SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs888428 | snp | A/G | 0.00277597 | 0.0371521 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483454 | TGATGCTCTGAGAAT[A/G]CAGAAACTTAGATCC | 80067 |
rs997666 | snp | C/T | 0.470327 | 0.118136 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452567 | GAAGTGCTCCTCTCA[C/T]GTCACCCTCCTGAGT | 80067 |
rs1185477 | snp | C/T | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462586 | AACAATAAATGAAAG[C/T]GCCTAAACTTTTACC | 80067 |
rs1476111 | snp | C/G | 0.393619 | 0.204631 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452100 | AAAGATTCTCCCTTC[C/G]AAAGGGATAAATTTT | 80067 |
rs1558936 | snp | C/T | 0.32768 | 0.237625 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471940 | ggagccttgacctct[C/T]ggcctcaatcaattc | 80067 |
rs1558937 | snp | A/G | 0.32768 | 0.237625 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471939 | gagccttgacctctt[A/G]gcctcaatcaattct | 80067 |
rs1861899 | snp | C/T | 0.355096 | 0.226837 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480473 | ATTTTTCCAAATTTA[C/T]AATTGAAAGAAAATC | 80067 |
rs1882378 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480753 | GAACTCTGGACCCAG[A/G]AGTCTAAATACCCAG | 80067 |
rs1921776 | snp | C/T | 0.461592 | 0.133149 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470393 | ACCTTTCACCACGCA[C/T]GTTACAGATCACCTT | 80067 |
rs1981788 | snp | C/T | 0.327445 | 0.237702 | intron-variant | DCAF17 | GRCh38.p7 | 2:171470829 | acggatatagaaggc[C/T]ggctgTATCTGTACG | 80067 |
rs2193621 | snp | C/T | 0.0444908 | 0.142359 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436215 | ctaacaactgataaa[C/T]ggatacgtaaaatgt | 80067 |
rs2356709 | snp | A/G | 0.461481 | 0.133325 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438282 | atggctcagaatgtg[A/G]tctaccttggtgaac | 80067 |
rs2356781 | snp | A/G | 0.327445 | 0.237702 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480499 | AAAATTTTTTAAAAT[A/G]AGAGAATACGGTAAT | 80067 |
rs3054497 | in-del | -/ATA | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466593 | TTTTCATTGAGAATA[-/ATA]TTAGAGATCAAAATT | 80067 |
rs3731979 | snp | C/T | 0.00205205 | 0.0319658 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482148 | CCTTTACTTGGGTTG[C/T]CTTTATTTAACATTC | 80067 |
rs3731980 | snp | A/G | 0.00531452 | 0.0512739 | DCAF17 | 2 | allele_origin=G(germline)/A(germline) | 2:171480091 | ATCTATTTGAGTAAC[A/G]GCTACCACAGAAAGC | 80067 |
rs3731981 | snp | A/G | 0.347954 | 0.230011 | DCAF17 | 2 | allele_origin=G(germline)/A(germline) | 2:171480031 | TTTGAAAGTCTTTGG[A/G]ATAGATAGATAAAAT | 80067 |
rs3731982 | snp | C/T | 0.354881 | 0.226936 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479769 | ATAATTGAAATTCTC[C/T]ACAGTGACAGCAAAT | 80067 |
rs3731983 | snp | C/T | 0.350574 | 0.228877 | DCAF17 | 2 | allele_origin=T(germline)/C(germline) | 2:171473883 | ACAACAATCCATTTC[C/T]TGGATCCCATTTTTT | 80067 |
rs3731984 | snp | A/T | 0.0518822 | 0.152477 | DCAF17 | 2 | allele_origin=T(germline)/A(germline) | 2:171453141 | AAGGTACAGCAAAAC[A/T]TGTTGTTGAATGCCT | 80067 |
rs3731985 | snp | A/T | 0.328148 | 0.237472 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452996 | CATATTATGAAAACA[A/T]CCATCTATCTAGATT | 80067 |
rs3795996 | snp | A/G | 0.0332515 | 0.12458 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481464 | GATGAGTTCTTAAAG[A/G]ATGGTATGGAATTTT | 80067 |
rs3795997 | snp | C/T | 0.00184672 | 0.0303307 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481492 | TTTGTTTGTTAAGGC[C/T]AGGAAAGACAGGGAG | 80067 |
rs3795998 | snp | A/G | 0.387914 | 0.208518 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481684 | TTGTATATAGTATCA[A/G]GAATTGGTTCTAGTT | 80067 |
rs3821084 | snp | A/C | 0.387784 | 0.208604 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481790 | TTAAGGTTTGCTTGG[A/C]ATCTTTTACATTAGC | 80067 |
rs4404240 | snp | A/T | 0.337841 | 0.23406 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463223 | CGATGGAGCGAGATT[A/T]TAAAAAAAAAAAAAA | 80067 |
rs4404241 | snp | A/T | 0.351418 | 0.228505 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463224 | GATGGAGCGAGATTT[A/T]AAAAAAAAAAAAAAA | 80067 |
rs4417688 | snp | A/G | 0.327914 | 0.237549 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463187 | GGTGAGTGAGACTGC[A/G]CCACTGCACTCCAGC | 80067 |
rs4458186 | snp | C/T | 0.32768 | 0.237625 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458701 | CTGAGCCTTGCTTGG[C/T]CACAGACCTTTAGCA | 80067 |
rs4496302 | snp | C/T | 0.350982 | 0.228698 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463183 | TTGCGGTGAGTGAGA[C/T]TGCGCCACTGCACTC | 80067 |
rs4522571 | snp | A/G | 0.328148 | 0.237472 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440924 | gctatgaggacagac[A/G]ggtggcacttccagg | 80067 |
rs4668385 | snp | A/G | 0.354019 | 0.227333 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450641 | GTTTCTTTATACACC[A/G]GGACACCTAGAAAAA | 80067 |
rs4668386 | snp | C/T | 0.32768 | 0.237625 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461202 | GTAATCCCAGCACTT[C/T]AGGAGGCTGACGCGG | 80067 |
rs4668387 | snp | C/T | 0.327445 | 0.237702 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476785 | ATTTGTTGAGTTTTA[C/T]TTCAGTACTTAAACT | 80067 |
rs5836336 | in-del | -/A | 0.5 | 0 | intron-variant, upstream-variant-2KB | METTL8, DCAF17 | GRCh38.p7 | 2:171432227 | GTCAAAAAAAAAAAA[-/A]TCCTGTGTCACAAGT | 80067 |
rs5836337 | in-del | -/T | 0.462253 | 0.132093 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461850 | CAACCAGTGATCTGC[-/T]TTTTTTTCACAGTAG | 80067 |
rs5836338 | in-del | -/AAT | 0.480223 | 0.0974544 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466589 | GCCTTTTTCATTGAG[-/AAT]AATATTAGAGATCAA | 80067 |
rs6433291 | snp | A/G | 0.391954 | 0.205789 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439031 | accAGaacactttag[A/G]tatttatgtctctct | 80067 |
rs6433292 | snp | C/G | 0.351635 | 0.228408 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439369 | ttttcctcttttatt[C/G]ccccagcttgggaag | 80067 |
rs6433293 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474828 | tttttaaatctgcct[A/G]tttctgcccttggcc | 80067 |
rs6713612 | snp | A/G | 0.354881 | 0.226936 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444798 | AAAGGATAAGAGGCT[A/G]TACGCTAAATTTATT | 80067 |
