SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs557525502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | THAP6, RCHY1 | GRCh38.p7 | 4:75516440 | GATAGGAAAAGGCCC[A/G]AGTGATAATTCTTTT | 25898 |
rs557573163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505523 | ATTAGAAGCTATGTG[C/T]AGATATGATATACAA | 25898 |
rs557660702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506104 | AAGAATAAAGGGAGG[A/G]AAAAAAAAAAATAGA | 25898 |
rs557806166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483442 | TGCCTAGGCCTGGGG[C/T]GTTAGGGAATGACTG | 25898 |
rs557875161 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493316 | TTCATTATTCATCTC[A/T]ATTTTCCTCACCACT | 25898 |
rs557945509 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75485600 | TTACGTCTAAAGTCT[A/T]AGCTGTGTGCTTTTG | 25898 |
rs557971511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509751 | AGATCTGATGGGTTT[A/G]TCAGGAGTTTCCACT | 25898 |
rs558057986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75501812 | GGCTCAGTGCGGTGG[C/T]TCACGCCTATAATCC | 25898 |
rs558128830 | snp | C/T | 0.000305033 | 0.012346 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494242 | GTCATGATTTGTTCA[C/T]TATGTAAAACACAAG | 25898 |
rs558190762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502560 | AAAAGAGAAAAGAAA[C/T]CTTCTAAAGAAGAAA | 25898 |
rs558263325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498142 | AAAAAACCAGAAACA[A/G]AAGAGAAGACGTAAG | 25898 |
rs558265811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484988 | GCCTTAAAAAAAAGA[C/T]GTTTTAAAAGGCAAA | 25898 |
rs558361104 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480731 | ACATCTGGACCAAGC[A/G]CAGTGGCTCATGCCT | 25898 |
rs558400042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489206 | TTATGACCAATGTTT[A/G]CTTTGTCGAAACCAT | 25898 |
rs558447765 | in-del | -/AAT | 0.0019976 | 0.0315406 | intron-variant | RCHY1 | GRCh38.p7 | 4:75487615 | TTCATATATATTCAT[-/AAT]ATATATATTCATAAT | 25898 |
rs558530556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497227 | GCAACCTAACATACA[G/T]GTGTTCAGTTGAGCC | 25898 |
rs558572435 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514631 | CGCTGGTTGGCCCCA[A/G]AGGAAAGGACGCTCA | 25898 |
rs558593702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505324 | AGAATCCGCACCCCA[A/G]GCACTGGGGACCCTG | 25898 |
rs558735076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489999 | CAAGCAGCATTTTAG[C/T]GTGGACAGTTTTTTC | 25898 |
rs558824844 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504662 | CTTGGTGCCCTTAAC[C/T]CCCAACATTGTTCAA | 25898 |
rs558868958 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514524 | TCGCTGCTAACGGTA[A/G]TAACTCTTAGGTTGC | 25898 |
rs558880702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490849 | TTAGGAACCTGGGAA[C/T]TTTCACACTATAAAA | 25898 |
rs558891066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499945 | AATGTTTCTAGCACA[A/C]ATATTTAAGCCTGGG | 25898 |
rs559155379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502816 | AAACATGAAAGAATG[A/G]CATGAAATAATCACT | 25898 |
rs559185415 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512487 | TGGATTTCATCCCCT[C/T]TGGCTACTCAGGGAC | 25898 |
rs559248973 | snp | C/T | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515880 | GCTCGAATATATTGC[C/T]CTCTCTATTTAGAAG | 25898 |
rs559291285 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494436 | AGACACACACACACA[C/T]TTCGGGTTTGATTTC | 25898 |
rs559302480 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486715 | AAAGGCATGTATTTA[A/C]AAAAATTCAGCTTCA | 25898 |
rs559581368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485174 | ATCCATACTGTGCCC[A/G]GGCATGGACATGGAC | 25898 |
rs559673299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504031 | TACGACTCTCAAAGT[C/T]CTCAAATGTATTTGA | 25898 |
rs559702068 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502534 | GCCAGAGTGAGACTC[C/T]GTCTCAAAAAAAAAG | 25898 |
rs559765565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496337 | AGAAGAACTAAGGGT[A/G]AGCTAGGAAGACATC | 25898 |
rs559842096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511628 | ATATTAAAAGATATA[C/T]TCAAGGGTTGAGATT | 25898 |
rs559881582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495810 | CAATTTTTGGTTTCC[A/G]AATGGATAATCAATT | 25898 |
rs559921920 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485917 | TCAGAGGTGTCTGTT[C/G]AATATAATTCAACAC | 25898 |
rs560107198 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483059 | AATAAAACCAAAATT[C/T]TTACACAAATAATAT | 25898 |
rs560107277 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75492215 | AATTCAAGACACTTA[A/C]CCAAGATCCAAAGAT | 25898 |
rs560273511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507456 | AAAGACAAATACTAA[A/G]GCAATAGAAACTACC | 25898 |
rs560297533 | in-del | -/A | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481814 | AATTTTGGGCAACCT[-/A]AAAAAAACTGTTTTC | 25898 |
rs560361475 | in-del | -/AT | 0.00438332 | 0.0466095 | intron-variant | RCHY1 | GRCh38.p7 | 4:75487616 | TCATATATATTCATA[-/AT]ATATATATTCATAAT | 25898 |
rs560362818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500092 | GCTGCAGTGAGTCAT[C/G]ATTGTGCGATTGCAC | 25898 |
rs560437026 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | THAP6, RCHY1 | GRCh38.p7 | 4:75516607 | ATCTGAATATTAAAA[C/T]GGAAAGTAACAAAAG | 25898 |
rs560535486 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496164 | AGACCTACCCTCCCA[A/T]CTGAAAAAATAATGA | 25898 |
rs560555683 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495736 | CTTGAACCACCATTA[C/T]TTTGGGTTTCTGTCA | 25898 |
rs560960454 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479361 | TAAACTATTCAACTA[A/G]TGAATACCTATTGCC | 25898 |
rs561105814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504965 | AAACACTGCCAAAGA[C/T]ATACTGCCTACACAT | 25898 |
rs561118514 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512434 | TTAGGAAGAACTGAC[A/G]GTCTATGTTTCTAAG | 25898 |
rs561179414 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480679 | AAAACAATAACATGA[C/T]TGGTTTGGCAGAATA | 25898 |
rs561190753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512462 | AAGGCCAACTCCTTC[A/G]CTTGTGCACTGGATT | 25898 |
rs561246332 | in-del | -/TGAAAATTCTGCAT | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495514 | AACAGAAGAGATACA[-/TGAAAATTCTGCAT]TGTACCCTCAAGAGG | 25898 |
rs561328708 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75479078 | ATCTATTACACAGAA[C/T]GGTGAGTATAATAAA | 25898 |
rs561334704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497351 | CCTACTCTAGTACCA[A/G]TCAATCACCAAGTTT | 25898 |
rs561401992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505637 | GAAAAAAAGGCCATA[C/T]ATATGATTTTTAAAA | 25898 |
rs561444015 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480904 | GCTGAGGTGGAAGGA[C/T]CAGTTCAGCCCAGGA | 25898 |
rs561471493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488839 | CCCAGCACTTTGGGA[A/G]ACCGAGGCGGGTGGA | 25898 |
rs561572444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507645 | AATGTCTAAATGGAA[A/G]AGGATATACATGCAA | 25898 |
rs561592597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509812 | ACCATGTAAGAAGTG[C/T]CTTTTGTCTCCCGCC | 25898 |
rs561699949 | snp | C/T | 1.80075e-05 | 0.00300057 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508979 | AATAAACTAAACATT[C/T]TGAGTTACCATTTGA | 25898 |
rs561723704 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483798 | CTACGTGGTTTTTAT[C/T]CTCGTATGCTGAAGT | 25898 |
rs561729633 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500989 | ATATATTTATAATTT[G/T]TATACATACTATATA | 25898 |
rs561855083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493499 | CAATGTTGCTACTTA[C/T]ACTGTTCTGCCTTAT | 25898 |
rs561865355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502012 | AGGAGGCAGAGGTTG[C/T]GGTGAGCCAAGACAG | 25898 |
rs561953149 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485064 | TTTGGCTTAGTTACT[A/G]TACTGCCCTGAAGGC | 25898 |
rs562212412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503559 | AATTAGCTGGCTGTG[A/G]TGGCGAGTGCCTGTA | 25898 |
rs562350161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510885 | CTGCTTATGCATTCA[A/G]ACAGTTGTGGCTGAA | 25898 |
rs562456423 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480763 | TAATCCTAGCCCTTG[A/G]AAGGCCGAGGTAGGA | 25898 |
rs562531953 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500038 | CCCAGCTACCCAGGA[A/G]GCTGAGGTGGGAGGA | 25898 |
rs562544289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499517 | GAAATATGGAAGCAA[C/T]CTTAGTGTCCATCAG | 25898 |
rs562668381 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490938 | AAATGGAGAGGAATT[A/G]GTCCATATTCTTTGT | 25898 |
rs562682094 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514789 | GGGTGCTCGCTGGCA[A/C]CTCGAAGTGCTTCTT | 25898 |
rs562728143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490403 | AGACTTTTTTTTTCC[C/T]GATCTGAGCTACTTA | 25898 |
rs562804202 | in-del | -/A | 0.0130921 | 0.0798413 | intron-variant | RCHY1 | GRCh38.p7 | 4:75487644 | AATATATATATTCAT[-/A]ATATATTCATAATAT | 25898 |
rs562991488 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515722 | AGTTTTAAGATATCA[A/G]AGACTTTAAGATATC | 25898 |
rs563209779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495727 | TCTGCCTTTCTTGAA[C/G]CACCATTACTTTGGG | 25898 |
rs563348766 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75486051 | CTACAAAGCAGAATC[A/C]AGCCCACTAGAGCTT | 25898 |
rs563369852 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485229 | TGAGTAAACTGCAAA[A/C]AATAAAAAAGAACGC | 25898 |
rs563636182 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497961 | GACTGGATTACCCCC[A/G]GGACAGACTTCACAA | 25898 |
rs563735918 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504102 | TTATCAGTGGTGTAT[C/T]TGAGATCTGGAATTA | 25898 |
rs563857956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497271 | TACATATTTTAAGAT[C/T]GTCCTAAAAGGCTTT | 25898 |
rs563874083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496595 | GACTGGGGAAACTCA[C/T]AATTCGCAGGCTCCG | 25898 |
rs563895870 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488168 | TTATTCCAAAATTAT[A/G]TGAGATTCTAAAATT | 25898 |
rs563977022 | snp | A/T | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512594 | CAAACATGCTGTAAT[A/T]CTTCCTCTCTTAAAG | 25898 |
rs564175651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500235 | TAGTCCAAAAATATG[C/T]ACACCTAATACATGT | 25898 |
rs564228069 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515602 | AGACAGTTCTACTTA[A/T]GTCTTCAATTTTGAA | 25898 |
rs564259998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500878 | AAAAAGACTGATTTT[C/T]AAACAAAAATACAGG | 25898 |
rs564323225 | snp | A/G | 8.27356e-05 | 0.00643125 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75508885 | CAAATGGCATATATC[A/G]CAATAATATTCTCCA | 25898 |
rs564400240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502323 | AGGCAGGTGGATCAC[A/G]AGGTCAGGAGATCGA | 25898 |
rs564400335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510750 | CATAAATTAAAAAGA[A/G]TAGGTTTTTAAAATA | 25898 |
rs564400648 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499248 | ACCCCAGTTAGAATG[G/T]CTTATATCATAAAAG | 25898 |
rs564462303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509970 | GAGCCTAAACAGCAA[A/G]CAGGCAACCTCTTCT | 25898 |
rs564464491 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501766 | CTTGGATATTTGCAC[C/T]GTACAATTAACAAGT | 25898 |
rs564495555 | snp | A/C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479701 | CTATGCACCAAAAAA[A/C/T]TCGTAAGGGTATTGT | 25898 |
rs564608513 | in-del | -/A | 0.178465 | 0.239547 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506640 | TAGGAGAAATACAGG[-/A]AAAAAAAAAAAGAGA | 25898 |
rs564798695 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505005 | CCTACTGTATATACG[A/G]CAGCGGTCACCAACC | 25898 |
rs564860028 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513434 | CAGGCGCGATCATCT[C/T]CATTTTACATACGGG | 25898 |
rs564928830 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | THAP6, RCHY1 | GRCh38.p7 | 4:75516654 | CTAAATATTATAATT[A/C]TCAAGACTAATAAAC | 25898 |
rs565206636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489629 | ATAATCACTGGAAGG[C/T]CTGTATACCTAATAA | 25898 |
rs565272080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502497 | GTGAGCCAAGATCGC[A/G]CCACTGCACTCCAGC | 25898 |
rs565274902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505698 | TACTTCCACAATGAC[A/G]AAATAGCTTCTATAG | 25898 |
rs565340499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509611 | TGTGTTCCCACCCAA[A/G]TCTCAACTTGAAATG | 25898 |
rs565433145 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481878 | TCTTATTATTTTACA[C/T]AATAATTTTCCCAAC | 25898 |
rs565482467 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490302 | TTATATTACTGACTG[A/C]CTCTGGCAAGTAATA | 25898 |
rs565661184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75492760 | ATGACAGTATAGTGG[A/G]GAGAAAAACCCTCAA | 25898 |
rs565663044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483426 | AAAGTGGATTAGTGG[G/T]TGCCTAGGCCTGGGG | 25898 |
rs565750607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483896 | ATTCTAATCTAAAAC[C/T]CAATACCATGTATGG | 25898 |
rs565796274 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479210 | ATTCTACACTGTAAA[C/T]ATATATCAAAACATC | 25898 |
rs565841054 | in-del | -/C | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514379 | GCACACCCCTCCCAG[-/C]CCCAGCGGCCACTAG | 25898 |
rs565997541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503100 | GATAATACTTTGTAG[A/C]AGGAAAGCGTCTTGC | 25898 |
rs566003861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75486773 | ATCACAAGGTCAGGA[A/G]TTTGAGACCAGCCTG | 25898 |
rs566103817 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480640 | TACTCACTCCTATTT[A/G]AAGATCCAATGATTC | 25898 |
rs566188257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495096 | TGTATTATATTTATA[C/T]ATCACCAATATCAAT | 25898 |
rs566197660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510970 | TATTTTAATAGCCTT[G/T]TTGGAGAATTATGGA | 25898 |
rs566398285 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490479 | TAGCATCTGTGTCAA[A/C]CCAGTATATATATAT | 25898 |
rs566410617 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481435 | ATCATCAAACATATT[C/T]GTTAACTTTGTTCCT | 25898 |
rs566466297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505304 | TTCCTAACAGGCCAT[A/G]CACCAGAATCCGCAC | 25898 |
rs566474576 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486265 | ACTGAGAAAACATTC[A/G]GGAGGGTACATCTGT | 25898 |
