SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13414 | snp | C/T | 0.286564 | 0.247312 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | RNF43, SUPT4H1, TSPOAP1-AS1 | GRCh38.p7 | 17:58354092 | GGAAAAGTTTTGTCT[C/T]AGAGCAAGGATGGAA | 54894 |
rs720236 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | RNF43 | GRCh38.p7 | 17:58408459 | TCCTTTGGATGCACG[C/T]TAATATCCTAAAATC | 54894 |
rs723991 | snp | A/G | 0.466618 | 0.124806 | intron-variant, upstream-variant-2KB | RNF43 | GRCh38.p7 | 17:58404678 | CAATAATAAGAAAAT[A/G]GTACTAGAAACAATT | 54894 |
rs757484 | snp | C/G | 0.168785 | 0.236441 | intron-variant | RNF43 | GRCh38.p7 | 17:58379736 | AGATAATTAGCTCTT[C/G]TTCTCCTTACCTTCT | 54894 |
rs917016 | snp | A/G | 0.160609 | 0.233472 | intron-variant | RNF43 | GRCh38.p7 | 17:58376795 | CATGAGCCCTCCACA[A/G]CCACACCCTTCTCAA | 54894 |
rs1047285 | snp | G/T | 0 | 0 | intron-variant | RNF43 | GRCh38.p7 | 17:58376405 | GATATAATTGTACTA[G/T]AAAGATCATGTTACt | 54894 |
rs1476596 | snp | C/T | 0.465578 | 0.126594 | intron-variant | RNF43 | GRCh38.p7 | 17:58407997 | ACAAAGATCTTCTTA[C/T]GTGTAGTAAATGAAT | 54894 |
rs1811202 | snp | A/C | 0.488726 | 0.0742286 | intron-variant | RNF43 | GRCh38.p7 | 17:58377074 | TCTGTCTTGGGAGGG[A/C]GGGGAAAAAATCAGA | 54894 |
rs1990008 | snp | C/G | 0.469148 | 0.120308 | intron-variant | RNF43 | GRCh38.p7 | 17:58382047 | TTTCTGGGGACTGAG[C/G]GCTGGTCAAAGGATT | 54894 |
rs2017770 | snp | A/G | | | intron-variant | RNF43 | GRCh38.p7 | 17:58401071 | TATCTCTGAAGTCAG[A/G]CCACCATGCAAAGTT | 54894 |
rs2018966 | snp | C/T | 0.16911 | 0.236552 | intron-variant | RNF43 | GRCh38.p7 | 17:58400204 | CCACCCCAGAACTCA[C/T]ATACTATTAGTCATT | 54894 |
rs2021733 | snp | A/G | 0.161596 | 0.233848 | intron-variant | RNF43 | GRCh38.p7 | 17:58411807 | CCACCACTTCTAAAA[A/G]TGATTACAGTCATAT | 54894 |
rs2107547 | snp | A/G | 0.274393 | 0.248807 | intron-variant | RNF43 | GRCh38.p7 | 17:58355382 | CTTAATGCATCTCTC[A/G]TGACTCCTGTCCTGT | 54894 |
rs2158459 | snp | C/T | 0.0130733 | 0.0797856 | intron-variant | RNF43 | GRCh38.p7 | 17:58355015 | CCTGACCCTCAATGA[C/T]CTCTTTCCTCCCCGC | 54894 |
rs2158460 | snp | C/G | 0.271837 | 0.249072 | intron-variant | RNF43 | GRCh38.p7 | 17:58355001 | ACCTCTTTCCTCCCC[C/G]CTCTCTAAATACAGG | 54894 |
rs2189681 | snp | C/G | 0.499987 | 0.00259581 | intron-variant | RNF43 | GRCh38.p7 | 17:58397545 | ctcctgagtagttgg[C/G]attacaggtgcctgc | 54894 |
