| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs1625 | snp | A/T | 0.400147 | 0.19989 | upstream-variant-2KB | BTBD3 | GRCh38.p7 | 20:11888961 | tggtcatttcaaggt[A/T]acttttcttctaCAG | 22903 |
| rs6660 | snp | C/T | 0.361474 | 0.223771 | utr-variant-3-prime | BTBD3 | GRCh38.p7 | 20:11926410 | TTCAAGACACTGTAG[C/T]CACTTGTGCATCAGT | 22903 |
| rs1043926 | snp | A/G | 0.363985 | 0.222503 | utr-variant-3-prime | BTBD3 | GRCh38.p7 | 20:11925532 | TATTTCCAGGACAAC[A/G]TTCTAAAAGTACAAT | 22903 |
| rs1232480 | snp | A/G | 0.446641 | 0.154377 | intron-variant | BTBD3 | GRCh38.p7 | 20:11907832 | CTGGCTCAATTCCCA[A/G]TTAGATCTTTTGACT | 22903 |
| rs1232481 | snp | G/T | 0.445592 | 0.155704 | intron-variant | BTBD3 | GRCh38.p7 | 20:11906203 | GGAATAACTTATTTT[G/T]GGCCAAAACTGGAAA | 22903 |
| rs1232482 | snp | C/T | 0.432063 | 0.171327 | intron-variant | BTBD3 | GRCh38.p7 | 20:11905995 | AATGAATTTACCTCA[C/T]CCTGCCTTCTAAGAA | 22903 |
| rs1232483 | snp | C/T | 0.445592 | 0.155704 | intron-variant | BTBD3 | GRCh38.p7 | 20:11905854 | ACCACTAGCAGATGT[C/T]GCTGGGAGGTTGCAG | 22903 |
| rs1232484 | snp | C/T | 0.441568 | 0.160629 | intron-variant | BTBD3 | GRCh38.p7 | 20:11904857 | gtacaaaacgttcat[C/T]gatatggttttagat | 22903 |
| rs1232485 | snp | A/T | 0.44306 | 0.158832 | intron-variant | BTBD3 | GRCh38.p7 | 20:11904751 | gaaaatgctattaaa[A/T]tattcttttccagct | 22903 |
| rs1232486 | snp | A/C | 0.441568 | 0.160629 | intron-variant | BTBD3 | GRCh38.p7 | 20:11904646 | tttaaattttGACAA[A/C]AGTATATTAATAGAT | 22903 |
| rs1232487 | snp | A/G | 0.451109 | 0.148509 | intron-variant | BTBD3 | GRCh38.p7 | 20:11898600 | atgtgctaggcactc[A/G]ggacacattaataaa | 22903 |
| rs1232488 | snp | C/T | 0.454182 | 0.144256 | intron-variant | BTBD3 | GRCh38.p7 | 20:11898090 | actgcatgcaacctc[C/T]gccttccaggttcaa | 22903 |
| rs1232489 | snp | C/T | 0.439363 | 0.163222 | intron-variant | BTBD3 | GRCh38.p7 | 20:11897794 | ggagggttttaagca[C/T]aatttgacttatgtt | 22903 |
| rs1232490 | snp | A/G | 0.437259 | 0.165632 | intron-variant | BTBD3 | GRCh38.p7 | 20:11897594 | actgattctggatac[A/G]ttttgaagacagaac | 22903 |
| rs1232491 | snp | A/G | 0.15698 | 0.23205 | intron-variant | BTBD3 | GRCh38.p7 | 20:11894849 | TTAGTCTTCCTCCCC[A/G]TCCACTTTTGACTGC | 22903 |
| rs1237445 | snp | C/T | 0.433527 | 0.169758 | intron-variant | BTBD3 | GRCh38.p7 | 20:11896048 | TCCAGATTAAGACGG[C/T]AAATTTAACACACAT | 22903 |
| rs1883792 | snp | A/G | 0.450105 | 0.149859 | intron-variant | BTBD3 | GRCh38.p7 | 20:11915737 | AGAGTGCTACAAAGA[A/G]GGGCATTATTACTCC | 22903 |
| rs1883793 | snp | C/T | 0.445724 | 0.155538 | intron-variant | BTBD3 | GRCh38.p7 | 20:11911583 | CATTATGAGATTTTT[C/T]TTTTCTGCAATTTTT | 22903 |
| rs1997808 | snp | A/G | 0 | 0 | intron-variant | BTBD3 | GRCh38.p7 | 20:11900376 | CCAACTGGGCTGTCC[A/G]TTAATGGCCTAAACT | 22903 |
