SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3636 | snp | C/G | 0.499789 | 0.146778 | intron-variant | WDR59 | GRCh38.p7 | 16:74903825 | ACTTTCTTGAACAAA[C/G]TGATTACGAAAGTGA | 79726 |
rs6927 | snp | A/G | 0.0193772 | 0.0965046 | utr-variant-3-prime, nc-transcript-variant | WDR59 | GRCh38.p7 | 16:74873709 | TACAATTTAAGTGTC[A/G]TATTTTAGAAGGCCA | 79726 |
rs14308 | snp | A/G | 0.23486 | 0.249541 | synonymous-codon, nc-transcript-variant | WDR59 | GRCh38.p7 | 16:74886293 | TTTATCATGCTGGTC[A/G]CGTTCTCGCTCACGG | 79726 |
rs713257 | snp | C/G | 0.451483 | 0.148002 | intron-variant | WDR59 | GRCh38.p7 | 16:74911496 | GAGCCTCTTCATACC[C/G]GTTCAGTCTGAGCAG | 79726 |
rs933724 | snp | A/G | 0.5 | 0 | downstream-variant-500B | WDR59 | GRCh38.p7 | 16:74873493 | AAAGTCAGTGCTCCG[A/G]TTTTTAAAGGAAATG | 79726 |
rs951574 | snp | A/G | 0.139903 | 0.224452 | intron-variant | WDR59 | GRCh38.p7 | 16:74955569 | GCCCTGAAAATCAGC[A/G]CAACCTCGGACATCC | 79726 |
rs951575 | snp | A/G | 0.454664 | 0.143571 | intron-variant | WDR59 | GRCh38.p7 | 16:74955442 | CCGAGGGTGAGAGGG[A/G]AATAAGGGTCCCGAG | 79726 |
rs1051432 | snp | C/G | 0.137867 | 0.223442 | utr-variant-3-prime, nc-transcript-variant | WDR59 | GRCh38.p7 | 16:74873752 | TCAGTAAATGTACCA[C/G]CTTCTAAAGCCATGA | 79726 |
rs1424115 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | WDR59 | GRCh38.p7 | 16:74919210 | CTCTCCCAACTGGCT[A/G]ATTCTACGCCTTGCC | 79726 |
rs1469129 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | WDR59 | GRCh38.p7 | 16:74910614 | CTCAGTGACAAGAGG[A/C]ATGGATTTCACTTCA | 79726 |
rs1469130 | snp | C/T | 0.496999 | 0.0386216 | intron-variant | WDR59 | GRCh38.p7 | 16:74910675 | TCAAAAGTATAAATC[C/T]TAACACTTTAAACcc | 79726 |
rs1559412 | snp | A/T | 0 | 0 | intron-variant | WDR59 | GRCh38.p7 | 16:74898791 | CCTGCTCCCACTGCT[A/T]TTTAAATAGGGACTC | 79726 |
rs1559413 | snp | C/G | 0.115438 | 0.210697 | intron-variant | WDR59 | GRCh38.p7 | 16:74902553 | CAAAGTGAAAATTAC[C/G]AGTCAATCTATTCTG | 79726 |
rs1808444 | snp | A/C | 0.485324 | 0.0843964 | intron-variant | WDR59 | GRCh38.p7 | 16:74874899 | GTGTAAAAAAAACAA[A/C]AAAAAACAGGCTGGG | 79726 |
rs1943063 | snp | A/C | 0.498158 | 0.0302955 | intron-variant | WDR59 | GRCh38.p7 | 16:74956163 | GTAACTAGCCAGCGG[A/C]CAAATGGCAGATGAC | 79726 |
rs1943064 | snp | A/G | 0.494692 | 0.0512434 | intron-variant | WDR59 | GRCh38.p7 | 16:74956106 | CTGGCGAGCTGGTGT[A/G]GAGTTGACCTTCATT | 79726 |
