SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs493519 | snp | C/T | 0.230017 | 0.2492 | intron-variant | WDR66 | GRCh38.p7 | 12:121959570 | TGCACACAGTCCAGC[C/T]TCTGTGTCCCCTCAG | 144406 |
rs525664 | snp | C/T | 0 | 0 | intron-variant | WDR66 | GRCh38.p7 | 12:121989358 | CTCAGGTGACAGCAG[C/T]CAAGGCCTGGCCTGG | 144406 |
rs529736 | snp | G/T | 0.496279 | 0.0429702 | intron-variant | WDR66 | GRCh38.p7 | 12:121946551 | gaaaaatctgtaaaa[G/T]cagctgggggccaag | 144406 |
rs567503 | snp | C/G | 0 | 0 | intron-variant | WDR66 | GRCh38.p7 | 12:121972187 | gcctgttacccagtt[C/G]caaagtcactttgac | 144406 |
rs657926 | snp | A/C | | | intron-variant | WDR66 | GRCh38.p7 | 12:121971480 | GCCGTAATAATCCCA[A/C]CCACTTGTGCTGAGT | 144406 |
rs658957 | snp | A/G | 0.497695 | 0.0338674 | utr-variant-3-prime, intron-variant | WDR66 | GRCh38.p7 | 12:121971758 | acagagccaaaccat[A/G]tcaCAAAGATTGGAG | 144406 |
rs671293 | snp | A/G | 0.492871 | 0.0592773 | intron-variant | WDR66 | GRCh38.p7 | 12:121972254 | aggaagatgtgggaa[A/G]gtttggaacttccta | 144406 |
rs686220 | snp | C/T | 0.499902 | 0.00698814 | intron-variant | WDR66 | GRCh38.p7 | 12:121948609 | CCTCAGCCTCCTGAG[C/T]AGTTGGGACTACCAG | 144406 |
rs693277 | snp | C/T | 0.221141 | 0.248329 | intron-variant | WDR66 | GRCh38.p7 | 12:121949831 | CACCATCACAGCTCA[C/T]TGCAGTCTCAAACTC | 144406 |
rs830115 | snp | A/G | 0.4087 | 0.193169 | intron-variant | WDR66 | GRCh38.p7 | 12:121976197 | ACATCGTGAAGCCTC[A/G]TCTCTACTAAAAATA | 144406 |
rs830116 | snp | C/T | 0.225893 | 0.248835 | intron-variant | WDR66 | GRCh38.p7 | 12:121974926 | GTGGGGGAGGCATCC[C/T]GTGTTCTGAAACCAC | 144406 |
rs830117 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | WDR66 | GRCh38.p7 | 12:121974410 | actataaaatgagac[A/G]attctgcctcacagc | 144406 |
rs830118 | snp | C/T | 0.494733 | 0.0510469 | intron-variant | WDR66 | GRCh38.p7 | 12:121974319 | tgataaaaacatacc[C/T]gagactgggcaattt | 144406 |
rs830120 | snp | A/G | 0.483655 | 0.0936489 | intron-variant | WDR66 | GRCh38.p7 | 12:121989748 | ATGGTTTCATGGACC[A/G]GTAGGACTGGGAGCA | 144406 |
rs830121 | snp | G/T | 0.406814 | 0.194704 | intron-variant | WDR66 | GRCh38.p7 | 12:121989255 | CTGCCCTGCATCAGA[G/T]CCCAGGTCTCAAACA | 144406 |
rs830122 | snp | A/G | 0.231482 | 0.249313 | intron-variant | WDR66 | GRCh38.p7 | 12:121988330 | atgttctaggattac[A/G]tggtggtgatgtctg | 144406 |
rs830123 | snp | C/T | 0.376791 | 0.215463 | intron-variant | WDR66 | GRCh38.p7 | 12:121988311 | tggtgatgtctgcac[C/T]actcggtggacattc | 144406 |
rs830124 | snp | A/G | 0.26326 | 0.249648 | intron-variant | WDR66 | GRCh38.p7 | 12:121957871 | TGTCCTAGCCACTGC[A/G]GTTAAAGGCACTGGA | 144406 |
rs830125 | snp | C/T | 0.145305 | 0.227022 | intron-variant | WDR66 | GRCh38.p7 | 12:121960003 | ccaggtatggtggca[C/T]gtgcctgtagtccta | 144406 |
rs830126 | snp | A/G | 0.230017 | 0.2492 | intron-variant | WDR66 | GRCh38.p7 | 12:121960217 | AAGATTATTTTTGAA[A/G]AAAATATTCTTAGTA | 144406 |