rs566519300 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505982 | GAAAGTACTCCTATG[C/T]TAGGGGGCCAAAATT | 25898 |
rs566571062 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482208 | AGAAATGAACTGCAC[A/G]CGTAGTGTCACTTAA | 25898 |
rs566593181 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514344 | ATAAAAACCACGCCC[A/T]GAGAAGCTGCGCCTC | 25898 |
rs566704330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498884 | ACTGATCTTGGCAAA[A/G]ATTTTTTTGTGTAAG | 25898 |
rs566927233 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485418 | AATCAATTTATATCT[A/C]TAAAGGAAATTTACA | 25898 |
rs566985445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507011 | GGGAACCAATACCTG[A/T]AAACTTAGAATTCTA | 25898 |
rs567110762 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500550 | TATTTTAAAACATAA[A/C]TCAGGAATAATACAC | 25898 |
rs567142194 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514375 | TCTAGCACACCCCTC[C/G]CAGCCCCAGCGGCCA | 25898 |
rs567213686 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482344 | GCACAGTGGCTTTCA[C/T]TCAATATAGAGCTAT | 25898 |
rs567403013 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503708 | AAAAAAAATTAATTA[A/T]AAAAAAAAAGAAAAT | 25898 |
rs567571354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503339 | ATTATGATTTTCAGA[C/T]GATGTACCATATGAA | 25898 |
rs567645146 | in-del | -/TC | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493461 | ATTAATGTCTATCTG[-/TC]TCTCTCTCTCTCTCA | 25898 |
rs567645832 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496680 | GCCCTTCTGTAGATC[C/T]ACCTAACAAATTAGA | 25898 |
rs567692456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504179 | ACAAGCTAGAACCTA[C/T]TAGAAATGTATCTAA | 25898 |
rs567730208 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488196 | ATTCTTTATGTCGGG[G/T]TATATGCTATCAGTC | 25898 |
rs567805806 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480357 | AGCGCTTCAATGATA[C/T]GGATGACTAGCTGTG | 25898 |
rs567976839 | in-del | -/A | 0.432504 | 0.170857 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498482 | AAAGCAATCCTGAGC[-/A]AAAAAAAAAAAAAAA | 25898 |
rs568013596 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75491857 | AAATTCAAGAGCTGA[C/G]ACTTCCAAAGTAAAA | 25898 |
rs568040990 | snp | G/T | 1.7719e-05 | 0.00297644 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490742 | CCAAATATTAAACAA[G/T]AATATATTAATTCAG | 25898 |
rs568041049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75500326 | AATAAGCTCTGGTGC[C/T]TATTTAATAACAATG | 25898 |
rs568127562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491486 | ATTCATCTACCCTAC[C/T]CATTTCAATATAAAT | 25898 |
rs568169348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75501567 | ATGCCTCCTAAAATG[C/T]CTACTTGAAGTGAAC | 25898 |
rs568254941 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75516148 | CTATTTTGTTAGATA[C/T]AATAAATCAAAACTG | 25898 |
rs568416573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510128 | CCTTGTTTTCAAACA[C/T]GGCAAAGACTGCCAG | 25898 |
rs568688346 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497642 | TCTGTTAAGTTTAAT[G/T]TGTCTTAAGTTTTTC | 25898 |
rs568700089 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75492632 | TCCCAGGTTTTTAAC[A/G]GAAGCACTTAATAGA | 25898 |
rs568704184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484682 | TGCCTACATTTACAA[A/G]TGTAAGTATTAGGCC | 25898 |
rs568715772 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75516074 | GTTCACTTGTTAAAG[A/G]TTTATTTTGCTGCTT | 25898 |
rs568871880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512639 | TGCCAGATCTCCCAG[C/T]AACCACATCTTTTTT | 25898 |
rs568885534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513588 | ATCAGGAAACTTCAA[C/T]TGAATACGTGCCAAT | 25898 |
rs569192325 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481288 | ACTTCCTTATTCAAA[A/G]AAGATTCAAATAGCT | 25898 |
rs569380332 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514533 | ACGGTAATAACTCTT[A/G]GGTTGCCTGTTTTCC | 25898 |
rs569537852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484491 | TGCAAATTTTGGCTT[C/T]TGGAAATTCACAGGG | 25898 |
rs569547694 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515095 | TGAGGGAAGGCTTCC[C/T]TGGGGAAGCGATGCA | 25898 |
rs569633258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483963 | AAAAGATGATCACTC[C/T]CCATAAGCCAAAAGG | 25898 |
rs569837171 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75503596 | GCTACTAGGGAGGCT[A/G]AGGCAGAATTGCTTG | 25898 |
rs570008980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495281 | TATAGATCATAAACA[C/G]ACTCTCCTATGTATA | 25898 |
rs570043995 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503668 | CTGCACTCCAGCCTG[C/G]GTGACAGAGTGGGAC | 25898 |
rs570112850 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75479064 | AATAAACTTTACTGA[A/T]CTATTACACAGAATG | 25898 |
rs570128101 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495820 | TTTCCGAATGGATAA[C/T]CAATTATCTTAATAC | 25898 |
rs570276020 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482235 | TTAAAGCAAAGCTTC[A/C]TGAAAATATAATACA | 25898 |
rs570352502 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479778 | TTCTGCGGCAGGGCA[A/G]CCTAACTTATTTCAG | 25898 |
rs570414834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490014 | TGTGGACAGTTTTTT[C/T]CCAAGATCATGAATC | 25898 |
rs570585450 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506606 | GAAAGTATCCAATTT[A/C]AGCATAAAGAAAATC | 25898 |
rs570624892 | in-del | -/ATCTT | 0.00676609 | 0.0577691 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485522 | TTAAGGTGACTGGCC[-/ATCTT]GTCTTAACTTTTACT | 25898 |
rs570675392 | snp | A/G | 1.64876e-05 | 0.00287116 | synonymous-codon, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75490640 | CTACTTCATCATCCA[A/G]CTGTCTCCAATACCT | 25898 |
rs570709503 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497041 | GACATAAAAACTACA[A/G]TGTCTGAGATTTAAA | 25898 |
rs570794004 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75503372 | GTCTCACTGAAAAAA[A/G]GGAATGAACAATATA | 25898 |
rs570810828 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | THAP6, RCHY1 | GRCh38.p7 | 4:75516675 | ACTAATAAACTAGTT[A/T]ACGAATCAATTTAGT | 25898 |
rs571105532 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481431 | CTGGATCATCAAACA[C/T]ATTTGTTAACTTTGT | 25898 |
rs571143235 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75503753 | TAGTCATTTATTAGG[A/C]AGGACTTCAAATTAC | 25898 |
rs571145575 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512500 | CTTTGGCTACTCAGG[C/G]ACAATGCCCTTACAG | 25898 |
rs571411992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496947 | TACAGGGCATTAAAA[A/G]TTATTATAACTGTAT | 25898 |
rs571601337 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488890 | GACCAGCCTGGCCAA[C/G]ATGGCGAAACACCGA | 25898 |
rs571633152 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480108 | TAATCATCGAGTTGA[C/T]GTGTCATGAACAAAT | 25898 |
rs571720834 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501382 | TGACTAAAGACAGTA[C/T]TTGTCAAACTTAATA | 25898 |
rs571985698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513921 | TCAGTCTACTTCGGC[A/G]GCAAAAGACGAATAA | 25898 |
rs572240361 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75516339 | CTATGTATTAAATGC[C/T]GTACTAAGCAATTTT | 25898 |
rs572351221 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484885 | AAACCAAAAAAAAAA[C/G]TGCATTTGAAAATGA | 25898 |
rs572369152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509616 | TCCCACCCAAATCTC[A/G]ACTTGAAATGTATCT | 25898 |
rs572381519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508669 | GCTGATAGTAAAAGA[A/G]ATACCGGTATTTATC | 25898 |
rs572539679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75496226 | ACTGAACATCAGGCA[A/G]CAACACAGAGTGATC | 25898 |
rs572624101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75487438 | CTATATAAATGACTA[C/T]ATATAAATATATATA | 25898 |
rs572625832 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497107 | GCTAACAAAAAGGTT[A/T]GTCAACTTGAAGGCA | 25898 |
rs572746649 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489087 | TCTAAAACAAACAAA[A/C]AAAAAAAGTCTGCAT | 25898 |
rs572783402 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515978 | GTTGCAAATAAATCA[A/G]AATGATTTTAGTTTC | 25898 |
rs572828703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504584 | TTCCAGTCAGTAGCA[A/G]GCTATTAGTAGTTAA | 25898 |
rs572875613 | snp | C/G | 0.000133609 | 0.00817232 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514145 | CCTGCCCAGCCCGCC[C/G]CAGCCCAACCTGACG | 25898 |
rs572956794 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480192 | TTGCTTTAAGTGCAT[G/T]ACTAGACAGCATAAA | 25898 |
rs573013368 | snp | A/C | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514581 | CAAATCTCAGGGCGT[A/C]GTTCGGCGCGAGGTT | 25898 |
rs573287098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506201 | AGGTTATCCATCCCT[A/C]CATTAACTGCCTTCT | 25898 |
rs573420167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499382 | GAGTCCTCAAAAAGA[A/C]TAAACATAGAGCTAC | 25898 |
rs573421480 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75508681 | AGAGATACCGGTATT[C/T]ATCAAAACTCACTTA | 25898 |
rs573484610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511291 | CCAAAAAAAGTCTTT[C/T]AAAAAGCTTCCAACC | 25898 |
rs573536038 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490761 | ATATTAATTCAGGTA[C/T]ACAAGAAGATGCAGG | 25898 |
rs573568772 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481679 | TACTGCTGTGAGGAC[A/T]AGGACTTTTATCTTT | 25898 |
rs573600970 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490254 | AAATAAAATGTACTT[A/T]AAAAGTCCCACCAGT | 25898 |
rs573674155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75502043 | TGCCATTGTACAACA[C/G]CCTGGGCAACAAGAG | 25898 |
rs573688230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509838 | CCGCCATGATTCTCA[A/G]GCCTCCCTAGCCATG | 25898 |
rs573938975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495420 | ACTTCTTCTACAATG[A/G]TAGGGTATTTAGCTA | 25898 |
rs573939013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485118 | AATGTTTATAAAATA[C/T]AGGCCCTTAGGTAAA | 25898 |
rs574062246 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75479163 | CCACAAAAAATGGTA[C/T]GAGGCAATAAATTTA | 25898 |
rs574126037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485905 | ATAGGAATGGCTTCA[C/G]AGGTGTCTGTTGAAT | 25898 |
rs574147187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511599 | GATCAAAACTTCCCA[C/T]GTCATTGAACAGCAT | 25898 |
rs574258145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512119 | CAGAAGCAGGTGAAT[A/G]TGGCTAGAGAAAAAG | 25898 |
rs574382814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512812 | TTGCCAAATCCAAAG[A/G]GCAATTCTCAGTTAT | 25898 |
rs574389634 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501502 | ACTCATTAAAAGCAA[A/C]TGCAGAAAATAAACA | 25898 |
rs574519004 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514793 | GCTCGCTGGCACCTC[G/T]AAGTGCTTCTTGCTT | 25898 |
rs574613110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491062 | TTGTTTAAAATTATT[A/C]AGATATTATTTCCTT | 25898 |
rs574649396 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495223 | AATATTTTCCTGTAT[-/A]AGCTTATGCTTTCTG | 25898 |
rs574672160 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75507289 | AAGAAGTGATAAACA[C/T]ATTATTCTAGTAAGC | 25898 |
rs574686296 | snp | A/G | 3.29516e-05 | 0.00405891 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515420 | AACTCTTAACATTCT[A/G]ATTTTCTTTCAGTTT | 25898 |
rs574693921 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511278 | GAAGAAAATCTCACC[-/A]AAAAAAGTCTTTTAA | 25898 |
rs574914908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484047 | GAAAGTCAAGACCCT[C/G]TGAATCTATTCTGGT | 25898 |
rs574916016 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487371 | GTTTAGAAAACTGAG[C/T]TTCGAAGAGTAAAGG | 25898 |
rs574958195 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512181 | GACACTTACTACCAC[A/G]TTTCCCTGGTCAATT | 25898 |
rs575011033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75495730 | GCCTTTCTTGAACCA[C/T]CATTACTTTGGGTTT | 25898 |
rs575204289 | in-del | -/ATAAT | 0.00279441 | 0.0372746 | intron-variant | RCHY1 | GRCh38.p7 | 4:75487613 | TATTCATATATATTC[-/ATAAT]ATATATATTCATAAT | 25898 |
rs575226390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75511987 | GAAATTCTCTAACCA[C/T]TACCTCCTCCCTAAC | 25898 |
rs575318337 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479329 | CAACTCCCATTTAAA[A/T]TTAATTCATTTCAAA | 25898 |
rs575390874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75487313 | AAAAAGAGGAGACAA[A/G]GGGAAACAGATTTTG | 25898 |
rs575538116 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75490316 | GACTCTGGCAAGTAA[C/T]ATGTAAACAATTCAG | 25898 |
rs575739852 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501752 | AGAAACTCAATATAC[A/T]TGGATATTTGCACTG | 25898 |
rs575790776 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506442 | TCAATACATTCAAAG[-/A]AAAAAAAGGTAAAGA | 25898 |
rs575801265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75504941 | TATTCAGGGTTATCA[C/T]AATACTGAAAACACT | 25898 |
rs575803743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489406 | TTATAAAATGTGTTT[C/T]TCTCATGGGACATTC | 25898 |
rs575850654 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480554 | ACTTACCCCACAGAA[-/T]TCATTGTAGTAATTA | 25898 |
rs575913665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483315 | AGAAAAGCACTAGTT[C/T]TTGAATAGTCACACT | 25898 |
rs575962761 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75499106 | AAAAAAGATTTAAAA[A/C]TAGTCCAAAGACCTG | 25898 |
rs576063909 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75498649 | ATGCATTTACGGCTA[A/T]CTCATATTCAAGAAA | 25898 |
rs576088480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | THAP6, RCHY1 | GRCh38.p7 | 4:75516463 | ATTCTTTTATCATCT[A/G]TAGATGAATAAATAC | 25898 |
rs576198915 | snp | C/G | 1.65943e-05 | 0.00288043 | missense, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75508913 | CCAAACAATGTGCTA[C/G]ATTCTTCACAAGTCT | 25898 |
rs576238770 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75493399 | ATTCTTATATTCTAT[C/T]GAACCTACTATACTG | 25898 |
rs576330363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509780 | CTTTTGCTTCTTCCT[C/G]ATTTTCTATTGCCAC | 25898 |
rs576398949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494248 | ATTTGTTCATTATGT[A/G]AAACACAAGTTTAGT | 25898 |
rs576423588 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75484248 | CCACTGCTCTCTTGC[A/T]GCCATTAGGAATCAT | 25898 |