rs1943066 | snp | A/G | 0.188 | 0.24219 | intron-variant | WDR59 | GRCh38.p7 | 16:74960161 | ttgtattttagtaga[A/G]acggggtttcaccgt | 79726 |
rs2011533 | snp | A/C | 0.498927 | 0.0231381 | intron-variant | WDR59 | GRCh38.p7 | 16:74955590 | ATAGAGTCTGCCTTT[A/C]ACTGTGGATGTCCGA | 79726 |
rs2042415 | snp | A/G | 0.232651 | 0.249397 | intron-variant, upstream-variant-2KB | WDR59 | GRCh38.p7 | 16:74944720 | GCCTCTTTTCCCCCA[A/G]GGTAGATCTGCACCA | 79726 |
rs2059266 | snp | A/G | 0.494855 | 0.0504572 | intron-variant | WDR59 | GRCh38.p7 | 16:74902133 | CACTGAACTATACAC[A/G]ACTTTGATTTGTGAA | 79726 |
rs2059267 | snp | C/T | 0.495135 | 0.0490805 | intron-variant | WDR59 | GRCh38.p7 | 16:74902638 | GAACTGCCTCTTGGA[C/T]TGAAAGACCTCCTTG | 79726 |
rs2059268 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | WDR59 | GRCh38.p7 | 16:74933760 | CAAGCTAATTTTGTA[A/T]TTTTAGTAGAGATGG | 79726 |
rs2081251 | snp | A/G | 0.111576 | 0.20818 | intron-variant | WDR59 | GRCh38.p7 | 16:74884498 | ggattataggtgtgc[A/G]ctagcacgcctggct | 79726 |
rs2081252 | snp | C/T | 0.31357 | 0.241783 | intron-variant | WDR59 | GRCh38.p7 | 16:74891864 | gggaggcggaggttg[C/T]ggtgagctgagatcg | 79726 |
rs2098743 | snp | C/T | 0.38821 | 0.208322 | intron-variant | WDR59 | GRCh38.p7 | 16:74884887 | CAGACCTCAGCTCCT[C/T]GGAGGCCTTCTCAAC | 79726 |
rs2156277 | snp | C/T | 0.464523 | 0.128375 | intron-variant, upstream-variant-2KB | WDR59 | GRCh38.p7 | 16:74958021 | TCCTGCGATGGCCAG[C/T]TGGCATCGTCCCATC | 79726 |
rs2187219 | snp | C/G | 0.499923 | 0.00618962 | intron-variant, upstream-variant-2KB | WDR59 | GRCh38.p7 | 16:74958095 | AGTATCAATAGGGGG[C/G]TGCAGAGACTTTACA | 79726 |
rs2288041 | snp | A/G | 0.424968 | 0.178567 | intron-variant | WDR59 | GRCh38.p7 | 16:74887548 | TTTACTGTGATAGGG[A/G]TACTCTTGCTGGAGG | 79726 |
rs2288042 | snp | G/T | 0.0788843 | 0.182262 | intron-variant | WDR59 | GRCh38.p7 | 16:74887495 | ACCACGTTCTGGGGG[G/T]CTTTGTGCCTTGCTG | 79726 |
rs2303250 | snp | A/G | 0.457504 | 0.139435 | intron-variant | WDR59 | GRCh38.p7 | 16:74909201 | GGCAGAGTCATCAGC[A/G]GGACTCTAAGCCTCC | 79726 |
rs2303251 | snp | C/G | 0.460027 | 0.135605 | intron-variant | WDR59 | GRCh38.p7 | 16:74909266 | CTCTGAGTAAAGACT[C/G]AAATCCAAGCTCATC | 79726 |
rs2303253 | snp | A/G | | | intron-variant | WDR59 | GRCh38.p7 | 16:74909330 | CACCCTCTTAGGATA[A/G]GTCCACAGACACCGA | 79726 |
rs2303254 | snp | A/G | 0.455621 | 0.142197 | intron-variant | WDR59 | GRCh38.p7 | 16:74909362 | TGGGCCTCAGACCCT[A/G]CCACGCTACCATGAA | 79726 |