rs830127 | snp | A/C | 0.192401 | 0.243274 | intron-variant | WDR66 | GRCh38.p7 | 12:121961047 | CCGCCCTTGCCTCCC[A/C]GTGTGCACGGGGAGG | 144406 |
rs830128 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | WDR66 | GRCh38.p7 | 12:121962887 | gtgaaggtgggaggc[A/G]tctggggtttgggaa | 144406 |
rs853758 | snp | A/T | 0.227074 | 0.248947 | intron-variant | WDR66 | GRCh38.p7 | 12:121970949 | GACCCCAGAGGGGCC[A/T]GGGGGCTGTACTGGC | 144406 |
rs853759 | snp | A/C | 0.23031 | 0.249223 | intron-variant | WDR66 | GRCh38.p7 | 12:121959950 | gcaacatggtgagac[A/C]ccccccatctctaca | 144406 |
rs865516 | snp | A/C | | | intron-variant | WDR66 | GRCh38.p7 | 12:121971524 | atgatacatggaact[A/C]actcagtgcaggccc | 144406 |
rs865517 | snp | A/G | 0 | 0 | intron-variant | WDR66 | GRCh38.p7 | 12:121969801 | ACGACTGAGAAGAAG[A/G]CAAACATTTCAGAAG | 144406 |
rs872781 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | WDR66 | GRCh38.p7 | 12:121996678 | TTTAAATTATTATTT[C/T]TTTAAGCTGCAAAGA | 144406 |
rs876934 | snp | C/T | 0.407502 | 0.194147 | upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | WDR66, PSMD9 | GRCh38.p7 | 12:121916942 | TTCCTCTTTAGGAAC[C/T]CACCAGAGGGCAGCA | 144406 |
rs876935 | snp | A/G | 0.067446 | 0.170804 | upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | WDR66, PSMD9 | GRCh38.p7 | 12:121917810 | TAAAAGAGACTGGAA[A/G]ATACGTGGAATTAGA | 144406 |
rs895958 | snp | C/T | 0.22263 | 0.248497 | intron-variant | WDR66 | GRCh38.p7 | 12:121940300 | TGAGAAAATGTATCT[C/T]ATCCCTGGAGATACT | 144406 |
rs1104151 | snp | C/G | | | intron-variant | WDR66 | GRCh38.p7 | 12:121972785 | ttcttccgccagagg[C/G]caggcgcggtagctc | 144406 |
rs1154513 | snp | C/T | 0.223522 | 0.248594 | intron-variant | WDR66 | GRCh38.p7 | 12:121954057 | CAAAGCATTTATCAA[C/T]ACGATATTTTATAAT | 144406 |
rs1154514 | snp | C/T | 0.339656 | 0.233371 | intron-variant | WDR66 | GRCh38.p7 | 12:121936982 | CTGGGCTTCCATGCC[C/T]GGTCAGCCGTGGTCT | 144406 |
rs1154517 | snp | C/G | 0.0973687 | 0.197999 | upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant | WDR66, PSMD9 | GRCh38.p7 | 12:121916799 | TGAGGCCTTGCTGCT[C/G]TGGATACGGAAATGG | 144406 |
rs1154519 | snp | C/G | 0.0973687 | 0.197999 | upstream-variant-2KB, downstream-variant-500B | WDR66, PSMD9 | GRCh38.p7 | 12:121918326 | CCGCAACCTTGGCAA[C/G]ATGGGGTGGAGAAGT | 144406 |
rs1169070 | snp | C/T | 0.32955 | 0.237006 | intron-variant | WDR66 | GRCh38.p7 | 12:121952013 | aggcgtgagccactg[C/T]acctggccCTAATAA | 144406 |
rs1169071 | snp | G/T | 0.32955 | 0.237006 | intron-variant | WDR66 | GRCh38.p7 | 12:121952178 | agactgaggtgagag[G/T]atcacttgagctcag | 144406 |
rs1169072 | snp | A/G | 0.490618 | 0.0678448 | intron-variant | WDR66 | GRCh38.p7 | 12:121963595 | GCATCCTAGAGTGGC[A/G]TCTCCTCCCTCCTGA | 144406 |
rs1169075 | snp | G/T | 0.21845 | 0.248001 | intron-variant | WDR66 | GRCh38.p7 | 12:121991748 | cctcggcctcccaaa[G/T]tgctgggattacagg | 144406 |