rs2189682 | snp | A/G | 0.161596 | 0.233848 | intron-variant | RNF43 | GRCh38.p7 | 17:58405178 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGTG | 54894 |
rs2240258 | snp | G/T | 0.225301 | 0.248777 | intron-variant | RNF43 | GRCh38.p7 | 17:58380822 | AGCCTCTGAGCAGGA[G/T]ACTAAGCCTGAAAGA | 54894 |
rs2240259 | snp | G/T | 0.277334 | 0.248501 | intron-variant | RNF43 | GRCh38.p7 | 17:58380768 | ATGTTAATGAAGCTA[G/T]TTCGCACTCTTGCAC | 54894 |
rs2254839 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | RNF43 | GRCh38.p7 | 17:58414236 | AAAGAATACATGTTT[A/G]GGAATAAGTTCTATA | 54894 |
rs2257205 | snp | A/G | 0.274325 | 0.248821 | missense, utr-variant-5-prime | RNF43 | GRCh38.p7 | 17:58370936 | CTCGACGGGCCCCCC[A/G]CCCCTGCCTGTCACT | 54894 |
rs2285989 | snp | C/G/T | 0.0228947 | 0.104514 | intron-variant | RNF43 | GRCh38.p7 | 17:58362726 | TAGCTATGTGCCTCC[C/G/T]GGGCTCCTGTGTTTC | 54894 |
rs2285990 | snp | A/G | 0.0105575 | 0.0718839 | missense | RNF43 | GRCh38.p7 | 17:58362569 | CGGTGCTGCGCATCC[A/G]GTGCCGCCCCCGCCA | 54894 |
rs2301867 | snp | A/T | 0.46845 | 0.121572 | intron-variant, utr-variant-5-prime | RNF43 | GRCh38.p7 | 17:58402713 | TAGTGTCACAGCCTC[A/T]TCTCTGGGACCTGAA | 54894 |
rs2428680 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | RNF43 | GRCh38.p7 | 17:58386540 | GAAGGGAAGAAACAC[A/G]TACTTTTGAGTGATT | 54894 |
rs2450509 | snp | C/T | 0.152667 | 0.230274 | intron-variant | RNF43 | GRCh38.p7 | 17:58368789 | TTACAATTTATTTTC[C/T]CATGAGATAACTTGT | 54894 |
rs2526367 | snp | A/G | 0.169435 | 0.236663 | intron-variant | RNF43 | GRCh38.p7 | 17:58393389 | atggagttttgctct[A/G]gatgcccaggctggg | 54894 |
rs2526368 | snp | A/C | 0.16911 | 0.236552 | intron-variant | RNF43 | GRCh38.p7 | 17:58392949 | gttgtttaagggtca[A/C]ctgTAATGTCAAATG | 54894 |
rs2526369 | snp | A/G | 0.16911 | 0.236552 | intron-variant | RNF43 | GRCh38.p7 | 17:58391752 | TGTGTCGGCATCTCT[A/G]TGAGGTGCTTTGGAA | 54894 |
rs2526370 | snp | C/G | 0.499839 | 0.00898417 | intron-variant | RNF43 | GRCh38.p7 | 17:58410275 | GAAGCCTGGCACCCA[C/G]AGAATAGAAGGAAGC | 54894 |
rs2526371 | snp | C/T | 0.215144 | 0.247558 | intron-variant | RNF43 | GRCh38.p7 | 17:58366184 | AGGTCTGGAAGCTTC[C/T]GTTTCTATTCCTTTG | 54894 |
rs2526372 | snp | C/T | 0.174288 | 0.23826 | intron-variant | RNF43 | GRCh38.p7 | 17:58363165 | GAGAGATCCTGGAAA[C/T]CCTCTAGTCCAACTT | 54894 |
rs2526373 | snp | A/G | 0.101658 | 0.201233 | intron-variant | RNF43 | GRCh38.p7 | 17:58362203 | AGTAAAATCTATAAT[A/G]TTTTAGATGGTGATA | 54894 |