rs2869879 | snp | A/G | 0.437824 | 0.164991 | intron-variant | WDR59 | GRCh38.p7 | 16:74906052 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 79726 |
rs2869880 | snp | C/T | 0.443598 | 0.158176 | intron-variant | WDR59 | GRCh38.p7 | 16:74904959 | TAAGGGGTCAAAGTT[C/T]GTTTTATTTTGTAGA | 79726 |
rs2870148 | snp | A/G | 0.0926964 | 0.194308 | intron-variant | WDR59 | GRCh38.p7 | 16:74874541 | ATCTGCTAGAGTCTT[A/G]AGAGGAAGACTTCCT | 79726 |
rs2904226 | snp | A/C | 0.35894 | 0.225016 | intron-variant | WDR59 | GRCh38.p7 | 16:74905822 | tattgattttctctt[A/C]atctgtggcttgtct | 79726 |
rs2904227 | snp | G/T | 0.359364 | 0.22481 | intron-variant | WDR59 | GRCh38.p7 | 16:74905772 | ttcaatgaacaaatt[G/T]tcctaattttgatga | 79726 |
rs2904327 | snp | C/G | 0.419296 | 0.183954 | intron-variant | WDR59 | GRCh38.p7 | 16:74884571 | CACTTGAGGCCAGGG[C/G]TTTGAGACCAGCCTG | 79726 |
rs3064646 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | WDR59 | GRCh38.p7 | 16:74943254 | TATTGCTCAACAATT[-/A]AAAAAAAAAAAAAGG | 79726 |
rs3743921 | snp | A/T | 0.446771 | 0.154211 | intron-variant | WDR59 | GRCh38.p7 | 16:74951618 | CCTGGCTTCCTCTTC[A/T]CTGCCTTAAGCTGAT | 79726 |
rs3781477 | snp | A/G | | | intron-variant | WDR59 | GRCh38.p7 | 16:74881641 | gcactttgggaggcc[A/G]aggcaggcagatcac | 79726 |
rs3814875 | snp | A/C | 0.406468 | 0.194981 | upstream-variant-2KB | WDR59 | GRCh38.p7 | 16:74985172 | ATTGGTTGACCCAAG[A/C]ATAGGCTCCGCCCCT | 79726 |
rs3835317 | in-del | -/T | | | intron-variant | WDR59 | GRCh38.p7 | 16:74921776 | GAGTAACAGCAGCCT[-/T]ATATAGTCCCTTTAC | 79726 |
rs3921019 | snp | C/T | 0.460925 | 0.134204 | intron-variant | WDR59 | GRCh38.p7 | 16:74959867 | CGTTTCCTTTGAAtt[C/T]cttcttttcttcttc | 79726 |
rs3937016 | snp | C/T | 0 | 0 | intron-variant | WDR59 | GRCh38.p7 | 16:74947095 | AAAGGTCAGTTCCAA[C/T]TAAGCAATGAAAACA | 79726 |
rs4405579 | snp | C/G | 0.451483 | 0.148002 | intron-variant | WDR59 | GRCh38.p7 | 16:74906358 | AGGACACTCACAACA[C/G]AATGGCTAAAGTTGA | 79726 |
rs4522442 | snp | C/G | 0 | 0 | intron-variant | WDR59 | GRCh38.p7 | 16:74906510 | AAAATACATCTATCT[C/G]ATGACTGAGGAATTC | 79726 |
rs4628995 | snp | C/T | 0.449473 | 0.150701 | intron-variant | WDR59 | GRCh38.p7 | 16:74906516 | catctatctgatgac[C/T]gaggaattctgctcc | 79726 |
rs4630577 | snp | C/G | 0.46875 | 0.121031 | intron-variant | WDR59 | GRCh38.p7 | 16:74984530 | CAGGCACTTTGCAAA[C/G]AGTGTTTCATCGAAT | 79726 |