rs576487020 | snp | A/C/T | 0.00358779 | 0.0422022 | intron-variant | RCHY1 | GRCh38.p7 | 4:75486839 | CAAAAATTAGCCAGG[A/C/T]GTAGTGGTGTGCGCT | 25898 |
rs576518732 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480744 | GCACAGTGGCTCATG[C/T]CTGTAATCCTAGCCC | 25898 |
rs576577330 | in-del | -/T | 0.0142736 | 0.0832652 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494529 | AGGATTTTATGTCTG[-/T]TCTACACAGAACCAC | 25898 |
rs576657214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75511441 | AGAAAATGTCTGCCA[A/G]CTACCCAAATGTGAA | 25898 |
rs576801108 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75488674 | CAGTGGTAGGCACCT[A/C]ACCTGGTATTTAAGA | 25898 |
rs576807759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498153 | AACAAAAGAGAAGAC[A/G]TAAGAACTCAGACCA | 25898 |
rs576851589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75506344 | GAACCAAACACCAAG[A/G]GAGAAAAAACAGAAA | 25898 |
rs576896790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75489946 | CACCCATGAGAGACC[C/T]TAAGACAAAGTTAAC | 25898 |
rs577055532 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514746 | GGCCCTGGGCTCAGC[C/G]GGTCCCGCGCGCTGC | 25898 |
rs577119485 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RCHY1 | GRCh38.p7 | 4:75498196 | GATAGATACTATTAC[A/G]AACAACTATTTAACC | 25898 |
rs577123565 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RCHY1 | GRCh38.p7 | 4:75501419 | GCTTCCAATATCTTT[C/T]GGCAGATTTTTTAAA | 25898 |
rs577161184 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504865 | GCTTTAAAATATTTT[C/T]TAAAGTAAAAAGAAT | 25898 |
rs577189958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75510617 | TTCTCATAGTTATAC[C/T]GCAGAACAGTAGTTC | 25898 |
rs577198393 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515266 | TTTCTCCTTATTAAA[C/G]AGTCAAGGCCCTGGA | 25898 |
rs577231673 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75483593 | TATATAATATGTGAA[C/T]TGTATCTTAATGAAG | 25898 |
rs577343503 | snp | C/T | 1.67975e-05 | 0.00289802 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491939 | TTTCAATACACTGTT[C/T]AAAAGAGAAATTCAC | 25898 |
rs577428627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75483477 | TGGGTATGAGTGTTT[C/T]CTTTTTGGGATGATA | 25898 |
rs577897988 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501807 | GAAAAGGCTCAGTGC[A/G]GTGGCTCACGCCTAT | 25898 |
rs577960064 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504058 | TTGAATTTGGTAATA[C/T]GTGTACAGAAGTAAT | 25898 |
rs577969743 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RCHY1 | GRCh38.p7 | 4:75487162 | GATGGATTTGTTTAC[A/T]AGGTTTTATTAAAAT | 25898 |
rs578016769 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RCHY1 | GRCh38.p7 | 4:75485916 | TTCAGAGGTGTCTGT[G/T]GAATATAATTCAACA | 25898 |
rs578136819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512248 | ATGATCATTTCACTT[C/T]TTCTCCTCTGGCTTT | 25898 |
rs578146819 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RCHY1 | GRCh38.p7 | 4:75497237 | ATACATGTGTTCAGT[A/T]GAGCCTAACGCTGCC | 25898 |
rs578237968 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RCHY1 | GRCh38.p7 | 4:75505432 | GCATGAGATGTGTAC[A/T]TTGCAGTAACAATAA | 25898 |
rs745362720 | snp | A/T | | | synonymous-codon, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491738 | CCTATGTAAAAGATG[A/T]CCACATGGCAAGACA | 25898 |
rs745427006 | snp | A/G | 1.64732e-05 | 0.0028699 | upstream-variant-2KB, missense, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515481 | GCTCCGCCATTGGAT[A/G]TGCTTCTCGCTGCTT | 25898 |
rs745471647 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75511397 | ACTGTCATTTTCATT[C/T]GTAGTGAGTCTCACT | 25898 |
rs745510205 | snp | C/T | 5.07988e-05 | 0.00503953 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491662 | AATATAAGATTATTT[C/T]AGTAAAACAAAAACT | 25898 |
rs745607381 | in-del | -/ATC | 1.75594e-05 | 0.00296301 | cds-indel, intron-variant, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75509252 | ATGATCTTCATTGTT[-/ATC]ATGACACAAGCGGCA | 25898 |
rs745699585 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512341 | GTAAACATACTTCCT[A/G]CTGACAGGCCTGAAA | 25898 |
rs745719441 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499068 | CCAAAATATATAAAG[A/G]GCTCAGACAACTTAA | 25898 |
rs745728783 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484555 | TTGCACATTTAAGTA[C/G]AGAAAAATCACTGGT | 25898 |
rs745766622 | in-del | -/TTAT | 1.6941e-05 | 0.00291036 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491656 | AAAGAAAATATAAGA[-/TTAT]TTTAGTAAAACAAAA | 25898 |
rs745784868 | snp | G/T | 1.6477e-05 | 0.00287024 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515410 | TCCGGTTACTAACTC[G/T]TAACATTCTAATTTT | 25898 |
rs745932336 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75509500 | CTTCAACATCACTAC[A/G]TCTGTATGAAGTTGA | 25898 |
rs745941204 | snp | A/G | 1.75004e-05 | 0.00295802 | intron-variant | RCHY1 | GRCh38.p7 | 4:75482675 | AGAGAATCTGAAAAG[A/G]GATTAATTCAAATTA | 25898 |
rs745943020 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75511066 | ATCGTATCAAGGAAT[A/G]TGATTGATATGATGC | 25898 |
rs745945908 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75496012 | GGCAATCCACTCTTC[A/G]TTGTCCTTCCTTCAA | 25898 |
rs745989293 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75507488 | AAACTGTAGATTGAA[A/G]CACGAACATATCCTA | 25898 |
rs745995389 | snp | C/T | 1.65677e-05 | 0.00287812 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482561 | GATCCAGTGAAATTC[C/T]ACGTCCTCCAGCTTG | 25898 |
rs746008297 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497141 | TAACAGAAACTATCC[A/G]AAATGAAATAGGAAG | 25898 |
rs746282163 | snp | A/G | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515127 | GCCGAGGGCTGAAAG[A/G]TGGGTAGGAGTTAGT | 25898 |
rs746384156 | snp | A/G | 1.81942e-05 | 0.00301609 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509299 | CACAGCAAGGTGCCT[A/G]ACACCCACGGAGAAA | 25898 |
rs746596177 | in-del | -/A | 6.8738e-05 | 0.0058621 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514124 | CTTAAATCCAAGCCT[-/A]AACCACCTGCCCAGC | 25898 |
rs746616242 | snp | A/G | 1.64735e-05 | 0.00286993 | upstream-variant-2KB, missense, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515471 | GTGAAATGCTGCTCC[A/G]CCATTGGATGTGCTT | 25898 |
rs746617830 | snp | C/T | 5.05318e-05 | 0.00502627 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490712 | AGCCTCTGAAAGAGA[C/T]AGAAAGGTTATTTTC | 25898 |
rs746621328 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75500086 | GTCAAGGCTGCAGTG[A/G]GTCATGATTGTGCGA | 25898 |
rs746634849 | snp | A/C | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513779 | CATGAAGCTGGCAGG[A/C]TATAAAACTTTACCA | 25898 |
rs746669127 | snp | C/T | 3.57935e-05 | 0.00423031 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514337 | CCCCAGGATAAAAAC[C/T]ACGCCCAGAGAAGCT | 25898 |
rs746784335 | in-del | -/TT | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481788 | AGGAATGAATGACTC[-/TT]TGAAGAAATAATTTT | 25898 |
rs746834048 | snp | A/G | 1.74452e-05 | 0.00295335 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491980 | GCTTAACTAGATTAA[A/G]ATGTCAGGTATAAAA | 25898 |
rs746851894 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484800 | AAATTATAATGGAAC[A/G]TCCCAAATGAACACT | 25898 |
rs746970435 | snp | C/T | 2.41595e-05 | 0.00347551 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494235 | TACTACAGTCATGAT[C/T]TGTTCATTATGTAAA | 25898 |
rs747073787 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75498887 | GATCTTGGCAAAGAT[G/T]TTTTTGTGTAAGATC | 25898 |
rs747105739 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481705 | TCTTTATTGTTCACT[A/G]TTGTCTCTACAGCAT | 25898 |
rs747147040 | snp | C/T | 1.69143e-05 | 0.00290807 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482518 | GAAAATGCCAAGTTC[C/T]CCAGTACTGTGTAGG | 25898 |
rs747166462 | in-del | -/ATCATG | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75488267 | CAAATTTCCTTGTCA[-/ATCATG]ATCATGTCTTTAACT | 25898 |
rs747167027 | snp | A/G | 1.76717e-05 | 0.00297247 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75509271 | TGACACAAGCGGCAA[A/G]TATAAAGCTTGTCAC | 25898 |
rs747385387 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504827 | ATCCTTTATTCTTTC[A/G]TCTGCACATTATTCA | 25898 |
rs747445375 | snp | C/T | 2.07967e-05 | 0.00322458 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509129 | AATTTTTTCAAACCA[C/T]CTTAATACAGCTTTT | 25898 |
rs747483124 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75492039 | ACTTACTAAAAATAA[C/T]AGCTAACATTAATAT | 25898 |
rs747596806 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501518 | TGCAGAAAATAAACA[C/T]TTCAAATATTTTTGA | 25898 |
rs747637751 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480051 | GAATGGTAAGGGATG[C/T]AGATTTTATTCTTAT | 25898 |
rs747797567 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502673 | TGATACATTATGGAA[C/T]CTTAATCTTATTTTT | 25898 |
rs748026806 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75488462 | TTTAGGACTTGGACT[C/G]GATAACAATTCCTAG | 25898 |
rs748059165 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75509710 | CTCTCCCGTGCCATT[C/G]TCGTGATAATGAATA | 25898 |
rs748169578 | in-del | -/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75490400 | TAAGACTTTTTTTTT[-/C]CCCGATCTGAGCTAC | 25898 |
rs748281279 | snp | A/G | 3.52044e-05 | 0.00419535 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75509260 | CATTGTTATCATGAC[A/G]CAAGCGGCAAGTATA | 25898 |
rs748419277 | snp | A/T | 3.55328e-05 | 0.00421487 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508971 | AAAACTGCAATAAAC[A/T]AAACATTTTGAGTTA | 25898 |
rs748499498 | snp | A/G | 0.000167539 | 0.00915104 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494198 | GCAAAACACATGAAA[A/G]CCAAAAGATTAGATT | 25898 |
rs748552864 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75505828 | ATCTCAGAGAGAAAG[C/T]AAATATACTGAGGCA | 25898 |
rs748554543 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75492260 | CCTTTGCATATTATG[G/T]ATGTTTTACTCCAAA | 25898 |
rs748572688 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75503320 | CCTATAAGCAATAAA[C/T]CAGATTATGATTTTC | 25898 |
rs748586221 | snp | C/T | 1.73039e-05 | 0.00294137 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514325 | CACCGATCCTTCCCC[C/T]AGGATAAAAACCACG | 25898 |
rs748610521 | snp | A/T | 1.65168e-05 | 0.00287369 | missense, nc-transcript-variant, intron-variant | RCHY1 | GRCh38.p7 | 4:75490683 | AGCAGAGTGCATACA[A/T]AATGGACATCTGTAG | 25898 |
rs748850196 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502817 | AACATGAAAGAATGA[C/T]ATGAAATAATCACTA | 25898 |
rs749109714 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484447 | TCGGGCAGAAGCACA[C/G]TAAATGGCAAAACAG | 25898 |
rs749141111 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75498946 | CAGACGGAATTACAT[A/C]AAGCTAAAAAGCTTC | 25898 |
rs749178150 | in-del | -/G | 1.76911e-05 | 0.0029741 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490742 | CCAAATATTAAACAA[-/G]AATATATTAATTCAG | 25898 |
rs749193562 | snp | C/T | 2.4677e-05 | 0.00351254 | intron-variant, upstream-variant-2KB | THAP6, RCHY1 | GRCh38.p7 | 4:75516731 | TCAATTATATAGCAA[C/T]AGTATTTGATTTTAA | 25898 |
rs749195011 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75511256 | TCATTAAAAGTCTTT[A/C]GGTATTGAAGAAAAT | 25898 |
rs749246579 | snp | C/G | 1.64732e-05 | 0.0028699 | upstream-variant-2KB, synonymous-codon, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515491 | TGGATGTGCTTCTCG[C/G]TGCTTGCCAAATTCG | 25898 |
rs749405829 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75485668 | GCCCTTTAGAAATGC[A/G]TATTTAGGGCTGCCT | 25898 |
rs749407099 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75494581 | ATTAATGGCATGGAT[A/G]TATACTAATTTTTTT | 25898 |
rs749480437 | snp | A/G | 1.85077e-05 | 0.00304196 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508770 | ATTTTAAAAACTATT[A/G]TTGCATATACATTAG | 25898 |
rs749729881 | snp | A/G | 1.65299e-05 | 0.00287483 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514173 | ACGGAAGCTTGTCAG[A/G]GAAGAGTCCATAGAA | 25898 |
rs749734790 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481478 | ATATTTAATTCCACT[A/G]CATGAGCCCAAAAAA | 25898 |
rs749761859 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514890 | AGCTAAACCGTGAGG[A/G]CAAAAAGTAAGGAAA | 25898 |
rs749810505 | snp | C/T | 4.96611e-05 | 0.00498278 | synonymous-codon, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482565 | CAGTGAAATTCTACG[C/T]CCTCCAGCTTGAGCA | 25898 |
rs749876880 | in-del | -/ACTT | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75508692 | TATTTATCAAAACTC[-/ACTT]AATTGGACACTTAAA | 25898 |
rs749940306 | in-del | -/TCTTG | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75485523 | TAAGGTGACTGGCCA[-/TCTTG]TCTTAACTTTTACTC | 25898 |
rs749984121 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506626 | TAAAGAAAATCAAAG[C/T]AGGAGAAATACAGGA | 25898 |
rs750035552 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75493545 | CTTGAACAAGTACGA[C/T]TTACACTTCACTTTA | 25898 |
rs750095188 | snp | C/G | 3.29511e-05 | 0.00405887 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515583 | CCATGTTATAAAAAG[C/G]AAAAGACAGTTCTAC | 25898 |
rs750135025 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495021 | AACCAATTTACTGGT[-/A]AAAAAATATATCATG | 25898 |
rs750217541 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479648 | ACACTCATTTTTTTT[A/T]TATACATACATCTTT | 25898 |
rs750274691 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75494928 | AGACAGGGACTGTAC[A/G]TTAATGAACTACTTG | 25898 |
rs750290438 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501103 | CAACCTCCCGCCCAC[A/G]GGTTCAAGCAATTCT | 25898 |
rs750296661 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514402 | GCCACTAGCGACAAT[A/T]TGGCTCCTAAGCACG | 25898 |
rs750308929 | in-del | -/TG | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75513956 | ACTGGCAGAGACCAC[-/TG]TGCAAGCCTAATCAC | 25898 |
rs750340269 | snp | A/C | 1.70831e-05 | 0.00292254 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514127 | TAAATCCAAGCCTAA[A/C]CACCTGCCCAGCCCG | 25898 |
rs750391215 | snp | C/T | 3.51679e-05 | 0.00419318 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75509241 | CGATCTAGTTGATGA[C/T]CTTCATTGTTATCAT | 25898 |
rs750470842 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75511812 | TGTGTCAACAGACTG[-/A]AAAAAAAAAAAAACA | 25898 |
rs750517898 | in-del | -/AT | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487656 | TCATATATATTCATA[-/AT]ATATATATTCATATA | 25898 |