| rs2206798 | snp | G/T | 0.449979 | 0.150028 | intron-variant, upstream-variant-2KB | BTBD3 | GRCh38.p7 | 20:11916797 | GGATCACGCTCATTT[G/T]TTCAAAGCACAGCAG | 22903 |
| rs2206799 | snp | C/G | 0.439641 | 0.162899 | upstream-variant-2KB | BTBD3 | GRCh38.p7 | 20:11890542 | TAAGCATTTATTGAA[C/G]ACTTGCACTGGCAGA | 22903 |
| rs2223708 | snp | A/G | 0.43978 | 0.162738 | upstream-variant-2KB | BTBD3 | GRCh38.p7 | 20:11889340 | tcagctgaagacctt[A/G]gtagaaaaatgctga | 22903 |
| rs2223709 | snp | A/G | 0.479177 | 0.0998894 | upstream-variant-2KB | BTBD3 | GRCh38.p7 | 20:11888819 | cccagttcatgaatc[A/G]ctaataaaagccaat | 22903 |
| rs2294967 | snp | C/T | 0.353587 | 0.22753 | intron-variant | BTBD3 | GRCh38.p7 | 20:11921950 | AGCTTAAATATGTAT[C/T]ATTCCTGTGCTTCTG | 22903 |
| rs2294968 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | BTBD3 | GRCh38.p7 | 20:11921061 | GCAGGTAAAACTGGT[G/T]TCTGTACATATATCT | 22903 |
| rs2327611 | snp | A/G | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11906252 | aaaaaaaaaaaaaGG[A/G]GTAATAATAAATGGA | 22903 |
| rs2746117 | snp | A/G | 0.479824 | 0.098392 | upstream-variant-2KB, intron-variant | BTBD3 | GRCh38.p7 | 20:11891180 | GCTGGCTTTCCGAGG[A/G]GGGGGGGGTCCCAGT | 22903 |
| rs2795021 | snp | A/G | 0.437401 | 0.165472 | intron-variant | BTBD3 | GRCh38.p7 | 20:11893157 | AAATGACCTATTTCT[A/G]TACTATTTTGTTCAG | 22903 |
| rs2795022 | snp | A/G | 0.437118 | 0.165792 | intron-variant | BTBD3 | GRCh38.p7 | 20:11892669 | AGTTATCAGTGCAAG[A/G]ATTGGGAAAGAATGA | 22903 |
| rs2876292 | snp | G/T | 0 | 0 | intron-variant | BTBD3 | GRCh38.p7 | 20:11906219 | TTATGGTATCAGTAG[G/T]GGAATAACTTATTTT | 22903 |
| rs3071747 | in-del | -/AAAA/AAAAA/G | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11906254 | aaaaaaaaaaaaaaa[-/AAAA/AAAAA/G]GGAGTAATAATAAAT | 22903 |
| rs3171277 | snp | A/C | 0 | 0 | utr-variant-3-prime | BTBD3 | GRCh38.p7 | 20:11926403 | CAGCTAATTCAAGAC[A/C]CTGTAGCCACTTGTG | 22903 |
| rs3177118 | snp | A/G | 0.48378 | 0.0885831 | utr-variant-3-prime | BTBD3 | GRCh38.p7 | 20:11924994 | TCGCTGCTGGCTTGT[A/G]CTGGTTTAGTGCCTG | 22903 |
| rs3215562 | in-del | -/A | 0.360632 | 0.224189 | intron-variant | BTBD3 | GRCh38.p7 | 20:11920950 | ATCCCCTACTGTGAA[-/A]GGTCTTGTCAGTGAC | 22903 |
| rs3762217 | snp | G/T | 0.128632 | 0.218563 | intron-variant | BTBD3 | GRCh38.p7 | 20:11907318 | GAGCCCCAGGACACA[G/T]TTAATAGGTATTCAG | 22903 |
| rs3762219 | snp | A/T | 0.447421 | 0.153379 | intron-variant | BTBD3 | GRCh38.p7 | 20:11908340 | TTTTTTTTTTTTTTT[A/T]AATAAGGTACTGACA | 22903 |
| rs3834758 | in-del | -/T | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11908339 | ttttttttttttttt[-/T]aaataaGGTACTGAC | 22903 |
| rs4142485 | snp | G/T | 0.445592 | 0.155704 | intron-variant | BTBD3 | GRCh38.p7 | 20:11909534 | CTTTGTAACTTCATG[G/T]ATGTTTAAGTTTTCC | 22903 |
| rs4813063 | snp | A/G | 0.351635 | 0.228408 | intron-variant | BTBD3 | GRCh38.p7 | 20:11910960 | CTTGATGAAAGCTCA[A/G]TTATTCTAATGTAGT | 22903 |
