| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs545261772 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950035 | CGCCAGCAAGAAAAT[C/G]GGTCGGAACTGGACT | 10422 |
| rs545301324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934389 | GAAAAAGCCAGGCAC[C/G]GTGGCTCATGCCTGT | 10422 |
| rs545337422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939215 | CCAAAAAAATTAAAA[A/G]AAAAAAAAAATGAAC | 10422 |
| rs545374342 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961536 | GGGAGCTGTAGTTCT[A/C]TGGTAGCTTCGTTCC | 10422 |
| rs545499610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956006 | TGGCCCAGCTCACGA[A/C]GCAACAGCCATGCTG | 10422 |
| rs545533999 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961941 | GAAGCCTAGGTTTGC[A/G]GGGCACCCAGAGGGG | 10422 |
| rs545565653 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958171 | CCTGTCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 10422 |
| rs545610716 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932738 | TAGGCGGAGGCAGCC[A/G]TGCTTGGGCTCAGGA | 10422 |
| rs545715031 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947255 | GTTCAGATTTGTGTG[G/T]TTTTTTTTTTCTTGA | 10422 |
| rs545828415 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947724 | CTTGCTGCCCCGCCC[C/T]GCAGGAACCCCCCCA | 10422 |
| rs545912883 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941172 | GCACTTTGGGAGGCC[A/G]GGGTGGGAGGATCAC | 10422 |
| rs546073040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933640 | TACAAAGGCCACACA[C/G]AGCTCACTGCTAAGT | 10422 |
| rs546230468 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933268 | AGATCAGAGAGCAGG[A/G]GCAGCTGCAGCACCT | 10422 |
| rs546287780 | snp | A/C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962563 | GTTAGCAATCTAACC[A/C/G]GGGAGGCTGTCTCTG | 10422 |
| rs546293812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937927 | CCTAAGCTGCTGGCG[C/T]AGTCTCCACCCCGCT | 10422 |
| rs546319851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938908 | GAATCATTCTTGAGT[A/C]AGTTTAATCAGAAAA | 10422 |
| rs546334392 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954527 | GATATCTGCATGGCC[C/G]TAGCTGAGGTACAAG | 10422 |
| rs546413610 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936534 | GGAGTCTTGCTCTGA[C/T]GCCCAGGCTAGAGTG | 10422 |
| rs546489285 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961645 | GGATCCCAAAGAAGT[A/C]ACGGGAAAAAGGAAT | 10422 |
| rs546518598 | in-del | -/AATAATTGTGCAAAG | 0.0023933 | 0.0345097 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954607 | GCACAGCACGGCCCC[-/AATAATTGTGCAAAG]AATTGGTGACAATCC | 10422 |
| rs546555284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939365 | CATAGCCGGCTGCAT[A/G]TGAAAGTAGGCAAAC | 10422 |
| rs546597368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934553 | TAATCCCAGCTACTC[A/G]GAAGGCTGAGGCAGG | 10422 |
| rs546682721 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936895 | TGAGGAAATAAACCA[C/G]AAACTGAACAACGGC | 10422 |
| rs546692081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935020 | GAGTAGCAGGGACTA[C/T]AGGTACGTGTGCCAC | 10422 |
| rs546744318 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956521 | TGTTCGTGCCCAAGT[C/T]GGTCCAGAGCTCCAC | 10422 |
| rs546901242 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949720 | CTGCGGCAGGCAGAA[A/C]TCGAGGACGGCCGCA | 10422 |
| rs546916776 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935617 | AGCCTGGGTGACAGA[G/T]CAAGACCCTGTCTCC | 10422 |
| rs546976974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945539 | AGGGGGAACTGCCCC[C/T]GGCTGCCCCTGGATC | 10422 |
| rs547064939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950378 | GACTCAGACAGATGC[A/G]CAGGCCAGAGGGATC | 10422 |
| rs547138493 | snp | A/G | 9.9595e-05 | 0.00705603 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945963 | CCGCAGGGCAGCCTC[A/G]TCCACACGCTCATCC | 10422 |
| rs547245043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933795 | CCCCACTCTCGGCAG[C/T]TGTCTGGCAGCCGCC | 10422 |
| rs547266280 | in-del | -/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933176 | TTCCCAGTGCGACAA[-/C]CACTTTTTTGTAAAC | 10422 |
| rs547306726 | snp | G/T | 0 | 0 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933337 | AGGTGAGGTCCACTC[G/T]GCCCGGTCTCGGGCC | 10422 |
| rs547309518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943211 | GATCGCTTGAGGTCA[A/G]GAGTTTGAGACGAGC | 10422 |
| rs547310859 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135963246 | GCCAGGAAGGTGTTG[G/T]GTAGTTTTGGACACG | 10422 |
| rs547388155 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938821 | GGGATGGTGGGGGGG[C/G]GATGTGGGCCACCAC | 10422 |
| rs547449260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960206 | GGTATAGACAGGAGG[C/T]CAGTCTGACACACAG | 10422 |
| rs547459908 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953255 | CTGTAAATGGCGAAT[G/T]CGTGGGTTGGTGAAC | 10422 |
| rs547472559 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955024 | GGAGTCTCTGGCTTT[G/T]CTCTGAAACAGAACT | 10422 |
| rs547489618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942603 | GCTGCAGTGAGCCAT[C/G]ATTGTGCCACCGCCA | 10422 |
| rs547630865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948266 | CCAAAACCACGAACT[C/T]ATCTCTGCTCCTTCT | 10422 |
| rs547646914 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944930 | ACAGGAGCCAGCTCA[A/G]CCCAAGGTCAGCCAT | 10422 |
| rs547672229 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943891 | AACCAAGCCCCTCAT[A/G]TTCTCACTTATAAGT | 10422 |
| rs547705677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944459 | ACAGAAACCTCCAAG[A/G]AGGAAGTAAAACCCG | 10422 |
| rs547752754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956681 | CCCAGCCGGAATCGT[C/G]GGGTGAGAGGAGAGG | 10422 |
| rs547887988 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962517 | ACTTTACTGCGCAGA[A/G]ATGAATAAGGCACAG | 10422 |
| rs547940451 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952204 | AGGGGACCCAAGCCC[A/G]GGGTGCTCTTCCTGG | 10422 |
| rs547987447 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135940212 | GCCACGTCAGTAAGT[A/G]CAATCTCAACGGAAA | 10422 |
| rs548027957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951350 | CAAAAATTATCTGGG[C/T]GTGGTGGCACACACC | 10422 |
| rs548142059 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135963093 | GGCTTCCAGTGGCCT[C/G]TGGGAGGGGAGGCCA | 10422 |
| rs548207512 | snp | C/T | 1.67598e-05 | 0.00289476 | missense | UBAC1 | GRCh38.p7 | 9:135947826 | GTCTGGACCGCGGCC[C/T]GGTCCATGTTGTAGG | 10422 |
| rs548224336 | snp | A/C | | | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933039 | CATGCTTGACATTAA[A/C]TCTGGGTTGAAACCT | 10422 |
| rs548279809 | snp | G/T | 3.30797e-05 | 0.00406679 | missense | UBAC1 | GRCh38.p7 | 9:135945168 | CCTCGGCCTCTGGGG[G/T]AGCTTGGCCAGGAAG | 10422 |
| rs548369094 | snp | A/G | 3.39593e-05 | 0.0041205 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939778 | GAGGACAGCACAGCC[A/G]TTAGCTCGCTGGGGG | 10422 |
| rs548485152 | snp | A/G | 4.94287e-05 | 0.00497111 | missense | UBAC1 | GRCh38.p7 | 9:135946325 | GCTAACAGCTTCTGC[A/G]CCACCTCGATGAGAG | 10422 |
| rs548583078 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936770 | AGTGCTGGGATTACA[C/G]GCGTGAGCCACCACG | 10422 |
| rs548594783 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941114 | TGTGCATGATCAGGT[A/C]AAAAGTCCCAGCCGG | 10422 |
| rs548718987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937138 | CTGCTCGGGTGGCAA[A/G]GGCCCTCCCAACATC | 10422 |
| rs548731926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958269 | AGCCAGAATGGTCTC[A/G]ATCTCCTGACCTTGT | 10422 |
| rs548971432 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937056 | ACAGGCGGCCAATAC[A/G]CTTCTGAAAGAAGGC | 10422 |
| rs548982740 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938417 | GTGCCTCCGCAAGAC[A/G]CCACCAGCAGCAGGC | 10422 |
| rs549058160 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934457 | TGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 10422 |
| rs549121487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933880 | GGTCAGCAGATGCAG[A/G]AAGGACACACACAGA | 10422 |
| rs549148668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935145 | CAAGTGATCCTCTTG[C/T]CTCAACCTCCCAAAG | 10422 |
| rs549228819 | snp | A/G/T | 4.94958e-05 | 0.00497452 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945133 | TCCCGCGGCAGCCTC[A/G/T]GAGGCAGCTGCTGTG | 10422 |
| rs549352737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949698 | GAGAAGAACAAGACA[A/C]CTGGTCCTGCGGCAG | 10422 |
| rs549355743 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939523 | GCCCACACTCACTCA[C/T]CACAGCCCCCACTCA | 10422 |
| rs549486039 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942022 | ACATTCTACGGAATG[C/T]TGTTCTGACACAGAG | 10422 |
| rs549537872 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939919 | CTCACAGCTCTGCTA[A/T]AACAGATCTTGGTTT | 10422 |
| rs549548761 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937280 | AAGCCGTCTCTACTA[A/C]AATACGAAAAATTAG | 10422 |
| rs549555173 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952416 | CCTTCTAGCTGGCAG[A/G]CTCCATGCTCGGCAC | 10422 |
| rs549584954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945446 | CTACCTTGAGACCCT[A/G]GGCAGAATCAGAAGC | 10422 |
| rs549593665 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941810 | CCTGTCTACCACTGG[G/T]AAGGGAGGGGCAGCA | 10422 |
| rs549687565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937516 | GGGTTCCCAGTGCCT[C/T]CCATCAAGAAAATAC | 10422 |
| rs549692003 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952777 | TGGGAATATTTGCAT[C/T]CCAAATAATCAACTC | 10422 |
| rs549705690 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952925 | GGTGGGGCTTGTCGC[A/G]AGTGCTCCCTCACCG | 10422 |
| rs549737666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947337 | GCTTACTGCAACCTC[C/T]GCCTCCCGGGTTCAA | 10422 |
| rs549845329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958207 | GCCCGCCACCACGCC[C/T]GGCTAATTTTTCTGT | 10422 |
| rs549864979 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946859 | CAGAACAGCTCCTGG[A/C]TACAGGGCCTAGAGG | 10422 |
| rs550009328 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932900 | AGCCGGCACGGAGCC[A/G]CGGGGATGTGGCCTC | 10422 |
| rs550129310 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961739 | AGTTAAGAAAAATAT[A/G]TCATTAAAATTAATT | 10422 |
| rs550327868 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944216 | GAAGCCGGGGGTTAC[A/G]CTGCGGGACATGGTG | 10422 |
| rs550360732 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950357 | GCAGCAGGCCTGGAA[A/G]GCAGCGACTCAGACA | 10422 |
| rs550405714 | snp | A/G | 1.66145e-05 | 0.00288218 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946236 | GGCCGGCAGTGAACC[A/G]CCCTGGAATGCAGCA | 10422 |
| rs550455047 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950477 | GGAAGAGCATGAAAA[A/T]ATCAGCGATAAGCCT | 10422 |
| rs550468404 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943587 | GAAATACCATTTGTC[C/T]CTGCAATTCCATTAC | 10422 |
| rs550526037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935474 | AAAAAAACGAGACCC[C/T]ATCTCAACAACAACA | 10422 |
| rs550701187 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135954947 | TTACATGGATGTGTG[A/T]GTCTAACACTGCACT | 10422 |
| rs550813377 | snp | A/C/G | 0.000150468 | 0.00867244 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933555 | GAGTGCCCACGCCCC[A/C/G]ACTCAGCCCACAGGC | 10422 |
| rs550984429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940453 | GGCGTGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 10422 |
| rs551096953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941061 | AAAGACTTCAGCTGG[C/G]GTGGAGCTCAGGAAG | 10422 |
| rs551117679 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935980 | GCAGTGAGCTGAGAT[C/T]GTGCCACTGCACTCC | 10422 |
| rs551275479 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957694 | GAGGACCCATCTTCA[C/T]GCGATCTAGGAAATG | 10422 |
| rs551524463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943836 | GGTCATGGATGAAGC[G/T]GGAAGCCACTGTCCT | 10422 |
| rs551545964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939059 | AAAAACTAATTAGCC[A/G]GGCATAGTGGTGCAT | 10422 |
| rs551569379 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951126 | CTTTTTATATTTTTT[-/G]TAGAGACAGGGTTTC | 10422 |
| rs551584790 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944504 | AGAGAGAAGGAAGAA[A/T]GGGGAGATGAGGCGC | 10422 |
| rs551640739 | snp | A/C/T | 5.10767e-05 | 0.00505333 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938396 | ATACCACTGTTAGCG[A/C/T]CTTCAGTGCCTCCGC | 10422 |
| rs551681753 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939411 | CGCCCGGGGCGCTCA[A/C/T]GAGTGAGGCTCCCAG | 10422 |
| rs551723714 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135954322 | TGGTGGCACATGCCC[A/G]TAGTCCCAGCTACTT | 10422 |
| rs551748670 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935045 | TGCCACCACTCCTGG[C/G]TGATTTTGTTTTTTT | 10422 |
| rs551790870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955114 | GCTGTTTTTCACAAA[C/T]ACTCTATAACAGAAC | 10422 |
| rs551838990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960861 | AAGGGGGAGAGTCGG[A/G]CAAACGGGCAGGAGG | 10422 |
| rs551895391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957242 | GGATGTTGGGGGGAC[A/G]CAGCTACTAGGAAGA | 10422 |
| rs551914707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941194 | GAGGATCACTTGAGG[C/T]CAGGAGTTTGAGACC | 10422 |
| rs551914856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946812 | GTCCTCCCCAGGCAG[A/G]AGGAGCCGTGGGATG | 10422 |
| rs552002682 | snp | A/G | 0.000332088 | 0.0128815 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946388 | TGTGGTGAAAAAAAA[A/G]GAGATCAATTCTCTA | 10422 |
| rs552076339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941739 | GGAGAGGGGCCTTGC[A/G]CTCACGGGCTGCAGG | 10422 |
| rs552185762 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960556 | CTCTTCATGAAGGAG[-/C]CTACGTTAATTCTCA | 10422 |
| rs552196809 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938113 | CTGCCAGCGCACGGC[A/G]ATCCTCAGCGCTGGA | 10422 |
| rs552233822 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952284 | CATGGGCCTAGCCCA[A/G]AAGAGTTTGACCTGC | 10422 |
| rs552306480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959531 | AGGCACACACCACCA[C/T]GCCCCGCTAATTTTT | 10422 |
| rs552323781 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937258 | ACCAGCCTGGCAAAC[A/G]TGGTGAAAGCCGTCT | 10422 |
| rs552401957 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938135 | AGCGCTGGATCCTCC[A/G]TATCGCCTCCGCAGC | 10422 |
| rs552404486 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932870 | GTGGCCCCGGTGCCC[A/G]CCCCGGGTCAGAGCA | 10422 |
| rs552433995 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958110 | GGAGTGCAGTGGCTT[C/G]ATCTCGGCTCACTGC | 10422 |
| rs552580179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937216 | AGGGAGGCTGAGGCA[C/G]GTGGATCACGAGGTC | 10422 |
| rs552580550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953857 | GAACAGCAGGGATTC[A/G]GCCGGGCGCAGTGGC | 10422 |
| rs552729815 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135948399 | CAGAGGACGAGGATG[C/G]AGGGATCAGCGGAGC | 10422 |
| rs552790739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955240 | CCTCCTGGCTCCAGC[A/G]CCCCCAGCAGTGCAC | 10422 |
| rs552827320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960521 | CTCTGCGGGAAAGGG[A/G]AAGAGGAAGGAGAAG | 10422 |
| rs553030725 | snp | C/G | 4.65994e-05 | 0.00482675 | intron-variant | UBAC1 | GRCh38.p7 | 9:135961011 | TGGGGGCAGGGGAGG[C/G]GGCCCGGCCTTACGT | 10422 |
| rs553046326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934031 | GGTTTTAACAGCTTT[A/G]CAAAACTGTTTCCCC | 10422 |
| rs553056074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934717 | CAAACTATAAGGTGC[A/G]AAACAGCTGTTTCAC | 10422 |
| rs553119397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939162 | AGTGTGATCACACCG[C/T]TGCACTCCAGCCTGG | 10422 |
| rs553142899 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955700 | CAGAATTGCTTCTTT[C/G]GTCTAGAAAGATCTG | 10422 |
| rs553216045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948504 | GGACAAGGAGCGAGC[C/T]TCAGGAGCTAGCGCT | 10422 |
| rs553254778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956412 | GCTTTCCTTTGAACA[C/T]GGGGGCTAGGCGCGT | 10422 |
| rs553295344 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961916 | CAGATCAGAGAGTCA[C/T]TGTTCCTGCGAAGCC | 10422 |
| rs553447347 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941929 | ATCTCATGACTTGTA[A/C]AGAAACCAAAGGCTA | 10422 |
| rs553590340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937286 | TCTCTACTAAAATAC[A/G]AAAAATTAGCCAGGC | 10422 |
| rs553608979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956720 | TTCTGTGTTTCACAA[A/G]ATACCCACAGTTTCC | 10422 |
| rs553694634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937053 | TCTACAGGCGGCCAA[C/T]ACGCTTCTGAAAGAA | 10422 |
| rs553722525 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947616 | TTCCAACTCTTACTT[G/T]GAAATAATTTTTGAT | 10422 |
| rs553724539 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954090 | GTTGCACTGAGCCAA[A/G]ATTGCACCACTGCAC | 10422 |
| rs553776455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941491 | CAGGAGCTCCAACAA[C/T]GAACTCTGGAAGAAC | 10422 |
| rs553781285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959122 | CATAAAAGAGTATCA[C/T]GATGGCCATGCACAT | 10422 |
| rs553850220 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947002 | TGCTGGGGAAAAGCC[A/T]CCATGCCCTGGTCAG | 10422 |
| rs553949991 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937614 | AAGGCAGCAGCAAAT[A/G]AGAGATTGTTTAAGG | 10422 |
| rs554004494 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947321 | CGATGATGCAATCTC[A/G]GCTTACTGCAACCTC | 10422 |
| rs554149502 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956373 | CCCTGATTCATGCAC[A/G]TGGCACTGGCTTGCG | 10422 |
| rs554228848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950687 | GGAGAGAGGGAGGTA[C/T]TATAGCCTCTTCATT | 10422 |
| rs554306914 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960094 | TAACGCACTCAACCT[C/G]TCAACACAGATACGT | 10422 |
| rs554314299 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949989 | AGGAATGCAGGCCGC[A/G]CCCAGGCCCTGAGAG | 10422 |
| rs554351212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945337 | AAGAAGAGCCTCTGC[C/T]ATGGTAGTGACTTCT | 10422 |
| rs554431723 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942768 | CCCTGGGAGAGGGTG[C/T]GCGCAGGGGCTGCCC | 10422 |
| rs554503652 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935889 | AAATTAGCCGGGCAC[A/G]GTGGCGGGCACCTGT | 10422 |
| rs554508002 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933617 | TAATGAAGAGGGTGC[A/G]TCTCCAATACAAAGG | 10422 |
| rs554707620 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940066 | CGCTTATGTGGACAC[A/G]AGGCAGTCAGGCCAA | 10422 |
| rs554760600 | snp | A/C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939385 | AGTAGGCAAACACAC[A/C/G]GCCTCCACCACGCCC | 10422 |
| rs554837259 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946169 | CAGCGCTTCCATAAA[A/G]CACTGAGGTTCCGGT | 10422 |
| rs554871721 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957832 | CAGGCTGGAGTGCAG[A/T]GGCGCGATCTCCGCT | 10422 |
| rs555076926 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135963364 | GCTGGAGACAAACAC[C/T]GGGCAGCCGGCCTGG | 10422 |
| rs555212384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951964 | AGGCTGTGGGGCAAC[A/G]GGTGTATGGTCAGAC | 10422 |
