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 |
rs57789217 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75498499 | AAAAAAAAAAAAAAA[-/A]CATAACTGGAGAGGC | 25898 |
rs57838127 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509876 | GTAAGTCCAATTAAA[C/T]CTCTTTTTCTTCCCA | 25898 |
rs58067589 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495416 | CTCCACTTCTTCTAC[A/G]ATGATAGGGTATTTA | 25898 |
rs58178148 | snp | A/C/G | 0.0832709 | 0.186283 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484437 | CCTGACTGGGTCGGG[A/C/G]AGAAGCACAGTAAAT | 25898 |
rs59144786 | in-del | -/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487279 | TTTTTGTTTACTTTT[-/T]GGGTAAATTTCAAAC | 25898 |
rs59581284 | snp | A/C | 0.463774 | 0.129618 | intron-variant | RCHY1 | GRCh38.p7 | 4:75487179 | GGTTTTATTAAAATT[A/C]GCTTTAGTCCTAACA | 25898 |
rs59968007 | snp | C/G | 0.0696718 | 0.173152 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506173 | CTAATCATATCAATG[C/G]TAAATTGGATTAAGG | 25898 |
rs62318618 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487820 | ATTCATAATATATAT[A/T]CATAATATATATATT | 25898 |
rs62318619 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487821 | TTCATAATATATATT[C/T]ATAATATATATATTC | 25898 |
rs62318620 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487824 | ATAATATATATTCAT[A/C]ATATATATATTCATA | 25898 |
rs62318629 | snp | A/G | 0.398354 | 0.201224 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497507 | CCTCTCTGACCACAT[A/G]GCAGAGCCAAGGTTG | 25898 |
rs62318630 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499646 | GGATGGAGGTCATTA[C/T]GTTAAGCGAAACAAG | 25898 |
rs62318632 | snp | C/T | 0.39527 | 0.203462 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512482 | TGCACTGGATTTCAT[C/T]CCCTTTGGCTACTCA | 25898 |
rs62318633 | snp | A/T | | | upstream-variant-2KB, splice-donor-variant, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514522 | CTTCGCTGCTAACGG[A/T]AATAACTCTTAGGTT | 25898 |
rs66464066 | in-del | -/CT | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482007 | ACTTTCTATAAAACA[-/CT]NGTTTCAATATAATT | 25898 |
rs67891124 | in-del | -/AAAT | 0.625 | 0.125 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479294 | CAAAGGACAAAAGAA[-/AAAT]AAAGTGGCATAGTTT | 25898 |
rs71203818 | in-del | -/TATATTCATAATATATATATTCATA | 0 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75487630 | ATATATATATTCATA[-/TATATTCATAATATATATATTCATA]ATATATATATTCATA | 25898 |
rs71203819 | in-del | -/ATTGCAGATTGAT | 0 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489564 | ATATTGCAGATTGAT[-/ATTGCAGATTGAT]GGTAATCAGATCCCC | 25898 |
rs71203820 | in-del | -/A | 0 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497769 | AATTAATGAAAAAAA[-/A]CTATAAACCAATGGA | 25898 |
rs71657364 | in-del | -/A | 0.5 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497762 | TTCCTGAAATTAATG[-/A]AAAAAAACTATAAAC | 25898 |
rs71699914 | in-del | -/AAAT | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479295 | AAAGGACAAAAGAAA[-/AAAT]AAGTGGCATAGTTTT | 25898 |
rs72209182 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75490495 | CAGTATATATATATT[-/A]TTTTTTTTGGCAAAT | 25898 |
rs72647441 | snp | C/T | 0.198324 | 0.244601 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485613 | CTTAGCTGTGTGCTT[C/T]TGAGATATACATTTT | 25898 |
rs72647449 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514949 | GAACTAACAAGACTG[G/T]TGGAGGAGGAAGACA | 25898 |
rs72866210 | snp | C/T | 0.0689305 | 0.172377 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479234 | AAACATCACATTGTA[C/T]TCCATATATATAATA | 25898 |
rs72866214 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481552 | TCCCACTCATCCATC[C/T]CCTATTTTCACACGC | 25898 |
rs72866215 | snp | G/T | 0.0689305 | 0.172377 | intron-variant | RCHY1 | GRCh38.p7 | 4:75482759 | AAATCATATTAAAGA[G/T]GTGAAAATACATACA | 25898 |
rs72866226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489034 | GAGCCGAGATTGTGC[C/T]ACTGCACTCCAGGCT | 25898 |
rs72866232 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498273 | CTTCTGAGATTGAAC[C/T]ACAAAAAAACCTCAA | 25898 |
rs72866234 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499613 | AATGAAATCCTGTAA[C/T]TTACAGCAACATGGA | 25898 |
rs72866236 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499883 | GGTGACTACGGTTTA[C/T]ATTAATTGATTATAC | 25898 |
rs72866238 | snp | A/C | 0.0689305 | 0.172377 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499931 | AGAGAATTAATTCAA[A/C]TGTTTCTAGCACAAA | 25898 |
rs72866241 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500203 | TTGATTATATGAATG[C/T]ACTGAATTACCACAT | 25898 |
rs72866248 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503823 | TGTGATAATATTCTT[C/G]CATCTTTTATGACGT | 25898 |
rs72866258 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508186 | AGAAAGGACTGAACA[C/T]GGAACACCTTGGGCT | 25898 |
rs72866268 | snp | A/G | 0.0103295 | 0.0711199 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514876 | TATTGCCAGTCACCA[A/G]CTAAACCGTGAGGAC | 25898 |
rs73827639 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | RCHY1 | GRCh38.p7 | 4:75501691 | AACATCTCCTAATTA[C/T]GTTCCACTGAACATG | 25898 |
rs73827640 | snp | C/G | 0.0524604 | 0.153226 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505808 | TGAGTGCTTGAAGGG[C/G]AAAGATCTCAGAGAG | 25898 |
rs73827642 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506561 | AGCAGATTCAATGCA[A/G]CAGAAGAGAGACCTG | 25898 |
rs73827644 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509490 | TAATTCTTCCCTTCA[A/G]CATCACTACGTCTGT | 25898 |
rs74337351 | snp | A/G | 0.161267 | 0.233723 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498975 | TCTGCACAGCACAGG[A/G]AAACAAACAAGTGAA | 25898 |
rs74459622 | snp | A/C | 0 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498483 | AAGCAATCCTGAGCA[A/C]AAAAAAAAAAAAAAA | 25898 |
rs74557489 | snp | C/T | 0.5 | 0 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75509234 | TTTAAAGCGATCTAG[C/T]TGATGATCTTCATTG | 25898 |
rs74670567 | in-del | -/T | 0.161267 | 0.233723 | intron-variant | RCHY1 | GRCh38.p7 | 4:75487938 | TATTTTGGTCAAGTA[-/T]TTTTAAATCTTCGAC | 25898 |
rs74688105 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497553 | CATTTTGGAGCTACC[A/C]ACCTTGCAAATCGTT | 25898 |
rs74707283 | snp | C/G | 0.5 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506423 | TCCTTTAAATCATCT[C/G]TGATCAATACATTCA | 25898 |
rs74868069 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497467 | TTACTCATTTTCTGT[C/T]ACTTTCCTTTGTCTG | 25898 |
rs74924378 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | RCHY1 | GRCh38.p7 | 4:75501571 | CTCCTAAAATGCCTA[C/T]TTGAAGTGAACATAA | 25898 |
rs74999917 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504717 | ACTGACATATTTGAG[A/C]ACACATTATCTTCAA | 25898 |
rs75140816 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507894 | AAAGTCAGCATACTG[A/G]TTACCTTTGGGGAAG | 25898 |
rs75206907 | snp | C/T | 0.159622 | 0.233092 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504135 | ATTGCATTTTGATGA[C/T]ACAAATACAAGAAGA | 25898 |
rs75376251 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510601 | GTCCTCCAACCCACT[A/C]TTCTCATAGTTATAC | 25898 |
rs75662726 | in-del | -/GGGG | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512903 | GCCTCTGGTATTTAA[-/GGGG]GGGGGGGGGGCGGGG | 25898 |
rs75963534 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75509122 | TTGATTAAATTTTTT[C/T]AAACCACCTTAATAC | 25898 |
rs76244619 | in-del | -/AA | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502987 | AAATAGAAAAAAAAA[-/AA]GGAAAATTTAGACAA | 25898 |
rs76668901 | in-del | -/AA | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75498131 | GACTAAAAAAAAAAA[-/AA]CCAGAAACAAAAGAG | 25898 |
rs76748341 | snp | C/T | 0.00314133 | 0.0395069 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508950 | CCTAAAAAAGAAACA[C/T]AATTAAAAACTGCAA | 25898 |
rs77217682 | in-del | -/T | 0.463774 | 0.129618 | intron-variant | RCHY1 | GRCh38.p7 | 4:75487275 | AATATTTTTGTTTAC[-/T]TTTTGGGTAAATTTC | 25898 |
rs77263141 | snp | C/G | 0.0807149 | 0.183963 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479222 | AAACATATATCAAAA[C/G]ATCACATTGTACTCC | 25898 |
rs77369924 | snp | A/C | 0.5 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506144 | ACAAAAAAAAAAAAA[A/C]CAAAAATTAGTCTCT | 25898 |
rs77486762 | snp | A/C | 0.5 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506143 | TACAAAAAAAAAAAA[A/C]ACAAAAATTAGTCTC | 25898 |
rs77511580 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512439 | AAGAACTGACAGTCT[A/G]TGTTTCTAAGGCCAA | 25898 |
rs77541232 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506385 | CCCATAGATAATCAA[A/G]ATATTGGAGTTATTA | 25898 |
rs77777051 | snp | A/G | 0.0887219 | 0.191022 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513449 | CCATTTTACATACGG[A/G]GTAGAGAGGAGCTAG | 25898 |
rs77865223 | snp | A/C | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515646 | GTCCTTTTTAAATAA[A/C]CTTTTTGTTAAATTT | 25898 |
rs77914119 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510947 | ATGTACACTGGAAAA[C/G]AAAGGAGTATTTTAA | 25898 |
rs77963446 | snp | A/C | 0.5 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498498 | AAAAAAAAAAAAAAA[A/C]ACATAACTGGAGAGG | 25898 |
rs77966089 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509497 | TCCCTTCAACATCAC[C/T]ACGTCTGTATGAAGT | 25898 |
rs78077394 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494867 | TGGTTACTTGTATTA[C/T]AGACAAACAAAAGAT | 25898 |
rs78091103 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500580 | CTATTAAACTCTGTA[C/T]GAAGCACTTGAATTG | 25898 |
rs78667157 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511657 | TTTGGTTAAAATTAA[C/T]GATTTTACTGCTTTA | 25898 |
rs79054166 | snp | A/C | 0.5 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511298 | AAGTCTTTTAAAAAG[A/C]TTCCAACCTCACAAA | 25898 |
rs79414828 | snp | A/T | 0.159951 | 0.233219 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510298 | CATCACCAACCTGCA[A/T]CACTCGCCTTGGAAT | 25898 |
rs79460824 | snp | C/T | 0.161267 | 0.233723 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496112 | AAAATTCTGCAGGGA[C/T]GTTTCCACTACTGCC | 25898 |
rs79499539 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75489565 | ATATTGCAGATTGAT[A/G]GTAATCAGATCCCCT | 25898 |
rs79780893 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488147 | GTGTTATATTTTTAT[C/T]AAGATTTATTCCAAA | 25898 |
rs80036361 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506716 | GTGGGAAAACGGTAC[A/G]GAAACATTATCTGAA | 25898 |
rs80099653 | snp | A/C | 0.16028 | 0.233346 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507666 | ATACATGCAAAAACT[A/C]ATCGAAAGAAAGCTG | 25898 |
rs80310198 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483108 | TTTAGTATACTGTTC[C/T]CTGTCTTCTCTGCCT | 25898 |
rs111434701 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515664 | TTTTGTTAAATTTGA[A/G]GTGACAATGTGATAC | 25898 |
rs111447343 | in-del | -/G | 0 | 0 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512997 | GTGGTTTATGGGGGG[-/G]CACCAAGATGTTAAA | 25898 |
rs111458716 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496553 | TACTCACACATGGCT[A/G]GGAACAGTGCCTGAT | 25898 |
rs111500393 | snp | C/T | 2.11195e-05 | 0.00324951 | intron-variant | RCHY1 | GRCh38.p7 | 4:75482717 | CCTTATAAATACAAG[C/T]AGCATTGTCTACTCA | 25898 |
rs111607608 | snp | C/T | 0 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498777 | CTCTCTCACCGTACA[C/T]AGAAATCAAATCAAA | 25898 |
rs111667316 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483668 | GCCTCTAGTCAATCA[C/T]ATGATTATCGGTTAG | 25898 |
rs111687955 | snp | C/T | 0.5 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506398 | AAGATATTGGAGTTA[C/T]TAGGCACAGTCCTTT | 25898 |
rs111808796 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514734 | GAGCTCGGCCCGGGC[C/T]CTGGGCTCAGCGGGT | 25898 |
rs111841082 | snp | A/T | 0.5 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489546 | TGGATTGCCTTGGTC[A/T]AAGATATTGCAGATT | 25898 |
rs112103682 | snp | C/T | 0.342134 | 0.232404 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488740 | GAACCTGGACAGCCA[C/T]CTGGCCCTTCCTAAA | 25898 |
rs112229643 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487280 | TTTTTGTTTACTTTT[G/T]GGTAAATTTCAAACA | 25898 |
rs112235071 | snp | A/G | 0.0298908 | 0.118541 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515860 | AATCTGAATGAAGGA[A/G]CTTTGCTCGAATATA | 25898 |
rs112359534 | snp | A/G | 0.00517822 | 0.0506191 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481016 | TAGATCTGGAAAACT[A/G]GTCTTTACTTATCTG | 25898 |
rs112473514 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495731 | CCTTTCTTGAACCAC[C/T]ATTACTTTGGGTTTC | 25898 |
rs112691533 | snp | A/G | 0.5 | 0 | missense, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75508869 | TCTTATCTTTGTCAA[A/G]CAAATGGCATATATC | 25898 |
rs112742417 | snp | G/T | 0 | 0 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514648 | GGAAAGGACGCTCAC[G/T]GGGCGCATCGTTACC | 25898 |
rs112771453 | in-del | -/G | 0.5 | 0 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75515019 | CCTGGAGAAGTGCTA[-/G]GAAGAAGTGTGTGTC | 25898 |
rs112842572 | snp | C/T | 0.5 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508978 | CAATAAACTAAACAT[C/T]TTGAGTTACCATTTG | 25898 |
rs112902827 | snp | A/T | 0.5 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485740 | AACTGATAGTCTGAA[A/T]GGTGAATAGAAAAAC | 25898 |
rs112906846 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482492 | ACCAAGGAAAGCCTT[C/T]TTCTATATCAGAAAA | 25898 |
rs113360061 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496569 | GGAACAGTGCCTGAT[C/T]CCATCAAACAGACTG | 25898 |
rs113393227 | snp | C/T | 0.5 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490549 | AGTGCCAACAAGGAG[C/T]CTACAAAGTTTTAAG | 25898 |
rs113588457 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482475 | ACACATGATAACACG[A/G]TACCAAGGAAAGCCT | 25898 |
rs113869775 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | THAP6, RCHY1 | GRCh38.p7 | 4:75516562 | AAAAATGAAATGAGG[C/G]CCATATATCTGCAGC | 25898 |
rs113874793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498772 | TGCTTCTCTCTCACC[A/G]TACACAGAAATCAAA | 25898 |
rs113968356 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491348 | AAAACTGCACTTCCT[A/G]GTATATATGGCCAGA | 25898 |
rs114204659 | snp | C/T | 0.029116 | 0.117091 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482393 | CCCTGAATCCTTACG[C/T]ACTTGTAATATGATT | 25898 |
