SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs922846 | snp | A/C | 0.093777 | 0.195178 | intron-variant | WDR17 | GRCh38.p7 | 4:176126528 | TGTGGGTTCTGCATC[A/C]GTGGATTGAACCAAC | 116966 |
rs1185564 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | WDR17 | GRCh38.p7 | 4:176095523 | AGCTTTTGTTCTGGC[A/C]TAGGAAGATACACAA | 116966 |
rs1385614 | snp | C/T | 0.499923 | 0.00618962 | intron-variant | WDR17 | GRCh38.p7 | 4:176071888 | CTCCATTCATCTTTC[C/T]GTATCTTTGAATCGG | 116966 |
rs1385615 | snp | C/T | 0.494013 | 0.0543839 | intron-variant | WDR17 | GRCh38.p7 | 4:176072032 | CTGCCATAATGACCT[C/T]ATTCTTCTCTACTTG | 116966 |
rs1385616 | snp | C/T | 0.349452 | 0.229367 | intron-variant | WDR17 | GRCh38.p7 | 4:176076622 | TCTGAATCATTGATA[C/T]GATTTTTTTTTGCAA | 116966 |
rs1385617 | snp | A/G | 0.3752 | 0.216391 | intron-variant | WDR17 | GRCh38.p7 | 4:176082929 | TACTTTTTCTGCTAC[A/G]TCAAGCCACTTTCAT | 116966 |
rs1471645 | snp | A/T | 0.426201 | 0.177351 | intron-variant | WDR17 | GRCh38.p7 | 4:176150941 | ATAATATGATCATTT[A/T]TTATAAAACATATCC | 116966 |
rs1482656 | snp | A/G | 0 | 0 | intron-variant | WDR17 | GRCh38.p7 | 4:176177824 | AATTTATTTTAGGCA[A/G]AAAGAGGCCACTTGT | 116966 |
rs1485522 | snp | C/T | 0.280785 | 0.248097 | intron-variant | WDR17 | GRCh38.p7 | 4:176076787 | CTCCTGAATGAGAGG[C/T]GGCCCATATAGGCTA | 116966 |
rs1485523 | snp | A/G | 0.499942 | 0.00539106 | intron-variant | WDR17 | GRCh38.p7 | 4:176077098 | CTATAATATATTGCT[A/G]AAGAGCTACACTTCC | 116966 |
rs1485524 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | WDR17 | GRCh38.p7 | 4:176070209 | TAGTGGATACGTTTC[A/G]TTAACATTTATATAT | 116966 |
rs1564616 | snp | A/C | 0.498253 | 0.0295011 | intron-variant | WDR17 | GRCh38.p7 | 4:176168433 | ACTAAACTTTACATA[A/C]ATGAGTCTTAACATA | 116966 |
rs1601425 | snp | C/T | | | intron-variant | WDR17 | GRCh38.p7 | 4:176107904 | ttttttccttccctc[C/T]ttccttccttttttc | 116966 |
rs1825233 | snp | A/G | 0.372592 | 0.217879 | upstream-variant-2KB | WDR17 | GRCh38.p7 | 4:176065833 | TGTAGCTGTCACGTG[A/G]GCCTCTGGGGCAGAC | 116966 |
rs1825234 | snp | C/G | 0.030278 | 0.119257 | utr-variant-5-prime, upstream-variant-2KB | WDR17 | GRCh38.p7 | 4:176065948 | GGCCCGGCCGCCCCG[C/G]CCCCGGGCGCCCTGA | 116966 |
rs1963008 | snp | A/T | 0.414741 | 0.188044 | intron-variant | WDR17 | GRCh38.p7 | 4:176094043 | TGCCATCACCAAGTT[A/T]GTCTTTATTATACTA | 116966 |
