SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs147368737 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020991 | AGTGAGAAGGCTGAC[A/G]GGGAACACGAAGAGG | 11169 |
rs147404759 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969336 | CAGCATTAAGACTCC[A/G]TTTCAAGAAAAAAAA | 11169 |
rs147421085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972845 | TGTTTATTAGATATT[C/G]GTCAGAGTGAAGCAG | 11169 |
rs147507097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989967 | TCACGCCCGGCAGAG[A/G]CAACATAAATTGATA | 11169 |
rs147517088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024580 | GAGAGATCAGATTGT[C/T]ACTGTGTCTGTGTAG | 11169 |
rs147524045 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992636 | GATATAATTTACAGC[C/T]AGGTGCTGTGACTCA | 11169 |
rs147580048 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014038 | CACTTAAACTTTAAA[A/G]ATAAAGTGCTAATTT | 11169 |
rs147580551 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948872 | TGTTCTGCAGCCTCC[A/G]CTGCTGATACCCAGG | 11169 |
rs147679941 | snp | C/T | 0.00122449 | 0.0247133 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999305 | CTATTTCATCTTTTC[C/T]AAAAAAACAAATCTC | 11169 |
rs147686808 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961086 | CTGAGGTTACAGACA[C/T]GAGCCATCACACCTG | 11169 |
rs147696014 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002846 | GATCCTCCTGCCTCA[A/G]CCTCCCAAAGTGCTG | 11169 |
rs147777028 | in-del | -/AATT | 0.280502 | 0.248132 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987401 | GCTAAAAATTAAAAC[-/AATT]AAGACAGAAACAATC | 11169 |
rs147784340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014498 | TATCCCTAGCACCAA[A/G]CAGTCTCTGACAGAA | 11169 |
rs147801026 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017728 | TTCATGATTCTATCC[A/T]AATGAGCTGCAAGAT | 11169 |
rs147833131 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963847 | CCAGGTGTGCTGGCT[C/T]ACACCTGTAATCCTA | 11169 |
rs147846070 | in-del | -/AAAAAAAAC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54994446 | AAGAGTAAAAAGAAA[-/AAAAAAAAC]CAGCCATAATCTTAA | 11169 |
rs147894278 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999043 | CAACTTTTTGTCTTC[C/T]CTGGAGTTAAGAAAC | 11169 |
rs147903595 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995364 | TTTATTGAATTTTGC[G/T]CTGTATTATTTCCTT | 11169 |
rs147937197 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985229 | AGAACAAAAAAATTA[A/T]CACAAAGTTAAAATA | 11169 |
rs147991811 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007949 | ATTTGAATAAACTGT[A/G]TATGTGACTCTCCAA | 11169 |
rs148045399 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012462 | TCATTCCCATATTTG[C/T]GTTACACAAAACATC | 11169 |
rs148064096 | in-del | -/T | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005734 | TCCAGAACAACATCA[-/T]TAAGGATCCTTCTCT | 11169 |
rs148105037 | snp | A/C/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991505 | TCATATTCAATGACA[A/C/T]TGACATGCTATTTGC | 11169 |
rs148161400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020546 | CTCTTTTCTTACCTA[C/T]ATTTACTCCTTCCCT | 11169 |
rs148203261 | snp | C/T | 0.000215612 | 0.0103807 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54957046 | TACCTGCTTAGGCTT[C/T]GGCTTTGGAATCAGA | 11169 |
rs148225510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004649 | GTAGAGACAGGGTTT[C/T]GCCATGTTTCCCAGG | 11169 |
rs148256968 | snp | A/G | 3.31252e-05 | 0.00406958 | missense | WDHD1 | GRCh38.p7 | 14:54991224 | TTACCATGAATCTGT[A/G]AGTGAGATGCAACGG | 11169 |
rs148257332 | snp | C/G | 0.0655868 | 0.168795 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980319 | ACAGAGTGAGACTCT[C/G]TCTCAAAAAAAAAAA | 11169 |
rs148316043 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954528 | GAGAAATGCTATTCA[C/T]ATAAAATTATTCATT | 11169 |
rs148321160 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022917 | GCAACCTCCACCTCC[C/T]GGGTTCAAGTGATTC | 11169 |
rs148368652 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959778 | AGCAAGATACCCTGT[A/G]TCCGCACCCCCCCCA | 11169 |
rs148370498 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989826 | CACCAGGTCCAGCTA[A/G]TTTCTGTATTTTTTT | 11169 |
rs148377688 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999433 | CACCTCTCCTGTTTT[C/T]AGCCCCACTTCTAGA | 11169 |
rs148475348 | snp | G/T | 0.261884 | 0.249717 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960646 | CTGGGATTACAGGCA[G/T]GAGCCACCATGCCCG | 11169 |
rs148485759 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002490 | CATTACTTAAAACTT[C/T]AATAAGCAAAAAATA | 11169 |
rs148519359 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983832 | CCAAAAAAAAAATTA[G/T]TTTTAAAGAAAAAAA | 11169 |
rs148528120 | snp | A/G | 0.00358779 | 0.0422022 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938710 | ATGAGTTGTGACTGT[A/G]CCACTGCACTTCAGC | 11169 |
rs148572722 | snp | C/T | 0.000447765 | 0.014956 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:54995686 | TCTTCATCATCCTCA[C/T]CATCATTTATAATCC | 11169 |
rs148632523 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994044 | AATGTTCAAGTGTTA[C/T]TGTAGCATGTAAGTT | 11169 |
rs148707409 | snp | A/G | 0.000250378 | 0.011186 | missense | WDHD1 | GRCh38.p7 | 14:54941534 | GTTTCTGATTTGTAG[A/G]AAAATCTAAAGGTTT | 11169 |
rs148727670 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949408 | AGGGTATCAGTGATC[A/G]AAGATCAAATGAATG | 11169 |
rs148749080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942703 | CCATTCATTTCATCT[A/G]TCTCTAAAATCTCTT | 11169 |
rs148760238 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981893 | TAAAAAAAGAAAAAA[C/T]ATTGGATTTGATATG | 11169 |
rs148815802 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018201 | TCCTCTAAATCTTAG[C/T]TGCATTTAGTTGAAA | 11169 |
rs148854813 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944139 | GTTGTTGTTATTATT[A/G]TTATTAGAGACGATG | 11169 |
rs148857416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007591 | AACTAGAGTATTTTC[C/T]GTGCAGAATAAACAA | 11169 |
rs148864034 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954336 | AGTAGAGATCAAGAA[A/G]ATAGGTAACATACTG | 11169 |
rs148953051 | snp | A/G | 9.88338e-05 | 0.00702902 | intron-variant, missense, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026768 | TGCCCATATCTCATT[A/G]GCTTCCGTGTGGCAG | 11169 |
rs148977236 | in-del | -/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998726 | TCACAACCACCCCAA[-/C]CCGCCATGCTTGCAT | 11169 |
rs149006835 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961906 | CAATGGCACGATCTC[A/G]GCTCACTGCTACCTC | 11169 |
rs149011490 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975884 | CTTTCTTTTAAAGGA[C/T]CTCTGAACAAAAAGA | 11169 |
rs149016360 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003783 | TGGCCAGGCTGGTCT[C/G]GAACTCCTGACCTCA | 11169 |
rs149020725 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987706 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 11169 |
rs149025928 | snp | A/G | 6.63207e-05 | 0.00575812 | missense | WDHD1 | GRCh38.p7 | 14:54955600 | GGACATATAGCTGGG[A/G]TTTCAGATAATACAT | 11169 |
rs149068494 | in-del | -/AT | 0.140581 | 0.224783 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941398 | CAAACTCTTTAAAAA[-/AT]ATATATATAATGAGT | 11169 |
rs149068687 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54971805 | CTGATATCCAGAGTC[C/T]ATAAGGAACTTAAAA | 11169 |
rs149109167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021995 | CCATAGATTAGTTTA[C/T]GTAATGAGCCCGTAA | 11169 |
rs149161941 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994955 | TCTTTATTGATCAAC[C/G]ACGATAGATATTTAT | 11169 |
rs149194560 | in-del | -/A | 0.0228947 | 0.104514 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959799 | ACCAAACAAAAAAAA[-/A]CAAACAAAAAAACCT | 11169 |
rs149216254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999358 | TGAAGATGGGGGAGG[A/G]CAGGTACCCAGCTTT | 11169 |
rs149224386 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947026 | CCAGCCTTGGTGACA[A/G]GGCAAGACTGTCTCA | 11169 |
rs149245094 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001116 | GGGAATCAACCAAAT[G/T]CAAATTTTTATATCC | 11169 |
rs149290095 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983300 | ATGTGAGCCACAAGT[C/G]TAATTTTTAATTTCC | 11169 |
rs149332555 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947678 | CTCATTGCAGCCTCC[A/G]TCTCCTGTGTTCAAG | 11169 |
rs149341510 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020098 | AGCAAAATCTCTATA[C/T]ACTCAGCTTTCTTTC | 11169 |
rs149343025 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952556 | CACTATCGTGAAAAC[A/G]GCCATCCTGTCCAAG | 11169 |
rs149385991 | snp | A/C/G | 0.000153988 | 0.00877328 | missense | WDHD1 | GRCh38.p7 | 14:54963141 | TCAGCAAGTTCCACA[A/C/G]AACGGAATTCTCGCT | 11169 |
rs149397122 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956077 | CTAAATTCCATGTTT[C/T]CTAAATGAATACAAT | 11169 |
rs149459761 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963661 | CACAATTAGCCAGGC[A/G]TGGTGGCGTGCGCCT | 11169 |
rs149483874 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939793 | CTGAAATACAATATA[C/T]ACAGATTATATCCTT | 11169 |
rs149500675 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015455 | CTTCCAGCTTCTGCC[A/G]TGGTCTCATTTGGTA | 11169 |
rs149543175 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980091 | ACACTTTGGGAGGCC[A/G]AGGCGGGAAGATCCC | 11169 |
rs149555683 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989468 | ATAGAGTATTTAATA[A/C]TATTTAAAAATAAAT | 11169 |
rs149619563 | snp | A/G | 9.90737e-05 | 0.00703754 | utr-variant-5-prime, synonymous-codon | WDHD1 | GRCh38.p7 | 14:55013590 | ACTTCCACAAGTCAC[A/G]ATAAAACTGTGAAGA | 11169 |
rs149662251 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990372 | GGAGGCCTAGGCAGG[C/T]GGATCACGAGGTCAG | 11169 |
rs149704172 | snp | C/T | 3.29712e-05 | 0.00406011 | missense | WDHD1 | GRCh38.p7 | 14:54987194 | GTCCTGCCATTGACA[C/T]CACAGGTCCAGCAAG | 11169 |
rs149721600 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942091 | CCGTCTCTACTAAAA[A/G]TACAAAAAAATTAGC | 11169 |
rs149777970 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003280 | TTTGGGAGGCTGAGA[C/T]AGGCAGATCACTAGA | 11169 |
rs149863963 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948709 | CTGCCTCCTCAGTGA[A/C]AGGTGGGTCCATGAT | 11169 |
rs149869285 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953764 | TAAGAAAATGTGGCA[C/T]ATATACACCATGGAA | 11169 |
rs149872071 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021907 | ATGATGGCATCTTCA[A/G]TGGTATAATCCTTCC | 11169 |
rs149926168 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957301 | CTGTTAAGTTTGTAT[G/T]GCCATCTCATCTTTA | 11169 |
rs149934042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969558 | TAATGAGTTCCAAAA[C/T]TGAATCGTAATAAAT | 11169 |
rs149936614 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998984 | GGCATTATTCCTATC[C/T]TTTTACACATACAGT | 11169 |
rs149998881 | in-del | -/TA/TATATATA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003599 | AACTATATATATATA[-/TA/TATATATA]GTTGCCCAGGCTGGA | 11169 |
rs150021228 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974624 | TGAGCTCTGGAGATC[A/G]AGACCAGCCTGGGCA | 11169 |
rs150031957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016833 | TCATTCCAAGTTTTC[C/T]GGTGCAAGCATAAAA | 11169 |
rs150035695 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945998 | TTTCTGAAAATATGC[-/A]AATTTTAAGTAATCT | 11169 |
rs150080999 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54973570 | GGCAGTGTGAATACC[C/T]CAAGTTTGAAAGAAT | 11169 |
rs150125538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976861 | GAAAATATGAAAACA[A/G]TCTGCAGTTATCAAT | 11169 |
rs150156276 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982767 | AAATGGTTGATATTT[C/T]AAAGACAAAGTGGAG | 11169 |
rs150179098 | snp | C/T | 4.95323e-05 | 0.00497631 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000891 | TAAATCATACCTTTC[C/T]ATGCAGTCTTTGGTT | 11169 |
rs150191927 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991907 | GTAAATGAATGAAGT[A/G]AGCCTATCAATTAAG | 11169 |
rs150193166 | snp | A/C | 0.0023933 | 0.0345097 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939268 | CCTCATCCTTTTGTC[A/C]AAAGGGACTACCTGG | 11169 |
rs150246023 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943856 | ATAAAAAAAAAAAAG[A/G]GGACAATTGCTTGTG | 11169 |
rs150312887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011040 | AAGAGCCAACCATGA[C/T]GACACCTTGATTTCA | 11169 |
rs150366303 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014818 | AAGTCAAAAAGATTC[A/G]TAAGAAAGATGGTAT | 11169 |
rs150402382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023265 | CCACATTAGAGTCTA[C/T]AGCTATGCCTTTCTA | 11169 |
rs150408044 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965828 | AGGCATGGTGGCACA[A/C]GCCTGTAGTCCCAGC | 11169 |
rs150419058 | snp | A/C | 3.29495e-05 | 0.00405877 | stop-gained | WDHD1 | GRCh38.p7 | 14:54989093 | AAGATCTGCTATTGT[A/C]TAATTCAAAGTGTTT | 11169 |
rs150462419 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971212 | TCCACAAAAGCAATT[A/G]CAACAAAAACAAAAA | 11169 |
rs150513970 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968058 | ATGTTATCACCAAGA[C/T]AAATGCTGATGAAGC | 11169 |
rs150528664 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990327 | CTCAGGCCAGGCGCG[A/G]TGGCTCACGCCTGTA | 11169 |
rs150571081 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974079 | GTGCATAAACCACCT[C/G]GAAGAGGAATTTAAA | 11169 |
rs150619409 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948414 | ATTATATCCCACTCC[C/T]GGCTCAGAGGGTCCC | 11169 |
rs150624333 | snp | A/G/T | 0.492696 | 0.0600805 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007250 | AAAAAAAAAAAAAAA[A/G/T]AAAAGAAAAGAAAAA | 11169 |
rs150633245 | snp | A/T | 1.67332e-05 | 0.00289246 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54963011 | TTCCACCTGGGTTGC[A/T]GTCAATTCGGCTGCC | 11169 |
rs150716456 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994212 | CAATTTCTTTAATAG[A/G]TACAATACTATTCAG | 11169 |
rs150727503 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005543 | GTCCTCTTCAGATTT[A/C]TGATGTAGATGCCAA | 11169 |
rs150733391 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953673 | AAAACACATGCACAC[A/G]TATGTTTATTGTGGC | 11169 |
rs150775376 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946056 | ACAGAACAAATCAAA[A/T]CAAGTAAAAATCAAG | 11169 |
rs150781215 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009080 | GATTACAGGCATGAG[A/C]CACTACGCCTGTCCA | 11169 |
rs150872294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959837 | TTTCCATCTAGCCAA[C/T]AAAAATTGTTTTATT | 11169 |
rs150892007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949526 | CAAATCTACGTTTGT[A/T]TGGTGTACCTGAAAG | 11169 |
rs150897262 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016732 | TGATTTAAACCTACA[C/T]AGCTGCATGTGGCTA | 11169 |
rs150906260 | snp | A/G | 0.000724876 | 0.019024 | utr-variant-5-prime, synonymous-codon | WDHD1 | GRCh38.p7 | 14:55010371 | GTTTGCATTTGTAGT[A/G]AAGCGAGTCAATATA | 11169 |
rs150942989 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982304 | GTGAGCCACCGCGCC[C/T]GGCCGATAATAATTT | 11169 |
rs150980864 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960899 | CGAACTCCTGGGCTC[A/T]AGATATCCTCCTGTC | 11169 |
rs151005525 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018684 | ACAAATTCTTAAAAA[G/T]TATGACTCTCCCAGC | 11169 |
rs151021045 | in-del | -/A | 0.0599851 | 0.162463 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982507 | AGGTAAGCAATTCTT[-/A]ACCTCGTAAAACAGG | 11169 |
rs151033940 | snp | A/C | 0.0193772 | 0.0965046 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938860 | GGTAAAAATGGCTAA[A/C]GGCACTTTGAGGGAA | 11169 |
rs151064706 | snp | C/G | 0.0295035 | 0.117819 | upstream-variant-2KB, utr-variant-5-prime | WDHD1, SOCS4 | GRCh38.p7 | 14:55027184 | CGGCGCCCTCCGCGT[C/G]GAAATTAGCCGGTTG | 11169 |
rs151100503 | in-del | -/TTA | 0.0433465 | 0.140692 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973856 | ATACTGAGTAGGATT[-/TTA]TTAAGTTACTTTCTA | 11169 |
rs151150140 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949015 | TACGTCACCATCATC[A/T]AAGACCAAAGATAGA | 11169 |
rs151212707 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987770 | TAGCTGGGACTACAG[A/G]TGGGTGCCACTGCAC | 11169 |
rs151246195 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965684 | TTTTAGGCTGGGCAC[A/G]GTGGCTCATGCCTGT | 11169 |
rs151256239 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006862 | AATTTATAATCCAAA[C/T]TTTTAAAAAGTAATT | 11169 |
rs151309439 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947281 | AGGCAGAGGTTGCAG[C/T]GAGCCGAGATTGTGC | 11169 |
rs151312413 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010708 | TTTCTTTTACTTCTG[G/T]TAAGAAAAATGTTTG | 11169 |
rs180673596 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974904 | GCCAGCAAGTTTTGC[C/T]TTTTCTTCTGTGTTG | 11169 |
rs180685124 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993329 | CTCACTATGTTGCCC[A/C/T]GGCTGGTCTTGAACT | 11169 |
rs180690586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953682 | GCACACGTATGTTTA[C/T]TGTGGCACTATTCAC | 11169 |
rs180696051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968603 | AGGATAAACAAGATC[A/G]ATAAACTCCTAGCTA | 11169 |
rs180704148 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985625 | GGAGCATGATCTATA[C/T]TTTTAAAAGATCACC | 11169 |
rs180718514 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003775 | TATCATGTTGGCCAG[G/T]CTGGTCTCGAACTCC | 11169 |
rs180726624 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019734 | ATTAGCCAGCTGTTG[C/T]GGAGGGCATCTGTGA | 11169 |
rs180750268 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011473 | CGGTTGCAGTGAGCT[A/G]AGACTGCGCCATTGC | 11169 |
rs180768287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945412 | ATAACACTATGAGAT[G/T]GATACAGTTATTATC | 11169 |
rs180768662 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961322 | CACCCCATCTCTATT[A/T]AAAAAAATAAAATAA | 11169 |
rs181105348 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997483 | AAAGTGTTTCTAAAT[C/G]CATACATTGAAAAAT | 11169 |
rs181187067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016023 | TTCTTGGTGTATCAG[C/T]AGATGCACTGGAGGA | 11169 |
rs181199885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982534 | CAGGGAAGCATTCTT[A/G]TTTTCCACCTATTCT | 11169 |
rs181228706 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019705 | GAAACCTTGTCTCTA[C/T]TAAAAATACAAAAAT | 11169 |
rs181229493 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940931 | TCAAAAAAATCCAGG[A/C]TATACAAACAGACAA | 11169 |
rs181246781 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002571 | GCTTGCACCCAAAAA[A/C]TGGAGAACTTGTAAT | 11169 |
rs181250218 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958064 | TAAAAAGAAACAAAA[A/C]ACAAACCTTCTCTAC | 11169 |
rs181258239 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988215 | GGTGACTAGTACATT[C/T]TTTGGTTTGTTTTTC | 11169 |
rs181271634 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965909 | TGCAGTAAGCCAAGA[A/C]TGCACAACTGCACTT | 11169 |
rs181277257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024332 | CTACCTCTGAAATAC[A/G]CCCTTCTTCAAGTGT | 11169 |
rs181292579 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012192 | TTAATGTATGTTGGT[A/C]ATTTACATTTTTTCT | 11169 |
rs181307131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970560 | GATTAGAAGAATCAA[C/T]ATCATTAAAATGACC | 11169 |
rs181315102 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949752 | CAGAGAGAAAGGTTA[A/G]GTTACCCACAAAGGG | 11169 |
rs181323631 | snp | C/T | 0.00062152 | 0.0176174 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984910 | AAGGTTATCCAACTA[C/T]AACGCAGTCTAAATT | 11169 |
rs181368143 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949307 | TAGAGAACTCCTCAA[A/C]TGACCTGATGGAGCT | 11169 |
rs181368533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965448 | CAAAAGGCAGGCATA[C/T]CTAACAGCCCGATCA | 11169 |
rs181376696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979928 | ATCTTGCAGATTTTT[C/G]TATATCATTATATAG | 11169 |
rs181383315 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996848 | CCAGGCTGGAGTGCA[A/G]TGGCGTGATCTCGGC | 11169 |
rs181415766 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953264 | ATCTACAAAGAACTC[A/T]AACAAATTTACAAGA | 11169 |
rs181534075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968452 | TGCATCTAGGGAAAC[C/T]AGATAAACGAGAACA | 11169 |
rs181535828 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940407 | AGATAAGGAATATTC[A/T]TGGTTCATTTATGTC | 11169 |
rs181662781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015294 | CCAGAGGCTGAGGCA[C/T]GAGAATCATTTGAAC | 11169 |
rs181675677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956640 | GAGTGAGCCTCTGTC[C/T]CAAAAAAGACAGGGG | 11169 |
rs181842845 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953128 | AAATTGACAGATGGG[A/G]TCTAATTAAACTAAA | 11169 |
rs181844845 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967900 | TGTTGGGATTACAGG[C/T]GTGAGCTACCCTGCC | 11169 |
rs181850936 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984310 | GACCAGCCTGGGCAA[A/C]ATGGCAAAACCCTGT | 11169 |
rs181858723 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55001661 | CAATCAAGATGAAGA[A/C]AACTAGTAAGTGAAG | 11169 |
rs181936699 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025486 | CCCACAAGTGTGGAG[A/G]GGCAACCCGCCCCTA | 11169 |
rs181944708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007844 | AAATGCCAAGCCATC[G/T]TGGATTGCCTTGGGC | 11169 |
rs181964094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971109 | GATTAAACACTTAAA[C/T]GTAAGACCTCAGAAT | 11169 |
rs181967958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988617 | AGGATACATATCAAA[C/T]TGTAAATAGCAGTTA | 11169 |
rs182038921 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958411 | GGATTACAAGCATGA[A/G]CCACCACGCCCGGTC | 11169 |
rs182077682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976352 | TCAGCCTCCCGAGCA[A/G]CTGGGACTACAGGCA | 11169 |
rs182084789 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962227 | TTCTCAGCTGGGCTA[A/C]AATAGCATTAAAACA | 11169 |
rs182101636 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993873 | TAAATGACGATAGCC[A/G]TAACTCTGTATAAAT | 11169 |
rs182166544 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55014425 | TAAGAATGTAAGAAA[C/G]ATGGGTATATAATCT | 11169 |
rs182239534 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949105 | AGCACCTCTCCCCCC[A/C/G]CAAAGGAACGCAGCT | 11169 |
rs182255171 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979073 | ATTACAAAAATGCTA[C/T]AGAGTCACCTAAGCT | 11169 |
rs182311432 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012454 | CCTACATCTCATTCC[A/C]ATATTTGCGTTACAC | 11169 |
rs182324096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994723 | CCAAAATCACACCAC[C/T]GCACTCCAGCCTGGG | 11169 |
rs182359332 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946018 | TTAAGTAATCTTAAC[A/G]TAAACCGATTTCCAG | 11169 |
rs182378917 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947774 | CTTTTGTATTTTTAA[C/T]AGAGATGGGGTTTCA | 11169 |
rs182385470 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975629 | GCTGGGATTACAGGC[C/G]TGAGCCACTGCACCC | 11169 |
rs182394595 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011790 | TGATGAAAATAGATA[A/C]CCTACTTTTATAATG | 11169 |
rs182443894 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959349 | GCTGCAGTGAGCCAT[A/G]ATCACGCCACTGCAC | 11169 |
rs182455480 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972261 | GCCTGGGAGACAGAG[C/T]GAGACTCGGTCTCAC | 11169 |
rs182512361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964712 | TAAAGGCATTTGCCC[A/G]GGGGTCAGGAATGCT | 11169 |
rs182524280 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942847 | TACCTTAAAAATACT[C/G]ATTACATTTTTAAGT | 11169 |
rs182546248 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996558 | TGAGCCATGATCTCA[A/C]CACTGCACTCCAGCC | 11169 |
rs182579740 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962425 | AGAGTTAAGGTGTAT[C/T]TGCGTAGATGTGTCA | 11169 |
rs182587496 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976006 | AAATTCTGTGAAATG[C/G]GTACACTGTGGTTTT | 11169 |
rs182591376 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994459 | AAACAGCCATAATCT[C/T]AATAATATAGTGCAT | 11169 |
rs182643207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963401 | TCTCCATGGCTTAAA[C/T]GAATAAAGTAATGGT | 11169 |
rs182660054 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946884 | TCCATCTCTACCAAA[A/G]AATAACAAAATTAGT | 11169 |
rs182748107 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005702 | TTGTGAAAGTTTCCC[C/T]TTAAGTTACGATGGG | 11169 |
rs182758152 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021269 | CAGAACCCTTCTGCC[A/T]GATTGCCTAAAGTCA | 11169 |
rs182890124 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54950950 | TTCTTTGAAACCAAC[A/G]AGAACAAAGACACAG | 11169 |
rs182893261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966889 | TTTTTAAAAGCTAAC[C/T]TGTTTCTTATTTAGA | 11169 |
rs182907537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990265 | GCAAAATCCTCAGAA[G/T]GGAAAACATCATATA | 11169 |
rs182954344 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027850 | TCTCTATTCAGATCC[C/T]ACCTAAAGTTTACTG | 11169 |
rs182962698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022427 | TAATAAATGTTCTTT[A/G]TGGCATTTTTCCCCC | 11169 |
rs183074919 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954759 | TTTGAGACAGAGTTT[C/T]GCTTTTGTTGCCCAG | 11169 |
rs183095828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986097 | AAAAGTCATAGACAC[C/T]GAGATGTATTTAAAG | 11169 |
rs183143201 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016818 | AATTTTGTTCATTTT[C/T]CATTCCAAGTTTTCT | 11169 |
rs183157684 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026229 | AGTGCGTAAGAATGG[A/G]ACTTGGAAAGATAAA | 11169 |
rs183175197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983229 | GTGTCTTTCAAATCA[C/T]CTGTCATAAGCCTCT | 11169 |
rs183180465 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54999111 | AAGATGATTTTTCCA[A/G]TCTCCTGCCTGAAAT | 11169 |
rs183238152 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990908 | TCTATGTAACAATGA[C/T]CATGAAGAATAAGGT | 11169 |
rs183241805 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942152 | GCTACTTGGGAGGCT[A/G]AGGCAGGAGACTAGA | 11169 |
rs183242310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009352 | GCAATTCAACCAACT[A/G]TATTGTTTTCCTATG | 11169 |
rs183254006 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971649 | GAAAGTCGAGGCTGC[A/G]GTGAGCCATGATCTC | 11169 |
rs183292815 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969228 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGG | 11169 |
rs183300333 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985755 | GTATTAGCAGAAGAA[A/T]TGAAAAGAGACAAAT | 11169 |
rs183304149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004458 | TAGCAACCAATGTTT[A/G]TTTTCTTTTTTTGAG | 11169 |
rs183337620 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939358 | TTTAGATCATAGCAC[A/C]GTCCCCAGAGCTGCA | 11169 |
rs183344624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020048 | TCTTCTTGACTCTTA[A/G]TCATTGAGTCTCATG | 11169 |
rs183351892 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028767 | GATTTTGCATGTATG[A/G]TAAAAGCTTGAGCCT | 11169 |
rs183354174 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960326 | GTGCCTGTCACCATG[C/T]CCGGCTAATTTTTAT | 11169 |
rs183356256 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938908 | AGGCTATGTAATAAT[A/G]TCATCTGTTAAATTT | 11169 |
rs183361085 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009967 | CTGGGATTACAGGCA[A/C]CCGCCACCACACCCA | 11169 |
rs183361412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972786 | AAGACTCCATTCCAA[A/G]AAAGAGAGACAGAAA | 11169 |
rs183361651 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954680 | CTATCCATCCATTTA[G/T]GTATTTACTTTTTCT | 11169 |
rs183369768 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005083 | TTTCAATCTCCTCAG[A/G]AACACTGTAGAAGTA | 11169 |
rs183483233 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958591 | TGGTGGATACCTTTC[A/T]GTCACCTTGTTTGCT | 11169 |
rs183486182 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939754 | AACCCTTTTGTAAAT[C/T]CTTGTTATTAGGTTG | 11169 |
rs183500985 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989376 | ATAGTTTCTGACAGG[A/T]GTCATAATACCAGAG | 11169 |
rs183587061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008921 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 11169 |
rs183736620 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011639 | AATTTTGTTATATTC[A/G]TGTGTGTGTTTGTGT | 11169 |
rs183757851 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955144 | GACAAATATGTATTT[G/T]CACATAAATAGAATA | 11169 |
rs183761610 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969658 | CTGGTACCAGTCCTA[A/C]TGAAAATATTCCAAA | 11169 |
rs183786183 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964061 | TGCAGTGAGTTACAA[A/T]CTTGCCACTGTACTC | 11169 |
rs183803802 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995326 | GTCTCATTGACTTTC[C/T]CTATAGGTTTTCTGT | 11169 |
rs183886477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016200 | GTTTTGTCCTTTATT[A/G]TATCAAATAACTAAC | 11169 |
rs183959576 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982912 | GCTCACTCCTGTAAT[A/C]CCAGCACTTTGAGAG | 11169 |
rs183967414 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996433 | GACAACATGATGAAA[A/C]CTCATCTCCACAAAA | 11169 |
rs183968558 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013972 | CTACTTCTATATTTA[C/T]CACTTTTTCACAAAA | 11169 |
rs183968635 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948193 | TCACTAGGGCTTGTC[A/G]GACAGTGGGCGCAGA | 11169 |
rs183983994 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977373 | ATGTATGCAGATAAC[A/G]TGATTTGTAAATACA | 11169 |
rs184010293 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017664 | ATCAATGTTCTTACT[A/G]TATTAGGAAATCTGT | 11169 |
rs184013596 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55012597 | ACTGCTATAAGAATC[C/T]CACAGACTGGGTAAT | 11169 |
rs184014420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974420 | TCTGGGCAACAGAGA[C/G]AGATTCTGTCTCAAA | 11169 |
rs184031552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993170 | TTACCCTGCCTGGAG[C/T]CCACTGTTGCAATCA | 11169 |
rs184103524 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945181 | AAGCCCCTTTGCCAT[C/G]GCCTCACCCTTGCTC | 11169 |
rs184112140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999561 | TTTTGAGAAGCTGAA[A/G]TGAGTTTCTCATCAT | 11169 |
rs184113528 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960745 | TCCTGACCTCAAGTG[A/C]TCCACCTGCCTCGGC | 11169 |
rs184118501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966660 | CCTTAATATGAGGCA[A/C]GCGTTAAATATTTAT | 11169 |
rs184124878 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942964 | CAACAAATGAGAAAC[A/T]TAAAATTGTAAATGA | 11169 |
rs184129133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997940 | GGGGAGGCCAGGCAC[A/G]GTGGCCCATGTCTGT | 11169 |
rs184179873 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978192 | ACTATTAAGATAGAC[A/T]GTGAATTCTTTAATT | 11169 |
rs184188460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996101 | AATAAGATTTTATTC[C/T]TCAGAAGTCATTCCC | 11169 |
rs184248007 | snp | C/T | 3.33751e-05 | 0.0040849 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013627 | ACAAATTAAAGTCAT[C/T]GGGCATGGTGTCTCA | 11169 |
rs184261632 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948303 | ATTCCCTTTCCTAGC[C/G]AAGCAAAGCTGTGAC | 11169 |
rs184266855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964456 | CCATACTGGCTAACA[C/T]GGTGAAACACAGTCT | 11169 |
rs184427287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001738 | AACTGTAAATATCTA[C/T]GCATGTAAGAGACAG | 11169 |
rs184489819 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953131 | TTGACAGATGGGATC[C/T]AATTAAACTAAAGAG | 11169 |
rs184498248 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018617 | GAATGGAGATAAAAA[G/T]ACAGAACCTATAAAA | 11169 |
rs184505564 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968133 | AAGCAAGTCTCAAAA[A/T]TTTTTTTTAAATTGA | 11169 |
rs184513629 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948898 | CCAGGCAGAGTCTGG[A/G]GTGGGCCTCCAGCAA | 11169 |
rs184513993 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984312 | CCAGCCTGGGCAACA[G/T]GGCAAAACCCTGTCT | 11169 |
rs184535123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978987 | ACTTTTTTTTCTTTT[C/T]TCATTCCTTTCATTG | 11169 |
rs184549747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023506 | TTCAACTTTTCTCTC[C/T]TAATGTCATGACTTT | 11169 |
rs184571165 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006299 | TTTACTTCTCTTGGT[A/G]GCATGTTAAAAGTTT | 11169 |
rs184644775 | snp | G/T | 0.0566069 | 0.158427 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955896 | GATTCCATGTTTTCC[G/T]TTTTTTTTTTTTTTT | 11169 |
rs184658439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987571 | AACTATATTGATATC[C/T]TTCCAGCCTTTTTTC | 11169 |
rs184662130 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964593 | GCAGTGAGCAGAGAT[C/G]GCGCCACTGCACTCC | 11169 |
rs184673712 | snp | A/G | 0.000362605 | 0.01346 | missense | WDHD1 | GRCh38.p7 | 14:54967351 | TAGCAACAGCAGGGC[A/G]TGGAAGGGTTGGGGG | 11169 |
rs184711972 | snp | A/C/G | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011328 | TGAGGTCAGGAGTTC[A/C/G]AGACCAGCCTAGCCA | 11169 |
rs184779577 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956661 | AAGACAGGGGGAGCA[C/G]GATAGTGATCTTGGA | 11169 |
rs184796275 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988198 | AGTAGAAAAAGCAAA[C/T]GGGTGACTAGTACAT | 11169 |
rs184813492 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952292 | AGGGAACTTCAGCAA[A/T]GTCTCAGGATACAAA | 11169 |
rs184821344 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983615 | AAGGCAGAGGTTGCA[A/G]TAAGCTGAGATCGCA | 11169 |
rs184831313 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023968 | ATATTTTATGGTAGT[A/T]AATGATAAAATACGC | 11169 |
rs184887484 | snp | G/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940492 | GTCAGCTGATTTTAT[G/T]TGATTGTTTCCTTCC | 11169 |
rs184904578 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54970273 | TTACTCTATACATAG[A/T]ATTGCTAAAGGGCTC | 11169 |
rs184922809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007024 | CTGAGCTCAGGAGTT[C/T]GAGACCAGCCTGGGC | 11169 |
rs185226830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016153 | CAATCTTCTAAAGAG[C/T]TTTTAGAGTAGTCTG | 11169 |
rs185268339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994548 | TACATTCTTTTTTTC[A/G]TATTGTCTTCAAAAT | 11169 |
rs185272086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019712 | TGTCTCTACTAAAAA[C/T]ACAAAAATTAGCCAG | 11169 |
rs185279331 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010625 | TGGAATGTGCATTAG[C/T]AAGAAAAATTTGCTA | 11169 |
rs185319770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944176 | TATGTTGCCCAGGCT[A/G]GTCACGAACTCCTGA | 11169 |
rs185339345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946951 | AGGAGGCTGAGGCAT[A/G]AGAATTGCTTGAACC | 11169 |
rs185340483 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973230 | TAGTATAGCCTTTTA[A/G]TCAGGACATTCTTGA | 11169 |
rs185354384 | snp | A/G | 6.62449e-05 | 0.00575483 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962449 | TGTGTCACTTTGCAG[A/G]TGACTTGCAAAATTT | 11169 |
rs185358233 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012367 | TAAAAGTCATCACAA[A/C]TAAAAAGCTTAGGGG | 11169 |
rs185358477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976213 | CATTAAAAATGCAAA[C/T]AAATATGAAGATGAA | 11169 |
rs185413518 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970577 | TCATTAAAATGACCA[C/T]ACTGTGTCTGCAGCA | 11169 |
rs185414184 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965096 | ACTTTTCTCTAAGAA[C/T]CTTTTTTCTCCAATT | 11169 |
rs185431668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996700 | CATAAAAACTACAAA[C/T]GTTAAGCCAATGGAA | 11169 |
rs185455787 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960433 | TCAGCCTCCCAAAGT[A/G]CTGGGATTACAGGTG | 11169 |
rs185469927 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992172 | CTGAGACAGGAGAAT[C/T]GCTTGAACCCGGGAG | 11169 |
rs185478380 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940083 | CATTATCAGAATAGT[A/G]ACTAACATTTATATA | 11169 |
rs185495332 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940979 | AATTTCCGAAACACA[A/G]AAGAAAAAGTCTCAC | 11169 |
rs185496349 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958257 | TCAGCCTCCCGAATT[G/T]CTGGGATTACAGGCG | 11169 |
rs185498617 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949368 | ATGCACAAGCCTCAG[G/T]AGCCAATTCAATCAA | 11169 |
rs185504317 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965571 | GTTACCTTGAGAGCC[A/C/T]GTTAAAACATAGACT | 11169 |
rs185505761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014550 | ATTAATAAATGAATA[C/G]ATGTATGAGCTCAAC | 11169 |
rs185519480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980407 | ATTTCTGAACATTTT[C/T]ATCACCCCAAAAAGA | 11169 |
rs185551896 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979134 | CTTTAGGTGCCACCC[A/C]AAATCTTTGCTCCTC | 11169 |
rs185570370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984174 | TATATTTCCTTCTTT[A/G]TAAGTTTTCTAATGA | 11169 |
rs185618104 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017697 | AACACAAAAGTACTT[C/G]AATTTGGAATTACAA | 11169 |
rs185698127 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967727 | CCAAGTTCAAGCAAT[C/T]CTCCCACCTCAGCCT | 11169 |
rs185806710 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015489 | TAACACACATAACAC[A/T]TGGTTAAATCTGTAA | 11169 |
rs185820831 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997043 | GATCCACCCGCCTCA[C/G]ACTCCCAAAGTGCTG | 11169 |
rs185879996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019817 | GAGGTTACAGTGAGC[C/T]GAGATCGTGCCACTG | 11169 |
rs185913972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985645 | AAAAGATCACCTAGG[C/T]TGCTCTGTGGAGAAT | 11169 |
rs186049628 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003884 | CTGTATATTTTTTAT[G/T]TACACTGTCTGCTCA | 11169 |
rs186066453 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949783 | AAGCCCATCAGACTA[A/C]CAGCTGATCTCTCGG | 11169 |
rs186072000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007655 | CACAAAACCCCAATA[C/T]GTGAAATTCTTAGAA | 11169 |
rs186075856 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982582 | TCTGTGGCAAATTAC[C/T]TGATTATCCCTTTTC | 11169 |
rs186139251 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020850 | ATGTATTATATACTG[C/T]ATCTGTACAATACAG | 11169 |
rs186197841 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966316 | CTCCAGCCTGGGTGA[C/T]AGAACGAGACTCCGT | 11169 |
rs186204995 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949165 | GAGAATGACTTTGAC[A/G]AGTTGAGAGAAGAAG | 11169 |
rs186217731 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997617 | TTGGATTTTCTAATT[A/T]AAAAAAATGGGGAGG | 11169 |
rs186218071 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54968530 | CAGAACTAAACAAAA[C/T]TGAGACTAAAGAATC | 11169 |
rs186235778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004560 | TGGGTTCAAGCAATT[C/T]TTATGCCTGAGACTC | 11169 |
rs186239055 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003584 | AAAAGAAAGAAAAAC[A/G]AACTATATATATATA | 11169 |
rs186256934 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024501 | GTTTACTCTTTTCTA[C/G]ACACCCATGTTTACT | 11169 |
rs186286670 | snp | A/C/T | 4.94458e-05 | 0.00497197 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008643 | CAAAGGAAAGACTTA[A/C/T]AACAGGGGCATCATG | 11169 |
rs186338224 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971149 | CCAGAAGAAACCCTA[A/G]CAAATACCCTTCAGG | 11169 |
rs186346966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988827 | TGCTATGTAGTTAGA[A/G]CATGTAATGAGGGAA | 11169 |
rs186350725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025803 | ACCATGATCCCTGGC[C/T]CCATTGGGCCTTTAC | 11169 |
rs186361850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953305 | CCCAATCAAAAAGTG[A/G]GCGAAGGATATGAGC | 11169 |
rs186388236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985466 | AGTATGGCCAGAACA[A/T]GGTAATGAGAAACAA | 11169 |
rs186456128 | snp | A/T | 0.00159617 | 0.0282053 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938550 | AAGACACACAGGAGT[A/T]TGAGACCAGCCTGGG | 11169 |
rs186463301 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974931 | GTTGGACCGGACTGT[C/T]TTCTGCATTTGAGGG | 11169 |
rs186469249 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993331 | CACTATGTTGCCCTG[A/G]CTGGTCTTGAACTCC | 11169 |
rs186470786 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953896 | CAAACACCGCATGTT[C/T]TCACTCATAGGTGAG | 11169 |
rs186472192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969052 | TTATTTATTTATTTA[C/T]TTTTGAGACGGAGTC | 11169 |
rs186579992 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012532 | CATTCCCGTTTTCTA[A/G]AACAATTCCTTAAGT | 11169 |
rs186596570 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942329 | CAGTTTCACATGCAG[C/T]TGTATGAAATAATAC | 11169 |
rs186630841 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939903 | GTATTATAAAATATA[A/T]ACAAAGCAAGTTGAG | 11169 |
rs186632368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955153 | GTATTTGCACATAAA[C/T]AGAATAATTTTGGAA | 11169 |
rs186635441 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995005 | TTTTCTTTGGAGATG[A/G]AGTCTTGCTCTGTTG | 11169 |
rs186642591 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969716 | TAAAGCCAGCATTAT[C/T]CTGATACCAAAATCT | 11169 |
rs186646726 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986882 | GCTGAAAGTTCTCTG[A/G]TCGTGCTTGCCAAAA | 11169 |
rs186667793 | snp | A/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026300 | ATCAGAGGAAAAAAT[A/T]GTTTTAAGCCGTCAA | 11169 |
rs186691102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009525 | CAACCTCTGTCTCCC[A/G]GGTTCAAGCAATTCT | 11169 |
rs186707056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958750 | AATAGTTGGTTCCTC[A/C]TCTTCCTCTACCTGA | 11169 |
rs186723298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989959 | GTGAGCCATCACGCC[C/T]GGCAGAGGCAACATA | 11169 |
rs186761742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942935 | CTTATTTATTTAGAC[A/G]CCATTTTATTGAACA | 11169 |
rs186766114 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54959756 | TCTGCTCCAGTCTGA[A/G]TGACAAAGCAAGATA | 11169 |
rs186773794 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972316 | AGATATGGTGGCTCA[G/T]GTCTGTAATCCCAGC | 11169 |
rs186784981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990362 | CAGCACTTTGGGAGG[C/T]CTAGGCAGGCGGATC | 11169 |
rs186886826 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008922 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 11169 |
rs186892529 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975813 | TGGTATTCAGGTGTG[C/T]ACCGATGTGACACGC | 11169 |
rs186929294 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972216 | GGAGGCGGAGCTTGC[A/G]GTGAGCCGAGATCAC | 11169 |
rs186949609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011894 | GTTTCCGACATTTGC[C/T]ATTGTTATGAATTGT | 11169 |
rs186981342 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946390 | TATCAACATCTGTGA[A/C/T]AAAATATTAGTTTCA | 11169 |
rs187008685 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978802 | CTGTCTCCAGAAATA[A/G]CTGAATTCTGCTTCA | 11169 |
rs187020111 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996374 | GCACTTTGGGAAGCC[A/G]AAGCAGGTGGATGCC | 11169 |
rs187029363 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013667 | TGCTAGCACTTTGGG[A/C]GTACAAGGTGGGAGG | 11169 |
rs187068170 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962254 | AACAGAGATCAACCA[C/T]ACATGTCTGTTTGAC | 11169 |
rs187095161 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994185 | CTATTTGAAGATTTT[A/C/T]AATTACAATCTCAAT | 11169 |
rs187198680 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962037 | AGATGGGGTTTCACC[A/G]TGTTGGCCAGGCTAG | 11169 |
rs187252114 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958418 | AAGCATGAGCCACCA[C/T]GCCCGGTCATCCAGC | 11169 |
rs187410135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945489 | CTATCCCAGGTTACA[C/T]AAACAGTAAAACTCA | 11169 |
rs187492118 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951471 | TCAATCTCTGAATAG[A/C]CCAATAACAGGCTCT | 11169 |
rs187501700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966984 | CCAGGTGTTATGGCA[C/T]AAAATGTATGGAGGC | 11169 |
rs187503565 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983522 | TATTAAAAATACAAA[A/T]ATTAGCCGAGTGTGG | 11169 |
rs187514993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017256 | AGAGTAGTCTAAACA[C/T]TCTTCTAAATGGTTT | 11169 |
rs187560938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991667 | CACTTGCAGTAAAAA[C/T]ATTAATTTTATTAAA | 11169 |
rs187569573 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963655 | TAAAAACACAATTAG[C/G]CAGGCGTGGTGGCGT | 11169 |
rs187585280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023049 | CATGCTCTGACCTCA[A/G]GTGATCCACCCACCT | 11169 |
rs187599190 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028986 | AAAGGGGTGCTTTGG[A/G]TGGGTATTTAGTGTT | 11169 |
rs187604531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010225 | AAAAAATTAAGTCAC[A/G]GTCCTGAAAACACTA | 11169 |
rs187608630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017681 | ATTAGGAAATCTGTG[A/G]AACACAAAAGTACTT | 11169 |
rs187618352 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954701 | TACTTTTTCTGATAG[C/G]CTTGCTATAGTATAA | 11169 |
rs187626536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948200 | GGCTTGTCGGACAGT[A/G]GGCGCAGAACAGGGG | 11169 |
rs187627468 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985791 | ATGTGTTATTCCATA[G/T]AATTGACATGATGAT | 11169 |
rs187650417 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983926 | ACATGTAATCAACAT[A/T]AAAAAATTGATTTTT | 11169 |
rs187722091 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952677 | CAAAAAAGAGCCCGC[A/G]TTGCCAAGTCACTCA | 11169 |
rs187773556 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005729 | TGGGAATCCAGAACA[A/T]CATCATAAGGATCCT | 11169 |
rs187778753 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950627 | TCCAGGAATTGAACT[C/T]AGCTCTGCACCAAGC | 11169 |
rs187792504 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969318 | GGCGTGAGCCACCGC[A/G]CCCAGCATTAAGACT | 11169 |
rs187794970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966742 | AAGTTTATTTTACAA[C/T]TTAAATTCTAGTGTG | 11169 |
rs187808029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005231 | TCCACATAGCACAGA[A/G]GAAAATCTGTGTGAC | 11169 |
rs187818976 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947881 | ACAGGCGTGAGCCAC[G/T]GTGCCAGGCCAAAAT | 11169 |
rs187841815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976607 | TCCATGTACCGCTAT[C/G]CACAGAAAGGAAATG | 11169 |
rs187874233 | snp | A/C | 0.00597247 | 0.0543191 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939474 | AATTAAGTATATGTC[A/C]ATTTTCTATAGTATA | 11169 |
rs187899728 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028174 | TTTTTCAATCTAGTT[C/G]CATTGTGAAAAGTTG | 11169 |
rs187917067 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967475 | AAAGTTTTCAAAAGT[C/T]AGTAACTTAGAATAG | 11169 |
rs187940695 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000269 | TAGTATTTAATGAAA[A/G]GTATTCCTTGGAAAG | 11169 |
rs188082348 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986589 | ACTCCAGCTAAAAGA[C/T]AGAGCCAACAAAAAA | 11169 |
rs188130060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022177 | TTACTAGCAAGATAC[C/T]TTCTGACTTCAGGCA | 11169 |
rs188135338 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025211 | CACAGCGCTTAATCC[C/T]TTACATTGTCTATGA | 11169 |
rs188161396 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954872 | TTTGCTGGGATTACA[G/T]GCATGTGCCACCAAG | 11169 |
rs188201643 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958370 | GACCTCAGGTGATCC[A/G]TCTGCCTTGGCCTCC | 11169 |
rs188214788 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971017 | CTCAATAAATGGTGC[G/T]GAGATAACTGGCTAA | 11169 |
rs188222027 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988445 | TAAGAAAACATTTTC[A/G]GGTGATAAAGAACAT | 11169 |
rs188232173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007726 | TTAAAGTGTCAAAGT[C/T]GCTTCTTTTAAATAG | 11169 |
rs188258568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014046 | CTTTAAAAATAAAGT[A/G]CTAATTTCCTTCTAT | 11169 |
rs188288978 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011395 | AAATTAGCCAGGCAT[G/T]GTGGTGGGCAGCCAG | 11169 |
rs188341640 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945232 | CATTAGGTGAAGCAC[A/C/G]GACACAGCACATTTG | 11169 |
rs188359253 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960785 | TGCTGGAATTACAGG[C/T]GTGAGCCACCACGCC | 11169 |
rs188365279 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974825 | ATGAGACTCTGTCTC[A/G]AAAAAATAAATAAAA | 11169 |
rs188372430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993232 | AAGAGATCCTCCTAC[C/T]TCAGCCTCCCAAGTA | 11169 |
rs188408156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013136 | GAGGCTGAACTGGGA[A/G]GACTGCTTGAGCCCA | 11169 |
rs188425661 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54977382 | GATAACGTGATTTGT[A/T]AATACAATTTTATAT | 11169 |
rs188496740 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948741 | CACAAGTAGCCTAAC[A/T]GGGAGGCACCCCCCA | 11169 |
rs188499070 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54964465 | CTAACACGGTGAAAC[A/C]CAGTCTCTATTAAAA | 11169 |
rs188581292 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943977 | ACAAAAAACCCATCA[C/T]CATTACATAATAATT | 11169 |
rs188589942 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998083 | CAGGGCGTGGTGGTG[A/G]GTGCCTGTTATCCTA | 11169 |
rs188598026 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972974 | TAAGGCATTCAAACA[A/C]GCCCATCATGAGTAG | 11169 |
rs188767273 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939143 | TGTAGGTTTGAGAGA[A/T]TCAAGATGAAAACTT | 11169 |
rs188799159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964184 | GGGTCTCCTAATTCA[C/T]AGTGTATTAGAACTA | 11169 |
rs188858647 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968405 | AAACACCTATATCAA[A/G]TTAGAAAGATCTCAA | 11169 |
rs188861738 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982957 | ATCACCTGATGCCAG[A/G]AGTTCAAAACCAGCC | 11169 |
rs188866129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960358 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT | 11169 |
rs188873882 | snp | A/C | 1.65389e-05 | 0.00287562 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002069 | CCTTATAGCCCACTG[A/C]AAGTGTCACTTTGTA | 11169 |
rs188897107 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018825 | CTTTGGGAGGCGAGA[C/T]CAGCCTGACCAACAA | 11169 |
rs188933221 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016292 | ACAACCCTTTCAGTG[C/G]TAATGAGCTAAAAAA | 11169 |
rs188944988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023793 | GAGGTGGCTATGAAA[C/T]TATTACAGTAATACA | 11169 |
rs189002404 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54970034 | CCAACATACTAGGCA[C/T]TGAAGGAACATAACT | 11169 |
rs189005603 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949226 | AGGAGGAAGTTCGAA[C/T]GCATCGCAAAGGAGC | 11169 |
rs189011795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987578 | TTGATATCTTTCCAG[C/T]CTTTTTTCTTTGCAC | 11169 |
rs189020250 | snp | A/G/T | 0.00954631 | 0.0685079 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006617 | CCTTTCAAATTTCTC[A/G/T]TATCTTTCTGTTGTC | 11169 |
rs189021939 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965315 | GGGACACAAGCACAG[C/G]AACTTTAAGACACCC | 11169 |
rs189059621 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54944815 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCTCAAA | 11169 |
rs189077459 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964626 | CCTGGGCAACAGAGC[A/G]AGACTTCGTTTCAAA | 11169 |
rs189094557 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996453 | TCTCCACAAAAAATT[A/T]GCCAGGCATGGTGGC | 11169 |
rs189163969 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953123 | AGCCAAAATTGACAG[A/T]TGGGATCTAATTAAA | 11169 |
rs189164215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967748 | ACCTCAGCCTCCCAA[A/G]TAGCTGGGACTACAG | 11169 |
rs189177221 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984233 | GGTGCAGTGGCTCGC[A/G]CCTGTAATCCCAGCA | 11169 |
rs189249959 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019727 | TACAAAAATTAGCCA[A/G]CTGTTGCGGAGGGCA | 11169 |
rs189365252 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979068 | AAAAGATTACAAAAA[C/T]GCTATAGAGTCACCT | 11169 |
rs189420441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970460 | ATCTAACCAAGGAGG[C/T]GAAAGATCTCTACAA | 11169 |
rs189455335 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948981 | AACAAAAAGGACATC[C/T]ATACCAAAACCCCAT | 11169 |
rs189468315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003768 | GGGGTCTTATCATGT[G/T]GGCCAGGCTGGTCTC | 11169 |
rs189586656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011698 | ACAAACATAAGATTA[C/T]ACTATATTAACTGTT | 11169 |
rs189692878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957420 | AAAACCATAGGTACT[C/T]AGAAGGTAAGTAGAA | 11169 |
rs189718590 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947722 | TCAGCCTCCCAAGTA[A/G]CTGGGATTACAGGCA | 11169 |
rs189734155 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976233 | ATGAAGATGAATTTC[C/T]TTATTTCCTTTTTAT | 11169 |
rs189739543 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994710 | AGGTTGCAGTGAGCC[A/C]AAATCACACCACCGC | 11169 |
rs189755987 | snp | A/C | 0.00597247 | 0.0543191 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941152 | GAACCAAACCCCTAG[A/C]AGGTATTAATGCACA | 11169 |
rs189757282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007028 | GCTCAGGAGTTCGAG[A/G]CCAGCCTGGGCAACA | 11169 |
rs189775826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012416 | CCAAAGTCCTTCTGA[A/G]TAAGTCTTCTTTCTC | 11169 |
rs189897678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992753 | GATTCCATCTCTACA[A/G]AAAATAAAAAATTAG | 11169 |
rs189969534 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024274 | CTCAAAGAAATCCTA[A/C]AATAATCACATCCAA | 11169 |
rs189976628 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960586 | CTTACTGCAACTCCC[C/T]ACTCCTGGATTCAAG | 11169 |
rs189998270 | snp | A/C/G | 0.00676609 | 0.0577691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988199 | GTAGAAAAAGCAAAC[A/C/G]GGTGACTAGTACATT | 11169 |
rs190049286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956366 | GGATAGGCTGGGTGC[A/G]GTGGCTCATGCCTGT | 11169 |
rs190078568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015057 | CCCTTCTATAGAGAG[C/T]AGATAGGAGGACTAT | 11169 |
rs190082256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979757 | CAGAGAAAAGTCTCC[C/T]ATACTATCCACTGAG | 11169 |
rs190153810 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953263 | AATCTACAAAGAACT[C/T]AAACAAATTTACAAG | 11169 |
rs190214767 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015629 | ATTCAGATGTAAGAC[A/C]CTAGGGATAGCTACT | 11169 |
rs190224368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011065 | ATTTCAGACTTCTTG[C/T]CTTCTGAACTGTGAG | 11169 |
rs190227848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945512 | AAAACTCAGACCTGG[G/T]ATCCAACAACCAGGC | 11169 |
rs190238632 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974045 | GGTTTTGATGACGAC[A/G]GAGTTTCCTGGAAAC | 11169 |
rs190240901 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996815 | TATTTTTTGACAGAG[A/T]GGAGTCTCGCTCTGT | 11169 |
rs190255994 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949381 | AGTAGCCAATTCAAT[A/C]AACTGGAAGAAAGGG | 11169 |
rs190269160 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965681 | TTATTTTAGGCTGGG[C/T]ACGGTGGCTCATGCC | 11169 |
rs190273219 | snp | A/G | 0.000399281 | 0.0141238 | missense | WDHD1 | GRCh38.p7 | 14:54981643 | TCCACGTATTACCAA[A/G]TCCTCTGTTAAGCAT | 11169 |
rs190283849 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997287 | TTTCAGTAGAGACGG[A/G]GTTTCCCCATGTTGG | 11169 |
rs190381078 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940317 | GTGCTCATAACCACT[A/G]TGCTATAATGTCTCT | 11169 |
rs190422790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946398 | TCTGTGACAAAATAT[C/T]AGTTTCAATAGTGGT | 11169 |
rs190426224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962265 | ACCACACATGTCTGT[C/T]TGACTTCTGTATCCA | 11169 |
rs190463137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020968 | GTCTTCATCCTTATC[A/G]TCTTCACAGTGAGAA | 11169 |
rs190503712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985856 | GGAAAGAGAAGAATC[A/G]AGGATAATTTTTAGA | 11169 |
rs190511707 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004678 | GGCTGGTCTTGAACT[C/G]GTGGCCTCAACTGAT | 11169 |
rs190539557 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001095 | TTTTTTTTCAAGAAT[G/T]TGGAGGGGAATCAAC | 11169 |
rs190542010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975062 | TATAGCACATCTAGT[C/T]GGTACTATAATAAAT | 11169 |
rs190643528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997772 | AAAAATTAGCCAGGC[A/G]TGGGGGCACAAGCCT | 11169 |
rs190656298 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966833 | TTTAAAACAGTTTCC[C/T]AGCTATCATAATTAA | 11169 |
rs190666352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983161 | AGAGTGAGACTCTGC[A/G]TCAAAAAAACCACAA | 11169 |
rs190676995 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998220 | AAAGAAAAAAAAAAA[A/T]TTTTAATGGAGGACT | 11169 |
rs190700919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025834 | ACACAGTATTGCCTC[C/T]GCTTACTATGCCAAC | 11169 |
rs190711008 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008885 | AACTGCAACCTCCGC[A/C]TCCCAGGTTCAAGCG | 11169 |
rs190720844 | snp | C/T | 0.0003911 | 0.0139784 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966427 | AAGAAATTCAACCTA[C/T]AGAAAAGCATTTAAC | 11169 |
rs190786708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985616 | TTGAGAAGAGGAGCA[C/T]GATCTATATTTTTAA | 11169 |
rs190790016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962197 | TGATACCCAGATCTG[C/T]CTTCAACATCTGTCT | 11169 |
rs190802958 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993868 | ATATGTAAATGACGA[C/T]AGCCGTAACTCTGTA | 11169 |
rs190868404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016159 | TCTAAAGAGCTTTTA[G/T]AGTAGTCTGAATGTT | 11169 |
rs190888142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982648 | CATTAGTTTCCGCAG[C/G]GTCTGGATCTAATTG | 11169 |
rs190967494 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54950202 | ACACAGAATGGCAAA[C/T]TGGATAAAGAGTCAA | 11169 |
rs191092851 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028554 | TATGTTGAATAAAGC[A/G]TGGTGAGATTTCTGG | 11169 |
rs191102711 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009859 | AGAGTCTCACTCTGT[C/T]GCCTAGGCTGGAATG | 11169 |
rs191126643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968587 | AAATTGATTTTTTGA[A/G]AGGATAAACAAGATC | 11169 |
rs191144859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959888 | TTTATAAAAGTTTCC[C/T]CTTTTGTCTCTCCTG | 11169 |
rs191150720 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972767 | CCAGCCTGGGCAACA[C/T]AGCAAGACTCCATTC | 11169 |
rs191158975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990838 | AATATATTATACTAG[C/T]AGTTGCCTTCTAAGA | 11169 |
rs191196702 | snp | C/T | | | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938835 | ATTCTCGATTGGATC[C/T]TAAACTGGGGGTAAA | 11169 |
rs191198312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954675 | TCTATCTATCCATCC[A/G]TTTATGTATTTACTT | 11169 |
rs191202748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969139 | CGCCTTCCAGGTTCA[C/T]GCAATTCTCCTGCCT | 11169 |
rs191209945 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985736 | AAGAGATGACATCCA[A/G]GTTGTATTAGCAGAA | 11169 |
rs191220051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004210 | TCCACTTCCTGGTAT[C/T]CATATCCTTGTGCTA | 11169 |
rs191227145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942936 | TTATTTATTTAGACG[C/T]CATTTTATTGAACAA | 11169 |
rs191295818 | snp | G/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939620 | TGGAAAAAAACAGGT[G/T]TACTATTATATAGCA | 11169 |
rs191367502 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972253 | GCACTCCAGCCTGGG[A/T]GACAGAGTGAGACTC | 11169 |
rs191377852 | snp | A/C | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009332 | ATACCTTTCACTTCA[A/C]CTCAGCAATTCAACC | 11169 |
rs191473406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964514 | TGTGGTGGCAGACAA[C/T]TGTAGTCCCAGCTAC | 11169 |
rs191512058 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939284 | AAAGGGACTACCTGG[C/T]ATCTGTTCCATGTTA | 11169 |
rs191526956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994208 | ATCTCAATTTCTTTA[A/G]TAGATACAATACTAT | 11169 |
rs191603285 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958825 | TTTGCTTTACATTCT[C/T]CCCCAATGCTTGCTT | 11169 |
rs191609912 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026398 | ACAGAACAGGCCACT[A/G]AATTTGACAAGTAGG | 11169 |
rs191623139 | snp | A/G | 0.00083647 | 0.0204337 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990083 | TTATTTAACATAACT[A/G]TAAATAAAATATTGA | 11169 |
rs191633300 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016558 | TTCTACTCCTGCAGA[A/T]GGTGATTTATATCTT | 11169 |
rs191675153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012141 | CCAATTTTAAAATTT[C/G]CATTTCTTTGCTTAC | 11169 |
rs191685469 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958566 | TCAGTGATCTCTACA[A/T]TGTCAAATCTGGTGG | 11169 |
rs191713415 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013961 | TTTTTGGAATGCTAC[C/T]TCTATATTTACCACT | 11169 |
rs191742990 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54978981 | GCTACTACTTTTTTT[C/T]CTTTTTTCATTCCTT | 11169 |
rs191754087 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996377 | CTTTGGGAAGCCGAA[A/G]CAGGTGGATGCCTTG | 11169 |
rs191776735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975878 | AATGTACTTTCTTTT[A/G]AAGGATCTCTGAACA | 11169 |
rs191866209 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967132 | GGCCTGGTGATCCCA[A/G]GCAGTCCTCTTCCCT | 11169 |
rs191870077 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944898 | CAGGCATAAGCCACC[A/G]TGCCTGGCCTCATAT | 11169 |
rs191871918 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54983541 | AGCCGAGTGTGGTGA[C/T]GCAAGCCTGTAATCC | 11169 |
rs191873685 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960676 | GGCTAATTTTTTTTT[G/T]TGTATTTTTAGTGGA | 11169 |
rs191882543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971310 | GGTCAGGTGCAATGG[C/T]TCACATCTGTAATCC | 11169 |
rs191892824 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006807 | AGTTCAAATGTTTCT[G/T]AAAGCATTTCAATAC | 11169 |
rs191923150 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017455 | TCAAGTGATTCTCCT[A/G]CCTCAGCCTCCCAAG | 11169 |
rs191963600 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023896 | ACTGCGGATGGTCTG[G/T]AAATGTTTGAGTGTG | 11169 |
rs191971448 | snp | A/G | 0.000844965 | 0.020537 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941699 | CCCACACCTTTGTAA[A/G]ATGGCAGGAGTGAAA | 11169 |
rs192012535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948247 | GTGAGCTGAAGCAGG[A/G]CAAGGCATCACCTCA | 11169 |
rs192030185 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964373 | AAGCCGGGCGCAGTG[C/G]CTCACACCTGTAATC | 11169 |
rs192036911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977518 | GCCTAGGGAACATAG[C/T]GAGACTGTGTCTCAA | 11169 |
rs192119672 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012574 | GTAGGTGTTTTAGTC[G/T]GTTCTGTACTGCTAT | 11169 |
rs192210429 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967479 | TTTTCAAAAGTTAGT[A/C]ACTTAGAATAGTAAT | 11169 |
rs192223340 | snp | C/T | 0.00255897 | 0.0356783 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000452 | TGTCTTCCAAATCCA[C/T]ATGATCACAGAAACA | 11169 |
rs192350902 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954972 | ATCCTCAGATGATCC[A/G]CCTGCTTCGGCTTCC | 11169 |
rs192364663 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986598 | AAAAGATAGAGCCAA[C/T]AAAAAAGTAAAAAGG | 11169 |
rs192407809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018370 | CATGAAAAGCTGAAA[C/T]GGTGAATGATTTCAT | 11169 |
rs192409125 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995277 | TGAGCCACCGTGCCC[A/G]GCCTTATTGATCTTG | 11169 |
rs192513823 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020026 | TTCCTTCCCTAATCT[C/G]ACCACCTCTTCTTGA | 11169 |
rs192599525 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952852 | TGATCTTTGACAAAC[A/C]TGACAAAAACAAGAA | 11169 |
rs192608328 | snp | A/C/G | 1.65853e-05 | 0.00287964 | missense | WDHD1 | GRCh38.p7 | 14:54955598 | GAGGACATATAGCTG[A/C/G]GGTTTCAGATAATAC | 11169 |
rs192620846 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969740 | AAAATCTGGCAAAGA[C/G]ACATCAAAAAGAGAA | 11169 |
rs192621686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017691 | CTGTGAAACACAAAA[A/G]TACTTGAATTTGGAA | 11169 |
rs192623574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984015 | CTCAGCCATATTTCA[A/G]GTGCTCAACAGACAC | 11169 |
rs192631096 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987012 | AGTGAACACAACAAA[A/G]TTATCTACATTTAAA | 11169 |
rs192636443 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005791 | TTTAGAATCAGCTCA[A/G]TTTGGTCCTCCTAGA | 11169 |
rs192659588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022202 | CAGGCACAAAGCATC[A/G]GTGAAACCAATCCAG | 11169 |
rs192660490 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55023232 | AGTTGTCAGATAATG[A/G]CTTCACTTTTTCTGG | 11169 |
rs192701189 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54939978 | ACTATAAATAAACCT[G/T]TACTTAAGATCTTGA | 11169 |
rs192724921 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969492 | AAATTCCTGGAAACA[G/T]AAAACTTCCCAAGAC | 11169 |
rs192735700 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948871 | CTGTTCTGCAGCCTC[C/T]GCTGCTGATACCCAG | 11169 |
rs192768003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974081 | GCATAAACCACCTGG[A/G]AGAGGAATTTAAAAA | 11169 |
rs192782391 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011300 | TTTGGGAGGCCAAGG[C/T]GGGTGGATCACGTGA | 11169 |
rs192798487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952247 | TTTAGAAAACCCCGT[C/T]GTCTCAGCCCAAAAT | 11169 |
rs192847239 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995980 | GAATTGTATTTATAT[C/T]TACACAATAAGACCC | 11169 |
rs192852201 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970216 | CAATCAAGTAAGATA[A/C]CAAAATAGGAAAAGA | 11169 |
rs192889242 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005359 | GGCTGCCTGGATCTG[C/G]TTAATGAAAGTTCCA | 11169 |
rs192923696 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960403 | TCAATCTCCTGACCT[C/G/T]GTGATCCACCCTCCT | 11169 |
rs192979579 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992935 | AAAAATTAATTAATT[A/T]AAAACAACATATAAT | 11169 |
rs193012339 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987894 | GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCGTG | 11169 |
rs193013162 | snp | A/G | 1.65542e-05 | 0.00287695 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013607 | TAAAACTGTGAAGAA[A/G]AGACACAAATTAAAG | 11169 |
rs193079870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991716 | TTTTTTTTTTAAAGT[C/T]CTGTGTGCTAAAATG | 11169 |
rs193149304 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947901 | CAGGCCAAAATTGTG[A/G]CTTTTCAAATTTAAC | 11169 |
rs193152154 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977262 | CTGTAGGGCTGCTGA[A/G]CTATTATAAAGTGTC | 11169 |
rs193161425 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54944150 | TATTATTATTAGAGA[C/T]GATGTCTCACTATGT | 11169 |
rs193165683 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972975 | AAGGCATTCAAACAC[A/G]CCCATCATGAGTAGT | 11169 |
rs193237690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010607 | CTAAATGTACAACTT[C/T]GCTGGAATGTGCATT | 11169 |
rs193301233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964018 | GAGCCTGAGACAGGA[A/G]GTTCACTAGAGCCCA | 11169 |
rs199512132 | snp | A/G | 0.000182148 | 0.00954153 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962894 | AAAGAGCTATGCAAA[A/G]ACCAACTTAACATTC | 11169 |
rs199522642 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974488 | ACAAAACCTGTTTTG[-/T]TTTTGTTTTTTTTTT | 11169 |
rs199531718 | in-del | -/AGG | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977008 | CAAGCTGGTCTTTAT[-/AGG]AGAAGTATTTATTCT | 11169 |
rs199563644 | in-del | -/TGTT | 0.0810805 | 0.184299 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011646 | TTATATTCGTGTGTG[-/TGTT]TGTGTGTATATATAT | 11169 |
rs199574542 | in-del | -/C | 0.0752113 | 0.178743 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959784 | TACCCTGTATCCGCA[-/C]CCCCCCCCACCAAAC | 11169 |
rs199578669 | in-del | -/ATAC | 0.0174175 | 0.0916809 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942265 | AAAATAAATAAATAA[-/ATAC]ATAAATAAATAAATA | 11169 |
rs199592202 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54973323 | TTATCAAATGCCCAC[C/T]AGAGTAATTAGAAAA | 11169 |
rs199629797 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983223 | TCCTCAGTGTCTTTC[-/A]AATCATCTGTCATAA | 11169 |
rs199634084 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | WDHD1 | GRCh38.p7 | 14:54962783 | CATCAGCTTCTCCAC[C/T]GTCCTCAGCATCTTC | 11169 |
rs199757650 | in-del | -/AAAAAAA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55013195 | GCAAGATCCCGTTTC[-/AAAAAAA]AAAAAAAAAAAAAAA | 11169 |
rs199851207 | snp | G/T | 0.000348834 | 0.0132021 | splice-acceptor-variant | WDHD1 | GRCh38.p7 | 14:55000994 | ACTATATTGAGGGTC[G/T]GTAAAGAAAAACAGT | 11169 |
rs199859365 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54963047 | TACAGCCAGTTCACT[C/T]AGTTTTTGAGCCAGT | 11169 |
rs199863099 | snp | A/G | 1.65949e-05 | 0.00288048 | missense | WDHD1 | GRCh38.p7 | 14:54941569 | TTTTTAGACAAATTC[A/G]GGTTCTCTTTTGCTT | 11169 |
rs199870655 | snp | A/G | 0.000694697 | 0.0186243 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54984847 | AAGGCACTGATCCCC[A/G]TCAAATCCTGTACCT | 11169 |
rs199873659 | snp | C/G | 0.0726307 | 0.176182 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024925 | TCTGAAATATGGCCT[C/G]GTGGGAAGGGAAAGA | 11169 |
rs199879918 | in-del | -/CTCA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993741 | TGCAATGCCACTCTT[-/CTCA]CTAATTTTTTTTGTT | 11169 |
rs199893292 | in-del | -/AAG | 0.380919 | 0.21298 | cds-indel, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939597 | TCTGGAAAAAAAAAA[-/AAG]AACACTGGAAAAAAA | 11169 |
rs199906739 | snp | C/T | 0.00053326 | 0.0163201 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984692 | TAACACTTTATATTA[C/T]ACTTGTTTTTTTTAA | 11169 |
rs199914676 | snp | C/T | 0.00199795 | 0.0315433 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989216 | AGAGTTCCACACCTA[C/T]AAACAGGTAAGATTA | 11169 |
rs199917355 | in-del | -/AAAG | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974516 | TTTTTTTGTTATATT[-/AAAG]AAAGAGTTTAAAAAT | 11169 |
rs199934312 | snp | A/G | 3.29777e-05 | 0.00406051 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962696 | GGAAAAGCCACATCC[A/G]TGATAGTTCTCATGA | 11169 |
rs199939907 | in-del | -/AAGTTGGAA | 0.0607341 | 0.163335 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949561 | AGGGAGAATGGAACC[-/AAGTTGGAA]AACACTCTGCAGGAT | 11169 |
rs199960828 | in-del | -/AAATA | 0.0158469 | 0.0875917 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938779 | AATAAATAAATAAAT[-/AAATA]AAAGTATTTACCTCT | 11169 |
rs199983052 | snp | A/G | 0.00128561 | 0.025321 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941721 | GGAGTGAAAAGGAAA[A/G]ATTTTTAGAAAATAA | 11169 |
rs200065489 | snp | C/T | 0.00199794 | 0.0315433 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54966589 | GTTGTGAAATATAAC[C/T]GAACGCCAAAATTGC | 11169 |
rs200084313 | snp | G/T | 0.000131922 | 0.00812056 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54989054 | ATCAGTGCTTTCACA[G/T]GCCAACAAAATAGCT | 11169 |
rs200097588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985929 | AGATGGGGAAACTAC[A/G]TAAGAAGCAAGCTTG | 11169 |
rs200112029 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54977910 | TTCCAAAGGGTTGTG[G/T]GGAAAAAAAAAAAAA | 11169 |
rs200141564 | snp | A/T | 3.33472e-05 | 0.0040832 | missense | WDHD1 | GRCh38.p7 | 14:54989200 | AGCGAATAATTCCAA[A/T]AGAGTTCCACACCTA | 11169 |
rs200177435 | in-del | -/TG | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974492 | AAACCTGTTTTGTTT[-/TG]TTTTTTTTTTTTTTG | 11169 |
rs200202401 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54992459 | CGTGCCACTGCACTC[C/T]AGGCTGGGTGACAGA | 11169 |
rs200204902 | in-del | -/ATAAC | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946038 | CCGATTTCCAGAAAA[-/ATAAC]AGAACAAATCAAAAC | 11169 |
rs200209739 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54952300 | TCAGCAAAGTCTCAG[G/T]ATACAAAATCAATGT | 11169 |
rs200226057 | snp | C/G | 0.000218927 | 0.0104602 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957024 | CAGATGAGGGTAGCT[C/G]AAACAGTACCTGCTT | 11169 |
