SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs9189 | snp | C/T | 0.021333 | 0.101051 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482209 | GAAATGAACTGCACG[C/T]GTAGTGTCACTTAAA | 25898 |
rs16732 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482008 | AAAATTATATTGAAA[C/G]TGTTTTATAGAAAGT | 25898 |
rs1046662 | snp | A/C | 0.465892 | 0.126058 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479373 | TTATAAGTGCCTGGC[A/C]ATAGGTATTCACTAG | 25898 |
rs1047970 | snp | A/G | 0.424659 | 0.17887 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482009 | TAAAATTATATTGAA[A/G]CTGTTTTATAGAAAG | 25898 |
rs1351093 | snp | C/T | 0 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485490 | CAAAGGTATGACTTA[C/T]TATATAAATTTAAAA | 25898 |
rs1351094 | snp | A/G | 0.396182 | 0.202807 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485210 | GCAGTTTACTCAGAA[A/G]TTAAACAGAAGTATC | 25898 |
rs1580297 | snp | C/T | 0.462909 | 0.131034 | downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75478576 | atgctgattttaata[C/T]tggctgttttaattt | 25898 |
rs1841932 | snp | G/T | 0.463343 | 0.130326 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479549 | ACTTTAGCTTATGTT[G/T]GAAGTAGTAGTTTGT | 25898 |
rs1841934 | snp | A/G | 0.434831 | 0.168337 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506366 | ATTATCTATGGGTAA[A/G]TTTTGTTTTCTGTTT | 25898 |
rs1904104 | snp | C/T | 0.395453 | 0.203331 | | | GRCh38.p7 | 4:75487951 | GCTTGTCAAGTGTGT[C/T]GAAGATTTAAAATAC | 25898 |
rs2045863 | snp | C/T | 0.472348 | 0.114286 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491569 | TTGTAAGATGTTTGA[C/T]TTTTTTGTGTGTGTG | 25898 |
rs2126852 | snp | A/G | 0.354235 | 0.227234 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481636 | CATCATATTTGATCA[A/G]TGTACTCATTTTTCT | 25898 |
rs2306176 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509361 | AGGAAGAAATTTTCT[C/T]TTTGTATTGCACACT | 25898 |
rs2306177 | snp | A/T | 0.363802 | 0.222596 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509142 | CTATTTTCTTTTTAA[A/T]AGCTGTATTAAGGTG | 25898 |
rs2867921 | snp | A/T | 0.463881 | 0.12944 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489896 | GTTCATTATCTCACA[A/T]TTCAGAAGGGACCCT | 25898 |
rs2903701 | snp | C/T | 0.390838 | 0.206555 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511674 | attttactgctttat[C/T]aacatttttaagtga | 25898 |
rs3210345 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482007 | AAATTATATTGAAAC[A/T]GTTTTATAGAAAGTT | 25898 |
rs3775531 | snp | C/G | 0.43309 | 0.17023 | intron-variant | RCHY1 | GRCh38.p7 | 4:75482854 | TTCATTTTCTGAATT[C/G]AGAGCCACCTTAATA | 25898 |
rs3775532 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482210 | CTTTAAGTGACACTA[C/T]GCGTGCAGTTCATTT | 25898 |
rs5859466 | in-del | -/A | 0.465788 | 0.126237 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506103 | AGGAAAAAAAAAAAA[-/A]TAGAACAGGACATAC | 25898 |
rs6535499 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503551 | aatacaaaaattagc[C/T]ggctgtggtggcgag | 25898 |
rs6815241 | snp | C/G | 0.440609 | 0.161766 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504647 | tcaactgagctggca[C/G]ttggtgcccttaacc | 25898 |
rs6816603 | snp | C/T | 0.440195 | 0.162252 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509663 | GTTGTGGGAGGGACT[C/T]AGAAGGAGGTAACTG | 25898 |
rs6818310 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RCHY1 | GRCh38.p7 | 4:75492906 | aaaataaaattaata[C/T]atatttCATTTGATT | 25898 |
rs6829753 | snp | A/G | 0.441841 | 0.160303 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510749 | tcataaattaaaaag[A/G]ataggtttttaaaat | 25898 |
