAGTCTCCCTAG[A/T]AGCTAGGACTAGAGG | 10152 |
| rs780234196 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404357 | ATAGTGTGAATACCA[A/G]CTGCCTTAATTGATA | 10152 |
| rs780267182 | snp | C/G | 2.36566e-05 | 0.00343915 | intron-variant | ABI2 | GRCh38.p7 | 2:203328649 | GCGAAGCATCCCCAG[C/G]TGGGCCGCGTCGGGG | 10152 |
| rs780278269 | snp | C/T | 1.66888e-05 | 0.00288862 | intron-variant | ABI2 | GRCh38.p7 | 2:203394683 | ATCATACAATACATA[C/T]GCTCTTCTTTTTGTA | 10152 |
| rs780303226 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328036 | GGAGGGAGCCGGCAG[A/G]AAGCCAGCTGAGCAG | 10152 |
| rs780354346 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357291 | CCTTGGGAGTATAAA[G/T]TAATTATTTAAGAGC | 10152 |
| rs780380870 | snp | A/G | 0.000163975 | 0.0090532 | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203396823 | CCTCCCCTTCCTGCT[A/G]CTTCTGCATCTGCCC | 10152 |
| rs780421251 | in-del | -/CT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422279 | CTGGGGACAGTAAGA[-/CT]CTGTCTCAATAAAAA | 10152 |
| rs780432085 | snp | A/G | 0.000194496 | 0.00985952 | intron-variant | ABI2 | GRCh38.p7 | 2:203351587 | GTCATGCAGGCTGGA[A/G]TGCAGTGGTGTGATC | 10152 |
| rs780448786 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413993 | GATAGAGTCCAAACT[A/G]CTGTAAGGCCCTTCC | 10152 |
| rs780465640 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203355658 | AACATGGAGAAACCC[C/T]GTCTTTACTAAAAAA | 10152 |
| rs780475664 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203413771 | TCAAAGATAATTCTT[C/T]GGAATTATCTTCAAA | 10152 |
| rs780554464 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359017 | ACTCTGTCTCAAAAA[A/C]ACAAAAAACAAAAGA | 10152 |
| rs780556400 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346821 | TGATGTATGATGAAA[C/T]GTCATTCCTTTATCT | 10152 |
| rs780580952 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203387604 | CTTTCTTGTACCTAA[C/T]ACCTGCTTCACTTAG | 10152 |
| rs780630035 | in-del | -/AACAACA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203392316 | ACCACCACCACCACC[-/AACAACA]ACAACAACAACAACA | 10152 |
| rs780642498 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203352521 | CCTGACCCTGTGTAG[A/G]GTTAGGCTAATACGT | 10152 |
| rs780661656 | snp | C/T | 1.67992e-05 | 0.00289816 | intron-variant | ABI2 | GRCh38.p7 | 2:203367051 | ATTTCACAAGTGAGA[C/T]CACAATATTTTCCTA | 10152 |
| rs780676003 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203396437 | AATTCAAAATGGAAA[A/T]CTGTTGTTTTTTAGT | 10152 |
| rs780703062 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203394326 | AAGGGAGAGGAGAAT[A/G]ATTAGTGCATTCATG | 10152 |
| rs780711393 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203356513 | AGCTGGGACTACAGG[C/T]GCGTGCTGCCACGCC | 10152 |
| rs780761150 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203431738 | CGGCGGGGCCTAGCT[A/G]TGTATAAATGATCCT | 10152 |
| rs780795206 | snp | C/G | 1.75715e-05 | 0.00296402 | intron-variant, upstream-variant-2KB | ABI2 | GRCh38.p7 | 2:203366854 | TTTTGAATTAATGAT[C/G]ACTGGTTTGTTTTTT | 10152 |
| rs780796180 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203411847 | CAATGAATTTCCCTT[G/T]GCCTGTTCAGGTAAC | 10152 |
| rs780837108 | snp | C/T | 6.68673e-05 | 0.0057818 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203402613 | CATGAATAGGCCTGC[C/T]TCTCGCCATACTCCC | 10152 |
| rs780839747 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427746 | GGATGTTCTTCATTG[C/T]CTGTGCTAAGGGGTT | 10152 |
| rs780853419 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203409899 | CTGAAAATCCAACCT[C/T]TTTCCACTAAGCACT | 10152 |
| rs780878420 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203418446 | GCTTTCAGGCTCACT[C/T]GTGGTTATTGGCAGG | 10152 |
| rs780895199 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203378053 | AAAGCTATTCTCATA[A/T]TTAGCCTAACATGCG | 10152 |
| rs780928845 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364295 | GACGGGGTTTCACCA[C/T]GTTGGTCAGGCTACT | 10152 |
| rs780980941 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203343305 | GGAAGCGGAGGTTGC[A/G]GTTAGCTGAGATTGC | 10152 |
| rs781111062 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203334086 | GTTGGGACTACAGGC[A/G]TGTGTCAGCATACCC | 10152 |
| rs781111487 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203341664 | ACAGTGAGCCTAGAT[G/T]GCACCACTGCACTCC | 10152 |
| rs781120979 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203351826 | CAGGAGTGAACTACC[A/G]CACCCAGCCGGTTTT | 10152 |
