SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8333 | snp | C/T | 0.489722 | 0.0709447 | synonymous-codon, upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2766231 | CGCCTTCGGGGCCAG[C/T]GGCGGGGGCCGCCCG | 56897 |
rs8912 | snp | A/G | 0.0295035 | 0.117819 | utr-variant-3-prime | WRNIP1 | GRCh38.p7 | 6:2785425 | AGAGTTCCATAGGTG[A/G]AGGCGCAGTTCTTTC | 56897 |
rs15217 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WRNIP1 | GRCh38.p7 | 6:2785441 | AGTTACACATTTATT[C/T]GAAAGAACTGCGCCT | 56897 |
rs160658 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2768971 | AACGCTAGAGACTTA[C/T]GAGCTTTGTTTACAA | 56897 |
rs160659 | snp | A/G | 0.482234 | 0.0925596 | intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2769404 | AACAAAGCCACTTAG[A/G]GATTTAAAAAAAAAT | 56897 |
rs160660 | snp | A/T | 0.398894 | 0.200825 | intron-variant, upstream-variant-2KB | WRNIP1, MYLK4 | GRCh38.p7 | 6:2770970 | TTCTGCATCATGAGT[A/T]CCACATGAGCTCGTT | 56897 |
rs160661 | snp | C/G | 0.046775 | 0.145601 | intron-variant, upstream-variant-2KB | WRNIP1, MYLK4 | GRCh38.p7 | 6:2771122 | GGAACATAATCTGGT[C/G]TGATGAGAGGCTATT | 56897 |
rs160662 | snp | A/G | 0.0726307 | 0.176182 | intron-variant, upstream-variant-2KB | WRNIP1, MYLK4 | GRCh38.p7 | 6:2772010 | CAATAATTAATATTG[A/G]TGACATGAAGTCAAT | 56897 |
rs160663 | snp | A/G | 0.046775 | 0.145601 | intron-variant, upstream-variant-2KB | WRNIP1, MYLK4 | GRCh38.p7 | 6:2772084 | TCCCCAGTCACTGCC[A/G]TGCAGGAATTTAAAG | 56897 |
rs160664 | snp | A/C | 0.483995 | 0.0880135 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2772842 | TCCCTGTTGACAGCT[A/C]TATATACATCCTTGT | 56897 |
rs160665 | snp | C/T | 0.484561 | 0.0864924 | intron-variant, downstream-variant-500B | WRNIP1 | GRCh38.p7 | 6:2773488 | AAAGCTCATTGTCTA[C/T]GCCATAGTTGCTTTG | 56897 |
rs160666 | snp | A/C | 0.397633 | 0.201754 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2773818 | TACAAGTCTTTGGAG[A/C]TCAAGAGAGTGAAAT | 56897 |
rs160667 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2774693 | ACAGACCCCTACCAA[A/G]TATAATGTAATTTGG | 56897 |
rs160668 | snp | C/G | 0.483923 | 0.0882034 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2774846 | AGCATCTGGGGCTCT[C/G]CCTTGGATATGTGCA | 56897 |
rs160695 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2780543 | TGTCTACATTGTGAC[A/G]TGAATGTGCCTCAGC | 56897 |
rs160696 | snp | A/C | 0.483708 | 0.088773 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2777746 | TAATTTCTGGTTGAG[A/C]AGTGATCCCCAGGCT | 56897 |
rs160697 | snp | A/G | 0.483418 | 0.0895317 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2776761 | AATACCATGGTATAT[A/G]AGGCTGCCCATCTCG | 56897 |
rs160698 | snp | A/G | | | intron-variant | WRNIP1 | GRCh38.p7 | 6:2776754 | ACTAGTAAATACCAT[A/G]GTATATAAGGCTGCC | 56897 |
rs160699 | snp | C/T | 0.483345 | 0.0897213 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2776069 | AGACTGGGAACACTC[C/T]TTCAAAATAGTTTGT | 56897 |
rs160700 | snp | C/T | 0.0178098 | 0.0926698 | downstream-variant-500B | WRNIP1 | GRCh38.p7 | 6:2786194 | CGGTTCTCCTCCTGC[C/T]GTTGCGTGATCCCTC | 56897 |