rs114251303 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488525 | ACTGCCAACCCAAGC[A/G]GGATAAAAATTGATT | 25898 |
rs114697927 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514908 | AAAAGTAAGGAAAAA[C/T]AGACACACTCCACCA | 25898 |
rs114934509 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485900 | AGTAAATAGGAATGG[C/T]TTCAGAGGTGTCTGT | 25898 |
rs114950888 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75501481 | GTTTTTCAGTATGCC[A/G]TATGCACTCATTAAA | 25898 |
rs115163427 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510616 | ATTCTCATAGTTATA[C/T]CGCAGAACAGTAGTT | 25898 |
rs115382086 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500793 | CAAACTTTCATGATA[C/T]ACCTAAGACAAAAAT | 25898 |
rs115416558 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506116 | AGGAAAAAAAAAAAA[A/T]AGAACAGGACATACA | 25898 |
rs115420443 | snp | A/G | 0.00517822 | 0.0506191 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480188 | AAAATTGCTTTAAGT[A/G]CATGACTAGACAGCA | 25898 |
rs115515664 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506297 | ATGTCCAACAATCAA[C/G]TAAAAAAAAAAATCA | 25898 |
rs115517494 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490207 | AAAAATCAGCAAATA[C/T]GTTCTCCTGAAATAA | 25898 |
rs115694407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | THAP6, RCHY1 | GRCh38.p7 | 4:75516624 | GAAAGTAACAAAAGC[A/G]TGAATTATGGTTTCC | 25898 |
rs115711002 | snp | C/T | 0.0111196 | 0.0737302 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481788 | AGGAATGAATGACTC[C/T]TTGAAGAAATAATTT | 25898 |
rs115852635 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499985 | GAAACCCCAACTCCA[C/T]AAAAAATTAGCTGGG | 25898 |
rs115969507 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512050 | TCCCTTCTCAGTTCC[C/T]CTACACTCATAGATA | 25898 |
rs116326063 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507377 | TAACTAACAAGCCTA[A/T]AGAGAATAAAAGCAA | 25898 |
rs116359504 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503858 | ACACCAAAATTTACT[C/T]AATATGGTTCATAAG | 25898 |
rs116372643 | snp | A/G | 0.0162398 | 0.0886349 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75516326 | ATCTGTAGACCTGCT[A/G]TGTATTAAATGCTGT | 25898 |
rs116406288 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503058 | ACTGAAGGTTCTCCA[C/T]CTAGGCAATATTTAC | 25898 |
rs116568271 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488185 | GAGATTCTAAAATTC[C/T]TTATGTCGGGGTATA | 25898 |
rs116631675 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506714 | AGGTGGGAAAACGGT[A/T]CAGAAACATTATCTG | 25898 |
rs116832617 | snp | C/G | 0.0142736 | 0.0832652 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480612 | TTGAAAACAGAAGAG[C/G]CTTATTATTATATAC | 25898 |
rs117225256 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480212 | GACAGCATAAACGAG[A/T]GATTGCATATGTACT | 25898 |
rs117457168 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493975 | GTTAATACTGCTTTT[C/T]AAAAAAGCAATATAG | 25898 |
rs137955612 | in-del | -/ATG | 0.0696718 | 0.173152 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509098 | AAAGAAATCTTATTT[-/ATG]ATACTTTTGATTAAA | 25898 |
rs138002199 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484098 | AACTGTTTCTCAATT[A/G]AGTTCTGTTAAATTT | 25898 |
rs138125830 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505551 | AATTCATTTTCACTT[A/G]TGTAGTGTTATTTTG | 25898 |
rs138127035 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479484 | TATGAAAATAGGTTT[C/T]AGTGAAGAAATAAAA | 25898 |
rs138246901 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498935 | TGAAACAAAAACAGA[C/T]GGAATTACATCAAGC | 25898 |
rs138287936 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480405 | ATAGAAGTTTAGATC[A/T]AAAGCAATGTGGTAA | 25898 |
rs139009808 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504947 | GGGTTATCATAATAC[G/T]GAAAACACTGCCAAA | 25898 |
rs139127899 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502798 | GAAAGACCTTTCATG[C/T]AGAAACATGAAAGAA | 25898 |
rs139214088 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484415 | ATCTAGCTAAAGACC[C/T]CTTATGCCTGACTGG | 25898 |
rs139269547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485348 | TGGAACTAAAGTATA[C/T]CTTTCTGGCATTCAA | 25898 |
rs139278088 | snp | A/C/G | 0.000465519 | 0.0152501 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491852 | ATTTTAAATTCAAGA[A/C/G]CTGAGACTTCCAAAG | 25898 |
rs139674856 | snp | A/G | 0.000230612 | 0.0107356 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515570 | CCAAATACTTTGGCC[A/G]TGTTATAAAAAGCAA | 25898 |
rs139867284 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514955 | ACAAGACTGGTGGAG[A/G]AGGAAGACATTAATA | 25898 |
rs139876815 | snp | C/T | 1.64969e-05 | 0.00287196 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514252 | TGACCTCGCTCTTGA[C/T]CGCTGGCGCCATCTT | 25898 |
rs139943147 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495541 | ATTGTACCCTCAAGA[A/G]GAAAAATATGCCTTC | 25898 |
rs140009975 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493808 | CTGTTTTAAAGTTAT[A/T]CTTAAAAGCAGTACC | 25898 |
rs140082616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75486110 | GGCTATTCTAGGAGG[A/G]GTTCCATCCTCCAAG | 25898 |
rs140233330 | snp | C/G | 0.000153988 | 0.00877328 | upstream-variant-2KB, missense, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515467 | AATGGTGAAATGCTG[C/G]TCCGCCATTGGATGT | 25898 |
rs140334281 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479323 | TTTGAACAACTCCCA[C/T]TTAAAATTAATTCAT | 25898 |
rs140346997 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503427 | GGTGGCCAGGCACAG[C/T]GGCTCACACCTGTAA | 25898 |
rs140368119 | snp | C/T | 5.02449e-05 | 0.00501198 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482536 | AGTACTGTGTAGGCT[C/T]GTCATTGCTGATCCA | 25898 |
rs140470958 | in-del | -/ATTGCAGATTGAT/TTGCAGATTGATA | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75489552 | CCTTGGTCAAAGATA[-/ATTGCAGATTGAT/TTGCAGATTGATA]TTGCAGATTGATGGT | 25898 |
rs140573894 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497738 | ATCTGAAATAGTAAT[A/G]GCCAAAACTTTCCTG | 25898 |
rs140621871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507605 | CTGTTTTACAAGACA[C/T]ATGACTTAAATGTAA | 25898 |
rs140668639 | snp | C/T | 0.000346583 | 0.0131595 | missense, nc-transcript-variant, intron-variant | RCHY1 | GRCh38.p7 | 4:75490675 | ATATCTAAAGCAGAG[C/T]GCATACATAATGGAC | 25898 |
rs140695710 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504999 | TGTGCACCTACTGTA[A/C/T]ATACGGCAGCGGTCA | 25898 |
rs140728731 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511343 | TTCCAAAATTCTAAT[G/T]TTTGTGTGAAAGCTT | 25898 |
rs140843880 | snp | A/G | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479905 | AAAATGTTAACAGTA[A/G]TTCTCTCTGAAAGAA | 25898 |
rs140923138 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511909 | CCAGGGTTCCATTCA[C/T]CACACTTTGAAAACC | 25898 |
rs141028669 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480999 | ACTTCAAAAAAAAGT[A/G]TTAGATCTGGAAAAC | 25898 |
rs141036251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504205 | TCTAAAATCTAGTAT[C/T]AGTTATTTACACGAT | 25898 |
rs141216118 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480132 | AACAAATACTTGAAG[C/T]AACCCTGGGTACCGA | 25898 |
rs141535565 | in-del | -/TTGTCAATCATGTCTT | 0.167809 | 0.236103 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488262 | AATAACCAAATTTCC[-/TTGTCAATCATGTCTT]TAACTATAACCATTT | 25898 |
rs141628043 | snp | C/T | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514771 | CGCTGCTCTTGGACG[C/T]CAGGGTGCTCGCTGG | 25898 |
rs141649385 | in-del | -/AC | 0.0693013 | 0.172766 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495905 | TTTGTCTGTGTATAT[-/AC]ACACACACATATTTA | 25898 |
rs141867840 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502172 | ATATTCACTCTGTAC[C/G]CAGGTCTAGTTCTTT | 25898 |
rs141943151 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497424 | AAGGCAAATGCTGAG[C/T]TGTAACCAATCCAGC | 25898 |
rs141953839 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500397 | TGTACATTACAGTAA[A/G]GATATATGTTCATTA | 25898 |
rs142057784 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494828 | TGCATGAGAGTAACC[A/G]TGTTCCCCACACTTT | 25898 |
rs142085367 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490757 | GAATATATTAATTCA[G/T]GTATACAAGAAGATG | 25898 |
rs142234827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488653 | CTATAATAACCCTTC[A/G]GTTATCAGTGGTAGG | 25898 |
rs142548879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503997 | TTATGAAGAAAGGTC[A/G]TCTTTTCTTCAACCA | 25898 |
rs142658745 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496653 | CAACAGTGGAGAATA[A/G]CCCTGGGATAAGCCC | 25898 |
rs142889758 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481588 | GAAGAAATATTCTAT[C/T]CATTTACAATAAGAC | 25898 |
rs142893367 | snp | C/T | 1.67184e-05 | 0.00289118 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491923 | TTCTGTCGGGACACA[C/T]TTTCAATACACTGTT | 25898 |
rs142909055 | snp | A/C/T | 0.00660433 | 0.0570873 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514130 | ATCCAAGCCTAACCA[A/C/T]CTGCCCAGCCCGCCC | 25898 |
rs143069371 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512247 | GATGATCATTTCACT[A/T]CTTCTCCTCTGGCTT | 25898 |
rs143149469 | in-del | -/G | 0.00636936 | 0.0560724 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489594 | CTTGGAGTGGAAAAC[-/G]TAAGTTGACCCCTTA | 25898 |
rs143240094 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515172 | GTGGCACAAAGAACA[C/T]GGTACCTGTTAGAAG | 25898 |
rs143329952 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484445 | GGTCGGGCAGAAGCA[A/C]AGTAAATGGCAAAAC | 25898 |
rs143415230 | snp | A/G | 0.00156375 | 0.0279182 | upstream-variant-2KB, synonymous-codon, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515518 | TTCGAAGTTAAAAGG[A/G]CTGACATTTCACGTG | 25898 |
rs143476896 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484182 | TACAGCTTTCAGTGA[A/C]CGCCAGGAGCACCAA | 25898 |
rs143522936 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483926 | GCTGAGAAGAGACAG[C/T]AACACATCTTAATTA | 25898 |
rs143628264 | snp | C/T | 0.029116 | 0.117091 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506431 | ATCATCTGTGATCAA[C/T]ACATTCAAAGAAAAA | 25898 |
rs143768682 | in-del | -/TAACT | 0.00795532 | 0.062565 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479781 | TGCGGCAGGGCAACC[-/TAACT]TATTTCAGGGACAGA | 25898 |
rs143807108 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510545 | TGGCTTCCTTTTTCT[G/T]CAACTCTCAGTTCCT | 25898 |
rs143844917 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RCHY1 | GRCh38.p7 | 4:75492612 | AGCACTGTGCCATGG[A/G]AGACTCCCAGGTTTT | 25898 |
rs143989077 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480427 | ATGTGGTAAAAGTGG[A/G]TTTGGAGTCAAACTT | 25898 |
rs144093791 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RCHY1 | GRCh38.p7 | 4:75482788 | CATAAGTCTAAAAAT[C/T]TCCAAAAGTAGAAAT | 25898 |
rs144308243 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485820 | CTTCTGTCTGTGTCT[A/G]TATTCCTATAGGTGT | 25898 |
rs144470234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508176 | AGGGACAAGAAGAAA[C/G]GACTGAACACGGAAC | 25898 |
rs144535183 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75516267 | AATAGCTCTGATCTC[C/T]AGAACTCCACACTGC | 25898 |
rs144594517 | snp | C/T | 0.00180202 | 0.0299627 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514167 | AACCTGACGGAAGCT[C/T]GTCAGGGAAGAGTCC | 25898 |
rs144610193 | snp | A/G | 0.0329836 | 0.124112 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479983 | ATACTTATGAAGTCA[A/G]AGAAAGAAAAAATAT | 25898 |
rs144689082 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481310 | CAAATAGCTCAAAGT[C/T]GGAAATACAACTGGT | 25898 |
rs144877628 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481144 | AAGAAGAGTGGAATA[C/T]AGAAGACAAGAAGGT | 25898 |
rs144936624 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510199 | GTTCAGCTATATCAG[A/T]CAGATGGCCACATGC | 25898 |
rs144961587 | snp | C/T | 0.00012328 | 0.00785013 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75509261 | ATTGTTATCATGACA[C/T]AAGCGGCAAGTATAA | 25898 |
rs145144708 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500070 | CACATAAACCTGGGA[C/G]GTCAAGGCTGCAGTG | 25898 |
rs145178243 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504468 | ATTTTCTCCTTATGA[C/T]TGTCCTAATATTTTT | 25898 |
rs145544069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496142 | CAAAGATAGAATAAC[A/G]GAGATCAGACCTACC | 25898 |
rs145565985 | in-del | -/AA | 0.0130921 | 0.0798413 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498581 | GCATGGTACTGGCAT[-/AA]AAAGAGACAAGTAGA | 25898 |
rs145639720 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505316 | CATGCACCAGAATCC[A/G]CACCCCAAGCACTGG | 25898 |
rs145833459 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491450 | TTCTATATCCAAGAC[A/G]CTTTGTCCTGTTTTA | 25898 |
rs145861196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511571 | CCTCTAATTTCAGTT[C/T]GCAGAAGTGTTTGAT | 25898 |
rs145898066 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497485 | TTTCCTTTGTCTGTC[C/T]ATAAATCCTCTCTGA | 25898 |
rs145966517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513022 | AAGATGTTAAATTCC[A/G]TTTTAGACCTCAAGT | 25898 |
rs146326212 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495421 | CTTCTTCTACAATGA[A/T]AGGGTATTTAGCTAG | 25898 |
rs146344451 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500743 | ACCTGTTCATCCTTG[C/T]CTTATAGATTTATTT | 25898 |
rs146474774 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75482838 | GAAAACTCTAAAAAG[C/T]TATTAAGGTGGCTCT | 25898 |
rs146492974 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RCHY1 | GRCh38.p7 | 4:75486966 | CCTGGGTGACAGAGA[A/G]AGACTCCGTCTAAAA | 25898 |
rs146666606 | snp | C/T | 0.00118137 | 0.0242753 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514287 | GGCCGTCGCCGCCAT[C/T]TCCTCCACCTCCCCT | 25898 |
rs146767521 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484292 | ATTCTAAAGCTCTGC[A/G]CATTTGTGTTTTGAG | 25898 |
rs146833150 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511055 | TGAAATCTGAAATCG[C/T]ATCAAGGAATATGAT | 25898 |
rs146851758 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515263 | ATGTTTCTCCTTATT[A/G]AAGAGTCAAGGCCCT | 25898 |
rs147031313 | in-del | -/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75494530 | AGGATTTTATGTCTG[-/T]TCTACACAGAACCAC | 25898 |
rs147212664 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503295 | TAATTATAATGATGG[C/T]GAAATCAATCCTATA | 25898 |
