SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs170896 | snp | G/T | 0.189261 | 0.242509 | upstream-variant-2KB | WDR47 | GRCh38.p7 | 1:109042258 | gggcggggaggggcg[G/T]ggaggggcgggccca | 22911 |
rs184605 | snp | A/G | 0.488666 | 0.0744214 | intron-variant | WDR47 | GRCh38.p7 | 1:109012603 | AAACAGAAAGGGAAT[A/G]CCTAAAGTTGACTTA | 22911 |
rs184606 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | WDR47 | GRCh38.p7 | 1:109002424 | TGCTCAAATATATAT[A/G]TTTTTTTCTAATGTT | 22911 |
rs189241 | snp | C/T | 0.499234 | 0.0195537 | intron-variant | WDR47 | GRCh38.p7 | 1:109012309 | ACAGGTGTGAGCCAC[C/T]GTGCTCGGCTCCCTT | 22911 |
rs337294 | snp | A/C | 0.0894459 | 0.191631 | intron-variant | WDR47 | GRCh38.p7 | 1:109012650 | ACAGACCAAAATGGA[A/C]GCTTAGCTGAGAGAC | 22911 |
rs337295 | snp | A/G | 0.490343 | 0.0688145 | intron-variant | WDR47 | GRCh38.p7 | 1:108997629 | gccaggcgtggtggt[A/G]ggcgcctgtagtccc | 22911 |
rs337296 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | WDR47 | GRCh38.p7 | 1:108992318 | TTGATTTGCATGATT[C/T]CGTGGGGTTCTCCGG | 22911 |
rs337297 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | WDR47 | GRCh38.p7 | 1:109002604 | CATTTCGGTCAGTCT[A/G]TTTCCGTGGAATAAA | 22911 |
rs337298 | snp | A/C | 0.188 | 0.24219 | intron-variant | WDR47 | GRCh38.p7 | 1:109000915 | atgcaaatgtgctta[A/C]aacagttctggcaca | 22911 |
rs337299 | snp | C/T | 0.296109 | 0.245711 | intron-variant | WDR47 | GRCh38.p7 | 1:109000380 | ctggcattacaggta[C/T]gcaccactatgcctg | 22911 |
rs337300 | snp | C/T | 0.302184 | 0.244493 | intron-variant | WDR47 | GRCh38.p7 | 1:108999198 | ctcttgttgcccagg[C/T]tggagtgcagtggcg | 22911 |
rs485675 | snp | A/G | 0.478188 | 0.10213 | intron-variant | WDR47 | GRCh38.p7 | 1:109025590 | aatacaaaaattagc[A/G]gagcgtggtggcacg | 22911 |
rs486689 | snp | A/G/T | | | intron-variant | WDR47 | GRCh38.p7 | 1:108987896 | GCTAAACTAAGCTCA[A/G/T]TTCATAAACACTCAA | 22911 |
rs487901 | snp | A/C | 0.301932 | 0.244547 | intron-variant | WDR47 | GRCh38.p7 | 1:108981962 | GCAAGGTGGCTCATG[A/C]CTATAATCCCAGCTA | 22911 |
rs489794 | snp | C/T | 0.363568 | 0.222716 | intron-variant | WDR47 | GRCh38.p7 | 1:108974019 | cgcaacatggcaaaa[C/T]tttgtctctacagaa | 22911 |
rs490208 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | WDR47 | GRCh38.p7 | 1:109027088 | TTAAGGCAGAGTCTC[C/G]CTCTGTTGCCCGGGC | 22911 |
rs490295 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | WDR47 | GRCh38.p7 | 1:109027758 | tgaactcctgacctc[A/G]tgatccacccgcctc | 22911 |
rs490681 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | WDR47 | GRCh38.p7 | 1:109006890 | CAATATGATTGAACT[A/G]CTATGGTGAACAAGA | 22911 |
rs494436 | snp | A/G | 0.32768 | 0.237625 | intron-variant | WDR47 | GRCh38.p7 | 1:108984862 | cagcctggcgacaga[A/G]tgagactctgtctca | 22911 |