rs200230664 | in-del | -/G | 0.176219 | 0.238865 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993757 | TCACTAATTTTTTTT[-/G]TTTTTCATAAAAAAG | 11169 |
rs200253655 | snp | A/G | 0.000903013 | 0.0212295 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955542 | GGTCACTGCATGCTA[A/G]ATTTCTCTATGTACT | 11169 |
rs200268686 | in-del | -/AC | 0.0142736 | 0.0832652 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976858 | TATGAAAATATGAAA[-/AC]AGTCTGCAGTTATCA | 11169 |
rs200273710 | in-del | -/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988238 | GTTTTTCCGTTTTTT[-/C]TTTCCTTTCTCGAAG | 11169 |
rs200286388 | in-del | -/TTCC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54995373 | TTTGCTCTGTATTAT[-/TTCC]TTCCTTCCATTTGCT | 11169 |
rs200329770 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54971825 | GAACTTAAAAAAAAA[-/A]TCAGCAGCAAAAAAC | 11169 |
rs200333560 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980187 | TGGGTGTGGTGGTGC[A/G]TGCCTGTAGTCCCAG | 11169 |
rs200333566 | snp | C/T | 0.000330874 | 0.012858 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991404 | GCATTGAAATATCTA[C/T]AACACAAAGGATCAT | 11169 |
rs200342914 | in-del | -/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54977087 | CAAAAAAATAAGGTT[-/G]TTTTTTTTTTGCCAA | 11169 |
rs200386217 | snp | A/C/T | 5.29613e-05 | 0.00514571 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963214 | AGATCAAATAACATC[A/C/T]AGTAAAACTTTTTAA | 11169 |
rs200410598 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008813 | TTTTTTTTTTTTTTT[C/T]TTTTTGAGACGGAGT | 11169 |
rs200424035 | in-del | -/A | 0.0433719 | 0.14073 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999305 | TCTTTTCTAAAAAAA[-/A]CAAATCTCCAACATT | 11169 |
rs200426794 | in-del | -/AA | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983959 | ATCTTTTTTCATGCT[-/AA]GTCTTCAAAATCCAG | 11169 |
rs200434634 | in-del | -/TTC | 0.0433465 | 0.140692 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017343 | TAGGAAAAATCAATA[-/TTC]TTTTTTTTTCTTTTT | 11169 |
rs200445471 | in-del | -/T | 0.498392 | 0.028309 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966163 | AAACCCCATCTCTAC[-/T]TAAAAAAAAAAAAAA | 11169 |
rs200449348 | in-del | -/CT | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958705 | TGACTTAGTTCCTTC[-/CT]CTCTGGACCTGTGGA | 11169 |
rs200535436 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980803 | AGTGAGACTCCACAT[A/T]AAAAAAAAAAAAAAA | 11169 |
rs200561268 | in-del | -/TATT | 0.0456336 | 0.143994 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969033 | GTAAGACCTTGTTTC[-/TATT]TATTTATTTATTTAT | 11169 |
rs200568830 | snp | C/T | 3.30431e-05 | 0.00406454 | missense | WDHD1 | GRCh38.p7 | 14:54984828 | GCTCTAGCAGTTGAA[C/T]TCCAAGGCACTGATC | 11169 |
rs200590281 | snp | C/T | 0.00031326 | 0.0125113 | missense | WDHD1 | GRCh38.p7 | 14:54957069 | GAATCAGAGGCTTTA[C/T]AATGGGAGACTTTTC | 11169 |
rs200591755 | snp | A/C/G/T | 0.00068089 | 0.0184398 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963191 | ATCCAAAAAGGGGGG[A/C/G/T]GGGGGGGAGATCAAA | 11169 |
rs200709670 | snp | G/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000631 | AAATTGCATAACCTT[G/T]CTCATGTTTCACCCT | 11169 |
rs200809120 | in-del | -/ATAA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54942281 | TAAATAAATAAATAA[-/ATAA]TAAAAATGAAACTTT | 11169 |
rs200829175 | snp | A/G | 0.00199806 | 0.0315443 | missense | WDHD1 | GRCh38.p7 | 14:54981612 | TTGCAGTGCTCTCTT[A/G]TATTACATATAGGAG | 11169 |
rs200829692 | snp | C/T | 0.00056311 | 0.0167701 | missense | WDHD1 | GRCh38.p7 | 14:54962534 | AGGAATTTGTACTTT[C/T]GGAAAACGAGTTCTG | 11169 |
rs200845681 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992054 | AGGTCGGGAGTTCCA[C/T]GTTGACCAGCCTGGC | 11169 |
rs200869931 | in-del | -/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972276 | TGAGACTCGGTCTCA[-/C]CAAAAAAAAAAAAAA | 11169 |
rs200882768 | snp | C/T | 0.00188511 | 0.0306431 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962888 | TTCAATAAAGAGCTA[C/T]GCAAAGACCAACTTA | 11169 |
rs200887287 | snp | A/C/T | 9.9231e-05 | 0.00704313 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54963104 | TTTAATGGCTAAATT[A/C/T]ACAGCATTTTGAGTC | 11169 |
rs200894779 | snp | A/C/T | 5.99251e-05 | 0.00547348 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987401 | TGCTAAAAATTAAAA[A/C/T]AAGACAGAAACAATC | 11169 |
rs200906758 | snp | A/C/G | 6.65979e-05 | 0.00577014 | missense | WDHD1 | GRCh38.p7 | 14:54963033 | TCGGCTGCCTTCTCT[A/C/G]CAGCCAGTTCACTTA | 11169 |
rs200919031 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988350 | ATATAAGAAAACATT[A/C]TTGGGTGATAAAGAC | 11169 |
rs200925562 | snp | A/C | 6.61102e-05 | 0.00574898 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962862 | GCTGTAACTAAGAGA[A/C]AATAATATTATTCAA | 11169 |
rs200940413 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012676 | TACAAGATTGAGGGG[C/T]TGGCATCTGGCAAGG | 11169 |
rs200963477 | snp | A/T | 0.000399281 | 0.0141238 | missense | WDHD1 | GRCh38.p7 | 14:54941665 | CCTTCACTTGCCGTT[A/T]CTCCTTTGGCTTTGT | 11169 |
rs201092969 | in-del | -/A | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026541 | CGATATACTACAACT[-/A]CCATGACGGCCCGAA | 11169 |
rs201110623 | snp | C/T | 6.59522e-05 | 0.0057421 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54987183 | CTGTTCTCCATGTCC[C/T]GCCATTGACACCACA | 11169 |
rs201139261 | snp | A/C | 1.66391e-05 | 0.00288431 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007271 | AAAAGAAAAATAAGA[A/C]TCACTTACCTTCCCA | 11169 |
rs201150906 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997747 | GAAACCCCGTCTCTA[C/T]TAAAAATGCAAAAAT | 11169 |
rs201210469 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001079 | TCAATTTTCTTTTCA[-/T]TTTTTTTTCAAGAAT | 11169 |
rs201255867 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54977913 | CAAAGGGTTGTGTGG[A/G]AAAAAAAAAAAAGCA | 11169 |
rs201260147 | in-del | -/A | 0.00993419 | 0.0697739 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961321 | CACCCCATCTCTATT[-/A]AAAAAAAATAAAATA | 11169 |
rs201260736 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54995153 | ACCCAGCTAATTTTT[-/T]GTATTTTTGTAGAGA | 11169 |
rs201296875 | snp | G/T | 0.00022372 | 0.010574 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957553 | TCTTTGTATACAAAT[G/T]TATTTAAATAATATA | 11169 |
rs201303959 | in-del | -/T | 0.0295035 | 0.117819 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027725 | GAAGGAATGACTTAA[-/T]TTCTGTTCCGGTTGG | 11169 |
rs201325863 | snp | A/C | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025861 | CAACATCACCACCCC[A/C]CCGCCACCACCACTC | 11169 |
rs201326855 | in-del | -/TTTGGTTC | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004283 | AACTTTCCATATACA[-/TTTGGTTC]TATTTATCTCTTTAA | 11169 |
rs201351516 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990487 | TGTAGTCCCAGCTAC[C/T]CGGGAGGCTGAGGCA | 11169 |
rs201423106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961750 | GTACTATAAGGTTTA[C/T]GCTCCCCACCAAAAA | 11169 |
rs201445432 | snp | A/G | 0.000296496 | 0.0121721 | missense | WDHD1 | GRCh38.p7 | 14:54991320 | GGGATGTTACAAGTG[A/G]TAGATTGTGAATGCT | 11169 |
rs201448829 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962448 | ATGTGTCACTTTGCA[C/G]ATGACTTGCAAAATT | 11169 |
rs201557672 | snp | A/C | 0.000137282 | 0.00828386 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956993 | TGAAGACAAACAGAT[A/C]CCATGCTGCTTACTG | 11169 |
rs201560985 | snp | C/T | | | missense | WDHD1 | GRCh38.p7 | 14:54981679 | CAATTCCTTCTGAAT[C/T]CACGTAACAAGGGGT | 11169 |
rs201564673 | in-del | -/TATATATC/TC/TT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003589 | AAGAAAAACGAACTA[-/TATATATC/TC/TT]TATATATATAGTTGC | 11169 |
rs201586593 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54979164 | TTCACACCAAAGTTC[-/T]TTTTTTTTTGAGATA | 11169 |
rs201603143 | in-del | -/AAAAAA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55013195 | GCAAGATCCCGTTTC[-/AAAAAA]AAAAAAAAAAAAAAA | 11169 |
rs201605402 | snp | C/T | 0.000659968 | 0.0181535 | missense | WDHD1 | GRCh38.p7 | 14:54962848 | TCTGTAGCAGTATTG[C/T]TGTAACTAAGAGAAA | 11169 |
rs201614471 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980821 | AAAAAAAAAAAAAAA[A/C]AAAACTCAGCTGGGC | 11169 |
rs201643518 | snp | C/T | 1.64849e-05 | 0.00287092 | missense | WDHD1 | GRCh38.p7 | 14:54941632 | TCAACCACACGTTTT[C/T]GCTTCTTTGCTTCAG | 11169 |
rs201658084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015071 | GTAGATAGGAGGACT[A/G]TAAGTCTCAGTTTGC | 11169 |
rs201679332 | in-del | -/TAAATAAA | | | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938785 | AAATAAATAAATAAA[-/TAAATAAA]AGTATTTACCTCTAA | 11169 |
rs201698337 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974494 | ACCTGTTTTGTTTTG[G/T]TTTTTTTTTTTTTGT | 11169 |
rs201722734 | snp | A/G | 4.96948e-05 | 0.00498447 | missense | WDHD1 | GRCh38.p7 | 14:54966476 | TTTATTTTACTCACC[A/G]CAAGCATTTTCATTA | 11169 |
rs201749860 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54952278 | CTCCTTAAGCTGATA[A/G]GGAACTTCAGCAAAG | 11169 |
rs201769435 | snp | A/G | 0.000230796 | 0.0107399 | stop-gained | WDHD1 | GRCh38.p7 | 14:54944364 | ACAATACTCTAAATC[A/G]AATCATTCCTTCTTT | 11169 |
rs201783479 | snp | A/G | 0.000208986 | 0.0102201 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54966562 | ACCATTTTTAGCTAA[A/G]TAATCAAGGTGGTTG | 11169 |
rs201859369 | snp | C/G | 0.00199792 | 0.0315431 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026696 | CCTAAAACGTTGTTT[C/G]TCAAAGAACCTTACC | 11169 |
rs201865649 | snp | C/T | 0.000244435 | 0.0110525 | missense, intron-variant | WDHD1 | GRCh38.p7 | 14:54995783 | CTCCATCAAAAAGAT[C/T]ATTATAATCCTTTTC | 11169 |
rs201895571 | snp | C/T | 3.31532e-05 | 0.0040713 | missense | WDHD1 | GRCh38.p7 | 14:54955615 | GTTTCAGATAATACA[C/T]TTTTAAGATTTTCTT | 11169 |
rs201947982 | in-del | -/T | 0.40263 | 0.198 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998631 | CATATTCTAGTAGAA[-/T]TTTTTTTTTTCACTT | 11169 |
rs201952894 | in-del | -/AAAAG/AG/G | 0.000164145 | 0.00905789 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007245 | TAAAAAAAAAAAAAA[-/AAAAG/AG/G]AAAAGAAAAGAAAAG | 11169 |
rs201981252 | snp | G/T | 1.65239e-05 | 0.00287431 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987132 | CAAGTCATAAAAGAC[G/T]GAAAAAAATCTACCT | 11169 |
rs201984413 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985690 | AAGAACTGAAGCTAA[A/G]AGACTAGTTAGGAGG | 11169 |
rs201994301 | in-del | -/T | 0.0162398 | 0.0886349 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022432 | ATGTTCTTTGTGGCA[-/T]TTTTTCCCCCCACAG | 11169 |
rs202021020 | in-del | -/A | 0.408359 | 0.193449 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970622 | CGAAGTCACAGCACC[-/A]AAAAAAAAAAAAAAG | 11169 |
rs202029430 | snp | C/T | 0.00688508 | 0.0582678 | missense | WDHD1 | GRCh38.p7 | 14:54941650 | TTCTTTGCTTCAGTT[C/T]CTTCACTTGCCGTTT | 11169 |
rs202102011 | in-del | -/AAAG | | | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939596 | CTCTGGAAAAAAAAA[-/AAAG]AACACTGGAAAAAAA | 11169 |
rs202105202 | in-del | -/T | 0.0314195 | 0.121337 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007230 | AGACTCCATCTCTAA[-/T]TAAAAAAAAAAAAAA | 11169 |
rs202140737 | snp | C/G | 0.00199792 | 0.0315431 | missense | WDHD1 | GRCh38.p7 | 14:54987202 | ATTGACACCACAGGT[C/G]CAGCAAGGCTGAATA | 11169 |
rs202160029 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019618 | CATGCCTGTAACCCC[-/A]AGCACTTTGGGAGGC | 11169 |
rs202190362 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016000 | CACCACACCCAGCCC[C/T]GATGGGCTTCTTGGT | 11169 |
rs202210324 | snp | A/G | 3.29484e-05 | 0.00405871 | missense | WDHD1 | GRCh38.p7 | 14:54991310 | AATGGCCTTTGGGAT[A/G]TTACAAGTGGTAGAT | 11169 |
rs202214344 | snp | C/T | 4.96184e-05 | 0.00498063 | missense | WDHD1 | GRCh38.p7 | 14:54963058 | CACTTAGTTTTTGAG[C/T]CAGTATTAATTTCCG | 11169 |
rs367558658 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54978474 | CCTGTAGTTCTACCT[A/G]CTCAGGAGACTGAGG | 11169 |
rs367634159 | snp | C/T | 2.0492e-05 | 0.00320087 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957548 | ATATTTCTTTGTATA[C/T]AAATGTATTTAAATA | 11169 |
rs367731286 | snp | A/G | 1.65351e-05 | 0.00287528 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54957196 | TGGTTCTTTGGAACT[A/G]GCTGATACCTAAAGA | 11169 |
rs367755494 | snp | A/G/T | 2.64603e-05 | 0.00363723 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987434 | ACTTTCATATGATAT[A/G/T]TACATATATATATAT | 11169 |
rs367764877 | snp | G/T | 1.91206e-05 | 0.00309192 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989252 | AAGTCTGAGAAAAAC[G/T]GAAGCTCCTAGAATC | 11169 |
rs367814457 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954397 | AGGAATACTCATATT[C/G]CTAAAGGTGTATAAA | 11169 |
rs367824710 | snp | C/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025462 | TCTCGTTCCACCTTA[C/G]GAGAAACACCCACAA | 11169 |
rs367837682 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54961262 | TTTGGGATGTGGAGG[G/T]GAGGAAATTGCTTGA | 11169 |
rs367861189 | snp | C/T | 1.79429e-05 | 0.00299518 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967426 | GTTCCATCATAAAAA[C/T]TTACTAACATGTCAT | 11169 |
rs367956717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994282 | TCTTTCAGAAAATTC[A/G]TCTATTTCATTTAAG | 11169 |
rs367965489 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951985 | TAGGTATTGATGGGA[C/T]GTATCTCAAAATAAT | 11169 |
rs367969433 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972208 | TGAACCCGGGAGGCG[A/G]AGCTTGCGGTGAGCC | 11169 |
rs367997621 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947123 | GGCGGGTGGATCACC[-/T]GAGGTCAGGAGTTCA | 11169 |
rs368036730 | snp | A/C/G | 0.0943545 | 0.197732 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025246 | AAGACCTTTGTTCAC[A/C/G]TGTTTGTCTGCTGAC | 11169 |
rs368088426 | snp | C/G | 1.64985e-05 | 0.0028721 | missense | WDHD1 | GRCh38.p7 | 14:54957064 | CTTTGGAATCAGAGG[C/G]TTTATAATGGGAGAC | 11169 |
rs368129551 | snp | G/T | 0.000646254 | 0.0179641 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010488 | TTAAGGTAAGAAACA[G/T]TAGCAAAACAAATCC | 11169 |
rs368132637 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54961961 | CCTGCTTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 11169 |
rs368151618 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003752 | TATTTTCAGTAGAGA[C/G]GGGGTCTTATCATGT | 11169 |
rs368204303 | snp | A/T | 0.0788843 | 0.182262 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998219 | CAAAGAAAAAAAAAA[A/T]TTTTTAATGGAGGAC | 11169 |
rs368209209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972820 | GGTGAAATGCCTAAT[A/G]TAGGTTAAGTGTTTA | 11169 |
rs368209721 | snp | A/C | 4.94735e-05 | 0.00497336 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55013565 | CTTCCCAAATCCTCA[A/C]ATCACCATCACTTCC | 11169 |
rs368213308 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54945865 | ATGTTTAACCCAGCA[A/G]CTATACGCCCCTCAC | 11169 |
rs368254694 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54952176 | GAAATAAAGGGTATT[C/T]AATTAGGAAAAGAGG | 11169 |
rs368266703 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54982056 | TGTGTACCCAGGCTG[C/G]AGGGCAGTGGCGCGA | 11169 |
rs368346537 | snp | C/T | 3.29658e-05 | 0.00405978 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000923 | CCACATTCCAAACTA[C/T]GATTAGACCATTAAT | 11169 |
rs368368535 | snp | A/G | 9.97009e-05 | 0.00705978 | missense | WDHD1 | GRCh38.p7 | 14:54941560 | GGTTTCTGCTTTTTA[A/G]ACAAATTCAGGTTCT | 11169 |
rs368396768 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971266 | CCAAAGAGCTTCTGC[A/G]CAGCAAAAGAAACTA | 11169 |
rs368447181 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997421 | CTTTTAAATGGAAGT[A/G]AACATAACTGTGCTC | 11169 |
rs368452934 | in-del | -/GGAGACAGAG | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55021422 | CTTTTTTTTTTTTTT[-/GGAGACAGAG]TTTTGCTTTGTTGGC | 11169 |
rs368454975 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965993 | TTTAACTGCAAGACC[A/T]ACTAGAAGATAGAAC | 11169 |
rs368472242 | snp | A/G/T | 0.000117049 | 0.00764939 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941707 | TTTGTAAAATGGCAG[A/G/T]AGTGAAAAGGAAAGA | 11169 |
rs368483589 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54949190 | AAGAAGGCTTCAGAC[A/G]ATCAAACCTCTCCGA | 11169 |
rs368486779 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008795 | CTATGATCCAAATAT[G/T]TCTTTTTTTTTTTTT | 11169 |
rs368534314 | snp | A/C/G | 0.000528048 | 0.0162404 | utr-variant-5-prime, synonymous-codon | WDHD1 | GRCh38.p7 | 14:55010416 | TTCAGGAAATGTGTG[A/C/G]ACTTGAATAGTATTA | 11169 |
rs368542276 | snp | A/C | 6.84006e-05 | 0.0058477 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987394 | TGAAGCTTGCTAAAA[A/C]TTAAAACAAGACAGA | 11169 |
rs368551600 | snp | C/T | 4.95626e-05 | 0.00497784 | missense | WDHD1 | GRCh38.p7 | 14:54963091 | AGCGAGAAGCATATT[C/T]AATGGCTAAATTCAC | 11169 |
rs368557502 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54964898 | CCTTATATGTGTTGT[A/T]CAAATAAAAAGGCTA | 11169 |
rs368559429 | snp | A/G | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940117 | GATTACTATGTGTCA[A/G]AAACTAAGGGCTTTC | 11169 |
rs368650936 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | WDHD1 | GRCh38.p7 | 14:54987289 | GCAGCAGCCCATCCT[C/T]GACCGAGACATATGG | 11169 |
rs368697937 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54941961 | TACTATTTAAAAATG[A/G]AACTTTTGGCCAGGC | 11169 |
rs368758306 | snp | A/C/T | 0.000106592 | 0.00729977 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000676 | AGGTTCTAAAAATAC[A/C/T]GTCAAGAAAAATATA | 11169 |
rs368766605 | snp | A/C | 1.75915e-05 | 0.00296571 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963209 | GGGGGAGATCAAATA[A/C]CATCAAGTAAAACTT | 11169 |
rs368816849 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966456 | ACTTTAACGTTTTCA[G/T]TATATTTATTTTACT | 11169 |
rs368819627 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941701 | CACACCTTTGTAAAA[C/T]GGCAGGAGTGAAAAG | 11169 |
rs368869027 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951046 | CACAAGAGAAAGCAG[A/G]AAATATCTAAAATTG | 11169 |
rs368904574 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55021967 | TTCTCTTCCATAGCA[A/G]TGACAATCCTTTCCA | 11169 |
rs368910961 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54955886 | CTACACTTCAGATTC[A/C]ATGTTTTCCTTTTTT | 11169 |
rs369017831 | snp | G/T | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027478 | CTCCGGGAGGTGAGT[G/T]GGGGAAGGGTGGCCG | 11169 |
rs369038111 | snp | C/T | | | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54984787 | AAGAGGGTCACCATG[C/T]AAAATTTGTTTTTTC | 11169 |
rs369050627 | snp | A/G | | | missense | WDHD1 | GRCh38.p7 | 14:54962842 | CTCCACTCTGTAGCA[A/G]TATTGCTGTAACTAA | 11169 |
rs369056533 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54987549 | ATTATGAAATACCCT[C/T]AAAATGAACTATATT | 11169 |
rs369094073 | in-del | -/CACCA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54986469 | CACCACACCACACCA[-/CACCA]TACCTGGTCCAGAAT | 11169 |
rs369158769 | snp | A/G | 1.70924e-05 | 0.00292334 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957682 | TGGTAGAAAATAGAT[A/G]ACTTCTGACATCTAT | 11169 |
rs369184965 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55006752 | AATATAAAATTAATT[C/T]ATTCATGCAAAATTT | 11169 |
rs369185284 | snp | C/G | 0.000153988 | 0.00877328 | splice-acceptor-variant | WDHD1 | GRCh38.p7 | 14:54962552 | AAAACGAGTTCTGTC[C/G]TACAGATTAAAATAA | 11169 |
rs369195298 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54973130 | ACACTATAAATACCA[C/T]AGGCAAATTTCATAT | 11169 |
rs369197345 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996008 | CCCAGTCCTTATTTC[A/G]AATGCCTTGTAGTCT | 11169 |
rs369256560 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996115 | CCTCAGAAGTCATTC[C/G]CTAGAAAAGAAGTGA | 11169 |
rs369256650 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015690 | ATTTCACGTTTTTGT[C/T]CCAATGGAATTTTTT | 11169 |
rs369269158 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974174 | TGCCTGTAATCCCAG[C/T]ACATAAGGAGGCTGA | 11169 |
rs369313602 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55006965 | GGCACGGTGGCTCAC[A/G]CCTGTAATACTAGCA | 11169 |
rs369355154 | snp | A/G | 1.67691e-05 | 0.00289556 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991445 | ATCACGAATACCAAT[A/G]ATTTGGAAAAAGGAA | 11169 |
rs369381589 | snp | C/T | 0.00131314 | 0.0255899 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957697 | GACTTCTGACATCTA[C/T]AATACTAGACAGAGT | 11169 |
rs369405430 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948233 | GTGGCACACCGAGTG[C/T]GAGCTGAAGCAGGGC | 11169 |
rs369412449 | snp | A/G | 0.000215333 | 0.010374 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002044 | TCAGGCAAACTACGC[A/G]TTAACTGCTCCTTAT | 11169 |
rs369469827 | in-del | -/TA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54969701 | CTCCAAATCACTCTA[-/TA]AAGCCAGCATTATCC | 11169 |
rs369559515 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996399 | GATGCCTTGAGCTCA[C/G]GAGTTCGAGACCAGC | 11169 |
rs369573046 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016587 | TTGTGAAGCATGATT[A/C]TTCCTAAGAACTCAG | 11169 |
rs369574032 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981512 | CTTTTTAAAAAGAGT[C/G]AACTTTAGACTTCTT | 11169 |
rs369596416 | snp | C/T | 1.68564e-05 | 0.00290309 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988978 | TAATTTCAACAACTG[C/T]ATCTAACAGTTCAAC | 11169 |
rs369629899 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985285 | TTGTTAGACTGGTTA[C/G]TCAGAAGTGACCTCT | 11169 |
rs369642815 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55007318 | CAAGTCTGCAGATTG[A/G]TTTTGCATTTATCAC | 11169 |
rs369663027 | snp | C/G/T | 0.000510981 | 0.0159763 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962700 | AAGCCACATCCATGA[C/G/T]AGTTCTCATGATTTA | 11169 |
rs369683922 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011804 | ACCCTACTTTTATAA[C/T]GGCTGCATAGTATTC | 11169 |
rs369698327 | in-del | -/A/AA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55007231 | GACTCCATCTCTAAT[-/A/AA]AAAAAAAAAAAAAAA | 11169 |
rs369805682 | snp | A/G | 9.51393e-05 | 0.00689642 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984678 | TCTTGAAGAATATCT[A/G]ACACTTTATATTATA | 11169 |
rs369862171 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026835 | AAAGCCAGTCTTATT[A/G]TTTCAAAAGAGAAAA | 11169 |
rs369870309 | snp | A/G | 0.000130306 | 0.0080707 | missense | WDHD1 | GRCh38.p7 | 14:54966584 | AGGTGGTTGTGAAAT[A/G]TAACTGAACGCCAAA | 11169 |
rs369874357 | snp | A/C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990574 | GCACTCCAGCCTGGG[A/C/G]AACAGAGCGAGACTC | 11169 |
rs369897077 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54999755 | ACAGGCACACACCAC[C/T]ACACTTGCCTAATTT | 11169 |
rs369909598 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958639 | CATAGCTGACTGTTC[C/T]TTACTTCTTGATACT | 11169 |
rs369945944 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55000378 | ACTATAGATTACTAC[C/T]CAGCATCTACTATAG | 11169 |
rs370007079 | snp | C/T | 0.000434899 | 0.0147398 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008755 | GCAAATGAATAAATG[C/T]TAACACAAAGGCCTC | 11169 |
rs370012580 | snp | A/C/T | 8.37354e-05 | 0.00647008 | missense | WDHD1 | GRCh38.p7 | 14:54963007 | CCTCTTCCACCTGGG[A/C/T]TGCTGTCAATTCGGC | 11169 |
rs370031987 | snp | A/G | 0.422969 | 0.180505 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007260 | AAAAAGAAAAGAAAA[A/G]AAAAATAAGAATCAC | 11169 |
rs370057188 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54959093 | AATTAAGAGCTTTCC[C/T]GGCATGGTGGCTTAA | 11169 |
rs370071656 | snp | A/C | 6.59609e-05 | 0.00574248 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962694 | TGGGAAAAGCCACAT[A/C]CATGATAGTTCTCAT | 11169 |
rs370105298 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55021029 | CTTACTGTCTCAGAG[A/G]TGGAAGAGGGGGAGG | 11169 |
rs370112256 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024425 | ATCCCTGTTGCCTCT[G/T]TCTCCATCCTTAATA | 11169 |
rs370114587 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55023534 | TTTTGTCTGCTTCTT[A/C]GGAGTATGTCCAGCA | 11169 |
rs370142582 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959405 | TGGCGGGGGGAAGAG[A/G]AGGGAGGGAGGGAGG | 11169 |
rs370145008 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54959445 | AGGGAGGGAGGGAGG[C/G]AGGCAGGCAGGCAGG | 11169 |
rs370161456 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004732 | TGCTGGGATTATGGG[C/T]GTGAGCCAGCGAGCC | 11169 |
rs370170236 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993935 | TAGAGTATAAAGGCT[A/C]CTGAGACCAAAACAT | 11169 |
rs370209803 | in-del | -/AGATTC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54955885 | CTACACTTCAGATTC[-/AGATTC]CATGTTTTCCTTTTT | 11169 |
rs370210535 | snp | C/G | 1.6473e-05 | 0.00286988 | intron-variant, synonymous-codon, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026773 | ATATCTCATTGGCTT[C/G]CGTGTGGCAGGCATG | 11169 |
rs370211594 | snp | A/G | 9.93706e-05 | 0.00704808 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981709 | TACCTAAACACCAAC[A/G]GAAAAATCACTTGGA | 11169 |
rs370217613 | snp | C/T | 1.64982e-05 | 0.00287208 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944305 | GGGAATTCACTAAGA[C/T]CTCAATCTCGGCACA | 11169 |
rs370252432 | snp | C/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000636 | GCATAACCTTTCTCA[C/T]GTTTCACCCTAAAAA | 11169 |
rs370266207 | snp | C/G | 1.64914e-05 | 0.00287149 | missense | WDHD1 | GRCh38.p7 | 14:54991252 | CGGTGTAGAACCTGA[C/G]TGAAATGGCTTTTGC | 11169 |
rs370284649 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993199 | CATGGCTCACTGCAG[C/G]CTCGACCTCTCGGGC | 11169 |
rs370296571 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975611 | GCCTTGCCCTCCCAA[A/G]GTGCTGGGATTACAG | 11169 |
rs370304514 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54987437 | TTCATATGATATTTA[C/T]ATATATATATATATA | 11169 |
rs370306787 | snp | A/C | 0.0941369 | 0.195465 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024838 | ACCCAGGGACACAAA[A/C]ACTGCGGAAGGCCGC | 11169 |
rs370345095 | in-del | -/A | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026436 | TAGTGATCTGACAAA[-/A]TTAATAATGTAAGAT | 11169 |
rs370367909 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55013669 | CTAGCACTTTGGGAG[C/T]ACAAGGTGGGAGGAT | 11169 |
rs370375068 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54970890 | CTGGTGCACAAACAG[A/C]AACACAGACCAGTGG | 11169 |
rs370450568 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54966336 | CGAGACTCCGTCGCA[A/C]AAAAAACAACAACAA | 11169 |
rs370458033 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020105 | TCTCTATATACTCAG[C/T]TTTCTTTCTGGTCAT | 11169 |
rs370491164 | snp | A/G | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941211 | TTTTCAAGGTTAAGA[A/G]ACAAATTCAAATTGG | 11169 |
rs370492600 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996479 | GTGGCATGTGTCTAT[A/G]GTCCCAGCTACCTGC | 11169 |
rs370501147 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54953660 | TCATGCTGCTATAAA[A/G]ACACATGCACACGTA | 11169 |
rs370631392 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963861 | TCACACCTGTAATCC[C/T]AGCACTTTGGAAGGC | 11169 |
rs370645370 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003308 | AGAGCTCAGGAGTTT[C/G]AGACTAGCCTGAGCA | 11169 |
rs370647986 | snp | C/T | 0.000153988 | 0.00877328 | missense | WDHD1 | GRCh38.p7 | 14:54957072 | TCAGAGGCTTTATAA[C/T]GGGAGACTTTTCATT | 11169 |
rs370665038 | snp | C/T | 1.64827e-05 | 0.00287073 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008673 | GTCCTCGAAATGTTT[C/T]CTGTTGGCTGCTATC | 11169 |
rs370697035 | snp | G/T | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011649 | TATTCGTGTGTGTGT[G/T]TGTGTGTATATATAT | 11169 |
rs370716250 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963259 | CTAGTAAAACTGAGA[C/T]AATAGTTTTCTAGCT | 11169 |
rs370729586 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011282 | CACCTGTAATCCCAG[C/T]ACTTTGGGAGGCCAA | 11169 |
rs370754307 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997547 | TAAGAAGATATTCAA[A/C]CATTCCATTTATAGT | 11169 |
rs370792481 | in-del | -/AA | 0.0170251 | 0.090679 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996215 | AACAAAATACTGCAT[-/AA]GATACATTTTCTTTA | 11169 |
rs370843677 | snp | C/T | 8.23988e-05 | 0.00641815 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000578 | TTCCGCATCAGTATA[C/T]GATATTCGACCACAA | 11169 |
rs370851666 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54949371 | CACAAGCCTCAGTAG[C/T]CAATTCAATCAACTG | 11169 |
rs370889586 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54945537 | CCAGGCAATTTGACT[A/C]CAAAGTCTATGTTTT | 11169 |
rs370962545 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54964323 | TCTTAATCGGGATGG[A/T]ACACTGCCTCAGGGG | 11169 |
rs370979449 | snp | C/T | 0.000312207 | 0.0124902 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002235 | TACATTAAATTGAAT[C/T]TGAAGAAGGAAAAAG | 11169 |
rs371013148 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55018464 | TCCTATTTTTAATTG[C/T]ATTAATTTATGTTCT | 11169 |
rs371014811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992561 | TTCTATTTGCCATTA[C/T]GAGCTTCACAACTTT | 11169 |
rs371022554 | snp | C/T | 3.30929e-05 | 0.0040676 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987122 | CATTTTACTTCAAGT[C/T]ATAAAAGACTGAAAA | 11169 |
rs371024179 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019185 | AGCAATACCATGGGA[C/G]AGACAGGCTAAGAAA | 11169 |
rs371038702 | snp | C/T | 3.31208e-05 | 0.00406931 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962462 | AGATGACTTGCAAAA[C/T]TTCCTTGATATTACA | 11169 |
rs371126586 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969508 | AAAACTTCCCAAGAC[G/T]GACTCAGAAAAAACA | 11169 |
rs371135552 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55007185 | GTGAGCCGAGATTGC[A/C]CCACTGCACTCCAGC | 11169 |
rs371181298 | snp | C/T | | | missense | WDHD1 | GRCh38.p7 | 14:54987265 | CGAAGAAGCAGGGCA[C/T]TAGTAGCGGCAGCAG | 11169 |
rs371199804 | in-del | -/AA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54994760 | GTGAGACTCCGCCTC[-/AA]AAAAAAAAAAAAAAA | 11169 |
rs371209985 | snp | C/T | 1.67846e-05 | 0.0028969 | missense | WDHD1 | GRCh38.p7 | 14:54957612 | AGGGATTTACTCGTC[C/T]TTGGCTGCTAAAGGT | 11169 |
rs371234810 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55006346 | CACATTTCTTGTACA[C/T]TTAACCTGTTACTGT | 11169 |
rs371258231 | snp | C/G | 1.65701e-05 | 0.00287833 | splice-acceptor-variant | WDHD1 | GRCh38.p7 | 14:54957205 | GGAACTGGCTGATAC[C/G]TAAAGAGCAAACTAG | 11169 |
rs371293649 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008797 | TGATCCAAATATTTC[-/T]TTTTTTTTTTTTTTT | 11169 |
rs371297691 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54992437 | AGAGGTTGCAGTGAA[C/T]CGAGATCGTGCCACT | 11169 |
rs371298022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946017 | TTTAAGTAATCTTAA[C/T]GTAAACCGATTTCCA | 11169 |
rs371351992 | snp | C/G/T | 1.72021e-05 | 0.0029327 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001033 | AATGATTTTGTAAAA[C/G/T]TTCAAACTAAATACT | 11169 |
rs371495860 | snp | C/T | 6.62065e-05 | 0.00575316 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002063 | ACTGCTCCTTATAGC[C/T]CACTGAAAGTGTCAC | 11169 |
rs371519572 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014179 | GCTCTCTAAACCCTC[C/T]GCCTCCCAGGCTCAA | 11169 |
rs371541612 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951581 | GAGGTACAAGGAGGA[A/G]CTGTTACCATTCCTT | 11169 |
rs371545991 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54952053 | CTGAATGGGCAAAAA[C/T]TGGAAGCATTCCCTT | 11169 |
rs371566246 | in-del | -/TTC | | | cds-indel | WDHD1 | GRCh38.p7 | 14:54962990 | ATCTTCTTCTTCTTC[-/TTC]CTCTTCCACCTGGGT | 11169 |
rs371574367 | in-del | -/AAA/AAC | 0.127944 | 0.218179 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966355 | AACAACAACAACAAC[-/AAA/AAC]AAAAAAAAACTTAAG | 11169 |
rs371577212 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025780 | TTTTCCTTCAGTTCT[C/T]TGAGCATACCATGAT | 11169 |
rs371577380 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939132 | TTCAAATTTTCTGTA[A/G]GTTTGAGAGATTCAA | 11169 |
rs371586744 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952768 | CACAGTACTGGTACC[A/T]AAACAGAGATACAGA | 11169 |
rs371637926 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010507 | CAAAACAAATCCAAA[C/T]GACTGGGAGTCTCTC | 11169 |
rs371678395 | snp | A/C/T | 0.000270295 | 0.0116223 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966446 | AAAGCATTTAACTTT[A/C/T]ACGTTTTCAGTATAT | 11169 |
rs371742027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015474 | TCTCATTTGGTAACA[C/T]AACACACATAACACA | 11169 |
rs371790833 | snp | A/G | 0.000153988 | 0.00877328 | missense | WDHD1 | GRCh38.p7 | 14:54987253 | ATAGTAAACAATCGA[A/G]GAAGCAGGGCACTAG | 11169 |
rs371815506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015290 | TACTCCAGAGGCTGA[A/G]GCATGAGAATCATTT | 11169 |
rs371883877 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962585 | CAATATAATGTAAAT[A/G]GGGAAAATATAGTCA | 11169 |
rs371965821 | snp | C/T | 0.000153988 | 0.00877328 | missense | WDHD1 | GRCh38.p7 | 14:54963111 | GCTAAATTCACAGCA[C/T]TTTGAGTCATTAGAT | 11169 |
rs372019823 | in-del | -/TAC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55023814 | CAGTAATACAGTATA[-/TAC]TACAGTTAATTTTAT | 11169 |
rs372023159 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003750 | TGTATTTTCAGTAGA[A/G]ACGGGGTCTTATCAT | 11169 |
rs372040759 | snp | C/T | 0.000153988 | 0.00877328 | missense | WDHD1 | GRCh38.p7 | 14:54941660 | CAGTTCCTTCACTTG[C/T]CGTTTCTCCTTTGGC | 11169 |
rs372078397 | snp | G/T | 1.6549e-05 | 0.0028765 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013604 | CAATAAAACTGTGAA[G/T]AAAAGACACAAATTA | 11169 |
rs372080525 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54986885 | GAAAGTTCTCTGGTC[A/G]TGCTTGCCAAAATGG | 11169 |
rs372085120 | snp | C/T | 0.000153988 | 0.00877328 | stop-gained | WDHD1 | GRCh38.p7 | 14:54941686 | TTGGCTTTGTTAGCC[C/T]ACACCTTTGTAAAAT | 11169 |
rs372094471 | snp | A/G | 1.64814e-05 | 0.00287061 | missense | WDHD1 | GRCh38.p7 | 14:54991371 | CCTCCTCTTTGAGAA[A/G]ACTAGAACCAGTTTT | 11169 |
rs372099280 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010085 | TGGCCTCCCAAAGTG[C/G]TGGGATTACAGGCGT | 11169 |
rs372104723 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988117 | CATAATTTTTTTCTT[G/T]ACATCTATCTACCTA | 11169 |
rs372135321 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54950033 | GGTACCAGCCACTGA[A/G]AAAACATGCCAAATT | 11169 |
rs372197427 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54950965 | GAGAACAAAGACACA[A/G]CATACCAGAATCTCT | 11169 |
rs372212737 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54978619 | ATGAATATACTTCTT[C/T]TGATACTAAATATGT | 11169 |
rs372262461 | snp | A/G | 1.65209e-05 | 0.00287405 | missense | WDHD1 | GRCh38.p7 | 14:54987380 | TAAAGTGCAGGCAGT[A/G]AAGCTTGCTAAAAAT | 11169 |
rs372302590 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54973169 | AGTCATTTAAAAAGA[C/T]GAAATCTCTTTTTGA | 11169 |
rs372319466 | snp | A/G | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940263 | AGTAGTAGGTAGAGA[A/G]GCGGGTCTCCGAACC | 11169 |
rs372324112 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954958 | GGTCTCGAACTCCCA[C/T]CCTCAGATGATCCGC | 11169 |
rs372326293 | snp | A/T | | | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938827 | AATGCATGATTCTCG[A/T]TTGGATCCTAAACTG | 11169 |
rs372420313 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981718 | ACCAACAGAAAAATC[A/T]CTTGGAGACATAGCT | 11169 |
rs372421435 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999928 | CATCCCTTCAACTGA[A/C]TTCTTTAACCTTATG | 11169 |
rs372455485 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985353 | CTGGAGCCTGCCATG[A/C]AAACATTAGGGGAAG | 11169 |
rs372509813 | snp | A/G | 8.34941e-05 | 0.00646065 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991435 | AATTAAGGGAATCAC[A/G]AATACCAATGATTTG | 11169 |
rs372517901 | snp | A/T | 0.000205135 | 0.0101255 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957683 | GGTAGAAAATAGATG[A/T]CTTCTGACATCTATA | 11169 |
rs372544481 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55022596 | CTGAGGTAGAAAAAT[C/T]GCTTGAACCCAGGAG | 11169 |
rs372580967 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55006317 | ATGTTAAAAGTTTCT[G/T]TATATAGATCTTTCA | 11169 |
rs372590430 | snp | A/G | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027824 | TCCGTTATGAAGAAA[A/G]TAACTTGTGTTCTCT | 11169 |
rs372597323 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991195 | TACTAAGAAGTTAAG[C/T]GTAGATCCAAGTCTT | 11169 |
rs372721275 | snp | A/T | 0.119627 | 0.213314 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007266 | AAAAGAAAAGAAAAA[A/T]AAGAATCACTTACCT | 11169 |
rs372726165 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003158 | AAGCAAAGAAAAAAA[-/A]TACATACTACATTTC | 11169 |
rs372732612 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011327 | GTGAGGTCAGGAGTT[C/T]GAGACCAGCCTAGCC | 11169 |
rs372762741 | snp | A/G | 1.67472e-05 | 0.00289367 | missense | WDHD1 | GRCh38.p7 | 14:54955661 | TTTTATTAGTTTGAG[A/G]ATTTCTTTTCTGGAA | 11169 |
rs372810047 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952325 | CAATGTGCAAAAATC[A/G]CAAGCATTCTTATAC | 11169 |
rs372815544 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55007231 | AGACTCCATCTCTAA[A/T]AAAAAAAAAAAAAAA | 11169 |
rs372873421 | snp | A/G | 7.35646e-05 | 0.00606439 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995571 | AAATATTAATCAACA[A/G]GGTAATCACATGCAC | 11169 |
rs372886136 | snp | C/T | 8.23866e-05 | 0.00641767 | missense | WDHD1 | GRCh38.p7 | 14:54981660 | CCTCTGTTAAGCATT[C/T]GAACAATTCCTTCTG | 11169 |
rs372982422 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54944552 | AGTTAGTAATCAACC[A/G]TAAGTCTCTGACATC | 11169 |
rs372986548 | snp | A/G | 1.66358e-05 | 0.00288402 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000484 | TTTGAAGAAACTGTT[A/G]TACCATACTCCCTTT | 11169 |
rs373015801 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948776 | GGGCAGACTGACACC[C/T]CACACGGCCGGGTAC | 11169 |
rs373033339 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54955887 | TACACTTCAGATTCC[A/G]TGTTTTCCTTTTTTT | 11169 |
rs373053541 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988331 | TTGAATTAACTGCAA[-/A]GGGATATAAGAAAAC | 11169 |
rs373068391 | snp | A/G | 3.42501e-05 | 0.0041381 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956996 | AGACAAACAGATCCC[A/G]TGCTGCTTACTGCAG | 11169 |
rs373083832 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992055 | GGTCGGGAGTTCCAC[A/G]TTGACCAGCCTGGCC | 11169 |
rs373096698 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958674 | CCTCTCTTGACTTCT[A/G]AGATACTGCATTCCC | 11169 |
rs373104897 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967966 | TAAAAGTGAAATCAG[C/T]TCTCTTCATATTTTC | 11169 |
rs373132123 | snp | A/G | 1.65551e-05 | 0.00287702 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54962505 | TTTCTCACCTGACTT[A/G]GCTGAAACATCAGAG | 11169 |
rs373178381 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958984 | AATTCATCATCTTCC[-/T]CTCTAAATCTGCTTT | 11169 |
rs373259564 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54966340 | ACTCCGTCGCACAAA[A/C]AACAACAACAACAAC | 11169 |
rs373292712 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024172 | CATGTTAAGGGTCAA[C/T]TGTATATTTCTATCT | 11169 |
rs373309475 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55000721 | TTAGGTAAATTTTAG[C/T]TAGGAAAGAATAAAT | 11169 |
rs373435535 | snp | C/T | 4.94535e-05 | 0.00497236 | missense | WDHD1 | GRCh38.p7 | 14:54991268 | TGAAATGGCTTTTGC[C/T]GGGGAGTTGGCATGG | 11169 |
rs373466116 | snp | C/G | 1.65263e-05 | 0.00287452 | missense | WDHD1 | GRCh38.p7 | 14:54991233 | ATCTGTGAGTGAGAT[C/G]CAACGGTGTAGAACC | 11169 |
rs373485755 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951093 | ATTAAAAGAACTAGA[A/G]AAGCAAGAGCAAACA | 11169 |
rs373521682 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974260 | AACCTCGTCTCTACA[A/G]AAAAATACAAAAAAT | 11169 |
rs373558249 | snp | A/C/G | 3.35454e-05 | 0.00409534 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989005 | CAACAGTGCCAAATT[A/C/G]TTCCTAATAATCTTG | 11169 |
rs373583242 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54979465 | CTGGCCCAATAGTCA[A/T]ATTTCTTGATAAGAG | 11169 |
rs373645648 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974291 | ACAAAAAATTTGCTA[G/T]GCATGGCAGCATGGA | 11169 |
rs373645827 | in-del | -/GTTT | 0.0134861 | 0.0810011 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963367 | ATTAATGGTGGGTCA[-/GTTT]GGCAGCATTTTTATG | 11169 |
rs373660862 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024773 | TTGTTAAACAGATGC[C/T]TGAAGGCAGCATGCT | 11169 |
rs373661289 | snp | C/T | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940934 | AAAAAATCCAGGCTA[C/T]ACAAACAGACAACTG | 11169 |
rs373693701 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55022779 | AATCTGCTGTCTCTT[C/G]GTCAGCAGAAGCTGA | 11169 |
rs373695546 | in-del | -/G | 0.000876296 | 0.0209136 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007250 | AAAAAAAAAAAAAAA[-/G]AAAAGAAAAGAAAAA | 11169 |
rs373705695 | snp | G/T | 4.0373e-05 | 0.00449276 | missense | WDHD1 | GRCh38.p7 | 14:54966605 | GAACGCCAAAATTGC[G/T]CCTATAAAAGCAAAT | 11169 |
rs373721103 | snp | A/G/T | 0.000702648 | 0.0187307 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963195 | AAAAAGGGGGGGGGG[A/G/T]GGGAGATCAAATAAC | 11169 |
rs373758820 | in-del | -/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988664 | TCTGGGAGGAGTTTT[-/C]ATTTTCCGAAACTTC | 11169 |
rs373819077 | snp | C/T | 1.66421e-05 | 0.00288458 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008739 | GAACAAAAAGAGTAA[C/T]GCAAATGAATAAATG | 11169 |
rs373881665 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997332 | AACTCCTGACCTCAG[A/G]TGATAAACCCACCTC | 11169 |
rs374032422 | snp | C/T | 6.6084e-05 | 0.00574784 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55007344 | ATCACATCGTTGCAT[C/T]TTTGTAGCAGTGGCC | 11169 |
rs374048690 | snp | C/T | 3.29506e-05 | 0.00405884 | missense | WDHD1 | GRCh38.p7 | 14:54962767 | TCTGGTTTTTCTTCA[C/T]CATCAGCTTCTCCAC | 11169 |
rs374054757 | snp | C/T | 4.9507e-05 | 0.00497504 | missense | WDHD1 | GRCh38.p7 | 14:54987151 | AAAAATCTACCTCTG[C/T]GATAAACAATGAAAA | 11169 |
rs374065524 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013841 | AGCCTGGAAGGTCAA[C/G]GCTGCAAGTGAACCA | 11169 |
rs374080773 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951324 | AGGGGATATCACCAC[C/T]GATCCCACAGAAATA | 11169 |
rs374083688 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54969229 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGGT | 11169 |
rs374091472 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54953574 | TGTGGCGATTCCTCA[A/G]GGATCTAGAACTAGA | 11169 |
rs374098293 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972207 | GTGAACCCGGGAGGC[A/G]GAGCTTGCGGTGAGC | 11169 |
rs374212029 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54992056 | GTCGGGAGTTCCACG[C/T]TGACCAGCCTGGCCA | 11169 |
rs374231735 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996997 | GGGTTTCACCATGTT[A/G]GCCAGGATGGTCTTG | 11169 |
rs374239564 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982195 | TTTGTATTTTTAGTA[C/G]AGACGGGGTTTCACC | 11169 |
rs374268890 | snp | G/T | 3.84978e-05 | 0.00438719 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000660 | CTAAAAATTAAAAAG[G/T]AGGTTCTAAAAATAC | 11169 |
rs374282891 | snp | C/T | 1.65614e-05 | 0.00287757 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962467 | ACTTGCAAAATTTCC[C/T]TGATATTACAAATTT | 11169 |
rs374286575 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997361 | TCGGCCTCCAAAAGT[G/T]CTGGGATTGTAGGCG | 11169 |
rs374308456 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014453 | TCTGCAACAATAAAA[A/T]AGGGACCGTATCTTC | 11169 |
rs374322328 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972620 | ATTCACTTTCATCCA[A/T]CAGTTTGGGAATTCT | 11169 |
rs374328357 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54994338 | ATTCATAATATTGCC[A/C]TTATGCCTTTGATAT | 11169 |
rs374330307 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952076 | ATTCCCTTTGAAAAC[C/T]GGCACAAGACAGGGA | 11169 |
rs374348180 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54999057 | CCCTGGAGTTAAGAA[A/T]CTCTCTCTTTACGTC | 11169 |
rs374403513 | snp | A/T | 1.6476e-05 | 0.00287014 | missense | WDHD1 | GRCh38.p7 | 14:54987288 | GGCAGCAGCCCATCC[A/T]TGACCGAGACATATG | 11169 |
rs374414493 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54970132 | CATTACCCTTAAGAA[C/T]TGGAATAAGACAAGG | 11169 |
rs374424035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969417 | AACCAAAACTGACAA[A/G]TGGGACCTAATTAGA | 11169 |
rs374427903 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55021074 | GCAGGAGAGGCAGGC[A/G]TACTTGGTGTGACCT | 11169 |
rs374442283 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951585 | TACAAGGAGGAGCTG[G/T]TACCATTCCTTCTGA | 11169 |
rs374497720 | snp | A/G | 0.000777303 | 0.0196989 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55002157 | CTTCTATATAGCTTA[A/G]CAGATTTTTCCACAG | 11169 |
rs374511540 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962867 | AACTAAGAGAAAATA[A/G]TATTATTCAATAAAG | 11169 |
rs374538765 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54986947 | TTCCACCTTGGAATT[A/C]TCTCTATAATATAGT | 11169 |
rs374544869 | snp | A/G/T | 5.07939e-05 | 0.00503933 | missense | WDHD1 | GRCh38.p7 | 14:54941506 | TACTCCTGCTTAAAT[A/G/T]CAAAAGCTGATAGTT | 11169 |
rs374555860 | in-del | -/CTTT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54976232 | TATGAAGATGAATTT[-/CTTT]ATTTCCTTTTTATTT | 11169 |
rs374603225 | in-del | -/CA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55012600 | GCTATAAGAATCCCA[-/CA]GACTGGGTAATTTAC | 11169 |
rs374634435 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967760 | CAAGTAGCTGGGACT[A/G]CAGATATATGCCACC | 11169 |
rs374634521 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55013398 | ATAAACAAAGGTATA[C/T]CTATATTCAAAAATA | 11169 |
rs374713419 | snp | A/G | 1.64936e-05 | 0.00287168 | missense | WDHD1 | GRCh38.p7 | 14:54941662 | GTTCCTTCACTTGCC[A/G]TTTCTCCTTTGGCTT | 11169 |
rs374739662 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008528 | GTTGAGTTAGCAGAA[A/G]ATTTTTTAGAGAGTT | 11169 |
rs374848061 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54950194 | ATTAAAAGACACAGA[A/C]TGGCAAATTGGATAA | 11169 |
rs374851903 | snp | A/C/T | 1.67478e-05 | 0.00289372 | missense, intron-variant | WDHD1 | GRCh38.p7 | 14:54995756 | GAAAATCACCAGCAT[A/C/T]ACTCATATCATCTCC | 11169 |
rs374852695 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015607 | CATTCAATAAAAAAC[A/G]GAATGGATTCAGATG | 11169 |
rs374899845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994148 | GTGTTATTGTAGCAT[A/G]TAAGTTGTTACAATA | 11169 |
rs374931650 | snp | A/G | 4.99804e-05 | 0.00499877 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962587 | ATATAATGTAAATGG[A/G]GAAAATATAGTCATC | 11169 |
rs374988591 | snp | A/G | 9.9481e-05 | 0.00705199 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002042 | ATTCAGGCAAACTAC[A/G]CATTAACTGCTCCTT | 11169 |
rs375007675 | snp | C/T | 4.94393e-05 | 0.00497164 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54957127 | GGATTTCTTGGATGA[C/T]TTGCCCATATTGTCT | 11169 |
rs375070885 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998000 | GTGGATCACCTGAGG[C/T]CAGGAATTCAAGACC | 11169 |
rs375102231 | snp | A/G | 3.30224e-05 | 0.00406326 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55013502 | TCAAAGCACATGAAT[A/G]TGCCTTTTCTCCAAC | 11169 |
rs375120584 | snp | C/T | 5.09152e-05 | 0.0050453 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957670 | CTTGCTTAATAATGG[C/T]AGAAAATAGATGACT | 11169 |
rs375130166 | snp | A/C | 8.49639e-05 | 0.00651727 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957674 | CTTAATAATGGTAGA[A/C]AATAGATGACTTCTG | 11169 |
rs375131662 | snp | C/G | 3.29538e-05 | 0.00405904 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026678 | AATGTTTTAACATTT[C/G]CACCTAAAACGTTGT | 11169 |
rs375137208 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965880 | AGAATCACTTGAACC[C/T]GGGAAGTGGAGGTTG | 11169 |
rs375242949 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958575 | TCTACATTGTCAAAT[C/G]TGGTGGATACCTTTC | 11169 |
rs375248357 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024880 | CCTAGGAAAGCCAGG[A/T]ATTGTCCAAGGTTTC | 11169 |
rs375258361 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54982014 | TTATTTATTATTATT[A/T]TTTTTTTTTTCGAGA | 11169 |
rs375275484 | snp | A/G | 6.59337e-05 | 0.0057413 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000594 | GATATTCGACCACAA[A/G]TAGGATGCCATGCCA | 11169 |
rs375277001 | snp | C/T | 1.74915e-05 | 0.00295727 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955532 | CTTTTTACTTGGTCA[C/T]TGCATGCTAAATTTC | 11169 |
rs375287868 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026140 | TGTAGTCCCCAGCAA[A/G]AGAGACACACAAGTA | 11169 |
rs375376934 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55006000 | CTCCCAAGTAGATGG[A/G]ACTACAGGAATATGC | 11169 |
rs375386274 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54984531 | CAAGATCTTATACAT[A/G]AAACAATGGCTACCT | 11169 |
rs375396182 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54962296 | CCATTAAGTAAAATG[A/C]CTGACACTCAATAGG | 11169 |
rs375441329 | in-del | -/AA/T/TA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980802 | AGTGAGACTCCACAT[-/AA/T/TA]AAAAAAAAAAAAAAA | 11169 |
rs375482833 | snp | A/T | 0.000153988 | 0.00877327 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955742 | TCTAGTATAATTTTA[A/T]ATGTTTTATAAGCAC | 11169 |
rs375573634 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005542 | GGTCCTCTTCAGATT[C/T]ATGATGTAGATGCCA | 11169 |
rs375612070 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997678 | AGCACTTTGGGAGGC[A/C]GAGGTGGGCAGATCA | 11169 |
rs375617546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996681 | AAGTTACTCCTATAG[A/G]ATGCATAAAAACTAC | 11169 |
rs375626261 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975923 | ATACCACTGAGTTGG[A/G]TTAGAAAATGCATTT | 11169 |
rs375674207 | snp | C/G | 5.05804e-05 | 0.00502868 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991199 | AAGAAGTTAAGTGTA[C/G]ATCCAAGTCTTACCA | 11169 |
rs375696927 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54981071 | AGCTGAGATCACGCC[A/T]CTACAATCCAGCCTG | 11169 |
rs375700038 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54944252 | CATAAGACACCATAC[C/T]CAGCCAAAAGGCATT | 11169 |
rs375703895 | snp | G/T | 1.65647e-05 | 0.00287786 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002051 | AACTACGCATTAACT[G/T]CTCCTTATAGCCCAC | 11169 |
rs375738819 | snp | A/T | 1.6945e-05 | 0.00291071 | missense | WDHD1 | GRCh38.p7 | 14:54955676 | AATTTCTTTTCTGGA[A/T]ATAGGATGCTGCAGA | 11169 |
rs375754720 | snp | A/G | 0.476852 | 0.105063 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007255 | AAAAAAAAAAGAAAA[A/G]AAAAGAAAAATAAGA | 11169 |
rs375808453 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024386 | ATCACTTTCTCAACC[A/G]TAACATTCAGAAATG | 11169 |
rs375832046 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981708 | GTACCTAAACACCAA[C/G]AGAAAAATCACTTGG | 11169 |
rs375834361 | snp | C/T | 0.000378984 | 0.0137604 | utr-variant-5-prime, synonymous-codon | WDHD1 | GRCh38.p7 | 14:55010380 | TGTAGTGAAGCGAGT[C/T]AATATACCATCTGGA | 11169 |
rs375836368 | snp | C/G | 1.65004e-05 | 0.00287227 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944303 | CTGGGAATTCACTAA[C/G]ATCTCAATCTCGGCA | 11169 |
rs375849616 | snp | C/T | 1.65181e-05 | 0.00287381 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55002101 | AACCTACCTGAGAGA[C/T]GAAATTATCTGAAAG | 11169 |
rs375854627 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54952340 | GCAAGCATTCTTATA[A/C]ACCAATAACAGACAA | 11169 |
rs375881174 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55022386 | CCTTCCTGCCTTAAA[G/T]CTTAGTGCTCACTTT | 11169 |
rs375883952 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54950991 | TCTCTGGGACACATT[C/T]AAAGCAGTGTGTAGA | 11169 |
rs375997142 | snp | C/T | 3.37849e-05 | 0.00410991 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966448 | AGCATTTAACTTTAA[C/T]GTTTTCAGTATATTT | 11169 |
rs376096921 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003915 | TGTCTTTGCTCATCT[G/T]TCTAATGGGTTTCTA | 11169 |
rs376107153 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982163 | AGGCACCCGCCACCA[C/T]GCCCAGCTAATTTTT | 11169 |
rs376107488 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025382 | CATATGCTGAACGCT[A/G]GTTCCCCGGGTCCCC | 11169 |
rs376128944 | snp | A/C | 0.141258 | 0.225111 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966355 | AAACAACAACAACAA[A/C]AAAAAAAAACTTAAG | 11169 |
rs376263085 | in-del | -/TTAT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55006229 | AACTGACATCTTTAT[-/TTAT]ATCAAATAATTCCTT | 11169 |
rs376280112 | snp | A/G | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028764 | GCAGATTTTGCATGT[A/G]TGGTAAAAGCTTGAG | 11169 |
rs376287014 | snp | C/G | 0.021333 | 0.101051 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986755 | TAGCATAGTGACGGG[C/G]ACTGAAGAAAGACAT | 11169 |
rs376299936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964437 | CAAGGTCAGGAGATC[A/G]AGACCATACTGGCTA | 11169 |
rs376305624 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54992287 | TTTGAGGTCAGGAGT[C/T]CGAGACCAGATTGAC | 11169 |
rs376318289 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949170 | TGACTTTGACGAGTT[C/G]AGAGAAGAAGGCTTC | 11169 |
rs376331354 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55013119 | CAGTCCTAGCTGCCC[A/G]GGAGGCTGAACTGGG | 11169 |
rs376333184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970607 | AACCTTGGTTTGCAT[A/C]GAAGTCACAGCACCA | 11169 |
rs376373600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958726 | GGACCTGTGGACTCA[C/T]TGTGTTCCAATAGTT | 11169 |
rs376378614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000048 | CTGTAACCAGAAGTC[G/T]AAACTAAGACTTGAA | 11169 |
rs376405178 | in-del | -/GAG | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010810 | AGCTAGTCTCAAAAT[-/GAG]GAGAAGGCATCAGAA | 11169 |
rs376415698 | in-del | -/TAAA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019577 | TTTACTTTAAAATAA[-/TAAA]GAGTAAGGCGGGGTG | 11169 |
rs376478101 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006999 | TGTGAGGCTGAGGTG[C/T]GTGGATTGCCTGAGC | 11169 |
rs376491693 | snp | C/T | 9.88647e-05 | 0.00703012 | missense | WDHD1 | GRCh38.p7 | 14:54987272 | GCAGGGCACTAGTAG[C/T]GGCAGCAGCCCATCC | 11169 |
rs376509836 | snp | A/G | 0.000313575 | 0.0125176 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54984754 | AATCCATGCAAGGTA[A/G]GATTTCCTTGTAAGA | 11169 |
rs376509974 | snp | C/T | 3.30978e-05 | 0.0040679 | missense | WDHD1 | GRCh38.p7 | 14:54944432 | GACAAAATATTACTT[C/T]TATTTTCTTCTAACC | 11169 |
rs376521617 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54983636 | TGAGATCGCATCATT[A/G]CACTCCAGCCTGGGC | 11169 |
rs376533354 | snp | C/G | | | missense | WDHD1 | GRCh38.p7 | 14:54987344 | AGTCTATTATCCACT[C/G]TTTGCTTGAATCCCA | 11169 |
rs376589623 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54955888 | ACACTTCAGATTCCA[A/T]GTTTTCCTTTTTTTT | 11169 |
rs376613336 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54956927 | TTCCCTAGCAAGACA[A/C]TTGTAAACAATCAGA | 11169 |
rs376626394 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54941874 | GCACATTAAAGATTT[A/G]CACTACTTTTATATC | 11169 |
rs376626739 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988977 | TTAATTTCAACAACT[A/G]TATCTAACAGTTCAA | 11169 |
rs376641504 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008079 | TCATTTACAAAACTT[-/A]AAAAGTTAAATATAA | 11169 |
rs376713727 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973170 | GTCATTTAAAAAGAC[A/G/T]AAATCTCTTTTTGAA | 11169 |
rs376721448 | snp | C/T | | | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938910 | GCTATGTAATAATAT[C/T]ATCTGTTAAATTTCT | 11169 |
rs376786739 | snp | A/C/T | 8.37477e-05 | 0.00647053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957232 | CTAGTGTTAGCACTG[A/C/T]ATGTTTAAAGAAGAA | 11169 |
rs376820357 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54979061 | CATTGCCAAAAGATT[A/T]CAAAAATGCTATAGA | 11169 |
rs376822788 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002008 | GTTTTCCATTCCAAT[A/C]ATATTTAACTGCAAC | 11169 |
rs376852613 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957030 | AGGGTAGCTGAAACA[C/G]TACCTGCTTAGGCTT | 11169 |
rs376893729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006488 | ACAATTTTGCTTCCA[C/G]TTACCTTACTAAATT | 11169 |
rs376902095 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024292 | TAATCACATCCAAAC[A/G]CAAACTCAATCTCCA | 11169 |
rs376906999 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963641 | AACCCCGTCTCTACT[A/G]AAAACACAATTAGCC | 11169 |
rs376937332 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54953608 | ACCATTTGACCCAGC[A/C]ATCCCATTACTGGGT | 11169 |
rs376981093 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963199 | AGGGGGGGGGGGGGG[-/A]GATCAAATAACATCA | 11169 |
rs376990051 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951687 | CCAAAGCCTGGCAGA[C/G]ACACAACAAAAAAAG | 11169 |
rs377007221 | snp | A/G/T | 6.66017e-05 | 0.00577038 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008740 | AACAAAAAGAGTAAC[A/G/T]CAAATGAATAAATGC | 11169 |
rs377053142 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948086 | CGGTTCCAAGATGGT[C/T]GAATAGGAAGAGCTT | 11169 |
rs377063976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994475 | AATAATATAGTGCAT[C/T]TAAAATACATATTAT | 11169 |
rs377085608 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993115 | ACCAATGAATTTTTT[G/T]ATTTTATTTTGTTTT | 11169 |
rs377091056 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003751 | GTATTTTCAGTAGAG[A/C]CGGGGTCTTATCATG | 11169 |
rs377126800 | snp | A/C/G | 9.90498e-05 | 0.00703677 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000611 | AGGATGCCATGCCAG[A/C/G]CCACAAATTGCATAA | 11169 |
rs377189859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011459 | AACCCGGGAGGCGGC[A/G]GTTGCAGTGAGCTGA | 11169 |
rs377207341 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980515 | ACGGATCAATATAAA[-/A]TACTATTAGTCCAGG | 11169 |
rs377259559 | snp | G/T | 3.29506e-05 | 0.00405884 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026803 | GTTTTCCTTTACCTA[G/T]CTGAAAATGTTTTAT | 11169 |
rs377307937 | in-del | -/TA | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994918 | CTCTCTTTCATTCTC[-/TA]TGTTAGTAATTTGTG | 11169 |
rs377336516 | snp | A/G | 6.68852e-05 | 0.00578257 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941706 | CTTTGTAAAATGGCA[A/G]GAGTGAAAAGGAAAG | 11169 |
rs377348129 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54953388 | GCTCATCATCACTGG[C/T]CATCAGAGAAATGCA | 11169 |
rs377390345 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54979667 | TTGTTTAAAAATTCA[A/T]TTTATTTAACTTTTG | 11169 |
rs377413776 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54986673 | GTCATGAGAAGAAGG[C/T]ATTTTCAATGGAATT | 11169 |
rs377432428 | in-del | -/AATT | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955301 | TAAAAACAAACAAAA[-/AATT]AATTACAAAATATAA | 11169 |
rs377477139 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975548 | AGACAGGGTTTCACC[A/G]TGTTGGCCAGGATAG | 11169 |
rs377481620 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940828 | TATGGTAGTAAATAT[A/G]TATTTTCTAGAAATA | 11169 |
rs377540562 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54968739 | TATTATGAACACTTC[C/T]ATGTGCACAAACCAG | 11169 |
rs377545579 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951224 | GCTGGTTTTTTGAAA[A/G]GATCAATAAAACTGA | 11169 |
rs377599332 | snp | A/G | 0.00138504 | 0.0262793 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007245 | ATAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 11169 |
rs377620212 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54969314 | TACAGGCGTGAGCCA[C/T]CGCGCCCAGCATTAA | 11169 |
rs377622390 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951555 | GATGGATTCACAGCC[A/G]AATTCTACCAGAGGT | 11169 |
rs377629774 | snp | A/G | 0.000434042 | 0.0147252 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013628 | CAAATTAAAGTCATC[A/G]GGCATGGTGTCTCAT | 11169 |
rs377638427 | snp | C/T | 3.29957e-05 | 0.00406162 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000511 | CTTTTACCTTACTGC[C/T]TGATGTCTTTCCACT | 11169 |
rs377641986 | snp | C/T | 1.65608e-05 | 0.00287752 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962482 | TTGATATTACAAATT[C/T]ATAAATATTTCTCAC | 11169 |
rs377648009 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54964079 | TGCCACTGTACTCTA[C/G]CCTGGGTAACAGAGT | 11169 |
rs377652098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996221 | ATACTGCATAAGATA[C/T]ATTTTCTTTATATTA | 11169 |
rs377700079 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54986492 | CTGGTCCAGAATCTA[C/T]GAATCTATTTCTTAC | 11169 |
rs377700717 | snp | A/C | 1.71581e-05 | 0.00292895 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002227 | CAAAAGTTTACATTA[A/C]ATTGAATTTGAAGAA | 11169 |
rs377710496 | snp | G/T | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028936 | AGATACTCATGGATG[G/T]ATAAAAGTAATTGTT | 11169 |
rs377731895 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55004546 | CAACCTCCGCCTCCT[C/G]GGTTCAAGCAATTCT | 11169 |
rs386381423 | in-del | -/AA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54966187 | AAAAAAAAAAAAAAA[-/AA]ATTAGCTAGGCGTGG | 11169 |
rs386777705 | multinucleotide-polymorphism | ACCTGTGTAGCCTTG/TCCTGTGTAGCCTTC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54942352 | AATAATACAGAAAGA[lengthTooLong]ACCCAGTTTTCCCCA | 11169 |
rs386777706 | multinucleotide-polymorphism | AAG/CAT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54984310 | GACCAGCCTGGGCAA[AAG/CAT]GGCAAAACCCTGTCT | 11169 |
rs386777707 | multinucleotide-polymorphism | AA/GG | | | upstream-variant-2KB, utr-variant-5-prime | WDHD1, SOCS4 | GRCh38.p7 | 14:55027372 | ACGAGGTGCAGGAGT[AA/GG]TTGGGCCTCCCCTCT | 11169 |
rs397803499 | in-del | -/A | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939598 | TGGAAAAAAAAAAAA[-/A]GAACACTGGAAAAAA | 11169 |
rs397838560 | in-del | -/TA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54973050 | TGATTTATATATATA[-/TA]GAACTCTTTCAACTT | 11169 |
rs397956863 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988241 | TTTCCGTTTTTTTTT[-/T]CCTTTCTCGAAGAGA | 11169 |
rs398025131 | in-del | -/T | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955915 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCAC | 11169 |
rs398025133 | in-del | -/A | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977925 | TGGAAAAAAAAAAAA[-/A]GCATGTTAAGAAAAA | 11169 |
rs398025134 | in-del | -/T | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997113 | TTTTTTTTTTTTTTT[-/T]GACACAGAGTCTCAC | 11169 |
rs398099361 | in-del | -/AA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996733 | TATAGTTTGGTATAA[-/AA]GTCTAATGAGAACAC | 11169 |
rs527237595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026926 | CGGTTTCCCCCACCC[A/G]AGTGACACCAGCGGG | 11169 |
rs527270106 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953850 | AACTGGGAACCATCA[C/T]TCTCAGCAAACTATC | 11169 |
rs527397607 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024366 | TGTTATTTGCAAGTG[C/G]AAGCATCACTTTCTC | 11169 |
rs527400315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949178 | ACGAGTTGAGAGAAG[A/G]AGGCTTCAGACGATC | 11169 |
rs527402019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943967 | CAAAAACAAAACAAA[A/G]AACCCATCACCATTA | 11169 |
rs527411722 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55027113 | CTGCGCCTGCGCCGA[A/C]CCGCCCACGCCCAGC | 11169 |
rs527463989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013212 | AAAAAAAAAAAAAAA[A/G]AAAAAATTGGTGGGG | 11169 |
rs527519448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013663 | ATAATGCTAGCACTT[C/T]GGGAGTACAAGGTGG | 11169 |
rs527525245 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006439 | TTGTATACAGGATAA[C/G]AATCCTGTATTTGTA | 11169 |
rs527554435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959149 | GCTGAGGAGGGAGGA[C/T]TGCTTGAGCCCAGTT | 11169 |
rs527587193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999735 | CTGAGTAGGAGCATG[A/G]AACTACAGGCACACA | 11169 |
rs527612624 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959728 | AGCTAGGACTGCATC[A/G]CTGCACTCCAACTCT | 11169 |
rs527630980 | in-del | -/CATGAGCCAC | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983798 | TGCTGGGATTATAGG[-/CATGAGCCAC]CATGCCCAGCCAAAA | 11169 |
rs527702125 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979275 | TCCCCTCTTAGCCTC[A/T]CAAGTAGCAGAGACT | 11169 |
rs527703975 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987470 | CAATCATGATATTCA[A/G]CAAAAAAACCAAATA | 11169 |
rs527735796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018585 | GTGAAGACCCTATTA[C/T]TGAAGAAGTGTACCC | 11169 |
rs527765013 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979914 | ATTTCACTTAACACA[A/T]CTTGCAGATTTTTCT | 11169 |
rs527828916 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972454 | GTGGTGGTGAACGCC[G/T]GTAATCCCAGCTACT | 11169 |
rs527850373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998298 | ATTAGCCCAGCTAAT[C/T]TTTGTATTTTTAGTA | 11169 |
rs527850661 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005712 | TTCCCTTTAAGTTAC[C/G]ATGGGAATCCAGAAC | 11169 |
rs527872319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958214 | TCACTGCAAAGTCCA[C/T]CTCCCAGGTTCAGGC | 11169 |
rs527879546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952342 | AAGCATTCTTATACA[C/G]CAATAACAGACAAAC | 11169 |
rs527881020 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948950 | AGGGTCCTGACTGTT[A/G]GAAGGAAAACTAACA | 11169 |
rs527905491 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998957 | TAATCCTCCCAATAA[A/C]CCCAAGTGGTTGGCA | 11169 |
rs527922117 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992348 | TACAAAAATTAGCCT[G/T]GCATGGTGGCGGGCA | 11169 |
rs527976057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993158 | GGTCTCGTTCTGTTA[C/T]CCTGCCTGGAGCCCA | 11169 |
rs528041060 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54953627 | CCATTACTGGGTATA[C/T]ACCCAAAGGATTATA | 11169 |
rs528076906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970584 | AATGACCATACTGTG[C/T]CTGCAGCAACCTTGG | 11169 |
rs528079592 | snp | C/T | 0.000166 | 0.00910892 | missense | WDHD1 | GRCh38.p7 | 14:54963126 | TTTTGAGTCATTAGA[C/T]CAGCAAGTTCCACAC | 11169 |
rs528131504 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011825 | CATAGTATTCCATTA[G/T]ATGGCTCCACCAAAA | 11169 |
rs528172396 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54979825 | TTTCATTCTTCTAGG[A/T]ATTCTTTTGCGTATG | 11169 |
rs528197220 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005160 | CTTCCTGGATCGGCA[A/T]CCACCACATCAATCC | 11169 |
rs528245292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991530 | ATTTGCCTCTTTCAC[C/T]GTGTTAAAGAGATGC | 11169 |
rs528249493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006101 | ACTCCTGAGCTCAAG[C/T]GGTCCTCCTGCCTCA | 11169 |
rs528250502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947151 | TCAAGACCAGCCTGA[A/C]CAACATGGAGAAACC | 11169 |
rs528305881 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941310 | AATCTGCAAAGATGA[C/T]AGTTTTTACATATGT | 11169 |
rs528308941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984969 | TTACTAGACTGACTA[A/G]CACTACTTTTTATGA | 11169 |
rs528343510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024052 | ATATTTCTAGGCTAC[A/G]TGGTTCGTCTGCTAG | 11169 |
rs528363918 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55001390 | CTCAGCCTCCCAGGT[A/T]GCTAGGGCTACAGGC | 11169 |
rs528400309 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017015 | ATAGAAAATCGCCCG[C/T]ATTAATTCCAATAAT | 11169 |
rs528414982 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978233 | AACTAACTAGATTCC[A/T]GAAAATGGACATGCA | 11169 |
rs528427378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969907 | AACATATGCAAATCA[A/G]TATATGCAATTCACT | 11169 |
rs528439470 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996656 | TAAGCAGATACACTG[A/C]AAAGATCCCAAGTTA | 11169 |
rs528596769 | snp | C/T | 4.95561e-05 | 0.00497751 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54991237 | GTGAGTGAGATGCAA[C/T]GGTGTAGAACCTGAC | 11169 |
rs528601859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946646 | GTGCCACCACACACA[C/T]CTGGCTGATTTTAAA | 11169 |
rs528685386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968759 | GCACAAACCAGAAAA[C/T]TTAGAGGAAATGGGC | 11169 |
rs528700910 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016042 | TGCACTGGAGGAGAC[G/T]TACAAAGTTACAGGT | 11169 |
rs528701072 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009645 | CTGTGTTGGCCAGGC[C/T]GGTCTTGAACTCCTG | 11169 |
rs528743357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969316 | CAGGCGTGAGCCACC[A/G]CGCCCAGCATTAAGA | 11169 |
rs528763094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961828 | CTCCCTGTACGCAAC[C/T]ATTTTCAACTCCTTT | 11169 |
rs528782165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003381 | CAGCCATTGTGGGCG[C/T]GTGCCTCTAGTCCCA | 11169 |
rs528824775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955422 | GTGGCTTCCTTATAG[C/T]CACAAGTGTCCAGAA | 11169 |
rs528853867 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012527 | TGAAACATTCCCGTT[G/T]TCTAGAACAATTCCT | 11169 |
rs528863605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005180 | CACATCAATCCCACT[C/G]AGTGAGCTCCCTTGC | 11169 |
rs528863910 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951952 | ACAACGCTTCATGCT[-/A]AAAAACTCTCAATAA | 11169 |
rs528893309 | snp | C/T | 1.70194e-05 | 0.00291709 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957677 | AATAATGGTAGAAAA[C/T]AGATGACTTCTGACA | 11169 |
rs528894510 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964436 | ACAAGGTCAGGAGAT[C/G]GAGACCATACTGGCT | 11169 |
rs528976860 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016001 | ACCACACCCAGCCCC[A/G]ATGGGCTTCTTGGTG | 11169 |
rs529021079 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960757 | GTGCTCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 11169 |
rs529056060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977727 | CAGGAGCTACTAGTA[C/T]AGACGGTTTCTAAAA | 11169 |
rs529131575 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54959122 | AAGCCTGTAATCCCA[A/G]CACTTTGGGAGGCTG | 11169 |
rs529184592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970682 | CCCCAAAGCAATCTA[C/T]AGATTCAACACTATT | 11169 |
rs529196091 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011893 | TGTTTCCGACATTTG[C/T]TATTGTTATGAATTG | 11169 |
rs529217600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997681 | ACTTTGGGAGGCCGA[A/G]GTGGGCAGATCACGA | 11169 |
rs529248008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971368 | GATTACTTGAGCCCA[A/G]GAGTTTGAGACCAGC | 11169 |
rs529252538 | in-del | -/AATA | 0.0166325 | 0.0896639 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019575 | GATTTACTTTAAAAT[-/AATA]AAGAGTAAGGCGGGG | 11169 |
rs529255225 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54943985 | CCCATCACCATTACA[C/T]AATAATTACTACATA | 11169 |
rs529320389 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991672 | GCAGTAAAAATATTA[A/T]TTTTATTAAATCTTG | 11169 |
rs529369834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024129 | TTGAAAAAAATCCAC[A/G]TATAAGTAGACATAC | 11169 |
rs529384833 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985070 | AAAGTCCTTATAAGT[A/G]GGCATTTATTCACTC | 11169 |
rs529389576 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947679 | TCATTGCAGCCTCCG[C/T]CTCCTGTGTTCAAGC | 11169 |
rs529393124 | snp | A/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941399 | AAACTCTTTAAAAAA[A/T]ATATATATAATGAGT | 11169 |
rs529463381 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54994152 | TATTGTAGCATGTAA[A/G]TTGTTACAATAAGCA | 11169 |
rs529469163 | snp | A/G | 3.38616e-05 | 0.00411456 | utr-variant-5-prime, synonymous-codon | WDHD1 | GRCh38.p7 | 14:55010446 | ATTAGAAACTGCAGT[A/G]ACCAGTTTTCCACTC | 11169 |
rs529487960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004141 | TAGTAAATACCTATA[C/T]ATAGACTCATCATGT | 11169 |
rs529548532 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996993 | GATGGGGTTTCACCA[G/T]GTTGGCCAGGATGGT | 11169 |
rs529553874 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54964836 | GAGAAACACTGCCAC[A/G]GGGAAAAGCTCCTCT | 11169 |
rs529580968 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955979 | CTCGGCTCACTGCAA[A/C]CTCCACCCTCCGAGT | 11169 |
rs529599901 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972147 | AGGCGTGGTGATGGG[C/T]GCCTGTAGTCCCAGC | 11169 |
rs529607397 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020859 | ATACTGTATCTGTAC[A/T]ATACAGCAATATAGA | 11169 |
rs529617989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003347 | AGACCCTGTCTCTAC[A/G]AAAAATAAAAAAATT | 11169 |
rs529647974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950921 | ATAACGAAATGAAGG[C/T]AGAAATAAAGATGTT | 11169 |