rs4887788 | snp | A/G | 0.238749 | 0.249747 | intron-variant | WDR59 | GRCh38.p7 | 16:74895543 | GCTAAGATTACAGGC[A/G]TGAGCCACCACGCCC | 79726 |
rs4887789 | snp | C/T | 0.450105 | 0.149859 | intron-variant | WDR59 | GRCh38.p7 | 16:74907351 | CACAGTGGGAGGTGA[C/T]TGGATCATGGGGGCG | 79726 |
rs4887790 | snp | C/T | 0.449345 | 0.150869 | intron-variant | WDR59 | GRCh38.p7 | 16:74907424 | GAGATTTGATGGTTT[C/T]ATAAGATCTGACAGT | 79726 |
rs4887791 | snp | C/T | 0.450357 | 0.149522 | intron-variant | WDR59 | GRCh38.p7 | 16:74907776 | TCAAAACAGGAAACA[C/T]GGAGCACTTCCAATG | 79726 |
rs4887792 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | WDR59 | GRCh38.p7 | 16:74912999 | agcgtgggcatcacc[A/G]ccatcatgaacatgt | 79726 |
rs4887793 | snp | A/T | 0 | 0 | intron-variant | WDR59 | GRCh38.p7 | 16:74927646 | AAATAAAACTTCTAA[A/T]AAACTTCTGATGTTT | 79726 |
rs4887794 | snp | G/T | 0.244205 | 0.249933 | intron-variant | WDR59 | GRCh38.p7 | 16:74930566 | CCTTGAAACAAACTT[G/T]ATGAAAGTTTTTTTT | 79726 |
rs4887795 | snp | C/T | 0.223819 | 0.248625 | intron-variant | WDR59 | GRCh38.p7 | 16:74930964 | TGTCTCGGAGCAAGA[C/T]TCCATCTCCAAAAAA | 79726 |
rs4887796 | snp | A/T | 0.498095 | 0.0308047 | intron-variant | WDR59 | GRCh38.p7 | 16:74965727 | AACCCCGATTTGCAA[A/T]TCGTTTCCAGAAATC | 79726 |
rs4887797 | snp | A/G | 0.485596 | 0.0836329 | intron-variant, upstream-variant-2KB | WDR59 | GRCh38.p7 | 16:74966000 | ACAACCCAATTCCAC[A/G]TTCACTTTTTTTATT | 79726 |
rs4887798 | snp | C/G | 0.0689305 | 0.172377 | intron-variant | WDR59 | GRCh38.p7 | 16:74984202 | GAATTGCTTGAATCC[C/G]GGAGGCGGAGGTTGC | 79726 |
rs4887799 | snp | C/G | 0.0119091 | 0.0762411 | upstream-variant-2KB | WDR59 | GRCh38.p7 | 16:74985409 | GGTGCCTGTTGTCCT[C/G]ACTAGCTCCTCGCTG | 79726 |
rs4888305 | snp | C/T | 0.119978 | 0.213528 | intron-variant | WDR59 | GRCh38.p7 | 16:74886476 | TCTCATAAGACAGCA[C/T]GTGGCCAATGGATTT | 79726 |
rs4888306 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | WDR59 | GRCh38.p7 | 16:74889124 | ATAAATTAAGCAAAC[C/T]TCAACTTGAAGTCAG | 79726 |
rs4888307 | snp | A/G | 0.227074 | 0.248947 | intron-variant | WDR59 | GRCh38.p7 | 16:74893160 | CACCAGTGAATATTG[A/G]TGGGATATCACTTCT | 79726 |
rs4888309 | snp | C/T | 0.44858 | 0.151875 | intron-variant | WDR59 | GRCh38.p7 | 16:74907669 | GCCTTCAGGGGTTTG[C/T]AGCAGGGAGGTTTGC | 79726 |
rs4888310 | snp | C/T | 0.000165022 | 0.00908206 | intron-variant | WDR59 | GRCh38.p7 | 16:74916309 | AGTCCGTGGAAATGA[C/T]TGTCATGTCTGATTA | 79726 |