| rs4813064 | snp | C/T | 0.122064 | 0.214785 | intron-variant | BTBD3 | GRCh38.p7 | 20:11920625 | AGACAGTGTGGTAGT[C/T]CACCAAGTGATCATA | 22903 |
| rs4814038 | snp | C/T | 0.446902 | 0.154045 | intron-variant | BTBD3 | GRCh38.p7 | 20:11900926 | CCATGTTAGCCAGGA[C/T]GGTCTCGATATCCTG | 22903 |
| rs4814039 | snp | A/C | 0.445855 | 0.155373 | intron-variant | BTBD3 | GRCh38.p7 | 20:11911035 | ATTAAGCAACCTAAA[A/C]AAAAGATTTCTTTCT | 22903 |
| rs4814040 | snp | A/C | 0.444931 | 0.15653 | intron-variant | BTBD3 | GRCh38.p7 | 20:11911352 | TTATATTAAGTAAAT[A/C]ACTATTTCTGGCAAA | 22903 |
| rs4814041 | snp | C/G | 0.361053 | 0.22398 | intron-variant | BTBD3 | GRCh38.p7 | 20:11920574 | AGTATGTGTTAAACA[C/G]GTTATAGAATCAGCT | 22903 |
| rs5840469 | in-del | -/T | 0.279726 | 0.248226 | upstream-variant-2KB, intron-variant | BTBD3 | GRCh38.p7 | 20:11892294 | TGCCCAGCCAAGGGC[-/T]TTTCCCCTTCTTTTA | 22903 |
| rs6033255 | snp | C/T | 0.396182 | 0.202807 | upstream-variant-2KB | BTBD3 | GRCh38.p7 | 20:11889143 | ttgtttgtttgtttg[C/T]ttgcttTTTGCAGTT | 22903 |
| rs6033256 | snp | G/T | 0.441841 | 0.160303 | intron-variant | BTBD3 | GRCh38.p7 | 20:11901797 | TATATAATGGTGTTC[G/T]GTTTGGCTTATAGGA | 22903 |
| rs6033257 | snp | C/T | 0 | 0 | intron-variant | BTBD3 | GRCh38.p7 | 20:11906796 | GAGGCATGCATTTTC[C/T]TACTGCCCTATACAC | 22903 |
| rs6033258 | snp | G/T | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11910187 | ACTTTGATGATCTGA[G/T]GGAGGAGATGTTCTT | 22903 |
| rs6033259 | snp | C/T | 0 | 0 | intron-variant | BTBD3 | GRCh38.p7 | 20:11913178 | TTGCTTTTTAGCGGC[C/T]TTGTAGTAAACCATG | 22903 |
| rs6033260 | snp | C/T | 0 | 0 | intron-variant | BTBD3 | GRCh38.p7 | 20:11921073 | AGAAACCAGTTTTAC[C/T]TGCAAGTATCCCCAC | 22903 |
| rs6033261 | snp | G/T | 0.379746 | 0.213696 | utr-variant-3-prime | BTBD3 | GRCh38.p7 | 20:11924037 | ATGAACAGAAATAAA[G/T]TGATAACAAGAGTTA | 22903 |
| rs6040967 | snp | C/T | 0.405776 | 0.195535 | intron-variant | BTBD3 | GRCh38.p7 | 20:11893451 | ACCTTGTAGTTCCAG[C/T]AGTGATGCTGGGCTG | 22903 |
| rs6040968 | snp | A/G | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11894209 | CGACCAAATGACGTA[A/G]GCTCAGTACGTAAGA | 22903 |
| rs6040969 | snp | A/G | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11894292 | tttcggatttactca[A/G]gttagatttatagca | 22903 |
| rs6040970 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTBD3 | GRCh38.p7 | 20:11894620 | CTAAAGAAGATTGAG[C/T]GTTTATCATGTTTTT | 22903 |
| rs6040971 | snp | A/G | 0.176219 | 0.238865 | intron-variant | BTBD3 | GRCh38.p7 | 20:11894621 | TAAAGAAGATTGAGT[A/G]TTTATCATGTTTTTA | 22903 |
| rs6040973 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | BTBD3 | GRCh38.p7 | 20:11898284 | CTTACCTCCTTGCTA[A/G]TCCTTGAACGTGGCA | 22903 |
| rs6040974 | snp | C/T | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11898569 | CTAGACTATAAATTC[C/T]TTGAGGTCGAGTATG | 22903 |
