SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1128044 | snp | C/G | 0.423881 | 0.179625 | utr-variant-3-prime | WDR5 | GRCh38.p7 | 9:134159126 | CCTGTGCTCCTGGCA[C/G]TGTGGCTTCCCGGTG | 11091 |
rs4130591 | snp | C/T | 0.274929 | 0.248754 | intron-variant | WDR5 | GRCh38.p7 | 9:134144569 | TACAGGTGGGAGACA[C/T]GGCACCCAACCTGTT | 11091 |
rs4130592 | snp | C/T | | | intron-variant | WDR5 | GRCh38.p7 | 9:134144454 | CGCTATCTTTGGCCT[C/T]TAGGATGCTCACAGA | 11091 |
rs11556387 | snp | C/T | 0.237882 | 0.249706 | utr-variant-3-prime | WDR5 | GRCh38.p7 | 9:134158945 | GGGGGACACCTGTGG[C/T]ATGGTAAGGCTCCCT | 11091 |
rs11556388 | snp | A/G | 0.0539704 | 0.155153 | utr-variant-3-prime | WDR5 | GRCh38.p7 | 9:134159283 | TGGCTGAGGGCACAG[A/G]TGCCTGGGTCTGTCC | 11091 |
rs11556389 | snp | C/T | 0.0535932 | 0.154675 | utr-variant-3-prime | WDR5 | GRCh38.p7 | 9:134159171 | AGTTAACAGCAGAGG[C/T]CGAGCGGGAGCCTCT | 11091 |
rs11556390 | snp | C/T | 0.48332 | 0.0897864 | synonymous-codon | WDR5 | GRCh38.p7 | 9:134139901 | GGAGGAGAAGAAGCC[C/T]GAGACCGAGGCCGCC | 11091 |
rs11556391 | snp | C/T | 0.4231 | 0.180378 | utr-variant-3-prime | WDR5 | GRCh38.p7 | 9:134158857 | CCCCCGTTCCCCGCC[C/T]CCAGCAACACTGAAC | 11091 |
rs28372151 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | WDR5 | GRCh38.p7 | 9:134152535 | GGGTGTGGCCTGAGG[A/G]TCTGTGACGGCCCGG | 11091 |
rs28377785 | snp | G/T | 0.0228947 | 0.104514 | intron-variant, upstream-variant-2KB | WDR5 | GRCh38.p7 | 9:134139265 | TGGAAGGCAGCCTCG[G/T]GCCAGCAGCCTGTGC | 11091 |
rs28399690 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | WDR5 | GRCh38.p7 | 9:134140338 | CGGGGTCGGAGGGTG[A/G]GGCGCTGGACCAAGG | 11091 |
rs28401385 | snp | A/G | 0.0970103 | 0.197722 | utr-variant-3-prime | WDR5 | GRCh38.p7 | 9:134158162 | AAGGTGTGGACCACC[A/G]GAAAGTTCTTAAAAG | 11091 |
rs28408860 | snp | C/T | 0.457037 | 0.140127 | upstream-variant-2KB | WDR5 | GRCh38.p7 | 9:134134467 | GAAGGGCTGGAAATA[C/T]TTTTGTTTTGGGGCT | 11091 |
rs28412245 | snp | A/G | 0.0970103 | 0.197722 | intron-variant | WDR5 | GRCh38.p7 | 9:134151730 | TAAACTGTGGCTTGT[A/G]TAGGAGAGATCCAGA | 11091 |
rs28413814 | snp | C/G | 0.274929 | 0.248754 | intron-variant | WDR5 | GRCh38.p7 | 9:134144127 | AGCCCTGATACTGCC[C/G]GGACGGACAGTGTGT | 11091 |
rs28415637 | snp | A/C | 0.422944 | 0.180528 | intron-variant | WDR5 | GRCh38.p7 | 9:134143164 | CCAGTCCTGGTGGGA[A/C]GTGTTGGAGGCTGGA | 11091 |