rs4888311 | snp | A/T | 0.370162 | 0.219229 | intron-variant | WDR59 | GRCh38.p7 | 16:74920395 | gtgggttaggtgggt[A/T]aaatatatatatata | 79726 |
rs4888312 | snp | C/G | 0.460563 | 0.156966 | intron-variant | WDR59 | GRCh38.p7 | 16:74924716 | AAGCCAAGAGTGAAA[C/G]TCGGAACTGCTTAAG | 79726 |
rs4888313 | snp | A/G | 0.455858 | 0.141853 | intron-variant | WDR59 | GRCh38.p7 | 16:74924740 | GCTTAAGTTTAGGAA[A/G]TTTTTTCAAAAATag | 79726 |
rs4888314 | snp | A/G | 0.455858 | 0.141853 | intron-variant | WDR59 | GRCh38.p7 | 16:74924808 | ctttttttaatagag[A/G]tgggatcttgccatg | 79726 |
rs4888315 | snp | C/T | 0.455977 | 0.141681 | intron-variant | WDR59 | GRCh38.p7 | 16:74926117 | caggctggagaacaa[C/T]ggtgtgatctcggct | 79726 |
rs4888316 | snp | C/G | 0.475081 | 0.108804 | intron-variant | WDR59 | GRCh38.p7 | 16:74932775 | ATTACAGGGGTGAGC[C/G]ACCATGCCCAGTCTT | 79726 |
rs4888317 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | WDR59 | GRCh38.p7 | 16:74935199 | CACACCACTGCAATC[C/G]AGCCTGGGCAACAGA | 79726 |
rs4888318 | snp | A/T | 0.456332 | 0.141164 | intron-variant | WDR59 | GRCh38.p7 | 16:74940340 | GCCAAGAATGCGCCA[A/T]TGCACTCCAGCCTGG | 79726 |
rs4888319 | snp | A/G | 0.0640965 | 0.167152 | intron-variant, upstream-variant-2KB | WDR59 | GRCh38.p7 | 16:74944194 | CCAGAGGCCAGGCGC[A/G]GTGGCTTGCACCTAT | 79726 |
rs4888320 | snp | G/T | 0.178144 | 0.239451 | intron-variant, upstream-variant-2KB | WDR59 | GRCh38.p7 | 16:74957966 | AGTGCAGAACAAATA[G/T]CACATAGAATCTCTG | 79726 |
rs4888321 | snp | A/C | 0.215446 | 0.2476 | intron-variant | WDR59 | GRCh38.p7 | 16:74960493 | ttcacatctgtaatc[A/C]cagcactttgggagg | 79726 |
rs4888322 | snp | C/T | 0.473909 | 0.111197 | intron-variant | WDR59 | GRCh38.p7 | 16:74960515 | tttgggaggctgagg[C/T]gggtggatcacccaa | 79726 |
rs4888323 | snp | C/T | 0.48666 | 0.0805725 | intron-variant | WDR59 | GRCh38.p7 | 16:74964371 | gcaacaagagcgaaa[C/T]atcatctcaaaaaaa | 79726 |
rs4888324 | snp | A/C | 0.4582 | 0.138394 | intron-variant | WDR59 | GRCh38.p7 | 16:74965719 | TTCCCAGAAACCCCG[A/C]TTTGCAAATCGTTTC | 79726 |
rs4888325 | snp | A/C | 0.4582 | 0.138394 | intron-variant | WDR59 | GRCh38.p7 | 16:74969649 | gctttagctcactgc[A/C]acctctgcctcccgc | 79726 |
rs4888327 | snp | A/C | 0.449473 | 0.150701 | intron-variant | WDR59 | GRCh38.p7 | 16:74974450 | acgctaggtgttcca[A/C]actgatattgtcatt | 79726 |