rs750531429 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75488989 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCTGGAG | 25898 |
rs750551513 | snp | A/G | 1.64963e-05 | 0.00287192 | synonymous-codon, missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514251 | CTGACCTCGCTCTTG[A/G]CCGCTGGCGCCATCT | 25898 |
rs750596873 | snp | A/T | 1.64931e-05 | 0.00287163 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75490651 | TCCAGCTGTCTCCAA[A/T]ACCTGGTCATATCTA | 25898 |
rs750796879 | snp | A/T | 1.9971e-05 | 0.00315992 | missense, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75494160 | TCAAACAATGGAAAA[A/T]ATCTTCCTTTGGACC | 25898 |
rs750949158 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75483964 | AAAGATGATCACTCT[C/T]CATAAGCCAAAAGGC | 25898 |
rs751037928 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481114 | CCAAGGAAACAGATG[-/T]AAGGGAAAGAACATA | 25898 |
rs751059640 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512464 | GCCAACTCCTTCACT[-/TG]TGTGCACTGGATTTC | 25898 |
rs751060863 | in-del | -/GGG | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512904 | CCTCTGGTATTTAAG[-/GGG]GGGGGGGGGGCGGGG | 25898 |
rs751120228 | snp | C/T | 1.7999e-05 | 0.00299987 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75509204 | TTCACAGTTTATGCA[C/T]TGCACTTCCTTCACT | 25898 |
rs751130557 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506732 | GAAACATTATCTGAA[C/G]AGAAACTGGCCAAAA | 25898 |
rs751362163 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514495 | GTCTCCGTCGTTGAC[C/G]TTAGTCGCAGTCTTC | 25898 |
rs751403277 | snp | C/T | 1.65704e-05 | 0.00287836 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75508903 | ATAATATTCTCCAAA[C/T]AATGTGCTACATTCT | 25898 |
rs751440802 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75503481 | GTGGGCGGATCACGA[C/G]GTCAGGAGATCAAGA | 25898 |
rs751511755 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75496437 | GGAGAGAGCTGCACA[A/G]AGAAACCTCTGAAAT | 25898 |
rs751577262 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512060 | GTTCCTCTACACTCA[C/T]AGATAACAATCCCAA | 25898 |
rs751604398 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75493957 | ATTTTAAAATATCTA[C/T]TTGTTAATACTGCTT | 25898 |
rs751732692 | snp | C/T | 1.67407e-05 | 0.00289311 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514143 | CACCTGCCCAGCCCG[C/T]CCCAGCCCAACCTGA | 25898 |
rs751736281 | snp | G/T | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513162 | TTCAGTGGAGCAATG[G/T]TCGTCAAGCCATGAC | 25898 |
rs751746079 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504698 | AAAAGCAGTTACAGA[A/G]GACACTGACATATTT | 25898 |
rs751752686 | snp | A/C | 1.6495e-05 | 0.0028718 | missense, stop-gained, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514243 | CAGCCCCGCTGACCT[A/C]GCTCTTGACCGCTGG | 25898 |
rs751765782 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499573 | GTATATGTACACTAC[A/G]GAGTATTACTCAGCC | 25898 |
rs751782476 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487811 | CATATATATATTCAT[-/A]ATATATATTCATAAT | 25898 |
rs751882842 | in-del | -/TAAAA | 1.71471e-05 | 0.00292801 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491977 | AAAGCTTAACTAGAT[-/TAAAA]TGTCAGGTATAAAAA | 25898 |
rs751941256 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75485444 | TTACATTTGTAAAGG[C/T]GTCTGTGTACATTAG | 25898 |
rs751967556 | snp | A/T | 1.65993e-05 | 0.00288086 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491801 | TAAATGAAATAAATG[A/T]TAGTGCTTGTATGAA | 25898 |
rs752053465 | snp | A/G | 1.6646e-05 | 0.00288491 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491883 | TAAAAAATATTTTAA[A/G]CCTACCTCCAAACAT | 25898 |
rs752175310 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486852 | GGCGTAGTGGTGTGC[A/G]CTTGTAGTCCCAGCT | 25898 |
rs752194301 | snp | A/G | 1.6546e-05 | 0.00287624 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75508876 | TTTGTCAAACAAATG[A/G]CATATATCGCAATAA | 25898 |
rs752199788 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75489698 | ATATGACTAAATGCC[A/G]CAAGGCTTTTATGCA | 25898 |
rs752228907 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75496748 | ACTTAACTGCATCCC[A/G]AAATAAAGCTCAAGA | 25898 |
rs752256528 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487064 | ATTAAAATACAGAAC[A/G]TTCAAAAGAAAGAAT | 25898 |
rs752350175 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504076 | TACAGAAGTAATGAT[-/A]AAGCCAAGACTTATC | 25898 |
rs752352710 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482326 | TTTCCAATCAAAACA[C/T]AAGCACAGTGGCTTT | 25898 |
rs752420078 | snp | C/T | 3.29728e-05 | 0.00406021 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75490613 | GATATTCTGATGGCA[C/T]AGGAGTCTGTGCTAC | 25898 |
rs752430283 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75489252 | ATCAAAACTTCACGT[A/G]CATTTCTGCTACCTG | 25898 |
rs752534973 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504495 | TTTTCTCTAGTTTAT[C/T]CTAAGAATATAGTAT | 25898 |
rs752626806 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75491254 | TCTTTTAGTTTACTA[C/T]ACTTGGCCAATATAA | 25898 |
rs752727588 | in-del | -/A | 1.65293e-05 | 0.00287479 | frameshift-variant, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482603 | GGATTCACAAATCTT[-/A]ACATTTCATGCCTAA | 25898 |
rs752757207 | snp | A/G | 1.65974e-05 | 0.0028807 | synonymous-codon, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491780 | ACGGGATGTGTGAAT[A/G]TCCTGTAAATGAAAT | 25898 |
rs752831133 | in-del | -/G | 1.66891e-05 | 0.00288864 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75508834 | CCTACAAATTCCACA[-/G]TTTTCACAGTGATAC | 25898 |
rs752910850 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502014 | GAGGCAGAGGTTGCG[C/G]TGAGCCAAGACAGTG | 25898 |
rs752912225 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75485572 | TTGGTTTGAGCAAAT[G/T]ATGGTACAATATTTA | 25898 |
rs753048584 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506978 | AATCAGAATATCTTT[A/G]AAGTGTTGGGAGGTC | 25898 |
rs753132506 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75508496 | AAAATTTATCCCAAT[C/T]CTCTACCTCAGTTGC | 25898 |
rs753136546 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495733 | TTTCTTGAACCACCA[A/T]TACTTTGGGTTTCTG | 25898 |
rs753197072 | snp | C/T | 0.000118756 | 0.00770479 | intron-variant, synonymous-codon, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491634 | CATTTCTTCATAACA[C/T]GTTCTGAAAGAAAAT | 25898 |
rs753202477 | snp | A/G | 3.29478e-05 | 0.00405867 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515552 | GATTTTGCTGTAGTT[A/G]AGCCAAATACTTTGG | 25898 |
rs753318993 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75483842 | CAGAAAATGTGTAAT[A/G]TAACCAAAAATTATC | 25898 |
rs753374006 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482425 | TATGCTGTGACACTA[A/G]TACAAAACACATCAA | 25898 |
rs753436846 | snp | A/G | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75516309 | GCATTCATTCACTAA[A/G]CATCTGTAGACCTGC | 25898 |
rs753567152 | snp | C/G/T | 3.298e-05 | 0.00406068 | synonymous-codon, missense, intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514235 | AGTGCTCGCAGCCCC[C/G/T]CTGACCTCGCTCTTG | 25898 |
rs753633804 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75492983 | CATATCTGATCATCA[C/G]TGGCATCTCTGAGTT | 25898 |
rs753703781 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75505406 | TCATGAAGTTTAATA[C/T]TTACCATGTAGCATG | 25898 |
rs753720281 | snp | C/T | 3.3849e-05 | 0.0041138 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514134 | AAGCCTAACCACCTG[C/T]CCAGCCCGCCCCAGC | 25898 |
rs753767205 | snp | C/G | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512211 | TCTCTCATTCTTCCA[C/G]AGTCTAAGACCTAAG | 25898 |
rs753768791 | snp | C/T | 1.65965e-05 | 0.00288062 | synonymous-codon, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482643 | CTGAACAGTGGATCG[C/T]CCATTACAGTCATTG | 25898 |
rs753826219 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486981 | AAGACTCCGTCTAAA[A/T]AAAAAATTTTGGTCT | 25898 |
rs753908519 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497316 | ACTGTAACCTAACTG[G/T]ATGTGTTTACCTACA | 25898 |
rs753913291 | snp | A/C | 3.41419e-05 | 0.00413156 | intron-variant, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491598 | AATTATTTTTAAAAT[A/C]CCAAACACTCACTCT | 25898 |
rs753918025 | snp | C/T | 3.29506e-05 | 0.00405884 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515428 | ACATTCTAATTTTCT[C/T]TCAGTTTTGTTATGA | 25898 |
rs753968715 | snp | A/G | 1.65086e-05 | 0.00287298 | missense, nc-transcript-variant, intron-variant | RCHY1 | GRCh38.p7 | 4:75490676 | TATCTAAAGCAGAGT[A/G]CATACATAATGGACA | 25898 |
rs753981989 | in-del | -/TG | 1.65719e-05 | 0.00287849 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75508905 | ATATTCTCCAAACAA[-/TG]TGTGCTACATTCTTC | 25898 |
rs754098635 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75483179 | GAGTAAACAGAGAGG[A/C]TCTTCGCTCATCCCT | 25898 |
rs754236215 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75498011 | AAAGAAATAATAAAG[A/G]GCAGAGCAGAAAAAA | 25898 |
rs754245076 | snp | C/T | 1.72442e-05 | 0.00293629 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508808 | TAGATAAGAACACTT[C/T]ACATACAGTACCTAC | 25898 |
rs754331631 | snp | A/T | 0.000136482 | 0.00825967 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514315 | CCTCACATTCCACCG[A/T]TCCTTCCCCCAGGAT | 25898 |
rs754431231 | snp | A/G | 1.68227e-05 | 0.00290018 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491944 | ATACACTGTTTAAAA[A/G]AGAAATTCACATTAA | 25898 |
rs754506053 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495683 | TGTTTAGCTACACAA[C/T]TCAGATTTATTTCCA | 25898 |
rs754611030 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481097 | ACTGCTGCTCTGGCC[A/G]GGCCAAGGAAACAGA | 25898 |
rs754615605 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75511874 | GCCTTGCAGAGCCCC[C/T]GAAAGGACTTCAGGA | 25898 |
rs754627645 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514501 | GTCGTTGACGTTAGT[C/T]GCAGTCTTCGCTGCT | 25898 |
rs754904273 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75503483 | GGGCGGATCACGAGG[C/T]CAGGAGATCAAGACC | 25898 |
rs754913934 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75488046 | TACAAAGGGCCCCTG[C/T]GGTATTCAAAAGAGA | 25898 |
rs754985591 | snp | A/C | 1.65974e-05 | 0.0028807 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482644 | TGAACAGTGGATCGT[A/C]CATTACAGTCATTGC | 25898 |
rs755021160 | snp | A/G | 1.70528e-05 | 0.00291995 | intron-variant, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491601 | TATTTTTAAAATCCC[A/G]AACACTCACTCTTTC | 25898 |
rs755078776 | in-del | -/TAGT | | | intron-variant, upstream-variant-2KB | THAP6, RCHY1 | GRCh38.p7 | 4:75516670 | TCAAGACTAATAAAC[-/TAGT]TAACGAATCAATTTA | 25898 |
rs755091162 | in-del | -/AATGCC | 1.70179e-05 | 0.00291696 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482505 | TTTTCTATATCAGAA[-/AATGCC]AATGCCAAGTTCTCC | 25898 |
rs755229173 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484204 | GAGCACCAAGGGGAC[C/T]CAGTAAGGTACCGTT | 25898 |
rs755239907 | in-del | -/TAAA | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506516 | ATAAATTTTATAACT[-/TAAA]TAAATAGATAACTTG | 25898 |
rs755249296 | snp | A/T | 1.76166e-05 | 0.00296783 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508966 | AATTAAAAACTGCAA[A/T]AAACTAAACATTTTG | 25898 |
rs755446859 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506868 | ATACTAACAACCAAT[A/G]ACTTAAAAAACAGCG | 25898 |
rs755500711 | snp | C/T | 1.64743e-05 | 0.00287 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515441 | CTTTCAGTTTTGTTA[C/T]GAGTTGCTAAAATGG | 25898 |
rs755509683 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75505800 | AGAGCAACTGAGTGC[C/T]TGAAGGGCAAAGATC | 25898 |
rs755529614 | snp | A/G | 2.50247e-05 | 0.00353719 | intron-variant, upstream-variant-2KB | THAP6, RCHY1 | GRCh38.p7 | 4:75516722 | AGCTTTAATTCAATT[A/G]TATAGCAATAGTATT | 25898 |
rs755619122 | snp | C/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514702 | CTCCGGTGGCGGGGA[C/G]CCTGGAGAAAGGGGC | 25898 |
rs755637978 | in-del | -/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75489807 | CTAGAATCTGGAGAC[-/T]GGGTCTCTGAGAACA | 25898 |
rs755777897 | snp | A/G | 8.34829e-05 | 0.00646022 | stop-gained, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491915 | TTGGACAATTCTGTC[A/G]GGACACATTTTCAAT | 25898 |
rs755852660 | snp | C/G | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515945 | ATTACAAGTTAAGAC[C/G]AAGGGATCTTTAGCT | 25898 |
rs755923774 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504604 | TTAGTAGTTAAGTTG[C/T]GGGGAGTTGAAAGTT | 25898 |
rs755995129 | snp | C/G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75489374 | GGGTTAACTCTATTA[C/G/T]AGTACCTAAAAGGTT | 25898 |
rs756129340 | snp | C/T | 3.35036e-05 | 0.00409276 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514297 | GCCATCTCCTCCACC[C/T]CCCCTCACATTCCAC | 25898 |
rs756131337 | snp | G/T | 1.80055e-05 | 0.00300041 | intron-variant | RCHY1 | GRCh38.p7 | 4:75482683 | TGAAAAGAGATTAAT[G/T]CAAATTAAGTATTTT | 25898 |
rs756147426 | in-del | -/CTT | 1.65825e-05 | 0.00287941 | cds-indel, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75508852 | TTCACAGTGATACTG[-/CTT]CTTATCTTTGTCAAA | 25898 |
rs756239245 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486943 | AAGATTGCTCCACTG[C/T]ACTCCAGCCTGGGTG | 25898 |
rs756279318 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501049 | AGTTTTGCTCTTGTT[A/G]CCCAGGCTGGAGTGC | 25898 |
rs756362130 | snp | C/G | 1.64939e-05 | 0.0028717 | synonymous-codon, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75490656 | CTGTCTCCAATACCT[C/G]GTCATATCTAAAGCA | 25898 |
rs756375632 | in-del | -/T | 3.63352e-05 | 0.00426219 | intron-variant | RCHY1 | GRCh38.p7 | 4:75482688 | AGAGATTAATTCAAA[-/T]TAAGTATTTTAAACC | 25898 |
rs756504499 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75505442 | TGTACTTTGCAGTAA[C/T]AATAACTTGAATGTC | 25898 |
rs756518432 | in-del | -/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75507617 | CACATGACTTAAATG[-/T]TAAGTATACAAAAAT | 25898 |
rs756595405 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75496924 | ACAGACACAGATGTT[A/C]GAATTAATACAGGGC | 25898 |
rs756622864 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480072 | TTATTCTTATTGTGA[A/C]TGAGAAGTGTTGAAG | 25898 |
rs756773513 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75503831 | TATTCTTCCATCTTT[C/T]ATGACGTTTGTACAC | 25898 |