rs28421319 | snp | C/T | 0.0228947 | 0.104514 | intron-variant, upstream-variant-2KB | WDR5 | GRCh38.p7 | 9:134139544 | TAAACTGCTGCATTC[C/T]TACAGACTTCTGGAT | 11091 |
rs28425680 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | WDR5 | GRCh38.p7 | 9:134140911 | CACCTACCGCTGGGG[A/G]GACGTAGCAGGCCGC | 11091 |
rs28425690 | snp | C/T | 0.237593 | 0.249692 | intron-variant | WDR5 | GRCh38.p7 | 9:134157426 | GCCCTGTGGGGTGCT[C/T]TGGGGCTTAGCATTG | 11091 |
rs28429050 | snp | C/T | 0.300673 | 0.244811 | intron-variant | WDR5 | GRCh38.p7 | 9:134151117 | CATGGGGCAGCAGGA[C/T]GGAGCTGTTGCTGAG | 11091 |
rs28434714 | snp | A/C | 0.144969 | 0.226867 | intron-variant | WDR5 | GRCh38.p7 | 9:134150974 | AGAAGGAGCAGGACC[A/C]ATGCAGGAAATGAGA | 11091 |
rs28436125 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | WDR5 | GRCh38.p7 | 9:134140468 | GCTGGTGCTGTTGGT[A/G]CTGAGTTTGGAGACT | 11091 |
rs28437234 | snp | C/G | 0.457853 | 0.138915 | intron-variant | WDR5 | GRCh38.p7 | 9:134137788 | CGACGGAGTTTCACT[C/G]TTTGGCCCAGGCTGG | 11091 |
rs28438574 | snp | C/G | 0.488424 | 0.0751925 | intron-variant | WDR5 | GRCh38.p7 | 9:134151700 | AGCAACAGGCTTCCC[C/G]CTCTGTGTTGGGGGT | 11091 |
rs28440102 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | WDR5 | GRCh38.p7 | 9:134144093 | TTGGAAGGCTTTGCC[C/T]GAGTGAGATGGCAGG | 11091 |
rs28451195 | snp | A/G | 0.23846 | 0.249734 | intron-variant | WDR5 | GRCh38.p7 | 9:134154293 | ACCTGCTCACGGCTG[A/G]TGTGCGTGGCTAGGC | 11091 |
rs28464304 | snp | A/G | 0.433382 | 0.169915 | upstream-variant-2KB | WDR5 | GRCh38.p7 | 9:134134664 | AGTTTCTCTGTTTGG[A/G]GGTTTAGAAAAGACC | 11091 |
rs28464405 | snp | A/C | | | intron-variant | WDR5 | GRCh38.p7 | 9:134137686 | AAAAAAACAAAAACA[A/C]AAAAAAAACACGCCA | 11091 |
rs28475221 | snp | G/T | 0.42263 | 0.180829 | intron-variant | WDR5 | GRCh38.p7 | 9:134137543 | CAAAAGATTGGCCGG[G/T]CGTAGTGGTACGCGC | 11091 |
rs28477108 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | WDR5 | GRCh38.p7 | 9:134144109 | GAGTGAGATGGCAGG[C/T]GAAGCCCTGATACTG | 11091 |
rs28485236 | snp | C/T | 0.261056 | 0.249755 | intron-variant | WDR5 | GRCh38.p7 | 9:134157113 | CGCTACTTCCTCACC[C/T]TCTGGCCCTGCATTT | 11091 |
rs28485412 | snp | A/G | 0.271972 | 0.249033 | intron-variant | WDR5 | GRCh38.p7 | 9:134145572 | GGCCGTTTGTGCGGG[A/G]TGGCTTTGGAGGGGA | 11091 |
rs28488634 | snp | C/T | 0.144969 | 0.226867 | intron-variant | WDR5 | GRCh38.p7 | 9:134145058 | CCACAGCTGCTGCTC[C/T]GTAGCTGTCTCCACT | 11091 |