rs147230092 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507522 | ACCTTAATAAAAAAC[A/G]AACTATATACTCCAA | 25898 |
rs147250391 | snp | C/G | 4.96931e-05 | 0.00498439 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482563 | TCCAGTGAAATTCTA[C/G]GTCCTCCAGCTTGAG | 25898 |
rs147336493 | snp | G/T | 0.00835141 | 0.0640778 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480784 | CGAGGTAGGAGAAAT[G/T]CTTGAGCCCAGGAGT | 25898 |
rs147549291 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490123 | GGGGTCTCCTGTGTG[C/T]ACTCCATAAAAATAA | 25898 |
rs147566005 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497274 | ATATTTTAAGATCGT[A/C]CTAAAAGGCTTTGCT | 25898 |
rs147797512 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497644 | TGTTAAGTTTAATTT[C/G]TCTTAAGTTTTTCTT | 25898 |
rs148086677 | in-del | -/GAAA | 0.0360663 | 0.129354 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507192 | GCTGGAGACCTACAG[-/GAAA]GAAGGGCAATAGAAA | 25898 |
rs148116038 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RCHY1 | GRCh38.p7 | 4:75501091 | TTTGGCTCACTGCAA[C/T]CTCCCGCCCACGGGT | 25898 |
rs148165238 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RCHY1 | GRCh38.p7 | 4:75492878 | CACTTTAGTCTTAAC[A/G]TTTCTTATTTATAAA | 25898 |
rs148181291 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480066 | TAGATTTTATTCTTA[C/T]TGTGAATGAGAAGTG | 25898 |
rs148299295 | in-del | -/CT | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482006 | AACTTTCTATAAAAC[-/CT]AGTTTCAATATAATT | 25898 |
rs148481981 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496334 | GTTAGAAGAACTAAG[A/C/G]GTGAGCTAGGAAGAC | 25898 |
rs148498504 | snp | C/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481534 | AGGAATATCCCATGC[C/G]CTTCCCACTCATCCA | 25898 |
rs148817515 | in-del | -/AAAAAAC | | | downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75478569 | GAATGTAAATTAAAA[-/AAAAAAC]CAGCCAATATTAAAA | 25898 |
rs148817787 | snp | A/C/G | 0.00557542 | 0.0525036 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483787 | ATTTGGCTTTGCTAC[A/C/G]TGGTTTTTATCCTCG | 25898 |
rs149202247 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510429 | CCAGGCCAGTGACTT[A/T]CCAATACACTGTGAC | 25898 |
rs149224296 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499428 | GTCCACTAAAAGTAC[A/G]TATCTAAGGGGAAAT | 25898 |
rs149346537 | in-del | -/A | 0.429538 | 0.173972 | intron-variant | RCHY1 | GRCh38.p7 | 4:75482884 | AAGGCAGATTTGAGC[-/A]AAAAAAAAAGCTTAT | 25898 |
rs149398625 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RCHY1 | GRCh38.p7 | 4:75492377 | CAGCACAGTACCTGT[A/G]TAAGATCAATTAAAT | 25898 |
rs149562582 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485719 | AATGAAACAGGTTAA[C/T]TGGTAAACTGATAGT | 25898 |
rs149591873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505736 | ACTCCTACTGAGAAC[C/T]AGAAAAACTCAATTT | 25898 |
rs149878244 | in-del | -/GATATTGCAGATT | 0.480775 | 0.0961398 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489548 | ATTGCCTTGGTCAAA[-/GATATTGCAGATT]GATATTGCAGATTGA | 25898 |
rs149926570 | snp | A/G | 1.77162e-05 | 0.0029762 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75509227 | CCTTCACTTTAAAGC[A/G]ATCTAGTTGATGATC | 25898 |
rs149965939 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502916 | AGAGTCCGCAGATAC[C/T]TTCTTTGTAGTTTTC | 25898 |
rs150159893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483587 | ATGAACTATATAATA[C/T]GTGAATTGTATCTTA | 25898 |
rs150231028 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511925 | CACACTTTGAAAACC[A/G]ATGCTACAGAACAAC | 25898 |
rs150260905 | in-del | -/AAAAAAACA | 0.0182019 | 0.0936463 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508090 | AACAAACTATATTTT[-/AAAAAAACA]AAAAAAACAAAAAAA | 25898 |
rs150299445 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489379 | AACTCTATTACAGTA[C/T]CTAAAAGGTTATTAT | 25898 |
rs150391867 | in-del | -/AC | 0.342806 | 0.232136 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498045 | AGAGTGAGACTAAAA[-/AC]ACAATACAAAAGACC | 25898 |
rs150459224 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498324 | AGACTGAAGCCATGA[C/T]AAAAAGTTTCACATC | 25898 |
rs150616046 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75493413 | TCGAACCTACTATAC[C/T]GCTAAGTAAATGATT | 25898 |
rs150740825 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480251 | TTTTGGACATGTTTG[A/G]ATCCTAAGTTAAAGA | 25898 |
rs150776823 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502796 | TAGAAAGACCTTTCA[C/T]GTAGAAACATGAAAG | 25898 |
rs150796639 | snp | C/T | 1.69327e-05 | 0.00290965 | splice-donor-variant, intron-variant | RCHY1 | GRCh38.p7 | 4:75508819 | ACTTTACATACAGTA[C/T]CTACAAATTCCACAG | 25898 |
rs150901164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485276 | TCTTAGTGGGCTCCA[C/T]CCTGAACTCAGTAAT | 25898 |
rs151044940 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511795 | TTTCCACCATCAATG[C/T]GTGTGTCAACAGACT | 25898 |
rs151057780 | snp | A/C | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481589 | AAGAAATATTCTATT[A/C]ATTTACAATAAGACA | 25898 |
rs151094131 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504176 | ATTACAAGCTAGAAC[C/T]TATTAGAAATGTATC | 25898 |
rs151322436 | snp | A/G | 0.00570002 | 0.0530803 | upstream-variant-2KB, synonymous-codon, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515524 | GTTAAAAGGACTGAC[A/G]TTTCACGTGTAAGAT | 25898 |
rs180796931 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505289 | CTGGGCGCAGCTCAG[G/T]TCCTAACAGGCCATG | 25898 |
rs180806892 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485018 | ATAAAAAGCTTAACT[A/G]ACTGATAAGACAAAT | 25898 |
rs181142183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75501163 | TACAGACATATACCA[A/C]CACGCCTGGCTAATT | 25898 |
rs181142726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510301 | CACCAACCTGCATCA[C/T]TCGCCTTGGAATTGT | 25898 |
rs181149568 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75479126 | CAAAAATATTAAGAG[C/T]AGATTTTAAGTGGTT | 25898 |
rs181179103 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489823 | GGGTCTCTGAGAACA[A/T]CATCAGAGAAAGACT | 25898 |
rs181293743 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484110 | ATTAAGTTCTGTTAA[A/G]TTTAATTTGTGTAAG | 25898 |
rs181425418 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504422 | GAAGACCTTTATGAT[G/T]ATCCATTTCCACTTA | 25898 |
rs181464926 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495337 | TTTATATTTTTCTTT[A/G]ATCCATTTGAAATTT | 25898 |
rs181549586 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75500437 | TAAGACCAGATGTTT[G/T]CCCGTATTTACCGAA | 25898 |
rs181627484 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491377 | GAAAAAAAAGAGGTA[A/T]CTACCTCAAATTGTG | 25898 |
rs181739898 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75505884 | TCCTTGGGAGATTTT[C/T]AGACCCTAAACTGTG | 25898 |
rs181747564 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75485803 | GAAAGCTCTAAGATC[C/T]GCTTCTGTCTGTGTC | 25898 |
rs181753208 | snp | A/C | 0.0287284 | 0.116357 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513677 | ACTTTCCTATGCATA[A/C]TTTCCTATTTAATGG | 25898 |
rs182027549 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490852 | GGAACCTGGGAACTT[A/T]CACACTATAAAACTT | 25898 |
rs182037495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511484 | TTTCAAGTAAAAAAT[A/G]CTGTTCCATGAAAAA | 25898 |
rs182193553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496921 | AGAACAGACACAGAT[A/G]TTAGAATTAATACAG | 25898 |
rs182238975 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494524 | ATTCTGAGGATTTTA[C/T]GTCTGTCTACACAGA | 25898 |
rs182293637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75501817 | AGTGCGGTGGCTCAC[A/G]CCTATAATCCCAGCA | 25898 |
rs182384034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503109 | TTGTAGCAGGAAAGC[A/G]TCTTGCACATTATAG | 25898 |
rs182642427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75487161 | GGATGGATTTGTTTA[C/G]AAGGTTTTATTAAAA | 25898 |
rs182648554 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498465 | AAAGACCCTGAATAG[A/T]CAAAGCAATCCTGAG | 25898 |
rs182687780 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506466 | GTAAAGAATTTCACC[A/T]GACAACTAGAAAATA | 25898 |
rs182781006 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481464 | CTGAAGTAAGAGGTA[C/T]ATTTAATTCCACTAC | 25898 |
rs182807912 | snp | C/G | 0.0158469 | 0.0875917 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514423 | CCTAAGCACGTGACC[C/G]GGGGCAGACGGATTT | 25898 |
rs182810393 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480268 | TCCTAAGTTAAAGAA[A/G]CAATCAGATTGTGAA | 25898 |
rs182943694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508195 | TGAACACGGAACACC[C/T]TGGGCTTTGACAGTA | 25898 |
rs182952622 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502917 | GAGTCCGCAGATACC[G/T]TCTTTGTAGTTTTCC | 25898 |
rs183121255 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RCHY1 | GRCh38.p7 | 4:75492430 | GCTATGATTGTTATA[A/C]CATTTTACAGTTAAA | 25898 |
rs183423942 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486786 | GAGTTTGAGACCAGC[A/C]TGGCCAATACAGTGA | 25898 |
rs183521604 | snp | C/T | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515113 | GGGAAGCGATGCAAG[C/T]CGAGGGCTGAAAGAT | 25898 |
rs183527522 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493643 | TATTAGATTTTTTTT[A/T]AAATAATGAAAAAGG | 25898 |
rs183543861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75492937 | CTAAAGTGCACCTCA[C/G]ACATACATTTTAACA | 25898 |
rs183659631 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499253 | AGTTAGAATGGCTTA[C/T]ATCATAAAAGACAGG | 25898 |
rs183728762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | THAP6, RCHY1 | GRCh38.p7 | 4:75516523 | TAAATATCCATTGAA[A/G]CTTTTCTTCCTTATA | 25898 |
rs183866772 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497259 | AACGCTGCCTCCTAC[A/G]TATTTTAAGATCGTC | 25898 |
rs183975833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493941 | ATATTCTGAGGTACA[C/T]ATTTTAAAATATCTA | 25898 |
rs184241189 | snp | C/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480068 | GATTTTATTCTTATT[C/G]TGAATGAGAAGTGTT | 25898 |
rs184385541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490252 | AAAAATAAAATGTAC[C/T]TAAAAAGTCCCACCA | 25898 |
rs184500513 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511050 | CAACATGAAATCTGA[A/T]ATCGTATCAAGGAAT | 25898 |
rs184594046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503994 | CAATTATGAAGAAAG[A/G]TCGTCTTTTCTTCAA | 25898 |
rs184606030 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483742 | GAATTATGAAACACT[C/T]CAGTGTAAATAAAAC | 25898 |
rs184739637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488644 | TCAAATTACCTATAA[C/T]AACCCTTCAGTTATC | 25898 |
rs184754304 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484921 | CCCAAATTAGACTCA[C/T]CTAAGAATGCCTATT | 25898 |
rs184792738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494276 | AGTCTCTGTAAAAAA[A/G]ATTTCCAGCCACAAT | 25898 |
rs184848577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504770 | TTTGGGTTTGCAGTG[C/T]TCAAATTCTTAGTAA | 25898 |
rs184884910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510258 | AAAAATCTCATCCCT[A/G]GAGTGACCATGTGGA | 25898 |
rs184900634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509108 | TATTTATGATACTTT[C/T]GATTAAATTTTTTCA | 25898 |
rs185025192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489422 | TCTCATGGGACATTC[C/T]TAGAGAAATCTCCAG | 25898 |
rs185205322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497096 | AGTTTGATATTGCTA[A/T]CAAAAAGGTTAGTCA | 25898 |
rs185335276 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RCHY1 | GRCh38.p7 | 4:75492431 | CTATGATTGTTATAC[C/G]ATTTTACAGTTAAAG | 25898 |
rs185674601 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495816 | TTGGTTTCCGAATGG[A/T]TAATCAATTATCTTA | 25898 |
rs185685738 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499876 | CCAGTAGGGTGACTA[C/T]GGTTTACATTAATTG | 25898 |
rs185699147 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503565 | CTGGCTGTGGTGGCG[A/T]GTGCCTGTAATCCCA | 25898 |
rs185815609 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500581 | TATTAAACTCTGTAC[A/G]AAGCACTTGAATTGC | 25898 |
rs185815891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483333 | GAATAGTCACACTAT[A/G]ATAAGCAGAAAATTT | 25898 |
rs185833524 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505594 | ATAGGATGAATCTTA[A/G]AAACAGAGCTCAGTA | 25898 |
rs185868673 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506075 | ATCTCCAAGGGACTA[C/T]GTCCTAGGAGCATAA | 25898 |
rs185875021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485907 | AGGAATGGCTTCAGA[A/G]GTGTCTGTTGAATAT | 25898 |
rs185966306 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RCHY1 | GRCh38.p7 | 4:75501300 | AGGCGTGAGCCACTG[C/T]GCCCAGCTCTTTTAA | 25898 |
rs186130770 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479181 | GGCAATAAATTTATT[A/G]CATTGATTTAATCAT | 25898 |
rs186215331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490857 | CTGGGAACTTTCACA[A/C]TATAAAACTTTTAAA | 25898 |
rs186230546 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513400 | CTTTAGTATATAATC[C/T]TCATACACTTTTATG | 25898 |
rs186639389 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514045 | CGCCTTGCCAAAAAC[A/G]TTCTCCTCAAGAAGA | 25898 |
rs186667544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75487375 | AGAAAACTGAGTTTC[A/G]AAGAGTAAAGGTTTT | 25898 |
rs186803665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494618 | TCCCTCAGAAAGATC[A/G]TAATTTATGATCTTT | 25898 |
rs186849699 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491518 | TTGCCATGCCCAATA[C/T]AGTATAAGTAACAAT | 25898 |
rs186917236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498555 | ACTACAAAGCTATTG[C/T]AATCAAATCAGCATG | 25898 |
rs187156272 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480194 | GCTTTAAGTGCATGA[A/C]TAGACAGCATAAACG | 25898 |
rs187247688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502928 | TACCTTCTTTGTAGT[C/T]TTCCTTGAACACAGT | 25898 |
rs187256874 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480546 | GAGGACAACACTTAC[C/T]CCACAGAATCATTGT | 25898 |
rs187297184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502587 | GAAAATCTACTTTTT[C/G]TTTAATAGAATAAAC | 25898 |
rs187485714 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509000 | TACCATTTGAATATC[C/T]AGAACTTATGTTCAA | 25898 |
rs187588845 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485604 | GTCTAAAGTCTTAGC[C/T]GTGTGCTTTTGAGAT | 25898 |