rs160701 | snp | A/G | 0.325563 | 0.238307 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2784878 | ATCCAGACTGTAGGC[A/G]CAAAAGGGGGATAAT | 56897 |
rs160702 | snp | A/G | 0.378174 | 0.214642 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2784821 | CCTGGTTTGCCTCTC[A/G]TTTCACCTCATGAGA | 56897 |
rs160703 | snp | A/G | 0.351344 | 0.228595 | synonymous-codon | WRNIP1 | GRCh38.p7 | 6:2784337 | AGGTCTGGCAGACCC[A/G]TCTGCGTTAACACAA | 56897 |
rs160704 | snp | C/G | 0.495745 | 0.0459295 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2784119 | CACAAGGAAACAGTT[C/G]TTAACACCACACAGT | 56897 |
rs167555 | snp | A/G | 0.492533 | 0.0606443 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2781697 | CTATAGAAGTCGTCA[A/G]ATTTCAGGTTATAAA | 56897 |
rs192874 | snp | A/G | 0 | 0 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2783684 | CGGGGGTAGCAGGAA[A/G]AATGTCTCAGGGCTA | 56897 |
rs315006 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2782715 | TTTTGCCCTTAAATA[C/T]GCCTTTTTTTAAAGC | 56897 |
rs315007 | snp | A/G | 0.467234 | 0.12373 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2782837 | AGCTGGTTAGTCCAC[A/G]TGTCGGTCCTTCTGG | 56897 |
rs316367 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2775841 | ATTTTCCCTTATTAT[A/G]AATAGTGTTTTATTA | 56897 |
rs458413 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | WRNIP1, MYLK4 | GRCh38.p7 | 6:2771649 | TATTGGAGCACTTCA[A/G]ATTTCTGGATTTTGG | 56897 |
rs466498 | snp | A/G | | | downstream-variant-500B | WRNIP1 | GRCh38.p7 | 6:2786195 | GGAGGGATCACGCAA[A/G]AGCAGGAGGAGAACC | 56897 |
rs869387 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | WRNIP1, MYLK4 | GRCh38.p7 | 6:2766716 | TTTTACAAGATGTGC[A/G]CTCTTAGATTTGATC | 56897 |
rs898768 | snp | C/T | 0.281313 | 0.248031 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2779648 | ATGTTGGTATTAAGC[C/T]TTCTACACAGGGCTG | 56897 |
rs898769 | snp | C/G | 0.257454 | 0.249889 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2779706 | AAGCTGCCCTGTTGA[C/G]AATCTAGAGGAGTTT | 56897 |
rs1059630 | snp | G/T | 0.2768 | 0.248559 | utr-variant-3-prime | WRNIP1 | GRCh38.p7 | 6:2785402 | CAACATTTTGTGCCA[G/T]AAATTTAAGAGTTCC | 56897 |
rs1317328 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WRNIP1, MYLK4 | GRCh38.p7 | 6:2766715 | GTTTTACAAGATGTG[A/C/G]GCTCTTAGATTTGAT | 56897 |
rs1461654 | snp | A/G | 0.0225045 | 0.103662 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2764642 | ATTACGTCCTAGACG[A/G]ATAGAAATGGAAAGA | 56897 |
rs1461655 | snp | G/T | 0.0410537 | 0.137264 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2764601 | AAAACAAGTGTGGTA[G/T]TCTGCATCTTTGAAT | 56897 |
rs2219633 | snp | C/T | 0 | 0 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2781307 | GCCTAGTGCCAGCGC[C/T]TTAAGAACCCCACAT | 56897 |
rs2279111 | snp | A/G | 0.32885 | 0.23724 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2764902 | TATTGGACGTGAACA[A/G]CAGAAAAAATACAAA | 56897 |