rs496147 | snp | C/T | 0.364609 | 0.222182 | intron-variant | WDR47 | GRCh38.p7 | 1:108972723 | aaggcaggcagatca[C/T]gaggtcaggagatca | 22911 |
rs501143 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | WDR47 | GRCh38.p7 | 1:109037292 | gcccaggctggagtg[C/T]gatggcgtgatgtcg | 22911 |
rs501148 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | WDR47 | GRCh38.p7 | 1:109038450 | ctcaagtgacctgcc[C/T]gccttggcttcccaa | 22911 |
rs503171 | snp | A/G | | | intron-variant | WDR47 | GRCh38.p7 | 1:109034618 | tccgtgctcctatga[A/G]aatctaatgccactg | 22911 |
rs504043 | snp | A/G | | | intron-variant | WDR47 | GRCh38.p7 | 1:109034530 | ctgctgtgcagctca[A/G]ttcctaacaggctgt | 22911 |
rs505470 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | WDR47 | GRCh38.p7 | 1:109017074 | GCCACATACATGCCA[C/T]TGCACATCAGCCTGG | 22911 |
rs506549 | snp | A/G | 0.33693 | 0.2344 | intron-variant | WDR47 | GRCh38.p7 | 1:109017221 | AAGCCTGGGCAACAT[A/G]GTGAAACCCTAACTC | 22911 |
rs507776 | snp | C/T | 0.302686 | 0.244385 | utr-variant-3-prime | WDR47 | GRCh38.p7 | 1:108970875 | CATCTTTAAACTCCA[C/T]AATGATCCTTAAGTG | 22911 |
rs516371 | snp | G/T | 0.336245 | 0.234652 | intron-variant | WDR47 | GRCh38.p7 | 1:109016849 | gcttgcttatatcag[G/T]ctcagtttctaatga | 22911 |
rs517843 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | WDR47 | GRCh38.p7 | 1:108980262 | AAATCAATGATCATG[A/G]ACTCAAATGTGCTGT | 22911 |
rs522297 | snp | A/G | | | intron-variant | WDR47 | GRCh38.p7 | 1:109034578 | caggagcgggactca[A/G]acagtaatgctccct | 22911 |
rs527378 | snp | A/G | 0.337841 | 0.23406 | intron-variant | WDR47 | GRCh38.p7 | 1:109036783 | cagtggcatgatctc[A/G]gctcactgcaagctc | 22911 |
rs536912 | snp | A/C | 0.32955 | 0.237006 | intron-variant | WDR47 | GRCh38.p7 | 1:108971725 | AGGGATAAATTACTA[A/C]CTACCTAATTATGCT | 22911 |
rs542417 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | WDR47 | GRCh38.p7 | 1:108972341 | aactattccaacagc[C/G]tcctcactgacattt | 22911 |
rs544636 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | WDR47 | GRCh38.p7 | 1:109016101 | CCAGACTTTTCAAGC[C/T]ACAGCCTTCTGTTTG | 22911 |
rs546907 | snp | C/T | 0.288127 | 0.247076 | intron-variant | WDR47 | GRCh38.p7 | 1:109034215 | ctgcaacctccgcct[C/T]ctgggttcaggtgat | 22911 |
rs551065 | snp | G/T | 0.32955 | 0.237006 | intron-variant | WDR47 | GRCh38.p7 | 1:108974097 | tacttgcagggctga[G/T]gtgggaggatcactt | 22911 |
rs560119 | snp | C/T | | | intron-variant | WDR47 | GRCh38.p7 | 1:108997748 | ttttgagatggagtc[C/T]tgctctgttgcccag | 22911 |
rs560215 | snp | C/T | | | intron-variant | WDR47 | GRCh38.p7 | 1:108997710 | tgcagtggcactatc[C/T]cggctcactgcaagc | 22911 |
rs561641 | snp | A/T | | | intron-variant | WDR47 | GRCh38.p7 | 1:108997714 | gcagtgagccgggat[A/T]gtgccactgcactcc | 22911 |
rs563642 | snp | C/T | | | intron-variant | WDR47 | GRCh38.p7 | 1:108988332 | AGCCCACTAGAAGTT[C/T]TAACAAATAGAGTTT | 22911 |