rs28489135 | snp | A/G | 0.0718919 | 0.175435 | intron-variant, upstream-variant-2KB | WDR5 | GRCh38.p7 | 9:134139143 | GCTGCTTTTCCAGAA[A/G]GCAGGATGTGGAAAT | 11091 |
rs28490920 | snp | C/T | 0.42357 | 0.179927 | intron-variant | WDR5 | GRCh38.p7 | 9:134145845 | CTTGTCTGCCCAAGT[C/T]GACTCCGCAGAGCAC | 11091 |
rs28491791 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | WDR5 | GRCh38.p7 | 9:134157714 | CGGCTGCTGTCCCCT[C/T]GCTCCCCTCCCCTGG | 11091 |
rs28493429 | snp | A/C | 0.281049 | 0.248064 | intron-variant | WDR5 | GRCh38.p7 | 9:134145651 | GAGCTTTAGAGACTT[A/C]GAGGCATGTGGCCCC | 11091 |
rs28495646 | snp | G/T | | | intron-variant | WDR5 | GRCh38.p7 | 9:134145097 | GTTTGTGGGGCTTTG[G/T]TTTTTTTTTTTTTTT | 11091 |
rs28501302 | snp | G/T | | | intron-variant | WDR5 | GRCh38.p7 | 9:134145951 | TCTTTTTTTTTTTTT[G/T]GTTTTTTAATATTTA | 11091 |
rs28505536 | snp | G/T | 0 | 0 | upstream-variant-2KB | WDR5 | GRCh38.p7 | 9:134134737 | CGATCTGAGAGCTGA[G/T]GTGGGGTGGAAGGAG | 11091 |
rs28507057 | snp | G/T | 0.0973687 | 0.197999 | intron-variant | WDR5 | GRCh38.p7 | 9:134154184 | GAGGCAGGTGATTCC[G/T]GAGAGTGCCCATGGC | 11091 |
rs28507484 | snp | A/C | 0 | 0 | intron-variant | WDR5 | GRCh38.p7 | 9:134137678 | GTCTCAAAAAAAAAA[A/C]AAAAACAAAAAAAAA | 11091 |
rs28508246 | snp | A/G | 0.422787 | 0.180679 | intron-variant | WDR5 | GRCh38.p7 | 9:134147448 | TCTGGAGACATTTTT[A/G]GTTGTCAGAGCTATA | 11091 |
rs28510147 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | WDR5 | GRCh38.p7 | 9:134155538 | TATTTGTAGGGTGGC[A/G]GTCTGCAAGTTAAAT | 11091 |
rs28510444 | snp | A/G | 0.0858192 | 0.188533 | utr-variant-3-prime | WDR5 | GRCh38.p7 | 9:134159066 | TTGGGTGCTAAGCGC[A/G]AGCCTCGCCGTCCCT | 11091 |
rs28522840 | snp | C/T | 0.472803 | 0.113397 | intron-variant | WDR5 | GRCh38.p7 | 9:134156681 | GTGCCCGTAGGGTGC[C/T]GTCGTCTTCCCCTTC | 11091 |
rs28523906 | snp | C/G | 0.0854556 | 0.188216 | intron-variant | WDR5 | GRCh38.p7 | 9:134150822 | CTAGCTACGTGGTGT[C/G]ATCTCGCGTTTAGTG | 11091 |
rs28526870 | snp | A/G | | | intron-variant | WDR5 | GRCh38.p7 | 9:134137723 | GACCCCACCGACGTA[A/G]AAACTTGGTGGGTGT | 11091 |
rs28529241 | snp | C/G | 0.371177 | 0.218669 | upstream-variant-2KB | WDR5 | GRCh38.p7 | 9:134134771 | AGCGTGTCACGGGCT[C/G]GGGATTCCGGCCCAG | 11091 |
rs28533919 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | WDR5 | GRCh38.p7 | 9:134137454 | TTGGGAGGCTGAGGC[A/G]GGCGGATTGCCTGAG | 11091 |
