SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6968 | snp | C/T | 0.0228194 | 0.10435 | synonymous-codon, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039012 | ATGACCATTGAGGAC[C/T]TGAATGAAGCTTTCC | 23510 |
rs9660 | snp | A/G | 0.341409 | 0.232689 | utr-variant-5-prime, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042651 | TTTTCAGGATCCCAA[A/G]ATGGCTGGGCGAAAA | 23510 |
rs1127088 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064397 | TGGGGACTTCTCCTT[C/T]TATGAAAGCCTCCTC | 23510 |
rs1466681 | snp | A/C | 0.362104 | 0.223456 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044960 | GATTTTAAAGTTACC[A/C]GGGAACCAAGCACCC | 23510 |
rs1491765 | snp | A/G | 0.357877 | 0.225527 | intron-variant | KCTD2 | GRCh38.p7 | 17:75032828 | TGGCCCTGGGGCAGA[A/G]TGCTGGATCCCAGCA | 23510 |
rs1802462 | snp | A/C | | | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038949 | TATTGGCCTCACCAA[A/C]CAATTGAGAATTTAT | 23510 |
rs1802463 | snp | C/T | | | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038997 | TTGAATGAAGCTTTC[C/T]CAGAAACCAAATTAG | 23510 |
rs1802465 | snp | C/G | | | missense, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038959 | AAAGTATCCCTATTG[C/G]CCTCACCAACCAATT | 23510 |
rs2291535 | snp | A/G | 0.320096 | 0.239972 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039408 | CCTGTCAGAGTGAGC[A/G]CCCCCACTCAGGGTA | 23510 |
rs2307008 | snp | A/G | 0.464416 | 0.128553 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046587 | GAGCGTCCCTCGGCA[A/G]GTTAACACTGTCTGC | 23510 |
rs2307009 | snp | A/C | 0.0715223 | 0.175059 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75046672 | GGACTGCACGAGACA[A/C]GGCTTGTGGCAGCGC | 23510 |
rs4076115 | snp | A/G | 0.131723 | 0.220251 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063741 | CTTTCTCCAGCAGCC[A/G]GGACCCTCTGGAGAG | 23510 |
rs4365317 | snp | C/G | 0.496968 | 0.0388195 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063725 | TGCAGCTTTGCCTCA[C/G]CTTTCTCCAGCAGCC | 23510 |
rs4435292 | snp | A/G | 0.366266 | 0.221319 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039698 | TGTTAGAAACAAGGA[A/G]TTGGAATTAGAAAAA | 23510 |
rs4447462 | snp | A/G | 0.357451 | 0.225731 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051388 | ctcccgggttcaagc[A/G]attttcctgcctcag | 23510 |
rs4788858 | snp | A/C | 0 | 0 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043238 | aaagaaaaggaaaGG[A/C]CAGTGTAGCTTTTCA | 23510 |
rs4789126 | snp | C/G | 0.378568 | 0.214407 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032295 | CATTTAGTCTTTCCC[C/G]TACAGAGGCTGTGGC | 23510 |
rs4789127 | snp | A/G | 0.378174 | 0.214642 | nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75032657 | GCTGGGAGTGAGGTT[A/G]GAGCTGTAAGATCCA | 23510 |
rs6146149 | in-del | -/CACACACACAC | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062744 | ACACACACACACACA[-/CACACACACAC]GCTTCTAAATCGTGG | 23510 |
rs7210163 | snp | A/G | 0.116138 | 0.211142 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035095 | AATTGGCCTCTCTAG[A/G]AGGTAGCTGCAGCCG | 23510 |
rs7210415 | snp | C/G | 0.420574 | 0.182769 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041773 | tgcctggctgaggca[C/G]gtggattgcttgagc | 23510 |
rs7211204 | snp | A/G | 0.49655 | 0.04139 | intron-variant | KCTD2 | GRCh38.p7 | 17:75050332 | actggcacaatcttg[A/G]ctcactgcaacctca | 23510 |
rs7211939 | snp | A/C | 0.0554779 | 0.157039 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052336 | tcatgcctgtaatcc[A/C]aacacttggaaggcc | 23510 |
rs7217434 | snp | A/G | 0.213333 | 0.247296 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044589 | tcaggtgatccaccc[A/G]cctcagccttgcaaa | 23510 |