rs3734499 | snp | A/G | 0.324619 | 0.238604 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2784563 | AAGGTTTCCCTCTCT[A/G]GGAGTCTAAGAGTCT | 56897 |
rs3734500 | snp | C/T | 0.292954 | 0.246282 | intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2768671 | AAAAGATGACATACA[C/T]GGAGTTTGAAAAGCT | 56897 |
rs3757086 | snp | C/T | 0.281577 | 0.247998 | intron-variant, downstream-variant-500B | WRNIP1 | GRCh38.p7 | 6:2773521 | AATACCTGAACACTA[C/T]TGCTTAGCCATACAA | 56897 |
rs3757088 | snp | C/T | 0.282105 | 0.24793 | intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2769707 | TTCTTCCACAGCAAG[C/T]ACTCAATCATATTAT | 56897 |
rs3757089 | snp | A/G | 0.269267 | 0.249256 | intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2769518 | ATGTATGATTAAAAA[A/G]TTACAAAAAAAAATT | 56897 |
rs3757090 | snp | C/T | 0.469148 | 0.120308 | intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2769415 | TTTTAATGTTTATTT[C/T]TTTTTAAATCCCTAA | 56897 |
rs3757092 | snp | C/G | 0.390651 | 0.206682 | intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2767977 | AAGACTGTTTAATGA[C/G]TGTGACAAATCTGCA | 56897 |
rs3757093 | snp | C/T | 0.398894 | 0.200825 | intron-variant, upstream-variant-2KB | WRNIP1, MYLK4 | GRCh38.p7 | 6:2766545 | CTTATCCAGGAGAGG[C/T]AGGCGGCTTCTTTCG | 56897 |
rs3757094 | snp | C/T | 0.458184 | 0.138417 | intron-variant, upstream-variant-2KB | WRNIP1, MYLK4 | GRCh38.p7 | 6:2766493 | CGACCATCAGCTGCA[C/T]CCACCGCCGAGATAA | 56897 |
rs3799239 | snp | A/T | 0.47023 | 0.118317 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2780727 | CCCGGCATGGTGAGA[A/T]TTTTTTAATGTCTTA | 56897 |
rs3799241 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2780189 | CCAAAGTCCCACAAA[A/T]GCTCAAGCAGCAGAA | 56897 |
rs3799243 | snp | A/G | 0.283684 | 0.24772 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2777738 | GATCACTGCTCAACC[A/G]GAAATTAGTTAGCAA | 56897 |
rs3799244 | snp | C/T | 0.283684 | 0.24772 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2777721 | AAATTAGTTAGCAAG[C/T]CTTCTGGAAGATGAT | 56897 |
rs3799245 | snp | A/C | 0.283421 | 0.247756 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2776919 | ACTTTAAAAAAATTT[A/C]CATTAAATTTTAAAA | 56897 |
rs3799248 | snp | G/T | 0.283421 | 0.247756 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2775853 | ATTATGTTGTTATAA[G/T]AAAACACTATTTATA | 56897 |
rs3823104 | snp | A/C | 0.472709 | 0.11358 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2783751 | CACATACACCAGGAA[A/C]TAAACGACTGAGCTC | 56897 |
rs3823106 | snp | C/T | 0.283684 | 0.24772 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2777030 | AACCTTACAGCTAAC[C/T]TAAAACAAAAACTGG | 56897 |
rs4083550 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2783070 | GGGGGACGAGTCTTC[C/T]GTTCTGGCTCTATCC | 56897 |
rs5873840 | in-del | -/G/T | 0.375 | 0.216506 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2777107 | GCTTTCATTCTGCTG[-/G/T]GAAATATCAAGTACA | 56897 |
rs6596916 | snp | C/T | 0.483708 | 0.088773 | intron-variant, upstream-variant-2KB | MYLK4, WRNIP1 | GRCh38.p7 | 6:2763395 | ggcagtaagcagcgc[C/T]tctcagggaggcttg | 56897 |
