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 |