rs6833496 | snp | A/G | 0.441977 | 0.16014 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490775 | ATACAAGAAGATGCA[A/G]GCTAACTGCCACATG | 25898 |
rs6835573 | snp | A/G | 0.462144 | 0.132269 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511219 | gttcacacatttaac[A/G]tgcaatatcaaaaaa | 25898 |
rs6835579 | snp | A/G | 0.441705 | 0.160466 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511243 | caaaaaatcatattc[A/G]ttaaaagtctttagg | 25898 |
rs6836107 | snp | A/G | 0.395635 | 0.2032 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488640 | caagtcaaattacct[A/G]taataacccttcagt | 25898 |
rs6838603 | snp | C/T | 0.389152 | 0.207694 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495840 | TATCTTAATACTACC[C/T]TTTCCTGATTTGAAA | 25898 |
rs6841882 | snp | C/T | 0.466824 | 0.124448 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488535 | caagcaggataaaaa[C/T]tgattgaataccaag | 25898 |
rs6845588 | snp | A/C | 0.396 | 0.202938 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507741 | aaaaagacacattat[A/C]taataataaatgggt | 25898 |
rs7657576 | snp | A/C | 0.462034 | 0.132445 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504175 | aattacaagctagaa[A/C]ctattagaaatgtat | 25898 |
rs7661260 | snp | A/T | 0.495927 | 0.0449436 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503707 | aaaaaaaaattaatt[A/T]aaaaaaaaaagaaaa | 25898 |
rs7661659 | snp | A/G | 0.440195 | 0.162252 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503915 | atgttaaagtactta[A/G]aaggaaacagatgat | 25898 |
rs7664140 | snp | G/T | 0.441977 | 0.16014 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513426 | TTATGAAACAGGCGC[G/T]ATCATCTCCATTTTA | 25898 |
rs7685936 | snp | A/G | 0.398354 | 0.201224 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504218 | atcagttatttacac[A/G]atgcacatgtgccag | 25898 |
rs7698352 | snp | A/T | 0.466308 | 0.125343 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483867 | ATTATCTAGCCAGAA[A/T]ACTAGGCTTTCCCAT | 25898 |
rs7698555 | snp | A/G | 0.0524604 | 0.153226 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481947 | TTACATTATAGAACT[A/G]ATGATACTGCCCTAA | 25898 |
rs7699102 | snp | C/G | 0.388964 | 0.20782 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504007 | aggtcgtcttttctt[C/G]aaccaaattacgact | 25898 |
rs10018377 | snp | A/G | 0.39527 | 0.203462 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500864 | GAATGTGCAGCTCCA[A/G]AAAGACTGATTTTCA | 25898 |
rs10020976 | snp | A/G | 0.398354 | 0.201224 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505909 | ACTGTGCTGTGACAA[A/G]CTAAGAAACTAAACA | 25898 |
rs10026125 | snp | C/G | 0.38821 | 0.208322 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504304 | ttgaagtacacaggt[C/G]tacttataagcagat | 25898 |
rs10031553 | snp | A/C | 0.441977 | 0.16014 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499494 | ctgcagcactattca[A/C]aatagctgaaatatg | 25898 |
rs10032148 | snp | A/G | 0.35207 | 0.228214 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484359 | ctgaattcagaagtc[A/G]caacaaaaactggac | 25898 |
rs10518139 | snp | C/T | 0.388964 | 0.20782 | intron-variant | RCHY1 | GRCh38.p7 | 4:75492191 | CACAAATAAGGAAAG[C/T]GACTTAGGAATTCAA | 25898 |
rs10518140 | snp | C/T | 0.390277 | 0.206936 | intron-variant | RCHY1 | GRCh38.p7 | 4:75492574 | AGATGTAATGTCTGA[C/T]TAAATCCAAGGAGGT | 25898 |
rs11422865 | in-del | -/T | 0.294832 | 0.245947 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490493 | ATATATTTTTTTTTT[-/T]GGCAAATTCAAGCAG | 25898 |
rs11722278 | snp | A/C | 0.318415 | 0.240457 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513217 | CGTACAGGCCTGAGA[A/C]TTGAACTTGCTTCTA | 25898 |