rs187656044 | snp | C/T | 0.000103643 | 0.00719797 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509135 | TTCAAACCACCTTAA[C/T]ACAGCTTTTAAAAAG | 25898 |
rs187679043 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75489046 | TGCCACTGCACTCCA[A/G]GCTGCACAACAAGAG | 25898 |
rs187784309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503303 | ATGATGGTGAAATCA[A/G]TCCTATAAGCAATAA | 25898 |
rs187797386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483560 | AAGCACCAAATTGTA[A/C]AATTTAAATGAATGA | 25898 |
rs187803884 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515165 | AGGCTTTGTGGCACA[A/G]AGAACATGGTACCTG | 25898 |
rs187836129 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493036 | GAGGATGCAATGAAT[A/T]AGTGTGTGCACACAC | 25898 |
rs187909080 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486832 | AAAAGTACAAAAATT[A/G]GCCAGGCGTAGTGGT | 25898 |
rs187955592 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511177 | CTGGAGAATACCAGT[G/T]CAGTGAGTTATTTAC | 25898 |
rs187963851 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490495 | CCAGTATATATATAT[A/T]TTTTTTTTGGCAAAT | 25898 |
rs188206429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | THAP6, RCHY1 | GRCh38.p7 | 4:75516574 | AGGGCCATATATCTG[C/T]AGCATGATTGGCAGA | 25898 |
rs188208067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507181 | CCAAAGATAATGCTG[A/G]AGACCTACAGGAAAG | 25898 |
rs188308266 | snp | C/T | 0.00116834 | 0.0241414 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494072 | AAACACTGTAATATT[C/T]TTAAAATTATACAAA | 25898 |
rs188499148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493716 | TGTATGTCTTAATTA[C/T]AAAAAGAAATAGTAA | 25898 |
rs188561704 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497332 | ATGTGTTTACCTACA[C/G]TAACCTACTCTAGTA | 25898 |
rs188764183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500791 | GACAAACTTTCATGA[C/T]ATACCTAAGACAAAA | 25898 |
rs188773424 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75478873 | AGACATTATACTAAA[C/T]GAAATAACCCAGGCA | 25898 |
rs188913542 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504330 | CAGATTTTCTTCTAC[C/G]TCTGCCACCCCTGAG | 25898 |
rs188919885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484018 | AGGTTGCAAGCTAAT[G/T]GCAACCAAATAAAGA | 25898 |
rs188970209 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503616 | AGAATTGCTTGAACC[A/C]AGGAGGCAGAGGTTG | 25898 |
rs189076999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513424 | TTTTATGAAACAGGC[A/G]CGATCATCTCCATTT | 25898 |
rs189285671 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499429 | TCCACTAAAAGTACA[A/T]ATCTAAGGGGAAATC | 25898 |
rs189302803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505136 | TATTAGATTCTCATA[A/C]GGAGTACACAACCTA | 25898 |
rs189485728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489687 | ACCAAACTCTGATAT[A/G]ACTAAATGCCGCAAG | 25898 |
rs189623840 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484963 | CTAAAAATATTTCAA[C/T]ATTTTTATTGCCTTA | 25898 |
rs189807681 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514980 | TTAATAAGAGCAATC[A/G]CTGCAATAAATGTAA | 25898 |
rs189840454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75492488 | ACTTCCAAAGTCACA[C/T]ATTAATAAGAGGCAG | 25898 |
rs189922755 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510281 | CATGTGGAGCAAAGC[C/T]TCATCACCAACCTGC | 25898 |
rs189990312 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495997 | TTTGATATGTGGAAC[A/G]GCAATCCACTCTTCG | 25898 |
rs190065598 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495219 | TCATCAATATTTTCC[G/T]GTATAGCTTATGCTT | 25898 |
rs190131186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503022 | AGAAAATAAATGCAA[A/G]AAGGCAGATAACCAT | 25898 |
rs190138702 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480676 | TTAAAAACAATAACA[G/T]GATTGGTTTGGCAGA | 25898 |
rs190156623 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500320 | TCTTATAATAAGCTC[C/T]GGTGCTTATTTAATA | 25898 |
rs190465185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494292 | ATTTCCAGCCACAAT[A/G]GAGAATATGGGATAA | 25898 |
rs190482986 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RCHY1 | GRCh38.p7 | 4:75486421 | TATATACTTTGGCAT[C/T]TTATTTTTATATAGT | 25898 |
rs190497966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506086 | ACTATGTCCTAGGAG[C/T]ATAAGAATAAAGGGA | 25898 |
rs190603309 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480007 | AAAATATTTAAGGGT[A/C]AAGTTATGTATTTTA | 25898 |
rs190636191 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480195 | CTTTAAGTGCATGAC[C/T]AGACAGCATAAACGA | 25898 |
rs190899064 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507971 | AATGTTGTGTTTCTT[A/G]ATCTGGGTAGTGGTT | 25898 |
rs190944645 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505655 | ATGATTTTTAAAATA[A/G]GCAAAATGAAACATA | 25898 |
rs190956013 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485791 | AGAATCCTTTAGGAA[A/G]GCTCTAAGATCTGCT | 25898 |
rs191016557 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RCHY1 | GRCh38.p7 | 4:75501458 | GAACTCAAAAATCCT[C/T]GAGGGTAGTTTTTCA | 25898 |
rs191131184 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75486956 | TGTACTCCAGCCTGG[A/G]TGACAGAGAAAGACT | 25898 |
rs191212830 | snp | C/T | 0.00211128 | 0.0324219 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494096 | ATACAAACTAAATTA[C/T]ATACCTTGTGTCTTC | 25898 |
rs191234811 | snp | A/C | 1.69364e-05 | 0.00290997 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491961 | GAAATTCACATTAAC[A/C]AAAGCTTAACTAGAT | 25898 |
rs191488359 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514081 | GTTCCAGGTGGAAAA[A/G]GTATCCTGAAAATCA | 25898 |
rs191558219 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498615 | AATTATGCAGAACAG[A/C]GAATCCACATATAAA | 25898 |
rs191695126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502908 | GGCATTAAAGAGTCC[A/G]CAGATACCTTCTTTG | 25898 |
rs192015295 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497140 | GTAACAGAAACTATC[C/T]GAAATGAAATAGGAA | 25898 |
rs192089339 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509901 | TTCCCAGTCTTGGGT[A/G]TGTCTTTATCAGCAG | 25898 |
rs192273879 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483177 | TTGAGTAAACAGAGA[G/T]GCTCTTCGCTCATCC | 25898 |
rs192417021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483652 | AACATAGCACACTTC[A/G]GCCTCTAGTCAATCA | 25898 |
rs192426834 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | THAP6, RCHY1 | GRCh38.p7 | 4:75516515 | TAAGATGCTAAATAT[A/C]CATTGAAACTTTTCT | 25898 |
rs192433970 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503644 | TTGCAGTGAGCCGAG[A/T]TCACGCCACTGCACT | 25898 |
rs192550710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509103 | AATCTTATTTATGAT[A/G]CTTTTGATTAAATTT | 25898 |
rs192556490 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75488415 | ATGAAAAGGACCCTG[A/T]CAAACTCTCTTAAAT | 25898 |
rs192697367 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503479 | AGGTGGGCGGATCAC[A/G]AGGTCAGGAGATCAA | 25898 |
rs192711922 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493887 | GTAAGTGATATAAGC[A/G]TTCTTACACTACAGA | 25898 |
rs192887859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489309 | GATTACATTCAATTG[C/T]CATTTTGAATGCATG | 25898 |
rs192913163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | THAP6, RCHY1 | GRCh38.p7 | 4:75516677 | TAATAAACTAGTTAA[C/T]GAATCAATTTAGTCA | 25898 |
rs193088792 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497794 | AATGGATTCAAAAAG[A/C]TCAACAAACCCTAAG | 25898 |
rs193102943 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499457 | ATCAGTACCTCAAAG[G/T]GTATCTGCACTCCCA | 25898 |
rs193183043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493612 | TAGATAGAATCAGTA[C/T]TATAATGTAATACTT | 25898 |
rs199546194 | in-del | -/GGGC | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512914 | TTAAGGGGGGGGGGG[-/GGGC]GGGGGAAGGCAAAAA | 25898 |
rs199643419 | in-del | -/AC | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482004 | AAAACTTTCTATAAA[-/AC]ACAGTTTCAATATAA | 25898 |
rs199658558 | snp | A/G | 9.93526e-05 | 0.00704744 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482564 | CCAGTGAAATTCTAC[A/G]TCCTCCAGCTTGAGC | 25898 |
rs199697353 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75494784 | CTGACCTCCAAATAG[A/T]CAGTACCAATTTATA | 25898 |
rs199762706 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479640 | CTTGATATACACTCA[-/T]TTTTTTTTTATACAT | 25898 |
rs199773737 | in-del | -/AAATAGG | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75505577 | GAATTAGAGTTAATC[-/AAATAGG]ATGAATCTTAGAAAC | 25898 |
rs199795746 | snp | C/T | 0.009925 | 0.0697424 | intron-variant, upstream-variant-2KB | THAP6, RCHY1 | GRCh38.p7 | 4:75516723 | GCTTTAATTCAATTA[C/T]ATAGCAATAGTATTT | 25898 |
rs199827703 | snp | A/G | 0.000153988 | 0.00877327 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75494106 | AATTATATACCTTGT[A/G]TCTTCCTTGAAGATT | 25898 |
rs199837515 | in-del | -/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75511587 | GCAGAAGTGTTTGAT[-/C]AAAACTTCCCATGTC | 25898 |
rs199904135 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75489548 | GATTGCCTTGGTCAA[A/T]GATATTGCAGATTGA | 25898 |
rs200101071 | snp | A/C | 5.08634e-05 | 0.00504273 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491645 | AACACGTTCTGAAAG[A/C]AAATATAAGATTATT | 25898 |
rs200241547 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489870 | CTAAAGCTTCTGGAC[-/T]TTGAACTTAGGTTCA | 25898 |
rs200249839 | snp | A/C | 0.00118842 | 0.0243474 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491564 | CACACCACACACACA[A/C]AAAAGTCAAACATCT | 25898 |
rs200337270 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483213 | ATAACAATAAGATGC[C/T]GTTTAAGAATTAATT | 25898 |
rs200440625 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488011 | AAGTCTTTTTTTTTT[-/A]ACCTCTAACTTTGGC | 25898 |
rs200625658 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510839 | TGAAAAATAACTATA[-/T]TTTTCCCCCCAAACA | 25898 |
rs200675122 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482004 | AAAAACTTTCTATAA[A/C]ACAGTTTCAATATAA | 25898 |
rs200764232 | in-del | -/TA | 0.16976 | 0.236773 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490483 | TCTGTGTCAAACCAG[-/TA]TATATATATATTTTT | 25898 |
rs200765087 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75489545 | CTGGATTGCCTTGGT[C/G]AAAGATATTGCAGAT | 25898 |
rs200791854 | in-del | -/ATA | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487496 | TAGTCATATATATTC[-/ATA]ATATATATATTCATA | 25898 |
rs200792030 | snp | C/T | 5.16791e-05 | 0.005083 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490728 | AGAAAGGTTATTTTC[C/T]AAATATTAAACAAGA | 25898 |
rs200818996 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75494785 | TGACCTCCAAATAGA[A/C]AGTACCAATTTATAC | 25898 |
rs200969877 | snp | C/T | 0.000446913 | 0.0149418 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514165 | CCAACCTGACGGAAG[C/T]TTGTCAGGGAAGAGT | 25898 |
rs201130612 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75489084 | CTGTCTAAAACAAAC[-/A]AAAAAAAAAAGTCTG | 25898 |
rs201182132 | snp | C/G | 0.343254 | 0.231956 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512912 | ATTTAAGGGGGGGGG[C/G]GGGGCGGGGGAAGGC | 25898 |
rs201278016 | snp | C/T | 3.33801e-05 | 0.00408521 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491914 | ATTGGACAATTCTGT[C/T]GGGACACATTTTCAA | 25898 |
rs201526982 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75510618 | TCTCATAGTTATACC[A/G]CAGAACAGTAGTTCT | 25898 |
rs201556958 | snp | C/T | 2.07717e-05 | 0.00322264 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509131 | TTTTTTCAAACCACC[C/T]TAATACAGCTTTTAA | 25898 |
rs201565465 | snp | C/T | 3.29533e-05 | 0.00405901 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515407 | CTTTCCGGTTACTAA[C/T]TCTTAACATTCTAAT | 25898 |
rs201674652 | snp | C/T | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75490634 | TCTGTGCTACTTCAT[C/T]ATCCAGCTGTCTCCA | 25898 |
rs201752755 | snp | A/G | 4.95995e-05 | 0.00497969 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482611 | CAAATCTTACATTTC[A/G]TGCCTAATATATGAA | 25898 |
rs201866310 | in-del | -/TC | 0.0158469 | 0.0875917 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75511977 | TTCCAAGCATGAAAT[-/TC]TCTAACCATTACCTC | 25898 |
rs201922601 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75489547 | GGATTGCCTTGGTCA[A/T]AGATATTGCAGATTG | 25898 |
rs201951635 | snp | C/G/T | 0.000360369 | 0.0134188 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514321 | ATTCCACCGATCCTT[C/G/T]CCCCAGGATAAAAAC | 25898 |
rs201960445 | in-del | -/A | 0.0189856 | 0.0955633 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510332 | TAAATGGAAAGAAAT[-/A]AAACCTTTACTCTTT | 25898 |
rs202075470 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506652 | CAGGAAAAAAAAAAA[C/T]AGACATGGGATGTAG | 25898 |
rs202218805 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75489566 | TATTGCAGATTGATG[G/T]TAATCAGATCCCCTT | 25898 |
rs367572583 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75511027 | CAACAACTCTTAAAG[G/T]GTAGTTGCAACATGA | 25898 |
rs367674831 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499848 | GAAGAAATAAGCCCT[A/G]GTGTTTGATAGACCA | 25898 |
rs367829154 | in-del | -/AA | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75511248 | AATCATATTCATTAA[-/AA]GTCTTTAGGTATTGA | 25898 |
rs367879399 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75503529 | GTGAAACCTCATCTC[C/T]ACTAAAAATACAAAA | 25898 |
rs367894456 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75494520 | ATATATTCTGAGGAT[C/T]TTATGTCTGTCTACA | 25898 |
rs367931469 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487630 | AATATATATATTCAT[-/A]ATATATATATTCATA | 25898 |
rs368017259 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514237 | TGCTCGCAGCCCCGC[C/T]GACCTCGCTCTTGAC | 25898 |
rs368131203 | snp | C/T | 0.000230779 | 0.0107395 | synonymous-codon, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75490608 | GTTCTGATATTCTGA[C/T]GGCATAGGAGTCTGT | 25898 |
rs368171667 | in-del | -/ATAT | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487554 | ATATATATATTCATA[-/ATAT]ATATATTCATAATAT | 25898 |
rs368200315 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495341 | TATTTTTCTTTAATC[C/T]ATTTGAAATTTGCTA | 25898 |
rs368222415 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480655 | AAAGATCCAATGATT[C/G]AATGATTAAAAACAA | 25898 |