rs529665013 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984116 | AGACACAACTTATTA[G/T]TGATTTGTATCACCT | 11169 |
rs529685873 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974178 | GTAATCCCAGTACAT[-/A]AAGGAGGCTGAGGTA | 11169 |
rs529687435 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940571 | TCTGCTTAGAAAACC[A/C]AAAATGTATGACATG | 11169 |
rs529709551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015502 | ACATGGTTAAATCTG[C/T]AAAATGACTAGTGAT | 11169 |
rs529728437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976457 | ATGCTTTGGCCTCCC[A/G]ATGTGTTGGGATTAC | 11169 |
rs529741283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968900 | TTTAAAGATTAGCCA[A/G]GTGTGGTGGTGTGTA | 11169 |
rs529817831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996108 | TTTTATTCCTCAGAA[A/G]TCATTCCCTAGAAAA | 11169 |
rs529882276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989773 | CAAGTGATTCTCCTC[C/T]CTCAGCCTCCTGTGT | 11169 |
rs529895286 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950060 | AATTGTAAAGACCAT[C/T]AAGGCTAGGAAGAAA | 11169 |
rs529903112 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945416 | CACTATGAGATGGAT[A/T]CAGTTATTATCTCCA | 11169 |
rs529928338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996508 | GCGAGGCTGAGGTAG[G/T]AGGGTCACCTGAACC | 11169 |
rs529935634 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958237 | GTTCAGGCGATTCTA[A/C]TGTCTCAGCCTCCCG | 11169 |
rs530021386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945814 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACTG | 11169 |
rs530117753 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967824 | TGGGGTTTTGCCATG[A/C/T]TGCCCAGGCTGGACT | 11169 |
rs530138674 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55006602 | AACATTCTCTTTCTT[C/T]CTTTCAAATTTCTCA | 11169 |
rs530179907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960853 | CACCCAGGCTGGAGT[A/G]CAGTGGTGCAACCAT | 11169 |
rs530200790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950895 | CCTGCTCCTGAATGA[C/G]TACTGGGTACATAAC | 11169 |
rs530220861 | snp | C/T | 0.000101196 | 0.0071125 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002199 | AACTATTAGAAAAGA[C/T]AAACAACGTAAACAA | 11169 |
rs530237511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020952 | GTAGATCATCATAAA[C/G]GTCTTCATCCTTATC | 11169 |
rs530263029 | snp | A/T | 0.00438332 | 0.0466095 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938586 | TGATGAAACCCATCT[A/T]TGTAAAAAAATACAA | 11169 |
rs530278332 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980794 | GGGTGACAGAGTGAG[A/G]CTCCACATAAAAAAA | 11169 |
rs530282869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020848 | CTATGTATTATATAC[C/T]GTATCTGTACAATAC | 11169 |
rs530311976 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54949090 | AATTCTAAAAATCAG[A/C]GCACCTCTCCCCCCC | 11169 |
rs530339955 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981837 | AAATAATCTAAGATT[A/T]TTACGTAAAATTTCA | 11169 |
rs530374965 | snp | C/G | 1.6486e-05 | 0.00287102 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967232 | AGTGTGTGTATCACA[C/G]GTGCTGTATTATCAA | 11169 |
rs530441083 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002967 | TGAGGAAAATAAAGA[A/C]AGAATCCTTCAAATA | 11169 |
rs530473147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010537 | CCATAGTTAAAAATC[C/T]GGTAAAAAACAAAAA | 11169 |
rs530487682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969812 | CTCAACAAAACACTA[A/G]CAAACCAAACCCAAC | 11169 |
rs530532264 | in-del | -/AAA | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943843 | AGAGGTTGTCTCTAT[-/AAA]AAAAAAAAAGAGGAC | 11169 |
rs530548153 | snp | A/T | 1.65244e-05 | 0.00287436 | missense | WDHD1 | GRCh38.p7 | 14:54963094 | GAGAAGCATATTTAA[A/T]GGCTAAATTCACAGC | 11169 |
rs530570643 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016944 | CATAGACAGCAAAAG[A/C]ACTTTCAAACAGTTA | 11169 |
rs530604126 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54955918 | TTTTTTTTTTTTTGA[C/G]ACGGAGTCTCACTCT | 11169 |
rs530616726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950777 | GCAAATGTAAAAGAA[C/T]AGAAATTATAACAAA | 11169 |
rs530633795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983518 | TCTCTATTAAAAATA[C/T]AAAAATTAGCCGAGT | 11169 |
rs530678314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946525 | GGGTCTTGCTTTGTC[A/G]CCCAGGCTGGAGTGC | 11169 |
rs530679345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990329 | CAGGCCAGGCGCGGT[A/G]GCTCACGCCTGTAAT | 11169 |
rs530681843 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996937 | GCTGGGACTACAGGC[A/G]CATGCCACCATGCCC | 11169 |
rs530734562 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008156 | ACGTATTTATTTGGC[A/C]CTAGAATACTGTGGA | 11169 |
rs530758192 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54964720 | TTTGCCCGGGGGTCA[C/G]GAATGCTAAAGAAGA | 11169 |
rs530760117 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005711 | TTTCCCTTTAAGTTA[C/T]GATGGGAATCCAGAA | 11169 |
rs530782470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002384 | CAAGGGATCTTCCTG[C/G]CTCAGCCTCCTAAGT | 11169 |
rs530891803 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990770 | ACATTCTGGTGGGTG[G/T]TGGAGTGAGGAAAAG | 11169 |
rs530945320 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961822 | GGCCCACTCCCTGTA[C/T]GCAACCATTTTCAAC | 11169 |
rs530949235 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950176 | AATGGGCTAAATGCT[A/C]CAATTAAAAGACACA | 11169 |
rs530996359 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021574 | GTTTTTGGTAGAGAC[C/T]GGGGTCTCATCATGT | 11169 |
rs531022155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996581 | CTCCAGCCTGGGTGA[C/T]AGAGTGAGACCCTGT | 11169 |
rs531048981 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55014577 | CAACTATCCAAACGT[A/G]TTTCAAATAACCATC | 11169 |
rs531053755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014606 | TCTGTATCTATCATA[A/G]CTTGTTTTAAACTTA | 11169 |
rs531125994 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939191 | TCTGATAATAAAACA[G/T]ATGGGAAACAAAGAG | 11169 |
rs531148891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974943 | TGTCTTCTGCATTTG[A/G]GGGGACTTTGCTCAC | 11169 |
rs531154790 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969245 | GGGTTTCACCGTGGT[A/C]TCGATCTCCTGACCT | 11169 |
rs531185279 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975102 | GTGAACACAACTAGG[-/A]AAAATGTCTAGTTTT | 11169 |
rs531205561 | in-del | -/GT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55021664 | GTGCTGGGATTACAG[-/GT]GTGAGCCACCGCGCC | 11169 |
rs531214265 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967901 | GTTGGGATTACAGGC[A/G]TGAGCTACCCTGCCC | 11169 |
rs531265449 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027811 | GCGACTCTATATATC[C/T]GTTATGAAGAAAGTA | 11169 |
rs531269148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944650 | TTTGAGACAGAGTCT[C/T]ACTCTGTCACCCAGC | 11169 |
rs531287126 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981884 | AGACCTAACTAAAAA[A/C]AGAAAAAACATTGGA | 11169 |
rs531417925 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959790 | TGTATCCGCACCCCC[A/C]CCACCAAACAAAAAA | 11169 |
rs531423143 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998993 | CCTATCTTTTTACAC[A/T]TACAGTATATTATGA | 11169 |
rs531456042 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945203 | CCCTTGCTCTCAGAG[A/C]TGACCTGCATCAGCA | 11169 |
rs531476219 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974487 | CCACAAAACCTGTTT[C/T]GTTTTGTTTTTTTTT | 11169 |
rs531479824 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54978728 | TTCTCTACTAATTCA[A/G]TTTTGCATCCTCTGA | 11169 |
rs531486520 | snp | A/C | | | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938579 | GGCAACATGATGAAA[A/C]CCATCTATGTAAAAA | 11169 |
rs531495810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001194 | TTATTTTCTAACCTC[A/C]CTTTTCAATAACATT | 11169 |
rs531497592 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994626 | ATTAGCCAGGCGTGG[C/T]GGCGCATGCCTGTAA | 11169 |
rs531557888 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979975 | AACAGCTTTGTCAAG[A/G]TATGATTCACATAAT | 11169 |
rs531607157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960294 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 11169 |
rs531617586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972486 | GGGAGGGTAAAGCAC[A/G]AGAATCTCTTGAACC | 11169 |
rs531668501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954403 | ACTCATATTGCTAAA[A/G]GTGTATAAAATGATA | 11169 |
rs531676517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973220 | ACTTAATTTATAGTA[C/T]AGCCTTTTAATCAGG | 11169 |
rs531720172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013710 | CAGGAGTTCAAGACT[A/G]GCCTGGATAATACAG | 11169 |
rs531723782 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019589 | TAATAAAGAGTAAGG[C/T]GGGGTGTGGTGGCTC | 11169 |
rs531723801 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55027030 | AGTGGGGACTCACCC[A/G]GGTGACCGAGCCTCC | 11169 |
rs531825257 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947369 | AAACCATGAGCCACT[A/G]TGCCCGGCCTATCAA | 11169 |
rs531844650 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948571 | TGGACTCCACCTCTG[C/G]GGGCAGGGCATAGCC | 11169 |
rs531859309 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971115 | ACACTTAAATGTAAG[A/G]CCTCAGAATATAAAA | 11169 |
rs531905544 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987554 | GAAATACCCTTAAAA[C/T]GAACTATATTGATAT | 11169 |
rs531915713 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943181 | TCTAACTGAGAGATT[C/G]TGCCTTCCTTCCTTC | 11169 |
rs531932695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989614 | AACAACAGACTTTTT[C/T]CCTAACTATTCTATG | 11169 |
rs531964358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986753 | CTTAGCATAGTGACG[C/G]GGACTGAAGAAAGAC | 11169 |
rs531992766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982445 | TTAGTACTCTTCTTC[C/T]TCTCTCTTCTTTTTG | 11169 |
rs531997617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942751 | CCCACTCCTACTTTA[C/T]TTCCCTGGCCATTTC | 11169 |
rs532055693 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996956 | GCCACCATGCCCAGC[C/T]AATTTTTGTATTTTT | 11169 |
rs532058365 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951180 | GATAGAGACACAAAA[A/C]AGCCTTCAAAAAATC | 11169 |
rs532066248 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021612 | GCTGATCTCAAACTC[C/G]TGACCTCAAGTGATC | 11169 |
rs532069259 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026389 | TCATTCCAAACAGAA[C/G]AGGCCACTGAATTTG | 11169 |
rs532090478 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014731 | ACAAAAATAACATAT[A/T]ATAAACAGCAAAAAA | 11169 |
rs532164555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960750 | ACCTCAAGTGCTCCA[C/T]CTGCCTCGGCCTCCC | 11169 |
rs532182277 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001587 | ATTTTCAAAGCAAAA[A/C]CTAAAAAATGTTATT | 11169 |
rs532183878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945751 | TCACCATATTGGCCA[A/G]GTGGGTCTCGAACTC | 11169 |
rs532196743 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954453 | TCTGGCATTGGAATT[A/G]TAAGTGCAGATTAAC | 11169 |
rs532250022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022047 | CTAGAGGTTGAATTC[A/G]AGACATTGTGTTTGG | 11169 |
rs532255897 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54959015 | TCTCTAGTGTTTCCT[C/G]ACTTAGGAAATGGCA | 11169 |
rs532268929 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939905 | ATTATAAAATATATA[C/T]AAAGCAAGTTGAGGA | 11169 |
rs532319203 | snp | C/G/T | 3.30154e-05 | 0.00406286 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55008705 | ATCACATCCACAATT[C/G/T]TGACTAGAAAATCAC | 11169 |
rs532373613 | snp | C/T | 4.96874e-05 | 0.0049841 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002045 | CAGGCAAACTACGCA[C/T]TAACTGCTCCTTATA | 11169 |
rs532435922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996015 | CTTATTTCAAATGCC[G/T]TGTAGTCTGGGGATG | 11169 |
rs532437668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967074 | CAGTCACACCCATTT[A/G]CTTTGTAGACAAAGT | 11169 |
rs532452201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949519 | AAAAGACCAAATCTA[C/T]GTTTGTTTGGTGTAC | 11169 |
rs532457532 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027646 | GAAAAGAAGGCGAGA[A/T]CTTCTAGAGCCTCTA | 11169 |
rs532463422 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944767 | TGGGATTACAGGCAT[A/G]CGCCACCACACCTGG | 11169 |
rs532495552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960328 | GCCTGTCACCATGCC[C/T]GGCTAATTTTTATGT | 11169 |
rs532521363 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020743 | AGTCAAAAATCCACA[G/T]AGAAGTTTTGATTAT | 11169 |
rs532528183 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013774 | AGCCAGGCATGGTTA[C/T]GTGTACCTGTAGTAC | 11169 |
rs532543211 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948952 | GGTCCTGACTGTTAG[A/C]AGGAAAACTAACAAA | 11169 |
rs532566985 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943252 | CTAATTTCCATGTGA[A/C]AGGCTGGAACAGAAC | 11169 |
rs532577431 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985799 | TTCCATAGAATTGAC[A/G]TGATGATATAATTTT | 11169 |
rs532598764 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014137 | GGCAGAGTCTCATTC[C/T]GTTGCCTAGGCAGTA | 11169 |
rs532651325 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55027062 | CCACTGAGGATCCAC[A/G]AGAGCTGCTTCCCGC | 11169 |
rs532663756 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007942 | AGGCTGCATTTGAAT[A/C]AACTGTATATGTGAC | 11169 |
rs532755360 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980089 | CAACACTTTGGGAGG[C/G]CGAGGCGGGAAGATC | 11169 |
rs532769020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988149 | TTACTTACCTACCTA[C/T]TTATCAAAACATGTA | 11169 |
rs532781646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958873 | AAATTGCTATACTTA[C/T]GCCAATGATTTTCAC | 11169 |
rs532823822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999604 | TAGCCTCCACTTTTT[C/T]ATTTTTATTTTTTAG | 11169 |
rs532826781 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54953402 | GCCATCAGAGAAATG[C/T]AAATCAAAACCACAG | 11169 |
rs532838238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953308 | AATCAAAAAGTGGGC[A/G]AAGGATATGAGCAGA | 11169 |
rs532872678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019957 | ATAACCTCAAGGAGT[C/T]AATGATTACCAACGC | 11169 |
rs532932075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952913 | GTGCTGGGAAAACTG[C/G]CTAGCCATATGTAGA | 11169 |
rs532945064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956232 | AGCCACTATTAAATA[C/T]GAATATACATCAGAA | 11169 |
rs532983913 | in-del | -/AA | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55027062 | CCACTGAGGATCCAC[-/AA]GAGCTGCTTCCCGCG | 11169 |
rs533001800 | in-del | -/AAAT/AAATAAAT | 0.164701 | 0.235618 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942263 | AAAAAATAAATAAAT[-/AAAT/AAATAAAT]AAATAAATAAATAAA | 11169 |
rs533005392 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012572 | CAGTAGGTGTTTTAG[C/T]CTGTTCTGTACTGCT | 11169 |
rs533099374 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54982319 | CGGCCGATAATAATT[C/T]TAAAGCCAATTTTAG | 11169 |
rs533109602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992278 | GGTAGATCATTTGAG[A/G]TCAGGAGTCCGAGAC | 11169 |
rs533166563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971475 | TTGTGCAATCCCATT[C/T]ACAATAGCCATATGC | 11169 |
rs533246416 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986616 | AAAAGTAAAAAGGGA[G/T]CTGCCAGTGAGGAAA | 11169 |
rs533269343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005891 | TATTTTTAAGGCAGG[A/G]TTTTGCTTTGTTGCC | 11169 |
rs533272547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017718 | GGAATTACAATTCAT[A/G]ATTCTATCCAAATGA | 11169 |
rs533281849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958423 | TGAGCCACCACGCCC[A/G]GTCATCCAGCCAAAT | 11169 |
rs533364754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947744 | TTACAGGCATGAGCC[A/G]CCATACCTGGCAAAC | 11169 |
rs533375042 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997488 | GTTTCTAAATCCATA[C/T]ATTGAAAAATACTTG | 11169 |
rs533427771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941935 | TTAGTTGCAAAATAC[C/T]ATAATTGCAGTACTA | 11169 |
rs533436699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991753 | GTGATGGTTGTCTTG[A/T]AAAAAAGCACTTATG | 11169 |
rs533442207 | in-del | -/T | 0.427819 | 0.185732 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993748 | CACTCTTCTCACTAA[-/T]TTTTTTTTGTTTTTC | 11169 |
rs533450159 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962612 | GTCATCCTCAATATA[C/T]AACAACCAGATAGCA | 11169 |
rs533466575 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942331 | GTTTCACATGCAGTT[C/G]TATGAAATAATACAG | 11169 |
rs533508214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971008 | GAATCCCTACTCAAT[A/T]AATGGTGCTGAGATA | 11169 |
rs533542174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025946 | ACTTGTCCAAAGAAG[C/G]CTTCCCTGACTCCTT | 11169 |
rs533560283 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956979 | ACAGTGAACAAAACT[A/G]AAGACAAACAGATCC | 11169 |
rs533607896 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020630 | CTCACATTTATATTC[-/T]TAGCCAGAACCTCAA | 11169 |
rs533608416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026628 | TATCCGCATGAGTCA[C/T]TTTTAGCTGACTGCA | 11169 |
rs533625924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951738 | CTGATGAACATCGAT[A/G]CAAAAATCCTCAGTA | 11169 |
rs533637717 | in-del | -/A | 0.00206569 | 0.0320714 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974092 | CTGGAAGAGGAATTT[-/A]AAAAAAAAAAAACAA | 11169 |
rs533658786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995128 | CTGGGATTACAGGCA[C/T]GTGCCACCACACCCA | 11169 |
rs533717508 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006048 | TTTCATTTTTTTGTG[C/G]AGACGAGGTCTTGCT | 11169 |
rs533736019 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965561 | GTGGTTCTCAGTTAC[A/C]TTGAGAGCCCGTTAA | 11169 |
rs533748019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994098 | AGATTTTCAATTACA[A/G]TCTCAATTTCTTCAT | 11169 |
rs533787142 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999277 | TAACCAGTGTCCCTA[C/G]ACCAAGGACAGTCTA | 11169 |
rs533805988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987751 | CTTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 11169 |
rs533853555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943300 | AAGGAATAGTCTCAT[C/G]TAGTATTTAATGTGT | 11169 |
rs533854242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993338 | TTGCCCTGGCTGGTC[C/T]TGAACTCCTGGCCTC | 11169 |
rs533873575 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948304 | TTCCCTTTCCTAGCC[A/C]AGCAAAGCTGTGACA | 11169 |
rs533895651 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978597 | CTCTAAAAAAAAAAA[A/C]CCGTTAATGAATATA | 11169 |
rs533933042 | in-del | -/C | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028422 | TGACCTAATTTTTTT[-/C]TTTTTGGAGATCATT | 11169 |
rs533933123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017731 | ATGATTCTATCCAAA[C/T]GAGCTGCAAGATAAC | 11169 |
rs533968069 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998694 | TCCATCTATGGCAGA[C/T]GAGGATCTGGTACCC | 11169 |
rs533970146 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015031 | TAATGCCAGAGTAAG[A/G]TGGTTAGGCTCCCTT | 11169 |
rs533983500 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952529 | CATTCCACGCTCATG[A/G]ATAGGAAGAATCACT | 11169 |
rs534018964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964041 | AGAGCCCAGGAGGTT[A/G]AGGCTGCAGTGAGTT | 11169 |
rs534043212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005419 | TCCAGTGGCAGCAGC[A/G]AACTTCAGCATGGCC | 11169 |
rs534045108 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012630 | ACAATGAACAGAAAT[A/T]TATTGTCTCATGATT | 11169 |
rs534049366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952989 | TCCAGATGGATTAAA[C/G]ACTTAAATGTTAGAT | 11169 |
rs534106109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991854 | ATGCCAGATAAACTA[C/T]GGTTATGCAGAATTG | 11169 |
rs534123681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947374 | ATGAGCCACTATGCC[C/T]GGCCTATCAATTTTC | 11169 |
rs534124597 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55018933 | GAGGCTGAGGCAGGA[A/G]AATTGCTTGAACCTG | 11169 |
rs534130690 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55013702 | CTTGAGGCCAGGAGT[A/T]CAAGACTAGCCTGGA | 11169 |
rs534157919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970452 | AGGAATATATCTAAC[C/T]AAGGAGGTGAAAGAT | 11169 |
rs534220919 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977845 | TATCGTAGTTTTTAA[C/G]AAGTTAAAATTCTTT | 11169 |
rs534252071 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024876 | TCTGCCTAGGAAAGC[A/C]AGGTATTGTCCAAGG | 11169 |
rs534265070 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55009056 | CACCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 11169 |
rs534327546 | snp | C/T | 1.65321e-05 | 0.00287502 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981527 | CAACTTTAGACTTCT[C/T]TTAATAGCCCACCTT | 11169 |
rs534335533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957888 | TATCTTCTGTTACTG[C/T]GGAAGAGTGGCAGCT | 11169 |
rs534420855 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | WDHD1 | GRCh38.p7 | 14:54991346 | ATGCTGCCTTCTTGA[C/T]CATCTTCCTCCTCCT | 11169 |
rs534422213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997866 | CAGTGAGCCGAGATC[A/G]CGCCATTGCACTCCA | 11169 |
rs534450581 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951937 | CTGTGACAAAATTCA[A/G]CAACGCTTCATGCTA | 11169 |
rs534503102 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941979 | CTTTTGGCCAGGCAC[A/G]GTGGCTCATGTCTGT | 11169 |
rs534536492 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54976305 | AGGGGCTGTATAACC[C/T]TGAACTCCTGGGTTC | 11169 |
rs534538089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017420 | CCATCTCGGGTCACT[A/G]CAACCTCCACTTCCC | 11169 |
rs534540071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976761 | ATAAATAATAAATAA[A/G]TAAATGTTCTACAAG | 11169 |
rs534557496 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54949259 | AAAACCTTGAAAAAA[C/G]ATTAGACGAATGGCT | 11169 |
rs534589647 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962071 | AGAACTCCTGACCTC[A/G]TTATCCGCCCACTCC | 11169 |
rs534629032 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003736 | GCCTGGCTAATTTTT[A/G]TATTTTCAGTAGAGA | 11169 |
rs534644023 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004749 | TGAGCCAGCGAGCCC[A/G]ACCCAATGTTTATTT | 11169 |
rs534646785 | snp | A/T | 1.67058e-05 | 0.00289009 | missense | WDHD1 | GRCh38.p7 | 14:54955656 | CTCAGTTTTATTAGT[A/T]TGAGAATTTCTTTTC | 11169 |
rs534653682 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997259 | CACAACCACACCTGG[A/C]TAATTTTTGTATTTT | 11169 |
rs534665840 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954571 | GTACTAGCAAAAGAC[C/T]GGTAACCATCTTTTG | 11169 |
rs534682399 | snp | C/G | 0.0733688 | 0.176922 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951182 | TAGAGACACAAAAAA[C/G]CCTTCAAAAAATCAA | 11169 |
rs534690014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945547 | TGACTCCAAAGTCTA[C/T]GTTTTTTTGTAGAGA | 11169 |
rs534700037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950273 | GCAGAGACACACATA[A/G]GCTCAAAATAAAGGG | 11169 |
rs534711553 | snp | A/G | | | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55013591 | CTTCCACAAGTCACA[A/G]TAAAACTGTGAAGAA | 11169 |
rs534711726 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983435 | CCCAGCACTTCAGGA[A/G]GTCGAGGCGGGTGGA | 11169 |
rs534719668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947110 | TTTGGGAGGCCAAGG[C/T]GGGTGGATCACCTGA | 11169 |
rs534738897 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54956687 | TTGGAAGTCAGAATC[G/T]GCTACAAAGTGTGTA | 11169 |
rs534765208 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939549 | TAATTAATTTATTTC[C/T]ATTTTCACTTTCATA | 11169 |
rs534770578 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948245 | GTGTGAGCTGAAGCA[A/G]GGCAAGGCATCACCT | 11169 |
rs534864014 | in-del | -/GGTGGATCACTTGA | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980562 | CATGCCTGTACTTTG[-/GGTGGATCACTTGA]GGTGGATCACTTGAG | 11169 |
rs534864255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009038 | CCGACCTTGTGATCC[A/G]CCCACCTCAGCCTCC | 11169 |
rs534880123 | snp | A/G | 1.65296e-05 | 0.00287481 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55007350 | TCGTTGCATTTTTGT[A/G]GCAGTGGCCAACTAA | 11169 |
rs534884391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001799 | AAAATTTCAGAGTCC[A/G]TGATCACAAGTCTCA | 11169 |
rs534918212 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54979047 | TTCTTTACTAAATTC[A/T]TTGCCAAAAGATTAC | 11169 |
rs534932253 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972550 | AATAAAGCAAGACTG[A/T]CACAAAAAAAAAAAA | 11169 |
rs534934221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010609 | AAATGTACAACTTTG[C/T]TGGAATGTGCATTAG | 11169 |
rs534989986 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989943 | TGCTGGGATTATAGG[C/T]GTGAGCCATCACGCC | 11169 |
rs535090687 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952154 | CAGGGCAATCAGGCA[C/G]GAGAAAGAAATAAAG | 11169 |
rs535150858 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952449 | AGGGATGTGAAGGAC[C/G]TCTTCAAAGAGAACT | 11169 |
rs535193580 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992473 | CTAGGCTGGGTGACA[C/G]AGCAAGACTCCCTCT | 11169 |
rs535208031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948006 | AGATCACCTGAGGTC[A/G]GGAGTTTGAGACCAG | 11169 |
rs535261326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002503 | TTCAATAAGCAAAAA[A/G]TAGGTGATAATTTGT | 11169 |
rs535276046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017106 | GAAAGTGAAATATCT[C/G]ACATCAGTGGGGATT | 11169 |
rs535348866 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956498 | CCAAAATTAGCTGGG[A/C]GTGATGTCAGGCCTC | 11169 |
rs535373417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963244 | AAGATACTGACACTA[C/T]TAGTAAAACTGAGAC | 11169 |
rs535436621 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965433 | ACTCAAAGAGGATGA[C/G]AAAAGGCAGGCATAT | 11169 |
rs535450941 | snp | C/G | 1.64795e-05 | 0.00287045 | missense | WDHD1 | GRCh38.p7 | 14:54991272 | ATGGCTTTTGCCGGG[C/G]AGTTGGCATGGGTCC | 11169 |
rs535474765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998457 | CTTAATTCACTTTTT[C/G]TTTTTACCAATGTTA | 11169 |
rs535476797 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988365 | CTTGGGTGATAAAGA[C/T]GTAGTGACAAAAATC | 11169 |
rs535477356 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946791 | GCTCACACCTGTAAC[A/C]CCAGCACTTTGGGAA | 11169 |
rs535512262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984630 | TAATTTATTCTTAAA[C/T]TAATTAGGAATAAAA | 11169 |
rs535546141 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940897 | AGCCAAATATACAAA[C/T]GAGAAAGTTTCATTT | 11169 |
rs535620390 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010665 | AAATTAATTCTACCT[G/T]AAGCAGCCTATCTCT | 11169 |
rs535632439 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003489 | CACTGCACTCCAGCC[C/T]GGGCAACAGAGTGAG | 11169 |
rs535662346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962637 | ATAGCAAAGAGGTCT[A/G]AAAAAAAGTATGAGT | 11169 |
rs535666168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970120 | AAAAGCTGGAAGCAT[C/T]ACCCTTAAGAATTGG | 11169 |
rs535695395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004423 | CTTTTCATTTTCCAC[A/G]TGGACTTTCCCTTTT | 11169 |
rs535755273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004779 | TTTCATCAACCTTAT[A/T]TCCATGTTGCTTAAG | 11169 |
rs535803399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975167 | AAACAGAAAAAGAAA[A/G]AAGGTCTCTGTTGGT | 11169 |
rs535803461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945690 | GGACTACAGGTACGC[A/G]CCACCACACCCAGCT | 11169 |
rs535819058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983704 | AAAAATTTTAAATAG[A/G]GATGGGATCTCACTA | 11169 |
rs535820518 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940355 | GCTACTAATTAAAAA[A/C]TAAAAAATGTATGTT | 11169 |
rs535830387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967689 | ACGGTGGTGTGATCA[C/T]GGCTCACTGAAGCCC | 11169 |
rs535889015 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947955 | GAGTGGTGGCTCACA[C/G]CTGTAATTCCAGCAC | 11169 |
rs535889487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009275 | CTTAAGCTTCTATTA[C/T]TTGCTAATCTAATTA | 11169 |
rs535950379 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002615 | AATATGATTACTTTT[C/T]TTTCCCCCAAGAGAC | 11169 |
rs536066114 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949797 | AACAGCTGATCTCTC[A/G]GCAGAAACTCTATGA | 11169 |
rs536077052 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982015 | TATTTATTATTATTA[A/T]TTTTTTTTTCGAGAT | 11169 |
rs536089133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996684 | TTACTCCTATAGGAT[A/G]CATAAAAACTACAAA | 11169 |
rs536091905 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997695 | AGGTGGGCAGATCAC[A/G]AGGTCAGGAGATCGA | 11169 |
rs536118486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020999 | GGCTGACGGGGAACA[C/T]GAAGAGGAGTTGGTC | 11169 |
rs536127352 | snp | C/T | 0.0770498 | 0.180522 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950406 | CAAAGAAGGCCATTA[C/T]ATAATGGTAAAGGGA | 11169 |
rs536137884 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982591 | AATTACCTGATTATC[A/C]CTTTTCTTATCTGTG | 11169 |
rs536163241 | in-del | -/AAAT | 0.0132831 | 0.080406 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938755 | GAGACCCTGTCTTTA[-/AAAT]AAATAAATAAATAAA | 11169 |
rs536175957 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014354 | CTTGACCTCCCAAAG[G/T]CAAGGGATTACAGAC | 11169 |
rs536181328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946214 | AACCAAAATTGAACA[C/T]TTCTTTCTTTGTTTT | 11169 |
rs536228501 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014974 | GACAAGCCAGGAAAG[A/T]AAAAGGAAAATGAAG | 11169 |
rs536245991 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55004435 | CACATGGACTTTCCC[-/T]TTTTTTTTAGCAACC | 11169 |
rs536254379 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954040 | GATGAGCACAGCACA[A/C]CAACATGGCACATGT | 11169 |
rs536292449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994780 | AAAAAAAAAAAATCC[A/G]GTTGCACTCATAACA | 11169 |
rs536318189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954496 | TGAATCCATCTTATA[G/T]CTATATATGCATCTG | 11169 |
rs536332846 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961164 | TACCTCTGCTTAAAA[C/T]CTACAACAGTCTCTC | 11169 |
rs536438483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013416 | ATATTCAAAAATATT[C/T]TTTCACTCAAGCATA | 11169 |
rs536441294 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944844 | AACTCCTGACCTCAC[A/G]TGATCTGCCCGCCTC | 11169 |
rs536447843 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028083 | TTTTTCTGCGTTTTT[A/G]TGATACCTTCCAGTA | 11169 |
rs536501263 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54973116 | AAAACCATGACTGCA[C/T]ACTATAAATACCACA | 11169 |
rs536519185 | snp | G/T | 0.00119737 | 0.0244387 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938894 | TTATTATAAAATACA[G/T]GCTATGTAATAATAT | 11169 |
rs536531384 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959441 | AGGAAGGGAGGGAGG[C/G]AGGCAGGCAGGCAGG | 11169 |
rs536555073 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022443 | GGCATTTTTCCCCCC[-/A]ACAGAATAGGGCACT | 11169 |
rs536629053 | snp | G/T | 1.66521e-05 | 0.00288544 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000843 | CAAATACAAAACTAA[G/T]AGAGATGAGCAAAGA | 11169 |
rs536686347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001612 | GTTATTATCCTAGAA[A/G]GAGAGACAATTCAAG | 11169 |
rs536695565 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54942059 | ACTGAGACCATCCTG[A/G]CTAACACAGTGAAAC | 11169 |
rs536762204 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002375 | TCCTGGGTTCAAGGG[A/T]TCTTCCTGGCTCAGC | 11169 |
rs536774214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956145 | ACCAATGACTAATCC[A/G]GGATCAAATACTTAT | 11169 |
rs536785391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949267 | GAAAAAAGATTAGAC[A/G]AATGGCTAACTAGAA | 11169 |
rs536864886 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975343 | GATCAGTAATTTCTC[A/G]TATTCATAATTTTTT | 11169 |
rs536874631 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973596 | AGAATCTTGTGGCAA[A/T]TCTGTCATAAATCTC | 11169 |
rs536904780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013843 | CCTGGAAGGTCAAGG[C/T]TGCAAGTGAACCATG | 11169 |
rs536937977 | snp | A/G | 3.58346e-05 | 0.00423273 | missense | WDHD1 | GRCh38.p7 | 14:54966573 | CTAAATAATCAAGGT[A/G]GTTGTGAAATATAAC | 11169 |
rs536990613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969124 | GCTCACTGCAAGCTC[C/T]GCCTTCCAGGTTCAC | 11169 |
rs537035397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009913 | GCAACCTCTGCCTCC[C/T]AGGTTCAAGTGATTC | 11169 |
rs537036442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949311 | GAACTCCTCAAATGA[C/T]CTGATGGAGCTGAAA | 11169 |
rs537078668 | snp | A/G | 9.88549e-05 | 0.00702977 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54989072 | CAACAAAATAGCTTC[A/G]TGGGAAAGATCTGCT | 11169 |
rs537122564 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949598 | ATACTATCCAGGAGA[A/G]CTTCCCCAACCTAGC | 11169 |
rs537125219 | in-del | -/G | 0.498158 | 0.0302955 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963185 | AAGCTAATCCAAAAA[-/G]GGGGGGGGGGGGGAG | 11169 |
rs537139464 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982095 | CACTGCAAGCTCCGC[C/G]TTCCAGGTTCAAGCC | 11169 |
rs537160266 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54938976 | AAATCTTTATTCTTA[C/G]GGTACATGCTGGGAA | 11169 |
rs537171251 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950531 | ACAAAGAGACTTAGA[C/T]TCCCACGCAATAATA | 11169 |
rs537201889 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951924 | ATGCAGAAAAGGCCT[G/T]TGACAAAATTCAACA | 11169 |
rs537235625 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007596 | GAGTATTTTCTGTGC[A/G]GAATAAACAAATGAT | 11169 |
rs537245824 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54981378 | AGTAAAGCAAGTGAC[C/T]GAAAACTTCAGAGTG | 11169 |
rs537249912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960040 | CACTCTTTACGCCCT[C/G]AACTCCTACACTCTC | 11169 |
rs537300914 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022294 | TTTCCCTTCAAGGCC[C/T]GGGGGTTAGTAGCTT | 11169 |
rs537355902 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55009679 | TCAGGTGATCTGCCC[A/G]CCTTGGCCTCCCAAA | 11169 |
rs537366948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015658 | CTTCTTTCAGTCCCA[A/G]TGGTGATGAGAGAAG | 11169 |
rs537476473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996161 | GTCCCTATAAAGTCT[A/G]TCATATTGTAAGACA | 11169 |
rs537504987 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020274 | TGAATCCACTTCAAG[G/T]TTTTCATTCTTACCA | 11169 |
rs537543380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989908 | TCCTCAAGTGACCAA[C/T]CCACCTTGGCCTCCC | 11169 |
rs537567411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013878 | CACCACTGCACTCCA[A/G]CCTGGGCAACAGAGC | 11169 |
rs537615608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993452 | CATAACAGAGCCGTA[A/G]GAGTTCACTGAAGTT | 11169 |
rs537621533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999858 | GCAATCCTCCCAAAG[G/T]GTTGGGATTACAGGT | 11169 |
rs537638950 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014264 | ATGCCTGGCTAATTT[A/C]TTTTTTGTAGAGACA | 11169 |
rs537691107 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54989590 | TTTCTTACAAATATG[A/G]ATGCAAATAACAACA | 11169 |
rs537698592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008227 | AAATTCCAAAGAAAA[A/G]CAATTATTAATTTGG | 11169 |
rs537740823 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987835 | TTTCACCATGTTGGT[A/C]AGGCTGGTCTCAAAC | 11169 |
rs537754156 | snp | C/T | 0.02016 | 0.0983543 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938622 | AGCCAGGTGTGGTGG[C/T]ATTTGCCTATACTCC | 11169 |
rs537789690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943419 | TTCCCCCTAGAGACC[C/T]GGTCTCACTCTGTCA | 11169 |
rs537806703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971690 | CGCACTGTAGCCTGG[A/G]TGACAGAATGAGACT | 11169 |
rs537824823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943998 | CATAATAATTACTAC[A/G]TATCCATATTACCAT | 11169 |
rs537832717 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012677 | ACAAGATTGAGGGGT[A/T]GGCATCTGGCAAGGG | 11169 |
rs537859405 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972905 | CTACTCTGATAAATA[C/T]GGTAACAGGTCAACG | 11169 |
rs537866271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980992 | GGTGCGCACCTATAA[C/T]CCCAGCTACTGGGGA | 11169 |
rs537875294 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964624 | AGCCTGGGCAACAGA[A/G]CGAGACTTCGTTTCA | 11169 |
rs537901466 | snp | A/T | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012194 | AATGTATGTTGGTCA[A/T]TTACATTTTTTCTTC | 11169 |
rs537918863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973725 | AAATTAGAAGAAACA[C/T]TGTGAGAAATGTTAA | 11169 |
rs537938914 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958673 | TCCTCTCTTGACTTC[C/T]GAGATACTGCATTCC | 11169 |
rs537980490 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966669 | GAGGCAAGCGTTAAA[C/T]ATTTATCTTAAGATA | 11169 |
rs538032444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942066 | CCATCCTGGCTAACA[C/T]AGTGAAACCCCGTCT | 11169 |
rs538051186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948369 | AATACTGTGCTTTTC[C/T]AATGGTCTTAGCAAA | 11169 |
rs538066147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978675 | GATTACAACTGTAAA[A/G]GCAAAACACACAGAA | 11169 |
rs538144469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979362 | GGTCTCACTATGTTG[C/T]CCAGGCTGGTCTCAA | 11169 |
rs538178942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965367 | TAAATATTCTAGACA[C/G]CAAACCTGGCCACTG | 11169 |
rs538232234 | in-del | -/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55022507 | GCCAACATGGCAAAA[-/C]CCCGTCTCTACTAAA | 11169 |
rs538270779 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026127 | GCTCTATTCTATCTG[C/T]AGTCCCCAGCAAAAG | 11169 |
rs538343964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006593 | CAAATAATGAACATT[C/T]TCTTTCTTCCTTTCA | 11169 |
rs538359506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008259 | CCAGTAATACGACAT[A/G]TAACAATTTATTACA | 11169 |
rs538401970 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941981 | TTTGGCCAGGCACGG[A/T]GGCTCATGTCTGTAA | 11169 |
rs538420941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987888 | CGCCTTGGCCTCCCA[A/G]AGTGCCGGGATTACA | 11169 |
rs538483349 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988312 | TAGTTGGCCAAGGCT[A/C]AGGTTGAATTAACTG | 11169 |
rs538501606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025807 | TGATCCCTGGCCCCA[C/T]TGGGCCTTTACACAC | 11169 |
rs538503295 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017986 | AGACCTCCTGGCCTC[A/C]AGCAATCCTCCCACC | 11169 |
rs538516335 | snp | A/G/T | 1.69341e-05 | 0.00290977 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54957598 | AGAGTTTACCTTAAA[A/G/T]GGATTTACTCGTCCT | 11169 |
rs538524166 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime | WDHD1, SOCS4 | GRCh38.p7 | 14:55027284 | GAGGCGATGACCGTG[A/G]CGGCTGGGTTGGGAC | 11169 |
rs538546325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981106 | ACAGAGCGAGACTCT[A/G]TCTTCTATTAGTCCT | 11169 |
rs538563351 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018655 | GGCTGAAGTATTTAC[C/T]CATTTCAATTAAAAC | 11169 |
rs538570417 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964080 | GCCACTGTACTCTAG[C/G]CTGGGTAACAGAGTG | 11169 |
rs538573703 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55007779 | TGTGGATATTAAGGC[A/G]TATTTGTGGAGGATA | 11169 |
rs538586875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020481 | TTCTTAGTCTCCTTA[A/G]CTGGATCCTCTTTAA | 11169 |
rs538607137 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54978600 | TAAAAAAAAAAAACC[A/G]TTAATGAATATACTT | 11169 |
rs538621196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020914 | AAAGAGGAGAAAAAA[C/T]ATTTACTATTTATTA | 11169 |
rs538634200 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006705 | ATAAGACTGTCTCCA[C/G]AGTTGTTCCATTAAG | 11169 |
rs538641729 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974498 | GTTTTGTTTTGTTTT[G/T]TTTTTTTTTGTTATA | 11169 |
rs538653409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966836 | AAAACAGTTTCCTAG[C/T]TATCATAATTAATGC | 11169 |
rs538694753 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006558 | TCTTGGGATTTACTC[A/G]TATACAAACATTTCC | 11169 |
rs538695072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000000 | GGGGGTTTCAGGAGG[A/G]ACAGCTATAAATGCA | 11169 |
rs538721020 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54982686 | GGAGAAAAAAATCTA[C/T]ACAAATGGAAGTTAT | 11169 |
rs538724361 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953670 | ATAAAAACACATGCA[A/C]ACGTATGTTTATTGT | 11169 |
rs538784700 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948841 | GCAGCAACATTTGCT[A/G]TTCACCAATATTTGC | 11169 |
rs538809636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979495 | GTTATCCACATATTC[C/T]ACTTTCATTTCTTTA | 11169 |
rs538821120 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943521 | TTCCCACCTCAACCT[C/G]CTGAGTAACTGGGAC | 11169 |
rs538872449 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55004876 | GGGGAGCCGCAGACC[A/G]GTCTTCTGTGGCAGG | 11169 |
rs538938361 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998557 | ATTTACTTCTCTACA[C/G]AATAAATCCTTCCAG | 11169 |
rs538954524 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027855 | ATTCAGATCCCACCT[A/C]AAGTTTACTGAAGTG | 11169 |
rs539007890 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985071 | AAGTCCTTATAAGTG[C/G]GCATTTATTCACTCA | 11169 |
rs539037822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948125 | AGCTCCCAGCATGAG[C/T]GATGCAGAAGACGGG | 11169 |
rs539119792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942108 | ACAAAAAAATTAGCC[A/G]GGCATGGTAGCGGGC | 11169 |
rs539124283 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000746 | ATAAATGACTTTTGA[C/T]AATAATTTATAAATA | 11169 |
rs539153417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953981 | CTGTTGTGGGGTGGG[A/G]GAAGTAGGGAGGGAT | 11169 |
rs539158426 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942911 | TCTTCCTCTTTTGCA[A/G]TGTAAAGTCTTATTT | 11169 |
rs539189281 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025862 | AACATCACCACCCCA[C/T]CGCCACCACCACTCA | 11169 |
rs539227688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018731 | GAGCCTGCCAAGTAC[C/T]TTAGAACCTAACATT | 11169 |
rs539290695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012742 | AAGAGAGGGCGAGAG[A/G]GAGAGCAAGAGGATC | 11169 |
rs539292718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019690 | CCTGGCCAACATGAC[A/G]AAACCTTGTCTCTAC | 11169 |
rs539295985 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972646 | ATTCTTAGTACTGTC[A/G]GTATGAGTTGTCAAA | 11169 |
rs539318128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957812 | AGCCAAAATAAAAGC[C/T]ATTAAATGTGAACCA | 11169 |
rs539334806 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006155 | AGGTGTGAGCCACCA[A/C]ACATAGGCTGTTGTT | 11169 |
rs539364117 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998632 | ATATTCTAGTAGAAT[A/T]TTTTTTTTTCACTTT | 11169 |
rs539378384 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952475 | GAACTACAAACCACT[A/G]CTCAATGAAATAAAA | 11169 |
rs539464074 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977807 | ATTATTGAATATAAC[A/T]GTTAAATGTTACCAG | 11169 |
rs539467048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986386 | CTATCCAGACTTGTA[C/T]TGAACTCCTGGGCTA | 11169 |
rs539501414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017347 | AAAAATCAATATTCT[C/T]TTTTTTTCTTTTTGA | 11169 |
rs539510101 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978948 | TCTATTTTCCTATTT[C/T]AGACAGGTGATCTAA | 11169 |
rs539596964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004868 | TGAGCAGTGGGGAGC[C/T]GCAGACCAGTCTTCT | 11169 |
rs539607509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990667 | CTATTCATGAAATAT[A/G]TATTTAATGTGCACT | 11169 |
rs539617592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997055 | TCAGACTCCCAAAGT[A/G]CTGGGATTACAGGCG | 11169 |
rs539645460 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963970 | TAAATTAGCTGGGCG[A/T]GGTGGCATGCACCTG | 11169 |
rs539683844 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952204 | AGGAAGTCAAATTGT[A/C]CCTGTTTGCAGATGA | 11169 |
rs539753664 | in-del | -/G | 0.00557542 | 0.0525036 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021070 | GAGGCAGGAGAGGCA[-/G]GGCATACTTGGTGTG | 11169 |
rs539771750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977061 | ACTCCCTTTGTTCCT[A/G]TATTTTAATACAAAA | 11169 |
rs539854600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969644 | AGATGCACAAAGAAC[C/T]GGTACCAGTCCTACT | 11169 |
rs539907493 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54977914 | AAAGGGTTGTGTGGA[-/A]AAAAAAAAAAAGCAT | 11169 |
rs539951606 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964366 | AAAAAGGAAGCCGGG[A/C]GCAGTGGCTCACACC | 11169 |
rs540026260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951137 | GCAGAAGGCAAGAAA[C/T]AACTGAGATCAGAGC | 11169 |
rs540062512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947664 | TGGCACAATCTTGGC[C/T]CATTGCAGCCTCCGT | 11169 |
rs540090023 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946943 | AGCTACTCAGGAGGC[A/T]GAGGCATGAGAATTG | 11169 |
rs540116693 | snp | A/G | 3.80909e-05 | 0.00436394 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984672 | TTTTCTTCTTGAAGA[A/G]TATCTAACACTTTAT | 11169 |
rs540150482 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55014669 | CCCTATCTACACACA[C/T]ACAAAAAAGCAAATA | 11169 |
rs540152304 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54983972 | CTAAGTCTTCAAAAT[A/C]CAGAGTATTTTACAC | 11169 |
rs540178252 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942164 | GCTGAGGCAGGAGAC[C/T]AGAGTGAACCCGGGA | 11169 |
rs540232088 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958239 | TCAGGCGATTCTACT[A/G]TCTCAGCCTCCCGAA | 11169 |
rs540285793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004904 | AGGCTGAGCACTCCA[C/G]TTTTCAGGAGGGAAC | 11169 |
rs540317875 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972039 | GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 11169 |
rs540335322 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55022748 | CTCCTCAATGATTTT[C/T]GTAATGGTGTCTGGG | 11169 |
rs540344539 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012849 | CTCATTACTTCTCAG[A/T]AGACCCCACCTCCCA | 11169 |
rs540417707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952244 | ATATTTAGAAAACCC[C/T]GTCGTCTCAGCCCAA | 11169 |
rs540489972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948138 | AGCGATGCAGAAGAC[A/G]GGTGATTTCTGCACT | 11169 |
rs540494103 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024520 | CCCATGTTTACTCTA[C/G]TCCAAGCTTCTATCA | 11169 |
rs540506577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977173 | CTCATATGTAAAAAT[C/T]GGGGAGAAGTGCTGG | 11169 |
rs540542109 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986419 | GCAACTCTCCCGCCT[C/T]GGCCTCCCAAAGTGC | 11169 |
rs540607707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990207 | AAAATTTATGCCAGG[C/T]CTATACTCTTCAAAT | 11169 |
rs540623347 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967135 | CTGGTGATCCCAAGC[A/T]GTCCTCTTCCCTCCC | 11169 |
rs540648522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996832 | GAGTCTCGCTCTGTC[A/G]CCAGGCTGGAGTGCA | 11169 |
rs540651133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963632 | ATATGGCAAAACCCC[A/G]TCTCTACTAAAAACA | 11169 |
rs540712687 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957328 | TTTAGAACTAAATAC[A/C]TTTGGTACAATCCAA | 11169 |
rs540735992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984030 | AGTGCTCAACAGACA[C/T]ACATACTAGTTATTG | 11169 |
rs540758899 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963519 | TTAAAAAATTCAAGG[A/G]GGAGGCTGGGCACGG | 11169 |
rs540767793 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947256 | AGACAGGAGAATCAC[G/T]TGAACCCAGAGGCAG | 11169 |
rs540785047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960758 | TGCTCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 11169 |
rs540829548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968522 | AATAACAGCAGAACT[A/G]AACAAAATTGAGACT | 11169 |
rs540846316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954788 | AGGCTGGAGTGCAGC[A/G]GTGTGATCTCAGATG | 11169 |
rs540848411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961400 | TGACTTGGCTCCTGC[C/T]CATCACTCCGAAACC | 11169 |
rs540879927 | in-del | -/CT | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988906 | GGTGTTTGTACCAAA[-/CT]CTTCTGAAATTTCAT | 11169 |
rs540936450 | in-del | -/AT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55014727 | AAATACAAAAATAAC[-/AT]ATAATAAACAGCAAA | 11169 |
rs540982109 | in-del | -/AAAC | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013385 | ATTATTTCATGAGAT[-/AAAC]AAAGGTATATCTATA | 11169 |
rs540985076 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54946828 | ATGGGCAAATCGCTT[C/G]AGGCCAAGAGTTTGA | 11169 |
rs541009901 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939083 | AACAATAAGACAAAC[G/T]AGAGGAAGGATATAC | 11169 |
rs541015095 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028347 | ACTTGGGATTTGTGG[A/G]AAAATAACCCACTGT | 11169 |
rs541029244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945786 | CCTCATGATCCACTC[A/G]CCTCGGCCTCCCAAA | 11169 |
rs541040196 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974236 | AGACCAGCTCGGGCT[A/T]CATAGCAAAACCTCG | 11169 |
rs541082166 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939937 | CCAAACACAAAATAC[A/T]TGTCTACAAACATGC | 11169 |
rs541156045 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022710 | ACAAACAAACAAAAA[A/T]CCTGTTCAGGCAGAT | 11169 |
rs541221361 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54976412 | ATGTTGCCCAGGCTA[C/G]CCTCAAACTCCTGGC | 11169 |
rs541273187 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003095 | AAAGGATTAGTAACA[C/G/T]ATAATAAAAACTTTA | 11169 |
rs541296885 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003012 | AAATGTATCTTCTTA[C/T]GCATTATTCTGAAGA | 11169 |
rs541334914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996468 | AGCCAGGCATGGTGG[C/T]ATGTGTCTATAGTCC | 11169 |
rs541337014 | in-del | -/AAATAAATAAAT | 0.0293864 | 0.1176 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942252 | AGACTCCGTCTCAAA[-/AAATAAATAAAT]AAATAAATAAATAAA | 11169 |
rs541355413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945086 | AACCTCACTTAGCCC[C/T]TGTGGCCTACCACAT | 11169 |
rs541360022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950056 | GCCAAATTGTAAAGA[C/T]CATCAAGGCTAGGAA | 11169 |
rs541409973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982199 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 11169 |
rs541427942 | snp | C/T | 5.03512e-05 | 0.00501728 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991447 | CACGAATACCAATGA[C/T]TTGGAAAAAGGAAAG | 11169 |
rs541504106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014473 | ACCGTATCTTCCTTG[C/T]CCACCATTGTATCCC | 11169 |
rs541511829 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941214 | TCAAGGTTAAGAAAC[A/G]AATTCAAATTGGTTG | 11169 |
rs541514951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977372 | CATGTATGCAGATAA[C/T]GTGATTTGTAAATAC | 11169 |
rs541565674 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008824 | TTTTCTTTTTGAGAC[A/G]GAGTCTCACTCTGTC | 11169 |
rs541567585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015163 | AAACATATTAGTATT[A/G]GTTGCATCAAAATTG | 11169 |
rs541642884 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008052 | AATATAAAATAACTG[A/G]ATTTATTCCCTTCAT | 11169 |
rs541645664 | snp | C/T | 5.56478e-05 | 0.00527454 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955734 | CAATAACATCTAGTA[C/T]AATTTTATATGTTTT | 11169 |
rs541692677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988496 | GGGGTTATCTGTGTA[C/T]ATACACCTTTGTCAA | 11169 |
rs541707905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950713 | TTCTGAGCACCACAT[C/T]GCACTTATTCCAACA | 11169 |
rs541771464 | snp | G/T | 0.0581099 | 0.160244 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951237 | AAAGATCAATAAAAC[G/T]GATAGACCGCTAGCA | 11169 |
rs541842202 | in-del | -/AAAT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54992968 | ATTAAAAACAAAAAC[-/AAAT]AATTTATATTAGATA | 11169 |
rs541878219 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55010227 | AAAATTAAGTCACGG[C/T]CCTGAAAACACTACC | 11169 |
rs541915340 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | WDHD1, SOCS4 | GRCh38.p7 | 14:55027280 | GGCGGAGGCGATGAC[C/T]GTGACGGCTGGGTTG | 11169 |
rs541915824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015950 | GTGATCCACCCACCT[C/T]GGCCTCTCAAAGTGC | 11169 |
rs541915996 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993551 | AATATCCACAATTAA[C/T]TGAATGTGCTATTAA | 11169 |
rs541943815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016931 | AGGGTGGTATGGCCA[C/T]AGACAGCAAAAGAAC | 11169 |
rs541954490 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54982017 | TTTATTATTATTATT[A/T]TTTTTTTCGAGATGG | 11169 |
rs541978869 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024398 | ACCGTAACATTCAGA[A/T]ATGTAGACGTTATCC | 11169 |
rs542086365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021542 | GCGTATGCCAACATA[C/T]CCAGCCAATTTTTTA | 11169 |
rs542091475 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996935 | TAGCTGGGACTACAG[A/G]CGCATGCCACCATGC | 11169 |
rs542154446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997401 | GTACCCAGACCCTCA[C/T]AAACCTTTTAAATGG | 11169 |
rs542156032 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946506 | GTTGTTGTTTTAAGA[C/G]AAAGGGTCTTGCTTT | 11169 |
rs542199513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975631 | TGGGATTACAGGCGT[A/G]AGCCACTGCACCCAA | 11169 |
rs542200029 | snp | C/T | 1.72767e-05 | 0.00293905 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008405 | CTCTATAGTCATAGC[C/T]ATAATACTACATGGA | 11169 |
rs542200049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001140 | TATATCCCTGTTCTA[C/T]ATTATTTCTAATTAT | 11169 |
rs542207081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015278 | TGTAATCCCAGCTAC[C/T]CCAGAGGCTGAGGCA | 11169 |
rs542258875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002005 | GTTGTTTTCCATTCC[A/G]ATAATATTTAACTGC | 11169 |
rs542265740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009581 | GGATTATAGGCACCC[A/G]CTACTATGCCCAGCT | 11169 |
rs542302947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995045 | GCATGCAGTTGACGC[A/G]ATCTCGGCTCACTGC | 11169 |
rs542340939 | in-del | -/AGTCAAATTTCTTGATA | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979460 | CTCGCCTGGCCCAAT[-/AGTCAAATTTCTTGATA]AGAGTTATCCACATA | 11169 |
rs542364469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003202 | ATCACTTAAATCTAG[A/G]ATGTACATTGTTAAA | 11169 |
rs542376107 | snp | A/G | 1.79825e-05 | 0.00299849 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989231 | CAAACAGGTAAGATT[A/G]AATATAAGTCTGAGA | 11169 |
rs542383316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981330 | TGATGGTAAGGTCAT[C/T]CTAATTATTTCTATT | 11169 |
rs542409855 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963542 | GGGCACGGTGGCTCA[C/T]GCCTGTAATACCAGT | 11169 |
rs542419008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945182 | AGCCCCTTTGCCATC[A/G]CCTCACCCTTGCTCT | 11169 |
rs542527407 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019473 | TTTTATTTGTGCCTT[C/T]TCTTTTTTGATTCAT | 11169 |
rs542532471 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982948 | GGCAGGTGGATCACC[C/T]GATGCCAGGAGTTCA | 11169 |
rs542606905 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55010032 | CCATGTTGGCCAGGC[C/T]GGTCTTGAACTCCTG | 11169 |
rs542671294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943121 | CATTCCTGGGGAAGT[A/G]AAACCTGAGGATTTA | 11169 |
rs542704213 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019590 | AATAAAGAGTAAGGC[A/G]GGGTGTGGTGGCTCA | 11169 |
rs542713849 | snp | A/C/T | 8.29489e-05 | 0.00643959 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:54995692 | TCATCCTCATCATCA[A/C/T]TTATAATCCCTTTTG | 11169 |
rs542729133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949187 | GAGAAGAAGGCTTCA[A/G]ACGATCAAACCTCTC | 11169 |
rs542735984 | in-del | -/GGAG | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959403 | CTGGCGGGGGGAAGA[-/GGAG]GGAGGGAGGGAGGGA | 11169 |
rs542805700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020607 | ATATTATGTTTATAA[A/G]GACAATTCTCACATT | 11169 |
rs542899260 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953242 | TGACAAAGGGCTAAT[A/C]TCCAGAATCTACAAA | 11169 |
rs542957589 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993757 | TCACTAATTTTTTTT[G/T]TTTTTCATAAAAAAG | 11169 |
rs542998396 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948491 | AACTACAAGGCGGCA[C/G]CCTCAGCCAGGAAAC | 11169 |
rs543041682 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947287 | AGGTTGCAGTGAGCC[A/G]AGATTGTGCCATTGC | 11169 |
rs543051402 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955133 | AACAAAAAATAGACA[A/G]ATATGTATTTGCACA | 11169 |
rs543052741 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988027 | GAGAGGGCAATCTCT[C/T]GATTAACAAAAAGCT | 11169 |
rs543055850 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026331 | AAAGTTAAAAAAAAA[A/T]AAGCAAAAAGGGAAA | 11169 |
rs543115645 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990078 | ATATTTTATTTAACA[C/T]AACTATAAATAAAAT | 11169 |
rs543153610 | in-del | -/TC | 0.00953873 | 0.0683987 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970467 | CAAGGAGGTGAAAGA[-/TC]TCTACAAGAACTACA | 11169 |
rs543154770 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948650 | AGCTTTGAAGAGAGT[A/C]GTGGTTCTCCCAGCA | 11169 |
rs543164197 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967046 | AGTAAGTCTTTCCCC[A/C]GTGGGTCTCTGACAG | 11169 |
rs543164322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974647 | CCTGGGCAACCTGGC[A/G]AAACACTGTCTCTAC | 11169 |
rs543168977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964886 | TGAAATATGTTTCCT[C/T]ATATGTGTTGTACAA | 11169 |
rs543190931 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996823 | GACAGAGTGGAGTCT[C/T]GCTCTGTCGCCAGGC | 11169 |
rs543241677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007845 | AATGCCAAGCCATCT[C/T]GGATTGCCTTGGGCA | 11169 |
rs543399651 | snp | C/T | 0.000131952 | 0.0081215 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944314 | CTAAGATCTCAATCT[C/T]GGCACAATTATCCTT | 11169 |
rs543499706 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974097 | AGAGGAATTTAAAAA[A/T]AAAAAAACAATGAAA | 11169 |
rs543509060 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949905 | ACTAAGCTTCATAAG[C/T]GAAGGAGAAATAAAA | 11169 |
rs543608041 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54953141 | GGATCTAATTAAACT[A/C]AAGAGCTTCTGCACA | 11169 |
rs543662972 | snp | G/T | 1.6483e-05 | 0.00287076 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008676 | CTCGAAATGTTTTCT[G/T]TTGGCTGCTATCCAT | 11169 |
rs543672547 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948929 | ACTCCAACAGACCTG[A/C]AGCTGAGGGTCCTGA | 11169 |
rs543731201 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949133 | GCTCCTCACCAGCAA[C/T]GGAACAAAGCTGGAC | 11169 |
rs543802108 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55027032 | TGGGGACTCACCCGG[G/T]TGACCGAGCCTCCGC | 11169 |
rs543804495 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | WDHD1, SOCS4 | GRCh38.p7 | 14:55027418 | GCCCAGACTGATGGC[G/T]ATGGTGATGGCAGCA | 11169 |
rs543826540 | snp | A/G | 0.000399281 | 0.0141238 | missense | WDHD1 | GRCh38.p7 | 14:54981553 | ACCTTAGTTGCTGGG[A/G]ATTTTCATGGATACC | 11169 |
rs543862026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012952 | TAAAAACACCACTGA[C/G]TTTTCCCTTAAAGGA | 11169 |
rs543878638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964960 | AAAGGAATAAAACTT[C/T]TTCTACAATAAACTG | 11169 |
rs543931559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006265 | TAAGAATATATGTTT[C/T]TATTTATCCAAGTCT | 11169 |
rs543947630 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958834 | CATTCTCCCCCAATG[C/G]TTGCTTACCCATGCT | 11169 |
rs543961214 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014052 | AAATAAAGTGCTAAT[G/T]TCCTTCTATAAAATA | 11169 |
rs543962842 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021218 | AACATAGAAGGGTCT[A/G]TGTTGTAAAATAAGT | 11169 |
rs543982867 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954949 | GGTCAGGCTGGTCTC[A/G]AACTCCCATCCTCAG | 11169 |
rs544010069 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025286 | ACAATTGTCTTGTGA[C/G]CCTGACACATCCCCC | 11169 |
rs544016151 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000263 | ACAAAATAGTATTTA[A/T]TGAAAGGTATTCCTT | 11169 |
rs544071931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026091 | CTTAAGCTCAAAGGA[A/G]GAAAAGACTGTGTCT | 11169 |
rs544133723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018936 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCTGGGA | 11169 |
rs544139111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994903 | ATAGTGATGGCCCAC[C/T]TCTCTTTCATTCTCT | 11169 |
rs544170171 | in-del | -/ATCTGGAATTTAACATTTT | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979529 | CCCATGCCCACCCCA[-/ATCTGGAATTTAACATTTT]ATCACTTTTATCAGA | 11169 |
rs544181501 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010759 | TAAGTGTTATAAAAA[A/G]GAAGGAGACTCAAGA | 11169 |
rs544184830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998144 | CTTCAACCCAGGAGG[C/T]GGAGGTTGCAGGGAG | 11169 |
rs544224895 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960460 | GGTGTGAGCCACCAC[A/G]CCCAGCTTGTAGTCT | 11169 |
rs544332498 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959619 | AGTACACACAAAAAA[G/T]TAACCAGGCATGGTG | 11169 |
rs544349644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999528 | AACTTCCAGAAACTA[C/T]AGTTTTAGAATTCAA | 11169 |
rs544384770 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55012935 | AAATCATAGCAGTGA[A/G]CTAAAAACACCACTG | 11169 |
rs544488670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979759 | GAGAAAAGTCTCCTA[C/T]ACTATCCACTGAGTT | 11169 |
rs544511772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971417 | CCTGTCTCTACAAAA[A/C]AATTTAAAAATTATC | 11169 |
rs544526725 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004988 | AGGTTGAGGAGCACC[A/G]AACTCAGGAGCTGGA | 11169 |
rs544541396 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011739 | TTTTTTTTACTTATT[G/T]TAAACTTATTTTCAA | 11169 |
rs544584905 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993290 | ACCTGGCTAATTTTT[A/G]AAGTTTTTTTGTAGA | 11169 |
rs544617357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957409 | AGGTATCTTTCAAAA[C/G]CATAGGTACTTAGAA | 11169 |
rs544655640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007656 | ACAAAACCCCAATAC[A/G]TGAAATTCTTAGAAT | 11169 |
rs544681248 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947717 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 11169 |
rs544681493 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55017272 | TCTTCTAAATGGTTT[C/T]ATCCTTTATTGTATC | 11169 |
rs544681503 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952608 | ATCCCCATCAAGCTA[C/T]CAATGACTTTCTTCA | 11169 |
rs544681700 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982173 | ACCACGCCCAGCTAA[-/T]TTTTTTTTTGTATTT | 11169 |
rs544789392 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54962387 | ACAAAAACATAAACA[C/T]ACACACACCAAAAGT | 11169 |
rs544804713 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019074 | ACTTCAAATTTATTC[A/C]GCATAAAATGCAACT | 11169 |
rs544911249 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972398 | GCCTGGCCAATGTGG[C/T]GAAAACCCATCTCTA | 11169 |
rs545043837 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959655 | CAACTGTAGTCATAG[A/C]TACTCAGTAGGGTGA | 11169 |
rs545047076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986637 | AGTGAGGAAAAATAT[C/T]GAAAGTATGATGTCA | 11169 |
rs545048918 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993706 | ATCCAGCTATCCTCT[A/G]TGATAGACATTACAA | 11169 |
rs545103953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960222 | GCCCAGGCTGGAGTG[A/C]GGTGGTATGATCTCA | 11169 |
rs545129886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954274 | CTGGGCAACAAGAGC[A/G]AAACTCCGTCTCAGA | 11169 |
rs545140931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994527 | TAAAAAATTTCCCAA[C/G]ATTTTTACATTCTTT | 11169 |
rs545145604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945245 | ACGGACACAGCACAT[G/T]TGTACATTTCATTAG | 11169 |
rs545152398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963691 | TGTAATCCCAGCTAC[C/T]CGGGAAGCTGAGGCA | 11169 |
rs545225505 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980325 | TGAGACTCTGTCTCA[A/C]AAAAAAAAAAGACAT | 11169 |
rs545252072 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019815 | CAGAGGTTACAGTGA[A/G]CCGAGATCGTGCCAC | 11169 |
rs545259112 | snp | C/T | 9.91048e-05 | 0.00703865 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026829 | TTTATAAAAGCCAGT[C/T]TTATTATTTCAAAAG | 11169 |
rs545295973 | snp | C/G | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55029086 | TGTTTTTGCTAGTAT[C/G]ATGTTTTCACAATTC | 11169 |
rs545317382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965023 | GCATAAAGGTGACAG[C/T]AGTGAGTACTACCTT | 11169 |
rs545338429 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949558 | GACAGGGAGAATGGA[A/T]CCAAGTTGGAAAACA | 11169 |
rs545356300 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958157 | TTGAGACAGAGTCTC[A/G]CTCTTGTTGCCCAAG | 11169 |
rs545361377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999371 | GGGCAGGTACCCAGC[C/T]TTGAACACAGATGTT | 11169 |
rs545425125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948207 | CGGACAGTGGGCGCA[A/G]AACAGGGGGTGTGGC | 11169 |
rs545484967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948436 | GAGGGTCCCATGCCC[A/G]TGGAGCCTCACTCAT | 11169 |
rs545487767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024412 | AAATGTAGACGTTAT[C/T]CCTGTTGCCTCTTTC | 11169 |
rs545573255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005089 | TCTCCTCAGGAACAC[C/T]GTAGAAGTAGAGATC | 11169 |
rs545573291 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54971298 | CAAGAGTAAACAGGT[C/T]AGGTGCAATGGCTCA | 11169 |
rs545599988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957476 | CTTTCTTCTGTTTCC[A/G]CACAGATCAGTCTTT | 11169 |
rs545684026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951409 | CTAGAAGACATGGAT[A/G]AATTCCTGGACACAC | 11169 |
rs545719495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947599 | ACTGTTCTTTTCTTT[C/T]TGTTTTTTCTGAGAT | 11169 |
rs545739609 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941275 | GCATCTCTGAAAGGC[C/T]CTGCATTTGGAGGCA | 11169 |
rs545791402 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996674 | AGATCCCAAGTTACT[C/G]CTATAGGATGCATAA | 11169 |
rs545807875 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55010115 | TGAGCCACCACAACC[A/G]GCCAAAGCAATATAT | 11169 |
rs545854080 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55018220 | ATTTAGTTGAAAACA[A/G]ACATCTTTAATCAAA | 11169 |
rs545882835 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005858 | TTTTTTTCCTTAGAG[C/G]CTTCAGATGAGACAT | 11169 |
rs545919575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007713 | CTACTATAAAATGTT[A/G]AAGTGTCAAAGTCGC | 11169 |
rs545929340 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010832 | AGGCATCAGAAGGCA[C/G]GGCCACAATGGCCAC | 11169 |
rs545940192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018073 | ACATACTTTCTCCCT[C/T]TGCTTGGAGTGATTG | 11169 |
rs545940238 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011784 | ATTTTCTGATGAAAA[C/T]AGATACCCTACTTTT | 11169 |
rs546023028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954920 | TTTTAATAGAGACAG[A/G]GTTTCTCCATGTTGG | 11169 |
rs546051506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015356 | CGCACTACTGTAGCC[C/T]GGGAAACAGCATGAC | 11169 |
rs546055466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022575 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGTAGA | 11169 |
rs546089751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984929 | GCAGTCTAAATTATT[C/T]TCTGTGAATTGATTT | 11169 |
rs546154596 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940398 | ATCATCACCAGATAA[A/G]GAATATTCTTGGTTC | 11169 |
rs546166872 | in-del | -/ACA | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015579 | CAAATCCTTTCGGGG[-/ACA]ACATGTGAGGCATTC | 11169 |
rs546168769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976292 | CAGGTTGGGGTGCAG[A/G]GGCTGTATAACCTTG | 11169 |
rs546169401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010192 | GATAAAAGAATATAT[A/G]AAGAAACAACAAACA | 11169 |
rs546170226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969273 | CCTTGTGATCCGCCC[A/G]CCTATGCCTCCCAAA | 11169 |
rs546237528 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962221 | TCTGTCTTCTCAGCT[G/T]GGCTAAAATAGCATT | 11169 |
rs546288247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951941 | GACAAAATTCAACAA[C/T]GCTTCATGCTAAAAA | 11169 |
rs546318470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950838 | AGAACTCAGCATTAG[A/G]AAACTCACCCAAAAC | 11169 |
rs546333592 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996939 | TGGGACTACAGGCGC[A/G]TGCCACCATGCCCAG | 11169 |
rs546397487 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998381 | GTGATCCACCGGCCT[A/C]GGCCTCCCAAAGTGC | 11169 |
rs546406034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975724 | TTTTTAAAGAGACGG[A/G]GTTTTGCTGTTGCCC | 11169 |
rs546489315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024059 | TAGGCTACATGGTTC[A/G]TCTGCTAGTTTTTTC | 11169 |
rs546496125 | in-del | -/TT | 0.00155039 | 0.0277991 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026829 | TTATAAAAGCCAGTC[-/TT]TTATTATTTCAAAAG | 11169 |
rs546555395 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003657 | CAACCTCTGCCTCCC[A/G]GGTTCAAGCAATTCT | 11169 |
rs546562071 | in-del | -/TACTGTATAAGATTCCCCTCAG | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976952 | AGTGCTTCAAATGCC[-/TACTGTATAAGATTCCCCTCAG]TAATTCAATTATTCT | 11169 |
rs546610641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963753 | TGCAGTGAGCCAAGA[C/T]TGCACCACTGCACTC | 11169 |
rs546615527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004754 | CAGCGAGCCCGACCC[A/C]ATGTTTATTTTTCAT | 11169 |
rs546674818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005161 | TTCCTGGATCGGCAT[C/T]CACCACATCAATCCC | 11169 |
rs546763161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946663 | TGGCTGATTTTAAAA[A/C]TTTTGGTAGAGATGG | 11169 |
rs546779380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016418 | TGACATTTACCACGG[A/G]GCTACAGTCATACTA | 11169 |
rs546800872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976762 | TAAATAATAAATAAA[C/T]AAATGTTCTACAAGG | 11169 |
rs546819870 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969563 | AGTTCCAAAATTGAA[G/T]CGTAATAAATAAAAA | 11169 |
rs546847550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003448 | TGAGTCCGGGAGGCA[A/G]AGGTTGCAGTGAATC | 11169 |
rs546862577 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977648 | TTCAAGTCCAGCCTG[C/G]ATAACGTAAGGAGAC | 11169 |
rs546879269 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54956373 | CTGGGTGCGGTGGCT[C/T]ATGCCTGTAATACCA | 11169 |
rs546909042 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003907 | TCTGCTCATGTCTTT[A/G]CTCATCTTTCTAATG | 11169 |
rs546934303 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950315 | TCTACCAAGCAAATG[A/G]AAAACAACAAAAGGC | 11169 |
rs546970340 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55000087 | GGTACATCTGCCAGG[C/T]AGGGTGAATAATGAA | 11169 |
rs546972498 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54968134 | AGCAAGTCTCAAAAA[C/T]TTTTTTTAAATTGAA | 11169 |
rs546977074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955958 | GCTGGAGTGCAGTGG[C/T]GCTATCTCGGCTCAC | 11169 |
rs546995062 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946091 | AACAAAGGTTCCTGA[A/G]TTTCCAAAAATTAAT | 11169 |
rs547014919 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003071 | GTATTCTTTCCATGA[C/T]TATCCAAAAAAGGAT | 11169 |
rs547039898 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961922 | GCTCACTGCTACCTC[C/T]ACCTCCTGAGTTCAA | 11169 |
rs547078504 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939048 | AAATCCTGTCTATAA[A/C]GCATACATGATAAAA | 11169 |
rs547121370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023281 | AGCTATGCCTTTCTA[C/T]TGCAATCCTATACCC | 11169 |
rs547138494 | snp | A/G | 3.3106e-05 | 0.0040684 | missense | WDHD1 | GRCh38.p7 | 14:54984728 | TTTATCTTGCCTTCA[A/G]CTGAAAACCCAATCC | 11169 |
