SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1830 | snp | A/G | 0.463451 | 0.130149 | utr-variant-3-prime, intron-variant | RNF6 | GRCh38.p7 | 13:26212948 | CTTTTAGATTTTAAA[A/G]CTAAATTTGAGAAAC | 6049 |
rs167288 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RNF6 | GRCh38.p7 | 13:26165645 | tcagcttgacctgta[C/T]gtgaaacatggagtc | 6049 |
rs167289 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | RNF6 | GRCh38.p7 | 13:26166947 | CACTATCACTATCAC[C/T]tgtaaggcctcccaa | 6049 |
rs167290 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF6 | GRCh38.p7 | 13:26146085 | ggggacttttggaca[C/T]tatctctgaatggac | 6049 |
rs167291 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | RNF6 | GRCh38.p7 | 13:26145301 | ttcccaccacattcc[C/G]atcacctgagcgtaa | 6049 |
rs172518 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | RNF6 | GRCh38.p7 | 13:26170018 | GATTTTTCTTTTTTT[A/G]CAAAAAGATTAAAGT | 6049 |
rs172519 | snp | A/C | 0.108048 | 0.20579 | intron-variant | RNF6 | GRCh38.p7 | 13:26153965 | GTATTTAAATTTATT[A/C]TCTACATTGAATTTA | 6049 |
rs177293 | snp | A/T | 0.200492 | 0.245049 | downstream-variant-500B, intron-variant | RNF6 | GRCh38.p7 | 13:26212608 | CTCTTAGAAACTGAA[A/T]ATCAATTGATAAAGT | 6049 |
rs182468 | snp | G/T | 0.376195 | 0.215812 | intron-variant | RNF6 | GRCh38.p7 | 13:26177960 | gacctcaggtggttt[G/T]cccaccttggcctcc | 6049 |
rs188527 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | RNF6 | GRCh38.p7 | 13:26166962 | ttgtaaggcctccca[A/G]gccatgtggaactta | 6049 |
rs188528 | snp | A/T | 0.182933 | 0.240836 | intron-variant | RNF6 | GRCh38.p7 | 13:26196839 | tcatttaaggaaatt[A/T]caggaagagggatgc | 6049 |
rs188529 | snp | A/G | 0.109814 | 0.206997 | intron-variant | RNF6 | GRCh38.p7 | 13:26146802 | gagatttgggtgtgg[A/G]cacagagccaaacca | 6049 |
rs190972 | snp | A/G | 0.306927 | 0.243432 | intron-variant | RNF6 | GRCh38.p7 | 13:26211249 | TAGATTGTGTTTTGT[A/G]TGGAAAATTCCCTGA | 6049 |
rs192749 | snp | A/T | 0.257454 | 0.249889 | intron-variant | RNF6 | GRCh38.p7 | 13:26209620 | ACTGTGAAGTGACAC[A/T]ATTTAGCCCCTCTGA | 6049 |
rs192750 | snp | C/G | 0.0399052 | 0.1355 | intron-variant | RNF6 | GRCh38.p7 | 13:26156359 | TCAGTTAATACATTG[C/G]TTACATAAGGTTTAA | 6049 |
rs192751 | snp | A/C | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26216788 | taaaaacctgtctct[A/C]ctaaaaatacaaaga | 6049 |
rs192752 | snp | A/T | 0.439918 | 0.162576 | intron-variant | RNF6 | GRCh38.p7 | 13:26137595 | tattcttatatatta[A/T]ttctttcaacataat | 6049 |
rs214429 | snp | C/T | 0.420415 | 0.182917 | intron-variant | RNF6 | GRCh38.p7 | 13:26179578 | agaatgtgctgagaa[C/T]gcagagccgtgagat | 6049 |
rs214430 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | RNF6 | GRCh38.p7 | 13:26166453 | tctatatcttgaaaa[A/C]cccatagtctcagcc | 6049 |
rs301047 | snp | C/T | 0.299136 | 0.245124 | synonymous-codon, intron-variant, utr-variant-3-prime | RNF6 | GRCh38.p7 | 13:26213977 | AATCTGTAGTGTTTG[C/T]ATTAGTGACTATGTA | 6049 |
rs301048 | snp | C/G | 0.256619 | 0.249912 | intron-variant | RNF6 | GRCh38.p7 | 13:26210853 | CAGCCAGCATTATGA[C/G]CCTTACTTAATTATC | 6049 |
rs301051 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | RNF6 | GRCh38.p7 | 13:26172745 | agataaggtttcact[A/G]tgttagccaggatgg | 6049 |
rs301052 | snp | C/T | 0.216349 | 0.247725 | intron-variant | RNF6 | GRCh38.p7 | 13:26172794 | gtgatccgcccacct[C/T]ggcctcccaaagtgc | 6049 |
rs301053 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | RNF6 | GRCh38.p7 | 13:26173694 | GATTTATTTCTTTGG[A/G]AAAAAAAAAagcatt | 6049 |
rs301054 | snp | C/T | 0.136847 | 0.222927 | intron-variant | RNF6 | GRCh38.p7 | 13:26173843 | GTAATCCTAGCTACT[C/T]GGGAGGCTGAGGCAG | 6049 |
rs301058 | snp | A/G | 0.404209 | 0.196773 | intron-variant | RNF6 | GRCh38.p7 | 13:26181754 | caaaaactgaagatg[A/G]ttgcatagaaaagCA | 6049 |
rs301059 | snp | C/G | 0.360421 | 0.224293 | intron-variant | RNF6 | GRCh38.p7 | 13:26181505 | AATGGGTTACACTAC[C/G]TGCAGTGGTTATGGC | 6049 |
rs301060 | snp | A/C | 0.405776 | 0.195535 | intron-variant | RNF6 | GRCh38.p7 | 13:26181377 | agtgactagattctt[A/C]aaggacaagacagac | 6049 |
rs301061 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | RNF6 | GRCh38.p7 | 13:26168012 | agaacacatggacac[A/T]aagaggaaaacaaga | 6049 |
rs301062 | snp | A/G | 0.25912 | 0.249834 | intron-variant | RNF6 | GRCh38.p7 | 13:26206512 | ATTCAAGTGCAGCCA[A/G]AAGCAGAAAAATCCA | 6049 |
rs301063 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF6 | GRCh38.p7 | 13:26202017 | CTAGTGGCACAAACC[A/G]CTCTTTCTTCCATTA | 6049 |
rs301064 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | RNF6 | GRCh38.p7 | 13:26197969 | ttatcttatgatttc[C/T]tctttcacctacaag | 6049 |
rs301065 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | RNF6 | GRCh38.p7 | 13:26196348 | atgttttatttcttc[C/T]tcatttttgaaagag | 6049 |
rs301066 | snp | C/T | 0.135484 | 0.22223 | intron-variant | RNF6 | GRCh38.p7 | 13:26195194 | taggatttccatccc[C/T]gcttacattgcccat | 6049 |
rs301067 | snp | A/G | 0.13446 | 0.221699 | intron-variant | RNF6 | GRCh38.p7 | 13:26195048 | aaatactgttttttg[A/G]ccattgtgatggtta | 6049 |
rs301068 | snp | A/T | 0.031825 | 0.122064 | intron-variant | RNF6 | GRCh38.p7 | 13:26191724 | TTATAAAGAGGTTTA[A/T]TTGACTGAGTTCTGC | 6049 |
rs301069 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | RNF6 | GRCh38.p7 | 13:26191223 | TGGAGATAAGAATGT[C/G]CCTTAGCCATTTTTT | 6049 |
rs301070 | snp | A/G | 0.434109 | 0.169127 | intron-variant | RNF6 | GRCh38.p7 | 13:26143878 | ctgtcatagtattcc[A/G]tacaacattgattct | 6049 |
rs301071 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | RNF6 | GRCh38.p7 | 13:26142062 | gttcatgttcttagc[A/C]cacgttttaatgggg | 6049 |
rs301072 | snp | A/C | 0.11228 | 0.208646 | intron-variant | RNF6 | GRCh38.p7 | 13:26133970 | accagataaaacaga[A/C]agtttaaatgatatc | 6049 |
rs474808 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | RNF6 | GRCh38.p7 | 13:26150309 | TTCAACCCATCCTGT[A/G]AAGACATGACATCAC | 6049 |
rs481432 | snp | A/G | 0.304188 | 0.244057 | intron-variant | RNF6 | GRCh38.p7 | 13:26205135 | TCAATACAGAGAAAT[A/G]CCTCTTCTAACCTAT | 6049 |
rs485250 | snp | C/G | 0.137527 | 0.223271 | intron-variant | RNF6 | GRCh38.p7 | 13:26157607 | AAGGGGCAAAAAAAG[C/G]CAAACAAGTCATCCT | 6049 |
rs485972 | snp | A/T | 0.496681 | 0.0405994 | intron-variant | RNF6 | GRCh38.p7 | 13:26186023 | TTTGTTTCATATCTA[A/T]GTTTATGTAGACTGC | 6049 |
rs498147 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | RNF6 | GRCh38.p7 | 13:26151256 | aaaaaGATATCAGAC[C/T]ATCTGGATTTAACTG | 6049 |
rs499911 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | RNF6 | GRCh38.p7 | 13:26165348 | tctccatgagagcct[C/T]acccctacagcaaac | 6049 |
rs499912 | snp | A/G | 0.265727 | 0.249505 | intron-variant | RNF6 | GRCh38.p7 | 13:26165347 | ctccatgagagcctc[A/G]cccctacagcaaact | 6049 |
rs504652 | snp | A/C | 0.299158 | 0.245119 | intron-variant | RNF6 | GRCh38.p7 | 13:26204916 | GCATCTGTGAGAGTC[A/C]AGCAGGTTTCAGATC | 6049 |
rs506272 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RNF6 | GRCh38.p7 | 13:26183943 | AGTATGTATATATAT[A/G]AATAATTATAAAAAA | 6049 |
rs508586 | snp | A/G | 0.298905 | 0.24517 | intron-variant | RNF6 | GRCh38.p7 | 13:26204915 | CATCTGTGAGAGTCA[A/G]GCAGGTTTCAGATCA | 6049 |
rs509054 | snp | G/T | 0.497091 | 0.0380279 | intron-variant | RNF6 | GRCh38.p7 | 13:26185810 | GCGTAGAGAACACAA[G/T]TTTAGAATCATGGCC | 6049 |
rs509915 | snp | G/T | 0.134119 | 0.221521 | intron-variant | RNF6 | GRCh38.p7 | 13:26185747 | GTAACAACTTTTTTT[G/T]GAGACAGGGTTTCGC | 6049 |
rs513289 | snp | A/G | 0.380919 | 0.21298 | intron-variant | RNF6 | GRCh38.p7 | 13:26177061 | ctggtggtccccgcc[A/G]atctttccttcttgg | 6049 |
rs522097 | snp | A/G | 0.265727 | 0.249505 | intron-variant | RNF6 | GRCh38.p7 | 13:26174611 | GAGACTCAAAAAAAA[A/G]AAAACAAACCCCAAA | 6049 |
rs524769 | snp | A/C | 0.084728 | 0.187577 | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26223357 | TGTAAATGTAAGCAG[A/C]AGAAAGATCTGGAAG | 6049 |
rs528413 | snp | A/C | 0.0718919 | 0.175435 | intron-variant | RNF6 | GRCh38.p7 | 13:26151941 | AGCTCTGGTGCCTTG[A/C]GTGAGGAAAAGACAG | 6049 |
rs530327 | snp | C/T | 0.135143 | 0.222054 | intron-variant | RNF6 | GRCh38.p7 | 13:26192279 | CTCTGTTCCTAGCCA[C/T]TGTTCTCTTTCCACT | 6049 |
rs538626 | snp | A/G | 0.039522 | 0.134904 | intron-variant | RNF6 | GRCh38.p7 | 13:26197954 | ctctttcacctacaa[A/G]ttatttaggatttgt | 6049 |
rs556026 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | RNF6 | GRCh38.p7 | 13:26173211 | TTAAAGCTATAGCTT[A/G]CAGTGGAGGTACTGA | 6049 |
rs559583 | snp | G/T | 0.141934 | 0.225437 | intron-variant | RNF6 | GRCh38.p7 | 13:26147257 | GACCCTAAAGGTAAA[G/T]TACAGTGTGTACCAA | 6049 |
rs564801 | snp | A/C | 0.302936 | 0.244331 | intron-variant | RNF6 | GRCh38.p7 | 13:26202998 | CAATCACACTTACCT[A/C]GTGGGGTTAAGTAAG | 6049 |
rs565258 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | RNF6 | GRCh38.p7 | 13:26161492 | aaaacattttactgc[A/G]ggacacaaaggggac | 6049 |
rs567571 | snp | A/T | 0.329084 | 0.237162 | intron-variant | RNF6 | GRCh38.p7 | 13:26164877 | taaaagttcaaaaaa[A/T]ttgcagcctgatgat | 6049 |
rs568487 | snp | C/G | 0.499722 | 0.0117779 | intron-variant | RNF6 | GRCh38.p7 | 13:26186427 | GACGCCCCCCGGCGC[C/G]TCCCGCTCTTGCTCT | 6049 |
rs586915 | snp | C/T | 0.236434 | 0.249632 | intron-variant | RNF6 | GRCh38.p7 | 13:26208933 | TGTCAAGAGGATCTT[C/T]CTATGACTCTAACTC | 6049 |
rs652568 | snp | A/G | 0.182296 | 0.240658 | intron-variant | RNF6 | GRCh38.p7 | 13:26218079 | TATAAGGAAAGTACT[A/G]TAAAAGAACTTCAAA | 6049 |
rs714454 | snp | A/G | 0.494484 | 0.0522255 | intron-variant | RNF6 | GRCh38.p7 | 13:26179056 | TGATAACTGGTGCAC[A/G]GTGTTCTTCTCCTAG | 6049 |
rs767831 | snp | A/T | 0.0678174 | 0.1712 | intron-variant | RNF6 | GRCh38.p7 | 13:26170633 | CATTTGGTTACCAGC[A/T]ACTTTCCCTCTGGGA | 6049 |
rs932751 | snp | A/G | 0.171704 | 0.237423 | intron-variant | RNF6 | GRCh38.p7 | 13:26188227 | GAACCACCAGTTTAC[A/G]CTTATAGAATCTAGT | 6049 |
rs959077 | snp | C/T | 0.4944 | 0.0526182 | intron-variant | RNF6 | GRCh38.p7 | 13:26179114 | TGCCAGACTAGGAAC[C/T]TTAGCAGAAACTGGC | 6049 |
rs1020025 | snp | A/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26157918 | gatggatggatggat[A/G]gatggatagatggat | 6049 |
rs1158461 | snp | A/G | 0.395818 | 0.203069 | intron-variant | RNF6 | GRCh38.p7 | 13:26171057 | ttttgatgaagtcct[A/G]tgtatctattttctc | 6049 |
rs1158462 | snp | G/T | 0.395087 | 0.203592 | intron-variant | RNF6 | GRCh38.p7 | 13:26170788 | CCAACCTTTGTAAGT[G/T]AATTCAGTTGGTTTG | 6049 |
rs1369837 | snp | A/G | 0.227369 | 0.248974 | intron-variant | RNF6 | GRCh38.p7 | 13:26139684 | TATATGCAGAAATAT[A/G]CCATTTTCTTGGACA | 6049 |
rs1369838 | snp | C/G | 0.227369 | 0.248974 | intron-variant | RNF6 | GRCh38.p7 | 13:26138932 | AATTTGAGGATACCC[C/G]TCTGACCAGATGTGA | 6049 |
rs1595150 | snp | A/G | 0.4941 | 0.0539917 | intron-variant | RNF6 | GRCh38.p7 | 13:26148902 | ccttcaaactgggac[A/G]ttggctttttcttgc | 6049 |
rs1629491 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | RNF6 | GRCh38.p7 | 13:26178422 | GGTCATGGGGATAGA[A/G]CCCTCATGAATGGGA | 6049 |
rs1629492 | snp | C/T | 0.340333 | 0.233109 | intron-variant | RNF6 | GRCh38.p7 | 13:26178419 | catggggatagagcc[C/T]tcatgaatgggacta | 6049 |
rs1656801 | snp | C/T | 0.109461 | 0.206758 | intron-variant | RNF6 | GRCh38.p7 | 13:26134465 | caaaaaacaaaaacc[C/T]caaccaaagcctgtt | 6049 |
rs1656802 | snp | A/C | 0.0399052 | 0.1355 | intron-variant | RNF6 | GRCh38.p7 | 13:26150942 | ATAACAAGAATTGAT[A/C]ATAAAATTAATAGTG | 6049 |
rs1810721 | snp | C/G | 0.420255 | 0.183066 | intron-variant | RNF6 | GRCh38.p7 | 13:26179226 | AGAATGCAAATTGTA[C/G]AGGTATGACTGCTAT | 6049 |
rs1810722 | snp | A/G | 0.4944 | 0.0526182 | intron-variant | RNF6 | GRCh38.p7 | 13:26179221 | GCAAATTGTACAGGT[A/G]TGACTGCTATGGCAG | 6049 |
rs1830860 | snp | C/T | 0.499759 | 0.0109798 | intron-variant | RNF6 | GRCh38.p7 | 13:26200531 | GTAATCCCAGCTACA[C/T]GGCTGAGGCAGGAGA | 6049 |
rs1830861 | snp | A/G | 0.395453 | 0.203331 | intron-variant | RNF6 | GRCh38.p7 | 13:26170446 | ATAGCTGCACAAAAC[A/G]GAAATGATGGCAGGA | 6049 |
rs1886454 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | RNF6 | GRCh38.p7 | 13:26175191 | CGGGGGGCTGAGGCA[A/G]GAGAATTGCTTGAAC | 6049 |
rs1886455 | snp | A/G | 0.378372 | 0.214524 | intron-variant | RNF6 | GRCh38.p7 | 13:26175079 | AAATAAAAAGGCACC[A/G]GACGCCAATGGGGAG | 6049 |
rs1924825 | snp | A/G | 0.231775 | 0.249335 | intron-variant | RNF6 | GRCh38.p7 | 13:26167776 | TTCCATGTCTTTGCT[A/G]TTATGAATAGTGCTG | 6049 |
rs2057564 | snp | C/T | 0.40595 | 0.195396 | intron-variant | RNF6 | GRCh38.p7 | 13:26188724 | gataagtgcttgaac[C/T]gaagaggcagaggtt | 6049 |
rs2057565 | snp | A/T | 0.400325 | 0.199756 | intron-variant | RNF6 | GRCh38.p7 | 13:26188673 | cactccagcctggca[A/T]cagagtgagacttca | 6049 |
rs2057566 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | RNF6 | GRCh38.p7 | 13:26187963 | ATCACTTGTTGACTT[C/T]TAGTTCTATTTTTTG | 6049 |
rs2057567 | snp | A/G | 0.2776 | 0.248472 | intron-variant | RNF6 | GRCh38.p7 | 13:26187912 | TTTACACTTCAGGCC[A/G]CTGTGGTCTCAAATA | 6049 |
rs2117930 | snp | C/T | 0.495407 | 0.0477027 | intron-variant | RNF6 | GRCh38.p7 | 13:26196789 | CCTACTTAACATTTC[C/T]GGTGGCTTGCTttct | 6049 |
rs2164453 | snp | A/G | 0.495407 | 0.0477027 | intron-variant | RNF6 | GRCh38.p7 | 13:26196891 | ctacattatacactc[A/G]ccttataatgctagt | 6049 |
rs2277426 | snp | G/T | 0.100231 | 0.200173 | utr-variant-5-prime, upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26222171 | AGAAGCCGGAAGCCC[G/T]TGCTGCAGCGTGGGG | 6049 |
rs2277427 | snp | A/C | 0.109814 | 0.206997 | utr-variant-5-prime, upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26222271 | CCGCCCACTTGGCGG[A/C]GGGGAGTCGCTCCGC | 6049 |
rs2419895 | snp | C/T | 0.227369 | 0.248974 | intron-variant | RNF6 | GRCh38.p7 | 13:26141006 | TGGGAAAATATTTCA[C/T]GATCATGGATTGGAA | 6049 |
rs2419896 | snp | A/T | 0.315758 | 0.241197 | intron-variant | RNF6 | GRCh38.p7 | 13:26165774 | ttggaatggctgtat[A/T]tacccaatgcctata | 6049 |
rs2419897 | snp | A/C | 0.328616 | 0.237317 | intron-variant | RNF6 | GRCh38.p7 | 13:26165875 | ttgtctcagatgaga[A/C]tttggactgtggact | 6049 |
rs2419899 | snp | A/C | 0.39527 | 0.203462 | intron-variant | RNF6 | GRCh38.p7 | 13:26170489 | ATTTTACTAACTATC[A/C]ATGCGTGAAGATGGA | 6049 |
rs2900999 | snp | C/T | 0.278133 | 0.248412 | intron-variant | RNF6 | GRCh38.p7 | 13:26158106 | ATAGATAGACAGAGA[C/T]TCCAGGACTCCAGGA | 6049 |
rs3030059 | in-del | -/TTTT | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26200423 | TTTTTTTTTTTTTTT[-/TTTT]GAGGCGGAGTTTTGC | 6049 |
rs3058499 | in-del | -/CTTCT | | | intron-variant | RNF6 | GRCh38.p7 | 13:26160541 | TCttcttctcttctt[-/CTTCT]ttttttttttttttt | 6049 |
rs3759468 | snp | C/T | 0.391769 | 0.205917 | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26222606 | CCCTTTCCCTTGCTG[C/T]GCTTTGGAACCTGGA | 6049 |
rs3759469 | snp | C/G | 0.357024 | 0.225933 | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26223183 | CTTTTGAGGAACTAC[C/G]ATATCCCCATTATTA | 6049 |
rs3834504 | in-del | -/AA | 0.49975 | 0.0111793 | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26223619 | ACTCCCTCTATATAT[-/AA]AACCCTATTTTAGCA | 6049 |
rs3837560 | in-del | -/T | 0.421684 | 0.181726 | utr-variant-3-prime | RNF6 | GRCh38.p7 | 13:26132130 | CATATTTAAGAATGC[-/T]TTTTTTTAATTACAT | 6049 |
rs3858760 | snp | C/T | 0.199254 | 0.244796 | upstream-variant-2KB, utr-variant-5-prime | RNF6 | GRCh38.p7 | 13:26222510 | CGCGTCGGTGTCGCT[C/T]GTTTGCCAGCCAGAC | 6049 |
rs3891621 | snp | C/T | 0.498673 | 0.0257246 | intron-variant | RNF6 | GRCh38.p7 | 13:26200768 | tgctcacactatcct[C/T]cattgccctattgga | 6049 |
rs3910433 | snp | A/G | 0.0527515 | 0.1536 | missense | RNF6 | GRCh38.p7 | 13:26219507 | TTATTAATGAACTCA[A/G]TGATGAAGATTATCG | 6049 |
rs3910434 | snp | C/T | 0.10237 | 0.201756 | utr-variant-5-prime, upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26222039 | CCCACAGCACACGTT[C/T]TCCGGACAGGAGGGC | 6049 |
rs3910435 | snp | C/T | 0.100231 | 0.200173 | utr-variant-5-prime, upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26222311 | GACGCAGTTTTCAGT[C/T]GCACGGGCGAGCTCC | 6049 |
rs3981341 | in-del | -/AA | 0.498945 | 0.022939 | intron-variant | RNF6 | GRCh38.p7 | 13:26174496 | AATACAAAAAAAAAA[-/AA]TTAGCTGAGCGTGGT | 6049 |
rs3981342 | in-del | -/GTGTGTGT | | | intron-variant | RNF6 | GRCh38.p7 | 13:26178628 | tgtgtgtgtgtgtgt[-/GTGTGTGT]gtgtgtggtgagaaa | 6049 |
rs4100617 | snp | A/G | 0.463559 | 0.129972 | intron-variant | RNF6 | GRCh38.p7 | 13:26209445 | AAACAAAAACAGGGA[A/G]AGAAGTGCCATACAT | 6049 |
rs4316612 | snp | C/G | 0.26518 | 0.249539 | intron-variant | RNF6 | GRCh38.p7 | 13:26172966 | atgagcaaaatatat[C/G]aacaaaagatatgaa | 6049 |
rs4371022 | snp | A/G | 0.498832 | 0.0241331 | intron-variant | RNF6 | GRCh38.p7 | 13:26188942 | TCAGAACAGATTTCT[A/G]AAGAGGTTGTATGCA | 6049 |
rs4545656 | snp | A/G | 0.370772 | 0.218893 | intron-variant | RNF6 | GRCh38.p7 | 13:26203604 | CTACGCATAAAGGCA[A/G]TATTAGAACTGGGCC | 6049 |
rs4630391 | snp | C/T | 0.351418 | 0.228505 | intron-variant | RNF6 | GRCh38.p7 | 13:26203687 | ACAATGCAGGCTGGG[C/T]GCAGTGGCTCACGCC | 6049 |
rs4638424 | snp | C/T | 0.401747 | 0.198678 | intron-variant | RNF6 | GRCh38.p7 | 13:26166602 | atgcaatctcattca[C/T]tcttgccacaaaaag | 6049 |
rs4769473 | snp | A/T | 0.377977 | 0.21476 | intron-variant | RNF6 | GRCh38.p7 | 13:26157281 | AATTTTAAAAATTTT[A/T]AAAAATGAAACTAGA | 6049 |
rs4769474 | snp | A/G | 0.377977 | 0.21476 | intron-variant | RNF6 | GRCh38.p7 | 13:26157315 | ATTAGAAGAAAATGT[A/G]GATAATTATTATATA | 6049 |
rs4769475 | snp | A/T | 0.377977 | 0.21476 | intron-variant | RNF6 | GRCh38.p7 | 13:26157576 | AACTAAGGCACAAAC[A/T]AGTAATTATTTTTAA | 6049 |
rs4769486 | snp | A/G | 0.463451 | 0.130149 | intron-variant | RNF6 | GRCh38.p7 | 13:26208959 | TGACAAAATGCTAAA[A/G]AAGAACAAACCAACA | 6049 |