rs568845 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | WDR47 | GRCh38.p7 | 1:108981020 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 22911 |
rs569922 | snp | C/G | 0.441158 | 0.161117 | intron-variant | WDR47 | GRCh38.p7 | 1:108973030 | ttcactaagttccag[C/G]cacattggcttcctg | 22911 |
rs570812 | snp | A/G | 0.441295 | 0.160954 | intron-variant | WDR47 | GRCh38.p7 | 1:108973113 | TGTGCTCTTCTCCTA[A/G]TATCCTGGCCTGGCT | 22911 |
rs570814 | snp | G/T | 0.441295 | 0.160954 | intron-variant | WDR47 | GRCh38.p7 | 1:108973114 | GTGCTCTTCTCCTAA[G/T]ATCCTGGCCTGGCTT | 22911 |
rs576821 | snp | C/G | 0.0368353 | 0.130617 | intron-variant | WDR47 | GRCh38.p7 | 1:108984741 | AAATCAGCTAGGCAT[C/G]GTGGTGCATGCCTGT | 22911 |
rs578262 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | WDR47 | GRCh38.p7 | 1:109023766 | ATTAAATGATATAAA[C/G]TTTGTGATTTACATG | 22911 |
rs705277 | snp | A/G | 0.253544 | 0.249975 | intron-variant | WDR47 | GRCh38.p7 | 1:108997310 | tagccagacatggtg[A/G]tgcaggcctatggtc | 22911 |
rs723281 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | WDR47 | GRCh38.p7 | 1:109012062 | TGGGCTCAAGTGATC[C/T]CCAGCCTCTAAAGTA | 22911 |
rs839877 | snp | A/G | 0.177182 | 0.23916 | intron-variant | WDR47 | GRCh38.p7 | 1:108981021 | TAGTCCCAGCTACTT[A/G]GGAGGCTGAGGCAGG | 22911 |
rs839878 | snp | A/C | 0.295343 | 0.245854 | intron-variant | WDR47 | GRCh38.p7 | 1:108984486 | CTATTGCATTTCAGC[A/C]TACTAGTCTACTTTT | 22911 |
rs839879 | snp | A/G | 0.247337 | 0.249986 | intron-variant | WDR47 | GRCh38.p7 | 1:108985239 | CATGTCTATCTCTGC[A/G]GCCTTATCAAACTCA | 22911 |
rs839880 | snp | A/G | 0.305934 | 0.243663 | intron-variant | WDR47 | GRCh38.p7 | 1:108997709 | agcttgcagtgagcc[A/G]agatagtgccactgc | 22911 |
rs1025996 | snp | C/T | 0.149665 | 0.228982 | intron-variant | WDR47 | GRCh38.p7 | 1:108982196 | TATCAAATAGATTGa[C/T]aattttaaaaataaa | 22911 |
rs1538137 | snp | G/T | 6.59261e-05 | 0.00574097 | missense | WDR47 | GRCh38.p7 | 1:108982669 | CGGTTGTATAAATGT[G/T]ACAATCCCCTGCTCC | 22911 |
rs1541186 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | WDR47 | GRCh38.p7 | 1:108981588 | TAACAAATGCAAGTA[C/T]TGTGAAAGAACTGAA | 22911 |
rs1625256 | snp | C/G | 0.296364 | 0.245663 | intron-variant | WDR47 | GRCh38.p7 | 1:109000237 | ACAAAAAGGGCAGGC[C/G]CAGTGGCTTACACCT | 22911 |
rs1765297 | snp | C/T | | | intron-variant | WDR47 | GRCh38.p7 | 1:109009922 | agaattgcttgaacc[C/T]gggagacggaggttg | 22911 |
rs1769728 | snp | A/C | 0 | 0 | intron-variant | WDR47 | GRCh38.p7 | 1:108989628 | GGCCTATAGCACATC[A/C]AAAATTACTAAAGAT | 22911 |
rs2359116 | snp | A/G | 0.490563 | 0.0680388 | intron-variant | WDR47 | GRCh38.p7 | 1:109010443 | tgtgccggtagtccc[A/G]gctactcagggggct | 22911 |