| rs781142101 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203405262 | AGTTGGTTAATCAGA[A/G]TACTTTTTGTAAACT | 10152 |
| rs781184372 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203404478 | CCCTTTTTATACATT[G/T]GCCTTTTAAACCATG | 10152 |
| rs781185664 | snp | A/G | 3.30426e-05 | 0.0040645 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203416942 | ACCGCCACCTGTGGA[A/G]GAACCAGTCTTTGAT | 10152 |
| rs781186521 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203394554 | AGAAGTGATACATTA[A/G]TAAAGACTGAAATTG | 10152 |
| rs781197578 | snp | C/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203346510 | CTGGTCTGTGTTTTG[C/G]GTTTATCCATTACTG | 10152 |
| rs781210589 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203416398 | CCTCCCCGGTTCCAG[C/T]GATTCTTGTGCCTTG | 10152 |
| rs781328344 | snp | C/T | 1.69596e-05 | 0.00291196 | intron-variant | ABI2 | GRCh38.p7 | 2:203411415 | ATCAGATTGTAGGCA[C/T]AAAATGTCATTTATA | 10152 |
| rs781343912 | in-del | -/GCGC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350892 | TGTGTGTGTGTGTGT[-/GCGC]GCGCGCATACTTTTA | 10152 |
| rs781353375 | snp | A/G | 0.000140223 | 0.00837209 | intron-variant | ABI2 | GRCh38.p7 | 2:203382233 | CAGGGCTGGATTTCC[A/G]TTCTTTGTTCTTATG | 10152 |
| rs781362113 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203399608 | GCAATCTCCGCCTCG[C/T]GGGTTCAAGCGATTC | 10152 |
| rs781365956 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203360824 | GAGTTTAGAACATTG[A/T]CTCAACACAAGGTTA | 10152 |
| rs781381707 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203414232 | TCAGCCTCGTGAGCA[G/T]CTGGGAATACACGTG | 10152 |
| rs781388356 | in-del | -/GAG/GAGGAG | 0.0173754 | 0.0915909 | utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328487 | CTCTGCGACCTGTAT[-/GAG/GAGGAG]GAGGAGGAGGAGGAG | 10152 |
| rs781401723 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203340319 | GGTCTAATGTACTGT[A/G]TAGTAACTATAGTTA | 10152 |
| rs781408647 | snp | A/G | 3.80699e-05 | 0.00436274 | synonymous-codon, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203391132 | CCCTATGTCAGGGAA[A/G]GGGACACTTGGGTGA | 10152 |
| rs781435258 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | ABI2 | GRCh38.p7 | 2:203427657 | AGATTAAGACTGATT[C/G]AGAAAAATCTGGGAT | 10152 |
| rs781460954 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428505 | TAAGTAGCTGCTGTT[A/C]GTCAGAATTAAAACC | 10152 |
| rs781542778 | in-del | -/T | 0.00229885 | 0.0338251 | intron-variant | ABI2 | GRCh38.p7 | 2:203351703 | ACTGTGCCCGGCTGA[-/T]TTTCGTATTTTTTGT | 10152 |
| rs781547843 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203381545 | ATATTGGGATTACAG[A/G]TGTAAGCCATCGTGC | 10152 |
| rs781554682 | snp | A/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203374720 | ATAATTGTAATTTAA[A/T]TGTTTATTTGAAACA | 10152 |
| rs781563059 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203411966 | AGTGAGGAATTGCTG[C/T]CACAGAGACCAGTGA | 10152 |
| rs781571651 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203347761 | GGGAAATTGTAGGTG[C/T]TTGTTTAGTTATTGG | 10152 |
| rs781624917 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421967 | GAGACTCTGTCTCAA[-/A]AAAAAAAAAAAAAAA | 10152 |
| rs781652240 | snp | A/G | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203395673 | GCAGTGGGAGTAGTG[A/G]AGGGAGCCACCCAAG | 10152 |
| rs781653562 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203359222 | TCTGCTATGACAGAT[G/T]AAGGTTTTTTTAAAT | 10152 |
| rs781668161 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203335579 | TGAATTATTTTATAA[A/G]TAGGATATAATTACA | 10152 |
| rs781691903 | snp | A/T | 3.79831e-05 | 0.00435776 | missense, utr-variant-5-prime, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203328626 | TGCGAGAACAACTAC[A/T]TACAGGTGCGAAGCA | 10152 |
| rs781703189 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350760 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAT | 10152 |
| rs781721868 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203381003 | TTCAGAGCTTTAGCT[A/G]AGTATTAATTTATGT | 10152 |
| rs781724421 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203396944 | CTCCAACTCCCCCTG[G/T]TGTTTCTTCCACTCC | 10152 |
| rs781754509 | in-del | -/TAAG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203380644 | TATGGTTTGAGTAAA[-/TAAG]TGTCGTGTAATCTTT | 10152 |