rs4770928 | snp | C/T | 0.386123 | 0.209692 | intron-variant | RNF6 | GRCh38.p7 | 13:26156720 | AAAACAAAAATAAAA[C/T]AAAAACTACTTAGAA | 6049 |
rs4770929 | snp | C/T | 0.176219 | 0.238865 | intron-variant | RNF6 | GRCh38.p7 | 13:26159469 | CTCTACTAAAAAATA[C/T]AAAAAATTAACCGGG | 6049 |
rs4770933 | snp | C/T | 0.405082 | 0.196086 | intron-variant | RNF6 | GRCh38.p7 | 13:26167685 | tactatttgacccag[C/T]gatcccattactgga | 6049 |
rs4770934 | snp | A/G | 0.394171 | 0.204242 | intron-variant | RNF6 | GRCh38.p7 | 13:26167895 | atcatatcctttgca[A/G]gaacatggatggaac | 6049 |
rs4770935 | snp | C/T | 0.394538 | 0.203982 | intron-variant | RNF6 | GRCh38.p7 | 13:26167901 | tcctttgcaagaaca[C/T]ggatggaactgaagg | 6049 |
rs4770936 | snp | A/G | 0.404733 | 0.196361 | intron-variant | RNF6 | GRCh38.p7 | 13:26170156 | GTGATTTACTTAAAT[A/G]CAAAAATAAGGCTTT | 6049 |
rs4770937 | snp | C/T | 0.395087 | 0.203592 | intron-variant | RNF6 | GRCh38.p7 | 13:26170264 | AAAAGCTTTGAAGAG[C/T]CAAGATCCTAACTAT | 6049 |
rs4770938 | snp | A/C | 0.367091 | 0.220884 | intron-variant | RNF6 | GRCh38.p7 | 13:26170271 | TTGAAGAGTCAAGAT[A/C]CTAACTATTATCAAG | 6049 |
rs4770939 | snp | A/T | 0.488545 | 0.074807 | intron-variant | RNF6 | GRCh38.p7 | 13:26175257 | GGCTAATTTTTGTAG[A/T]TTTAGTAGAGACGGG | 6049 |
rs4770940 | snp | C/T | 0.496175 | 0.0435625 | intron-variant | RNF6 | GRCh38.p7 | 13:26175289 | TTTGGCCATGTTGGC[C/T]AGGCTGGTCTCAAAC | 6049 |
rs4770941 | snp | C/T | 0.4944 | 0.0526182 | intron-variant | RNF6 | GRCh38.p7 | 13:26180703 | CCCTGATTAGAACCA[C/T]TGATGGCTATTGGGA | 6049 |
rs4770942 | snp | C/T | 0.4944 | 0.0526182 | intron-variant | RNF6 | GRCh38.p7 | 13:26180834 | ACCTGCTGCCACTGC[C/T]GTGCCAATATTCACC | 6049 |
rs4770943 | snp | C/T | 0.200492 | 0.245049 | intron-variant | RNF6 | GRCh38.p7 | 13:26180874 | TCAGTCCAGGGCCCA[C/T]TGGGTATTCTAAAGG | 6049 |
rs4770944 | snp | G/T | 0.4944 | 0.0526182 | intron-variant | RNF6 | GRCh38.p7 | 13:26180875 | CAGTCCAGGGCCCAC[G/T]GGGTATTCTAAAGGA | 6049 |
rs4770945 | snp | A/C | 0.420574 | 0.182769 | intron-variant | RNF6 | GRCh38.p7 | 13:26180894 | TATTCTAAAGGAACC[A/C]GAAGGGGAGAGGCTA | 6049 |
rs4770946 | snp | C/T | 0.444133 | 0.157519 | intron-variant | RNF6 | GRCh38.p7 | 13:26183874 | ATATTTTTATATATA[C/T]AAAATATAGGTTTTT | 6049 |
rs4770948 | snp | A/C | 0.499121 | 0.020948 | intron-variant | RNF6 | GRCh38.p7 | 13:26189871 | TCTAATCCAATCACT[A/C]CTCTGACAGTTTAGC | 6049 |
rs4770949 | snp | C/T | 0.499121 | 0.020948 | intron-variant | RNF6 | GRCh38.p7 | 13:26190959 | AGTCATATGAAATGT[C/T]GGAATAGAGTGACCA | 6049 |
rs4770950 | snp | C/T | 0.499104 | 0.0211472 | intron-variant | RNF6 | GRCh38.p7 | 13:26191015 | GAATCATCATCCAGC[C/T]CCAGTGTTCAGTAGG | 6049 |
rs4770951 | snp | A/C | 0.499104 | 0.0211472 | intron-variant | RNF6 | GRCh38.p7 | 13:26191158 | CAGGAGTGGTTTAAT[A/C]GATTGTTCAATACAC | 6049 |
rs4770952 | snp | A/G | 0.49655 | 0.04139 | intron-variant | RNF6 | GRCh38.p7 | 13:26191226 | AAATGGCTAAGGGAC[A/G]TTCTTATCTCCAACC | 6049 |
rs4770953 | snp | C/T | 0.499539 | 0.0151687 | intron-variant | RNF6 | GRCh38.p7 | 13:26197703 | aagatccattttcac[C/T]tgtttaattaatgtc | 6049 |
rs4770954 | snp | A/G | 0.499653 | 0.0131743 | intron-variant | RNF6 | GRCh38.p7 | 13:26197853 | acatggtgaaacccc[A/G]tctGttctctgatca | 6049 |
rs4770956 | snp | C/T | 0.498794 | 0.0245311 | intron-variant | RNF6 | GRCh38.p7 | 13:26198743 | acatagaatataata[C/T]gaaatacttttaaaa | 6049 |
rs4770957 | snp | C/T | 0.495213 | 0.048687 | intron-variant | RNF6 | GRCh38.p7 | 13:26199647 | atttgtatatgtatg[C/T]agatataaattacaa | 6049 |
rs4770958 | snp | A/G | 0.476401 | 0.106032 | intron-variant | RNF6 | GRCh38.p7 | 13:26208106 | TTTAGGTGTGTGCAG[A/G]AAAGAATTTACATGG | 6049 |
rs4770959 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | RNF6 | GRCh38.p7 | 13:26210338 | ATTCCAATGGAGAGA[C/T]GCAGGAAGATTAAAA | 6049 |
rs4770960 | snp | A/G | 0.462909 | 0.131034 | intron-variant | RNF6 | GRCh38.p7 | 13:26216997 | TAGCTATTATATGAC[A/G]TCATTCTGATTTCAT | 6049 |
rs5004282 | snp | A/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26170487 | GCATTTTACTAACTA[A/T]CCATGCGTGAAGATG | 6049 |
rs5802364 | in-del | -/G | 0.395087 | 0.203592 | intron-variant | RNF6 | GRCh38.p7 | 13:26170496 | TAACTATCCATGCGT[-/G]AAGATGGAGGAACAA | 6049 |
rs5802366 | in-del | -/A | 0.36335 | 0.222827 | intron-variant | RNF6 | GRCh38.p7 | 13:26202630 | ACTAAAAATAAATTT[-/A]AAAAAAATACAAAAC | 6049 |
rs6491112 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | RNF6 | GRCh38.p7 | 13:26141766 | aatgaaaaacctgaa[A/G]ctataaaaattctaa | 6049 |
rs6491113 | snp | A/G | 0.393619 | 0.204631 | intron-variant | RNF6 | GRCh38.p7 | 13:26155520 | CTACAACATCATATG[A/G]GTTAGGTATGGGTAT | 6049 |
rs6491114 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | RNF6 | GRCh38.p7 | 13:26176281 | TAAGCATACTCTTCC[C/T]AGTCTCTTCTCTTTT | 6049 |
rs7139682 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF6 | GRCh38.p7 | 13:26150842 | TCAATGCCTGAAATC[A/G]TAAGAAAAATCATCA | 6049 |
rs7317124 | snp | G/T | 0.47852 | 0.101384 | intron-variant | RNF6 | GRCh38.p7 | 13:26204116 | atcgtcaacaagtgt[G/T]tccccaataaatttc | 6049 |
rs7318762 | snp | C/T | 0.485324 | 0.0843964 | intron-variant | RNF6 | GRCh38.p7 | 13:26175401 | TGATTTTTGAGAGGA[C/T]ACCTGACGCGAAGAG | 6049 |
rs7319418 | snp | C/T | 0.392696 | 0.205275 | intron-variant | RNF6 | GRCh38.p7 | 13:26154087 | TTACCTGCAATATAG[C/T]AATGAACAAGAAGAA | 6049 |
rs7320035 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF6 | GRCh38.p7 | 13:26154456 | GTCATGATATCTAAA[C/T]ACATCCAAAGGGGAA | 6049 |
rs7320117 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | RNF6 | GRCh38.p7 | 13:26168552 | GAAGTTTTGCAGAAA[A/G]TGTTCTTACAGGGGT | 6049 |
rs7320397 | snp | A/G | 0.386694 | 0.20932 | intron-variant | RNF6 | GRCh38.p7 | 13:26156491 | TATTATAGTTAAAAT[A/G]CCACATATGTATTTG | 6049 |
rs7321667 | snp | A/G | 0.394171 | 0.204242 | intron-variant | RNF6 | GRCh38.p7 | 13:26156076 | TAAGTGGCAGAAAAC[A/G]TAGAATGGATCAAAA | 6049 |
rs7322847 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RNF6 | GRCh38.p7 | 13:26181168 | tggttccattccccg[C/T]ccctgtgcacccagg | 6049 |
rs7324092 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RNF6 | GRCh38.p7 | 13:26184977 | GAACTTGTAGGTATT[A/G]TTATCATTTTattga | 6049 |
rs7326198 | snp | A/G | 0.369346 | 0.219673 | intron-variant | RNF6 | GRCh38.p7 | 13:26199427 | aactaaatgaaaaca[A/G]caacaataaaaactg | 6049 |
rs7327409 | snp | C/T | 0.430732 | 0.172731 | intron-variant | RNF6 | GRCh38.p7 | 13:26156530 | GCTGTGTGCATATTA[C/T]TGTGTGTTATCAAAC | 6049 |
rs7327585 | snp | A/G/T | 0.0225045 | 0.103662 | intron-variant | RNF6 | GRCh38.p7 | 13:26166290 | tttcttttgtaaatt[A/G/T]ctcagtctctggtat | 6049 |
rs7327712 | snp | C/T | 0.360421 | 0.224293 | intron-variant | RNF6 | GRCh38.p7 | 13:26148783 | aaatccccagatctg[C/T]agggtgagttgacaa | 6049 |
rs7327946 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | RNF6 | GRCh38.p7 | 13:26145372 | ggtttggctttgtgt[C/T]cccacccaaatctca | 6049 |
rs7329094 | snp | A/G | 0.268995 | 0.249277 | intron-variant | RNF6 | GRCh38.p7 | 13:26141926 | caaaagaaactatca[A/G]aagagtacagacaac | 6049 |
rs7329751 | snp | A/C | 0.0501905 | 0.150254 | intron-variant | RNF6 | GRCh38.p7 | 13:26220930 | CAATTTCACCTGTAA[A/C]ACTAAATTACAAATT | 6049 |
rs7331202 | snp | C/T | 0.286825 | 0.247273 | intron-variant | RNF6 | GRCh38.p7 | 13:26141670 | ttttgggaaaactgg[C/T]taaccatatgcagaa | 6049 |
rs7332725 | snp | C/G | 0.377977 | 0.21476 | intron-variant | RNF6 | GRCh38.p7 | 13:26158124 | CAGGACTCCAGGAAG[C/G]TAGGAGAGAGGAGCC | 6049 |
rs7333334 | snp | G/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26164411 | atatctactttatag[G/T]atattaagtctgcct | 6049 |
rs7333766 | snp | G/T | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26164637 | CAGTATAAACCACTG[G/T]TATTTTGTGTACCTG | 6049 |
rs7334003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26149565 | gcactccagcctggg[A/C]aacagggtgagactc | 6049 |
rs7337724 | snp | C/T | 0.112983 | 0.209108 | intron-variant | RNF6 | GRCh38.p7 | 13:26161839 | TAGCAGAAAATCCCA[C/T]TGTGTCTTCTCTTTC | 6049 |
rs7338440 | snp | A/C | 0.365024 | 0.221967 | intron-variant | RNF6 | GRCh38.p7 | 13:26200895 | catgggagttcagca[A/C]gactcaaagtaagta | 6049 |
rs7981522 | snp | A/G | 0.368733 | 0.220005 | intron-variant | RNF6 | GRCh38.p7 | 13:26168164 | caagagtttccctat[A/G]taacaaacctgcaca | 6049 |
rs7982053 | snp | A/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26168473 | TGTCGTTTTTGGGCA[A/G]GGGTAGGACCACGTC | 6049 |
rs7982318 | snp | A/G | 0.395087 | 0.203592 | intron-variant | RNF6 | GRCh38.p7 | 13:26168661 | TCTAAATGCCCAAGG[A/G]CAAATGAGTAGATCC | 6049 |
rs7982824 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | RNF6 | GRCh38.p7 | 13:26134041 | gtcattactgcaaga[C/T]gggggataaagtacc | 6049 |
rs7982836 | snp | A/G | 0.495213 | 0.048687 | intron-variant | RNF6 | GRCh38.p7 | 13:26193046 | aaatggggaaaactg[A/G]gttaggggaaccagt | 6049 |
rs7982890 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | RNF6 | GRCh38.p7 | 13:26140246 | acaaaaacttcagcc[A/G]aaattaattgaaagg | 6049 |
rs7983335 | snp | A/G | 0.394721 | 0.203852 | intron-variant | RNF6 | GRCh38.p7 | 13:26168150 | atcaatccccatgac[A/G]agagtttccctatgt | 6049 |
rs7984239 | snp | A/G | 0.394721 | 0.203852 | intron-variant | RNF6 | GRCh38.p7 | 13:26168649 | TCTCCTTCACTTTCT[A/G]AATGCCCAAGGGCAA | 6049 |
rs7985629 | snp | C/T | 0.415399 | 0.187465 | intron-variant | RNF6 | GRCh38.p7 | 13:26172259 | TAACCGATGCTGGAA[C/T]AGCTGGTTAGCACTA | 6049 |
rs7985782 | snp | C/G | 0.414905 | 0.187899 | intron-variant | RNF6 | GRCh38.p7 | 13:26172272 | aacagctggttagca[C/G]tatggaaaaaaatac | 6049 |
rs7985823 | snp | C/T | 0.416218 | 0.186739 | intron-variant | RNF6 | GRCh38.p7 | 13:26172330 | aatacatcccagata[C/T]gctaaaggtctaaat | 6049 |
rs7987427 | snp | C/G | 0.394538 | 0.203982 | intron-variant | RNF6 | GRCh38.p7 | 13:26169082 | GTACCCTGGGAAAAG[C/G]CTGCACTCCCAGCCA | 6049 |
rs7987921 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF6 | GRCh38.p7 | 13:26207875 | CCCCACACGGATGCA[A/G]AGCAGACTTTTCTGC | 6049 |
rs7988010 | snp | G/T | 0.392696 | 0.205275 | intron-variant | RNF6 | GRCh38.p7 | 13:26154973 | aggcagaagttgcag[G/T]gggccaagatcacac | 6049 |
rs7988263 | snp | A/T | 0.394721 | 0.203852 | intron-variant | RNF6 | GRCh38.p7 | 13:26168283 | ATCTCAGTGGACTGC[A/T]TGGTAATGGCTATGA | 6049 |
rs7988938 | snp | C/T | 0.404907 | 0.196224 | intron-variant | RNF6 | GRCh38.p7 | 13:26169205 | TCATGCACCCCATCC[C/T]CTCCCTGCTTCACAG | 6049 |
rs7990091 | snp | A/G | 0.299411 | 0.245069 | intron-variant | RNF6 | GRCh38.p7 | 13:26173001 | taatttagagaagga[A/G]aaaagccaggtggat | 6049 |
rs7990167 | snp | A/T | 0.0101775 | 0.0706056 | missense, intron-variant | RNF6 | GRCh38.p7 | 13:26215274 | CTACCATTGAAATTC[A/T]CTGAGGTTTGGCTTC | 6049 |
rs7990711 | snp | A/G | 0.394904 | 0.203722 | intron-variant | RNF6 | GRCh38.p7 | 13:26169819 | AGCCAATTAGCAAAT[A/G]CAGATAGGCTACAGT | 6049 |
rs7991682 | snp | C/T | 0.266819 | 0.249434 | intron-variant | RNF6 | GRCh38.p7 | 13:26172574 | tttgagatggaatct[C/T]gctctgtcgcccagg | 6049 |
rs7992166 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RNF6 | GRCh38.p7 | 13:26187851 | gcctcagcctcccaa[C/T]tagctgggactacag | 6049 |
rs7992921 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RNF6 | GRCh38.p7 | 13:26151571 | CCCGGCCCAGATGGT[C/T]TGATATCCTGATATC | 6049 |
rs7994119 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | RNF6 | GRCh38.p7 | 13:26152370 | GGTCTTCCTTGGTCC[A/G]TCGGATTACGTTTCT | 6049 |
rs7994386 | snp | C/T | 0.314057 | 0.241654 | intron-variant | RNF6 | GRCh38.p7 | 13:26169215 | CATCCCCTCCCTGCT[C/T]CACAGACTCTAGGTG | 6049 |
rs7995185 | snp | C/T | 0.095934 | 0.196885 | intron-variant | RNF6 | GRCh38.p7 | 13:26155247 | gcaccccagcctggg[C/T]ggcaaagcaaagctc | 6049 |
rs7997304 | snp | C/T | 0.239326 | 0.249772 | intron-variant | RNF6 | GRCh38.p7 | 13:26173196 | TGCATGCCCCACAGT[C/T]CAGTACCTCCACTGT | 6049 |
rs7997849 | snp | C/G | 0.394904 | 0.203722 | intron-variant | RNF6 | GRCh38.p7 | 13:26167480 | ataattagagaaatg[C/G]aaatcaaaaccataa | 6049 |
rs7998024 | snp | C/T | 0.135484 | 0.22223 | intron-variant | RNF6 | GRCh38.p7 | 13:26204261 | agcactttggaaggc[C/T]gaggcgggtggatca | 6049 |
rs7998188 | snp | C/G | 0.472896 | 0.113214 | intron-variant | RNF6 | GRCh38.p7 | 13:26174198 | CATTTAGGACTCAGG[C/G]CACTGATTTCATCCT | 6049 |
rs8000254 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | RNF6 | GRCh38.p7 | 13:26170011 | CAAATGGGATTTTTC[C/T]TTTTTTGCAAAAAGA | 6049 |
rs8000542 | snp | G/T | 0.106987 | 0.205054 | intron-variant | RNF6 | GRCh38.p7 | 13:26201466 | GCAAGCAACAATAAC[G/T]GAGGCAGAAGATAAA | 6049 |
rs8002764 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RNF6 | GRCh38.p7 | 13:26180308 | TGTCTGTTTGTCTTC[C/T]TACTAGGGTGTCTCA | 6049 |
rs9319280 | snp | G/T | 0.36315 | 0.222928 | intron-variant | RNF6 | GRCh38.p7 | 13:26204824 | TGAGAGGTATTCAAT[G/T]CTAATTGAAGTAGTT | 6049 |
rs9319281 | snp | G/T | 0.341235 | 0.232758 | intron-variant | RNF6 | GRCh38.p7 | 13:26208750 | TAATCTGATCCCAAT[G/T]GGTTGGAGTAAAGAA | 6049 |
rs9319282 | snp | A/C | 0.39214 | 0.205661 | intron-variant | RNF6 | GRCh38.p7 | 13:26216037 | ACTCAGTCATTTTTG[A/C]AACTAGGTATTTCTG | 6049 |
rs9507673 | snp | C/T | 0.434687 | 0.168495 | intron-variant | RNF6 | GRCh38.p7 | 13:26153306 | ATAACCTCCCTTCTC[C/T]GGGTTTAAGTGATTT | 6049 |
rs9507677 | snp | A/C | 0.394721 | 0.203852 | intron-variant | RNF6 | GRCh38.p7 | 13:26169419 | CTGACCAGAGAGGAG[A/C]TCCCTGACCAAGGCA | 6049 |
rs9507682 | snp | A/G | 0.493658 | 0.0559517 | intron-variant | RNF6 | GRCh38.p7 | 13:26192045 | AATGGCTGAAGTTAA[A/G]TGAGCAGAGGAACAA | 6049 |
rs9507683 | snp | C/T | 0.499598 | 0.0141716 | intron-variant | RNF6 | GRCh38.p7 | 13:26194978 | ataccctcacagatg[C/T]acctaggatcaatgc | 6049 |
rs9507686 | snp | C/T | 0.046775 | 0.145601 | intron-variant | RNF6 | GRCh38.p7 | 13:26218060 | CTCTACATACTTCAT[C/T]TAGTTTGAAGTTCTT | 6049 |
rs9512116 | snp | A/G | 0.306679 | 0.24349 | intron-variant | RNF6 | GRCh38.p7 | 13:26132666 | AACTTTAATAAAAAG[A/G]AAAGAGGTAGAAACA | 6049 |
rs9512120 | snp | C/T | 0.432504 | 0.170857 | intron-variant | RNF6 | GRCh38.p7 | 13:26146416 | attgcatttaggttt[C/T]caattaagtggtcat | 6049 |
rs9512124 | snp | A/G | 0.232943 | 0.249417 | intron-variant | RNF6 | GRCh38.p7 | 13:26147231 | cttttgaagtgtagt[A/G]catgccctcattggt | 6049 |
rs9512125 | snp | C/T | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26149895 | ATATATATATATATA[C/T]ACACACACAGTGTAT | 6049 |
rs9512129 | snp | C/T | 0.424814 | 0.178718 | intron-variant | RNF6 | GRCh38.p7 | 13:26158909 | ACCATCTCTAACTTG[C/T]GCATAATTTATGATC | 6049 |
rs9512130 | snp | A/T | 0.406641 | 0.194842 | intron-variant | RNF6 | GRCh38.p7 | 13:26159055 | CAGCTAATAGAAGTA[A/T]AAATATACTACAATA | 6049 |
rs9512137 | snp | C/T | 0.394721 | 0.203852 | intron-variant | RNF6 | GRCh38.p7 | 13:26169370 | GCAAGGGGAGATCCA[C/T]CTGAGAGTGTCTTGG | 6049 |
rs9512138 | snp | A/T | 0.394721 | 0.203852 | intron-variant | RNF6 | GRCh38.p7 | 13:26169461 | CCCCTCAGCTTGGCT[A/T]AACTGTACATGGGTT | 6049 |
rs9512139 | snp | A/C | 0.394721 | 0.203852 | intron-variant | RNF6 | GRCh38.p7 | 13:26169469 | CTTGGCTTAACTGTA[A/C]ATGGGTTTCTTCCAG | 6049 |
rs9512140 | snp | A/T | 0.394721 | 0.203852 | intron-variant | RNF6 | GRCh38.p7 | 13:26169566 | GTACATTTTTCCTCT[A/T]TCTTCTTTGAAATAT | 6049 |
rs9512142 | snp | A/G | 0.385359 | 0.210185 | intron-variant | RNF6 | GRCh38.p7 | 13:26176343 | cacccaggctggagt[A/G]caatggcacaatcat | 6049 |
rs9512143 | snp | A/G | 0.470132 | 0.118498 | intron-variant | RNF6 | GRCh38.p7 | 13:26183674 | AGCCATGCAGTAAAA[A/G]ATAGTTTTGGACTAA | 6049 |
rs9512144 | snp | C/T | 0.474544 | 0.10991 | intron-variant | RNF6 | GRCh38.p7 | 13:26184942 | GTGAGCTCCAAAGTG[C/T]GCTGCAGGAAATTAT | 6049 |
rs9512145 | snp | C/T | 0.498774 | 0.02473 | intron-variant | RNF6 | GRCh38.p7 | 13:26190397 | GTGAGGTGGGGGCAT[C/T]GTTTTTCTACCTATC | 6049 |
rs9512148 | snp | A/G | 0.498794 | 0.0245311 | intron-variant | RNF6 | GRCh38.p7 | 13:26191569 | CATGATAGTGAATGA[A/G]TTCTCACAAGATCTG | 6049 |
rs9512149 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | RNF6 | GRCh38.p7 | 13:26193347 | TGAGAAGAGGTCAGT[A/T]ATACggaaggaaagc | 6049 |
rs9512150 | snp | A/G | 0.498774 | 0.02473 | intron-variant | RNF6 | GRCh38.p7 | 13:26197633 | aacacccagttacct[A/G]tgtaggaatcagaat | 6049 |
rs9512152 | snp | C/T | 0.499539 | 0.0151687 | intron-variant | RNF6 | GRCh38.p7 | 13:26198511 | tgtcatataaactaa[C/T]catcacagcatctat | 6049 |
rs9512153 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNF6 | GRCh38.p7 | 13:26206869 | aggtccacattatga[C/T]tctcatgggccctcg | 6049 |
rs9512154 | snp | G/T | 0.046775 | 0.145601 | intron-variant | RNF6 | GRCh38.p7 | 13:26212171 | GTAGACCCATCCTCC[G/T]GGGCCATGAAAAATG | 6049 |
rs9551249 | snp | C/T | 0.37138 | 0.218556 | intron-variant | RNF6 | GRCh38.p7 | 13:26196883 | aaacaaaaactagca[C/T]tataaggtgagtgta | 6049 |
rs9553751 | snp | C/G | 0.492582 | 0.0604491 | intron-variant | RNF6 | GRCh38.p7 | 13:26140702 | caaattatctctcat[C/G]attgatgatatgatt | 6049 |
rs9553752 | snp | C/T | 0.432797 | 0.170544 | intron-variant | RNF6 | GRCh38.p7 | 13:26144964 | tgtcttcaacaccat[C/T]gatcagtgtgatatt | 6049 |
rs9553755 | snp | G/T | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26157368 | TTTAAACTTTGCAGA[G/T]AAACCAGAGAACACA | 6049 |
rs9553756 | snp | C/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26160544 | TCTTCTCTTCTTCTT[C/T]TTTTTTTTTTTTTTT | 6049 |
rs9553757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26163995 | AGAGCTATAGTAGCT[A/G]TCACAAAAATAGGAT | 6049 |
rs9553758 | snp | A/G | 0.496483 | 0.0417852 | intron-variant | RNF6 | GRCh38.p7 | 13:26186434 | GAGCGGGACGCGCCG[A/G]GGGGCGTCTGCGTGG | 6049 |
rs9553759 | snp | G/T | 0.49703 | 0.0384237 | intron-variant | RNF6 | GRCh38.p7 | 13:26186465 | CACGTGGGCCCCGCA[G/T]CCAGTCGCGCTACCG | 6049 |