| rs6040975 | snp | C/T | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11898607 | ATGTGTCCTGAGTGC[C/T]TAGCACATAGAAGAT | 22903 |
| rs6040976 | snp | A/G | 0.445987 | 0.155207 | intron-variant | BTBD3 | GRCh38.p7 | 20:11900056 | TTTCTATGATGCTAT[A/G]TAAGTAAGAGCATTC | 22903 |
| rs6040977 | snp | C/T | 0.452965 | 0.145963 | intron-variant | BTBD3 | GRCh38.p7 | 20:11901784 | TTAGGGATGTCAATA[C/T]ATAATGGTGTTCGGT | 22903 |
| rs6040978 | snp | G/T | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11901997 | TCTAGTAAAAGACTA[G/T]ACCCTTGAACAACTT | 22903 |
| rs6040979 | snp | A/G | 0.441568 | 0.160629 | intron-variant | BTBD3 | GRCh38.p7 | 20:11902159 | gaacataaacagtca[A/G]taaacgcatattttg | 22903 |
| rs6040980 | snp | A/C | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11904193 | aattggctcacagtt[A/C]tgcaggctctacagg | 22903 |
| rs6040981 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | BTBD3 | GRCh38.p7 | 20:11905484 | tactattgcatcTCC[C/T]AGAGATTCCCCATGA | 22903 |
| rs6040982 | snp | A/C | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11908212 | ATGTAAATTGTGATC[A/C]CCATTTTCAGAGATT | 22903 |
| rs6074365 | snp | A/G | 0.451359 | 0.148171 | intron-variant | BTBD3 | GRCh38.p7 | 20:11912046 | GCTCACCCCAAATCT[A/G]AAGTACAATTCAAGG | 22903 |
| rs6074366 | snp | G/T | 0.451608 | 0.147832 | intron-variant | BTBD3 | GRCh38.p7 | 20:11915558 | GCTGAGATTCTGGGT[G/T]ACTAATAGGCTCCCT | 22903 |
| rs6074367 | snp | C/T | 0 | 0 | intron-variant | BTBD3 | GRCh38.p7 | 20:11915634 | ACCTGCATTACTTGC[C/T]TTATTACCGTGGTAA | 22903 |
| rs6074368 | snp | C/T | 0 | 0 | intron-variant | BTBD3 | GRCh38.p7 | 20:11915710 | CCATGCTCATCAGTC[C/T]TTACATACATTGGAG | 22903 |
| rs6078381 | snp | C/T | 0.44546 | 0.155869 | intron-variant | BTBD3 | GRCh38.p7 | 20:11902880 | CAGCTACATGTTTTA[C/T]CCATTAATGAAATAC | 22903 |
| rs6078382 | snp | A/C | 0.435694 | 0.167385 | intron-variant | BTBD3 | GRCh38.p7 | 20:11903146 | CCAACAAACTGTTTT[A/C]TTCTATTTAGTATAT | 22903 |
| rs6078383 | snp | A/G | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11908377 | TTGCCACTCTTTGAA[A/G]ATGTATTTTGACTTT | 22903 |
| rs6078384 | snp | C/T | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11910444 | CAGCCCCATTCAGGC[C/T]TTTTTGAAAGGGACC | 22903 |
| rs6078385 | snp | C/T | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11910508 | ACTATTTTCAAGTAC[C/T]TAGTAGAAAGTCATA | 22903 |
| rs6078386 | snp | A/G | 0 | 0 | intron-variant | BTBD3 | GRCh38.p7 | 20:11911885 | TAGTATTCCAAACAA[A/G]GTGCACACTGAGACA | 22903 |
| rs6078387 | snp | A/G | 0 | 0 | intron-variant | BTBD3 | GRCh38.p7 | 20:11912088 | TCTGTGTGGTGAAAA[A/G]GTGGCTTAATGAAAC | 22903 |
| rs6078388 | snp | A/G | 0 | 0 | intron-variant | BTBD3 | GRCh38.p7 | 20:11912281 | CAGGAGGCTGTCTCA[A/G]GAAGTGGGCACAGCA | 22903 |