rs756898771 | snp | A/G | 1.64732e-05 | 0.0028699 | upstream-variant-2KB, missense, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515474 | AAATGCTGCTCCGCC[A/G]TTGGATGTGCTTCTC | 25898 |
rs756920124 | snp | A/G | 6.58968e-05 | 0.00573969 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515577 | CTTTGGCCATGTTAT[A/G]AAAAGCAAAAGACAG | 25898 |
rs756945297 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75491533 | TAGTATAAGTAACAA[C/T]GTTTGTCCACCTCCC | 25898 |
rs756955843 | snp | C/G | 1.69473e-05 | 0.0029109 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491654 | TGAAAGAAAATATAA[C/G]ATTATTTTAGTAAAA | 25898 |
rs756996711 | snp | A/C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504703 | CAGTTACAGAGGACA[A/C/T]TGACATATTTGAGCA | 25898 |
rs757036478 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75490020 | CAGTTTTTTCCCAAG[A/G]TCATGAATCAAGACT | 25898 |
rs757112932 | in-del | -/AG | 1.96976e-05 | 0.00313822 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509149 | ATACAGCTTTTAAAA[-/AG]AAAATAGAAATGTCA | 25898 |
rs757160685 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512228 | GTCTAAGACCTAAGA[C/T]TTAGATGATCATTTC | 25898 |
rs757183752 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75493057 | GTGCACACACACTAC[A/G]CATGCTTTGGAAACC | 25898 |
rs757247940 | snp | A/G | 1.65719e-05 | 0.00287849 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75508905 | AATATTCTCCAAACA[A/G]TGTGCTACATTCTTC | 25898 |
rs757394394 | snp | A/G | 9.2465e-05 | 0.00679882 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509308 | GTGCCTAACACCCAC[A/G]GAGAAAAAAGAGATA | 25898 |
rs757398616 | snp | C/T | 1.69605e-05 | 0.00291204 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482666 | AGTCATTGCAGAGAA[C/T]CTGAAAAGAGATTAA | 25898 |
rs757499951 | snp | C/T | 1.64944e-05 | 0.00287175 | missense, synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514247 | CCCGCTGACCTCGCT[C/T]TTGACCGCTGGCGCC | 25898 |
rs757615967 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497098 | TTTGATATTGCTAAC[A/G]AAAAGGTTAGTCAAC | 25898 |
rs757627792 | snp | A/G/T | 3.3204e-05 | 0.00407444 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491805 | TGAAATAAATGTTAG[A/G/T]GCTTGTATGAAGACA | 25898 |
rs757701925 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75510602 | TCCTCCAACCCACTA[C/T]TCTCATAGTTATACC | 25898 |
rs757762193 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481532 | CCAGGAATATCCCAT[A/G]CCCTTCCCACTCATC | 25898 |
rs757773847 | snp | C/T | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75516314 | CATTCACTAAGCATC[C/T]GTAGACCTGCTATGT | 25898 |
rs757777112 | snp | C/T | 3.30907e-05 | 0.00406746 | missense, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75508883 | AACAAATGGCATATA[C/T]CGCAATAATATTCTC | 25898 |
rs757784088 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75498179 | GACCACAGAAATACA[A/C]AGATAGATACTATTA | 25898 |
rs757799467 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75509585 | TCCCACAACACCTGA[C/T]ATGCTTTGGCTGTGT | 25898 |
rs757860531 | snp | C/T | 1.66515e-05 | 0.00288539 | synonymous-codon, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491892 | TTTTAAGCCTACCTC[C/T]AAACATATTGGACAA | 25898 |
rs758036503 | snp | G/T | 6.65713e-05 | 0.00576899 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491878 | CAAAGTAAAAAATAT[G/T]TTAAGCCTACCTCCA | 25898 |
rs758123996 | snp | A/G | 1.79184e-05 | 0.00299314 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514335 | TCCCCCAGGATAAAA[A/G]CCACGCCCAGAGAAG | 25898 |
rs758128206 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75493718 | TATGTCTTAATTATA[A/G]AAAGAAATAGTAAAA | 25898 |
rs758130844 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75493475 | TGTCTCTCTCTCTCT[C/G]AACAGCTACAATGTT | 25898 |
rs758243197 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75485838 | TTCCTATAGGTGTTA[C/T]GTGTATGTGATAACA | 25898 |
rs758335354 | in-del | -/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487819 | TATTCATAATATATA[-/T]TCATAATATATATAT | 25898 |
rs758366808 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514451 | TTTCCGGTTCCCGGG[A/G]CTACGAGGCGGAAGC | 25898 |
rs758522189 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502738 | TTCACATTATCAATC[A/T]TTCCCAACTATCCTA | 25898 |
rs758532156 | snp | A/C | 1.68519e-05 | 0.0029027 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514137 | CCTAACCACCTGCCC[A/C]GCCCGCCCCAGCCCA | 25898 |
rs758856687 | snp | A/C/G | 3.39151e-05 | 0.00411784 | intron-variant, missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491635 | ATTTCTTCATAACAC[A/C/G]TTCTGAAAGAAAATA | 25898 |
rs758898989 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499506 | TCAAAATAGCTGAAA[C/T]ATGGAAGCAACCTTA | 25898 |
rs758946669 | snp | A/G | 3.31956e-05 | 0.0040739 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491794 | TGTCCTGTAAATGAA[A/G]TAAATGTTAGTGCTT | 25898 |
rs758955723 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484023 | GCAAGCTAATTGCAA[C/T]CAAATAAAGAAAGTC | 25898 |
rs759015755 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75483627 | TTATTTCCAAAAATT[A/G]TCTACATGGAACATA | 25898 |
rs759102524 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75508450 | ACCTGTATTTCTTGA[A/T]AATTTTTTAAATACT | 25898 |
rs759143626 | snp | C/T | 1.70886e-05 | 0.00292301 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490723 | GAGATAGAAAGGTTA[C/T]TTTCCAAATATTAAA | 25898 |
rs759194216 | snp | A/T | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515735 | CAGAGACTTTAAGAT[A/T]TCAGAGACTGGTTTA | 25898 |
rs759293948 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482298 | GGCTTCCAAAAAACT[A/G]ACACTAAAGGAATTT | 25898 |
rs759303169 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499929 | AAAGAGAATTAATTC[-/A]AATGTTTCTAGCACA | 25898 |
rs759357057 | snp | A/T | 6.62339e-05 | 0.00575435 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490561 | GAGTCTACAAAGTTT[A/T]AAGTATTGATTCTAC | 25898 |
rs759365132 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75483641 | TATCTACATGGAACA[C/T]AGCACACTTCGGCCT | 25898 |
rs759399021 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501837 | TAATCCCAGCACTTT[A/G]GGAGGCCAAGGTGGG | 25898 |
rs759415425 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499492 | TACTGCAGCACTATT[C/G]AAAATAGCTGAAATA | 25898 |
rs759471729 | snp | A/G | 3.29468e-05 | 0.00405861 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515537 | ACATTTCACGTGTAA[A/G]ATTTTGCTGTAGTTA | 25898 |
rs759497582 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504348 | TGCCACCCCTGAGAT[A/G]GCAAAGCCAATCTCT | 25898 |
rs759571888 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75494683 | AGACATCACTTAGTT[A/C]ACATGTTGATTATTT | 25898 |
rs759702691 | snp | G/T | 1.65954e-05 | 0.00288053 | synonymous-codon, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491768 | ATGAGCAACAACACG[G/T]GATGTGTGAATGTCC | 25898 |
rs759771052 | snp | C/T | 1.66421e-05 | 0.00288458 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491868 | CTGAGACTTCCAAAG[C/T]AAAAAATATTTTAAG | 25898 |
rs759813055 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75500662 | TCCAGATGAGAGTCA[A/G]ATATATCTTAGATGA | 25898 |
rs759837584 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75491522 | CATGCCCAATATAGT[A/G]TAAGTAACAATGTTT | 25898 |
rs760044137 | in-del | -/AAA | 1.66832e-05 | 0.00288814 | splice-donor-variant | RCHY1 | GRCh38.p7 | 4:75491723 | AAGATGTTACTTTAC[-/AAA]CTATGTAAAAGATGT | 25898 |
rs760047591 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501849 | TTTGGGAGGCCAAGG[A/T]GGGAGGATCACCTGA | 25898 |
rs760060750 | in-del | -/A | 8.02295e-05 | 0.00633311 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75494155 | CATTTCAAACAATGG[-/A]AAAAAATCTTCCTTT | 25898 |
rs760125041 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75489542 | TGACTGGATTGCCTT[C/G]GTCAAAGATATTGCA | 25898 |
rs760137553 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486821 | CCGTCTCTACTAAAA[A/G]TACAAAAATTAGCCA | 25898 |
rs760330539 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499357 | CAGCCACTGTGGCAA[C/T]CTGAATGGAGAGTCC | 25898 |
rs760331669 | snp | G/T | 6.6223e-05 | 0.00575388 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482630 | CTAATATATGAAACT[G/T]AACAGTGGATCGTCC | 25898 |
rs760415345 | snp | A/C | 1.66374e-05 | 0.00288417 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490542 | AAATAAGAGTGCCAA[A/C]AAGGAGTCTACAAAG | 25898 |
rs760573479 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502287 | GGCTCACACCTGTAA[C/T]CCCAGCACTTTGGGA | 25898 |
rs760670413 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75505307 | CTAACAGGCCATGCA[A/C]CAGAATCCGCACCCC | 25898 |
rs760671203 | snp | C/T | 1.64909e-05 | 0.00287144 | missense, intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514210 | ACCTTTAGGAGACAT[C/T]CTCTGTCATAGTGCT | 25898 |
rs760809296 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502053 | CAACAGCCTGGGCAA[C/T]AAGAGTGAAACTCTG | 25898 |
rs760833209 | in-del | -/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75482896 | GAGCAAAAAAAAAGC[-/T]TATTTTAAAATAGTT | 25898 |
rs760840278 | snp | A/T | 1.6476e-05 | 0.00287014 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515419 | TAACTCTTAACATTC[A/T]AATTTTCTTTCAGTT | 25898 |
rs760844175 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480523 | TAAACCTCAGCTTTC[C/T]TGTCTATGAGGACAA | 25898 |
rs760885259 | snp | C/T | 1.9991e-05 | 0.0031615 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75494164 | ACAATGGAAAAAATC[C/T]TCCTTTGGACCAATC | 25898 |
rs760894768 | snp | A/G | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515313 | GCTGCAGGTGTTAGA[A/G]GAAGATATTTGTCTT | 25898 |
rs760900302 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75503272 | TTGAGAACCAGTGCT[C/T]TGGACTCTAATTATA | 25898 |
rs760932325 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75508446 | AATCACCTGTATTTC[C/T]TGATAATTTTTTAAA | 25898 |
rs760934130 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75490009 | TTTAGTGTGGACAGT[G/T]TTTTCCCAAGATCAT | 25898 |
rs761059644 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75510363 | AATCTACATCACTGT[G/T]GGGTTTTTTCATTAC | 25898 |
rs761320512 | snp | A/G | 3.49834e-05 | 0.00418216 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514107 | AATCAGGTTAACCTC[A/G]AACTTAAATCCAAGC | 25898 |
rs761404956 | in-del | -/CT | 1.64768e-05 | 0.00287021 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515407 | CTTTCCGGTTACTAA[-/CT]CTTAACATTCTAATT | 25898 |
rs761424779 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75500193 | TTAGCCTGATTTGAT[C/T]ATATGAATGCACTGA | 25898 |
rs761667516 | snp | C/T | 1.66313e-05 | 0.00288364 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491739 | CTATGTAAAAGATGT[C/T]CACATGGCAAGACAT | 25898 |
rs761688603 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479628 | AGAAATGAACAACTT[G/T]ATATACACTCATTTT | 25898 |
rs761764942 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506495 | TAACAAGAATGAAGA[C/T]AAAATATAAATTTTA | 25898 |
rs761770151 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479553 | ACTACTACTTCCAAC[A/G]TAAGCTAAAGTTAAT | 25898 |
rs761800030 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75496085 | TAGAATAGGCTGTCA[A/G]ACTCCATAAGTAAAA | 25898 |
rs762051389 | snp | A/G | 1.8149e-05 | 0.00301234 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508788 | GCATATACATTAGAA[A/G]CAATTAGATAAGAAC | 25898 |
rs762143992 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75485967 | GCTTGTTTTGGGTTT[A/T]GAACCTCTAGATTCT | 25898 |
rs762232778 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75511864 | AGTAGTTTTGGCCTT[A/G]CAGAGCCCCTGAAAG | 25898 |
rs762267902 | snp | A/G | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515549 | TAAGATTTTGCTGTA[A/G]TTAAGCCAAATACTT | 25898 |
rs762333928 | snp | A/C | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512507 | TACTCAGGGACAATG[A/C]CCTTACAGTTTTCTC | 25898 |
rs762344467 | snp | A/G | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515241 | TACTCGGGGTACACA[A/G]CTAAATATGTTTCTC | 25898 |
rs762388678 | snp | A/G | 4.0808e-05 | 0.00451689 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75494148 | ATAAGTTACATTTCA[A/G]ACAATGGAAAAAATC | 25898 |
rs762481961 | snp | C/T | 1.9176e-05 | 0.00309639 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509334 | AGATATAGTAAGAAG[C/T]AAAAGAAACTAAGTG | 25898 |
rs762565041 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486656 | ACAATTCCCTATAAG[A/G]AGTGTAAAAACAAGC | 25898 |
rs762643630 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495077 | ATCAATGTTTTCATT[C/T]GCATGTATTATATTT | 25898 |
rs762724679 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75496293 | ATTGCTCATTTATTG[C/T]CTAGAGAGTTTTGAG | 25898 |
rs762802775 | snp | A/C/G/T | 0.000444762 | 0.0149062 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515418 | CTAACTCTTAACATT[A/C/G/T]TAATTTTCTTTCAGT | 25898 |
rs762823185 | snp | G/T | 3.59991e-05 | 0.00424243 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490747 | TATTAAACAAGAATA[G/T]ATTAATTCAGGTATA | 25898 |
rs762871786 | snp | C/T | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75490625 | GCATAGGAGTCTGTG[C/T]TACTTCATCATCCAG | 25898 |
rs762944664 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481974 | CTAATTGAGCCAAAC[A/G]TAGAAAACTTTGGAA | 25898 |
rs762999317 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480809 | AGGAGTTCAAGACCA[C/G]CCTGGACTTTGTTTC | 25898 |
rs763011973 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75505188 | ACAATAGGGTTTGTG[C/T]TCCTATGAGAATCTA | 25898 |
rs763176548 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75492562 | CTTAATTTGACAAGA[C/T]GTAATGTCTGATTAA | 25898 |
rs763191378 | snp | A/G | 3.32845e-05 | 0.00407936 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491876 | TCCAAAGTAAAAAAT[A/G]TTTTAAGCCTACCTC | 25898 |
rs763245514 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512006 | CTCCTCCCTAACTTA[C/T]TCCAAGTCTCCCCTT | 25898 |
rs763321153 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75485326 | TTAAATTTTTAAAAA[C/T]GATCTATGGAACTAA | 25898 |
rs763357127 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75479048 | TCAGTTAGACAAGAG[A/G]AATAAACTTTACTGA | 25898 |
rs763424735 | in-del | -/A | 3.32837e-05 | 0.00407931 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491868 | TGAGACTTCCAAAGT[-/A]AAAAAATATTTTAAG | 25898 |
rs763469263 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512691 | CCCCAAGAATACCCT[A/G]TAAGTGCTATTTTCA | 25898 |