rs1976031 | snp | C/T | 0.420574 | 0.182769 | intron-variant | WDR17 | GRCh38.p7 | 4:176168006 | gcacgtgccaccatg[C/T]ccgggcaatttttgt | 116966 |
rs2062137 | snp | G/T | 0.322245 | 0.239334 | downstream-variant-500B | WDR17 | GRCh38.p7 | 4:176183235 | ttgtttttatttttg[G/T]tttttgagacctagt | 116966 |
rs2062138 | snp | G/T | 0.385168 | 0.210309 | downstream-variant-500B | WDR17 | GRCh38.p7 | 4:176183171 | gcaatctcagctcac[G/T]gcaagctccgcctcc | 116966 |
rs2062139 | snp | A/G | 0 | 0 | intron-variant | WDR17 | GRCh38.p7 | 4:176171888 | GACACAAAAAATGTA[A/G]AAGCTCTAAAAGTTT | 116966 |
rs2128422 | snp | A/G | 0.418653 | 0.184544 | intron-variant | WDR17 | GRCh38.p7 | 4:176158223 | AACTGGCCTCCTCAT[A/G]TCTGCTATTGACCTT | 116966 |
rs2128425 | snp | C/T | 0.422 | 0.181428 | intron-variant | WDR17 | GRCh38.p7 | 4:176142910 | cctgggcagcaagag[C/T]gaaactccgtcctca | 116966 |
rs2128426 | snp | C/T | 0.478104 | 0.102316 | intron-variant, downstream-variant-500B | WDR17 | GRCh38.p7 | 4:176163526 | GTGCTTGAAACACTA[C/T]GGAATTACAACTGGG | 116966 |
rs2170576 | snp | A/G | 0.498568 | 0.0267188 | intron-variant | WDR17 | GRCh38.p7 | 4:176163865 | CCTAATAGAGCCTCC[A/G]TAATAATGGATTGTT | 116966 |
rs2333396 | snp | C/T | 0.247905 | 0.249991 | intron-variant | WDR17 | GRCh38.p7 | 4:176110774 | TACGAGAAATAGAGA[C/T]GTAAGGTTTAATGCT | 116966 |
rs2333397 | snp | C/T | 0.276999 | 0.249036 | intron-variant | WDR17 | GRCh38.p7 | 4:176110807 | ACTCCAAGTCACACT[C/T]TATGTGTGGTGCAAA | 116966 |
rs2333398 | snp | A/G | 0.304688 | 0.243945 | intron-variant | WDR17 | GRCh38.p7 | 4:176111288 | AATTTCTATTTCACT[A/G]GAGTTCCTGTCACTG | 116966 |
rs2333399 | snp | C/T | 0.440746 | 0.161604 | intron-variant | WDR17 | GRCh38.p7 | 4:176123653 | atatgggaaaggaca[C/T]ggggcttccgtgctg | 116966 |
rs2333401 | snp | A/T | 0.372592 | 0.217879 | utr-variant-5-prime, upstream-variant-2KB | WDR17 | GRCh38.p7 | 4:176065970 | gcgcccTGAGCGAGC[A/T]GGCGGGGAGGGCGGG | 116966 |
rs2877924 | snp | A/G | 0.403334 | 0.197456 | intron-variant | WDR17 | GRCh38.p7 | 4:176162015 | CTTTTAAAAAGTATT[A/G]GTTTGCTTTTATAAT | 116966 |
rs2877925 | snp | A/G | 0.499295 | 0.0187567 | intron-variant | WDR17 | GRCh38.p7 | 4:176165186 | aaaaaaaaaaaaccc[A/G]ttactaaaaatacaa | 116966 |
rs3112289 | snp | A/G | 0 | 0 | intron-variant | WDR17 | GRCh38.p7 | 4:176133012 | TTATTCAGAAATGAA[A/G]AATTGTCTTGTTGAA | 116966 |
rs3112290 | snp | A/G | | | intron-variant | WDR17 | GRCh38.p7 | 4:176132996 | AATTGTCTTGTTGAA[A/G]ACCCACTGCCAGATT | 116966 |