rs1169076 | snp | C/T | 0.495135 | 0.0490805 | intron-variant | WDR66 | GRCh38.p7 | 12:121991578 | AGgcttcacaatgac[C/T]gggaggtcttgttca | 144406 |
rs1169077 | snp | C/T | 0.231189 | 0.249291 | intron-variant | WDR66 | GRCh38.p7 | 12:121987106 | AACAGAAATTGTCCC[C/T]GTGCTTCTTGGCTCA | 144406 |
rs1169078 | snp | C/G | 0.490453 | 0.0684267 | intron-variant | WDR66 | GRCh38.p7 | 12:121978348 | ggagtgcagtggcac[C/G]atctcggctcactgt | 144406 |
rs1169079 | snp | C/T | 0.495407 | 0.0477027 | intron-variant | WDR66 | GRCh38.p7 | 12:121974014 | agatttgggtggaga[C/T]acagccaaaccatat | 144406 |
rs1169080 | snp | A/C | 0.228253 | 0.249052 | intron-variant | WDR66 | GRCh38.p7 | 12:121972964 | tggttacataggcaa[A/C]tttctacagttgggt | 144406 |
rs1169081 | snp | A/C | 0.438461 | 0.164264 | missense | WDR66 | GRCh38.p7 | 12:121968006 | AGATCTGAAGTCCCA[A/C]CTAGAAAGGAACACA | 144406 |
rs1177588 | snp | A/G | 0.499923 | 0.00618962 | intron-variant | WDR66 | GRCh38.p7 | 12:121951261 | CATCTCAAGAAAAAA[A/G]AAGTCATAATCATTT | 144406 |
rs1177589 | snp | A/G | 0.497586 | 0.0346604 | intron-variant | WDR66 | GRCh38.p7 | 12:121966027 | tcctaaccccaagca[A/G]tcctcccaccttagc | 144406 |
rs1182927 | snp | A/G | 0.251814 | 0.249993 | intron-variant | WDR66 | GRCh38.p7 | 12:122001463 | GAAGGTGATTGTTTA[A/G]CTCTTGAGGCTAAGC | 144406 |
rs1183898 | snp | C/T | 0 | 0 | intron-variant | WDR66 | GRCh38.p7 | 12:121954672 | caaaaaaaaAAACCT[C/T]TTTTGGATGTATATG | 144406 |
rs1184893 | snp | A/G | 0.499999 | 0.000798721 | intron-variant | WDR66 | GRCh38.p7 | 12:121965905 | gctcactgcagcctc[A/G]acctcccaggctcaa | 144406 |
rs1185260 | snp | A/G | 0.221439 | 0.248363 | intron-variant | WDR66 | GRCh38.p7 | 12:121951342 | TAGATATTTCCCAAG[A/G]CAGCAAGTTCTCTTA | 144406 |
rs1185641 | snp | A/G | | | intron-variant | WDR66 | GRCh38.p7 | 12:121994302 | cggggcggctggccg[A/G]gcggggggctgaccc | 144406 |
rs1375653 | snp | A/G | 0.499923 | 0.00618962 | intron-variant | WDR66 | GRCh38.p7 | 12:121950408 | cattgtgaatgtatg[A/G]aacaccgctgaattg | 144406 |
rs1375654 | snp | A/G | 0.499902 | 0.00698814 | intron-variant | WDR66 | GRCh38.p7 | 12:121947805 | CTGGCAAAAGCAAGT[A/G]CATGAGGCAGACTTC | 144406 |
rs1375655 | snp | A/G | 0.499908 | 0.00678851 | intron-variant | WDR66 | GRCh38.p7 | 12:121947784 | GGCAGACTTCACAAA[A/G]CCTGAAAATCAGCCT | 144406 |
rs1523260 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WDR66 | GRCh38.p7 | 12:121946859 | TGCAGCAGTGGCTCA[C/T]GCCTATAATCCCTGC | 144406 |
rs1630694 | snp | C/G | 0.0744748 | 0.178019 | intron-variant | WDR66 | GRCh38.p7 | 12:121948859 | AAACAGAAAAGATAC[C/G]GCATTTCGTAAAAAA | 144406 |
rs1630699 | snp | C/G | 0.499908 | 0.00678851 | intron-variant | WDR66 | GRCh38.p7 | 12:121948852 | AAAGATACCGCATTT[C/G]GTAAAAAAAAATAGG | 144406 |
rs1667580 | snp | C/T | 0.220544 | 0.248259 | intron-variant | WDR66 | GRCh38.p7 | 12:121939182 | CACAATCAGATTTGT[C/T]TGGGAAAACATCACA | 144406 |
rs1667583 | snp | A/G | 0.220544 | 0.248259 | intron-variant | WDR66 | GRCh38.p7 | 12:121932300 | TCTTCTGTAAAATGG[A/G]TATATGAATACCCAC | 144406 |