rs763470302 | snp | A/G | 1.82221e-05 | 0.00301839 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75509195 | TTGAATTTTTTCACA[A/G]TTTATGCACTGCACT | 25898 |
rs763525870 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499381 | AGAGTCCTCAAAAAG[A/G]CTAAACATAGAGCTA | 25898 |
rs763559185 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75500393 | TTCTTGTACATTACA[A/G]TAAGGATATATGTTC | 25898 |
rs763656246 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75492503 | CATTAATAAGAGGCA[A/G]AATTAAACTGGAGCT | 25898 |
rs763838172 | snp | A/C | 5.35432e-05 | 0.00517385 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491562 | CCCACACCACACACA[A/C]AAAAAAGTCAAACAT | 25898 |
rs763912369 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75491421 | TTTAAGAGAAACATA[C/T]GGCAAAAGTGTAGTT | 25898 |
rs763945632 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75505339 | AGCACTGGGGACCCT[A/G]ATATAAGGCACTCCC | 25898 |
rs763998575 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504638 | CTCAGATTTTCAACT[A/G]AGCTGGCACTTGGTG | 25898 |
rs764006534 | in-del | -/G | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512848 | CAAACAGCTGCATTT[-/G]GACCCAGCTGACCAC | 25898 |
rs764033960 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501810 | AAGGCTCAGTGCGGT[A/G]GCTCACGCCTATAAT | 25898 |
rs764122747 | snp | A/G | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515358 | GATTTTGTGTTTCCT[A/G]AAACACCGGGAAAGG | 25898 |
rs764169229 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75483051 | TCTCAATTAATAAAA[A/C]CAAAATTTTTACACA | 25898 |
rs764176162 | snp | A/G | 1.6577e-05 | 0.00287893 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514279 | TCTTCCCGGGCCGTC[A/G]CCGCCATCTCCTCCA | 25898 |
rs764400752 | in-del | -/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484965 | AAAAATATTTCAATA[-/T]TTTTATTGCCTTAAA | 25898 |
rs764422478 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486975 | CAGAGAAAGACTCCG[C/T]CTAAAAAAAAAATTT | 25898 |
rs764519934 | snp | A/G | 3.29478e-05 | 0.00405867 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515559 | CTGTAGTTAAGCCAA[A/G]TACTTTGGCCATGTT | 25898 |
rs764560495 | in-del | -/TTTT | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75479140 | GTAGATTTTAAGTGG[-/TTTT]TTTACCACAAAAAAT | 25898 |
rs764568328 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497923 | GAAAGAAAAGAAGAC[A/G]TGCACAGGAGAAAAA | 25898 |
rs764571392 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75508655 | TATAGCTTGATTGTG[C/G]TGATAGTAAAAGAGA | 25898 |
rs764705537 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75510389 | ATTACAGCAACTTTA[C/T]CATTACAAGTATATC | 25898 |
rs764752696 | snp | A/G | 1.66054e-05 | 0.00288139 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491800 | GTAAATGAAATAAAT[A/G]TTAGTGCTTGTATGA | 25898 |
rs764888747 | in-del | -/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495971 | TTGAATTACTATAGC[-/T]TTTATCATGTTTTGA | 25898 |
rs764896720 | snp | C/T | 1.66123e-05 | 0.00288199 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482647 | ACAGTGGATCGTCCA[C/T]TACAGTCATTGCAGA | 25898 |
rs764924377 | snp | A/G | 1.65499e-05 | 0.00287657 | missense, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75508868 | TTCTTATCTTTGTCA[A/G]ACAAATGGCATATAT | 25898 |
rs764927720 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506524 | TATAACTTAAATAAA[A/T]AGATAACTTGGTAGG | 25898 |
rs764951841 | snp | C/T | 6.59685e-05 | 0.00574281 | synonymous-codon, missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514242 | GCAGCCCCGCTGACC[C/T]CGCTCTTGACCGCTG | 25898 |
rs764965664 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75493193 | CTTTTATCTTCAAAA[A/C]ATTTACAATCTACTA | 25898 |
rs765018773 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75505527 | GAAGCTATGTGTAGA[C/T]ATGATATACAAAATA | 25898 |
rs765057410 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75494906 | AATTTGCATTTCACA[A/G]ATAATGAGACAGGGA | 25898 |
rs765105411 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479612 | AAGACCCCAGAAACT[A/C]AGAAATGAACAACTT | 25898 |
rs765231464 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480660 | TCCAATGATTCAATG[A/G]TTAAAAACAATAACA | 25898 |
rs765231913 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75488968 | TAATCCCAGCTACTT[C/G]GGAGGCTGAGGCAGG | 25898 |
rs765316749 | snp | C/G | 1.65968e-05 | 0.00288065 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491774 | AACAACACGGGATGT[C/G]TGAATGTCCTGTAAA | 25898 |
rs765416676 | snp | A/T | 1.64741e-05 | 0.00286998 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515548 | GTAAGATTTTGCTGT[A/T]GTTAAGCCAAATACT | 25898 |
rs765423165 | snp | A/G | 1.66402e-05 | 0.00288441 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491869 | TGAGACTTCCAAAGT[A/G]AAAAATATTTTAAGC | 25898 |
rs765587676 | snp | C/T | 2.07851e-05 | 0.00322368 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509137 | CAAACCACCTTAATA[C/T]AGCTTTTAAAAAGAA | 25898 |
rs765734565 | snp | A/C/G | 3.2948e-05 | 0.00405871 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515442 | TTTCAGTTTTGTTAT[A/C/G]AGTTGCTAAAATGGT | 25898 |
rs765758060 | snp | A/T | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515835 | TCAATGTTGTTTACA[A/T]GTAGTTTACAATCTG | 25898 |
rs765995631 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495346 | TTCTTTAATCCATTT[C/G]AAATTTGCTATATAT | 25898 |
rs766041795 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75496377 | ATGATGAGCTGAGAC[A/C]GTCTAGAGAAACCAA | 25898 |
rs766150066 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514455 | CGGTTCCCGGGGCTA[C/G]GAGGCGGAAGCGAAG | 25898 |
rs766157023 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499293 | ATGCTGGTGAGGATA[C/T]AGAGAAAGTGGAACC | 25898 |
rs766289961 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75503451 | CCTGTAATTCCAGCA[C/T]TTTGGGAGGCCAAGG | 25898 |
rs766392966 | snp | A/G | 1.69046e-05 | 0.00290723 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514306 | TCCACCTCCCCTCAC[A/G]TTCCACCGATCCTTC | 25898 |
rs766486122 | snp | C/T | 1.64906e-05 | 0.00287142 | missense, intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514234 | TAGTGCTCGCAGCCC[C/T]GCTGACCTCGCTCTT | 25898 |
rs766523775 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502907 | AGGCATTAAAGAGTC[C/T]GCAGATACCTTCTTT | 25898 |
rs766543131 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506393 | TAATCAAGATATTGG[-/A]GTTATTAGGCACAGT | 25898 |
rs766615920 | snp | A/T | 1.77303e-05 | 0.00297739 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508796 | ATTAGAAGCAATTAG[A/T]TAAGAACACTTTACA | 25898 |
rs766650178 | snp | C/T | 3.42818e-05 | 0.00414001 | intron-variant, splice-donor-variant | RCHY1 | GRCh38.p7 | 4:75491582 | AAGTCAAACATCTTA[C/T]AATTATTTTTAAAAT | 25898 |
rs766699336 | in-del | -/A | 0.000237067 | 0.0108847 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491960 | GAAATTCACATTAAC[-/A]AAAAGCTTAACTAGA | 25898 |
rs766774341 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512054 | TTCTCAGTTCCTCTA[C/T]ACTCATAGATAACAA | 25898 |
rs766784183 | snp | C/T | 2.00347e-05 | 0.00316495 | missense, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75494166 | AATGGAAAAAATCTT[C/T]CTTTGGACCAATCCT | 25898 |
rs766791932 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486713 | GCAAAGGCATGTATT[G/T]AAAAAAATTCAGCTT | 25898 |
rs766811336 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75500401 | CATTACAGTAAGGAT[A/G]TATGTTCATTACCAA | 25898 |
rs766863296 | snp | C/G | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512840 | TATCTTACTCAAACA[C/G]CTGCATTTGACCCAG | 25898 |
rs766901064 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75496601 | GGAAACTCATAATTC[A/G]CAGGCTCCGGGTGGA | 25898 |
rs766908278 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75489164 | TATATATAAAATTTA[C/T]ATATATTGCTAAATT | 25898 |
rs766924672 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486574 | AGGGTTTTCACTGGA[A/C]ATTAGGATTACTAAG | 25898 |
rs766959827 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75485327 | TAAATTTTTAAAAAC[A/G]ATCTATGGAACTAAA | 25898 |
rs766971150 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75510287 | GAGCAAAGCCTCATC[A/C]CCAACCTGCATCACT | 25898 |
rs767054543 | in-del | -/GG | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512905 | CTCTGGTATTTAAGG[-/GG]GGGGGGGGGGCGGGG | 25898 |
rs767100801 | in-del | -/AA | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487024 | CTTAACGGTTGTTTC[-/AA]ATTGAAGGAATAAAA | 25898 |
rs767151434 | snp | C/T | 1.73836e-05 | 0.00294813 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514117 | ACCTCAAACTTAAAT[C/T]CAAGCCTAACCACCT | 25898 |
rs767197281 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482315 | CACTAAAGGAATTTC[C/T]AATCAAAACACAAGC | 25898 |
rs767208371 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497614 | TTTAAACTCTGTTAA[A/G]TTTAATTTAAACTCT | 25898 |
rs767252436 | snp | A/C | 1.65359e-05 | 0.00287536 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482614 | ATCTTACATTTCATG[A/C]CTAATATATGAAACT | 25898 |
rs767308337 | snp | C/T | 1.66043e-05 | 0.00288129 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491758 | ATGGCAAGACATGAG[C/T]AACAACACGGGATGT | 25898 |
rs767348534 | snp | A/G | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515741 | CTTTAAGATATCAGA[A/G]ACTGGTTTACAAAAA | 25898 |
rs767397649 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504361 | ATAGCAAAGCCAATC[C/T]CTCTTCTTCCTCCCT | 25898 |
rs767567684 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75507982 | TCTTGATCTGGGTAG[C/T]GGTTACAAAGGCATG | 25898 |
rs767575059 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479418 | TTTAGTACTTAGTAA[A/T]TTTATTTTGATGCAT | 25898 |
rs767583245 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513244 | TCTAATAATGAGGCA[A/G]TGACCAGCAAGGCTG | 25898 |
rs767669621 | snp | A/C/G/T | 3.30023e-05 | 0.00406205 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514192 | GAGTCCATAGAAGGC[A/C/G/T]TCACCTTTAGGAGAC | 25898 |
rs767784574 | snp | A/C/T | 5.01671e-05 | 0.00500814 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514295 | CCGCCATCTCCTCCA[A/C/T]CTCCCCTCACATTCC | 25898 |
rs767798073 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504852 | TATTCACAAAAGGGC[C/T]TTAAAATATTTTTTA | 25898 |
rs767828872 | in-del | -/AATA | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75479088 | CAGAATGGTGAGTAT[-/AATA]AATAATGCATTGTAC | 25898 |
rs767894419 | snp | C/G | 1.66815e-05 | 0.00288799 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491910 | ACATATTGGACAATT[C/G]TGTCGGGACACATTT | 25898 |
rs767956901 | in-del | -/CA | 1.67447e-05 | 0.00289345 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75508830 | AGTACCTACAAATTC[-/CA]CAGTTTTCACAGTGA | 25898 |
rs767966826 | snp | A/G | 2.02452e-05 | 0.00318154 | missense, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75494151 | AGTTACATTTCAAAC[A/G]ATGGAAAAAATCTTC | 25898 |
rs768019668 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499653 | GGTCATTATGTTAAG[C/T]GAAACAAGCCAACCA | 25898 |
rs768029864 | in-del | -/AG | 1.65266e-05 | 0.00287455 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514176 | GAAGCTTGTCAGGGA[-/AG]AGTCCATAGAAGGCG | 25898 |
rs768124304 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495575 | TCACCTAACTAGCCT[C/T]TCTACAGACCAGAAT | 25898 |
rs768148110 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512454 | ATGTTTCTAAGGCCA[A/G]CTCCTTCACTTGTGC | 25898 |
rs768263732 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501453 | CAAAAGAACTCAAAA[A/T]TCCTCGAGGGTAGTT | 25898 |
rs768265692 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484801 | AATTATAATGGAACG[A/T]CCCAAATGAACACTT | 25898 |
rs768272734 | snp | A/G | | | downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75478645 | AGCAATCCCACTTCT[A/G]GACATATAGCTAAAG | 25898 |
rs768358520 | in-del | -/A | 1.65993e-05 | 0.00288086 | frameshift-variant, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491770 | GAGCAACAACACGGG[-/A]TGTGTGAATGTCCTG | 25898 |
rs768402365 | snp | A/G | 1.64735e-05 | 0.00286993 | upstream-variant-2KB, synonymous-codon, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515497 | TGCTTCTCGCTGCTT[A/G]CCAAATTCGAAGTTA | 25898 |
rs768403364 | snp | A/C | 4.02755e-05 | 0.00448733 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509346 | AAGCAAAAGAAACTA[A/C]GTGTGCAATACAAAA | 25898 |
rs768593302 | snp | A/C | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515406 | GCTTTCCGGTTACTA[A/C]CTCTTAACATTCTAA | 25898 |
rs768630029 | snp | C/G | 1.66827e-05 | 0.00288809 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491724 | AAGATGTTACTTTAC[C/G]TATGTAAAAGATGTC | 25898 |
rs768805287 | snp | C/T | 4.80654e-05 | 0.00490208 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75494124 | TTCCTTGAAGATTCA[C/T]AGCTAGGCATAAGTT | 25898 |
rs768913412 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481918 | GGAATACCTCAAAAG[A/C]AAGAAAATTTCTTTT | 25898 |
rs769018604 | snp | A/C | 1.65151e-05 | 0.00287355 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514263 | TTGACCGCTGGCGCC[A/C]TCTTCCCGGGCCGTC | 25898 |
rs769022200 | in-del | -/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75489348 | TTGTATAGAAGGTAT[-/C]CCATGCAAGAGGGTT | 25898 |
rs769032217 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75482984 | GATGAATACCTGATA[C/T]TTATAATTCAAAATA | 25898 |
rs769050347 | snp | C/T | 1.84879e-05 | 0.00304033 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508771 | TTTTAAAAACTATTA[C/T]TGCATATACATTAGA | 25898 |
rs769072596 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75492149 | CAATGAAAATGTCAA[C/T]AAACATTATTGAGAT | 25898 |
rs769245883 | snp | A/T | 1.66286e-05 | 0.0028834 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490531 | CAGGAGGGCAAAAAT[A/T]AGAGTGCCAACAAGG | 25898 |
rs769288472 | snp | C/T | 1.68781e-05 | 0.00290495 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491677 | TAGTAAAACAAAAAC[C/T]GTCTCCACTATTTTC | 25898 |
rs769390212 | in-del | -/TT | 1.64766e-05 | 0.0028702 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515410 | TCCGGTTACTAACTC[-/TT]AACATTCTAATTTTC | 25898 |
rs769409775 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75507767 | TGGGTCAATCATACA[C/G]GAAAATGTAATAATT | 25898 |
rs769444225 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499279 | ACAGGGAATAACAGA[A/T]GCTGGTGAGGATATA | 25898 |
rs769448766 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484150 | CAAACAGCTGGCATC[A/G]GAAGTGGGATTTGAA | 25898 |