rs368299505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502134 | TAACAAAGCTTTTAT[A/G]ACTGCAAAAGCCTTT | 25898 |
rs368365451 | snp | C/G | 0.000132286 | 0.00813176 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482576 | TACGTCCTCCAGCTT[C/G]AGCAGTATTATAGGA | 25898 |
rs368450293 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488421 | AGGACCCTGACAAAC[C/T]CTCTTAAATATAGAC | 25898 |
rs368517028 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75493140 | CATTAGCATAGCTTG[C/T]CATCACCCCAAACTC | 25898 |
rs368527752 | snp | C/T | 4.53648e-05 | 0.00476239 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494225 | GATTATTTTTTACTA[C/T]AGTCATGATTTGTTC | 25898 |
rs368815747 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481581 | GCTTAGGGAAGAAAT[A/C]TTCTATTCATTTACA | 25898 |
rs368841470 | snp | A/G | 3.29533e-05 | 0.00405901 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515415 | TTACTAACTCTTAAC[A/G]TTCTAATTTTCTTTC | 25898 |
rs368916977 | snp | C/G | 3.30006e-05 | 0.00406192 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514254 | ACCTCGCTCTTGACC[C/G]CTGGCGCCATCTTCC | 25898 |
rs369006663 | in-del | -/AT | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487667 | ATAATATATATATTC[-/AT]ATATATATTCATAAT | 25898 |
rs369046790 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75496855 | TAACCAGGCAACAAA[A/G]AGGCAGAAAAACACA | 25898 |
rs369060868 | snp | C/G/T | 4.99624e-05 | 0.00499791 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514290 | CGTCGCCGCCATCTC[C/G/T]TCCACCTCCCCTCAC | 25898 |
rs369145958 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510792 | TAAAAGTAACAAACT[C/T]ATTACTTGTTAACAT | 25898 |
rs369214354 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504371 | CAATCTCTCTTCTTC[C/T]TCCCTCTTTTCAGCC | 25898 |
rs369242412 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502103 | CTGAGAAGGGATTTT[A/G]ATTAAATTCAGCATT | 25898 |
rs369408765 | snp | G/T | 0.000232423 | 0.0107776 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508793 | TACATTAGAAGCAAT[G/T]AGATAAGAACACTTT | 25898 |
rs369421285 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75505089 | TTGGGGGATGGTTTC[A/G]GGATGAAACTGTTCC | 25898 |
rs369627358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502358 | ATGCTGGCTAACACG[C/G]TGAAACCCCGTCTCT | 25898 |
rs369645169 | snp | C/T | 9.97075e-05 | 0.00706002 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491839 | TAAACATCCAAGTAT[C/T]TTAAATTCAAGAGCT | 25898 |
rs369658625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489631 | AATCACTGGAAGGCC[C/T]GTATACCTAATAATA | 25898 |
rs369731008 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486266 | CTGAGAAAACATTCG[A/G]GAGGGTACATCTGTG | 25898 |
rs369812068 | snp | C/T | 6.67468e-05 | 0.00577658 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491721 | AAAAAGATGTTACTT[C/T]ACCTATGTAAAAGAT | 25898 |
rs369983795 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75490145 | TAAAAATAAGTCTAA[C/G]ATGGAATAAAAAGGG | 25898 |
rs370044880 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487824 | ATAATATATATTCAT[-/A]ATATATATATTCATA | 25898 |
rs370095600 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502988 | AATAGAAAAAAAAAA[-/A]GGAAAATTTAGACAA | 25898 |
rs370233531 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499891 | CGGTTTACATTAATT[G/T]ATTATACATTTCAAA | 25898 |
rs370315111 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480183 | ATTTGAAAATTGCTT[A/T]AAGTGCATGACTAGA | 25898 |
rs370501938 | in-del | -/TGTAATAGACT | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75498109 | AAAATCAAAAAAAAA[-/TGTAATAGACT]AAAAAAAAAAAAACC | 25898 |
rs370536165 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497362 | ACCAATCAATCACCA[A/G]GTTTCATCCAATCAC | 25898 |
rs370657823 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506562 | GCAGATTCAATGCAG[C/T]AGAAGAGAGACCTGG | 25898 |
rs370727427 | in-del | -/CAGGAC | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506121 | AAAAAAAAAATAGAA[-/CAGGAC]ATACAAAAAAAAAAA | 25898 |
rs370747865 | snp | A/C | 1.6522e-05 | 0.00287414 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514178 | AGCTTGTCAGGGAAG[A/C]GTCCATAGAAGGCGT | 25898 |
rs370748281 | in-del | -/GAT | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75509100 | AGAAATCTTATTTAT[-/GAT]ACTTTTGATTAAATT | 25898 |
rs370839561 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75492442 | ATACCATTTTACAGT[C/T]AAAGCAGTGGAGGCC | 25898 |
rs370857175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502357 | CATGCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 25898 |
rs371053990 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506130 | ATAGAACAGGACATA[A/C]AAAAAAAAAAAAAAC | 25898 |
rs371122538 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499537 | GTGTCCATCAGTGGA[A/T]GAATGGATAAAGAAA | 25898 |
rs371227626 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514482 | GAAGGCAGACGCAGT[C/G/T]TCCGTCGTTGACGTT | 25898 |
rs371250778 | snp | A/C | 1.6517e-05 | 0.00287372 | missense, nc-transcript-variant, intron-variant | RCHY1 | GRCh38.p7 | 4:75490680 | TAAAGCAGAGTGCAT[A/C]CATAATGGACATCTG | 25898 |
rs371416161 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482541 | TGTGTAGGCTCGTCA[C/T]TGCTGATCCAGTGAA | 25898 |
rs371638162 | snp | A/G | 0.000543501 | 0.0164759 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515558 | GCTGTAGTTAAGCCA[A/G]ATACTTTGGCCATGT | 25898 |
rs371645197 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75488728 | TGGACTCATGGAGAA[C/T]CTGGACAGCCACCTG | 25898 |
rs371652476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511064 | AAATCGTATCAAGGA[A/G]TATGATTGATATGAT | 25898 |
rs371802092 | in-del | -/AT | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487631 | ATATATATATTCATA[-/AT]ATATATATTCATATA | 25898 |
rs371933050 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481226 | AAATTTCAACAAAAG[A/G]AGAAATAAATGTGCC | 25898 |
rs371938310 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504018 | TCTTCAACCAAATTA[C/T]GACTCTCAAAGTTCT | 25898 |
rs371946175 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483063 | AAACCAAAATTTTTA[A/C]ACAAATAATATTTTT | 25898 |
rs371988206 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495794 | ATACAGTTTGAAGAG[G/T]CAATTTTTGGTTTCC | 25898 |
rs371992356 | snp | C/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514255 | CCTCGCTCTTGACCG[C/T]TGGCGCCATCTTCCC | 25898 |
rs371997588 | snp | C/T | 3.3168e-05 | 0.00407221 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482641 | AACTGAACAGTGGAT[C/T]GTCCATTACAGTCAT | 25898 |
rs372027777 | in-del | -/G | 0.00438332 | 0.0466095 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496421 | ACAGAGCATCAGATA[-/G]GGAGAGAGCTGCACA | 25898 |
rs372107342 | in-del | -/AT | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487717 | TCATAATATATATTC[-/AT]ATATATATATTCATA | 25898 |
rs372110501 | in-del | -/ATATATATATTC | 0.393987 | 0.204372 | intron-variant | RCHY1 | GRCh38.p7 | 4:75487881 | TAATATATATTCATA[-/ATATATATATTC]ATATATATATTCATA | 25898 |
rs372253230 | snp | A/T | 6.64651e-05 | 0.00576438 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491815 | GTTAGTGCTTGTATG[A/T]AGACAATATAAACAT | 25898 |
rs372325516 | in-del | -/A/AG | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75490494 | CCAGTATATATATAT[-/A/AG]TTTTTTTTTGGCAAA | 25898 |
rs372405343 | in-del | -/AT | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487578 | ATAATATATATATTC[-/AT]ATATATATTCATAAT | 25898 |
rs372499929 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490755 | AAGAATATATTAATT[C/T]AGGTATACAAGAAGA | 25898 |
rs372576903 | in-del | -/CA | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75498048 | GTGAGACTAAAAACA[-/CA]ATACAAAAGACCAAT | 25898 |
rs372596588 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501135 | CTGCCTCAGCCCCCC[A/G]AATAGCTGGGATTAC | 25898 |
rs372904277 | in-del | -/CTT | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484539 | TCTTCAATTCTTCTT[-/CTT]GCACATTTAAGTAGA | 25898 |
rs372924512 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504401 | CTACTCAACATGAAG[A/C]AGGATGAAGACCTTT | 25898 |
rs373112261 | snp | A/G | 0.000153988 | 0.00877328 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515567 | AAGCCAAATACTTTG[A/G]CCATGTTATAAAAAG | 25898 |
rs373159683 | snp | A/T | 1.64743e-05 | 0.00287 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515443 | TTCAGTTTTGTTATG[A/T]GTTGCTAAAATGGTG | 25898 |
rs373405255 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514429 | CACGTGACCCGGGGC[A/G]GACGGATTTCCGGTT | 25898 |
rs373505417 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486851 | AGGCGTAGTGGTGTG[C/T]GCTTGTAGTCCCAGC | 25898 |
rs373579068 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487839 | AATATATATATTCAT[-/A]ATATATATTCATAAT | 25898 |
rs373623446 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75483890 | TTTCCCATTCTAATC[C/T]AAAACTCAATACCAT | 25898 |
rs373688801 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75500130 | TGGGCAACAGAGCAA[A/G]ACCCTTTCTCAAAAA | 25898 |
rs373795131 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487640 | TTCATAATATATATA[A/T]TCATATATATTCATA | 25898 |
rs373872182 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75490493 | AACCAGTATATATAT[-/A]TTTTTTTTTTGGCAA | 25898 |
rs373885844 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75485784 | GCAAATGAGAATCCT[C/T]TAGGAAAGCTCTAAG | 25898 |
rs374012222 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502511 | CGCCACTGCACTCCA[A/G]CCTGGGCGCCAGAGT | 25898 |
rs374029900 | snp | C/T | 1.67203e-05 | 0.00289134 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482657 | GTCCATTACAGTCAT[C/T]GCAGAGAATCTGAAA | 25898 |
rs374064698 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480468 | CCCAACTCCAACATA[C/T]AGTGTCTGTTATTTA | 25898 |
rs374184455 | in-del | -/AGAA | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75507195 | GGAGACCTACAGGAA[-/AGAA]GGGCAATAGAAACGG | 25898 |
rs374215600 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75510901 | ACAGTTGTGGCTGAA[G/T]TACAAAAAGAAACTC | 25898 |
rs374307152 | snp | C/T | | | downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75478629 | AATTACCATATGATC[C/T]AGCAATCCCACTTCT | 25898 |
rs374316282 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503257 | AAAAACTCTCCCCAG[A/T]TGAGAACCAGTGCTC | 25898 |
rs374406012 | in-del | -/AT/ATATATATTCATATATATTCATAAT | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487592 | ATATATATATTCATA[-/AT/ATATATATTCATATATATTCATAAT]ATATATATTCATATA | 25898 |
rs374417153 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481449 | TTGTTAACTTTGTTC[C/T]TGAAGTAAGAGGTAT | 25898 |
rs374426686 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514493 | CAGTCTCCGTCGTTG[A/G]CGTTAGTCGCAGTCT | 25898 |
rs374573916 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499475 | ATCTGCACTCCCATG[C/T]TTACTGCAGCACTAT | 25898 |
rs374605285 | in-del | -/A | 0.372391 | 0.217992 | intron-variant | RCHY1 | GRCh38.p7 | 4:75487867 | AATATATATATTCAT[-/A]ATATATATTCATAAT | 25898 |
rs374655826 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75488596 | CAGCCAGTACTGAAA[C/T]TGTTTAGATTTCAAT | 25898 |
rs374671709 | in-del | -/TC | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487636 | ATATTCATAATATAT[-/TC]ATATTCATATATATT | 25898 |
rs374834456 | snp | C/G | 0.000118071 | 0.00768254 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490714 | CCTCTGAAAGAGATA[C/G]AAAGGTTATTTTCCA | 25898 |
rs374960686 | snp | A/C | 1.69329e-05 | 0.00290967 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482517 | AGAAAATGCCAAGTT[A/C]TCCAGTACTGTGTAG | 25898 |
rs375114747 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487259 | TATTAATAAGACAGT[G/T]AAATATTTTTGTTTA | 25898 |
rs375281016 | snp | A/G | 1.65061e-05 | 0.00287277 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514187 | GGGAAGAGTCCATAG[A/G]AGGCGTCACCTTTAG | 25898 |
rs375307890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494842 | CATGTTCCCCACACT[C/T]TGGGTAACATGGTTA | 25898 |
rs375392806 | in-del | -/AT | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487732 | ATATATATATTCATA[-/AT]ATATATATTCATATA | 25898 |
rs375769703 | snp | A/C | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513851 | CCATTATCTCCACTT[A/C]CATTATTTCATCACA | 25898 |
rs375797369 | snp | C/T | | | synonymous-codon, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482592 | AGCAGTATTATAGGA[C/T]TCACAAATCTTACAT | 25898 |
rs375969785 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509872 | AACTGTAAGTCCAAT[G/T]AAACCTCTTTTTCTT | 25898 |
rs376115200 | in-del | -/ATAT | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487528 | ATATATATATTCATA[-/ATAT]ATATATTCATAATAT | 25898 |
rs376157308 | in-del | -/CA | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495914 | GTATATACACACACA[-/CA]TATTTATCTATTCGT | 25898 |
rs376282741 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479975 | TATAACCTATACTTA[A/T]GAAGTCAGAGAAAGA | 25898 |
rs376373598 | snp | A/G | 3.32237e-05 | 0.00407563 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491827 | ATGAAGACAATATAA[A/G]CATCCAAGTATTTTA | 25898 |
rs376391786 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489016 | GGAGGCAGAGGTTGC[A/T]GTGAGCCGAGATTGT | 25898 |
rs376434149 | snp | C/G | 6.46336e-05 | 0.00568442 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494210 | AAAGCCAAAAGATTA[C/G]ATTATTTTTTACTAC | 25898 |
rs376442326 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75490076 | TCAATTTGTTCCTTG[C/T]TTATGATTCTGTGAA | 25898 |
rs376447608 | snp | G/T | 1.64768e-05 | 0.00287021 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515411 | CCGGTTACTAACTCT[G/T]AACATTCTAATTTTC | 25898 |
rs376527201 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497715 | GGAAGGAGGAGGACC[A/G]AAAAAACATCTGAAA | 25898 |
rs376594181 | snp | C/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514261 | TCTTGACCGCTGGCG[C/T]CATCTTCCCGGGCCG | 25898 |
rs376664965 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514465 | GGCTACGAGGCGGAA[C/G]CGAAGGCAGACGCAG | 25898 |
rs376740411 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75511980 | CAAGCATGAAATTCT[-/CT]AACCATTACCTCCTC | 25898 |
rs376765109 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497289 | CCTAAAAGGCTTTGC[G/T]GTACATAGTTAACTG | 25898 |
rs376857743 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75483501 | GATGATAAAAATGTT[C/G]TAAAATTGTGGTGAT | 25898 |
rs376860837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504906 | TAAATGGTAAATGGC[A/G]ATGACTAATTTTTCT | 25898 |