rs6718740 | snp | C/G | 0.392325 | 0.205532 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440567 | caacagagcgagaca[C/G]tgtctcaaaaaaTTT | 80067 |
rs6720250 | snp | A/T | 0.32768 | 0.237625 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458958 | AGAAAATTATATACA[A/T]GTCTATAAATATAGT | 80067 |
rs6729749 | snp | G/T | 0.0479149 | 0.147179 | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469753 | GATAAGTGCAAAAAG[G/T]GAGTTAAGGGGGGAG | 80067 |
rs6730160 | snp | C/T | 0.0479149 | 0.147179 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171470066 | tctcactctggtgcc[C/T]agcctagagtgcagt | 80067 |
rs6737818 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171450868 | ttacaggtgaggatt[C/T]tgagccccagagaag | 80067 |
rs6740733 | snp | G/T | 0.32768 | 0.237625 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456788 | tcttggcttgactgt[G/T]gttgttgtataggaa | 80067 |
rs6741663 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472692 | GTTTCTGCCTCCCCC[C/T]AGACTATAAGCTTCT | 80067 |
rs6741806 | snp | A/G | 0.328148 | 0.237472 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444727 | AGGTCTTTGAATCTG[A/G]TTGGCTGTCCTTTAG | 80067 |
rs6743290 | snp | A/G | 0.355096 | 0.226837 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171470072 | TCTGGTGCCTAGCCT[A/G]GAGTGCAGTGGCACA | 80067 |
rs6751956 | snp | C/T | 0.396327 | 0.202703 | DCAF17, METTL8 | 2 | allele_origin=T(germline)/C(germline) | 2:171435106 | TAAATTTAAGAATGT[C/T]TGGACAACTCATTCC | 80067 |
rs7563499 | snp | A/G | 0.0748431 | 0.178382 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433987 | GGCCGAGAAGCTTGT[A/G]AGTACCGGGGCAGTG | 80067 |
rs7564602 | snp | C/T | 0.0718919 | 0.175435 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474890 | cactagccaaggcta[C/T]agtaatagcccactc | 80067 |
rs7568037 | snp | C/T | 0.334138 | 0.239331 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445495 | TCTCTTAAGAAAAAC[C/T]AGGAGCATTTTGAAT | 80067 |
rs7572334 | snp | A/C | 0.35445 | 0.227135 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171477142 | AAGAAAGTTGACTAT[A/C]TTGAGTTTGTCTTTT | 80067 |
rs7572973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441645 | gaaaacagggagcct[C/T]gtactcttggctgca | 80067 |
rs7576894 | snp | C/T | 0.325091 | 0.238456 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442740 | taacaattagctaag[C/T]gtagtagcatgagct | 80067 |
rs7591821 | snp | A/C | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469633 | atttattgagggcct[A/C]ccatgtgccagacaT | 80067 |
rs7594714 | snp | A/G | 0.426507 | 0.177046 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445808 | CCACCTTGGCCTCCT[A/G]AGTAGCTGGGACTAC | 80067 |
rs7599416 | snp | A/C | 0.040671 | 0.13668 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441632 | gagtggaagcttgga[A/C]aacagggagcctcgt | 80067 |
rs7600478 | snp | C/T | 0.422158 | 0.181278 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491110 | AGGGTGGGAGGATCA[C/T]GAGGTCAGGAGTTCG | 80067 |
rs7606658 | snp | A/C | 0.35445 | 0.227135 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473496 | CAAATGATTTATTCT[A/C]TTTGTGTATCAGTTT | 80067 |
rs9646734 | snp | C/T | 0.133777 | 0.221342 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465937 | TTTGCATACTTTAAA[C/T]ATTTAATCTTCTTTC | 80067 |
rs9678149 | snp | A/G | 0.32768 | 0.237625 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460121 | CGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCTA | 80067 |
rs9678164 | snp | A/G | 0.32768 | 0.237625 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460310 | CCTGGGCGATTGAGC[A/G]AGATTCCATCTCAAA | 80067 |
rs9679537 | snp | A/T | 0.327914 | 0.237549 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460275 | TTGCAGTGAGCCGAG[A/T]TCGTGCCACTGCACT | 80067 |
rs9679547 | snp | A/T | 0.277778 | 0.248452 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460543 | attattattattatt[A/T]Attttgagacagggt | 80067 |
rs9789380 | snp | A/G | 0.42263 | 0.180829 | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485236 | TCCACACATTCTCCA[A/G]CATGTGTGGTTGTTA | 80067 |
rs9789572 | snp | A/G | 0.388025 | 0.208445 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484817 | AAATTTACCTGTTCT[A/G]AACTTCATATGAGTG | 80067 |
rs9789596 | snp | C/T | 0.326506 | 0.238006 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488772 | TACCAGCTGGACTCA[C/T]GATCCAGTAGTTTCC | 80067 |
rs10177689 | snp | G/T | 0.114387 | 0.210022 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479162 | TAAATCCATATAAAT[G/T]TTTATGTCTTAGGGT | 80067 |
rs10445722 | snp | C/G | 0.328148 | 0.237472 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446973 | ACTGAAATGTATTGT[C/G]TTTACTATCAAGAAC | 80067 |
rs10445762 | snp | A/G | 0.198944 | 0.244731 | intron-variant | DCAF17 | GRCh38.p7 | 2:171447045 | TAGAGATTTCTGACC[A/G]AATTAAGGAACACTG | 80067 |
rs10460358 | snp | A/G | 0.463234 | 0.130503 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439284 | ccttctggtattccc[A/G]ttatgtggatgttat | 80067 |
rs10490604 | snp | C/G | 0.425432 | 0.178112 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457403 | TTTTTATACAATTCA[C/G]CAGCTTAATCAAAAA | 80067 |
rs10515933 | snp | A/G | 0.327914 | 0.237549 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468652 | ATCTGTTTTCAGGAG[A/G]TATATGTGGCCCGCA | 80067 |
rs11311213 | in-del | -/T | 0.0482946 | 0.147699 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479535 | AAAAGGATTTTTTTT[-/T]AAAGGTGGTAAAAAG | 80067 |
rs11366327 | in-del | -/A | 0.32768 | 0.237625 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473624 | ATCTCTTGGGTTATT[-/A]ACTCCTGTTTGTGAG | 80067 |
rs11449615 | in-del | -/T | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477454 | AATAATTTTTTTTTT[-/T]GCCCATTCTGGCATT | 80067 |
rs11677265 | snp | A/G | 0.0146672 | 0.084371 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474256 | GTCTTAGTTAATTCT[A/G]TAGGGTTAATAAGAA | 80067 |
rs11677562 | snp | A/G | 0.463343 | 0.130326 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444745 | GGCTGTCCTTTAGGA[A/G]AAACGGAACTCATAA | 80067 |
rs11696032 | snp | C/T | 0.379354 | 0.213933 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454245 | GATCTAGAATTAAAA[C/T]AGATTGGCTACTTTA | 80067 |