rs6596917 | snp | A/G | 0.483636 | 0.0889627 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2763434 | aggagtccccagttg[A/G]ggggaggctcaggca | 56897 |
rs6900099 | snp | C/T | 0.264906 | 0.249555 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2763504 | gcctggcgagaagtg[C/T]tgtcccaagtgctaa | 56897 |
rs6904325 | snp | A/G | 0.449091 | 0.151204 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2764173 | TTTTGGTAGTTTCAC[A/G]TTACATGATGATTAA | 56897 |
rs6905699 | snp | C/T | 0.0333695 | 0.124785 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2764234 | AATCTTATTTTTGAG[C/T]CTAACTTTTTTAGTT | 56897 |
rs6906234 | snp | C/T | 0.0603597 | 0.1629 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2764492 | CATTCTCCCTCAATT[C/T]ATTTACCTCTTCTAG | 56897 |
rs6907679 | snp | C/T | 0.0352966 | 0.128072 | intron-variant, upstream-variant-2KB | WRNIP1, MYLK4 | GRCh38.p7 | 6:2767187 | agggcagttaggata[C/T]tgtgagtctagaaag | 56897 |
rs6917574 | snp | C/T | 0.0490535 | 0.14873 | synonymous-codon, upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2766075 | cgccgcggcggggAG[C/T]GCGTCTCCGCGCAGC | 56897 |
rs6922354 | snp | A/G | 0.284471 | 0.247612 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2763651 | gcccgcgcctctccc[A/G]ccatacttccccaca | 56897 |
rs6922514 | snp | A/G | 0.281841 | 0.247964 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2763701 | ggccttggcccgccc[A/G]ggaaagagctcccat | 56897 |
rs6922870 | snp | C/G | 0 | 0 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2772676 | TGTTAGCAATTCTAA[C/G]AAGAAGTTAAGTTAG | 56897 |
rs6923007 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2767493 | TTCCTGGAATGAATT[C/G]CCCTTTTTGTGCCTT | 56897 |
rs6923119 | snp | A/C | 0 | 0 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2780959 | tctcaaaattgcttt[A/C]tggagatagctatta | 56897 |
rs6926930 | snp | A/T | 0.44858 | 0.151875 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2763802 | agcgagcgaggactg[A/T]gagggctgccagaat | 56897 |
rs6927585 | snp | A/G | 0.449091 | 0.151204 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2764181 | GTTTCACGTTACATG[A/G]TGATTAAAGTTTAAC | 56897 |
rs6931824 | snp | A/T | 0.0329836 | 0.124112 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2777341 | TAGTAGGGATGATGA[A/T]TGTAATGTAATCAAC | 56897 |
rs6942236 | snp | A/G | 0.267364 | 0.249396 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2763674 | tccccacaagctgag[A/G]gagccagctccggcc | 56897 |
rs7750399 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2782849 | CACGTGTCGGTCCTT[C/T]TGGGACCCTGCCACA | 56897 |
rs7755438 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2784267 | GTCGCCTGCACATAG[A/G]CCAGGAGGACAGTGT | 56897 |
rs7773410 | snp | A/C/T | 0.0661207 | 0.171646 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2780454 | GCTTTTTGGCTTTAG[A/C/T]GTGCCTCAGCTGATG | 56897 |
rs9328128 | snp | C/T | 0.454544 | 0.143743 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2775197 | TACAGAGGATGGACC[C/T]ACTGCTCGGTTTTTC | 56897 |