rs376922873 | in-del | -/CAC | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484240 | TTTGTGTCCACTGCT[-/CAC]CTCTTGCAGCCATTA | 25898 |
rs376996872 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499385 | TCCTCAAAAAGACTA[A/C]ACATAGAGCTACCAT | 25898 |
rs377277339 | snp | C/G | 1.65323e-05 | 0.00287505 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514172 | GACGGAAGCTTGTCA[C/G]GGAAGAGTCCATAGA | 25898 |
rs377369247 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75498354 | CAAAGAAAAGCCCAC[A/T]ATCTGATGGCTTCAC | 25898 |
rs377417374 | snp | C/T | 1.77278e-05 | 0.00297718 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75509226 | TCCTTCACTTTAAAG[C/T]GATCTAGTTGATGAT | 25898 |
rs377623937 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502175 | TTCACTCTGTACCCA[A/G]GTCTAGTTCTTTTTT | 25898 |
rs397819176 | in-del | -/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75490503 | ATATATTTTTTTTTT[-/T]GGCAAATTCAAGCAG | 25898 |
rs398063698 | in-del | -/GGGG | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512913 | TTTAAGGGGGGGGGG[-/GGGG]CGGGGGAAGGCAAAA | 25898 |
rs398107515 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506115 | AGGAAAAAAAAAAAA[-/A]TAGAACAGGACATAC | 25898 |
rs527245634 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514383 | ACCCCTCCCAGCCCC[A/G]GCGGCCACTAGCGAC | 25898 |
rs527258948 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75503619 | ATTGCTTGAACCCAG[A/G]AGGCAGAGGTTGCAG | 25898 |
rs527364847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506569 | CAATGCAGCAGAAGA[A/G]AGACCTGGAAGTTAA | 25898 |
rs527397725 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506004 | GCCAAAATTTGGAGT[A/C]CAGATTCCACCACGA | 25898 |
rs527456510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507491 | CTGTAGATTGAAACA[C/T]GAACATATCCTAACT | 25898 |
rs527580375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491192 | ATCTAATTTTAATAT[C/T]TTTTCCATTAATAAA | 25898 |
rs527592788 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490493 | AACCAGTATATATAT[A/T]TTTTTTTTTTGGCAA | 25898 |
rs527600473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500100 | GAGTCATGATTGTGC[A/G]ATTGCACTCCAGCCT | 25898 |
rs527803619 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483676 | TCAATCACATGATTA[A/T]CGGTTAGTATTCCAA | 25898 |
rs527976412 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75501389 | AGACAGTATTTGTCA[A/C]ACTTAATAGATTTTG | 25898 |
rs528108445 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75486589 | AATTAGGATTACTAA[G/T]AGTTAAAACTGTAGT | 25898 |
rs528202253 | snp | A/C | 0.00119737 | 0.0244387 | downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75478728 | CATTATTCACAACAG[A/C]TAAGATATGGAAGCA | 25898 |
rs528227169 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75510448 | ATACACTGTGACCTT[A/G]CAGATCCACTCATTT | 25898 |
rs528352959 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481113 | GGCCAAGGAAACAGA[G/T]GAAGGGAAAGAACAT | 25898 |
rs528360524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504202 | GTATCTAAAATCTAG[C/T]ATCAGTTATTTACAC | 25898 |
rs528416410 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484714 | CAGAAGCAGCACTTT[A/C/T]TAAACATTTTATAGA | 25898 |
rs528418182 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512472 | CCTTCACTTGTGCAC[A/T]GGATTTCATCCCCTT | 25898 |
rs528450988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496742 | CAAGTAACTTAACTG[C/T]ATCCCAAAATAAAGC | 25898 |
rs528462215 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504996 | TACTGTGCACCTACT[A/G]TATATACGGCAGCGG | 25898 |
rs528514939 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75503205 | CTGGTTACAACAGCT[A/G]AAAATGTCTCCAGGC | 25898 |
rs528575286 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498501 | AAAAAAAAAAAAAAC[A/G]TAACTGGAGAGGCTT | 25898 |
rs528730675 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489445 | ATCTCCAGTGACACA[C/G]GTACTTATTTCACTG | 25898 |
rs528822524 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480977 | GCCTAAATGACAGAG[C/T]AAAACCACTTCAAAA | 25898 |
rs528863714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500392 | ATTCTTGTACATTAC[A/G]GTAAGGATATATGTT | 25898 |
rs528993985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75492697 | ATAACTGAAAAACAA[C/T]ATAACAAAAAAAACC | 25898 |
rs529119192 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496275 | AAGTAAGTGAGCCCT[-/A]AAATTGCTCATTTAT | 25898 |
rs529120376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483802 | GTGGTTTTTATCCTC[A/G]TATGCTGAAGTATCT | 25898 |
rs529134109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493601 | AATTCTTACAGTAGA[C/T]AGAATCAGTACTATA | 25898 |
rs529162843 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75510067 | TTTATTAATCATCAA[C/T]CTCATATCTAATATT | 25898 |
rs529199637 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512445 | TGACAGTCTATGTTT[C/T]TAAGGCCAACTCCTT | 25898 |
rs529221109 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75479147 | TTAAGTGGTTTTTTT[A/G]CCACAAAAAATGGTA | 25898 |
rs529225053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484361 | GAATTCAGAAGTCGC[A/C]ACAAAAACTGGACTG | 25898 |
rs529364082 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75485720 | ATGAAACAGGTTAAT[C/T]GGTAAACTGATAGTC | 25898 |
rs529419238 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502322 | AAGGCAGGTGGATCA[C/T]GAGGTCAGGAGATCG | 25898 |
rs529439605 | snp | C/T | 0 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503069 | TCCACCTAGGCAATA[C/T]TTACATTTTGAACCA | 25898 |
rs529539109 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495775 | TAAATCCATACTCTA[A/T]TGAATACAGTTTGAA | 25898 |
rs529540961 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485526 | GGTGACTGGCCATCT[G/T]GTCTTAACTTTTACT | 25898 |
rs529553065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495031 | ACTGGTAAAAAATAT[A/T]TCATGAATATTAGTT | 25898 |
rs529739452 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486041 | AGACCTGTAGCTACA[A/G]AGCAGAATCAAGCCC | 25898 |
rs529778421 | snp | C/T | 3.34269e-05 | 0.00408807 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514293 | CGCCGCCATCTCCTC[C/T]ACCTCCCCTCACATT | 25898 |
rs529795649 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513637 | TAAGAAGTTTTCTCA[G/T]AGTAACAATACATGC | 25898 |
rs529845799 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75488790 | TAAAAGTTCTGCATT[C/T]CAGCCAGGCAAGGTG | 25898 |
rs529869333 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505917 | GTGACAAGCTAAGAA[A/T]CTAAACAGAGAGCAA | 25898 |
rs529932246 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499541 | CCATCAGTGGATGAA[A/C/T]GGATAAAGAAAATAT | 25898 |
rs529933827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489751 | CAAGTAAAGAAAATT[C/T]TGATGGTCCAATGAC | 25898 |
rs529944396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498785 | CCGTACACAGAAATC[A/G]AATCAAAATGGATTA | 25898 |
rs530067474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490404 | GACTTTTTTTTTCCC[A/G]ATCTGAGCTACTTAA | 25898 |
rs530242875 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482164 | GTCAAGACTACTACT[G/T]AAAATTAAGTGCAGT | 25898 |
rs530316252 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | THAP6, RCHY1 | GRCh38.p7 | 4:75516553 | AATGTGAGAAAAAAT[A/G]AAATGAGGGCCATAT | 25898 |
rs530474297 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515825 | CCAAAGAAATTCAAT[A/G]TTGTTTACATGTAGT | 25898 |
rs530631872 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75485453 | TAAAGGTGTCTGTGT[A/G]CATTAGGAACTCTTA | 25898 |
rs530698686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511711 | CTTTTTAAAAAAACT[A/G]TAGGTGTAGTATAGT | 25898 |
rs530898157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503678 | GCCTGGGTGACAGAG[C/T]GGGACTCCATCTCAA | 25898 |
rs531005717 | snp | A/C | | | downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75478828 | CCCTATAAAAGAAAG[A/C]AATCCTGTCACTTGT | 25898 |
rs531019731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496640 | AAGGATATTGCCTCA[A/G]CAGTGGAGAATAGCC | 25898 |
rs531042870 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488169 | TATTCCAAAATTATA[A/T]GAGATTCTAAAATTC | 25898 |
rs531118061 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487032 | TTGTTTCAAATTGAA[A/G]GAATAAAAAAGTGTA | 25898 |
rs531222507 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495870 | ATGTCACTTTTGCCA[C/T]AAATTCATATGTATA | 25898 |
rs531254448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488804 | TCCAGCCAGGCAAGG[C/T]GGCTCATCACTCCTA | 25898 |
rs531300113 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506641 | TAGGAGAAATACAGG[A/G]AAAAAAAAAAGAGAC | 25898 |
rs531427241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500298 | CCACTTCTGCTATGC[A/G]ACTCTGTCTTATAAT | 25898 |
rs531444821 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514681 | TGACGGGTCCTCCCT[C/T]TCTCCCTCCGGTGGC | 25898 |
rs531458594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483746 | TATGAAACACTCCAG[C/T]GTAAATAAAACAAAA | 25898 |
rs531561256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491386 | GAGGTAACTACCTCA[A/G]ATTGTGGGAGGAGAC | 25898 |
rs531566698 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500887 | GATTTTCAAACAAAA[A/T]TACAGGAATTAATAC | 25898 |
rs531777404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509984 | AACAGGCAACCTCTT[C/T]TTAGACATTTCCAGA | 25898 |
rs531886618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502331 | GGATCACGAGGTCAG[A/G]AGATCGAGACCATGC | 25898 |
rs531991518 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479716 | TTCGTAAGGGTATTG[C/T]TATTTTACTTTTTTC | 25898 |
rs532161457 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488903 | AACATGGCGAAACAC[A/C/T]GACTCTACTAAAAAT | 25898 |
rs532274054 | snp | A/C/G | 6.61567e-05 | 0.00575107 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514271 | TGGCGCCATCTTCCC[A/C/G]GGCCGTCGCCGCCAT | 25898 |
rs532279894 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505053 | TGGTTTCATGGAAGA[A/C]AATTTTTCCATGGAC | 25898 |
rs532452795 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490367 | TCTAGTGTTGGGAAA[A/C]ACTACATAAAGGTAT | 25898 |
rs532565775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498643 | AAATGTATGCATTTA[C/T]GGCTAACTCATATTC | 25898 |
rs532649122 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481119 | GGAAACAGATGAAGG[C/G]AAAGAACATAAGAAG | 25898 |
rs533305360 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497109 | TAACAAAAAGGTTAG[A/T]CAACTTGAAGGCACA | 25898 |
rs533344165 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486452 | ATAGAAAAACTAAAT[A/G]TATTTAGATATCTTA | 25898 |
rs533466686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511629 | TATTAAAAGATATAT[C/T]CAAGGGTTGAGATTT | 25898 |
rs533471260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75486781 | GTCAGGAGTTTGAGA[C/T]CAGCCTGGCCAATAC | 25898 |
rs533593858 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504061 | AATTTGGTAATATGT[C/G]TACAGAAGTAATGAT | 25898 |
rs533626110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488083 | TGATTATTTGATCTG[A/T]TAAATTACATAGGAA | 25898 |
rs533630950 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489161 | ATGTATATATAAAAT[G/T]TATATATATTGCTAA | 25898 |
rs533639530 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498890 | CTTGGCAAAGATTTT[A/T]TTGTGTAAGATCTCA | 25898 |
rs533761661 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480698 | TTTGGCAGAATAATA[C/T]CAAACATAAAAAGTA | 25898 |
rs533884442 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514617 | CAGCGGCGCGGAGAC[G/T]CTGGTTGGCCCCAGA | 25898 |
rs533887608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497873 | ATCAAAACCAGAGAC[A/G]AAGAAAAAAAATCTT | 25898 |
rs534006177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507074 | AAAAAAGACATTTTT[C/T]AGAGACAAAAAAAAC | 25898 |
rs534010046 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515906 | AGAAGTAGATCAAGC[A/G]TAGGTTATAGAGAAA | 25898 |
rs534070445 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515206 | GAAGGAAAATGTACA[A/G]GCCAACAAAATTGAA | 25898 |
rs534090860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507863 | ACTATATGATTCCAT[C/T]CATTAAAAACTTCCA | 25898 |
rs534214260 | snp | C/T | 0.000664573 | 0.0182166 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491838 | ATAAACATCCAAGTA[C/T]TTTAAATTCAAGAGC | 25898 |
rs534225371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500560 | CATAAATCAGGAATA[A/G]TACACTATTAAACTC | 25898 |
rs534405483 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506882 | TGACTTAAAAAACAG[C/T]GAGAGGAGGATAAAA | 25898 |
rs534905315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495880 | TGCCATAAATTCATA[G/T]GTATAAATATTTGTC | 25898 |
rs534966242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503712 | AAAATTAATTAAAAA[A/G]AAAAAGAAAATATGG | 25898 |
rs534991734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75486994 | AAAAAAAAATTTTGG[C/T]CTAGTTTGAAGTTAC | 25898 |
rs535135254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488316 | TTCCACAGTTAACTG[C/T]TTAATTCTGATGCAG | 25898 |
rs535195291 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483381 | TATAATTTGGAAAAT[A/C]ATTATTTAAAAAATA | 25898 |
rs535313324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513749 | CCTACGTCTGAACAT[C/G]TGCACTGCCTTTAAC | 25898 |
rs535379347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512838 | GTTATCTTACTCAAA[C/T]AGCTGCATTTGACCC | 25898 |
rs535531340 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501073 | GGAGTGCAATGGCAC[A/G]ATTTTGGCTCACTGC | 25898 |
rs535541312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493002 | CATCTCTGAGTTGAT[A/G]GAATGTAAATGCTGA | 25898 |
rs535625832 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493997 | GCAATATAGTTGCAC[C/T]TGGAAATACATGAAA | 25898 |
rs535626165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484048 | AAAGTCAAGACCCTC[C/T]GAATCTATTCTGGTT | 25898 |
rs535660471 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506137 | AGGACATACAAAAAA[A/C]AAAAAAACAAAAATT | 25898 |
rs535830476 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479995 | TCAGAGAAAGAAAAA[A/G]TATTTAAGGGTAAAG | 25898 |
rs535864601 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508343 | AATTCCTTATACACC[A/G]ACATGTCAACAGTAG | 25898 |
rs535893852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512029 | CTCCCCTTGCAACAC[C/T]CTAGTTCCCTTCTCA | 25898 |
rs535926537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497088 | TAATGGCAAGTTTGA[C/T]ATTGCTAACAAAAAG | 25898 |