rs1667584 | snp | C/T | 0.221141 | 0.248329 | intron-variant | WDR66 | GRCh38.p7 | 12:121950490 | TGTGTTTTGGTTTTG[C/T]TCTACAAttttttat | 144406 |
rs1667586 | snp | C/T | 0.499918 | 0.00638925 | intron-variant | WDR66 | GRCh38.p7 | 12:121944273 | GGACATATGGCTGCA[C/T]AACCATATTTCCCTG | 144406 |
rs1667588 | snp | A/C | | | intron-variant | WDR66 | GRCh38.p7 | 12:121952350 | tcactgtagccttga[A/C]cacctgggctcaagt | 144406 |
rs1678951 | snp | C/T | 0.223225 | 0.248562 | intron-variant | WDR66 | GRCh38.p7 | 12:121945708 | TCTTGCTCTGTCACC[C/T]AGGCTGGAGTGCAGT | 144406 |
rs1678952 | snp | A/C | 0.499902 | 0.00698814 | intron-variant | WDR66 | GRCh38.p7 | 12:121947245 | TTTTTGTTAAACTGT[A/C]TATTAAGCATTTTAA | 144406 |
rs1678953 | snp | A/G | 0.499908 | 0.00678851 | intron-variant | WDR66 | GRCh38.p7 | 12:121947307 | ATTCTTTTTTAAGTA[A/G]AGCTATCTGCTGAGA | 144406 |
rs1678966 | snp | C/G | 0.221159 | 0.248331 | intron-variant | WDR66 | GRCh38.p7 | 12:121976442 | CCCCATTAACACCTG[C/G]TAGGTTAAGAGCAAC | 144406 |
rs1678967 | snp | A/G | 0.221141 | 0.248329 | intron-variant | WDR66 | GRCh38.p7 | 12:121920910 | ctggagtgcaatggt[A/G]tgatcttggctcact | 144406 |
rs1678968 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | WDR66 | GRCh38.p7 | 12:121920984 | CTCCCAAGTAGCTGG[A/G]ATTACAGGCGCCTGC | 144406 |
rs1678969 | snp | C/T | 0.220544 | 0.248259 | intron-variant | WDR66 | GRCh38.p7 | 12:121933568 | AATTTCAGCACAGGC[C/T]GTGGCCAAGGAGGCT | 144406 |
rs1720030 | snp | A/G | 0.499913 | 0.00658888 | intron-variant | WDR66 | GRCh38.p7 | 12:121947053 | TTGGAGCCCCAGAAG[A/G]AGAATAAAGAAAGAA | 144406 |
rs1720033 | snp | C/T | 0.330016 | 0.236849 | intron-variant | WDR66 | GRCh38.p7 | 12:121946438 | acatccttgaagata[C/T]gaactgctgaaagaa | 144406 |
rs1720037 | snp | G/T | 0.329317 | 0.237084 | intron-variant | WDR66 | GRCh38.p7 | 12:121944323 | CAACATTCCTCTTGC[G/T]CCTAAAAAATTTTTT | 144406 |
rs1720056 | snp | A/T | | | intron-variant | WDR66 | GRCh38.p7 | 12:121952348 | tcacttgagcccagg[A/T]gttcaaggctgcagt | 144406 |
rs1720066 | snp | G/T | 0.448452 | 0.152042 | intron-variant | WDR66 | GRCh38.p7 | 12:121926076 | AGATCAAGACCATCC[G/T]GGCTAACACGGTGAA | 144406 |
rs1720067 | snp | A/G | 0.225597 | 0.248806 | intron-variant | WDR66 | GRCh38.p7 | 12:121925875 | CCTAGGTGACAGAGC[A/G]AGACTCCACCTCAAA | 144406 |
rs1720068 | snp | A/G | 0.447291 | 0.153545 | intron-variant | WDR66 | GRCh38.p7 | 12:121925789 | ATTTTTGGTTCTGCC[A/G]TTTTGGTTCCGCAGT | 144406 |
rs1720071 | snp | C/T | 0 | 0 | missense | WDR66 | GRCh38.p7 | 12:121923898 | GTATCCGACATCCAG[C/T]CCAAAGCAGGGATCT | 144406 |
rs1814592 | snp | A/G | 0.407502 | 0.194147 | intron-variant | WDR66 | GRCh38.p7 | 12:122000281 | TTGGGGCCGGGCGCA[A/G]TGGCTCATGCCTGTA | 144406 |
rs1824949 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | WDR66 | GRCh38.p7 | 12:121980254 | GAGACACCTGCCCAC[A/G]TCTTAGCTGTCATCT | 144406 |