rs11729106 | snp | C/G | 0.395818 | 0.203069 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494835 | gagtaaccatgttcc[C/G]cacactttgggtaac | 25898 |
rs11729704 | snp | A/C | 0 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500114 | cgattgcactccagc[A/C]tgggcaacagagcaa | 25898 |
rs11729929 | snp | A/G | 0.463774 | 0.129618 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488873 | cgaggtcaggagttc[A/G]agaccagcctggcca | 25898 |
rs11730978 | snp | A/T | 0.463774 | 0.129618 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488815 | aaggtggctcatcac[A/T]cctataatcccagca | 25898 |
rs11731909 | snp | A/C | 0.159292 | 0.232964 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495819 | GTTTCCGAATGGATA[A/C]TCAATTATCTTAATA | 25898 |
rs11732511 | snp | C/T | 0.395635 | 0.2032 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500568 | AGGAATAATACACTA[C/T]TAAACTCTGTACGAA | 25898 |
rs11735018 | snp | C/T | 0.426201 | 0.177351 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499861 | ctggtgtttgataga[C/T]cagtagggtgactac | 25898 |
rs11735057 | snp | A/C | 0 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499956 | cacaaaTATTTAagc[A/C]tgggcaacaagggga | 25898 |
rs12639787 | snp | C/T | 0 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510843 | aaataactatatttt[C/T]cCCCCCaaacagctg | 25898 |
rs12644911 | snp | C/T | 0.342358 | 0.232314 | downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75478861 | caggaacctggaaga[C/T]attatactaaatgaa | 25898 |
rs12648354 | snp | A/G | 0.396 | 0.202938 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511373 | tgaattttatcactg[A/G]caacaaatactgtca | 25898 |
rs13103964 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75511922 | caccacactttgaaa[A/C]ccAATGCTACAGAAC | 25898 |
rs13112378 | snp | A/G | 0.463774 | 0.129618 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500090 | AGGCTGCAGTGAGTC[A/G]TGATTGTGCGATTGC | 25898 |
rs13134862 | snp | A/G | 0.462472 | 0.13174 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500686 | TAGATGAAGCAATAG[A/G]GTCAAGAGTAGAAAT | 25898 |
rs13137105 | snp | A/G | 0.462363 | 0.131916 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491177 | TTTTCAATTATTTTC[A/G]TCTAATTTTAATATC | 25898 |
rs13144397 | snp | A/C | 0 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499571 | tggtatatgtacact[A/C]cggagtattactcag | 25898 |
rs13145288 | snp | A/T | 0.441977 | 0.16014 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499979 | CAAGGGGAAACCCCA[A/T]CTCCACAAAAAATTA | 25898 |
rs17000594 | snp | A/G | 0.161267 | 0.233723 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494355 | TAAGCACTATACACA[A/G]AGTGGTATCTACCCT | 25898 |
rs17000595 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | RCHY1 | GRCh38.p7 | 4:75501602 | TTATTTGTCTATAAC[A/G]TGAGTCACATATTAC | 25898 |
rs17000597 | snp | C/T | 0.159622 | 0.233092 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502106 | AGAAGGGATTTTGAT[C/T]AAATTCAGCATTTAA | 25898 |
rs17278863 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489572 | AGATTGATGGTAATC[A/G]GATCCCCTTGGAGTG | 25898 |
rs17279298 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505940 | GAGAGCAACAGGTAA[A/G]AGCCTAAGAAACTAA | 25898 |
rs28507535 | snp | A/G | 0.426201 | 0.177351 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510562 | AACTCTCAGTTCCTT[A/G]ACTTTGTCATTTCCA | 25898 |
rs28509772 | snp | C/T | 0.289942 | 0.246789 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499894 | TTTACATTAATTGAT[C/T]ATACATTTCAAACTA | 25898 |
rs28877578 | snp | A/G | 0.462472 | 0.13174 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499766 | ACCAGAAGCCTACAA[A/G]GGTAGGGAGGATGGG | 25898 |