rs547149699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022061 | CGAGACATTGTGTTT[A/G]GGGGCAAGTATACCA | 11169 |
rs547199700 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990946 | TATTGCCAAGAAATA[C/T]TGCAAGATAGTAATA | 11169 |
rs547252727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961899 | TGGAGTGCAATGGCA[C/T]GATCTCGGCTCACTG | 11169 |
rs547308445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981975 | GCCACCTGCTGGAAG[A/T]TAATAATAATTTCAT | 11169 |
rs547312934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955456 | CCACTACCAATGCCA[A/G]TGTATTATTTGTATT | 11169 |
rs547330393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996082 | TGTATATGCCAAAAT[A/G]TAAAATAAGATTTTA | 11169 |
rs547359479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949520 | AAAGACCAAATCTAC[A/G]TTTGTTTGGTGTACC | 11169 |
rs547362332 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55017491 | AGTATTACAGGCACG[C/T]ACCACCCACACCTGG | 11169 |
rs547364201 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988264 | CGAAGAGAGATTTTA[A/T]ATTTAATCCATCATG | 11169 |
rs547379767 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021617 | TCTCAAACTCCTGAC[C/T]TCAAGTGATCCATCT | 11169 |
rs547477176 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968035 | CATTAATACCTGTCA[C/T]GGAATCCATGTTATC | 11169 |
rs547480546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960356 | TGTATTTTTAGTAGA[C/G]ACGGGGTTTCACTGT | 11169 |
rs547514091 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55027033 | GGGGACTCACCCGGG[A/T]GACCGAGCCTCCGCC | 11169 |
rs547526805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954455 | TGGCATTGGAATTAT[A/G]AGTGCAGATTAACTT | 11169 |
rs547542442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000749 | AATGACTTTTGACAA[C/T]AATTTATAAATAATA | 11169 |
rs547570577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953985 | TGTGGGGTGGGGGAA[A/G]TAGGGAGGGATAGCA | 11169 |
rs547588642 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55022319 | TAGCTTTATAAATAA[C/T]GGCAGTTCTGATCAC | 11169 |
rs547655758 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54971559 | AAGAACTACAAAACA[C/T]TGTTGAAAGAAACCA | 11169 |
rs547697592 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944768 | GGGATTACAGGCATG[C/T]GCCACCACACCTGGC | 11169 |
rs547760086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945323 | TAATGCAAATATTTA[A/T]CATTTACTGATCACT | 11169 |
rs547812467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976463 | TGGCCTCCCGATGTG[C/T]TGGGATTACAGCTGT | 11169 |
rs547815991 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014138 | GCAGAGTCTCATTCT[A/G]TTGCCTAGGCAGTAT | 11169 |
rs547900890 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001588 | TTTTCAAAGCAAAAC[A/C]TAAAAAATGTTATTA | 11169 |
rs547980411 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55027063 | CACTGAGGATCCACA[A/G]GAGCTGCTTCCCGCG | 11169 |
rs547993948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988183 | ATCCAAAAAATATTA[A/C]GTAGAAAAAGCAAAC | 11169 |
rs548005630 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950061 | ATTGTAAAGACCATC[A/G]AGGCTAGGAAGAAAC | 11169 |
rs548020061 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982597 | CTGATTATCCCTTTT[C/T]TTATCTGTGGCTTCA | 11169 |
rs548126502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990326 | ACTCAGGCCAGGCGC[A/G]GTGGCTCACGCCTGT | 11169 |
rs548143511 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54964362 | AAATAAAAAGGAAGC[C/T]GGGCGCAGTGGCTCA | 11169 |
rs548150989 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013810 | ACTTGGGAGGCTGCA[C/G]TAGGAAGATAACTTG | 11169 |
rs548163709 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54956712 | TGTGTAACAACTCAC[A/G]AGGCAGAATAGGGAG | 11169 |
rs548174919 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945939 | TTAAGGTTAAAAAAA[A/T]TTTTATTAAAAAATT | 11169 |
rs548192643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954507 | TATAGCTATATATGC[A/C]TCTGTGAGAAATGCT | 11169 |
rs548193353 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983481 | AGTTCAAGACCAGCC[A/T]GGCCAGCATGGTAAA | 11169 |
rs548253557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954817 | TGACTGCAATCTCCG[C/T]GTCCCGGGTTCAAGT | 11169 |
rs548343272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989784 | CCTCCCTCAGCCTCC[C/T]GTGTAGCTGTGGTTA | 11169 |
rs548599398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001703 | AAGCCATTGCTGACC[C/T]ACTGGGCTTATGTTT | 11169 |
rs548652897 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime | WDHD1, SOCS4 | GRCh38.p7 | 14:55027138 | CCCAGCGCAGGTCCC[G/T]ACAGAGGTCGCCGGG | 11169 |
rs548664261 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948796 | CGGCCGGGTACCCCT[A/C]TGAGACGAGGCTTCC | 11169 |
rs548668357 | in-del | -/T | 0.02016 | 0.0983543 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944089 | GAAAAAGGCTTTTCC[-/T]TTTTTTTTTAGTTGT | 11169 |
rs548702886 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943392 | TGAATTCATTTTTAC[A/T]TATTAATTTTTTTCC | 11169 |
rs548712361 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027690 | TCGTGCCCTCACCTT[A/G]TCGCTTCTGTAGAGA | 11169 |
rs548722939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996144 | GATATTAATATGATA[A/C]AGTCCCTATAAAGTC | 11169 |
rs548768153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981841 | AATCTAAGATTATTA[C/T]GTAAAATTTCATTAA | 11169 |
rs548810322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988632 | TTGTAAATAGCAGTT[A/C]TATCTGAGAGTAGAA | 11169 |
rs548823220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999760 | CACACACCACCACAC[C/T]TGCCTAATTTTTATT | 11169 |
rs548851038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020137 | CTTCTGGGGTCACTG[C/T]TTCCTCTTCAGCCCT | 11169 |
rs548853249 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944557 | GTAATCAACCATAAG[C/T]CTCTGACATCTATTA | 11169 |
rs548855017 | snp | A/G | 1.64808e-05 | 0.00287057 | missense | WDHD1 | GRCh38.p7 | 14:54967344 | GATAATATAGCAACA[A/G]CAGGGCGTGGAAGGG | 11169 |
rs548886683 | snp | A/G | 4.94499e-05 | 0.00497217 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000593 | CGATATTCGACCACA[A/G]GTAGGATGCCATGCC | 11169 |
rs548932226 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979327 | TGGGTAATTAAAAAA[A/T]TTTTTTTTTGTTGAA | 11169 |
rs548937439 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008142 | GCAATTAGTCTTCAA[C/T]GTATTTATTTGGCAC | 11169 |
rs548959921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953889 | AAAAAACCAAACACC[A/G]CATGTTCTCACTCAT | 11169 |
rs548985613 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55017585 | TGACCTCAAGTGATA[A/C]ACCTACCTCAGCTTT | 11169 |
rs548999730 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54961840 | ACCATTTTCAACTCC[-/T]TTTTTTTTTTTTTTG | 11169 |
rs549011631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979925 | CACATCTTGCAGATT[C/T]TTCTATATCATTATA | 11169 |
rs549029072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994139 | AATGTTCAAGTGTTA[C/T]TGTAGCATGTAAGTT | 11169 |
rs549101631 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006095 | TGTCAAACTCCTGAG[C/T]TCAAGCGGTCCTCCT | 11169 |
rs549126116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952351 | TATACACCAATAACA[A/G]ACAAACAGAGAGCCA | 11169 |
rs549137123 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971676 | TCTCATCTCACCACC[A/G]CACTGTAGCCTGGGT | 11169 |
rs549183892 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012633 | ATGAACAGAAATTTA[A/T]TGTCTCATGATTCTG | 11169 |
rs549200128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964595 | AGTGAGCAGAGATCG[C/T]GCCACTGCACTCCAG | 11169 |
rs549234115 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959193 | GGTAACATAGGGAGA[A/C]CCTGTCTCTACAAAA | 11169 |
rs549269359 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978598 | TCTAAAAAAAAAAAA[A/C]CGTTAATGAATATAC | 11169 |
rs549292024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992349 | ACAAAAATTAGCCTG[A/G]CATGGTGGCGGGCAC | 11169 |
rs549297379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953505 | GTGGAGAAATAGGAA[C/T]ACTTTTACACTGTTG | 11169 |
rs549316978 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976192 | AACAATGAGAGCAAA[-/C]AGAGGCATTAAAAAT | 11169 |
rs549333371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947966 | CACACCTGTAATTCC[A/G]GCACTTTGGGAGGCC | 11169 |
rs549353239 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948053 | AAACCTCGTCTCTAC[C/T]AAAGATACAAAATTA | 11169 |
rs549372089 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021460 | GCCAGCCTGGAATGT[A/G]CAGCGGCACAATCTC | 11169 |
rs549440552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020870 | GTACAATACAGCAAT[A/G]TAGAGAAAAAATATA | 11169 |
rs549464684 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972465 | CGCCTGTAATCCCAG[A/C]TACTCGGGAGGGTAA | 11169 |
rs549467016 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972148 | GGCGTGGTGATGGGC[A/G]CCTGTAGTCCCAGCT | 11169 |
rs549483431 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54943842 | AGAGGTTGTCTCTAT[-/A]AAAAAAAAAAAAGAG | 11169 |
rs549488759 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013228 | AAAAAATTGGTGGGG[A/C]AAGTTATGGCATTAT | 11169 |
rs549507998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021575 | TTTTTGGTAGAGACC[A/G]GGGTCTCATCATGTT | 11169 |
rs549508040 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014272 | CTAATTTATTTTTTG[G/T]AGAGACAGGGTGTCC | 11169 |
rs549509098 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54944134 | TCTTTGTTGTTGTTA[C/T]TATTATTATTAGAGA | 11169 |
rs549575945 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55000213 | TAAGGCTAATTCAGA[A/G]TAGAAACAGTTTGCA | 11169 |
rs549586484 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54964915 | AAATAAAAAGGCTAC[-/T]AGTTCCTGGACCACA | 11169 |
rs549590331 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028371 | CCACTGTTGATCTCC[C/T]GAAAGAGCAGTGGTA | 11169 |
rs549597146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993167 | CTGTTACCCTGCCTG[A/G]AGCCCACTGTTGCAA | 11169 |
rs549612408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982367 | ATCAGAAGGCTCCCG[C/T]TTGAGAAACATTTAG | 11169 |
rs549616114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994678 | AGGCACAAGAATCAC[C/T]TGAATCCAGGAGGCG | 11169 |
rs549657539 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939236 | TCACTGATTAAGATG[C/T]TTTCTACATGGATGG | 11169 |
rs549677425 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995211 | GTCTTGAACTCCTGA[A/C]CTCAAGTGATCTGCC | 11169 |
rs549678917 | snp | A/G | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942630 | AGGAATGTTATATAA[A/G]TGAGTATATATTCTT | 11169 |
rs549728808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972534 | GCACTCCAGCCTGGG[C/T]AATAAAGCAAGACTG | 11169 |
rs549736407 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974486 | ACCACAAAACCTGTT[C/T]TGTTTTGTTTTTTTT | 11169 |
rs549738130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988769 | CTTAACAATGTAAAA[A/G]AAAAATCCCATCTCT | 11169 |
rs549743265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025734 | TCTCTCACTAAACTC[C/T]GCATCACTCTCCACA | 11169 |
rs549762999 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027822 | TATCCGTTATGAAGA[A/T]AGTAACTTGTGTTCT | 11169 |
rs549806235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944723 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 11169 |
rs549830029 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988255 | TTCCTTTCTCGAAGA[C/G]AGATTTTAAATTTAA | 11169 |
rs549903737 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959792 | TATCCGCACCCCCCC[A/C/T]ACCAAACAAAAAAAA | 11169 |
rs549907659 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013332 | ATCTCAAAAAAAAAT[G/T]GTAGGGCAAGTTACG | 11169 |
rs549964230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948594 | GCATAGCCGAACAAA[A/G]GCAGCAGAAACCTCT | 11169 |
rs549997653 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959225 | CAAAAAACAACAAAA[A/C]AAAAAACCCAAACCA | 11169 |
rs550077827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949031 | AAGACCAAAGATAGA[C/T]GAAACCATAAAGATT | 11169 |
rs550088750 | snp | C/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025855 | CTATGCCAACATCAC[C/G]ACCCCACCGCCACCA | 11169 |
rs550140614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949204 | CGATCAAACCTCTCC[A/G]AGCTAAAGGAGGAAG | 11169 |
rs550147193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979401 | CCTCCAGCATTCCTC[C/T]CGCCTTGGGCTCCCA | 11169 |
rs550178254 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952457 | GAAGGACCTCTTCAA[A/G]GAGAACTACAAACCA | 11169 |
rs550203794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019884 | AACAAAAAAGAAATC[C/T]GCTATCAGTGTCTGG | 11169 |
rs550213443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013725 | AGCCTGGATAATACA[C/G]AGAGACCTAGTCTCT | 11169 |
rs550364284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017698 | ACACAAAAGTACTTG[A/G]ATTTGGAATTACAAT | 11169 |
rs550388372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987563 | TTAAAATGAACTATA[C/T]TGATATCTTTCCAGC | 11169 |
rs550410698 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943218 | CAGAAGTTTATCAGA[A/T]GCAAGCCAGCCACCT | 11169 |
rs550451890 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979987 | AAGATATGATTCACA[A/T]AATATTGAGTTCACA | 11169 |
rs550537603 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019650 | AAGGCTGGTGGATCA[A/G]TTGAGGTCAGGAGTT | 11169 |
rs550550138 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005839 | ATTTTACTTTGTTTT[A/C]TTTTTTTTTTCCTTA | 11169 |
rs550584334 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998545 | TCCACAGCCCCAATT[A/T]ACTTCTCTACAGAAT | 11169 |
rs550658486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999030 | TTCCTTTCTTTTACA[A/G]CTTTTTGTCTTCCCT | 11169 |
rs550689877 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54961410 | CCTGCCCATCACTCC[A/G]AAACCCTTCAGCACC | 11169 |
rs550709029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993206 | CACTGCAGCCTCGAC[C/T]TCTCGGGCTCAAGAG | 11169 |
rs550758453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978347 | TAGCACTTTGGAAGG[C/G]TGATGCAAGAGGATC | 11169 |
rs550758925 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941428 | GTTTCCCAAAGACTC[A/G]AGTCTATATTCAAAG | 11169 |
rs550784699 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54953888 | CAAAAAACCAAACAC[C/T]GCATGTTCTCACTCA | 11169 |
rs550797490 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990794 | GGAAAAGGGTCAGAC[C/T]TTTCCCCCCATAGTA | 11169 |
rs550817519 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008248 | ATTAATTTGGCCCAG[A/T]AATACGACATATAAC | 11169 |
rs550819286 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955955 | CAGGCTGGAGTGCAG[C/T]GGCGCTATCTCGGCT | 11169 |
rs550819366 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970712 | TCCTATCAAATTACC[A/G]ATGTCATTTTTCACA | 11169 |
rs550822452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004651 | AGAGACAGGGTTTCG[C/T]CATGTTTCCCAGGCT | 11169 |
rs550824593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997026 | TGATCTCTTGACCTC[A/G]TGATCCACCCGCCTC | 11169 |
rs550885861 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997696 | GGTGGGCAGATCACG[A/G]GGTCAGGAGATCGAG | 11169 |
rs550887178 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012530 | AACATTCCCGTTTTC[C/T]AGAACAATTCCTTAA | 11169 |
rs550906146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956054 | AGGCACCTGCCACCG[C/T]GGCTGGCCTAAATTC | 11169 |
rs550943247 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55023995 | ACGCTAGTATCTACA[A/T]AGATTTTATGCACTC | 11169 |
rs550994985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947311 | CCATTGCATTGCAGT[C/G]TGGGCAACAAGAGCA | 11169 |
rs551017679 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988212 | ACGGGTGACTAGTAC[A/C]TTTTTTGGTTTGTTT | 11169 |
rs551054880 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54959782 | AGATACCCTGTATCC[A/G]CACCCCCCCCACCAA | 11169 |
rs551092379 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943274 | GAACAGAACACCAGT[A/C]TTTTTCCCAAAAGGA | 11169 |
rs551095222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977760 | CTTCTAAGTGTAAAA[C/G]CTGTAATTTACAGTC | 11169 |
rs551103691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941857 | TATTACTTAAATGCA[A/G]AGCACATTAAAGATT | 11169 |
rs551110239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948284 | AAGCGCAAGGGGTCA[A/G]AAAATTCCCTTTCCT | 11169 |
rs551170787 | snp | A/C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55014595 | TCAAATAACCATCTG[A/C/T]ATCTATCATAACTTG | 11169 |
rs551191558 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971927 | AACGGTGGGTCACAC[C/T]CATAATCCCAGAACT | 11169 |
rs551201700 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54999683 | CTTGCTGTAGCCTCA[A/G]CCTCCTGGGCTCTAG | 11169 |
rs551233518 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956848 | TCCCACCTCAGCCTC[A/C]TGAGTATCTGGGACT | 11169 |
rs551235291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026618 | ATTATTCCTCTATCC[A/G]CATGAGTCATTTTTA | 11169 |
rs551273347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950925 | CGAAATGAAGGCAGA[A/C]ATAAAGATGTTCTTT | 11169 |
rs551334466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951616 | AACTATTCCAATCAA[C/T]AGAAAAAGAGGGAAT | 11169 |
rs551338792 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012410 | TAATTTCCAAAGTCC[G/T]TCTGAATAAGTCTTC | 11169 |
rs551347948 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999628 | TTTTTAGATGGGGTA[A/T]CACTGTCATCCAGGC | 11169 |
rs551355218 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958911 | CTCTTGACCAGAATA[A/C]TTCCCTGAGCTCCTG | 11169 |
rs551376504 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953364 | CAGCCAACAGACACA[G/T]GAAAAAATGCTCATC | 11169 |
rs551449377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994059 | TTGTAGCATGTAAGT[C/T]GTTACAATAAGCACT | 11169 |
rs551527903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971511 | CACAAAATACCTAGG[A/G]TATATCTAACCAAGG | 11169 |
rs551618629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991769 | AAAAAAGCACTTATG[A/C]AATTGTTTGAGTTGT | 11169 |
rs551634683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964543 | ACTCGGGAGGCTGAG[A/G]CAGGAGAATGGCGTG | 11169 |
rs551674402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997774 | AAATTAGCCAGGCGT[A/G]GGGGCACAAGCCTGT | 11169 |
rs551679731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992295 | CAGGAGTCCGAGACC[A/C]GATTGACCTACATAG | 11169 |
rs551684332 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006333 | TATATAGATCTTTCA[C/T]ATTTCTTGTACATTT | 11169 |
rs551697559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958514 | ATATAGCACTTCCAG[C/T]TCTACCACCCTACAG | 11169 |
rs551703102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951854 | CGCAAATAAATAAAC[A/G]TAATCCAGCATATAA | 11169 |
rs551830003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025553 | GCATCCATGAGTGCT[C/T]CTTTTCCAATTCATC | 11169 |
rs551865183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979238 | CTCACTGTAACCTCA[A/G]CCTCCTGGGCTCAAG | 11169 |
rs551957541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946546 | GCTGGAGTGCAGTGG[C/T]ATAATCAGCTCACTG | 11169 |
rs551968279 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961330 | CTCTATTAAAAAAAA[-/T]AAAATAAAATAAAAA | 11169 |
rs551994905 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54944860 | TGATCTGCCCGCCTC[C/G]GCTTCCCAAACTGCT | 11169 |
rs552015881 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004738 | GATTATGGGCGTGAG[C/G]CAGCGAGCCCGACCC | 11169 |
rs552030902 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952311 | TCAGGATACAAAATC[A/C]ATGTGCAAAAATCGC | 11169 |
rs552084658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947346 | GAAAAAAGTGTTAAG[C/T]GGAAAAAAAACCATG | 11169 |
rs552127886 | in-del | -/AA | 0.0663949 | 0.169674 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974092 | TGGAAGAGGAATTTA[-/AA]AAAAAAAAAAAACAA | 11169 |
rs552134059 | snp | G/T | 1.67114e-05 | 0.00289057 | missense | WDHD1 | GRCh38.p7 | 14:54941530 | GATAGTTTCTGATTT[G/T]TAGAAAAATCTAAAG | 11169 |
rs552146176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947872 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCA | 11169 |
rs552163292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023065 | GTGATCCACCCACCT[C/T]GGCCTCCCAAAATGC | 11169 |
rs552171517 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949666 | ATGCCACAAAGATAC[G/T]CCTCGAGAAGAGCAA | 11169 |
rs552191855 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983926 | ACATGTAATCAACAT[-/A]AAAAAATTGATTTTT | 11169 |
rs552207658 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016994 | CAATGTCATCAGGAG[A/T]TTTAAATAGAAAATC | 11169 |
rs552253816 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977561 | CTTTATTAGCTGATA[A/C]TAAATGTAGAGCTAC | 11169 |
rs552264756 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959577 | AGACCAGCTTCGGCA[A/C]CAAAGCAAGCTCCTC | 11169 |
rs552279536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003359 | TACAAAAAATAAAAA[A/G]ATTAGCCAGCCATTG | 11169 |
rs552298570 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008419 | CCATAATACTACATG[C/G]AAAGTGGTTCAATTA | 11169 |
rs552362821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022295 | TTCCCTTCAAGGCCC[A/G]GGGGTTAGTAGCTTT | 11169 |
rs552368915 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940089 | CAGAATAGTAACTAA[C/G]ATTTATATAAAAGAT | 11169 |
rs552371404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950211 | GGCAAATTGGATAAA[A/G]AGTCAAGACCCATCA | 11169 |
rs552387053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991109 | AGTGCTCCAGGCTAC[C/T]TAATCAAAGTTTTTA | 11169 |
rs552395591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975933 | GTTGGGTTAGAAAAT[A/G]CATTTAAAGTTAAAA | 11169 |
rs552414155 | in-del | -/ATTTTGCTCTGTATTATTTCCTTCC | 0.0562307 | 0.157967 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995357 | TGTCAATTTTATTGA[-/ATTTTGCTCTGTATTATTTCCTTCC]ATTTGCTTGGGGTTT | 11169 |
rs552559104 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961823 | GCCCACTCCCTGTAC[A/G]CAACCATTTTCAACT | 11169 |
rs552595713 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996173 | TCTGTCATATTGTAA[C/G]ACAGTCTCTCATTTA | 11169 |
rs552620784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009615 | TTTTGTATTTTTAAT[A/G]GAGACGAGGTTTCAC | 11169 |
rs552656029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996586 | GCCTGGGTGACAGAG[C/T]GAGACCCTGTCTCAA | 11169 |
rs552667615 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965058 | AGACAAGAGTGGCAA[A/T]TTGCTCTGTGGTCTC | 11169 |
rs552727704 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990335 | AGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 11169 |
rs552729480 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951197 | GCCTTCAAAAAATCA[A/G]TGAATCCAGGAGCTG | 11169 |
rs552800152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008947 | GATTACAGGTGTGCA[C/T]CACCATGCCCAGCTA | 11169 |
rs552826699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961036 | TCTCAAACGTCTGGT[C/T]TCAAGTGATCCTTCC | 11169 |
rs552831860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967914 | GCGTGAGCTACCCTG[A/C]CCAACCTCACATCTC | 11169 |
rs552838379 | snp | A/G | 1.71581e-05 | 0.00292895 | missense | WDHD1 | GRCh38.p7 | 14:54955687 | TGGAAATAGGATGCT[A/G]CAGATGCCTATAAAA | 11169 |
rs552858046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969239 | GAGACGGGGTTTCAC[C/T]GTGGTCTCGATCTCC | 11169 |
rs552861485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002396 | CTGGCTCAGCCTCCT[A/G]AGTAGCTGGGACTAC | 11169 |
rs552969439 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026433 | AACTAGTGATCTGAC[-/A]AAATTAATAATGTAA | 11169 |
rs553023862 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55012523 | TTAATGAAACATTCC[C/G]GTTTTCTAGAACAAT | 11169 |
rs553052355 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945563 | GTTTTTTTGTAGAGA[C/T]GGAGTCTAGCTCTTT | 11169 |
rs553054018 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942078 | ACACAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 11169 |
rs553136514 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55010208 | AAGAAACAACAAACA[A/G]CAAAAAATTAAGTCA | 11169 |
rs553174647 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022437 | TCTTTGTGGCATTTT[C/T]CCCCCCACAGAATAG | 11169 |
rs553242027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015765 | GTGCAGTGGTGCTAT[C/T]ACAGCTCACTGCAAC | 11169 |
rs553272997 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960298 | TCAGCCTCCCAAGTA[C/G]CTGGGATTACAGGTG | 11169 |
rs553282161 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956560 | TGAGAATTGCTTGAA[-/C]CCAGGAGACAGAGGC | 11169 |
rs553336924 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004282 | TAACTTTCCATATAC[A/C]TTTGGTTCTATTTAT | 11169 |
rs553348369 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996370 | CTCAGCACTTTGGGA[A/C]GCCGAAGCAGGTGGA | 11169 |
rs553357522 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974573 | CTCACTCCTGTAATA[A/T]CCCAGCACTTTGGGA | 11169 |
rs553360135 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014348 | GCCTGTCTTGACCTC[C/T]CAAAGTCAAGGGATT | 11169 |
rs553372330 | snp | A/C | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975603 | ATCTGCCTGCCTTGC[A/C]CTCCCAAGGTGCTGG | 11169 |
rs553383430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982817 | AGAACATGAATCTCC[A/G]AAAAGAGAAATATTT | 11169 |
rs553387872 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949777 | AAAGGGAAGCCCATC[A/G]GACTAACAGCTGATC | 11169 |
rs553411626 | snp | C/T | | | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54963029 | CAATTCGGCTGCCTT[C/T]TCTACAGCCAGTTCA | 11169 |
rs553437269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968541 | AAAATTGAGACTAAA[A/G]AATCCATACAAAGGA | 11169 |
rs553473564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974500 | TTTGTTTTGTTTTTT[G/T]TTTTTTTGTTATATT | 11169 |
rs553497219 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965594 | CATAGACTGATGGGC[A/G]AAAGCAAAAGGGAAG | 11169 |
rs553533101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967646 | TTTTTTTTGAGACAG[G/T]GTCTCACTGTGTTGC | 11169 |
rs553544515 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988313 | AGTTGGCCAAGGCTC[A/G]GGTTGAATTAACTGC | 11169 |
rs553564810 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54966452 | TTTAACTTTAACGTT[C/T]TCAGTATATTTATTT | 11169 |
rs553627283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945124 | GTAGGCTCTTTTTCT[A/G]TTTCCCCAAACCAGC | 11169 |
rs553640012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954971 | CATCCTCAGATGATC[C/T]GCCTGCTTCGGCTTC | 11169 |
rs553642581 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026865 | AGCAGCGAGGCTAGG[C/G]ATAGGAAGAGAGCTT | 11169 |
rs553644449 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949100 | ATCAGAGCACCTCTC[C/T]CCCCCCAAAGGAACG | 11169 |
rs553658027 | snp | C/T | 1.65457e-05 | 0.00287621 | missense | WDHD1 | GRCh38.p7 | 14:54989187 | TCATCATTATAGCAG[C/T]GAATAATTCCAATAG | 11169 |
rs553724521 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959388 | GGATGACAGTCACAC[C/T]CTGGCGGGGGGAAGA | 11169 |
rs553807758 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016415 | TGTTGACATTTACCA[C/T]GGGGCTACAGTCATA | 11169 |
rs553818328 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55018955 | TTGAACCTGGGAGGC[A/C]GAGGTTACAGTGGGC | 11169 |
rs553850339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960234 | GTGCGGTGGTATGAT[C/T]TCACCTCACTGCAAG | 11169 |
rs553853010 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953171 | AGCAAAAGAAACTAC[A/C]ATCAGAGTGAACAGG | 11169 |
rs553866105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001846 | AATAAAGGCTAACTA[C/T]TGATCATTTTAGAAC | 11169 |
rs553915646 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960561 | CTGGAGTGCAGTGGC[A/G]TGATCTCCACTTACT | 11169 |
rs553957014 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | WDHD1, SOCS4 | GRCh38.p7 | 14:55027293 | ACCGTGACGGCTGGG[C/T]TGGGACCGGAACGCC | 11169 |
rs553972471 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026392 | TTCCAAACAGAACAG[A/G]CCACTGAATTTGACA | 11169 |
rs553974993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943590 | TTTTGTAGAGATGGT[A/G]TATCACTATGTTGTC | 11169 |
rs554005174 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994722 | GCCAAAATCACACCA[A/C]CGCACTCCAGCCTGG | 11169 |
rs554030384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944119 | TCATGATCGTTATTA[C/T]CTTTGTTGTTGTTAT | 11169 |
rs554043451 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55022072 | GTTTGGGGGCAAGTA[C/T]ACCAGTTTGACACCT | 11169 |
rs554044286 | in-del | -/AAATAAAT | 0.00641404 | 0.0562662 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938755 | GAGACCCTGTCTTTA[-/AAATAAAT]AAATAAATAAATAAA | 11169 |
rs554055439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965683 | ATTTTAGGCTGGGCA[C/T]GGTGGCTCATGCCTG | 11169 |
rs554174091 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953672 | AAAAACACATGCACA[C/T]GTATGTTTATTGTGG | 11169 |
rs554230588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968180 | TATTCTGAGACCATA[A/G]TAAAATAAAAATAGA | 11169 |
rs554232187 | snp | A/G | 4.95536e-05 | 0.00497738 | stop-gained, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55002095 | TTGTAAAACCTACCT[A/G]AGAGATGAAATTATC | 11169 |
rs554237575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948862 | CAATATTTGCTGTTC[C/T]GCAGCCTCCGCTGCT | 11169 |
rs554280326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003558 | AAAGCCAATTGTGTA[C/T]ATATGTATAAAAAAG | 11169 |
rs554300792 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54989647 | AAAATAAATACATAC[A/T]TTTTAAGAAAACATA | 11169 |
rs554325603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971960 | GGGAGGCTGAGGTGG[A/G]TGGATCACTTGAAAC | 11169 |
rs554356947 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974091 | CTGGAAGAGGAATTT[-/A]AAAAAAAAAAAAACA | 11169 |
rs554380480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974625 | GAGCTCTGGAGATCG[A/G]GACCAGCCTGGGCAA | 11169 |
rs554414229 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012743 | AGAGAGGGCGAGAGG[C/G]AGAGCAAGAGGATCA | 11169 |
rs554443818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975180 | AAGAAGGTCTCTGTT[A/G]GTAGAGAGCAAATTA | 11169 |
rs554477337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006162 | AGCCACCACACATAG[C/G]CTGTTGTTTTATATG | 11169 |
rs554477376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013366 | TTATCATACATTTTA[A/G]AATATTATTTCATGA | 11169 |
rs554492815 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954058 | ACATGGCACATGTGT[A/G/T]CATATGTAACAAACC | 11169 |
rs554538705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006785 | ACTTCAAAATGAATC[C/T]TGAAAAAGTTCAAAT | 11169 |
rs554558201 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949106 | GCACCTCTCCCCCCC[A/C]AAAGGAACGCAGCTC | 11169 |
rs554605296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953034 | ACCCCAGAAGAAAAC[C/T]TAGGCAATACCATTC | 11169 |
rs554605309 | in-del | -/AGAC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54981253 | TTTTATTAAAATAAA[-/AGAC]AGTAATAAAAGGTGA | 11169 |
rs554658479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981388 | GTGACTGAAAACTTC[A/G]GAGTGAATATGAACA | 11169 |
rs554696767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955009 | GCTGAGATTATAGGC[A/G]TGAGCCACCATGCCC | 11169 |
rs554726625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995311 | AAGAACCAGCTTTTG[C/G]TCTCATTGACTTTCT | 11169 |
rs554758001 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028104 | CCTTCCAGTATCAAT[A/C]ACATTTATTTTATTA | 11169 |
rs554771022 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55012734 | GAAAGGTAAAGAGAG[A/G]GCGAGAGGGAGAGCA | 11169 |
rs554779440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988918 | AAACTCTTCTGAAAT[C/T]TCATATTACAAAAAA | 11169 |
rs554804242 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944848 | CCTGACCTCACGTGA[C/T]CTGCCCGCCTCGGCT | 11169 |
rs554821178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021011 | ACACGAAGAGGAGTT[A/G]GTCTTACTGTCTCAG | 11169 |
rs554826465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014367 | AGTCAAGGGATTACA[A/G]ACATGAGTCACCATG | 11169 |
rs554832112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953744 | TCATCAATGATAGAC[C/T]AGATTAAGAAAATGT | 11169 |
rs554848930 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967690 | CGGTGGTGTGATCAC[A/G]GCTCACTGAAGCCCC | 11169 |
rs554887839 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008486 | TTTCCTGCTAACTCT[C/G]TTACTGAATAAAACA | 11169 |
rs554947835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994861 | CTAGTGGCTACTATA[C/T]ATTGGATAGCACAAA | 11169 |
rs554951015 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975584 | AACTCCTGACCTCAG[C/G]GTGATCTGCCTGCCT | 11169 |
rs554999074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988354 | AAGAAAACATTCTTG[A/G]GTGATAAAGACGTAG | 11169 |
rs555084389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018892 | TCCAGGCATGGTGGC[A/G]CATGCCTGTAATCCC | 11169 |
rs555109249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965799 | TGTTTCTACTAAAAA[C/T]ACAAAAATTAGCCAG | 11169 |
rs555140907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999298 | GGACAGTCTATTTCA[C/T]CTTTTCTAAAAAAAC | 11169 |
rs555154181 | snp | C/G | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012854 | TACTTCTCAGTAGAC[C/G]CCACCTCCCACCACT | 11169 |
rs555170296 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964910 | TGTACAAATAAAAAG[C/G]CTACTAGTTCCTGGA | 11169 |
rs555170950 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959453 | AGGGAGGCAGGCAGG[C/G]AGGCAGGCAGGCAGG | 11169 |
rs555277383 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000216 | GGCTAATTCAGAGTA[A/G]AAACAGTTTGCAGGC | 11169 |
rs555374011 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942243 | GCGAGAGCAAGACTC[C/T]GTCTCAAAAAATAAA | 11169 |
rs555377952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979720 | GCTCAATTTACATGC[C/T]CAAAAAGTATAAAAA | 11169 |
rs555413657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005471 | GATATGACACTGACA[C/T]TGAAAGAGTTTTCAA | 11169 |
rs555439576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963638 | CAAAACCCCGTCTCT[A/G]CTAAAAACACAATTA | 11169 |
rs555443333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980229 | GCTAAGGTGGGAGGA[C/T]CGCTTGAGCCCAGGA | 11169 |
rs555445204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972044 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACGAGGT | 11169 |
rs555520656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985259 | AATGTGATACAGAAT[A/G]TCAGAGTGGTTTGTT | 11169 |
rs555551107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952548 | GGAAGAATCACTATC[A/G]TGAAAACGGCCATCC | 11169 |
rs555584253 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977937 | AAAAGCATGTTAAGA[A/C]AAAAAAAGCCAGCTG | 11169 |
rs555589332 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993348 | TGGTCTTGAACTCCT[A/G]GCCTCAAGCAATCCT | 11169 |
rs555614285 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953022 | AAAACCATAAAAACC[A/C]CAGAAGAAAACCTAG | 11169 |
rs555648712 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987018 | CACAACAAAATTATC[G/T]ACATTTAAAGATTAC | 11169 |
rs555652963 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986510 | ATCTATTTCTTACTG[C/T]GGCAAAGCAGACAAA | 11169 |
rs555687086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011657 | TGTGTGTTTGTGTGT[A/G]TATATATATGTATTT | 11169 |
rs555691063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019760 | TGTGATCCCAGCTAC[C/T]TGGGAGGCTGAGGAG | 11169 |
rs555739164 | in-del | -/ATT | 0.00358779 | 0.0422022 | cds-indel | WDHD1 | GRCh38.p7 | 14:54940069 | ACCAACAGCATCATC[-/ATT]ATCAGAATAGTAACT | 11169 |
rs555744987 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012212 | ACATTTTTTCTTCTG[C/G]GAACGCATTTTCTAA | 11169 |
rs555752543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020319 | CCAATGGCCTCCACA[C/T]TGCTAAATCTAATGG | 11169 |
rs555758353 | snp | C/T | 0.000148813 | 0.00862464 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013600 | GTCACAATAAAACTG[C/T]GAAGAAAAGACACAA | 11169 |
rs555759366 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964058 | GGCTGCAGTGAGTTA[A/C]AATCTTGCCACTGTA | 11169 |
rs555770391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017428 | GGTCACTGCAACCTC[C/T]ACTTCCCAGGTTCAA | 11169 |
rs555779829 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54994761 | TGAGACTCCGCCTCA[-/A]AAAAAAAAAAAAAAA | 11169 |
rs555836991 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | WDHD1, SOCS4 | GRCh38.p7 | 14:55027235 | AGGGAGGGAGCTGAA[A/C]ACGGAAGTGGTGGCG | 11169 |
rs555842090 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945791 | TGATCCACTCGCCTC[A/G]GCCTCCCAAAGTGCT | 11169 |
rs555873719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981051 | GTGAGGCGGAGCTTG[C/T]AGTGAGCTGAGATCA | 11169 |
rs555887803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957889 | ATCTTCTGTTACTGC[A/G]GAAGAGTGGCAGCTC | 11169 |
rs555888675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023724 | TTAAGCAGATACAAC[C/G]TCATACAGTGTTTTA | 11169 |
rs555928280 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994150 | GTTATTGTAGCATGT[A/C/G]AGTTGTTACAATAAG | 11169 |
rs555998154 | snp | C/T | 1.64947e-05 | 0.00287177 | missense | WDHD1 | GRCh38.p7 | 14:54941600 | TTTCTTCCTGGTTTT[C/T]TGTTTCATCACTTTC | 11169 |
rs556016690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024306 | CGCAAACTCAATCTC[C/T]ACCCACAGCTCTACC | 11169 |
rs556041485 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953556 | AACCATTGTGGAAGG[C/T]GGTGTGGCGATTCCT | 11169 |
rs556072037 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54944797 | GCTAATTTTTTGCAT[A/G]GGGTTTCACCATGTT | 11169 |
rs556073352 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017780 | CCATACTTGTCAAAT[G/T]TTCAGATTTTATTTA | 11169 |
rs556092512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942996 | GTTCTAAATGACGCT[A/G]AAGGTGTTTAAACCA | 11169 |
rs556180096 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972920 | TGGTAACAGGTCAAC[A/G]GGGCAAAGACTGTCT | 11169 |
rs556203469 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999352 | TGCATGTGAAGATGG[C/G]GGAGGGCAGGTACCC | 11169 |
rs556223202 | snp | A/G | | | stop-gained | WDHD1 | GRCh38.p7 | 14:54995639 | CTAGGATGTGACTTC[A/G]CTGTCTAGGACGACC | 11169 |
rs556242806 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54965956 | AGCGAAACTCCGCCT[A/T]AAAAAAAAAAAAGAA | 11169 |
rs556242882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973749 | ATGTTAATTGCCTAA[A/G]CATTTTTTTCTAAAA | 11169 |
rs556274922 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993525 | TTCTGAGTCTTGGTG[A/C]AACATCAAAGAATAT | 11169 |
rs556349224 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948393 | TAGCAAACGGCACAC[C/T]AGGAGATTATATCCC | 11169 |
rs556356973 | snp | A/G | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028716 | CTTATCAATCAAGCC[A/G]TTTGATTCATAGGTT | 11169 |
rs556384592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987873 | CTCAGGTCATCTGTC[C/G]GCCTTGGCCTCCCAA | 11169 |
rs556442269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971834 | AAAAAAATCAGCAGC[A/G]AAAAACAAATATCCC | 11169 |
rs556442284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964099 | GGTAACAGAGTGAGA[A/C]CCTTTCTCTAAAAAA | 11169 |
rs556498695 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54976135 | GACCACTAGGCCACA[C/T]TGGCTTTCCAGAGAA | 11169 |
rs556521537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006124 | CTGCCTCAGCCTCCC[A/G]AAGTGCTGGGATTAT | 11169 |
rs556549837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958716 | CTTCCTCTCTGGACC[C/T]GTGGACTCATTGTGT | 11169 |
rs556617396 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948019 | TCAGGAGTTTGAGAC[C/T]AGCCTGACCAACATG | 11169 |
rs556624342 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005590 | GATGTACTGTCCCAT[C/G]TGGAAGACAAAGCTG | 11169 |
rs556656394 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55004576 | TTATGCCTGAGACTC[C/T]CAAGTAGCTGGGATT | 11169 |
rs556660032 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978071 | TTGCAAATAAATAAT[G/T]TCATATACCTCTAAG | 11169 |
rs556716145 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54989664 | TTTAAGAAAACATAA[-/T]TTTTTTTTTTTTTTG | 11169 |
rs556750736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024934 | TGGCCTCGTGGGAAG[A/G]GAAAGACCTGACCGT | 11169 |
rs556808158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018022 | AGCGCACAAACCGAT[A/G]TTAATTAAATACACA | 11169 |
rs556827692 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951293 | AGAATCAAATAGATG[C/T]AATAAAAAATGATAA | 11169 |
rs556829882 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940596 | GACATGATTAAACCT[G/T]GTTTGTTCAATATAA | 11169 |
rs556854299 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012703 | AAGGGTCTTCTTATT[G/T]CATCATCCCATCTTG | 11169 |
rs556891051 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022508 | CCAACATGGCAAAAC[A/C]CCGTCTCTACTAAAA | 11169 |
rs557011541 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016632 | ACTTTCTGAGGTGAT[G/T]AAAATGGTCTATACC | 11169 |
rs557056669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992492 | AAGACTCCCTCTCAA[A/G]AAATAAAAACAAGAA | 11169 |
rs557121537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011455 | CCTGAACCCGGGAGG[C/T]GGCGGTTGCAGTGAG | 11169 |
rs557184501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004794 | TTCCATGTTGCTTAA[A/G]AGCCTGTGCAAGAAC | 11169 |
rs557251815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983529 | AATACAAAAATTAGC[C/T]GAGTGTGGTGACGCA | 11169 |
rs557257456 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54949432 | ATGAATGAAATGAAG[C/T]GAGAAGAAAAGTTTA | 11169 |
rs557318366 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997972 | ACCCTAGCACTTTGG[A/G]GGGCTGCGGTGGGTG | 11169 |
rs557336267 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942119 | AGCCGGGCATGGTAG[C/T]GGGCGCCTGTAGTCC | 11169 |
rs557337654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015967 | GCCTCTCAAAGTGCT[C/G]GGATTATAGGCATGA | 11169 |
rs557348300 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946311 | TCTGACTCAACCTTC[G/T]GAGTGGCTAGGACTA | 11169 |
rs557403128 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010094 | AAAGTGCTGGGATTA[C/G/T]AGGCGTGAGCCACCA | 11169 |
rs557424600 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942930 | AAAGTCTTATTTATT[C/T]AGACGCCATTTTATT | 11169 |
rs557447781 | in-del | -/AC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54962383 | AAAACAAAAACATAA[-/AC]ACACACACACACCAA | 11169 |
rs557492712 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024997 | AAAAGAGGAAGGAAT[G/T]CCTCTTGCAGTTGAG | 11169 |
rs557493575 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969625 | AAAATCACAGCTGAA[C/T]TCTAGATGCACAAAG | 11169 |
rs557542209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949806 | TCTCTCGGCAGAAAC[C/T]CTATGAGCCAGAAGA | 11169 |
rs557545016 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945667 | TGCCTCAGCCTCCCA[A/C]ACAGCTGGGACTACA | 11169 |
rs557548872 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015446 | TTCTTTGTACTTCCA[C/G]CTTCTGCCATGGTCT | 11169 |
rs557674188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998019 | GAATTCAAGACCAGC[C/G]TGGCTAACATGGTGA | 11169 |
rs557676833 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54981389 | TGACTGAAAACTTCA[C/G]AGTGAATATGAACAA | 11169 |
rs557718220 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939678 | TCAAAGTTCTGATTT[G/T]TAAGTTAAACCAAGT | 11169 |
rs557738987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010833 | GGCATCAGAAGGCAC[A/G]GCCACAATGGCCACT | 11169 |
rs557740342 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022308 | CCGGGGGTTAGTAGC[-/T]TTATAAATAATGGCA | 11169 |
rs557745435 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017359 | TCTTTTTTTTTCTTT[G/T]TGAAACAGGGCCTTG | 11169 |
rs557781436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986396 | TTGTATTGAACTCCT[A/G]GGCTAAAGCAACTCT | 11169 |
rs557810382 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011481 | GTGAGCTGAGACTGC[C/G]CCATTGCACTCCAGC | 11169 |
rs557819267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025906 | CTTAATGCCTGCTCC[A/G]TCTTCAGATGGCGTC | 11169 |
rs557853869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979511 | ACTTTCATTTCTTTA[C/T]CTCCCATGCCCACCC | 11169 |
rs557882636 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018803 | GCTCACGCCTGTAAT[A/C]CCAGCACTTTGGGAG | 11169 |
rs558028851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952506 | GAGGACACAAACAAA[C/T]GGAAGAACATTCCAC | 11169 |
rs558053775 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992043 | CAGATCACTTAAGGT[C/T]GGGAGTTCCACGTTG | 11169 |
rs558076881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016769 | ACTGTATTGGACAGC[A/G]CAGCATTAAAAGAAA | 11169 |
rs558116994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992661 | GACTCACGCTTGTAA[C/T]TGCAGCACTTTGGGA | 11169 |
rs558118815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977814 | AATATAACAGTTAAA[C/T]GTTACCAGCTGTAAT | 11169 |
rs558126312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984709 | CTTGTTTTTTTTAAA[C/T]AAATTTATCTTGCCT | 11169 |
rs558166118 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969654 | AGAACTGGTACCAGT[A/C]CTACTGAAAATATTC | 11169 |
rs558199101 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026239 | AATGGGACTTGGAAA[A/G]ATAAAAGGGACCAGA | 11169 |
rs558233670 | snp | C/G | 1.65488e-05 | 0.00287647 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962885 | TTATTCAATAAAGAG[C/G]TATGCAAAGACCAAC | 11169 |
rs558263061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990698 | GTATCATACCTTGTT[C/T]CAAATCCTAAGAACA | 11169 |
rs558271506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003708 | AGCTGGGACTACAGG[C/T]GCACACCACCACGCC | 11169 |
rs558323821 | in-del | -/AAATAAAT | 0.0139241 | 0.0822689 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938762 | GTCTTTAAAATAAAT[-/AAATAAAT]AAATAAATAAATAAA | 11169 |
rs558341420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946377 | TTCTGATTAAGTATA[C/T]CAACATCTGTGACAA | 11169 |
rs558346575 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946616 | AGACTCTCAAGCAGT[A/T]GGGACTACAGGCATG | 11169 |
rs558363628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950574 | AACACCCCACTGTCA[A/G]CATTAGACAGATCAA | 11169 |
rs558379915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968429 | ATCTCAAATTAACAA[C/T]CTAACATTGCATCTA | 11169 |
rs558386314 | in-del | -/AGAGA | 0.00993419 | 0.0697739 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951273 | AATAAAGAAGAAAAG[-/AGAGA]AGAATCAAATAGATG | 11169 |
rs558459241 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975344 | ATCAGTAATTTCTCA[C/T]ATTCATAATTTTTTT | 11169 |
rs558478994 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949312 | AACTCCTCAAATGAC[C/G]TGATGGAGCTGAAAA | 11169 |
rs558483962 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941108 | GAAAGAGGACTATTG[C/T]CCTTCCTTGCACATG | 11169 |
rs558493742 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54942077 | AACACAGTGAAACCC[C/T]GTCTCTACTAAAAAT | 11169 |
rs558570519 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54978129 | AATCTTACTTGAATA[A/G]GCATTAGGCAGAATA | 11169 |
rs558606480 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945529 | TCCAACAACCAGGCA[A/C]TTTGACTCCAAAGTC | 11169 |
rs558621761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009946 | CTGCCTCAGCTTCCC[A/G]AGTAGCTGGGATTAC | 11169 |
rs558642822 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54982858 | GAGACAGAGATGACA[A/G]GTGATTTAAAATAAG | 11169 |
rs558647643 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997169 | GGCGTGATCTTGGCT[C/G]ACTGCAAACTTCATC | 11169 |
rs558655194 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986919 | GATTTAGACATGGAA[A/G]TAATTAACCAAATTC | 11169 |
rs558736696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021740 | TGAAATTACTTCGCT[C/T]CCTTATCTTTTTTGC | 11169 |
rs558748071 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004921 | TTTCAGGAGGGAACT[G/T]CTAAATAGGCACAGA | 11169 |
rs558772517 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028785 | AAAGCTTGAGCCTCC[G/T]AGTTTAACAGTCCTG | 11169 |
rs558805233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982682 | CTTCGGAGAAAAAAA[C/T]CTATACAAATGGAAG | 11169 |
rs558819014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949148 | CGGAACAAAGCTGGA[C/T]GGAGAATGACTTTGA | 11169 |
rs558829674 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54950297 | TAAAGGGATGGAGGA[A/G]GATCTACCAAGCAAA | 11169 |
rs558830698 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988321 | AAGGCTCAGGTTGAA[C/T]TAACTGCAAAGGGAT | 11169 |
rs558871489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015675 | GGTGATGAGAGAAGT[A/G]TTTCACGTTTTTGTT | 11169 |
rs558915151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960469 | CACCACGCCCAGCTT[A/G]TAGTCTCTTTATTTT | 11169 |
rs558937418 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028205 | CAAACACACAGGCAA[A/G]CCGTCGTGTTCTTAC | 11169 |
rs558979636 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954582 | AGACCGGTAACCATC[G/T]TTTGTCCACAAGTAG | 11169 |
rs558999915 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989667 | AGAAAACATAATTTT[-/A]TTTTTTTTTTTGGAG | 11169 |
rs559033586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974734 | TGGGAGGCTGAGGCA[C/T]AAGAATCACTTGAAC | 11169 |
rs559053977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989915 | GTGACCAACCCACCT[C/T]GGCCTCCCAAAGTGC | 11169 |
rs559085665 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014184 | CTAAACCCTCCGCCT[-/C]CCAGGCTCAAGTGAT | 11169 |
rs559086753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954793 | GGAGTGCAGCGGTGT[A/G]ATCTCAGATGACTGC | 11169 |
rs559179689 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022828 | CCTTTCTCTTTCTTT[C/T]TTTTTTTTTTTTTGA | 11169 |
rs559258711 | in-del | -/AAAT | 0.453834 | 0.144747 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942260 | TCTCAAAAAATAAAT[-/AAAT]AAATAAATAAATAAA | 11169 |
rs559329073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022127 | GGGTGGCCAGGGGCA[C/T]TGCCCAACATTAAAA | 11169 |
rs559332419 | in-del | -/TG | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55013473 | ATCAATTGATATAAC[-/TG]TTTTTACTACCTTCA | 11169 |
rs559358504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996490 | CTATAGTCCCAGCTA[C/T]CTGCGAGGCTGAGGT | 11169 |
rs559375962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950059 | AAATTGTAAAGACCA[C/T]CAAGGCTAGGAAGAA | 11169 |
rs559403395 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54939960 | AAACATGCTTTCCAA[C/T]GTACTATAAATAAAC | 11169 |
rs559466643 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940563 | TATTAGTCTCTGCTT[A/T]GAAAACCAAAAATGT | 11169 |
rs559471681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943911 | GCCATGATCACACCA[C/T]GACACTCCTGCCTGG | 11169 |
rs559489059 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54978008 | ACTTGTAATATTAAA[C/T]GAAATGAAGAAGCAA | 11169 |
rs559489313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007778 | CTGTGGATATTAAGG[C/T]ATATTTGTGGAGGAT | 11169 |
rs559526086 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54979452 | TGAGCCACCTCGCCT[C/G]GCCCAATAGTCAAAT | 11169 |
rs559529671 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967783 | ATGCCACCATGCCTG[C/G]CTAACTTTTGTATTT | 11169 |
rs559555557 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027512 | CCTGGCCTCGCAGGC[C/T]GGGGTCTTGTTCCTG | 11169 |
rs559598743 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003178 | TACTACATTTCCTTG[A/G]GCTCAATTATCACTT | 11169 |
rs559600154 | in-del | -/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005998 | GTCTCCCAAGTAGAT[-/G]GGACTACAGGAATAT | 11169 |
rs559661247 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014169 | CATGATTATAGCTCT[A/C]TAAACCCTCCGCCTC | 11169 |
rs559679811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967219 | AGGATAATTTTAAAG[C/T]GTGTGTATCACAGGT | 11169 |
rs559733450 | snp | C/T | 4.97055e-05 | 0.00498501 | missense | WDHD1 | GRCh38.p7 | 14:54944439 | TATTACTTCTATTTT[C/T]TTCTAACCACATCTG | 11169 |
rs559846694 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958459 | CAAGAACTGTTGACA[A/C]TATTATCATTTCCTC | 11169 |
rs559936368 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009566 | CCTCCCAAGTAGCCG[A/G]GATTATAGGCACCCG | 11169 |
rs559979160 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988506 | GTGTATATACACCTT[G/T]GTCAACTCATCAAAT | 11169 |
rs559988462 | snp | A/C | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012286 | TCTACCTTAAATGCG[A/C]CTGGGTTTGGAAAAA | 11169 |
rs559991146 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020802 | GAGTAGAAGCCTTAC[C/T]GATAACATAAACAAT | 11169 |
rs560002112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006429 | TGGCTATTGTTTGTA[C/T]ACAGGATAACAATCC | 11169 |
rs560012391 | in-del | -/AG | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986356 | TTTAAAAATAGAAAC[-/AG]GGGCTTGCTATTGCT | 11169 |
rs560013571 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974239 | CCAGCTCGGGCTACA[C/T]AGCAAAACCTCGTCT | 11169 |
rs560024549 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994962 | TGATCAACCACGATA[G/T]ATATTTATTAATTTT | 11169 |
rs560052479 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990084 | TATTTAACATAACTA[C/T]AAATAAAATATTGAC | 11169 |
rs560102118 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000451 | GTGTCTTCCAAATCC[A/C]TATGATCACAGAAAC | 11169 |
rs560105388 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982249 | CTCCTGACCTTGTGA[G/T]CCACCCGCCTCAGCC | 11169 |
rs560109881 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54992680 | AGCACTTTGGGAGGC[G/T]GGGGAGGGAATATCA | 11169 |
rs560124773 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974851 | TAAAAATGCCAAACT[A/G]GAGAAAACTAGGTCG | 11169 |
rs560142319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953848 | GAAACTGGGAACCAT[C/T]ATTCTCAGCAAACTA | 11169 |
rs560170271 | snp | C/T | 4.94279e-05 | 0.00497107 | missense | WDHD1 | GRCh38.p7 | 14:54987293 | CAGCCCATCCTTGAC[C/T]GAGACATATGGCTTC | 11169 |
rs560251136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019238 | TACCAGAAATGATTA[C/T]CTTACATATGTTAAC | 11169 |
rs560278851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993737 | AGATTGCAATGCCAC[C/T]CTTCTCACTAATTTT | 11169 |
rs560297838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957533 | TCTCATCATTTGGAA[A/G]TATTTCTTTGTATAC | 11169 |
rs560299725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964315 | TCAGTACTTCTTAAT[C/T]GGGATGGTACACTGC | 11169 |
rs560300501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954310 | TAAATAAATACAAAG[A/C]AATCCAGCATAGTAG | 11169 |
rs560321492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948462 | CTCATTGCTAGCACA[A/G]CAGTCTGAGATTGAA | 11169 |
rs560330905 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015482 | GGTAACATAACACAC[A/G]TAACACATGGTTAAA | 11169 |
rs560432479 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958852 | GCTTACCCATGCTCA[C/T]GGTTTAAATTGCTAT | 11169 |
rs560443230 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993132 | TTTTATTTTGTTTTT[A/T]TCTGAGACAGGGTCT | 11169 |
rs560450957 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994512 | ACATGTACTCAATAT[-/A]AAAAAATTTCCCAAG | 11169 |
rs560511660 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948213 | GTGGGCGCAGAACAG[C/G]GGGTGTGGCACACCG | 11169 |
rs560529411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998292 | TGTGAAATTAGCCCA[A/G]CTAATTTTTGTATTT | 11169 |
rs560651433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979871 | TACATATTCTTATTC[C/T]TTCCCCACTTTTACA | 11169 |
rs560677491 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55000159 | GCTCAGTAAAGCTGT[C/T]TGACTAAGCAGAGGA | 11169 |
rs560678490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994147 | AGTGTTATTGTAGCA[C/T]GTAAGTTGTTACAAT | 11169 |
rs560707275 | in-del | -/AGGC | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959441 | GGAAGGGAGGGAGGG[-/AGGC]AGGCAGGCAGGCAGG | 11169 |
rs560810110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998941 | CTATACATAATTCAC[C/T]TAATCCTCCCAATAA | 11169 |
rs560852948 | snp | A/C/G | 0.00199529 | 0.0315338 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952675 | ACCAAAAAAGAGCCC[A/C/G]CATTGCCAAGTCACT | 11169 |
rs560896694 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955010 | CTGAGATTATAGGCG[G/T]GAGCCACCATGCCCA | 11169 |
rs560997434 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980464 | ATCATTTTATACATA[A/T]GCCAGCAGCAGTACT | 11169 |
rs561001064 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972471 | TAATCCCAGCTACTC[A/G]GGAGGGTAAAGCACG | 11169 |
rs561002883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007784 | ATATTAAGGCATATT[C/T]GTGGAGGATATTTCT | 11169 |
rs561012472 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988663 | TTCTGGGAGGAGTTT[G/T]CATTTTCCGAAACTT | 11169 |
rs561030700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944558 | TAATCAACCATAAGT[A/C]TCTGACATCTATTAT | 11169 |
rs561032242 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960271 | CTCCCGGGTTCACGC[A/C]ATTCTCCTGCCTCAG | 11169 |
rs561062033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973217 | TCCACTTAATTTATA[C/G]TATAGCCTTTTAATC | 11169 |
rs561089122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013685 | ACAAGGTGGGAGGAT[C/T]GCTTGAGGCCAGGAG | 11169 |
rs561106789 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020925 | AAAATATTTACTATT[C/T]ATTAAGTGGAAGTAG | 11169 |
rs561108848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958820 | TTCTTTTTGCTTTAC[A/G]TTCTCCCCCAATGCT | 11169 |
rs561113387 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966260 | GAATTGCGTGAACCC[A/G]GGAGGCAGAGGTTGC | 11169 |
rs561114423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988050 | AAAAAGCTGAAAAAA[C/T]ATTTTCTTTTCTTTT | 11169 |
rs561136567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943769 | AACATACAGGAACTT[A/G]TAGAGATTAAAACAG | 11169 |
rs561156967 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019489 | TCTTTTTTGATTCAT[G/T]ACTCTTGCTAAAGCA | 11169 |
rs561173773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953250 | GGCTAATATCCAGAA[C/T]CTACAAAGAACTCAA | 11169 |
rs561234266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026343 | AAATAAGCAAAAAGG[A/G]AAATAGCATCACTAA | 11169 |
rs561246085 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024260 | CTCTAGGTGAATATC[G/T]CAAAGAAATCCTACA | 11169 |
rs561297643 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55027002 | CATCTCCTTGGTGGA[C/G]GCGGGCAGCCGGAGT | 11169 |
rs561298329 | snp | C/T | 0.00206675 | 0.0320796 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000985 | GACCAGGTTACTATA[C/T]TGAGGGTCTGTAAAG | 11169 |
rs561351789 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948260 | GGGCAAGGCATCACC[A/T]CACCCGGGAAGCGCA | 11169 |
rs561360593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019865 | CAGAGCTAGACTCCA[C/T]CTCAACAAAAAAGAA | 11169 |
rs561374557 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005097 | GGAACACTGTAGAAG[C/G/T]AGAGATCAGGCATGA | 11169 |
rs561452526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958288 | CCTGCTACCACGCCC[A/G]GCTAATTTTTGTATT | 11169 |
rs561508329 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002283 | ATATATTTACAAGAC[A/T]TAAAAGCAAATTAGT | 11169 |
rs561616902 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948560 | GCCTGCCTCTGTGGA[C/T]TCCACCTCTGGGGGC | 11169 |
rs561642706 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958062 | CTTAAAAAGAAACAA[A/G]AAACAAACCTTCTCT | 11169 |
rs561648363 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005681 | AGGACATAGAGGTTC[C/T]AGACATTGTGAAAGT | 11169 |
rs561651994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987494 | CCAAATAGTTTACTT[C/G]CTATTATACACTAGT | 11169 |
rs561677508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018305 | ACTTATGCACAGGAA[C/G]ACACTGAAATTTATC | 11169 |
rs561699884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971320 | AATGGCTCACATCTG[C/T]AATCCCAGCACTTTG | 11169 |
rs561705199 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941389 | CAGTTGCTTCAAACT[C/G]TTTAAAAAATATATA | 11169 |
rs561738631 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012524 | TAATGAAACATTCCC[A/G]TTTTCTAGAACAATT | 11169 |
rs561808410 | snp | G/T | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027748 | CCGGTTGGTTCTCTT[G/T]GTACCTGAAGGTATA | 11169 |
rs561814610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006221 | TAGGGAAGAACTGAC[A/G]TCTTTATTTATATCA | 11169 |
rs561848550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970661 | AAGAAAGAAAAAGAC[C/G]ATACTCCCCAAAGCA | 11169 |
rs561914427 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978265 | GAAATCACTGAGAAC[A/C]ACCTACACTATAAGA | 11169 |
rs561931221 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941784 | CAGGTAATATTTTTA[A/T]ATATAAAGCAGAATA | 11169 |
rs562029037 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011004 | ACAGGAATGGAACAT[A/C]TTCTCCCTCAGAGCC | 11169 |
rs562030550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947276 | CCCAGAGGCAGAGGT[G/T]GCAGTGAGCCGAGAT | 11169 |
rs562030889 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004028 | TACTGTGACTAATAT[G/T]TTGTACCATGCAAAA | 11169 |
rs562067568 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016850 | GTGCAAGCATAAAAA[C/G]TGAAGTGACTGTTAA | 11169 |
rs562093070 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951541 | AAAGTCCAGGACCAG[A/C]TGGATTCACAGCCAA | 11169 |
rs562094229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004643 | TTTTTAGTAGAGACA[A/G]GGTTTCGCCATGTTT | 11169 |
rs562098434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012981 | GAAAAAAGGGAACAT[C/T]TAAACCTTTCTTGGA | 11169 |
rs562101851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016138 | GAAAATAGAGTTAAG[C/G]AATCTTCTAAAGAGC | 11169 |
rs562181968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962311 | CCTGACACTCAATAG[A/G]CATTTTATAAACATC | 11169 |
rs562189360 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985032 | TTAGAAACACAGTAA[A/G]ATGTTACATGGACTC | 11169 |
rs562320124 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940381 | ATGTTTTCCTAACTT[C/T]AATCATCACCAGATA | 11169 |
rs562329966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016843 | TTTTCTGGTGCAAGC[A/G]TAAAAAGTGAAGTGA | 11169 |
rs562370269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955959 | CTGGAGTGCAGTGGC[A/G]CTATCTCGGCTCACT | 11169 |
rs562372174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018425 | GGAATATCTTGACTT[G/T]TGGGAAGAATATTTT | 11169 |
rs562394890 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960895 | CCCTCGAACTCCTGG[A/G]CTCAAGATATCCTCC | 11169 |
rs562422939 | snp | A/G/T | 0.00755907 | 0.0610114 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021600 | CATGTTGGCCAGGCT[A/G/T]ATCTCAAACTCCTGA | 11169 |
rs562431675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018971 | GAGGTTACAGTGGGC[C/T]GAGATGGTGCCATTG | 11169 |
rs562433020 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016388 | ATGAAAATATAACTT[C/G]AATAAAATGTTTGTT | 11169 |
rs562451327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964974 | TTTTCTACAATAAAC[C/T]GAGTTTTCTTAATAC | 11169 |
rs562452876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959639 | CAGGCATGGTGATGC[A/G]CAACTGTAGTCATAG | 11169 |
rs562479727 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951598 | TGTTACCATTCCTTC[A/T]GAAACTATTCCAATC | 11169 |
rs562552073 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992233 | CAGTGGCTCAGGCCT[A/G]TAATCCCAGCACTTT | 11169 |
rs562601768 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939023 | ATGCATATTCCAAAT[C/G]GTTCAGGAAAAATCC | 11169 |
rs562603707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979764 | AAGTCTCCTATACTA[C/T]CCACTGAGTTTCTCT | 11169 |
rs562615086 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993000 | TAATAAAAAGTGTCA[A/G]TATAAAGAGGATCTA | 11169 |
rs562615857 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993899 | TAAATAAATGCTCTC[A/G]GAAGGGTCCTCAAAA | 11169 |
rs562618039 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997907 | CAAGAGCGGAACTCC[A/G]TCTCAAAAAAAAAAA | 11169 |
rs562639741 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024607 | GTAGAAAGAAGTAGA[A/C]ATAAGAGACTCCATT | 11169 |
rs562702376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979155 | TTTGCTCCTCTTCAC[A/G]CCAAAGTTCTTTTTT | 11169 |
rs562727392 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970490 | AGAACTACAAAACAC[G/T]GTTGAAAGAAATCAC | 11169 |
rs562812362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985647 | AAGATCACCTAGGCT[G/T]CTCTGTGGAGAATGG | 11169 |
rs562821178 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997771 | CAAAAATTAGCCAGG[C/T]GTGGGGGCACAAGCC | 11169 |
rs562822550 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941906 | CAATCTAAGCTTTGC[C/T]TATATTAATCATATT | 11169 |
rs562847704 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948662 | AGTAGTGGTTCTCCC[A/G]GCACAGAGTTTGAGA | 11169 |
rs562897051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011132 | CAATTTGTTACAGCA[A/G]CCTTAGTAAACTAAT | 11169 |
rs562898750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947057 | AAAAAAGTGTTAGGC[A/G]GGCCAGGCATGGTGG | 11169 |
rs562900162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952621 | TATCAATGACTTTCT[C/T]CACAGAATTGGAAAA | 11169 |
rs562923795 | snp | A/G | 1.65162e-05 | 0.00287365 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54963086 | CCGAGAGCGAGAAGC[A/G]TATTTAATGGCTAAA | 11169 |
rs562954982 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54971038 | AACTGGCTAACCACA[C/T]GCAGAATGAAACTGG | 11169 |
rs562986993 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956911 | ACAGAATTGAACCCA[A/C]TTCCCTAGCAAGACA | 11169 |
rs563006788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969461 | GCACAGCAAAGAAAA[C/T]CTAGAGGAAATGGAT | 11169 |
rs563012485 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947347 | AAAAAAGTGTTAAGC[A/G]GAAAAAAAACCATGA | 11169 |
rs563027909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017489 | CTAGTATTACAGGCA[C/T]GCACCACCCACACCT | 11169 |
rs563109892 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950097 | CAATTAATGAGCAAA[A/G]TAACCAGCTAACATC | 11169 |
rs563114397 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011741 | TTTTTTACTTATTGT[A/C]AACTTATTTTCAACT | 11169 |
rs563174388 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945979 | ACCATAACCATTTGC[C/T]CAATTTCTGAAAATA | 11169 |
rs563235181 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946524 | AGGGTCTTGCTTTGT[C/T]GCCCAGGCTGGAGTG | 11169 |
rs563261921 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954690 | ATTTATGTATTTACT[C/T]TTTCTGATAGCCTTG | 11169 |
rs563294325 | snp | C/T | 8.28466e-05 | 0.00643556 | missense | WDHD1 | GRCh38.p7 | 14:54984858 | CCCCATCAAATCCTG[C/T]ACCTAATGAGAAAAT | 11169 |
rs563365975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016942 | GCCATAGACAGCAAA[A/G]GAACTTTCAAACAGT | 11169 |
rs563475467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996936 | AGCTGGGACTACAGG[C/T]GCATGCCACCATGCC | 11169 |
rs563504554 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028333 | TTGGCTTAAAAACAA[C/G]TTGGGATTTGTGGAA | 11169 |
rs563506884 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028707 | TCATTTTCTCTTATC[A/G]ATCAAGCCATTTGAT | 11169 |
rs563547370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009588 | AGGCACCCGCTACTA[C/T]GCCCAGCTCATTTTT | 11169 |
rs563564669 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021571 | TATGTTTTTGGTAGA[C/G]ACCGGGGTCTCATCA | 11169 |
rs563568685 | snp | A/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026119 | TCTGGTTCGCTCTAT[A/T]CTATCTGTAGTCCCC | 11169 |
rs563574025 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961817 | CCCCAGGCCCACTCC[C/T]TGTACGCAACCATTT | 11169 |
rs563595126 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951142 | AGGCAAGAAATAACT[A/G]AGATCAGAGCAGAAC | 11169 |
rs563635227 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991456 | CAATGATTTGGAAAA[A/G]GGAAAGCATTATGGA | 11169 |
rs563635334 | snp | A/G | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955353 | CCACAATTTAAAAAT[A/G]TACAATTTATTAAAG | 11169 |
rs563680762 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54953326 | GGATATGAGCAGACA[C/T]TTCTCAAAAGAAGAC | 11169 |
rs563683792 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960942 | ATACCTGGGACTACC[A/G]GTGTGTACTACCATG | 11169 |
rs563685851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945190 | TGCCATCGCCTCACC[C/G]TTGCTCTCAGAGCTG | 11169 |
rs563782325 | in-del | -/AA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54979321 | CATGCCTGGGTAATT[-/AA]AAAAATTTTTTTTTG | 11169 |
rs563811956 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003833 | CCTCCCAAAGTGCTG[C/G]GATTATAGGCGTGAG | 11169 |
rs563862195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963708 | GGGAAGCTGAGGCAG[A/G]AGAATCGCTTGAACC | 11169 |
rs563875924 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938665 | GCTGAAGCAGGAGGA[C/T]CACCTCAGCCCAGGG | 11169 |
rs563921897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969888 | TGGGATGTAAGGTTG[A/G]TTCAACATATGCAAA | 11169 |
rs563981150 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958495 | CCATACATTCCTCCA[C/T]ACAATATAGCACTTC | 11169 |
rs564001851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014553 | AATAAATGAATAGAT[A/G]TATGAGCTCAACTAT | 11169 |
rs564016834 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941285 | AAGGCCCTGCATTTG[A/G]AGGCAGAGTAATCTG | 11169 |
rs564027426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017001 | ATCAGGAGTTTTAAA[C/T]AGAAAATCGCCCGTA | 11169 |
rs564069645 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55013330 | CCATCTCAAAAAAAA[A/C]TGGTAGGGCAAGTTA | 11169 |
rs564090708 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017660 | AAAAATCAATGTTCT[A/T]ACTATATTAGGAAAT | 11169 |
rs564214225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012445 | TCCAAGTAACCTACA[G/T]CTCATTCCCATATTT | 11169 |
rs564279486 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951457 | AACGAGGAAGAAGTT[C/G]AATCTCTGAATAGAC | 11169 |
rs564326145 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54956038 | AGGTAGCTGGGATTA[C/T]AGGCACCTGCCACCG | 11169 |
rs564343069 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963877 | AGCACTTTGGAAGGC[C/G]AAGGCAGAGGGACTG | 11169 |
rs564360519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015357 | GCACTACTGTAGCCT[A/G]GGAAACAGCATGACA | 11169 |
rs564374760 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955931 | GAGACGGAGTCTCAC[G/T]CTGTTGCCCAGGCTG | 11169 |
rs564393448 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996940 | GGGACTACAGGCGCA[C/T]GCCACCATGCCCAGC | 11169 |
rs564405617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985483 | GTAATGAGAAACAAC[A/G]GTAAGAGATGAGGTT | 11169 |
rs564423467 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016025 | CTTGGTGTATCAGCA[A/G]ATGCACTGGAGGAGA | 11169 |
rs564423571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009635 | CGAGGTTTCACTGTG[C/T]TGGCCAGGCTGGTCT | 11169 |
rs564514702 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024097 | TAGAAACTGCCAAAA[A/G]TTTTCTAATATGTGT | 11169 |
rs564521479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975775 | GGCTCCAGTGATCCT[C/T]CTGCCCCTGTCTTTT | 11169 |
rs564545209 | snp | A/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026874 | GCTAGGGATAGGAAG[A/T]GAGCTTAGTCTCCTC | 11169 |
rs564567908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020625 | CAATTCTCACATTTA[C/T]ATTCTTAGCCAGAAC | 11169 |
rs564576223 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960614 | AAGCAATTCTCCTGC[C/T]TCAGCCTCCCGAGTA | 11169 |
rs564599146 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990817 | CCATAGTACTTGCCA[C/T]CTTCTAATATATTAT | 11169 |
rs564602091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991136 | TTTAAAAATATGTTT[C/T]ATCCAAAAAAATTAA | 11169 |
rs564676960 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55017330 | TTCTACAGTGCTGTA[C/G]GAAAAATCAATATTC | 11169 |
rs564696048 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949465 | GAAAAAAGAGTAAAA[A/T]GAAACAAACAAAGCC | 11169 |
rs564725401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967738 | CAATCCTCCCACCTC[A/G]GCCTCCCAAGTAGCT | 11169 |
rs564728038 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968735 | AGACTATTATGAACA[A/C]TTCTATGTGCACAAA | 11169 |
rs564728985 | in-del | -/TTT | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016324 | TATATCAAGTACATA[-/TTT]AATAAAAGATTAAAT | 11169 |
rs564757366 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976347 | TTACCTCAGCCTCCC[A/G]AGCAGCTGGGACTAC | 11169 |
rs564789454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969315 | ACAGGCGTGAGCCAC[C/T]GCGCCCAGCATTAAG | 11169 |
rs564793625 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961827 | ACTCCCTGTACGCAA[A/C]CATTTTCAACTCCTT | 11169 |