rs2590998 | snp | A/G | 0.0364509 | 0.129988 | | | GRCh38.p7 | 1:109005222 | TAGAAACTAGGCTTC[A/G]CCATGTTACCCAGGT | 22911 |
rs2590999 | snp | C/G | 0.33693 | 0.2344 | | | GRCh38.p7 | 1:108989585 | AGTCGTTTTTCCTCC[C/G]TTTTTCTCTTATCTA | 22911 |
rs2591000 | snp | C/T | 0.327211 | 0.237778 | | | GRCh38.p7 | 1:108989236 | GGGGTTTGGTTGAGT[C/T]TGACCATACCTAGTG | 22911 |
rs2786625 | snp | A/T | | | intron-variant | WDR47 | GRCh38.p7 | 1:109023209 | ctccgtctcaaaaaa[A/T]aaaataaaataaaat | 22911 |
rs2790738 | snp | C/T | | | intron-variant | WDR47 | GRCh38.p7 | 1:108988780 | tttttttttttgaga[C/T]ggagtatcgctctac | 22911 |
rs2839742 | snp | C/T | 0.0110494 | 0.0735024 | intron-variant | WDR47 | GRCh38.p7 | 1:109025141 | AGATGAGTACATTTT[C/T]TCCCTCAGCTAGAgg | 22911 |
rs3835721 | in-del | -/C | | | intron-variant | WDR47 | GRCh38.p7 | 1:108982876 | ACCATATTTCTAAAC[-/C]ATTATTCTTGACCAG | 22911 |
rs3861912 | snp | A/G | 0.150333 | 0.229274 | intron-variant | WDR47 | GRCh38.p7 | 1:108974216 | AAAAACAGGCTGGGC[A/G]TGGTGGCTCACGCCT | 22911 |
rs3861913 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | WDR47 | GRCh38.p7 | 1:109029986 | TTTGGTTAGAAAGCT[A/G/T]CCAGTGATATTTTTT | 22911 |
rs4255409 | snp | G/T | 0.0685596 | 0.171987 | intron-variant | WDR47 | GRCh38.p7 | 1:109029723 | cgcccgggtaatttt[G/T]ttaaaaaaatattta | 22911 |
rs4336879 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | WDR47 | GRCh38.p7 | 1:109006161 | GTGATCTGCCACCCT[C/T]GGCCTCCCAAAGTGC | 22911 |
rs4971327 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | WDR47 | GRCh38.p7 | 1:109000230 | AGCCACTGCGCCTGC[C/G]CTTTTTGTTTTTTAA | 22911 |
rs5776961 | in-del | -/A | 0.276534 | 0.248588 | intron-variant | WDR47 | GRCh38.p7 | 1:109006363 | GCGCCATTGCAGTCC[-/A]GCCTGGGCAATAAGA | 22911 |
rs5776962 | in-del | -/A | 0 | 0 | intron-variant | WDR47 | GRCh38.p7 | 1:109021544 | AAAAAAAAAAAAAAA[-/A]GGCGCAAGTATAAAA | 22911 |
rs6537733 | snp | A/G | 0.497473 | 0.0354532 | intron-variant | WDR47 | GRCh38.p7 | 1:109004190 | GAGTGGCACAAACCC[A/G]GGAGGCGGAGCTTGC | 22911 |
rs6604758 | snp | A/T | 0.148326 | 0.228391 | intron-variant | WDR47 | GRCh38.p7 | 1:109038496 | agatagggttttgcc[A/T]tgttgcccaggctgg | 22911 |
rs6660713 | snp | A/G | | | intron-variant | WDR47 | GRCh38.p7 | 1:109035859 | ttactatgctaccca[A/G]actacagtgtagttg | 22911 |
rs6669151 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | WDR47 | GRCh38.p7 | 1:109035883 | gtagttgctattgcc[A/G]ggcctgttcatagca | 22911 |
rs6671194 | snp | G/T | 0.0626037 | 0.165477 | intron-variant | WDR47 | GRCh38.p7 | 1:109034205 | cgcctcctgggttca[G/T]gtgattctactgcct | 22911 |
rs7418395 | snp | A/G | | | intron-variant | WDR47 | GRCh38.p7 | 1:109029776 | cagttctctgcctca[A/G]cctctccgataagct | 22911 |
rs7517768 | snp | C/T | | | intron-variant | WDR47 | GRCh38.p7 | 1:109037529 | tgccattctcctgcc[C/T]cagcctctctgagta | 22911 |