rs9553760 | snp | A/G | 0.495963 | 0.0447464 | intron-variant | RNF6 | GRCh38.p7 | 13:26186675 | GCTATACCTTCGGCC[A/G]CAGGTAGCGCGTTCC | 6049 |
rs9553761 | snp | C/T | 0.496616 | 0.0409947 | intron-variant | RNF6 | GRCh38.p7 | 13:26186690 | ACAGGTAGCGCGTTC[C/T]TTCGCTGTGCTGACC | 6049 |
rs9553762 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RNF6 | GRCh38.p7 | 13:26186697 | GCGCGTTCCTTCGCT[A/G]TGCTGACCGTCGATC | 6049 |
rs9553763 | snp | C/T | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26186774 | GGGACCTttcttctt[C/T]tttttttttttttct | 6049 |
rs9553764 | snp | C/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26186784 | ttcttcttttttttt[C/T]tttctttttttgaga | 6049 |
rs9553765 | snp | A/C | 0.298905 | 0.24517 | intron-variant | RNF6 | GRCh38.p7 | 13:26189108 | CCGAGGCAGGTGGAT[A/C]ACCTGAGGTCAGGAG | 6049 |
rs9578964 | snp | A/G | 0.0345262 | 0.126772 | downstream-variant-500B | RNF6 | GRCh38.p7 | 13:26131825 | CAGCTACTCGGGAAG[A/G]TGAGGCAGGAGAATT | 6049 |
rs9578965 | snp | A/C | 0.0341408 | 0.126114 | downstream-variant-500B | RNF6 | GRCh38.p7 | 13:26132028 | TCAAACCTTTCAACA[A/C]CTTGTTCTTCCCACT | 6049 |
rs9578966 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | RNF6 | GRCh38.p7 | 13:26132921 | tctttggtggttctg[C/T]ggtggggggtgccag | 6049 |
rs9578967 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | RNF6 | GRCh38.p7 | 13:26136245 | TTATAGTCCTGTGTG[A/T]TTACTCTTTAACCCC | 6049 |
rs9578968 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | RNF6 | GRCh38.p7 | 13:26143632 | ctaggggagaaacag[A/C]accatatattggatg | 6049 |
rs9578969 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RNF6 | GRCh38.p7 | 13:26154681 | TAGGTGTACATATAT[A/G]TTAAGGCAATAAGCA | 6049 |
rs9578970 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | RNF6 | GRCh38.p7 | 13:26166108 | cctttcctgtgcttt[C/T]ctagtgatagtgaat | 6049 |
rs9578971 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | RNF6 | GRCh38.p7 | 13:26166749 | acaaggtgaaacccc[A/G]tctctaccaaatata | 6049 |
rs9578972 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | RNF6 | GRCh38.p7 | 13:26167117 | tggaagacaaactag[A/G]caataccattctgga | 6049 |
rs9578973 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | RNF6 | GRCh38.p7 | 13:26173118 | CGGTGAGGTAGAAAC[C/T]GGCAGAGTACACATA | 6049 |
rs9578975 | snp | A/C | 0.497855 | 0.0326773 | intron-variant | RNF6 | GRCh38.p7 | 13:26189405 | CTCTAAATCAAATAA[A/C]AGGCTTAGTGTGAGT | 6049 |
rs9578976 | snp | C/T | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26189542 | AGAAGGGAAACTATT[C/T]TCATTTAAAGGCAGT | 6049 |
rs9578977 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RNF6 | GRCh38.p7 | 13:26220551 | CTATTCAGTAAGTCA[C/T]ACTAAAGCAATGGTT | 6049 |
rs9578978 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | RNF6 | GRCh38.p7 | 13:26220808 | CAGTGAAGCAACTGT[A/G]CAACTCTGCCTCTCG | 6049 |
rs9581545 | snp | C/T | 0.0352966 | 0.128072 | downstream-variant-500B | RNF6 | GRCh38.p7 | 13:26131754 | CATATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 6049 |
rs9581546 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RNF6 | GRCh38.p7 | 13:26132577 | TATTGCACTCACTAG[A/G]TAATAAAATAATGCA | 6049 |
rs9581547 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | RNF6 | GRCh38.p7 | 13:26135276 | ATAGCTTCAAAACAA[C/T]ATGTTTAAGGGTTCA | 6049 |
rs9581548 | snp | C/T | 0.286825 | 0.247273 | intron-variant | RNF6 | GRCh38.p7 | 13:26135322 | GAATTTTATAGCACA[C/T]ACTTTTTATAGCAAT | 6049 |
rs9581549 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | RNF6 | GRCh38.p7 | 13:26138480 | atatatttttttctt[C/T]gtaactccttgtttt | 6049 |
rs9581550 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | RNF6 | GRCh38.p7 | 13:26139050 | tatcttatatgtttc[A/G]acatcttaaaattct | 6049 |
rs9581551 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RNF6 | GRCh38.p7 | 13:26139467 | gaatattgtTATAAA[C/T]TCTTGTCAATATCCA | 6049 |
rs9581552 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RNF6 | GRCh38.p7 | 13:26139641 | TCAGTTTGAAGGAAA[C/T]TGACATCTTTATAAT | 6049 |
rs9581555 | snp | A/C | 0.286303 | 0.24735 | intron-variant | RNF6 | GRCh38.p7 | 13:26142100 | tctcaaaagaagaca[A/C]agaagcagtcaccaa | 6049 |
rs9581556 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | RNF6 | GRCh38.p7 | 13:26145017 | agattcctgtgaacc[A/G]aattgtgacacagag | 6049 |
rs9581558 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RNF6 | GRCh38.p7 | 13:26145592 | ttggcttccccttca[C/T]cttccaccatgattg | 6049 |
rs9581559 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RNF6 | GRCh38.p7 | 13:26145854 | gcctttcccaccaca[A/G]tggacctcactctac | 6049 |
rs9581560 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | RNF6 | GRCh38.p7 | 13:26147097 | tacagggcccatatc[A/C]atcaattcagcctga | 6049 |
rs9581561 | snp | C/G | 0.286564 | 0.247312 | intron-variant | RNF6 | GRCh38.p7 | 13:26148008 | aagaactgcctgaga[C/G]tgggtaatttataaa | 6049 |
rs9581562 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RNF6 | GRCh38.p7 | 13:26149401 | gaccatcctggctaa[C/T]acagtgaaaccccat | 6049 |
rs9581563 | snp | A/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26149941 | atatatacacagtgt[A/G]tatataatgtgtata | 6049 |
rs9581564 | snp | C/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26149995 | atgtgtatatatata[C/T]aACATAGTAAGTATT | 6049 |
rs9581566 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RNF6 | GRCh38.p7 | 13:26153851 | GAACTGCGGGCCAGA[A/G]CATCTATTGCTCATC | 6049 |
rs9581568 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | RNF6 | GRCh38.p7 | 13:26155994 | AACAGCATGAAAGCC[A/G]CTTTTAAAAGAGAGA | 6049 |
rs9581569 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | RNF6 | GRCh38.p7 | 13:26163989 | ATGAAAAGAGCTATA[A/G]TAGCTGTCACAAAAA | 6049 |
rs9581570 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | RNF6 | GRCh38.p7 | 13:26166730 | ttcaagaccaacctg[G/T]gcaacaaggtgaaac | 6049 |
rs9581571 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | RNF6 | GRCh38.p7 | 13:26173104 | GATTGGCAAGACCAC[A/G]GTGAGGTAGAAACCG | 6049 |
rs9581572 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | RNF6 | GRCh38.p7 | 13:26177067 | aggaaagatcggcgg[A/G]gaccaccagagctag | 6049 |
rs9581573 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | RNF6 | GRCh38.p7 | 13:26178365 | ctcatgtggtgaaac[A/G]ggagaggggtctctc | 6049 |
rs9581574 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | RNF6 | GRCh38.p7 | 13:26180945 | CTTCCTGCACTTCCT[A/G]TAGTCGGagatgttc | 6049 |
rs9581575 | snp | C/T | 0.493568 | 0.0563433 | intron-variant | RNF6 | GRCh38.p7 | 13:26182019 | AGTTCCTCCATATTT[C/T]TAAAAAAATCTTCAT | 6049 |
rs9581576 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | RNF6 | GRCh38.p7 | 13:26182063 | TTTAAGGCTTATTTT[A/G]TAAAACTCTTCTGAT | 6049 |
rs9581577 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | RNF6 | GRCh38.p7 | 13:26184369 | TCTCCCTCAGTTTAG[C/T]CTCTGCATAAAGGCA | 6049 |
rs9581578 | snp | C/G | 0.108402 | 0.206034 | intron-variant | RNF6 | GRCh38.p7 | 13:26186422 | GCCGCAGAGCAAGAG[C/G]GGGACGCGCCGGGGG | 6049 |
rs9581579 | snp | A/C | 0.108402 | 0.206034 | intron-variant | RNF6 | GRCh38.p7 | 13:26186693 | GGTAGCGCGTTCCTT[A/C]GCTGTGCTGACCGTC | 6049 |
rs9581580 | snp | G/T | 0.496483 | 0.0417852 | intron-variant | RNF6 | GRCh38.p7 | 13:26186859 | CTCGGCTCACTGCAA[G/T]TTCCGCCTCCCAGGT | 6049 |
rs9581581 | snp | A/G | 0.480302 | 0.0972668 | intron-variant | RNF6 | GRCh38.p7 | 13:26187122 | GGCCTGAGGTCCGGG[A/G]CTGGGGCTGTCCCCG | 6049 |
rs9581582 | snp | G/T | 0.388964 | 0.20782 | intron-variant | RNF6 | GRCh38.p7 | 13:26187139 | TGGGGCTGTCCCCGC[G/T]TCCTGTTTCTGCCAT | 6049 |
rs9581583 | snp | A/C | 0.499437 | 0.0167637 | intron-variant | RNF6 | GRCh38.p7 | 13:26189336 | CCATCTCAAAAAAAA[A/C]GCTTCCTATTGTAAT | 6049 |
rs9581584 | snp | A/G | 0.115438 | 0.210697 | intron-variant | RNF6 | GRCh38.p7 | 13:26194319 | gaaagattaacAAAT[A/G]Caaggataatatcta | 6049 |
rs9581585 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | RNF6 | GRCh38.p7 | 13:26200927 | aaagtaatcatgtta[C/T]ttttcaaaaaattaa | 6049 |
rs9581586 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RNF6 | GRCh38.p7 | 13:26202405 | AGGATCAAATTAAGA[C/T]CATAATTAGATGATT | 6049 |
rs9581587 | snp | A/C | 0.36315 | 0.222928 | intron-variant | RNF6 | GRCh38.p7 | 13:26202946 | TTTATGAAGCCCTTA[A/C]CACATGCCAAGGACT | 6049 |
rs9581588 | snp | C/G | 0.36315 | 0.222928 | intron-variant | RNF6 | GRCh38.p7 | 13:26203162 | TTGTAAATTACCTCT[C/G]GAGAGCATCCTGTTC | 6049 |
rs9581589 | snp | C/T | 0.363359 | 0.222822 | intron-variant | RNF6 | GRCh38.p7 | 13:26205115 | GGCTCATCATTTTGT[C/T]CTGAATAGGTTAGAA | 6049 |
rs9581590 | snp | A/C | 0.0644693 | 0.167566 | intron-variant | RNF6 | GRCh38.p7 | 13:26209592 | GAATTGACACTACCT[A/C]GAAAACCTGAACTCA | 6049 |
rs9581591 | snp | C/T | 0.387074 | 0.209071 | intron-variant | RNF6 | GRCh38.p7 | 13:26210802 | TAAATTATGAATTCA[C/T]GTTAAATATTGAAAG | 6049 |
rs10161810 | snp | A/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26155865 | TTCAGTTTAAGGGGC[A/G]GACAGGGCAGAAGGA | 6049 |
rs10220204 | snp | G/T | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26147254 | tcattggtacacact[G/T]tactttacctttagg | 6049 |
rs10467433 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RNF6 | GRCh38.p7 | 13:26206264 | TAGATGGATGCAGTG[A/G]GAGACAAGACAAAGA | 6049 |
rs10467680 | snp | C/T | 0.362732 | 0.22314 | intron-variant | RNF6 | GRCh38.p7 | 13:26206283 | ACAAGACAAAGAGCA[C/T]ACAGCCCAAGCCACC | 6049 |
rs10467681 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | RNF6 | GRCh38.p7 | 13:26207005 | tcttggtatgtgact[G/T]gttttaaaagaaatt | 6049 |
rs10507349 | snp | A/G | 0.351418 | 0.228505 | intron-variant | RNF6 | GRCh38.p7 | 13:26207391 | GCTGAGGAGTGACAA[A/G]TCGAAATGAGGCTTG | 6049 |
rs10507350 | snp | C/T | 0.0883596 | 0.190715 | intron-variant | RNF6 | GRCh38.p7 | 13:26209102 | CAGTTTTAAGGAAAG[C/T]GTATTGTCAAAAAGT | 6049 |
rs10507351 | snp | A/G | 0.124491 | 0.216211 | intron-variant | RNF6 | GRCh38.p7 | 13:26210714 | GAGGCAAATAGCCAC[A/G]TGATTGACTCCCTAA | 6049 |
rs10507352 | snp | A/T | 0.0973687 | 0.197999 | intron-variant | RNF6 | GRCh38.p7 | 13:26220548 | CATCTATTCAGTAAG[A/T]CACACTAAAGCAATG | 6049 |
rs10507364 | snp | C/T | 0.135143 | 0.222054 | intron-variant | RNF6 | GRCh38.p7 | 13:26187245 | TCCTAGCCTTCGGAC[C/T]GGGAACCTGATAGGA | 6049 |
rs10605347 | in-del | -/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26157996 | AGATAGATAGATAGA[-/T]AGAAGAAGTCATTGG | 6049 |
rs10606579 | in-del | -/ATAC | | | intron-variant | RNF6 | GRCh38.p7 | 13:26149892 | TATATATATATATAT[-/ATAC]ACACACACAGTGTAT | 6049 |
rs10628120 | in-del | -/TATAT | 0.0170251 | 0.090679 | intron-variant | RNF6 | GRCh38.p7 | 13:26183902 | TACTTATTTATATAT[-/TATAT]GTAATATATACAATA | 6049 |
rs10674426 | in-del | -/A/AA/AAA | | | intron-variant | RNF6 | GRCh38.p7 | 13:26173965 | AAAAAAAAAAAAAAA[-/A/AA/AAA]GCAAAGAAAAAATTC | 6049 |
rs10682446 | in-del | -/TT/TTT/TTTT | 0.29046 | 0.246704 | intron-variant | RNF6 | GRCh38.p7 | 13:26151621 | TCTTTTTTTTTTTTT[-/TT/TTT/TTTT]GGCAGAGGAGACATT | 6049 |
rs10690747 | in-del | -/A/TA/TATA | 0.215446 | 0.2476 | intron-variant | RNF6 | GRCh38.p7 | 13:26149920 | GTGTATATATATATA[-/A/TA/TATA]CACAGTGTATATATA | 6049 |
rs10712832 | in-del | -/A | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26170240 | AATGCTGGATTTTAC[-/A]AAAAAAAAAAAAGCT | 6049 |
rs11149432 | snp | A/C | 0.496905 | 0.0392151 | intron-variant | RNF6 | GRCh38.p7 | 13:26186876 | TCCGCCTCCCAGGTT[A/C]ACGCCATTCTCCTGC | 6049 |
rs11149433 | snp | A/T | 0.121022 | 0.21416 | intron-variant | RNF6 | GRCh38.p7 | 13:26199148 | tgtatatgaaaatgc[A/T]aaggacctagggcag | 6049 |
rs11363090 | in-del | -/A | 0.100588 | 0.200439 | intron-variant | RNF6 | GRCh38.p7 | 13:26153787 | TTTTGGAGGTGCCAT[-/A]AAATGACCGAAATTG | 6049 |
rs11404502 | in-del | -/A | 0.498346 | 0.0287064 | intron-variant | RNF6 | GRCh38.p7 | 13:26189730 | AAGCTCCTTGGAGAT[-/A]AGAGATTTCACAGTC | 6049 |
rs11558132 | snp | G/T | 0.461813 | 0.132798 | utr-variant-5-prime | RNF6 | GRCh38.p7 | 13:26221326 | TATTGCTTCAGATGG[G/T]CAGCTCTCAAAAAAG | 6049 |
rs11616732 | snp | G/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26152777 | TTACATAGATCATTG[G/T]TACAGACATTAGAGA | 6049 |
rs11616801 | snp | A/T | 0.416218 | 0.186739 | intron-variant | RNF6 | GRCh38.p7 | 13:26183803 | TCACAGAAAGTATAG[A/T]TTACTTTGCTTGAAA | 6049 |
rs11616950 | snp | C/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26134910 | tatttttaaaaaGAT[C/G]ATGTATTACTTTAAC | 6049 |
rs11617020 | snp | A/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26184016 | TATATATATATATAT[A/T]TATTTTTTTTTTTTT | 6049 |
rs11617021 | snp | A/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26184018 | TATATATATATATAT[A/T]TTTTTTTTTTTTTTT | 6049 |
rs11617261 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | RNF6 | GRCh38.p7 | 13:26183891 | aaatataggtttttt[A/T]atacttatttatata | 6049 |
rs11617826 | snp | C/T | 0.478685 | 0.10101 | intron-variant | RNF6 | GRCh38.p7 | 13:26206304 | CCAAGCCACCATCTG[C/T]CTGGCAGGGTGGCAC | 6049 |
rs11618206 | snp | A/C | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26177765 | ATCTCTGCCAAAAGG[A/C]TACGGCAAGCCACTA | 6049 |
rs11618995 | snp | C/T | 0.426354 | 0.177198 | intron-variant | RNF6 | GRCh38.p7 | 13:26200137 | ataaatatttgctgt[C/T]tgtaagatacccagt | 6049 |
rs11619338 | snp | C/T | 0.368733 | 0.220005 | intron-variant | RNF6 | GRCh38.p7 | 13:26171694 | ggtacaaaaatacaa[C/T]gagatatgattcagt | 6049 |
rs11620064 | snp | C/T | 0.474272 | 0.110462 | intron-variant | RNF6 | GRCh38.p7 | 13:26183847 | CTACAATATATTCCT[C/T]GAATTATTTATATAT | 6049 |
rs11839581 | snp | A/G | 0.461148 | 0.133852 | intron-variant | RNF6 | GRCh38.p7 | 13:26211694 | ACCTGTGAGGCGGAG[A/G]TTGCAGCGAGCCGAG | 6049 |
rs11839733 | snp | A/T | 0.161596 | 0.233848 | intron-variant | RNF6 | GRCh38.p7 | 13:26190282 | caggatcatctccct[A/T]ttttaagatttttaa | 6049 |
rs11840509 | snp | C/T | 0.109814 | 0.206997 | intron-variant | RNF6 | GRCh38.p7 | 13:26161685 | TACTGAATTATCTTA[C/T]TGGTTCTAACACTTT | 6049 |
rs12017414 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | RNF6 | GRCh38.p7 | 13:26157898 | gatggatggatggat[A/G]gatggatggatggat | 6049 |
rs12100295 | snp | C/T | 0.494315 | 0.0530107 | intron-variant | RNF6 | GRCh38.p7 | 13:26180337 | CAAGCAACCCTGCAA[C/T]ATGTCAAGAGTGTGG | 6049 |
rs12100329 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | RNF6 | GRCh38.p7 | 13:26172366 | aagcaaaactttaaa[A/C]attcaaaagaaaaca | 6049 |
rs12184690 | snp | A/T | 0.115788 | 0.21092 | intron-variant | RNF6 | GRCh38.p7 | 13:26197828 | caggagactgagacc[A/T]tcctggctaacatgg | 6049 |
rs12427601 | snp | C/T | 0.494609 | 0.0516363 | intron-variant | RNF6 | GRCh38.p7 | 13:26181271 | gaactgcagagcacc[C/T]ccaggatgtgcactc | 6049 |
rs12427602 | snp | C/T | 0.494568 | 0.0518327 | intron-variant | RNF6 | GRCh38.p7 | 13:26181327 | ttgggaacaccaaga[C/T]tgggatgccataggc | 6049 |
rs12428716 | snp | C/T | 0.0510282 | 0.151361 | synonymous-codon | RNF6 | GRCh38.p7 | 13:26215501 | TTGGTTCCCATTTTG[C/T]CCACTTCGAGTTGCA | 6049 |
rs12429453 | snp | C/T | 0.400147 | 0.19989 | intron-variant | RNF6 | GRCh38.p7 | 13:26207882 | CGGATGCAGAGCAGA[C/T]TTTTCTGCCTTGCTT | 6049 |
rs12430305 | snp | C/T | 0.0707826 | 0.174302 | intron-variant | RNF6 | GRCh38.p7 | 13:26186844 | gtgtagtggcgcgat[C/T]tcggctcactgcaat | 6049 |
rs12430350 | snp | C/T | 0.494526 | 0.0520291 | intron-variant | RNF6 | GRCh38.p7 | 13:26181247 | ctgcctggggtacta[C/T]aatggcctgaactgc | 6049 |
rs12430355 | snp | C/T | 0.494568 | 0.0518327 | intron-variant | RNF6 | GRCh38.p7 | 13:26181269 | ctgaactgcagagca[C/T]ctccaggatgtgcac | 6049 |
rs12430404 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | RNF6 | GRCh38.p7 | 13:26199625 | aaacatatatctaca[A/G]acatatatttgtata | 6049 |
rs12431318 | snp | A/G | 0.494442 | 0.0524218 | intron-variant | RNF6 | GRCh38.p7 | 13:26181219 | CATGGCTTCCAGATT[A/G]GAGTCGGGGGCTCTG | 6049 |
rs12583735 | snp | C/T | 0.496681 | 0.0405994 | intron-variant | RNF6 | GRCh38.p7 | 13:26189324 | CAGAGCCAGACTCCA[C/T]CTCAAAAAAAACGCT | 6049 |
rs12853169 | snp | G/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26134883 | CTACATATGTTTCTG[G/T]attatttatattatt | 6049 |
rs12854952 | snp | A/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26160687 | ggctagggttgccct[A/C]acaaaatactacaga | 6049 |
rs12854953 | snp | A/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26160688 | gctagggttgcccta[A/C]caaaatactacagac | 6049 |
rs12855191 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF6 | GRCh38.p7 | 13:26163048 | gggcgcggtggctca[C/T]gcctgtaatcccagc | 6049 |
rs12857368 | snp | A/T | 0.394904 | 0.203722 | intron-variant | RNF6 | GRCh38.p7 | 13:26172042 | ctaaatagtatattt[A/T]aaaatgattaaaatg | 6049 |
rs12864596 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26160681 | ttagatggctagggt[C/G/T]gccctaacaaaatac | 6049 |
rs12865499 | snp | C/G | 0.400325 | 0.199756 | intron-variant | RNF6 | GRCh38.p7 | 13:26209555 | AGAAGTCACAAACCT[C/G]ATCAGATCCAAGCTA | 6049 |
rs12869931 | snp | A/G | 0.362941 | 0.223034 | intron-variant | RNF6 | GRCh38.p7 | 13:26206528 | TGGCTGCACTTGAAT[A/G]GTATTTCAGAAACAT | 6049 |
rs12871868 | snp | A/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26149966 | tgtatatatatatac[A/C]cagtgtatatataat | 6049 |
rs12873928 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | RNF6 | GRCh38.p7 | 13:26134987 | AGATTGGTAAACAAA[C/T]GTGAATAGACAAATG | 6049 |
rs12873948 | snp | A/G | 0.351635 | 0.228408 | intron-variant | RNF6 | GRCh38.p7 | 13:26205639 | TAACATCAGTTGCCA[A/G]GACACAAACAACTCT | 6049 |
rs12874823 | snp | A/T | 0.104149 | 0.203046 | intron-variant | RNF6 | GRCh38.p7 | 13:26193059 | tgggttaggggaacc[A/T]gtttgagctgtggcg | 6049 |
rs12874929 | snp | A/G | 0.351418 | 0.228505 | intron-variant | RNF6 | GRCh38.p7 | 13:26207470 | AGAGATGATGGCAAG[A/G]ATCTATGTGAGAAAT | 6049 |