| rs555285675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946528 | GGGCAAGGCAGGGGA[C/T]TGGCAGGGCCAAGAG | 10422 |
| rs555309449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938576 | AGGAAGAGCTAGTCC[A/G]CTTTTCTCTGCAGAC | 10422 |
| rs555355903 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948440 | CAGGCCAAGAGCAGA[C/G]CATGGACGCAAGACC | 10422 |
| rs555448046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939135 | TGGGCCCAGGAGGTC[A/G]AGGCTGCAGTGAGTG | 10422 |
| rs555498163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959932 | CACAGCCAGTGCGTT[C/G]CAGAAGGGGGCTTGC | 10422 |
| rs555507442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948076 | TCTGTGCAAGGCCCA[A/G]GGACAGCAGACGTGT | 10422 |
| rs555523159 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944259 | CACTCATCACCAGCA[A/G]AAGCAAACTCAGAAT | 10422 |
| rs555571513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955189 | TTTTGTGCTCGTGTC[C/T]AGCTCAGAACACTGA | 10422 |
| rs555755952 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934853 | AACCACACAGATGAT[C/T]ATTTATCTGAGGAAG | 10422 |
| rs555817324 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-5-prime | UBAC1 | GRCh38.p7 | 9:135961357 | CCCGCCGCCGCAGCA[A/G]CCGCCGGGGGCGCGC | 10422 |
| rs555839356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946454 | TCCCCTGTCCTAGAA[C/T]TCTTGATTCTGAGAG | 10422 |
| rs555848547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936208 | AAAAAGAAAAAGTTA[C/T]TGGACAGACCCCAAG | 10422 |
| rs555934025 | snp | G/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949310 | AGCCAACTCATAAGA[G/T]TTACAGAAAGAGAAA | 10422 |
| rs555942804 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944170 | AAGCATTTGTCTCCA[C/T]GGAACCCTGTGCAGG | 10422 |
| rs555946489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947400 | GGGATTACAGGTGCC[C/T]GCCACTACGCCCGGC | 10422 |
| rs555985431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936879 | ATTCTGCCCATCAGT[A/G]TGAGGAAATAAACCA | 10422 |
| rs556023900 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961849 | CTGCTGTAGAACGGA[C/G]GCTCTCCAAAGAACT | 10422 |
| rs556036375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957965 | ATTTTTAGTACAGAA[A/G]GGGTATTGCCATGTT | 10422 |
| rs556235886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943576 | ACCTAGAAACAGAAA[C/T]ACCATTTGTCCCTGC | 10422 |
| rs556522805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947527 | GAATTCTATCTAAAC[A/G]TTTTGCCAAACTCAG | 10422 |
| rs556584396 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943281 | AAAAATTAGCTGGGC[A/G]TGGTGGGTGTGTGCC | 10422 |
| rs556601062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947158 | CAGCACGTGCCTGCC[C/T]TGCCTGCTGCGGCGT | 10422 |
| rs556652978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955739 | TTTTAAATGAAAACA[A/G]CAGATCCATTGTTTC | 10422 |
| rs556692396 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135951979 | GGGTGTATGGTCAGA[C/T]CCCGCTGTTTATATT | 10422 |
| rs556759576 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949529 | AGAGGAAGGGGAGGC[A/G]GCTGGTGCAGGGAGG | 10422 |
| rs556854787 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135945305 | CGGACCAGGGCCTTC[A/G]CCTCCTGTCCATTCC | 10422 |
| rs556903946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937706 | GCCACACCGGAGGGA[A/G]GGATGAGGTGCATAG | 10422 |
| rs556998301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956221 | ACTGAGTGCAAACTC[C/T]AGGAGGAAGTTGGAG | 10422 |
| rs557124642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935384 | GGCACAATGGCTCTC[A/G]CCTACAATCCCAGCA | 10422 |
| rs557146874 | snp | A/G | 8.76555e-05 | 0.00661967 | missense | UBAC1 | GRCh38.p7 | 9:135945245 | ATGGCCTGAGGCACC[A/G]ACATGCTGCAAGGCA | 10422 |
| rs557162151 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949793 | ATGAGCAGGACACAG[G/T]CCACTCTGGGGTCAG | 10422 |
| rs557234504 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944683 | CCGCAGAGAGGCTGC[A/C]GAACAGGGGGGGCTT | 10422 |
| rs557302213 | snp | C/G/T | 0.000169179 | 0.0091957 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939773 | GCCTAGAGGACAGCA[C/G/T]AGCCGTTAGCTCGCT | 10422 |
| rs557455870 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937656 | CGGCAAAACTCTACC[A/G]GGAAGCAGAGAGGTA | 10422 |
| rs557591197 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135963292 | TGGGGGCATTCACAC[A/G]GAGGTGGCCTGGAGG | 10422 |
| rs557592178 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135932973 | AAGACAGGAAATAGG[A/T]AAAGGGACTTTATTA | 10422 |
| rs557631009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946182 | AAGCACTGAGGTTCC[A/G]GTCAGTGGTCAGTGC | 10422 |
| rs557650913 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135953997 | TACAAAAATTAGCCA[A/G]GCGTGGTGGCGCATG | 10422 |
| rs557683732 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943730 | ACGGATAAGAAAAGA[A/C]ACCGGATAGACTGAA | 10422 |
| rs557708351 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135960042 | TACTATGGTAAGAAC[A/T]GAAGTTTATCCTTAG | 10422 |
| rs557721875 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932742 | CGGAGGCAGCCGTGC[C/T]TGGGCTCAGGACCTG | 10422 |
| rs557812282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942771 | TGGGAGAGGGTGTGC[A/G]CAGGGGCTGCCCTGG | 10422 |
| rs557901779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953574 | CCACCCGCCTCGGCC[A/T]CCCAAAGTGCTGGGA | 10422 |
| rs557905242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947999 | TCTGCCCAAGAAAGA[C/T]TCCGTCTCCTTTAGG | 10422 |
| rs557918949 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937293 | TAAAATACGAAAAAT[C/T]AGCCAGGCGTGGTAG | 10422 |
| rs557978565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938517 | TACCGTGAAGACAAA[C/T]GCAGTCTGGATTCAC | 10422 |
| rs558021739 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960582 | TCTCAGCTCTCAAAG[A/C]TGCTGCTGAAAAAAA | 10422 |
| rs558053052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934168 | CACATGGACGCACTT[C/T]AGCATAAGTGGCCCC | 10422 |
| rs558240886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951474 | CAGCCTGGGCAACAG[A/C]GTGAGATCCTGTCTC | 10422 |
| rs558280222 | in-del | -/GA | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135948399 | CAGAGGACGAGGATG[-/GA]GGGATCAGCGGAGCT | 10422 |
| rs558379988 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940679 | TTCGTTTTTGGGGAA[C/G]GACATACATTTTCTG | 10422 |
| rs558381539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940133 | GGATAAGACTGTCTC[A/G]GCAGCCACCGCAGGT | 10422 |
| rs558475268 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135953067 | ACACGCAGGTGAAGG[C/T]GGACAGCAGCGCGGG | 10422 |
| rs558480288 | snp | A/G | 8.81096e-05 | 0.00663679 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955439 | AAATAGAAATTTCAA[A/G]GTAGAAAATAAGTAA | 10422 |
| rs558594400 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949679 | CCAGACCAAGGGACA[C/G]ATCGAGAAGAACAAG | 10422 |
| rs558643918 | in-del | -/AAAA | 0.00398564 | 0.0444627 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936026 | GCGAGATTCCATCTC[-/AAAA]AAAAAAAAAAAAAGA | 10422 |
| rs558682222 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936137 | CATGGACAGTGGCGC[A/C]ATCACTGCACTCTAG | 10422 |
| rs558945450 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952747 | ACTGTTTCGGATTTC[A/G]GGTTTTTTCAGATTT | 10422 |
| rs559087791 | snp | C/T | 0.00010001 | 0.00707071 | missense | UBAC1 | GRCh38.p7 | 9:135953729 | AGTGGTGATGGAGCA[C/T]GCTTTTTTATCAATA | 10422 |
| rs559234051 | snp | C/G | 5.03639e-05 | 0.00501791 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938378 | GCAAAGCCAAGAGCA[C/G]CAATACCACTGTTAG | 10422 |
| rs559235201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946573 | GGACTGAAGCCAGTG[A/G]AAAGGGACAGGAACG | 10422 |
| rs559375903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933808 | AGCTGTCTGGCAGCC[A/G]CCAGGGCTCAAAAAT | 10422 |
| rs559466888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948110 | CAGCGTCTGCTCTGA[C/T]GTAAATAAGAGTGAA | 10422 |
| rs559483972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949633 | CCTCCAGACAGTTTC[C/T]CCTCCTGGCACCCGA | 10422 |
| rs559563879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944327 | CTCCATGGAAAACAC[A/G]AGCTCCGCAGGTGAG | 10422 |
| rs559603169 | in-del | -/CACT | 0.0170251 | 0.090679 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939498 | ACTCACCACAGCCCA[-/CACT]CACTCAGCCCACACT | 10422 |
| rs559617037 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960838 | GCGTCCAGAGGTGTG[C/G]GATCCGAAAGGGGGA | 10422 |
| rs559625451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943804 | CATAAAAAGGAACGA[A/G]ATCACGTCCTTTGCA | 10422 |
| rs559722994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934297 | TTGGCTCTGTTCATG[A/G]TTGGACAATCCCCAG | 10422 |
| rs559743862 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936380 | ATCCCTACCTCACAC[A/C]ACACACATACTTCTA | 10422 |
| rs559745128 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135954658 | AGGCATTTTAACCGG[C/T]TCAGTTCTGAAAAAG | 10422 |
| rs559787053 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961472 | CCGCCGGGGGCGCGC[C/T]GTGGCCACCGCAAAG | 10422 |
| rs559939310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952219 | AGGGTGCTCTTCCTG[A/G]GTACCCATGGTCCCA | 10422 |
| rs560002012 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135933611 | GCTTCCTAATGAAGA[C/G]GGTGCGTCTCCAATA | 10422 |
| rs560110853 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958121 | GCTTGATCTCGGCTC[A/C]CTGCAAGTCCCACCT | 10422 |
| rs560137894 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938094 | ACCTGCATGGCAGGA[A/C]GTGCTGCCAGCGCAC | 10422 |
| rs560260950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942223 | AACCTCAGAGCACAA[A/G]GGACCCAGCTGGAGA | 10422 |
| rs560338772 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942080 | AAGATCTTAGGAAAA[C/T]GAGCACGTTAAGATT | 10422 |
| rs560372593 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937427 | GCCTGGGTGACAAGG[A/C]GAGACTCTGTCTCAA | 10422 |
| rs560448879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937141 | CTCGGGTGGCAAAGG[C/G]CCTCCCAACATCCAG | 10422 |
| rs560633941 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933228 | CGGCCTTACACACTA[A/C]CGTCACCAAAGTTTA | 10422 |
| rs560692742 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932861 | CATGCTGCGGTGGCC[C/T]CGGTGCCCGCCCCGG | 10422 |
| rs560732007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944435 | GCCATCTGAGCATGT[C/T]GGAGACAGACAGAAA | 10422 |
| rs560777194 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935467 | CCTGAGCAAAAAAAC[A/G]AGACCCCATCTCAAC | 10422 |
| rs560965956 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957528 | ACTCTGCTTCTTTGT[A/T]CTCGGCAGAAGCTGG | 10422 |
| rs561029028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939330 | GAGCCATCTATCCAA[C/T]TGTCTCACTTTAAAA | 10422 |
| rs561030165 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935421 | AAGGCAGAGGTGGGG[G/T]GAGCGCTTGAAGCCA | 10422 |
| rs561076686 | snp | A/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961584 | GTTCCCACCCGGGGC[A/T]CTCACCACGTGGGAC | 10422 |
| rs561194923 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962089 | CACTTCCTTGTAAAA[A/T]CCAGTTTTAGCGAAG | 10422 |
| rs561235844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935938 | GGCTGAGGCAGGAGA[A/G]TGGCGTGAACCCGGT | 10422 |
| rs561403124 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956887 | GCACTTTCTAAACCC[A/G]GTAGCAGGCTCAGCC | 10422 |
| rs561407694 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940840 | CTAATCCCTGAAAGG[A/T]CAGATCCCACTCTCT | 10422 |
| rs561716487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933762 | GGTGGGCAGTGTGCC[C/T]GTGCGTGCTCATGGC | 10422 |
| rs561742395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947752 | CCACAGCAATCCCCC[A/C]CACGGGGACCCCATG | 10422 |
| rs561775846 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933305 | GTCCAGGGCTGAGGC[A/G]CTGAAGGTGAGTTTC | 10422 |
| rs561798863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953231 | GAGAACCCCTTATAA[C/T]CACATCTACTGTAAA | 10422 |
| rs561813365 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957844 | CAGTGGCGCGATCTC[C/T]GCTTATTGCAACCTC | 10422 |
| rs561823113 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941462 | CAATTGCCTTCCTGA[A/G]CCACACCCTAATCCA | 10422 |
| rs561969632 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955006 | GAAACCTGCAGAACC[C/T]CTGGAGTCTCTGGCT | 10422 |
| rs561996595 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135963054 | GCGGGGGAGCAATGC[A/G]GAGGGAGAGGAAGAG | 10422 |
| rs561999144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943797 | ATGCAGCCATAAAAA[C/G]GAACGAGATCACGTC | 10422 |
| rs562080173 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955472 | CGTAATTCTAATAAT[A/T]TAGGACCTGGCATCC | 10422 |
| rs562114674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935851 | CTAACACGGTGAAAC[C/G]CTGTCTCTACTAAAA | 10422 |
| rs562176774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935491 | TCTCAACAACAACAA[A/C]AAAAATAGCTGGGCA | 10422 |
| rs562205299 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135963040 | GGCAGGGCATCCTTG[C/T]GGGGGAGCAATGCGG | 10422 |
| rs562331979 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960640 | ACTGCCGGAAAGTCC[C/T]GAGGCCCTGCTCCGT | 10422 |
| rs562476456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957503 | ACGGAAGCACTAGGA[C/T]GACCGTGTCACTCTG | 10422 |
| rs562709751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946624 | GCTGGCCCGATACTC[A/G]GCCTGTGCCCTGTGA | 10422 |
| rs562797570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952100 | GACTCAGGGACAGGC[A/G]GAGGCAGGCCCAGAT | 10422 |
| rs562916118 | in-del | -/AC | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941230 | GGCCAACATGGGAAA[-/AC]CCCATCTCTACTAAA | 10422 |
| rs563040445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937372 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGGG | 10422 |
| rs563206630 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938148 | CCGTATCGCCTCCGC[A/G]GCACCTATTTGTCCT | 10422 |
| rs563242279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943867 | CAGCAAACTAACACA[A/G]GAACAAAAAACCAAG | 10422 |
| rs563254336 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936461 | AAAATAAAAGGAAAA[C/T]GTGTTTCTGACTTTC | 10422 |
| rs563261217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948583 | GGCAACTCCCAGAGA[A/G]CTGGGCTTGAGACCC | 10422 |
| rs563271917 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947107 | TTGGACTGGCATCAG[A/G]TGAAGTTGGAAGCCA | 10422 |
| rs563310081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934426 | AACACTTTGGGAGGC[C/T]GAAGCAGGCGGATCA | 10422 |
| rs563608181 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934813 | TGAAAGAGTTGAACA[A/C]AAAGATAAAGAGTTA | 10422 |
| rs563634311 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939882 | CAACAGCACTGAGGA[C/T]GCTGTCCGTCCACGT | 10422 |
| rs563847773 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950629 | ATTATACTAGTAATG[A/G]AAACCCTGAGATCTT | 10422 |
| rs563892383 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950397 | GCCAGAGGGATCTGG[A/T]GGGAGGGAACACCCC | 10422 |
| rs563905902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947297 | GCTCTTGCTGCCGAG[A/G]CTGGAGTACGATGAT | 10422 |
| rs563912828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948128 | AAATAAGAGTGAAGC[A/G]GTAGGTGAGGGGCAG | 10422 |
| rs564130893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953213 | ACAGGCTCTGCCGGG[A/G]GAGAGAACCCCTTAT | 10422 |
| rs564180069 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957977 | GAAGGGGTATTGCCA[C/T]GTTGGCCAGGCTGGA | 10422 |
| rs564383445 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947734 | CGCCCCGCAGGAACC[C/T]CCCCACAGCAATCCC | 10422 |
| rs564468605 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960101 | CTCAACCTGTCAACA[C/T]AGATACGTCGTAACT | 10422 |
| rs564538187 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937498 | GACAACCCAACGAGC[C/T]CTGGGTTCCCAGTGC | 10422 |
| rs564687763 | snp | A/C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932853 | GCCTCCCACATGCTG[A/C/T]GGTGGCCCCGGTGCC | 10422 |
| rs564703880 | in-del | -/T | 0.0166325 | 0.0896639 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940553 | CACTGCACTGCAGCC[-/T]TGGGCGACAGAGCGA | 10422 |
| rs564739928 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952733 | TGCCCGGGACCAGAA[C/T]TGTTTCGGATTTCGG | 10422 |
| rs564748957 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933701 | CCATCGGATGCACCC[A/T]TCAAATCAGATCTGA | 10422 |
| rs564751376 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962359 | CTCCCCACTGCAAGC[A/C]CCCTTGGCAGTGGTC | 10422 |
| rs564866249 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962914 | GAGTGGGGGAAGCTA[C/G]AGGGCTTGGAGGAGC | 10422 |
| rs564982479 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935821 | CACGAGGTCAGGAGA[G/T]CAAGACCATCCTGGC | 10422 |
| rs565098279 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952040 | GGTCAAACTGTAATC[G/T]GAGAACTGTGAATGC | 10422 |
| rs565173693 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956939 | AGCCTGGAGCTGGGC[C/T]GGGGCACCACCCCAG | 10422 |
| rs565244235 | snp | A/C/G | 0.000432123 | 0.014693 | missense, synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945981 | CACACGCTCATCCTC[A/C/G]TCCTCGTCCAGCATT | 10422 |
| rs565431055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941512 | CTGGAAGAACCCACC[A/G]CACAATATTTTGATA | 10422 |
| rs565450658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937066 | AATACGCTTCTGAAA[A/G]AAGGCCAGCCTTCAA | 10422 |
| rs565503396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942679 | AAAAGAGAAACTTTT[A/G]CATGCAGAGCTAACC | 10422 |
| rs565518193 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940980 | AGCACTGCACCCCGC[A/G]GACGGTGCACGTCCA | 10422 |
| rs565576122 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932956 | GGCACCAAGAAAAGA[C/T]GAAGACAGGAAATAG | 10422 |
| rs565626102 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938831 | GGGGGGGATGTGGGC[C/T]ACCACAGGGACCTCC | 10422 |
| rs565769658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956104 | ACCCGGGCAGGGAAC[A/G]GGAGGCAACACATGG | 10422 |
| rs565792042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959791 | CGATGGTTGTTCAGA[C/T]GGCAAAATCATGCAG | 10422 |
| rs565825605 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948292 | CTTCTGGAAGCTCCT[A/G]AAGGGCAGTCATGGC | 10422 |
| rs565899330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944474 | GAGGAAGTAAAACCC[A/G]AATCAAAGAACAGGA | 10422 |
| rs565903847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938072 | GGACTACACCCGCAG[A/G]ATGCCAACCTGCATG | 10422 |
| rs565936558 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944134 | CTTAACATTAAATTA[A/T]ATTTTAAAAGAAACA | 10422 |
| rs565958440 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954345 | AGCTACTTGGGAGAC[G/T]GAGGTGGGAGGACTG | 10422 |
| rs566078948 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950910 | CCAGCCTGGGCAACA[C/T]GGTGAGACCCCATGT | 10422 |
| rs566101922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938502 | CCCTGGAAGGGACTC[C/T]ACCGTGAAGACAAAC | 10422 |
| rs566218794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951383 | TGGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 10422 |
| rs566240838 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934104 | TGTGAAGGAGCACGC[A/G]TTCTGCCAGCCCCTC | 10422 |