rs7522923 | snp | G/T | 0.0611083 | 0.163768 | intron-variant | WDR47 | GRCh38.p7 | 1:109007426 | tcagcctcccaaagt[G/T]ctgggattacaggtg | 22911 |
rs7523984 | snp | C/T | 0.336702 | 0.234484 | intron-variant | WDR47 | GRCh38.p7 | 1:109022670 | gctcactggaacctc[C/T]gtctccctggttcaa | 22911 |
rs7524891 | snp | C/T | | | intron-variant | WDR47 | GRCh38.p7 | 1:109037677 | AACCttttataaaat[C/T]tttttagaaaatttt | 22911 |
rs7524892 | snp | G/T | | | intron-variant | WDR47 | GRCh38.p7 | 1:109037672 | tttataaaatttttt[G/T]agaaaattttataGA | 22911 |
rs7526309 | snp | C/T | 0.301681 | 0.2446 | intron-variant | WDR47 | GRCh38.p7 | 1:109022773 | tatttttagtagagg[C/T]gggatttcaccatgt | 22911 |
rs7531651 | snp | A/G | 0.277067 | 0.24853 | intron-variant | WDR47 | GRCh38.p7 | 1:109022746 | tgtgccaccatgccc[A/G]gttaatttttatatt | 22911 |
rs7538033 | snp | G/T | | | intron-variant | WDR47 | GRCh38.p7 | 1:109037646 | ataGAATTGGGTTGG[G/T]ttttttttttttttt | 22911 |
rs7538212 | snp | C/G | | | intron-variant | WDR47 | GRCh38.p7 | 1:109037480 | cgccaccaagcccgg[C/G]taattttttatattt | 22911 |
rs7540472 | snp | A/G | 0.296109 | 0.245711 | intron-variant, upstream-variant-2KB | WDR47 | GRCh38.p7 | 1:109017817 | aatggcacaatctcg[A/G]ctcactgcaccctct | 22911 |
rs7541010 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | WDR47 | GRCh38.p7 | 1:109032354 | cgcctggctaatctt[C/T]tgtatttttagtaga | 22911 |
rs7542809 | snp | G/T | | | intron-variant | WDR47 | GRCh38.p7 | 1:109028363 | ctaatttttgttggg[G/T]ttttttttttttttt | 22911 |
rs7550159 | snp | C/T | | | intron-variant | WDR47 | GRCh38.p7 | 1:109007869 | agcactttgggaggc[C/T]gaggtgggcagatca | 22911 |
rs9658938 | snp | C/T | 0.149999 | 0.229128 | intron-variant | WDR47 | GRCh38.p7 | 1:108979933 | acagcacgaggtgag[C/T]gacaaatgagtgagc | 22911 |
rs9659682 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | WDR47 | GRCh38.p7 | 1:108989805 | gttcaagcgattctc[C/T]tgcctcagcctccca | 22911 |
rs9659778 | snp | A/G | 0.14665 | 0.227637 | intron-variant | WDR47 | GRCh38.p7 | 1:108994352 | cagtgagctgagatt[A/G]caccactgcattcca | 22911 |
rs9660938 | snp | A/G | 0.146985 | 0.227789 | intron-variant | WDR47 | GRCh38.p7 | 1:108998376 | ggcatggtggtggac[A/G]cttgtggtccccgct | 22911 |
rs9697335 | snp | G/T | | | intron-variant | WDR47 | GRCh38.p7 | 1:109032996 | ATTTAACTCTTTATG[G/T]GTGTTTTACTTAGTC | 22911 |
rs9697550 | snp | A/G | 0.089084 | 0.191327 | upstream-variant-2KB | WDR47 | GRCh38.p7 | 1:109042479 | AAAATAGCACGAACA[A/G]GATTGTCGCCTGCAA | 22911 |
rs9697705 | snp | G/T | | | intron-variant | WDR47 | GRCh38.p7 | 1:109032922 | TTCTGTTGAATGGAA[G/T]ATTTACGTTTTGTAA | 22911 |
rs9697801 | snp | C/T | 0.0854556 | 0.188216 | intron-variant | WDR47 | GRCh38.p7 | 1:109036612 | gctgaccccgtgatc[C/T]gcttgcctcggcctt | 22911 |