rs11887983 | snp | A/T | 0.00917871 | 0.0671201 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478121 | TGTGTCCTTGCATTG[A/T]GAATTTCATATTAAT | 80067 |
rs11901352 | snp | G/T | 0.040671 | 0.13668 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471608 | tcttttatgtaaaat[G/T]taataataCCACTAT | 80067 |
rs12052810 | snp | G/T | 0.462472 | 0.13174 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451085 | TTTAATTTTACCTTG[G/T]TTAGATAACTACATC | 80067 |
rs12151641 | snp | A/T | 0.388903 | 0.207861 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483539 | AGAAAACAAAACAAA[A/T]CCTATCCTATTTACT | 80067 |
rs12471094 | snp | A/G | 0.462472 | 0.13174 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466414 | CCTTTTTTTCACAAT[A/G]TAGGAAGTGGAAGCC | 80067 |
rs12612865 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468306 | GTGGTAGTAGTGACT[A/G]TCCTGTAATAAAGCT | 80067 |
rs12620294 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439815 | cacccataatcccag[A/C]tactccagaggccaa | 80067 |
rs12620336 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439867 | tgggaggtggaggtt[C/G]cagtgagttgtgatt | 80067 |
rs12620343 | snp | C/T | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440053 | tgtagccccaaactc[C/T]tgcactccagtgatc | 80067 |
rs13005833 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469593 | TTTAAAAATGGCTTA[A/G]GCGTTGATTTGTCAT | 80067 |
rs13024497 | snp | A/G | 0.247277 | 0.249985 | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447401 | atggagtcttctgtc[A/G]ccaggctggagtgca | 80067 |
rs13031705 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439512 | atttcttttttttcc[C/T]ttttttttttttttt | 80067 |
rs13396824 | snp | A/T | 0.114036 | 0.209795 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449506 | TTTTAACTATTAGTT[A/T]TATAAATTAGATGTA | 80067 |
rs13402901 | snp | A/G | 0.114036 | 0.209795 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465386 | TTTCATTTTGTTTTC[A/G]ATTTTGGGGTTTGCT | 80067 |
rs13404032 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451533 | GTGTCTTGTCTGATG[C/T]ACCTTTTTAATAATT | 80067 |
rs13404120 | snp | G/T | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451628 | gttgccaggctagag[G/T]gtcgtggtgagctct | 80067 |
rs13417427 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439419 | aaactcactgattct[G/T]tccttggctgcatcc | 80067 |
rs16859388 | snp | A/G | 0.0170251 | 0.090679 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433706 | AGCAATTATCGCAAA[A/G]CCAGTCAGTGTCCCC | 80067 |
rs16859390 | snp | A/T | 0.0729998 | 0.176553 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458603 | TCATTTTACTCCTAT[A/T]CATCATGTGCCTTGC | 80067 |
rs16859392 | snp | G/T | 0.0766824 | 0.180169 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461638 | TCTTTTATAACTCAC[G/T]TGTTAAGAAATCAAC | 80067 |
rs16859394 | snp | C/G | 0.0766824 | 0.180169 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468107 | AAATTGCTATACCTT[C/G]TATTTATGCATCTAA | 80067 |
rs16859404 | snp | G/T | 0.0320164 | 0.122406 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483889 | GTTCGGCATGAACTT[G/T]TGCCAAATTTCCTCC | 80067 |
rs16859405 | snp | A/G | 0.078151 | 0.181571 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488641 | CAGCTGTTACACAAC[A/G]TCTACTTGAAGATGT | 80067 |
rs16859410 | snp | G/T | 0.078151 | 0.181571 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489433 | TACAAATTCTCACAA[G/T]GACATATAGCTGACG | 80067 |
rs17220419 | snp | C/T | 0.328148 | 0.237472 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448582 | TTGTGGTTTATTTAT[C/T]TGGCATTTGAATATT | 80067 |
rs17220440 | snp | A/G | 0.337841 | 0.23406 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449638 | GAATACTCTTAGATC[A/G]AAAACAATTTTTATT | 80067 |
rs17220608 | snp | G/T | 0.32768 | 0.237625 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459664 | TTTTTCCTTAACATT[G/T]TATTAGTAATAGACC | 80067 |
rs17220657 | snp | C/T | 0.32768 | 0.237625 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459980 | TGAAATGGGTTATTT[C/T]GGACAGAGTTTTTCC | 80067 |
rs17220699 | snp | A/G | 0.32768 | 0.237625 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462833 | TATTATTATATCATC[A/G]TATACAAAAGATTGG | 80067 |
rs17220734 | snp | C/T | 0.327445 | 0.237702 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466687 | CATTTTTTGCATTTA[C/T]TGGGAAAGGTATTTC | 80067 |
rs17220817 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468283 | AGTTAACTTGTCTGA[C/T]GATAATAGTGGTAGT | 80067 |
rs17221346 | snp | C/T | 0.405391 | 0.195841 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483909 | AAATTTCCTCCAAAG[C/T]TCTCAAAAGGCAAGG | 80067 |
rs17221367 | snp | C/G | 0.389378 | 0.207543 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484226 | GTTTACTTATATCAT[C/G]CATCTTTTAGAATCC | 80067 |
rs17221402 | snp | A/G | 0.329317 | 0.237084 | intron-variant | DCAF17 | GRCh38.p7 | 2:171485748 | GTAGTATTCTAGGCC[A/G]GATATGTTGTGATAG | 80067 |
rs17286415 | snp | A/G | 0.327914 | 0.237549 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451212 | CTGTATGCCCCTGAA[A/G]CCAAGCAAACTATTT | 80067 |
rs17286660 | snp | C/T | 0.327445 | 0.237702 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467082 | ATGTTTATGCCTGTC[C/T]CTTCTTTTTCCTCAA | 80067 |
rs17287442 | snp | C/G | 0.174288 | 0.23826 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491511 | GGGTGTTTTTCACCT[C/G]CTGGTGGCCGTGGAT | 80067 |
rs28420126 | snp | C/T | 0.465788 | 0.126237 | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447675 | CCACTTCTTTTTTTC[C/T]TTTTTATCTAGAAAC | 80067 |
rs28453686 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450964 | GAGTCCCTGCTCTTA[C/T]GCACTGTAGTAAGCT | 80067 |
rs28663293 | snp | A/G | 0.110872 | 0.20771 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449151 | GTAGCTGGGATTTTG[A/G]GTGTGCACCCCATGC | 80067 |
rs28742013 | snp | A/G | 0.393619 | 0.204631 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450808 | TGTATTTACTAATTT[A/G]ATCTTCAGCACACTC | 80067 |
rs28791188 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455507 | AGAGCAGCATGATTT[A/G]TAATCCTTTGGGTAT | 80067 |
rs28795154 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455761 | GCATTTCTCTGATGG[C/T]CAGTGATGATGAGCA | 80067 |
rs28799322 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455703 | TTTTTTATGATCGCC[A/G]TTCTAACTGGTGTGA | 80067 |