rs564861468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983174 | GCGTCAAAAAAACCA[C/T]AAACACAAAAACAAA | 11169 |
rs564907838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945240 | GAAGCACGGACACAG[C/T]ACATTTGTACATTTC | 11169 |
rs564929235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950017 | ATGGAAAGGAACAAC[C/T]GGTACCAGCCACTGA | 11169 |
rs564949696 | snp | C/T | 1.65021e-05 | 0.00287241 | utr-variant-5-prime, synonymous-codon | WDHD1 | GRCh38.p7 | 14:55008698 | GCTATCCATCACATC[C/T]ACAATTTTGACTAGA | 11169 |
rs564962985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982427 | TCTTTACGAAATTTA[C/T]CTTTAGTACTCTTCT | 11169 |
rs565057177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967059 | CCAGTGGGTCTCTGA[C/T]AGTCACACCCATTTA | 11169 |
rs565093898 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | WDHD1, SOCS4 | GRCh38.p7 | 14:55027431 | GCGATGGTGATGGCA[A/G]CAGTTACTCGCACAA | 11169 |
rs565096024 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001526 | CCTCAGCCTCTCAAA[C/G]TGCTGGGATTACAGG | 11169 |
rs565131959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954445 | CAGAACAATCTGGCA[C/T]TGGAATTATAAGTGC | 11169 |
rs565169668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948937 | AGACCTGCAGCTGAG[A/G]GTCCTGACTGTTAGA | 11169 |
rs565192335 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974190 | ACATAAGGAGGCTGA[C/G]GTAGGCAGATCGCTT | 11169 |
rs565217806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943791 | TTAAAACAGTAAACC[A/G]TCAAAAAATTAACCA | 11169 |
rs565268399 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002654 | TCTGTCACCCAGGCT[A/G]GAGTGCAGTGGTGTG | 11169 |
rs565306336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953772 | TGTGGCACATATACA[C/T]CATGGAATACTATAC | 11169 |
rs565359535 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947498 | TAAAGTCATTAAGAA[A/T]ATAAGATATACTTTA | 11169 |
rs565363018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014123 | TTATAAAATTTTGAG[A/G]CAGAGTCTCATTCTG | 11169 |
rs565427918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009219 | AGATTTCCCATTATG[C/T]TAAAATACAAACACT | 11169 |
rs565473042 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54971530 | ATCTAACCAAGGAGG[C/T]GAAAGATCTCTACAA | 11169 |
rs565527556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975108 | ACAACTAGGAAAAAT[A/G]TCTAGTTTTCAAGCA | 11169 |
rs565539501 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988837 | TTAGAGCATGTAATG[A/C]GGGAATCATTATGGC | 11169 |
rs565566938 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014961 | TTTACCTGGAGCAGA[A/C]AAGCCAGGAAAGAAA | 11169 |
rs565569603 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55027038 | CTCACCCGGGTGACC[A/G]AGCCTCCGCCACTGA | 11169 |
rs565606258 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980569 | GTACTTTGGGTGGAT[C/G]ACTTGAGGTGGATCA | 11169 |
rs565611962 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988442 | ATATAAGAAAACATT[C/T]TCGGGTGATAAAGAA | 11169 |
rs565653020 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939335 | GTTGCTGCACAGATA[G/T]GAGAGGCTTTAGATC | 11169 |
rs565672015 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951472 | CAATCTCTGAATAGA[A/C]CAATAACAGGCTCTG | 11169 |
rs565702534 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949232 | AAGTTCGAACGCATC[A/G]CAAAGGAGCTAAAAA | 11169 |
rs565710927 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972469 | TGTAATCCCAGCTAC[C/T]CGGGAGGGTAAAGCA | 11169 |
rs565711103 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981067 | AGTGAGCTGAGATCA[C/T]GCCACTACAATCCAG | 11169 |
rs565747622 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54982731 | ATTAAAGCCTGAATG[A/C]CTAATAGAAAACACA | 11169 |
rs565763433 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944830 | TCAGGCTGGTCTCAA[A/T]CTCCTGACCTCACGT | 11169 |
rs565765742 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54949241 | GCATCGCAAAGGAGC[-/T]TAAAAACCTTGAAAA | 11169 |
rs565780176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968884 | AATTGCTACAAAAAT[G/T]TTTAAAGATTAGCCA | 11169 |
rs565797651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961112 | ACCTGGCCAGTAGTC[C/T]ATTATCTGTTCTTCT | 11169 |
rs565877538 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975416 | ACAGTGGCGCAATCT[C/T]GGCTCACTGCAACCT | 11169 |
rs565920018 | in-del | -/AC | 0.0123036 | 0.0774623 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003596 | ACGAACTATATATAT[-/AC]ATAGTTGCCCAGGCT | 11169 |
rs565925208 | in-del | -/C | 0.0115144 | 0.0749975 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020646 | TAGCCAGAACCTCAA[-/C]CCTGAACTCTGGAAG | 11169 |
rs565930571 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989749 | ACCGCAACCTCTGCC[A/T]CCTGGATTCAAGTGA | 11169 |
rs565963382 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997552 | AGATATTCAACCATT[C/G]CATTTATAGTCCTAA | 11169 |
rs565965990 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001159 | ATTTCTAATTATATT[C/T]GATACAAGACAAAGT | 11169 |
rs565966042 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938885 | AGGGAAATTTTATTA[C/T]AAAATACAGGCTATG | 11169 |
rs565983851 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028688 | ATTGATGTCCACACA[C/T]CTGTCATTTTCTCTT | 11169 |
rs565992671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974533 | AGAAAGAGTTTAAAA[A/G]TGCCAAAATAATCAG | 11169 |
rs566028433 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001605 | AAAAAATGTTATTAT[C/G]CTAGAAAGAGAGACA | 11169 |
rs566038490 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54986311 | TATAGAACAGTTATA[C/T]AGAATATATTTCTTT | 11169 |
rs566040185 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007558 | CCTTCAAAGGTATGA[A/T]GAGTACAAATCTTAA | 11169 |
rs566088773 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000776 | AATATAAATTTAATT[A/T]TACTTTCATTCTGAC | 11169 |
rs566089861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995302 | ATCTTGTCAAAGAAC[A/C]AGCTTTTGGTCTCAT | 11169 |
rs566101653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007967 | TGTGACTCTCCAAAT[C/T]AAATGTGACCCATAA | 11169 |
rs566112306 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | WDHD1, SOCS4 | GRCh38.p7 | 14:55027103 | GCTCACCACACTGCG[C/T]CTGCGCCGACCCGCC | 11169 |
rs566216733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943279 | GAACACCAGTCTTTT[C/T]CCCAAAAGGAATAGT | 11169 |
rs566268763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980726 | TAGAAGAATAGCTTG[A/G]ACTCAAAGTGGAGGT | 11169 |
rs566291706 | in-del | -/AAAT | 0.379622 | 0.213771 | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938758 | CCCTGTCTTTAAAAT[-/AAAT]AAATAAATAAATAAA | 11169 |
rs566292785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005345 | TGTGGCTCCTAAAAG[A/G]CTGCCTGGATCTGGT | 11169 |
rs566303659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013369 | TCATACATTTTAAAA[C/T]ATTATTTCATGAGAT | 11169 |
rs566308476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953394 | CATCACTGGCCATCA[A/G]AGAAATGCAAATCAA | 11169 |
rs566346088 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55014762 | AATCTATATAAAGAG[C/T]TGTGGATGTTCAAAA | 11169 |
rs566351591 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005920 | CCTAGGCTGGAGTAC[A/G]GTGACAAGATCATAG | 11169 |
rs566370183 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003844 | GCTGGGATTATAGGC[A/G]TGAGCCACTGTGCCC | 11169 |
rs566370337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948732 | TCCATGATCCACAAG[C/T]AGCCTAACTGGGAGG | 11169 |
rs566478598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986953 | CTTGGAATTCTCTCT[A/G]TAATATAGTTCTATT | 11169 |
rs566566189 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026627 | CTATCCGCATGAGTC[A/G]TTTTTAGCTGACTGC | 11169 |
rs566599170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980176 | CAAAAAGTAGCTGGG[C/T]GTGGTGGTGCGTGCC | 11169 |
rs566645257 | in-del | -/A | 0.109993 | 0.207119 | intron-variant | WDHD1 | GRCh38.p7 | 14:54983681 | CTAATTTATTCCTTA[-/A]AAAAAAAAAAAATTT | 11169 |
rs566682550 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54941703 | CACCTTTGTAAAATG[A/G]CAGGAGTGAAAAGGA | 11169 |
rs566701915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54999725 | CCTCAGCCTTCTGAG[C/T]AGGAGCATGAAACTA | 11169 |
rs566722302 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980195 | GTGGTGCGTGCCTGT[A/C]GTCCCAGCTACTTGG | 11169 |
rs566727083 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991825 | ATACAACACTACTTT[A/T]ACTTAAAAAACACAT | 11169 |
rs566759667 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952955 | GGATCCATTCCTCAC[A/G]TCTTATACAAAAATT | 11169 |
rs566790855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992327 | GAAACCCCGTCTCTA[C/T]TAAAATACAAAAATT | 11169 |
rs566790925 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985223 | ACAAAAAGAACAAAA[A/C]AATTATCACAAAGTT | 11169 |
rs566802741 | in-del | -/AAG | | | cds-indel, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939074 | TAAAATGTCAACAAT[-/AAG]ACAAACTAGAGGAAG | 11169 |
rs566847558 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018539 | TCCAAAAGAATCATA[C/G]ACAACTTGATGAATT | 11169 |
rs566851344 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978466 | AGCCTGTGCCTGTAG[A/T]TCTACCTACTCAGGA | 11169 |
rs566900465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026639 | GTCATTTTTAGCTGA[C/T]TGCACATATAAAGTT | 11169 |
rs566906087 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960884 | AGCCTACTGCACCCT[C/T]GAACTCCTGGGCTCA | 11169 |
rs566912543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971081 | CACCATGTGCAAAAA[C/T]TAACTCAAGATGGAT | 11169 |
rs566937387 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972025 | GACATGTAATCCCAG[C/G]ACTTTGGGAGGCCGA | 11169 |
rs566985067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964021 | CCTGAGACAGGAGGT[C/T]CACTAGAGCCCAGGA | 11169 |
rs567010094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997634 | AAAAAATGGGGAGGC[C/T]GGGCATGGTGTCTCA | 11169 |
rs567024295 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020214 | CAAAATCAAAACCAC[A/G]TAGTGTCAACCTCAC | 11169 |
rs567049609 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54968377 | CAATGTTAAGAGGAA[C/T]GTTTATAGCACTAAA | 11169 |
rs567061212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024291 | ATAATCACATCCAAA[C/T]GCAAACTCAATCTCC | 11169 |
rs567081835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977833 | ACCAGCTGTAATTAT[C/T]GTAGTTTTTAACAAG | 11169 |
rs567104463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947349 | AAAAGTGTTAAGCGG[A/G]AAAAAAACCATGAGC | 11169 |
rs567124768 | snp | A/C | 3.53176e-05 | 0.00420209 | missense | WDHD1 | GRCh38.p7 | 14:54995606 | TCAAATTCTTACCAA[A/C]TGAGTTTTCATCATC | 11169 |
rs567133129 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003688 | CCTGCCTCAGCCTCC[C/T]GAGCAGCTGGGACTA | 11169 |
rs567196263 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960309 | AGTAGCTGGGATTAC[A/T]GGTGCCTGTCACCAT | 11169 |
rs567210958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943403 | TTACTTATTAATTTT[C/T]TTCCCCCTAGAGACC | 11169 |
rs567239055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949002 | AAAACCCCATGTGTA[C/T]GTCACCATCATCAAA | 11169 |
rs567280124 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980255 | CAGGATGTCACTGAA[A/G]TGAGCCTGAAGTGAG | 11169 |
rs567320126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971686 | CCACCGCACTGTAGC[C/T]TGGGTGACAGAATGA | 11169 |
rs567329290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959194 | GTAACATAGGGAGAC[C/T]CTGTCTCTACAAAAA | 11169 |
rs567404145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973719 | TTAACAAAATTAGAA[A/G]AAACACTGTGAGAAA | 11169 |
rs567509657 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953534 | TGGTGGGACTGTAAA[C/G]TAGTTCAACCATTGT | 11169 |
rs567599343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987809 | TTTTTGCATTTTTAG[G/T]AGAGATGCAGTTTCA | 11169 |
rs567614103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018631 | AGACAGAACCTATAA[A/C]AATACTGAGGCTGAA | 11169 |
rs567642260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013248 | TATGGCATTATCATG[C/T]ATTTTAAAATATTAT | 11169 |
rs567653456 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971131 | CCTCAGAATATAAAA[A/T]TCCCAGAAGAAACCC | 11169 |
rs567655305 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979328 | GGGTAATTAAAAAAA[A/T]TTTTTTTTGTTGAAA | 11169 |
rs567710976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964607 | TCGCGCCACTGCACT[C/T]CAGCCTGGGCAACAG | 11169 |
rs567761842 | snp | C/G/T | 0.00053718 | 0.0163803 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957567 | TGTATTTAAATAATA[C/G/T]AAAACATCACTTGGA | 11169 |
rs567809832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979580 | CACCGTTAACCTCCA[C/T]GTAGCCAAATTAAGA | 11169 |
rs567814097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947981 | AGCACTTTGGGAGGC[C/T]AAGGTGGGCAGATCA | 11169 |
rs567819420 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952445 | TACAAGGGATGTGAA[C/G]GACCTCTTCAAAGAG | 11169 |
rs567860939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985983 | TGTGAGCAAATTAAG[C/T]CTGAAATGTCTGTCC | 11169 |
rs567870468 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017843 | AAAAAACATGTTTTG[C/T]TTCTGTTTTTGTTGC | 11169 |
rs567882352 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024110 | AAATTTTCTAATATG[A/T]GTATTGAAAAAAATC | 11169 |
rs567895499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942011 | ATCCCAGCACTTTGG[A/G]AGGCCGAGGTGGGTG | 11169 |
rs567896271 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024906 | GTTTCTCCCCATGTG[A/G]TAGTCTGAAATATGG | 11169 |
rs567899826 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947953 | AGGAGTGGTGGCTCA[A/C]ACCTGTAATTCCAGC | 11169 |
rs567936421 | snp | A/G | 0.00795532 | 0.062565 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940584 | CCAAAAATGTATGAC[A/G]TGATTAAACCTTGTT | 11169 |
rs567941826 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998080 | TAGCAGGGCGTGGTG[G/T]TGGGTGCCTGTTATC | 11169 |
rs567960462 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972200 | GAATGGGGTGAACCC[A/G]GGAGGCGGAGCTTGC | 11169 |
rs568012363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004755 | AGCGAGCCCGACCCA[A/G]TGTTTATTTTTCATC | 11169 |
rs568024882 | in-del | -/CT | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977482 | AAGGTGGGAGGATCA[-/CT]CGAGGTTAGTTCAAG | 11169 |
rs568048667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991892 | GGCAAACATTTTCTT[A/G]TAAATGAATGAAGTG | 11169 |
rs568066964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947505 | ATTAAGAAAATAAGA[C/T]ATACTTTATTATTAT | 11169 |
rs568076849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997908 | AAGAGCGGAACTCCG[C/T]CTCAAAAAAAAAAAA | 11169 |
rs568126413 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54961270 | GTGGAGGTGAGGAAA[C/T]TGCTTGAGTTTGAGA | 11169 |
rs568130721 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54959262 | AACTAGCCAGACATG[A/G]TGACACATGCCTGTG | 11169 |
rs568137574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998409 | TGCTGGGATTACAGC[C/T]GTGAGCCACCGTGCC | 11169 |
rs568152323 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969580 | GTAATAAATAAAAAA[A/C]CTATCAACCAAAAAA | 11169 |
rs568173227 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018620 | TGGAGATAAAAAGAC[-/AG]AACCTATAAAAATAC | 11169 |
rs568187515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010659 | TTAGAAAAATTAATT[C/T]TACCTTAAGCAGCCT | 11169 |
rs568218347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962623 | TATACAACAACCAGA[G/T]AGCAAAGAGGTCTGA | 11169 |
rs568245587 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54956896 | TGCCTAGCTGCAAAA[A/G]CAGAATTGAACCCAC | 11169 |
rs568251557 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977680 | CTGTTTCTAAATAAA[A/T]AAATAAAAAGGGCTC | 11169 |
rs568253041 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55006426 | AAATGGCTATTGTTT[A/G]TATACAGGATAACAA | 11169 |
rs568266435 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009725 | GCATGAGCCACGACG[A/C]CAGCCCTAAAATAAT | 11169 |
rs568277826 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951914 | ATCTCAATAGATGCA[C/G]AAAAGGCCTGTGACA | 11169 |
rs568354154 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975628 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 11169 |
rs568391014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978168 | CCTCATAGGTTCAAA[C/T]CTTAACCTACTATTA | 11169 |
rs568392927 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54949375 | AGCCTCAGTAGCCAA[C/T]TCAATCAACTGGAAG | 11169 |
rs568427917 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950911 | TACTGGGTACATAAC[A/G]AAATGAAGGCAGAAA | 11169 |
rs568469911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946670 | TTTTAAAACTTTTGG[C/T]AGAGATGGGGTCTCC | 11169 |
rs568525987 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940874 | AAGATAATATTAAGA[C/T]CATATCAAGCCAAAT | 11169 |
rs568529575 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984344 | TACAAAAAATACAAA[A/T]ATTAGCTAGGCATGG | 11169 |
rs568576503 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947667 | CACAATCTTGGCTCA[C/T]TGCAGCCTCCGTCTC | 11169 |
rs568619564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948271 | CACCTCACCCGGGAA[A/G]CGCAAGGGGTCAGAA | 11169 |
rs568648108 | in-del | -/GG | 0.00837171 | 0.0641543 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963185 | AAGCTAATCCAAAAA[-/GG]GGGGGGGGGGGGAGA | 11169 |
rs568664280 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950363 | TCTCTGATAAAACAG[A/T]CTTTAAACCAACAAA | 11169 |
rs568709308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990382 | GCAGGCGGATCACGA[A/G]GTCAGGAGATCGAGA | 11169 |
rs568712012 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955501 | TTGCATAATTTTGTA[A/T]TGCTGCTACTGTATA | 11169 |
rs568715371 | snp | C/T | 0 | 0 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005840 | TTTTACTTTGTTTTC[C/T]TTTTTTTTTCCTTAG | 11169 |
rs568763618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991628 | CTAACTGTATTAGTC[A/G]TTACTGCATTGTTAA | 11169 |
rs568827546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998574 | ATAAATCCTTCCAGC[G/T]CTTTTAGTTGTTTCT | 11169 |
rs568841221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986164 | CAAACTGCATATTTT[C/G]ACCTAAGAGTCATGG | 11169 |
rs568879384 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980350 | GACATAATTCAGTGG[-/T]TTTTTTTGTATATTC | 11169 |
rs568884496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023456 | TGTGAGCAACCGCAA[C/T]TGCAGACCTCAATCT | 11169 |
rs568945303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024176 | TTAAGGGTCAATTGT[A/G]TATTTCTATCTCTAG | 11169 |
rs568955151 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54966292 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 11169 |
rs568977047 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004838 | TCAGTGGTTGTTCCT[A/G]TGCATTCAGTGGTCT | 11169 |
rs569017101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009610 | CTCATTTTTGTATTT[G/T]TAATAGAGACGAGGT | 11169 |
rs569017916 | snp | A/G | 1.6566e-05 | 0.00287797 | missense | WDHD1 | GRCh38.p7 | 14:54957047 | ACCTGCTTAGGCTTC[A/G]GCTTTGGAATCAGAG | 11169 |
rs569062409 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011952 | TTGAAAATAGCCAGA[A/G]ATGACTGTGTACATT | 11169 |
rs569063560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996747 | AAGTCTAATGAGAAC[A/G]CCATTAACAGATTAA | 11169 |
rs569072223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970865 | AAGGCTAGTGAAAAA[A/G]AACATGGCACTGGTG | 11169 |
rs569129388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963892 | CAAGGCAGAGGGACT[C/G]CTAGAGGCCAGGAGT | 11169 |
rs569255961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991750 | AGTGTGATGGTTGTC[C/T]TGAAAAAAAGCACTT | 11169 |
rs569277893 | snp | A/G | 9.62955e-05 | 0.00693819 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941454 | CAAAGATGAGTAAAA[A/G]AAAATCCATTACTTC | 11169 |
rs569280532 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977035 | TATTCTTTCAATCTA[A/C]TTATCAGCTAACTCC | 11169 |
rs569284976 | in-del | -/TAC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54944614 | CTTGTTAATTCATGT[-/TAC]TTTTTTTTTTTTTTT | 11169 |
rs569285582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978392 | ATTAGAGGTCAATCT[A/G]GGCAAGATGGTGAGA | 11169 |
rs569304506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977771 | AAAAGCTGTAATTTA[C/T]AGTCCATTATTTCTT | 11169 |
rs569309509 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969107 | GCAGTGGCACGATCT[C/T]GGCTCACTGCAAGCT | 11169 |
rs569387638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004151 | CTATATATAGACTCA[C/T]CATGTAGAAGCAAGC | 11169 |
rs569457945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950517 | GTCCTTAGAGACCTA[C/T]AAAGAGACTTAGACT | 11169 |
rs569496591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984665 | GAAATAATTTTCTTC[C/T]TGAAGAATATCTAAC | 11169 |
rs569588201 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975280 | AGAAGAAACAATACT[C/T]GGTAAACTGAAGTTC | 11169 |
rs569652540 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968313 | AAATATTCTTTGAAA[A/T]AAATGAAAACAGACA | 11169 |
rs569681514 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974576 | ACTCCTGTAATATCC[C/T]AGCACTTTGGGAGCC | 11169 |
rs569697716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954521 | CATCTGTGAGAAATG[C/T]TATTCATATAAAATT | 11169 |
rs569719653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945495 | CAGGTTACACAAACA[G/T]TAAAACTCAGACCTG | 11169 |
rs569721766 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998332 | ACGGGGTTTCGTCAT[C/G]TTGGCCAGGCTGGTC | 11169 |
rs569724120 | snp | G/T | | | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008344 | TGCCACACTCTGACA[G/T]ATCCATCACAACTAG | 11169 |
rs569724445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010525 | CTGGGAGTCTCTCCA[C/T]AGTTAAAAATCCGGT | 11169 |
rs569822253 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949574 | CCAAGTTGGAAAACA[C/G]TCTGCAGGATACTAT | 11169 |
rs569839366 | snp | A/G | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027549 | AGGCTCTCCTCCCAG[A/G]AAACAATATCCGGAT | 11169 |
rs569841083 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55000391 | ACTCAGCATCTACTA[C/T]AGTAACATGAAAGGT | 11169 |
rs569843281 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028773 | GCATGTATGGTAAAA[G/T]CTTGAGCCTCCGAGT | 11169 |
rs569907285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021719 | ATGTCTCCAAGGTCT[A/G]TATCTTGAAATTACT | 11169 |
rs569915498 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940061 | ATGAAATAACCAACA[A/G]CATCATCATTATCAG | 11169 |
rs569949967 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026067 | CAATGCCTGTCAATC[C/T]AAAAAGACCTTAAGC | 11169 |
rs569959969 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990512 | GAGGCAGGAGAATGG[C/T]GTGAACCTGGGAGGC | 11169 |
rs569968462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022273 | CTAAGAGACTGGAGT[C/T]TATCTTTTCCCTTCA | 11169 |
rs570019129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001721 | TGGGCTTATGTTTCC[C/T]TAACTGTAAATATCT | 11169 |
rs570082231 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002337 | GACGGTGTCTCACTA[C/T]GTTGCCCAGGTTGGT | 11169 |
rs570122331 | in-del | -/GAA | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951448 | CCAAGACTAAACGAG[-/GAA]GAAGTTCAATCTCTG | 11169 |
rs570145831 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54946455 | TTTTTGTATAACCAA[A/C]TGATAGTATGAAAAA | 11169 |
rs570171836 | snp | A/G | 1.65499e-05 | 0.00287657 | missense | WDHD1 | GRCh38.p7 | 14:54963108 | ATGGCTAAATTCACA[A/G]CATTTTGAGTCATTA | 11169 |
rs570185271 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014261 | ACCATGCCTGGCTAA[G/T]TTATTTTTTGTAGAG | 11169 |
rs570199376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013861 | CAAGTGAACCATGAC[A/G]GCACCACTGCACTCC | 11169 |
rs570207419 | in-del | -/ATAA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54942278 | TAAATAAATAAATAA[-/ATAA]TAAAAATGAAACTTT | 11169 |
rs570246738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008176 | AATACTGTGGACTTT[G/T]ATCACAAAAACAGTA | 11169 |
rs570263866 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940264 | GTAGTAGGTAGAGAA[A/G]CGGGTCTCCGAACCT | 11169 |
rs570275269 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54960420 | TGATCCACCCTCCTC[A/G]GCCTCCCAAAGTGCT | 11169 |
rs570289072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959924 | GTGCTAGCCCCTTGC[A/G]GTTTGGTGCCTCCCT | 11169 |
rs570392742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956242 | AAATACGAATATACA[G/T]CAGAACTATCTGGGT | 11169 |
rs570417134 | in-del | -/TCGAGACCAGCCTGGACAACA | 0.00676609 | 0.0577691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996403 | CTTGAGCTCAGGAGT[-/TCGAGACCAGCCTGGACAACA]TCGAGACCAGCCTGG | 11169 |
rs570438968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997252 | AGGCCTACACAACCA[C/T]ACCTGGCTAATTTTT | 11169 |
rs570455190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951167 | CAGAACTGAAGGAGA[C/T]AGAGACACAAAAAAG | 11169 |
rs570509709 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004748 | GTGAGCCAGCGAGCC[C/T]GACCCAATGTTTATT | 11169 |
rs570544430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975939 | TTAGAAAATGCATTT[A/G]AAGTTAAAAGAATAA | 11169 |
rs570559728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945542 | CAATTTGACTCCAAA[A/G]TCTATGTTTTTTTGT | 11169 |
rs570572051 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997826 | TGAGGCAGGAGAATC[A/T]CTTGAACCCGGGAAG | 11169 |
rs570653867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984281 | GGGTGGATCACTTGC[A/G]CCTAGGAGTTTGAGA | 11169 |
rs570657166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023103 | ACAGGTGTGAGCCAT[C/T]ACACCCGGCCATCTT | 11169 |
rs570686686 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953929 | CTGAACAATGAGAAC[A/C/G]CTTGGACACAGGAAG | 11169 |
rs570696507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55015682 | AGAGAAGTATTTCAC[A/G]TTTTTGTTCCAATGG | 11169 |
rs570743651 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949696 | ACTCCAAGACACATA[A/G]TTGTCAGATTCACCA | 11169 |
rs570753438 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952283 | TAAGCTGATAGGGAA[C/G]TTCAGCAAAGTCTCA | 11169 |
rs570759251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016382 | TTGATAATGAAAATA[C/T]AACTTGAATAAAATG | 11169 |
rs570812069 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955421 | TGTGGCTTCCTTATA[G/T]TCACAAGTGTCCAGA | 11169 |
rs570832534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996599 | AGTGAGACCCTGTCT[C/T]AAAATAAATAAATTT | 11169 |
rs570863019 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989916 | TGACCAACCCACCTT[G/T]GCCTCCCAAAGTGCT | 11169 |
rs570872669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950234 | ACCCATCAGTGTGCT[A/G]TATTCAGGAGACCCA | 11169 |
rs570918717 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997446 | GTGCTCTGAAAACTG[A/C]TGTTTAATAAAATGA | 11169 |
rs570958504 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54961875 | GGAGTCTCACTCCAT[C/T]GCCCAGGCTGGAGTG | 11169 |
rs570964141 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988231 | TTTGGTTTGTTTTTC[C/T]GTTTTTTTTTCCTTT | 11169 |
rs570995451 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54983627 | GCAGTAAGCTGAGAT[C/T]GCATCATTGCACTCC | 11169 |
rs570996641 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022011 | GTAATGAGCCCGTAA[A/C]GGCCTGTATGAACTC | 11169 |
rs571028434 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014663 | TATGTGCCCTATCTA[C/T]ACACATACAAAAAAG | 11169 |
rs571053147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968031 | GTACCATTAATACCT[C/G]TCATGGAATCCATGT | 11169 |
rs571063052 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54977087 | AAAAAAATAAGGTTG[-/T]TTTTTTTTTTGCCAA | 11169 |
rs571115748 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994694 | TGAATCCAGGAGGCG[A/G]AGGTTGCAGTGAGCC | 11169 |
rs571120485 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961043 | CGTCTGGTCTCAAGT[G/T]ATCCTTCCACCTTGG | 11169 |
rs571142063 | snp | C/G | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012431 | ATAAGTCTTCTTTCT[C/G]CAAGTAACCTACATC | 11169 |
rs571157527 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55018859 | AGAAACCCCATCTCT[A/G]CTAAAAATACTAAAT | 11169 |
rs571162628 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981905 | AAACATTGGATTTGA[A/T]ATGACTAAAATTTAC | 11169 |
rs571189907 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995261 | GCTGGGATTATAGAC[A/G/T]TGAGCCACCGTGCCC | 11169 |
rs571208039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996217 | CAAAATACTGCATAA[A/G]ATACATTTTCTTTAT | 11169 |
rs571225067 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974496 | CTGTTTTGTTTTGTT[G/T]TTTTTTTTTTTGTTA | 11169 |
rs571235364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944728 | GGGTTCAAGCGATTC[C/T]CCTGCCTCAGCCTCC | 11169 |
rs571340447 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953973 | ACTTGGGCCTGTTGT[C/G]GGGTGGGGGAAGTAG | 11169 |
rs571353267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975040 | AGCCTCATTTATCTT[G/T]GTGTGGTATAGCACA | 11169 |
rs571514786 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949042 | TAGATGAAACCATAA[A/C]GATTGGGGAAAAAAC | 11169 |
rs571525503 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime | WDHD1, SOCS4 | GRCh38.p7 | 14:55027254 | GAAGTGGTGGCGGCG[C/G]CCAGGGAACCGGCGG | 11169 |
rs571574735 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949211 | ACCTCTCCGAGCTAA[A/T]GGAGGAAGTTCGAAC | 11169 |
rs571579194 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54971847 | GCAAAAAACAAATAT[A/C]CCCAATAAAAAGTGG | 11169 |
rs571580435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944082 | AAAAACAGAAAAAGG[C/T]TTTTCCTTTTTTTTT | 11169 |
rs571674613 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959812 | AACAAAAAAAACAAA[A/C]AAAAAAACCTTTCCA | 11169 |
rs571677066 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959323 | AGATCGCTTGGGTCT[G/T]GGGGGTTGAGGCTGC | 11169 |
rs571690291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013732 | ATAATACAGAGAGAC[C/T]TAGTCTCTACAAAAA | 11169 |
rs571717329 | snp | A/G | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027920 | TAGCCTTGAGCACTT[A/G]CATTTGATCCATGCA | 11169 |
rs571737191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001139 | TTATATCCCTGTTCT[A/G]TATTATTTCTAATTA | 11169 |
rs571786995 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025836 | ACAGTATTGCCTCTG[C/T]TTACTATGCCAACAT | 11169 |
rs571904969 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967915 | CGTGAGCTACCCTGC[C/T]CAACCTCACATCTCA | 11169 |
rs571910595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981295 | GTTTAATCAGAATTC[C/T]TCTCCCTGTGTGGCT | 11169 |
rs571941944 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54944954 | GGATCAATGAACTGG[A/G]AAATCCTTTGTAAGG | 11169 |
rs571969220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019689 | GCCTGGCCAACATGA[C/T]GAAACCTTGTCTCTA | 11169 |
rs571970627 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014350 | CTGTCTTGACCTCCC[A/T]AAGTCAAGGGATTAC | 11169 |
rs572158368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948203 | TTGTCGGACAGTGGG[C/T]GCAGAACAGGGGGTG | 11169 |
rs572170402 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944124 | ATCGTTATTATCTTT[C/G]TTGTTGTTATTATTA | 11169 |
rs572186531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019824 | CAGTGAGCCGAGATC[A/G]TGCCACTGCACTCCA | 11169 |
rs572189229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020605 | AAATATTATGTTTAT[A/G]AGGACAATTCTCACA | 11169 |
rs572190155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954694 | ATGTATTTACTTTTT[C/G]TGATAGCCTTGCTAT | 11169 |
rs572201456 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005839 | TTTTACTTTGTTTTC[-/T]TTTTTTTTTTCCTTA | 11169 |
rs572211862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974067 | CCTGGAAACTATGTG[C/T]ATAAACCACCTGGAA | 11169 |
rs572245458 | snp | A/G | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940971 | ACATAGGAAATTTCC[A/G]AAACACAAAAGAAAA | 11169 |
rs572250152 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | WDHD1, SOCS4 | GRCh38.p7 | 14:55027324 | GAAGCGGGGTTGGGG[A/G]TGGCAGAAAAGCATC | 11169 |
rs572277171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966857 | TAATTAATGCTCAGA[C/G]AATTTGGTAAACAAG | 11169 |
rs572359140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958783 | CTCAAATGTTGGAGA[C/T]TCCCTAGGCTTAAGC | 11169 |
rs572367930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993745 | ATGCCACTCTTCTCA[C/T]TAATTTTTTTTGTTT | 11169 |
rs572373966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994213 | AATTTCTTTAATAGA[C/T]ACAATACTATTCAGG | 11169 |
rs572473283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952656 | ACTTTAAAGTTCATA[C/T]GGAACCAAAAAAGAG | 11169 |
rs572633646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964363 | AATAAAAAGGAAGCC[A/G]GGCGCAGTGGCTCAC | 11169 |
rs572706063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006193 | TGAATGTTATCAAAA[C/G]TATAGATTAATTTAG | 11169 |
rs572715096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953176 | AAGAAACTACCATCA[C/G]AGTGAACAGGCAACC | 11169 |
rs572776389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025138 | GGAGGTGGGACCTGC[A/G]GGCAGCAATACTGCT | 11169 |
rs572790307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025927 | AGATGGCGTCTCAAG[A/G]AACACTTGTCCAAAG | 11169 |
rs572796367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979059 | TTCATTGCCAAAAGA[C/T]TACAAAAATGCTATA | 11169 |
rs572798266 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955411 | CATTAATATTTGTGG[C/T]TTCCTTATAGTCACA | 11169 |
rs572820806 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962078 | CTGACCTCGTTATCC[A/G]CCCACTCCGGCCTCC | 11169 |
rs572855901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018820 | CAGCACTTTGGGAGG[C/T]GAGACCAGCCTGACC | 11169 |
rs572875308 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010957 | ACAAGGCAAGGAATG[C/T]TGAGGATTGCCACAC | 11169 |
rs572937931 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979554 | TAACATTTTATCACT[G/T]TTATCAGAGTCACCG | 11169 |
rs572953808 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998038 | CTAACATGGTGAAAC[A/C]CTGTCTCTACTAAAA | 11169 |
rs572971810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952233 | GACATGATTGTATAT[C/T]TAGAAAACCCCGTCG | 11169 |
rs572993990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952521 | CGGAAGAACATTCCA[C/T]GCTCATGGATAGGAA | 11169 |
rs573030726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992693 | GCTGGGGAGGGAATA[C/T]CACTTGAGGCCAGGA | 11169 |
rs573032406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947626 | AGATGGAGTCTCACT[C/T]TGTTGCCCAGGCTGG | 11169 |
rs573057106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948137 | GAGCGATGCAGAAGA[C/T]GGGTGATTTCTGCAC | 11169 |
rs573088366 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54992044 | AGATCACTTAAGGTC[A/G]GGAGTTCCACGTTGA | 11169 |
rs573103442 | snp | C/T | 0.00047882 | 0.0154655 | missense | WDHD1 | GRCh38.p7 | 14:54984747 | AAAACCCAATCCATG[C/T]AAGGTAGGATTTCCT | 11169 |
rs573128621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55017415 | TGGCACCATCTCGGG[C/T]CACTGCAACCTCCAC | 11169 |
rs573149204 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970369 | TATACACCAATAATG[C/T]TCGAGCTGAGAGTCA | 11169 |
rs573150600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985499 | GTAAGAGATGAGGTT[A/G]GAGAGGCAGGCAAAG | 11169 |
rs573192761 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004640 | ATATTTTTAGTAGAG[A/T]CAGGGTTTCGCCATG | 11169 |
rs573200736 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016406 | TAAAATGTTTGTTGA[C/T]ATTTACCACGGGGCT | 11169 |
rs573214350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54986414 | CTAAAGCAACTCTCC[C/T]GCCTCGGCCTCCCAA | 11169 |
rs573287096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004891 | AGTCTTCTGTGGCAG[A/G]CTGAGCACTCCAGTT | 11169 |
rs573291613 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942993 | GAGGTTCTAAATGAC[A/G]CTAAAGGTGTTTAAA | 11169 |
rs573324816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963623 | GCCTGGCCAATATGG[C/T]AAAACCCCGTCTCTA | 11169 |
rs573341789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019735 | TTAGCCAGCTGTTGC[A/G]GAGGGCATCTGTGAT | 11169 |
rs573390714 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965905 | AGGTTGCAGTAAGCC[A/G]AGACTGCACAACTGC | 11169 |
rs573446894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54977088 | AAAAAAATAAGGTTG[G/T]TTTTTTTTTGCCAAT | 11169 |
rs573449017 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54957509 | TGCCTCCAAGTCTGG[A/G]GAGAGTCATCTCATC | 11169 |
rs573466013 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54992621 | GTAACAACACTAGCA[G/T]ATATAATTTACAGCC | 11169 |
rs573502585 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963532 | GGGGGAGGCTGGGCA[C/T]GGTGGCTCACGCCTG | 11169 |
rs573527746 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941131 | TGCACATGACAAAAA[C/T]CAAATGAACCAAACC | 11169 |
rs573579519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990146 | TGACTACTGATAGCA[A/G]TAAAAAGTTTTATTA | 11169 |
rs573613596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026002 | ATGTTTATCACTGCA[C/T]ATATTACTTGTTTCT | 11169 |
rs573622882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55012931 | ATTCAAATCATAGCA[A/G]TGAGCTAAAAACACC | 11169 |
rs573649642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964917 | ATAAAAAGGCTACTA[A/G]TTCCTGGACCACAAG | 11169 |
rs573658793 | snp | A/C | 1.64961e-05 | 0.00287189 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55013575 | CCTCACATCACCATC[A/C]CTTCCACAAGTCACA | 11169 |
rs573665332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004961 | CACACCATCAGACCA[C/G]TCTGCAACCTCAGGT | 11169 |
rs573733262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980877 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGATCAC | 11169 |
rs573754212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54972902 | TATCTACTCTGATAA[A/G]TATGGTAACAGGTCA | 11169 |
rs573776640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993426 | TTCCCAGCCAGACCA[A/G]TGAATCTTAACATAA | 11169 |
rs573787492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998775 | CCAATTCTCCCAATA[C/T]AGATAGATATATCCT | 11169 |
rs573811020 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942255 | CTCCGTCTCAAAAAA[A/T]AAATAAATAAATAAA | 11169 |
rs573833067 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55022130 | TGGCCAGGGGCATTG[C/T]CCAACATTAAAAGAA | 11169 |
rs573860590 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019371 | AATTATACCTTTGTT[C/T]CAAATTTTCAAAACT | 11169 |
rs573872281 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54942972 | GAGAAACATAAAATT[G/T]TAAATGAGGTTCTAA | 11169 |
rs573918540 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012293 | TAAATGCGCCTGGGT[G/T]TGGAAAAAATATGAA | 11169 |
rs573925833 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948336 | ACAGCACCTGGAAAA[C/T]TGGGTCACCCCCACC | 11169 |
rs573965064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979114 | TTCAAAGACTTTTTA[C/T]CCTCCTTTAGGTGCC | 11169 |
rs574079419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957395 | CCCAAGAAAGACAGA[A/G]GTATCTTTCAAAACC | 11169 |
rs574087467 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972996 | CATGAGTAGTGCTCT[C/T]GCAGCTGATTTATTA | 11169 |
rs574087525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947111 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACCTGAG | 11169 |
rs574132288 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WDHD1 | GRCh38.p7 | 14:55016860 | AAAAAGTGAAGTGAC[C/T]GTTAATGGGTTGTCT | 11169 |
rs574140070 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952258 | CCGTCGTCTCAGCCC[A/C]AAATCTCCTTAAGCT | 11169 |
rs574247562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970473 | GGTGAAAGATCTCTA[C/T]AAGAACTACAAAACA | 11169 |
rs574306145 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54991487 | ATCTAGTAACTTTTT[C/T]ATTCATATTCAATGA | 11169 |
rs574308714 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963654 | CTAAAAACACAATTA[C/G]CCAGGCGTGGTGGCG | 11169 |
rs574327130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997331 | GAACTCCTGACCTCA[A/G]GTGATAAACCCACCT | 11169 |
rs574347010 | snp | C/T | 5.20124e-05 | 0.00509936 | missense | WDHD1 | GRCh38.p7 | 14:54955694 | AGGATGCTGCAGATG[C/T]CTATAAAAACAAACA | 11169 |
rs574391043 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988802 | CATTACTAACTATGC[C/G]ATGTCATTTTGCTAT | 11169 |
rs574408303 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956483 | TCTCTACTAAAAATA[A/C]CAAAATTAGCTGGGC | 11169 |
rs574410341 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950671 | ATCTACGGAACTCTC[C/T]ACCCCAAATCAACAG | 11169 |
rs574495768 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941212 | TTTCAAGGTTAAGAA[A/G]CAAATTCAAATTGGT | 11169 |
rs574496538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54985338 | GACATGAACTGCAAG[C/T]TGGAGCCTGCCATGC | 11169 |
rs574512649 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | WDHD1 | GRCh38.p7 | 14:55014247 | TACAGGCGCATGCCA[C/T]CATGCCTGGCTAATT | 11169 |
rs574584503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954823 | CAATCTCCGCGTCCC[A/G]GGTTCAAGTGATTCT | 11169 |
rs574599952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55023769 | TTAAGCTTACCGAAA[C/T]AGCAACAGGAGGTGG | 11169 |
rs574660323 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54979279 | CTCTTAGCCTCTCAA[A/G]TAGCAGAGACTATAG | 11169 |
rs574678225 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990519 | GAGAATGGCGTGAAC[C/T]TGGGAGGCGGAGCTT | 11169 |
rs574717871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021984 | GACAATCCTTTCCAT[A/G]GATTAGTTTATGTAA | 11169 |
rs574741769 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028315 | AATGAAGAGGAAGAA[G/T]GATTGGCTTAAAAAC | 11169 |
rs574774333 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004389 | ACTGAATTATTTGCA[C/T]CACTTTTCTTTTTCA | 11169 |
rs574810982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54968544 | ATTGAGACTAAAGAA[C/T]CCATACAAAGGATCA | 11169 |
rs574814456 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939134 | CAAATTTTCTGTAGG[A/T]TTGAGAGATTCAAGA | 11169 |
rs574951075 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54976104 | CAGGCAGTGTCACTC[C/G]AGAGCTCGAGCTCTG | 11169 |
rs575023870 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | WDHD1 | GRCh38.p7 | 14:54970534 | AAATGGAAACACATT[C/T]CACACTCATGGATTA | 11169 |
rs575064170 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989949 | GATTATAGGCGTGAG[A/C]CATCACGCCCGGCAG | 11169 |
rs575082187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54945623 | TTGGCTTACTGCAAC[C/T]TCCACCTTCCAGGTT | 11169 |
rs575131089 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954739 | CTTTTTGTTTTTTTG[G/T]TTTTTTTGAGACAGA | 11169 |
rs575144632 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988870 | AAACAGACATATGTT[C/G]TGAGGTATTTTGGGT | 11169 |
rs575155600 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54951342 | TCCCACAGAAATACA[A/C]ACTACCATCAAAGAA | 11169 |
rs575186617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54947085 | TGGCTCACACCTGTA[A/G]TCCCTGCACTTTGGG | 11169 |
rs575186728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952189 | TTCAATTAGGAAAAG[A/G]GGAAGTCAAATTGTA | 11169 |
rs575255269 | snp | C/G | 0.0715223 | 0.175059 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024953 | AGACCTGACCGTCCC[C/G]TAAAGGGTCTGTGCT | 11169 |
rs575266707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54978098 | TAAGATAATGACATT[C/T]ACTAACAAAATGAAT | 11169 |
rs575281687 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958402 | ACAGTGCTGGGATTA[C/T]AAGCATGAGCCACCA | 11169 |
rs575332332 | snp | A/C | 0.000709788 | 0.0188252 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987142 | AAGACTGAAAAAAAT[A/C]TACCTCTGTGATAAA | 11169 |
rs575352880 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55004486 | GAGATAGAGTCTCGC[A/T]CTATCACCTGAGCTA | 11169 |
rs575354910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010538 | CATAGTTAAAAATCC[A/G]GTAAAAAACAAAAAA | 11169 |
rs575355317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55024408 | TCAGAAATGTAGACG[C/T]TATCCCTGTTGCCTC | 11169 |
rs575395016 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55012874 | CTCCCACCACTGTTA[C/T]GTTGGGGATTAAGTT | 11169 |
rs575482578 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55022023 | TAAAGGCCTGTATGA[A/T]CTCCTCATCTAGAGG | 11169 |
rs575581960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010130 | GGCCAAAGCAATATA[C/T]TTCAATTCAAAAAGA | 11169 |
rs575589031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002019 | CAATAATATTTAACT[A/G]CAACTGTATTCAGGC | 11169 |
rs575591907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54997979 | CACTTTGGGGGGCTG[C/T]GGTGGGTGGATCACC | 11169 |
rs575622979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962217 | AACATCTGTCTTCTC[A/C]GCTGGGCTAAAATAG | 11169 |
rs575645684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003873 | CCAGCTACCAACTGT[A/G]TATTTTTTATGTACA | 11169 |
rs575684214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955812 | ATTCTTATACTAACA[C/T]GTGAAATCTGGAGTT | 11169 |
rs575690790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010719 | TCTGGTAAGAAAAAT[A/G]TTTGAATAGTACTTC | 11169 |
rs575726905 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54945961 | TAAAAAATTACTAGT[A/G]TGACCATAACCATTT | 11169 |
rs575778763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54969633 | AGCTGAATTCTAGAT[A/G]CACAAAGAACTGGTA | 11169 |
rs575814652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54990583 | CCTGGGCAACAGAGC[A/G]AGACTCCATCTCAAA | 11169 |
rs575839726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974636 | ATCGAGACCAGCCTG[A/G]GCAACCTGGCGAAAC | 11169 |
rs575900546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967709 | CACTGAAGCCCCAAC[C/G]TCCCAAGTTCAAGCA | 11169 |
rs575910329 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940385 | TTTCCTAACTTTAAT[A/C]ATCACCAGATAAGGA | 11169 |
rs575955307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54946344 | AGAGTGCACAGCCAC[C/T]TGGCTAAAACTGGAC | 11169 |
rs575985139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961321 | ACACCCCATCTCTAT[C/T]AAAAAAAATAAAATA | 11169 |
rs575991600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975672 | ATAATTAAAGGAAAA[C/T]AGGAAAATTTTATAT | 11169 |
rs576010381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949132 | AGCTCCTCACCAGCA[A/G]CGGAACAAAGCTGGA | 11169 |
rs576166733 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949431 | AATGAATGAAATGAA[A/G]CGAGAAGAAAAGTTT | 11169 |
rs576225082 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949868 | AAAAGAATTTTCAAC[C/T]CAGAATTTCATATCC | 11169 |
rs576228992 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025616 | ACATCTCTCTGCTTC[A/T]AGCCTTTAATACCTT | 11169 |
rs576276341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021100 | GACCTTATAAAAACA[C/T]ATCATAATTTCCGTC | 11169 |
rs576349571 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948927 | AAACTCCAACAGACC[G/T]GCAGCTGAGGGTCCT | 11169 |
rs576349766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954155 | GCCAGGCATGGTGGC[A/G]TATGCCTGCAATCCC | 11169 |
rs576404655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944244 | ATTACAGGCATAAGA[C/T]ACCATACCCAGCCAA | 11169 |
rs576443614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981435 | ACTATGGAAAGCAAG[C/T]AATTGGACTAAGATA | 11169 |
rs576459653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54994889 | AAATCTACAGATCTA[C/T]AGTGATGGCCCACCT | 11169 |
rs576507654 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990595 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 11169 |
rs576526152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982076 | CAGTGGCGCGATCTC[C/G]GCCCACTGCAAGCTC | 11169 |
rs576527409 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:55006880 | TTAAAAAGTAATTAA[A/C]AAAACTATTTTTACA | 11169 |
rs576553360 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | WDHD1, SOCS4 | GRCh38.p7 | 14:55027382 | GGAGTGGTTGGGCCT[A/C]CCCTCTCCACTTAAG | 11169 |
rs576569686 | snp | C/T | 6.58935e-05 | 0.00573955 | missense | WDHD1 | GRCh38.p7 | 14:54991325 | GTTACAAGTGGTAGA[C/T]TGTGAATGCTGCCTT | 11169 |
rs576677404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54961368 | AAAATCCTTAATATG[A/G]CCTACACAGATCTGC | 11169 |
rs576733735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55003714 | GACTACAGGCGCACA[C/T]CACCACGCCTGGCTA | 11169 |
rs576739183 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950018 | TGGAAAGGAACAACC[A/G]GTACCAGCCACTGAA | 11169 |
rs576741492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000251 | CTGAGACCTGATACA[A/T]AATAGTATTTAATGA | 11169 |
rs576750362 | snp | C/T | 3.33256e-05 | 0.00408187 | missense | WDHD1 | GRCh38.p7 | 14:54955649 | TCACTTCCTCAGTTT[C/T]ATTAGTTTGAGAATT | 11169 |
rs576794954 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | WDHD1 | GRCh38.p7 | 14:54993266 | GGGATTACAGGCACA[C/T]GTCACCACACCTGGC | 11169 |
rs576795440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54996831 | GGAGTCTCGCTCTGT[C/T]GCCAGGCTGGAGTGC | 11169 |
rs576809791 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54950626 | ATCCAGGAATTGAAC[A/T]CAGCTCTGCACCAAG | 11169 |
rs576819802 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54979413 | CTCCCGCCTTGGGCT[C/T]CCAAAGTGTTGGGAT | 11169 |
rs576851531 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939055 | GTCTATAAAGCATAC[A/G]TGATAAAATGTCAAC | 11169 |
rs577061696 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55017210 | TTTGGCAGGAAATAG[C/T]GTTCAGCAGTCCTGC | 11169 |
rs577142860 | snp | C/T | 0.00013238 | 0.00813465 | missense | WDHD1 | GRCh38.p7 | 14:54944433 | ACAAAATATTACTTC[C/T]ATTTTCTTCTAACCA | 11169 |
rs577143414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009395 | CAAGAGAAACTCCAA[A/G]ATATTCTGACTGTAC | 11169 |
rs577151946 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028233 | TACCGTGGGTGGCAT[C/T]GTGTGAGGCGTTGTT | 11169 |
rs577187586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55020435 | TAAACATCCTTCTTG[C/T]CTTTCAGTTCTCTAC | 11169 |
rs577209754 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55009961 | GAGTAGCTGGGATTA[C/T]AGGCACCCGCCACCA | 11169 |
rs577214358 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021312 | GCACTACTTCTTCTA[A/C]ATCTTCTTCCTTATC | 11169 |
rs577214767 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028943 | CATGGATGTATAAAA[A/G]TAATTGTTATTAATA | 11169 |
rs577233158 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54982726 | ATATTATTAAAGCCT[G/T]AATGACTAATAGAAA | 11169 |
rs577235238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54974744 | AGGCATAAGAATCAC[G/T]TGAACCCGGAAGGAG | 11169 |
rs577254406 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013916 | TATCTCAAGGAAAAA[A/G]AAAAGTCACCTAGTT | 11169 |
rs577276547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55021857 | AGCAGGAATTTGTTT[C/T]GGGCTCGATGGCCTT | 11169 |
rs577298945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54975482 | CCTCCCAAGTAGCTG[A/G]GATTACAGGCATCTG | 11169 |
rs577327202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001060 | TACTCATTTTATTAC[C/T]AAATTCAATTTTCTT | 11169 |
rs577339416 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954984 | TCCGCCTGCTTCGGC[C/T]TCCCAAAGTGCTGAG | 11169 |
rs577343576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954271 | AGCCTGGGCAACAAG[A/G]GCGAAACTCCGTCTC | 11169 |
rs577378310 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016105 | GAAATATAGTAGAAT[C/T]AATAAGAAATAAAGG | 11169 |
rs577389024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001791 | CTTCCTCTAAAATTT[A/C]AGAGTCCATGATCAC | 11169 |
rs577421116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987874 | TCAGGTCATCTGTCC[A/G]CCTTGGCCTCCCAAA | 11169 |
rs577427765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54954667 | CTTATTTTTCTATCT[A/C]TCCATCCATTTATGT | 11169 |
rs577453123 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54981412 | ATGAACAAATTCCTA[A/G]TTTAGTGACTATGGA | 11169 |
rs577461395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018987 | GAGATGGTGCCATTG[A/C]ACTCCAGCCTGGGCA | 11169 |
rs577486808 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027492 | TGGGGGAAGGGTGGC[C/T]GCTGCCTGGCCTCGC | 11169 |
rs577490557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54949337 | TGAAAACCATGGCAC[A/G]AGAACTACGTGACGA | 11169 |
rs577521302 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956617 | CACTCCATCCAGCCT[-/G]GGTGACAGAGTGAGC | 11169 |
rs577523357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55019762 | TGATCCCAGCTACTT[C/G]GGAGGCTGAGGAGAG | 11169 |
rs577540141 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013349 | TAGGGCAAGTTACGG[C/T]ATTATCATACATTTT | 11169 |
rs577557844 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | WDHD1 | GRCh38.p7 | 14:54973909 | AGAGCACCAATTCGC[A/T]TTTTTTTATCCTTTC | 11169 |
rs577575081 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54998847 | TCATGTAAATGCTAT[A/T]CATGGCTGAATAATA | 11169 |
rs577595773 | snp | C/G | 0.000547879 | 0.0165421 | missense | WDHD1 | GRCh38.p7 | 14:54995618 | CAACTGAGTTTTCAT[C/G]ATCTTCTAGGATGTG | 11169 |
rs577665960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000421 | TAATTTTCCAAGAAA[A/G]TAAGGCAGTTTGTGG | 11169 |
rs577680535 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54953809 | AAAAAAGGATGAATT[A/C]ATGTCCTTTGTAGGG | 11169 |
rs577684387 | in-del | -/CCCATG | 0.00199481 | 0.0315187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979514 | TTCATTTCTTTACCT[-/CCCATG]CCCACCCCAATCTGG | 11169 |
rs577751493 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026186 | AATCAACATAGAAGC[G/T]ACAGTGGAAGCCGTG | 11169 |
rs577757798 | snp | C/T | 1.64781e-05 | 0.00287033 | missense | WDHD1 | GRCh38.p7 | 14:54987242 | GAACCCCTCCAATAG[C/T]AAACAATCGAAGAAG | 11169 |
rs577763362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54959654 | ACAACTGTAGTCATA[A/G]CTACTCAGTAGGGTG | 11169 |
rs577773581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54979799 | GAGGTAACTATTATT[A/G]TTAGTTTCCTTTTCA | 11169 |
rs577829344 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54980324 | GTGAGACTCTGTCTC[A/T]AAAAAAAAAAAGACA | 11169 |
rs577898372 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54948838 | CAGGCAGCAACATTT[C/G]CTGTTCACCAATATT | 11169 |
rs577900769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943078 | AAAGCAAGTATCTAC[A/G]TTACTAGGTGCCTGT | 11169 |
rs577939434 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | WDHD1 | GRCh38.p7 | 14:54943487 | GCAGCCTTGACCTCC[G/T]GGGCTCAAGTAAGTG | 11169 |
rs577953690 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54964652 | TCAAAAAAAAAAAAA[G/T]AAATAAAAAGGAATA | 11169 |
rs577969231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | WDHD1 | GRCh38.p7 | 14:54952624 | CAATGACTTTCTTCA[C/T]AGAATTGGAAAAAAC | 11169 |
rs578193666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55005667 | CCTCCTTCATTTGCA[A/G]GACATAGAGGTTCTA | 11169 |
rs578194737 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:55018040 | AATTAAATACACAAA[A/C]AATACTAGCATTGCA | 11169 |
rs578223610 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | WDHD1 | GRCh38.p7 | 14:54958100 | ATTCCTTCCAGTCAC[C/T]ATTTTCTCTCGCCTC | 11169 |
rs745339765 | snp | A/G | 5.32652e-05 | 0.0051604 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995832 | GAACAAATTAATACA[A/G]ATTATAAAGTAAAAG | 11169 |
rs745356547 | in-del | -/TTTAAA | 6.12526e-05 | 0.00553377 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008291 | AAATGGGCAAAAAAC[-/TTTAAA]TTTAAATTGCTGAGT | 11169 |
rs745370099 | snp | A/T | 1.66468e-05 | 0.00288498 | missense | WDHD1 | GRCh38.p7 | 14:54962957 | TATTTCTTACCCAGC[A/T]TTCAGCTTTTTTCTG | 11169 |
rs745380893 | snp | C/T | 1.6483e-05 | 0.00287076 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008639 | GGATCAAAGGAAAGA[C/T]TTAAAACAGGGGCAT | 11169 |
rs745385364 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55004846 | TGTTCCTATGCATTC[A/G]GTGGTCTGAGCAGTG | 11169 |
rs745408547 | snp | C/G | 1.65091e-05 | 0.00287303 | stop-gained | WDHD1 | GRCh38.p7 | 14:54962850 | TGTAGCAGTATTGCT[C/G]TAACTAAGAGAAAAT | 11169 |
rs745419241 | snp | A/G | 8.31428e-05 | 0.00644705 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981492 | ATAAAAAGAATTTCA[A/G]CATACTTTTTAAAAA | 11169 |
rs745446031 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54977633 | AAAAAAGGACTCTTG[-/T]TCAAGTCCAGCCTGG | 11169 |
rs745505589 | in-del | -/AGGCGAGACC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55018817 | TCCCAGCACTTTGGG[-/AGGCGAGACC]AGCCTGACCAACAAT | 11169 |
rs745507195 | snp | C/G | 1.71637e-05 | 0.00292943 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008392 | AAACAATACATTTCT[C/G]TATAGTCATAGCCAT | 11169 |
rs745519040 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005977 | TCAAGTGATACTCCT[A/G]CCTCAGTCTCCCAAG | 11169 |
rs745526519 | snp | A/G | 3.30186e-05 | 0.00406303 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54967364 | GCGTGGAAGGGTTGG[A/G]GGAAACCGAGAACCT | 11169 |
rs745543508 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54943173 | CTTCCACTTCTAACT[A/G]AGAGATTGTGCCTTC | 11169 |
rs745594811 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026192 | CATAGAAGCGACAGT[A/G]GAAGCCGTGCAATCG | 11169 |
rs745600208 | snp | A/G | 3.41099e-05 | 0.00412962 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002221 | CGTAAACAAAAGTTT[A/G]CATTAAATTGAATTT | 11169 |
rs745607774 | snp | A/C | 1.65318e-05 | 0.002875 | missense | WDHD1 | GRCh38.p7 | 14:54966492 | CAAGCATTTTCATTA[A/C]AAGTTCCTGTTGCTC | 11169 |
rs745651196 | snp | A/G | 1.68692e-05 | 0.00290419 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013644 | GGCATGGTGTCTCAT[A/G]CCTATAATGCTAGCA | 11169 |
rs745683224 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54978570 | AGCATGGGCAAATGA[C/G]TGATACCCTGGCTCT | 11169 |
rs745720805 | snp | G/T | 1.6495e-05 | 0.0028718 | missense | WDHD1 | GRCh38.p7 | 14:54987369 | ATCCCAAGAACTAAA[G/T]TGCAGGCAGTGAAGC | 11169 |
rs745720933 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963996 | ACCTGCAGTCTTATC[C/T]ACTCAGGAGCCTGAG | 11169 |
rs745736560 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980142 | CCAGCCTAGGCAACA[C/T]GGTGAAACCCTGTCT | 11169 |
rs745760010 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974414 | CTCCAGTCTGGGCAA[C/G]AGAGAGAGATTCTGT | 11169 |
rs745767617 | snp | A/G | 1.65121e-05 | 0.00287329 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000506 | ACTCCCTTTTACCTT[A/G]CTGCTTGATGTCTTT | 11169 |
rs745771031 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55012812 | GGCATCAATCCAATC[A/G]TGAGGCCAGAGCCCT | 11169 |
rs745834637 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998756 | TGTACACTACTCTCC[A/G]ACCCCAATTCTCCCA | 11169 |
rs745848052 | in-del | -/AAAGGGA | 1.7024e-05 | 0.00291749 | frameshift-variant | WDHD1 | GRCh38.p7 | 14:54957595 | GGAAGAGTTTACCTT[-/AAAGGGA]TTTACTCGTCCTTGG | 11169 |
rs745864183 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55000339 | CTTGGGAGACATCAG[G/T]TTGAACAAGTAAGAA | 11169 |
rs745879169 | snp | C/G | 4.99921e-05 | 0.00499935 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981731 | TCACTTGGAGACATA[C/G]CTACATGTTGTTAAA | 11169 |
rs745947255 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951756 | AAAATCCTCAGTAAA[A/C]TACTGGCAAACCAAA | 11169 |
rs745969498 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54989896 | CTCCAACTCCTATCC[A/T]CAAGTGACCAACCCA | 11169 |
rs745970852 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55021727 | AAGGTCTATATCTTG[A/C]AATTACTTCGCTCCC | 11169 |
rs745995189 | snp | C/T | 1.65616e-05 | 0.00287759 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962473 | AAAATTTCCTTGATA[C/T]TACAAATTTATAAAT | 11169 |
rs746060661 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55022702 | CAAAACAAACAAACA[A/T]ACAAAAAACCTGTTC | 11169 |
rs746068062 | snp | A/G | 1.67083e-05 | 0.00289031 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007262 | AAAGAAAAGAAAAGA[A/G]AAATAAGAATCACTT | 11169 |
rs746147054 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55010177 | CAAAAACCTTTACTA[C/G]ATAAAAGAATATATG | 11169 |
rs746189843 | snp | C/T | 1.64933e-05 | 0.00287165 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000901 | CTTTCCATGCAGTCT[C/T]TGGTTTCCACATTCC | 11169 |
rs746205633 | snp | C/T | 4.94686e-05 | 0.00497311 | missense | WDHD1 | GRCh38.p7 | 14:54989056 | CAGTGCTTTCACATG[C/T]CAACAAAATAGCTTC | 11169 |
rs746215825 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54962284 | CTTCTGTATCCACCA[C/T]TAAGTAAAATGCCTG | 11169 |
rs746232191 | snp | C/T | 1.71211e-05 | 0.00292579 | intron-variant | WDHD1 | GRCh38.p7 | 14:54956997 | GACAAACAGATCCCA[C/T]GCTGCTTACTGCAGA | 11169 |
rs746242979 | snp | C/G | 1.91547e-05 | 0.00309467 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000659 | CCTAAAAATTAAAAA[C/G]TAGGTTCTAAAAATA | 11169 |
rs746287396 | snp | C/T | 1.67075e-05 | 0.00289023 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54963149 | TTCCACACAACGGAA[C/T]TCTCGCTCCAGTTTA | 11169 |
rs746303000 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998355 | GGCTGGTCTTGAACT[C/T]CTGACCTCAGGTGAT | 11169 |
rs746322679 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948252 | CTGAAGCAGGGCAAG[G/T]CATCACCTCACCCGG | 11169 |
rs746369539 | snp | C/T | 1.64819e-05 | 0.00287066 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55010364 | CCACATGGTTTGCAT[C/T]TGTAGTGAAGCGAGT | 11169 |
rs746403455 | snp | C/T | 1.65007e-05 | 0.00287229 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54984763 | AAGGTAGGATTTCCT[C/T]GTAAGAGGAAGAGGG | 11169 |
rs746431321 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54984370 | CATGGTGGCACATGC[C/T]TGTAGTCCCAGCTAC | 11169 |
rs746440437 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54968519 | TAAAATAACAGCAGA[A/G]CTAAACAAAATTGAG | 11169 |
rs746458827 | snp | A/G | 1.65149e-05 | 0.00287353 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54987378 | ACTAAAGTGCAGGCA[A/G]TGAAGCTTGCTAAAA | 11169 |
rs746492905 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958196 | CAATGGTGTGATCTC[A/G]GCTCACTGCAAAGTC | 11169 |
rs746547956 | snp | G/T | 1.72677e-05 | 0.00293829 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955552 | TGCTAAATTTCTCTA[G/T]GTACTGACCTTTGGT | 11169 |
rs746561491 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55007491 | CTCAGAAAAATGCAA[C/T]TTAATGCACCTTAAT | 11169 |
rs746577427 | snp | C/T | 1.64817e-05 | 0.00287064 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000526 | TTGATGTCTTTCCAC[C/T]GGGGTCACAAACATT | 11169 |
rs746615345 | snp | A/T | 8.33646e-05 | 0.00645564 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008745 | AAAGAGTAACGCAAA[A/T]GAATAAATGCTAACA | 11169 |
rs746632418 | snp | A/T | 3.59189e-05 | 0.00423771 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995852 | TAAAGTAAAAGTGAA[A/T]GATTTAGAAAAACTC | 11169 |
rs746692441 | snp | C/T | 1.66726e-05 | 0.00288722 | missense | WDHD1 | GRCh38.p7 | 14:54962967 | CCAGCATTCAGCTTT[C/T]TTCTGAAATCTTCTT | 11169 |
rs746746117 | snp | C/G | 1.64961e-05 | 0.00287189 | missense | WDHD1 | GRCh38.p7 | 14:54991382 | AGAAGACTAGAACCA[C/G]TTTTTAGCATTGAAA | 11169 |
rs746753301 | in-del | -/TAC | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026531 | ATAACTTTGTCGATA[-/TAC]TACAACTACCATGAC | 11169 |
rs746761598 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55012848 | TCTCATTACTTCTCA[A/G]TAGACCCCACCTCCC | 11169 |
rs746762776 | snp | A/C | 1.65603e-05 | 0.00287747 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962485 | ATATTACAAATTTAT[A/C]AATATTTCTCACCTG | 11169 |
rs746782032 | snp | C/T | 0.000281688 | 0.0118644 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55007366 | GCAGTGGCCAACTAA[C/T]AGCACATGTCTAATT | 11169 |
rs746811760 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55014126 | TAAAATTTTGAGGCA[A/G]AGTCTCATTCTGTTG | 11169 |
rs746818922 | in-del | -/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54969343 | AAGACTCCGTTTCAA[-/G]AAAAAAAAAAAAAAA | 11169 |
rs746838104 | snp | A/G | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027985 | TTATGCTTTTCTTGT[A/G]TCTTCATTCTCCATA | 11169 |
rs746848106 | in-del | -/CTAAAGGTAA | 1.67629e-05 | 0.00289503 | frameshift-variant | WDHD1 | GRCh38.p7 | 14:54957620 | ACTCGTCCTTGGCTG[-/CTAAAGGTAA]CTGCACCTTTCACAA | 11169 |
rs746894766 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54949345 | ATGGCACGAGAACTA[C/T]GTGACGAATGCACAA | 11169 |
rs746963566 | snp | C/G | 1.68408e-05 | 0.00290175 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988987 | CAACTGTATCTAACA[C/G]TTCAACAGTGCCAAA | 11169 |
rs746983873 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003162 | AAAGAAAAAAAATAC[A/G]TACTACATTTCCTTG | 11169 |
rs746984841 | snp | C/T | 3.31005e-05 | 0.00406807 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54966511 | TTCCTGTTGCTCTTT[C/T]GTTGCTTGATTTTTA | 11169 |
rs746986795 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003827 | CCTCAGCCTCCCAAA[C/G]TGCTGGGATTATAGG | 11169 |
rs747009757 | snp | C/T | 1.77871e-05 | 0.00298215 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55010460 | TGACCAGTTTTCCAC[C/T]CTAAAAGAAAAATTA | 11169 |
rs747024803 | snp | C/G | 3.36895e-05 | 0.00410412 | missense | WDHD1 | GRCh38.p7 | 14:54963154 | CACAACGGAATTCTC[C/G]CTCCAGTTTACAAGA | 11169 |
rs747050465 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55023004 | TAATTTTTTGCATTT[G/T]TAGTAGAGACAGGGT | 11169 |
rs747145089 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54986216 | GCATTTTAAAAAATG[-/A]AAATAAAAAAATTTA | 11169 |
rs747149254 | snp | A/C | 1.65004e-05 | 0.00287227 | missense | WDHD1 | GRCh38.p7 | 14:54984790 | AGGGTCACCATGCAA[A/C]ATTTGTTTTTTCTTT | 11169 |
rs747180886 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54941741 | TTAGAAAATAACAAA[C/T]AAGAAGTAAATGATT | 11169 |
rs747194472 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54962350 | GACCATAGCTTCACA[A/G]ACAACATCTGAGATT | 11169 |
rs747221447 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997386 | TAGGCGTTAGCCACC[A/G]TACCCAGACCCTCAT | 11169 |
rs747233658 | snp | C/T | 1.64876e-05 | 0.00287116 | missense | WDHD1 | GRCh38.p7 | 14:54941642 | GTTTTCGCTTCTTTG[C/T]TTCAGTTCCTTCACT | 11169 |
rs747236249 | snp | C/G | 1.74327e-05 | 0.00295229 | missense | WDHD1 | GRCh38.p7 | 14:54995610 | ATTCTTACCAACTGA[C/G]TTTTCATCATCTTCT | 11169 |
rs747256768 | snp | A/T | 3.29783e-05 | 0.00406055 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962693 | ATGGGAAAAGCCACA[A/T]CCATGATAGTTCTCA | 11169 |
rs747269908 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996406 | TGAGCTCAGGAGTTC[A/G]AGACCAGCCTGGACA | 11169 |
rs747272781 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998605 | TTGCTACTTCTTCCA[C/T]ACCTGTAAATCATAT | 11169 |
rs747292488 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963472 | TACATACCACTTTAA[G/T]CTACTAATTGCAAGA | 11169 |
rs747303317 | snp | A/G | 3.58912e-05 | 0.00423607 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991164 | TAACTATAGTAAGAA[A/G]AAAGTGCTGAAAACC | 11169 |
rs747336167 | in-del | -/TA | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940320 | TCATAACCACTGTGC[-/TA]TATAATGTCTCTGAT | 11169 |
rs747369046 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948857 | TTCACCAATATTTGC[C/T]GTTCTGCAGCCTCCG | 11169 |
rs747412482 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54986042 | CTGGATGTGTAAGTC[G/T]GGAGACACAAGGAGA | 11169 |
rs747414607 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54987543 | AAAGTAATTATGAAA[C/T]ACCCTTAAAATGAAC | 11169 |
rs747422541 | snp | A/C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985114 | AGAGAGCTTACTACA[A/C/T]GCCAGCATTGGCCTA | 11169 |
rs747435948 | snp | G/T | 1.70621e-05 | 0.00292074 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001026 | AATAAATAATGATTT[G/T]GTAAAATTTCAAACT | 11169 |
rs747436093 | snp | A/G | 3.30945e-05 | 0.0040677 | missense | WDHD1 | GRCh38.p7 | 14:54989188 | CATCATTATAGCAGC[A/G]AATAATTCCAATAGA | 11169 |
rs747479515 | snp | A/G | 1.64838e-05 | 0.00287083 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000933 | AACTATGATTAGACC[A/G]TTAATACTACCTGCA | 11169 |
rs747486715 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55018607 | AGTGTACCCTGAATG[C/G]AGATAAAAAGACAGA | 11169 |
rs747502545 | in-del | -/AG | 4.9445e-05 | 0.00497193 | frameshift-variant, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008647 | GGAAAGACTTAAAAC[-/AG]GGGCATCATGTCCTC | 11169 |
rs747506862 | in-del | -/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947346 | AAAAAAGTGTTAAGC[-/G]GGAAAAAAAACCATG | 11169 |
rs747520742 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55006159 | GTGAGCCACCACACA[C/T]AGGCTGTTGTTTTAT | 11169 |
rs747522092 | snp | C/T | 3.3561e-05 | 0.00409626 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013469 | TCATATCAATTGATA[C/T]AACTGTTTTTACTAC | 11169 |
rs747527362 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54971265 | ACCAAAGAGCTTCTG[C/T]GCAGCAAAAGAAACT | 11169 |
rs747578834 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54957937 | TAATCCCTTTACTTG[A/T]GTTCTGCATCCCATG | 11169 |
rs747595111 | snp | C/T | 1.64895e-05 | 0.00287132 | missense | WDHD1 | GRCh38.p7 | 14:54989169 | TCTATGGCATTGTCT[C/T]GCTCATCATTATAGC | 11169 |
rs747613572 | snp | C/G | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028497 | CAATATCATTGGCTA[C/G]AGTACATAGAGTTCA | 11169 |
rs747686438 | snp | C/G/T | 4.0005e-05 | 0.00447227 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995586 | GGGTAATCACATGCA[C/G/T]AAAGTCAAATTCTTA | 11169 |
rs747711027 | in-del | -/A | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026292 | TTTAGGAATCAGAGG[-/A]AAAAAATTGTTTTAA | 11169 |
rs747727402 | snp | C/T | 4.9948e-05 | 0.00499715 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989019 | TCTTCCTAATAATCT[C/T]GAGTTTACCTTGCTA | 11169 |
rs747791135 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947098 | TAATCCCTGCACTTT[A/G]GGAGGCCAAGGCGGG | 11169 |
rs747829304 | snp | C/G | 1.65173e-05 | 0.00287374 | missense | WDHD1 | GRCh38.p7 | 14:54984810 | GTTTTTTCTTTTTCC[C/G]CAGCTCTAGCAGTTG | 11169 |
rs747853086 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015583 | TCCTTTCGGGGACAA[C/T]ATGTGAGGCATTCAA | 11169 |
rs747869043 | in-del | -/C | 3.50398e-05 | 0.00418553 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963194 | AAAAAGGGGGGGGGG[-/C]GGGGAGATCAAATAA | 11169 |
rs747873858 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54968114 | AACCACATGCTTGGC[C/T]GTAAAGCAAGTCTCA | 11169 |
rs747886442 | snp | G/T | 1.65146e-05 | 0.0028735 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944289 | AGAATTTTTTAAATC[G/T]GGGAATTCACTAAGA | 11169 |
rs747893581 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967546 | CTCTTTTTAAAAAAG[C/T]GTTTTAGGCTTGACT | 11169 |
rs747906428 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954782 | TTGCCCAGGCTGGAG[G/T]GCAGCGGTGTGATCT | 11169 |
rs747998241 | in-del | -/AAG | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54987512 | ATTATACACTAGTAT[-/AAG]AAGTTGCTTTAAAAA | 11169 |
rs748039498 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54956052 | ACAGGCACCTGCCAC[C/T]GCGGCTGGCCTAAAT | 11169 |
rs748047739 | snp | A/G | 3.32801e-05 | 0.00407908 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55007374 | CAACTAATAGCACAT[A/G]TCTAATTGGTAAAAA | 11169 |
rs748065481 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55004428 | CATTTTCCACATGGA[C/T]TTTCCCTTTTTTTTT | 11169 |
rs748092913 | snp | C/T | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941364 | TACTACATTATCTTA[C/T]AAAGACAAACAGTTG | 11169 |
rs748120001 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963197 | AAAGGGGGGGGGGGG[C/G]GAGATCAAATAACAT | 11169 |
rs748120507 | snp | A/T | 6.59141e-05 | 0.00574045 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967256 | TTATCAAATTCAAAG[A/T]GTCAAGGTAAGACTT | 11169 |
rs748140348 | snp | C/T | 1.74718e-05 | 0.00295561 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001040 | TTGTAAAATTTCAAA[C/T]TAAATACTCATTTTA | 11169 |
rs748145516 | snp | C/G/T | 8.28183e-05 | 0.00643453 | missense | WDHD1 | GRCh38.p7 | 14:54962525 | AAACATCAGAGGAAT[C/G/T]TGTACTTTTGGAAAA | 11169 |
rs748146482 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997739 | AACACAGTGAAACCC[C/T]GTCTCTACTAAAAAT | 11169 |
rs748186277 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54991409 | GAAATATCTACAACA[C/T]AAAGGATCATAATTA | 11169 |
rs748211914 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55012668 | CTGGACACTACAAGA[C/T]TGAGGGGTTGGCATC | 11169 |
rs748215995 | snp | C/T | 6.59381e-05 | 0.00574149 | missense | WDHD1 | GRCh38.p7 | 14:54987197 | CTGCCATTGACACCA[C/T]AGGTCCAGCAAGGCT | 11169 |
rs748222389 | in-del | -/T | 1.65759e-05 | 0.00287883 | frameshift-variant | WDHD1 | GRCh38.p7 | 14:54955614 | GTTTCAGATAATACA[-/T]TTTTTAAGATTTTCT | 11169 |
rs748222745 | snp | C/T | 3.29592e-05 | 0.00405938 | missense | WDHD1 | GRCh38.p7 | 14:54957135 | TGGATGATTTGCCCA[C/T]ATTGTCTAAAATATT | 11169 |
rs748229336 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54970318 | TTGGTAAAGTTTCAG[A/G]ATACAAAATCAATAT | 11169 |