rs28535008 | snp | C/G | 0.261332 | 0.249743 | intron-variant | WDR5 | GRCh38.p7 | 9:134157665 | CCTGTGGCCTCCTGC[C/G]CCTGTCCCCCAACCG | 11091 |
rs28538491 | snp | C/T | 0.145642 | 0.227177 | intron-variant | WDR5 | GRCh38.p7 | 9:134152847 | GGCTGTGGTCAGGAT[C/T]GAGGAGGCCTCTTCT | 11091 |
rs28540854 | snp | C/T | 0.317692 | 0.240661 | downstream-variant-500B | WDR5 | GRCh38.p7 | 9:134160031 | GGGTGGGAGGGCGGC[C/T]GCCCTGGGGCTTTGT | 11091 |
rs28541450 | snp | A/C | | | intron-variant | WDR5 | GRCh38.p7 | 9:134137684 | AAAAAAAAACAAAAA[A/C]AAAAAAAAAACACGC | 11091 |
rs28542945 | snp | A/C | 0.264358 | 0.249587 | intron-variant | WDR5 | GRCh38.p7 | 9:134150934 | AGTGACAAAAATGCT[A/C]AGATGTTTAGGAATG | 11091 |
rs28549758 | snp | C/T | 0.4231 | 0.180378 | intron-variant | WDR5 | GRCh38.p7 | 9:134147998 | CGTCTCTCCTAAAAA[C/T]ATATATATATAAAAA | 11091 |
rs28549934 | snp | A/C | 0.47023 | 0.118317 | intron-variant | WDR5 | GRCh38.p7 | 9:134151716 | CTCTGTGTTGGGGGT[A/C]AACTGTGGCTTGTGT | 11091 |
rs28550794 | snp | A/G | 0.0599851 | 0.162463 | downstream-variant-500B | WDR5 | GRCh38.p7 | 9:134160337 | TGTGAAGAGTGTGGC[A/G]CCCCCCAGTTTCCTG | 11091 |
rs28562287 | snp | A/T | 0.0425688 | 0.139543 | intron-variant | WDR5 | GRCh38.p7 | 9:134142329 | TAATAATACTCTGTT[A/T]TAGGGCAAGTGTCTG | 11091 |
rs28562648 | snp | C/T | 0.209693 | 0.246729 | intron-variant | WDR5 | GRCh38.p7 | 9:134150957 | TAGGAATGCGGCTAG[C/T]GAGAAGGAGCAGGAC | 11091 |
rs28562957 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | WDR5 | GRCh38.p7 | 9:134139529 | TGCATTTTGTTTGCA[C/T]AAACTGCTGCATTCC | 11091 |
rs28564554 | snp | C/T | 0.249886 | 0.25 | intron-variant | WDR5 | GRCh38.p7 | 9:134140251 | CCCCCACCCTGGCTG[C/T]GATCCTGACGCACAG | 11091 |
rs28565058 | snp | C/T | 0.144969 | 0.226867 | intron-variant | WDR5 | GRCh38.p7 | 9:134156773 | TGGAGCTGGTCACTG[C/T]GCTGCCGACTCAGAC | 11091 |
rs28567437 | snp | A/G | 0.4231 | 0.180378 | intron-variant | WDR5 | GRCh38.p7 | 9:134146126 | CCCTCCACCATGCCC[A/G]GCTAATTTTTTTTTA | 11091 |
rs28570290 | snp | C/T | 0.2462 | 0.249971 | intron-variant | WDR5 | GRCh38.p7 | 9:134145773 | ATCATCCACAGCCCT[C/T]GCGCCCTCCTTGCAC | 11091 |
rs28572025 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | WDR5 | GRCh38.p7 | 9:134156731 | GCCCCGCTGAGGAAC[C/T]GCTGCTAAGAGCTCT | 11091 |
rs28578388 | snp | A/T | 0.0372196 | 0.131242 | upstream-variant-2KB | WDR5 | GRCh38.p7 | 9:134134937 | GCCCTGAAGGACCAG[A/T]CAGGGACCTTGCCTT | 11091 |