rs7218004 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | KCTD2 | GRCh38.p7 | 17:75032748 | GAGCCCCGGGCGGGC[A/G]GGTTGGGGGAACATG | 23510 |
rs7218157 | snp | A/C | 0.489492 | 0.0717183 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030949 | AACAATACAAAAATA[A/C]AATTAGCCAGGCGTG | 23510 |
rs7218282 | snp | A/G | 0.0592355 | 0.161582 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030687 | TGTATAAATTTCTTA[A/G]ACTGTTCTATATGAT | 23510 |
rs7219493 | snp | C/T | 0.464629 | 0.128197 | upstream-variant-2KB, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75048093 | ATATCACACTGCTTT[C/T]CTATAGTCCTGGTCG | 23510 |
rs7223981 | snp | A/T | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031750 | ccccacctataaact[A/T]ggggggtttttttgt | 23510 |
rs7224300 | snp | A/G | 0.278133 | 0.248412 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033161 | TTCAAATGAGACTGC[A/G]TCTCGCTATGTTGCC | 23510 |
rs7503086 | snp | A/C | 0 | 0 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039894 | gaatcatatgctata[A/C]tcttctttttcttgt | 23510 |
rs8064912 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037361 | aaaaaaaaaaaaaaa[A/G]aaagaaaTGGCAGAA | 23510 |
rs8065776 | snp | A/G | 0.421209 | 0.182174 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055815 | ccagcctgggcaaca[A/G]gagcgaaactcccat | 23510 |
rs8073270 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035852 | aaacaaacaaacaaa[C/T]aaacaaaAAACTCCA | 23510 |
rs8077242 | snp | C/G | 0 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036757 | TCAGATCCTCAGCGG[C/G]ATGGCTGAGTGCCAG | 23510 |
rs8077664 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037017 | GATTTCTCGAGGGTT[A/G]TCAGGCATTGTTGCT | 23510 |
rs8078243 | snp | A/C | 0.140242 | 0.224618 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036706 | CTGCATTTTTTCTCA[A/C]ATCCCTGCGCTTTCA | 23510 |
rs8079265 | snp | A/G | 0.209693 | 0.246729 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037067 | CTGCAAAAATGGGCC[A/G]GGTGCGGTGGCTCAC | 23510 |
rs8079749 | snp | C/G | 0.0283406 | 0.115616 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031727 | ctaacctctctgaac[C/G]ttagtttccccacct | 23510 |
rs8080887 | snp | A/G | 0.162581 | 0.234218 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75040504 | AGCACCTTGAATTGT[A/G]AAGAAATTCTGATTT | 23510 |
rs9891685 | snp | A/G | 0.292008 | 0.246445 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037283 | CGGGAGGCAAAGGTT[A/G]CAATGAGCAGAAATC | 23510 |
rs9900856 | snp | A/G | 0.464841 | 0.127841 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037832 | AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 23510 |
rs9904728 | snp | C/T | 0.320096 | 0.239972 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034540 | GTGCTCCTTGATAGG[C/T]GTTCAACCATAGTGC | 23510 |
rs9905052 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | KCTD2 | GRCh38.p7 | 17:75035189 | CCTTCGTGGTCGGAA[C/T]GTTTTAATCCCTGCA | 23510 |
rs9906330 | snp | A/G | 0.401924 | 0.198543 | intron-variant | KCTD2 | GRCh38.p7 | 17:75053342 | TGCTTACCAGATGGC[A/G]GGAGGAGGCGCCCAG | 23510 |
rs9911825 | snp | C/T | 0.166832 | 0.235761 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057369 | TGGCATCTTAAATAC[C/T]TGGGACTTTGACAGC | 23510 |
rs9915277 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031231 | GGCTCATATGCAGGA[C/T]GTACAAAATTTCCTA | 23510 |
rs9915968 | snp | C/G | 0.496937 | 0.0390173 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063521 | TGCACCCTCCAAGAC[C/G]TGCAGCAGATGCAAA | 23510 |
rs10512598 | snp | C/T | 0.320575 | 0.239832 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75042037 | CAAAGGCCTTGTGGT[C/T]GATTGAACTGTAAAT | 23510 |
rs10533801 | in-del | -/AC | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75062700 | CCCCCCTCACCCCCA[-/AC]ACACACACACACACA | 23510 |