rs12875445 | snp | A/C | 0.196149 | 0.244131 | intron-variant | RNF6 | GRCh38.p7 | 13:26172112 | TAACTGATATTATAA[A/C]ATGTTAAAATTAAAC | 6049 |
rs13378638 | snp | C/T | 0.0861826 | 0.188849 | intron-variant | RNF6 | GRCh38.p7 | 13:26179661 | attcagggtcctgtc[C/T]tCCTGCAATGCATTc | 6049 |
rs17071948 | snp | A/G | 0.3752 | 0.216391 | intron-variant | RNF6 | GRCh38.p7 | 13:26187402 | TGAGAATGTCAGCCC[A/G]TGAGCTCTGGTGTGC | 6049 |
rs17071954 | snp | A/G | 0.124144 | 0.21601 | intron-variant | RNF6 | GRCh38.p7 | 13:26220090 | AAGGGATACTGGGAT[A/G]ATATAATTTACATTT | 6049 |
rs17083313 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | RNF6 | GRCh38.p7 | 13:26134982 | AAAAAAGATTGGTAA[A/G]CAAACGTGAATAGAC | 6049 |
rs17083316 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | RNF6 | GRCh38.p7 | 13:26150757 | ACAATAATACTTTTA[C/T]GTACAAGGCTATACT | 6049 |
rs17083319 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | RNF6 | GRCh38.p7 | 13:26152067 | TAACCTGGCCTCGGC[C/T]AACACCTTGAGCTGC | 6049 |
rs17083321 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | RNF6 | GRCh38.p7 | 13:26152613 | CATGCTATGTGTCCT[C/T]TACACGTGTTTACTG | 6049 |
rs17083325 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | RNF6 | GRCh38.p7 | 13:26152741 | AAACTTCCTGGGAGA[A/G]ACAAAACTAGTTATA | 6049 |
rs17083327 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | RNF6 | GRCh38.p7 | 13:26152823 | TGGACTATAGCATTT[A/G]GTGAAGTTTGGAGGA | 6049 |
rs17083332 | snp | G/T | 0.0980852 | 0.198549 | intron-variant | RNF6 | GRCh38.p7 | 13:26155940 | CTTCCTGGGTCACTC[G/T]TAGATAATTCTGCTC | 6049 |
rs17083341 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | RNF6 | GRCh38.p7 | 13:26156891 | AGTTTATATAACATG[A/G]GGAGAGCATTACAAA | 6049 |
rs17083343 | snp | A/G | 0.103438 | 0.202533 | intron-variant | RNF6 | GRCh38.p7 | 13:26157390 | GAGAACACAATGGCA[A/G]TGGGTGTAATTTGAC | 6049 |
rs17083419 | snp | C/T | 0.117537 | 0.212022 | intron-variant | RNF6 | GRCh38.p7 | 13:26205145 | AGAGGTATTTCTCTG[C/T]ATTGAGCTTCAGTTA | 6049 |
rs17083434 | snp | A/G | 0.0988009 | 0.199095 | utr-variant-3-prime, intron-variant | RNF6 | GRCh38.p7 | 13:26213315 | ATATACACCTATGGT[A/G]TGCTGCATATTAAAT | 6049 |
rs17083436 | snp | C/T | 0.0318036 | 0.122026 | missense, intron-variant, utr-variant-3-prime | RNF6 | GRCh38.p7 | 13:26214014 | AGTTCACTATCAATA[C/T]TGTTATGCTCATAGT | 6049 |
rs17083445 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | RNF6 | GRCh38.p7 | 13:26219282 | TTCACCTTATAAAAT[A/G]CAGAAGCCAGTGATT | 6049 |
rs17083465 | snp | A/C | 0.0955749 | 0.196603 | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26223981 | GTACAACGACTTCAG[A/C]TATTGTGAACACACA | 6049 |
rs17083467 | snp | C/G | 0.0955749 | 0.196603 | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26224435 | TTTATTGGATTGGTA[C/G]CTGGCCTTTGTAGTG | 6049 |
rs17433427 | snp | A/T | 0.239614 | 0.249784 | intron-variant | RNF6 | GRCh38.p7 | 13:26150456 | GAAAACATGATTAAA[A/T]ACCTCCCTGTACCTG | 6049 |
rs17433548 | snp | C/G | 0.225301 | 0.248777 | intron-variant | RNF6 | GRCh38.p7 | 13:26152046 | GTAACACACCAACCT[C/G]TTTTATAACCTGGCC | 6049 |
rs17433785 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RNF6 | GRCh38.p7 | 13:26154213 | TTTTCCATTGATATT[C/T]GGAACTCTAAAACAA | 6049 |
rs17433862 | snp | C/G | 0.225893 | 0.248835 | intron-variant | RNF6 | GRCh38.p7 | 13:26155611 | CCTGATTCTGCCTCT[C/G]AAAGGCAAGCCAGAG | 6049 |
rs17435452 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | RNF6 | GRCh38.p7 | 13:26190705 | TGTTCTATTCATCAA[C/T]TGAACATTTGAACAC | 6049 |
rs17435472 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | RNF6 | GRCh38.p7 | 13:26190845 | TCCTCAAAGGATGCA[A/G]TGGCCAGTGGATTCA | 6049 |
rs17436547 | snp | A/C | 0.462034 | 0.132445 | intron-variant | RNF6 | GRCh38.p7 | 13:26221373 | TTCAATAAACTGTTT[A/C]TTTAAAGGCCAGGAA | 6049 |
rs17511627 | snp | A/C | 0.290977 | 0.246619 | intron-variant | RNF6 | GRCh38.p7 | 13:26150190 | TTTTGTTAAACGCAC[A/C]ATGAGCAATTCCGGA | 6049 |
rs17526316 | snp | G/T | 0.371785 | 0.218331 | intron-variant | RNF6 | GRCh38.p7 | 13:26189665 | AGCACATTGGATGAT[G/T]AAACTTCAGACTGAG | 6049 |
rs28372677 | snp | A/C | 0.0197687 | 0.0974348 | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26223036 | AGACAGAGACCTACT[A/C]AGCATCTTAACTAAC | 6049 |
rs28415708 | snp | A/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26148930 | AGGCCAGCATGCAGG[A/G]GGAATTCTCTCTTGC | 6049 |
rs28452974 | snp | A/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26149870 | ATATAATGTGTGTGT[A/G]TATATATATATATAT | 6049 |
rs28567000 | snp | A/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26184020 | tatatatatatatat[A/T]ttttttttttttttt | 6049 |
rs28600376 | snp | C/T | | | missense, intron-variant | RNF6 | GRCh38.p7 | 13:26214669 | CTCCAGGACGGATCC[C/T]TCTCACTTGAAGGTC | 6049 |
rs28608845 | snp | C/T | | | synonymous-codon, intron-variant, missense | RNF6 | GRCh38.p7 | 13:26214670 | TCCAGGACGGATCCT[C/T]CTCACTTGAAGGTCC | 6049 |
rs28610109 | snp | C/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26186788 | TCTTTTTTTTTTTTT[C/T]TTTTTTTGAGACGGA | 6049 |
rs28684858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26149006 | TTGGATAAAATCCAC[A/G]CACATTATGGAGTAT | 6049 |
rs28710828 | snp | A/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26204492 | ACAGAGCGAGACTCC[A/C]CCTCAAAAAAAAAAA | 6049 |
rs28731044 | snp | C/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26186786 | CTTCTTTTTTTTTTT[C/T]TCTTTTTTTGAGACG | 6049 |
rs28752326 | snp | C/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26197575 | ACACTGCTCAAGCCC[C/T]CTACTTGCTCTCCCT | 6049 |
rs28753934 | snp | A/T | 0.0345262 | 0.126772 | intron-variant | RNF6 | GRCh38.p7 | 13:26137029 | AAAATAACAACTCAC[A/T]TTCTCATTACTGAGG | 6049 |
rs33971902 | in-del | -/CC | | | intron-variant | RNF6 | GRCh38.p7 | 13:26170488 | CATTTTACTAACTAT[-/CC]ATGCGTGAAGATGGA | 6049 |
rs34015717 | in-del | -/G | 0.353154 | 0.227726 | intron-variant | RNF6 | GRCh38.p7 | 13:26205291 | CATTAAAAAATACAA[-/G]ACTATTTTGCCTTGT | 6049 |
rs34068231 | snp | A/G | 0.459687 | 0.136129 | intron-variant | RNF6 | GRCh38.p7 | 13:26211702 | GGCGGAGGTTGCAGC[A/G]AGCCGAGATAGTGCC | 6049 |
rs34079341 | in-del | -/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26158598 | CTGAAAATGACTATG[-/C]CAGATTTATATTGAT | 6049 |
rs34129998 | in-del | -/C | | | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26222740 | GCCTCCAGCGATCCT[-/C]CCCTCCTCATCCCAG | 6049 |
rs34172697 | in-del | -/A | | | intron-variant | RNF6 | GRCh38.p7 | 13:26196634 | TGAGACTCTTTCTCC[-/A]AAAAATAAATAAATA | 6049 |
rs34181435 | snp | A/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26135753 | GTGGTAGGCCTAGGA[A/G]GTGGTGTTTGCATCA | 6049 |
rs34238147 | snp | A/G | 0.352721 | 0.227922 | intron-variant | RNF6 | GRCh38.p7 | 13:26202118 | TAAACTTGGAGAACC[A/G]AGGCCTGTTTCAGGT | 6049 |
rs34246040 | in-del | -/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26189800 | CTCTCTGCTCAATTT[-/G]TGCTGTAACCACTTC | 6049 |
rs34266173 | in-del | -/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26162275 | AGCTTAGAACCCACT[-/G]GGAATCATTCAAACT | 6049 |
rs34266191 | in-del | -/T/TT | 0.662578 | 0.0374088 | intron-variant | RNF6 | GRCh38.p7 | 13:26144381 | ATGGAAATATCTTCA[-/T/TT]TTTTTTTTTTTTCAC | 6049 |
rs34336773 | in-del | -/A | 0.319376 | 0.240181 | intron-variant | RNF6 | GRCh38.p7 | 13:26141426 | GAGCAAGACTCTGTC[-/A]AAAAAAAAAAAAAAA | 6049 |
rs34343015 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF6 | GRCh38.p7 | 13:26210357 | GGAAGATTAAAAGTT[C/T]ATTAGATGTTCTTGT | 6049 |
rs34366530 | in-del | -/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26139417 | CAAACCTGATGTTTT[-/C]CCCTGTGGCCCTGTG | 6049 |
rs34380865 | snp | A/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26177827 | GCCTCCCAGCTCTAG[A/C]TATGCCCTACTCCAC | 6049 |
rs34400633 | in-del | -/AGAC | | | intron-variant | RNF6 | GRCh38.p7 | 13:26157960 | AGCTAGCTAGAAGAT[-/AGAC]AGATAGATAGATAGA | 6049 |
rs34449426 | in-del | -/A | | | intron-variant | RNF6 | GRCh38.p7 | 13:26151739 | TAGAATATGAGAAAT[-/A]AAAGTTCCCAATAGT | 6049 |
rs34507728 | snp | A/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26150030 | TGTATATATATATAC[A/C]CAGTGTATATATAAT | 6049 |
rs34521580 | in-del | -/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26147085 | GAATGGACTAATACA[-/G]GGGCCCATATCAATC | 6049 |
rs34584161 | snp | A/G | 0.355096 | 0.226837 | intron-variant | RNF6 | GRCh38.p7 | 13:26202862 | AACTGGATATGAGTC[A/G]GCAACAAAAGTCCTT | 6049 |
rs34611426 | snp | C/T | 0.12623 | 0.217212 | missense, intron-variant | RNF6 | GRCh38.p7 | 13:26214921 | AATTATGATAAACAG[C/T]GCCACTCTGTCTCTG | 6049 |
rs34640458 | in-del | -/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26154422 | GTGTAGAGTTAACAT[-/G]GGAAAACCAGAGATC | 6049 |
rs34642088 | in-del | -/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26211505 | GCTCATGCCTATAAT[-/C]CCCAGCACTTTGGGA | 6049 |
rs34701644 | snp | C/T | 0.352721 | 0.227922 | intron-variant | RNF6 | GRCh38.p7 | 13:26205293 | TTAAAAAATACAAGA[C/T]TATTTTGCCTTGTTT | 6049 |
rs34728580 | in-del | -/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26139709 | ATATATTTAGTCCTT[-/C]CCTTGCTGTCTTTTA | 6049 |
rs34753443 | in-del | -/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26209671 | GGATTGTTACCCACT[-/G]GGGGAGAAGGTGAGC | 6049 |
rs34838281 | in-del | -/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26145364 | GTGATCTGGTTTGGC[-/T]TTTGTGTCCCCACCC | 6049 |
rs34849782 | in-del | -/A | | | intron-variant | RNF6 | GRCh38.p7 | 13:26197299 | TAGAGTATTTACCTT[-/A]AAAAGCTTACAACTA | 6049 |
rs34897738 | snp | A/T | 0.36315 | 0.222928 | intron-variant | RNF6 | GRCh38.p7 | 13:26203574 | ATGCTTCCCCCAGGC[A/T]GCTCCTAGCAGTGAC | 6049 |
rs34900385 | snp | A/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26150336 | TGAAGCTCGCGAATA[A/C]CGATAGCTAGCGATT | 6049 |
rs34921709 | in-del | -/T | 0.94845 | 0.0951144 | intron-variant | RNF6 | GRCh38.p7 | 13:26207478 | TGGCAAGAATCTATG[-/T]GAGAAATAGTGACAA | 6049 |
rs35078889 | in-del | -/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26150876 | TAAGAGAGTTATATA[-/T]TTTTCCTGTTGGGGA | 6049 |
rs35106908 | in-del | -/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26203571 | GCCATGCTTCCCCCA[-/G]GCAGCTCCTAGCAGT | 6049 |
rs35139305 | in-del | -/AT | 0.350764 | 0.228794 | intron-variant | RNF6 | GRCh38.p7 | 13:26209786 | GTGAGAAGATGTGAG[-/AT]ATATATATATATATA | 6049 |
rs35172799 | in-del | -/A | 0.0876345 | 0.190099 | intron-variant | RNF6 | GRCh38.p7 | 13:26159625 | GTGAAACTCCATCTC[-/A]AAAAAAAAAATTATT | 6049 |
rs35193957 | in-del | -/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26179806 | ACTGACACGATCTCA[-/G]GGGCAACATCATTGA | 6049 |
rs35276113 | in-del | -/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26175370 | CAGGCGTGAGCCACT[-/G]GCACCCAGCCTCAGG | 6049 |
rs35328831 | snp | C/T | 0.362313 | 0.223351 | intron-variant | RNF6 | GRCh38.p7 | 13:26206204 | CACCACCCTCCCCAC[C/T]GCCCCCCGTCCCTGC | 6049 |
rs35351669 | in-del | -/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26209656 | GCTGCATGTGATTTT[-/G]GGATTGTTACCCACT | 6049 |
rs35375072 | snp | G/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26145620 | TTGTAAGTTTCCTGA[G/T]GCCTCCCCAGAAGCA | 6049 |
rs35391825 | in-del | -/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26162532 | GACTGATCATCTCAT[-/G]GGAAGAACACAGAAC | 6049 |
rs35400818 | in-del | -/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26156502 | AATACCACATATGTA[-/T]TTTGTCAAGAGAGCT | 6049 |
rs35447394 | in-del | -/A | | | intron-variant | RNF6 | GRCh38.p7 | 13:26173789 | AACCCCGGCTCTACT[-/A]AAAATACAGAAATTA | 6049 |
rs35478692 | in-del | -/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26173998 | AAGCAAATATAACAA[-/C]AATGTTAAAAGTTGT | 6049 |
rs35507213 | in-del | -/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26158283 | GGGATCCAAATGGCT[-/C]CACCTTGGGTCAGAC | 6049 |
rs35577507 | in-del | -/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26205357 | AAGCTCTCCAGATAA[-/C]CTAAGAAATTCTGAG | 6049 |
rs35669290 | in-del | -/A | | | intron-variant | RNF6 | GRCh38.p7 | 13:26135419 | TAAATTACATCCACT[-/A]CAATAGTGCTGAGAT | 6049 |
rs35706716 | in-del | -/TATAT | | | intron-variant | RNF6 | GRCh38.p7 | 13:26183903 | TTTATACTTATTTAT[-/TATAT]ATATGTAATATATAC | 6049 |
rs35733787 | in-del | -/T | | | intron-variant, utr-variant-5-prime | RNF6 | GRCh38.p7 | 13:26221597 | AGGCCTTCCTTCCTA[-/T]TCCCGTTCCCATTCG | 6049 |
rs35750258 | in-del | -/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26183650 | CTGAGAAGGTAAAAT[-/G]GGAATGTTAGCCATG | 6049 |
rs35751313 | in-del | -/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26190031 | CAGGTCTCACGGGGC[-/G]TAAAATCAAGGTGTT | 6049 |
rs35765366 | in-del | -/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26140524 | ACCATCTATGACAAA[-/C]CCCACAGCCAACATC | 6049 |
rs35773834 | in-del | -/A | | | intron-variant | RNF6 | GRCh38.p7 | 13:26207231 | GAGAACAGCATGGGC[-/A]AAAAAAAAAAAAGTA | 6049 |
rs35855043 | snp | A/G | 0.407502 | 0.194147 | intron-variant | RNF6 | GRCh38.p7 | 13:26208296 | CCTCCTGGGAGTCTG[A/G]AATTTTGGTATGTGC | 6049 |
rs35868020 | in-del | -/A | | | intron-variant | RNF6 | GRCh38.p7 | 13:26196072 | TTCTAAAATTTTATC[-/A]AAAACTTACAGATCC | 6049 |
rs35868766 | in-del | -/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26139870 | AGAGACTGGGTCTCA[-/C]CTGTGTCCCCCAGGG | 6049 |
rs35907080 | in-del | -/A | | | intron-variant | RNF6 | GRCh38.p7 | 13:26174357 | ACGTAAAGGGACAGC[-/A]AAACTGAAATAGGCT | 6049 |
rs35942116 | in-del | -/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26187732 | GCTCTATTTGATTTT[-/G]GGGGGTTTTTTAAGA | 6049 |
rs35981749 | in-del | -/A | 0.499325 | 0.0183582 | intron-variant | RNF6 | GRCh38.p7 | 13:26189327 | CCATCTCAAAAAAAA[-/A]CGCTTCCTATTGTAA | 6049 |
rs36000975 | in-del | -/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26209725 | TGGAATTGCACAGAA[-/G]GGTGGCTGGATTAGG | 6049 |
rs36160805 | in-del | -/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26200372 | ATGAGCCCCACACTT[-/G]GGTTTAATATTCTGC | 6049 |
rs45472692 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-5-prime | RNF6 | GRCh38.p7 | 13:26221277 | AACACGCTTTTAACA[C/T]ATGCCATGGTATCCA | 6049 |
rs45551031 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-5-prime, upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26222183 | CCCGTGCTGCAGCGT[A/G]GGGTCGTCCAGCTGG | 6049 |
rs55672336 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | RNF6 | GRCh38.p7 | 13:26140123 | ATTTTGGGGATGGGG[A/T]TTAATATAGACAATC | 6049 |
rs55703219 | snp | C/T | 0.101658 | 0.201233 | intron-variant | RNF6 | GRCh38.p7 | 13:26190646 | CTTGTATCCCCATAA[C/T]ACACCCAACACATGA | 6049 |
rs55713738 | in-del | -/TC | 0.395087 | 0.203592 | intron-variant | RNF6 | GRCh38.p7 | 13:26170487 | GCATTTTACTAACTA[-/TC]CCATGCGTGAAGATG | 6049 |
rs55750307 | snp | A/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26157946 | GATAGATGGATGGCT[A/G]GCTAGCTAGAAGATA | 6049 |
rs55757744 | snp | A/G | 0.495213 | 0.048687 | intron-variant | RNF6 | GRCh38.p7 | 13:26200261 | ATATCCATACAAATA[A/G]CTAAAATCAAAAAGC | 6049 |
rs55767001 | in-del | -/T/TT | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26144392 | TTCATTTTTTTTTTT[-/T/TT]CACTATTTCAGAGAG | 6049 |
rs55936108 | snp | G/T | 0.494733 | 0.0510469 | intron-variant | RNF6 | GRCh38.p7 | 13:26186031 | CATAAACATAGATAT[G/T]AAACAAACACAAAAT | 6049 |
rs55972548 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RNF6 | GRCh38.p7 | 13:26172835 | GGCGTGAGCCACCGC[A/G]CCCGGCCTAGAATAT | 6049 |
rs56024174 | snp | A/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26157938 | GATAGATGGATAGAT[A/G]GATGGCTAGCTAGCT | 6049 |
rs56038404 | in-del | -/TGATTAAACATTTTT | | | intron-variant | RNF6 | GRCh38.p7 | 13:26182357 | CCTCAAATTAAATTT[-/TGATTAAACATTTTT]GGCAAAAATGTTACA | 6049 |
rs56055612 | snp | A/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26157956 | TGGCTAGCTAGCTAG[A/C]AGATAGATAGATAGA | 6049 |
rs56107121 | snp | C/T | 0.4944 | 0.0526182 | intron-variant | RNF6 | GRCh38.p7 | 13:26181092 | CCATCAGCCTTCCAG[C/T]CTAGGAAGGGGGGTC | 6049 |
rs56116523 | snp | A/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26157944 | TGGATAGATGGATGG[A/C]TAGCTAGCTAGAAGA | 6049 |
rs56137727 | snp | A/G | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26157926 | GATGGATGGATGGAT[A/G]GATGGATAGATGGAT | 6049 |
rs56159536 | in-del | -/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26172561 | CTTTTTTTTTTTTTT[-/T]GAGATGGAATCTTGC | 6049 |
rs56195292 | snp | G/T | 0.0926964 | 0.194308 | intron-variant | RNF6 | GRCh38.p7 | 13:26158062 | GAAAGACAAATGGAT[G/T]AATAGATGAAACATG | 6049 |
rs56213113 | snp | A/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26212144 | CCATTCCATTGTGTT[A/C]TATATGCTGTAGTAG | 6049 |
rs56421053 | in-del | -/CCGCTTCCTGTTTCTGCCATCAGTGGGGCCACAGGCC | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26187135 | GGACTGGGGCTGTCC[lengthTooLong]TGAAGACGGCTTGTA | 6049 |
rs56677274 | in-del | -/TG | | | intron-variant | RNF6 | GRCh38.p7 | 13:26178642 | GTGTGTGTGTGTGTG[-/TG]GTGAGAAAGCTTAAG | 6049 |
rs56750324 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | RNF6 | GRCh38.p7 | 13:26167752 | ACACATGCACACATA[C/T]GCTCATTGCAGCACT | 6049 |
rs56875324 | in-del | -/A | 0.465473 | 0.126772 | intron-variant | RNF6 | GRCh38.p7 | 13:26206917 | GGCCCCTTCCTCCTT[-/A]AAAAAAAAAAATTAA | 6049 |
rs57022456 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | RNF6 | GRCh38.p7 | 13:26159101 | GCTGTAAATTTTAAC[-/A]AAAAAATTGCTAAGA | 6049 |
rs57023715 | in-del | -/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26157964 | TAGCTAGAAGATAGA[-/T]AGATAGATAGATAGA | 6049 |
rs57056845 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | RNF6 | GRCh38.p7 | 13:26186041 | GATATGAAACAAACA[C/T]AAAATGTATGTTTTA | 6049 |