rs4234875 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | WDR17 | GRCh38.p7 | 4:176174930 | GCTTAAACTCCTAGG[A/G]TTTATTGATCTTTCA | 116966 |
rs4269125 | snp | A/G | 0.498034 | 0.0312882 | intron-variant | WDR17 | GRCh38.p7 | 4:176165782 | ATTAAACATTTTTCA[A/G]TTAACTATATGTCTT | 116966 |
rs4276243 | snp | A/G | 0.434398 | 0.168811 | utr-variant-3-prime | WDR17 | GRCh38.p7 | 4:176181822 | TTTTTATGTATAAAA[A/G]ATGAAGAAAAAATTT | 116966 |
rs4299535 | snp | A/T | 0.498525 | 0.0271165 | intron-variant | WDR17 | GRCh38.p7 | 4:176165743 | AGCAGTTCAAACTCA[A/T]AACATAGTATGTTAC | 116966 |
rs4370079 | snp | A/T | 0.0955749 | 0.196603 | intron-variant | WDR17 | GRCh38.p7 | 4:176165749 | TCAAACTCATAACAT[A/T]GTATGTTACATAATA | 116966 |
rs4384996 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | WDR17 | GRCh38.p7 | 4:176167135 | GTCTTTATTCCTATT[C/T]TATATTCATTATATT | 116966 |
rs4388031 | snp | C/T | 0.0455781 | 0.143916 | intron-variant | WDR17 | GRCh38.p7 | 4:176166171 | TTTTATTTAAGAACA[C/T]ATTCCTTTAAAATGT | 116966 |
rs4444774 | snp | C/T | 0.317451 | 0.240729 | intron-variant | WDR17 | GRCh38.p7 | 4:176172685 | TTCTGCAGGCTGTAC[C/T]GGAAGCATGGCACTG | 116966 |
rs4473612 | snp | A/C | 0 | 0 | intron-variant | WDR17 | GRCh38.p7 | 4:176066400 | GTATATGTCTAGAGC[A/C]TAGGTTGCTGTTCTC | 116966 |
rs4475089 | snp | A/G | 0.49975 | 0.0111793 | intron-variant | WDR17 | GRCh38.p7 | 4:176170678 | CAGTTAGCTAAGACC[A/G]CTTTTAATGATAGGG | 116966 |
rs4536876 | snp | C/T | 0.452965 | 0.145963 | utr-variant-3-prime | WDR17 | GRCh38.p7 | 4:176181686 | CAATCCTACTGTCAT[C/T]CTTTTTATTTTAAAA | 116966 |
rs4538426 | snp | G/T | 0.499628 | 0.0138642 | intron-variant | WDR17 | GRCh38.p7 | 4:176172354 | TTTAGTAACATTGTT[G/T]TCAAATCAATTATTT | 116966 |
rs4543067 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | WDR17 | GRCh38.p7 | 4:176175739 | ATTTTTTGTATTTTT[C/T]TAGTAGAGACGGGGT | 116966 |
rs4582106 | snp | C/G | 0.0633504 | 0.166319 | intron-variant, downstream-variant-500B | WDR17 | GRCh38.p7 | 4:176163605 | CACATATTCCCACAT[C/G]TTAAAATTCCGCATA | 116966 |
rs4690659 | snp | C/G | 0.44333 | 0.158505 | intron-variant | WDR17 | GRCh38.p7 | 4:176111961 | GGGTAGTCCATTAGA[C/G]ATCATTATAGTAAAA | 116966 |
rs4690661 | snp | A/G | 0.0128824 | 0.0792165 | missense, nc-transcript-variant | WDR17 | GRCh38.p7 | 4:176151875 | GGTATTGGTGTACCT[A/G]CTAAAGAGGAAAGAC | 116966 |
rs4690662 | snp | A/C | 0.439224 | 0.163383 | intron-variant | WDR17 | GRCh38.p7 | 4:176157261 | ATTATTATGTAATTA[A/C]CTTTCTTCTGACATT | 116966 |