rs2526374 | snp | A/C | 0.478863 | 0.100608 | missense | RNF43 | GRCh38.p7 | 17:58358524 | GCACAAGGCTGGGGA[A/C]TGAGCCACCTCCAAT | 54894 |
rs2632506 | snp | G/T | 0.16911 | 0.236552 | intron-variant | RNF43 | GRCh38.p7 | 17:58390047 | AGAGCACATGACGGG[G/T]TGCAGGGCAGCATGT | 54894 |
rs2632509 | snp | C/T | 0.158302 | 0.232576 | intron-variant | RNF43 | GRCh38.p7 | 17:58410526 | TACTCTGTACTTCTT[C/T]TAAAGGCTGGCATCA | 54894 |
rs2632510 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | RNF43 | GRCh38.p7 | 17:58413197 | CCAGAAGTGTAAACC[A/G]TGTGTCCCTAACACA | 54894 |
rs2632511 | snp | A/G | 0.162253 | 0.234095 | intron-variant | RNF43 | GRCh38.p7 | 17:58413628 | GTAAGATTTGCCAGA[A/G]TGAGAAAAACGATAG | 54894 |
rs2632512 | snp | C/T | 0.160609 | 0.233472 | intron-variant | RNF43 | GRCh38.p7 | 17:58374461 | GCAGTGGTGCAATCT[C/T]GGCTTGCTGCAACCT | 54894 |
rs2632513 | snp | C/T | 0.359575 | 0.224707 | intron-variant | RNF43 | GRCh38.p7 | 17:58370691 | ACCTTCATCCCAGCA[C/T]GCTCCCCATCCCACC | 54894 |
rs2632514 | snp | C/T | 0.152667 | 0.230274 | intron-variant | RNF43 | GRCh38.p7 | 17:58369073 | GTGTGTGTGTGTGTG[C/T]GTGTATGAGAGAGAG | 54894 |
rs2632515 | snp | C/T | 0.152667 | 0.230274 | intron-variant | RNF43 | GRCh38.p7 | 17:58367522 | TACCATGGAGGCCAC[C/T]ACCTGGTAGTAAAGA | 54894 |
rs2632517 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | RNF43 | GRCh38.p7 | 17:58363113 | TGGGCAAGTTTTCCC[C/T]CGTCTTTGGGCCTCA | 54894 |
rs2632519 | snp | C/T | 0.470618 | 0.117591 | downstream-variant-500B, upstream-variant-2KB, nc-transcript-variant | RNF43, SUPT4H1, TSPOAP1-AS1 | GRCh38.p7 | 17:58352403 | GCCCGCTGACTACCC[C/T]ACACAGCCTCCGCCG | 54894 |
rs2632528 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | RNF43 | GRCh38.p7 | 17:58401816 | TTTTTTTTATGCTAG[C/G]AATATATGGATAAAA | 54894 |
rs2632529 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | RNF43 | GRCh38.p7 | 17:58398328 | CCAGTCTCTTATATT[A/G]TTTCATGCCAAAAAT | 54894 |
rs2632530 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | RNF43 | GRCh38.p7 | 17:58395963 | AGGCTACATCCTAAC[A/G]GTTGTGTCTTCCCAT | 54894 |
rs2680687 | snp | C/T | 0.16911 | 0.236552 | intron-variant | RNF43 | GRCh38.p7 | 17:58414605 | ATAAAGAATAGGCCA[C/T]GTATGAATGACTTAC | 54894 |
rs2680688 | snp | A/G | 0.378372 | 0.214524 | intron-variant | RNF43 | GRCh38.p7 | 17:58373163 | GGAGAAGGCTGGACC[A/G]TGTGGGGAGGGTCGA | 54894 |
rs2680692 | snp | A/G | 0 | 0 | intron-variant | RNF43 | GRCh38.p7 | 17:58371279 | CAAGCTCTTCATTTA[A/G]GTCCCCTCTGGGACA | 54894 |