rs57166295 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | RNF6 | GRCh38.p7 | 13:26146876 | TAGGTGACTGAATCA[C/T]GGGGGCAGACATCCC | 6049 |
rs57180402 | snp | C/T | 0.446771 | 0.154211 | intron-variant | RNF6 | GRCh38.p7 | 13:26176802 | AGCCAAGTGTGATGG[C/T]ACATGCCTGTAATCC | 6049 |
rs57251514 | in-del | -/TAAA | | | intron-variant | RNF6 | GRCh38.p7 | 13:26196663 | AAATAAATAAATAAA[-/TAAA]ACATTTTCAGATAAC | 6049 |
rs57373126 | in-del | -/ATATATATATATAT | | | intron-variant | RNF6 | GRCh38.p7 | 13:26148658 | TATATATATATATAT[-/ATATATATATATAT]GAGGGAGATATATAT | 6049 |
rs57465135 | in-del | -/A | 0.378174 | 0.214642 | intron-variant | RNF6 | GRCh38.p7 | 13:26137654 | AGAGATAGAAATTAT[-/A]AAAAAAAAAAAAACA | 6049 |
rs57585322 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF6 | GRCh38.p7 | 13:26204733 | TCCTAGTTTATTTCC[A/G]TGTAAGAAGGGCCTA | 6049 |
rs57919560 | in-del | -/AGA | | | intron-variant | RNF6 | GRCh38.p7 | 13:26157957 | GGCTAGCTAGCTAGA[-/AGA]TAGATAGATAGATAG | 6049 |
rs58041266 | in-del | -/ATATAT/ATATATAT | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26148671 | TATATATATATATAT[-/ATATAT/ATATATAT]GAGGGAGATATATAT | 6049 |
rs58323298 | snp | C/T | 0.124491 | 0.216211 | intron-variant | RNF6 | GRCh38.p7 | 13:26190149 | GTGGCCCTCTTCCTC[C/T]GTCTTCAAAGCCAGC | 6049 |
rs58930862 | snp | C/T | 0.227074 | 0.248947 | intron-variant | RNF6 | GRCh38.p7 | 13:26149101 | GCCCAGAATAATGTA[C/T]GACCAAATATCTGAG | 6049 |
rs59062361 | in-del | -/A | | | intron-variant | RNF6 | GRCh38.p7 | 13:26137667 | TAAAAAAAAAAAAAA[-/A]CAAATAGAAACTCTG | 6049 |
rs59314474 | in-del | -/AT/TA | | | intron-variant | RNF6 | GRCh38.p7 | 13:26209787 | ATATATATATATATA[-/AT/TA]CTGGGCAGCCAAGAA | 6049 |
rs59322318 | in-del | -/TG | | | intron-variant | RNF6 | GRCh38.p7 | 13:26178641 | GTGTGTGTGTGTGTG[-/TG]GTGAGAAAGCTTAAG | 6049 |
rs59571565 | snp | A/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26200426 | TTTTTTTTTTTTTTT[A/T]GAGGCGGAGTTTTGC | 6049 |
rs59761171 | in-del | -/C | 0.0383715 | 0.133092 | intron-variant | RNF6 | GRCh38.p7 | 13:26196747 | TGAAGGGAAAGTATA[-/C]CAGATAGAGATGCAA | 6049 |
rs60017283 | in-del | -/AAAAA | | | downstream-variant-500B | RNF6 | GRCh38.p7 | 13:26131946 | AAAAAAAAAAAAAAA[-/AAAAA]GATCCTCCTAAGAAA | 6049 |
rs60144279 | snp | A/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26188785 | CAGGCACATGCCACC[A/C]TGCCCGGTTAATTTT | 6049 |
rs60381245 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | RNF6 | GRCh38.p7 | 13:26172589 | TGCTCTGTCGCCCAG[G/T]CTGGAGTGCAGTGGC | 6049 |
rs60472311 | snp | A/G | 0.226484 | 0.248892 | intron-variant | RNF6 | GRCh38.p7 | 13:26153375 | TGCACCACCACGTCC[A/G]GCTAATTTTTGTATT | 6049 |
rs60520219 | snp | A/G | 0.102014 | 0.201495 | intron-variant | RNF6 | GRCh38.p7 | 13:26216824 | GCCAGGCATGGTGGC[A/G]TGCGCCTGTAATCCC | 6049 |
rs60829328 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | RNF6 | GRCh38.p7 | 13:26170568 | AATAAAGCCCAGATC[A/G]TCTTAGTGTGATCTT | 6049 |
rs61096715 | snp | A/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26219155 | TTTAAGTCATATTTT[A/T]TTTGTATAAAAATTA | 6049 |
rs61102619 | in-del | -/GGC | 0.0337553 | 0.125452 | intron-variant | RNF6 | GRCh38.p7 | 13:26195271 | AGGCTGCCTTTGGGG[-/GGC]GGCTTATTAGTAGAC | 6049 |
rs61109483 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | RNF6 | GRCh38.p7 | 13:26186541 | GCGCACACACATGCA[C/T]GTGCACGAGCGCACG | 6049 |
rs61144258 | in-del | -/A | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26141443 | AAAAAAAAAAAAAAA[-/A]TGCAGCCAGAGGCAA | 6049 |
rs61179356 | snp | A/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26200770 | CAATAGGGCAATGGA[A/G]GATAGTGTGAGCAGA | 6049 |
rs61193604 | snp | A/G | 0.447162 | 0.153712 | intron-variant | RNF6 | GRCh38.p7 | 13:26176803 | GCCAAGTGTGATGGC[A/G]CATGCCTGTAATCCC | 6049 |
rs61383574 | in-del | -/C | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26211729 | GCCACTGCACTCAAG[-/C]CCTGGGCAACAGAGT | 6049 |
rs61558413 | snp | A/C/T | 0.0205511 | 0.0992634 | intron-variant | RNF6 | GRCh38.p7 | 13:26183149 | AAGACATGCTGTTCT[A/C/T]TAGAAATCTGTTATA | 6049 |
rs61591240 | in-del | -/GGAT | | | intron-variant | RNF6 | GRCh38.p7 | 13:26157925 | GATGGATGGATGGAT[-/GGAT]AGATGGATAGATGGA | 6049 |
rs61619744 | snp | A/C | 0.225893 | 0.248835 | intron-variant | RNF6 | GRCh38.p7 | 13:26154004 | CTCTAATTTCAGCTA[A/C]ATGAAATTCTTACGA | 6049 |
rs61687531 | in-del | -/CAG | | | intron-variant | RNF6 | GRCh38.p7 | 13:26135343 | TTATAGCAATAATAG[-/CAG]TCACCTGGCTTCCCT | 6049 |
rs61740522 | snp | G/T | 4.9436e-05 | 0.00497148 | synonymous-codon, intron-variant | RNF6 | GRCh38.p7 | 13:26214835 | ATCTTGCTCTAAAAA[G/T]ACTCGAGTTCTACCT | 6049 |
rs61753154 | snp | C/T | 0.00974514 | 0.0691202 | synonymous-codon | RNF6 | GRCh38.p7 | 13:26219491 | ATGGTCTCTCATAAG[C/T]CGATAATCTTCATCA | 6049 |
rs61760896 | snp | C/T | 0.0001977 | 0.00994037 | missense, intron-variant, utr-variant-3-prime | RNF6 | GRCh38.p7 | 13:26214633 | GAGTTCTATTTGCAA[C/T]ACTATCCCGATCTCT | 6049 |
rs61760897 | snp | A/G | 0.00579886 | 0.0535332 | missense, intron-variant | RNF6 | GRCh38.p7 | 13:26215391 | TAATCTTCTCCATGA[A/G]TTTCAAATCCTCTAT | 6049 |
rs61944944 | snp | C/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26136574 | ATTTTGGAGGAAAAG[C/T]CACAAAGAATAACAC | 6049 |
rs61944945 | snp | C/T | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26139347 | CTTTTTTATGGAAAC[C/T]CCAATAAATGCTCTG | 6049 |
rs61944946 | snp | A/G | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26140499 | AAGGAACATACCTCA[A/G]AATAATATGAACCAT | 6049 |
rs61944947 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | RNF6 | GRCh38.p7 | 13:26142108 | GAAGACAAAGAAGCA[A/G]TCACCAAACATATAA | 6049 |
rs61944948 | snp | C/T | 0.0912534 | 0.193131 | intron-variant | RNF6 | GRCh38.p7 | 13:26142269 | AAGGGAACACACTTA[C/T]ACACTGTTGGTGGGA | 6049 |
rs61944950 | snp | A/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26159625 | GTGAAACTCCATCTC[A/C]AAAAAAAAAATTATT | 6049 |
rs61946760 | snp | A/G | 0.238171 | 0.24972 | intron-variant | RNF6 | GRCh38.p7 | 13:26169624 | CGGCCTTAAGACCCA[A/G]GAAATGTCTTTCTGA | 6049 |
rs61946761 | snp | C/T | 0.447032 | 0.153878 | intron-variant | RNF6 | GRCh38.p7 | 13:26176412 | CTCCCACCTCGACCT[C/T]CCAAAGTCATTGGAT | 6049 |
rs61946763 | snp | A/G | 0.388964 | 0.20782 | intron-variant | RNF6 | GRCh38.p7 | 13:26182494 | ATTTCTTCATTGTAA[A/G]TGGTATTTTTCCATT | 6049 |
rs61946764 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF6 | GRCh38.p7 | 13:26183171 | TCTGTTATATGCTTT[C/T]GCTCTAAAAGTATTT | 6049 |
rs61946796 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | RNF6 | GRCh38.p7 | 13:26189260 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 6049 |
rs61946798 | snp | A/G/T | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26205221 | CATGGAGTACTTGGA[A/G/T]TACAATAAGTACATG | 6049 |
rs61946807 | snp | A/C | | | missense, intron-variant | RNF6 | GRCh38.p7 | 13:26215263 | TGTTGGAACTACTAC[A/C]ATTGAAATTCACTGA | 6049 |
rs61946808 | snp | C/T | 0.0352966 | 0.128072 | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26223321 | ACTAAAATGGAAATA[C/T]ATAAAACAGCCTAGA | 6049 |
rs62847660 | snp | C/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26160541 | TCTTCTTCTCTTCTT[C/T]TTCTTTTTTTTTTTT | 6049 |
rs66536727 | in-del | -/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26186775 | GGACCTTTCTTCTTC[-/T]TTTTTTTTTTTTCTT | 6049 |
rs67032068 | in-del | -/A | 0.414905 | 0.187899 | intron-variant | RNF6 | GRCh38.p7 | 13:26172278 | TGGTTAGCACTATGG[-/A]AAAAAATACAGATCT | 6049 |
rs67295740 | in-del | -/TC | | | intron-variant | RNF6 | GRCh38.p7 | 13:26160532 | TCCAGCCTATCTTCT[-/TC]TCTTCTTCTTCTTTT | 6049 |
rs67656503 | in-del | -/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26183885 | TATATAAAATATAGG[-/T]TTTTTTATACTTATT | 6049 |
rs67674065 | snp | A/G | 0.22263 | 0.248497 | intron-variant | RNF6 | GRCh38.p7 | 13:26187358 | GCCTTGGGGATCGCG[A/G]AGCAGGAGGCTTACT | 6049 |
rs68194307 | snp | A/G | 0.485596 | 0.0836329 | intron-variant | RNF6 | GRCh38.p7 | 13:26145450 | GACTGAATCATGGGG[A/G]GGGGGGGGGACTTCC | 6049 |
rs71080231 | in-del | -/TACA | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26149893 | ATATATATATATATA[-/TACA]CACACACAGTGTATA | 6049 |
rs71080233 | in-del | -/A | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26153160 | AAAAGAAAAAAAAAA[-/A]GAAAAGACTAAAGAT | 6049 |
rs71080234 | in-del | -/TATTT | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26153211 | TATTTTATTTTATTT[-/TATTT]TATTTTATGTATTTT | 6049 |
rs71080237 | in-del | -/TGTGTG | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26178637 | GTGTGTGTGTGTGTG[-/TGTGTG]GTGAGAAAGCTTAAG | 6049 |
rs71080239 | in-del | -/A | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26204497 | GCGAGACTCCACCTC[-/A]AAAAAAAAAAAAAAA | 6049 |
rs71188711 | in-del | -/A | 0.5 | 0 | downstream-variant-500B | RNF6 | GRCh38.p7 | 13:26131925 | AGAGAGACTCCATAT[-/A]AAAAAAAAAAAAAAA | 6049 |
rs71188712 | in-del | -/G | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26145446 | AGGTGACTGAATCAT[-/G]GGGGGGGGGGGGGAC | 6049 |
rs71188713 | in-del | -/C | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26153503 | GCATGAGCCACCGCA[-/C]CCCAGTCAAGATATT | 6049 |
rs71188715 | in-del | -/A | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26206164 | GCCCTTTGACTGGGG[-/A]AACCCTTCCCATCCG | 6049 |
rs71188717 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RNF6 | GRCh38.p7 | 13:26221964 | CCCCGGCGTCTCCAG[A/G]AAGTAGTGGTGGGAC | 6049 |
rs71733531 | in-del | -/A | | | downstream-variant-500B | RNF6 | GRCh38.p7 | 13:26131950 | AAAAAAAAAAAAAAA[-/A]GATCCTCCTAAGAAA | 6049 |
rs71771342 | in-del | -/ACTTGGAGTACAATAAGTACATGGAGT | | | intron-variant | RNF6 | GRCh38.p7 | 13:26205214 | ATAAGTACATGGAGT[-/ACTTGGAGTACAATAAGTACATGGAGT]CAGAACTTTACAAAA | 6049 |
rs71813042 | in-del | -/TA | 0.416766 | 0.18625 | intron-variant | RNF6 | GRCh38.p7 | 13:26150049 | TGTATATATAATGTG[-/TA]TATATATATATATAC | 6049 |
rs72166737 | in-del | -/TAA | 0.0501905 | 0.150254 | utr-variant-3-prime, intron-variant, cds-indel | RNF6 | GRCh38.p7 | 13:26213114 | ATATTGCTTGCTGTC[-/TAA]TAAGTTAGATTGTCA | 6049 |
rs72420363 | in-del | -/AGC | 0.227369 | 0.248974 | intron-variant | RNF6 | GRCh38.p7 | 13:26135341 | TTTTATAGCAATAAT[-/AGC]AGTCACCTGGCTTCC | 6049 |
rs73158235 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RNF6 | GRCh38.p7 | 13:26136764 | AAAAATATGGCCTCA[C/G]TGGGGAGGCCAGTGA | 6049 |
rs73158236 | snp | A/G | 0.231775 | 0.249335 | intron-variant | RNF6 | GRCh38.p7 | 13:26137520 | CAAAGTCTAGACTTT[A/G]GGCTTATTAGACAGA | 6049 |
rs73158238 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | RNF6 | GRCh38.p7 | 13:26141927 | AAAAGAAACTATCAG[A/T]AGAGTACAGACAACC | 6049 |
rs73158239 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | RNF6 | GRCh38.p7 | 13:26146195 | GGAGAAGTGTTAACA[A/G]TATGAATTTTTGGCA | 6049 |
rs73158240 | snp | A/C/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26147761 | TCTTATTTTCAGCAA[A/C/T]CTCAGGTCTGTGGCT | 6049 |
rs73158244 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | RNF6 | GRCh38.p7 | 13:26159837 | AATACAATAACGAAT[A/G]TAAGGAGTATATGAA | 6049 |
rs73158245 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF6 | GRCh38.p7 | 13:26161990 | CTTTTGTCTAAACAT[C/T]ACCTATCTAGGCTAT | 6049 |
rs73158247 | snp | A/G | 0.16618 | 0.23553 | intron-variant | RNF6 | GRCh38.p7 | 13:26164742 | TTACTGCCTCTCATG[A/G]ATGAGATCTTGCTTT | 6049 |
rs73158254 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | RNF6 | GRCh38.p7 | 13:26170770 | TTGTATGATTCTTAA[C/T]CACAAACCAACTGAA | 6049 |
rs73158256 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | RNF6 | GRCh38.p7 | 13:26171320 | GTAGTCATTAGGGAA[A/G]CGCAAATCAAAACCA | 6049 |
rs73158279 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RNF6 | GRCh38.p7 | 13:26187595 | CTTATTGGGTGACTT[A/G]GTGGGTATGTTAATG | 6049 |
rs73158289 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | RNF6 | GRCh38.p7 | 13:26194429 | CCAGAGGCATAGGCT[C/T]GCTAAAAGACTAATA | 6049 |
rs73158290 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | RNF6 | GRCh38.p7 | 13:26195152 | CAACTATGATTAATG[A/G]ATAAAGTAGACAGCA | 6049 |
rs73158291 | snp | C/T | 0.140919 | 0.224948 | intron-variant | RNF6 | GRCh38.p7 | 13:26195626 | ACAGAAAATCAAAGA[C/T]AAATTAAAAATCCTG | 6049 |
rs73158293 | snp | A/G | 0.499846 | 0.00878459 | intron-variant | RNF6 | GRCh38.p7 | 13:26198130 | TGTGTGTGTGTGTGT[A/G]TATATATATATATAC | 6049 |
rs73158296 | snp | C/T | 0.078151 | 0.181571 | intron-variant | RNF6 | GRCh38.p7 | 13:26199762 | CTATAGAGAGAGAGA[C/T]AGATGAAGATACATT | 6049 |
rs73158297 | snp | C/T | 0.140919 | 0.224948 | intron-variant | RNF6 | GRCh38.p7 | 13:26200101 | TAATCTTGCACTTCC[C/T]GACCTCCAGAACTGT | 6049 |
rs73158301 | snp | A/T | | | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26223620 | CTCCCTCTATATATA[A/T]AACCCTATTTTAGCA | 6049 |
rs73482829 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | RNF6 | GRCh38.p7 | 13:26135668 | TAATGGTAAATATGA[A/G]ATGTGACTCCTAAGG | 6049 |
rs73482830 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | RNF6 | GRCh38.p7 | 13:26136818 | CCTTTCCTCTATAAA[A/G]AACACAATGAGAAAA | 6049 |
rs73482838 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | RNF6 | GRCh38.p7 | 13:26144337 | ATTAAAGTTCTCCTT[G/T]GCTGAGGTGACCCCT | 6049 |
rs73482839 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RNF6 | GRCh38.p7 | 13:26145289 | GATCTATTTGTCTTA[C/T]GCTCAGGTGATCGGA | 6049 |
rs73482854 | snp | C/G | 0.0379877 | 0.132479 | intron-variant | RNF6 | GRCh38.p7 | 13:26157076 | CAGTGCTGGGGAAAC[C/G]GGGAATGACTGCTAG | 6049 |
rs73482877 | snp | A/G | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26174596 | TGAATCCGGGAGGCG[A/G]AGACTCAAAAAAAAG | 6049 |
rs73489456 | snp | C/T | 0.0174175 | 0.0916809 | downstream-variant-500B | RNF6 | GRCh38.p7 | 13:26131968 | TCCTCCTAAGAAACT[C/T]GTAGTGGAAAATGTG | 6049 |
rs74040354 | snp | C/G | 0.0644693 | 0.167566 | intron-variant | RNF6 | GRCh38.p7 | 13:26144895 | CTTCCATTTGGCAAT[C/G]GAGTGCTATTGTGCA | 6049 |
rs74040359 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | RNF6 | GRCh38.p7 | 13:26156341 | GCTATAAGCCATTAC[A/G]CATCAGTTAATACAT | 6049 |
rs74040375 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RNF6 | GRCh38.p7 | 13:26157906 | GATGGATGGATGGAT[A/G]GATGGATGGATGGAT | 6049 |
rs74040380 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | RNF6 | GRCh38.p7 | 13:26168467 | ATGAAGTGTCGTTTT[G/T]GGGCAGGGGTAGGAC | 6049 |
rs74040404 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | RNF6 | GRCh38.p7 | 13:26192578 | ATTAGATTATGTGAT[A/G]TTTTTACATCTGTCA | 6049 |
rs74241261 | snp | A/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26189730 | TAAGCTCCTTGGAGA[A/T]AGAGATTTCACAGTC | 6049 |
rs74318308 | snp | C/G | 0.0111196 | 0.0737302 | upstream-variant-2KB, utr-variant-5-prime | RNF6 | GRCh38.p7 | 13:26222498 | CACTTAACTCTGCGC[C/G]TCGGTGTCGCTCGTT | 6049 |
rs74415080 | snp | A/G | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26143272 | TAAGGGATCTCCTGT[A/G]TTCTAGACTCTTCCT | 6049 |
rs74417622 | snp | G/T | 0.127599 | 0.217986 | intron-variant | RNF6 | GRCh38.p7 | 13:26211713 | CAGCGAGCCGAGATA[G/T]TGCCACTGCACTCAA | 6049 |
rs74512319 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RNF6 | GRCh38.p7 | 13:26204023 | CAGCCTCCTTCCTTC[C/T]CTTTCTTCTCTGGAA | 6049 |
rs74518983 | snp | A/C | 0.0399052 | 0.1355 | intron-variant | RNF6 | GRCh38.p7 | 13:26190640 | CCTCACCTTGTATCC[A/C]CATAACACACCCAAC | 6049 |
rs74580298 | snp | A/G | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26136109 | CAGTGACCTACATCA[A/G]TAATTGTTCCTCAAA | 6049 |
rs74680701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26175819 | CCGATTTGAAAATGC[A/G]CATGGAAAACAACAG | 6049 |
rs74851210 | snp | A/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26137232 | TGAAAATGTCTACAG[A/T]AAAGTGCATTAATAT | 6049 |
rs74886408 | snp | A/C | 0.0667028 | 0.170006 | intron-variant | RNF6 | GRCh38.p7 | 13:26176938 | GACTCGGTCTCAAAA[A/C]AACAAACTAACATAC | 6049 |
rs74919728 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RNF6 | GRCh38.p7 | 13:26189476 | TATCTGTGTTCATAC[A/G]AAATTTCATATTTCA | 6049 |
rs75026201 | snp | A/G | 0.104859 | 0.203554 | intron-variant | RNF6 | GRCh38.p7 | 13:26187420 | AGCTCTGGTGTGCAA[A/G]AAAAATGCCTCTTTT | 6049 |
rs75158260 | snp | G/T | 0.111576 | 0.20818 | intron-variant | RNF6 | GRCh38.p7 | 13:26176115 | TAAGGCGTGAGGCCT[G/T]ATGTGAACTAATGAA | 6049 |
rs75285054 | snp | A/G | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26143278 | ATCTCCTGTATTCTA[A/G]ACTCTTCCTTATCTA | 6049 |
rs75497456 | snp | G/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26137237 | ATGTCTACAGAAAAG[G/T]GCATTAATATTGCAG | 6049 |
rs75526494 | in-del | -/AAA | | | intron-variant | RNF6 | GRCh38.p7 | 13:26170250 | TTTACAAAAAAAAAA[-/AAA]GCTTTGAAGAGTCAA | 6049 |
rs75626353 | snp | A/T | 0.102014 | 0.201495 | intron-variant | RNF6 | GRCh38.p7 | 13:26216228 | GTCTATAAACTGGAG[A/T]TAATAATAGAATCAA | 6049 |
rs75629890 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RNF6 | GRCh38.p7 | 13:26216253 | AATCAATCTCATAGG[A/G]TTATCCTGAGGATAA | 6049 |
rs75888585 | snp | C/G | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26195273 | GCTGCCTTTGGGGGG[C/G]GGCTTATTAGTAGAC | 6049 |
rs75894900 | snp | A/C | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26170241 | ATGCTGGATTTTACA[A/C]AAAAAAAAAAAGCTT | 6049 |
rs75905910 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF6 | GRCh38.p7 | 13:26170799 | AATTAACTTACAAAG[G/T]TTGGAGAAAGGGAAT | 6049 |
rs75962186 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF6 | GRCh38.p7 | 13:26158114 | ACAGAGACTCCAGGA[C/T]TCCAGGAAGGTAGGA | 6049 |
rs75978135 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | RNF6 | GRCh38.p7 | 13:26200196 | CAGACCAAGGCAATA[C/T]CTGACATCATCAATC | 6049 |