| rs566258009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950705 | TAGCCTCTTCATTAA[G/T]AAGTCAATAGAGACT | 10422 |
| rs566360418 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135963131 | TGGAGGGTGTGGGCC[C/T]AAGAGTGAAATCAAG | 10422 |
| rs566386626 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934335 | AACAATCCTCTGGTG[C/T]TCTGATTAAAAGTCT | 10422 |
| rs566477231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956691 | ATCGTGGGGTGAGAG[A/G]AGAGGGGCTGCACTT | 10422 |
| rs566550236 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956606 | GCACAGCACACCACC[A/G]CACAGCACAGCACCG | 10422 |
| rs566622525 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940602 | AAAAAAAAAAATCCT[A/C]AAACTAATTTTTTAA | 10422 |
| rs566653543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941128 | TCAAAAGTCCCAGCC[A/G]GGAGCAGTGGCTCAC | 10422 |
| rs566723458 | snp | A/G | 0.000106362 | 0.00729176 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955274 | GCCTGCTGCCAACCC[A/G]CCCGCCCACAGCAGC | 10422 |
| rs566757882 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936124 | GGGGCAGATCTTGCA[A/T]GGACAGTGGCGCCAT | 10422 |
| rs566906665 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957903 | CCTCAGCCTCCTGAG[G/T]AGGTGGGATTACAGG | 10422 |
| rs567161474 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953256 | TGTAAATGGCGAATG[C/T]GTGGGTTGGTGAACA | 10422 |
| rs567203194 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960503 | AGAGCTCCAAGCAGC[C/T]GGCTCTGCGGGAAAG | 10422 |
| rs567286034 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938467 | TCTGTGAGTTCCTGT[A/T]GAGCCCCCAGGGCTG | 10422 |
| rs567508143 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949146 | TGAGCCAGGACAGAC[A/G]GCCCACGGAGGAACA | 10422 |
| rs567529122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949152 | AGGACAGACGGCCCA[C/T]GGAGGAACACACCAG | 10422 |
| rs567532853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935183 | ATTACAGGCATGAGC[A/C]ACCATGCCCAACCTG | 10422 |
| rs567577876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944547 | TCCACACACACAGGC[A/G]CAGGGACCCTTCAGC | 10422 |
| rs567612608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955677 | CCCTACTGACAATTC[C/G]CGGCCACCAGAATTG | 10422 |
| rs567777010 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934090 | TCTGTTCCACCCACT[A/G]TGAAGGAGCACGCGT | 10422 |
| rs567777592 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939958 | CTAAAGCCGAGGAAG[C/T]GCAGGGATGACTGTA | 10422 |
| rs567875951 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135940512 | ATGAACCTGGAAGGC[A/G]GAGCTTGCAGTGAGC | 10422 |
| rs567889640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943967 | ACACACCGGGGCCCA[C/T]CAGGGGGTCTGGGGG | 10422 |
| rs567929648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937283 | CCGTCTCTACTAAAA[C/T]ACGAAAAATTAGCCA | 10422 |
| rs568058370 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135960508 | TCCAAGCAGCCGGCT[C/T]TGCGGGAAAGGGGAA | 10422 |
| rs568058902 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941855 | GCCTCAAGTCAGAGC[G/T]CTCCAATCCTTTCTC | 10422 |
| rs568086816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952939 | CGAGTGCTCCCTCAC[C/T]GGCCACTCTCTGCAT | 10422 |
| rs568095680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946873 | GCTACAGGGCCTAGA[A/G]GTCAGGCGTCAGCTG | 10422 |
| rs568174282 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956425 | CACGGGGGCTAGGCG[C/T]GTCGGCTCACCATTT | 10422 |
| rs568494138 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961774 | CTGTTTCTTTTAACC[C/T]TTTTAAGATAGAATT | 10422 |
| rs568551379 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939020 | CAAGATCAGCCTGGG[A/C/G]AACAAAGGGAGATCT | 10422 |
| rs568582980 | snp | C/G | 0.000385076 | 0.0138705 | missense | UBAC1 | GRCh38.p7 | 9:135947830 | GGACCGCGGCCCGGT[C/G]CATGTTGTAGGAGGG | 10422 |
| rs568656860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956284 | TACAAAGATCTCACA[A/G]CCAACTGCTGGCAGG | 10422 |
| rs568694979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943617 | CTGGGTATATACCCA[A/G]AGGAATAGAAATCAT | 10422 |
| rs568746275 | snp | A/G | 0.000152332 | 0.00872598 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938175 | TCCTGCAAGGGAACC[A/G]GCCAGCCTCCCCGAC | 10422 |
| rs568770965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948246 | GCTGCAGCTGAGCCC[C/T]GAGGCCAAAACCACG | 10422 |
| rs568816188 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956686 | CCGGAATCGTGGGGT[A/G]AGAGGAGAGGGGCTG | 10422 |
| rs569101222 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935808 | GAGACGGGCGGATCA[A/C/T]GAGGTCAGGAGATCA | 10422 |
| rs569135111 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962144 | GAACTCCCAGCCTCA[A/G]TATCAGATCACCCTG | 10422 |
| rs569166254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945773 | TCTTCAAAACCCCAC[A/G]TTAGAAATGATTCAG | 10422 |
| rs569230172 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936017 | GGTGACAGAGCGAGA[G/T]TCCATCTCAAAAAAA | 10422 |
| rs569282494 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940498 | GGCAGGAGAATGGCA[C/T]GAACCTGGAAGGCGG | 10422 |
| rs569366743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936642 | GGGATTACAGGTGCA[C/T]ACCACCATGCCCAAC | 10422 |
| rs569532665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952432 | CTCCATGCTCGGCAC[A/G]GGCTCAGGCCCTGCT | 10422 |
| rs569549507 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949381 | CAGGACTAAATTTCC[C/T]AGAACTCAAACATCT | 10422 |
| rs569626709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938100 | ATGGCAGGACGTGCT[A/G]CCAGCGCACGGCGAT | 10422 |
| rs569807459 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955166 | AGAATGCTTTTAGTC[G/T]ATCTCGTTTTTGTGC | 10422 |
| rs569810001 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944514 | AAGAATGGGGAGATG[A/G]GGCGCGGGCGAGGAA | 10422 |
| rs570010737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960351 | AAGTGTCTCCGCGAG[A/G]AGACCCTACTCCTGG | 10422 |
| rs570059890 | snp | G/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135945493 | GCAAGCGGACCCAGA[G/T]ATATCTGCTGAGGGC | 10422 |
| rs570104915 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934635 | ACTGCACTCCAGCCT[G/T]GGCAGCAGAGTGAGA | 10422 |
| rs570278248 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941745 | GGGCCTTGCGCTCAC[G/T]GGCTGCAGGACGTCG | 10422 |
| rs570317832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941275 | GCTGGGCGTGGTGGC[A/G]GGCACCTGTAATCCC | 10422 |
| rs570355511 | snp | G/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938966 | GTAATCCCAGCACTT[G/T]GGAAGCCAAAGCAGG | 10422 |
| rs570369865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957576 | GCCCCAACCAAGGCC[A/G]CTGGAGTAGGGAGGC | 10422 |
| rs570377162 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947970 | AAAGACGATGACAAC[A/T]GAATCAGCGGAGCTC | 10422 |
| rs570415996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940132 | TGGATAAGACTGTCT[C/T]GGCAGCCACCGCAGG | 10422 |
| rs570481869 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952287 | GGGCCTAGCCCAAAA[A/G]AGTTTGACCTGCTCT | 10422 |
| rs570572115 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958922 | GTGGGATACAATCTC[A/C]ATTTAAAGTAGAATA | 10422 |
| rs570650657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937239 | ACGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCA | 10422 |
| rs570657591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958425 | TCCACTCCAGGGCAA[C/T]GGAAGCTAGAGGCCA | 10422 |
| rs570795664 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932875 | CCCGGTGCCCGCCCC[A/G]GGTCAGAGCAGCCGG | 10422 |
| rs570965679 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961666 | AAAAAGGAATGTAAG[G/T]CATCTCGATAATGTT | 10422 |
| rs571130478 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935023 | TAGCAGGGACTACAG[C/G]TACGTGTGCCACCAC | 10422 |
| rs571155780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942785 | CGCAGGGGCTGCCCT[A/G]GGAGGGCGGGGTCTG | 10422 |
| rs571208981 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955711 | CTTTGGTCTAGAAAG[A/T]TCTGGAAAATAATTT | 10422 |
| rs571256494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934609 | AGCTGGCAGTGAGCC[A/G]AGATTGCGCCACTGC | 10422 |
| rs571296111 | snp | A/G | 4.56777e-05 | 0.00477878 | intron-variant | UBAC1 | GRCh38.p7 | 9:135961013 | GGGGCAGGGGAGGGG[A/G]CCCGGCCTTACGTGC | 10422 |
| rs571482731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956581 | ATACAGCCCGACACA[C/T]GACAGCACAGCACAG | 10422 |
| rs571546037 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949736 | TCGAGGACGGCCGCA[C/T]GCTCCCCGGGCCTGG | 10422 |
| rs571548231 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135933839 | CATCTTCCCCAACAA[C/T]TCCACTTCCAATCCC | 10422 |
| rs571672196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945597 | CAGAAGCAGGGCAAG[C/T]AACTCACACGGGAAT | 10422 |
| rs571681350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951239 | CGTGGGCCACCGCAC[C/T]CAGCCAAGACTGCTA | 10422 |
| rs571747235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940407 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 10422 |
| rs571783262 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935959 | TGAACCCGGTAGGCG[A/G]AGCTTGCAGTGAGCT | 10422 |
| rs571963680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947238 | CCCAAAATAACTCAC[A/G]GGTTCAGATTTGTGT | 10422 |
| rs572037660 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947554 | TCAGGGCCGGATTGA[C/T]GTTTTCCCAGGGGTA | 10422 |
| rs572063044 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949713 | CCTGGTCCTGCGGCA[A/G]GCAGAACTCGAGGAC | 10422 |
| rs572124203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947617 | TCCAACTCTTACTTG[A/G]AAATAATTTTTGATT | 10422 |
| rs572187382 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953387 | AGTGGCACGATCTCG[G/T]CTCACTGCAACCTCT | 10422 |
| rs572198064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943665 | TGCACACGTATGTTC[A/G]CTGCAGCACTACTCA | 10422 |
| rs572245610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944207 | CTGAGCTGCGAAGCC[A/G]GGGGTTACACTGCGG | 10422 |
| rs572261050 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953435 | GATTCTCCTGCCTCA[A/G]CCTCCTGAGCTGCTG | 10422 |
| rs572293470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953152 | AGAGGCAGGTTTTCC[A/G]TGCTGGTCCCGTGAG | 10422 |
| rs572347186 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959123 | ATAAAAGAGTATCAT[C/G]ATGGCCATGCACATC | 10422 |
| rs572547251 | in-del | -/A | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939211 | ACTCCAAAAAAATTA[-/A]AAAAAAAAAAAAAAT | 10422 |
| rs572561573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933620 | TGAAGAGGGTGCGTC[C/T]CCAATACAAAGGCCA | 10422 |
| rs572616547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960031 | ATGCGAGCAGCTACT[A/G]TGGTAAGAACTGAAG | 10422 |
| rs572713220 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934436 | GAGGCCGAAGCAGGC[A/G]GATCATGAGGTCAGG | 10422 |
| rs572835055 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949528 | CAGAGGAAGGGGAGG[A/C]GGCTGGTGCAGGGAG | 10422 |
| rs572839612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945827 | CGTCACCCACGGTGG[A/G]AGCCCCACAAAACCA | 10422 |
| rs572921472 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945347 | TCTGCTATGGTAGTG[A/G]CTTCTCCAGCATCAG | 10422 |
| rs572952813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940085 | CAGTCAGGCCAACTT[C/T]AGACCCTTTCAGGTT | 10422 |
| rs573035427 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935797 | TTTGGGAGGCCGAGA[C/T]GGGCGGATCACGAGG | 10422 |
| rs573056635 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962865 | TGGAAGCTGGTGGAG[C/G]AGAAAGGGGAGGAAC | 10422 |
| rs573098704 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935422 | AGGCAGAGGTGGGGG[A/G]AGCGCTTGAAGCCAG | 10422 |
| rs573130780 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135963372 | CAAACACTGGGCAGC[C/T]GGCCTGGGCCACGTA | 10422 |
| rs573172622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956889 | ACTTTCTAAACCCGG[C/T]AGCAGGCTCAGCCTG | 10422 |
| rs573281210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954952 | TGGATGTGTGTGTCT[A/G]ACACTGCACTGGGAT | 10422 |
| rs573398003 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957233 | AGGCTGAGGGGATGT[C/T]GGGGGGACGCAGCTA | 10422 |
| rs573449102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941500 | CAACAATGAACTCTG[A/G]AAGAACCCACCGCAC | 10422 |
| rs573452496 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936069 | GTTAAAACAATGAAG[C/G]TCTTGTCTATAATAT | 10422 |
| rs573490884 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946181 | AAAGCACTGAGGTTC[C/T]GGTCAGTGGTCAGTG | 10422 |
| rs573509297 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952065 | GAATGCTGCCTGCAG[C/T]AGTTCCCAGAAACAG | 10422 |
| rs573509901 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940893 | ATCTTTGGCAGTTTT[C/G]CGGCCACCATAAGGT | 10422 |
| rs573571448 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135948855 | TGGGTGAATTACTTG[A/G]GGTCAGGAGTTCGAG | 10422 |
| rs573731811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954600 | GAGGCAGGCACAGCA[C/T]GGCCCCAATAATTGT | 10422 |
| rs573878642 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135943801 | AGCCATAAAAAGGAA[C/G]GAGATCACGTCCTTT | 10422 |
| rs573894620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948098 | CAGACGTGTCCTCAG[C/T]GTCTGCTCTGACGTA | 10422 |
| rs573947343 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956388 | GTGGCACTGGCTTGC[A/G]GGAGTCCTGCTTTCC | 10422 |
| rs573949341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949577 | TCACGTACTGCATAC[A/G]GCTGGCACCCCCTCC | 10422 |
| rs574010351 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948480 | TCCTAGAACTGCATC[C/G]GTGGCAGGGGACAAG | 10422 |
| rs574088504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939138 | GCCCAGGAGGTCGAG[A/G]CTGCAGTGAGTGTGA | 10422 |
| rs574172965 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936907 | CCAGAAACTGAACAA[C/G]GGCATCTGCAACACA | 10422 |
| rs574232511 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936247 | CACTAACATCCTAAG[G/T]TATACAAACAGCTGG | 10422 |
| rs574295764 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961855 | TAGAACGGAGGCTCT[C/T]CAAAGAACTTGGCTT | 10422 |
| rs574299823 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135960747 | GCTGGCGTGTACAGG[A/G]CTCGGCCGGGCGGCT | 10422 |
| rs574431151 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135958086 | GAGTCTCTCTCCGTC[A/G]CCCAGGCTGGAGTGC | 10422 |
| rs574511388 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953257 | GTAAATGGCGAATGC[A/G]TGGGTTGGTGAACAA | 10422 |
| rs574703330 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBAC1 | GRCh38.p7 | 9:135940536 | AGTGAGCCAAGATCG[C/T]GCCACTGCACTGCAG | 10422 |
| rs574766660 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939401 | GCCTCCACCACGCCC[A/G]GGGCGCTCACGAGTG | 10422 |
| rs574880501 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955757 | GATCCATTGTTTCCT[A/G]ATGACCTAAAGATCT | 10422 |
| rs574884221 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947168 | CTGCCCTGCCTGCTG[C/T]GGCGTCCACGTGAGC | 10422 |
| rs575001017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135942821 | TACACACAGACAGAA[C/T]GTGCGCCTTGGGCCC | 10422 |
| rs575113475 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934533 | GGCGTGGTGGCAGGC[A/G]CCTATAATCCCAGCT | 10422 |
| rs575161922 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933070 | ACCTCCGTCAAATAA[A/C]AAGTGGACTCTCCAA | 10422 |
| rs575174857 | snp | A/G | 0.000197198 | 0.00992774 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955458 | GAAAATAAGTAAATC[A/G]TAATTCTAATAATAT | 10422 |
| rs575200526 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950100 | TTCCCCAGCCTCAGA[A/C]AGGAAGGCAGCCCTT | 10422 |
| rs575345520 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949543 | CGGCTGGTGCAGGGA[G/T]GAGCGGCTCAGAGCT | 10422 |
| rs575357808 | in-del | -/T | 0.323908 | 0.238825 | intron-variant | UBAC1 | GRCh38.p7 | 9:135936499 | GGGTTTTCCTTTTTC[-/T]TTTTTTTTTTTTTTG | 10422 |
| rs575512305 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939297 | AGAATTCCGTATTTT[A/T]AAATTTTTATACTGT | 10422 |
| rs575608295 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937754 | CCCAAAGCTGAATAG[C/T]AGATACATGGCTATT | 10422 |
| rs575706174 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962061 | GGCTCCTGAACCTTC[C/T]ACATCATCTGTACAC | 10422 |
| rs575732729 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947473 | GGCCAGGCTGGTCTC[A/G]AACTTCTGACCTCAG | 10422 |
| rs575743217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945411 | ACAGGTGCGACGGAA[A/G]CGCTGGTCCTTGCCT | 10422 |
| rs575779255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950893 | AGCCCAGGAGTTCAA[A/G]ACCAGCCTGGGCAAC | 10422 |
| rs575781135 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956884 | TGGGCACTTTCTAAA[A/C]CCGGTAGCAGGCTCA | 10422 |
| rs575807965 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946158 | CAGGCCCTCATCAGC[A/G]CTTCCATAAAGCACT | 10422 |
| rs575892978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135957379 | TTTGCAGGCTAGTTC[A/G]TTTGTCAAGTTCAGA | 10422 |
| rs575942535 | snp | C/T | 3.32773e-05 | 0.00407892 | missense | UBAC1 | GRCh38.p7 | 9:135945908 | TCAGCTGAAGGGCCT[C/T]GGTGGCTCTGTTCTC | 10422 |
| rs575950594 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135932974 | AGACAGGAAATAGGA[A/T]AAGGGACTTTATTAA | 10422 |
| rs576056616 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135951767 | GTGAGCTGAGATCAC[A/G]CCACTGCACTCTAGC | 10422 |
| rs576125973 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937690 | CGCGGCCACGGCGAC[A/G]GCCACACCGGAGGGA | 10422 |
| rs576170454 | snp | G/T | 0.000461878 | 0.0151897 | missense | UBAC1 | GRCh38.p7 | 9:135938300 | AGAGAGGACTGTCGG[G/T]GTCGATGCCCTTGTC | 10422 |
| rs576245099 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948003 | CCCAAGAAAGACTCC[A/G]TCTCCTTTAGGAGCC | 10422 |
| rs576286353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959865 | CCCTTGAACGCAGGA[A/G]GCTCAGCCCCCTCCT | 10422 |
| rs576302856 | snp | C/T | 1.70179e-05 | 0.00291696 | missense | UBAC1 | GRCh38.p7 | 9:135955402 | TTGGGATCTTCTAAG[C/T]TCCCATGAGCACACT | 10422 |
| rs576303956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947736 | CCCCGCAGGAACCCC[C/T]CCACAGCAATCCCCC | 10422 |
| rs576330645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135954445 | CGACACCCTGTCTCA[A/G]AAGAGCATGGGTTCC | 10422 |
| rs576339610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960610 | AAAACCTCACCCCAA[C/G]AGCAAAAAGGTACAA | 10422 |
| rs576437802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933721 | ATCAGATCTGATCAC[A/G]GAGAGTCATGCACTC | 10422 |
| rs576449122 | snp | G/T | 1.82151e-05 | 0.00301782 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945856 | CAGGCCCCAGGTGTC[G/T]CCGGCAAGGGAAGGA | 10422 |
| rs576514055 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943674 | ATGTTCACTGCAGCA[C/G]TACTCACAATAGCAA | 10422 |
| rs576559330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946128 | ATCAACAGGAGTTGC[C/T]GGTGAGGCAGGCCCC | 10422 |
| rs576595356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135934191 | GTGGCCCCAGGTCTA[C/T]AGGCTCCAGGGACAG | 10422 |
| rs576854000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935823 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 10422 |
| rs577148241 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135940895 | CTTTGGCAGTTTTCC[A/G]GCCACCATAAGGTGG | 10422 |