rs2680693 | snp | A/G | 0 | 0 | intron-variant | RNF43 | GRCh38.p7 | 17:58369907 | CTCACAGGACCTTTA[A/G]ACCTTTGCCTGTGAC | 54894 |
rs2680694 | snp | C/T | 0.16911 | 0.236552 | intron-variant | RNF43 | GRCh38.p7 | 17:58392508 | TCCCTACAACTAAGA[C/T]GTATAAATCTAAAGT | 54894 |
rs2680695 | snp | A/G | 0.161596 | 0.233848 | intron-variant | RNF43 | GRCh38.p7 | 17:58393302 | gtcccagctacttgg[A/G]acgctgaggcaggag | 54894 |
rs2680696 | snp | C/T | 0.161596 | 0.233848 | intron-variant | RNF43 | GRCh38.p7 | 17:58395652 | CTAAATAAAAAAGAG[C/T]AGACTTGTTTTGCAG | 54894 |
rs2680697 | snp | A/T | 0.169435 | 0.236663 | intron-variant | RNF43 | GRCh38.p7 | 17:58401350 | ATATTGGAACATCCA[A/T]GTGTTTGGGTATGCA | 54894 |
rs2680698 | snp | C/T | 0.449345 | 0.150869 | intron-variant | RNF43 | GRCh38.p7 | 17:58368023 | CTTTTTTAGCTCACC[C/T]CTCTAAGCCAGCCTC | 54894 |
rs2680699 | snp | A/G | 0.449218 | 0.151037 | intron-variant | RNF43 | GRCh38.p7 | 17:58367983 | ATCTGTAAAAGGGGA[A/G]TAATAATGGGACTTG | 54894 |
rs2680700 | snp | A/C | 0.372189 | 0.218105 | intron-variant | RNF43 | GRCh38.p7 | 17:58363181 | AGACTCCTGGAGCTG[A/C]GAGAGATCCTGGAAA | 54894 |
rs2680701 | snp | C/T | 0.252616 | 0.249986 | missense | RNF43 | GRCh38.p7 | 17:58360940 | CCTCTTCCCAGGATC[C/T]GCTTCAGCAGAGAAC | 54894 |
rs2680702 | snp | C/T | 0.400504 | 0.199621 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | RNF43, SUPT4H1, TSPOAP1-AS1 | GRCh38.p7 | 17:58354188 | ATTTCTGCTGGACTT[C/T]ATCTGGGCAGAGGAA | 54894 |
rs2680703 | snp | C/T | 0.441158 | 0.161117 | downstream-variant-500B, upstream-variant-2KB, nc-transcript-variant | RNF43, SUPT4H1, TSPOAP1-AS1 | GRCh38.p7 | 17:58352312 | AGCCTCCCCGCCTGC[C/T]GGCGGGAGAAACCAT | 54894 |
rs2680705 | snp | A/G | 0.163892 | 0.234703 | upstream-variant-2KB, utr-variant-5-prime | RNF43 | GRCh38.p7 | 17:58418223 | ACCTCCCAAAGATTG[A/G]AAAGAAAATAACAGT | 54894 |
rs2680707 | snp | C/T | 0.165853 | 0.235413 | intron-variant | RNF43 | GRCh38.p7 | 17:58378280 | TATTTATTTTTGAGA[C/T]AGGGTCTTGCTCTGT | 54894 |
rs2680708 | snp | A/G | 0.499942 | 0.00539106 | intron-variant | RNF43 | GRCh38.p7 | 17:58378759 | GGGGTGCTGGTGAGC[A/G]AAAGAGCTGACAAGA | 54894 |
rs2680711 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | RNF43 | GRCh38.p7 | 17:58404896 | ACTTTCTAAAATGTA[C/T]CAATCAGTCCCTGTT | 54894 |
rs2877877 | snp | A/G | 0.293037 | 0.246268 | utr-variant-3-prime, upstream-variant-2KB, intron-variant | RNF43, SUPT4H1, TSPOAP1-AS1 | GRCh38.p7 | 17:58354169 | TTCTACCTTCATTCC[A/G]TCCTTCCTCTGCCCA | 54894 |