rs76154673 | snp | C/T | 0.352721 | 0.227922 | intron-variant | RNF6 | GRCh38.p7 | 13:26203351 | TCAAGAAATAGATAA[C/T]AGATTGCAGGTGGTT | 6049 |
rs76389185 | snp | G/T | | | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26223596 | ATGTCCCTTTTGGGG[G/T]CTCCCATACTCCCTC | 6049 |
rs76390961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF6 | GRCh38.p7 | 13:26136018 | AGTCTGGAGAATCAT[A/G]AGCCAAATAAACCTC | 6049 |
rs76392965 | snp | A/G | 0.124837 | 0.216412 | intron-variant | RNF6 | GRCh38.p7 | 13:26198814 | GCTCAAAATACAAAA[A/G]TCAATTGTACAGGTA | 6049 |
rs76443192 | snp | C/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26174652 | AAAGTTACTCACCCC[C/T]TTAGGCTGGGGAGAC | 6049 |
rs76470452 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | RNF6 | GRCh38.p7 | 13:26164448 | ATGTGTCTCCATTGT[C/T]CCCTTTTTTAACCCT | 6049 |
rs76470547 | snp | C/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26157964 | TAGCTAGAAGATAGA[C/T]AGATAGATAGATAGA | 6049 |
rs76523439 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | RNF6 | GRCh38.p7 | 13:26201808 | TAAAATAATAACTTA[A/T]GGTTAAATGAGGCCC | 6049 |
rs76569396 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF6 | GRCh38.p7 | 13:26132473 | AATAAAACCAAAGAG[A/G]GAAAAATAAAAGTAG | 6049 |
rs76703346 | snp | C/G | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26147687 | AGAGTAGAACTCCCT[C/G]TGAAGCTGGGAGTTT | 6049 |
rs76797834 | snp | G/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26160669 | TTGGATGATGTATTA[G/T]ATGGCTAGGGTTGCC | 6049 |
rs76853305 | snp | C/G | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26176158 | AGGACAGAGGGGTTG[C/G]CTGGTAAACTCTCTG | 6049 |
rs76854714 | snp | A/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26137234 | AAAATGTCTACAGAA[A/G]AGTGCATTAATATTG | 6049 |
rs76903109 | snp | A/C | 0.225597 | 0.248806 | intron-variant | RNF6 | GRCh38.p7 | 13:26160098 | TGCCCCTCTAGAAAA[A/C]AAAATTGCCTTAAAT | 6049 |
rs76918296 | snp | A/T | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26155369 | TTTCTTTTTTTTTTT[A/T]AATTCTACTTTGTGT | 6049 |
rs76958022 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | RNF6 | GRCh38.p7 | 13:26179940 | AGGCAAGAAGTTGCT[A/G]AAGAATCAAAGAAGG | 6049 |
rs76967235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF6 | GRCh38.p7 | 13:26138808 | ATCTATTTAGCATAA[A/G]AGAAGGCAGGTTTGT | 6049 |
rs76992390 | snp | C/G | 0.227074 | 0.248947 | intron-variant | RNF6 | GRCh38.p7 | 13:26146315 | TGCATTGACACTGCT[C/G]TTCATTATGGTAACC | 6049 |
rs77030346 | snp | C/T | 0.109814 | 0.206997 | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26222973 | CTCCCAACATTCCTC[C/T]CTCTGATTTTATTTC | 6049 |
rs77152643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26142901 | TCACAATCAACACAG[C/T]TTATGTTACATGATA | 6049 |
rs77354185 | snp | C/G | 0.227369 | 0.248974 | intron-variant | RNF6 | GRCh38.p7 | 13:26134764 | TTCCCAGAAATCAAA[C/G]TCTGTAATTGCACTT | 6049 |
rs77443961 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | RNF6 | GRCh38.p7 | 13:26201597 | ATAAAGCACTTGTTT[G/T]ATTCAATTCTACATT | 6049 |
rs77548022 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RNF6 | GRCh38.p7 | 13:26190150 | TGGCCCTCTTCCTCC[A/G]TCTTCAAAGCCAGCA | 6049 |
rs77562004 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF6 | GRCh38.p7 | 13:26208753 | TCTGATCCCAATTGG[C/T]TGGAGTAAAGAAGGT | 6049 |
rs77593332 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | RNF6 | GRCh38.p7 | 13:26181126 | TCCTGTACTTGACAA[G/T]GCACCGGACTAGATC | 6049 |
rs77612507 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF6 | GRCh38.p7 | 13:26181692 | GACCAAGGGGATTCC[C/T]CTTGGCATCAAGCAG | 6049 |
rs77631085 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF6 | GRCh38.p7 | 13:26191893 | AAGCATTGCTATAAA[A/G]ATGACATTTGAGTAA | 6049 |
rs77676730 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | RNF6 | GRCh38.p7 | 13:26184769 | CTTACATTTTCTATG[A/G]GTGAAAATAACGTAG | 6049 |
rs77697732 | snp | A/G | 0.227369 | 0.248974 | intron-variant | RNF6 | GRCh38.p7 | 13:26158719 | TAGGTGAATGTCTGT[A/G]TGTGGGTGTGTGTGT | 6049 |
rs77756616 | snp | C/T | 0.122411 | 0.214991 | intron-variant | RNF6 | GRCh38.p7 | 13:26178919 | ACTTATTTCACTTAG[C/T]ATAATGTCCTCCAGA | 6049 |
rs77876950 | snp | C/T | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26186776 | GACCTTTCTTCTTCT[C/T]TTTTTTTTTTTCTTT | 6049 |
rs78105491 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | RNF6 | GRCh38.p7 | 13:26143368 | AAAGTAACTGTCTTA[C/T]TTGCCTGTTGATTCA | 6049 |
rs78105823 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | RNF6 | GRCh38.p7 | 13:26132213 | TTCAAAGCCAAGTAC[A/G]ATATGAACAAGTACA | 6049 |
rs78127460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26170301 | GCCAAAATTTAATCA[A/G]AAGCAAAATCCAGAT | 6049 |
rs78177864 | snp | A/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26137235 | AAATGTCTACAGAAA[A/G]GTGCATTAATATTGC | 6049 |
rs78300986 | snp | A/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26173948 | GAGCGAGACTCCGTC[A/T]CAAAAAAAAAAAAAA | 6049 |
rs78315084 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | RNF6 | GRCh38.p7 | 13:26191803 | TACAGTTGGTGATAT[A/G]TGTTATGGAGGAATA | 6049 |
rs78376826 | snp | C/T | 0.2768 | 0.248559 | intron-variant | RNF6 | GRCh38.p7 | 13:26147181 | CACATGTTCCCCAGC[C/T]TTCTGCCTGTGCATA | 6049 |
rs78545974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF6 | GRCh38.p7 | 13:26170370 | GAATTTCCCCTGACT[C/T]GTTGACGGTCCTATA | 6049 |
rs78564163 | snp | A/T | 0.5 | 0 | downstream-variant-500B | RNF6 | GRCh38.p7 | 13:26131924 | GAGAGAGACTCCATA[A/T]AAAAAAAAAAAAAAA | 6049 |
rs78637150 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF6 | GRCh38.p7 | 13:26171893 | ATAATAGAAGTTATC[A/G]GGGCTAGGGGAAGGG | 6049 |
rs78676723 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF6 | GRCh38.p7 | 13:26145204 | CAAGTGATAAAATCA[C/T]ATCTGGTGCAACAGC | 6049 |
rs79006540 | snp | C/T | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26155359 | CCATGGTATGTTTCT[C/T]TTTTTTTTTTAATTC | 6049 |
rs79041288 | snp | A/G | 0.119281 | 0.213102 | intron-variant | RNF6 | GRCh38.p7 | 13:26200034 | CTTATGAAGACAGCC[A/G]TCTATGAACCAGAAA | 6049 |
rs79224917 | snp | A/G | 0.228253 | 0.249052 | intron-variant | RNF6 | GRCh38.p7 | 13:26143892 | ATGGAATACTATGAC[A/G]GTGGATAAGGCATTC | 6049 |
rs79282962 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RNF6 | GRCh38.p7 | 13:26192909 | CGCACAGAAACTGTA[A/C]TATAATAAACGTGGT | 6049 |
rs79369778 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | RNF6 | GRCh38.p7 | 13:26156628 | TTTTAAAAAACAAAT[G/T]TTCAAATAACAGAAA | 6049 |
rs79418394 | snp | A/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26156404 | GAAGGAAACGACAGA[A/C]ACAAAATGGTGGAGA | 6049 |
rs79611419 | snp | G/T | 0.0599851 | 0.162463 | intron-variant | RNF6 | GRCh38.p7 | 13:26134976 | TTAACAAAAAAAGAT[G/T]GGTAAACAAACGTGA | 6049 |
rs79738614 | in-del | -/T/TT | | | intron-variant | RNF6 | GRCh38.p7 | 13:26144391 | TTCATTTTTTTTTTT[-/T/TT]CACTATTTCAGAGAG | 6049 |
rs79803113 | snp | A/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26193967 | AGTAGATTATTATCT[A/T]GAATAAGAACGGAAC | 6049 |
rs79888139 | snp | A/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26153160 | TCTGTCTCAAGAAAA[A/G]AAAAAAAAAAGAAAA | 6049 |
rs79956134 | snp | A/C | | | intron-variant | RNF6 | GRCh38.p7 | 13:26147584 | TCAAAATTTAGGAGT[A/C]AATGTCCTCAGCTTC | 6049 |
rs80087748 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | RNF6 | GRCh38.p7 | 13:26180648 | GTCTGTCTCTGACTT[C/T]ATGTCCGTATTCCAG | 6049 |
rs80220761 | snp | C/T | 0.230603 | 0.249246 | intron-variant | RNF6 | GRCh38.p7 | 13:26162160 | GATATAAAAACTAAC[C/T]AACGCAGAGCCACAC | 6049 |
rs80241917 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF6 | GRCh38.p7 | 13:26184342 | GGCCGCCTCAAATTA[C/T]ATTCTAATCAGTCTC | 6049 |
rs80274387 | snp | A/G | 0.114387 | 0.210022 | intron-variant | RNF6 | GRCh38.p7 | 13:26176106 | GTGGTTGTCTAAGGC[A/G]TGAGGCCTGATGTGA | 6049 |
rs111228367 | in-del | -/T | 0.0752113 | 0.178743 | intron-variant | RNF6 | GRCh38.p7 | 13:26193660 | AGGTAGTTGGAAGGG[-/T]AAGTAAAATCAAGAG | 6049 |
rs111241960 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | RNF6 | GRCh38.p7 | 13:26166791 | CAGGCATGGTGGTGC[A/G]TGCCTGTAATCCCAG | 6049 |
rs111293705 | snp | A/G | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26200702 | GAGCCACCATGCCTG[A/G]CCTGAAATTCTTAAT | 6049 |
rs111314589 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RNF6 | GRCh38.p7 | 13:26142535 | CACCATGGAATACTA[C/T]GCAGCCATAAAAAGA | 6049 |
rs111332183 | snp | A/C | 0.5 | 0 | missense, intron-variant | RNF6 | GRCh38.p7 | 13:26214740 | CTGCTGGATTCTTCT[A/C]CTTCTTCTACTGTTA | 6049 |
rs111347479 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | RNF6 | GRCh38.p7 | 13:26140070 | ATGTCTACAAACTTG[C/T]TAATCTCTTTGTTAA | 6049 |
rs111403417 | snp | C/T | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26178863 | CTATTTTAGATCCCA[C/T]ATATAAGTGAGATCA | 6049 |
rs111424416 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | RNF6 | GRCh38.p7 | 13:26166541 | ATACAAAAATCCCTA[A/G]CATTCCTATACACCA | 6049 |
rs111488997 | in-del | -/TATTT | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26153191 | ACTAAAGATGTAAGA[-/TATTT]TATTTTATTTTATTT | 6049 |
rs111564273 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF6 | GRCh38.p7 | 13:26156838 | AAATCAGTAGACCCT[C/T]GTTACCTACACTGAA | 6049 |
rs111599883 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | RNF6 | GRCh38.p7 | 13:26145035 | TTGTGACACAGAGTT[C/G]ATATACTCCTGAAGT | 6049 |
rs111652519 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF6 | GRCh38.p7 | 13:26143648 | ACCATATATTGGATG[C/T]TGATGCAGAGAATGT | 6049 |
rs111655819 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF6 | GRCh38.p7 | 13:26149448 | AAAAATTAGCTGAGC[A/G]TGGTGGCAGGCGCCT | 6049 |
rs111666817 | snp | C/T | 0.114036 | 0.209795 | intron-variant | RNF6 | GRCh38.p7 | 13:26184069 | TCTCGCTCTGTTGCT[C/T]AGGCTGGAGTGCAGT | 6049 |
rs111706868 | snp | C/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26160537 | CCTATCTTCTTCTCT[C/T]CTTCTTCTTTTTTTT | 6049 |
rs111718552 | snp | A/C/G | 0.0244538 | 0.107838 | intron-variant | RNF6 | GRCh38.p7 | 13:26211619 | GAAAATTCGCCGGGC[A/C/G]TGGTGGCGCATGTCT | 6049 |
rs111727886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26179728 | CCTCACACACCCAGC[A/G]ACCTCCTTGGATCCA | 6049 |
rs111749740 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | RNF6 | GRCh38.p7 | 13:26199684 | AATACTCCTAATACA[C/T]AAAGAATTATTGCAA | 6049 |
rs111762057 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RNF6 | GRCh38.p7 | 13:26177280 | AGCGACTCTACTTCA[C/T]TGACTCCCATTCACT | 6049 |
rs111790811 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RNF6 | GRCh38.p7 | 13:26182449 | TTATTGATGATAAAT[G/T]GATCATCTAATTAAA | 6049 |
rs111799222 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | RNF6 | GRCh38.p7 | 13:26194961 | GTTAATCTCCTTTGG[C/T]GATACCCTCACAGAT | 6049 |
rs111809400 | snp | C/G | 0.0729998 | 0.176553 | intron-variant | RNF6 | GRCh38.p7 | 13:26166731 | TCAAGACCAACCTGG[C/G]CAACAAGGTGAAACC | 6049 |
rs111812058 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | RNF6 | GRCh38.p7 | 13:26148403 | TTGTGATAATTTGCA[G/T]ATTTCTATGGCCAGA | 6049 |
rs111816388 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | RNF6 | GRCh38.p7 | 13:26169599 | ATAAATCTTCTTAAG[A/T]GTCTCTTGCCGGCCT | 6049 |
rs111843437 | snp | C/T | 0.00716266 | 0.059414 | utr-variant-5-prime, upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26222239 | CAGGCCCCAGCCCTT[C/T]TTTCCCGACAGCCAC | 6049 |
rs111857740 | snp | C/T | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26161813 | AACGCACTCTTCCCC[C/T]TTGCCCTGCCTAGCA | 6049 |
rs111865527 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF6 | GRCh38.p7 | 13:26161910 | GGGAATCCAATGTCA[C/T]GTTGTCAGTTGACCC | 6049 |
rs111892986 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | RNF6 | GRCh38.p7 | 13:26156879 | GTAACAGATGGGAGT[C/T]TATATAACATGGGGA | 6049 |
rs111980610 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | RNF6 | GRCh38.p7 | 13:26163289 | TGCACTCCAGCCTGG[A/G]AGACAGAGAGAGACT | 6049 |
rs112087406 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF6 | GRCh38.p7 | 13:26186665 | CCGCAGCGGCGCTAT[A/G]CCTTCGGCCACAGGT | 6049 |
rs112115155 | snp | A/G | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26201412 | AGGTGGAATGGAGGA[A/G]GGGTAATTCTTTCAA | 6049 |
rs112128789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26173829 | GGTGGTGTATGCCTG[C/T]AATCCTAGCTACTCG | 6049 |
rs112172241 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | RNF6 | GRCh38.p7 | 13:26188941 | CTCAGAACAGATTTC[C/T]GAAGAGGTTGTATGC | 6049 |
rs112291698 | snp | A/G | 0.039522 | 0.134904 | intron-variant | RNF6 | GRCh38.p7 | 13:26173279 | ATATGCATTTCAGCC[A/G]TGCTTGTAACAGTGA | 6049 |
rs112297672 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RNF6 | GRCh38.p7 | 13:26152808 | AGGGAGAAGTCAGCA[C/T]GGACTATAGCATTTG | 6049 |
rs112299048 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | RNF6 | GRCh38.p7 | 13:26166603 | TGCAATCTCATTCAC[A/T]CTTGCCACAAAAAGA | 6049 |
rs112388573 | snp | C/T | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26159420 | ACAAGGTCAGCAGAT[C/T]GAGACCATCCTGGAT | 6049 |
rs112466268 | snp | A/T | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26164878 | AAAAGTTCAAAAAAT[A/T]TGCAGCCTGATGATG | 6049 |
rs112471447 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | RNF6 | GRCh38.p7 | 13:26135263 | CATCAGAGAACTAAT[A/T]GCTTCAAAACAATAT | 6049 |
rs112525150 | snp | A/G | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26187268 | TGATAGGAGACGAAT[A/G]GAAAGGGGGAAAGCC | 6049 |
rs112600131 | snp | A/G | 0.239037 | 0.24976 | downstream-variant-500B | RNF6 | GRCh38.p7 | 13:26131755 | ATATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 6049 |
rs112608841 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | RNF6 | GRCh38.p7 | 13:26182675 | CTGGGCATGGTGGCA[C/T]ACACCTGTAGTCCCA | 6049 |
rs112629958 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RNF6 | GRCh38.p7 | 13:26168750 | GGCATAGTGGCTCAC[A/G]CCAATAATCCTAGCA | 6049 |
rs112644265 | snp | C/T | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26133669 | TCTAAAATTTCTAGC[C/T]GGATGTTTCTTGTAC | 6049 |
rs112776933 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RNF6 | GRCh38.p7 | 13:26177062 | CAAGAAGGAAAGATC[A/G]GCGGGGACCACCAGA | 6049 |
rs112842895 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | RNF6 | GRCh38.p7 | 13:26190014 | TGCATTAGAAATCCA[A/G]CACAGGTCTCACGGG | 6049 |
rs112879755 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF6 | GRCh38.p7 | 13:26137708 | GCCCAATAACTGAAA[C/T]GAGAAATTCACTAGA | 6049 |
rs112917635 | snp | C/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26181270 | TGAACTGCAGAGCAC[C/T]TCCAGGATGTGCACT | 6049 |
rs112924946 | snp | C/T | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26219733 | TTGGCTTTGTATTTT[C/T]AACTTGCAGTTTTTC | 6049 |
rs113096888 | snp | A/G | 0.311369 | 0.242351 | intron-variant | RNF6 | GRCh38.p7 | 13:26165989 | ttgggagggaccagg[A/G]gtggaatgttatggt | 6049 |
rs113102214 | snp | C/G | 0.0379877 | 0.132479 | intron-variant | RNF6 | GRCh38.p7 | 13:26180645 | AAAGTCTGTCTCTGA[C/G]TTTATGTCCGTATTC | 6049 |
rs113102717 | snp | A/G | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26182349 | TCTTTGCTTCCTCAA[A/G]TTAAATTTGGCAAAA | 6049 |
rs113122741 | snp | A/T | 0 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26160528 | TGCATCCAGCCTATC[A/T]TCTTCTCTTCTTCTT | 6049 |
rs113151595 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RNF6 | GRCh38.p7 | 13:26142493 | TCCATCAGTGGTGGA[C/T]TGGATAAAGAAAATG | 6049 |
rs113288161 | snp | A/G | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26132485 | GAGAGAAAAATAAAA[A/G]TAGAAGTTTAATGTA | 6049 |
rs113357626 | snp | A/G | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26193711 | GCATACTGAAGGAAT[A/G]ATCCAGTACAAGAAT | 6049 |
rs113390269 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | RNF6 | GRCh38.p7 | 13:26173442 | AGATCTCAAAAACCT[A/T]AGAGTGATGTGAAAA | 6049 |
rs113531188 | snp | A/G | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26165255 | GCCTGCCAGTGCACC[A/G]AAGTCAAGAATTGAG | 6049 |
rs113556749 | snp | G/T | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26201065 | ATTCATGCTGATAAT[G/T]AATAGCATGAATAGC | 6049 |
rs113594946 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RNF6 | GRCh38.p7 | 13:26181512 | CCACTGCAGGTAGTG[C/T]AACCCATTGGGTGGA | 6049 |
rs113604471 | snp | A/G | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26193985 | ATAAGAACGGAACAG[A/G]AAGTAATGGAATTTT | 6049 |
rs113615660 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | RNF6 | GRCh38.p7 | 13:26145904 | AGGATTTTTCCAGCT[A/G]CTTGTGTATTCCAGA | 6049 |
rs113743717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF6 | GRCh38.p7 | 13:26218692 | CTAATCTTTAGTAAC[C/T]TATAGAAGACAAATG | 6049 |
rs113773605 | snp | C/G | 0.0704125 | 0.17392 | intron-variant | RNF6 | GRCh38.p7 | 13:26199304 | CATATGCTGCTGGTA[C/G]AAATGGATATCCATA | 6049 |
rs113831161 | snp | A/G/T | 0.00557542 | 0.0525036 | intron-variant | RNF6 | GRCh38.p7 | 13:26171765 | ATGAAACTTCAAGAC[A/G/T]TTATGCTTGGTGAAA | 6049 |
rs113863442 | snp | A/G | 0.5 | 0 | intron-variant | RNF6 | GRCh38.p7 | 13:26154129 | CTTTGGTAAACTGCA[A/G]GTACAAAAATCGAGG | 6049 |
rs113946897 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RNF6 | GRCh38.p7 | 13:26135665 | TAATAATGGTAAATA[C/T]GAAATGTGACTCCTA | 6049 |
rs113982202 | snp | C/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26151495 | CTCAAACTCCTGACC[C/T]CAGGTGATCCACCTG | 6049 |
rs114008142 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF6 | GRCh38.p7 | 13:26215808 | TACATAGTTACAAAG[C/T]TTTAAATACTATTTA | 6049 |