rs4690663 | snp | A/G | 0.497151 | 0.037632 | intron-variant | WDR17 | GRCh38.p7 | 4:176171222 | ACTTATATAACTTTT[A/G]GAATTTTAAAATAGG | 116966 |
rs4690664 | snp | C/T | 0.095934 | 0.196885 | intron-variant | WDR17 | GRCh38.p7 | 4:176171292 | TAGTCTATTTAAAAA[C/T]GATATTTAAATGGGA | 116966 |
rs4690665 | snp | A/G | 0.388616 | 0.208052 | intron-variant | WDR17 | GRCh38.p7 | 4:176174757 | CATGACATTAGAGCA[A/G]TTTCTCTTGCTAAGA | 116966 |
rs5016793 | snp | G/T | 0.353803 | 0.227431 | intron-variant | WDR17 | GRCh38.p7 | 4:176130935 | AATATATAAAAATAA[G/T]CACAGTGATATTTAT | 116966 |
rs5016794 | snp | C/T | 0.353587 | 0.22753 | intron-variant | WDR17 | GRCh38.p7 | 4:176130926 | GGGATAAATAATATA[C/T]AAAAATAATCACAGT | 116966 |
rs5016795 | snp | A/G | 0.353587 | 0.22753 | intron-variant | WDR17 | GRCh38.p7 | 4:176130913 | GAAGACAAAATATGG[A/G]ATAAATAATATATAA | 116966 |
rs5016796 | snp | C/T | 0.433527 | 0.169758 | intron-variant | WDR17 | GRCh38.p7 | 4:176130824 | GGTCTTATAATTTAC[C/T]GTAGTGTCATTATTT | 116966 |
rs5016797 | snp | C/T | 0.352721 | 0.227922 | intron-variant | WDR17 | GRCh38.p7 | 4:176130793 | CCATATTCCAGTGTA[C/T]AATTAATAATCGATT | 116966 |
rs5016798 | snp | A/T | 0.277778 | 0.248452 | intron-variant | WDR17 | GRCh38.p7 | 4:176130762 | aaaaaaaaaaaaaaa[A/T]aCTGAGAAATATTTT | 116966 |
rs5016799 | snp | A/G | 0.286042 | 0.247388 | intron-variant | WDR17 | GRCh38.p7 | 4:176130614 | GCCGGGCGTGGTGGC[A/G]GGAGCCTGTAGTCCC | 116966 |
rs6419995 | snp | G/T | 0.477004 | 0.104734 | intron-variant | WDR17 | GRCh38.p7 | 4:176110243 | GCCTCCCAGGTTCAC[G/T]CCATTCTCCTGCCTC | 116966 |
rs6553907 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | WDR17 | GRCh38.p7 | 4:176067203 | GTTTTGAAGGCAGAC[A/G]TCTGAGATAGGTGGT | 116966 |
rs6553908 | snp | A/T | 0.280785 | 0.248097 | intron-variant | WDR17 | GRCh38.p7 | 4:176067387 | TTTAAAGCAATGACT[A/T]ATTTCAAAGGGCATA | 116966 |
rs6553909 | snp | G/T | 0.496483 | 0.0417852 | intron-variant | WDR17 | GRCh38.p7 | 4:176067435 | TTGAGTTCTGCAAAC[G/T]TAATTATGTAAAAAT | 116966 |
rs6553910 | snp | A/C | 0.499937 | 0.0055907 | intron-variant | WDR17 | GRCh38.p7 | 4:176075048 | TTAATTTTTAAATGC[A/C]GAAACATAAGTCTGA | 116966 |
rs6553911 | snp | A/C | 0.499937 | 0.0055907 | intron-variant | WDR17 | GRCh38.p7 | 4:176075188 | TTTCAATTTTATGAT[A/C]TATTTTAACAAAAAA | 116966 |
rs6553912 | snp | A/G | 0.499937 | 0.0055907 | intron-variant | WDR17 | GRCh38.p7 | 4:176075258 | TTTTTTAATTATAAG[A/G]TGACTGAGTCAATTT | 116966 |