rs11077772 | snp | C/T | 0.37778 | 0.214877 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75039603 | TAGCCAGACTTCTCT[C/T]TGGTGGAGCCACTGA | 23510 |
rs11077773 | snp | C/T | 0.470908 | 0.117046 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063978 | TTGCCAAATGTGTTA[C/T]GTTGTGTCTCAGAGA | 23510 |
rs11312083 | in-del | -/T | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044034 | GCACACGTTGTGCAC[-/T]TTTTTTTTTTTTTTT | 23510 |
rs11538852 | snp | G/T | 0.130351 | 0.219509 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75065663 | TGTTTCTGCACAGTT[G/T]TAACTGCTCTTGGGG | 23510 |
rs11538853 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064699 | TTTTACAGCTGTAAA[G/T]TGTTAGATGAACTGC | 23510 |
rs11538854 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75063366 | TCTGGGGGATGAGGG[C/T]GGAAGGCCTAGCTCC | 23510 |
rs11651848 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KCTD2 | GRCh38.p7 | 17:75052618 | atcccagctacttgg[A/G]aggctgaggcagcag | 23510 |
rs11867756 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033130 | TTTAATAATTTTTTT[C/T]CTtttttttcttttt | 23510 |
rs11869630 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033131 | ttaataatttttttt[C/T]Ttttttttctttttt | 23510 |
rs11870474 | snp | A/C | 0.164873 | 0.23506 | intron-variant | KCTD2 | GRCh38.p7 | 17:75034715 | GCGGTGCCCTGTAAC[A/C]CCGAGAAGAAGTGCT | 23510 |
rs11871228 | snp | A/G | 0.409552 | 0.192466 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051547 | CCTTGGCCTCCCGAA[A/G]TGCTGCGATTACAGG | 23510 |
rs12103574 | snp | A/G | 0.166832 | 0.235761 | intron-variant | KCTD2 | GRCh38.p7 | 17:75056554 | AGATTCTGAAGGCTT[A/G]TGGATTTATACCCCT | 23510 |
rs12150430 | snp | A/G | 0.362941 | 0.223034 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058824 | ataaataggccgggc[A/G]cggtggctcatgcct | 23510 |
rs12232542 | snp | C/T | 0.31357 | 0.241783 | intron-variant, downstream-variant-500B | KCTD2 | GRCh38.p7 | 17:75060662 | CGGCCAGGGAGGGCG[C/T]GCGTGCGAGGGCGGG | 23510 |
rs12600475 | snp | A/C | 0 | 0 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049654 | GTGAGTGTCTGTAGT[A/C]TGAAGAAGCAAGACA | 23510 |
rs12602540 | snp | A/G | 0.32955 | 0.237006 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064016 | TTCTGTGACTCTCTT[A/G]GAAATGCCTTGACTG | 23510 |
rs12602633 | snp | C/G | 0.336702 | 0.234484 | utr-variant-3-prime, nc-transcript-variant | KCTD2 | GRCh38.p7 | 17:75064590 | TCCCTAGGACCCTCA[C/G]TCTCCTTGTTTCTCT | 23510 |
rs12936866 | snp | A/G | 0.397994 | 0.201489 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055955 | AGAATCGCTTGAACT[A/G]AGATAGCAGAGGTTG | 23510 |
rs12938569 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant, utr-variant-3-prime | KCTD2 | GRCh38.p7 | 17:75060070 | TGGGAAGTGTGGTGC[A/G]GCCGTTTCCCCTACT | 23510 |
rs12938889 | snp | A/C | 0.362313 | 0.223351 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75043834 | ATTTACTTATGTGTA[A/C]AATGGGCATTATCAG | 23510 |
rs12939787 | snp | C/G | 0.132409 | 0.220618 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044071 | actctgtcccccggg[C/G]tggagtgcagtggca | 23510 |
rs12940199 | snp | C/T | 0.399073 | 0.200692 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058664 | attagccaggcttag[C/T]ggcaggcgcctgtaa | 23510 |
rs12940952 | snp | A/G | 0.170733 | 0.237101 | intron-variant | KCTD2 | GRCh38.p7 | 17:75051346 | ctggagtgcaatggc[A/G]ctatcacagctcact | 23510 |
rs12943148 | snp | C/G | 0.40157 | 0.198813 | intron-variant | KCTD2 | GRCh38.p7 | 17:75055637 | tcaggagttcaagac[C/G]agcctgactaacatg | 23510 |
rs12943281 | snp | A/G | 0.160609 | 0.233472 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033999 | GAAAGTTCCTTTTAC[A/G]GAATTTTTTATTTCT | 23510 |