rs28849697 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171456004 | TTTGCTGTGCAGAAG[A/C]TCCTTAGTTTAATTA | 80067 |
rs34033840 | in-del | -/CC | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171478144 | TATTAATACTTCCCC[-/CC]ATATCCTGGGGTAGA | 80067 |
rs34063621 | in-del | -/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171480561 | GCATGCGGGATTCCC[-/C]AGGTACTCTTGTATA | 80067 |
rs34127006 | snp | C/G | 0.0792508 | 0.182605 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457056 | CATCCTTGTCTTGTG[C/G]TGGTTTTCAAGGGGA | 80067 |
rs34153130 | in-del | -/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171446889 | ATGAAAAATATAACA[-/C]AAAAAGCCTAATTTC | 80067 |
rs34159763 | in-del | -/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171445778 | CCTCTACCTCCTGGG[-/G]CTCAGGTGATCCTTC | 80067 |
rs34238683 | in-del | -/A/C | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467728 | GAGCGAGACTGTCTC[-/A/C]AAAAAAAAAAAAAAA | 80067 |
rs34316002 | in-del | -/C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486181 | GGCTACACTTTTTTT[-/C/T]CTCAGAAAAACCAAC | 80067 |
rs34501466 | in-del | -/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171477975 | TCTTTTTATTTCTTT[-/G]CCATATGATAGAATG | 80067 |
rs34579689 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171472765 | TAGTCTGATACCTAG[-/T]AACATAGTAGCCTAT | 80067 |
rs34630185 | in-del | -/A | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171458862 | TTTTCCAAGAAAAAA[-/A]TTTTTACCATGACAT | 80067 |
rs34800947 | in-del | -/A | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171476854 | AATCCTTTTTCCCTT[-/A]CTCAGAGTTTTGAAG | 80067 |
rs35114893 | in-del | -/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171471775 | TTCCAGCACTTTGGG[-/G]AGGCCTAGGCAGGCA | 80067 |
rs35118788 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171465190 | TGACAGAGTGAAACT[-/T]CTGTCTCAAAAAGGA | 80067 |
rs35132997 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171460424 | TTTTATCCCTTTTTT[-/T]AGAAAGAAGACTGGA | 80067 |
rs35237908 | in-del | -/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455053 | ATGTGTCATGGGGGT[-/C]TTGTTGTACAGATTA | 80067 |
rs35241834 | in-del | -/T | 0.387074 | 0.209071 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435563 | TTGGAAGTACTTGCC[-/T]TTTTTTTTTTTTTTT | 80067 |
rs35257768 | in-del | -/GAGA | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487745 | ATAGAAAGAGAGAGA[-/GAGA]CTTACTATGTTATGT | 80067 |
rs35261185 | in-del | -/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171473428 | GGGCAACATAGCGAG[-/C]ACTCTATCTCTATTT | 80067 |
rs35281870 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171479474 | GGTTGGATTTCATTT[-/T]CCTAATATTCTCCCT | 80067 |
rs35364813 | in-del | -/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436488 | TCTTGTCAACACTTG[-/G]ATGTGTGACTCACAG | 80067 |
rs35398558 | in-del | -/A | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171463874 | AAAAGGCAAGTTAAA[-/A]GACTTATTTCTTCCC | 80067 |
rs35412246 | snp | G/T | 0.0792508 | 0.182605 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457214 | AATTGTTCTCTCTGT[G/T]CCTGTAGGTTAAGTA | 80067 |
rs35459663 | in-del | -/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171440741 | ATTTTTGTCTCCCCC[-/C]ATTGTTGGCTCCAGT | 80067 |
rs35602810 | in-del | -/C | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436744 | GTCTTTTTACTTTCC[-/C]TGATGTTATTGTTTG | 80067 |
rs35640081 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171449008 | ACCCTCTATCATTTG[G/T]CTTTTTTTTTTCTTT | 80067 |
rs36112363 | snp | G/T | 0.404498 | 0.196546 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472948 | TTCCCAGTGCTTCTG[G/T]ATATAAGGTAATACA | 80067 |
rs41268699 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443909 | AGCTAATGTATAATT[A/G]TCTTAGTGTTTAAGA | 80067 |
rs41268701 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171469083 | ATCAAGTTCTTTATT[C/T]TCTACCTCTCAAATA | 80067 |
rs55715902 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442478 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAA | 80067 |
rs55716501 | snp | A/C | 0.02016 | 0.0983543 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470471 | CCTTGATGTCATGGC[A/C]ATCAGGGGACAATGT | 80067 |
rs55770977 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171471920 | CTTGGGAGGCTGAGG[C/T]GAGAGAATTGATTGA | 80067 |
rs55974181 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438303 | CTTGGTGAACGTTTC[A/G]TGTAAGCTTGAGAAG | 80067 |
rs55987027 | snp | A/G | 0.267091 | 0.249415 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449689 | TAAAATTATGTATGT[A/G]TTTAAATAGGGATAT | 80067 |
rs55999882 | snp | A/G | 0.392325 | 0.205532 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440272 | TTGGTTGAGGGCTAT[A/G]TATGATATGATATAT | 80067 |
rs56037346 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171460676 | GCTGGGACTACAGGT[G/T]CATGCCACCACACCC | 80067 |
rs56100423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478709 | TAGGACCATTTTTAG[G/T]TAGAAACATTAGAGT | 80067 |
rs56410960 | snp | A/G | 0.3512 | 0.228601 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438801 | GAGTGCAGTGGCACA[A/G]TCATAGCTCACTGTA | 80067 |
rs56851249 | snp | A/T | 0.469544 | 0.119585 | intron-variant | DCAF17 | GRCh38.p7 | 2:171485942 | GGAAAGGAGGGGGAC[A/T]CTCAGCCTCCTATAT | 80067 |
rs57099324 | snp | A/G | 0.348354 | 0.22984 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450900 | TAAGTAACTTATCCA[A/G]CATCATAGTGTTGGT | 80067 |
rs57136707 | snp | C/G | 0.0475351 | 0.146656 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459399 | GTTCAGAGTTCATCT[C/G]AGGAATCCAAGGATG | 80067 |
rs57259754 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486067 | TCAGCAATAGCCTGT[A/G]ATATTTGTCTGATAC | 80067 |
rs57410416 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | DCAF17 | GRCh38.p7 | 2:171485906 | CTCATTATAACCTGA[A/G]TCCTATAGAAGGGTG | 80067 |
rs57764747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447424 | GGAGTGCAGTGGCAC[A/G]ATCTCAGCTCACCGC | 80067 |
rs57999878 | snp | A/G | 0.00611388 | 0.0549505 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483587 | AGGAGATACCGCTCT[A/G]TTTAGACAAATTAAG | 80067 |