rs1971955 | snp | A/G | 0.370568 | 0.219005 | intron-variant | WDR66 | GRCh38.p7 | 12:121982531 | tgataggcatgcgcc[A/G]tcttgcctggctaat | 144406 |
rs2004863 | snp | A/T | 0.093777 | 0.195178 | intron-variant | WDR66 | GRCh38.p7 | 12:121921155 | ATAAAAAGAATGTCA[A/T]GTTTCTGACCAGGCA | 144406 |
rs2004864 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | WDR66 | GRCh38.p7 | 12:121921139 | GTTTCTGACCAGGCA[C/T]GGTGGCTCATGCCTG | 144406 |
rs2076860 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | WDR66 | GRCh38.p7 | 12:121997236 | GGGTGTTGTGGCGTA[C/T]GCCTTTGCATTCACG | 144406 |
rs2167066 | snp | A/T | | | intron-variant | WDR66 | GRCh38.p7 | 12:121935638 | TGTCAAAAGGCTGGT[A/T]GGcttatcacgagaa | 144406 |
rs2177330 | snp | C/G | 0.199254 | 0.244796 | intron-variant | WDR66 | GRCh38.p7 | 12:121964965 | CATTTAGTACTCATG[C/G]TGCTGTGCAACCCCC | 144406 |
rs2247139 | snp | A/G | 0.234109 | 0.249494 | intron-variant | WDR66 | GRCh38.p7 | 12:121942368 | catgtcatagcatgc[A/G]tcagtgcttcattcc | 144406 |
rs2272135 | snp | C/T | 0.407845 | 0.193868 | upstream-variant-2KB, downstream-variant-500B | WDR66, PSMD9 | GRCh38.p7 | 12:121918251 | GACGGTTGTGTGCTG[C/T]ATCCATGAGACCTGG | 144406 |
rs2309275 | snp | C/T | 0.409212 | 0.192748 | intron-variant | WDR66 | GRCh38.p7 | 12:121962907 | gggtttgggaaatgc[C/T]gcgaaggctggtgag | 144406 |
rs2309276 | snp | G/T | 0.0839998 | 0.186933 | intron-variant | WDR66 | GRCh38.p7 | 12:121977818 | aaaaaaattagccgg[G/T]cgtggtggtgggcgc | 144406 |
rs2309277 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | WDR66 | GRCh38.p7 | 12:121977819 | aaaaaattagccggg[C/T]gtggtggtgggcgcc | 144406 |
rs2442439 | snp | C/T | 0.44651 | 0.154543 | intron-variant | WDR66 | GRCh38.p7 | 12:121923046 | GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 144406 |
rs2620331 | snp | C/T | | | intron-variant | WDR66 | GRCh38.p7 | 12:121949364 | ggagatgaggtctca[C/T]tatgttgcccaggct | 144406 |
rs2620353 | snp | A/G | 0.233235 | 0.249437 | intron-variant | WDR66 | GRCh38.p7 | 12:121967529 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 144406 |
rs2688409 | snp | C/T | 0.447938 | 0.152711 | intron-variant | WDR66 | GRCh38.p7 | 12:121924518 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA | 144406 |
rs2688411 | snp | G/T | 0.499923 | 0.00618962 | intron-variant | WDR66 | GRCh38.p7 | 12:121943678 | gatctccccaccttg[G/T]cctcccaaaatgttg | 144406 |
rs2922797 | snp | C/T | 0.499918 | 0.00638925 | intron-variant | WDR66 | GRCh38.p7 | 12:121943182 | GGGACTATAGGCATG[C/T]GCCACCACACCCAGG | 144406 |
rs2948663 | snp | C/G | 0.499918 | 0.00638925 | intron-variant | WDR66 | GRCh38.p7 | 12:121943288 | TCTCACTTTGTCACC[C/G]AGGCTGGAGTGCAGT | 144406 |
rs2948664 | snp | A/C | 0.499918 | 0.00638925 | intron-variant | WDR66 | GRCh38.p7 | 12:121943228 | CCTCCCAGGTTCAAG[A/C]AATTCTCATGCCTCA | 144406 |
rs2948666 | snp | A/T | 0.499928 | 0.00598999 | intron-variant | WDR66 | GRCh38.p7 | 12:121952420 | ATTTTTTTTTTTTTT[A/T]TATACAGGGTCTTGT | 144406 |