rs114020164 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | RNF6 | GRCh38.p7 | 13:26160190 | AATTAAAGAGAATCT[A/G]CTTAGTATCAAAATT | 6049 |
rs114020915 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF6 | GRCh38.p7 | 13:26173507 | TAAATGTTTAAAAAG[C/T]CCTACAATTTCATAT | 6049 |
rs114026154 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | RNF6 | GRCh38.p7 | 13:26140446 | TCAGTAAAATCCAAC[A/C]TCCCTTCATGATAAA | 6049 |
rs114095378 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF6 | GRCh38.p7 | 13:26174230 | TCGGTGCCTGTCTCA[C/T]AGGATTTCGAGGGCA | 6049 |
rs114310462 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RNF6 | GRCh38.p7 | 13:26220081 | TAATGAGCAAAGGGA[C/T]ACTGGGATGATATAA | 6049 |
rs114358188 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | RNF6 | GRCh38.p7 | 13:26152032 | CCAACCTTCTGCGGG[A/T]AACACACCAACCTCT | 6049 |
rs114365565 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RNF6 | GRCh38.p7 | 13:26181003 | CCAGGTATTGTAACC[C/T]AGTCTGTTTGTCCAG | 6049 |
rs114386671 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RNF6 | GRCh38.p7 | 13:26143388 | CTGTTGATTCAGAAG[A/C]ATGAGGAGCCCAAAG | 6049 |
rs114387003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26192911 | CACAGAAACTGTAAT[A/G]TAATAAACGTGGTAT | 6049 |
rs114387984 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | RNF6 | GRCh38.p7 | 13:26158006 | ATAGATAGAAGAAGT[C/T]ATTGGATGGATAAAT | 6049 |
rs114388761 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | RNF6 | GRCh38.p7 | 13:26172851 | CCCGGCCTAGAATAT[A/G]TCTTTACTGTATATA | 6049 |
rs114391154 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF6 | GRCh38.p7 | 13:26193840 | TTTGAAGCACAGACA[A/G]TATGTGAGAAAAGAG | 6049 |
rs114391352 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | RNF6 | GRCh38.p7 | 13:26135759 | GGCCTAGGAGGTGGT[A/G]TTTGCATCATGGGGG | 6049 |
rs114423490 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | RNF6 | GRCh38.p7 | 13:26137542 | TTAGACAGAACTTTT[C/T]ATCAGTTATGTTGAG | 6049 |
rs114449839 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | RNF6 | GRCh38.p7 | 13:26137821 | AAACAGCATGCATAA[A/T]AAATTAAGAAAAACA | 6049 |
rs114456061 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | RNF6 | GRCh38.p7 | 13:26164855 | GTTTTATAACAGAAG[A/C]AGAGCATAAAAGTTC | 6049 |
rs114465547 | snp | A/G | 0.0111196 | 0.0737302 | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26223212 | TATGCTGGGCACCTG[A/G]ATAACAAGCTACATG | 6049 |
rs114533312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF6 | GRCh38.p7 | 13:26208388 | AGCTTTTCTGGTAGA[C/T]AACACTTCTCTCATG | 6049 |
rs114551346 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF6 | GRCh38.p7 | 13:26221457 | TTTTGTTAGACACAT[C/T]TAGAAAATTAGATCC | 6049 |
rs114555353 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | RNF6 | GRCh38.p7 | 13:26197915 | AAGGTTTTCAGGAAG[A/C]CCCCGTAACATCTTG | 6049 |
rs114632229 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | RNF6 | GRCh38.p7 | 13:26190723 | AACATTTGAACACCT[A/G]TGATATGTGGGTGCT | 6049 |
rs114655096 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RNF6 | GRCh38.p7 | 13:26202602 | AGCTTCTTATCTCTT[A/G]CTTCACAGCATCACT | 6049 |
rs114688292 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | RNF6 | GRCh38.p7 | 13:26146979 | AGGTCTTACCAGCCA[C/T]GATTCTTGTACAGCC | 6049 |
rs114691721 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF6 | GRCh38.p7 | 13:26195928 | TTATTCATCAGCATC[A/G]TAATGAGATAAACCC | 6049 |
rs114717968 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | RNF6 | GRCh38.p7 | 13:26210611 | AAATTAGAAAAATAT[A/C]TTTAGGAGGAATTAA | 6049 |
rs114722355 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF6 | GRCh38.p7 | 13:26139493 | GTAGCATTGACCACC[C/T]TGTGTCACCACTCAG | 6049 |
rs114728440 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RNF6 | GRCh38.p7 | 13:26152809 | GGGAGAAGTCAGCAT[A/G]GACTATAGCATTTGG | 6049 |
rs114732803 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | RNF6 | GRCh38.p7 | 13:26146029 | AAACCCCTACTTTAA[C/G]TGGTAGACCACAGTG | 6049 |
rs114756556 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | RNF6 | GRCh38.p7 | 13:26176251 | TCTTCTCTAACTGTA[C/G]TTTTCCTTTTGCTTT | 6049 |
rs114770774 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RNF6 | GRCh38.p7 | 13:26148937 | CATGCAGGAGGAATT[C/T]TCTCTTGCTCAGGGA | 6049 |
rs114884131 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RNF6 | GRCh38.p7 | 13:26205462 | GACTGGACTAGTTCA[A/G]AAAATGCCTTTCCAT | 6049 |
rs114886374 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | RNF6 | GRCh38.p7 | 13:26160932 | CAGTCAGAATGGATC[A/G]GGGCTGACTTTAATG | 6049 |
rs114887674 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | RNF6 | GRCh38.p7 | 13:26199105 | CCCAATGTTCTTTTA[C/T]ATAGACATTAACAAG | 6049 |
rs114901119 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF6 | GRCh38.p7 | 13:26184945 | AGCTCCAAAGTGCGC[C/T]GCAGGAAATTATTTT | 6049 |
rs114919624 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF6 | GRCh38.p7 | 13:26153892 | TCAGCCCCAAAATGG[A/G]ATTTCAGTGTCTCAC | 6049 |
rs114920288 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | RNF6 | GRCh38.p7 | 13:26136463 | CTGCTTCCATTTAAC[C/T]TCAACAGTTAGGGGA | 6049 |
rs114960872 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RNF6 | GRCh38.p7 | 13:26146249 | GGACTCAGCAACACA[A/G]GTTTGGAAGTCTGGA | 6049 |
rs114962511 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | RNF6 | GRCh38.p7 | 13:26158146 | AGAGGAGCCAGGGAA[A/G]CTACAGTAACCTCAG | 6049 |
rs114965935 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF6 | GRCh38.p7 | 13:26152216 | ACATTCAACACGTTT[C/T]ACAATTCAAAACATA | 6049 |
rs114990048 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | RNF6 | GRCh38.p7 | 13:26207811 | GGGGCACTCCTGCTA[A/C/T]CCATTCTGGCCCCTT | 6049 |
rs115005424 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | RNF6 | GRCh38.p7 | 13:26174250 | TTTCGAGGGCAAGAG[G/T]CTGGAATGAAAGAGG | 6049 |
rs115118579 | snp | C/G/T | 0.0126979 | 0.078662 | intron-variant | RNF6 | GRCh38.p7 | 13:26179627 | AGTGGGAAGGAGAAG[C/G/T]GCTATGTCTGCCAAG | 6049 |
rs115138525 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNF6 | GRCh38.p7 | 13:26190355 | ATTTATAGATTCTAG[A/G]TATTAGGATGTAAAC | 6049 |
rs115195399 | snp | A/C | 0.0298908 | 0.118541 | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26223159 | TTTGTTCTTTCATTT[A/C]TGCATTAACTTTTGA | 6049 |
rs115221674 | snp | A/C/G | 0.0205511 | 0.0992634 | intron-variant | RNF6 | GRCh38.p7 | 13:26162512 | GTCTCCTTTTTTGCT[A/C/G]CACCTGACTGATCAT | 6049 |
rs115221849 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | RNF6 | GRCh38.p7 | 13:26167930 | GGCTATTATCCTTAG[C/T]AAACTAACACAGGAA | 6049 |
rs115239929 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RNF6 | GRCh38.p7 | 13:26157941 | AGATGGATAGATGGA[C/T]GGCTAGCTAGCTAGA | 6049 |
rs115241887 | snp | A/T | 0.0622301 | 0.165053 | intron-variant | RNF6 | GRCh38.p7 | 13:26192595 | TTTTACATCTGTCAT[A/T]CTAGCAGACTCTATT | 6049 |
rs115246310 | snp | G/T | 0.0310518 | 0.120672 | intron-variant | RNF6 | GRCh38.p7 | 13:26181781 | TTTGTGCTCCAGTGG[G/T]ATGCTACAGGTTCTT | 6049 |
rs115316014 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RNF6 | GRCh38.p7 | 13:26172350 | AAGGTCTAAATAGGA[A/G]AAGCAAAACTTTAAA | 6049 |
rs115323307 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | RNF6 | GRCh38.p7 | 13:26164798 | CATGTCTGCTTAAAC[A/G]ATCTTCTCCTGAATG | 6049 |
rs115395834 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | RNF6 | GRCh38.p7 | 13:26195038 | ACTCAGTTATTAACC[A/C]TCACAATGGCCAAAA | 6049 |
rs115431554 | snp | A/C | 0.0441095 | 0.141807 | intron-variant | RNF6 | GRCh38.p7 | 13:26185052 | CCCAAGCTGTAGTGA[A/C]GTGGCACAAACACGG | 6049 |
rs115435381 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | RNF6 | GRCh38.p7 | 13:26149245 | TACATCAAAAGTTCA[A/T]TCTGAATAATTCAAT | 6049 |
rs115452404 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | RNF6 | GRCh38.p7 | 13:26156308 | TTAAGGGGACGATCC[A/T]CAAATGAAGACACAA | 6049 |
rs115469820 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | RNF6 | GRCh38.p7 | 13:26187073 | TGAGCCACCGCGCCC[A/G]GCAAGCGTCAGGGAC | 6049 |
rs115473129 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RNF6 | GRCh38.p7 | 13:26202734 | ATGATCAAGAATAAA[A/C]ATAGTATGGTACATT | 6049 |
rs115523392 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RNF6 | GRCh38.p7 | 13:26137070 | AAGCTACAGCTCCTT[C/T]GAAAATCCTCATTCC | 6049 |
rs115529638 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | RNF6 | GRCh38.p7 | 13:26184898 | TCCACCAGTAGAGGG[A/C]AGCCCTCTCCCTACA | 6049 |
rs115565593 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | RNF6 | GRCh38.p7 | 13:26158687 | CCATTACATAAAATT[G/T]TATATCTATGTCTCA | 6049 |
rs115672746 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF6 | GRCh38.p7 | 13:26144937 | ATGGCTTGGTGGGTC[C/T]AGTCAGCATAATGTC | 6049 |
rs115694857 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | RNF6 | GRCh38.p7 | 13:26188137 | CCAGACCATCACAAC[G/T]GTCTTGTGGCTCATG | 6049 |
rs115728167 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RNF6 | GRCh38.p7 | 13:26139599 | ACCTGTTTAACACTT[C/T]GGTTGGAATTGCAAT | 6049 |
rs115731319 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF6 | GRCh38.p7 | 13:26207257 | AGTATGAAAGGCAAG[A/G]TGAGATACCCTGCGA | 6049 |
rs115810165 | snp | A/C | 0.0554779 | 0.157039 | intron-variant | RNF6 | GRCh38.p7 | 13:26182745 | GGGAGATCAAGGCCA[A/C]AATGAGCCATGATCA | 6049 |
rs115838871 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | RNF6 | GRCh38.p7 | 13:26157271 | CAAATTAATAAATTT[A/T]AAAAATTTTAAAAAA | 6049 |
rs115886566 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | RNF6 | GRCh38.p7 | 13:26197523 | TTTACATTGGCCAAC[C/G]CTTGTACCCATTTTT | 6049 |
rs115945347 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF6 | GRCh38.p7 | 13:26146506 | CCAGAGCTACTCACA[A/G]TTTTATTTCTCACAG | 6049 |
rs115980656 | snp | A/G | 0.102726 | 0.202016 | downstream-variant-500B, intron-variant | RNF6 | GRCh38.p7 | 13:26212723 | ATGAAATATTAGTGG[A/G]GGGTGAATAAACCAC | 6049 |
rs115989735 | snp | A/G | 0.180702 | 0.240204 | intron-variant | RNF6 | GRCh38.p7 | 13:26165173 | CTGAAAGGGGCCAAC[A/G]TAGAACTTGGGACAT | 6049 |
rs115990750 | snp | C/T | 0.0217236 | 0.101931 | utr-variant-3-prime | RNF6 | GRCh38.p7 | 13:26132305 | AAAAAAAACTGTTTG[C/T]GAAGAGAAAGATAAT | 6049 |
rs115993442 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | RNF6 | GRCh38.p7 | 13:26168614 | TTTTAAGCCTTGCAT[A/G]GTTCATAGCCAGCTC | 6049 |
rs116043485 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF6 | GRCh38.p7 | 13:26148131 | CTTCTTCACAAGGGG[A/G]CAGGAAAGAGAATGA | 6049 |
rs116082471 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | RNF6 | GRCh38.p7 | 13:26140061 | TTGCAAAATATGTCT[A/G]CAAACTTGCTAATCT | 6049 |
rs116141232 | snp | A/C | 0.0995161 | 0.199636 | intron-variant | RNF6 | GRCh38.p7 | 13:26153105 | TTGCAGTGAGCTAAG[A/C]TCTTTCCACTGCACT | 6049 |
rs116156635 | snp | C/T | 0.030665 | 0.119967 | intron-variant | RNF6 | GRCh38.p7 | 13:26139321 | AAGCTGTTTCCTCTG[C/T]CCTGCCTTGCCTTTT | 6049 |
rs116212859 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | RNF6 | GRCh38.p7 | 13:26162163 | ATAAAAACTAACCAA[C/T]GCAGAGCCACACCTC | 6049 |
rs116224758 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | RNF6 | GRCh38.p7 | 13:26205119 | CATCATTTTGTCCTG[A/C]ATAGGTTAGAAGAGG | 6049 |
rs116240549 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF6 | GRCh38.p7 | 13:26146689 | TGGACCACCTTTTCA[C/T]CTATGTTTCAGCCAA | 6049 |
rs116298066 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26224107 | GTTGAGTGGAAAAGA[C/T]ATATGTGTCTCTTCC | 6049 |
rs116308434 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | RNF6 | GRCh38.p7 | 13:26185831 | TTCTCTACGCCTAAC[A/T]ACGAACCTTGTGCCT | 6049 |
rs116384597 | snp | A/C | 0.030665 | 0.119967 | intron-variant | RNF6 | GRCh38.p7 | 13:26138948 | GGGTATCCTCAAATT[A/C]TTCTTCTTCTTTGTA | 6049 |
rs116385432 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RNF6 | GRCh38.p7 | 13:26168628 | TAGTTCATAGCCAGC[A/T]CATCCTCTCCTTCAC | 6049 |
rs116452557 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | RNF6 | GRCh38.p7 | 13:26205047 | GAGTCCCTGGAGCAA[C/T]GTGATAAATTGGCCC | 6049 |
rs116461828 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | RNF6 | GRCh38.p7 | 13:26151053 | TGTTAAATAAAAAGG[A/G]GAAGGAAAGTCTTAG | 6049 |
rs116470063 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF6 | GRCh38.p7 | 13:26197440 | AGGGCCTCTATCTCT[C/T]AGTCTCTGTGGAGGT | 6049 |
rs116478004 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | RNF6 | GRCh38.p7 | 13:26167245 | TGCACAGCAAAGGAA[A/C]CTATCTAGAGTAAAT | 6049 |
rs116489590 | snp | A/G | 0.0376037 | 0.131863 | utr-variant-3-prime | RNF6 | GRCh38.p7 | 13:26132278 | GTTGTCATATTCTAT[A/G]TTCCATAAAAGAAAA | 6049 |
rs116523356 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | RNF6 | GRCh38.p7 | 13:26186648 | CTCAGCTCTCACAGG[A/G]CCCGCAGCGGCGCTA | 6049 |
rs116524827 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | RNF6 | GRCh38.p7 | 13:26190042 | GGGGCTAAAATCAAG[G/T]TGTTGGCAGGACTGT | 6049 |
rs116536064 | snp | C/T | 0.0115144 | 0.0749975 | utr-variant-3-prime, intron-variant | RNF6 | GRCh38.p7 | 13:26213281 | ACTGAATATTTTAAC[C/T]TTAAAATTATATACC | 6049 |
rs116540336 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF6 | GRCh38.p7 | 13:26154562 | ATTGAGTAGCTGCCA[C/T]ATACTGGTATTTATC | 6049 |
rs116551910 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | RNF6 | GRCh38.p7 | 13:26198608 | GGCAATGATGTCCAC[C/T]CTCACCACTTCTACT | 6049 |
rs116633252 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | RNF6 | GRCh38.p7 | 13:26152236 | TTCAAAACATATGAA[A/G]GGATTCAGTGTGAAA | 6049 |
rs116643344 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF6 | GRCh38.p7 | 13:26171117 | TCAAGAAAATGGAAA[A/G]ACAACAGAATGGGAG | 6049 |
rs116683468 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RNF6 | GRCh38.p7 | 13:26202265 | ATGAGACAATGAGCA[C/T]GGAATCTCTTCAGAT | 6049 |
rs116699481 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RNF6 | GRCh38.p7 | 13:26168149 | AATCAATCCCCATGA[C/T]AAGAGTTTCCCTATG | 6049 |
rs116699772 | snp | A/C | 0.0622301 | 0.165053 | intron-variant | RNF6 | GRCh38.p7 | 13:26189375 | GGATGAAAATATGCC[A/C]CCTTGCCTCAATTAC | 6049 |
rs116700646 | snp | G/T | 0.0622301 | 0.165053 | intron-variant | RNF6 | GRCh38.p7 | 13:26193792 | GGATGGTTGAAGAAT[G/T]GTTGATTGAACAAAT | 6049 |
rs116707681 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RNF6 | GRCh38.p7 | 13:26216046 | TTTTTGCAACTAGGT[A/G]TTTCTGTAATCTTAG | 6049 |
rs116710782 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | RNF6 | GRCh38.p7 | 13:26210873 | AATGCTGGCTGAAAC[G/T]AAAAAAATCTAGGAA | 6049 |
rs116715251 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | RNF6 | GRCh38.p7 | 13:26153229 | TTTTATGTATTTTTT[C/T]CCAAGATGGAGTCTT | 6049 |
rs116716350 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF6 | GRCh38.p7 | 13:26181975 | TAATCAAGGATCAAA[C/T]AGCTAGCCTTCTTTA | 6049 |
rs116732611 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | RNF6 | GRCh38.p7 | 13:26145741 | AGAACAAACTAATAC[G/T]ATGGGGCACTGATCT | 6049 |
rs116762748 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | RNF6 | GRCh38.p7 | 13:26205484 | CCTTTCCATGGGATA[G/T]ATATCCATTTTCCTC | 6049 |
rs116765547 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | RNF6 | GRCh38.p7 | 13:26203497 | TGCTGTGAGAAGCAC[A/G]ACTGACTGAGAGCCT | 6049 |
rs116771795 | snp | A/G/T | 0.0209421 | 0.100162 | intron-variant | RNF6 | GRCh38.p7 | 13:26152196 | TTTATTTTTGAATAT[A/G/T]TAACACATTCAACAC | 6049 |
rs116782751 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | RNF6 | GRCh38.p7 | 13:26195808 | CACCCACACCCACAC[A/C]CACATACATACAATT | 6049 |
rs116786402 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | RNF6 | GRCh38.p7 | 13:26137288 | CAATTGGGGTAAATA[A/G]TAGATTAACTAAAGA | 6049 |
rs116840358 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | RNF6 | GRCh38.p7 | 13:26169332 | GAAGGGCAAGGAGTA[A/G]GGAAAGACGAAAGGG | 6049 |
rs116903359 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF6 | GRCh38.p7 | 13:26151892 | TTCTCTGGGGTGCAG[C/T]TCCAAGCTGGTCCCT | 6049 |
rs116907566 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF6 | GRCh38.p7 | 13:26164763 | ATCTTGCTTTCCCAC[A/G]TATTACTGTTTATTT | 6049 |
rs116913662 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | RNF6 | GRCh38.p7 | 13:26200200 | CCAAGGCAATACCTG[A/T]CATCATCAATCATTA | 6049 |
rs116920953 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF6 | GRCh38.p7 | 13:26195207 | GCAGGGATGGAAATC[C/T]TAAGAATCAAAATGA | 6049 |
rs116965581 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RNF6 | GRCh38.p7 | 13:26199614 | CTGAGAGGATAAAAC[A/G]TATATCTACAGACAT | 6049 |
rs117004461 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | RNF6 | GRCh38.p7 | 13:26149316 | CAGACGGCCAGGCAT[G/T]GTGGCTCACGCCTGT | 6049 |
rs117024318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26218335 | TCTTTGCATTCATTC[C/T]TCTGTCCTATACTGC | 6049 |
rs117040005 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RNF6 | GRCh38.p7 | 13:26167055 | TGAGAACATGCTAAC[A/G]CAATGGGTTAAAGAC | 6049 |
rs117040712 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RNF6 | GRCh38.p7 | 13:26218988 | AATACTTCATTATAT[C/G]GGTCATCAATATACA | 6049 |
rs117046294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26154326 | AGAGCTATTTTGTCT[G/T]TTTTTGAAAGTACTG | 6049 |
rs117055926 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RNF6 | GRCh38.p7 | 13:26134137 | GAGTTCTGACCCTCC[C/T]GTAGACCTTTCCTGA | 6049 |
rs117061691 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF6 | GRCh38.p7 | 13:26143251 | TGGTAATACTGAGAG[A/G]TGCCTTAAGGGATCT | 6049 |
rs117066315 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | RNF6 | GRCh38.p7 | 13:26169252 | CAGGCTCAGGGAGCC[A/G]TGGAGACTAGGATGA | 6049 |