| rs577150448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135952053 | TCTGAGAACTGTGAA[C/T]GCTGCCTGCAGCAGT | 10422 |
| rs577152866 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | UBAC1 | GRCh38.p7 | 9:135959289 | TGGACTTGTGGATAT[-/A]AACCGAACCCCTGAG | 10422 |
| rs577388961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947128 | TTGGAAGCCAGCCGT[C/T]CTCCCACCCCGGCAC | 10422 |
| rs577508648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135937086 | CCAGCCTTCAAGATC[A/G]GGGCACGGCCATCGC | 10422 |
| rs577532892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135941514 | GGAAGAACCCACCGC[A/G]CAATATTTTGATATC | 10422 |
| rs577545372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960546 | GAGAAGGGGCCTCTT[A/C]ATGAAGGAGCCTACG | 10422 |
| rs577742534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948409 | GGATGGAGGGATCAG[C/T]GGAGCTACAAAGGCT | 10422 |
| rs577767896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135948522 | AGGAGCTAGCGCTCC[A/G]TCCCCCGCCACCCTG | 10422 |
| rs577856163 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944700 | AACAGGGGGGGCTTG[C/T]GGATGAGTGGTCAGA | 10422 |
| rs577903396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938709 | TGCCCAGCTTGCCTG[C/T]GGTCCTGTTATGGGC | 10422 |
| rs577917687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135935358 | ATTGCAATTGAAAAA[C/T]ACATGTGCCAGGCAC | 10422 |
| rs577929305 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944334 | GAAAACACGAGCTCC[C/G]CAGGTGAGGCCACAG | 10422 |
| rs577929885 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135960045 | TATGGTAAGAACTGA[A/G]GTTTATCCTTAGAGA | 10422 |
| rs577931179 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135949300 | CACGCCTACCAGCCA[A/C]CTCATAAGAGTTACA | 10422 |
| rs578021081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944631 | GGACACCCCCGACGG[C/T]AAATGACCCTCCCGG | 10422 |
| rs578111875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBAC1 | GRCh38.p7 | 9:135956421 | TGAACACGGGGGCTA[C/G]GCGCGTCGGCTCACC | 10422 |
| rs578149790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950814 | TTATGAGTGGTTGGG[C/T]CGGGCATGGTGGTTC | 10422 |
| rs578227916 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBAC1 | GRCh38.p7 | 9:135950020 | CAGCCCCCAGCTGGC[C/T]GCCAGCAAGAAAATG | 10422 |
| rs745320692 | in-del | -/CACGCT | 6.64137e-05 | 0.00576216 | cds-indel | UBAC1 | GRCh38.p7 | 9:135945968 | GGGCAGCCTCGTCCA[-/CACGCT]CATCCTCGTCCTCGT | 10422 |
| rs745371399 | snp | C/T | 1.65127e-05 | 0.00287334 | missense | UBAC1 | GRCh38.p7 | 9:135945050 | TCAGCCCGAAACTCC[C/T]TTTTCCTCCGGATCT | 10422 |
| rs745372763 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957537 | CTTTGTTCTCGGCAG[A/C]AGCTGGGGTATGGCA | 10422 |
| rs745424837 | in-del | -/ACTG | | | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932601 | AACAAACAGCTCGGA[-/ACTG]ACTGCTTCCAGCAAC | 10422 |
| rs745580720 | snp | A/G | 7.8373e-05 | 0.00625942 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960979 | GGTCCGCAGTCGGAG[A/G]GGTCCGGAGCGGGTG | 10422 |
| rs745599369 | snp | A/T | 1.66103e-05 | 0.00288182 | missense | UBAC1 | GRCh38.p7 | 9:135945975 | CTCGTCCACACGCTC[A/T]TCCTCGTCCTCGTCC | 10422 |
| rs745601029 | snp | C/T | 2.62003e-05 | 0.00361932 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135961049 | GCAGCGCTCCTTGAG[C/T]TTCTCCACCGAGGTG | 10422 |
| rs745629536 | in-del | -/CCAACTTCAGA | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135940077 | CACGAGGCAGTCAGG[-/CCAACTTCAGA]CCAACTTCAGACCCT | 10422 |
| rs745736259 | in-del | -/AGC | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959334 | GCTCAGGGAGGACAC[-/AGC]AGCACCTCAGAGAAG | 10422 |
| rs745891693 | snp | C/T | 1.79725e-05 | 0.00299766 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953792 | CAACACACTGGTTAT[C/T]ACTTCATATCCACAA | 10422 |
| rs745927233 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135955710 | TCTTTGGTCTAGAAA[A/G]ATCTGGAAAATAATT | 10422 |
| rs745957966 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943381 | TCACTGATCATTAGA[A/G]AAATGCAAATCAAAA | 10422 |
| rs745980714 | snp | C/T | 2.44909e-05 | 0.00349926 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945286 | TCCAACATCCCCAGA[C/T]TAACGGACCAGGGCC | 10422 |
| rs746028418 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934427 | ACACTTTGGGAGGCC[A/G]AAGCAGGCGGATCAT | 10422 |
| rs746116039 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944610 | CCTGAGCGGCCCCTC[A/G]CTCATGGACACCCCC | 10422 |
| rs746124698 | snp | G/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934944 | GGAGTGCAGTGGAGT[G/T]ATCATGGCTCACTGC | 10422 |
| rs746137736 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135960119 | ATACGTCGTAACTTA[C/T]CACATGGAGTCGCCA | 10422 |
| rs746138674 | snp | C/T | 1.70915e-05 | 0.00292326 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945879 | GGGAAGGAGGTGGCC[C/T]CCCACGCACTGGTTC | 10422 |
| rs746152739 | snp | C/G | 3.33233e-05 | 0.00408173 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933537 | GGAAAACAGAGCCAG[C/G]CTGAGTGCCCACGCC | 10422 |
| rs746204797 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937826 | TGTATGTACGTATCT[A/C]ACAATAAAAATAAAC | 10422 |
| rs746345989 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135948297 | GGAAGCTCCTGAAGG[A/G]CAGTCATGGCAGTAG | 10422 |
| rs746428531 | snp | C/T | 0.000141922 | 0.00842264 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947775 | ACCCCATGCACCCGC[C/T]GCCGCTCTGGGCTGA | 10422 |
| rs746438831 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135954592 | TGGCCCAGGAGGCAG[A/G]CACAGCACGGCCCCA | 10422 |
| rs746455366 | snp | G/T | 1.64993e-05 | 0.00287218 | missense | UBAC1 | GRCh38.p7 | 9:135946367 | TTCCGGAGTTCTGTC[G/T]GGAACTGTGGTGAAA | 10422 |
| rs746506797 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135940834 | CCTCTCCTAATCCCT[C/G]AAAGGTCAGATCCCA | 10422 |
| rs746730543 | snp | G/T | 1.68216e-05 | 0.00290009 | missense | UBAC1 | GRCh38.p7 | 9:135955388 | GATGGGTTATACTTT[G/T]GGGATCTTCTAAGCT | 10422 |
| rs746800431 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959199 | CCCATGTCGATGCAG[C/T]GTGGGGTCCACAGGA | 10422 |
| rs746841119 | snp | A/G | 1.66313e-05 | 0.00288364 | missense | UBAC1 | GRCh38.p7 | 9:135945910 | AGCTGAAGGGCCTTG[A/G]TGGCTCTGTTCTCCG | 10422 |
| rs746903030 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949547 | TGGTGCAGGGAGGAG[C/T]GGCTCAGAGCTGCCT | 10422 |
| rs746986351 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950963 | TCAGGTGTGGTGGCA[A/C]ACACCTATAGTCCCA | 10422 |
| rs746991346 | snp | A/G | 1.77593e-05 | 0.00297982 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135947894 | ATCTGGAGCTTTCTG[A/G]TCTTGTTTTTTCTAC | 10422 |
| rs747005393 | snp | G/T | 1.65002e-05 | 0.00287225 | missense | UBAC1 | GRCh38.p7 | 9:135938238 | TAGCAATGTTTTCGG[G/T]TTGGTCAGGCCCAGC | 10422 |
| rs747077069 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942758 | AGAAAGCTAGCCCTG[A/G]GAGAGGGTGTGCGCA | 10422 |
| rs747134054 | snp | C/T | 1.66172e-05 | 0.00288242 | missense | UBAC1 | GRCh38.p7 | 9:135953706 | CTGAGACATCAGCCA[C/T]CTTGGGAAGTGGTGA | 10422 |
| rs747154918 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135954267 | CCTGGACAACATGGC[A/G]AGACCCCATCTCTAC | 10422 |
| rs747184089 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942480 | CACAGGGAGATCCCT[A/T]TCTGTACAAAATTTT | 10422 |
| rs747276028 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943309 | GCCTGTAGTCCCAGC[C/T]ACTCAGGAGGCTGAG | 10422 |
| rs747291545 | snp | A/C | 1.65855e-05 | 0.00287967 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945187 | TTGGCCAGGAAGAGG[A/C]GTGTCTATGGTCGGG | 10422 |
| rs747308603 | in-del | -/TCAG | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939505 | ACAGCCCACACTCAC[-/TCAG]CCCACACTCACTCAT | 10422 |
| rs747362112 | snp | C/T | 1.65072e-05 | 0.00287286 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135933403 | GAACAACGCCACCTA[C/T]GTGCGATTTAGTGTC | 10422 |
| rs747378427 | snp | A/C | 1.66513e-05 | 0.00288537 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933533 | GCAGGGAAAACAGAG[A/C]CAGCCTGAGTGCCCA | 10422 |
| rs747611086 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938500 | CTCCCTGGAAGGGAC[A/T]CTACCGTGAAGACAA | 10422 |
| rs747614396 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937676 | GCAGAGAGGTAAGCC[A/G]CGGCCACGGCGACGG | 10422 |
| rs747806415 | snp | C/T | 1.65806e-05 | 0.00287924 | missense | UBAC1 | GRCh38.p7 | 9:135939693 | CATTCTGCTGGTTGT[C/T]GTTCACTCTGAGGGC | 10422 |
| rs747834943 | snp | C/T | 1.64817e-05 | 0.00287064 | missense | UBAC1 | GRCh38.p7 | 9:135946355 | GACACCAGTATCTTC[C/T]GGAGTTCTGTCTGGA | 10422 |
| rs747944649 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934161 | CCTGACACACATGGA[C/T]GCACTTCAGCATAAG | 10422 |
| rs748000452 | snp | C/G/T | 3.57649e-05 | 0.00422864 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955245 | TGGCTCCAGCGCCCC[C/G/T]AGCAGTGCACGATGC | 10422 |
| rs748078884 | snp | A/G | 8.32175e-05 | 0.00644995 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135955359 | CCTCTCTGAGGCAGC[A/G]TGGATTAATTTATGA | 10422 |
| rs748133629 | snp | C/T | 0.000168677 | 0.00918204 | missense | UBAC1 | GRCh38.p7 | 9:135947806 | CACTCACGTCTCTCA[C/T]GTTGGTCTGGACCGC | 10422 |
| rs748162848 | snp | C/G | 1.65146e-05 | 0.0028735 | missense | UBAC1 | GRCh38.p7 | 9:135938310 | GTCGGGGTCGATGCC[C/G]TTGTCCAGCTCCTCC | 10422 |
| rs748217454 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937015 | GGCCAAACGCTGAGC[A/G]GAAGGTCTCTCACAG | 10422 |
| rs748235426 | in-del | -/AT | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961735 | ATTGAGTTAAGAAAA[-/AT]ATGTCATTAAAATTA | 10422 |
| rs748242866 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962979 | ACTAACGGTGTGACC[A/G]GGTGGCAGAATGAAT | 10422 |
| rs748314724 | in-del | -/CTGA | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956787 | TGGACGGAGAGAAGG[-/CTGA]CTATTTTCTTGCTCT | 10422 |
| rs748330766 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135951529 | AAAAATTAATGTAGG[A/C]CAGGCGCAATGGCTC | 10422 |
| rs748401748 | snp | A/G | 1.70968e-05 | 0.00292371 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953674 | ATTGCAAACTTTGAA[A/G]TTTACCTTTTCTTCT | 10422 |
| rs748419066 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952854 | AAAAGTTTCAGACTG[C/T]GCTGCATTTCTGCGT | 10422 |
| rs748695545 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135946099 | CTGAGCTCCACCTGC[A/C]CGCCCTCAGGCACAT | 10422 |
| rs748761834 | snp | C/T | 1.65425e-05 | 0.00287593 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933382 | CTGTGGCCTGATAGC[C/T]GAGTGGAACAACGCC | 10422 |
| rs748766783 | snp | C/G | 3.3865e-05 | 0.00411477 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960990 | GGAGGGGTCCGGAGC[C/G]GGTGTTGGGGGCAGG | 10422 |
| rs748772114 | snp | A/G | 2.2893e-05 | 0.00338319 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135961073 | CGAGGTGTCCTCGGT[A/G]GCCTCCTCCAGCCAC | 10422 |
| rs748887183 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935961 | AACCCGGTAGGCGGA[A/G]CTTGCAGTGAGCTGA | 10422 |
| rs748911934 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947719 | CTCCTCTTGCTGCCC[C/T]GCCCCGCAGGAACCC | 10422 |
| rs748933533 | snp | A/G | 1.70298e-05 | 0.00291798 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946025 | GACAGGGCCATGAGG[A/G]CTCCAGCCTCAGGTT | 10422 |
| rs748963297 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135954075 | ACCTGGGAGGCGGAG[C/G]TTGCACTGAGCCAAG | 10422 |
| rs749104374 | snp | C/T | 3.34627e-05 | 0.00409026 | missense | UBAC1 | GRCh38.p7 | 9:135939675 | GCCCAACACTCACCG[C/T]GGCATTCTGCTGGTT | 10422 |
| rs749126335 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943200 | CGAGGCGGGCAGATC[A/G]CTTGAGGTCAGGAGT | 10422 |
| rs749223058 | in-del | -/T | 1.66218e-05 | 0.00288281 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946231 | CCAAGGCCGGCAGTG[-/T]AACCGCCCTGGAATG | 10422 |
| rs749229996 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958577 | TCATTCCCCTCCAGG[C/G]AGATGGAAAAGAGGA | 10422 |
| rs749289432 | snp | C/G | 1.66153e-05 | 0.00288225 | missense | UBAC1 | GRCh38.p7 | 9:135953711 | ACATCAGCCATCTTG[C/G]GAAGTGGTGATGGAG | 10422 |
| rs749305382 | in-del | -/TTTTT | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135953300 | ACTTCTTTATAATTC[-/TTTTT]TTTTTAAGTTTGTAT | 10422 |
| rs749360546 | snp | C/G | 1.67584e-05 | 0.00289464 | missense | UBAC1 | GRCh38.p7 | 9:135945891 | GCCCCCCACGCACTG[C/G]TTCAGCTGAAGGGCC | 10422 |
| rs749371302 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935011 | CAGTCCCCTGAGTAG[A/C]AGGGACTACAGGTAC | 10422 |
| rs749450890 | in-del | -/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942253 | GTGACTGCTCCACTT[-/G]GGACAGGCTTCCAGG | 10422 |
| rs749478431 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961663 | GGGAAAAAGGAATGT[A/G]AGGCATCTCGATAAT | 10422 |
| rs749568524 | snp | C/T | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962969 | TGTGAGAGCCACTAA[C/T]GGTGTGACCAGGTGG | 10422 |
| rs749607529 | snp | A/G | 1.72107e-05 | 0.00293343 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947786 | CCGCCGCCGCTCTGG[A/G]CTGACACTCACGTCT | 10422 |
| rs749649926 | snp | C/T | 4.94482e-05 | 0.00497209 | missense | UBAC1 | GRCh38.p7 | 9:135945068 | TTCCTCCGGATCTTC[C/T]TGAAGATTTCCGTCA | 10422 |
| rs749704638 | snp | A/G | 1.68295e-05 | 0.00290077 | missense | UBAC1 | GRCh38.p7 | 9:135947863 | GGTTGGCGGTGGCCC[A/G]CAGTATGGCCTCTTT | 10422 |
| rs749744979 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135955892 | ATAAGAGGAGCGCTC[A/G]GCATGACTGCTCTCA | 10422 |
| rs749889958 | snp | A/G | 1.6768e-05 | 0.00289546 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135947848 | TGTTGTAGGAGGGCA[A/G]GTTGGCGGTGGCCCG | 10422 |
| rs749979721 | snp | G/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943990 | TCTGGGGGAGGGAGA[G/T]CATCATGAAAAATAG | 10422 |
| rs749997868 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135933643 | AAAGGCCACACAGAG[C/T]TCACTGCTAAGTGTG | 10422 |
| rs750079741 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959100 | GCTCTCATTTCCTAT[C/T]TCCTTTCATAAAAGA | 10422 |
| rs750102428 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934592 | ATGAACCAGGGAGGC[A/G]GAGCTGGCAGTGAGC | 10422 |
| rs750104973 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944261 | CTCATCACCAGCAGA[A/G]GCAAACTCAGAATCA | 10422 |
| rs750190641 | snp | A/G | 1.65927e-05 | 0.00288029 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933360 | CTCGGGCCGCACCAG[A/G]GGGCTGCTGTGGCCT | 10422 |
| rs750216733 | snp | G/T | 0.000141183 | 0.00840069 | utr-variant-5-prime | UBAC1 | GRCh38.p7 | 9:135961175 | CATCCCGCCGCCGCC[G/T]CAGGGGCCTGCGCCC | 10422 |
| rs750269610 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952702 | AACAGTGCAGCTGAG[C/T]ATCCCTCATCTGAAA | 10422 |
| rs750278348 | snp | A/G | 4.95479e-05 | 0.0049771 | missense | UBAC1 | GRCh38.p7 | 9:135933455 | AGCATGACAGGCCCC[A/G]TTTCTGGATCATTCA | 10422 |
| rs750303199 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941978 | CCCCTCAAGCCTTGA[A/C]CACCTTGTGATGATT | 10422 |
| rs750436422 | snp | C/G | 1.65293e-05 | 0.00287479 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946256 | GGAATGCAGCATCGG[C/G]GTTGACTCATACCAT | 10422 |
| rs750497566 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939979 | GATGACTGTAGTTAG[A/C]AGAGCCGGGGGGCAG | 10422 |
| rs750561711 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947363 | TTCAAGTGATTCTCC[C/T]GTCTCAGCCTCCTGA | 10422 |
| rs750664752 | in-del | -/CAG | 1.6661e-05 | 0.00288621 | cds-indel | UBAC1 | GRCh38.p7 | 9:135938346 | GGGCTTCCGGTCCCC[-/CAG]CAGCCACTCGCACTG | 10422 |
| rs750673904 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957219 | ACACAAAACTGGCCA[C/G]GCTGAGGGGATGTTG | 10422 |
| rs750696347 | snp | A/G | 1.75136e-05 | 0.00295914 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955432 | TGGGGAAAAATAGAA[A/G]TTTCAAGGTAGAAAA | 10422 |
| rs750715582 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935895 | GCCGGGCACGGTGGC[A/G]GGCACCTGTAGTCCC | 10422 |
| rs750786364 | snp | A/G/T | 3.32581e-05 | 0.00407776 | missense | UBAC1 | GRCh38.p7 | 9:135945944 | AGCCCATCTCCGTGA[A/G/T]CTGCCGCAGGGCAGC | 10422 |
| rs750804459 | snp | C/T | 1.6659e-05 | 0.00288604 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945990 | ATCCTCGTCCTCGTC[C/T]AGCATTGCTGCAGGG | 10422 |
| rs750849955 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937436 | ACAAGGCGAGACTCT[A/G]TCTCAAAAAAAAAAA | 10422 |
| rs751054344 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952577 | CACGTGCAAGTGGAC[A/G]GTGCAGACCATGAAT | 10422 |
| rs751080291 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943625 | ATACCCAAAGGAATA[C/G]AAATCATTCTGTTAT | 10422 |
| rs751142322 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135953321 | TTTTAAGTTTGTATT[C/T]ATTTATTTAATTTTG | 10422 |
| rs751144505 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942042 | CTGACACAGAGAGAT[A/G]ACGGGAGGGAATGGC | 10422 |
| rs751192323 | snp | C/T | | | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932603 | CAAACAGCTCGGAAC[C/T]GACTGCTTCCAGCAA | 10422 |
| rs751260777 | snp | C/T | 3.34879e-05 | 0.0040918 | missense | UBAC1 | GRCh38.p7 | 9:135947831 | GACCGCGGCCCGGTC[C/T]ATGTTGTAGGAGGGC | 10422 |
| rs751290448 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135945756 | CACATATTTAAGGTA[A/C]CTCTTCAAAACCCCA | 10422 |
| rs751374269 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936785 | GGCGTGAGCCACCAC[A/G]CCCAGCCATGGAGGG | 10422 |
| rs751399220 | snp | G/T | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962794 | TGGGGCATTTTTAAC[G/T]CAGGAAGCAGAAGTA | 10422 |
| rs751502328 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949037 | CACTCAAGCCTGGGT[A/G]AGTGACAGTGAGACA | 10422 |
| rs751525391 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937353 | GGCTGAGGCAGGAGA[A/G]TTGCTTGAACCTGGG | 10422 |
| rs751568350 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938181 | AAGGGAACCAGCCAG[C/T]CTCCCCGACCCGAGA | 10422 |
| rs751584109 | snp | C/T | 3.43083e-05 | 0.00414161 | missense | UBAC1 | GRCh38.p7 | 9:135961026 | GGGCCCGGCCTTACG[C/T]GCTTGAGGCAGCGCT | 10422 |
| rs751728072 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939013 | AGGAGTTCAAGATCA[C/G]CCTGGGCAACAAAGG | 10422 |
| rs751769479 | snp | A/C | 1.77329e-05 | 0.0029776 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953784 | CGTATATCCAACACA[A/C]TGGTTATCACTTCAT | 10422 |
| rs751850591 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135955524 | TGGGTTTTCTTATGA[A/G]CTAAGAAATTACACC | 10422 |
| rs751854832 | in-del | -/CA | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939481 | CTCACAGCCCACACT[-/CA]CACTCACCACAGCCC | 10422 |
| rs751971761 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958377 | AAACTCATTAACTAC[C/G]TGTTGTACAAGACAG | 10422 |
| rs752023777 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956242 | GAAGTTGGAGCAGAC[A/G]GCCATGACCCCTTCC | 10422 |
| rs752051504 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958917 | GCAGAGTGGGATACA[A/C]TCTCAATTTAAAGTA | 10422 |
| rs752061508 | snp | A/G/T | 6.73428e-05 | 0.00580237 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938193 | CAGCCTCCCCGACCC[A/G/T]AGACTTAGCATAAAG | 10422 |
| rs752147984 | in-del | -/A | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947687 | CTCACCGGCTTCCCC[-/A]AATCCTCCCAGAGAA | 10422 |
| rs752202096 | snp | A/T | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962599 | TGCCTGCAGGCTTTT[A/T]TTCTGTCCACACCAT | 10422 |