rs4888328 | snp | C/T | 0.387263 | 0.208947 | intron-variant | WDR59 | GRCh38.p7 | 16:74976004 | GTTAAAATACACATA[C/T]ATAAATTTATTTAAA | 79726 |
rs5001472 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | WDR59 | GRCh38.p7 | 16:74881082 | AGACCAAGCGCATCA[C/T]ATACCACAGTCAGAA | 79726 |
rs5001473 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | WDR59 | GRCh38.p7 | 16:74881108 | CAGAAACAAAAACAA[A/C]AAAAAATCATCTTAT | 79726 |
rs5001474 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | WDR59 | GRCh38.p7 | 16:74881195 | TGAAACCATGAGCCC[C/T]GTCTGTAAATATTGA | 79726 |
rs5001475 | snp | A/C | 0.0410537 | 0.137264 | intron-variant | WDR59 | GRCh38.p7 | 16:74881242 | CTCAAATTTGCTATG[A/C]TGAAGTCTGTGGATA | 79726 |
rs5001476 | snp | C/G | 0.0410537 | 0.137264 | intron-variant | WDR59 | GRCh38.p7 | 16:74881284 | TTGCAGACAAGATTA[C/G]CACAGAGGAAACTGC | 79726 |
rs5023507 | snp | A/C/T | 1.66941e-05 | 0.00288908 | intron-variant | WDR59 | GRCh38.p7 | 16:74909790 | ACAAAACACCAAAGC[A/C/T]TAAGTTGGTATGACA | 79726 |
rs5023508 | snp | C/T | 0.000568961 | 0.016857 | intron-variant | WDR59 | GRCh38.p7 | 16:74909783 | AAATGAAACAAAACA[C/T]CAAAGCCTAAGTTGG | 79726 |
rs5817931 | in-del | -/A/AA | 0.501053 | 0.0874226 | intron-variant | WDR59 | GRCh38.p7 | 16:74902438 | GTTTGTAGTAAAAAA[-/A/AA]GGCCATACCATCAAA | 79726 |
rs6564182 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | WDR59 | GRCh38.p7 | 16:74915060 | TTCCACAGGCTAAGC[A/G]AACAAAGAAGTTTTG | 79726 |
rs6564183 | snp | C/G | 0.347914 | 0.230028 | intron-variant | WDR59 | GRCh38.p7 | 16:74915150 | GCACAGCCCAGCACA[C/G]CACAGCACAGCACAG | 79726 |
rs6564184 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | WDR59 | GRCh38.p7 | 16:74915217 | CCAAGTCAACTCTGT[C/T]CCCAACTTCAGCAGC | 79726 |
rs6564185 | snp | A/G | 0.33303 | 0.235809 | intron-variant | WDR59 | GRCh38.p7 | 16:74946104 | caggcgtgagccacc[A/G]cacccggccacattc | 79726 |
rs6564186 | snp | C/T | 0.45574 | 0.142025 | intron-variant | WDR59 | GRCh38.p7 | 16:74953209 | aggggcagtggctca[C/T]gcctgtaatcccagc | 79726 |
rs6564187 | snp | C/T | 0.486984 | 0.079614 | intron-variant | WDR59 | GRCh38.p7 | 16:74960279 | gaggttgcagtgagc[C/T]gacatcgcgccactg | 79726 |
rs6564188 | snp | C/T | 0.441977 | 0.16014 | intron-variant | WDR59 | GRCh38.p7 | 16:74968057 | atgcaaaaggacaaa[C/T]attatatgactccac | 79726 |
rs7184327 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | WDR59 | GRCh38.p7 | 16:74976613 | cacctggctaatttt[C/T]tgtatttttagtaga | 79726 |