rs535947951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505159 | ACAACCTAGATCCCT[C/T]GAATGCACAGTTCAC | 25898 |
rs536032181 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488539 | CAGGATAAAAATTGA[C/T]TGAATACCAAGAAAA | 25898 |
rs536150126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489019 | GGCAGAGGTTGCAGT[A/G]AGCCGAGATTGTGCC | 25898 |
rs536202308 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512682 | ACAGCTAAACCCCAA[C/G]AATACCCTATAAGTG | 25898 |
rs536265136 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482391 | GACCCTGAATCCTTA[C/T]GTACTTGTAATATGA | 25898 |
rs536401934 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515160 | GCAAAAGGCTTTGTG[A/G]CACAAAGAACATGGT | 25898 |
rs536501736 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480657 | AGATCCAATGATTCA[A/G]TGATTAAAAACAATA | 25898 |
rs536607136 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75507394 | GAGAATAAAAGCAAA[C/T]AGGAAAGCAACAGAT | 25898 |
rs536740341 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479715 | ATTCGTAAGGGTATT[C/G]TTATTTTACTTTTTT | 25898 |
rs536802533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510504 | ACCATAACGTAGTTC[A/G]TTCCTTAAAGATTTT | 25898 |
rs536817218 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506142 | ATACAAAAAAAAAAA[A/C]AACAAAAATTAGTCT | 25898 |
rs536874401 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514553 | GCCTGTTTTCCCCCA[A/G]TCGCTACCCGCCCAA | 25898 |
rs536993422 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499336 | TTGTAGAAATATAAA[G/T]TAATACAGCCACTGT | 25898 |
rs537080357 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484597 | AGGAAATATGAGAGC[A/C]AAAGCCAAGATTCAA | 25898 |
rs537387418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502623 | CTATTCTGTTTGCAA[C/T]TATCATATGGGTCCA | 25898 |
rs537411014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495342 | ATTTTTCTTTAATCC[A/G]TTTGAAATTTGCTAT | 25898 |
rs537547248 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75486916 | CCCTGGAGGCAGAGG[C/T]TGCAGTGAGCCAAGA | 25898 |
rs537665069 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482255 | AATATAATACACTTC[G/T]ATGAATGTATCAGTG | 25898 |
rs537669775 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75479086 | CACAGAATGGTGAGT[A/T]TAATAAATAATGCAT | 25898 |
rs537810295 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75516097 | TGCTGCTTTTGTGCC[A/T]GGCACTGTCCTATGT | 25898 |
rs537904914 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481572 | TTTTCACACGCTTAG[G/T]GAAGAAATATTCTAT | 25898 |
rs537927955 | snp | C/T | 8.78418e-05 | 0.0066267 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75509248 | GTTGATGATCTTCAT[C/T]GTTATCATGACACAA | 25898 |
rs537945609 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499767 | CCAGAAGCCTACAAG[A/G]GTAGGGAGGATGGGG | 25898 |
rs537951917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490038 | ATGAATCAAGACTTC[C/T]CTGTAATTATGACTC | 25898 |
rs537952691 | snp | A/G | | | upstream-variant-2KB, missense, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515466 | AAATGGTGAAATGCT[A/G]CTCCGCCATTGGATG | 25898 |
rs538145905 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75489560 | CAAAGATATTGCAGA[C/T]TGATGGTAATCAGAT | 25898 |
rs538150060 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484010 | TATGCTTTAGGTTGC[A/C]AGCTAATTGCAACCA | 25898 |
rs538260477 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515287 | AGGCCCTGGAAAATG[A/T]TGTAAGCAAAGCTGC | 25898 |
rs538326845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512514 | GGACAATGCCCTTAC[A/G]GTTTTCTCACTCTCT | 25898 |
rs538351212 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495388 | GATTGCTACTTGTCC[C/G]TAAATTTCTATTCTC | 25898 |
rs538388259 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511926 | ACACTTTGAAAACCA[A/G]TGCTACAGAACAACG | 25898 |
rs538414432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504281 | TTGACCCCTTGAACA[A/G]CACAAATTTGAAGTA | 25898 |
rs538421615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496052 | AGCTATTGTGAATTT[C/T]CTCTTACAAATGAAC | 25898 |
rs538591934 | in-del | -/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486295 | TGTCCTAATTTCAAA[-/T]TTTTTTTCAGTAATT | 25898 |
rs538915676 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488430 | ACAAACTCTCTTAAA[A/T]ATAGACTTCTGACAA | 25898 |
rs538928267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496958 | AAAAGTTATTATAAC[C/T]GTATACCATTACATT | 25898 |
rs539056051 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480109 | AATCATCGAGTTGAC[A/G]TGTCATGAACAAATA | 25898 |
rs539141607 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant | RCHY1 | GRCh38.p7 | 4:75501985 | CGGGAGGCTGAGGCA[-/G]GACTTGAACCCAGGA | 25898 |
rs539176128 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75513983 | ATCACTTCCCAAGAA[A/G]GGTTTTGCTTTAAAG | 25898 |
rs539383221 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505437 | AGATGTGTACTTTGC[A/C]GTAACAATAACTTGA | 25898 |
rs539415029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502535 | CCAGAGTGAGACTCC[A/G]TCTCAAAAAAAAAGA | 25898 |
rs539444636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75492768 | ATAGTGGGGAGAAAA[A/C]CCCTCAAAATAATAA | 25898 |
rs539467040 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483439 | GGTTGCCTAGGCCTG[A/G]GGCGTTAGGGAATGA | 25898 |
rs539473119 | in-del | -/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75490130 | CCTGTGTGCACTCCA[-/T]AAAAATAAGTCTAAG | 25898 |
rs539539098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493994 | AAAGCAATATAGTTG[C/T]ACTTGGAAATACATG | 25898 |
rs539552587 | snp | A/C/T | 4.0711e-05 | 0.00451156 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494184 | TTGGACCAATCCTAG[A/C/T]AAAACACATGAAAGC | 25898 |
rs539807258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75487512 | TAATATATATATTCA[C/T]AATATATATATTCAT | 25898 |
rs539839326 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75483103 | TTAGGTTTAGTATAC[C/T]GTTCCCTGTCTTCTC | 25898 |
rs540103995 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481393 | TGGTAAAGCTATTAC[A/G]GAGATAACAGTGTCA | 25898 |
rs540204367 | snp | A/G | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515629 | TGAACTTTAGTTCCC[A/G]AGTCCTTTTTAAATA | 25898 |
rs540231093 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481004 | AAAAAAAAGTATTAG[A/T]TCTGGAAAACTAGTC | 25898 |
rs540366131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506256 | AAAAAAAATAGCATC[A/G]AGAGCTTAATAAATT | 25898 |
rs540437258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490288 | CCAACCCTAGTCAGT[C/T]ATATTACTGACTGAC | 25898 |
rs540462177 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495291 | AAACAGACTCTCCTA[C/T]GTATACTTCTAGTAC | 25898 |
rs540540482 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502439 | CAGTTACTTGGGAGG[C/T]TGAGGCAGGAAAAAG | 25898 |
rs540576122 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505691 | TAACTTCTACTTCCA[A/C]AATGACGAAATAGCT | 25898 |
rs540622573 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509856 | CTCCCTAGCCATGTG[G/T]AACTGTAAGTCCAAT | 25898 |
rs541190548 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494403 | TTTTTCTATAAAATT[A/G]CAAAAAGAGAGAAAC | 25898 |
rs541217910 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503595 | AGCTACTAGGGAGGC[A/T]GAGGCAGAATTGCTT | 25898 |
rs541331312 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499028 | AAACTATTTGCAAAC[C/T]ATCCACCTGACAAGG | 25898 |
rs541334307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485126 | TAAAATATAGGCCCT[C/T]AGGTAAAGCTGACTT | 25898 |
rs541493317 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75498698 | CAGAAAAAGGACAAT[C/T]TCTTCAATAAATGGT | 25898 |
rs541657093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511605 | AACTTCCCATGTCAT[C/T]GAACAGCATATTAAA | 25898 |
rs541747412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504019 | CTTCAACCAAATTAC[A/G]ACTCTCAAAGTTCTC | 25898 |
rs541750784 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501975 | GCCAGCTACTCGGGA[A/G]GCTGAGGCAGGACTT | 25898 |
rs541783424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491176 | CTTTTCAATTATTTT[C/T]ATCTAATTTTAATAT | 25898 |
rs541969595 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75492192 | ACAAATAAGGAAAGT[C/G]ACTTAGGAATTCAAG | 25898 |
rs542023429 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514799 | TGGCACCTCGAAGTG[C/T]TTCTTGCTTCCTCCC | 25898 |
rs542042267 | snp | G/T | 0.00130055 | 0.0254673 | upstream-variant-2KB, missense, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515486 | GCCATTGGATGTGCT[G/T]CTCGCTGCTTGCCAA | 25898 |
rs542083530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512194 | ACGTTTCCCTGGTCA[A/G]TTCTCTCATTCTTCC | 25898 |
rs542166522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500770 | ATTTAATGAACTAAA[A/G]GCAATGACAAACTTT | 25898 |
rs542238637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503552 | ATACAAAAATTAGCT[A/G]GCTGTGGTGGCGAGT | 25898 |
rs542361301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496148 | TAGAATAACGGAGAT[C/T]AGACCTACCCTCCCA | 25898 |
rs542405039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75486310 | TTTTTTTTCAGTAAT[C/T]TAAAATCTTATAGTC | 25898 |
rs542691203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75487350 | GCTGTCTCAGGACTT[C/T]TAATTGTTTAGAAAA | 25898 |
rs542785315 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479339 | TTAAAATTAATTCAT[C/T]TCAAATTAAACTATT | 25898 |
rs542789920 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514104 | GAAAATCAGGTTAAC[C/T]TCAAACTTAAATCCA | 25898 |
rs543005901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513379 | CTGTTAAACACTATA[C/T]ACGCCCTTTAGTATA | 25898 |
rs543270502 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480857 | TTAGCTGGGCATGGT[A/G]GCACACACCTGTAGT | 25898 |
rs543277866 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75508369 | AGTAGCTTGTCTGTG[A/G]TTAGGCTCTGGTTAT | 25898 |
rs543389865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489407 | TATAAAATGTGTTTC[C/T]CTCATGGGACATTCC | 25898 |
rs543599363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75501948 | CCAGGCATGGTGGCA[C/G]ATGCCTGTAATGCCA | 25898 |
rs543622572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509790 | TTCCTCATTTTCTAT[C/T]GCCACCACCATGTAA | 25898 |
rs543653522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510813 | TTGTTAACATAAATA[A/G]CATGTTTTAATGAAA | 25898 |
rs543662076 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500893 | CAAACAAAAATACAG[G/T]AATTAATACATTCAA | 25898 |
rs543692113 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501816 | CAGTGCGGTGGCTCA[C/T]GCCTATAATCCCAGC | 25898 |
rs543770417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485055 | TACTAGCCTTTTGGC[C/T]TAGTTACTATACTGC | 25898 |
rs543787041 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493492 | ACAGCTACAATGTTG[A/C]TACTTATACTGTTCT | 25898 |
rs543787611 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480219 | TAAACGAGTGATTGC[A/G]TATGTACTCTGCATT | 25898 |
rs543947998 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480758 | GCCTGTAATCCTAGC[C/T]CTTGGAAGGCCGAGG | 25898 |
rs544038672 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75494685 | ACATCACTTAGTTCA[A/C]ATGTTGATTATTTTT | 25898 |
rs544158239 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507217 | CAATAGAAACGGTAA[A/C]TATATAACAACAATA | 25898 |
rs544252791 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75509846 | ATTCTCAGGCCTCCC[C/T]AGCCATGTGGAACTG | 25898 |
rs544449344 | snp | C/G | 1.73782e-05 | 0.00294767 | intron-variant | RCHY1 | GRCh38.p7 | 4:75482674 | CAGAGAATCTGAAAA[C/G]AGATTAATTCAAATT | 25898 |
rs544736240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490400 | TTAAGACTTTTTTTT[C/T]CCCGATCTGAGCTAC | 25898 |
rs544745876 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503516 | CCTGGCTAACAAAGT[G/T]AAACCTCATCTCTAC | 25898 |
rs544757885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485224 | ATTTCTGAGTAAACT[G/T]CAAACAATAAAAAAG | 25898 |
rs544831100 | in-del | -/G | 0.393803 | 0.204501 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512996 | AATTGTGTGGTTTAT[-/G]GGGGGGCACCAAGAT | 25898 |
rs544895270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483483 | TGAGTGTTTCCTTTT[C/T]GGGATGATAAAAATG | 25898 |
rs544906117 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484740 | ATAGAAGGATAAAAT[G/T]CCATTTGCTTATAGA | 25898 |
rs545068488 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495723 | AACTTCTGCCTTTCT[G/T]GAACCACCATTACTT | 25898 |
rs545282018 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479286 | TTAATAACACAAAGG[A/G]CAAAAGAAAAAGTGG | 25898 |
rs545537899 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497714 | GGGAAGGAGGAGGAC[C/T]GAAAAAACATCTGAA | 25898 |
rs545552202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512280 | AAACTCTAACAACTC[C/T]TCCTCCTTAACACTC | 25898 |
rs545638306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512987 | ACACAGATCTAATTG[C/T]GTGGTTTATGGGGGG | 25898 |
rs545638317 | snp | A/C | 0 | 0 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504068 | TAATATGTGTACAGA[A/C]GTAATGATAAGCCAA | 25898 |
rs545646519 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480456 | TTGGATCTGATTCCC[A/C]ACTCCAACATATAGT | 25898 |
rs545665243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488703 | GAGGACACAAATCCA[A/G]TGTTAAGCATGGACT | 25898 |
rs545755946 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75488475 | CTGGATAACAATTCC[C/T]AGAACTCTAATGGAG | 25898 |
rs545758351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483684 | ATGATTATCGGTTAG[C/T]ATTCCAAAAGTGATT | 25898 |
rs545806041 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75507087 | TTCAGAGACAAAAAA[A/T]ACTGAGAGAATGTAT | 25898 |
rs545941985 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515599 | AAAAGACAGTTCTAC[C/T]TAAGTCTTCAATTTT | 25898 |
rs545975037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508674 | TAGTAAAAGAGATAC[C/T]GGTATTTATCAAAAC | 25898 |
rs545986895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498353 | TCAAAGAAAAGCCCA[C/T]AATCTGATGGCTTCA | 25898 |
rs546034283 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75516343 | GTATTAAATGCTGTA[C/G]TAAGCAATTTTCTGG | 25898 |
rs546037982 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507521 | TACCTTAATAAAAAA[A/C]GAACTATATACTCCA | 25898 |
rs546146807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493130 | TGGCTATCTCCATTA[A/G]CATAGCTTGCCATCA | 25898 |