| rs752249200 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939117 | TGAGGCAGGAGGATC[A/G]CTTGGGCCCAGGAGG | 10422 |
| rs752249674 | snp | C/G | 3.31033e-05 | 0.00406823 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135933487 | CCACTGGGTGCTGTT[C/G]AGTGGGTTCTCCAGC | 10422 |
| rs752249984 | snp | C/T | 9.10938e-05 | 0.00674823 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945858 | GGCCCCAGGTGTCTC[C/T]GGCAAGGGAAGGAGG | 10422 |
| rs752438404 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135945019 | GGCGACAGGTCTAGT[A/T]ACACATACCCGAGCA | 10422 |
| rs752473971 | snp | C/T | 3.65938e-05 | 0.00427733 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947761 | TCCCCCACACGGGGA[C/T]CCCATGCACCCGCCG | 10422 |
| rs752631024 | snp | C/T | 3.2963e-05 | 0.00405961 | missense | UBAC1 | GRCh38.p7 | 9:135945105 | CTCTGGCCTCCTCAT[C/T]GGTGGCGCTGGCTCC | 10422 |
| rs752696645 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135945607 | GCAAGTAACTCACAC[A/G]GGAATCCTGAGAAGA | 10422 |
| rs752710207 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135946617 | ACTCAGTGCTGGCCC[A/G]ATACTCAGCCTGTGC | 10422 |
| rs752808556 | snp | A/G | 1.70598e-05 | 0.00292055 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939640 | CACTCACTCACCACA[A/G]CCCACACTCACTCAC | 10422 |
| rs752823105 | snp | C/T | 1.66679e-05 | 0.00288681 | missense | UBAC1 | GRCh38.p7 | 9:135938359 | CCCAGCAGCCACTCG[C/T]ACTGCAAAGCCAAGA | 10422 |
| rs752850329 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937675 | AGCAGAGAGGTAAGC[C/T]GCGGCCACGGCGACG | 10422 |
| rs752900954 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947314 | TGGAGTACGATGATG[C/T]AATCTCGGCTTACTG | 10422 |
| rs752939978 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938106 | GGACGTGCTGCCAGC[A/G]CACGGCGATCCTCAG | 10422 |
| rs753093230 | in-del | -/CGAGCATCAGCCCGAAACTCCCT | 1.67812e-05 | 0.0028966 | splice-acceptor-variant | UBAC1 | GRCh38.p7 | 9:135939760 | AGGGAAATGACGGCC[-/CGAGCATCAGCCCGAAACTCCCT]TAGAGGACAGCACAG | 10422 |
| rs753133937 | snp | A/T | 1.75176e-05 | 0.00295947 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953775 | AAAACAACACGTATA[A/T]CCAACACACTGGTTA | 10422 |
| rs753157749 | snp | C/T | | | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933264 | AATAAGATCAGAGAG[C/T]AGGAGCAGCTGCAGC | 10422 |
| rs753211895 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941368 | CCAAGATCGCACCAC[C/T]GTACTCCAGCCTGGG | 10422 |
| rs753252750 | in-del | -/CCGCCGCCGCAGGGGCCTGCGC | 4.64608e-05 | 0.00481957 | utr-variant-5-prime | UBAC1 | GRCh38.p7 | 9:135961167 | TGCACGAACATCCCG[-/CCGCCGCCGCAGGGGCCTGCGC]CCGCCACCCGGGCCC | 10422 |
| rs753369099 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934655 | GCAGAGTGAGACTCC[A/G]TCTCAAAAAATAAAA | 10422 |
| rs753479509 | snp | C/T | 1.65255e-05 | 0.00287445 | missense | UBAC1 | GRCh38.p7 | 9:135933464 | GGCCCCGTTTCTGGA[C/T]CATTCATCCACTGGG | 10422 |
| rs753568383 | snp | A/C/G | 0.000133271 | 0.00816197 | utr-variant-5-prime | UBAC1 | GRCh38.p7 | 9:135961199 | TGCGCCCGCCACCCG[A/C/G]GCCCCTGAAGGTCAC | 10422 |
| rs753683257 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135953631 | CCTGTAATTCTTAAA[C/T]GTAGACTTCTACCAA | 10422 |
| rs753763205 | snp | C/T | 1.84804e-05 | 0.00303971 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947751 | CCCACAGCAATCCCC[C/T]ACACGGGGACCCCAT | 10422 |
| rs753771096 | snp | A/G | 8.83228e-05 | 0.00664482 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955278 | GCTGCCAACCCGCCC[A/G]CCCACAGCAGCCTTA | 10422 |
| rs753820308 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949418 | CCAGAGTCAATGTGC[C/T]GGACATAGCAAAGAG | 10422 |
| rs753851636 | in-del | -/A | 1.68576e-05 | 0.00290319 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939664 | CACTCACCACAGCCC[-/A]ACACTCACCGCGGCA | 10422 |
| rs753891681 | snp | C/G | 4.37149e-05 | 0.00467499 | intron-variant | UBAC1 | GRCh38.p7 | 9:135961015 | GGCAGGGGAGGGGGC[C/G]CGGCCTTACGTGCTT | 10422 |
| rs753900824 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957406 | CAGAATACAGACTAC[A/G]AAATGCAGTTTTCCA | 10422 |
| rs753923065 | snp | C/T | 3.32094e-05 | 0.00407475 | missense | UBAC1 | GRCh38.p7 | 9:135945949 | ATCTCCGTGAGCTGC[C/T]GCAGGGCAGCCTCGT | 10422 |
| rs754106186 | snp | A/G | 3.34966e-05 | 0.00409233 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946000 | TCGTCCAGCATTGCT[A/G]CAGGGAGACGACAGG | 10422 |
| rs754108985 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936900 | AAATAAACCAGAAAC[C/T]GAACAACGGCATCTG | 10422 |
| rs754151062 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938526 | GACAAACGCAGTCTG[A/G]ATTCACTGCCGTGCG | 10422 |
| rs754196005 | snp | C/G/T | 6.65973e-05 | 0.00577019 | missense | UBAC1 | GRCh38.p7 | 9:135938357 | CCCCCAGCAGCCACT[C/G/T]GCACTGCAAAGCCAA | 10422 |
| rs754217269 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950377 | CGACTCAGACAGATG[C/T]GCAGGCCAGAGGGAT | 10422 |
| rs754331370 | in-del | -/TTGAG | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961721 | AATATTTTGTATCTA[-/TTGAG]TTAAGAAAAATATGT | 10422 |
| rs754345574 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937537 | AAGAAAATACTCCAC[A/C]ACCCCCACAAAGAAC | 10422 |
| rs754445931 | snp | A/C/G | 9.92185e-05 | 0.00704276 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933383 | TGTGGCCTGATAGCC[A/C/G]AGTGGAACAACGCCA | 10422 |
| rs754447322 | snp | A/G | 3.57226e-05 | 0.00422611 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953659 | CAACCAAGGTCCCCA[A/G]TTGCAAACTTTGAAA | 10422 |
| rs754496149 | snp | A/T | 1.70487e-05 | 0.0029196 | missense | UBAC1 | GRCh38.p7 | 9:135945227 | TGTTCAATTAGCCAC[A/T]CCATGGCCTGAGGCA | 10422 |
| rs754515414 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135960644 | CCGGAAAGTCCCGAG[A/G]CCCTGCTCCGTCGGC | 10422 |
| rs754521237 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935479 | AACGAGACCCCATCT[C/T]AACAACAACAAAAAA | 10422 |
| rs754564905 | snp | C/G | 1.65419e-05 | 0.00287588 | missense | UBAC1 | GRCh38.p7 | 9:135933477 | GATCATTCATCCACT[C/G]GGTGCTGTTCAGTGG | 10422 |
| rs754604165 | snp | C/T | 1.65012e-05 | 0.00287234 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135946276 | ACTCATACCATTCGC[C/T]TTCTTAAACAATTCC | 10422 |
| rs754637940 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135948926 | AAGACAAAAATAAGC[C/T]CGGTGTCCTGGTGCA | 10422 |
| rs754655002 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950557 | GGAAAAATACAGCTG[C/T]GTAAGAAGGATAGAT | 10422 |
| rs754784851 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135945470 | CAGAAGCCCATGTCT[A/C]AGGAGAGGCAAGCGG | 10422 |
| rs754845885 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943298 | GGTGGGTGTGTGCCT[A/G]TAGTCCCAGCTACTC | 10422 |
| rs754910346 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944522 | GGAGATGAGGCGCGG[A/G]CGAGGAAGGTCCACA | 10422 |
| rs754922697 | snp | C/T | 1.69608e-05 | 0.00291206 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939776 | TAGAGGACAGCACAG[C/T]CGTTAGCTCGCTGGG | 10422 |
| rs754926143 | snp | A/G | 6.7784e-05 | 0.00582129 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945011 | CTCTGCCTGGCGACA[A/G]GTCTAGTAACACATA | 10422 |
| rs754962440 | snp | A/G | 0.000149416 | 0.00864209 | missense | UBAC1 | GRCh38.p7 | 9:135945950 | TCTCCGTGAGCTGCC[A/G]CAGGGCAGCCTCGTC | 10422 |
| rs754986839 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947255 | GTTCAGATTTGTGTG[-/T]TTTTTTTTTTCTTGA | 10422 |
| rs755128041 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936928 | CTGCAACACAAATAA[C/T]GGGAAAAGGGTCAGC | 10422 |
| rs755162494 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135946516 | AGGATCAGCTGAGGG[C/G]AAGGCAGGGGATTGG | 10422 |
| rs755192732 | snp | A/G | 1.68105e-05 | 0.00289914 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946007 | GCATTGCTGCAGGGA[A/G]ACGACAGGGCCATGA | 10422 |
| rs755349598 | snp | A/G | 1.68434e-05 | 0.00290197 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135947866 | TGGCGGTGGCCCGCA[A/G]TATGGCCTCTTTATC | 10422 |
| rs755454900 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956537 | GGTCCAGAGCTCCAC[A/G]ACTCCACTCTATTAT | 10422 |
| rs755491474 | in-del | -/CT | 1.6543e-05 | 0.00287597 | frameshift-variant | UBAC1 | GRCh38.p7 | 9:135939718 | GAGGGCATCTATCAC[-/CT]CTTTCTCGTCGAACC | 10422 |
| rs755543444 | snp | C/G | 0.000278663 | 0.0118006 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953647 | GTAGACTTCTACCAA[C/G]CAAGGTCCCCAATTG | 10422 |
| rs755602519 | snp | C/T | 1.65438e-05 | 0.00287605 | missense | UBAC1 | GRCh38.p7 | 9:135945171 | CGGCCTCTGGGGGAG[C/T]TTGGCCAGGAAGAGG | 10422 |
| rs755614140 | snp | C/G | 4.94556e-05 | 0.00497246 | missense | UBAC1 | GRCh38.p7 | 9:135945113 | TCCTCATCGGTGGCG[C/G]TGGCTCCCGCGGCAG | 10422 |
| rs755700495 | snp | G/T | 3.30764e-05 | 0.00406659 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945163 | GGCCCCCTCGGCCTC[G/T]GGGGGAGCTTGGCCA | 10422 |
| rs755897670 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947566 | TGACGTTTTCCCAGG[A/G]GTATCTATCTTTTCA | 10422 |
| rs755969393 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942288 | GATGTAAACTTGGCT[C/T]CCTAGGAGACAAGCA | 10422 |
| rs755972865 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135953457 | GAGCTGCTGGGACTA[C/T]AGGCATGAGCCACCA | 10422 |
| rs756062632 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943157 | GGGCGCAGTGTCTCA[C/T]ACCTGTAATCCCAGC | 10422 |
| rs756089005 | snp | A/T | 1.65176e-05 | 0.00287376 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946263 | AGCATCGGGGTTGAC[A/T]CATACCATTCGCCTT | 10422 |
| rs756117221 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135955740 | TTTAAATGAAAACAG[C/T]AGATCCATTGTTTCC | 10422 |
| rs756139461 | snp | C/G | 1.66663e-05 | 0.00288667 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135955338 | GGTCCTGGCATCACT[C/G]AGCACCCTCTCTGAG | 10422 |
| rs756205016 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956470 | AACACTGATGGTGCC[A/G]TGTGATGAAGACTGA | 10422 |
| rs756255399 | snp | C/T | 3.2994e-05 | 0.00406152 | missense | UBAC1 | GRCh38.p7 | 9:135945123 | TGGCGCTGGCTCCCG[C/T]GGCAGCCTCGGAGGC | 10422 |
| rs756297140 | snp | C/T | 1.70516e-05 | 0.00291985 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945880 | GGAAGGAGGTGGCCC[C/T]CCACGCACTGGTTCA | 10422 |
| rs756300826 | snp | A/C/T | 5.28074e-05 | 0.00513823 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955438 | AAAATAGAAATTTCA[A/C/T]GGTAGAAAATAAGTA | 10422 |
| rs756418366 | snp | A/G | 4.98666e-05 | 0.00499308 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938214 | TAGCATAAAGAAGGC[A/G]CACATACCTAGCAAT | 10422 |
| rs756524923 | snp | A/C | 1.66391e-05 | 0.00288431 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135938349 | CTTCCGGTCCCCCAG[A/C]AGCCACTCGCACTGC | 10422 |
| rs756559054 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135948893 | TGGCCAACATGGTGA[A/T]ACCCCATCTCTACTA | 10422 |
| rs756622970 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958049 | ACAGGTATAATTTTC[-/T]TTTTTTTTTTTTTTT | 10422 |
| rs756652641 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958371 | TTTCTAAAACTCATT[A/T]ACTACCTGTTGTACA | 10422 |
| rs756772580 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942150 | ATGGCAAGAAAGTAT[A/T]TGACTAACAACCTCC | 10422 |
| rs756827411 | snp | A/G | 6.70039e-05 | 0.0057877 | missense | UBAC1 | GRCh38.p7 | 9:135947844 | TCCATGTTGTAGGAG[A/G]GCAGGTTGGCGGTGG | 10422 |
| rs756862421 | snp | G/T | | | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932660 | CAAAATAAATTCATT[G/T]TCTCATTTTAAGACA | 10422 |
| rs756865350 | in-del | -/GTGGTTCAGCTGAAGGGCCTTGGTG | 1.76415e-05 | 0.00296992 | frameshift-variant | UBAC1 | GRCh38.p7 | 9:135945249 | CTGAGGCACCGACAT[-/GTGGTTCAGCTGAAGGGCCTTGGTG]GCTGCAAGGCAAGAG | 10422 |
| rs756902719 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941760 | GGGCTGCAGGACGTC[A/G]GGCCCTGCCAGCTCT | 10422 |
| rs756903589 | in-del | -/CTAA | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135951103 | CTTGTGCCAACAAGC[-/CTAA]CTAACTTTTTATATT | 10422 |
| rs756958762 | snp | A/G | 3.2963e-05 | 0.00405961 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945109 | GGCCTCCTCATCGGT[A/G]GCGCTGGCTCCCGCG | 10422 |
| rs757070958 | snp | C/G | 4.97905e-05 | 0.00498926 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933357 | GGTCTCGGGCCGCAC[C/G]AGGGGGCTGCTGTGG | 10422 |
| rs757126651 | snp | G/T | | | utr-variant-5-prime | UBAC1 | GRCh38.p7 | 9:135961339 | CTCAGCGGTCGCCTC[G/T]CTCCCGCCGCCGCAG | 10422 |
| rs757154378 | snp | A/G | 3.37035e-05 | 0.00410495 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946010 | TTGCTGCAGGGAGAC[A/G]ACAGGGCCATGAGGG | 10422 |
| rs757163651 | snp | A/C | 1.80224e-05 | 0.00300181 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955464 | AAGTAAATCGTAATT[A/C]TAATAATATAGGACC | 10422 |
| rs757194636 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135951053 | CAGTGAGGTGAGATC[A/G]TACCACACACTCCAG | 10422 |
| rs757255406 | snp | A/C | 3.35632e-05 | 0.0040964 | missense | UBAC1 | GRCh38.p7 | 9:135961028 | GCCCGGCCTTACGTG[A/C]TTGAGGCAGCGCTCC | 10422 |
| rs757343161 | snp | A/G | 1.68247e-05 | 0.00290035 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939765 | AAATGACGGCCTAGA[A/G]GACAGCACAGCCGTT | 10422 |
| rs757400901 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135955568 | AAGAATTCCCACTAA[C/T]GGTAGATGCCAAATG | 10422 |
| rs757465241 | snp | C/G/T | 0.000142102 | 0.00842808 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953787 | ATATCCAACACACTG[C/G/T]TTATCACTTCATATC | 10422 |
| rs757485364 | snp | G/T | 1.71223e-05 | 0.00292589 | missense | UBAC1 | GRCh38.p7 | 9:135955304 | CCTTACCTTGGTCCT[G/T]GATGTTCTCTTCCAG | 10422 |
| rs757513433 | snp | A/C | 8.53352e-05 | 0.00653148 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945268 | GCAAGGCAAGAGACT[A/C]TTTCCAACATCCCCA | 10422 |
| rs757523909 | snp | A/G | 1.7345e-05 | 0.00294486 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945873 | CGGCAAGGGAAGGAG[A/G]TGGCCCCCCACGCAC | 10422 |
| rs757672904 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937753 | GCCCAAAGCTGAATA[A/G]TAGATACATGGCTAT | 10422 |
| rs757715627 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135946654 | AGGAAACCGTCGGCC[C/T]AGCTGGCGCAGGTGC | 10422 |
| rs757834779 | snp | A/G | | | missense | UBAC1 | GRCh38.p7 | 9:135953718 | CCATCTTGGGAAGTG[A/G]TGATGGAGCACGCTT | 10422 |
| rs757839358 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938192 | CCAGCCTCCCCGACC[A/C]GAGACTTAGCATAAA | 10422 |
| rs757839708 | snp | C/T | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962784 | AGTCCTGGAATGGGG[C/T]ATTTTTAACGCAGGA | 10422 |
| rs757839856 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949156 | CAGACGGCCCACGGA[A/G]GAACACACCAGAACA | 10422 |
| rs757909852 | snp | C/G | 8.44716e-05 | 0.00649836 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938187 | ACCAGCCAGCCTCCC[C/G]GACCCGAGACTTAGC | 10422 |
| rs757970080 | in-del | -/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950063 | ACTCTGCCAACCGCC[-/G]GAAGACCTCAGAAGC | 10422 |
| rs757998241 | snp | C/T | 8.53206e-05 | 0.00653093 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939785 | GCACAGCCGTTAGCT[C/T]GCTGGGGGCGGCAGG | 10422 |
| rs758046874 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941901 | ATCTCGATCCCTACT[A/G]GACGACTGCCTGATC | 10422 |
| rs758056101 | snp | A/C | 5.43848e-05 | 0.00521435 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947768 | CACGGGGACCCCATG[A/C]ACCCGCCGCCGCTCT | 10422 |
| rs758172218 | snp | C/T | 1.67761e-05 | 0.00289617 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945023 | ACAGGTCTAGTAACA[C/T]ATACCCGAGCATCAG | 10422 |
| rs758269812 | snp | A/G | 1.76378e-05 | 0.00296961 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955440 | AATAGAAATTTCAAG[A/G]TAGAAAATAAGTAAA | 10422 |
| rs758281854 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934916 | GACAGCGACTTGCTT[C/T]GTTGCCCAGGCTGGA | 10422 |
| rs758365843 | snp | A/G | 3.33244e-05 | 0.0040818 | missense | UBAC1 | GRCh38.p7 | 9:135938360 | CCAGCAGCCACTCGC[A/G]CTGCAAAGCCAAGAG | 10422 |
| rs758581135 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938116 | CCAGCGCACGGCGAT[A/C]CTCAGCGCTGGATCC | 10422 |
| rs758622794 | snp | A/G | 0.000728129 | 0.0190666 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939654 | AGCCCACACTCACTC[A/G]CCACAGCCCAACACT | 10422 |
| rs758637895 | snp | A/G | 8.78495e-05 | 0.00662699 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953779 | CAACACGTATATCCA[A/G]CACACTGGTTATCAC | 10422 |
| rs758647305 | snp | C/G | 1.67323e-05 | 0.00289239 | missense | UBAC1 | GRCh38.p7 | 9:135953690 | TTTACCTTTTCTTCT[C/G]CTGAGACATCAGCCA | 10422 |
| rs758693151 | snp | A/G | | | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932472 | ATCTAAATCTCAAAA[A/G]CAATGAAAAGACCTA | 10422 |
| rs758729908 | in-del | -/AC | 3.36579e-05 | 0.00410217 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945020 | GCGACAGGTCTAGTA[-/AC]ACATACCCGAGCATC | 10422 |
| rs758828429 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950796 | TGTTAAAAATAACAA[C/G]AGTTATGAGTGGTTG | 10422 |
| rs758938327 | snp | A/G | 1.78576e-05 | 0.00298806 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945253 | AGGCACCGACATGCT[A/G]CAAGGCAAGAGACTC | 10422 |
| rs759028384 | snp | A/G | 3.31625e-05 | 0.00407188 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135933505 | TGGGTTCTCCAGCAT[A/G]TCTTCAAATGCTGCA | 10422 |
| rs759040007 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947126 | AGTTGGAAGCCAGCC[A/G]TCCTCCCACCCCGGC | 10422 |
| rs759062641 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936370 | TACAAAGAAGATCCC[C/T]ACCTCACACCACACA | 10422 |
| rs759192500 | snp | A/G | 0.000181334 | 0.0095202 | missense | UBAC1 | GRCh38.p7 | 9:135938263 | CCCAGCTGCACCACC[A/G]GGTTATCCAGGATGG | 10422 |
| rs759239504 | snp | A/G | 1.71293e-05 | 0.00292649 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135955410 | TTCTAAGCTCCCATG[A/G]GCACACTGGGGAAAA | 10422 |
| rs759268780 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135948736 | GTCCACACCCAAAGC[A/G]CAGTGCCCCAGCCAG | 10422 |
| rs759299540 | snp | A/G | 1.69292e-05 | 0.00290935 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938176 | CCTGCAAGGGAACCA[A/G]CCAGCCTCCCCGACC | 10422 |
| rs759329495 | snp | C/T | 1.66062e-05 | 0.00288146 | missense | UBAC1 | GRCh38.p7 | 9:135945922 | TTGGTGGCTCTGTTC[C/T]CCGGAAAGCCCATCT | 10422 |
| rs759473006 | in-del | -/TT | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957773 | TTTATGAACTCCTTC[-/TT]TTTTTTTTTTTTTTT | 10422 |
| rs759491200 | in-del | -/TTTTT | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947200 | CTGCAAACACTTTTC[-/TTTTT]TAACTTAGAATGTTC | 10422 |
| rs759515215 | in-del | -/A | | | utr-variant-5-prime | UBAC1 | GRCh38.p7 | 9:135961353 | CGCTCCCGCCGCCGC[-/A]GCAGCCGCCGGGGGC | 10422 |
| rs759517728 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956177 | CCGAGCAGCGCTCAC[A/G]GGGGACCTGGGAAGC | 10422 |
| rs759548642 | in-del | -/CAATGTTTTCGGGTTGGTCAGGCC/CAATGTTTTCGGGTTGGTCAGGCCCAGCTGCACCACCGGGTTATC | 3.32073e-05 | 0.00407465 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933518 | TGTCTTCAAATGCTG[lengthTooLong]CAGGGAAAACAGAGC | 10422 |
| rs759561933 | snp | A/G | 6.60066e-05 | 0.00574447 | missense | UBAC1 | GRCh38.p7 | 9:135933408 | ACGCCACCTACGTGC[A/G]ATTTAGTGTCTGGAA | 10422 |
| rs759573505 | snp | C/T | 1.67792e-05 | 0.00289643 | missense | UBAC1 | GRCh38.p7 | 9:135947821 | TGTTGGTCTGGACCG[C/T]GGCCCGGTCCATGTT | 10422 |