rs28579703 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | WDR5 | GRCh38.p7 | 9:134157163 | CGAGAGCAGGGGGTT[C/T]GAGCCCTTGTGGAAA | 11091 |
rs28580780 | snp | C/G | 0.465996 | 0.12588 | upstream-variant-2KB | WDR5 | GRCh38.p7 | 9:134135347 | GGAAGGGCTGGCCCC[C/G]GGAGAGCCCGCTGCG | 11091 |
rs28581991 | snp | C/T | 0.498009 | 0.0314867 | intron-variant, upstream-variant-2KB | WDR5 | GRCh38.p7 | 9:134139785 | TTAAAATATAGTTTG[C/T]TTCTTGGCTCCCTGT | 11091 |
rs28585632 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | WDR5 | GRCh38.p7 | 9:134140245 | TAGTTGCCCCCACCC[C/T]GGCTGCGATCCTGAC | 11091 |
rs28588875 | snp | C/T | 0.423413 | 0.180077 | intron-variant | WDR5 | GRCh38.p7 | 9:134145007 | TTTAAATAACTGGTA[C/T]CACATCACAGCTGCT | 11091 |
rs28593202 | snp | A/G | 0.144969 | 0.226867 | intron-variant | WDR5 | GRCh38.p7 | 9:134143902 | ACCGCTCCATTTCAC[A/G]AAGTGGCCAGAAAGT | 11091 |
rs28594106 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | WDR5 | GRCh38.p7 | 9:134140211 | AGAGTCTCTGTAGGA[A/C]CCAGAAAACATCTCT | 11091 |
rs28595141 | snp | A/G | 0.145642 | 0.227177 | utr-variant-3-prime | WDR5 | GRCh38.p7 | 9:134159590 | CATCTGGAGATGTAT[A/G]TCCTGTGGTTTCCCC | 11091 |
rs28597926 | snp | C/T | 0.264084 | 0.249603 | intron-variant | WDR5 | GRCh38.p7 | 9:134149108 | GTGGACACGCACACT[C/T]GAAATCTGTTTCCCA | 11091 |
rs28602914 | snp | C/T | 0.462253 | 0.132093 | intron-variant | WDR5 | GRCh38.p7 | 9:134143268 | CCGAGAGGCCGGGCG[C/T]GGCGGCTCACGCCTG | 11091 |
rs28603051 | snp | A/T | 0.375 | 0.216506 | intron-variant | WDR5 | GRCh38.p7 | 9:134143828 | CCAAAACTCTGTCTT[A/T]AAAAAAAAAAAAAAA | 11091 |
rs28604373 | snp | A/G | 0.475702 | 0.107512 | intron-variant | WDR5 | GRCh38.p7 | 9:134153008 | GTCTCCAGTACACTC[A/G]CCTCTGAGGCTCTGG | 11091 |
rs28605038 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | WDR5 | GRCh38.p7 | 9:134156320 | AGCAGGCGGGGCTGT[C/T]CCCATTGGGAGAGGA | 11091 |
rs28610172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | WDR5 | GRCh38.p7 | 9:134139083 | TCTTTTTTCGTTCCC[C/T]TGCAGTGTGAGTCCT | 11091 |
rs28610236 | snp | C/T | 0.432063 | 0.171327 | upstream-variant-2KB | WDR5 | GRCh38.p7 | 9:134133979 | TATGGCAGGTGAAAA[C/T]AGAAGAGAAAATAAG | 11091 |
rs28620240 | snp | C/T | 0.0980852 | 0.198549 | intron-variant | WDR5 | GRCh38.p7 | 9:134151049 | GAGATGAGGCGGCTC[C/T]GGAGAGGCCCTCCCG | 11091 |