rs58182652 | snp | C/G | 0.421842 | 0.181577 | intron-variant | DCAF17 | GRCh38.p7 | 2:171490595 | AAGTGCAATGAAATG[C/G]TTAATCTCATGGTCA | 80067 |
rs58267868 | snp | A/G | 0.422787 | 0.180679 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487562 | CCAAGTAGCTGGGAC[A/G]ACAGGTGTGCACCAT | 80067 |
rs58367130 | snp | C/G/T | 0.115088 | 0.210473 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446946 | ATGGTGTGACCAATA[C/G/T]GAAGGGTCAAGACTG | 80067 |
rs58536060 | snp | A/G | 0.355525 | 0.226637 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478506 | AGAGGATGTGAGGGC[A/G]TGATAAATCAGTTCA | 80067 |
rs58560571 | snp | A/C | 0.0748431 | 0.178382 | intron-variant | DCAF17 | GRCh38.p7 | 2:171470841 | GCCGGCCTTCTATAT[A/C]CGTGGGTTCCACATC | 80067 |
rs58636477 | in-del | -/T | 0.351853 | 0.228311 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458135 | TCGACTAAAGTATGA[-/T]TTTTTTTTTTAGTGA | 80067 |
rs58796565 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439485 | CTCTTATGGTGTTTT[C/T]TGATTTCTAGTATTT | 80067 |
rs58806459 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486131 | TGTTATTCCTGATTA[C/G]AGACAACATTGAATT | 80067 |
rs58808521 | snp | G/T | 0.0908922 | 0.192833 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471274 | TTAGTCAGAAGAGTA[G/T]ATAACTAAAAAAAAT | 80067 |
rs59019079 | snp | A/C | 0.0368353 | 0.130617 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472558 | TAAGGCTCATTTCAA[A/C]CTTTTTTTAACTCCC | 80067 |
rs59195571 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487510 | CTCATTCCAGCCTCC[A/G]CCTCCCGGATTCAAG | 80067 |
rs59559275 | in-del | -/CTTT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487001 | CTACGAGGTATAATT[-/CTTT]GTATGGACATACGCT | 80067 |
rs59737276 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171456377 | TCTGTTCTTGTACCA[C/G]TACCATGCTGTTTTG | 80067 |
rs59827170 | snp | A/G | 0.00352536 | 0.041836 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484943 | GCTGAGTATTCTTTC[A/G]TATGAATATATCACA | 80067 |
rs59960186 | snp | A/G | 0.350982 | 0.228698 | intron-variant | DCAF17 | GRCh38.p7 | 2:171436957 | TTTTGTATTTTTGGT[A/G]GAGACCGGGTTTCTC | 80067 |
rs59994598 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171470951 | GATTATATGCAAATA[C/T]TGCACCATTTTATAT | 80067 |
rs60392491 | in-del | -/A | 0.428333 | 0.175206 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443349 | TATTTTAATCTTGTT[-/A]TTTTTTTATATGAAT | 80067 |
rs60439518 | snp | A/G | 0.32768 | 0.237625 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457744 | ATTATTCTGAGGGAT[A/G]TGTGCCGCACTTCCA | 80067 |
rs60601337 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444241 | CAATAATACTAATAG[A/G]TATGATGATTATCAA | 80067 |
rs60830980 | in-del | -/TTGACTG | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438365 | TTCTGTTTGATCCAG[-/TTGACTG]ATGGTACCTTTCAGT | 80067 |
rs60837517 | snp | A/C | 0.0748431 | 0.178382 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455161 | CACCCTCCGATAGGC[A/C]CGAGTGTGTGTTGTT | 80067 |
rs61731491 | snp | A/G | 0.0256438 | 0.110292 | DCAF17 | 2 | allele_origin=G(germline)/A(germline) | 2:171468988 | TAATAAGAAGAAACA[A/G]AAAGGAGTTTTCCAT | 80067 |
rs62183467 | snp | A/G | 0.327914 | 0.237549 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435705 | CCAGATTCAAAAACT[A/G]TCAAGATTTGCCACA | 80067 |
rs62183468 | snp | A/G | 0.327914 | 0.237549 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435752 | CACTTTTCCTTTTGC[A/G]TGACCTCTTTTAAAG | 80067 |
rs62183470 | snp | G/T | 0.350982 | 0.228698 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437350 | TAGAAAGACTTTTCT[G/T]TCTTCATTGCAAGGC | 80067 |
rs62183471 | snp | A/G | 0.3512 | 0.228601 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437396 | AAAAATCAATTGACC[A/G]TAGACACTTTTGGAT | 80067 |
rs62183472 | snp | A/G | 0.328148 | 0.237472 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438052 | CACAAATGTTGATAC[A/G]TTGTATGTGCATTTT | 80067 |
rs62183492 | snp | C/G | 0.355096 | 0.226837 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439728 | AGGCTAGGAGTTCGA[C/G]ACCAGCCTGGCCAAC | 80067 |
rs62183493 | snp | A/T | 0.328148 | 0.237472 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441539 | CTATACTGACCCAAT[A/T]CTCAGCCCCAGCAAT | 80067 |
rs62183494 | snp | A/G | 0.32885 | 0.23724 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445930 | TCAAGTGATCTGCCC[A/G]CCTTGGCCTCCCAAA | 80067 |
rs62183495 | snp | C/T | 0.328148 | 0.237472 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448154 | CCTTTTTTTTTGAGA[C/T]GGGATCTCACTCTGT | 80067 |
rs62183497 | snp | A/G | 0.327914 | 0.237549 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451759 | TTTTGTATTTTTACT[A/G]GAGACGGGGTTTCAC | 80067 |
rs62183498 | snp | A/G | 0.32768 | 0.237625 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454430 | GCTGGGACTACAGGC[A/G]CCTGCCACCACACCC | 80067 |
rs62183499 | snp | A/G | 0.32768 | 0.237625 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454688 | GGTCATTTGAGGTTA[A/G]GAGATCAATACCAGC | 80067 |
rs62183501 | snp | A/G | 0.116488 | 0.211364 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459052 | TGGTGGCTCATGCCC[A/G]TAATCCCAGCACTTT | 80067 |
rs62183502 | snp | A/C | 0.32768 | 0.237625 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459419 | ATCCAAGGATGGTTT[A/C]ATGTTTACAAATTTA | 80067 |
rs62183503 | snp | C/T | 0.327445 | 0.237702 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467411 | AAGTCAAAAGTTTGG[C/T]TGGGCACAGTGGCTC | 80067 |
rs62183504 | snp | A/G | 0.420255 | 0.183066 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468630 | CCAGTTTCAATCTCT[A/G]CTCACCTGCGGGCCA | 80067 |
rs62183506 | snp | A/G | 0.328148 | 0.237472 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475458 | ACAGAGTAGATGCTC[A/G]GTATTTGTTGAATAA | 80067 |
rs62183507 | snp | C/T | 0.327445 | 0.237702 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478435 | CTTTATGGTTTTTGC[C/T]TCATTTTTTACTTGC | 80067 |
rs62183509 | snp | G/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482040 | ACCTGATTAACCAGA[G/T]AAAATTTTTGGCTTA | 80067 |
rs62183537 | snp | A/G | 0.422315 | 0.181128 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486596 | TATTTAAAGTACACA[A/G]TTTGATAAGTTTTGC | 80067 |
rs62183539 | snp | A/T | 0.32627 | 0.238082 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489336 | AGGATGGGAAACATT[A/T]CTGTAATAGAAAAGT | 80067 |