rs769511270 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486337 | AGTCATATGTTTAAG[C/T]AAATAATCATAAAAC | 25898 |
rs769792633 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75509713 | TCCCGTGCCATTCTC[A/G]TGATAATGAATAAAA | 25898 |
rs769822561 | snp | A/G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497290 | CTAAAAGGCTTTGCT[A/G/T]TACATAGTTAACTGT | 25898 |
rs770001329 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75505848 | ATACTGAGGCAAAGT[C/T]AATAGTCTCTACTTC | 25898 |
rs770001439 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75492351 | TATTGAAATTTACTA[A/C]ATGCCATGTTCAGCA | 25898 |
rs770002032 | in-del | -/AC | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75496229 | GAACATCAGGCAACA[-/AC]ACAGAGTGATCTGTG | 25898 |
rs770048264 | snp | C/T | 7.04697e-05 | 0.00593548 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494065 | ATTGCAAAAACACTG[C/T]AATATTTTTAAAATT | 25898 |
rs770051038 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75505070 | ATTTTTCCATGGACC[G/T]AGGTTGGGGGATGGT | 25898 |
rs770087676 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75494281 | CTGTAAAAAAAATTT[C/T]CAGCCACAATGGAGA | 25898 |
rs770347832 | snp | C/T | 1.66106e-05 | 0.00288184 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514283 | CCCGGGCCGTCGCCG[C/T]CATCTCCTCCACCTC | 25898 |
rs770410354 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514014 | GTACGAAGCAGGTAG[A/G]AAAGGTGGGGCTTAT | 25898 |
rs770473576 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512609 | ACTTCCTCTCTTAAA[A/G]AGGAAAAAATATGGT | 25898 |
rs770474837 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75509908 | TCTTGGGTATGTCTT[C/T]ATCAGCAGTGTGAAA | 25898 |
rs770514215 | snp | A/G | 1.6615e-05 | 0.00288223 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490545 | TAAGAGTGCCAACAA[A/G]GAGTCTACAAAGTTT | 25898 |
rs770566740 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497465 | CCTTACTCATTTTCT[A/G]TCACTTTCCTTTGTC | 25898 |
rs770572957 | snp | C/T | 2.46412e-05 | 0.00350998 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494238 | TACAGTCATGATTTG[C/T]TCATTATGTAAAACA | 25898 |
rs770615395 | in-del | -/CAAA | 6.82739e-05 | 0.00584229 | intron-variant, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491600 | TTATTTTTAAAATCC[-/CAAA]CACTCACTCTTTCAA | 25898 |
rs770647120 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501591 | AGTGAACATAATTAT[C/T]TGTCTATAACGTGAG | 25898 |
rs770741277 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75489681 | TCCACTACCAAACTC[C/T]GATATGACTAAATGC | 25898 |
rs770809381 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484844 | TAAGAAGTGCATTTG[A/C]TGATGGCCATAAGCT | 25898 |
rs770926812 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75498961 | CAAGCTAAAAAGCTT[C/T]TGCACAGCACAGGGA | 25898 |
rs770965995 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75483558 | AAAAGCACCAAATTG[A/T]ACAATTTAAATGAAT | 25898 |
rs771015357 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482207 | TAGAAATGAACTGCA[C/T]GCGTAGTGTCACTTA | 25898 |
rs771083653 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75494472 | TTAATGGATTCTTTC[C/T]ACAGATGCCATTCTG | 25898 |
rs771111964 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479213 | CTACACTGTAAACAT[A/G]TATCAAAACATCACA | 25898 |
rs771120306 | snp | C/G | 1.64735e-05 | 0.00286993 | upstream-variant-2KB, missense, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515531 | GGACTGACATTTCAC[C/G]TGTAAGATTTTGCTG | 25898 |
rs771418645 | snp | C/T | 7.10922e-05 | 0.00596163 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75509279 | GCGGCAAGTATAAAG[C/T]TTGTCACAGCAAGGT | 25898 |
rs771526823 | in-del | -/AGAC | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75494781 | AACTGACCTCCAAAT[-/AGAC]AGACAGTACCAATTT | 25898 |
rs771563171 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502847 | AATGCATAATCCTTC[A/G]GTTTTCTTTCTGTAC | 25898 |
rs771616228 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501802 | GTTCTGAAAAGGCTC[A/C]GTGCGGTGGCTCACG | 25898 |
rs771621543 | snp | C/T | 1.66441e-05 | 0.00288474 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490539 | CAAAAATAAGAGTGC[C/T]AACAAGGAGTCTACA | 25898 |
rs771671194 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512059 | AGTTCCTCTACACTC[-/AT]AGATAACAATCCCAA | 25898 |
rs771712615 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499310 | GAGAAAGTGGAACCC[C/T]TGTATACTACTTGTA | 25898 |
rs771757523 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75511399 | TGTCATTTTCATTTG[C/T]AGTGAGTCTCACTTT | 25898 |
rs771963438 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504090 | ATAAGCCAAGACTTA[C/T]CAGTGGTGTATTTGA | 25898 |
rs772033826 | snp | G/T | 0.000136105 | 0.00824828 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491967 | CACATTAACAAAAGC[G/T]TAACTAGATTAAAAT | 25898 |
rs772036533 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75505205 | CCTATGAGAATCTAA[C/T]GCTACTACTGATGTG | 25898 |
rs772092456 | in-del | -/C | 1.69106e-05 | 0.00290775 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491670 | ATTATTTTAGTAAAA[-/C]AAAAACTGTCTCCAC | 25898 |
rs772147664 | in-del | -/AA | 3.70982e-05 | 0.00430671 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509312 | CTAACACCCACGGAG[-/AA]AAAAGAGATATAGTA | 25898 |
rs772251208 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75511099 | CTTTTCTTCCTTGGT[C/T]ACATTAAAATCTATT | 25898 |
rs772308675 | in-del | -/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484265 | CATTAGGAATCATGG[-/T]TAAGTTCTCAGATTC | 25898 |
rs772316505 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481597 | TTCTATTCATTTACA[A/G]TAAGACATCCACTCC | 25898 |
rs772328999 | snp | A/G | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515220 | AAGCCAACAAAATTG[A/G]AATCATACTCGGGGT | 25898 |
rs772369704 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497170 | AGAAAAGGGAATTTT[C/T]TTAAAACGACAGAGC | 25898 |
rs772410653 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75503018 | AAGCAGAAAATAAAT[A/G]CAAAAAGGCAGATAA | 25898 |
rs772426947 | snp | C/T | 1.66012e-05 | 0.00288103 | missense, nc-transcript-variant, splice-acceptor-variant, intron-variant | RCHY1 | GRCh38.p7 | 4:75490700 | ATGGACATCTGTAGC[C/T]TCTGAAAGAGATAGA | 25898 |
rs772464133 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497566 | CCCACCTTGCAAATC[A/G]TTCTTTGCTCAATTA | 25898 |
rs772556650 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501230 | GTCAGGCTGGTCTCA[A/G]ACTCCCAACCTCAGG | 25898 |
rs772576644 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486490 | ATAATTTAAGGAAAC[A/T]TCCTTCCAAAAAATT | 25898 |
rs772587125 | snp | G/T | 1.65509e-05 | 0.00287666 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482629 | CCTAATATATGAAAC[G/T]GAACAGTGGATCGTC | 25898 |
rs772628207 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501578 | AATGCCTACTTGAAG[C/T]GAACATAATTATTTG | 25898 |
rs772812767 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75485242 | AACAATAAAAAAGAA[C/T]GCTGTCTTTCCCCTA | 25898 |
rs772909394 | snp | A/G | 3.32668e-05 | 0.00407827 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491856 | TAAATTCAAGAGCTG[A/G]GACTTCCAAAGTAAA | 25898 |
rs772935631 | snp | A/G | 1.66217e-05 | 0.0028828 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490540 | AAAAATAAGAGTGCC[A/G]ACAAGGAGTCTACAA | 25898 |
rs773116913 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482474 | GACACATGATAACAC[A/G]ATACCAAGGAAAGCC | 25898 |
rs773137511 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75479767 | ATAGATACAAATTCT[A/G]CGGCAGGGCAACCTA | 25898 |
rs773302923 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504324 | TATAAGCAGATTTTC[C/T]TCTACCTCTGCCACC | 25898 |
rs773341036 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497322 | ACCTAACTGGATGTG[C/T]TTACCTACAGTAACC | 25898 |
rs773347011 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480754 | TCATGCCTGTAATCC[C/T]AGCCCTTGGAAGGCC | 25898 |
rs773374603 | snp | C/G | 1.64999e-05 | 0.00287222 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509126 | TTAAATTTTTTCAAA[C/G]CACCTTAATACAGCT | 25898 |
rs773481410 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75492486 | GAACTTCCAAAGTCA[A/C]ACATTAATAAGAGGC | 25898 |
rs773516255 | snp | C/T | | | downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75478882 | ACTAAATGAAATAAC[C/T]CAGGCACAAAAAGGT | 25898 |
rs773537667 | snp | A/G/T | 3.55791e-05 | 0.00421765 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508795 | CATTAGAAGCAATTA[A/G/T]ATAAGAACACTTTAC | 25898 |
rs773553543 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75490512 | TTTTTTTGGCAAATT[C/T]AAGCAGGAGGGCAAA | 25898 |
rs773673880 | in-del | -/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75486112 | CTATTCTAGGAGGGG[-/T]TCCATCCTCCAAGCA | 25898 |
rs773680363 | snp | A/T | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512690 | ACCCCAAGAATACCC[A/T]ATAAGTGCTATTTTC | 25898 |
rs773711804 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75500360 | AACTGGTTACTTCCT[C/T]ACTTTTTAAAAAGCT | 25898 |
rs773776967 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497841 | AAAACTATACAATGG[-/A]ATGTCATAATCTAAT | 25898 |
rs773796599 | snp | A/T | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514046 | GCCTTGCCAAAAACG[A/T]TCTCCTCAAGAAGAA | 25898 |
rs773835573 | in-del | -/G | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75516144 | CTAGCTATTTTGTTA[-/G]ATATAATAAATCAAA | 25898 |
rs773845367 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75508444 | AAAATCACCTGTATT[A/T]CTTGATAATTTTTTA | 25898 |
rs773933189 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75509930 | AGTGTGAAAACAGAC[C/T]AATATAACACCCCAA | 25898 |
rs773999077 | snp | C/T | 1.651e-05 | 0.0028731 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514184 | TCAGGGAAGAGTCCA[C/T]AGAAGGCGTCACCTT | 25898 |
rs774004795 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75488590 | CTAAAGCAGCCAGTA[C/T]TGAAATTGTTTAGAT | 25898 |
rs774055446 | in-del | -/CT | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75510914 | AAGTACAAAAAGAAA[-/CT]CTGGCCTCACACAAA | 25898 |
rs774120386 | snp | C/T | 3.33372e-05 | 0.00408258 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491727 | ATGTTACTTTACCTA[C/T]GTAAAAGATGTCCAC | 25898 |
rs774147886 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501803 | TTCTGAAAAGGCTCA[C/G]TGCGGTGGCTCACGC | 25898 |
rs774212407 | snp | A/G | 1.66291e-05 | 0.00288345 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491849 | AGTATTTTAAATTCA[A/G]GAGCTGAGACTTCCA | 25898 |
rs774235909 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499332 | CTACTTGTAGAAATA[C/T]AAATTAATACAGCCA | 25898 |
rs774476900 | in-del | -/AAA | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75483309 | ATGCAAGAAAAGCAC[-/AAA]TAGTTTTTGAATAGT | 25898 |
rs774525221 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506185 | ATGCTAAATTGGATT[A/C]AGGTTATCCATCCCT | 25898 |
rs774561166 | snp | G/T | 1.85177e-05 | 0.00304278 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508773 | TTAAAAACTATTATT[G/T]CATATACATTAGAAG | 25898 |
rs774602156 | snp | A/G | 2.18114e-05 | 0.00330231 | missense, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75494133 | GATTCATAGCTAGGC[A/G]TAAGTTACATTTCAA | 25898 |
rs774693673 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75489526 | GCAAAACTAACTGAA[A/T]TGACTGGATTGCCTT | 25898 |
rs774811290 | snp | C/T | 1.65323e-05 | 0.00287505 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482610 | ACAAATCTTACATTT[C/T]ATGCCTAATATATGA | 25898 |
rs774895941 | snp | C/T | 1.6863e-05 | 0.00290365 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491683 | AACAAAAACTGTCTC[C/T]ACTATTTTCAAACAT | 25898 |
rs774954100 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75511584 | TTTGCAGAAGTGTTT[A/G]ATCAAAACTTCCCAT | 25898 |
rs775059842 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502849 | TGCATAATCCTTCGG[C/T]TTTCTTTCTGTACTG | 25898 |
rs775064533 | snp | A/C | 2.06892e-05 | 0.00321623 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509138 | AAACCACCTTAATAC[A/C]GCTTTTAAAAAGAAA | 25898 |
rs775160120 | in-del | -/TTACT | 1.67136e-05 | 0.00289076 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491715 | ATTGAGAAAAAGATG[-/TTACT]TTACCTATGTAAAAG | 25898 |
rs775265012 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75500051 | GAGGCTGAGGTGGGA[C/G]GATCACATAAACCTG | 25898 |
rs775277133 | snp | A/G | | | downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75479023 | GATGCTGATCAAAGG[A/G]TACAAAATATCAGTT | 25898 |
rs775285001 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512210 | TTCTCTCATTCTTCC[-/AG]AGTCTAAGACCTAAG | 25898 |
rs775357741 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75483678 | AATCACATGATTATC[A/G]GTTAGTATTCCAAAA | 25898 |
rs775478571 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502222 | AAAGATGAATATTTT[A/G]TGACATTTATTCTTT | 25898 |
rs775521704 | snp | A/C | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515299 | ATGATGTAAGCAAAG[A/C]TGCAGGTGTTAGAAG | 25898 |
rs775586648 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480609 | ATGTTGAAAACAGAA[A/G]AGCCTTATTATTATA | 25898 |
rs775623260 | snp | A/C | 1.66421e-05 | 0.00288458 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491874 | CTTCCAAAGTAAAAA[A/C]TATTTTAAGCCTACC | 25898 |
rs775631489 | snp | C/T | | | missense, intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514219 | AGACATCCTCTGTCA[C/T]AGTGCTCGCAGCCCC | 25898 |
rs775712537 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75496067 | TCTCTTACAAATGAA[C/T]TTTAGAATAGGCTGT | 25898 |
rs775768928 | in-del | -/A | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484716 | GAAGCAGCACTTTTT[-/A]AACATTTTATAGAAG | 25898 |
rs775861951 | snp | C/T | 5.62551e-05 | 0.00530324 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509324 | GAGAAAAAAGAGATA[C/T]AGTAAGAAGCAAAAG | 25898 |
rs775887886 | in-del | -/ATA | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487796 | ATAATATATATATTC[-/ATA]ATATATATATTCATA | 25898 |
rs775899161 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504055 | TATTTGAATTTGGTA[A/G]TATGTGTACAGAAGT | 25898 |
rs775921619 | in-del | -/AA | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75479121 | CATTTCAAAAATATT[-/AA]GAGTAGATTTTAAGT | 25898 |
rs775966363 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495018 | TTTTAACCAATTTAC[C/T]GGTAAAAAATATATC | 25898 |
rs775972110 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75488688 | TAACCTGGTATTTAA[A/G]AGGACACAAATCCAA | 25898 |