rs748289137 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024136 | AAATCCACGTATAAG[C/T]AGACATACACAATTC | 11169 |
rs748305997 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980802 | GAGTGAGACTCCACA[-/T]AAAAAAAAAAAAAAA | 11169 |
rs748313757 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985352 | GCTGGAGCCTGCCAT[A/G]CAAACATTAGGGGAA | 11169 |
rs748318970 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996473 | GGCATGGTGGCATGT[A/G]TCTATAGTCCCAGCT | 11169 |
rs748379965 | snp | A/G | 1.82877e-05 | 0.00302383 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010467 | TTTTCCACTCTAAAA[A/G]AAAAATTAAGGTAAG | 11169 |
rs748409316 | snp | G/T | 1.64958e-05 | 0.00287187 | missense | WDHD1 | GRCh38.p7 | 14:54944392 | TTTTATTATGTCTGC[G/T]TCATCTGAAAAGTCA | 11169 |
rs748423622 | snp | G/T | 3.31296e-05 | 0.00406985 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987109 | CTCAAGTAATTTCCA[G/T]TTTACTTCAAGTCAT | 11169 |
rs748454405 | snp | C/T | 1.65263e-05 | 0.00287452 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981529 | ACTTTAGACTTCTTT[C/T]AATAGCCCACCTTAG | 11169 |
rs748478108 | snp | C/T | 4.9445e-05 | 0.00497193 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008657 | AAAACAGGGGCATCA[C/T]GTCCTCGAAATGTTT | 11169 |
rs748518830 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54949070 | AACAGAGCAAAAAAG[C/G]TGAAAATTCTAAAAA | 11169 |
rs748521172 | snp | A/C | 1.91035e-05 | 0.00309053 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941461 | GAGTAAAAAAAAATC[A/C]ATTACTTCCCTAGGG | 11169 |
rs748530453 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54987814 | GCATTTTTAGTAGAG[A/G]TGCAGTTTCACCATG | 11169 |
rs748534070 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54971435 | TTTAAAAATTATCCA[C/G]GTGTGGTGGCATGTG | 11169 |
rs748556760 | in-del | -/C | 3.36471e-05 | 0.00410151 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010303 | TCTGATGTCAAAGAG[-/C]CTTACCTAGATCCAG | 11169 |
rs748561021 | in-del | -/TTTGT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005831 | GGTACTTTATTTTAC[-/TTTGT]TTTCTTTTTTTTTTC | 11169 |
rs748574565 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019956 | CATAACCTCAAGGAG[C/T]CAATGATTACCAACG | 11169 |
rs748579553 | snp | A/G | 3.46374e-05 | 0.00416143 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991186 | CTGAAAACCTACTAA[A/G]AAGTTAAGTGTAGAT | 11169 |
rs748621639 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54959269 | CAGACATGGTGACAC[A/T]TGCCTGTGGTCCTAG | 11169 |
rs748668601 | snp | C/T | 8.27931e-05 | 0.00643348 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55002167 | GCTTAACAGATTTTT[C/T]CACAGGAATTGCCAG | 11169 |
rs748698948 | snp | A/T | 1.66441e-05 | 0.00288474 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957219 | CCTAAAGAGCAAACT[A/T]GTGTTAGCACTGTAT | 11169 |
rs748709066 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008253 | TTTGGCCCAGTAATA[A/C]GACATATAACAATTT | 11169 |
rs748709123 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54994485 | TGCATTTAAAATACA[G/T]ATTATCATTTCAACA | 11169 |
rs748750044 | snp | C/T | 3.29614e-05 | 0.00405951 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962728 | TTATGGGCTTGAAAA[C/T]GTATCTCACCAGGCT | 11169 |
rs748769721 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967647 | TTTTTTTGAGACAGG[G/T]TCTCACTGTGTTGCC | 11169 |
rs748772724 | in-del | -/AA | 1.8248e-05 | 0.00302054 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989237 | GGTAAGATTAAATAT[-/AA]GTCTGAGAAAAACTG | 11169 |
rs748778959 | snp | G/T | 1.64874e-05 | 0.00287113 | missense | WDHD1 | GRCh38.p7 | 14:54967354 | CAACAGCAGGGCGTG[G/T]AAGGGTTGGGGGAAA | 11169 |
rs748820770 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54967280 | AAGACTTCCACATAC[C/T]TCCATTTGTCCTTTC | 11169 |
rs748824420 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016003 | CACACCCAGCCCCGA[A/T]GGGCTTCTTGGTGTA | 11169 |
rs748872228 | snp | C/T | 3.30442e-05 | 0.0040646 | missense | WDHD1 | GRCh38.p7 | 14:54989181 | TCTTGCTCATCATTA[C/T]AGCAGCGAATAATTC | 11169 |
rs748884104 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55022783 | TGCTGTCTCTTGGTC[-/A]GCAGAAGCTGATTCT | 11169 |
rs748896449 | snp | C/T | 3.29582e-05 | 0.00405931 | missense | WDHD1 | GRCh38.p7 | 14:54957117 | TAAGTGCAGTGGATT[C/T]CTTGGATGATTTGCC | 11169 |
rs748912499 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55017190 | ACAGTAATACAAATA[A/C]AAACTTTGGCAGGAA | 11169 |
rs748975040 | in-del | -/ATTAAATTGAATTTGAAGAA | 1.70956e-05 | 0.00292361 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002223 | TAAACAAAAGTTTAC[-/ATTAAATTGAATTTGAAGAA]GGAAAAAGGCACAAA | 11169 |
rs749002719 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54957379 | TCCCAAATACCACAT[A/C]CCCAAGAAAGACAGA | 11169 |
rs749016814 | snp | C/T | 1.64822e-05 | 0.00287068 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54987216 | TCCAGCAAGGCTGAA[C/T]ACCTCTTTTTGAACC | 11169 |
rs749023176 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954587 | GGTAACCATCTTTTG[C/T]CCACAAGTAGAGAAC | 11169 |
rs749030406 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54956309 | TGGGGTCTGAGTATA[C/T]ATATTTTTAAAAAGT | 11169 |
rs749044207 | snp | C/T | 1.64868e-05 | 0.00287109 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55013519 | GCCTTTTCTCCAACA[C/T]TAATGAACTTAGGAT | 11169 |
rs749066240 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54991567 | GGTGCAAAAGCAATG[G/T]TGGGTAAAATTCCTG | 11169 |
rs749093915 | snp | A/C | 5.01995e-05 | 0.00500972 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995820 | GCTAGATACCTTGAA[A/C]AAATTAATACAAATT | 11169 |
rs749114619 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55023440 | TCATTTATCTTGAAA[C/T]TGTGAGCAACCGCAA | 11169 |
rs749120527 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54976645 | TCTAAATATGCCAAC[A/G]TGTTAAGCAAAACTG | 11169 |
rs749145282 | snp | A/C | 1.65496e-05 | 0.00287655 | missense | WDHD1 | GRCh38.p7 | 14:54944429 | TCAGACAAAATATTA[A/C]TTCTATTTTCTTCTA | 11169 |
rs749149126 | snp | C/T | 1.65002e-05 | 0.00287225 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008618 | ATTACCAGAAAGATG[C/T]CCTTAGGATCAAAGG | 11169 |
rs749156653 | in-del | -/ACAA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55006469 | ATAACAATCCTGTAT[-/ACAA]ACAATTTTGCTTCCA | 11169 |
rs749179236 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54943112 | GCGCCCTGCCATTCC[A/T]GGGGAAGTGAAACCT | 11169 |
rs749191479 | snp | C/T | 1.66078e-05 | 0.00288161 | synonymous-codon, intron-variant | WDHD1 | GRCh38.p7 | 14:54995706 | ATTTATAATCCCTTT[C/T]GAAAAAGAAGGGATC | 11169 |
rs749204341 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025863 | ACATCACCACCCCAC[C/T]GCCACCACCACTCAT | 11169 |
rs749228402 | in-del | -/CTT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55021303 | TGTTTTCTGGCACTA[-/CTT]CTTCTACATCTTCTT | 11169 |
rs749269827 | snp | C/T | 1.64857e-05 | 0.00287099 | stop-gained | WDHD1 | GRCh38.p7 | 14:54962830 | AACCTTGGTTGGCTC[C/T]ACTCTGTAGCAGTAT | 11169 |
rs749269870 | snp | C/T | 1.64977e-05 | 0.00287203 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944306 | GGAATTCACTAAGAT[C/T]TCAATCTCGGCACAA | 11169 |
rs749293911 | snp | C/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55027012 | GTGGACGCGGGCAGC[C/G]GGAGTGGGGACTCAC | 11169 |
rs749304434 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54962695 | GGGAAAAGCCACATC[C/T]ATGATAGTTCTCATG | 11169 |
rs749369782 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016100 | ATAGTGAAATATAGT[-/A]GAATTAATAAGAAAT | 11169 |
rs749375360 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948021 | AGGAGTTTGAGACCA[C/G]CCTGACCAACATGGA | 11169 |
rs749471772 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020070 | AGTCTCATGAGGTTC[A/G]TGGTGAGGCACAAGC | 11169 |
rs749492890 | snp | C/G | 1.67318e-05 | 0.00289234 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013634 | AAAGTCATCGGGCAT[C/G]GTGTCTCATGCCTAT | 11169 |
rs749547161 | snp | A/G/T | 3.55122e-05 | 0.00421367 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963200 | GGGGGGGGGGGGGGA[A/G/T]ATCAAATAACATCAA | 11169 |
rs749562074 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55007816 | TAGTCAATTACATTC[A/G]TATTCTCTCTAGAAA | 11169 |
rs749575010 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54973015 | GCTGATTTATTAAAA[A/T]GCATTAATTAATCAC | 11169 |
rs749597728 | snp | G/T | 1.65323e-05 | 0.00287505 | missense | WDHD1 | GRCh38.p7 | 14:54963061 | TTAGTTTTTGAGCCA[G/T]TATTAATTTCCGAGA | 11169 |
rs749627191 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000545 | GTCACAAACATTCTC[C/T]AGAAGCCCTAGATTT | 11169 |
rs749639667 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974800 | CCACTGTACTAGCCT[A/G]GATGACAGAATGAGA | 11169 |
rs749664768 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008492 | GCTAACTCTCTTACT[G/T]AATAAAACAAAGGTT | 11169 |
rs749677111 | snp | A/T | 1.67694e-05 | 0.00289558 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008760 | TGAATAAATGCTAAC[A/T]CAAAGGCCTCTCCTA | 11169 |
rs749722378 | snp | C/T | 1.67435e-05 | 0.00289335 | missense | WDHD1 | GRCh38.p7 | 14:54962995 | CTTCTTCTTCTTCCT[C/T]TTCCACCTGGGTTGC | 11169 |
rs749737758 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54981572 | TTCATGGATACCAAC[C/T]ACCCAGTAGTGATCA | 11169 |
rs749751030 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54961258 | CAACTTTGGGATGTG[A/G]AGGTGAGGAAATTGC | 11169 |
rs749765010 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54946332 | GCTAGGACTACAAGA[C/G]TGCACAGCCACCTGG | 11169 |
rs749776537 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947185 | TCTCTACTAAAAATA[C/G]AAAATTAGTCGGGCA | 11169 |
rs749779210 | snp | C/T | 3.29538e-05 | 0.00405904 | missense | WDHD1 | GRCh38.p7 | 14:54991358 | TGACCATCTTCCTCC[C/T]CCTCTTTGAGAAGAC | 11169 |
rs749791388 | in-del | -/CT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55004015 | AGTTTGTCATTTGTA[-/CT]GTGACTAATATTTTG | 11169 |
rs749851632 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996825 | CAGAGTGGAGTCTCG[C/T]TCTGTCGCCAGGCTG | 11169 |
rs749879999 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55001014 | AGAAAAACAGTTAAT[A/C]AATAATGATTTTGTA | 11169 |
rs749927804 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985794 | TGTTATTCCATAGAA[C/T]TGACATGATGATATA | 11169 |
rs750002596 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54992640 | TAATTTACAGCCAGG[-/T]GCTGTGACTCACGCT | 11169 |
rs750004293 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54987026 | AATTATCTACATTTA[A/C]AGATTACACGGATTC | 11169 |
rs750022751 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019736 | TAGCCAGCTGTTGCG[C/G]AGGGCATCTGTGATC | 11169 |
rs750048513 | snp | C/T | 1.97939e-05 | 0.00314588 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941445 | GTCTATATTCAAAGA[C/T]GAGTAAAAAAAAATC | 11169 |
rs750089585 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948786 | ACACCTCACACGGCC[A/G]GGTACCCCTCTGAGA | 11169 |
rs750111288 | snp | A/G | 1.8392e-05 | 0.00303243 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957573 | TAAATAATATAAAAC[A/G]TCACTTGGAAGAGTT | 11169 |
rs750116018 | snp | A/G | 1.95421e-05 | 0.00312581 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007243 | TAATAAAAAAAAAAA[A/G]AAAAAAGAAAAGAAA | 11169 |
rs750130580 | snp | G/T | 1.66502e-05 | 0.00288527 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000840 | AAACAAATACAAAAC[G/T]AATAGAGATGAGCAA | 11169 |
rs750156695 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020809 | AGCCTTACTGATAAC[A/G]TAAACAATTAACACA | 11169 |
rs750197539 | snp | A/T | 1.8239e-05 | 0.0030198 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955726 | GAATACTGCAATAAC[A/T]TCTAGTATAATTTTA | 11169 |
rs750239457 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993998 | CTTTAAAAAGCACAA[C/T]ATAGCACTGCACATT | 11169 |
rs750240222 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960223 | CCCAGGCTGGAGTGC[A/G]GTGGTATGATCTCAC | 11169 |
rs750254975 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008018 | AACCCAAGGCCCAAC[A/G]CATGGTCATTACATT | 11169 |
rs750293371 | snp | A/C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960662 | GAGCCACCATGCCCG[A/C/G]CTAATTTTTTTTTTT | 11169 |
rs750324555 | snp | A/C/G | 6.62564e-05 | 0.0057554 | missense | WDHD1 | GRCh38.p7 | 14:54963109 | TGGCTAAATTCACAG[A/C/G]ATTTTGAGTCATTAG | 11169 |
rs750333965 | snp | A/T | 1.65795e-05 | 0.00287914 | missense | WDHD1 | GRCh38.p7 | 14:54955623 | TAATACATTTTTAAG[A/T]TTTTCTTCTTTCACT | 11169 |
rs750344719 | snp | A/G | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028144 | TTTTTCTGTTGAAGA[A/G]GTTTCCCTATTGTTT | 11169 |
rs750357463 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54946860 | ACCAGCCTGGCCAAC[A/G]TGGCAAACTCCATCT | 11169 |
rs750363975 | snp | A/G | 1.69536e-05 | 0.00291145 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984708 | ACTTGTTTTTTTTAA[A/G]CAAATTTATCTTGCC | 11169 |
rs750366661 | snp | C/T | 1.7093e-05 | 0.00292339 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010285 | TCTAACATTATTTCC[C/T]TTTCTGATGTCAAAG | 11169 |
rs750419303 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996281 | ATAAAAATAAAGTGA[C/T]AGAACCAATAGAAAA | 11169 |
rs750447193 | snp | C/G | 1.76129e-05 | 0.00296752 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008318 | TTGCTGAGTTTACCT[C/G]ATCTGAAATTTGCCA | 11169 |
rs750464027 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54955757 | TATGTTTTATAAGCA[C/T]GTTCTGAAAAATGTG | 11169 |
rs750473906 | in-del | -/AG | 0.000107535 | 0.00733183 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007249 | AAAAAAAAAAAAAAA[-/AG]AAAAGAAAAGAAAAA | 11169 |
rs750592451 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54955891 | CTTCAGATTCCATGT[A/T]TTCCTTTTTTTTTTT | 11169 |
rs750608161 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005223 | TGGTAGTGTCCACAT[A/G]GCACAGAGGAAAATC | 11169 |
rs750672065 | snp | A/G | 1.9347e-05 | 0.00311017 | missense | WDHD1 | GRCh38.p7 | 14:54966594 | GAAATATAACTGAAC[A/G]CCAAAATTGCTCCTA | 11169 |
rs750698200 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985308 | GACCTCTCAGAAAGT[-/A]AAAGTTTAAGCTGAG | 11169 |
rs750719421 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54976138 | CACTAGGCCACATTG[G/T]CTTTCCAGAGAAGCA | 11169 |
rs750790135 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026514 | CCTCTGGAAGTACGA[C/T]TATAACTTTGTCGAT | 11169 |
rs750790569 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011172 | TGTTTACTTTTTCCT[C/T]CTTTACAGTCTTCTT | 11169 |
rs750800058 | snp | A/G | 1.64912e-05 | 0.00287147 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54987177 | GAAAAGCTGTTCTCC[A/G]TGTCCTGCCATTGAC | 11169 |
rs750848674 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963348 | GGAATTACAATTAAT[C/T]ACAATTAATGGTGGG | 11169 |
rs750852653 | snp | A/T | 3.2969e-05 | 0.00405998 | missense | WDHD1 | GRCh38.p7 | 14:54944356 | TTCAGTTGACAATAC[A/T]CTAAATCGAATCATT | 11169 |
rs750855027 | snp | A/C | 3.31835e-05 | 0.00407316 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984870 | CTGTACCTAATGAGA[A/C]AATGTAAATATAAAT | 11169 |
rs750861475 | snp | C/T | 1.6728e-05 | 0.00289201 | missense, intron-variant | WDHD1 | GRCh38.p7 | 14:54995753 | TTAGAAAATCACCAG[C/T]ATTACTCATATCATC | 11169 |
rs750899119 | in-del | -/ATTT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54973077 | AACTTATGTACTCCG[-/ATTT]ATTTATTAGAAAAGC | 11169 |
rs750938008 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | WDHD1 | GRCh38.p7 | 14:54962774 | TTTCTTCATCATCAG[C/T]TTCTCCACTGTCCTC | 11169 |
rs750944356 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54964927 | TACTAGTTCCTGGAC[C/T]ACAAGTAACACTTTA | 11169 |
rs750952369 | snp | C/G | 1.70965e-05 | 0.00292369 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941729 | AAGGAAAGATTTTTA[C/G]AAAATAACAAATAAG | 11169 |
rs750954258 | in-del | -/AAG | 1.80213e-05 | 0.00300172 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941742 | TAGAAAATAACAAAT[-/AAG]AAGTAAATGATTTAT | 11169 |
rs750993389 | snp | A/C | 1.65844e-05 | 0.00287957 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:54995679 | CATGAGGTCTTCATC[A/C]TCCTCATCATCATTT | 11169 |
rs751007261 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54999892 | AGTCACTGCAGCAGA[C/G]CTCAAAATTATTTTT | 11169 |
rs751013750 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997013 | GCCAGGATGGTCTTG[A/T]TCTCTTGACCTCGTG | 11169 |
rs751033840 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974489 | CAAAACCTGTTTTGT[-/T]TTTGTTTTTTTTTTT | 11169 |
rs751044409 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988890 | GTATTTTGGGTGTGC[C/T]GGTGTTTGTACCAAA | 11169 |
rs751067589 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939804 | TATACACAGATTATA[C/T]CCTTAAGCATTAGGT | 11169 |
rs751108960 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963298 | TCCCTAATTCTAAGA[C/T]GCACATTTTTACAAG | 11169 |
rs751109944 | snp | C/T | 1.65151e-05 | 0.00287355 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54984745 | TGAAAACCCAATCCA[C/T]GCAAGGTAGGATTTC | 11169 |
rs751117505 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54949793 | GACTAACAGCTGATC[G/T]CTCGGCAGAAACTCT | 11169 |
rs751117536 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020969 | TCTTCATCCTTATCG[C/T]CTTCACAGTGAGAAG | 11169 |
rs751131173 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974033 | GCTAATTTGGTGGGT[C/T]TTGATGACGACGGAG | 11169 |
rs751142967 | snp | G/T | 1.67548e-05 | 0.00289432 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010306 | GATGTCAAAGAGCCT[G/T]ACCTAGATCCAGCAG | 11169 |
rs751161193 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993223 | CTCGGGCTCAAGAGA[C/T]CCTCCTACCTCAGCC | 11169 |
rs751242780 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54981701 | ACAAGGGGTACCTAA[A/T]CACCAACAGAAAAAT | 11169 |
rs751247153 | snp | A/G | 1.66966e-05 | 0.00288929 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991436 | ATTAAGGGAATCACG[A/G]ATACCAATGATTTGG | 11169 |
rs751272929 | snp | G/T | 3.3042e-05 | 0.00406447 | missense | WDHD1 | GRCh38.p7 | 14:54941587 | TTCTCTTTTGCTTTT[G/T]CTTCCTGGTTTTCTG | 11169 |
rs751353706 | snp | C/T | 9.88826e-05 | 0.00703076 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967241 | ATCACAGGTGCTGTA[C/T]TATCAAATTCAAAGT | 11169 |
rs751357803 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965620 | GGAAGTAGCCCTAGA[A/G]ATGTTTATTCCTGCA | 11169 |
rs751385409 | snp | C/G/T | 0.000109059 | 0.00738372 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989234 | ACAGGTAAGATTAAA[C/G/T]ATAAGTCTGAGAAAA | 11169 |
rs751411015 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54943324 | AATGTGTAAGTAGAT[A/T]CAATTTTTAAAAATT | 11169 |
rs751438464 | snp | A/C | 3.29625e-05 | 0.00405958 | missense | WDHD1 | GRCh38.p7 | 14:54989152 | TATCATGGAACTCCA[A/C]ATCTATGGCATTGTC | 11169 |
rs751453166 | in-del | -/CATCAGATTGTCAGAATGAAAGTATAAT | 1.74718e-05 | 0.00295561 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001040 | TGTAAAATTTCAAAC[-/CATCAGATTGTCAGAATGAAAGTATAAT]TAAATACTCATTTTA | 11169 |
rs751458496 | snp | C/T | 3.70982e-05 | 0.00430671 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955732 | TGCAATAACATCTAG[C/T]ATAATTTTATATGTT | 11169 |
rs751504055 | in-del | -/AT | 0.0212403 | 0.100842 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987438 | TCATATGATATTTAC[-/AT]ATATATATATATAAG | 11169 |
rs751515640 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016766 | GCTACTGTATTGGAC[A/G]GCGCAGCATTAAAAG | 11169 |
rs751571622 | snp | C/T | 1.65806e-05 | 0.00287924 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000871 | AGAAGAGACAAAAGA[C/T]ACACTAAATCATACC | 11169 |
rs751572994 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54992075 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCTGTCT | 11169 |
rs751601474 | snp | A/T | 3.36253e-05 | 0.00410019 | missense, intron-variant | WDHD1 | GRCh38.p7 | 14:54995762 | CACCAGCATTACTCA[A/T]ATCATCTCCATCAAA | 11169 |
rs751606367 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002043 | TTCAGGCAAACTACG[C/T]ATTAACTGCTCCTTA | 11169 |
rs751631584 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958572 | ATCTCTACATTGTCA[A/C]ATCTGGTGGATACCT | 11169 |
rs751658380 | snp | A/G | 3.31076e-05 | 0.0040685 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962889 | TCAATAAAGAGCTAT[A/G]CAAAGACCAACTTAA | 11169 |
rs751659124 | snp | C/G | 1.65861e-05 | 0.00287972 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:54995687 | CTTCATCATCCTCAT[C/G]ATCATTTATAATCCC | 11169 |
rs751675391 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026647 | TAGCTGACTGCACAT[A/G]TAAAGTTTAAGGATA | 11169 |
rs751681428 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | WDHD1 | GRCh38.p7 | 14:54962786 | CAGCTTCTCCACTGT[C/T]CTCAGCATCTTCTTC | 11169 |
rs751690616 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54944107 | TTTTTTTAGTTGTCA[G/T]GATCGTTATTATCTT | 11169 |
rs751705216 | snp | C/T | 6.7245e-05 | 0.0057981 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008565 | AAATATATTTTTAAA[C/T]ATATTCAGGAAAAAC | 11169 |
rs751734336 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993448 | TTAACATAACAGAGC[C/T]GTAAGAGTTCACTGA | 11169 |
rs751734507 | snp | C/T | 1.64798e-05 | 0.00287047 | missense | WDHD1 | GRCh38.p7 | 14:54967342 | AGGATAATATAGCAA[C/T]AGCAGGGCGTGGAAG | 11169 |
rs751762438 | snp | C/T | 1.71305e-05 | 0.00292659 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008338 | GAAATTTGCCACACT[C/T]TGACAGATCCATCAC | 11169 |
rs751763669 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54978151 | GGCAGAATAGTAAAA[A/C]TCCTCATAGGTTCAA | 11169 |
rs751792183 | snp | A/G | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027821 | ATATCCGTTATGAAG[A/G]AAGTAACTTGTGTTC | 11169 |
rs751860191 | snp | C/T | 9.92178e-05 | 0.00704266 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55002150 | AGATTCTCTTCTATA[C/T]AGCTTAACAGATTTT | 11169 |
rs751880297 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55013428 | ATTTTTTCACTCAAG[C/T]ATAAAAATCACATGC | 11169 |
rs751885307 | snp | A/C | 1.64727e-05 | 0.00286986 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026705 | TTGTTTCTCAAAGAA[A/C]CTTACCTCCCAGAAT | 11169 |
rs751886178 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54979515 | TCATTTCTTTACCTC[C/T]CATGCCCACCCCAAT | 11169 |
rs751917338 | snp | A/G | 3.29506e-05 | 0.00405884 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54987294 | AGCCCATCCTTGACC[A/G]AGACATATGGCTTCA | 11169 |
rs751963710 | snp | C/T | 1.65531e-05 | 0.00287686 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54957202 | TTTGGAACTGGCTGA[C/T]ACCTAAAGAGCAAAC | 11169 |
rs751965645 | in-del | -/TCT/TCTTCT | 0.00205508 | 0.0319905 | cds-indel | WDHD1 | GRCh38.p7 | 14:54962975 | AGCTTTTTTCTGAAA[-/TCT/TCTTCT]TCTTCTTCTTCTTCT | 11169 |
rs752001321 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55001419 | GCATGCACCACCACA[C/T]ATGGCTAATTTTTTA | 11169 |
rs752013575 | snp | A/G | | | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938454 | CCAGAGAATCACTTG[A/G]ACCCAAAAGGCAGAG | 11169 |
rs752061940 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54966458 | TTTAACGTTTTCAGT[A/C]TATTTATTTTACTCA | 11169 |
rs752074222 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54978665 | AATATTCAGTGATTA[A/C]AACTGTAAAGGCAAA | 11169 |
rs752077765 | snp | C/T | 0.000106328 | 0.0072906 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944497 | ATTATGTGAAAACAT[C/T]TTATACTTAAGACAG | 11169 |
rs752078780 | snp | C/T | 1.65296e-05 | 0.00287481 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000981 | GGGAGACCAGGTTAC[C/T]ATATTGAGGGTCTGT | 11169 |
rs752122303 | snp | C/G | | | missense | WDHD1 | GRCh38.p7 | 14:54987268 | AGAAGCAGGGCACTA[C/G]TAGCGGCAGCAGCCC | 11169 |
rs752138232 | snp | C/T | 1.64868e-05 | 0.00287109 | missense | WDHD1 | GRCh38.p7 | 14:54987188 | CTCCATGTCCTGCCA[C/T]TGACACCACAGGTCC | 11169 |
rs752240002 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54961962 | CTGCTTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 11169 |
rs752264036 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55009860 | GAGTCTCACTCTGTC[A/G]CCTAGGCTGGAATGC | 11169 |
rs752335690 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996718 | TAAGCCAATGGAAAT[G/T]TATAGTTTGGTATAA | 11169 |
rs752356810 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54983024 | ACAACATTAGCCAGG[C/T]GTGGTGGTATGTGCC | 11169 |
rs752361365 | snp | A/G | 1.6582e-05 | 0.00287936 | utr-variant-5-prime, synonymous-codon | WDHD1 | GRCh38.p7 | 14:55010431 | GACTTGAATAGTATT[A/G]TTAGAAACTGCAGTG | 11169 |
rs752424848 | snp | A/G | 1.65965e-05 | 0.00288062 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008593 | AACACAAAAAGAGAA[A/G]GAAAAAATAATTACC | 11169 |
rs752462317 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997793 | GCACAAGCCTGTAAT[C/T]CCAGCTACTCAGGAG | 11169 |
rs752510107 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985764 | GAAGAAATGAAAAGA[A/G]ACAAATTTAGAATGT | 11169 |
rs752510618 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54983974 | AAGTCTTCAAAATCC[A/G]GAGTATTTTACACAT | 11169 |
rs752526924 | snp | C/T | 4.94311e-05 | 0.00497123 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54962820 | TTGATTTCTGAACCT[C/T]GGTTGGCTCCACTCT | 11169 |
rs752528613 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948635 | ATGTCCCTGTCTGAC[A/G]GCTTTGAAGAGAGTA | 11169 |
rs752530015 | snp | A/G | 1.76173e-05 | 0.00296788 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967416 | GTAAAGAAAAGTTCC[A/G]TCATAAAAATTTACT | 11169 |
rs752535072 | in-del | -/A | 1.65408e-05 | 0.00287578 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002068 | CCTTATAGCCCACTG[-/A]AAAGTGTCACTTTGT | 11169 |
rs752579257 | in-del | -/TAAG | 3.33589e-05 | 0.00408391 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007266 | AAAAGAAAAGAAAAA[-/TAAG]AATCACTTACCTTCC | 11169 |
rs752587360 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54970482 | TCTCTACAAGAACTA[C/T]AAAACACTGTTGAAA | 11169 |
rs752634802 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54945967 | ATTACTAGTATGACC[A/G]TAACCATTTGCCCAA | 11169 |
rs752639327 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54969595 | CCTATCAACCAAAAA[A/C]AGCCCTGGACCAGAA | 11169 |
rs752645855 | snp | C/T | 0.000115492 | 0.00759819 | missense | WDHD1 | GRCh38.p7 | 14:54957177 | CTGAATTCATTGACA[C/T]GGCTGGTTCTTTGGA | 11169 |
rs752682306 | in-del | -/AC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003586 | AAGAAAGAAAAACGA[-/AC]TATATATATATAGTT | 11169 |
rs752693737 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54979849 | GCGTATGTAAAGCAA[A/G]TACAATTACATATTC | 11169 |
rs752745772 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55027078 | AGAGCTGCTTCCCGC[C/G]CTTCGGCTCGCTCAC | 11169 |
rs752764070 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | WDHD1 | GRCh38.p7 | 14:54987302 | CTTGACCGAGACATA[C/T]GGCTTCAATATCCTC | 11169 |
rs752790577 | snp | A/G | 1.6588e-05 | 0.00287988 | missense | WDHD1 | GRCh38.p7 | 14:54955597 | GGAGGACATATAGCT[A/G]GGGTTTCAGATAATA | 11169 |
rs752792512 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948510 | CAGCCAGGAAACTCG[-/A]ACTGGGTGGAGCCCA | 11169 |
rs752798398 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54994827 | AACCACATTTCAAGT[A/G]CTCAACAGCTACATG | 11169 |
rs752812605 | in-del | -/T | 0.000144162 | 0.00848884 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984697 | TTTATATTATACTTG[-/T]TTTTTTTTAAACAAA | 11169 |
rs752840211 | snp | A/T | 3.32834e-05 | 0.00407929 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000483 | TTTTGAAGAAACTGT[A/T]GTACCATACTCCCTT | 11169 |
rs752858757 | snp | C/T | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028048 | AATGATATTCTTTCA[C/T]TTGTACTTATCTTTG | 11169 |
rs752867538 | snp | A/G | 1.65762e-05 | 0.00287886 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962915 | CTTAACATTCAAGAC[A/G]GTAAAGGAAAATTCA | 11169 |
rs752921160 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980741 | AACTCAAAGTGGAGG[C/T]TGTAGTGAACTGAGA | 11169 |
rs752924360 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965223 | GCAGGTCTCTGCCCT[A/C]TGGGGCATAAAGTCT | 11169 |
rs752939992 | snp | C/T | 1.76375e-05 | 0.00296958 | missense, intron-variant | WDHD1 | GRCh38.p7 | 14:54995785 | CCATCAAAAAGATCA[C/T]TATAATCCTTTTCCA | 11169 |
rs752945796 | snp | G/T | 3.29707e-05 | 0.00406008 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55013552 | TCATCATCCAAGTCT[G/T]CCCAAATCCTCACAT | 11169 |
rs752947324 | snp | C/T | 3.29489e-05 | 0.00405874 | missense | WDHD1 | GRCh38.p7 | 14:54991337 | AGATTGTGAATGCTG[C/T]CTTCTTGACCATCTT | 11169 |
rs752948789 | snp | C/G | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028990 | GGGTGCTTTGGGTGG[C/G]TATTTAGTGTTTTTT | 11169 |
rs752964193 | in-del | -/AA | 6.85248e-05 | 0.00585301 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963180 | CAAGAAAGCTAATCC[-/AA]AAAGGGGGGGGGGGG | 11169 |
rs752999159 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55001833 | AAACTCACTTAACAA[C/T]AAAGGCTAACTACTG | 11169 |
rs753022883 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002740 | CTCCCAAATAGCTAG[A/G]ACTACAGCCCAACTA | 11169 |
rs753023266 | snp | A/G | | | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938723 | GTGCCACTGCACTTC[A/G]GCCTGGGTGACAGAG | 11169 |
rs753037708 | snp | C/T | 1.65699e-05 | 0.00287831 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55007287 | TCACTTACCTTCCCA[C/T]TTTTTGGCTGCCAAG | 11169 |
rs753055436 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939840 | CAAAAGAAATCGCGG[G/T]TTTTGCCACTGAAAT | 11169 |
rs753072001 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55007247 | AAAAAAAAAAAAAAA[A/G]AAGAAAAGAAAAGAA | 11169 |
rs753132175 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54989316 | ATAATTAAATTTGTA[C/T]TAAGATTTAGGTTTT | 11169 |
rs753163628 | snp | A/G | 1.68454e-05 | 0.00290214 | missense | WDHD1 | GRCh38.p7 | 14:54957605 | ACCTTAAAGGGATTT[A/G]CTCGTCCTTGGCTGC | 11169 |
rs753193086 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55017654 | AGCCAGAAAAATCAA[A/T]GTTCTTACTATATTA | 11169 |
rs753236993 | snp | C/G | 1.6473e-05 | 0.00286988 | intron-variant, synonymous-codon, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026755 | GTGTCCCTCTGTATG[C/G]CCATATCTCATTGGC | 11169 |
rs753260937 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974333 | AGCTACTCGGAAGGC[A/G]GAGGACGGAGGATCG | 11169 |
rs753280783 | snp | A/T | 1.67643e-05 | 0.00289515 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966455 | AACTTTAACGTTTTC[A/T]GTATATTTATTTTAC | 11169 |
rs753302772 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012387 | AAGCTTAGGGGTTTA[C/T]AGATAATTAATTTCC | 11169 |
rs753307723 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55022448 | TTTTTCCCCCCACAG[A/G]ATAGGGCACTTTAGT | 11169 |
rs753316910 | in-del | -/T | 1.68868e-05 | 0.0029057 | frameshift-variant | WDHD1 | GRCh38.p7 | 14:54941577 | CAAATTCAGGTTCTC[-/T]TTTGCTTTTTCTTCC | 11169 |
rs753345230 | snp | C/T | 3.31752e-05 | 0.00407265 | missense | WDHD1 | GRCh38.p7 | 14:54963043 | TCTCTACAGCCAGTT[C/T]ACTTAGTTTTTGAGC | 11169 |
rs753364355 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54999631 | TTAGATGGGGTATCA[C/T]TGTCATCCAGGCTGG | 11169 |
rs753392367 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948755 | CTGGGAGGCACCCCC[C/G]AGTAGGGGCAGACTG | 11169 |
rs753408851 | snp | A/T | 1.65173e-05 | 0.00287374 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55002107 | CCTGAGAGATGAAAT[A/T]ATCTGAAAGATCAAA | 11169 |
rs753481218 | snp | A/G | 1.65269e-05 | 0.00287457 | missense | WDHD1 | GRCh38.p7 | 14:54957191 | ATGGCTGGTTCTTTG[A/G]AACTGGCTGATACCT | 11169 |
rs753505564 | snp | A/C | 1.71743e-05 | 0.00293033 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010276 | GCCTTTTGTTCTAAC[A/C]TTATTTCCTTTTCTG | 11169 |
rs753530365 | snp | C/G/T | 0.000105113 | 0.00724896 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963194 | CAAAAAGGGGGGGGG[C/G/T]GGGGAGATCAAATAA | 11169 |
rs753549666 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55018266 | TTTTGAAGCTTTTAG[C/T]GAAATGCAATTCATG | 11169 |
rs753598931 | snp | C/T | 4.97764e-05 | 0.00498856 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000490 | GAAACTGTTGTACCA[C/T]ACTCCCTTTTACCTT | 11169 |
rs753636160 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019457 | TTTATCTCTAATATT[A/G]TTTTATTTGTGCCTT | 11169 |
rs753642920 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947228 | CCTGTAATCACAGCT[-/A]CTCAGGAGGCTGAGA | 11169 |
rs753652385 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54970814 | AAAAACAACAAAGCT[C/G]GAGGCATCACATTAC | 11169 |
rs753661614 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005793 | TAGAATCAGCTCAAT[G/T]TGGTCCTCCTAGACA | 11169 |
rs753676710 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960280 | TCACGCCATTCTCCT[A/G]CCTCAGCCTCCCAAG | 11169 |
rs753679196 | in-del | -/TGAAAATGTTTTATAAA | 1.64757e-05 | 0.00287012 | intron-variant, splice-acceptor-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026805 | TTTCCTTTACCTATC[-/TGAAAATGTTTTATAAA]AGCCAGTCTTATTAT | 11169 |
rs753714902 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55007147 | GCAGGAGAATTGCTA[G/T]AACCTGGGAGGCAGA | 11169 |
rs753734370 | in-del | -/AAAAAG | 3.35647e-05 | 0.00409649 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007386 | ATGTCTAATTGGTAA[-/AAAAAG]AAAAAGAAAATTTCT | 11169 |
rs753736531 | snp | A/G | 1.66037e-05 | 0.00288125 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962938 | AAAATTCAAACAACT[A/G]AATTATTTCTTACCC | 11169 |
rs753754012 | snp | A/C | 1.78461e-05 | 0.0029871 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967424 | AAGTTCCATCATAAA[A/C]ATTTACTAACATGTC | 11169 |
rs753755329 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958653 | CCTTACTTCTTGATA[C/G]TTTGTCCTCTCTTGA | 11169 |
rs753782686 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54971831 | TAAAAAAAAATCAGC[A/G]GCAAAAAACAAATAT | 11169 |
rs753783074 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54944153 | TATTATTAGAGACGA[C/T]GTCTCACTATGTTGC | 11169 |
rs753785155 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993693 | AGTAGATGAGAGAAT[C/G]CAGCTATCCTCTATG | 11169 |
rs753834649 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967159 | CCCTCCCTGCTACCC[C/G]TATTTATGTAATTAT | 11169 |
rs753873682 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54989409 | ACAATTACTTATTAT[G/T]TCCTTGGTGAGAATA | 11169 |
rs753888418 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54982490 | ACTCTGTCCCCAACT[A/C]CTAGGTAAGCAATTC | 11169 |
rs753904750 | snp | A/G | 1.82417e-05 | 0.00302002 | missense | WDHD1 | GRCh38.p7 | 14:54966579 | AATCAAGGTGGTTGT[A/G]AAATATAACTGAACG | 11169 |
rs753927031 | snp | A/G | 3.41583e-05 | 0.00413255 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007254 | AAAAAAAAAAAGAAA[A/G]GAAAAGAAAAATAAG | 11169 |
rs753949065 | in-del | -/AT | 1.75225e-05 | 0.00295989 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987425 | AACAATCAAACTTTC[-/AT]ATGATATTTACATAT | 11169 |
rs753962729 | snp | A/C | 1.70411e-05 | 0.00291895 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987420 | ACAGAAACAATCAAA[A/C]TTTCATATGATATTT | 11169 |
rs753968191 | in-del | -/A | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940982 | TCCGAAACACAAAAG[-/A]AAAAAGTCTCACCTA | 11169 |
rs754021561 | in-del | -/AAG | 0.00011616 | 0.00762015 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000867 | GCAAAGAAGAGACAA[-/AAG]ATACACTAAATCATA | 11169 |
rs754027340 | snp | C/T | 1.64841e-05 | 0.00287085 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000595 | ATATTCGACCACAAG[C/T]AGGATGCCATGCCAG | 11169 |
rs754045365 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951031 | ATAGCACTAAATGCC[C/T]ACAAGAGAAAGCAGA | 11169 |
rs754054868 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002871 | GTGCTGAGATTACAG[A/C]GTGAGACACCATGCC | 11169 |
rs754073042 | snp | A/G | 1.79787e-05 | 0.00299817 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955721 | AACATGAATACTGCA[A/G]TAACATCTAGTATAA | 11169 |
rs754083889 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | WDHD1 | GRCh38.p7 | 14:54987334 | TTCTGAGGCAAGTCT[A/G]TTATCCACTCTTTGC | 11169 |
rs754094941 | snp | A/G | 1.65121e-05 | 0.00287329 | missense | WDHD1 | GRCh38.p7 | 14:54984750 | ACCCAATCCATGCAA[A/G]GTAGGATTTCCTTGT | 11169 |
rs754141878 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54956966 | TCCTATATCTGAAAC[A/G]GTGAACAAAACTGAA | 11169 |
rs754155600 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54989580 | AAAATTGAGTTTTCT[A/T]ACAAATATGGATGCA | 11169 |
rs754238492 | snp | C/G | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941046 | TAAAAGACGTCATCC[C/G]CTAGGTCTAGTAGAA | 11169 |
rs754248340 | snp | A/G | 1.65811e-05 | 0.00287929 | stop-gained | WDHD1 | GRCh38.p7 | 14:54962549 | TGGAAAACGAGTTCT[A/G]TCCTACAGATTAAAA | 11169 |
rs754262492 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975890 | TTTAAAGGATCTCTG[A/T]ACAAAAAGAAAGCAT | 11169 |
rs754318177 | snp | C/T | 2.13541e-05 | 0.0032675 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008268 | CGACATATAACAATT[C/T]ATTACAGAAATGGGC | 11169 |
rs754321555 | snp | G/T | 1.64936e-05 | 0.00287168 | missense | WDHD1 | GRCh38.p7 | 14:54941602 | TCTTCCTGGTTTTCT[G/T]TTTCATCACTTTCAT | 11169 |
rs754351282 | snp | C/T | 5.0045e-05 | 0.005002 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966653 | ACTATCACCTTAATA[C/T]GAGGCAAGCGTTAAA | 11169 |
rs754373627 | snp | A/C | 1.65146e-05 | 0.0028735 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55007325 | GCAGATTGATTTTGC[A/C]TTTATCACATCGTTG | 11169 |
rs754384966 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54977646 | TGTTCAAGTCCAGCC[G/T]GGATAACGTAAGGAG | 11169 |
rs754395531 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972695 | CATGGTAGTGGGCAC[C/T]TGTAATCCCAGATAT | 11169 |
rs754414603 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020596 | CACAGTAATAAATAT[A/T]ATGTTTATAAGGACA | 11169 |
rs754437681 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010917 | TAAATGCAGCATCCA[C/T]GCCAGAGACTGCAGT | 11169 |
rs754450603 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960260 | GCAAGCTCTGCCTCC[C/T]GGGTTCACGCCATTC | 11169 |
rs754498690 | snp | C/T | 1.65864e-05 | 0.00287974 | missense | WDHD1 | GRCh38.p7 | 14:54963121 | CAGCATTTTGAGTCA[C/T]TAGATCAGCAAGTTC | 11169 |
rs754530198 | snp | A/C | 0.000133298 | 0.00816279 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55010315 | GAGCCTTACCTAGAT[A/C]CAGCAGCAATTTTAG | 11169 |
rs754549586 | snp | C/T | 1.65468e-05 | 0.00287631 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55010424 | ATGTGTGGACTTGAA[C/T]AGTATTATTAGAAAC | 11169 |
rs754583330 | snp | A/G | 1.65151e-05 | 0.00287355 | missense | WDHD1 | GRCh38.p7 | 14:54984746 | GAAAACCCAATCCAT[A/G]CAAGGTAGGATTTCC | 11169 |
rs754596318 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008240 | AAGCAATTATTAATT[C/T]GGCCCAGTAATACGA | 11169 |
rs754623742 | snp | C/G | 1.65616e-05 | 0.00287759 | missense | WDHD1 | GRCh38.p7 | 14:54963049 | CAGCCAGTTCACTTA[C/G]TTTTTGAGCCAGTAT | 11169 |
rs754634801 | snp | C/T | 1.67514e-05 | 0.00289403 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991441 | GGGAATCACGAATAC[C/T]AATGATTTGGAAAAA | 11169 |
rs754640072 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993256 | CCAAGTAGGTGGGAT[C/T]ACAGGCACACGTCAC | 11169 |
rs754645663 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960916 | GATATCCTCCTGTCC[A/C]AGCCTCCCAAATACC | 11169 |
rs754665637 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54946030 | AACGTAAACCGATTT[C/T]CAGAAAAATAACAGA | 11169 |
rs754669751 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55009697 | TTGGCCTCCCAAAGG[A/G]CTGGGATTACAGGCA | 11169 |
rs754675116 | snp | C/G | 1.6534e-05 | 0.00287519 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981702 | CAAGGGGTACCTAAA[C/G]ACCAACAGAAAAATC | 11169 |
rs754676341 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963322 | TTACAAGTTTTAACA[C/T]CTCTGAAATTGGAAT | 11169 |
rs754741092 | snp | C/T | 4.94393e-05 | 0.00497164 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967251 | CTGTATTATCAAATT[C/T]AAAGTGTCAAGGTAA | 11169 |
rs754767711 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015514 | CTGTAAAATGACTAG[C/T]GATAAGCTATCTCCC | 11169 |
rs754798136 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965873 | AGGCAGGAGAATCAC[C/T]TGAACCCGGGAAGTG | 11169 |
rs754851272 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003167 | AAAAAAATACATACT[A/G]CATTTCCTTGAGCTC | 11169 |
rs754861561 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980343 | AAAAAAAAGACATAA[A/T]TCAGTGGTTTTTTTG | 11169 |
rs754891618 | snp | A/G | 1.64852e-05 | 0.00287094 | missense | WDHD1 | GRCh38.p7 | 14:54957075 | GAGGCTTTATAATGG[A/G]AGACTTTTCATTATT | 11169 |
rs754891673 | in-del | -/TGCCATCAGATTGTCAGAATG | 1.75197e-05 | 0.00295966 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001041 | GTAAAATTTCAAACT[-/TGCCATCAGATTGTCAGAATG]AAATACTCATTTTAT | 11169 |
rs754928782 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016879 | AATGGGTTGTCTCCA[C/T]TATCAAAAGAACTTT | 11169 |
rs754932992 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55006031 | CACCACACCTGGCTA[A/C]TTTTCATTTTTTTGT | 11169 |
rs754946585 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55023863 | ACTGCATCTTTATGT[C/T]TGTTTACATTTCTCT | 11169 |
rs754947946 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54955991 | CAACCTCCACCCTCC[A/G]AGTTCAAGTGGTTCT | 11169 |
rs754956031 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54969498 | CTGGAAACATAAAAC[C/T]TCCCAAGACTGACTC | 11169 |
rs754962572 | snp | C/G | 3.29717e-05 | 0.00406015 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54987192 | ATGTCCTGCCATTGA[C/G]ACCACAGGTCCAGCA | 11169 |
rs754968236 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54987962 | CACATAGAAGATAGT[-/A]AAAATCCATGAAGTG | 11169 |
rs754986700 | snp | C/T | 8.98481e-05 | 0.00670194 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944504 | GAAAACATTTTATAC[C/T]TAAGACAGAGTTTAA | 11169 |
rs755014451 | snp | C/T | 1.65765e-05 | 0.00287888 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000873 | AAGAGACAAAAGATA[C/T]ACTAAATCATACCTT | 11169 |
rs755088406 | snp | C/T | 1.65784e-05 | 0.00287905 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987096 | AACAGCAAAAAAGCT[C/T]AAGTAATTTCCATTT | 11169 |
rs755109011 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55021040 | AGAGGTGGAAGAGGG[A/G]GAGGAAGTAGAGGAG | 11169 |
rs755111640 | snp | A/C | 1.64879e-05 | 0.00287118 | missense | WDHD1 | GRCh38.p7 | 14:54944368 | TACTCTAAATCGAAT[A/C]ATTCCTTCTTTTATT | 11169 |
rs755146505 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997649 | CGGGCATGGTGTCTC[A/T]TGCCTGTAATCCCAG | 11169 |
rs755153766 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54956499 | CAAAATTAGCTGGGC[A/G]TGATGTCAGGCCTCT | 11169 |
rs755164960 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55001663 | ATCAAGATGAAGAAA[-/A]CTAGTAAGTGAAGTG | 11169 |
rs755166729 | snp | A/T | 4.95421e-05 | 0.00497681 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944287 | TAAGAATTTTTTAAA[A/T]CTGGGAATTCACTAA | 11169 |
rs755180743 | snp | A/G | 5.02391e-05 | 0.00501169 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008573 | TTTTAAACATATTCA[A/G]GAAAAACACAAAAAG | 11169 |
rs755198864 | snp | A/C | 4.94246e-05 | 0.0049709 | stop-gained | WDHD1 | GRCh38.p7 | 14:54962798 | TGTCCTCAGCATCTT[A/C]TTCAACTTGATTTCT | 11169 |
rs755216994 | snp | C/T | 1.65899e-05 | 0.00288005 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:54995690 | CATCATCCTCATCAT[C/T]ATTTATAATCCCTTT | 11169 |
rs755231118 | in-del | -/C | 1.64768e-05 | 0.00287021 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955517 | TGCTGCTACTGTATA[-/C]TTTTTACTTGGTCAC | 11169 |
rs755237866 | snp | A/C | 1.70697e-05 | 0.00292139 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008345 | GCCACACTCTGACAG[A/C]TCCATCACAACTAGC | 11169 |
rs755247207 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963482 | TTTAATCTACTAATT[A/G]CAAGAAAATTAAGAA | 11169 |
rs755298397 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965120 | TCCAATTTTAAAATT[A/G]AAAGTCTGGACCATT | 11169 |
rs755299653 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55000059 | AGTCTAAACTAAGAC[A/T]TGAATATAAATAGGT | 11169 |
rs755324832 | snp | C/G | 1.76724e-05 | 0.00297252 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957580 | TATAAAACATCACTT[C/G]GAAGAGTTTACCTTA | 11169 |
rs755352618 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54986063 | CACAAGGAGAGGGTA[C/G]GGTTGGTGCTATCAA | 11169 |
rs755352705 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55001560 | GAGCCACTGTGCCCA[A/G]CCACTGGCACAATTT | 11169 |
rs755385627 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954458 | CATTGGAATTATAAG[A/T]GCAGATTAACTTGAA | 11169 |
rs755405003 | snp | A/G | 1.654e-05 | 0.00287571 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55002152 | ATTCTCTTCTATATA[A/G]CTTAACAGATTTTTC | 11169 |
rs755444518 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54987464 | TATAAGCAATCATGA[C/T]ATTCAACAAAAAAAC | 11169 |
rs755449494 | snp | C/T | 1.65658e-05 | 0.00287795 | missense | WDHD1 | GRCh38.p7 | 14:54957204 | TGGAACTGGCTGATA[C/T]CTAAAGAGCAAACTA | 11169 |
rs755456320 | snp | C/T | | | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938457 | GAGAATCACTTGAAC[C/T]CAAAAGGCAGAGGCT | 11169 |
rs755506785 | snp | A/T | 6.68304e-05 | 0.0057802 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013473 | ATCAATTGATATAAC[A/T]GTTTTTACTACCTTC | 11169 |
rs755506947 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939813 | ATTATATCCTTAAGC[A/G]TTAGGTTGGCACAAA | 11169 |
rs755509761 | snp | C/G/T | 0.000124121 | 0.00787705 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963196 | AAAAGGGGGGGGGGG[C/G/T]GGAGATCAAATAACA | 11169 |
rs755554700 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019932 | ATCAAGACTTCATCA[G/T]CTTTATGACATAACC | 11169 |
rs755613196 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947103 | CCTGCACTTTGGGAG[G/T]CCAAGGCGGGTGGAT | 11169 |
rs755655193 | snp | A/C | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940287 | CCGAACCTAGGTAAT[A/C]TGGCTTTGGAATCTG | 11169 |
rs755663977 | snp | A/G/T | 9.90335e-05 | 0.00703619 | stop-gained, synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000894 | ATCATACCTTTCCAT[A/G/T]CAGTCTTTGGTTTCC | 11169 |
rs755694523 | snp | A/C/G/T | 0.00236936 | 0.034344 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963187 | GCTAATCCAAAAAGG[A/C/G/T]GGGGGGGGGGGAGAT | 11169 |
rs755705654 | snp | C/T | 1.72305e-05 | 0.00293513 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013444 | ATAAAAATCACATGC[C/T]AGTATCATTTCATAT | 11169 |
rs755738777 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948150 | GACGGGTGATTTCTG[C/T]ACTTCCAACTGAGGT | 11169 |
rs755759447 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54983025 | CAACATTAGCCAGGC[A/G]TGGTGGTATGTGCCT | 11169 |
rs755767252 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54968941 | CAGCTGCTCAGAAGA[C/G]TGAGATGGGAAGATT | 11169 |
rs755794857 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997867 | AGTGAGCCGAGATCG[C/T]GCCATTGCACTCCAG | 11169 |
rs755827163 | snp | A/G | 1.65086e-05 | 0.00287298 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54944413 | TGAAAAGTCAGGATT[A/G]TCAGACAAAATATTA | 11169 |
rs755830340 | snp | C/T | 1.65924e-05 | 0.00288027 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55010432 | ACTTGAATAGTATTA[C/T]TAGAAACTGCAGTGA | 11169 |
rs755872149 | in-del | -/A | 1.65244e-05 | 0.00287436 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002084 | AAAGTGTCACTTTGT[-/A]AAACCTACCTGAGAG | 11169 |
rs755882561 | snp | A/G | 1.65883e-05 | 0.00287991 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008594 | ACACAAAAAGAGAAG[A/G]AAAAAATAATTACCA | 11169 |
rs755893430 | in-del | -/A | 1.65729e-05 | 0.00287857 | frameshift-variant, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55007286 | ATCACTTACCTTCCC[-/A]CTTTTTGGCTGCCAA | 11169 |
rs755924064 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55004448 | CCTTTTTTTTTAGCA[A/C]CCAATGTTTATTTTC | 11169 |
rs755934408 | snp | C/T | 1.65781e-05 | 0.00287902 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962917 | TAACATTCAAGACAG[C/T]AAAGGAAAATTCAAA | 11169 |
rs755936617 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008395 | CAATACATTTCTCTA[C/T]AGTCATAGCCATAAT | 11169 |
rs755947232 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55018114 | ATCTTTAAGCCTTTG[A/G]AGAGCGAGCGACTCT | 11169 |
rs755988473 | snp | C/T | 5.10582e-05 | 0.00505237 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008357 | CAGATCCATCACAAC[C/T]AGCTGATGCCTGCAG | 11169 |
rs755989968 | snp | C/T | 1.76499e-05 | 0.00297063 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967417 | TAAAGAAAAGTTCCA[C/T]CATAAAAATTTACTA | 11169 |
rs755991594 | snp | A/T | 1.64789e-05 | 0.0028704 | missense | WDHD1 | GRCh38.p7 | 14:54962823 | ATTTCTGAACCTTGG[A/T]TGGCTCCACTCTGTA | 11169 |
rs756029375 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54957358 | AATTAAGAATGATAC[G/T]TATATTCCCAAATAC | 11169 |
rs756052166 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005687 | TAGAGGTTCTAGACA[C/T]TGTGAAAGTTTCCCT | 11169 |
rs756087639 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54943100 | GGTGCCTGTGCTGCG[A/C]CCTGCCATTCCTGGG | 11169 |
rs756100025 | snp | C/T | 3.34185e-05 | 0.00408756 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966459 | TTAACGTTTTCAGTA[C/T]ATTTATTTTACTCAC | 11169 |
rs756106521 | in-del | -/GGG | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963185 | AAGCTAATCCAAAAA[-/GGG]GGGGGGGGGGGAGAT | 11169 |
rs756117541 | snp | C/T | 4.94523e-05 | 0.00497229 | missense | WDHD1 | GRCh38.p7 | 14:54967350 | ATAGCAACAGCAGGG[C/T]GTGGAAGGGTTGGGG | 11169 |
rs756192704 | snp | C/T | 6.59011e-05 | 0.00573988 | missense | WDHD1 | GRCh38.p7 | 14:54987311 | GACATATGGCTTCAA[C/T]ATCCTCATTCTGAGG | 11169 |
rs756220291 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965233 | GCCCTCTGGGGCATA[A/G]AGTCTAGTGTAAGAC | 11169 |
rs756224323 | snp | A/C/G | 3.69414e-05 | 0.00429763 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963198 | AAGGGGGGGGGGGGG[A/C/G]AGATCAAATAACATC | 11169 |
rs756228188 | in-del | -/G | 1.6892e-05 | 0.00290615 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957245 | TGTATGTTTAAAGAA[-/G]AAAAATAAAATCCCA | 11169 |
rs756231737 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | WDHD1, SOCS4 | GRCh38.p7 | 14:55027286 | GGCGATGACCGTGAC[G/T]GCTGGGTTGGGACCG | 11169 |
rs756265714 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55001990 | ATACAACAGCCAGGA[C/G]TTGTTTTCCATTCCA | 11169 |
rs756273832 | snp | A/G | 4.28936e-05 | 0.00463087 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966621 | CCTATAAAAGCAAAT[A/G]AAATTGCTTAAGGCC | 11169 |
rs756317200 | snp | C/T | 1.64844e-05 | 0.00287087 | missense | WDHD1 | GRCh38.p7 | 14:54987203 | TTGACACCACAGGTC[C/T]AGCAAGGCTGAATAC | 11169 |
rs756368489 | snp | C/G | 2.03056e-05 | 0.00318628 | missense, intron-variant | WDHD1 | GRCh38.p7 | 14:54995809 | TTTTCCACTCTGCTA[C/G]ATACCTTGAACAAAT | 11169 |
rs756432892 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963685 | TGCGCCTGTAATCCC[-/A]GCTACTCGGGAAGCT | 11169 |
rs756438770 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015336 | AGGATGCAGTGAGCC[A/G]AGATCGCACTACTGT | 11169 |
rs756448850 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954542 | ATATAAAATTATTCA[C/T]TGCAGTACTGTCTGT | 11169 |
rs756471609 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54950114 | AACCAGCTAACATCA[A/T]AATGACAGGATCAAA | 11169 |
rs756500928 | in-del | -/ATG | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951302 | TAGATGCAATAAAAA[-/ATG]ATAAAGGGGATATCA | 11169 |
rs756551964 | snp | C/T | 3.36327e-05 | 0.00410063 | missense | WDHD1 | GRCh38.p7 | 14:54957608 | TTAAAGGGATTTACT[C/T]GTCCTTGGCTGCTAA | 11169 |
rs756559647 | snp | C/T | 4.96824e-05 | 0.00498385 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962450 | GTGTCACTTTGCAGA[C/T]GACTTGCAAAATTTC | 11169 |
rs756571869 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55021363 | AACTCATTTCTATCA[A/G]ATTGTCTTCTGCTAA | 11169 |
rs756573207 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939859 | TGCCACTGAAATGGC[A/G]AAACTGCATTTACTT | 11169 |
rs756601265 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54992214 | AAAAAAAAAGAGCTG[A/G]GCACAGTGGCTCAGG | 11169 |
rs756604244 | in-del | -/AGA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54949173 | CTTTGACGAGTTGAG[-/AGA]AGAAGGCTTCAGACG | 11169 |
rs756605614 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974551 | CCAAAATAATCAGGC[A/G]TGGTGGCTCACTCCT | 11169 |
rs756606309 | snp | G/T | 1.80922e-05 | 0.00300762 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941474 | TCCATTACTTCCCTA[G/T]GGTCACTTTCTTCCT | 11169 |
rs756619414 | snp | A/C | 1.65996e-05 | 0.00288089 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55002179 | TTTCCACAGGAATTG[A/C]CAGTAACTATTAGAA | 11169 |
rs756620350 | snp | A/G | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940973 | ATAGGAAATTTCCGA[A/G]ACACAAAAGAAAAAG | 11169 |
rs756660498 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960993 | TTTACTTTTTGTAGA[C/G]ATAGGGTTTCATTGT | 11169 |
rs756660554 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975872 | TCACAAAATGTACTT[G/T]CTTTTAAAGGATCTC | 11169 |
rs756682083 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998318 | TATTTTTAGTAGAGA[C/T]GGGGTTTCGTCATGT | 11169 |
rs756726171 | snp | A/G | 1.6489e-05 | 0.00287128 | missense | WDHD1 | GRCh38.p7 | 14:54967357 | CAGCAGGGCGTGGAA[A/G]GGTTGGGGGAAACCG | 11169 |
rs756728502 | snp | C/T | 3.29457e-05 | 0.00405854 | intron-variant, missense, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026766 | TATGCCCATATCTCA[C/T]TGGCTTCCGTGTGGC | 11169 |
rs756747555 | in-del | -/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54969071 | TGAGACGGAGTCTCG[-/C]TTTGTTGCCCAGGCT | 11169 |
rs756780591 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948760 | AGGCACCCCCCAGTA[A/G]GGGCAGACTGACACC | 11169 |
rs756791562 | snp | A/G | 4.95462e-05 | 0.00497701 | missense | WDHD1 | GRCh38.p7 | 14:54991238 | TGAGTGAGATGCAAC[A/G]GTGTAGAACCTGACT | 11169 |
rs756839155 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54984230 | CCGGGTGCAGTGGCT[C/G]GCGCCTGTAATCCCA | 11169 |
rs756850004 | snp | G/T | 3.99848e-05 | 0.00447111 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989261 | AAAAACTGAAGCTCC[G/T]AGAATCAGTAAGCCA | 11169 |
rs756886988 | snp | C/G | 1.6517e-05 | 0.00287372 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55002119 | AATTATCTGAAAGAT[C/G]AAATTGATGACTCCA | 11169 |
rs756938458 | snp | A/G | 1.67919e-05 | 0.00289753 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001008 | CTGTAAAGAAAAACA[A/G]TTAATAAATAATGAT | 11169 |
rs756939179 | in-del | -/AG | 1.68289e-05 | 0.00290072 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007391 | CTAATTGGTAAAAAA[-/AG]AAAATTTCTTTCCTT | 11169 |
rs756950873 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55018297 | AAAACAAAACTTATG[A/C]ACAGGAAGACACTGA | 11169 |
rs756963583 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54969709 | CACTCTATAAAGCCA[A/G]CATTATCCTGATACC | 11169 |
rs756967856 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985765 | AAGAAATGAAAAGAG[A/T]CAAATTTAGAATGTG | 11169 |
rs756979571 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54957481 | TTCTGTTTCCACACA[C/G]ATCAGTCTTTCATGC | 11169 |
rs756992449 | in-del | AGATTCCATGTTTTCC/CATGTTTTCCTT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54955886 | CTACACTTCAGATTC[AGATTCCATGTTTTCC/CATGTTTTCCTT]TTTTTTTTTTTTTTT | 11169 |
rs757022989 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54970875 | AAAAAGAACATGGCA[C/G]TGGTGCACAAACAGA | 11169 |
rs757031731 | snp | C/G | 1.65641e-05 | 0.00287781 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000495 | TGTTGTACCATACTC[C/G]CTTTTACCTTACTGC | 11169 |
rs757038064 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011983 | CTAATTTTAATACAC[A/G]GTATCAATTTGCTCT | 11169 |
rs757043605 | snp | C/T | 1.65707e-05 | 0.00287838 | missense | WDHD1 | GRCh38.p7 | 14:54955613 | GGGTTTCAGATAATA[C/T]ATTTTTAAGATTTTC | 11169 |
rs757069418 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54989570 | AAATATTTCAAAAAT[C/T]GAGTTTTCTTACAAA | 11169 |
rs757080911 | snp | A/G | 1.65176e-05 | 0.00287376 | utr-variant-5-prime, synonymous-codon | WDHD1 | GRCh38.p7 | 14:55008712 | CCACAATTTTGACTA[A/G]AAAATCACTAAGAAC | 11169 |
rs757132056 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54981303 | AGAATTCCTCTCCCT[C/G]TGTGGCTGAAATGAT | 11169 |
rs757136927 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015192 | GGCTAGGGTGGAGCC[-/T]TGACCAACATGGCAA | 11169 |
rs757154970 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993844 | TAAATTTCTGAATTT[C/T]AATTTCTAATATGTA | 11169 |
rs757173565 | snp | C/T | 0.000116814 | 0.00764154 | missense | WDHD1 | GRCh38.p7 | 14:54963025 | CTGTCAATTCGGCTG[C/T]CTTCTCTACAGCCAG | 11169 |
rs757175747 | snp | G/T | 1.75443e-05 | 0.00296173 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955521 | GCTACTGTATACTTT[G/T]TACTTGGTCACTGCA | 11169 |
rs757227161 | snp | C/T | 1.66349e-05 | 0.00288395 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962949 | AACTAAATTATTTCT[C/T]ACCCAGCATTCAGCT | 11169 |
rs757246274 | snp | C/T | 3.31274e-05 | 0.00406972 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962466 | GACTTGCAAAATTTC[C/T]TTGATATTACAAATT | 11169 |
rs757267757 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55027052 | CGAGCCTCCGCCACT[A/G]AGGATCCACAAGAGC | 11169 |
rs757284441 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54945871 | AACCCAGCAGCTATA[C/T]GCCCCTCACTAGGCT | 11169 |
rs757284841 | snp | C/G | 3.29712e-05 | 0.00406011 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008632 | GTCCTTAGGATCAAA[C/G]GAAAGACTTAAAACA | 11169 |
rs757313019 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967896 | AAAGTGTTGGGATTA[C/T]AGGCGTGAGCTACCC | 11169 |
rs757361817 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54955470 | AATGTATTATTTGTA[G/T]TAAGGAATAACAGCA | 11169 |
rs757371770 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015202 | GGAGCCTGACCAACA[C/T]GGCAAAACCCTGAGT | 11169 |
rs757388357 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54989619 | CAGACTTTTTTCCTA[A/T]CTATTCTATGATAAA | 11169 |
rs757429900 | snp | A/T | 1.64743e-05 | 0.00287 | intron-variant, synonymous-codon, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026782 | TGGCTTCCGTGTGGC[A/T]GGCATGTTTTCCTTT | 11169 |
rs757469617 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002872 | TGCTGAGATTACAGC[A/G]TGAGACACCATGCCT | 11169 |
rs757471082 | snp | A/C | 0.000183253 | 0.00957043 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987430 | TCAAACTTTCATATG[A/C]TATTTACATATATAT | 11169 |
rs757492275 | snp | A/G | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940066 | ATAACCAACAGCATC[A/G]TCATTATCAGAATAG | 11169 |
rs757512913 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974806 | TACTAGCCTGGATGA[C/T]AGAATGAGACTCTGT | 11169 |
rs757518680 | snp | C/T | 0.000215423 | 0.0103762 | missense | WDHD1 | GRCh38.p7 | 14:54984860 | CCATCAAATCCTGTA[C/T]CTAATGAGAAAATGT | 11169 |
rs757527014 | snp | A/C | 1.64822e-05 | 0.00287068 | missense | WDHD1 | GRCh38.p7 | 14:54987359 | CTTTGCTTGAATCCC[A/C]AGAACTAAAGTGCAG | 11169 |
rs757544648 | snp | C/T | 3.29989e-05 | 0.00406182 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000607 | AAGTAGGATGCCATG[C/T]CAGACCACAAATTGC | 11169 |
rs757569739 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55022557 | TGTGGTGGTGTATGC[C/T]TGTAATCCCAGCTAC | 11169 |
rs757595655 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990802 | GTCAGACTTTTCCCC[C/T]CATAGTACTTGCCAC | 11169 |
rs757597701 | snp | A/G | 6.65768e-05 | 0.00576923 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54963140 | ATCAGCAAGTTCCAC[A/G]CAACGGAATTCTCGC | 11169 |
rs757601909 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993940 | TATAAAGGCTACTGA[C/G]ACCAAAACATTTGAG | 11169 |
rs757619347 | snp | A/G | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941056 | CATCCCCTAGGTCTA[A/G]TAGAAACATATAGAG | 11169 |
rs757648868 | snp | C/G | 1.651e-05 | 0.0028731 | stop-gained | WDHD1 | GRCh38.p7 | 14:54984751 | CCCAATCCATGCAAG[C/G]TAGGATTTCCTTGTA | 11169 |
rs757648930 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975918 | CATAAATACCACTGA[A/G]TTGGGTTAGAAAATG | 11169 |
rs757659990 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024053 | TATTTCTAGGCTACA[C/T]GGTTCGTCTGCTAGT | 11169 |
rs757683351 | snp | C/T | 0.000181307 | 0.00951949 | missense | WDHD1 | GRCh38.p7 | 14:54941626 | CTTTCATCAACCACA[C/T]GTTTTCGCTTCTTTG | 11169 |
rs757683509 | in-del | -/TATT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54969037 | GACCTTGTTTCTATT[-/TATT]TATTTATTTATTTAT | 11169 |
rs757717927 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54995895 | GGTAAACTTTTAATA[A/T]GCACCTATAAATTCT | 11169 |
rs757741909 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55017750 | CTGCAAGATAACACA[C/T]CAACAAAAAAGAAGC | 11169 |
rs757759336 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54962575 | TAAAATAAAGCAATA[C/T]AATGTAAATGGGGAA | 11169 |
rs757797749 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55018476 | TTGTATTAATTTATG[C/T]TCTGTGCCAGAATGA | 11169 |
rs757797874 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985907 | ATTGTTAGTAAGCCA[C/T]TTACTAAGATGGGGA | 11169 |
rs757804827 | snp | A/G | 1.65767e-05 | 0.00287891 | missense | WDHD1 | GRCh38.p7 | 14:54963117 | TTCACAGCATTTTGA[A/G]TCATTAGATCAGCAA | 11169 |
rs757861218 | in-del | -/T | 3.42604e-05 | 0.00413872 | frameshift-variant, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008338 | AAATTTGCCACACTC[-/T]TGACAGATCCATCAC | 11169 |
rs757876681 | snp | C/T | 1.65146e-05 | 0.0028735 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55007330 | TTGATTTTGCATTTA[C/T]CACATCGTTGCATTT | 11169 |
rs757877143 | snp | C/T | 1.64773e-05 | 0.00287026 | missense | WDHD1 | GRCh38.p7 | 14:54991359 | GACCATCTTCCTCCT[C/T]CTCTTTGAGAAGACT | 11169 |
rs757884205 | snp | G/T | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012050 | TATGTATGATAATAC[G/T]TACTTCTCAAAGCCC | 11169 |
rs757884287 | snp | C/T | 3.32519e-05 | 0.00407736 | missense | WDHD1 | GRCh38.p7 | 14:54963037 | CTGCCTTCTCTACAG[C/T]CAGTTCACTTAGTTT | 11169 |
rs757899929 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947242 | TACTCAGGAGGCTGA[G/T]ACAGGAGAATCACTT | 11169 |
rs757915328 | snp | C/T | 1.64972e-05 | 0.00287199 | missense | WDHD1 | GRCh38.p7 | 14:54981687 | TCTGAATCCACGTAA[C/T]AAGGGGTACCTAAAC | 11169 |
rs757935064 | snp | C/T | 3.30535e-05 | 0.00406518 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987131 | TCAAGTCATAAAAGA[C/T]TGAAAAAAATCTACC | 11169 |
rs757998081 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55014298 | TGTCCCTACGTTGCC[C/T]AGGCTGGTCTTGAGC | 11169 |
rs758004374 | snp | A/G | 0.000119019 | 0.00771333 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941448 | TATATTCAAAGATGA[A/G]TAAAAAAAAATCCAT | 11169 |
rs758036762 | snp | A/C | 1.90239e-05 | 0.00308408 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007244 | AATAAAAAAAAAAAA[A/C]AAAAAGAAAAGAAAA | 11169 |
rs758037928 | snp | G/T | 1.66241e-05 | 0.00288302 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981495 | AAAAGAATTTCAACA[G/T]ACTTTTTAAAAAGAG | 11169 |
rs758055902 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972451 | GGTGTGGTGGTGAAC[A/G]CCTGTAATCCCAGCT | 11169 |
rs758075723 | snp | C/G | 1.93407e-05 | 0.00310966 | missense | WDHD1 | GRCh38.p7 | 14:54966595 | AAATATAACTGAACG[C/G]CAAAATTGCTCCTAT | 11169 |
rs758078455 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990132 | GACCTATGACTTGAT[G/T]ACTACTGATAGCAAT | 11169 |
rs758089981 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008063 | ACTGAATTTATTCCC[C/T]TCATTTACAAAACTT | 11169 |
rs758112213 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958963 | ACATTCTACTCACCT[G/T]ACAGTAATTCATCAT | 11169 |
rs758129091 | snp | C/T | 1.68502e-05 | 0.00290255 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988980 | ATTTCAACAACTGTA[C/T]CTAACAGTTCAACAG | 11169 |
rs758147441 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54945965 | AAATTACTAGTATGA[C/T]CATAACCATTTGCCC | 11169 |
rs758160163 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | WDHD1 | GRCh38.p7 | 14:54989115 | AAAGTGTTTGATAAG[C/T]GTGTTGCATGGTGTA | 11169 |
rs758165325 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960228 | GCTGGAGTGCGGTGG[C/T]ATGATCTCACCTCAC | 11169 |
rs758192026 | snp | A/C/G | 3.67642e-05 | 0.00428731 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955731 | CTGCAATAACATCTA[A/C/G]TATAATTTTATATGT | 11169 |
rs758194323 | snp | A/G | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028153 | TGAAGAGGTTTCCCT[A/G]TTGTTTTTTTCAATC | 11169 |
rs758205489 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980165 | CCCTGTCTCTACAAA[A/T]AGTAGCTGGGTGTGG | 11169 |
rs758323545 | in-del | -/G/GG | 0.208893 | 0.248868 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963184 | AAGCTAATCCAAAAA[-/G/GG]GGGGGGGGGGGGGGA | 11169 |
rs758329771 | snp | G/T | 1.66299e-05 | 0.00288352 | missense | WDHD1 | GRCh38.p7 | 14:54955639 | TTTTCTTCTTTCACT[G/T]CCTCAGTTTTATTAG | 11169 |
rs758330373 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54981098 | CCTGGGCAACAGAGC[A/G]AGACTCTGTCTTCTA | 11169 |
rs758400444 | snp | A/C | 3.30551e-05 | 0.00406528 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000615 | TGCCATGCCAGACCA[A/C]AAATTGCATAACCTT | 11169 |
rs758404036 | snp | A/T | 5.20269e-05 | 0.00510007 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941734 | AAGATTTTTAGAAAA[A/T]AACAAATAAGAAGTA | 11169 |
rs758412166 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967176 | ATTTATGTAATTATA[C/T]AGTAATGAATATTCA | 11169 |
rs758453678 | snp | C/T | 1.70799e-05 | 0.00292227 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010286 | CTAACATTATTTCCT[C/T]TTCTGATGTCAAAGA | 11169 |
rs758467168 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55004297 | ATTTGGTTCTATTTA[A/T]CTCTTTAACAGGTAT | 11169 |
rs758491385 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54942884 | AAACACAATCACAGA[A/C]TTTGCCAAGTCTCTT | 11169 |
rs758526404 | snp | G/T | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941173 | TTAATGCACAAAGGT[G/T]TTAATACCTTGGCTT | 11169 |
rs758526993 | snp | G/T | 1.66693e-05 | 0.00288693 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962593 | TGTAAATGGGGAAAA[G/T]ATAGTCATCCTCAAT | 11169 |
rs758569604 | snp | A/C | | | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54991315 | CCTTTGGGATGTTAC[A/C]AGTGGTAGATTGTGA | 11169 |
rs758586031 | snp | C/T | 1.65241e-05 | 0.00287433 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55007346 | CACATCGTTGCATTT[C/T]TGTAGCAGTGGCCAA | 11169 |
rs758587161 | snp | C/T | 1.65627e-05 | 0.00287769 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962476 | ATTTCCTTGATATTA[C/T]AAATTTATAAATATT | 11169 |
rs758612574 | snp | C/T | 6.59348e-05 | 0.00574135 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967236 | TGTGTATCACAGGTG[C/T]TGTATTATCAAATTC | 11169 |
rs758627685 | in-del | -/T | 1.64874e-05 | 0.00287113 | frameshift-variant | WDHD1 | GRCh38.p7 | 14:54944333 | ACAATTATCCTTACC[-/T]TTCTTTCTTCAGTTG | 11169 |
rs758630200 | in-del | -/GA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54955916 | TTTTTTTTTTTTTTT[-/GA]GACGGAGTCTCACTC | 11169 |
rs758631928 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024187 | TTGTATATTTCTATC[A/T]CTAGCTCACATTTTT | 11169 |
rs758747635 | snp | A/G | 1.64789e-05 | 0.0028704 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54957121 | TGCAGTGGATTTCTT[A/G]GATGATTTGCCCATA | 11169 |
rs758749660 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026575 | AACAATAATCTAAAG[A/G]AATATGTGTGCCATT | 11169 |
rs758781353 | snp | C/T | 3.38421e-05 | 0.00411338 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013463 | ATCATTTCATATCAA[C/T]TGATATAACTGTTTT | 11169 |
rs758800696 | snp | A/C/G/T | 0.0013849 | 0.0262838 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963188 | CTAATCCAAAAAGGG[A/C/G/T]GGGGGGGGGGAGATC | 11169 |
rs758801459 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54999924 | TAATCATCCCTTCAA[C/T]TGACTTCTTTAACCT | 11169 |
rs758823127 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963357 | ATTAATTACAATTAA[C/T]GGTGGGTCAGTTTGG | 11169 |
rs758832389 | snp | A/T | 1.72824e-05 | 0.00293954 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55010452 | AACTGCAGTGACCAG[A/T]TTTCCACTCTAAAAG | 11169 |
rs758845102 | snp | C/T | 1.64906e-05 | 0.00287142 | missense | WDHD1 | GRCh38.p7 | 14:54987178 | AAAAGCTGTTCTCCA[C/T]GTCCTGCCATTGACA | 11169 |
rs758847861 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55023553 | GTATGTCCAGCATCA[C/T]TAGTGGCACTTCATA | 11169 |
rs758855892 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998375 | CCTCAGGTGATCCAC[C/T]GGCCTCGGCCTCCCA | 11169 |
rs758881243 | snp | A/C | 1.65877e-05 | 0.00287986 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:54995685 | GTCTTCATCATCCTC[A/C]TCATCATTTATAATC | 11169 |
rs758917896 | in-del | -/AAA | | | cds-indel, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939587 | GTCCCAATTCTCTGG[-/AAA]AAAAAAAAAGAACAC | 11169 |
rs758964884 | snp | C/T | 1.65943e-05 | 0.00288043 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984873 | TACCTAATGAGAAAA[C/T]GTAAATATAAATCAG | 11169 |
rs758994107 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003617 | TGCCCAGGCTGGAGA[G/T]AAGTAGTGCCATCTT | 11169 |
rs758994190 | snp | A/G | | | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54989075 | CAAAATAGCTTCGTG[A/G]GAAAGATCTGCTATT | 11169 |
rs759008045 | snp | A/C/G/T | 0.0130021 | 0.0796624 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963186 | AGCTAATCCAAAAAG[A/C/G/T]GGGGGGGGGGGGAGA | 11169 |
rs759095635 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54952790 | AGATACAGACCAATG[G/T]AACAGAACAGAGCCC | 11169 |
rs759097029 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975703 | TGACTTAAATTAATG[C/T]TTTTTTTTTTAAAGA | 11169 |
rs759100856 | snp | C/G | 1.65386e-05 | 0.00287559 | missense | WDHD1 | GRCh38.p7 | 14:54984843 | CTCCAAGGCACTGAT[C/G]CCCATCAAATCCTGT | 11169 |
rs759163289 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55022195 | CTGACTTCAGGCACA[A/C]AGCATCAGTGAAACC | 11169 |
rs759183586 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54949808 | TCTCGGCAGAAACTC[C/T]ATGAGCCAGAAGAGA | 11169 |
rs759204288 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019535 | CTACCCCCAATAAAC[C/T]AGATTTTAGTTATAA | 11169 |
rs759221684 | snp | C/T | 1.65919e-05 | 0.00288022 | missense | WDHD1 | GRCh38.p7 | 14:54995661 | AGGACGACCTGAAGC[C/T]ATCATGAGGTCTTCA | 11169 |
rs759256842 | snp | C/G | 3.2956e-05 | 0.00405918 | missense | WDHD1 | GRCh38.p7 | 14:54962740 | AAATGTATCTCACCA[C/G]GCTTATGTATTTCTG | 11169 |
rs759271733 | snp | A/G | 1.69086e-05 | 0.00290758 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957246 | GTATGTTTAAAGAAG[A/G]AAAATAAAATCCCAA | 11169 |
rs759306697 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996612 | CTCAAAATAAATAAA[G/T]TTTTAGATCATTTCA | 11169 |
rs759310504 | in-del | -/GAG | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972665 | TGAGTTGTCAAAAAA[-/GAG]AAAAAAATCAGGCAT | 11169 |
rs759324586 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54945849 | TGGCCCAGAGTCTCT[C/T]ATGTTTAACCCAGCA | 11169 |
rs759342111 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010714 | TTACTTCTGGTAAGA[A/G]AAATGTTTGAATAGT | 11169 |
rs759356441 | snp | A/C | 6.68159e-05 | 0.00577957 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991208 | AGTGTAGATCCAAGT[A/C]TTACCATGAATCTGT | 11169 |
rs759379364 | snp | A/G | 9.92507e-05 | 0.00704383 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002065 | TGCTCCTTATAGCCC[A/G]CTGAAAGTGTCACTT | 11169 |
rs759389211 | in-del | -/CTA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54973265 | GATACTAAGTAGAAG[-/CTA]CTAGACCCTAGGGTT | 11169 |
rs759394480 | snp | A/G | 9.89054e-05 | 0.00703157 | missense | WDHD1 | GRCh38.p7 | 14:54957159 | AAATATTAGTTGAAC[A/G]TGCTGAATTCATTGA | 11169 |
rs759429081 | snp | C/T | 3.45369e-05 | 0.00415539 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013436 | ACTCAAGCATAAAAA[C/T]CACATGCCAGTATCA | 11169 |
rs759437092 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985502 | AGAGATGAGGTTGGA[C/G]AGGCAGGCAAAGGTC | 11169 |
rs759451789 | snp | A/C/G/T | 0.00209572 | 0.0323087 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963192 | TCCAAAAAGGGGGGG[A/C/G/T]GGGGGGAGATCAAAT | 11169 |
rs759483028 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948552 | GGAGTCCTGCCTGCC[A/T]CTGTGGACTCCACCT | 11169 |
rs759490382 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55006955 | AATCATGCCAGGCAC[A/G]GTGGCTCACGCCTGT | 11169 |
rs759503748 | snp | A/G | 1.64846e-05 | 0.0028709 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55013546 | GGATCATCATCATCC[A/G]AGTCTTCCCAAATCC | 11169 |
rs759510212 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54983892 | ATTTCATCGAAGATA[C/T]CTCAAATATTATCAT | 11169 |