| rs759574278 | in-del | -/TCT | 2.11182e-05 | 0.00324941 | cds-indel | UBAC1 | GRCh38.p7 | 9:135961141 | CCTTGCCCGCGAAGA[-/TCT]TCTCCTCCTGCACGA | 10422 |
| rs759607873 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944751 | TTTTTCAAAAGGTGA[C/T]GAATGTGGCAACACA | 10422 |
| rs759609498 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956972 | CAGGCCGTCCTCGGA[C/T]GTCTCAGGTGGCCGG | 10422 |
| rs759643367 | snp | C/T | 6.10842e-05 | 0.00552616 | missense | UBAC1 | GRCh38.p7 | 9:135961131 | AGCCGCAGCACCTTG[C/T]CCGCGAAGATCTTCT | 10422 |
| rs759730820 | snp | C/T | 8.30889e-05 | 0.00644496 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946235 | AGGCCGGCAGTGAAC[C/T]GCCCTGGAATGCAGC | 10422 |
| rs759775036 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958731 | CATTCAAATACACAA[C/T]TCGAGGGTTCTCTTT | 10422 |
| rs759813376 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947293 | TTTCGCTCTTGCTGC[C/T]GAGGCTGGAGTACGA | 10422 |
| rs759828797 | snp | C/T | 1.7134e-05 | 0.00292689 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939627 | TTACCACAGCCCACA[C/T]TCACTCACCACAGCC | 10422 |
| rs759877665 | snp | G/T | 1.64762e-05 | 0.00287016 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135946300 | CAATTCCACTGCATC[G/T]GGGTTCAGCGCTAAC | 10422 |
| rs759911867 | snp | A/G | 1.65578e-05 | 0.00287726 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135939730 | CACCTCTTTCTCGTC[A/G]AACCCCATCTCCATC | 10422 |
| rs759961467 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952312 | TGCTCTTTCTCTGGG[A/G]TGAACACTCTCCTTA | 10422 |
| rs759975018 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135960333 | AGGTGAATAAACTTT[A/T]AAAAGTGTCTCCGCG | 10422 |
| rs760011439 | snp | G/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942549 | TGTAAGAGCTACTCA[G/T]GAGGCTGAAGTAGCA | 10422 |
| rs760049030 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941705 | GCCCATGGGGGCAAA[A/G]ACTTGCTTGTGGGCA | 10422 |
| rs760064855 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962970 | GTGAGAGCCACTAAC[A/G]GTGTGACCAGGTGGC | 10422 |
| rs760205646 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944626 | CTCATGGACACCCCC[A/G]ACGGCAAATGACCCT | 10422 |
| rs760332249 | snp | C/T | 3.67884e-05 | 0.00428869 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945848 | CACAAAACCAGGCCC[C/T]AGGTGTCTCCGGCAA | 10422 |
| rs760352632 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936987 | AATAAGAAAACAATC[C/G]AAGAGAAAAGCAGGC | 10422 |
| rs760357805 | snp | G/T | 3.39058e-05 | 0.00411725 | missense | UBAC1 | GRCh38.p7 | 9:135953753 | ATCAATAATAGGACA[G/T]CTAGAAAAAACAACA | 10422 |
| rs760404401 | snp | C/T | 1.65176e-05 | 0.00287376 | missense | UBAC1 | GRCh38.p7 | 9:135933456 | GCATGACAGGCCCCG[C/T]TTCTGGATCATTCAT | 10422 |
| rs760433738 | snp | A/G | 5.17652e-05 | 0.00508723 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945291 | CATCCCCAGACTAAC[A/G]GACCAGGGCCTTCGC | 10422 |
| rs760557555 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938601 | GCAGACCCTGGTGTC[A/G]CAGGGATCACTGACT | 10422 |
| rs760739241 | snp | C/T | 1.74793e-05 | 0.00295624 | missense | UBAC1 | GRCh38.p7 | 9:135945093 | CCGTCAGCTCATCTC[C/T]GGCCTCCTCATCGGT | 10422 |
| rs760763052 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135955239 | CCCTCCTGGCTCCAG[C/T]GCCCCCAGCAGTGCA | 10422 |
| rs760766514 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957774 | TTATGAACTCCTTCT[-/T]TTTTTTTTTTTTTTT | 10422 |
| rs760815470 | in-del | -/T | 0.000120796 | 0.00777069 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947942 | AGTCTGAGGTGAACG[-/T]TAAGAGCAGCAAAAA | 10422 |
| rs760844776 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941626 | GCTCATTTCTACCTC[A/G]GCCCAGGAAATGATG | 10422 |
| rs760941555 | in-del | -/CACT | 0.00012007 | 0.00774728 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939625 | ACTTACCACAGCCCA[-/CACT]CACTCACCACAGCCC | 10422 |
| rs760945842 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957925 | GATTACAGGAGTCCG[C/T]GACCATGCCAGGCTA | 10422 |
| rs760966311 | snp | A/G | 1.66779e-05 | 0.00288768 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945992 | CCTCGTCCTCGTCCA[A/G]CATTGCTGCAGGGAG | 10422 |
| rs761011641 | snp | G/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135960193 | TCAGATCATGTCAGG[G/T]ATAGACAGGAGGTCA | 10422 |
| rs761056870 | snp | A/G | 3.96904e-05 | 0.00445462 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135961106 | GGCGCCGTCGGACGC[A/G]CAGATGTGCAGCCGC | 10422 |
| rs761057186 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135963270 | GGACACGGGGACCTG[A/G]ATGTGCTGGGGGCAT | 10422 |
| rs761114192 | snp | C/T | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962320 | CACTTGCCCTTGCTG[C/T]ATTGGGAGTTGAGCC | 10422 |
| rs761145356 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135951810 | AGCGAAACTCTGTCT[C/G]AAAAATAATAAAATA | 10422 |
| rs761236236 | snp | A/C | 1.64754e-05 | 0.00287009 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938408 | GCGCCTTCAGTGCCT[A/C]CGCAAGACGCCACCA | 10422 |
| rs761353059 | in-del | -/GACGCCCAGGCTAGA | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936532 | GTGGAGTCTTGCTCT[-/GACGCCCAGGCTAGA]GTGCAGTGGCACGAT | 10422 |
| rs761449598 | snp | A/G | 1.66527e-05 | 0.00288549 | missense | UBAC1 | GRCh38.p7 | 9:135953726 | GGAAGTGGTGATGGA[A/G]CACGCTTTTTTATCA | 10422 |
| rs761488750 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135955200 | TGTCCAGCTCAGAAC[A/G]CTGACTCCTGTGGGT | 10422 |
| rs761515438 | snp | C/G | | | missense | UBAC1 | GRCh38.p7 | 9:135946338 | GCGCCACCTCGATGA[C/G]AGACACCAGTATCTT | 10422 |
| rs761565388 | snp | A/C | | | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135932998 | TTATTAAAGAAAAGT[A/C]ATCTGTGAGTGACTA | 10422 |
| rs761622527 | snp | A/G | 1.66746e-05 | 0.00288739 | missense | UBAC1 | GRCh38.p7 | 9:135945200 | GGCGTGTCTATGGTC[A/G]GGTCTTCTGCGTGTT | 10422 |
| rs761772268 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947178 | TGCTGCGGCGTCCAC[A/G]TGAGCACTGCAAACA | 10422 |
| rs761781996 | snp | C/T | 1.65021e-05 | 0.00287241 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135933436 | GAAGATTCTAGAGAT[C/T]TGCAGCATGACAGGC | 10422 |
| rs761844836 | in-del | -/A | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937440 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 10422 |
| rs761855076 | snp | C/T | 0.000328061 | 0.0128032 | utr-variant-5-prime | UBAC1 | GRCh38.p7 | 9:135961168 | GCACGAACATCCCGC[C/T]GCCGCCGCAGGGGCC | 10422 |
| rs761862298 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938051 | GGGCCCCACAGTGAC[A/G]TAGCGGGACTACACC | 10422 |
| rs761920615 | snp | C/T | 3.39138e-05 | 0.00411774 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946422 | GTCCACCAAACCTAC[C/T]TGGATCTATGACTTG | 10422 |
| rs761974975 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959868 | TTGAACGCAGGAGGC[C/T]CAGCCCCCTCCTTGG | 10422 |
| rs761987920 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949991 | GAATGCAGGCCGCGC[C/T]CAGGCCCTGAGAGCA | 10422 |
| rs762006426 | snp | C/G/T | 3.4159e-05 | 0.00413262 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945006 | AGCGACTCTGCCTGG[C/G/T]GACAGGTCTAGTAAC | 10422 |
| rs762008573 | snp | C/T | 1.69212e-05 | 0.00290866 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135947801 | GCTGACACTCACGTC[C/T]CTCATGTTGGTCTGG | 10422 |
| rs762037918 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958172 | CTGTCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 10422 |
| rs762042255 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939824 | GAACCAGTGACCTGC[A/G]TGCAGAGGGGCCCGC | 10422 |
| rs762127829 | snp | A/T | 1.74613e-05 | 0.00295472 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955428 | ACACTGGGGAAAAAT[A/T]GAAATTTCAAGGTAG | 10422 |
| rs762149290 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944021 | TAGTGCATGCTGGGC[-/T]TTCATACCTAGGTGA | 10422 |
| rs762287376 | snp | G/T | 5.9072e-05 | 0.00543438 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960998 | CCGGAGCGGGTGTTG[G/T]GGGCAGGGGAGGGGG | 10422 |
| rs762294104 | snp | A/C | 1.66366e-05 | 0.0028841 | stop-gained | UBAC1 | GRCh38.p7 | 9:135945986 | GCTCATCCTCGTCCT[A/C]GTCCAGCATTGCTGC | 10422 |
| rs762376348 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135960251 | TGACCTTACTGAGTC[C/T]TTTAGAGACTCGAGA | 10422 |
| rs762464285 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135948477 | GCCTCCTAGAACTGC[A/G]TCGGTGGCAGGGGAC | 10422 |
| rs762649982 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135953279 | GGTGAACAACTAGTA[C/T]AGAGAACTTCTTTAT | 10422 |
| rs762695333 | snp | A/G | 5.02651e-05 | 0.00501299 | missense | UBAC1 | GRCh38.p7 | 9:135947827 | TCTGGACCGCGGCCC[A/G]GTCCATGTTGTAGGA | 10422 |
| rs762697493 | snp | C/T | | | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932727 | GAGGCCAGAGGTAGG[C/T]GGAGGCAGCCGTGCT | 10422 |
| rs762737613 | snp | A/G | 1.65553e-05 | 0.00287705 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135938328 | GTCCAGCTCCTCCGG[A/G]GAGGGCTTCCGGTCC | 10422 |
| rs762755602 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135945659 | CTACGAACGGGATTC[A/C]CCTTGAGTTCTCATA | 10422 |
| rs762792820 | in-del | -/C | 1.67019e-05 | 0.00288975 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933550 | GCCTGAGTGCCCACG[-/C]CCCCCACTCAGCCCA | 10422 |
| rs762852665 | snp | A/G | 4.07125e-05 | 0.0045116 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947918 | TTTCTACACAGAAAC[A/G]TAATCAGAAAGTCTG | 10422 |
| rs762904759 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957646 | AAGAGTAGTGACTTC[A/G]TTTCTGCTTGTACCT | 10422 |
| rs763008295 | snp | A/G | 1.66846e-05 | 0.00288826 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933548 | CCAGCCTGAGTGCCC[A/G]CGCCCCCACTCAGCC | 10422 |
| rs763010954 | snp | C/T | 1.65031e-05 | 0.00287251 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945142 | AGCCTCGGAGGCAGC[C/T]GCTGTGGCCCCCTCG | 10422 |
| rs763033698 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936639 | GCTGGGATTACAGGT[C/G]CATACCACCATGCCC | 10422 |
| rs763115728 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935690 | TGTAAAAGAAGAAAT[A/G]CAATGGCCAACAGAA | 10422 |
| rs763154837 | snp | C/T | 6.69781e-05 | 0.00578659 | missense | UBAC1 | GRCh38.p7 | 9:135939756 | CCATCAGGGAAATGA[C/T]GGCCTAGAGGACAGC | 10422 |
| rs763247432 | snp | A/G | 1.64762e-05 | 0.00287016 | missense | UBAC1 | GRCh38.p7 | 9:135946310 | GCATCTGGGTTCAGC[A/G]CTAACAGCTTCTGCG | 10422 |
| rs763307940 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135954778 | ACTGGCTTGGAGCTT[C/G]ATGGTCATCTCAGCG | 10422 |
| rs763322555 | snp | A/G | 1.72856e-05 | 0.00293982 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944980 | CATGGCGCCACCTCA[A/G]GGGAAGACACAGCGA | 10422 |
| rs763335908 | snp | C/T | 3.34325e-05 | 0.00408842 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946406 | GATCAATTCTCTAAA[C/T]GTCCACCAAACCTAC | 10422 |
| rs763403059 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943340 | GCAGGAAGAATCCAG[C/G]CTGGGCGACAGAGCA | 10422 |
| rs763427370 | snp | A/G | 1.73625e-05 | 0.00294634 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955421 | CATGAGCACACTGGG[A/G]AAAAATAGAAATTTC | 10422 |
| rs763537888 | in-del | -/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941599 | TCACTAGCTTCAATA[-/G]GAAGTACTGTCGCTC | 10422 |
| rs763639946 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952528 | GCTTCTAGGGCAGCC[A/G]GTAAACAACACACTG | 10422 |
| rs763727765 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135953283 | AACAACTAGTATAGA[C/G]AACTTCTTTATAATT | 10422 |
| rs763748955 | snp | A/G | 1.6486e-05 | 0.00287102 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135938273 | CCACCGGGTTATCCA[A/G]GATGGCCTGAAAGAG | 10422 |
| rs763837126 | snp | A/G | 3.31428e-05 | 0.00407066 | missense | UBAC1 | GRCh38.p7 | 9:135938332 | AGCTCCTCCGGAGAG[A/G]GCTTCCGGTCCCCCA | 10422 |
| rs763897954 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957203 | AGGGGCTCACTCCTT[C/T]ACACAAAACTGGCCA | 10422 |
| rs763914470 | in-del | -/CA | 1.67142e-05 | 0.00289081 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933555 | GAGTGCCCACGCCCC[-/CA]CTCAGCCCACAGGCA | 10422 |
| rs763915734 | snp | A/G | 2.10999e-05 | 0.003248 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947926 | CAGAAACGTAATCAG[A/G]AAGTCTGAGGTGAAC | 10422 |
| rs763939738 | snp | A/G | 1.65902e-05 | 0.00288008 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933355 | CCGGTCTCGGGCCGC[A/G]CCAGGGGGCTGCTGT | 10422 |
| rs763985932 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135945678 | TGAGTTCTCATACAA[C/T]GGCCCAAAGAGAATT | 10422 |
| rs764003661 | snp | C/T | 1.65141e-05 | 0.00287346 | missense | UBAC1 | GRCh38.p7 | 9:135945147 | CGGAGGCAGCTGCTG[C/T]GGCCCCCTCGGCCTC | 10422 |
| rs764061847 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135960697 | TTCCCGATCTGCCCC[-/T]TACCTCCCTGCGTGG | 10422 |
| rs764087510 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135948963 | TAATCCCAGCTACCC[A/G]GGAGGCTGAGGCAGG | 10422 |
| rs764187378 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947409 | GGTGCCTGCCACTAC[A/G]CCCGGCTAATTTTTG | 10422 |
| rs764207966 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938992 | GCAGGAGGATCGATT[A/G]AAGCCAGGAGTTCAA | 10422 |
| rs764217434 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135960159 | TGCAGCCTCCTTCAA[A/C]CTAAATTCTGCCAAG | 10422 |
| rs764230613 | snp | A/G | 6.90834e-05 | 0.00587681 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944983 | GGCGCCACCTCAAGG[A/G]AAGACACAGCGACTC | 10422 |
| rs764276955 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938145 | CCTCCGTATCGCCTC[C/T]GCAGCACCTATTTGT | 10422 |
| rs764311518 | snp | C/G | 1.64765e-05 | 0.00287019 | missense | UBAC1 | GRCh38.p7 | 9:135946317 | GGTTCAGCGCTAACA[C/G]CTTCTGCGCCACCTC | 10422 |
| rs764367147 | snp | A/C/G | 0.0001005 | 0.00708814 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135939757 | CATCAGGGAAATGAC[A/C/G]GCCTAGAGGACAGCA | 10422 |
| rs764384291 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942770 | CTGGGAGAGGGTGTG[C/T]GCAGGGGCTGCCCTG | 10422 |
| rs764396142 | snp | C/G | | | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933350 | TCTGCCCGGTCTCGG[C/G]CCGCACCAGGGGGCT | 10422 |
| rs764449387 | snp | A/G | 1.76789e-05 | 0.00297307 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945866 | GTGTCTCCGGCAAGG[A/G]AAGGAGGTGGCCCCC | 10422 |
| rs764632974 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943375 | TCAACATCACTGATC[A/G]TTAGAGAAATGCAAA | 10422 |
| rs764637025 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934484 | GCTAATACGGTAAAA[C/T]CCTGTCTCTACTAAA | 10422 |
| rs764767870 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135948740 | ACACCCAAAGCGCAG[C/T]GCCCCAGCCAGCCAC | 10422 |
| rs764779714 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135945556 | GCTGCCCCTGGATCT[C/T]GGATTATTCATTTTA | 10422 |
| rs764782293 | snp | C/T | 1.69083e-05 | 0.00290755 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938182 | AGGGAACCAGCCAGC[C/T]TCCCCGACCCGAGAC | 10422 |
| rs764950355 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950712 | TTCATTAAGAAGTCA[A/G]TAGAGACTAAAGTTG | 10422 |
| rs764981951 | snp | G/T | 1.64857e-05 | 0.00287099 | missense | UBAC1 | GRCh38.p7 | 9:135938264 | CCAGCTGCACCACCG[G/T]GTTATCCAGGATGGC | 10422 |
| rs765077151 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956983 | CGGACGTCTCAGGTG[C/G]CCGGGCAGACGCCCT | 10422 |
| rs765117685 | snp | G/T | 1.90109e-05 | 0.00308303 | missense | UBAC1 | GRCh38.p7 | 9:135945098 | AGCTCATCTCTGGCC[G/T]CCTCATCGGTGGCGC | 10422 |
| rs765132757 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956285 | ACAAAGATCTCACAG[C/T]CAACTGCTGGCAGGG | 10422 |
| rs765143018 | snp | A/G | 3.68793e-05 | 0.00429398 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947756 | AGCAATCCCCCACAC[A/G]GGGACCCCATGCACC | 10422 |
| rs765163186 | snp | A/G | 1.68752e-05 | 0.00290471 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945016 | CCTGGCGACAGGTCT[A/G]GTAACACATACCCGA | 10422 |
| rs765207507 | snp | A/G | 6.9847e-05 | 0.0059092 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135961025 | GGGGCCCGGCCTTAC[A/G]TGCTTGAGGCAGCGC | 10422 |
| rs765248761 | in-del | -/A | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949059 | GTGAGACACCATCTC[-/A]AAAAAAAAAAAAAAA | 10422 |
| rs765264040 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944777 | ACACAGAGGAAACTG[A/G]GGCGCCTGGATTCAA | 10422 |
| rs765270601 | in-del | -/CTC | 2.18957e-05 | 0.00330868 | cds-indel | UBAC1 | GRCh38.p7 | 9:135961145 | GCCCGCGAAGATCTT[-/CTC]CTCCTGCACGAACAT | 10422 |
| rs765295995 | snp | A/G | | | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933061 | TTGAAACCTACCTCC[A/G]TCAAATAACAAGTGG | 10422 |
| rs765365824 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135933592 | GTGACTTTCCTCTTC[A/G]GCAGCTTCCTAATGA | 10422 |
| rs765474323 | snp | G/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952427 | GCAGGCTCCATGCTC[G/T]GCACGGGCTCAGGCC | 10422 |
| rs765478902 | snp | A/C | 0.000238475 | 0.010917 | missense | UBAC1 | GRCh38.p7 | 9:135961142 | CTTGCCCGCGAAGAT[A/C]TTCTCCTCCTGCACG | 10422 |
| rs765524905 | snp | C/G | 1.70816e-05 | 0.00292242 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939635 | GCCCACACTCACTCA[C/G]CACAGCCCACACTCA | 10422 |
| rs765566625 | snp | G/T | 1.66682e-05 | 0.00288684 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135939748 | CCCCATCTCCATCAG[G/T]GAAATGACGGCCTAG | 10422 |
| rs765619089 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135953095 | GGGAGTGAACCGTCA[C/T]GCAGGATGTGTCCCT | 10422 |
| rs765685887 | in-del | -/C | 8.28e-05 | 0.00643375 | frameshift-variant | UBAC1 | GRCh38.p7 | 9:135939733 | CTCTTTCTCGTCGAA[-/C]CCCATCTCCATCAGG | 10422 |
| rs765698401 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939017 | GTTCAAGATCAGCCT[C/G]GGCAACAAAGGGAGA | 10422 |
| rs765761147 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944078 | ATGGCACATGTTTAC[C/T]TATGTAACAAACCTG | 10422 |
| rs765762757 | snp | G/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942560 | CTCAGGAGGCTGAAG[G/T]AGCATCATTTGAGCC | 10422 |
| rs765866029 | snp | C/T | 1.75274e-05 | 0.0029603 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945244 | CATGGCCTGAGGCAC[C/T]GACATGCTGCAAGGC | 10422 |
| rs765936323 | snp | A/G | 3.36033e-05 | 0.00409884 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945211 | GGTCGGGTCTTCTGC[A/G]TGTTCAATTAGCCAC | 10422 |
| rs765939590 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956157 | CACACACACCACAGC[C/T]ACCTCCGAGCAGCGC | 10422 |
| rs765952805 | snp | A/G | 3.30486e-05 | 0.00406487 | missense | UBAC1 | GRCh38.p7 | 9:135933462 | CAGGCCCCGTTTCTG[A/G]ATCATTCATCCACTG | 10422 |
| rs766030222 | snp | A/C | 1.72582e-05 | 0.00293748 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953764 | GACATCTAGAAAAAA[A/C]AACACGTATATCCAA | 10422 |
| rs766194212 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938613 | GTCGCAGGGATCACT[A/G]ACTGCTGCCGCTTCC | 10422 |
| rs766244489 | snp | A/G | 1.69415e-05 | 0.00291041 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938172 | TTGTCCTGCAAGGGA[A/G]CCAGCCAGCCTCCCC | 10422 |
| rs766262091 | snp | C/T | 1.69694e-05 | 0.0029128 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946423 | TCCACCAAACCTACT[C/T]GGATCTATGACTTGC | 10422 |
| rs766397102 | in-del | -/A | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936975 | CCTTTCTGAATGAAT[-/A]AGAAAACAATCCAAG | 10422 |