rs33923711 | in-del | -/GGG | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512914 | GCCTCTGGTATTTAA[-/GGG]GGGGGGGGGGGCGGG | 25898 |
rs34047546 | in-del | -/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75482789 | TAAGTCTAAAAATTT[-/C]CCAAAAGTAGAAATT | 25898 |
rs34377379 | in-del | -/TA | 0.0755793 | 0.179102 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480528 | CTCAGCTTTCTTGTC[-/TA]TGAGGACAACACTTA | 25898 |
rs34389789 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486244 | GACTACTTGAGACTC[-/A]AGATGACTGAGAAAA | 25898 |
rs34389833 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483944 | CACATCTTAATTAAA[C/T]GAAAAAAGATGATCA | 25898 |
rs34627803 | in-del | -/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75496553 | ACTCACACATGGCTA[-/G]GGAACAGTGCCTGAT | 25898 |
rs34862587 | in-del | -/AGAC | 0.462582 | 0.131564 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494782 | AACTGACCTCCAAAT[-/AGAC]AGTACCAATTTATAC | 25898 |
rs34895675 | in-del | -/C | 0.441977 | 0.16014 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504270 | AGTAAATACAGTTGA[-/C]CCCTTGAACAACACA | 25898 |
rs35093715 | in-del | -/AT | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487867 | ATATATATATTCATA[-/AT]ATATATATTCATAAT | 25898 |
rs35101784 | in-del | -/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75490469 | TCATCACATTAGCAT[-/C]CTGTGTCAAACCAGT | 25898 |
rs35216484 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501330 | ATATTTTTATTATCT[-/A]AAAAATAATAGTCAT | 25898 |
rs35316729 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486817 | AACCCCGTCTCTACT[-/A]AAAGTACAAAAATTA | 25898 |
rs35403414 | snp | A/G | 0.0314385 | 0.121371 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480385 | GTGAGGGGTATTTTA[A/G]CAAAATAGAAGTTTA | 25898 |
rs35545040 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75508938 | AAGTCTGTTGGGCCT[-/A]AAAAAGAAACATAAT | 25898 |
rs35718300 | in-del | -/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75508221 | AGTATTGGTAACATT[-/C]CCTTTCCTAAACTCG | 25898 |
rs35851256 | in-del | -/A | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515556 | TGCTGTAGTTAAGCC[-/A]AAATACTTTGGCCAT | 25898 |
rs35931543 | snp | A/T | 0.39527 | 0.203462 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511769 | AGATACTAGCAATAC[A/T]AAACAGTGCTTTTCC | 25898 |
rs35953782 | in-del | -/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75488767 | AAATCCTTAAAGCTT[-/C]CCATTATTAAAAGTT | 25898 |
rs36016390 | in-del | -/C | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75516399 | GGGCCCTTTTTATCG[-/C]AGGATAAATTCTGGA | 25898 |
rs36082473 | snp | C/T | 0.0162871 | 0.0887597 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514275 | GCCATCTTCCCGGGC[C/T]GTCGCCGCCATCTCC | 25898 |
rs55879565 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506629 | AGAAAATCAAAGTAG[A/G]AGAAATACAGGAAAA | 25898 |
rs56077838 | snp | A/G | 0.25045 | 0.25 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503638 | CAGAGGTTGCAGTGA[A/G]CCGAGATCACGCCAC | 25898 |
rs57129862 | in-del | -/TAAA | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479297 | AGGACAAAAGAAAAA[-/TAAA]GTGGCATAGTTTTGA | 25898 |
rs57275697 | snp | C/T | 0.390464 | 0.206809 | intron-variant | RCHY1 | GRCh38.p7 | 4:75486871 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 25898 |
rs57535583 | in-del | -/ACAG | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75494784 | CTGACCTCCAAATAG[-/ACAG]TACCAATTTATACTT | 25898 |
rs57675155 | snp | A/G/T | 0.0696718 | 0.173152 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504722 | CATATTTGAGCACAC[A/G/T]TTATCTTCAACTTGG | 25898 |