rs759532090 | snp | A/G | 1.65154e-05 | 0.00287358 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000976 | CCACAGGGAGACCAG[A/G]TTACTATATTGAGGG | 11169 |
rs759548126 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020555 | TACCTATATTTACTC[C/G]TTCCCTAGGTGACTT | 11169 |
rs759553388 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54959781 | AAGATACCCTGTATC[C/T]GCACCCCCCCCACCA | 11169 |
rs759602266 | in-del | -/AA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019780 | AGGCTGAGGAGAGAG[-/AA]TCACTTGAACCCAGG | 11169 |
rs759612233 | snp | A/T | 5.01308e-05 | 0.00500628 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000468 | ATGATCACAGAAACA[A/T]TTTGAAGAAACTGTT | 11169 |
rs759619331 | snp | A/G | 3.29886e-05 | 0.00406118 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008690 | TGTTGGCTGCTATCC[A/G]TCACATCCACAATTT | 11169 |
rs759645684 | snp | A/G | 1.73561e-05 | 0.00294581 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967410 | CTGTTAGTAAAGAAA[A/G]GTTCCATCATAAAAA | 11169 |
rs759747928 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | WDHD1 | GRCh38.p7 | 14:54981597 | TGATCAGATTTTCCT[C/T]TGCAGTGCTCTCTTG | 11169 |
rs759771810 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003114 | ATAAAAACTTTATTT[A/T]AAAAAATTTTTAAAT | 11169 |
rs759782184 | snp | C/T | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028897 | GATGACACCTACCTC[C/T]GTCGCATTGTTAGAG | 11169 |
rs759787600 | snp | A/G | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027945 | CATGCAATATCTGCT[A/G]AAGTCTTGGCCACTA | 11169 |
rs759798883 | snp | C/T | 3.29538e-05 | 0.00405904 | missense | WDHD1 | GRCh38.p7 | 14:54991281 | GCCGGGGAGTTGGCA[C/T]GGGTCCATCATAAAA | 11169 |
rs759809311 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54946532 | GCTTTGTCGCCCAGG[C/T]TGGAGTGCAGTGGTA | 11169 |
rs759845930 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54982308 | GCCACCGCGCCCGGC[C/T]GATAATAATTTTAAA | 11169 |
rs759853959 | snp | G/T | 1.64728e-05 | 0.00286987 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026708 | TTTCTCAAAGAACCT[G/T]ACCTCCCAGAATCAT | 11169 |
rs759882202 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980544 | GGACCAGGTACGGTG[C/G]CTCATGCCTGTACTT | 11169 |
rs759910496 | in-del | -/T | 8.31995e-05 | 0.00644925 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981490 | CATAAAAAGAATTTC[-/T]AACATACTTTTTAAA | 11169 |
rs759941491 | snp | C/G | 6.91443e-05 | 0.0058794 | missense | WDHD1 | GRCh38.p7 | 14:54966558 | CATAACCATTTTTAG[C/G]TAAATAATCAAGGTG | 11169 |
rs760001554 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002668 | TGGAGTGCAGTGGTG[G/T]GATCACAGCTTACTG | 11169 |
rs760002961 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54944528 | AGTTTAAAGTGCCTC[A/G]TGATTTTAAGTTAGT | 11169 |
rs760006892 | snp | C/T | 0.00028166 | 0.0118638 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54966475 | ATTTATTTTACTCAC[C/T]GCAAGCATTTTCATT | 11169 |
rs760033927 | snp | A/C | 1.78439e-05 | 0.00298691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963219 | AAATAACATCAAGTA[A/C]AACTTTTTAAAGATA | 11169 |
rs760057118 | snp | C/G | 4.94246e-05 | 0.0049709 | missense | WDHD1 | GRCh38.p7 | 14:54987296 | CCCATCCTTGACCGA[C/G]ACATATGGCTTCAAT | 11169 |
rs760083329 | snp | A/C | 0.000471921 | 0.0153537 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008767 | ATGCTAACACAAAGG[A/C]CTCTCCTAAAAGCTA | 11169 |
rs760086043 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016150 | AAGCAATCTTCTAAA[G/T]AGCTTTTAGAGTAGT | 11169 |
rs760109967 | snp | A/G | 1.65075e-05 | 0.00287289 | missense | WDHD1 | GRCh38.p7 | 14:54957183 | TCATTGACATGGCTG[A/G]TTCTTTGGAACTGGC | 11169 |
rs760112437 | snp | A/T | 1.66424e-05 | 0.0028846 | missense | WDHD1 | GRCh38.p7 | 14:54955589 | TGTTTTGAGGAGGAC[A/T]TATAGCTGGGGTTTC | 11169 |
rs760182052 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54995584 | CAGGGTAATCACATG[A/C]ACAAAGTCAAATTCT | 11169 |
rs760190763 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954948 | TGGTCAGGCTGGTCT[C/T]GAACTCCCATCCTCA | 11169 |
rs760229773 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54943493 | TTGACCTCCTGGGCT[C/T]AAGTAAGTGATCTTC | 11169 |
rs760242285 | snp | A/T | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012185 | CTTACATTTAATGTA[A/T]GTTGGTCATTTACAT | 11169 |
rs760265544 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54978840 | CCAACAAAACAGAAG[C/T]CAAAAACAGAAGATA | 11169 |
rs760267202 | snp | C/T | | | missense | WDHD1 | GRCh38.p7 | 14:54962994 | TCTTCTTCTTCTTCC[C/T]CTTCCACCTGGGTTG | 11169 |
rs760292606 | snp | A/G/T | 6.99876e-05 | 0.00591522 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963193 | CCAAAAAGGGGGGGG[A/G/T]GGGGGAGATCAAATA | 11169 |
rs760341113 | in-del | -/A | 0.00119346 | 0.0243989 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941449 | TATTCAAAGATGAGT[-/A]AAAAAAAAATCCATT | 11169 |
rs760347733 | snp | C/T | 3.29859e-05 | 0.00406102 | missense | WDHD1 | GRCh38.p7 | 14:54987169 | TAAACAATGAAAAGC[C/T]GTTCTCCATGTCCTG | 11169 |
rs760390252 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54964451 | CGAGACCATACTGGC[C/T]AACACGGTGAAACAC | 11169 |
rs760402958 | snp | A/C/G | 3.36017e-05 | 0.00409877 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54944461 | CCACATCTGGAACCC[A/C/G]GTCTTTGGCCTAAAA | 11169 |
rs760447412 | snp | A/T | 1.66829e-05 | 0.00288811 | missense | WDHD1 | GRCh38.p7 | 14:54941537 | TCTGATTTGTAGAAA[A/T]ATCTAAAGGTTTCTG | 11169 |
rs760502630 | snp | G/T | 1.69052e-05 | 0.00290728 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957658 | AAAAAAGAAACCCTT[G/T]CTTAATAATGGTAGA | 11169 |
rs760504052 | in-del | -/A | 1.64728e-05 | 0.00286987 | intron-variant, splice-donor-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026708 | TTCTCAAAGAACCTT[-/A]ACCTCCCAGAATCAT | 11169 |
rs760509829 | snp | C/T | 3.29522e-05 | 0.00405894 | missense | WDHD1 | GRCh38.p7 | 14:54981645 | CACGTATTACCAAGT[C/T]CTCTGTTAAGCATTC | 11169 |
rs760528441 | snp | A/G | 0.000115857 | 0.00761018 | missense | WDHD1 | GRCh38.p7 | 14:54991226 | ACCATGAATCTGTGA[A/G]TGAGATGCAACGGTG | 11169 |
rs760529367 | snp | C/G | 1.64751e-05 | 0.00287007 | missense | WDHD1 | GRCh38.p7 | 14:54991305 | CATAAAATGGCCTTT[C/G]GGATGTTACAAGTGG | 11169 |
rs760550603 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000566 | CCCTAGATTTCCTTC[C/T]GCATCAGTATACGAT | 11169 |
rs760567365 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54971615 | CATTTGCAGATCCTG[A/C]GGTGGATCACTGAGC | 11169 |
rs760584412 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988212 | CGGGTGACTAGTACA[-/T]TTTTTTGGTTTGTTT | 11169 |
rs760594634 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019269 | ATTTAGATCATATGT[C/T]TAATGTTTGGATAAT | 11169 |
rs760644021 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54970493 | ACTACAAAACACTGT[C/T]GAAAGAAATCACAGA | 11169 |
rs760653685 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026674 | GATAAATGTTTTAAC[A/G]TTTGCACCTAAAACG | 11169 |
rs760685400 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54957291 | CTTGAAATTTCTGTT[-/A]AGTTTGTATTGCCAT | 11169 |
rs760694666 | snp | C/G | 4.00593e-05 | 0.00447527 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000666 | ATTAAAAAGTAGGTT[C/G]TAAAAATACTGTCAA | 11169 |
rs760696408 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54994870 | ACTATATATTGGATA[C/G]CACAAATCTACAGAT | 11169 |
rs760696833 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55009065 | CTCCCAAAGTGCTGG[C/G]ATTACAGGCATGAGC | 11169 |
rs760700498 | snp | A/C | 1.68267e-05 | 0.00290053 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987416 | CAAGACAGAAACAAT[A/C]AAACTTTCATATGAT | 11169 |
rs760749229 | snp | A/T | 1.64808e-05 | 0.00287057 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955710 | CTATAAAAACAAACA[A/T]GAATACTGCAATAAC | 11169 |
rs760749872 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996174 | CTGTCATATTGTAAG[A/C]CAGTCTCTCATTTAC | 11169 |
rs760788050 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54961461 | GCTTTTCACACCACC[A/C]TTTTGCAGCCTTCAG | 11169 |
rs760795036 | snp | C/G | 1.72359e-05 | 0.00293558 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010262 | AACAAATAAACAAGG[C/G]CTTTTGTTCTAACAT | 11169 |
rs760883001 | snp | C/T | 6.63053e-05 | 0.00575745 | missense | WDHD1 | GRCh38.p7 | 14:54962546 | TTTTGGAAAACGAGT[C/T]CTGTCCTACAGATTA | 11169 |
rs760924063 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54981518 | AAAAAGAGTCAACTT[G/T]AGACTTCTTTTAATA | 11169 |
rs760941255 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54982418 | ACAAAGTGATCTTTA[C/T]GAAATTTATCTTTAG | 11169 |
rs760959220 | snp | A/C | 1.67329e-05 | 0.00289243 | stop-gained | WDHD1 | GRCh38.p7 | 14:54963019 | GGGTTGCTGTCAATT[A/C]GGCTGCCTTCTCTAC | 11169 |
rs760973216 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54968708 | TTCCACAGAAATACA[A/G]AAGATCCTCAGAGAC | 11169 |
rs760997425 | snp | C/T | 1.65089e-05 | 0.00287301 | utr-variant-5-prime, synonymous-codon | WDHD1 | GRCh38.p7 | 14:55008704 | CATCACATCCACAAT[C/T]TTGACTAGAAAATCA | 11169 |
rs761006505 | snp | C/T | 2.43336e-05 | 0.00348801 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966651 | CAACTATCACCTTAA[C/T]ATGAGGCAAGCGTTA | 11169 |
rs761010386 | in-del | -/TGGAAAATTAC | 1.68354e-05 | 0.00290128 | frameshift-variant, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000633 | TTGCATAACCTTTCT[-/TGGAAAATTAC]CATGTTTCACCCTAA | 11169 |
rs761036473 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | WDHD1 | GRCh38.p7 | 14:54967300 | TTTGTCCTTTCTCTG[C/T]TGCAATCTGACAGTA | 11169 |
rs761044562 | in-del | -/AAAAG | 0.000164145 | 0.00905789 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007246 | TAAAAAAAAAAAAAA[-/AAAAG]AAAAGAAAAGAAAAA | 11169 |
rs761080040 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990680 | ATATATTTAATGTGC[A/G]CTGTATCATACCTTG | 11169 |
rs761110598 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54953243 | GACAAAGGGCTAATA[C/T]CCAGAATCTACAAAG | 11169 |
rs761139664 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54955072 | ATAAAATAAGCTACA[A/G]AAGCTATTGTTAAGT | 11169 |
rs761142283 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | WDHD1 | GRCh38.p7 | 14:54989087 | GTGGGAAAGATCTGC[C/T]ATTGTATAATTCAAA | 11169 |
rs761143902 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55017529 | TCGTATTTTCATAGA[G/T]ATGGGGTTTCACCAT | 11169 |
rs761150082 | snp | C/G | 1.6554e-05 | 0.00287693 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55007293 | ACCTTCCCACTTTTT[C/G]GCTGCCAAGCAAGTC | 11169 |
rs761167775 | snp | A/G | 1.69925e-05 | 0.00291478 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957673 | GCTTAATAATGGTAG[A/G]AAATAGATGACTTCT | 11169 |
rs761170010 | in-del | -/TCCATGATAGT | 1.64876e-05 | 0.00287116 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962693 | ATGGGAAAAGCCACA[-/TCCATGATAGT]TCTCATGATTTATGG | 11169 |
rs761200766 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54956648 | CTCTGTCTCAAAAAA[G/T]ACAGGGGGAGCAGGA | 11169 |
rs761202707 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54999085 | GTCTTTTCTCTTAGA[A/C]AAATTCCCCAAAGAT | 11169 |
rs761251367 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55012999 | AACCTTTCTTGGAAG[C/T]ATTATTTTCCTGCAT | 11169 |
rs761267041 | snp | A/T | 1.64743e-05 | 0.00287 | missense | WDHD1 | GRCh38.p7 | 14:54991311 | ATGGCCTTTGGGATG[A/T]TACAAGTGGTAGATT | 11169 |
rs761268702 | snp | A/C | 4.98931e-05 | 0.00499441 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007274 | AGAAAAATAAGAATC[A/C]CTTACCTTCCCACTT | 11169 |
rs761291977 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54991718 | TTTTTTTTAAAGTTC[C/T]GTGTGCTAAAATGAG | 11169 |
rs761304947 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965849 | TAGTCCCAGCTACTC[A/G]GAAGGTTGAGGCAGG | 11169 |
rs761319303 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54942175 | AGACTAGAGTGAACC[C/T]GGGAGGTGGAGCCTG | 11169 |
rs761319962 | snp | A/T | 0.00720727 | 0.0595961 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007233 | ACTCCATCTCTAATA[A/T]AAAAAAAAAAAAAAA | 11169 |
rs761368033 | snp | C/G | | | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000962 | CAGCTAAATATTGCC[C/G]ACAGGGAGACCAGGT | 11169 |
rs761385687 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54949231 | GAAGTTCGAACGCAT[C/T]GCAAAGGAGCTAAAA | 11169 |
rs761400331 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54999745 | GCATGAAACTACAGG[C/T]ACACACCACCACACT | 11169 |
rs761400569 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975369 | TTTTTTTTTTTTGAG[A/G]CAGAGTTTCCCTCTG | 11169 |
rs761449456 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996901 | GGTTCAAGCGATTCT[C/T]CTGCCTCAGTCTCCC | 11169 |
rs761455247 | in-del | -/C | 0.000412749 | 0.0143598 | frameshift-variant | WDHD1 | GRCh38.p7 | 14:54941591 | CTTTTGCTTTTTCTT[-/C]CTGGTTTTCTGTTTC | 11169 |
rs761473476 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026440 | GATCTGACAAAATTA[A/G]TAATGTAAGATGCAG | 11169 |
rs761473569 | snp | C/T | 3.33128e-05 | 0.00408109 | missense | WDHD1 | GRCh38.p7 | 14:54966530 | GCTTGATTTTTAGTG[C/T]TCTCTTCATATTCAT | 11169 |
rs761534076 | snp | A/T | 0.000188377 | 0.00970325 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987395 | GAAGCTTGCTAAAAA[A/T]TAAAACAAGACAGAA | 11169 |
rs761534377 | snp | G/T | 1.69103e-05 | 0.00290773 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966444 | GAAAAGCATTTAACT[G/T]TAACGTTTTCAGTAT | 11169 |
rs761576285 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002433 | ACACCACTGTGCCAG[A/G]CGCAAATCTGTATTT | 11169 |
rs761607935 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54986752 | TCTTAGCATAGTGAC[C/G]GGGACTGAAGAAAGA | 11169 |
rs761619725 | snp | A/G | 9.88663e-05 | 0.00703018 | stop-gained | WDHD1 | GRCh38.p7 | 14:54981661 | CTCTGTTAAGCATTC[A/G]AACAATTCCTTCTGA | 11169 |
rs761620792 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55013721 | GACTAGCCTGGATAA[C/T]ACAGAGAGACCTAGT | 11169 |
rs761650326 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55021897 | TTCTATAACAATGAT[C/G]GCATCTTCAATGGTA | 11169 |
rs761660247 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016726 | CTTAATTGATTTAAA[A/C]CTACATAGCTGCATG | 11169 |
rs761696556 | snp | G/T | 3.43348e-05 | 0.00414321 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010277 | CCTTTTGTTCTAACA[G/T]TATTTCCTTTTCTGA | 11169 |
rs761717191 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020731 | CAACCCCTAAACAGT[A/C]AAAAATCCACATAGA | 11169 |
rs761723101 | snp | C/T | 1.81823e-05 | 0.0030151 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984694 | ACACTTTATATTATA[C/T]TTGTTTTTTTTAAAC | 11169 |
rs761732250 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988627 | TCAAATTGTAAATAG[C/T]AGTTATATCTGAGAG | 11169 |
rs761736330 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54971914 | ATACAAGGCTGGGAA[C/T]GGTGGGTCACACCCA | 11169 |
rs761787791 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54973906 | AGCAGAGCACCAATT[C/T]GCATTTTTTTATCCT | 11169 |
rs761814688 | in-del | -/AC | 1.6759e-05 | 0.00289469 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001005 | GGTCTGTAAAGAAAA[-/AC]AGTTAATAAATAATG | 11169 |
rs761829030 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005871 | AGCCTTCAGATGAGA[C/T]ATTTTATTTTTAAGG | 11169 |
rs761837413 | snp | G/T | 2.62898e-05 | 0.0036255 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966657 | TCACCTTAATATGAG[G/T]CAAGCGTTAAATATT | 11169 |
rs761890357 | snp | A/G | 3.29489e-05 | 0.00405874 | missense | WDHD1 | GRCh38.p7 | 14:54989100 | GCTATTGTATAATTC[A/G]AAGTGTTTGATAAGT | 11169 |
rs761909342 | snp | C/T | 3.39807e-05 | 0.00412179 | missense | WDHD1 | GRCh38.p7 | 14:54989212 | CAATAGAGTTCCACA[C/T]CTACAAACAGGTAAG | 11169 |
rs761916745 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54983770 | GTGATCCTCCTGCCT[C/T]GGCCTCCCAGAGTGC | 11169 |
rs761962898 | snp | A/T | 0.000131855 | 0.0081185 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963177 | TTACAAGAAAGCTAA[A/T]CCAAAAAGGGGGGGG | 11169 |
rs761963520 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948390 | TCTTAGCAAACGGCA[C/T]ACCAGGAGATTATAT | 11169 |
rs761968590 | snp | A/C | 1.64876e-05 | 0.00287116 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000948 | ATTAATACTACCTGC[A/C]GCTAAATATTGCCCA | 11169 |
rs762020548 | snp | G/T | 1.66181e-05 | 0.00288249 | missense | WDHD1 | GRCh38.p7 | 14:54957042 | ACAGTACCTGCTTAG[G/T]CTTCGGCTTTGGAAT | 11169 |
rs762024112 | snp | A/G | 1.64849e-05 | 0.00287092 | missense | WDHD1 | GRCh38.p7 | 14:54944354 | TCTTCAGTTGACAAT[A/G]CTCTAAATCGAATCA | 11169 |
rs762062825 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958255 | TCTCAGCCTCCCGAA[C/T]TGCTGGGATTACAGG | 11169 |
rs762089468 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54991890 | TTGGCAAACATTTTC[C/T]TGTAAATGAATGAAG | 11169 |
rs762091182 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54970268 | CTATATTACTCTATA[C/T]ATAGAATTGCTAAAG | 11169 |
rs762103451 | snp | C/T | 1.6537e-05 | 0.00287545 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962870 | TAAGAGAAAATAATA[C/T]TATTCAATAAAGAGC | 11169 |
rs762134175 | snp | C/T | 0.000154264 | 0.00878113 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54941496 | TTTCTTCCTTTACTC[C/T]TGCTTAAATGCAAAA | 11169 |
rs762147435 | snp | A/C/G | 7.23961e-05 | 0.00601611 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955724 | ATGAATACTGCAATA[A/C/G]CATCTAGTATAATTT | 11169 |
rs762150872 | snp | A/C | 1.64757e-05 | 0.00287012 | missense | WDHD1 | GRCh38.p7 | 14:54962766 | TTCTGGTTTTTCTTC[A/C]TCATCAGCTTCTCCA | 11169 |
rs762185719 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54943663 | TTGGCCTCCCAAAGT[C/G]CTAGGATTACAGGCT | 11169 |
rs762245654 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54942558 | CCAAGCCCCAACTCC[G/T]ACTCCAACCCCTGGC | 11169 |
rs762269977 | snp | C/T | 3.45578e-05 | 0.00415665 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008410 | TAGTCATAGCCATAA[C/T]ACTACATGGAAAGTG | 11169 |
rs762269992 | snp | C/G | 1.65842e-05 | 0.00287955 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:54995672 | AAGCCATCATGAGGT[C/G]TTCATCATCCTCATC | 11169 |
rs762276040 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55006634 | ATCTTTCTGTTGTCT[A/G]ACTGTATCAGTTAGT | 11169 |
rs762281286 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | WDHD1 | GRCh38.p7 | 14:54967314 | GTTGCAATCTGACAG[C/T]AAGGAAGCTTAAAGG | 11169 |
rs762295617 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026446 | ACAAAATTAATAATG[C/T]AAGATGCAGGGAAGG | 11169 |
rs762384174 | snp | A/C | 3.40849e-05 | 0.00412811 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007400 | AAAAAAAGAAAATTT[A/C]TTTCCTTTATGAAAA | 11169 |
rs762387671 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55014476 | GTATCTTCCTTGTCC[A/G]CCATTGTATCCCTAG | 11169 |
rs762392646 | snp | A/C | 2.07656e-05 | 0.00322217 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008285 | TTACAGAAATGGGCA[A/C]AAAACTTTAAATTTA | 11169 |
rs762403948 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55001157 | TTATTTCTAATTATA[C/T]TCGATACAAGACAAA | 11169 |
rs762410003 | snp | C/T | 1.66549e-05 | 0.00288568 | missense | WDHD1 | GRCh38.p7 | 14:54995645 | TGTGACTTCGCTGTC[C/T]AGGACGACCTGAAGC | 11169 |
rs762412722 | in-del | -/GA | 3.65544e-05 | 0.00427503 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963198 | AAGGGGGGGGGGGGG[-/GA]GATCAAATAACATCA | 11169 |
rs762423552 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54979115 | TCAAAGACTTTTTAT[C/G]CTCCTTTAGGTGCCA | 11169 |
rs762459039 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002578 | CCCAAAAAATGGAGA[A/G]CTTGTAATTACTAGT | 11169 |
rs762465074 | snp | C/T | 1.66927e-05 | 0.00288895 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991434 | TAATTAAGGGAATCA[C/T]GAATACCAATGATTT | 11169 |
rs762500276 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020835 | ACACATATTTTGTCT[A/T]TGTATTATATACTGT | 11169 |
rs762502534 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988799 | TTGCATTACTAACTA[C/T]GCCATGTCATTTTGC | 11169 |
rs762569265 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005814 | CTCCTAGACATCTTA[C/T]TGGTACTTTATTTTA | 11169 |
rs762595451 | snp | C/T | 1.65703e-05 | 0.00287834 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54941574 | AGACAAATTCAGGTT[C/T]TCTTTTGCTTTTTCT | 11169 |
rs762622925 | snp | A/G | 1.6569e-05 | 0.00287824 | missense | WDHD1 | GRCh38.p7 | 14:54962536 | GAATTTGTACTTTTG[A/G]AAAACGAGTTCTGTC | 11169 |
rs762652327 | snp | A/T | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940697 | TGTTGATGCTGATAA[A/T]CAGAGTATCCCACCA | 11169 |
rs762664927 | snp | A/C | 1.66065e-05 | 0.00288149 | splice-donor-variant | WDHD1 | GRCh38.p7 | 14:55007278 | AAATAAGAATCACTT[A/C]CCTTCCCACTTTTTG | 11169 |
rs762672299 | snp | C/T | 2.26657e-05 | 0.00336635 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966636 | AAAATTGCTTAAGGC[C/T]AACTATCACCTTAAT | 11169 |
rs762709903 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990258 | TAAAAAGGCAAAATC[C/T]TCAGAATGGAAAACA | 11169 |
rs762746517 | snp | C/T | 1.65157e-05 | 0.0028736 | missense | WDHD1 | GRCh38.p7 | 14:54957057 | GCTTCGGCTTTGGAA[C/T]CAGAGGCTTTATAAT | 11169 |
rs762788842 | snp | C/G | 3.30164e-05 | 0.00406289 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000972 | TTGCCCACAGGGAGA[C/G]CAGGTTACTATATTG | 11169 |
rs762822740 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55009406 | CCAAAATATTCTGAC[C/T]GTACAGCCCAAGTTC | 11169 |
rs762850002 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997559 | CAACCATTCCATTTA[C/T]AGTCCTAAAAGTTTG | 11169 |
rs762854516 | snp | C/T | 1.65247e-05 | 0.00287438 | missense | WDHD1 | GRCh38.p7 | 14:54984831 | CTAGCAGTTGAACTC[C/T]AAGGCACTGATCCCC | 11169 |
rs762865916 | snp | A/G | 3.11832e-05 | 0.0039485 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963181 | AAGAAAGCTAATCCA[A/G]AAAGGGGGGGGGGGG | 11169 |
rs762867163 | in-del | -/AAAT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54942255 | TCCGTCTCAAAAAAT[-/AAAT]AAATAAATAAATAAA | 11169 |
rs762872279 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55017789 | TCAAATTTTCAGATT[G/T]TATTTATATCTAGAA | 11169 |
rs762873725 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996345 | CAGCATGGTGGCTCA[C/T]ACCTGTAATCTCAGC | 11169 |
rs762930866 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54982513 | AGCAATTCTTACCTC[C/G]TAAAACAGGGAAGCA | 11169 |
rs762950965 | snp | C/T | 0.000131796 | 0.00811668 | missense | WDHD1 | GRCh38.p7 | 14:54962779 | TCATCATCAGCTTCT[C/T]CACTGTCCTCAGCAT | 11169 |
rs762951108 | in-del | -/G | 3.2994e-05 | 0.00406152 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010496 | GAAACATTAGCAAAA[-/G]CAAATCCAAATGACT | 11169 |
rs762974745 | snp | A/T | 1.64814e-05 | 0.00287061 | utr-variant-5-prime, synonymous-codon | WDHD1 | GRCh38.p7 | 14:55010395 | CAATATACCATCTGG[A/T]ACTCCTTCAGGAAAT | 11169 |
rs762992891 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965389 | TGGCCACTGGTCACA[A/G]ATAAATTTTCATCAC | 11169 |
rs762999877 | snp | A/G | 1.64762e-05 | 0.00287016 | missense | WDHD1 | GRCh38.p7 | 14:54967329 | TAAGGAAGCTTAAAG[A/G]ATAATATAGCAACAG | 11169 |
rs763002038 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967530 | CATATATAACAAATA[C/T]CTCTTTTTAAAAAAG | 11169 |
rs763021263 | snp | C/T | 1.65512e-05 | 0.00287669 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54967379 | GGGAAACCGAGAACC[C/T]TTACAAGGAATGCAC | 11169 |
rs763040959 | in-del | -/T | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028999 | GGTGGGTATTTAGTG[-/T]TTTTTTGTTTAAAGT | 11169 |
rs763051454 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54970421 | TACAATAGTCATACA[C/T]GTACATAAAATACCT | 11169 |
rs763102946 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54971524 | GGATATATCTAACCA[A/T]GGAGGTGAAAGATCT | 11169 |
rs763108281 | snp | A/C/G | 4.94526e-05 | 0.00497235 | stop-gained, missense | WDHD1 | GRCh38.p7 | 14:54957155 | TCTAAAATATTAGTT[A/C/G]AACGTGCTGAATTCA | 11169 |
rs763165100 | in-del | -/TT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54999065 | TTAAGAAACTCTCTC[-/TT]TACGTCTTTTCTCTT | 11169 |
rs763189690 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026552 | AACTACCATGACGGC[C/T]CGAATCAAACAATAA | 11169 |
rs763208229 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54945466 | GAGGCTCAGAGATGT[C/G]AAATAACCTATCCCA | 11169 |
rs763226330 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54959512 | TTGTGCCTGTAATCC[A/G]AAAATTTTGGGAGGC | 11169 |
rs763242392 | snp | A/G | 4.26685e-05 | 0.0046187 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995862 | GTGAATGATTTAGAA[A/G]AACTCAATTACTAAA | 11169 |
rs763272917 | snp | C/T | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027700 | ACCTTGTCGCTTCTG[C/T]AGAGATAAAGAAGGA | 11169 |
rs763344565 | snp | C/T | 1.69986e-05 | 0.0029153 | splice-acceptor-variant | WDHD1 | GRCh38.p7 | 14:54944471 | AACCCGGTCTTTGGC[C/T]TAAAATCACAATTAT | 11169 |
rs763444191 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55013285 | AGATTAAAAAAAGGT[A/G]TATCTATATTCAAAA | 11169 |
rs763482681 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010854 | AATGGCCACTGCCCT[A/G]TGTTTCCACAACAAA | 11169 |
rs763530127 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54977618 | AACTGTTCAACATTT[A/G]AAAAAGGACTCTTGT | 11169 |
rs763541385 | in-del | -/TT | 1.66095e-05 | 0.00288175 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962941 | ATTCAAACAACTAAA[-/TT]ATTTCTTACCCAGCA | 11169 |
rs763541804 | snp | A/C | 1.65132e-05 | 0.00287339 | stop-gained | WDHD1 | GRCh38.p7 | 14:54957186 | TTGACATGGCTGGTT[A/C]TTTGGAACTGGCTGA | 11169 |
rs763629174 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026349 | GCAAAAAGGGAAATA[A/G]CATCACTAAAGGCAT | 11169 |
rs763656267 | snp | A/G | 1.6729e-05 | 0.00289209 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54963016 | CCTGGGTTGCTGTCA[A/G]TTCGGCTGCCTTCTC | 11169 |
rs763684749 | snp | A/T | 1.6492e-05 | 0.00287154 | utr-variant-5-prime, synonymous-codon | WDHD1 | GRCh38.p7 | 14:55013569 | CCAAATCCTCACATC[A/T]CCATCACTTCCACAA | 11169 |
rs763719232 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012285 | ATCTACCTTAAATGC[A/G]CCTGGGTTTGGAAAA | 11169 |
rs763730019 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972485 | CGGGAGGGTAAAGCA[C/T]GAGAATCTCTTGAAC | 11169 |
rs763783160 | in-del | -/T | 1.65703e-05 | 0.00287834 | frameshift-variant | WDHD1 | GRCh38.p7 | 14:54941574 | GACAAATTCAGGTTC[-/T]TCTTTTGCTTTTTCT | 11169 |
rs763797885 | in-del | -/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975538 | TTTTTAGTAGAGACA[-/G]GGTTTCACCATGTTG | 11169 |
rs763813410 | in-del | -/A | 0.00125562 | 0.0250246 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007384 | ACATGTCTAATTGGT[-/A]AAAAAAAGAAAATTT | 11169 |
rs763821390 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | WDHD1 | GRCh38.p7 | 14:54981649 | TATTACCAAGTCCTC[C/T]GTTAAGCATTCGAAC | 11169 |
rs763866505 | snp | A/G | 6.58957e-05 | 0.00573964 | missense | WDHD1 | GRCh38.p7 | 14:54991307 | TAAAATGGCCTTTGG[A/G]ATGTTACAAGTGGTA | 11169 |
rs763876876 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55018162 | TCCTACTGTAATAAT[C/G]GTATTATTATTATTA | 11169 |
rs763902704 | snp | A/G | 1.64931e-05 | 0.00287163 | stop-gained | WDHD1 | GRCh38.p7 | 14:54987170 | AAACAATGAAAAGCT[A/G]TTCTCCATGTCCTGC | 11169 |
rs763911495 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958642 | AGCTGACTGTTCCTT[A/C]CTTCTTGATACTTTG | 11169 |
rs763922952 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985712 | GTTAGGAGGCTACTA[C/T]GACAGTCCAAGAGAT | 11169 |
rs763964946 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019393 | TTCAAAACTATTGGC[A/C]TAAGGGTGTCAATGT | 11169 |
rs764020311 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55006978 | ACGCCTGTAATACTA[A/G]CATTTTGTGAGGCTG | 11169 |
rs764058184 | snp | C/T | 1.76855e-05 | 0.00297362 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967418 | AAAGAAAAGTTCCAT[C/T]ATAAAAATTTACTAA | 11169 |
rs764073413 | snp | A/G | 1.74039e-05 | 0.00294985 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002237 | CATTAAATTGAATTT[A/G]AAGAAGGAAAAAGGC | 11169 |
rs764088623 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55013382 | AATATTATTTCATGA[C/G]ATAAACAAAGGTATA | 11169 |
rs764132001 | in-del | -/A | 1.64727e-05 | 0.00286986 | intron-variant, frameshift-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026724 | CCTCCCAGAATCATC[-/A]AAAACAGACCTCCGT | 11169 |
rs764139403 | snp | A/C | 3.39184e-05 | 0.00411802 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987419 | GACAGAAACAATCAA[A/C]CTTTCATATGATATT | 11169 |
rs764142038 | snp | C/T | 1.94312e-05 | 0.00311693 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957565 | AATGTATTTAAATAA[C/T]ATAAAACATCACTTG | 11169 |
rs764150751 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54982448 | GTACTCTTCTTCCTC[C/T]CTCTTCTTTTTGTTG | 11169 |
rs764179070 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980982 | CAGGCGTGATGGTGC[A/G]CACCTATAATCCCAG | 11169 |
rs764183315 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54946859 | GACCAGCCTGGCCAA[A/C]GTGGCAAACTCCATC | 11169 |
rs764189794 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54979661 | GCTGCTTTGTTTAAA[A/T]ATTCAATTTATTTAA | 11169 |
rs764202240 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967830 | TTTGCCATGTTGCCC[A/G]GGCTGGACTCGAACT | 11169 |
rs764261527 | in-del | -/CAAT | 3.34052e-05 | 0.00408674 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987412 | AAAACAAGACAGAAA[-/CAAT]CAAACTTTCATATGA | 11169 |
rs764265883 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005319 | CACTGGGATTAGTCA[C/T]CATAAGAAGCTGTGG | 11169 |
rs764272507 | snp | C/T | 3.59054e-05 | 0.00423691 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955719 | CAAACATGAATACTG[C/T]AATAACATCTAGTAT | 11169 |
rs764294133 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54984261 | GCACTTTAGGAGGCC[A/G]AGGTGGGTGGATCAC | 11169 |
rs764312894 | snp | C/T | 1.66288e-05 | 0.00288343 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000485 | TTGAAGAAACTGTTG[C/T]ACCATACTCCCTTTT | 11169 |
rs764313667 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965033 | GACAGTAGTGAGTAC[C/T]ACCTTTTGGAGACAA | 11169 |
rs764345461 | in-del | -/TCC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960905 | CCTGGGCTCAAGATA[-/TCC]TCCTGTCCCAGCCTC | 11169 |
rs764356153 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015159 | TTTAAAACATATTAG[C/T]ATTAGTTGCATCAAA | 11169 |
rs764365116 | in-del | -/ACTATAGTAGA | 1.72006e-05 | 0.00293258 | frameshift-variant, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000639 | AACCTTTCTCATGTT[-/ACTATAGTAGA]TCACCCTAAAAATTA | 11169 |
rs764385745 | snp | C/T | 1.72133e-05 | 0.00293366 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010267 | ATAAACAAGGCCTTT[C/T]GTTCTAACATTATTT | 11169 |
rs764442319 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016282 | GAAAACCAACACAAC[C/T]CTTTCAGTGGTAATG | 11169 |
rs764451506 | snp | A/G | 1.65627e-05 | 0.00287769 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962451 | TGTCACTTTGCAGAT[A/G]ACTTGCAAAATTTCC | 11169 |
rs764452676 | snp | A/G | 5.01685e-05 | 0.00500817 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54963020 | GGTTGCTGTCAATTC[A/G]GCTGCCTTCTCTACA | 11169 |
rs764483479 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54968856 | CACCACCCTGGGCAA[A/C]AAAATGAGACCCAAT | 11169 |
rs764483995 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020471 | TAGCTACTCTTTCTT[A/G]GTCTCCTTAGCTGGA | 11169 |
rs764521930 | snp | A/G | 1.78436e-05 | 0.00298688 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007427 | AAAATCCCCCCCAAA[A/G]TATATGCAGAACTGA | 11169 |
rs764531409 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55023880 | GTTTACATTTCTCTT[A/G]ACTGCGGATGGTCTG | 11169 |
rs764533068 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54991810 | AAGTGATTTTTTTTC[A/G]TACAACACTACTTTT | 11169 |
rs764534809 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54956826 | AACTCCTGGGCTCAA[A/G]TGATCCTCCCACCTC | 11169 |
rs764551315 | snp | C/T | 1.65781e-05 | 0.00287902 | missense | WDHD1 | GRCh38.p7 | 14:54962548 | TTGGAAAACGAGTTC[C/T]GTCCTACAGATTAAA | 11169 |
rs764559076 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990768 | TTACATTCTGGTGGG[A/T]GGTGGAGTGAGGAAA | 11169 |
rs764605200 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975887 | TCTTTTAAAGGATCT[C/T]TGAACAAAAAGAAAG | 11169 |
rs764606339 | snp | A/G | 0.000122683 | 0.00783112 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966652 | AACTATCACCTTAAT[A/G]TGAGGCAAGCGTTAA | 11169 |
rs764646749 | snp | A/G | 1.65151e-05 | 0.00287355 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55007323 | CTGCAGATTGATTTT[A/G]CATTTATCACATCGT | 11169 |
rs764656187 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54989090 | GGAAAGATCTGCTAT[C/T]GTATAATTCAAAGTG | 11169 |
rs764671649 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54973075 | TCAACTTATGTACTC[C/T]GATTTATTTATTAGA | 11169 |
rs764702898 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55013080 | ACAAATTTTGGGGTG[A/G]TCAGGTATGGTGGCA | 11169 |
rs764779956 | snp | A/G | 7.61905e-05 | 0.00617166 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957568 | GTATTTAAATAATAT[A/G]AAACATCACTTGGAA | 11169 |
rs764811446 | in-del | -/G | 3.29745e-05 | 0.00406031 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962702 | GCCACATCCATGATA[-/G]TTCTCATGATTTATG | 11169 |
rs764812470 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026703 | CGTTGTTTCTCAAAG[A/G]ACCTTACCTCCCAGA | 11169 |
rs764815226 | in-del | -/TATAGA | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012385 | AAAAGCTTAGGGGTT[-/TATAGA]TAATTAATTTCCAAA | 11169 |
rs764834140 | snp | A/T | 0.000592836 | 0.0172066 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007234 | CTCCATCTCTAATAA[A/T]AAAAAAAAAAAAAAA | 11169 |
rs764864862 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954281 | ACAAGAGCGAAACTC[C/T]GTCTCAGAAAAAATA | 11169 |
rs764887194 | snp | C/T | 1.65318e-05 | 0.002875 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55002144 | ACTCCAAGATTCTCT[C/T]CTATATAGCTTAACA | 11169 |
rs764925682 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948763 | CACCCCCCAGTAGGG[A/G]CAGACTGACACCTCA | 11169 |
rs764926590 | in-del | -/AA | 1.65438e-05 | 0.00287605 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026840 | CAGTCTTATTATTTC[-/AA]AAGAGAAAAGCAGCG | 11169 |
rs764966417 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54986989 | ACATTTTCATTTTCA[C/T]TGCTGCTAGTGAACA | 11169 |
rs764969473 | snp | C/G | 3.33639e-05 | 0.00408422 | missense | WDHD1 | GRCh38.p7 | 14:54966532 | TTGATTTTTAGTGCT[C/G]TCTTCATATTCATAA | 11169 |
rs764976870 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54949419 | GATCAAAGATCAAAT[G/T]AATGAAATGAAGCGA | 11169 |
rs765025679 | snp | C/T | 5.36284e-05 | 0.00517797 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984698 | TTTATATTATACTTG[C/T]TTTTTTTAAACAAAT | 11169 |
rs765050592 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54945908 | AAATGAATCCTAAAT[A/G]AAAAGTCTAAACTTT | 11169 |
rs765061571 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972038 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 11169 |
rs765066014 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008010 | AACCATCTAACCCAA[A/G]GCCCAACGCATGGTC | 11169 |
rs765096443 | snp | A/C/G | 6.59256e-05 | 0.00574101 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55010393 | GTCAATATACCATCT[A/C/G]GAACTCCTTCAGGAA | 11169 |
rs765161014 | snp | C/T | 1.66607e-05 | 0.00288619 | missense | WDHD1 | GRCh38.p7 | 14:54963030 | AATTCGGCTGCCTTC[C/T]CTACAGCCAGTTCAC | 11169 |
rs765182371 | snp | A/C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54973918 | ATTCGCATTTTTTTA[A/C/T]CCTTTCCTTAGCTTT | 11169 |
rs765184243 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54959856 | AATTGTTTTATTTAT[C/G]TCGTTTCTGAAAATA | 11169 |
rs765191077 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54994897 | AGATCTATAGTGATG[A/G]CCCACCTCTCTTTCA | 11169 |
rs765214266 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993045 | CCAATATTATCAATT[C/T]ATATGTTACAAAATT | 11169 |
rs765214901 | snp | G/T | 1.71284e-05 | 0.00292642 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010282 | TGTTCTAACATTATT[G/T]CCTTTTCTGATGTCA | 11169 |
rs765237753 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54983773 | ATCCTCCTGCCTCGG[A/C]CTCCCAGAGTGCTGG | 11169 |
rs765252528 | snp | A/T | 0.000103983 | 0.00720975 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989218 | AGTTCCACACCTACA[A/T]ACAGGTAAGATTAAA | 11169 |
rs765285084 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020086 | TGGTGAGGCACAAGC[-/A]AAATCTCTATATACT | 11169 |
rs765321455 | snp | C/T | 2.66138e-05 | 0.00364776 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966658 | CACCTTAATATGAGG[C/T]AAGCGTTAAATATTT | 11169 |
rs765328801 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016631 | AACTTTCTGAGGTGA[C/T]GAAAATGGTCTATAC | 11169 |
rs765332122 | in-del | -/TTTG | 1.73788e-05 | 0.00294772 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001039 | TTGTAAAATTTCAAA[-/TTTG]CTAAATACTCATTTT | 11169 |
rs765360632 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54969188 | AGACTACAGGTGCCC[A/G]CCACCACGCCCAGCT | 11169 |
rs765386317 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005881 | TGAGACATTTTATTT[C/T]TAAGGCAGGGTTTTG | 11169 |
rs765417872 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985245 | CACAAAGTTAAAATA[A/C]TGTGATACAGAATGT | 11169 |
rs765427576 | in-del | -/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947372 | CCATGAGCCACTATG[-/C]CCGGCCTATCAATTT | 11169 |
rs765430334 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54989102 | TATTGTATAATTCAA[A/G]GTGTTTGATAAGTGT | 11169 |
rs765437634 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55007926 | CTTTAAAACCTTTAT[G/T]AGGCTGCATTTGAAT | 11169 |
rs765469070 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54942605 | TCCATCTTGATCATG[C/T]TGTCATTTCAGGAAT | 11169 |
rs765496031 | in-del | -/AAG | 7.24192e-05 | 0.006017 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007248 | AAAAAAAAAAAAAAA[-/AAG]AAAAGAAAAGAAAAA | 11169 |
rs765500220 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972842 | AAGTGTTTATTAGAT[A/T]TTGGTCAGAGTGAAG | 11169 |
rs765583637 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024081 | AGTTTTTTCAAATTG[C/T]TAGAAACTGCCAAAA | 11169 |
rs765589405 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005205 | CCTTGCTGTTGCATG[G/T]GATGGTAGTGTCCAC | 11169 |
rs765596601 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958409 | TGGGATTACAAGCAT[A/G]AGCCACCACGCCCGG | 11169 |
rs765637858 | snp | C/T | 1.64841e-05 | 0.00287085 | missense | WDHD1 | GRCh38.p7 | 14:54944355 | CTTCAGTTGACAATA[C/T]TCTAAATCGAATCAT | 11169 |
rs765640574 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54979205 | CGCCTAGACAGGAGT[A/G]CAGAGGTGTGATCAT | 11169 |
rs765648305 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54943740 | TCTTTTCTTGGGGTA[G/T]TCTCCTAACTTAAAA | 11169 |
rs765650588 | in-del | -/G | 1.64863e-05 | 0.00287104 | frameshift-variant | WDHD1 | GRCh38.p7 | 14:54941641 | CGTTTTCGCTTCTTT[-/G]CTTCAGTTCCTTCAC | 11169 |
rs765673363 | snp | A/G | 3.6412e-05 | 0.00426669 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008309 | AAATTTAAATTGCTG[A/G]GTTTACCTGATCTGA | 11169 |
rs765678335 | snp | A/G | 1.65836e-05 | 0.0028795 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984866 | AATCCTGTACCTAAT[A/G]AGAAAATGTAAATAT | 11169 |
rs765678544 | snp | C/T | 0.000200381 | 0.0100075 | missense, intron-variant | WDHD1 | GRCh38.p7 | 14:54995747 | TGTCATTTAGAAAAT[C/T]ACCAGCATTACTCAT | 11169 |
rs765738151 | snp | C/T | 1.7315e-05 | 0.00294231 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008413 | TCATAGCCATAATAC[C/T]ACATGGAAAGTGGTT | 11169 |
rs765769805 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54967316 | TGCAATCTGACAGTA[A/G]GGAAGCTTAAAGGAT | 11169 |
rs765772108 | snp | A/C | 1.66443e-05 | 0.00288477 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962583 | AGCAATATAATGTAA[A/C]TGGGGAAAATATAGT | 11169 |
rs765794949 | snp | A/T | 1.65855e-05 | 0.00287967 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:54995677 | ATCATGAGGTCTTCA[A/T]CATCCTCATCATCAT | 11169 |
rs765821001 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002605 | TAGTACTTTAAATAT[A/G]ATTACTTTTTTTTCC | 11169 |
rs765854758 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54949725 | CAAAGTTGAAATGAA[A/G]GAAAAAATGTTCAGA | 11169 |
rs765862892 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993749 | CACTCTTCTCACTAA[-/T]TTTTTTTGTTTTTCA | 11169 |
rs765891230 | snp | C/T | 0.000149595 | 0.00864726 | missense | WDHD1 | GRCh38.p7 | 14:54995650 | CTTCGCTGTCTAGGA[C/T]GACCTGAAGCCATCA | 11169 |
rs765895245 | snp | A/G | 1.65222e-05 | 0.00287417 | missense | WDHD1 | GRCh38.p7 | 14:54984740 | TCAGCTGAAAACCCA[A/G]TCCATGCAAGGTAGG | 11169 |
rs766006154 | snp | C/T | 1.65902e-05 | 0.00288008 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55007280 | ATAAGAATCACTTAC[C/T]TTCCCACTTTTTGGC | 11169 |
rs766018884 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975587 | TCCTGACCTCAGGGT[A/G]ATCTGCCTGCCTTGC | 11169 |
rs766033684 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54973981 | TAAATATCCCCGTCA[C/T]AGAAGAATTCAAGGA | 11169 |
rs766053969 | snp | C/T | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940710 | AATCAGAGTATCCCA[C/T]CAAGAGCACATGATG | 11169 |
rs766063683 | snp | A/G | 4.94295e-05 | 0.00497115 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54989135 | TGCATGGTGTATGGA[A/G]GTATCATGGAACTCC | 11169 |
rs766077709 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55009564 | AGCCTCCCAAGTAGC[C/T]GGGATTATAGGCACC | 11169 |
rs766079090 | snp | G/T | 9.88403e-05 | 0.00702925 | missense | WDHD1 | GRCh38.p7 | 14:54991326 | TTACAAGTGGTAGAT[G/T]GTGAATGCTGCCTTC | 11169 |
rs766118485 | snp | C/T | 6.61059e-05 | 0.00574879 | missense | WDHD1 | GRCh38.p7 | 14:54941585 | GGTTCTCTTTTGCTT[C/T]TTCTTCCTGGTTTTC | 11169 |
rs766157221 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55022056 | GAATTCGAGACATTG[C/T]GTTTGGGGGCAAGTA | 11169 |
rs766188244 | snp | C/G | 2.06349e-05 | 0.00321202 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010497 | GAAACATTAGCAAAA[C/G]AAATCCAAATGACTG | 11169 |
rs766223184 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54989834 | CAGCTAATTTCTGTA[-/T]TTTTTTTAGTAGAGA | 11169 |
rs766237707 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960698 | TTTAGTGGAGATGTG[C/G]TTTCACCATTTTGGC | 11169 |
rs766254449 | snp | A/C/T | 3.30209e-05 | 0.00406319 | stop-gained, missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000973 | TGCCCACAGGGAGAC[A/C/T]AGGTTACTATATTGA | 11169 |
rs766265045 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026890 | GAGCTTAGTCTCCTC[C/T]AGGGCCCGTTCTCCG | 11169 |
rs766326836 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54982572 | ACTCAGGAAATCTGT[A/G]GCAAATTACCTGATT | 11169 |
rs766333980 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54961668 | GCTCTTTTCATATTC[C/T]ACATGTTTTTTAAGT | 11169 |
rs766335932 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54946994 | GTTGCAGTGAGCTGA[C/G]ATTGCACCAGTGGAC | 11169 |
rs766341358 | snp | A/G | 1.65644e-05 | 0.00287783 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54963110 | GGCTAAATTCACAGC[A/G]TTTTGAGTCATTAGA | 11169 |
rs766341681 | snp | A/G | 0.000100859 | 0.00710066 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008562 | AGGAAATATATTTTT[A/G]AACATATTCAGGAAA | 11169 |
rs766341694 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55018966 | AGGCAGAGGTTACAG[C/T]GGGCCGAGATGGTGC | 11169 |
rs766371601 | snp | A/C | 0.000165295 | 0.00908956 | missense | WDHD1 | GRCh38.p7 | 14:54984838 | TTGAACTCCAAGGCA[A/C]TGATCCCCATCAAAT | 11169 |
rs766380860 | snp | A/G | 1.65957e-05 | 0.00288055 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000867 | GCAAAGAAGAGACAA[A/G]AGATACACTAAATCA | 11169 |
rs766388960 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947567 | ATGAGATATATTATG[A/G]TAAAAATGAAATTGT | 11169 |
rs766392836 | snp | C/T | 9.94909e-05 | 0.00705235 | missense | WDHD1 | GRCh38.p7 | 14:54967383 | AACCGAGAACCTTTA[C/T]AAGGAATGCACCTGT | 11169 |
rs766398734 | in-del | -/AA | 0.000166218 | 0.0091149 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013619 | GAAAAGACACAAATT[-/AA]AGTCATCGGGCATGG | 11169 |
rs766413425 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55006896 | AAAACTATTTTTACA[C/G]TCAAAGTTGAAAAGG | 11169 |
rs766414302 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54970455 | AATATATCTAACCAA[C/G]GAGGTGAAAGATCTC | 11169 |
rs766472231 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005548 | CTTCAGATTTATGAT[A/G]TAGATGCCAACACTT | 11169 |
rs766501251 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958561 | GGCCCTCAGTGATCT[C/T]TACATTGTCAAATCT | 11169 |
rs766554165 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54959605 | CTCTCTCTACAAAAA[A/G]TACACACAAAAAATT | 11169 |
rs766563471 | snp | C/T | 1.64773e-05 | 0.00287026 | missense | WDHD1 | GRCh38.p7 | 14:54967336 | GCTTAAAGGATAATA[C/T]AGCAACAGCAGGGCG | 11169 |
rs766584884 | in-del | -/CCATAATCACGCCACTGCACTCTAACCTGGATGA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54959345 | TGAGGCTGCAGTGAG[lengthTooLong]CAGTCACACCCTGGC | 11169 |
rs766648559 | in-del | -/AAC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54966341 | CTCCGTCGCACAAAA[-/AAC]AACAACAACAACAAA | 11169 |
rs766683103 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54945531 | CAACAACCAGGCAAT[G/T]TGACTCCAAAGTCTA | 11169 |
rs766689970 | snp | A/G | 1.80941e-05 | 0.00300778 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989233 | AACAGGTAAGATTAA[A/G]TATAAGTCTGAGAAA | 11169 |
rs766771532 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54966273 | CCGGGAGGCAGAGGT[C/T]GCAGTGAGCCGAGAT | 11169 |
rs766833112 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965021 | TTGCATAAAGGTGAC[A/G]GTAGTGAGTACTACC | 11169 |
rs766856202 | snp | C/G | 8.39948e-05 | 0.00648 | missense, intron-variant | WDHD1 | GRCh38.p7 | 14:54995760 | ATCACCAGCATTACT[C/G]ATATCATCTCCATCA | 11169 |
rs766861010 | snp | A/G | 6.95628e-05 | 0.00589717 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944487 | TAAAATCACAATTAT[A/G]TGAAAACATTTTATA | 11169 |
rs766871184 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55014526 | GAAACCTTAATAAAT[A/G]TTTGTTGAATTAATA | 11169 |
rs766905700 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55001273 | CACCATTTTATTTTA[G/T]TTTTAGAGTCAGGGT | 11169 |
rs766910357 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54944181 | TGCCCAGGCTGGTCA[C/T]GAACTCCTGAGCTCA | 11169 |
rs766916146 | snp | C/T | 6.59435e-05 | 0.00574172 | missense | WDHD1 | GRCh38.p7 | 14:54944363 | GACAATACTCTAAAT[C/T]GAATCATTCCTTCTT | 11169 |
rs766956655 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974326 | TAGCTTTAGCTACTC[A/G]GAAGGCGGAGGACGG | 11169 |
rs766965401 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975827 | GCACCGATGTGACAC[A/G]CTCTCAAATGAATTT | 11169 |
rs766968345 | snp | C/T | 1.64836e-05 | 0.0028708 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008678 | CGAAATGTTTTCTGT[C/T]GGCTGCTATCCATCA | 11169 |
rs766975944 | in-del | -/AAC | 1.69037e-05 | 0.00290716 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966446 | AAAGCATTTAACTTT[-/AAC]GTTTTCAGTATATTT | 11169 |
rs767030158 | snp | G/T | 1.65671e-05 | 0.00287807 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55010429 | TGGACTTGAATAGTA[G/T]TATTAGAAACTGCAG | 11169 |
rs767040316 | in-del | -/AAAC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54992964 | ATTAATTAAAAACAA[-/AAAC]AAATAATTTATATTA | 11169 |
rs767047924 | snp | C/T | 1.72644e-05 | 0.00293801 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013439 | CAAGCATAAAAATCA[C/T]ATGCCAGTATCATTT | 11169 |
rs767077470 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975749 | TTGCCCAGGCTGTCT[A/G]CAAACTCCTGGGCTC | 11169 |
rs767078751 | snp | C/T | 1.65037e-05 | 0.00287256 | missense | WDHD1 | GRCh38.p7 | 14:54987149 | AAAAAAATCTACCTC[C/T]GTGATAAACAATGAA | 11169 |
rs767128391 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54995415 | TTTCTCTTTTTCTAG[C/T]CTGCCATAGCAGAAG | 11169 |
rs767131948 | snp | C/T | 1.65913e-05 | 0.00288017 | missense | WDHD1 | GRCh38.p7 | 14:54995663 | GACGACCTGAAGCCA[C/T]CATGAGGTCTTCATC | 11169 |
rs767142111 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55023676 | AGGCAATTTACTGGA[A/G]AGACAAACTGCTCAT | 11169 |
rs767152214 | in-del | -/AAC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54966343 | CGTCGCACAAAAAAC[-/AAC]AACAACAACAACAAA | 11169 |
rs767190296 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55009779 | ATGCTTTCAGTATTA[C/T]AAAATAGGCCATCTG | 11169 |
rs767216225 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993340 | GCCCTGGCTGGTCTT[C/G]AACTCCTGGCCTCAA | 11169 |
rs767274013 | snp | A/G | 0.000131937 | 0.00812103 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944315 | TAAGATCTCAATCTC[A/G]GCACAATTATCCTTA | 11169 |
rs767307294 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948073 | ATACAAAATTAAGCG[A/G]TTCCAAGATGGTCGA | 11169 |
rs767313152 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010736 | TTGAATAGTACTTCT[A/G]TGGATCCTAAGTGTT | 11169 |
rs767322977 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54968235 | ACCACACAAATTACA[C/T]GGAAAGTAAACAACA | 11169 |
rs767329171 | snp | C/G | 3.36995e-05 | 0.00410471 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941716 | TGGCAGGAGTGAAAA[C/G]GAAAGATTTTTAGAA | 11169 |
rs767399091 | snp | C/G | 1.66131e-05 | 0.00288206 | missense | WDHD1 | GRCh38.p7 | 14:54991216 | TCCAAGTCTTACCAT[C/G]AATCTGTGAGTGAGA | 11169 |
rs767400786 | snp | A/G/T | 8.2417e-05 | 0.00641892 | missense | WDHD1 | GRCh38.p7 | 14:54967347 | AATATAGCAACAGCA[A/G/T]GGCGTGGAAGGGTTG | 11169 |
rs767427987 | in-del | -/AG | 1.7086e-05 | 0.00292279 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007254 | AAAAAAAAAAAGAAA[-/AG]AAAAGAAAAATAAGA | 11169 |
rs767428426 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54962310 | GCCTGACACTCAATA[A/G]GCATTTTATAAACAT | 11169 |
rs767431091 | snp | C/G | 1.64958e-05 | 0.00287187 | stop-gained | WDHD1 | GRCh38.p7 | 14:54957173 | CGTGCTGAATTCATT[C/G]ACATGGCTGGTTCTT | 11169 |
rs767458116 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998947 | ATAATTCACTTAATC[C/T]TCCCAATAACCCCAA | 11169 |
rs767462000 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54969524 | GACTCAGAAAAAACA[C/G]AAATTCTGAACAAAC | 11169 |
rs767484161 | snp | C/T | 1.64792e-05 | 0.00287042 | missense | WDHD1 | GRCh38.p7 | 14:54957086 | ATGGGAGACTTTTCA[C/T]TATTTGTAGTTCGAC | 11169 |
rs767510072 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974489 | ACAAAACCTGTTTTG[-/T]TTTGTTTTTTTTTTT | 11169 |
rs767517768 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55018018 | CAGCAGCGCACAAAC[C/T]GATGTTAATTAAATA | 11169 |
rs767521295 | in-del | -/AGTTTAA | 1.83256e-05 | 0.00302696 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944513 | TTATACTTAAGACAG[-/AGTTTAA]AGTGCCTCATGATTT | 11169 |
rs767523454 | snp | A/G | 1.82968e-05 | 0.00302457 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989237 | GGTAAGATTAAATAT[A/G]AGTCTGAGAAAAACT | 11169 |
rs767534567 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54994819 | TTTGAACTAACCACA[C/T]TTCAAGTGCTCAACA | 11169 |
rs767553682 | snp | C/T | 3.34225e-05 | 0.0040878 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000469 | TGATCACAGAAACAT[C/T]TTGAAGAAACTGTTG | 11169 |
rs767569925 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55007911 | CTTATTTCGTACCTC[C/G]TTTAAAACCTTTATT | 11169 |
rs767618163 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993640 | TCTTTATACACTTCA[A/G]ACAAAAACAATGTAT | 11169 |
rs767659600 | snp | A/G | | | splice-donor-variant | WDHD1 | GRCh38.p7 | 14:55013483 | ATAACTGTTTTTACT[A/G]CCTTCAAAGCACATG | 11169 |
rs767676278 | snp | A/T | 1.64958e-05 | 0.00287187 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008691 | GTTGGCTGCTATCCA[A/T]CACATCCACAATTTT | 11169 |
rs767717429 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54946641 | GGCATGTGCCACCAC[A/C]CACACCTGGCTGATT | 11169 |
rs767724567 | snp | G/T | 1.65644e-05 | 0.00287783 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962902 | ATGCAAAGACCAACT[G/T]AACATTCAAGACAGT | 11169 |
rs767741898 | snp | A/G | 1.66175e-05 | 0.00288244 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008589 | GAAAAACACAAAAAG[A/G]GAAGGAAAAAATAAT | 11169 |
rs767785024 | snp | A/T | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028000 | ATCTTCATTCTCCAT[A/T]TTGGTACAGCAGCCT | 11169 |
rs767785144 | in-del | -/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015527 | AGTGATAAGCTATCT[-/C]CCCTTTTCCTACCCT | 11169 |
rs767787159 | in-del | -/A | 0.444444 | 0.157135 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963180 | CAAGAAAGCTAATCC[-/A]AAAAGGGGGGGGGGG | 11169 |
rs767847859 | snp | A/G | 0.000117959 | 0.00767892 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966449 | GCATTTAACTTTAAC[A/G]TTTTCAGTATATTTA | 11169 |
rs767892550 | snp | A/G | 0.000395483 | 0.0140565 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007246 | TAAAAAAAAAAAAAA[A/G]AAAGAAAAGAAAAGA | 11169 |
rs767896647 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54959473 | AGGCAGGCAGGCAGG[A/C]AATTTCTAGCTGAGC | 11169 |
rs767918578 | snp | C/T | 1.75832e-05 | 0.00296501 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967415 | AGTAAAGAAAAGTTC[C/T]ATCATAAAAATTTAC | 11169 |
rs767924597 | snp | C/T | | | missense | WDHD1 | GRCh38.p7 | 14:54966572 | GCTAAATAATCAAGG[C/T]GGTTGTGAAATATAA | 11169 |
rs767938020 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003660 | CCTCTGCCTCCCAGG[G/T]TCAAGCAATTCTCCT | 11169 |
rs767947644 | snp | A/G | 1.73456e-05 | 0.00294491 | missense | WDHD1 | GRCh38.p7 | 14:54966560 | TAACCATTTTTAGCT[A/G]AATAATCAAGGTGGT | 11169 |
rs767957997 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003145 | TAGGTTTTTTTGTAA[A/G]CAAAGAAAAAAAATA | 11169 |
rs767960392 | snp | C/T | 1.66352e-05 | 0.00288398 | missense | WDHD1 | GRCh38.p7 | 14:54955590 | GTTTTGAGGAGGACA[C/T]ATAGCTGGGGTTTCA | 11169 |
rs767968499 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | WDHD1 | GRCh38.p7 | 14:54987299 | ATCCTTGACCGAGAC[A/G]TATGGCTTCAATATC | 11169 |
rs767972033 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002711 | CTGGGGTCAAAGGAT[C/G]CTCCTGCTTCAGCCT | 11169 |
rs767992947 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026145 | TCCCCAGCAAAAGAG[A/G]CACACAAGTATTTTT | 11169 |
rs768002659 | snp | A/C/G | 3.85195e-05 | 0.00438846 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987405 | AAAAATTAAAACAAG[A/C/G]CAGAAACAATCAAAC | 11169 |
rs768024781 | in-del | -/CAC | 1.65334e-05 | 0.00287514 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981702 | CAAGGGGTACCTAAA[-/CAC]CAACAGAAAAATCAC | 11169 |
rs768055555 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954484 | TTGAACCATACATGA[A/T]TCCATCTTATAGCTA | 11169 |
rs768068666 | snp | A/G | 6.66756e-05 | 0.0057735 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54955650 | CACTTCCTCAGTTTT[A/G]TTAGTTTGAGAATTT | 11169 |
rs768069495 | snp | A/G/T | 1.64803e-05 | 0.00287052 | stop-gained, missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000579 | TCCGCATCAGTATAC[A/G/T]ATATTCGACCACAAG | 11169 |
rs768092361 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant, synonymous-codon, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026716 | AGAACCTTACCTCCC[A/G]GAATCATCAAAACAG | 11169 |
rs768146033 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54992994 | ATTAGATAATAAAAA[C/G]TGTCAGTATAAAGAG | 11169 |
rs768166924 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980210 | AGTCCCAGCTACTTG[G/T]AAGGCTAAGGTGGGA | 11169 |
rs768197761 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55012899 | TAAGTTTCCAACACA[C/T]GCTTTTAGGGGAACA | 11169 |
rs768206414 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990325 | AACTCAGGCCAGGCG[C/T]GGTGGCTCACGCCTG | 11169 |
rs768216660 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54978929 | TTCCAGAACTGATGA[A/G]ATGTCTATTTTCCTA | 11169 |
rs768248334 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958209 | TCGGCTCACTGCAAA[A/G]TCCACCTCCCAGGTT | 11169 |
rs768269446 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54964702 | TATTCTGAACTAAAG[A/G]CATTTGCCCGGGGGT | 11169 |
rs768294222 | in-del | -/AATGTA | 1.66294e-05 | 0.00288347 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962576 | AAAATAAAGCAATAT[-/AATGTA]AATGGGGAAAATATA | 11169 |
rs768312915 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54944991 | CAAAAGGATCACTCA[C/T]GTTTGTATTTTCCAA | 11169 |
rs768319799 | snp | A/G | 1.71446e-05 | 0.0029278 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955558 | ATTTCTCTATGTACT[A/G]ACCTTTGGTTTTCAG | 11169 |
rs768362382 | snp | A/G | 3.29549e-05 | 0.00405911 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54987273 | CAGGGCACTAGTAGC[A/G]GCAGCAGCCCATCCT | 11169 |
rs768368377 | snp | C/G | 1.64814e-05 | 0.00287061 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000528 | GATGTCTTTCCACTG[C/G]GGTCACAAACATTCT | 11169 |
rs768392384 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965675 | TTTTATTTATTTTAG[C/G]CTGGGCACGGTGGCT | 11169 |
rs768396223 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54977381 | AGATAACGTGATTTG[C/T]AAATACAATTTTATA | 11169 |
rs768398203 | snp | A/G | 1.64882e-05 | 0.00287121 | missense | WDHD1 | GRCh38.p7 | 14:54941647 | CGCTTCTTTGCTTCA[A/G]TTCCTTCACTTGCCG | 11169 |
rs768426128 | snp | C/T | 5.01199e-05 | 0.00500574 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008753 | ACGCAAATGAATAAA[C/T]GCTAACACAAAGGCC | 11169 |
rs768448600 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55014193 | CCGCCTCCCAGGCTC[A/C]AGTGATCAAACCACT | 11169 |
rs768451350 | snp | A/C | 1.66477e-05 | 0.00288506 | missense | WDHD1 | GRCh38.p7 | 14:54941550 | AAAATCTAAAGGTTT[A/C]TGCTTTTTAGACAAA | 11169 |
rs768451691 | in-del | -/TG | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55004376 | GTTTTATTATCTAAC[-/TG]AATTATTTGCATCAC | 11169 |
rs768453557 | in-del | -/C | 5.24939e-05 | 0.00512291 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963192 | CCAAAAAGGGGGGGG[-/C]GGGGGGAGATCAAAT | 11169 |
rs768466067 | snp | A/G | 3.32171e-05 | 0.00407522 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55007372 | GCCAACTAATAGCAC[A/G]TGTCTAATTGGTAAA | 11169 |
rs768469483 | snp | C/T | 1.69152e-05 | 0.00290814 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957659 | AAAAAGAAACCCTTG[C/T]TTAATAATGGTAGAA | 11169 |
rs768492858 | snp | A/G | 3.66589e-05 | 0.00428113 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995853 | AAAGTAAAAGTGAAT[A/G]ATTTAGAAAAACTCA | 11169 |
rs768506864 | snp | C/T | 1.65559e-05 | 0.00287709 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962492 | AAATTTATAAATATT[C/T]CTCACCTGACTTAGC | 11169 |
rs768512851 | snp | C/T | | | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000628 | CACAAATTGCATAAC[C/T]TTTCTCATGTTTCAC | 11169 |
rs768514299 | snp | C/T | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940318 | TGCTCATAACCACTG[C/T]GCTATAATGTCTCTG | 11169 |
rs768517319 | snp | A/T | 0.000299825 | 0.0122402 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007272 | AAAGAAAAATAAGAA[A/T]CACTTACCTTCCCAC | 11169 |
rs768520659 | snp | A/G | 3.31181e-05 | 0.00406914 | missense | WDHD1 | GRCh38.p7 | 14:54966515 | TGTTGCTCTTTTGTT[A/G]CTTGATTTTTAGTGC | 11169 |
rs768522134 | snp | A/T | 1.64988e-05 | 0.00287213 | missense | WDHD1 | GRCh38.p7 | 14:54991383 | GAAGACTAGAACCAG[A/T]TTTTAGCATTGAAAT | 11169 |
rs768567732 | snp | A/C/G | 0.000115362 | 0.00759408 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55010376 | CATTTGTAGTGAAGC[A/C/G]AGTCAATATACCATC | 11169 |
rs768589005 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54949351 | CGAGAACTACGTGAC[A/G]AATGCACAAGCCTCA | 11169 |
rs768622672 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947460 | ATGTGAAAACCACAG[C/G]CACTCCCTCAAACTG | 11169 |
rs768639539 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002363 | TTGGTCTCTAACTCC[C/T]GGGTTCAAGGGATCT | 11169 |
rs768757036 | snp | A/T | 1.79551e-05 | 0.0029962 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010463 | CCAGTTTTCCACTCT[A/T]AAAGAAAAATTAAGG | 11169 |
rs768793163 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997438 | ACATAACTGTGCTCT[A/G]AAAACTGATGTTTAA | 11169 |
rs768804419 | snp | A/C/T | 3.43928e-05 | 0.00414674 | missense | WDHD1 | GRCh38.p7 | 14:54995616 | ACCAACTGAGTTTTC[A/C/T]TCATCTTCTAGGATG | 11169 |
rs768807129 | snp | C/T | 1.67052e-05 | 0.00289004 | missense | WDHD1 | GRCh38.p7 | 14:54957035 | AGCTGAAACAGTACC[C/T]GCTTAGGCTTCGGCT | 11169 |
rs768807330 | snp | A/C/G/T | 0.00515587 | 0.0505255 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963189 | TAATCCAAAAAGGGG[A/C/G/T]GGGGGGGGGAGATCA | 11169 |
rs768818439 | snp | A/T | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011812 | TTTATAATGGCTGCA[A/T]AGTATTCCATTATAT | 11169 |
rs768906882 | in-del | -/AAAG/AG/G | 0.00220272 | 0.0331211 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007246 | AAAAAAAAAAAAAAA[-/AAAG/AG/G]AAAGAAAAGAAAAGA | 11169 |
rs768916889 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54970123 | AGCTGGAAGCATTAC[C/T]CTTAAGAATTGGAAT | 11169 |
rs768918739 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948359 | CCCCCACCCTAATAC[C/T]GTGCTTTTCCAATGG | 11169 |
rs768959329 | snp | C/T | 3.75679e-05 | 0.00433388 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984685 | GAATATCTAACACTT[C/T]ATATTATACTTGTTT | 11169 |
rs768992961 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54943139 | ACCTGAGGATTTAAC[G/T]GGTACACCACACACA | 11169 |
rs769016883 | in-del | -/TC | 1.64822e-05 | 0.00287068 | frameshift-variant, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008673 | GTCCTCGAAATGTTT[-/TC]TGTTGGCTGCTATCC | 11169 |
rs769036676 | snp | C/G | 1.78921e-05 | 0.00299094 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991170 | TAGTAAGAAAAAAGT[C/G]CTGAAAACCTACTAA | 11169 |
rs769036711 | snp | A/C | 1.64751e-05 | 0.00287007 | missense | WDHD1 | GRCh38.p7 | 14:54967311 | TCTGTTGCAATCTGA[A/C]AGTAAGGAAGCTTAA | 11169 |
rs769039932 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958024 | TGACTTTTCCCTATT[C/T]ATTGGCCCCTAAAGT | 11169 |
rs769089712 | snp | C/T | 1.66158e-05 | 0.0028823 | missense | WDHD1 | GRCh38.p7 | 14:54989196 | TAGCAGCGAATAATT[C/T]CAATAGAGTTCCACA | 11169 |
rs769111454 | in-del | -/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005082 | TTTTCAATCTCCTCA[-/G]GAACACTGTAGAAGT | 11169 |
rs769134913 | in-del | -/TTTTC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988052 | AAAGCTGAAAAAATA[-/TTTTC]TTTTCTTTTGAAAAG | 11169 |
rs769141787 | in-del | -/A/GGGA | 0.000281185 | 0.0118544 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963195 | AAAAGGGGGGGGGGG[-/A/GGGA]GGGAGATCAAATAAC | 11169 |
rs769146082 | snp | C/T | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940095 | AGTAACTAACATTTA[C/T]ATAAAAGATTACTAT | 11169 |
rs769158091 | in-del | -/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54961156 | CATGCTATACCTCTG[-/C]CTTAAAACCTACAAC | 11169 |
rs769190669 | in-del | -/AAT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951521 | ATAGCCTACCAACCA[-/AAT]AAAAAGTCCAGGACC | 11169 |
rs769209845 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55018656 | GCTGAAGTATTTACC[C/T]ATTTCAATTAAAACA | 11169 |
rs769250965 | snp | C/T | 1.64811e-05 | 0.00287059 | missense | WDHD1 | GRCh38.p7 | 14:54957131 | TTCTTGGATGATTTG[C/T]CCATATTGTCTAAAA | 11169 |
rs769268369 | snp | C/T | 1.64838e-05 | 0.00287083 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000938 | TGATTAGACCATTAA[C/T]ACTACCTGCAGCTAA | 11169 |
rs769273518 | snp | A/C/T | 4.98586e-05 | 0.00499272 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007275 | GAAAAATAAGAATCA[A/C/T]TTACCTTCCCACTTT | 11169 |
rs769334411 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54943598 | AGATGGTGTATCACT[A/G]TGTTGTCTAGGCTGG | 11169 |
rs769356594 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002436 | CCACTGTGCCAGGCG[C/T]AAATCTGTATTTTAA | 11169 |
rs769373563 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002429 | GCATACACCACTGTG[C/G]CAGGCGCAAATCTGT | 11169 |
rs769429849 | snp | A/C | 1.65138e-05 | 0.00287343 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54989042 | CCTTGCTAGTTCATC[A/C]GTGCTTTCACATGCC | 11169 |
rs769447484 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015606 | GCATTCAATAAAAAA[C/T]GGAATGGATTCAGAT | 11169 |
rs769460226 | in-del | -/T | 1.68593e-05 | 0.00290334 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988977 | TAATTTCAACAACTG[-/T]TATCTAACAGTTCAA | 11169 |
rs769461332 | snp | C/G | 2.17934e-05 | 0.00330094 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966627 | AAAGCAAATAAAATT[C/G]CTTAAGGCCAACTAT | 11169 |
rs769487727 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55009434 | TTCTAAGTAAAATAA[-/T]TTTTTTTTTTTTTTT | 11169 |
rs769506329 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997911 | GCGGAACTCCGTCTC[-/A]AAAAAAAAAAAATGG | 11169 |
rs769545634 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939589 | CCAATTCTCTGGAAA[-/A]AAAAAAAAAGAACAC | 11169 |
rs769556220 | snp | C/T | 1.76802e-05 | 0.00297318 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000644 | TTTCTCATGTTTCAC[C/T]CTAAAAATTAAAAAG | 11169 |
rs769568489 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003229 | TAAAAGTTCACATGG[C/G]CTGGGTGTGGTAGCT | 11169 |
rs769570115 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55004384 | ATCTAACTGAATTAT[A/T]TGCATCACTTTTCTT | 11169 |
rs769572760 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016917 | GATCAGGTGCGTTCA[C/G]GGTGGTATGGCCATA | 11169 |
rs769589909 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55018544 | AAGAATCATAGACAA[C/T]TTGATGAATTTTGTC | 11169 |
rs769608054 | snp | C/T | 1.65946e-05 | 0.00288046 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:54995693 | CATCCTCATCATCAT[C/T]TATAATCCCTTTTGA | 11169 |
rs769609075 | snp | A/T | 0.000428372 | 0.0146288 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987396 | AAGCTTGCTAAAAAT[A/T]AAAACAAGACAGAAA | 11169 |
rs769618478 | snp | G/T | 1.65012e-05 | 0.00287234 | missense | WDHD1 | GRCh38.p7 | 14:54941672 | TTGCCGTTTCTCCTT[G/T]GGCTTTGTTAGCCCA | 11169 |
rs769620914 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954313 | ATAAATACAAAGAAA[C/T]CCAGCATAGTAGAGA | 11169 |
rs769660474 | snp | C/G | 1.6519e-05 | 0.00287388 | missense | WDHD1 | GRCh38.p7 | 14:54984819 | TTTTCCCCAGCTCTA[C/G]CAGTTGAACTCCAAG | 11169 |
rs769663026 | snp | A/T | 1.69919e-05 | 0.00291473 | missense | WDHD1 | GRCh38.p7 | 14:54995622 | TGAGTTTTCATCATC[A/T]TCTAGGATGTGACTT | 11169 |
rs769691492 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54989999 | CACTTGGAAAACTTA[C/T]CTTCCACTGATGTCC | 11169 |
rs769789521 | snp | A/G | 1.68038e-05 | 0.00289855 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007385 | ACATGTCTAATTGGT[A/G]AAAAAAGAAAATTTC | 11169 |
rs769823329 | in-del | -/AACCAC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54971031 | CTGAGATAACTGGCT[-/AACCAC]ATGCAGAATGAAACT | 11169 |
rs769824757 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975285 | AAACAATACTTGGTA[A/T]ACTGAAGTTCAGCTC | 11169 |
rs769844127 | snp | A/C | 1.6501e-05 | 0.00287232 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000964 | GCTAAATATTGCCCA[A/C]AGGGAGACCAGGTTA | 11169 |
rs769901415 | snp | A/C/G/T | 0.000542017 | 0.0164555 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963190 | AATCCAAAAAGGGGG[A/C/G/T]GGGGGGGGAGATCAA | 11169 |
rs769902169 | snp | C/T | 1.64768e-05 | 0.00287021 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967270 | GTGTCAAGGTAAGAC[C/T]TCCACATACCTCCAT | 11169 |
rs769926279 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985375 | TAGGGGAAGGAACAC[A/G]GAAGTGGATGGAGGG | 11169 |
rs769947401 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948412 | AGATTATATCCCACT[C/G]CTGGCTCAGAGGGTC | 11169 |
rs769947426 | snp | C/G | 1.66515e-05 | 0.00288539 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957220 | CTAAAGAGCAAACTA[C/G]TGTTAGCACTGTATG | 11169 |
rs769958767 | snp | A/T | 1.65482e-05 | 0.00287643 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987121 | CCATTTTACTTCAAG[A/T]CATAAAAGACTGAAA | 11169 |
rs769978553 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55000244 | GGCCAAACTGAGACC[C/T]GATACAAAATAGTAT | 11169 |
rs769978786 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54986555 | CTGACCTAGAGAGTA[A/G]TAGAGAAAAAGGGGA | 11169 |
rs770000104 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019971 | TCAATGATTACCAAC[A/G]CATTTCTTACTACCT | 11169 |
rs770000548 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948899 | CAGGCAGAGTCTGGA[G/T]TGGGCCTCCAGCAAA | 11169 |
rs770001597 | in-del | -/AAGGAAATAATGTTAG | 4.05375e-05 | 0.0045019 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010494 | AAGAAACATTAGCAA[-/AAGGAAATAATGTTAG]AACAAATCCAAATGA | 11169 |
rs770004503 | snp | A/G | 8.23988e-05 | 0.00641815 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54957136 | GGATGATTTGCCCAT[A/G]TTGTCTAAAATATTA | 11169 |
rs770027531 | in-del | -/A | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010576 | AATCTAGTTCATATC[-/A]AGAGAAAAATTATCA | 11169 |
rs770036425 | snp | C/T | 1.64808e-05 | 0.00287057 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008663 | GGGGCATCATGTCCT[C/T]GAAATGTTTTCTGTT | 11169 |
rs770075010 | snp | C/T | 1.64966e-05 | 0.00287194 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55013505 | AAGCACATGAATATG[C/T]CTTTTCTCCAACATT | 11169 |
rs770092016 | snp | C/T | 1.67643e-05 | 0.00289515 | missense | WDHD1 | GRCh38.p7 | 14:54962986 | TGAAATCTTCTTCTT[C/T]TTCTTCCTCTTCCAC | 11169 |
rs770102115 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54971483 | TCCCATTTACAATAG[C/T]CATATGCACACACAC | 11169 |
rs770102948 | snp | C/G | 2.83499e-05 | 0.00376486 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963178 | TACAAGAAAGCTAAT[C/G]CAAAAAGGGGGGGGG | 11169 |
rs770109204 | in-del | -/ATAATTTTTTTTTTTTTTTTG | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55009430 | CAAGTTCTAAGTAAA[-/ATAATTTTTTTTTTTTTTTTG]AGACAGAGTTTCACT | 11169 |
rs770144968 | snp | A/G | 1.65384e-05 | 0.00287557 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962872 | AGAGAAAATAATATT[A/G]TTCAATAAAGAGCTA | 11169 |
rs770146933 | snp | C/G | 1.64898e-05 | 0.00287135 | missense | WDHD1 | GRCh38.p7 | 14:54981544 | TAATAGCCCACCTTA[C/G]TTGCTGGGGATTTTC | 11169 |
rs770203568 | snp | G/T | 1.89629e-05 | 0.00307914 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010478 | AAAAGAAAAATTAAG[G/T]TAAGAAACATTAGCA | 11169 |
rs770271728 | snp | C/G/T | 3.30471e-05 | 0.00406481 | missense | WDHD1 | GRCh38.p7 | 14:54967371 | AGGGTTGGGGGAAAC[C/G/T]GAGAACCTTTACAAG | 11169 |
rs770316655 | snp | A/T | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027665 | CTAGAGCCTCTAATC[A/T]TGGCATCCTTCGTGC | 11169 |
rs770371073 | snp | G/T | 1.71349e-05 | 0.00292697 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991190 | AAACCTACTAAGAAG[G/T]TAAGTGTAGATCCAA | 11169 |
rs770381901 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025455 | CTAAGTCTCTCGTTC[C/T]ACCTTACGAGAAACA | 11169 |
rs770383222 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54946180 | TCATCTACTTCTAAA[A/C]AGCTATTTTTAAAAA | 11169 |
rs770408841 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016014 | CCGATGGGCTTCTTG[G/T]TGTATCAGCAGATGC | 11169 |
rs770485970 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54989807 | GTGGTTACAGGTGCA[-/T]TGCCACCAGGTCCAG | 11169 |
rs770488875 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54956312 | GGTCTGAGTATATAT[A/G]TTTTTAAAAAGTGAT | 11169 |
rs770498321 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980981 | CCAGGCGTGATGGTG[C/T]GCACCTATAATCCCA | 11169 |
rs770518463 | snp | C/T | 4.95037e-05 | 0.00497488 | missense | WDHD1 | GRCh38.p7 | 14:54962845 | CACTCTGTAGCAGTA[C/T]TGCTGTAACTAAGAG | 11169 |
rs770518512 | snp | A/G | 1.64963e-05 | 0.00287192 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944309 | ATTCACTAAGATCTC[A/G]ATCTCGGCACAATTA | 11169 |
rs770524547 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967676 | CCCAGGCTAAAGCAC[A/G]GTGGTGTGATCACGG | 11169 |
rs770529919 | snp | C/T | 2.34717e-05 | 0.00342568 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966645 | TAAGGCCAACTATCA[C/T]CTTAATATGAGGCAA | 11169 |
rs770543854 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54941936 | TAGTTGCAAAATACT[A/G]TAATTGCAGTACTAT | 11169 |
rs770565630 | in-del | -/T | 1.64851e-05 | 0.00287093 | frameshift-variant | WDHD1 | GRCh38.p7 | 14:54991268 | GAAATGGCTTTTGCC[-/T]GGGGAGTTGGCATGG | 11169 |
rs770571480 | snp | C/G | 1.64808e-05 | 0.00287057 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962729 | TATGGGCTTGAAAAT[C/G]TATCTCACCAGGCTT | 11169 |
rs770608091 | snp | C/T | 3.295e-05 | 0.00405881 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54967292 | TACCTCCATTTGTCC[C/T]TTCTCTGTTGCAATC | 11169 |
rs770660918 | snp | C/T | 3.30551e-05 | 0.00406528 | missense | WDHD1 | GRCh38.p7 | 14:54989184 | TGCTCATCATTATAG[C/T]AGCGAATAATTCCAA | 11169 |