rs117096692 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF6 | GRCh38.p7 | 13:26165266 | CACCGAAGTCAAGAA[C/T]TGAGGTTTGGGAACC | 6049 |
rs117169636 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RNF6 | GRCh38.p7 | 13:26180083 | TAACCCAAATGACAC[A/C]CTGTTCTACCCCCAG | 6049 |
rs117192041 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | RNF6 | GRCh38.p7 | 13:26141125 | GGAATTAGAAAAAAC[A/T]ATTCTAAAATTCATA | 6049 |
rs117200936 | snp | A/C | 0.0111272 | 0.0738324 | intron-variant | RNF6 | GRCh38.p7 | 13:26175977 | ATTCCAGGGAAAGCC[A/C]GGAGTGAACTTGCTC | 6049 |
rs117345449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26173162 | ATACAACCATTGTAG[A/G]GAGAGCAAGTTTAGG | 6049 |
rs117358813 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | RNF6 | GRCh38.p7 | 13:26204589 | AAGCAGGCTTGGCAA[A/T]TAACTGAGAAATTTT | 6049 |
rs117393781 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF6 | GRCh38.p7 | 13:26133902 | TTTGATATATATGAC[A/G]AAGATTTTCAATTGA | 6049 |
rs117438590 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF6 | GRCh38.p7 | 13:26203425 | TGATTGTTTCTAAAT[A/G]TGCTAAGGATGTTAA | 6049 |
rs117443901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26196909 | GTGTATAATGTAGGT[A/G]TAGAAATCAAAGATA | 6049 |
rs117455601 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | RNF6 | GRCh38.p7 | 13:26202747 | AAAATAGTATGGTAC[A/C]TTTAGAAAGGAAAAA | 6049 |
rs117504350 | snp | A/C | 0.0798611 | 0.183174 | intron-variant | RNF6 | GRCh38.p7 | 13:26191213 | TTTAGAAGGAAAAAA[A/C]TGGCTAAGGGACATT | 6049 |
rs117529256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF6 | GRCh38.p7 | 13:26151108 | TGACACTATCACGTG[A/G]TAGAAAAGTCACCAG | 6049 |
rs117532564 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RNF6 | GRCh38.p7 | 13:26144662 | GTAGTGCTGCAGCTG[A/C]ACACATTCAGGTATT | 6049 |
rs117701301 | snp | A/C | 0.0509478 | 0.151255 | intron-variant | RNF6 | GRCh38.p7 | 13:26147566 | ACTGACAAAGAAGAC[A/C]CATCAAAATTTAGGA | 6049 |
rs117733839 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RNF6 | GRCh38.p7 | 13:26190788 | CAGACAAGGTTTACT[A/G]CTGTTAATGTGACCT | 6049 |
rs117739456 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RNF6 | GRCh38.p7 | 13:26204151 | ATGTATAATTCTGTC[C/T]TGGTGTTCACTTCTC | 6049 |
rs117756845 | snp | G/T | 0.0494327 | 0.149241 | intron-variant | RNF6 | GRCh38.p7 | 13:26165815 | TTCTAGGAAGTAACT[G/T]ACTTGCTTTTGATTT | 6049 |
rs117801823 | snp | C/G | 0.0142736 | 0.0832652 | upstream-variant-2KB, utr-variant-5-prime | RNF6 | GRCh38.p7 | 13:26222425 | CGGCCGCTCAGCGCT[C/G]GTGGCAGCCGCGTAG | 6049 |
rs117802215 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF6 | GRCh38.p7 | 13:26183266 | GTAAAACTTGACACA[C/T]GAGAACAGATTCACT | 6049 |
rs117823756 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RNF6 | GRCh38.p7 | 13:26135555 | TCTGTCTCTCTATCC[A/G]GATTAGCTGTTGCTA | 6049 |
rs117860153 | snp | C/G | 0.0399052 | 0.1355 | intron-variant | RNF6 | GRCh38.p7 | 13:26194796 | AGGAAGGGTCCAGCA[C/G]TGGAGAAAGATGTAG | 6049 |
rs117900579 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF6 | GRCh38.p7 | 13:26217508 | TGGGAGAGTAAGCGA[C/T]ACATCCTACTCTCAC | 6049 |
rs117905588 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | RNF6 | GRCh38.p7 | 13:26166433 | CTGTTTGCAGACAAC[A/G]TGATTCTATATCTTG | 6049 |
rs117921772 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RNF6 | GRCh38.p7 | 13:26153996 | ATTTGAAACTCTAAT[G/T]TCAGCTAAATGAAAT | 6049 |
rs117926831 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | RNF6 | GRCh38.p7 | 13:26161410 | TGTATGAATGGTTTG[G/T]GTAAAGTTGACCTTC | 6049 |
rs117949812 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | RNF6 | GRCh38.p7 | 13:26193696 | TTTTAAAATACCCTT[A/G]CATACTGAAGGAATG | 6049 |
rs117973148 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF6 | GRCh38.p7 | 13:26181528 | AACCCATTGGGTGGA[A/G]ATGTCCACGTCCAGT | 6049 |
rs117994752 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RNF6 | GRCh38.p7 | 13:26190734 | ACCTATGATATGTGG[A/G]TGCTATTCTAGGCTC | 6049 |
rs118013708 | snp | C/T | 0.0166325 | 0.0896639 | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26224209 | TCCAATCAAGTGATT[C/T]ACCAGGTAGGAAGTT | 6049 |
rs118046009 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | RNF6 | GRCh38.p7 | 13:26149809 | TCAGCCATTAGCTTG[A/T]CTGTGCCTCAATTTA | 6049 |
rs118062667 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF6 | GRCh38.p7 | 13:26210585 | CAGACATATGATAGA[A/G]CAAAGTTGTAAAATT | 6049 |
rs118071926 | snp | C/G | 0.0189856 | 0.0955633 | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26223217 | TGGGCACCTGGATAA[C/G]AAGCTACATGCAGTC | 6049 |
rs118082671 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | RNF6 | GRCh38.p7 | 13:26187099 | GGGACCTTTCTAGAG[C/T]CTTGCTTGGCCTGAG | 6049 |
rs118097991 | snp | A/G | 0.031825 | 0.122064 | intron-variant | RNF6 | GRCh38.p7 | 13:26175080 | TCCCCATTGGCGTCC[A/G]GTGCCTTTTTATTTT | 6049 |
rs118148133 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF6 | GRCh38.p7 | 13:26144703 | TGTGCAGAACTATCC[A/G]TAAACTGTCTTCTCT | 6049 |
rs118165919 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF6 | GRCh38.p7 | 13:26168160 | ATGACAAGAGTTTCC[C/T]TATGTAACAAACCTG | 6049 |
rs121434522 | snp | A/G | | | missense | RNF6 | GRCh38.p7 | 13:26215577 | ACTCAGAAGTCCCTA[A/G]AGAAAGTTCACATGA | 6049 |
rs121434523 | snp | A/G | | | missense, intron-variant | RNF6 | GRCh38.p7 | 13:26215158 | AATGGAATTGGGGGA[A/G]CAGCTGGCATTCCTC | 6049 |
rs121434524 | snp | A/G | | | missense, intron-variant | RNF6 | GRCh38.p7 | 13:26215151 | TTGGGGGAGCAGCTG[A/G]CATTCCTCGAGCTAA | 6049 |
rs137871932 | in-del | -/TTCT | 0.296364 | 0.245663 | intron-variant | RNF6 | GRCh38.p7 | 13:26186772 | CAGGGACCTTTCTTC[-/TTCT]TTTTTTTTTTTTCTT | 6049 |
rs137901397 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RNF6 | GRCh38.p7 | 13:26138358 | TAAATACTAAAGGGG[G/T]TTATTCAGCCTGAAA | 6049 |
rs137905210 | in-del | -/A | 0.0252325 | 0.109451 | intron-variant | RNF6 | GRCh38.p7 | 13:26193778 | AAGCAGTTTTGCTGG[-/A]ATGGTTGAAGAATGG | 6049 |
rs137925110 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF6 | GRCh38.p7 | 13:26171409 | AAATAGCAAGTGTTC[A/T]TTAAGATATGGAGAA | 6049 |
rs138037036 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26177754 | TCCTATCTACCATCT[A/C]TGCCAAAAGGCTACG | 6049 |
rs138050403 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF6 | GRCh38.p7 | 13:26157196 | AACCATCAAACTGTA[C/T]ACTTTAAATTGGGCA | 6049 |
rs138076879 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF6 | GRCh38.p7 | 13:26175499 | TGACCTACTGGGTAC[A/C]TGCAGGATAGCCTTA | 6049 |
rs138089796 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF6 | GRCh38.p7 | 13:26150588 | TACTATCATAGTTCT[C/T]ATGACACCTAGTAAG | 6049 |
rs138094219 | in-del | -/GT | | | intron-variant | RNF6 | GRCh38.p7 | 13:26158725 | AATGTCTGTGTGTGG[-/GT]GTGTGTGTGTGTATT | 6049 |
rs138117088 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RNF6 | GRCh38.p7 | 13:26221420 | CACTCTGCTGCAAAG[C/G]CAAAGCAAATTCTCC | 6049 |
rs138203243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26220036 | ACATTAATTACAAAT[C/T]TTAGGCTTGAATTAT | 6049 |
rs138204371 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26165936 | TTTGGGGACTGTTGG[G/T]AAGGCATGATTGGTT | 6049 |
rs138213113 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF6 | GRCh38.p7 | 13:26215829 | ATACTATTTATGCAA[C/T]GCTATGGAGAAATCC | 6049 |
rs138254571 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RNF6 | GRCh38.p7 | 13:26154322 | TTCTAGAGCTATTTT[G/T]TCTTTTTTTGAAAGT | 6049 |
rs138254956 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | RNF6 | GRCh38.p7 | 13:26188287 | GCAAGGGAGGCAATT[A/G]TAACAATATCCCTCC | 6049 |
rs138294612 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | RNF6 | GRCh38.p7 | 13:26184251 | TTAGCCAGGATGGTC[C/T]CGATCTCCTGACCTC | 6049 |
rs138379662 | snp | C/T | 0.00420878 | 0.0456801 | missense, intron-variant, utr-variant-3-prime | RNF6 | GRCh38.p7 | 13:26214167 | AAATTGTTTGGATTT[C/T]GCAACTGCCTGCCAC | 6049 |
rs138410419 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RNF6 | GRCh38.p7 | 13:26199090 | AATCCCACTCAAAAT[C/T]CCAATGTTCTTTTAC | 6049 |
rs138415461 | in-del | -/CCCCGCTTCCTGTTTCTGCCATCAGTGGGGCCACAGG | 0.47023 | 0.118317 | intron-variant | RNF6 | GRCh38.p7 | 13:26187133 | CGGGACTGGGGCTGT[lengthTooLong]CCTGAAGACGGCTTG | 6049 |
rs138446136 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF6 | GRCh38.p7 | 13:26142706 | ATGGGAACGATAGAC[A/G]TGGGGGACTCCAAGA | 6049 |
rs138446230 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF6 | GRCh38.p7 | 13:26194871 | GCTTTATAGGCTAGC[A/G]GTGCTGGCAGCTGAT | 6049 |
rs138468421 | snp | A/G | 0.00356828 | 0.0420881 | synonymous-codon, intron-variant | RNF6 | GRCh38.p7 | 13:26215354 | ATGATCTCTGTTACT[A/G]TCTGAAAGTGGAATG | 6049 |
rs138480965 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | RNF6 | GRCh38.p7 | 13:26173585 | CAGATGAAAATCATG[C/G]ACAACACATTCATAT | 6049 |
rs138490734 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | RNF6 | GRCh38.p7 | 13:26142443 | TTCATCACAGCACTA[C/T]TCACAATAGCAAAAA | 6049 |
rs138499094 | snp | C/T | 9.42729e-05 | 0.00686495 | utr-variant-3-prime | RNF6 | GRCh38.p7 | 13:26132386 | TGAGGTGCTTCACAG[C/T]CTATTTTTCCAGATA | 6049 |
rs138507764 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26209486 | CCATTTCACTGTATC[A/G/T]GGTAGGCAGGAGAAG | 6049 |
rs138508581 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RNF6 | GRCh38.p7 | 13:26168322 | AAGTGAGAGCAGAGC[C/T]CACTCAGGCAGACAG | 6049 |
rs138559746 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF6 | GRCh38.p7 | 13:26203926 | CCACTGCACTCCAGC[C/T]TGGGCGACAGAGCGA | 6049 |
rs138590823 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF6 | GRCh38.p7 | 13:26204554 | AAGAAAAGGGAAACA[A/G]TAACTCCTTTGGTCT | 6049 |
rs138681221 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26179950 | TTGCTAAAGAATCAA[A/T]GAAGGATCCTCAGGT | 6049 |
rs138738790 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF6 | GRCh38.p7 | 13:26161371 | AAAAAGTCCTACTGT[A/G]ATTCTGAATAAAATT | 6049 |
rs138742866 | snp | C/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26219363 | ATATTTTCATAAAGA[C/G]AAGCAAGGAAAAAGA | 6049 |
rs138772710 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF6 | GRCh38.p7 | 13:26157933 | GGATGGATAGATGGA[C/T]AGATGGATGGCTAGC | 6049 |
rs138783453 | snp | G/T | 1.6477e-05 | 0.00287024 | missense, intron-variant, utr-variant-3-prime | RNF6 | GRCh38.p7 | 13:26214287 | GAGGAACCTTCCCTG[G/T]GCTGGCTCCTGTTGT | 6049 |
rs138786530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26194372 | CTATCCCATCAAAAG[C/G]GAGGAGAAGAAAAAC | 6049 |
rs138863852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26158512 | GTGAAAGTTGGTCTA[C/T]TTATAAATATCTACT | 6049 |
rs138864245 | snp | C/T | 3.29457e-05 | 0.00405854 | missense, intron-variant | RNF6 | GRCh38.p7 | 13:26215295 | GTTTGGCTTCTTGTT[C/T]GCCTAGCCACAGGAC | 6049 |
rs138925339 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RNF6 | GRCh38.p7 | 13:26209687 | GGGGAGAAGGTGAGC[A/G]CATTTGGAATTGCAC | 6049 |
rs138932655 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26200273 | ATAGCTAAAATCAAA[A/T]AGCCTGACAATATTG | 6049 |
rs138938228 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF6 | GRCh38.p7 | 13:26136985 | GCTCTATTTCCATCC[A/C]CTGCTTTCTAGCTCA | 6049 |
rs138991755 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF6 | GRCh38.p7 | 13:26163517 | CCTACCTGTAAGTAT[C/T]TACATCTAAGAATGA | 6049 |
rs139090182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26196050 | TTGAAGATAAAATGG[C/G]CAAAATTTTCTAAAA | 6049 |
rs139101846 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | RNF6 | GRCh38.p7 | 13:26131783 | ATACAAAAATTAGCC[A/G]GGCGTGCTGGTGGAA | 6049 |
rs139142019 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | RNF6 | GRCh38.p7 | 13:26167728 | AATATAAATTGTTCT[A/G]CCATAAAGACACATG | 6049 |
rs139174482 | snp | A/G | 0.00154801 | 0.0277779 | synonymous-codon, intron-variant | RNF6 | GRCh38.p7 | 13:26214799 | TGGGGTATATGCAGT[A/G]CCTCTGCGTTCTCGT | 6049 |
rs139195331 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26201175 | CATTTTATTTTGCAC[G/T]GAGTCCAGCAAATTA | 6049 |
rs139216748 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF6 | GRCh38.p7 | 13:26168654 | TTCACTTTCTAAATG[C/T]CCAAGGGCAAATGAG | 6049 |
rs139284595 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | RNF6 | GRCh38.p7 | 13:26166017 | GGTTTGGCTGTGTCC[C/G]CACCTAAATCTCATC | 6049 |
rs139302917 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | RNF6 | GRCh38.p7 | 13:26172744 | CAGATAAGGTTTCAC[C/T]ATGTTAGCCAGGATG | 6049 |
rs139340455 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RNF6 | GRCh38.p7 | 13:26159206 | AGGGACATTATATTG[C/T]CTTTGAGCCAAAATG | 6049 |
rs139400623 | in-del | -/G | | | intron-variant | RNF6 | GRCh38.p7 | 13:26142738 | AGGGAGGGATGGATG[-/G]GGGGAAAGTGCTAAA | 6049 |
rs139427344 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26182073 | ATTTTATAAAACTCT[A/T]CTGATAATTTAATTG | 6049 |
rs139442945 | in-del | -/TCTTCTTC | 0.183568 | 0.241012 | intron-variant | RNF6 | GRCh38.p7 | 13:26160526 | ACTGCATCCAGCCTA[-/TCTTCTTC]TCTTCTTCTTCTTTT | 6049 |
rs139446591 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26223639 | CCTATTTTAGCATGT[A/G]TTCATGTATTTAACA | 6049 |
rs139515136 | snp | A/C | 0.0345262 | 0.126772 | intron-variant | RNF6 | GRCh38.p7 | 13:26166726 | GGAGTTCAAGACCAA[A/C]CTGGGCAACAAGGTG | 6049 |
rs139529247 | in-del | -/A | 0.0295035 | 0.117819 | intron-variant | RNF6 | GRCh38.p7 | 13:26163729 | TCCCTGATTGTACCT[-/A]AAAATTTATTGTTAT | 6049 |
rs139551586 | snp | C/T | 0.000839789 | 0.0204741 | synonymous-codon | RNF6 | GRCh38.p7 | 13:26218551 | GTCAGGCTGAGATGC[C/T]AGTTGTTCCTTGACG | 6049 |
rs139595924 | in-del | -/ATTG | 0.210605 | 0.246877 | intron-variant | RNF6 | GRCh38.p7 | 13:26184987 | TATTGTTATCATTTT[-/ATTG]ATTGATTGATTGATT | 6049 |
rs139608117 | in-del | -/A | 0.0232847 | 0.105357 | intron-variant | RNF6 | GRCh38.p7 | 13:26138470 | GACAGTTATATATAT[-/A]TTTTTTCTTTGTAAC | 6049 |
rs139630066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26147830 | CTTTCAGGTCATTTA[C/T]GTGGCACTTTAGCTG | 6049 |
rs139631937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26181192 | ACCCAGGAAAAGCAG[C/G]ACCAGGGAAAGCATG | 6049 |
rs139652857 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | RNF6 | GRCh38.p7 | 13:26176564 | TTTATTTGAAAATAG[G/T]GTCTCTGCCAATGTA | 6049 |
rs139664667 | snp | A/C | 0.000345972 | 0.0131479 | missense, intron-variant, utr-variant-3-prime | RNF6 | GRCh38.p7 | 13:26214373 | TCTTTGAAGTTCTGA[A/C]TCAGAATCGGCCTCC | 6049 |
rs139753084 | snp | C/T | | | intron-variant | RNF6 | GRCh38.p7 | 13:26144907 | AATGGAGTGCTATTG[C/T]GCATGCCCAATTTTA | 6049 |
rs139781407 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RNF6 | GRCh38.p7 | 13:26172345 | CGCTAAAGGTCTAAA[C/T]AGGAAAAGCAAAACT | 6049 |
rs139796866 | snp | C/T | 0.000428308 | 0.0146277 | missense, intron-variant, synonymous-codon | RNF6 | GRCh38.p7 | 13:26214662 | CTATTTTCTCCAGGA[C/T]GGATCCTTCTCACTT | 6049 |
rs139814011 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF6 | GRCh38.p7 | 13:26174910 | GTGGATTGGGGCCCA[C/T]TCTAACGGCCTCGGT | 6049 |
rs139836261 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF6 | GRCh38.p7 | 13:26184843 | ATCTGTGGACTCCTG[C/G]AGAAGGCAGGCGATC | 6049 |
rs139884741 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF6 | GRCh38.p7 | 13:26200918 | AGTAAGTAAAAAGTA[A/G]TCATGTTATTTTTCA | 6049 |
rs139900676 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF6 | GRCh38.p7 | 13:26135830 | TGAGTGAGTTTTCAC[C/T]CTATAATTTCGTTGC | 6049 |
rs139904932 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RNF6 | GRCh38.p7 | 13:26197265 | AACACCTGGGGAAAG[G/T]TCCCTGACCTCCCTT | 6049 |
rs140080683 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26154696 | GTTAAGGCAATAAGC[A/T]AGACTTATTCCACAT | 6049 |
rs140096450 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | RNF6 | GRCh38.p7 | 13:26222664 | TCTGTCTGTCTGTCT[A/G]TCTCTATTTGAGACA | 6049 |
rs140115641 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF6 | GRCh38.p7 | 13:26217360 | TGTAGTGATGATGGT[A/G]CATGTGAAAGAGTTT | 6049 |
rs140231578 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | RNF6 | GRCh38.p7 | 13:26186262 | ATCAAAACATTTCTG[G/T]AAATCTGACACATCT | 6049 |
rs140248078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF6 | GRCh38.p7 | 13:26190880 | TTCATCATCATCAGT[A/G]TCAACATTGTGATCT | 6049 |
rs140267704 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF6 | GRCh38.p7 | 13:26187280 | AATAGAAAGGGGGAA[A/G]GCCCTGGAAAATTAA | 6049 |
rs140396861 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF6 | GRCh38.p7 | 13:26164942 | AATTCAAGCCAGCTG[C/T]AGAAATTTGCATAAG | 6049 |
rs140451922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26198689 | TATATATTGAAAAGG[A/G]AAAAGCAAAAGTATC | 6049 |
rs140451976 | in-del | -/AAT | 0.0569829 | 0.158885 | intron-variant | RNF6 | GRCh38.p7 | 13:26171379 | GGTGGCTATTATAAA[-/AAT]AATAATAACAGAAAA | 6049 |
rs140452510 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RNF6 | GRCh38.p7 | 13:26160918 | TCTTATAAGGCCACC[A/T]GTCAGAATGGATCGG | 6049 |
rs140554839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26203565 | GCCCAGGCCATGCTT[C/T]CCCCAGGCAGCTCCT | 6049 |
rs140604899 | in-del | -/TTTT | | | intron-variant | RNF6 | GRCh38.p7 | 13:26200406 | CACTGTTTGAAATTC[-/TTTT]TTTTTTTTTTTTTTT | 6049 |
rs140606771 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF6 | GRCh38.p7 | 13:26146992 | CATGATTCTTGTACA[A/G]CCTGCAAAACTGTGA | 6049 |
rs140618145 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RNF6 | GRCh38.p7 | 13:26143734 | CTGTGACTGAGTCTT[C/G]AAAAGCCTATTTTAC | 6049 |
rs140629071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF6 | GRCh38.p7 | 13:26217546 | CGTGGACCTCCTTCC[C/T]ACCAGCTAGAACCTA | 6049 |