rs546172792 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75478835 | AAAGAAAGAAATCCT[A/G]TCACTTGTGACAGGA | 25898 |
rs546632287 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497445 | CCAATCCAGCTGTTT[C/T]CATACCTTACTCATT | 25898 |
rs546925851 | in-del | -/AAC | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489819 | GACTGGGTCTCTGAG[-/AAC]AACATCAGAGAAAGA | 25898 |
rs546970620 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488399 | GGAGGTTCATGAAAG[C/G]ATGAAAAGGACCCTG | 25898 |
rs547156757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488884 | GTTCAAGACCAGCCT[A/G]GCCAACATGGCGAAA | 25898 |
rs547555293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75492725 | ACCATAACAAAAAAA[C/T]AGATGTAAGTTTTTG | 25898 |
rs547561927 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RCHY1 | GRCh38.p7 | 4:75492968 | TCCCCACAATTACAA[C/T]ATATCTGATCATCAG | 25898 |
rs547606221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502514 | CACTGCACTCCAGCC[C/T]GGGCGCCAGAGTGAG | 25898 |
rs547624638 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75496697 | CCTAACAAATTAGAA[A/G]AGTAAATCCCAGAAA | 25898 |
rs547663027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75486707 | CAAGTTGCAAAGGCA[G/T]GTATTTAAAAAAATT | 25898 |
rs547669760 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506131 | TAGAACAGGACATAC[-/A]AAAAAAAAAAAAACA | 25898 |
rs547724074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485537 | ATCTTGTCTTAACTT[C/T]TACTCACACCATTTT | 25898 |
rs547815102 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495776 | AAATCCATACTCTAA[A/T]GAATACAGTTTGAAG | 25898 |
rs547925223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495052 | AATATTAGTTATTTA[C/T]ATAATGAATATCAAT | 25898 |
rs547932486 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498794 | GAAATCAAATCAAAA[A/T]GGATTAAAGACTTAA | 25898 |
rs547986877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503092 | TTGAACCAGATAATA[C/T]TTTGTAGCAGGAAAG | 25898 |
rs548006684 | snp | A/C | 1.78688e-05 | 0.00298899 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514336 | CCCCCAGGATAAAAA[A/C]CACGCCCAGAGAAGC | 25898 |
rs548056199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490461 | TTCCATTAATCATCA[C/T]ATTAGCATCTGTGTC | 25898 |
rs548117837 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499579 | GTACACTACGGAGTA[C/T]TACTCAGCCATTAAA | 25898 |
rs548158332 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513647 | TCTCAGAGTAACAAT[A/C]CATGCTTATTAGGCA | 25898 |
rs548278752 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482194 | TTCTATCAAGAACTA[A/G]AAATGAACTGCACGC | 25898 |
rs548366060 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515826 | CAAAGAAATTCAATG[C/T]TGTTTACATGTAGTT | 25898 |
rs548626802 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507691 | AAGCTGATATAGATA[C/G]AGTAGAGCCTAGGGC | 25898 |
rs548726192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484631 | GAAAATGGGATCCTT[A/C]ATTTCTGAAGAACTG | 25898 |
rs548769467 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75478549 | ACACTTGTGCACTGA[C/T]GTTGGGAATGTAAAT | 25898 |
rs549118475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512449 | AGTCTATGTTTCTAA[A/G]GCCAACTCCTTCACT | 25898 |
rs549263916 | in-del | -/ATTT | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479174 | GGTATGAGGCAATAA[-/ATTT]ATTACATTGATTTAA | 25898 |
rs549286803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511730 | GTGTAGTATAGTTCA[A/G]TGCCACTGTCTTGAT | 25898 |
rs549350259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495842 | TCTTAATACTACCCT[C/T]TCCTGATTTGAAATG | 25898 |
rs549412984 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480327 | AAAAATGAAAGGTTA[A/C]TCTATCAAATCATGA | 25898 |
rs549464349 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502495 | CAGTGAGCCAAGATC[A/G]CGCCACTGCACTCCA | 25898 |
rs549505472 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487058 | GTGTAGATTAAAATA[C/T]AGAACGTTCAAAAGA | 25898 |
rs549542285 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479956 | ACCTTCTTTCTTATA[G/T]AGGTATAACCTATAC | 25898 |
rs549756835 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515709 | AATTTAGTTTAAAAG[C/T]TTTAAGATATCAGAG | 25898 |
rs549802212 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499796 | GGCAGGGGAGGGGAT[G/T]AAGAAAAGTTGATTA | 25898 |
rs549802254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507617 | ACACATGACTTAAAT[A/G]TAAGTATACAAAAAT | 25898 |
rs549814356 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506682 | GTAAAAAGATCTATG[C/G]GATGGAGTCTCAGAA | 25898 |
rs549891083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | THAP6, RCHY1 | GRCh38.p7 | 4:75516719 | GGCAGCTTTAATTCA[A/G]TTATATAGCAATAGT | 25898 |
rs550095958 | snp | C/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514722 | GAGAAAGGGGCGGAG[C/G]TCGGCCCGGGCCCTG | 25898 |
rs550356163 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505057 | TTCATGGAAGACAAT[A/T]TTTCCATGGACCGAG | 25898 |
rs550359903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510033 | AAATAATAAAGATTA[C/T]ATTCTTATTTTACTA | 25898 |
rs550471773 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75485540 | TTGTCTTAACTTTTA[C/T]TCACACCATTTTTTC | 25898 |
rs550508457 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513507 | TAAGATTTGGGGATA[A/G]GGCGGTTGAGGTTCC | 25898 |
rs550583336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498644 | AATGTATGCATTTAC[A/G]GCTAACTCATATTCA | 25898 |
rs550625472 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512579 | ATTTCCTAGAATATA[C/T]AAACATGCTGTAATA | 25898 |
rs550659506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489668 | ATCTCATGTATCTTC[C/T]ACTACCAAACTCTGA | 25898 |
rs550812228 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502691 | TAATCTTATTTTTCC[C/T]AATTTTGGTATTTCA | 25898 |
rs550963028 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514986 | AGAGCAATCACTGCA[A/G]TAAATGTAAGATTAC | 25898 |
rs550974890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488941 | TTAGCCAGGTGTGGT[A/G]GCGGGCACCTGTAAT | 25898 |
rs550979863 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502269 | AAGAAGGCCAGCTGC[A/G]GTGGCTCACACCTGT | 25898 |
rs551012724 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497877 | AAACCAGAGACAAAG[-/A]AAAAAAATCTTAAAA | 25898 |
rs551020178 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481985 | AAACATAGAAAACTT[G/T]GGAAAAAACTTTCTA | 25898 |
rs551110342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75492769 | TAGTGGGGAGAAAAA[C/T]CCTCAAAATAATAAG | 25898 |
rs551137330 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513358 | ATTTACTTCAGGGAA[C/T]GCGCCCTGTTAAACA | 25898 |
rs551497325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484453 | AGAAGCACAGTAAAT[A/G]GCAAAACAGCAGGGG | 25898 |
rs551617163 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495256 | TCTTGTTTAGGAAAC[C/T]TTTGTAACCTATAGA | 25898 |
rs551626849 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479769 | AGATACAAATTCTGC[A/G]GCAGGGCAACCTAAC | 25898 |
rs551663045 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75479013 | GAAAAGGGGAGATGC[C/T]GATCAAAGGGTACAA | 25898 |
rs551794124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503238 | TGCCAGATATCACCT[A/G]GGAAAAAACTCTCCC | 25898 |
rs551806563 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511054 | ATGAAATCTGAAATC[A/G]TATCAAGGAATATGA | 25898 |
rs551839235 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75505671 | GCAAAATGAAACATA[C/T]ATTGTAACTTCTACT | 25898 |
rs551847464 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486570 | TCCTAGGGTTTTCAC[A/T]GGAAATTAGGATTAC | 25898 |
rs552103658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499654 | GTCATTATGTTAAGC[A/G]AAACAAGCCAACCAC | 25898 |
rs552193355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506022 | GATTCCACCACGAAA[A/G]AGATGGGCCTGGTAA | 25898 |
rs552205454 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514386 | CCTCCCAGCCCCAGC[G/T]GCCACTAGCGACAAT | 25898 |
rs552242145 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491987 | TAGATTAAAATGTCA[A/G]GTATAAAAATATTAA | 25898 |
rs552278683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498912 | AAGATCTCAAAAGCA[C/T]GCACAACTGAAACAA | 25898 |
rs552331471 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506604 | TGGAAAGTATCCAAT[G/T]TAAGCATAAAGAAAA | 25898 |
rs552674123 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75482725 | ATACAAGTAGCATTG[C/T]CTACTCATAATCCCT | 25898 |
rs552882598 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503718 | AATTAAAAAAAAAAA[A/G]AAAATATGGTATCCT | 25898 |
rs552902084 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75483443 | GCCTAGGCCTGGGGC[A/G]TTAGGGAATGACTGC | 25898 |
rs553023411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495929 | CATATTTATCTATTC[A/G]TCTATTCCTGCACAA | 25898 |
rs553137079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503478 | AAGGTGGGCGGATCA[C/T]GAGGTCAGGAGATCA | 25898 |
rs553334665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485915 | CTTCAGAGGTGTCTG[C/T]TGAATATAATTCAAC | 25898 |
rs553587703 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512910 | GTATTTAAGGGGGGG[A/G]GGGGGGCGGGGGAAG | 25898 |
rs553594043 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75508426 | GTTTTTTCCAATTTT[C/T]ATAAAATCACCTGTA | 25898 |
rs553643228 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480156 | GTACCGAAGCCTAGA[A/G]ACTTTGAGTACATTT | 25898 |
rs553674525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513790 | CAGGCTATAAAACTT[C/T]ACCACAGGAGCTGAA | 25898 |
rs553750553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508468 | TTTTTTAAATACTAA[C/T]TTTTACAAAGGAAAA | 25898 |
rs553756186 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482458 | CTAATGCATAGATGA[C/T]GACACATGATAACAC | 25898 |
rs553877869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493023 | TAAATGCTGAGGTGA[A/G]GATGCAATGAATTAG | 25898 |
rs553902042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484744 | AAGGATAAAATGCCA[C/T]TTGCTTATAGAAATG | 25898 |
rs553948606 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483400 | ATTTAAAAAATATGA[A/T]CTAAATGGAGAAAGT | 25898 |
rs553961877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484060 | CTCTGAATCTATTCT[A/G]GTTCAGGGCTGCCTG | 25898 |
rs553995467 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495514 | AACAGAAGAGATACA[A/T]GAAAATTCTGCATTG | 25898 |
rs554060467 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75498152 | AAACAAAAGAGAAGA[C/T]GTAAGAACTCAGACC | 25898 |
rs554123744 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75500441 | ACCAGATGTTTGCCC[A/G]TATTTACCGAAAACT | 25898 |
rs554129630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75501574 | CTAAAATGCCTACTT[A/G]AAGTGAACATAATTA | 25898 |
rs554269301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512707 | TAAGTGCTATTTTCA[A/G]TTCCACTCCTCCCAT | 25898 |
rs554357726 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488568 | AATACTTTGCCAGAT[C/T]TTCACACTAAAGCAG | 25898 |
rs554578154 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480670 | CAATGATTAAAAACA[A/G]TAACATGATTGGTTT | 25898 |
rs554611375 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514561 | TCCCCCAATCGCTAC[C/G]CGCCCAAATCTCAGG | 25898 |
rs554648972 | in-del | -/TCT | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504509 | CCTAAGAATATAGTA[-/TCT]TATAATACATATAAC | 25898 |
rs554855677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499367 | GGCAATCTGAATGGA[A/G]AGTCCTCAAAAAGAC | 25898 |
rs555125165 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501211 | ACAGGGTTTCTCCAT[C/G]TTGGTCAGGCTGGTC | 25898 |
rs555132206 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506970 | AACCATGGAATCAGA[A/G]TATCTTTAAAGTGTT | 25898 |
rs555262168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511153 | ATGTTTTACTCATGC[A/G]TTGGTCATCTGGAGA | 25898 |
rs555591786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502629 | TGTTTGCAATTATCA[C/T]ATGGGTCCATTGAAC | 25898 |
rs555723188 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482473 | CGACACATGATAACA[C/T]GATACCAAGGAAAGC | 25898 |
rs555886092 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490068 | CTTATCTCTCAATTT[A/G]TTCCTTGCTTATGAT | 25898 |
rs555981415 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495188 | TAGCCATTTTTAATT[A/G]CTATGTGGTAAAAAG | 25898 |
rs555988873 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512062 | TCCTCTACACTCATA[C/G]ATAACAATCCCAACC | 25898 |
rs556134788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489393 | ACCTAAAAGGTTATT[A/G]TAAAATGTGTTTCTC | 25898 |
rs556208420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499087 | CAGACAACTTAATAA[C/T]AAAAAAAAAGATTTA | 25898 |
rs556286677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507225 | ACGGTAAATATATAA[C/T]AACAATAGCATATAA | 25898 |
rs556348825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75501539 | ATATTTTTGAACAAT[A/G]ACAAAAGATAAAATG | 25898 |
rs556349883 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482281 | CAGTGGCAAACATCA[C/T]TGGCTTCCAAAAAAC | 25898 |
rs556511201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508187 | GAAAGGACTGAACAC[A/G]GAACACCTTGGGCTT | 25898 |
rs556511650 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495687 | TAGCTACACAACTCA[C/G]ATTTATTTCCATGAG | 25898 |
rs556523658 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75516102 | CTTTTGTGCCAGGCA[C/G]TGTCCTATGTGTTAG | 25898 |
rs556526062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503538 | CATCTCTACTAAAAA[C/T]ACAAAAATTAGCTGG | 25898 |
rs556665378 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510891 | ATGCATTCAAACAGT[C/T]GTGGCTGAAGTACAA | 25898 |
rs556669633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511927 | CACTTTGAAAACCAA[C/T]GCTACAGAACAACGG | 25898 |
rs556728653 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479902 | GTTAAAATGTTAACA[C/G]TAGTTCTCTCTGAAA | 25898 |
rs556735677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496990 | AAAAAGTATTAAATA[C/T]GAAAAATATGTTTAA | 25898 |
rs557104473 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480116 | GAGTTGACGTGTCAT[G/T]AACAAATACTTGAAG | 25898 |
rs557117012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75487239 | TGAACAAAGATTTCA[C/T]GTAGTATTAATAAGA | 25898 |
rs557314996 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480605 | ACAGATGTTGAAAAC[A/G]GAAGAGCCTTATTAT | 25898 |
rs557379481 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507123 | GCAGGACCTCACTAA[A/C]AGAAACACTAAAGAC | 25898 |