rs770687936 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54991593 | TCCTGGTGCCTTGGC[A/T]CCAATCAAGGCAGTG | 11169 |
rs770738966 | snp | A/C | 3.29685e-05 | 0.00405995 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55013542 | CTTAGGATCATCATC[A/C]TCCAAGTCTTCCCAA | 11169 |
rs770743965 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019425 | TTCACGTATTTTGAA[A/G]CCTATATTGTACCTT | 11169 |
rs770747803 | snp | A/T | 1.64803e-05 | 0.00287052 | missense | WDHD1 | GRCh38.p7 | 14:54987225 | GCTGAATACCTCTTT[A/T]TGAACCCCTCCAATA | 11169 |
rs770770896 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996537 | CCTGGAAGGTCAGGG[C/G]TGCAGTGAGCCATGA | 11169 |
rs770798853 | in-del | -/AAAAA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55013197 | AAGATCCCGTTTCAA[-/AAAAA]AAAAAAAAAAAAAAA | 11169 |
rs770808195 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998458 | TTAATTCACTTTTTG[-/T]TTTTACCAATGTTAC | 11169 |
rs770822692 | snp | A/C | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010550 | TCCGGTAAAAAACAA[A/C]AAACCTTAAAAATCT | 11169 |
rs770823111 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55023487 | ACAGTACATTATCAG[A/G]CAATTCAACTTTTCT | 11169 |
rs770838567 | snp | A/G | 1.66112e-05 | 0.00288189 | missense, intron-variant | WDHD1 | GRCh38.p7 | 14:54995710 | ATAATCCCTTTTGAA[A/G]AAGAAGGGATCTCAA | 11169 |
rs770842839 | snp | A/T | 2.50441e-05 | 0.00353857 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995821 | CTAGATACCTTGAAC[A/T]AATTAATACAAATTA | 11169 |
rs770848832 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54986601 | AGATAGAGCCAACAA[A/C]AAAGTAAAAAGGGAG | 11169 |
rs770913221 | snp | C/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025919 | CCGTCTTCAGATGGC[C/G]TCTCAAGAAACACTT | 11169 |
rs770967134 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948031 | GACCAGCCTGACCAA[C/T]ATGGAGAAACCTCGT | 11169 |
rs771057475 | snp | A/G | 5.02769e-05 | 0.00501358 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54957625 | TCCTTGGCTGCTAAA[A/G]GTAACTGCACCTTTC | 11169 |
rs771060783 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020244 | CTAATTCAAATTCCT[C/T]CCCTTCCATTATCTT | 11169 |
rs771114210 | snp | C/T | 5.01853e-05 | 0.005009 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013636 | AGTCATCGGGCATGG[C/T]GTCTCATGCCTATAA | 11169 |
rs771131331 | in-del | -/A | | | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938512 | CACTCCAGCCTGGGC[-/A]AACAGAAAGACTGTC | 11169 |
rs771140825 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008505 | CTGAATAAAACAAAG[A/G]TTGAAAAGTTGAGTT | 11169 |
rs771151508 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54973076 | CAACTTATGTACTCC[A/G]ATTTATTTATTAGAA | 11169 |
rs771158260 | snp | C/G | 1.64784e-05 | 0.00287035 | missense | WDHD1 | GRCh38.p7 | 14:54991274 | GGCTTTTGCCGGGGA[C/G]TTGGCATGGGTCCAT | 11169 |
rs771159517 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54964614 | ACTGCACTCCAGCCT[A/G]GGCAACAGAGCGAGA | 11169 |
rs771164306 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938938 | TCTTTGGAGTAATTA[A/T]GGCATTGTAATTATG | 11169 |
rs771204476 | snp | A/G | 4.95823e-05 | 0.00497882 | missense | WDHD1 | GRCh38.p7 | 14:54963063 | AGTTTTTGAGCCAGT[A/G]TTAATTTCCGAGAGC | 11169 |
rs771209480 | snp | C/T | 1.68672e-05 | 0.00290402 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002203 | ATTAGAAAAGATAAA[C/T]AACGTAAACAAAAGT | 11169 |
rs771212885 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55007873 | GCAGACTTAACTGTT[C/G]CCTCTGCCAATCTGG | 11169 |
rs771240445 | snp | C/T | 1.67136e-05 | 0.00289076 | missense | WDHD1 | GRCh38.p7 | 14:54955657 | TCAGTTTTATTAGTT[C/T]GAGAATTTCTTTTCT | 11169 |
rs771255542 | snp | C/G | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028637 | ATAGCTACAAAATGC[C/G]TTCACTATAATATCT | 11169 |
rs771261193 | snp | C/T | 1.65086e-05 | 0.00287298 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55010337 | CAATTTTAGTACCAT[C/T]CCCATTAAAGACCAC | 11169 |
rs771263596 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996014 | CCTTATTTCAAATGC[C/G]TTGTAGTCTGGGGAT | 11169 |
rs771266333 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54994632 | CAGGCGTGGTGGCGC[A/T]TGCCTGTAATCCCAG | 11169 |
rs771268548 | in-del | -/AAT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985241 | TTATCACAAAGTTAA[-/AAT]AATGTGATACAGAAT | 11169 |
rs771272564 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015843 | AGCTGGGACTGCAGG[C/G]GTGCGCCACCACACC | 11169 |
rs771277764 | snp | C/G | 1.68289e-05 | 0.00290072 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008765 | AAATGCTAACACAAA[C/G]GCCTCTCCTAAAAGC | 11169 |
rs771293841 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54946348 | TGCACAGCCACCTGG[C/T]TAAAACTGGACATTT | 11169 |
rs771293876 | snp | A/C | 1.6861e-05 | 0.00290348 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54955572 | TGACCTTTGGTTTTC[A/C]GTGTTTTGAGGAGGA | 11169 |
rs771330961 | snp | C/T | 1.66106e-05 | 0.00288184 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981720 | CAACAGAAAAATCAC[C/T]TGGAGACATAGCTAC | 11169 |
rs771402659 | snp | A/G | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55029084 | CTTGTTTTTGCTAGT[A/G]TCATGTTTTCACAAT | 11169 |
rs771410422 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947215 | ATGGTTGCGCATGCC[C/T]GTAATCACAGCTACT | 11169 |
rs771458514 | snp | C/G | 0.000284659 | 0.0119268 | missense | WDHD1 | GRCh38.p7 | 14:54963001 | CTTCTTCCTCTTCCA[C/G]CTGGGTTGCTGTCAA | 11169 |
rs771475796 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54978923 | TTCCCTTTCCAGAAC[A/T]GATGAAATGTCTATT | 11169 |
rs771496445 | snp | C/G | 1.66665e-05 | 0.00288669 | missense | WDHD1 | GRCh38.p7 | 14:54962962 | CTTACCCAGCATTCA[C/G]CTTTTTTCTGAAATC | 11169 |
rs771500865 | snp | C/G | 8.98325e-05 | 0.00670136 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995841 | AATACAAATTATAAA[C/G]TAAAAGTGAATGATT | 11169 |
rs771511351 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | WDHD1 | GRCh38.p7 | 14:54981579 | ATACCAACCACCCAG[C/T]AGTGATCAGATTTTC | 11169 |
rs771547746 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55006111 | TCAAGCGGTCCTCCT[A/G]CCTCAGCCTCCCAAA | 11169 |
rs771608828 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54943442 | CTCTGTCACCCATGC[C/T]GGAGTACAGTGACAC | 11169 |
rs771637033 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54991705 | GCTTACACAGATTTT[C/T]TTTTTAAAGTTCTGT | 11169 |
rs771657965 | snp | C/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026207 | GGAAGCCGTGCAATC[C/G]AGCAGTAGTGCGTAA | 11169 |
rs771661103 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954854 | CCTGCCTCAGCCTTC[C/T]GATTTGCTGGGATTA | 11169 |
rs771663310 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54969923 | TATATGCAATTCACT[A/G]CATCAACAGAATTAA | 11169 |
rs771668517 | snp | C/G | 8.23825e-05 | 0.00641751 | missense | WDHD1 | GRCh38.p7 | 14:54962747 | TCTCACCAGGCTTAT[C/G]TATTTCTGGTTTTTC | 11169 |
rs771685194 | snp | G/T | 1.66302e-05 | 0.00288355 | synonymous-codon, intron-variant | WDHD1 | GRCh38.p7 | 14:54995718 | TTTTGAAAAAGAAGG[G/T]ATCTCAACTGCATTG | 11169 |
rs771686362 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54977317 | ATTGTCTGTAGACCA[A/C]ATACAAAAATAGTTT | 11169 |
rs771690054 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54992807 | TAGTCCTAGCTACCC[A/G]GAAGGCTGAGTGGGA | 11169 |
rs771713401 | in-del | -/CC | 1.68898e-05 | 0.00290596 | frameshift-variant | WDHD1 | GRCh38.p7 | 14:54957601 | TTTACCTTAAAGGGA[-/CC]TTTACTCGTCCTTGG | 11169 |
rs771716229 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54957723 | AGAGTATTTTAATCC[C/G]CATTAAATGAAAACA | 11169 |
rs771741672 | snp | A/T | 6.59163e-05 | 0.00574054 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026810 | TTTACCTATCTGAAA[A/T]TGTTTTATAAAAGCC | 11169 |
rs771757942 | snp | C/G | 1.651e-05 | 0.0028731 | missense | WDHD1 | GRCh38.p7 | 14:54967365 | CGTGGAAGGGTTGGG[C/G]GAAACCGAGAACCTT | 11169 |
rs771786376 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998767 | CTCCGACCCCAATTC[C/T]CCCAATATAGATAGA | 11169 |
rs771802871 | snp | A/G | 1.68221e-05 | 0.00290014 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957643 | AACTGCACCTTTCAC[A/G]AAAAAGAAACCCTTG | 11169 |
rs771861571 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54957879 | CAGATCTTTTATCTT[C/T]TGTTACTGCGGAAGA | 11169 |
rs771875212 | snp | A/G | 3.429e-05 | 0.00414051 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002223 | TAAACAAAAGTTTAC[A/G]TTAAATTGAATTTGA | 11169 |
rs771901948 | snp | C/T | 1.65359e-05 | 0.00287536 | missense | WDHD1 | GRCh38.p7 | 14:54966503 | ATTAAAAGTTCCTGT[C/T]GCTCTTTTGTTGCTT | 11169 |
rs771904356 | snp | C/T | 0.000223669 | 0.0105728 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008401 | ATTTCTCTATAGTCA[C/T]AGCCATAATACTACA | 11169 |
rs771910147 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54964286 | TCAAGATTTTTAGTA[G/T]CATTTATCTATAATC | 11169 |
rs771920339 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025576 | AATTCATCCTCCATG[C/T]ATTTTCTCAAAAACA | 11169 |
rs771946439 | snp | C/T | 1.64779e-05 | 0.00287031 | missense | WDHD1 | GRCh38.p7 | 14:54987250 | CCAATAGTAAACAAT[C/T]GAAGAAGCAGGGCAC | 11169 |
rs771948503 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954035 | TAAATGATGAGCACA[C/G]CACACCAACATGGCA | 11169 |
rs771973802 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012039 | TATCCAGCCACTATG[C/T]ATGATAATACTTACT | 11169 |
rs772006065 | snp | C/T | 3.29674e-05 | 0.00405988 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026661 | TATAAAGTTTAAGGA[C/T]AAATGTTTTAACATT | 11169 |
rs772028635 | snp | A/G | 1.64993e-05 | 0.00287218 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54987374 | AAGAACTAAAGTGCA[A/G]GCAGTGAAGCTTGCT | 11169 |
rs772061657 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55012828 | TGAGGCCAGAGCCCT[A/C]ATGGTCTCATTACTT | 11169 |
rs772107209 | snp | C/G | 1.68522e-05 | 0.00290272 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008768 | TGCTAACACAAAGGC[C/G]TCTCCTAAAAGCTAT | 11169 |
rs772117402 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55021762 | CTTTTTTGCCATACC[C/T]ACAATCTCCTTCATG | 11169 |
rs772155946 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55000392 | CTCAGCATCTACTAT[A/G]GTAACATGAAAGGTA | 11169 |
rs772162708 | in-del | -/CAT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988099 | CACCCATTGCTTTCC[-/CAT]CATAATTTTTTTCTT | 11169 |
rs772178779 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008900 | CTCCCAGGTTCAAGC[C/G]ATTCTCCTGCCTCAG | 11169 |
rs772184774 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951830 | GGGATGCAAGGCTAG[C/T]TCAACATTCGCAAAT | 11169 |
rs772195239 | snp | A/G | 3.29723e-05 | 0.00406018 | stop-gained | WDHD1 | GRCh38.p7 | 14:54941633 | CAACCACACGTTTTC[A/G]CTTCTTTGCTTCAGT | 11169 |
rs772207508 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55022769 | GGTGTCTGGGAATCT[A/G]CTGTCTCTTGGTCAG | 11169 |
rs772210391 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974948 | TCTGCATTTGAGGGG[A/C]CTTTGCTCACATCTC | 11169 |
rs772211011 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54992790 | ATGGTGGCATGCATC[G/T]GTAGTCCTAGCTACC | 11169 |
rs772239593 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54989948 | GGATTATAGGCGTGA[A/G]CCATCACGCCCGGCA | 11169 |
rs772313379 | snp | A/G | 1.70052e-05 | 0.00291587 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981747 | CTACATGTTGTTAAA[A/G]GAACCCTATTTCAAA | 11169 |
rs772322783 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54964891 | TATGTTTCCTTATAT[A/G]TGTTGTACAAATAAA | 11169 |
rs772337041 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54961384 | CCTACACAGATCTGC[A/G]TGACTTGGCTCCTGC | 11169 |
rs772359648 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996107 | ATTTTATTCCTCAGA[A/C]GTCATTCCCTAGAAA | 11169 |
rs772359951 | snp | A/T | 1.64849e-05 | 0.00287092 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54991375 | CTCTTTGAGAAGACT[A/T]GAACCAGTTTTTAGC | 11169 |
rs772366370 | snp | A/C/G | 8.23763e-05 | 0.00641733 | missense | WDHD1 | GRCh38.p7 | 14:54981633 | CATATAGGAGTCCAC[A/C/G]TATTACCAAGTCCTC | 11169 |
rs772379707 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54983586 | GCTGAAGCAGGAGAA[C/T]TGCTGGAACCCGGAA | 11169 |
rs772387287 | in-del | -/AATA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003098 | GGATTAGTAACATAT[-/AATA]AAAACTTTATTTTAA | 11169 |
rs772406154 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54994374 | GTAGCACTGCCATAC[A/G]GACATATAATGTGAG | 11169 |
rs772407051 | in-del | -/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55009993 | CCCAGCTAATTTTTT[-/G]GTATTAGTAGAGACG | 11169 |
rs772591338 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54966023 | CTTTACAAGGGAAAA[C/T]ACCACCAGATAAAAC | 11169 |
rs772602263 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54984424 | GGCTTAAGCCCAGGA[A/G]GTGGAGGTTGCAGTG | 11169 |
rs772637479 | in-del | -/AAG | | | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939596 | TCTGGAAAAAAAAAA[-/AAG]AAGAACACTGGAAAA | 11169 |
rs772688105 | snp | A/G | 0.000165131 | 0.00908505 | missense | WDHD1 | GRCh38.p7 | 14:54963079 | TTAATTTCCGAGAGC[A/G]AGAAGCATATTTAAT | 11169 |
rs772692841 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55014465 | AAATAGGGACCGTAT[A/C]TTCCTTGTCCACCAT | 11169 |
rs772693219 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980876 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCAGATCA | 11169 |
rs772697058 | snp | A/T | 1.66081e-05 | 0.00288163 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991418 | ACAACACAAAGGATC[A/T]TAATTAAGGGAATCA | 11169 |
rs772755043 | in-del | -/ATTACTCATATCATCTCCATCAAAAAGATCATTATAATCCTTTTCCA | 1.6728e-05 | 0.00289201 | frameshift-variant, intron-variant | WDHD1 | GRCh38.p7 | 14:54995753 | TAGAAAATCACCAGC[lengthTooLong]ATTACTCATATCATC | 11169 |
rs772756905 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003233 | AGTTCACATGGGCTG[C/G]GTGTGGTAGCTCAGG | 11169 |
rs772759062 | snp | C/T | 1.64991e-05 | 0.00287215 | missense | WDHD1 | GRCh38.p7 | 14:54984782 | AGAGGAAGAGGGTCA[C/T]CATGCAAAATTTGTT | 11169 |
rs772767825 | snp | A/G | 5.03461e-05 | 0.00501702 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007386 | CATGTCTAATTGGTA[A/G]AAAAAGAAAATTTCT | 11169 |
rs772827383 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967625 | TCTCACATCTCACTT[C/G]ATTTATTTTTTTTGA | 11169 |
rs772893819 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55022018 | GCCCGTAAAGGCCTG[A/T]ATGAACTCCTCATCT | 11169 |
rs772933244 | snp | A/G | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940672 | TTCAAAGTCTTGCTC[A/G]GTAAAGTACTGTTGA | 11169 |
rs772950765 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954799 | CAGCGGTGTGATCTC[A/T]GATGACTGCAATCTC | 11169 |
rs772952119 | snp | A/G | 2.21786e-05 | 0.00332999 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966632 | AAATAAAATTGCTTA[A/G]GGCCAACTATCACCT | 11169 |
rs772990006 | in-del | -/AAAAAA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55013196 | CAAGATCCCGTTTCA[-/AAAAAA]AAAAAAAAAAAAAAA | 11169 |
rs773005112 | snp | G/T | 1.71126e-05 | 0.00292506 | missense | WDHD1 | GRCh38.p7 | 14:54966552 | CATATTCATAACCAT[G/T]TTTAGCTAAATAATC | 11169 |
rs773075177 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993149 | CTGAGACAGGGTCTC[A/G]TTCTGTTACCCTGCC | 11169 |
rs773088704 | snp | C/T | 1.94945e-05 | 0.003122 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010486 | AATTAAGGTAAGAAA[C/T]ATTAGCAAAACAAAT | 11169 |
rs773160680 | snp | A/C/G | 3.40566e-05 | 0.00412642 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991193 | CCTACTAAGAAGTTA[A/C/G]GTGTAGATCCAAGTC | 11169 |
rs773191177 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975506 | GCATCTGCCACCAGG[C/T]CTGGCTAATTTTTGT | 11169 |
rs773215794 | in-del | -/ATTCAA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54955881 | AAAACTACACTTCAG[-/ATTCAA]ATTCCATGTTTTCCT | 11169 |
rs773251565 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019103 | CTCTAAACAAGGCTA[C/T]AGCTAATTTTTTATG | 11169 |
rs773262282 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55018855 | ATGGAGAAACCCCAT[C/T]TCTACTAAAAATACT | 11169 |
rs773274484 | snp | A/C | 1.64765e-05 | 0.00287019 | missense | WDHD1 | GRCh38.p7 | 14:54967327 | AGTAAGGAAGCTTAA[A/C]GGATAATATAGCAAC | 11169 |
rs773303842 | in-del | -/AG | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54946671 | TTTAAAACTTTTGGT[-/AG]AGATGGGGTCTCCCT | 11169 |
rs773309396 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985497 | CGGTAAGAGATGAGG[C/T]TGGAGAGGCAGGCAA | 11169 |
rs773314133 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54961527 | CTTCTGCTCCTGTTC[C/T]CATGCACCTTTGCCT | 11169 |
rs773314219 | in-del | -/AGT | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026414 | ATTTGACAAGTAGGC[-/AGT]AGTAACTAGTGATCT | 11169 |
rs773344977 | snp | A/T | 3.29641e-05 | 0.00405968 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962716 | AGTTCTCATGATTTA[A/T]GGGCTTGAAAATGTA | 11169 |
rs773355666 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010701 | TCTAATTTTTCTTTT[A/G]CTTCTGGTAAGAAAA | 11169 |
rs773371260 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948959 | ACTGTTAGAAGGAAA[A/G]CTAACAAACAAAAAG | 11169 |
rs773372858 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54970416 | CCATTTACAATAGTC[A/T]TACATGTACATAAAA | 11169 |
rs773374028 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947888 | TGAGCCACTGTGCCA[C/G]GCCAAAATTGTGACT | 11169 |
rs773387167 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988536 | TGGGTGCATTTTATT[A/G]TAAATAAATTACATC | 11169 |
rs773388672 | snp | G/T | 1.77662e-05 | 0.0029804 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989227 | CCTACAAACAGGTAA[G/T]ATTAAATATAAGTCT | 11169 |
rs773426387 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54971503 | TGCACACACACAAAA[C/T]ACCTAGGATATATCT | 11169 |
rs773485208 | in-del | -/AGGAAATAATGTT | 2.02632e-05 | 0.00318295 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010495 | AGAAACATTAGCAAA[-/AGGAAATAATGTT]ACAAATCCAAATGAC | 11169 |
rs773529633 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020052 | CTTGACTCTTAATCA[C/T]TGAGTCTCATGAGGT | 11169 |
rs773538762 | snp | C/T | 3.38301e-05 | 0.00411265 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54944467 | CTGGAACCCGGTCTT[C/T]GGCCTAAAATCACAA | 11169 |
rs773540775 | snp | C/T | 1.67497e-05 | 0.00289389 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54962987 | GAAATCTTCTTCTTC[C/T]TCTTCCTCTTCCACC | 11169 |
rs773555951 | in-del | -/TC | 1.64751e-05 | 0.00287007 | frameshift-variant | WDHD1 | GRCh38.p7 | 14:54962775 | TCTTCATCATCAGCT[-/TC]TCTCCACTGTCCTCA | 11169 |
rs773600347 | snp | A/G | 0.000725175 | 0.0190279 | utr-variant-5-prime, synonymous-codon | WDHD1 | GRCh38.p7 | 14:55013518 | TGCCTTTTCTCCAAC[A/G]TTAATGAACTTAGGA | 11169 |
rs773617202 | snp | C/G/T | 3.36486e-05 | 0.00410163 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008557 | TTAGTAGGAAATATA[C/G/T]TTTTAAACATATTCA | 11169 |
rs773617406 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54946191 | TAAACAGCTATTTTT[A/G]AAAAGAAAACCAAAA | 11169 |
rs773630939 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55006797 | ATCTTGAAAAAGTTC[A/T]AATGTTTCTTAAAGC | 11169 |
rs773659240 | snp | A/C | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027681 | TGGCATCCTTCGTGC[A/C]CTCACCTTGTCGCTT | 11169 |
rs773667062 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54945397 | CTCATTTAAATGACA[A/G]TAACACTATGAGATG | 11169 |
rs773667099 | snp | A/G | 1.65444e-05 | 0.00287609 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962877 | AAATAATATTATTCA[A/G]TAAAGAGCTATGCAA | 11169 |
rs773684051 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993203 | GCTCACTGCAGCCTC[A/G]ACCTCTCGGGCTCAA | 11169 |
rs773700665 | snp | C/T | 0.000188299 | 0.00970124 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995855 | AGTAAAAGTGAATGA[C/T]TTAGAAAAACTCAAT | 11169 |
rs773723572 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954935 | GGTTTCTCCATGTTG[A/G]TCAGGCTGGTCTCGA | 11169 |
rs773728020 | snp | G/T | 4.94336e-05 | 0.00497135 | missense | WDHD1 | GRCh38.p7 | 14:54981562 | GCTGGGGATTTTCAT[G/T]GATACCAACCACCCA | 11169 |
rs773772728 | snp | A/G | 1.6596e-05 | 0.00288058 | missense | WDHD1 | GRCh38.p7 | 14:54995659 | CTAGGACGACCTGAA[A/G]CCATCATGAGGTCTT | 11169 |
rs773785669 | in-del | -/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963186 | AGCTAATCCAAAAAG[-/G]GGGGGGGGGGGGAGA | 11169 |
rs773837777 | snp | C/G | 1.64795e-05 | 0.00287045 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962733 | GGCTTGAAAATGTAT[C/G]TCACCAGGCTTATGT | 11169 |
rs773839239 | snp | C/T | 1.65332e-05 | 0.00287512 | missense | WDHD1 | GRCh38.p7 | 14:54984839 | TGAACTCCAAGGCAC[C/T]GATCCCCATCAAATC | 11169 |
rs773867943 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980358 | TTCAGTGGTTTTTTT[A/G]TATATTCACAGAATT | 11169 |
rs773887393 | in-del | -/AA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54943570 | GCCAGGCTAATTTTT[-/AA]AAATTTTTGTAGAGA | 11169 |
rs773891221 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | WDHD1 | GRCh38.p7 | 14:54967299 | ATTTGTCCTTTCTCT[A/G]TTGCAATCTGACAGT | 11169 |
rs773895399 | snp | A/C | 1.75514e-05 | 0.00296233 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007420 | CTTTATGAAAATCCC[A/C]CCCAAAATATATGCA | 11169 |
rs773896002 | snp | C/G | 1.66197e-05 | 0.00288263 | missense, intron-variant | WDHD1 | GRCh38.p7 | 14:54995713 | ATCCCTTTTGAAAAA[C/G]AAGGGATCTCAACTG | 11169 |
rs773916091 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990788 | GAGTGAGGAAAAGGG[-/T]CAGACTTTTCCCCCC | 11169 |
rs773951042 | snp | C/T | 1.71211e-05 | 0.00292579 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008380 | GCCTGCAGGAATAAA[C/T]AATACATTTCTCTAT | 11169 |
rs773976515 | snp | A/G | 6.59837e-05 | 0.00574348 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944310 | TTCACTAAGATCTCA[A/G]TCTCGGCACAATTAT | 11169 |
rs773980749 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54968461 | GGAAACTAGATAAAC[A/G]AGAACACACTAACCC | 11169 |
rs773989378 | snp | C/T | 4.94539e-05 | 0.00497238 | missense | WDHD1 | GRCh38.p7 | 14:54957158 | AAAATATTAGTTGAA[C/T]GTGCTGAATTCATTG | 11169 |
rs774002059 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54991620 | AGTGGCACCTAACTG[G/T]ATTAGTCGTTACTGC | 11169 |
rs774079174 | snp | C/T | 1.64846e-05 | 0.0028709 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55013543 | TTAGGATCATCATCA[C/T]CCAAGTCTTCCCAAA | 11169 |
rs774104416 | snp | A/T | 1.77099e-05 | 0.00297568 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963202 | GGGGGGGGGGGGAGA[A/T]CAAATAACATCAAGT | 11169 |
rs774145970 | in-del | -/AA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015379 | GCATGACACTGTCTC[-/AA]AAAAAAAAAAAAAAA | 11169 |
rs774160091 | snp | A/G | 1.65743e-05 | 0.00287869 | missense | WDHD1 | GRCh38.p7 | 14:54962542 | GTACTTTTGGAAAAC[A/G]AGTTCTGTCCTACAG | 11169 |
rs774190937 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54961767 | CTCCCCACCAAAAAA[A/G]GGCCAGCAGTGCCTT | 11169 |
rs774204927 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54952723 | AAGCTGGAGGCATCA[C/T]GCTACCTGACTTCAA | 11169 |
rs774270841 | snp | G/T | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010563 | AAAAAACCTTAAAAA[G/T]CTAGTTCATATCAAG | 11169 |
rs774278032 | snp | A/G | 1.65261e-05 | 0.0028745 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987133 | AAGTCATAAAAGACT[A/G]AAAAAAATCTACCTC | 11169 |
rs774291560 | snp | G/T | 8.23771e-05 | 0.0064173 | missense | WDHD1 | GRCh38.p7 | 14:54981582 | CCAACCACCCAGTAG[G/T]GATCAGATTTTCCTT | 11169 |
rs774296740 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54970991 | ACAAGGAACTGGGAA[A/T]GGAATCCCTACTCAA | 11169 |
rs774303702 | snp | A/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026100 | AAAGGAGGAAAAGAC[A/T]GTGTCTGGTTCGCTC | 11169 |
rs774340731 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54973129 | CACACTATAAATACC[A/G]CAGGCAAATTTCATA | 11169 |
rs774359492 | snp | C/T | 1.64904e-05 | 0.00287139 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008684 | GTTTTCTGTTGGCTG[C/T]TATCCATCACATCCA | 11169 |
rs774367392 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55007875 | AGACTTAACTGTTCC[C/T]TCTGCCAATCTGGAG | 11169 |
rs774370269 | snp | A/G | 6.6706e-05 | 0.00577482 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010512 | CAAATCCAAATGACT[A/G]GGAGTCTCTCCATAG | 11169 |
rs774374615 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963968 | AATAAATTAGCTGGG[C/T]GTGGTGGCATGCACC | 11169 |
rs774395338 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011959 | TAGCCAGAAATGACT[A/G]TGTACATTCTAATTT | 11169 |
rs774401108 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998901 | AGTATGCCAAACTTA[G/T]GAAGTGTGCTAGACA | 11169 |
rs774431101 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020535 | TATCCTTGAACCTCT[A/T]TTCTTACCTATATTT | 11169 |
rs774464778 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948417 | ATATCCCACTCCTGG[C/T]TCAGAGGGTCCCATG | 11169 |
rs774476139 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990589 | CAACAGAGCGAGACT[C/G]CATCTCAAAAAAAAA | 11169 |
rs774480923 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54971605 | AATGGAAAGACATTT[A/G]CAGATCCTGAGGTGG | 11169 |
rs774491092 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54994663 | CTACTCAGGAGGCTG[A/T]GGCACAAGAATCACT | 11169 |
rs774541445 | snp | A/C | 1.66338e-05 | 0.00288386 | missense | WDHD1 | GRCh38.p7 | 14:54967388 | AGAACCTTTACAAGG[A/C]ATGCACCTGTTAGTA | 11169 |
rs774582429 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54992383 | TAATCCCAGCTACTC[A/C]GGAGGCTGAGGCAGG | 11169 |
rs774592096 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54945598 | TATGCTGGAGTACAG[G/T]GGCTCTGTATTGGCT | 11169 |
rs774622630 | snp | G/T | 1.64779e-05 | 0.00287031 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54991276 | CTTTTGCCGGGGAGT[G/T]GGCATGGGTCCATCA | 11169 |
rs774643579 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54946427 | GTAATTCCTTAAAAT[C/T]TCAAAAGTAAGTTTT | 11169 |
rs774683045 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55004981 | CAACCTCAGGTTGAG[A/G]AGCACCGAACTCAGG | 11169 |
rs774690721 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008569 | ATATTTTTAAACATA[C/T]TCAGGAAAAACACAA | 11169 |
rs774692841 | snp | A/G | 1.6834e-05 | 0.00290116 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957239 | TAGCACTGTATGTTT[A/G]AAGAAGAAAAATAAA | 11169 |
rs774745123 | snp | A/G | 1.69189e-05 | 0.00290846 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002207 | GAAAAGATAAACAAC[A/G]TAAACAAAAGTTTAC | 11169 |
rs774745273 | snp | G/T | 6.68695e-05 | 0.00578189 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991207 | AAGTGTAGATCCAAG[G/T]CTTACCATGAATCTG | 11169 |
rs774746054 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996055 | TATAGGGACTGACAT[A/G]TAAACAAATACTGTA | 11169 |
rs774752625 | snp | A/T | 1.67217e-05 | 0.00289147 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000463 | TCCATATGATCACAG[A/T]AACATTTTGAAGAAA | 11169 |
rs774759876 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947247 | AGGAGGCTGAGACAG[A/G]AGAATCACTTGAACC | 11169 |
rs774764897 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016032 | TATCAGCAGATGCAC[C/T]GGAGGAGACGTACAA | 11169 |
rs774772732 | snp | A/G | 6.86436e-05 | 0.00585808 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987397 | AGCTTGCTAAAAATT[A/G]AAACAAGACAGAAAC | 11169 |
rs774802718 | snp | A/G | 1.66796e-05 | 0.00288782 | missense | WDHD1 | GRCh38.p7 | 14:54955585 | TCAGTGTTTTGAGGA[A/G]GACATATAGCTGGGG | 11169 |
rs774828027 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000567 | CCTAGATTTCCTTCC[A/G]CATCAGTATACGATA | 11169 |
rs774871349 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55023719 | GTGTTTTAAGCAGAT[A/G]CAACCTCATACAGTG | 11169 |
rs774872199 | snp | A/G | 0.000488269 | 0.0156172 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008766 | AATGCTAACACAAAG[A/G]CCTCTCCTAAAAGCT | 11169 |
rs774885295 | snp | A/C | 1.65201e-05 | 0.00287398 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54963071 | AGCCAGTATTAATTT[A/C]CGAGAGCGAGAAGCA | 11169 |
rs774901132 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002609 | ACTTTAAATATGATT[A/T]CTTTTTTTTCCCCCA | 11169 |
rs774913360 | snp | A/C | 4.9467e-05 | 0.00497303 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55013560 | CAAGTCTTCCCAAAT[A/C]CTCACATCACCATCA | 11169 |
rs774936839 | snp | A/T | 1.65916e-05 | 0.00288019 | stop-gained | WDHD1 | GRCh38.p7 | 14:54944444 | CTTCTATTTTCTTCT[A/T]ACCACATCTGGAACC | 11169 |
rs774955499 | in-del | -/T | 1.64749e-05 | 0.00287005 | frameshift-variant | WDHD1 | GRCh38.p7 | 14:54991350 | GCCTTCTTGACCATC[-/T]TTCCTCCTCCTCTTT | 11169 |
rs774961197 | snp | C/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025605 | CAAACCTGATCACAT[C/G]TCTCTGCTTCAAGCC | 11169 |
rs775008910 | in-del | -/TAGCTAAATAATCAAGGTGGTTTTG | 1.71596e-05 | 0.00292908 | frameshift-variant | WDHD1 | GRCh38.p7 | 14:54966554 | ATTCATAACCATTTT[-/TAGCTAAATAATCAAGGTGGTTTTG]TAGCTAAATAATCAA | 11169 |
rs775056853 | snp | A/G | 1.64779e-05 | 0.00287031 | stop-gained | WDHD1 | GRCh38.p7 | 14:54987251 | CAATAGTAAACAATC[A/G]AAGAAGCAGGGCACT | 11169 |
rs775082916 | in-del | -/A | 0.00119346 | 0.0243989 | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941450 | TATTCAAAGATGAGT[-/A]AAAAAAAATCCATTA | 11169 |
rs775084538 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54957836 | TGAACCACCCCAACG[A/T]GCCACTATGAAACAT | 11169 |
rs775130952 | snp | C/T | 3.295e-05 | 0.00405881 | missense | WDHD1 | GRCh38.p7 | 14:54991304 | TCATAAAATGGCCTT[C/T]GGGATGTTACAAGTG | 11169 |
rs775138773 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54964425 | ACAGGTGGATCACAA[A/G]GTCAGGAGATCGAGA | 11169 |
rs775155938 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954902 | GCCTGGCTAATTTTG[G/T]ATTTTTAATAGAGAC | 11169 |
rs775192726 | snp | C/T | 3.33472e-05 | 0.0040832 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995848 | ATTATAAAGTAAAAG[C/T]GAATGATTTAGAAAA | 11169 |
rs775204680 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54943463 | ACAGTGACACAATCA[C/T]GGCTCACTGCAGCCT | 11169 |
rs775209858 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54962903 | TGCAAAGACCAACTT[A/G]ACATTCAAGACAGTA | 11169 |
rs775240435 | in-del | -/GGC | 1.68661e-05 | 0.00290392 | cds-indel | WDHD1 | GRCh38.p7 | 14:54957603 | TACCTTAAAGGGATT[-/GGC]TACTCGTCCTTGGCT | 11169 |
rs775242426 | snp | A/G | 1.68474e-05 | 0.00290231 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957648 | CACCTTTCACAAAAA[A/G]GAAACCCTTGCTTAA | 11169 |
rs775249146 | snp | C/T | 1.65386e-05 | 0.00287559 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54966505 | TAAAAGTTCCTGTTG[C/T]TCTTTTGTTGCTTGA | 11169 |
rs775267826 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54958110 | GTCACCATTTTCTCT[C/T]GCCTCCTCCATCCAG | 11169 |
rs775277440 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54971879 | CAAAGGACATGAACA[A/G]ACACTTTTCAAAAGA | 11169 |
rs775309673 | snp | A/T | 1.66294e-05 | 0.00288347 | missense, intron-variant | WDHD1 | GRCh38.p7 | 14:54995720 | TTGAAAAAGAAGGGA[A/T]CTCAACTGCATTGTC | 11169 |
rs775309889 | snp | C/T | 1.64811e-05 | 0.00287059 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008654 | CTTAAAACAGGGGCA[C/T]CATGTCCTCGAAATG | 11169 |
rs775324197 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012060 | AATACTTACTTCTCA[A/G]AGCCCTCACTATTAC | 11169 |
rs775365350 | snp | C/T | 4.07009e-05 | 0.00451096 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957552 | TTCTTTGTATACAAA[C/T]GTATTTAAATAATAT | 11169 |
rs775370465 | snp | C/G/T | 3.29621e-05 | 0.00405958 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55010375 | GCATTTGTAGTGAAG[C/G/T]GAGTCAATATACCAT | 11169 |
rs775428591 | snp | C/T | 3.29614e-05 | 0.00405951 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026673 | GGATAAATGTTTTAA[C/T]ATTTGCACCTAAAAC | 11169 |
rs775445552 | in-del | -/TTGT | 6.6223e-05 | 0.00575388 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026690 | TTTGCACCTAAAACG[-/TTGT]TTCTCAAAGAACCTT | 11169 |
rs775469379 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55021408 | GTCTATTAGCGTTCC[-/T]TTTTTTTTTTTTTGG | 11169 |
rs775477580 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019249 | ATTATCTTACATATG[C/T]TAACATTTAGATCAT | 11169 |
rs775488138 | snp | A/G | 1.64819e-05 | 0.00287066 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000587 | AGTATACGATATTCG[A/G]CCACAAGTAGGATGC | 11169 |
rs775519110 | snp | C/T | 6.60633e-05 | 0.00574694 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002090 | TCACTTTGTAAAACC[C/T]ACCTGAGAGATGAAA | 11169 |
rs775522802 | in-del | -/C | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028164 | CCCTATTGTTTTTTT[-/C]AATCTAGTTCCATTG | 11169 |
rs775526469 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55000431 | AGAAAGTAAGGCAGT[C/T]TGTGGTGTCTTCCAA | 11169 |
rs775546290 | snp | C/T | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54940747 | ACTGCAATACTGTCA[C/T]AGCAGTGTCTTCAGT | 11169 |
rs775586928 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54982366 | AATCAGAAGGCTCCC[G/T]CTTGAGAAACATTTA | 11169 |
rs775612803 | snp | G/T | 3.44424e-05 | 0.0041497 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010261 | AAACAAATAAACAAG[G/T]CCTTTTGTTCTAACA | 11169 |
rs775629587 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960525 | TATTATTTTAGATGA[A/T]GTCTCACTCTGTCAC | 11169 |
rs775702763 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997176 | TCTTGGCTCACTGCA[A/G]ACTTCATCTCCCAGG | 11169 |
rs775753988 | snp | A/G | 1.66866e-05 | 0.00288842 | missense | WDHD1 | GRCh38.p7 | 14:54941536 | TTCTGATTTGTAGAA[A/G]AATCTAAAGGTTTCT | 11169 |
rs775780969 | snp | C/G | 4.94605e-05 | 0.0049727 | missense | WDHD1 | GRCh38.p7 | 14:54991376 | TCTTTGAGAAGACTA[C/G]AACCAGTTTTTAGCA | 11169 |
rs775821999 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55017509 | CACCCACACCTGGCT[A/G]AATTTCGTATTTTCA | 11169 |
rs775891082 | in-del | -/TTGGAAAATTACCTT | 1.67953e-05 | 0.00289782 | cds-indel, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000632 | ATTGCATAACCTTTC[-/TTGGAAAATTACCTT]TCATGTTTCACCCTA | 11169 |
rs775918333 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005028 | TCACCCTGAAATTCC[C/T]CCTTGGTCACAGCCT | 11169 |
rs775921985 | snp | C/T | 9.43841e-05 | 0.006869 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966646 | AAGGCCAACTATCAC[C/T]TTAATATGAGGCAAG | 11169 |
rs775968467 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005437 | CTTCAGCATGGCCTT[C/T]GGACCAGTATTCCTG | 11169 |
rs775974945 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54968650 | AAGAGGGAAGCTCCA[C/T]ATAAGCACAATCAGA | 11169 |
rs775996424 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967806 | TTGTATTTTCAGTAG[C/T]GATGGGGTTTTGCCA | 11169 |
rs776005256 | snp | C/G | 1.95356e-05 | 0.00312529 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000663 | AAAATTAAAAAGTAG[C/G]TTCTAAAAATACTGT | 11169 |
rs776094196 | snp | A/G | 1.69902e-05 | 0.00291458 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966428 | AGAAATTCAACCTAT[A/G]GAAAAGCATTTAACT | 11169 |
rs776097151 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002321 | GTTTCTGTTTTTAAG[-/A]GACGGTGTCTCACTA | 11169 |
rs776103574 | in-del | -/TTAAAGGGCCTCATAAAAAGAAT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54981465 | AAAAGACAAATACAC[-/TTAAAGGGCCTCATAAAAAGAAT]TTCAACATACTTTTT | 11169 |
rs776168307 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54956537 | CAACTCCTCGGGAGG[C/T]TGAGGCATGAGAATT | 11169 |
rs776175473 | snp | A/C | 3.31587e-05 | 0.00407164 | missense | WDHD1 | GRCh38.p7 | 14:54966520 | CTCTTTTGTTGCTTG[A/C]TTTTTAGTGCTCTCT | 11169 |
rs776192305 | snp | C/T | 1.64757e-05 | 0.00287012 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026682 | TTTTAACATTTGCAC[C/T]TAAAACGTTGTTTCT | 11169 |
rs776200347 | in-del | -/C | 1.74977e-05 | 0.00295779 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963193 | CAAAAAGGGGGGGGG[-/C]GGGGGAGATCAAATA | 11169 |
rs776260273 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002419 | GGGACTACAGGCATA[C/T]ACCACTGTGCCAGGC | 11169 |
rs776324852 | in-del | -/G | 4.99455e-05 | 0.00499702 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962584 | CAATATAATGTAAAT[-/G]GGGGAAAATATAGTC | 11169 |
rs776329139 | snp | A/C/T | 3.41607e-05 | 0.00413273 | missense | WDHD1 | GRCh38.p7 | 14:54955561 | TCTCTATGTACTGAC[A/C/T]TTTGGTTTTCAGTGT | 11169 |
rs776343206 | snp | C/G | 1.65064e-05 | 0.00287279 | missense | WDHD1 | GRCh38.p7 | 14:54991389 | TAGAACCAGTTTTTA[C/G]CATTGAAATATCTAC | 11169 |
rs776350326 | snp | A/C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954248 | CCAAGATCGTGCCAA[A/C/T]GCACTCCAGCCTGGG | 11169 |
rs776429190 | snp | A/G | 1.64787e-05 | 0.00287038 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000533 | CTTTCCACTGGGGTC[A/G]CAAACATTCTCTAGA | 11169 |
rs776466373 | in-del | -/TTATCTTCTG | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54957872 | GTATGTACAGATCTT[-/TTATCTTCTG]TTACTGCGGAAGAGT | 11169 |
rs776482249 | snp | C/T | 3.32851e-05 | 0.00407939 | missense | WDHD1 | GRCh38.p7 | 14:54941551 | AAATCTAAAGGTTTC[C/T]GCTTTTTAGACAAAT | 11169 |
rs776563344 | snp | C/T | 1.64844e-05 | 0.00287087 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000941 | TTAGACCATTAATAC[C/T]ACCTGCAGCTAAATA | 11169 |
rs776583270 | snp | A/C | 0.000282892 | 0.0118898 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007273 | AAGAAAAATAAGAAT[A/C]ACTTACCTTCCCACT | 11169 |
rs776615718 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55007946 | TGCATTTGAATAAAC[C/T]GTATATGTGACTCTC | 11169 |
rs776616159 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948386 | ATGGTCTTAGCAAAC[A/G]GCACACCAGGAGATT | 11169 |
rs776616525 | snp | A/G | 1.82627e-05 | 0.00302175 | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55010466 | GTTTTCCACTCTAAA[A/G]GAAAAATTAAGGTAA | 11169 |
rs776643538 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55004977 | TCTGCAACCTCAGGT[C/T]GAGGAGCACCGAACT | 11169 |
rs776664756 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997511 | AATACTTGATATGAG[G/T]AAATTAATAACTAAG | 11169 |
rs776671818 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55021864 | ATTTGTTTCGGGCTC[A/G]ATGGCCTTCAGAGCT | 11169 |
rs776710009 | snp | C/T | | | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55007319 | AAGTCTGCAGATTGA[C/T]TTTGCATTTATCACA | 11169 |
rs776715227 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947515 | TAAGATATACTTTAT[C/T]ATTATTTTTCTCCCT | 11169 |
rs776722857 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54968972 | AATTGAGCTTGGGAG[A/G]TTGAGGCTGCAGTGA | 11169 |
rs776789497 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54983755 | AACTCCTGGGCTCAA[C/G]TGATCCTCCTGCCTC | 11169 |
rs776847144 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54985201 | GGTAGAAGACAAATT[A/T]AAAAACACAAAAAGA | 11169 |
rs776945408 | snp | A/G | 1.65141e-05 | 0.00287346 | missense | WDHD1 | GRCh38.p7 | 14:54967366 | GTGGAAGGGTTGGGG[A/G]AAACCGAGAACCTTT | 11169 |
rs776952671 | snp | C/T | 1.76468e-05 | 0.00297037 | missense | WDHD1 | GRCh38.p7 | 14:54963165 | TCTCGCTCCAGTTTA[C/T]AAGAAAGCTAATCCA | 11169 |
rs776961781 | in-del | -/AG | 1.65844e-05 | 0.00287957 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008732 | TCACTAAGAACAAAA[-/AG]AGTAACGCAAATGAA | 11169 |
rs776990167 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54984875 | CCTAATGAGAAAATG[C/T]AAATATAAATCAGGC | 11169 |
rs777003411 | snp | A/G | 3.30535e-05 | 0.00406518 | missense | WDHD1 | GRCh38.p7 | 14:54963096 | GAAGCATATTTAATG[A/G]CTAAATTCACAGCAT | 11169 |
rs777022313 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54962757 | CTTATGTATTTCTGG[C/T]TTTTCTTCATCATCA | 11169 |
rs777034162 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55017704 | AAGTACTTGAATTTG[A/G]AATTACAATTCATGA | 11169 |
rs777071898 | snp | A/G | 3.29506e-05 | 0.00405884 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54967313 | TGTTGCAATCTGACA[A/G]TAAGGAAGCTTAAAG | 11169 |
rs777119529 | snp | A/C/T | 3.92459e-05 | 0.00442964 | intron-variant | WDHD1 | GRCh38.p7 | 14:54989257 | TGAGAAAAACTGAAG[A/C/T]TCCTAGAATCAGTAA | 11169 |
rs777157520 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54991845 | AAAAAACACATGCCA[A/G]ATAAACTACGGTTAT | 11169 |
rs777166055 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988061 | AAAATATTTTCTTTT[C/G]TTTTGAAAAGAAAAA | 11169 |
rs777190712 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026374 | AGGCATGGAAGGATA[C/T]CATTCCAAACAGAAC | 11169 |
rs777198934 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54942010 | AATCCCAGCACTTTG[A/G]GAGGCCGAGGTGGGT | 11169 |
rs777270437 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54939586 | GTCCCAATTCTCTGG[-/A]AAAAAAAAAAAAGAA | 11169 |
rs777274148 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947133 | TCACCTGAGGTCAGG[A/G]GTTCAAGACCAGCCT | 11169 |
rs777299947 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54943656 | TCCTGCCTTGGCCTC[C/G]CAAAGTGCTAGGATT | 11169 |
rs777320118 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54968255 | AGTAAACAACATACT[C/T]CAGAATGACTTTTGA | 11169 |
rs777335892 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015915 | TGTTGGCCAGGCTGG[C/T]CTTGAACTCCTGACC | 11169 |
rs777340784 | snp | A/G | 1.64798e-05 | 0.00287047 | missense | WDHD1 | GRCh38.p7 | 14:54957134 | TTGGATGATTTGCCC[A/G]TATTGTCTAAAATAT | 11169 |
rs777346365 | in-del | -/GT | 1.6476e-05 | 0.00287014 | frameshift-variant | WDHD1 | GRCh38.p7 | 14:54989126 | TAAGTGTGTTGCATG[-/GT]GTATGGAGGTATCAT | 11169 |
rs777349691 | snp | G/T | 1.64789e-05 | 0.0028704 | missense | WDHD1 | GRCh38.p7 | 14:54957113 | CGACTAAGTGCAGTG[G/T]ATTTCTTGGATGATT | 11169 |
rs777375220 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54956233 | GCCACTATTAAATAC[A/G]AATATACATCAGAAC | 11169 |
rs777388267 | snp | C/T | 1.6476e-05 | 0.00287014 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967272 | GTCAAGGTAAGACTT[C/T]CACATACCTCCATTT | 11169 |
rs777415376 | in-del | -/GA | 1.65642e-05 | 0.00287782 | frameshift-variant, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55002095 | TTGTAAAACCTACCT[-/GA]GAGATGAAATTATCT | 11169 |
rs777473861 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54983040 | GTGGTGGTATGTGCC[C/T]GTAGTCCCAGATACT | 11169 |
rs777509066 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55004543 | CTGCAACCTCCGCCT[C/T]CTGGGTTCAAGCAAT | 11169 |
rs777518955 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55006669 | CCAAAATGTTAGGTA[C/T]TAATGGTGAGAATGG | 11169 |
rs777539662 | snp | C/T | 0.000351636 | 0.013255 | synonymous-codon, intron-variant | WDHD1 | GRCh38.p7 | 14:54995811 | TTCCACTCTGCTAGA[C/T]ACCTTGAACAAATTA | 11169 |
rs777563045 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54969655 | GAACTGGTACCAGTC[C/T]TACTGAAAATATTCC | 11169 |
rs777601480 | snp | A/G | 5.10547e-05 | 0.0050522 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008358 | AGATCCATCACAACT[A/G]GCTGATGCCTGCAGG | 11169 |
rs777616054 | snp | A/C | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55025812 | CCTGGCCCCATTGGG[A/C]CTTTACACACAGTAT | 11169 |
rs777616778 | in-del | -/TATT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54969034 | GTAAGACCTTGTTTC[-/TATT]TATTTATTTATTTAT | 11169 |
rs777635617 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005753 | GGATCCTTCTCTGGG[C/T]AGTGCAGAAAGCCCT | 11169 |
rs777647240 | snp | C/T | 1.65315e-05 | 0.00287498 | missense | WDHD1 | GRCh38.p7 | 14:54944426 | TTGTCAGACAAAATA[C/T]TACTTCTATTTTCTT | 11169 |
rs777671336 | snp | C/T | 1.65507e-05 | 0.00287664 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008601 | AAGAGAAGGAAAAAA[C/T]AATTACCAGAAAGAT | 11169 |
rs777681218 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55000296 | AAAGGCATTATATGG[A/G]GAGAAAAAAGTTTCT | 11169 |
rs777697391 | snp | G/T | 1.67013e-05 | 0.0028897 | intron-variant | WDHD1 | GRCh38.p7 | 14:54957226 | AGCAAACTAGTGTTA[G/T]CACTGTATGTTTAAA | 11169 |
rs777718809 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008823 | TTTTTCTTTTTGAGA[C/T]GGAGTCTCACTCTGT | 11169 |
rs777720111 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974061 | GAGTTTCCTGGAAAC[C/T]ATGTGCATAAACCAC | 11169 |
rs777733614 | snp | A/C | 1.66012e-05 | 0.00288103 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962933 | AAAGGAAAATTCAAA[A/C]AACTAAATTATTTCT | 11169 |
rs777769448 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54976599 | CCCGAACTTCCATGT[A/C]CCGCTATCCACAGAA | 11169 |
rs777786564 | snp | A/G | 1.64808e-05 | 0.00287057 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54962826 | TCTGAACCTTGGTTG[A/G]CTCCACTCTGTAGCA | 11169 |
rs777789717 | in-del | -/CAC | 0.000200337 | 0.0100064 | cds-indel, intron-variant | WDHD1 | GRCh38.p7 | 14:54995747 | TGTCATTTAGAAAAT[-/CAC]CAGCATTACTCATAT | 11169 |
rs777833940 | in-del | -/TT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55000740 | GAAAGAATAAATGAC[-/TT]TTGACAATAATTTAT | 11169 |
rs777887532 | snp | C/T | 1.66899e-05 | 0.00288871 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966461 | AACGTTTTCAGTATA[C/T]TTATTTTACTCACCG | 11169 |
rs777898164 | snp | A/G | 1.88988e-05 | 0.00307393 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944521 | AAGACAGAGTTTAAA[A/G]TGCCTCATGATTTTA | 11169 |
rs777932827 | snp | C/G | 1.64757e-05 | 0.00287012 | missense | WDHD1 | GRCh38.p7 | 14:54987326 | TATCCTCATTCTGAG[C/G]CAAGTCTATTATCCA | 11169 |
rs777969806 | snp | C/T | 1.65504e-05 | 0.00287662 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981705 | GGGGTACCTAAACAC[C/T]AACAGAAAAATCACT | 11169 |
rs777977455 | in-del | -/AAAAAAAAAAAAAAA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54972554 | AAGCAAGACTGTCAC[-/AAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 11169 |
rs777979268 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967090 | CTTTGTAGACAAAGT[A/C]CCTGGAAGCAGTGAT | 11169 |
rs777986168 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54989442 | ATACATATATACTTA[C/T]TAATTAGCAAATAGA | 11169 |
rs777996917 | snp | C/T | 1.66682e-05 | 0.00288684 | intron-variant | WDHD1 | GRCh38.p7 | 14:55002189 | AATTGCCAGTAACTA[C/T]TAGAAAAGATAAACA | 11169 |
rs777999647 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55002073 | ATAGCCCACTGAAAG[C/T]GTCACTTTGTAAAAC | 11169 |
rs778015504 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015442 | CCTCTTCTTTGTACT[C/T]CCAGCTTCTGCCATG | 11169 |
rs778031896 | in-del | -/AC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54950264 | ATGTCATGTGCAGAG[-/AC]ACACATAAGCTCAAA | 11169 |
rs778034445 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54949174 | TTTGACGAGTTGAGA[C/G]AAGAAGGCTTCAGAC | 11169 |
rs778051192 | snp | A/G | 1.67211e-05 | 0.00289142 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013632 | TTAAAGTCATCGGGC[A/G]TGGTGTCTCATGCCT | 11169 |
rs778077406 | in-del | -/GTTT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988220 | CTAGTACATTTTTTG[-/GTTT]GTTTTTCCGTTTTTT | 11169 |
rs778093004 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | WDHD1 | GRCh38.p7 | 14:54991347 | TGCTGCCTTCTTGAC[C/T]ATCTTCCTCCTCCTC | 11169 |
rs778114177 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015792 | CAACCTCTGCCTCCC[A/G]GGTTCAAGTGATTCT | 11169 |
rs778114726 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954546 | AAAATTATTCATTGC[A/C]GTACTGTCTGTACTA | 11169 |
rs778115860 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54976697 | ATACTGAGAAGTGTT[G/T]CTTCCAATCTTTGAA | 11169 |
rs778206997 | in-del | -/AG | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948889 | TGCTGATACCCAGGC[-/AG]AGTCTGGAGTGGGCC | 11169 |
rs778211907 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54992229 | GGCACAGTGGCTCAG[G/T]CCTGTAATCCCAGCA | 11169 |
rs778262544 | snp | A/T | 1.91904e-05 | 0.00309755 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967440 | ATTTACTAACATGTC[A/T]TAAAAACTACAAAAT | 11169 |
rs778270647 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54961059 | ATCCTTCCACCTTGG[C/G]CTCTCAAAATGCTGA | 11169 |
rs778299008 | in-del | -/TT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55022284 | AGTTTATCTTTTCCC[-/TT]TTCAAGGCCCGGGGG | 11169 |
rs778352315 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948785 | GACACCTCACACGGC[C/T]GGGTACCCCTCTGAG | 11169 |
rs778369530 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55010011 | ATTAGTAGAGACGGG[A/G]TTTTGCCATGTTGGC | 11169 |
rs778414691 | snp | A/G | 3.36118e-05 | 0.00409936 | stop-gained | WDHD1 | GRCh38.p7 | 14:54957609 | TAAAGGGATTTACTC[A/G]TCCTTGGCTGCTAAA | 11169 |
rs778456966 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54957507 | CATGCCTCCAAGTCT[A/G]GGGAGAGTCATCTCA | 11169 |
rs778459077 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954725 | AGTATAAAGAAGTTC[-/T]TTTTGTTTTTTTGGT | 11169 |
rs778493279 | snp | G/T | 1.65108e-05 | 0.00287317 | missense | WDHD1 | GRCh38.p7 | 14:54991239 | GAGTGAGATGCAACG[G/T]TGTAGAACCTGACTG | 11169 |
rs778496517 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55007125 | CCCAGCTACTCGGGA[A/G]GCTGAGGCAGGAGAA | 11169 |
rs778501980 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54943142 | TGAGGATTTAACTGG[G/T]ACACCACACACATTC | 11169 |
rs778537780 | in-del | -/CT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024019 | TGCACTCATGACATA[-/CT]TTTTCTTAATTTTTC | 11169 |
rs778543841 | in-del | -/AAAAAAAAAAAAAG | 3.07489e-05 | 0.00392091 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007237 | CATCTCTAATAAAAA[-/AAAAAAAAAAAAAG]AAAAGAAAAGAAAAA | 11169 |
rs778548364 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55005955 | CTGCAGCCTTAATCT[C/G]CTGGGCTCAAGTGAT | 11169 |
rs778549850 | snp | A/G | 3.29717e-05 | 0.00406015 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55008633 | TCCTTAGGATCAAAG[A/G]AAAGACTTAAAACAG | 11169 |
rs778551736 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54984350 | AAATACAAAAATTAG[C/G]TAGGCATGGTGGCAC | 11169 |
rs778554516 | snp | A/G | 3.59182e-05 | 0.00423767 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991162 | ATTAACTATAGTAAG[A/G]AAAAAGTGCTGAAAA | 11169 |
rs778590539 | snp | C/G | 3.29804e-05 | 0.00406068 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54967358 | AGCAGGGCGTGGAAG[C/G]GTTGGGGGAAACCGA | 11169 |
rs778603137 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54969801 | ATATAAAAATCCTCA[A/G]CAAAACACTAGCAAA | 11169 |
rs778648933 | in-del | -/A | 1.71755e-05 | 0.00293044 | splice-donor-variant | WDHD1 | GRCh38.p7 | 14:54957589 | CACTTGGAAGAGTTT[-/A]ACCTTAAAGGGATTT | 11169 |
rs778663933 | snp | C/T | 1.65463e-05 | 0.00287626 | missense | WDHD1 | GRCh38.p7 | 14:54957198 | GTTCTTTGGAACTGG[C/T]TGATACCTAAAGAGC | 11169 |
rs778675361 | in-del | -/TTC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988054 | AGCTGAAAAAATATT[-/TTC]TTTTCTTTTGAAAAG | 11169 |
rs778686685 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54986477 | CACACCACACCATAC[C/T]TGGTCCAGAATCTAT | 11169 |
rs778708775 | snp | C/T | 3.36027e-05 | 0.00409881 | | | GRCh38.p7 | 14:55013638 | TCATCGGGCATGGTG[C/T]CTCATGCCTATAATG | 11169 |
rs778718513 | snp | A/C | 2.59629e-05 | 0.00360288 | | | GRCh38.p7 | 14:54995829 | CTTGAACAAATTAAT[A/C]CAAATTATAAAGTAA | 11169 |
rs778733650 | snp | A/G | | | | | GRCh38.p7 | 14:54970987 | AAAAACAAGGAACTG[A/G]GAAAGGAATCCCTAC | 11169 |
rs778741594 | snp | A/T | 1.6483e-05 | 0.00287076 | | | GRCh38.p7 | 14:54987362 | TGCTTGAATCCCAAG[A/T]ACTAAAGTGCAGGCA | 11169 |
rs778744920 | snp | C/T | | | | | GRCh38.p7 | 14:54980026 | ACCAGCCATATCATA[C/T]GGTAAGTATACAATT | 11169 |
rs778772865 | in-del | -/C | 0.000140032 | 0.00836637 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007416 | TTCCTTTATGAAAAT[-/C]CCCCCCCAAAATATA | 11169 |
rs778775318 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998544 | CTCCACAGCCCCAAT[C/T]TACTTCTCTACAGAA | 11169 |
rs778775434 | snp | C/T | 1.648e-05 | 0.0028705 | missense | WDHD1 | GRCh38.p7 | 14:54987230 | ATACCTCTTTTTGAA[C/T]CCCTCCAATAGTAAA | 11169 |
rs778781871 | snp | C/T | 1.66402e-05 | 0.00288441 | splice-donor-variant | WDHD1 | GRCh38.p7 | 14:54962951 | CTAAATTATTTCTTA[C/T]CCAGCATTCAGCTTT | 11169 |
rs778789951 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54954592 | CCATCTTTTGTCCAC[A/C]AGTAGAGAACTACAT | 11169 |
rs778813357 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54978442 | TTTTAAAAATTAGCC[A/G]GGTGTGGTAGCCTGT | 11169 |
rs778857825 | snp | C/T | 1.65422e-05 | 0.0028759 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000499 | GTACCATACTCCCTT[C/T]TACCTTACTGCTTGA | 11169 |
rs778936251 | snp | C/T | 1.75468e-05 | 0.00296194 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955524 | ACTGTATACTTTTTA[C/T]TTGGTCACTGCATGC | 11169 |
rs778958660 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | WDHD1, SOCS4 | GRCh38.p7 | 14:55027129 | CCGCCCACGCCCAGC[G/T]CAGGTCCCGACAGAG | 11169 |
rs778995580 | snp | A/G | 4.98285e-05 | 0.00499117 | intron-variant | WDHD1 | GRCh38.p7 | 14:55008735 | CTAAGAACAAAAAGA[A/G]TAACGCAAATGAATA | 11169 |
rs779031121 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant, missense, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026784 | GCTTCCGTGTGGCAG[A/G]CATGTTTTCCTTTAC | 11169 |
rs779046378 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55012736 | AAGGTAAAGAGAGGG[A/C]GAGAGGGAGAGCAAG | 11169 |
rs779046581 | snp | C/T | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028137 | TGAGACGTTTTTCTG[C/T]TGAAGAGGTTTCCCT | 11169 |
rs779105569 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54955502 | TGCATAATTTTGTAT[G/T]GCTGCTACTGTATAC | 11169 |
rs779128193 | snp | A/G | 4.95454e-05 | 0.00497697 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55007337 | TGCATTTATCACATC[A/G]TTGCATTTTTGTAGC | 11169 |
rs779129173 | snp | C/T | 1.66944e-05 | 0.0028891 | missense | WDHD1 | GRCh38.p7 | 14:54963144 | GCAAGTTCCACACAA[C/T]GGAATTCTCGCTCCA | 11169 |
rs779129674 | snp | C/G | 1.64798e-05 | 0.00287047 | missense | WDHD1 | GRCh38.p7 | 14:54991368 | CCTCCTCCTCTTTGA[C/G]AAGACTAGAACCAGT | 11169 |
rs779131431 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55003098 | GGATTAGTAACATAT[A/G]ATAAAAACTTTATTT | 11169 |
rs779132524 | snp | A/G | 1.88156e-05 | 0.00306715 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000656 | CACCCTAAAAATTAA[A/G]AAGTAGGTTCTAAAA | 11169 |
rs779142189 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55010169 | TTTGTCCTCAAAAAC[C/G]TTTACTAGATAAAAG | 11169 |
rs779148562 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993984 | TAAACTCTATATGAC[C/T]TTAAAAAGCACAACA | 11169 |
rs779165440 | snp | A/G | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941123 | TCCTTCCTTGCACAT[A/G]ACAAAAACCAAATGA | 11169 |
rs779168075 | snp | C/T | 1.65373e-05 | 0.00287548 | missense | WDHD1 | GRCh38.p7 | 14:54966487 | CACCGCAAGCATTTT[C/T]ATTAAAAGTTCCTGT | 11169 |
rs779224335 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55017779 | GCCATACTTGTCAAA[A/T]TTTCAGATTTTATTT | 11169 |
rs779230851 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974879 | TCGTGTCCAGATTAA[C/T]CTTGCCCCAGCCAGC | 11169 |
rs779235605 | snp | A/G | 0.000117492 | 0.00766369 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55010441 | GTATTATTAGAAACT[A/G]CAGTGACCAGTTTTC | 11169 |
rs779238502 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996829 | GTGGAGTCTCGCTCT[A/G]TCGCCAGGCTGGAGT | 11169 |
rs779273034 | snp | A/G | 1.6953e-05 | 0.0029114 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941722 | GAGTGAAAAGGAAAG[A/G]TTTTTAGAAAATAAC | 11169 |
rs779288848 | snp | C/T | 6.59446e-05 | 0.00574177 | utr-variant-5-prime, synonymous-codon | WDHD1 | GRCh38.p7 | 14:55010350 | ATCCCCATTAAAGAC[C/T]ACATGGTTTGCATTT | 11169 |
rs779311719 | in-del | -/TTC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55016349 | GATTAAATACTAAAT[-/TTC]TTCTTCTCAGGAAAG | 11169 |
rs779368519 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54948204 | TGTCGGACAGTGGGC[A/G]CAGAACAGGGGGTGT | 11169 |
rs779440760 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54969206 | ACCACGCCCAGCTAA[C/T]GTTTTGTATTTTTAG | 11169 |
rs779451419 | snp | C/G | 1.66012e-05 | 0.00288103 | missense | WDHD1 | GRCh38.p7 | 14:54963040 | CCTTCTCTACAGCCA[C/G]TTCACTTAGTTTTTG | 11169 |
rs779477643 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998345 | ATGTTGGCCAGGCTG[C/G]TCTTGAACTCCTGAC | 11169 |
rs779491604 | snp | C/G | 8.31608e-05 | 0.00644775 | intron-variant | WDHD1 | GRCh38.p7 | 14:54981723 | CAGAAAAATCACTTG[C/G]AGACATAGCTACATG | 11169 |
rs779501021 | snp | A/G | | | downstream-variant-500B | WDHD1 | GRCh38.p7 | 14:54938444 | GAGGCCGAGGCCAGA[A/G]AATCACTTGAACCCA | 11169 |
rs779514064 | snp | A/G | 1.64841e-05 | 0.00287085 | missense | WDHD1 | GRCh38.p7 | 14:54941627 | TTTCATCAACCACAC[A/G]TTTTCGCTTCTTTGC | 11169 |
rs779537321 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960906 | CTGGGCTCAAGATAT[C/T]CTCCTGTCCCAGCCT | 11169 |
rs779543600 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012216 | TTTTTCTTCTGGGAA[C/T]GCATTTTCTAATTAT | 11169 |
rs779559197 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54971161 | CTAGCAAATACCCTT[C/T]AGGATATTGGCCTTG | 11169 |
rs779566656 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54983516 | TGTCTCTATTAAAAA[C/T]ACAAAAATTAGCCGA | 11169 |
rs779573098 | snp | C/T | 8.36593e-05 | 0.00646704 | intron-variant | WDHD1 | GRCh38.p7 | 14:54995582 | AACAGGGTAATCACA[C/T]GCACAAAGTCAAATT | 11169 |
rs779634984 | snp | C/T | 1.72973e-05 | 0.00294081 | intron-variant | WDHD1 | GRCh38.p7 | 14:54955550 | CATGCTAAATTTCTC[C/T]ATGTACTGACCTTTG | 11169 |
rs779686451 | snp | A/C | 1.66771e-05 | 0.00288761 | missense | WDHD1 | GRCh38.p7 | 14:54962963 | TTACCCAGCATTCAG[A/C]TTTTTTCTGAAATCT | 11169 |
rs779706276 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019847 | GCACTCCAGCCTGGG[C/T]GACAGAGCTAGACTC | 11169 |
rs779710325 | snp | C/T | 1.706e-05 | 0.00292057 | intron-variant | WDHD1 | GRCh38.p7 | 14:55010288 | AACATTATTTCCTTT[C/T]CTGATGTCAAAGAGC | 11169 |
rs779710468 | snp | C/T | 3.29652e-05 | 0.00405974 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000525 | CTTGATGTCTTTCCA[C/T]TGGGGTCACAAACAT | 11169 |
rs779779586 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990275 | CAGAATGGAAAACAT[C/G]ATATAACCAACACAG | 11169 |
rs779779745 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54959042 | GGCACCATCATTCAC[G/T]CAAGTACTCAAGCCA | 11169 |
rs779814229 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980186 | CTGGGTGTGGTGGTG[C/T]GTGCCTGTAGTCCCA | 11169 |
rs779829069 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54944571 | GTCTCTGACATCTAT[C/T]ATATAAAGTAAGGAA | 11169 |
rs779831094 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960229 | CTGGAGTGCGGTGGT[A/G]TGATCTCACCTCACT | 11169 |
rs779863151 | snp | C/G | 3.29875e-05 | 0.00406112 | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026824 | AATGTTTTATAAAAG[C/G]CAGTCTTATTATTTC | 11169 |
rs779867172 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965459 | CATATCTAACAGCCC[A/G]ATCAAAGTTCTTAAG | 11169 |
rs779867527 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54981171 | AAAAGCAGCTTAATT[A/G]TATATTTCAATTCTC | 11169 |
rs779882735 | snp | A/G | 0.0234835 | 0.105784 | intron-variant | WDHD1 | GRCh38.p7 | 14:55007269 | AGAAAAGAAAAATAA[A/G]AATCACTTACCTTCC | 11169 |
rs779886635 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54995044 | GGCATGCAGTTGACG[C/T]GATCTCGGCTCACTG | 11169 |
rs779886940 | snp | C/T | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028221 | CCGTCGTGTTCTTAC[C/T]GTGGGTGGCATTGTG | 11169 |
rs779893526 | snp | C/G | 1.66632e-05 | 0.0028864 | missense | WDHD1 | GRCh38.p7 | 14:54955645 | TCTTTCACTTCCTCA[C/G]TTTTATTAGTTTGAG | 11169 |
rs779911298 | snp | A/G | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55027774 | GTATAATTAATTAAT[A/G]CTCAATTAATGCTTA | 11169 |
rs779940978 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54977040 | TTTCAATCTACTTAT[C/T]AGCTAACTCCCTTTG | 11169 |
rs779992083 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967431 | ATCATAAAAATTTAC[C/T]AACATGTCATAAAAA | 11169 |
rs779999164 | snp | A/C | 1.68647e-05 | 0.0029038 | intron-variant | WDHD1 | GRCh38.p7 | 14:54988985 | AACAACTGTATCTAA[A/C]AGTTCAACAGTGCCA | 11169 |
rs780034781 | in-del | -/GGGG | 0.0101428 | 0.0704878 | intron-variant | WDHD1 | GRCh38.p7 | 14:54963185 | AAGCTAATCCAAAAA[-/GGGG]GGGGGGGGGGAGATC | 11169 |
rs780136618 | snp | C/T | 1.75594e-05 | 0.00296301 | intron-variant | WDHD1 | GRCh38.p7 | 14:54941737 | ATTTTTAGAAAATAA[C/T]AAATAAGAAGTAAAT | 11169 |
rs780156639 | snp | A/C | 1.65471e-05 | 0.00287633 | missense, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000618 | CATGCCAGACCACAA[A/C]TTGCATAACCTTTCT | 11169 |
rs780180224 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015802 | TCCCGGGTTCAAGTG[-/A]ATTCTCCTGCCTCAG | 11169 |
rs780189511 | snp | C/T | 8.33507e-05 | 0.00645511 | intron-variant | WDHD1 | GRCh38.p7 | 14:54962595 | TAAATGGGGAAAATA[C/T]AGTCATCCTCAATAT | 11169 |
rs780189991 | snp | A/G | 1.64871e-05 | 0.00287111 | missense | WDHD1 | GRCh38.p7 | 14:54941641 | CGTTTTCGCTTCTTT[A/G]CTTCAGTTCCTTCAC | 11169 |
rs780206255 | snp | A/T | 1.64819e-05 | 0.00287066 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967240 | TATCACAGGTGCTGT[A/T]TTATCAAATTCAAAG | 11169 |
rs780218124 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963459 | TTTGATGAAATATTA[C/T]ATACCACTTTAATCT | 11169 |
rs780246544 | snp | G/T | 4.94972e-05 | 0.00497455 | missense | WDHD1 | GRCh38.p7 | 14:54984786 | GAAGAGGGTCACCAT[G/T]CAAAATTTGTTTTTT | 11169 |
rs780255746 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55024214 | TTTTCTCTGAGCTTG[A/G]GACACAATTATCCAA | 11169 |
rs780276355 | snp | C/T | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011448 | AGAATCACCTGAACC[C/T]GGGAGGCGGCGGTTG | 11169 |
rs780304215 | snp | A/G | 3.29587e-05 | 0.00405934 | missense | WDHD1 | GRCh38.p7 | 14:54957123 | CAGTGGATTTCTTGG[A/G]TGATTTGCCCATATT | 11169 |
rs780328805 | snp | A/G | 0.000151191 | 0.00869324 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013468 | TTCATATCAATTGAT[A/G]TAACTGTTTTTACTA | 11169 |
rs780347606 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54962326 | GCATTTTATAAACAT[C/G]TGTTAAATGACCATA | 11169 |
rs780376690 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54944616 | GTTAATTCATGTTAC[-/T]TTTTTTTTTTTTTTT | 11169 |
rs780388619 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020994 | GAGAAGGCTGACGGG[C/G]AACACGAAGAGGAGT | 11169 |
rs780389014 | snp | A/T | 1.70566e-05 | 0.00292027 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001022 | AGTTAATAAATAATG[A/T]TTTTGTAAAATTTCA | 11169 |
rs780394975 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998465 | ACTTTTTGTTTTTAC[C/G]AATGTTACACATGCA | 11169 |
rs780397900 | in-del | -/AA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54996245 | TATATTATCTCAGTT[-/AA]AGTTAGTGTTTTGAT | 11169 |
rs780443996 | snp | A/G | 1.6483e-05 | 0.00287076 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000924 | CACATTCCAAACTAT[A/G]ATTAGACCATTAATA | 11169 |
rs780448613 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54978122 | AATGAATAATCTTAC[C/T]TGAATAAGCATTAGG | 11169 |
rs780537327 | snp | A/G | 3.3083e-05 | 0.00406699 | intron-variant | WDHD1 | GRCh38.p7 | 14:55000882 | AAGATACACTAAATC[A/G]TACCTTTCCATGCAG | 11169 |
rs780545891 | in-del | -/C | 1.65293e-05 | 0.00287479 | splice-donor-variant | WDHD1 | GRCh38.p7 | 14:55008607 | AGGAAAAAATAATTA[-/C]CAGAAAGATGTCCTT | 11169 |
rs780551382 | in-del | -/TTACT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54977129 | GTACTCTCTACCAAA[-/TTACT]TTAATCTTTTTGGAC | 11169 |
rs780573477 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54997262 | AACCACACCTGGCTA[A/G]TTTTTGTATTTTCAG | 11169 |
rs780600143 | in-del | -/A | 4.94654e-05 | 0.00497295 | frameshift-variant | WDHD1 | GRCh38.p7 | 14:54944364 | CAATACTCTAAATCG[-/A]AATCATTCCTTCTTT | 11169 |
rs780633099 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54960950 | GACTACCGGTGTGTA[C/T]TACCATGCCTGGCTA | 11169 |
rs780639683 | snp | C/T | 1.75943e-05 | 0.00296595 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55010457 | CAGTGACCAGTTTTC[C/T]ACTCTAAAAGAAAAA | 11169 |
rs780688267 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54947056 | AAAAAAAGTGTTAGG[C/T]GGGCCAGGCATGGTG | 11169 |
rs780755654 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55018596 | ATTATTGAAGAAGTG[C/T]ACCCTGAATGGAGAT | 11169 |
rs780757028 | snp | A/G | 1.65941e-05 | 0.00288041 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54963124 | CATTTTGAGTCATTA[A/G]ATCAGCAAGTTCCAC | 11169 |
rs780758989 | snp | C/T | 1.6679e-05 | 0.00288777 | missense | WDHD1 | GRCh38.p7 | 14:54955652 | CTTCCTCAGTTTTAT[C/T]AGTTTGAGAATTTCT | 11169 |
rs780761629 | snp | C/G | 1.66272e-05 | 0.00288328 | intron-variant | WDHD1 | GRCh38.p7 | 14:54984889 | GTAAATATAAATCAG[C/G]CATCAAAGGTTATCC | 11169 |
rs780761652 | snp | C/T | 1.67444e-05 | 0.00289343 | missense | WDHD1 | GRCh38.p7 | 14:54963153 | ACACAACGGAATTCT[C/T]GCTCCAGTTTACAAG | 11169 |
rs780768195 | in-del | -/TACA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963457 | GATTTGATGAAATAT[-/TACA]TACCACTTTAATCTA | 11169 |
rs780781504 | snp | A/G | | | upstream-variant-2KB, intron-variant | WDHD1, SOCS4 | GRCh38.p7 | 14:55028306 | TTGTATATGAATGAA[A/G]AGGAAGAATGATTGG | 11169 |
rs780848543 | snp | A/G | 1.65954e-05 | 0.00288053 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55000623 | CAGACCACAAATTGC[A/G]TAACCTTTCTCATGT | 11169 |
rs780903435 | snp | A/G | 1.6628e-05 | 0.00288335 | utr-variant-5-prime, synonymous-codon | WDHD1 | GRCh38.p7 | 14:55010317 | GCCTTACCTAGATCC[A/G]GCAGCAATTTTAGTA | 11169 |
rs780908142 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54967490 | TAGTAACTTAGAATA[A/G]TAATATTATAATAGC | 11169 |
rs780999275 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55004332 | CTATTCATAACTCAA[G/T]AGCAAACTTATAATT | 11169 |
rs781018444 | snp | C/T | 1.66233e-05 | 0.00288295 | synonymous-codon, utr-variant-5-prime | WDHD1 | GRCh38.p7 | 14:55007373 | CCAACTAATAGCACA[C/T]GTCTAATTGGTAAAA | 11169 |
rs781026114 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54982964 | GATGCCAGGAGTTCA[A/T]AACCAGCCTAGCCAA | 11169 |
rs781033982 | in-del | -/G | 1.76428e-05 | 0.00297003 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001044 | AAATTTCAAACTAAA[-/G]TACTCATTTTATTAC | 11169 |
rs781034476 | snp | A/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015579 | CAAATCCTTTCGGGG[A/C]CAACATGTGAGGCAT | 11169 |
rs781073588 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54951859 | ATAAATAAACGTAAT[C/T]CAGCATATAAACAGA | 11169 |
rs781124051 | snp | A/C | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55011870 | TCTCAATTGAAAGAC[A/C]CTTCAATTGTTTCCG | 11169 |
rs781218285 | snp | C/T | 3.2987e-05 | 0.00406108 | missense | WDHD1 | GRCh38.p7 | 14:54944382 | TCATTCCTTCTTTTA[C/T]TATGTCTGCTTCATC | 11169 |
rs781228763 | snp | A/G | 1.65704e-05 | 0.00287836 | intron-variant | WDHD1 | GRCh38.p7 | 14:54987098 | CAGCAAAAAAGCTCA[A/G]GTAATTTCCATTTTA | 11169 |
rs781236453 | snp | A/G | 1.64787e-05 | 0.00287038 | intron-variant | WDHD1 | GRCh38.p7 | 14:54967253 | GTATTATCAAATTCA[A/G]AGTGTCAAGGTAAGA | 11169 |
rs781322213 | snp | C/G | 1.65296e-05 | 0.00287481 | utr-variant-5-prime, missense | WDHD1 | GRCh38.p7 | 14:55013492 | TTTACTACCTTCAAA[C/G]CACATGAATATGCCT | 11169 |
rs781325997 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55027003 | ATCTCCTTGGTGGAC[A/G]CGGGCAGCCGGAGTG | 11169 |
rs781334083 | snp | G/T | 6.43894e-05 | 0.00567367 | intron-variant | WDHD1 | GRCh38.p7 | 14:54966620 | TCCTATAAAAGCAAA[G/T]AAAATTGCTTAAGGC | 11169 |
rs781336031 | snp | A/G | 1.64838e-05 | 0.00287083 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54989162 | CTCCACATCTATGGC[A/G]TTGTCTTGCTCATCA | 11169 |
rs781339435 | snp | C/T | 1.64779e-05 | 0.00287031 | missense | WDHD1 | GRCh38.p7 | 14:54962818 | ACTTGATTTCTGAAC[C/T]TTGGTTGGCTCCACT | 11169 |
rs781400484 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55000151 | TTAAAGTTGCTCAGT[A/G]AAGCTGTTTGACTAA | 11169 |
rs781402776 | snp | C/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55001772 | AAACAGACCAACAAC[C/G]TTTCTTCCTCTAAAA | 11169 |
rs781413732 | in-del | -/AGA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54998187 | TCCAGCCTGGGCAAC[-/AGA]AGGAGACTTTGCCTC | 11169 |
rs781413986 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55012663 | GAAGGCTGGACACTA[C/T]AAGATTGAGGGGTTG | 11169 |
rs781460496 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54963533 | GGGGAGGCTGGGCAC[A/G]GTGGCTCACGCCTGT | 11169 |
rs781502719 | snp | C/T | 1.64876e-05 | 0.00287116 | synonymous-codon | WDHD1 | GRCh38.p7 | 14:54991258 | AGAACCTGACTGAAA[C/T]GGCTTTTGCCGGGGA | 11169 |
rs781525190 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54986156 | TGGTTTCTCAAACTG[C/T]ATATTTTGACCTAAG | 11169 |
rs781548764 | snp | C/T | 1.65143e-05 | 0.00287348 | intron-variant | WDHD1 | GRCh38.p7 | 14:54944288 | AAGAATTTTTTAAAT[C/T]TGGGAATTCACTAAG | 11169 |
rs781560002 | snp | A/C | 3.31851e-05 | 0.00407326 | intron-variant | WDHD1 | GRCh38.p7 | 14:55013613 | TGTGAAGAAAAGACA[A/C]AAATTAAAGTCATCG | 11169 |
rs781582295 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54987510 | CTATTATACACTAGT[A/G]TAAGAAGTTGCTTTA | 11169 |
rs781585462 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965143 | GGACCATTCACTCTT[G/T]TCAACAAATATCGAG | 11169 |
rs781603996 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54953619 | CAGCAATCCCATTAC[-/T]GGGTATATACCCAAA | 11169 |
rs781625378 | snp | A/T | 1.74595e-05 | 0.00295456 | intron-variant | WDHD1 | GRCh38.p7 | 14:54991183 | GTGCTGAAAACCTAC[A/T]AAGAAGTTAAGTGTA | 11169 |
rs781627153 | in-del | -/C | 1.66056e-05 | 0.00288141 | frameshift-variant | WDHD1 | GRCh38.p7 | 14:54955595 | GAGGAGGACATATAG[-/C]TGGGGTTTCAGATAA | 11169 |
rs781725906 | snp | A/C | 0.000121226 | 0.00778448 | intron-variant | WDHD1 | GRCh38.p7 | 14:55001037 | ATTTTGTAAAATTTC[A/C]AACTAAATACTCATT | 11169 |
rs781735428 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019953 | TGACATAACCTCAAG[G/T]AGTCAATGATTACCA | 11169 |
rs781758441 | snp | A/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55020012 | CTCAGAGAGCAACAT[A/T]CCTTCCCTAATCTGA | 11169 |
rs781766153 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55008798 | TGATCCAAATATTTC[-/T]TTTTTTTTTTTTTTC | 11169 |
rs781769618 | snp | G/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55021273 | ACCCTTCTGCCAGAT[G/T]GCCTAAAGTCAATTT | 11169 |
rs796071805 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54965956 | AGCGAAACTCCGCCT[-/A]AAAAAAAAAAAAGAA | 11169 |
rs796106446 | in-del | -/C | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54980817 | AAAAAAAAAAAAAAA[-/C]AAAAAAAACTCAGCT | 11169 |
rs796214473 | in-del | -/TG | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993756 | CTCACTAATTTTTTT[-/TG]TTTTTCATAAAAAAG | 11169 |
rs796214528 | in-del | -/C | | | intron-variant, upstream-variant-2KB | WDHD1, SOCS4 | GRCh38.p7 | 14:55026543 | ATATACTACAACTAC[-/C]ATGACGGCCCGAATC | 11169 |
rs796268164 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988764 | AGCACTTAACAATGT[-/A]AAAAAAAAAATCCCA | 11169 |
rs796321500 | in-del | AG/CATAATCACGCCACTGCACTCTAACCTGGATGACAGTCACA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54959346 | AGGCTGCAGTGAGCC[lengthTooLong]CCTGGCGGGGGGAAG | 11169 |
rs796356449 | in-del | -/A | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54988329 | GGTTGAATTAACTGC[-/A]AAGGGATATAAGAAA | 11169 |
rs796458807 | multinucleotide-polymorphism | AT/GC | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54986588 | ACTCCAGCTAAAAGA[AT/GC]GAGCCAACAAAAAAG | 11169 |
rs796462112 | multinucleotide-polymorphism | GT/TG | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974493 | ACCTGTTTTGTTTTG[GT/TG]TTTTTTTTTTTTGTT | 11169 |
rs796598892 | in-del | GTT/TG | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54974493 | ACCTGTTTTGTTTTG[GTT/TG]TTTTTTTTTTTGTTA | 11169 |
rs796644276 | in-del | -/AT | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54993046 | CAATATTATCAATTC[-/AT]ATGTTACAAAATTAA | 11169 |
rs796651921 | in-del | -/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54975352 | TTCTCATATTCATAA[-/T]TTTTTTTTTTTTTGA | 11169 |
rs796714102 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54964003 | GTCTTATCTACTCAG[A/G]AGCCTGAGACAGGAG | 11169 |
rs796741333 | snp | A/G | | | utr-variant-3-prime | WDHD1 | GRCh38.p7 | 14:54941058 | TCCCCTAGGTCTAGT[A/G]GAAACATATAGAGAA | 11169 |
rs796819690 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54968795 | CCTGTAATCCCAATA[C/T]TTTTGGAGGCAAAGG | 11169 |
rs796850888 | snp | C/T | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55015300 | GCTGAGGCATGAGAA[C/T]CATTTGAACCCAGGA | 11169 |
rs796907754 | in-del | -/AA | | | intron-variant | WDHD1 | GRCh38.p7 | 14:55019872 | AGACTCCATCTCAAC[-/AA]AAAAGAAATCCGCTA | 11169 |
rs796945238 | snp | A/G | | | intron-variant | WDHD1 | GRCh38.p7 | 14:54990394 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGTCTA | 11169 |
rs796998528 | snp | A/G | | | intron-variant, upstream-variant-2KB | WDHD1 | GRCh38.p7 | 14:55012390 | CTTAGGGGTTTATAG[A/G]TAATTAATTTCCAAA | 11169 |