| rs781764603 | in-del | -/ATT | | | cds-indel, nc-transcript-variant | ABI2 | GRCh38.p7 | 2:203428550 | AATATAATGAATAAG[-/ATT]AATAGGCCAAAATAT | 10152 |
| rs796077707 | in-del | -/AGAGCTAGGTATTGAAAGGCAGTGGC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203373803 | AAGTAATTCTTCTCA[-/AGAGCTAGGTATTGAAAGGCAGTGGC]AGAGCTAGGTATTGA | 10152 |
| rs796117080 | in-del | -/TTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203357046 | AGCGTTTTTAAAATT[-/TTT]GTCTGTTTTTAAAAA | 10152 |
| rs796117154 | in-del | G/TT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384316 | TTTTTTTTTTTTTTT[G/TT]TTTTTTGAGACAGGG | 10152 |
| rs796178683 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384316 | TTTTTTTTTTTTTTT[-/G]TTTTTTTTGAGACAG | 10152 |
| rs796201753 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384311 | TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTGA | 10152 |
| rs796264851 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384312 | TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTGAG | 10152 |
| rs796278569 | in-del | -/AA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203329314 | CTGTTTCTTAGAGAG[-/AA]TTGGGAAGATGAACC | 10152 |
| rs796279472 | in-del | G/TTTT | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384314 | TTTTTTTTTTTTTTT[G/TTTT]TTTTTTGAGACAGGG | 10152 |
| rs796296789 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384307 | TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 10152 |
| rs796307037 | in-del | -/GC | | | intron-variant | ABI2 | GRCh38.p7 | 2:203350900 | TGTGTGTGCGCGCGC[-/GC]ATACTTTTAGGTGTT | 10152 |
| rs796357135 | in-del | -/CA | | | intron-variant | ABI2 | GRCh38.p7 | 2:203421964 | AGTGAGACTCTGTCT[-/CA]AAAAAAAAAAAAAAA | 10152 |
| rs796368086 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203375911 | GCCATTTTCTAAAGG[C/T]ATGTTTTCTTCTGCC | 10152 |
| rs796445764 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422428 | GTGACTATGATGATG[A/G]AGAGAAGTCGAGTGT | 10152 |
| rs796459850 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203425228 | TTTCTTTTTCTTTTA[-/T]TTTTTCTTTTTTGAG | 10152 |
| rs796499769 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203341535 | CCTTGGCCAAGATGG[C/T]GAAACCCCATCTCTA | 10152 |
| rs796506385 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203376451 | ATCATATAGCCAAAC[G/T]AAATTATTTTGACTT | 10152 |
| rs796508669 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203408179 | ACTTTTTTTTTTTTT[-/T]GAGATGGAGTTTTGC | 10152 |
| rs796519162 | snp | A/C | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422735 | TTGGAGTGGTAGGGG[A/C]AGAAGGAATATGGCT | 10152 |
| rs796555880 | in-del | -/AG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203417963 | AATATATCTTTAAAA[-/AG]AGAGAGAGAGAGAGA | 10152 |
| rs796586813 | in-del | -/A | | | intron-variant | ABI2 | GRCh38.p7 | 2:203397071 | GTTGTACTTCGTATT[-/A]AAAAAAAAATAAGAA | 10152 |
| rs796613546 | in-del | -/TTTTGTTTTTG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384291 | TGTTTTTGTTTTTGT[-/TTTTGTTTTTG]TTTTTTTTTTTTTTT | 10152 |
| rs796647883 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203398567 | CCAAGGTATAACTTA[-/T]GTACAGTAAAATTCA | 10152 |
| rs796726581 | snp | C/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203330490 | GTGGATGGTACATAC[C/T]TAGTAGGAGAGGCTG | 10152 |
| rs796727273 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203422126 | CATGGCGATACCCTC[A/G]TCTCTACAAAAAATT | 10152 |
| rs796733330 | in-del | -/TTG | | | intron-variant | ABI2 | GRCh38.p7 | 2:203344541 | CGGCTAATTTTTGCT[-/TTG]TTGTTGTTGTTGTTG | 10152 |
| rs796810069 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203403903 | ATTACAGGCACCCAC[A/G]ACCACACCCAGCTAA | 10152 |
| rs796812057 | snp | A/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203339598 | AAAAAAAAAAAAAAA[A/G]AAAAAGAAAAAAAGA | 10152 |
| rs796819546 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384302 | TTTGTTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 10152 |
| rs796885512 | in-del | -/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203364091 | CTTTGTCCATTCATC[-/T]TTTTTTTTTTTTTTA | 10152 |
| rs796934320 | in-del | -/G | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384301 | TTTGTTTTTTTTTTT[-/G]TTTTTTTTTTTTTTT | 10152 |
| rs796995948 | snp | G/T | | | intron-variant | ABI2 | GRCh38.p7 | 2:203384297 | TTGTTTTTGTTTTTT[G/T]TTTTTTTTTTTTTTT | 10152 |