rs28620999 | snp | A/G | 0.236616 | 0.249641 | intron-variant | WDR5 | GRCh38.p7 | 9:134155309 | AGGATGCCTCCAGAC[A/G]TGCCGCCTCACCCCT | 11091 |
rs28623667 | snp | A/G | 0.370162 | 0.219229 | intron-variant | WDR5 | GRCh38.p7 | 9:134137126 | CCTGGGCTCCACCTC[A/G]GGGACTGAGGGACTC | 11091 |
rs28626085 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | WDR5 | GRCh38.p7 | 9:134140949 | CACGTAGCAGGCGGG[C/T]GTGTCTCCTCCTGGA | 11091 |
rs28626222 | snp | A/G | 0.0854556 | 0.188216 | intron-variant | WDR5 | GRCh38.p7 | 9:134148621 | CAGCTCCGTGTAGAC[A/G]CTGACGTGTGCTGTT | 11091 |
rs28626885 | snp | A/C | 0.145305 | 0.227022 | utr-variant-3-prime | WDR5 | GRCh38.p7 | 9:134158756 | AAGGCTCCCCTGGGG[A/C]AAGAGGGCGGAAGGT | 11091 |
rs28634919 | snp | A/T | 0 | 0 | intron-variant | WDR5 | GRCh38.p7 | 9:134149199 | CATGCATGACCCCCC[A/T]TCGGTCTTGAGAAGA | 11091 |
rs28635910 | snp | A/C | 0.471004 | 0.116864 | intron-variant | WDR5 | GRCh38.p7 | 9:134157205 | ACTGCTTCTCCCTCC[A/C]TGTGAGCAGCTTCAC | 11091 |
rs28637300 | snp | C/T | 0.144969 | 0.226867 | utr-variant-3-prime | WDR5 | GRCh38.p7 | 9:134158764 | CCTGGGGAAAGAGGG[C/T]GGAAGGTTTCTTTGG | 11091 |
rs28644346 | snp | A/C | 0.000477952 | 0.0154515 | synonymous-codon | WDR5 | GRCh38.p7 | 9:134142395 | CTGCAACTTCAATCC[A/C]CAGTCCAACCTTATT | 11091 |
rs28648812 | snp | A/G | 0.423257 | 0.180228 | intron-variant | WDR5 | GRCh38.p7 | 9:134142176 | GCAGGGGCATGGGGC[A/G]GGGGTGGGTGGGGGA | 11091 |
rs28654852 | snp | A/T | 0.0429648 | 0.14013 | intron-variant | WDR5 | GRCh38.p7 | 9:134144180 | GTCTGAGCCCCGCAC[A/T]TAGCTGGGCCACAAG | 11091 |
rs28654988 | snp | C/T | 0.144969 | 0.226867 | intron-variant | WDR5 | GRCh38.p7 | 9:134154257 | AGGGGCCCCCGGGCC[C/T]ATGGGCTTGAGGTGT | 11091 |
rs28657441 | snp | A/G | 0.0482373 | 0.14762 | utr-variant-5-prime | WDR5 | GRCh38.p7 | 9:134139869 | TCCTGTGCGGCCAGC[A/G]TCAGAGCCATGGCGA | 11091 |
rs28657551 | snp | A/T | 0.0524604 | 0.153226 | intron-variant | WDR5 | GRCh38.p7 | 9:134148010 | AAATATATATATATA[A/T]AAATTAGCTGGGCGT | 11091 |
rs28665545 | snp | C/G | 0.144969 | 0.226867 | intron-variant | WDR5 | GRCh38.p7 | 9:134154225 | AGGAGGCCTGTATTC[C/G]TAAAGTCCTGGTGTC | 11091 |
rs28673958 | snp | A/C | 0.144969 | 0.226867 | intron-variant | WDR5 | GRCh38.p7 | 9:134148740 | GTGAGGATGCGTCAC[A/C]ATCCCGGGCAGGTGA | 11091 |
rs28687115 | snp | C/T | 0.0426181 | 0.139616 | intron-variant | WDR5 | GRCh38.p7 | 9:134141467 | TGGATGACTAGACAA[C/T]TGTGTCCTGCTCTTA | 11091 |