| rs766439659 | in-del | -/CACT | 8.51448e-05 | 0.0065242 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939645 | ACTCACCACAGCCCA[-/CACT]CACTCACCACAGCCC | 10422 |
| rs766450579 | snp | A/C | 0.00471534 | 0.0483264 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939772 | GGCCTAGAGGACAGC[A/C]CAGCCGTTAGCTCGC | 10422 |
| rs766502016 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949332 | AAAGAGAAAAGAAAA[C/G]AAGGAGATCAAAAAA | 10422 |
| rs766567460 | in-del | -/A | 0.000136519 | 0.0082608 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953758 | TAATAGGACATCTAG[-/A]AAAAACAACACGTAT | 10422 |
| rs766569387 | snp | A/C | 4.48682e-05 | 0.00473625 | intron-variant | UBAC1 | GRCh38.p7 | 9:135961014 | GGGCAGGGGAGGGGG[A/C]CCGGCCTTACGTGCT | 10422 |
| rs766581659 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941211 | AGGAGTTTGAGACCA[A/G]CCTGGCCAACATGGG | 10422 |
| rs766613763 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962429 | ACCATGCTCCTAAAT[A/G]TGAATTTTGTAGTTC | 10422 |
| rs766621728 | snp | G/T | 1.66971e-05 | 0.00288934 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945996 | GTCCTCGTCCAGCAT[G/T]GCTGCAGGGAGACGA | 10422 |
| rs766766825 | snp | G/T | 1.66218e-05 | 0.00288281 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946231 | CCCAAGGCCGGCAGT[G/T]AACCGCCCTGGAATG | 10422 |
| rs766768799 | snp | C/G | 3.32563e-05 | 0.00407763 | missense | UBAC1 | GRCh38.p7 | 9:135938352 | CCGGTCCCCCAGCAG[C/G]CACTCGCACTGCAAA | 10422 |
| rs766856613 | snp | C/T | 5.23866e-05 | 0.00511767 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938409 | CGCCTTCAGTGCCTC[C/T]GCAAGACGCCACCAG | 10422 |
| rs766904899 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952024 | AAGTCTGAACACCAA[C/T]GGTCAAACTGTAATC | 10422 |
| rs767019836 | snp | A/G | 1.88216e-05 | 0.00306764 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953632 | CTGTAATTCTTAAAT[A/G]TAGACTTCTACCAAC | 10422 |
| rs767020532 | snp | C/G | 1.83602e-05 | 0.00302982 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953652 | CTTCTACCAACCAAG[C/G]TCCCCAATTGCAAAC | 10422 |
| rs767050882 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942931 | TTTGTCTCAATGGGA[C/T]CTAACTAAAGAGCTT | 10422 |
| rs767092892 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135955216 | CTGACTCCTGTGGGT[A/G]GACCACCCCCTCCTG | 10422 |
| rs767147659 | snp | C/T | 1.65343e-05 | 0.00287521 | missense | UBAC1 | GRCh38.p7 | 9:135945162 | TGGCCCCCTCGGCCT[C/T]TGGGGGAGCTTGGCC | 10422 |
| rs767182749 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943943 | CATGGACACAGTGAG[A/G]GGAACATCACACACC | 10422 |
| rs767191956 | snp | C/T | 1.65323e-05 | 0.00287505 | missense | UBAC1 | GRCh38.p7 | 9:135945161 | GTGGCCCCCTCGGCC[C/T]CTGGGGGAGCTTGGC | 10422 |
| rs767274716 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959294 | TTGTGGATATAAACC[A/G]AACCCCTGAGGAGCT | 10422 |
| rs767345723 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944250 | CAGGGGCCCCACTCA[C/T]CACCAGCAGAAGCAA | 10422 |
| rs767351518 | snp | A/G | 3.31892e-05 | 0.00407351 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933358 | GTCTCGGGCCGCACC[A/G]GGGGGCTGCTGTGGC | 10422 |
| rs767353493 | snp | G/T | 0.000150692 | 0.0086789 | missense | UBAC1 | GRCh38.p7 | 9:135945205 | GTCTATGGTCGGGTC[G/T]TCTGCGTGTTCAATT | 10422 |
| rs767494944 | snp | A/C | 0.00109927 | 0.0234186 | utr-variant-5-prime | UBAC1 | GRCh38.p7 | 9:135961171 | CGAACATCCCGCCGC[A/C]GCCGCAGGGGCCTGC | 10422 |
| rs767572966 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135939113 | AGGCTGAGGCAGGAG[A/G]ATCGCTTGGGCCCAG | 10422 |
| rs767750116 | snp | A/G | 1.7465e-05 | 0.00295503 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955429 | CACTGGGGAAAAATA[A/G]AAATTTCAAGGTAGA | 10422 |
| rs767849206 | snp | C/T | 1.65004e-05 | 0.00287227 | missense | UBAC1 | GRCh38.p7 | 9:135945087 | AGATTTCCGTCAGCT[C/T]ATCTCTGGCCTCCTC | 10422 |
| rs767865163 | in-del | -/TGT | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957139 | AGTAACTGGAATTTC[-/TGT]TACTCTCAAGACTGA | 10422 |
| rs767901096 | snp | C/T | 1.64947e-05 | 0.00287177 | missense | UBAC1 | GRCh38.p7 | 9:135938294 | CCTGAAAGAGAGGAC[C/T]GTCGGGGTCGATGCC | 10422 |
| rs767903630 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935179 | TACAATTACAGGCAT[A/G]AGCCACCATGCCCAA | 10422 |
| rs767912104 | snp | G/T | 9.45805e-05 | 0.00687614 | intron-variant | UBAC1 | GRCh38.p7 | 9:135961010 | TTGGGGGCAGGGGAG[G/T]GGGCCCGGCCTTACG | 10422 |
| rs767951254 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959018 | AATTAGCATTGCATC[A/G]GAACTGGCTGCCTAA | 10422 |
| rs768074234 | snp | A/T | 1.67242e-05 | 0.00289168 | missense | UBAC1 | GRCh38.p7 | 9:135938341 | GGAGAGGGCTTCCGG[A/T]CCCCCAGCAGCCACT | 10422 |
| rs768101590 | snp | C/T | 1.66241e-05 | 0.00288302 | missense | UBAC1 | GRCh38.p7 | 9:135945982 | ACACGCTCATCCTCG[C/T]CCTCGTCCAGCATTG | 10422 |
| rs768149118 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936061 | GAATACAAGTTAAAA[C/T]AATGAAGGTCTTGTC | 10422 |
| rs768174940 | snp | A/G | | | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135938331 | CAGCTCCTCCGGAGA[A/G]GGCTTCCGGTCCCCC | 10422 |
| rs768262551 | snp | C/T | 0.000224669 | 0.0105964 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135961076 | GGTGTCCTCGGTGGC[C/T]TCCTCCAGCCACTCG | 10422 |
| rs768301041 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135938025 | CACACCACGATCAGA[A/G]CCTGACCTGCGGGCC | 10422 |
| rs768362970 | snp | A/G | | | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932921 | ATGTGGCCTCTCGGG[A/G]ACGCACGGGTTTCTT | 10422 |
| rs768375719 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936462 | AAATAAAAGGAAAAC[A/G]TGTTTCTGACTTTCG | 10422 |
| rs768397870 | in-del | -/A | 0.000149965 | 0.00865795 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946379 | TCTGGAACTGTGGTG[-/A]AAAAAAAAGGAGATC | 10422 |
| rs768453676 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952542 | CAGTAAACAACACAC[C/T]GCACGGTGTTCCTAA | 10422 |
| rs768568700 | snp | C/T | 1.66374e-05 | 0.00288417 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135953722 | CTTGGGAAGTGGTGA[C/T]GGAGCACGCTTTTTT | 10422 |
| rs768587091 | snp | C/T | 1.81276e-05 | 0.00301056 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953799 | CTGGTTATCACTTCA[C/T]ATCCACAAAATGGCA | 10422 |
| rs768588787 | snp | A/G | 3.32651e-05 | 0.00407817 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945196 | AAGAGGCGTGTCTAT[A/G]GTCGGGTCTTCTGCG | 10422 |
| rs768592795 | in-del | -/A | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936187 | CCTATTTCTATTAGG[-/A]AAAAAAAAAAGAAAA | 10422 |
| rs768609928 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135933850 | ACAACTCCACTTCCA[A/G]TCCCACCCCGAGAAG | 10422 |
| rs768683277 | snp | A/G | 1.65023e-05 | 0.00287244 | missense | UBAC1 | GRCh38.p7 | 9:135938236 | CCTAGCAATGTTTTC[A/G]GGTTGGTCAGGCCCA | 10422 |
| rs768728979 | in-del | -/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943657 | AGATATGTGCACACG[-/T]TATGTTCACTGCAGC | 10422 |
| rs768791883 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935888 | AAAATTAGCCGGGCA[C/T]GGTGGCGGGCACCTG | 10422 |
| rs768893306 | snp | C/T | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961808 | AATTGCCTACATGGC[C/T]GCTGTGATATTTCTT | 10422 |
| rs768906137 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949846 | ACTGTGGGGAAAGAG[C/T]ATGATCCTTGGTGGG | 10422 |
| rs768987034 | snp | A/G | 1.67279e-05 | 0.002892 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946407 | ATCAATTCTCTAAAT[A/G]TCCACCAAACCTACT | 10422 |
| rs769040602 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943623 | ATATACCCAAAGGAA[C/T]AGAAATCATTCTGTT | 10422 |
| rs769070055 | snp | A/G | 1.65053e-05 | 0.0028727 | missense | UBAC1 | GRCh38.p7 | 9:135946274 | TGACTCATACCATTC[A/G]CCTTCTTAAACAATT | 10422 |
| rs769107317 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135935012 | AGTCCCCTGAGTAGC[A/G]GGGACTACAGGTACG | 10422 |
| rs769215567 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958515 | TCATAAAACCCCTCC[C/T]TGATTCAGGAGTGCA | 10422 |
| rs769225877 | snp | C/T | 1.72193e-05 | 0.00293417 | missense | UBAC1 | GRCh38.p7 | 9:135955414 | AAGCTCCCATGAGCA[C/T]ACTGGGGAAAAATAG | 10422 |
| rs769457200 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135946199 | TCAGTGGTCAGTGCG[C/T]GGAGCTGCAGACGCT | 10422 |
| rs769474421 | snp | A/G | 7.82626e-05 | 0.00625501 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960980 | GTCCGCAGTCGGAGG[A/G]GTCCGGAGCGGGTGT | 10422 |
| rs769495289 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941301 | ATCCCAGCTACTCGG[A/G]AGCCTGAGGCAGGAG | 10422 |
| rs769545064 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135946819 | CCAGGCAGGAGGAGC[C/T]GTGGGATGGACCGGA | 10422 |
| rs769550460 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135951769 | GAGCTGAGATCACGC[C/G]ACTGCACTCTAGCTT | 10422 |
| rs769555889 | snp | C/T | 1.66059e-05 | 0.00288144 | missense | UBAC1 | GRCh38.p7 | 9:135945923 | TGGTGGCTCTGTTCT[C/T]CGGAAAGCCCATCTC | 10422 |
| rs769574057 | snp | C/T | 3.3248e-05 | 0.00407712 | missense | UBAC1 | GRCh38.p7 | 9:135945980 | CCACACGCTCATCCT[C/T]GTCCTCGTCCAGCAT | 10422 |
| rs769694348 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943484 | GAGGCTGTGGAGAAA[C/T]AGGAACGCTTTTACA | 10422 |
| rs769786565 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934428 | CACTTTGGGAGGCCG[A/G]AGCAGGCGGATCATG | 10422 |
| rs769798475 | snp | G/T | 1.81836e-05 | 0.00301521 | missense | UBAC1 | GRCh38.p7 | 9:135947899 | GAGCTTTCTGGTCTT[G/T]TTTTTTCTACACAGA | 10422 |
| rs769817767 | snp | A/G | 7.56554e-05 | 0.00614996 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945289 | AACATCCCCAGACTA[A/G]CGGACCAGGGCCTTC | 10422 |
| rs769872373 | snp | A/G | 1.64996e-05 | 0.0028722 | missense | UBAC1 | GRCh38.p7 | 9:135933425 | TTTAGTGTCTGGAAG[A/G]TTCTAGAGATCTGCA | 10422 |
| rs769879966 | in-del | -/AACAA | 1.67245e-05 | 0.00289171 | splice-acceptor-variant | UBAC1 | GRCh38.p7 | 9:135945999 | TCGTCCAGCATTGCT[-/AACAA]GCAGGGAGACGACAG | 10422 |
| rs769880741 | snp | A/G | 1.6679e-05 | 0.00288777 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933544 | AGAGCCAGCCTGAGT[A/G]CCCACGCCCCCACTC | 10422 |
| rs769939345 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944518 | ATGGGGAGATGAGGC[A/G]CGGGCGAGGAAGGTC | 10422 |
| rs770159632 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934741 | GTTTCACACACAGGG[C/T]GGGGAACTTAATTTC | 10422 |
| rs770219279 | snp | C/T | 1.64928e-05 | 0.00287161 | missense | UBAC1 | GRCh38.p7 | 9:135945059 | AACTCCCTTTTCCTC[C/T]GGATCTTCTTGAAGA | 10422 |
| rs770269637 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135954615 | CGGCCCCAATAATTG[A/T]GCAAAGAATTGGTGA | 10422 |
| rs770296296 | in-del | -/CT | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941419 | TCAAAAAAGAAAAAA[-/CT]CTGTATTTTCTATTT | 10422 |
| rs770397714 | snp | C/G/T | 1.73924e-05 | 0.00294888 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953769 | CTAGAAAAAACAACA[C/G/T]GTATATCCAACACAC | 10422 |
| rs770405115 | in-del | -/G | 1.65949e-05 | 0.00288048 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933358 | TCTCGGGCCGCACCA[-/G]GGGGGCTGCTGTGGC | 10422 |
| rs770475269 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135948677 | CCAGTGGCAGGGGAG[C/G]GGGGCAGACACAGCC | 10422 |
| rs770480644 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135945531 | GGGACCACAGGGGGA[A/G]CTGCCCCCGGCTGCC | 10422 |
| rs770666580 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949743 | CGGCCGCACGCTCCC[C/T]GGGCCTGGCAGTTGC | 10422 |
| rs770677062 | snp | C/T | 1.66175e-05 | 0.00288244 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945915 | AAGGGCCTTGGTGGC[C/T]CTGTTCTCCGGAAAG | 10422 |
| rs770769047 | snp | C/G | 1.64914e-05 | 0.00287149 | missense | UBAC1 | GRCh38.p7 | 9:135938246 | TTTTCGGGTTGGTCA[C/G]GCCCAGCTGCACCAC | 10422 |
| rs770921508 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135940977 | TGCAGCACTGCACCC[C/G]GCGGACGGTGCACGT | 10422 |
| rs770991018 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944607 | CAGCCTGAGCGGCCC[A/C]TCGCTCATGGACACC | 10422 |
| rs771048282 | snp | A/C/G | 8.30884e-05 | 0.00644504 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135953710 | GACATCAGCCATCTT[A/C/G]GGAAGTGGTGATGGA | 10422 |
| rs771075771 | snp | G/T | 7.93037e-05 | 0.00629647 | missense | UBAC1 | GRCh38.p7 | 9:135961111 | CGTCGGACGCGCAGA[G/T]GTGCAGCCGCAGCAC | 10422 |
| rs771078162 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135954282 | GAGACCCCATCTCTA[C/T]GAAAATATAAAAAAT | 10422 |
| rs771134734 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936156 | ACTGCACTCTAGCCT[C/G]GGTGACAGAGAAAGA | 10422 |
| rs771166453 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942520 | AAAATTAGCCCTGTG[A/T]GGTGGTGCGTGCCTG | 10422 |
| rs771284285 | snp | C/T | 1.66538e-05 | 0.00288559 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933534 | CAGGGAAAACAGAGC[C/T]AGCCTGAGTGCCCAC | 10422 |
| rs771351768 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937269 | AAACATGGTGAAAGC[C/T]GTCTCTACTAAAATA | 10422 |
| rs771410214 | snp | A/G | 3.29533e-05 | 0.00405901 | missense | UBAC1 | GRCh38.p7 | 9:135946295 | TTAAACAATTCCACT[A/G]CATCTGGGTTCAGCG | 10422 |
| rs771432476 | snp | G/T | 3.30262e-05 | 0.0040635 | missense | UBAC1 | GRCh38.p7 | 9:135946369 | CCGGAGTTCTGTCTG[G/T]AACTGTGGTGAAAAA | 10422 |
| rs771601866 | snp | A/G | | | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932586 | AGAAGAGAAGTTCAA[A/G]ACAAACAGCTCGGAA | 10422 |
| rs771750430 | snp | C/G | 1.65644e-05 | 0.00287783 | missense | UBAC1 | GRCh38.p7 | 9:135939699 | GCTGGTTGTTGTTCA[C/G]TCTGAGGGCATCTAT | 10422 |
| rs771764428 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957351 | CTGGGGGTGCTTCCT[C/T]ATGATCCTAAAGTTT | 10422 |
| rs771806528 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958620 | TGCCGGCGTCAGCAC[A/G]CACTGGGGACCTGGC | 10422 |
| rs771896575 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947213 | TCTTTTTTAACTTAG[A/G]ATGTTCTGACCCAAA | 10422 |
| rs771903287 | snp | A/C | 3.68175e-05 | 0.00429038 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945846 | CCCACAAAACCAGGC[A/C]CCAGGTGTCTCCGGC | 10422 |
| rs771987300 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962981 | TAACGGTGTGACCAG[A/G]TGGCAGAATGAATGG | 10422 |
| rs772011133 | snp | C/T | 1.66969e-05 | 0.00288932 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933549 | CAGCCTGAGTGCCCA[C/T]GCCCCCACTCAGCCC | 10422 |
| rs772046835 | snp | C/T | 8.34913e-05 | 0.00646055 | missense | UBAC1 | GRCh38.p7 | 9:135955375 | TGGATTAATTTATGA[C/T]GGGTTATACTTTTGG | 10422 |
| rs772168865 | snp | C/T | 1.70081e-05 | 0.00291612 | missense | UBAC1 | GRCh38.p7 | 9:135947878 | GCAGTATGGCCTCTT[C/T]ATCTGGAGCTTTCTG | 10422 |
| rs772238646 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961857 | GAACGGAGGCTCTCC[A/G]AAGAACTTGGCTTTA | 10422 |
| rs772398105 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941489 | TCCAGGAGCTCCAAC[A/T]ATGAACTCTGGAAGA | 10422 |
| rs772412160 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952883 | GTTTGGATTTTCCGA[C/T]GGGGATGCTGAGGCT | 10422 |
| rs772515940 | snp | A/G | 9.94464e-05 | 0.00705077 | missense | UBAC1 | GRCh38.p7 | 9:135945185 | GCTTGGCCAGGAAGA[A/G]GCGTGTCTATGGTCG | 10422 |
| rs772576192 | snp | A/C | 1.6473e-05 | 0.00286988 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946223 | AGACGCTCCCCAAGG[A/C]CGGCAGTGAACCGCC | 10422 |
| rs772637592 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937018 | CAAACGCTGAGCGGA[A/G]GGTCTCTCACAGCCA | 10422 |
| rs772654331 | snp | A/G | 1.65463e-05 | 0.00287626 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135939709 | GTTCACTCTGAGGGC[A/G]TCTATCACCTCTTTC | 10422 |
| rs772676369 | snp | C/T | 1.64901e-05 | 0.00287137 | missense | UBAC1 | GRCh38.p7 | 9:135946293 | TCTTAAACAATTCCA[C/T]TGCATCTGGGTTCAG | 10422 |
| rs772700200 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961978 | GCCGCCCTTGGTGCA[A/G]GTGATGCCAGGCAGA | 10422 |
| rs772757887 | snp | C/G | 1.71387e-05 | 0.00292729 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938402 | CTGTTAGCGCCTTCA[C/G]TGCCTCCGCAAGACG | 10422 |
| rs772852686 | snp | A/C/T | 3.35747e-05 | 0.00409712 | missense | UBAC1 | GRCh38.p7 | 9:135945210 | TGGTCGGGTCTTCTG[A/C/T]GTGTTCAATTAGCCA | 10422 |
| rs772887986 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135946519 | ATCAGCTGAGGGCAA[A/G]GCAGGGGATTGGCAG | 10422 |
| rs772930319 | in-del | -/CC | | | utr-variant-5-prime | UBAC1 | GRCh38.p7 | 9:135961349 | GCCTCGCTCCCGCCG[-/CC]GCAGCAGCCGCCGGG | 10422 |
| rs773032794 | snp | A/G | 1.78809e-05 | 0.00299001 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955250 | CCAGCGCCCCCAGCA[A/G]TGCACGATGCCTGCT | 10422 |
| rs773038986 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959941 | TGCGTTCCAGAAGGG[C/G]GCTTGCCAAGCTTGC | 10422 |
| rs773120524 | snp | C/T | 3.6806e-05 | 0.00428971 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945847 | CCACAAAACCAGGCC[C/T]CAGGTGTCTCCGGCA | 10422 |
| rs773352233 | snp | A/G | 0.000171872 | 0.00926856 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135947885 | GGCCTCTTTATCTGG[A/G]GCTTTCTGGTCTTGT | 10422 |
| rs773436911 | snp | C/T | 1.65436e-05 | 0.00287602 | missense | UBAC1 | GRCh38.p7 | 9:135945089 | ATTTCCGTCAGCTCA[C/T]CTCTGGCCTCCTCAT | 10422 |
| rs773494291 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941572 | ACTGAATTCAAGGAC[A/C]GGATGCCCTCCTCAC | 10422 |
| rs773526936 | snp | G/T | 1.64982e-05 | 0.00287208 | missense | UBAC1 | GRCh38.p7 | 9:135945131 | GCTCCCGCGGCAGCC[G/T]CGGAGGCAGCTGCTG | 10422 |
| rs773583551 | snp | A/T | 1.98057e-05 | 0.00314682 | missense | UBAC1 | GRCh38.p7 | 9:135961102 | ACTCGGCGCCGTCGG[A/T]CGCGCAGATGTGCAG | 10422 |
| rs773795129 | snp | A/G | 6.87817e-05 | 0.00586397 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946038 | GGGCTCCAGCCTCAG[A/G]TTCAGGGGCCTTATC | 10422 |
| rs773799936 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135963136 | GGTGTGGGCCCAAGA[A/G]TGAAATCAAGGATGA | 10422 |
| rs773881513 | snp | C/T | 1.66269e-05 | 0.00288326 | missense | UBAC1 | GRCh38.p7 | 9:135945983 | CACGCTCATCCTCGT[C/T]CTCGTCCAGCATTGC | 10422 |
| rs774074645 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135954963 | GTCTAACACTGCACT[A/G]GGATGCCAACATCAC | 10422 |
| rs774108343 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957918 | TAGGTGGGATTACAG[A/G]AGTCCGCGACCATGC | 10422 |
| rs774128934 | snp | C/T | 2.36863e-05 | 0.00344131 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947941 | AAAGTCTGAGGTGAA[C/T]GTAAGAGCAGCAAAA | 10422 |
| rs774147287 | snp | A/G | 1.66418e-05 | 0.00288455 | missense | UBAC1 | GRCh38.p7 | 9:135953724 | TGGGAAGTGGTGATG[A/G]AGCACGCTTTTTTAT | 10422 |
| rs774158352 | snp | A/G | | | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932928 | CTCTCGGGGACGCAC[A/G]GGTTTCTTGTGCGGC | 10422 |
| rs774195204 | in-del | -/A | 0.000149965 | 0.00865795 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946380 | TCTGGAACTGTGGTG[-/A]AAAAAAAGGAGATCA | 10422 |
| rs774198092 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958609 | GGAAAAAATCATGCC[A/G]GCGTCAGCACGCACT | 10422 |
| rs774235177 | snp | C/G | 6.66556e-05 | 0.00577264 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945199 | AGGCGTGTCTATGGT[C/G]GGGTCTTCTGCGTGT | 10422 |
| rs774326445 | in-del | -/ACAGC | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956582 | ACAGCCCGACACACG[-/ACAGC]ACAGCACAGCACAGC | 10422 |