rs6553915 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | WDR17 | GRCh38.p7 | 4:176144723 | AAATGTTTTAATTGC[C/T]GTATTCATATTCCAC | 116966 |
rs6810394 | snp | A/G | 1.65198e-05 | 0.00287395 | missense | WDR17 | GRCh38.p7 | 4:176162106 | AGTAAAGAACTGGCA[A/G]AATGGTATTTTCAAG | 116966 |
rs6810644 | snp | A/T | 0.497959 | 0.0318836 | upstream-variant-2KB | WDR17 | GRCh38.p7 | 4:176064882 | TATCCATCAAGAATT[A/T]ATTGAAGACCTGCTA | 116966 |
rs6811204 | snp | A/G | 0.499933 | 0.00579035 | intron-variant | WDR17 | GRCh38.p7 | 4:176072162 | TGCTTAGATAACACT[A/G]CCTGCCAAGCATGTA | 116966 |
rs6812514 | snp | A/T | 0.367503 | 0.220665 | intron-variant | WDR17 | GRCh38.p7 | 4:176140368 | CGTAAAAACTTGTTT[A/T]TAGTTGTGTAGATGC | 116966 |
rs6812750 | snp | C/T | 0.367503 | 0.220665 | intron-variant | WDR17 | GRCh38.p7 | 4:176140319 | TGGAGAGTAGTATTT[C/T]GGTTTCACAGGTGAT | 116966 |
rs6813271 | snp | C/T | 0.441841 | 0.160303 | intron-variant | WDR17 | GRCh38.p7 | 4:176126693 | gtgatgtggcttgac[C/T]gtgtctccaccaaaa | 116966 |
rs6814389 | snp | C/T | 0.496517 | 0.0415876 | intron-variant | WDR17 | GRCh38.p7 | 4:176067681 | AAAGCCATAAATTAA[C/T]TTAGGCCAGAAAAAC | 116966 |
rs6815166 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | WDR17 | GRCh38.p7 | 4:176115126 | ATAGCACTGTGAAAG[G/T]CTCATTATATGCTAA | 116966 |
rs6818449 | snp | C/T | 0.499971 | 0.00379382 | intron-variant | WDR17 | GRCh38.p7 | 4:176072715 | TTTTTTGCATAGCTC[C/T]GAGCACATAGTATAT | 116966 |
rs6818456 | snp | C/T | 0.499913 | 0.00658888 | intron-variant | WDR17 | GRCh38.p7 | 4:176072721 | GCATAGCTCCGAGCA[C/T]ATAGTATATTTACAC | 116966 |
rs6822582 | snp | G/T | 0.473451 | 0.112115 | utr-variant-5-prime, upstream-variant-2KB | WDR17 | GRCh38.p7 | 4:176065857 | GGCAGACCCTGGAGA[G/T]CGGGCTCGCGGCGCC | 116966 |
rs6823265 | snp | A/C | 0.284995 | 0.247539 | intron-variant | WDR17 | GRCh38.p7 | 4:176107228 | gaaatgcaaatcaaa[A/C]gaacaataagacacc | 116966 |
rs6825591 | snp | A/G | 0.102014 | 0.201495 | intron-variant | WDR17 | GRCh38.p7 | 4:176151722 | aattccgctctatta[A/G]ttatttcaaaatatg | 116966 |
rs6826405 | snp | C/T | 0.106987 | 0.205054 | intron-variant | WDR17 | GRCh38.p7 | 4:176151394 | CCCTCCCGTGTCCCA[C/T]CCCCACACACACCCC | 116966 |
rs6826418 | snp | C/T | 0.106987 | 0.205054 | intron-variant | WDR17 | GRCh38.p7 | 4:176151409 | CCCCCACACACACCC[C/T]AAAATATTATGTTTA | 116966 |