rs776032936 | snp | A/T | 1.64768e-05 | 0.00287021 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515408 | TTTCCGGTTACTAAC[A/T]CTTAACATTCTAATT | 25898 |
rs776143068 | in-del | -/T | 1.66056e-05 | 0.00288141 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491811 | AAATGTTAGTGCTTG[-/T]ATGAAGACAATATAA | 25898 |
rs776232775 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75499401 | ACATAGAGCTACCAT[A/G]TGATCCAGCAAGTCC | 25898 |
rs776254600 | snp | A/G | 3.39893e-05 | 0.00412232 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490719 | GAAAGAGATAGAAAG[A/G]TTATTTTCCAAATAT | 25898 |
rs776307800 | snp | C/G | 3.31631e-05 | 0.00407191 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490553 | CCAACAAGGAGTCTA[C/G]AAAGTTTTAAGTATT | 25898 |
rs776331292 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484901 | TGCATTTGAAAATGA[A/G]GGCTCCCAAATTAGA | 25898 |
rs776387337 | in-del | -/ACTC | 1.64776e-05 | 0.00287028 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515406 | GCTTTCCGGTTACTA[-/ACTC]TTAACATTCTAATTT | 25898 |
rs776571759 | snp | A/T | 1.66219e-05 | 0.00288283 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514286 | GGGCCGTCGCCGCCA[A/T]CTCCTCCACCTCCCC | 25898 |
rs776706014 | in-del | -/TT | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75485964 | TGAGCTTGTTTTGGG[-/TT]TTGAACCTCTAGATT | 25898 |
rs776715962 | snp | C/T | | | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515365 | TGTTTCCTAAAACAC[C/T]GGGAAAGGGAAAATA | 25898 |
rs776770876 | snp | A/G/T | 1.64735e-05 | 0.00286993 | upstream-variant-2KB, splice-donor-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515533 | ACTGACATTTCACGT[A/G/T]TAAGATTTTGCTGTA | 25898 |
rs776858859 | snp | A/G | 3.32088e-05 | 0.00407471 | missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491767 | CATGAGCAACAACAC[A/G]GGATGTGTGAATGTC | 25898 |
rs776894486 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504217 | TATCAGTTATTTACA[C/T]GATGCACATGTGCCA | 25898 |
rs776963900 | snp | A/T | 1.6501e-05 | 0.00287232 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509134 | TTTCAAACCACCTTA[A/T]TACAGCTTTTAAAAA | 25898 |
rs777053671 | snp | A/G | 1.78768e-05 | 0.00298966 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75509287 | TATAAAGCTTGTCAC[A/G]GCAAGGTGCCTAACA | 25898 |
rs777141002 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75511777 | GCAATACTAAACAGT[A/G]CTTTTCCACCATCAA | 25898 |
rs777455122 | snp | A/C | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514854 | CAAAATATGTACTGA[A/C]ATTCACTATTGCCAG | 25898 |
rs777599886 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75491976 | AAAAGCTTAACTAGA[C/T]TAAAATGTCAGGTAT | 25898 |
rs777634322 | snp | A/G | 4.61659e-05 | 0.00480425 | intron-variant | RCHY1 | GRCh38.p7 | 4:75494227 | TTATTTTTTACTACA[A/G]TCATGATTTGTTCAT | 25898 |
rs777672629 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513643 | GTTTTCTCAGAGTAA[C/T]AATACATGCTTATTA | 25898 |
rs777672866 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75485654 | TGACCTAAGAATTGG[C/G]CCTTTAGAAATGCAT | 25898 |
rs777695754 | snp | A/G | 3.52827e-05 | 0.00420001 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75509266 | TATCATGACACAAGC[A/G]GCAAGTATAAAGCTT | 25898 |
rs777724401 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75501097 | TCACTGCAACCTCCC[A/G]CCCACGGGTTCAAGC | 25898 |
rs777795487 | in-del | -/GAAAGA | 1.66413e-05 | 0.0028845 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490704 | ACATCTGTAGCCTCT[-/GAAAGA]GATAGAAAGGTTATT | 25898 |
rs778110214 | in-del | -/CAAA | 1.65515e-05 | 0.00287671 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75508866 | GCTTCTTATCTTTGT[-/CAAA]CAAATGGCATATATC | 25898 |
rs778120136 | snp | C/T | 1.67964e-05 | 0.00289792 | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514140 | AACCACCTGCCCAGC[C/T]CGCCCCAGCCCAACC | 25898 |
rs778207897 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75507145 | ACTAAAGACAATTCT[C/T]TAAGCAGAAGAAAAG | 25898 |
rs778241913 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481414 | AACAGTGTCAAAGTC[A/G]GCTGGATCATCAAAC | 25898 |
rs778293097 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480101 | AGGATTTTAATCATC[A/G]AGTTGACGTGTCATG | 25898 |
rs778296812 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75496927 | GACACAGATGTTAGA[A/T]TTAATACAGGGCATT | 25898 |
rs778302476 | snp | C/G | 6.58924e-05 | 0.0057395 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515447 | GTTTTGTTATGAGTT[C/G]CTAAAATGGTGAAAT | 25898 |
rs778302521 | snp | C/G | 1.67646e-05 | 0.00289517 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490710 | GTAGCCTCTGAAAGA[C/G]ATAGAAAGGTTATTT | 25898 |
rs778419522 | snp | C/T | 1.68969e-05 | 0.00290657 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491954 | TAAAAGAGAAATTCA[C/T]ATTAACAAAAGCTTA | 25898 |
rs778574542 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75503893 | CAAACGTTGAAGGCA[A/G]GTACATATGTTAAAG | 25898 |
rs778817323 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75490202 | ATCTCAAAAATCAGC[A/G]AATATGTTCTCCTGA | 25898 |
rs778832896 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75507484 | ACCAAAACTGTAGAT[C/T]GAAACACGAACATAT | 25898 |
rs778874126 | snp | A/T | 6.78714e-05 | 0.00582504 | intron-variant, missense, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491629 | TTCAACATTTCTTCA[A/T]AACACGTTCTGAAAG | 25898 |
rs778879251 | in-del | -/CA | 1.83724e-05 | 0.00303082 | frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75509191 | CATGTTGAATTTTTT[-/CA]CAGTTTATGCACTGC | 25898 |
rs779038657 | in-del | -/CT | 1.70246e-05 | 0.00291754 | intron-variant, splice-donor-variant, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75491610 | AATCCCAAACACTCA[-/CT]CTTTCAACATTTCTT | 25898 |
rs779129335 | snp | C/G/T | 4.99133e-05 | 0.00499546 | intron-variant | RCHY1 | GRCh38.p7 | 4:75490536 | GGGCAAAAATAAGAG[C/G/T]GCCAACAAGGAGTCT | 25898 |
rs779178725 | snp | C/G | 0.000611121 | 0.0174696 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514265 | GACCGCTGGCGCCAT[C/G]TTCCCGGGCCGTCGC | 25898 |
rs779205074 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481566 | CCCCTATTTTCACAC[G/T]CTTAGGGAAGAAATA | 25898 |
rs779210341 | snp | C/G | 1.77338e-05 | 0.00297768 | intron-variant | RCHY1 | GRCh38.p7 | 4:75508970 | AAAAACTGCAATAAA[C/G]TAAACATTTTGAGTT | 25898 |
rs779265679 | snp | C/T | 2.01595e-05 | 0.0031748 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509348 | GCAAAAGAAACTAAG[C/T]GTGCAATACAAAAAG | 25898 |
rs779544795 | snp | C/T | 4.95528e-05 | 0.00497734 | missense, nc-transcript-variant, intron-variant | RCHY1 | GRCh38.p7 | 4:75490681 | AAAGCAGAGTGCATA[C/T]ATAATGGACATCTGT | 25898 |
rs779594062 | snp | C/T | 3.32408e-05 | 0.00407668 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491830 | AAGACAATATAAACA[C/T]CCAAGTATTTTAAAT | 25898 |
rs779628550 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75505697 | CTACTTCCACAATGA[C/T]GAAATAGCTTCTATA | 25898 |
rs779761521 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481573 | TTTCACACGCTTAGG[A/G]AAGAAATATTCTATT | 25898 |
rs779774144 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75507148 | AAAGACAATTCTTTA[A/C]GCAGAAGAAAAGTAA | 25898 |
rs779880883 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75490370 | AGTGTTGGGAAAAAC[G/T]ACATAAAGGTATTCT | 25898 |
rs779910070 | snp | A/G | 4.94189e-05 | 0.00497062 | upstream-variant-2KB, missense, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515490 | TTGGATGTGCTTCTC[A/G]CTGCTTGCCAAATTC | 25898 |
rs779952988 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487374 | TAGAAAACTGAGTTT[C/T]GAAGAGTAAAGGTTT | 25898 |
rs780004396 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502499 | GAGCCAAGATCGCGC[C/T]ACTGCACTCCAGCCT | 25898 |
rs780021064 | snp | A/G | 3.51247e-05 | 0.0041906 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75509255 | ATCTTCATTGTTATC[A/G]TGACACAAGCGGCAA | 25898 |
rs780070041 | in-del | -/C | 5.73082e-05 | 0.00535265 | intron-variant | RCHY1 | GRCh38.p7 | 4:75509334 | AGATATAGTAAGAAG[-/C]AAAAGAAACTAAGTG | 25898 |
rs780132255 | snp | C/T | 2.04397e-05 | 0.00319678 | intron-variant | RCHY1 | GRCh38.p7 | 4:75482713 | TAAACCTTATAAATA[C/T]AAGTAGCATTGTCTA | 25898 |
rs780230772 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497273 | CATATTTTAAGATCG[C/T]CCTAAAAGGCTTTGC | 25898 |
rs780233974 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75510979 | AGCCTTTTTGGAGAA[G/T]TATGGATATCATTCT | 25898 |
rs780243063 | snp | C/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484105 | TCTCAATTAAGTTCT[C/G]TTAAATTTAATTTGT | 25898 |
rs780308570 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75482847 | AAAAAGCTATTAAGG[G/T]GGCTCTGAATTCAGA | 25898 |
rs780463078 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75498735 | AAAAACAGGATACCA[C/T]ATGCAGAAGCATGAA | 25898 |
rs780544022 | snp | A/C | 3.29957e-05 | 0.00406162 | missense, synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514253 | GACCTCGCTCTTGAC[A/C]GCTGGCGCCATCTTC | 25898 |
rs780584128 | snp | G/T | | | downstream-variant-500B | RCHY1 | GRCh38.p7 | 4:75478823 | TTCAGCCCTATAAAA[G/T]AAAGAAATCCTGTCA | 25898 |
rs780702849 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484103 | TTTCTCAATTAAGTT[C/T]TGTTAAATTTAATTT | 25898 |
rs780717529 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75480021 | TAAAGTTATGTATTT[C/T]AAGTTTTGCATACTG | 25898 |
rs780729665 | snp | C/T | 1.64732e-05 | 0.0028699 | upstream-variant-2KB, missense, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515480 | TGCTCCGCCATTGGA[C/T]GTGCTTCTCGCTGCT | 25898 |
rs780731915 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513877 | TCACACACCTGAACG[A/G]AAAACCCCAGTACAG | 25898 |
rs780768466 | snp | A/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495689 | GCTACACAACTCAGA[A/T]TTATTTCCATGAGAA | 25898 |
rs780774153 | snp | A/G | 1.64746e-05 | 0.00287002 | upstream-variant-2KB, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75515579 | TTGGCCATGTTATAA[A/G]AAGCAAAAGACAGTT | 25898 |
rs780776121 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | RCHY1, THAP6 | GRCh38.p7 | 4:75514523 | TTCGCTGCTAACGGT[A/G]ATAACTCTTAGGTTG | 25898 |
rs780832420 | snp | C/T | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75513069 | ACATCTCAGTAGAAA[C/T]TGAATCATAAGGATA | 25898 |
rs780862189 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75502618 | TCATTCTATTCTGTT[C/T]GCAATTATCATATGG | 25898 |
rs780909610 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75481973 | CCTAATTGAGCCAAA[C/T]ATAGAAAACTTTGGA | 25898 |
rs781057818 | snp | A/T | 1.69367e-05 | 0.00290999 | intron-variant | RCHY1 | GRCh38.p7 | 4:75491659 | GAAAATATAAGATTA[A/T]TTTAGTAAAACAAAA | 25898 |
rs781080541 | in-del | -/AA | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487083 | AAAAGAAAGAATTTT[-/AA]AAGTTTATAAGGGAA | 25898 |
rs781101333 | snp | A/C | 3.34169e-05 | 0.00408746 | stop-lost, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482539 | ACTGTGTAGGCTCGT[A/C]ATTGCTGATCCAGTG | 25898 |
rs781134147 | snp | A/G | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512142 | AGAAAAAGCATCACC[A/G]TCCTTGCTGGTTCAT | 25898 |
rs781215465 | snp | C/T | 1.64947e-05 | 0.00287177 | missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant, intron-variant | RCHY1, THAP6 | GRCh38.p7 | 4:75514249 | CGCTGACCTCGCTCT[C/T]GACCGCTGGCGCCAT | 25898 |
rs781270546 | snp | A/C | 8.31124e-05 | 0.00644587 | intron-variant, splice-donor-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75514153 | GCCCGCCCCAGCCCA[A/C]CCTGACGGAAGCTTG | 25898 |
rs781282918 | in-del | -/GTGTA | 1.68303e-05 | 0.00290084 | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482527 | AAGTTCTCCAGTACT[-/GTGTA]GGCTCGTCATTGCTG | 25898 |
rs781297110 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497103 | TATTGCTAACAAAAA[A/G]GTTAGTCAACTTGAA | 25898 |
rs781372878 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75483249 | TAGTGCTAAGTAAGA[A/G]CCTGAAAAATAACAA | 25898 |
rs781427959 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75498941 | AAAAACAGACGGAAT[C/T]ACATCAAGCTAAAAA | 25898 |
rs781541293 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504914 | AAATGGCGATGACTA[A/C]TTTTTCTAGTATATT | 25898 |
rs781573843 | in-del | -/AC | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75495904 | TTTGTCTGTGTATAT[-/AC]ACACACACACATATT | 25898 |
rs781605722 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75484291 | GATTCTAAAGCTCTG[A/C]GCATTTGTGTTTTGA | 25898 |
rs781654123 | snp | A/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75500672 | AGTCAGATATATCTT[A/C]GATGAAGCAATAGGG | 25898 |
rs781715374 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75506883 | GACTTAAAAAACAGC[G/T]AGAGGAGGATAAAAG | 25898 |
rs796094134 | in-del | -/AT | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75487758 | ATATATATATTCATA[-/AT]ATATATATTCATATA | 25898 |
rs796101110 | in-del | -/C | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75504273 | AAATACAGTTGACCC[-/C]TTGAACAACACAAAT | 25898 |
rs796132761 | in-del | CTGC/GT | | | utr-variant-3-prime, nc-transcript-variant | RCHY1 | GRCh38.p7 | 4:75482008 | CTTTCTATAAAACAG[CTGC/GT]TCAATATAATTTTAT | 25898 |
rs796180163 | snp | A/G | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497578 | ATCGTTCTTTGCTCA[A/G]TTAAACTCTGTTAAG | 25898 |
rs796250931 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75497208 | AGCTGTGAGACAACT[G/T]CAAGCAACCTAACAT | 25898 |
rs796251449 | in-del | -/AA | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75511246 | AAAATCATATTCATT[-/AA]AAGTCTTTAGGTATT | 25898 |
rs796492564 | in-del | C/GGGG | | | intron-variant, upstream-variant-2KB | RCHY1, THAP6 | GRCh38.p7 | 4:75512909 | GTATTTAAGGGGGGG[C/GGGG]GGGCGGGGGAAGGCA | 25898 |
rs796574547 | snp | G/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75505074 | TTCCATGGACCGAGG[G/T]TGGGGGATGGTTTCG | 25898 |
rs796602996 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75485844 | TAGGTGTTATGTGTA[C/T]GTGATAACATTTGGT | 25898 |
rs796650328 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75505335 | CCCAAGCACTGGGGA[C/T]CCTGATATAAGGCAC | 25898 |
rs796651747 | multinucleotide-polymorphism | AT/TG | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75498376 | GGCTTCACTGCTGAA[AT/TG]ATAGCAAACATTTAA | 25898 |
rs797014860 | snp | C/T | | | intron-variant | RCHY1 | GRCh38.p7 | 4:75483997 | AGAAACAACCTTTTA[C/T]GCTTTAGGTTGCAAG | 25898 |