| rs774357275 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949877 | CCTCAACTAATCAGG[C/T]AGGTCCTTAAAAGGG | 10422 |
| rs774442826 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958156 | GGTTCACACCATTCT[C/T]CTGTCTCAGCCTCCC | 10422 |
| rs774521558 | snp | C/T | 9.88549e-05 | 0.00702977 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135946324 | CGCTAACAGCTTCTG[C/T]GCCACCTCGATGAGA | 10422 |
| rs774548617 | snp | C/T | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135961829 | GATATTTCTTTTGCA[C/T]TGCACTGCTGTAGAA | 10422 |
| rs774663698 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943695 | ACAATAGCAAAGACA[C/T]AGAATCAACTCAAAT | 10422 |
| rs774679512 | snp | A/G | 3.44021e-05 | 0.00414727 | intron-variant | UBAC1 | GRCh38.p7 | 9:135944994 | AAGGGAAGACACAGC[A/G]ACTCTGCCTGGCGAC | 10422 |
| rs774753473 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934520 | AAAAAATTAGCTGGG[C/T]GTGGTGGCAGGCGCC | 10422 |
| rs774792710 | snp | C/T | 0.000184723 | 0.00960872 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960995 | GGTCCGGAGCGGGTG[C/T]TGGGGGCAGGGGAGG | 10422 |
| rs774793762 | snp | G/T | | | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932696 | CATGTTTTTTAAAAT[G/T]AAAAAAAAGGAGGAA | 10422 |
| rs774835102 | snp | C/T | 1.64819e-05 | 0.00287066 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945079 | CTTCTTGAAGATTTC[C/T]GTCAGCTCATCTCTG | 10422 |
| rs774875410 | snp | A/G | 0.000155727 | 0.00882265 | intron-variant | UBAC1 | GRCh38.p7 | 9:135960981 | TCCGCAGTCGGAGGG[A/G]TCCGGAGCGGGTGTT | 10422 |
| rs775058848 | snp | G/T | 1.72889e-05 | 0.0029401 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955418 | TCCCATGAGCACACT[G/T]GGGAAAAATAGAAAT | 10422 |
| rs775241604 | snp | C/G/T | 3.29702e-05 | 0.00406008 | missense | UBAC1 | GRCh38.p7 | 9:135938265 | CAGCTGCACCACCGG[C/G/T]TTATCCAGGATGGCC | 10422 |
| rs775283038 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937949 | CACCCCGCTGGCCCT[C/T]GGAAAGCCACTGGCA | 10422 |
| rs775309340 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957583 | CCAAGGCCGCTGGAG[C/T]AGGGAGGCCCTCACA | 10422 |
| rs775357252 | snp | C/T | 2.02312e-05 | 0.00318044 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947917 | TTTTCTACACAGAAA[C/T]GTAATCAGAAAGTCT | 10422 |
| rs775399721 | snp | G/T | 1.6552e-05 | 0.00287676 | missense | UBAC1 | GRCh38.p7 | 9:135938327 | TGTCCAGCTCCTCCG[G/T]AGAGGGCTTCCGGTC | 10422 |
| rs775444698 | in-del | -/A | 3.32781e-05 | 0.00407897 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933528 | TGCTGCAGGGAAAAC[-/A]AGAGCCAGCCTGAGT | 10422 |
| rs775491699 | in-del | -/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135954156 | AAAAAAAAAAAAAAA[-/G]GAAGAAGAGCAGGGC | 10422 |
| rs775550015 | in-del | -/CTGC | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958287 | TCCTGACCTTGTGAT[-/CTGC]CTGCCTGTCTTGGCC | 10422 |
| rs775599471 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135948247 | CTGCAGCTGAGCCCC[A/G]AGGCCAAAACCACGA | 10422 |
| rs775604253 | in-del | -/AACCTGAATGAACA | 1.67486e-05 | 0.00289379 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946000 | CGTCCAGCATTGCTG[-/AACCTGAATGAACA]CAGGGAGACGACAGG | 10422 |
| rs775604863 | in-del | -/AT | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943542 | ACCACTGTGGAAGAC[-/AT]GTGGTGATTCCTCAA | 10422 |
| rs775617022 | snp | C/G | 3.33712e-05 | 0.00408466 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933546 | AGCCAGCCTGAGTGC[C/G]CACGCCCCCACTCAG | 10422 |
| rs775629434 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958734 | TCAAATACACAACTC[A/G]AGGGTTCTCTTTTCT | 10422 |
| rs775687453 | snp | C/G | 1.66319e-05 | 0.00288369 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946391 | GGTGAAAAAAAAGGA[C/G]ATCAATTCTCTAAAT | 10422 |
| rs775731673 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135946309 | TGCATCTGGGTTCAG[C/T]GCTAACAGCTTCTGC | 10422 |
| rs775779052 | snp | A/G | 1.73201e-05 | 0.00294274 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939806 | GGGCGGCAGGAGGCC[A/G]AGGAACCAGTGACCT | 10422 |
| rs775786396 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943191 | TTGGGAGGCCGAGGC[A/G]GGCAGATCGCTTGAG | 10422 |
| rs775806898 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135953250 | ATCTACTGTAAATGG[C/T]GAATGCGTGGGTTGG | 10422 |
| rs775896941 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135954677 | GTTCTGAAAAAGTCT[A/G]TGAGGGTGGAGAGTT | 10422 |
| rs776199785 | in-del | -/A | 3.32016e-05 | 0.00407427 | splice-acceptor-variant | UBAC1 | GRCh38.p7 | 9:135933517 | ATGTCTTCAAATGCT[-/A]GCAGGGAAAACAGAG | 10422 |
| rs776281205 | snp | C/G/T | 7.0969e-05 | 0.00595652 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955273 | TGCCTGCTGCCAACC[C/G/T]GCCCGCCCACAGCAG | 10422 |
| rs776338703 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135946881 | GCCTAGAGGTCAGGC[A/G]TCAGCTGTCCCTACT | 10422 |
| rs776349782 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135945532 | GGACCACAGGGGGAA[A/C]TGCCCCCGGCTGCCC | 10422 |
| rs776362606 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135936344 | ACCATTCTCAAGTTT[C/T]AGAATTTGGGTACAA | 10422 |
| rs776531601 | snp | C/G | 1.66076e-05 | 0.00288158 | missense | UBAC1 | GRCh38.p7 | 9:135945921 | CTTGGTGGCTCTGTT[C/G]TCCGGAAAGCCCATC | 10422 |
| rs776538614 | snp | A/G | 1.65007e-05 | 0.00287229 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945136 | CGCGGCAGCCTCGGA[A/G]GCAGCTGCTGTGGCC | 10422 |
| rs776634638 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135943347 | GAATCCAGCCTGGGC[A/G]ACAGAGCAAGGCTCA | 10422 |
| rs776716031 | in-del | -/GTGCTTGAGGCAGCGCTC | 1.72424e-05 | 0.00293614 | splice-acceptor-variant | UBAC1 | GRCh38.p7 | 9:135955415 | GCTCCCATGAGCACA[-/GTGCTTGAGGCAGCGCTC]CTGGGGAAAAATAGA | 10422 |
| rs776741960 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942542 | GCGTGCCTGTAAGAG[C/T]TACTCAGGAGGCTGA | 10422 |
| rs776827663 | snp | G/T | 1.66037e-05 | 0.00288125 | missense | UBAC1 | GRCh38.p7 | 9:135945191 | CCAGGAAGAGGCGTG[G/T]CTATGGTCGGGTCTT | 10422 |
| rs776842593 | snp | C/T | 1.65034e-05 | 0.00287253 | missense | UBAC1 | GRCh38.p7 | 9:135933407 | AACGCCACCTACGTG[C/T]GATTTAGTGTCTGGA | 10422 |
| rs776871746 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958701 | ATGACATCCAGGGAC[C/T]GGCTTCCAGAGAGAC | 10422 |
| rs776872389 | snp | C/G | 1.6477e-05 | 0.00287024 | missense | UBAC1 | GRCh38.p7 | 9:135946299 | ACAATTCCACTGCAT[C/G]TGGGTTCAGCGCTAA | 10422 |
| rs776959045 | snp | G/T | 2.01867e-05 | 0.00317694 | missense | UBAC1 | GRCh38.p7 | 9:135961129 | GCAGCCGCAGCACCT[G/T]GCCCGCGAAGATCTT | 10422 |
| rs776969749 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135963334 | ACAGGACTGAAGTTG[A/G]GGAGAGAGGCCTGGG | 10422 |
| rs776997731 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934388 | AGAAAAAGCCAGGCA[C/T]GGTGGCTCATGCCTG | 10422 |
| rs777017082 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941212 | GGAGTTTGAGACCAG[C/T]CTGGCCAACATGGGA | 10422 |
| rs777046871 | snp | C/T | 1.66203e-05 | 0.00288268 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946234 | AAGGCCGGCAGTGAA[C/T]CGCCCTGGAATGCAG | 10422 |
| rs777225483 | snp | G/T | | | missense | UBAC1 | GRCh38.p7 | 9:135939691 | GGCATTCTGCTGGTT[G/T]TTGTTCACTCTGAGG | 10422 |
| rs777227623 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950946 | AAAAATACAAAAATT[A/T]GTCAGGTGTGGTGGC | 10422 |
| rs777264759 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937776 | ATGGCTATTAGTTTT[A/C]TTCTTCTTTAAAGTT | 10422 |
| rs777269536 | snp | A/G | | | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932594 | AGTTCAAAACAAACA[A/G]CTCGGAACTGACTGC | 10422 |
| rs777339804 | snp | A/C | 3.6075e-05 | 0.00424691 | intron-variant | UBAC1 | GRCh38.p7 | 9:135947770 | CGGGGACCCCATGCA[A/C]CCGCCGCCGCTCTGG | 10422 |
| rs777379288 | snp | A/G | 0.000181283 | 0.00951887 | missense | UBAC1 | GRCh38.p7 | 9:135945074 | CGGATCTTCTTGAAG[A/G]TTTCCGTCAGCTCAT | 10422 |
| rs777421952 | snp | C/G | 1.65636e-05 | 0.00287776 | missense | UBAC1 | GRCh38.p7 | 9:135945039 | ATACCCGAGCATCAG[C/G]CCGAAACTCCCTTTT | 10422 |
| rs777491053 | snp | C/G | 1.66977e-05 | 0.00288939 | missense | UBAC1 | GRCh38.p7 | 9:135955376 | GGATTAATTTATGAT[C/G]GGTTATACTTTTGGG | 10422 |
| rs777661814 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135934934 | TGCCCAGGCTGGAGT[A/G]CAGTGGAGTGATCAT | 10422 |
| rs777705289 | snp | A/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135949479 | TATTCCAGAACACTA[A/T]AGCACACCAGATGGC | 10422 |
| rs777722565 | snp | C/T | 3.5832e-05 | 0.00423258 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955457 | AGAAAATAAGTAAAT[C/T]GTAATTCTAATAATA | 10422 |
| rs777814244 | snp | A/G | 3.33394e-05 | 0.00408272 | missense | UBAC1 | GRCh38.p7 | 9:135953694 | CCTTTTCTTCTGCTG[A/G]GACATCAGCCATCTT | 10422 |
| rs777977997 | snp | A/G | 1.65833e-05 | 0.00287948 | missense | UBAC1 | GRCh38.p7 | 9:135945186 | CTTGGCCAGGAAGAG[A/G]CGTGTCTATGGTCGG | 10422 |
| rs778140859 | snp | A/G | | | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932483 | AAAAACAATGAAAAG[A/G]CCTAGATGTGTGGAG | 10422 |
| rs778150317 | snp | A/G/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135946650 | TGTGAGGAAACCGTC[A/G/T]GCCCAGCTGGCGCAG | 10422 |
| rs778175496 | snp | A/C | 1.76058e-05 | 0.00296692 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953780 | AACACGTATATCCAA[A/C]ACACTGGTTATCACT | 10422 |
| rs778185807 | in-del | -/TCT | 3.2975e-05 | 0.00406035 | cds-indel | UBAC1 | GRCh38.p7 | 9:135945063 | CCCTTTTCCTCCGGA[-/TCT]TCTTGAAGATTTCCG | 10422 |
| rs778263400 | snp | A/C | 1.81388e-05 | 0.00301149 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945259 | CGACATGCTGCAAGG[A/C]AAGAGACTCTTTCCA | 10422 |
| rs778343639 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958350 | CCGTGCTCAGCCAGG[C/T]ATAATTTTCTAAAAC | 10422 |
| rs778364038 | snp | C/T | 1.66394e-05 | 0.00288434 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933528 | ATGCTGCAGGGAAAA[C/T]AGAGCCAGCCTGAGT | 10422 |
| rs778413716 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937642 | AGGAGACACAAATAC[A/G]GCAAAACTCTACCGG | 10422 |
| rs778454623 | snp | C/T | 1.94532e-05 | 0.00311869 | utr-variant-5-prime | UBAC1 | GRCh38.p7 | 9:135961205 | CGCCACCCGGGCCCC[C/T]GAAGGTCACCGGGAA | 10422 |
| rs778455085 | snp | A/C | 1.64789e-05 | 0.0028704 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135946345 | CTCGATGAGAGACAC[A/C]AGTATCTTCCGGAGT | 10422 |
| rs778522992 | snp | A/G | 1.65529e-05 | 0.00287683 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135933484 | CATCCACTGGGTGCT[A/G]TTCAGTGGGTTCTCC | 10422 |
| rs778565596 | snp | A/C/G/T | 4.94837e-05 | 0.00497393 | missense, synonymous-codon | UBAC1 | GRCh38.p7 | 9:135946282 | ACCATTCGCCTTCTT[A/C/G/T]AACAATTCCACTGCA | 10422 |
| rs778614560 | snp | C/T | 1.69778e-05 | 0.00291352 | intron-variant | UBAC1 | GRCh38.p7 | 9:135939777 | AGAGGACAGCACAGC[C/T]GTTAGCTCGCTGGGG | 10422 |
| rs778651680 | snp | A/G | 3.32049e-05 | 0.00407448 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135939688 | CGCGGCATTCTGCTG[A/G]TTGTTGTTCACTCTG | 10422 |
| rs778677616 | snp | A/T | 1.82324e-05 | 0.00301925 | intron-variant | UBAC1 | GRCh38.p7 | 9:135953801 | GGTTATCACTTCATA[A/T]CCACAAAATGGCATA | 10422 |
| rs778844896 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959547 | GCCCCGCTAATTTTT[C/T]GTATTTTAGTTGAGA | 10422 |
| rs778884675 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944579 | CTGCAGACTGTGCCA[C/T]GGAGGCGGCTGGCAG | 10422 |
| rs778901485 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135944179 | TCTCCACGGAACCCT[A/G]TGCAGGGAAGACCTG | 10422 |
| rs778924692 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135946077 | AACATTTGCAGCAAT[C/T]ATCTGTCTGAGCTCC | 10422 |
| rs779016344 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135937008 | AAAAGCAGGCCAAAC[A/G]CTGAGCGGAAGGTCT | 10422 |
| rs779199942 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962975 | AGCCACTAACGGTGT[A/G]ACCAGGTGGCAGAAT | 10422 |
| rs779266338 | in-del | -/CT | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135950164 | TTTCAGCTCGAGACC[-/CT]GAGCACAGAAACCAG | 10422 |
| rs779301708 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957465 | ACCCACAGTCCACGT[A/G]TCACCAGCACACCAG | 10422 |
| rs779366012 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947580 | GGGTATCTATCTTTT[C/T]AATCCTGCCTTCAGA | 10422 |
| rs779390710 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135956567 | TCTACCTCAGCACCA[C/T]ACAGCCCGACACACG | 10422 |
| rs779402032 | snp | G/T | 1.68681e-05 | 0.00290409 | missense | UBAC1 | GRCh38.p7 | 9:135947869 | CGGTGGCCCGCAGTA[G/T]GGCCTCTTTATCTGG | 10422 |
| rs779482330 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135954070 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCACTGAG | 10422 |
| rs779493435 | snp | C/G | 3.31049e-05 | 0.00406834 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945175 | CTCTGGGGGAGCTTG[C/G]CCAGGAAGAGGCGTG | 10422 |
| rs779577837 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947678 | ACAGACCCGCTCACC[A/G]GCTTCCCCAAATCCT | 10422 |
| rs779655739 | snp | A/G | 3.30759e-05 | 0.00406655 | missense | UBAC1 | GRCh38.p7 | 9:135945167 | CCCTCGGCCTCTGGG[A/G]GAGCTTGGCCAGGAA | 10422 |
| rs779693189 | snp | C/T | 9.75277e-05 | 0.00698243 | utr-variant-5-prime | UBAC1 | GRCh38.p7 | 9:135961186 | CGCCGCAGGGGCCTG[C/T]GCCCGCCACCCGGGC | 10422 |
| rs779717112 | snp | A/G | 2.40688e-05 | 0.00346898 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135961061 | GAGCTTCTCCACCGA[A/G]GTGTCCTCGGTGGCC | 10422 |
| rs779745711 | snp | C/G | 1.65485e-05 | 0.00287645 | utr-variant-3-prime | UBAC1 | GRCh38.p7 | 9:135933381 | GCTGTGGCCTGATAG[C/G]CGAGTGGAACAACGC | 10422 |
| rs779848343 | snp | C/G | | | downstream-variant-500B | UBAC1 | GRCh38.p7 | 9:135932777 | CCAGGAATACGGGCT[C/G]AGCTCCAGTCCCTTA | 10422 |
| rs779932040 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135947414 | CTGCCACTACGCCCG[A/G]CTAATTTTTGGTATT | 10422 |
| rs779974201 | snp | A/G | 6.80122e-05 | 0.00583108 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946024 | CGACAGGGCCATGAG[A/G]GCTCCAGCCTCAGGT | 10422 |
| rs780053889 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135953509 | ATTTTTAGTAGAGCC[A/G]GGGTTTCACCATATT | 10422 |
| rs780063954 | snp | C/G/T | 3.38165e-05 | 0.00411185 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938387 | AGAGCACCAATACCA[C/G/T]TGTTAGCGCCTTCAG | 10422 |
| rs780086830 | snp | A/G | 3.34806e-05 | 0.00409136 | missense | UBAC1 | GRCh38.p7 | 9:135939674 | AGCCCAACACTCACC[A/G]CGGCATTCTGCTGGT | 10422 |
| rs780163525 | snp | A/C | 1.66477e-05 | 0.00288506 | missense | UBAC1 | GRCh38.p7 | 9:135955343 | TGGCATCACTCAGCA[A/C]CCTCTCTGAGGCAGC | 10422 |
| rs780192015 | snp | A/C | 1.6599e-05 | 0.00288084 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938216 | GCATAAAGAAGGCGC[A/C]CATACCTAGCAATGT | 10422 |
| rs780195283 | snp | C/T | 3.3216e-05 | 0.00407515 | missense | UBAC1 | GRCh38.p7 | 9:135945946 | CCCATCTCCGTGAGC[C/T]GCCGCAGGGCAGCCT | 10422 |
| rs780287060 | snp | A/G | 3.29984e-05 | 0.00406179 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135938298 | AAAGAGAGGACTGTC[A/G]GGGTCGATGCCCTTG | 10422 |
| rs780311054 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135946195 | CCGGTCAGTGGTCAG[C/T]GCGTGGAGCTGCAGA | 10422 |
| rs780415263 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135948904 | GTGAAACCCCATCTC[C/T]ACTAAAAAGACAAAA | 10422 |
| rs780451579 | snp | G/T | 3.29728e-05 | 0.00406021 | missense | UBAC1 | GRCh38.p7 | 9:135945114 | CCTCATCGGTGGCGC[G/T]GGCTCCCGCGGCAGC | 10422 |
| rs780628051 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135942198 | CACAACACACGAGAG[C/T]GCGAAGTCCAACCTC | 10422 |
| rs780650075 | in-del | -/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952455 | CCCTGCTGTGGGGTA[-/G]GGACACGCCACTTGC | 10422 |
| rs780807817 | snp | A/G | | | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135933421 | GCGATTTAGTGTCTG[A/G]AAGATTCTAGAGATC | 10422 |
| rs780815399 | snp | A/G | | | upstream-variant-2KB | UBAC1 | GRCh38.p7 | 9:135962931 | GGGCTTGGAGGAGCC[A/G]GGTCAGAGCATTAAG | 10422 |
| rs780823748 | snp | A/C | 1.67556e-05 | 0.0028944 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135947846 | CATGTTGTAGGAGGG[A/C]AGGTTGGCGGTGGCC | 10422 |
| rs780861570 | in-del | -/CACGCTCATCCT | | | cds-indel | UBAC1 | GRCh38.p7 | 9:135945967 | GGGCAGCCTCGTCCA[-/CACGCTCATCCT]CACGCTCATCCTCGT | 10422 |
| rs780919176 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135957526 | TCACTCTGCTTCTTT[A/G]TTCTCGGCAGAAGCT | 10422 |
| rs781000813 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135958442 | GAAGCTAGAGGCCAC[C/T]ACGGTGATCCCAATT | 10422 |
| rs781076532 | snp | C/G | | | utr-variant-5-prime | UBAC1 | GRCh38.p7 | 9:135961367 | CAGCAGCCGCCGGGG[C/G]CGCGCCGTCGCGGCC | 10422 |
| rs781102640 | snp | A/G | 0.000108352 | 0.00735964 | intron-variant | UBAC1 | GRCh38.p7 | 9:135955467 | TAAATCGTAATTCTA[A/G]TAATATAGGACCTGG | 10422 |
| rs781103525 | snp | C/T | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135954303 | TATAAAAAATAGTTG[C/T]GCATGGTGGCACATG | 10422 |
| rs781110799 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135941130 | AAAAGTCCCAGCCGG[C/G]AGCAGTGGCTCACGC | 10422 |
| rs781189264 | snp | A/G | 3.23138e-05 | 0.00401944 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135961031 | CGGCCTTACGTGCTT[A/G]AGGCAGCGCTCCTTG | 10422 |
| rs781190332 | snp | A/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135952661 | GAAATAGACAAGACA[A/G]GCAGAACTCAGCCTC | 10422 |
| rs781191124 | snp | C/T | 1.66076e-05 | 0.00288158 | synonymous-codon | UBAC1 | GRCh38.p7 | 9:135945972 | AGCCTCGTCCACACG[C/T]TCATCCTCGTCCTCG | 10422 |
| rs781206315 | snp | A/C | 2.28506e-05 | 0.00338006 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945279 | GACTCTTTCCAACAT[A/C]CCCAGACTAACGGAC | 10422 |
| rs781207645 | snp | A/C | 1.6869e-05 | 0.00290417 | intron-variant | UBAC1 | GRCh38.p7 | 9:135946012 | GCTGCAGGGAGACGA[A/C]AGGGCCATGAGGGCT | 10422 |
| rs781296337 | snp | A/G | 1.66593e-05 | 0.00288607 | intron-variant | UBAC1 | GRCh38.p7 | 9:135933536 | GGGAAAACAGAGCCA[A/G]CCTGAGTGCCCACGC | 10422 |
| rs781324855 | snp | G/T | 1.6473e-05 | 0.00286988 | missense | UBAC1 | GRCh38.p7 | 9:135955315 | TCCTGGATGTTCTCT[G/T]CCAGGATGGTCCTGG | 10422 |
| rs781500099 | snp | C/T | 1.7208e-05 | 0.00293321 | intron-variant | UBAC1 | GRCh38.p7 | 9:135945877 | AAGGGAAGGAGGTGG[C/T]CCCCCACGCACTGGT | 10422 |
| rs781539936 | snp | C/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135953902 | CCAGCACTTTGGGAG[C/G]CTGAGGCGGGCAAAT | 10422 |
| rs781545794 | snp | C/T | 1.66374e-05 | 0.00288417 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938213 | TTAGCATAAAGAAGG[C/T]GCACATACCTAGCAA | 10422 |
| rs781652177 | snp | G/T | 1.66421e-05 | 0.00288458 | intron-variant | UBAC1 | GRCh38.p7 | 9:135938212 | CTTAGCATAAAGAAG[G/T]CGCACATACCTAGCA | 10422 |
| rs781653164 | snp | A/C | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135946678 | CAGGTGCAGGGCAAG[A/C]TGAAGACCCTCTCTG | 10422 |
| rs781695132 | snp | C/T | 1.6517e-05 | 0.00287372 | splice-acceptor-variant | UBAC1 | GRCh38.p7 | 9:135946373 | AGTTCTGTCTGGAAC[C/T]GTGGTGAAAAAAAAG | 10422 |
| rs796120901 | in-del | -/A | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135960598 | TGCTGCTGAAAAAAA[-/A]CCTCACCCCAACAGC | 10422 |
| rs796234104 | in-del | -/G | | | intron-variant | UBAC1 | GRCh38.p7 | 9:135959372 | AGGGTTTTTTGTCTG[-/G]TTTTTTTTTTTTTTT | 10422 |