rs67351517 | in-del | -/CTTTT | 0.031825 | 0.122064 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171477186 | TCTTTTCTGAGTTTC[-/CTTTT]AAGTTTTTATTGATG | 80067 |
rs71407938 | in-del | -/C | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467726 | AGAGCGAGACTGTCT[-/C]CAAAAAAAAAAAAAA | 80067 |
rs72237176 | in-del | -/T | 0.423726 | 0.179776 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486174 | GAATTTTGGCTACAC[-/T]TTTTTTTCTCAGAAA | 80067 |
rs72471696 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455980 | CTATTCACTCTGATG[A/G]TAGTTTCTTTTGCTG | 80067 |
rs72625234 | snp | C/G | 0.181659 | 0.240478 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486731 | TCCCAAGACAACCTC[C/G]GATCTGTTTCTGTAA | 80067 |
rs72882321 | snp | C/T | 0.173965 | 0.238157 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442152 | TTCATTCTTGTGAAA[C/T]TGTTTGGTTTAAACT | 80067 |
rs72882324 | snp | C/G | 0.16976 | 0.236773 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450875 | TGAGGATTCTGAGCC[C/G]CAGAGAAGCTAAGTA | 80067 |
rs72882329 | snp | A/T | 0.093417 | 0.194889 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454036 | ACGTATATATTTAAT[A/T]AAGTTAAGCAGCAGT | 80067 |
rs72882335 | snp | A/G | 0.093417 | 0.194889 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466304 | AAAGTTATTTTGTAT[A/G]CTTTATGTTAAAATT | 80067 |
rs72882344 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473750 | ATTCCACTTTAACTG[A/G]TTAATATTTTTTCTT | 80067 |
rs72882347 | snp | A/G | 0.133435 | 0.221162 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474583 | ATTCTGCATGATTCT[A/G]TTTATTCCTTTGGCT | 80067 |
rs72882349 | snp | A/T | 0.0287284 | 0.116357 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475424 | ACCTATAACCCCAGC[A/T]CTAAGCATAGTCCTT | 80067 |
rs72882352 | snp | A/G | | | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485523 | GTTCTAAGGGCACGT[A/G]TTCCACCGTTTCACA | 80067 |
rs73022930 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438510 | TCTATCCGTGTTTGC[C/T]ACATTGTGTTTTGAT | 80067 |
rs73022941 | snp | G/T | 0.0106757 | 0.0722763 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457934 | GGATTGGACTTCCAG[G/T]CTTTTCTCAGGTGAT | 80067 |
rs73022949 | snp | A/T | 0.0766824 | 0.180169 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462416 | ATGATCAAAGGATAT[A/T]GTTTAAAAGAAACAG | 80067 |
rs73022955 | snp | C/T | 0.030665 | 0.119967 | intron-variant | DCAF17 | GRCh38.p7 | 2:171490609 | GGTTAATCTCATGGT[C/T]ACACCTCTGAGAAAT | 80067 |
rs73976158 | snp | C/T | 0.116488 | 0.211364 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457384 | TCTTCATTTAAGTAG[C/T]TTGTTTTTGATTAAG | 80067 |
rs73976159 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461960 | GATATTATATTTGAG[A/T]TTCGTTTCATGTTGT | 80067 |
rs73976160 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464321 | GTGTTGGCAGAGGTA[A/G]CCTCCCTCTGAAGGC | 80067 |
rs73976162 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467824 | GTTTAAGGGTGAACC[A/G]TTTGTGTTTTTTTCC | 80067 |
rs73976164 | snp | A/G | 0.0383715 | 0.133092 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470390 | ATCACCTTTCACCAC[A/G]CACGTTACAGATCAC | 80067 |
rs73976165 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473615 | AGATATGGTATCTCT[C/T]GGGTTATTAACTCCT | 80067 |
rs73976167 | snp | C/G | 0.00761208 | 0.0612217 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480951 | GTGTGAAAAGGACTC[C/G]ATATGATTGTGTTTT | 80067 |
rs73976168 | snp | A/G | 0.00167863 | 0.0289223 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482119 | GGTCCTTGACTTTTA[A/G]TAATCATTCTTTAGA | 80067 |
rs73976170 | snp | C/G | 0.0037085 | 0.042901 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483297 | CTACATGCCCACCTA[C/G]TTAACAGGTACTAGT | 80067 |
rs73976174 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488214 | ACCTGCCAAGATAAT[A/G]TGCATCTATAAATTG | 80067 |
rs73976175 | snp | C/T | 0.118933 | 0.212888 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489243 | TCTGTTGTCTTTGTA[C/T]TAGTCTCACTTCTGA | 80067 |
rs73976177 | snp | A/G | 0.124837 | 0.216412 | utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171490870 | GGGAGTTCAGAGTCC[A/G]CACAGAACAGTCTTG | 80067 |
rs73976178 | snp | C/T | 0.0314385 | 0.121371 | utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171490987 | AACTTGGATCCTGGG[C/T]TCAGATTTCTTCATA | 80067 |
rs74268270 | in-del | -/TTTT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466739 | ACTGTTTTTTTTTTT[-/TTTT]CTATTTTGAATTCCT | 80067 |
rs74484035 | snp | G/T | 0.039522 | 0.134904 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438594 | TGACACCTTTTTCAT[G/T]ATCTTATGCCCACTT | 80067 |
rs74516180 | in-del | -/AAC | 0.327914 | 0.237549 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448429 | ACTTAATAAAATAAT[-/AAC]TAATTCATAATAATA | 80067 |
rs74526549 | snp | A/G | 0.0759472 | 0.179459 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456880 | TTAAGAAGCTTTTGG[A/G]TTAGACAATGGGGTT | 80067 |
rs74562960 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453804 | TGCATAGTTATTTAT[G/T]GAGCTCTCCTACTGG | 80067 |
rs74620944 | in-del | -/AA | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443043 | GGGAGTAAAAAAAAA[-/AA]CCATAAAGGGTTTTT | 80067 |
rs74780004 | snp | A/G | 0.0018577 | 0.0304204 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484826 | TGTTCTAAACTTCAT[A/G]TGAGTGAAATTATAC | 80067 |
rs74809805 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462466 | TTAGGGGAGTGCAAA[G/T]CTCAATGTCACTGAT | 80067 |
rs74845295 | snp | A/G | 0.5 | 0 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491337 | AAAAAGAAAAGAAAA[A/G]AAAAAAAGAAGTCAC | 80067 |
rs74956216 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171467249 | ACAGATGAACCGCAT[A/C]GCCTAGAAATATGGA | 80067 |
rs75066774 | snp | A/G | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452699 | AGACTCCTAGCCTCA[A/G]GCGATCCTCCTGCCT | 80067 |
rs75082854 | snp | G/T | 0.0741063 | 0.177655 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472753 | AGGTATGAATGCCTA[G/T]TCTGATACCTAGAAC | 80067 |
rs75189609 | snp | A/G | 0.325327 | 0.238382 | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447686 | TTTCCTTTTTATCTA[A/G]AAACAGAGTCTTGCT | 80067 |