rs9392425 | snp | C/T | 0.453209 | 0.145623 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2763689 | ggagccagctccggc[C/T]ttggcccgcccagga | 56897 |
rs9503298 | snp | A/G | 0.143959 | 0.226396 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2783679 | GTGGGCGGGGGTAGC[A/G]GGAAGAATGTCTCAG | 56897 |
rs10631379 | in-del | -/AAC | 0 | 0 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2764573 | CAAAAGCAAAAAATA[-/AAC]ACATGGTAATTCATT | 56897 |
rs10701160 | in-del | -/AAC | 0.0505692 | 0.150756 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2764572 | ACAAAAGCAAAAAAT[-/AAC]AACATGGTAATTCAT | 56897 |
rs11242798 | snp | A/T | 0.352287 | 0.228117 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2783762 | TTTATTTCCTGGTGT[A/T]TGTGCTTTTGAATGT | 56897 |
rs11297192 | in-del | -/T | 0.0337553 | 0.125452 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2780022 | GTGTGCACTTATCTG[-/T]TTTTGTAGAACTGCA | 56897 |
rs11378197 | in-del | -/C | 0.149665 | 0.228982 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2783080 | GAACAGAAGACTCGT[-/C]CCCCCTCCACTCTTG | 56897 |
rs11755120 | snp | C/T | 0 | 0 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2783187 | GACAGCCACAGGTTT[C/T]TGCTGCAGCAGCCTC | 56897 |
rs11757037 | snp | C/T | 0 | 0 | downstream-variant-500B | WRNIP1 | GRCh38.p7 | 6:2785781 | TTTCCTGCCTGGATG[C/T]TAGGTACCAGCGTTG | 56897 |
rs12111319 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2778890 | TGGAACATGTTTTCC[A/G]TACACGGTAATGAGG | 56897 |
rs12208216 | snp | A/G | 0.172028 | 0.23753 | intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2769354 | TGTTTATTTAAATGG[A/G]TTTCTGAAATAAAAG | 56897 |
rs12527929 | snp | G/T | 0.282632 | 0.247861 | intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2768582 | CAGCATTCTTCCGAG[G/T]TCAAGTTGCTTTTGG | 56897 |
rs13193327 | snp | A/G | 0.445064 | 0.156365 | intron-variant, upstream-variant-2KB | MYLK4, WRNIP1 | GRCh38.p7 | 6:2763379 | gccctgggtgccgtg[A/G]ggcagtaagcagcgc | 56897 |
rs13193342 | snp | A/G | 0.290201 | 0.246747 | intron-variant, upstream-variant-2KB | MYLK4, WRNIP1 | GRCh38.p7 | 6:2763429 | cgcgcaggagtcccc[A/G]gttggggggaggctc | 56897 |
rs13196532 | snp | C/T | 0.459914 | 0.13578 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2763492 | gaggcaactacggcc[C/T]ggcgagaagtgctgt | 56897 |
rs13207957 | snp | A/C | 0.290201 | 0.246747 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2763448 | ggggggaggctcagg[A/C]atggcaggcctgagc | 56897 |
rs13210509 | snp | A/G | 0.182614 | 0.240747 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2763781 | caaggcagaggaggc[A/G]ctgagagcgagcgag | 56897 |
rs13216410 | snp | C/T | 0.426354 | 0.177198 | upstream-variant-2KB, intron-variant | WRNIP1, MYLK4 | GRCh38.p7 | 6:2765336 | AACGGCCACGGACTA[C/T]ACTTACTTACATGCC | 56897 |
rs17135709 | snp | G/T | 0.27008 | 0.249192 | intron-variant | WRNIP1 | GRCh38.p7 | 6:2781566 | GTTGTGATTATTTTT[G/T]TATATGCCACCTAGT | 56897 |
rs17228987 | snp | C/T | 0.331179 | 0.236453 | downstream-variant-500B | WRNIP1 | GRCh38.p7 | 6:2785902 | CTTGTTGAAAGTTAA[C/T]TCTGATCTCTTTAAA | 56897 |