rs12946754 | snp | C/T | 0.131038 | 0.219882 | intron-variant | KCTD2 | GRCh38.p7 | 17:75049571 | CGCTTTGCAGATAAC[C/T]TCAGGAGTTCTTTCC | 23510 |
rs12949127 | snp | A/T | 0.166832 | 0.235761 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058977 | gtggcgggtgcctgt[A/T]gtcccagctacttgg | 23510 |
rs12949352 | snp | A/G | 0.123105 | 0.215401 | intron-variant | KCTD2 | GRCh38.p7 | 17:75054143 | ctacctcagcctacc[A/G]agtagctgggactac | 23510 |
rs12949451 | snp | A/C | 0.251578 | 0.249995 | intron-variant | KCTD2 | GRCh38.p7 | 17:75036224 | gggcccggccaggga[A/C]tggagttttgtctgc | 23510 |
rs12950279 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047229 | TGCGCGCGggcagca[A/G]cggtggcggcggcgg | 23510 |
rs12950646 | snp | C/G | 0.494315 | 0.0530107 | intron-variant, upstream-variant-2KB | ATP5H, KCTD2 | GRCh38.p7 | 17:75045375 | aggagacagggtttt[C/G]agatcaaccggtctg | 23510 |
rs12951145 | snp | A/G | 0.213635 | 0.247341 | intron-variant | KCTD2 | GRCh38.p7 | 17:75037981 | ATGAACCCATGAGGT[A/G]AAGGTTGCAGTGAGC | 23510 |
rs12952376 | snp | C/T | 0.49724 | 0.037049 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75047242 | cagcggtggcggcgg[C/T]ggtccaagatggcgg | 23510 |
rs16967530 | snp | C/T | 0.0166325 | 0.0896639 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75030674 | GATTGCTCTGGCATG[C/T]ATAAATTTCTTAAAC | 23510 |
rs28412160 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044495 | TAGGCGTGAGCCACC[A/G]CGCCCGGCCCTAATT | 23510 |
rs28438465 | snp | A/G | 0.0865458 | 0.189163 | downstream-variant-500B, intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75038720 | GCCTCAGTAAGTGGC[A/G]CCTACACAGCCCGTC | 23510 |
rs28497354 | snp | A/G | 0.19646 | 0.2442 | intron-variant | KCTD2 | GRCh38.p7 | 17:75033169 | AGACTGCATCTCGCT[A/G]TGTTGCCCAGGCTGG | 23510 |
rs28501229 | snp | C/T | 0.20111 | 0.245173 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041905 | TAAGAAGGGGTGAAC[C/T]GGCCCAGGTCAGAAA | 23510 |
rs28576234 | snp | C/T | 0.351853 | 0.228311 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044480 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCG | 23510 |
rs28587464 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75044634 | GGCATGAGCCACCGC[A/G]CCCGGCCTGCATTTT | 23510 |
rs28648787 | snp | A/G | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041371 | AAAAAAAAAAAAAAA[A/G]AAGAGCAGAGAGGTG | 23510 |
rs28694537 | snp | A/G | 0.0854556 | 0.188216 | intron-variant | KCTD2 | GRCh38.p7 | 17:75057860 | GTCACTGCACCCGGC[A/G]ATCGTTATACCTCTT | 23510 |
rs28797168 | snp | A/G | 0.084728 | 0.187577 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058516 | CTCAAAAATAATAAT[A/G]AGGCTGGGTGCGGTG | 23510 |
rs34037833 | in-del | -/G | | | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75032496 | GGGTAGTGTGGGAGT[-/G]GGGGGTGTGACATGG | 23510 |
rs34316730 | in-del | -/A | 0.397994 | 0.201489 | intron-variant | KCTD2 | GRCh38.p7 | 17:75058338 | AAAAGGAAAAAAAAA[-/A]TAAAAAATTAGCTGG | 23510 |
rs34415927 | snp | A/G | 0.0154538 | 0.0865337 | upstream-variant-2KB | KCTD2 | GRCh38.p7 | 17:75031542 | GGGAGAACTGGCAGG[A/G]TAACAGCATGTCACT | 23510 |
rs34551845 | in-del | -/A | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75036222 | TGGGCCCGGCCAGGG[-/A]ACTGGAGTTTTGTCT | 23510 |
rs34581230 | in-del | -/C | | | intron-variant | KCTD2 | GRCh38.p7 | 17:75059636 | AGCAGCAATCCCAGG[-/C]CCCCGTTCAAGGGGT | 23510 |
rs34600095 | in-del | -/A | | | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041731 | CAAACATTTAACTTG[-/A]AAAGCCCCCTGGGGC | 23510 |
rs34603178 | snp | A/G | 0.362523 | 0.223246 | intron-variant | ATP5H, KCTD2 | GRCh38.p7 | 17:75041097 | GGCATGGTGGCTCAC[A/G]CCTGTACTCCCAGCA | 23510 |