rs75205514 | in-del | -/AT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171480487 | GTAAATTTGGAAAAA[-/AT]TTTTTTAAAATAAGA | 80067 |
rs75227314 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479256 | TGCATAGTGATTGAG[A/G]GAAACATGCTATGCC | 80067 |
rs75241025 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | METTL8, DCAF17 | GRCh38.p7 | 2:171432227 | TGGCAAAGCAACGTC[A/C]AAAAAAAAAAATCCT | 80067 |
rs75244294 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171470843 | CGGCCTTCTATATCC[A/G]TGGGTTCCACATCTG | 80067 |
rs75246237 | snp | A/T | 0.32768 | 0.237625 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466023 | ACATGTATCTAAATT[A/T]AAAAAAATTTTTTTA | 80067 |
rs75279562 | snp | G/T | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454302 | AATTTTTTTTTTTTT[G/T]GAGACAGAGTCTTGC | 80067 |
rs75295568 | snp | G/T | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445145 | CTATTTTTTTTTTTT[G/T]AGACGGTCTCTCTTT | 80067 |
rs75584578 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441086 | TTAGCCTGTATCTCC[A/G]CTGAGTCTACCAGTC | 80067 |
rs75594139 | snp | C/T | 0.328148 | 0.237472 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440522 | CAAGGCTGCTCGAGC[C/T]GTCAGCATGCCACTG | 80067 |
rs75633126 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433826 | TCCTAATACAAAAGC[A/G]CAGTTTACCGTCCCC | 80067 |
rs75774601 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467273 | ATATGGAAAAAATTA[A/G]GAAAAAGGTACATGA | 80067 |
rs75833923 | snp | A/G | 0.00018952 | 0.00973262 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484136 | TTTGTTTGTGGTGAT[A/G]ATCAGTATTAGTAGT | 80067 |
rs75894811 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483996 | AAGTGCTTAATAATC[A/G]TTTTTTACTGATGAT | 80067 |
rs75984729 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444682 | CTTATTCTAAGAAAT[A/G]CACTTAGGAAATACT | 80067 |
rs75992229 | in-del | -/GTTGACT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438364 | ATTCTGTTTGATCCA[-/GTTGACT]GATGGTACCTTTCAG | 80067 |
rs76059736 | snp | C/T | 0.116838 | 0.211584 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437395 | CAAAAATCAATTGAC[C/T]ATAGACACTTTTGGA | 80067 |
rs76077445 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486942 | ATACTGTGGCCTTTC[A/G]ATGGACATTTCAGTT | 80067 |
rs76137360 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443292 | GGAAATGAACCAAAA[C/T]GTTAATAAGGGTTAT | 80067 |
rs76205813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468763 | TTTATTTCCTTGAAC[A/T]TAGTAATTTTTCATT | 80067 |
rs76335624 | snp | A/G | 0.039522 | 0.134904 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448932 | CATTACCAGATCTCA[A/G]TTAATAAACCTATTT | 80067 |
rs76347150 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473323 | GAAAATATTGGAAAA[G/T]GTCAGGTGCAGTGGC | 80067 |
rs76397917 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476626 | GCTGATCATTACCTA[C/T]TTCAGTGGCACCTGT | 80067 |
rs76533507 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437533 | TGGTGGAATTAACCA[C/T]TGAAAGCATCTGGGC | 80067 |
rs76652855 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488080 | GTTAATGCCTTGAAC[C/G]TATTTTAGTTCAATG | 80067 |
rs76755350 | snp | A/T | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463316 | TAAAAAAAAAAAAAA[A/T]ATCGGTGCAAAACTG | 80067 |
rs76806294 | snp | C/G | 0.046775 | 0.145601 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433946 | CCTCCCGGCACCTGG[C/G]CAGAACCTCCCAGGG | 80067 |
rs76819661 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470397 | TTCACCACGCACGTT[A/G]CAGATCACCTTTTAC | 80067 |
rs76871216 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451074 | TAAGTAGTTCCTTTA[A/G]TTTTACCTTGTTTAG | 80067 |
rs76931660 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477756 | AAGATTGTGCCACTA[C/T]AGTGAGGCAAGATCG | 80067 |
rs77022385 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488166 | CATAAAAGTAACAGT[C/T]GGTGAAAGTGAAATT | 80067 |
rs77033804 | in-del | -/CTC | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486727 | TCCCAAGACAACCTC[-/CTC]GGATCTGTTTCTGTA | 80067 |
rs77105072 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439103 | TCTTATTGTTCCCCT[A/G]TATAGTTAAGGTGCT | 80067 |
rs77108896 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438365 | TTCTGTTTGATCCAG[A/T]TGACTGATGGTACCT | 80067 |
rs77176791 | snp | A/G | 0.00222758 | 0.0332991 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482635 | CAAGAGTGTTTCAGA[A/G]TAGGATGTCTTAAGA | 80067 |
rs77193647 | snp | A/G/T | 0.00438332 | 0.0466095 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451881 | AGTTTAATTCTATAC[A/G/T]TTATCATATGTTAAT | 80067 |
rs77284169 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443674 | TAGAAGAACCAGTTA[C/T]TATTAACATATTGCA | 80067 |
rs77288528 | snp | A/G | 0.0905309 | 0.192535 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436327 | TTTCACTTCTCCTAG[A/G]TTATACCTAGGAATG | 80067 |
rs77399420 | snp | A/C | 0.328382 | 0.237395 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440006 | CCCAGGCTAGAGTGC[A/C]GTGGCTTTTCACAGG | 80067 |
rs77471594 | snp | A/G | 0.183886 | 0.241099 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461382 | CAGTGAGCCGAGATC[A/G]TGCCACTGCACTCCA | 80067 |
rs77479345 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480291 | GTCAGTCCAGACTCA[C/T]CTATGCCAATGACCA | 80067 |
rs77509790 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452643 | ATTTTTTGTATAAAC[A/G]AGGTCTCACTATTTC | 80067 |
rs77634005 | snp | A/G | 0.32768 | 0.237625 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476335 | CAATCCTAAGAAAAA[A/G]GAATAGTATTTTCAG | 80067 |
rs77708089 | snp | A/T | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451044 | AGAACTCTAGCATTA[A/T]AAAAAAAAAAAAGTT | 80067 |
rs77760038 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459592 | CATTATATTTTTAGG[A/T]GAAATGCCAAAGGAT | 80067 |
rs77778526 | snp | A/C | 0.138886 | 0.22395 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487433 | TACTTATTTTTCTTT[A/C]TTTATTTTGAGACGG | 80067 |
rs78076961 | snp | C/T | 0.0337553 | 0.125452 | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469717 | AAAAATAAGATGCAA[C/T]GTATTAAGTACAGTG | 80067 |