| rs6078389 | snp | A/T | 0 | 0 | intron-variant | BTBD3 | GRCh38.p7 | 20:11913038 | CAAAAACAAAACACT[A/T]TTCCCTCATAACTTA | 22903 |
| rs6078391 | snp | A/G | 0.450734 | 0.149016 | intron-variant | BTBD3 | GRCh38.p7 | 20:11913354 | CAGCGTCCTCACTGC[A/G]GTTCCTTCCTTCCAT | 22903 |
| rs6078392 | snp | C/T | 0 | 0 | intron-variant | BTBD3 | GRCh38.p7 | 20:11921916 | GAAGTGTTTTATATC[C/T]TGAAATAAGGACAGT | 22903 |
| rs6104805 | snp | C/T | 0 | 0 | intron-variant | BTBD3 | GRCh38.p7 | 20:11913989 | CCGTATGCCCAACAC[C/T]TAATACACTGCATAG | 22903 |
| rs6104806 | snp | C/T | 0 | 0 | intron-variant | BTBD3 | GRCh38.p7 | 20:11914059 | GATGGACTTCTTGGC[C/T]TATTTACCTCATTAG | 22903 |
| rs6104807 | snp | C/T | 0.455144 | 0.142885 | intron-variant | BTBD3 | GRCh38.p7 | 20:11915511 | TTCAACCTTGAATAC[C/T]GTATGAAATGCAGAT | 22903 |
| rs6104808 | snp | C/T | 0 | 0 | utr-variant-3-prime | BTBD3 | GRCh38.p7 | 20:11926489 | ATAAATATGAAGTAC[C/T]TCATGTTGAATGTTA | 22903 |
| rs6109170 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | BTBD3 | GRCh38.p7 | 20:11891184 | GCTTTCCGAGGGGGG[G/T]GGGGTCCCAGTGGGG | 22903 |
| rs6109171 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | BTBD3 | GRCh38.p7 | 20:11895038 | ATGAAGCGCTCCTAT[A/G]CCGCCGCTGCCTCCT | 22903 |
| rs6109172 | snp | C/T | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11899701 | TGTGTTTCTAGGCTC[C/T]TTTTGTGTCCTTCAA | 22903 |
| rs6109173 | snp | C/T | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11899711 | GGCTCCTTTTGTGTC[C/T]TTCAAATCCAAGAAT | 22903 |
| rs6109174 | snp | C/T | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11899753 | ATCAGACTCACTTTC[C/T]TCCTCTTTCTTAATA | 22903 |
| rs6109175 | snp | C/T | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11900013 | AAATATACCTAGCTC[C/T]TTGTGTATATTTGAT | 22903 |
| rs6109176 | snp | A/G | 0.441841 | 0.160303 | intron-variant | BTBD3 | GRCh38.p7 | 20:11901838 | CTCAAGATAAGGACA[A/G]CCTATATTTTGATTT | 22903 |
| rs6109178 | snp | A/G | 0 | 0 | intron-variant | BTBD3 | GRCh38.p7 | 20:11912795 | agatgtggaaaatga[A/G]gctcacaaatactga | 22903 |
| rs6109179 | snp | A/G | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11912817 | AAATACTGACCTTAA[A/G]GTCACTTGTTGTTAG | 22903 |
| rs6109180 | snp | A/G | 0 | 0 | intron-variant | BTBD3 | GRCh38.p7 | 20:11913011 | TTGCTCAGTATTGAA[A/G]GGACAAATAAGCAAA | 22903 |
| rs6109181 | snp | A/G | | | intron-variant | BTBD3 | GRCh38.p7 | 20:11913080 | TACTCTCCTCTGTTA[A/G]GTTATGTTAATCATT | 22903 |
| rs6109182 | snp | C/T | 0.450105 | 0.149859 | intron-variant | BTBD3 | GRCh38.p7 | 20:11914439 | AAAGCCATGGCTTCT[C/T]TTTCTAGAAAAATAA | 22903 |
| rs6109183 | snp | C/T | 0.450105 | 0.149859 | intron-variant | BTBD3 | GRCh38.p7 | 20:11914959 | CTGGGTGAATCTCTT[C/T]CATCTTATAGCTGAG | 22903 |
| rs6109184 | snp | A/G | 0.449979 | 0.150028 | intron-variant, upstream-variant-2KB | BTBD3 | GRCh38.p7 | 20:11916767 | GGGTGCATTTGCCTG[A/G]GGGGTAGCAAATGGC | 22903 |