rs3030929 | in-del | -/CTTAACTTA | | | intron-variant | RNF43 | GRCh38.p7 | 17:58377045 | TCTCCCTGTGTCCTC[-/CTTAACTTA]TTTGTTCTGATTTTT | 54894 |
rs3030932 | in-del | -/CCC | | | intron-variant | RNF43 | GRCh38.p7 | 17:58380240 | GAGTACCACTGAGCC[-/CCC]TTGTTTAGCTAGGTC | 54894 |
rs3030936 | in-del | -/A | 0 | 0 | intron-variant | RNF43 | GRCh38.p7 | 17:58401839 | AAAAAAAAAAAAAAA[-/A]CCTATAATCTAATAC | 54894 |
rs3744093 | snp | A/G | 0.481874 | 0.0934578 | missense, intron-variant | RNF43 | GRCh38.p7 | 17:58415439 | GCAGAACAGAAAGCT[A/G]TTATCAGAGTGATCC | 54894 |
rs3785492 | snp | A/G | 0.283684 | 0.24772 | intron-variant | RNF43 | GRCh38.p7 | 17:58410702 | CTTATAATGTAACAT[A/G]TTTCATCACCTTTCT | 54894 |
rs3785493 | snp | A/C | 0.226484 | 0.248892 | intron-variant | RNF43 | GRCh38.p7 | 17:58394758 | ACTGGAGAGGTAACT[A/C]TTGCAGGTACACTTC | 54894 |
rs3837804 | in-del | -/GCAAGTCTCTAAGACTC | 0.274124 | 0.248833 | intron-variant | RNF43 | GRCh38.p7 | 17:58399421 | CTTGGAAATTATCCC[-/GCAAGTCTCTAAGACTC]TCAGTTCCCTATCTG | 54894 |
rs3837805 | in-del | -/T | 0.499982 | 0.00299515 | intron-variant | RNF43 | GRCh38.p7 | 17:58388703 | AAGATCCATCTCCTT[-/T]GACAAATCCTGTAGG | 54894 |
rs4793583 | snp | G/T | 0.4776 | 0.103433 | intron-variant | RNF43 | GRCh38.p7 | 17:58374046 | GATTGTTCTATGCAC[G/T]TTTTCATATTAACTC | 54894 |
rs4793585 | snp | A/G | 0.466412 | 0.125164 | intron-variant | RNF43 | GRCh38.p7 | 17:58393150 | cggtgacttatgcct[A/G]taatcccagcacttt | 54894 |
rs4793588 | snp | A/C | 0.161924 | 0.233971 | intron-variant | RNF43 | GRCh38.p7 | 17:58393690 | AATTTAATGTTTGCG[A/C]TTCATTGTAATACTT | 54894 |
rs4793941 | snp | A/G | 0.468249 | 0.121932 | intron-variant | RNF43 | GRCh38.p7 | 17:58395005 | GTGGCACATGGTGCT[A/G]TGCAGGCAAGTATAT | 54894 |
rs4793942 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | RNF43 | GRCh38.p7 | 17:58395059 | TCGGTTTGCTGTATA[A/G]TAAGTCTGTTTGGAC | 54894 |
rs4793946 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | RNF43 | GRCh38.p7 | 17:58416987 | GCAGAGGGAGGGGGG[A/G]AAAAGGAATTTCAAA | 54894 |
rs5821226 | in-del | -/CTTAA | 0.488726 | 0.0742286 | intron-variant | RNF43 | GRCh38.p7 | 17:58377045 | TCTCCCTGTGTCCTC[-/CTTAA]CTTATTTGTTCTGAT | 54894 |
rs5821227 | in-del | -/ACTTA | | | intron-variant | RNF43 | GRCh38.p7 | 17:58377049 | CCTGTGTCCTCCTTA[-/ACTTA]TTTGTTCTGATTTTT | 54894 |
rs5821228 | in-del | -/A | 0.468349 | 0.121752 | intron-variant | RNF43 | GRCh38.p7 | 17:58381910 | CTTGGTTCTATAGAG[-/A]AAAAAAAATGGCACC | 54894 |