rs6827241 | snp | C/T | 0.480931 | 0.0957637 | intron-variant | WDR17 | GRCh38.p7 | 4:176106702 | ctcacatctgtgatc[C/T]gggcactttgggagg | 116966 |
rs6829241 | snp | C/G | 0.436976 | 0.165952 | intron-variant | WDR17 | GRCh38.p7 | 4:176109399 | ACAGGTGTCATTAGA[C/G]GAGGAGGAAAGTTTC | 116966 |
rs6829868 | snp | A/C | 0.499965 | 0.00419314 | intron-variant | WDR17 | GRCh38.p7 | 4:176070809 | GCATGAGCCTCTGTG[A/C]CTGGCCCTGTTTTTG | 116966 |
rs6830231 | snp | A/G | 0.499965 | 0.00419314 | intron-variant | WDR17 | GRCh38.p7 | 4:176070953 | AATATGCCAGCATTA[A/G]GTGACTTTCTGCCCA | 116966 |
rs6831148 | snp | A/G | 0.49607 | 0.0441545 | intron-variant | WDR17 | GRCh38.p7 | 4:176067714 | TGCTCCCAGTAGAGG[A/G]GAGACTAGGGCTAGA | 116966 |
rs6832331 | snp | C/G | 0.110167 | 0.207236 | intron-variant | WDR17 | GRCh38.p7 | 4:176092420 | aaaaccttcaaaaaa[C/G]tgggtgtaggaggaa | 116966 |
rs6834458 | snp | G/T | 0.367503 | 0.220665 | intron-variant | WDR17 | GRCh38.p7 | 4:176140413 | GGATAAAAAGCCTTT[G/T]CAAGGAGAAATAAAG | 116966 |
rs6836094 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | WDR17 | GRCh38.p7 | 4:176110331 | tacttttagtagaga[C/T]ggggtttcaccatgt | 116966 |
rs6837815 | snp | A/G | 0.371785 | 0.218331 | intron-variant | WDR17 | GRCh38.p7 | 4:176149417 | tgggactacaatcac[A/G]tgccaccacacccag | 116966 |
rs6838194 | snp | A/G | 0.107341 | 0.205301 | intron-variant | WDR17 | GRCh38.p7 | 4:176149588 | TCTAATGGTTATTCa[A/G]ttttatattcatatt | 116966 |
rs6841227 | snp | A/G | 0.364817 | 0.222075 | intron-variant | WDR17 | GRCh38.p7 | 4:176114932 | CTGTAATAGAGAAAC[A/G]AGAAGTTCAGAGTGA | 116966 |
rs6844703 | snp | A/G | 0.499933 | 0.00579035 | intron-variant | WDR17 | GRCh38.p7 | 4:176073301 | gatgttccccttact[A/G]tgtccatgtgttctc | 116966 |
rs6847592 | snp | C/T | 0.28052 | 0.24813 | intron-variant | WDR17 | GRCh38.p7 | 4:176070311 | TATGTTGGCTCAGAG[C/T]GTAATATTTGACTTA | 116966 |
rs6848054 | snp | A/C | 0.354665 | 0.227036 | intron-variant | WDR17 | GRCh38.p7 | 4:176138777 | TGATTGTGGAAACCC[A/C]GCATTTTAGTATCAA | 116966 |
rs6848995 | snp | G/T | 0.499933 | 0.00579035 | intron-variant | WDR17 | GRCh38.p7 | 4:176072913 | TTTTAATAGACATTT[G/T]TAGGTACTTTTATTG | 116966 |
rs6849006 | snp | A/G | 0.367503 | 0.220665 | intron-variant | WDR17 | GRCh38.p7 | 4:176142778 | GAGTAAGGTACTAAA[A/G]CCTAATTATACTTGT | 116966 |
rs6849468 | snp | A/G | 0.372391 | 0.217992 | intron-variant | WDR17 | GRCh38.p7 | 4:176143021 | agtagctgggattat[A/G]ggcatgcgccaccac | 116966 |