rs5821229 | in-del | -/A | | | intron-variant | RNF43 | GRCh38.p7 | 17:58401824 | ATATATTCCTAGCAT[-/A]AAAAAAAAAAAAAAA | 54894 |
rs6503859 | snp | C/G | 0.419296 | 0.183954 | intron-variant | RNF43 | GRCh38.p7 | 17:58383491 | tatttttggtaaaga[C/G]agggtctccctgtgt | 54894 |
rs6503862 | snp | A/T | 0.163892 | 0.234703 | intron-variant | RNF43 | GRCh38.p7 | 17:58406770 | CTTTTTTTTTTTTTT[A/T]AAATAGCAAAATAAG | 54894 |
rs7211294 | snp | A/G | 0.390651 | 0.206682 | intron-variant | RNF43 | GRCh38.p7 | 17:58385422 | CCTATTTCAGTTAAC[A/G]GCACCACCATTTTCC | 54894 |
rs7215531 | snp | A/T | 0.400504 | 0.199621 | intron-variant | RNF43 | GRCh38.p7 | 17:58416013 | TAAACAGCTAAGGCC[A/T]TGCATCAAAGGTGAG | 54894 |
rs7216856 | snp | A/G | 0.425277 | 0.178263 | intron-variant | RNF43 | GRCh38.p7 | 17:58394934 | TATGGAGGCACAATG[A/G]TTCAGCTATTCCACC | 54894 |
rs7218637 | snp | A/G | 0.184521 | 0.241273 | intron-variant | RNF43 | GRCh38.p7 | 17:58368606 | aaatcccagctactc[A/G]ggaggctgaggcagg | 54894 |
rs7219031 | snp | A/G | 0.152667 | 0.230274 | intron-variant | RNF43 | GRCh38.p7 | 17:58368547 | gcgagactccatctc[A/G]ttaaaaaaaaaaaaa | 54894 |
rs7219859 | snp | A/G | 0.301681 | 0.2446 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | RNF43, SUPT4H1, TSPOAP1-AS1 | GRCh38.p7 | 17:58353389 | ATTTGCCCAAGGTCT[A/G]AGTCACTGAAGTATG | 54894 |
rs7221205 | snp | A/G | 0.42803 | 0.175514 | intron-variant | RNF43 | GRCh38.p7 | 17:58408438 | TTAAGTACTAAGAAG[A/G]TAAGGTCCTTTGGAT | 54894 |
rs7502645 | snp | A/G | | | intron-variant | RNF43 | GRCh38.p7 | 17:58400349 | CAGTCTTGCTTAGTT[A/G]TGTTAAGCTGATGCC | 54894 |
rs7502856 | snp | G/T | 0 | 0 | intron-variant | RNF43 | GRCh38.p7 | 17:58356047 | AGGGAGATAGTGGTG[G/T]GGTACTGGCAGCACT | 54894 |
rs8065321 | snp | A/C | 0.0554779 | 0.157039 | intron-variant | RNF43 | GRCh38.p7 | 17:58366905 | atctcagctcactgc[A/C]gtttccgcctcccgg | 54894 |
rs8067183 | snp | A/G | 0.419456 | 0.183806 | intron-variant | RNF43 | GRCh38.p7 | 17:58384662 | TGGCTTCTGGGCATC[A/G]GTTTCAGGTACTAAA | 54894 |
rs8070135 | snp | A/G | 0.439363 | 0.163222 | intron-variant | RNF43 | GRCh38.p7 | 17:58381702 | AGTAGCATCTCTTGC[A/G]CTCCTAGGAACTAAA | 54894 |
rs8072522 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | RNF43 | GRCh38.p7 | 17:58400313 | AAAGCCTTGTCCTTT[C/T]GGCTACATTAAAAAT | 54894 |
rs8078280 | snp | A/G | 0.274929 | 0.248754 | intron-variant | RNF43 | GRCh38.p7 | 17:58395771 | CAAAGGGATGACTAT[A/G]AACATTTTATCAACA | 54894 |