rs78383460 | snp | C/T | 0.078151 | 0.181571 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488810 | ATTTCTGTAGAAAGT[C/T]TTGAGTGCCTCTGCC | 80067 |
rs78488864 | snp | C/T | 0.00139625 | 0.0263852 | intron-variant, missense, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473914 | TCTCTAGAATCTGAC[C/T]GGATCTATTTCCATC | 80067 |
rs78561668 | snp | A/G | 0.000374672 | 0.0136819 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484090 | GTAGTTCTTCATTCA[A/G]TGGTTAGCAGTCATT | 80067 |
rs78632393 | snp | A/G/T | 0.0298908 | 0.118541 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171475821 | TTTATGCTTCGTAGT[A/G/T]ATCAGTCTACCTCTC | 80067 |
rs78683074 | snp | A/G | 0.0752113 | 0.178743 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171433087 | CAGCTCAGGGTGCAA[A/G]GTGGGAACCAACCCT | 80067 |
rs78854579 | snp | A/G | 0.02016 | 0.0983543 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475531 | GCACTTTGGGAGGCC[A/G]AAGCAGGAGGATCCC | 80067 |
rs78854848 | snp | C/T | 0.117188 | 0.211804 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448082 | TCCATCTAAAGGAAA[C/T]AAGTCCTGTGGTAAA | 80067 |
rs78939846 | snp | C/T | 0.354235 | 0.227234 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450180 | AAGTGAGAGCTAAGC[C/T]TTGAGGATGCAAAGG | 80067 |
rs79017245 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452571 | TGCTCCTCTCACGTC[A/G]CCCTCCTGAGTAGCT | 80067 |
rs79030073 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486999 | AAGCTACGAGGTATA[A/T]TTGTATGGACATACG | 80067 |
rs79037488 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452498 | CATGTCTGATGCCCA[C/G]GCTGGAGTGCAATGG | 80067 |
rs79085683 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466411 | GCCCCTTTTTTTCAC[A/C]ATGTAGGAAGTGGAA | 80067 |
rs79122560 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453704 | CTTGTGGAGCAGTTA[C/T]ATGGGAGGAAAGAAG | 80067 |
rs79242373 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451853 | CCACCACTCCTGGCT[A/G]AGAATTTTTTTAAGT | 80067 |
rs79275087 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436649 | TTTTTTTTTTTTTTT[-/TT]ACAAAAATCCTTACA | 80067 |
rs79531093 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433742 | CCACCCAAGGACAAG[C/G/T]CTCCGGGAAAGAGTA | 80067 |
rs79581001 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465325 | CGATTTGAAATCATT[C/T]TTCTATAGGATTAAG | 80067 |
rs79604508 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450153 | AACCAGACATTGTAT[C/T]TTCTCACTCATAAGT | 80067 |
rs79629880 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437958 | TAGAAACTTAGATTA[C/T]GATTTGAAGTCTTTC | 80067 |
rs79728590 | in-del | -/CAAAA | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171467727 | AGAGCGAGACTGTCT[-/CAAAA]AAAAAAAAAAAAAAA | 80067 |
rs79843945 | snp | A/G | 0.351418 | 0.228505 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467034 | CCCTTTTCTTAAAAG[A/G]TTAAAAAAATAAGCA | 80067 |
rs80057381 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450687 | GTGTCTCCCCTTGGC[A/G]GAGTCTGTTGTAGTT | 80067 |
rs80076920 | snp | C/T | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449019 | TTTGTCTTTTTTTTT[C/T]CTTTTTTAAGACAAG | 80067 |
rs80320833 | snp | A/G | 0.116488 | 0.211364 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171475660 | CTTAGCTCCTCAGGA[A/G]TCTGGGGCAGGAGGA | 80067 |
rs80336595 | snp | G/T | 0.00112087 | 0.0236469 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434467 | CTTTCCCTGGGCCCC[G/T]CCGGGAAAGTCTGGG | 80067 |
rs111259008 | snp | A/G | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171447053 | TCTGACCAAATTAAG[A/G]AACACTGTTTTCCTG | 80067 |
rs111298984 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444858 | ACATAAAGTTTTAGT[A/T]TTCTGGAGCTGCTGC | 80067 |
rs111492750 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488200 | ACTCAGGACACTCTA[C/T]CTGCCAAGATAATAT | 80067 |
rs111508787 | in-del | -/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481136 | GAGATAATTGTAACC[-/C]TAAGAGACTTTTAGC | 80067 |
rs111528974 | snp | C/T | 0.000711744 | 0.0188511 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472852 | GTAGGAAATATGGCA[C/T]CATTTCATTTTACAT | 80067 |
rs111530397 | snp | A/G | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462204 | AAAACCCAAAGCCAT[A/G]AAAGAAGAGATTGAT | 80067 |
rs111539500 | snp | A/C | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438713 | GTATCTTTTGCCATT[A/C]CTTTACTTTTAATCT | 80067 |
rs111556008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456189 | TGAGTTAATTTTTGC[A/G]TATGGTGTAAGGAAG | 80067 |
rs111567371 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171433216 | AGGCAGTACCCTGGG[A/G]TACCTGGTGAAAACC | 80067 |
rs111587613 | snp | A/G | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437741 | ATTGTTTTAACGTCC[A/G]TGAGATCGGTAGTGA | 80067 |
rs111619436 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439310 | GTTATACCTTCTCCA[A/G]TTTTCCTGTAATACT | 80067 |
rs111642937 | snp | C/T | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444100 | TTCATGGAATGTTAA[C/T]GGGTGTCAGAGGAGT | 80067 |
rs111705129 | snp | A/G | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489746 | GAGCTCTGCCTCCCA[A/G]GTTCACGCCATTCTC | 80067 |
rs111737117 | in-del | -/T | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463221 | GGCGATGGAGCGAGA[-/T]TTTAAAAAAAAAAAA | 80067 |
rs111845477 | snp | A/G | 0.093417 | 0.194889 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454371 | CCCACTGCAATCTCT[A/G]CCTCCTGGGTTCAAA | 80067 |
rs111862462 | in-del | -/AA | 0 | 0 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171477266 | ATTGGGGTAATATAT[-/AA]GTCTTTAAAAATCAC | 80067 |
rs111958561 | snp | A/G | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451731 | CAGGCGTGCACCACC[A/G]GGCCCAGCTAATTTT | 80067 |
rs111986627 | snp | C/T | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452177 | TCTAACTTTTAGTTA[C/T]AGCAGTTTTGATTGG | 80067 |
rs111992140 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489720 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCGAGCT | 80067 |
rs111993581 | in-del | -/T | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438653 | CGACTTTGTCTGAAA[-/T]TAGTATAGCTACTCC | 80067 |
rs112006982 | snp | C/T | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440615 | ATTGGATAAAAAGAA[C/T]TAAATAGGCCTTTAG | 80067 |
rs112045336 | snp | A/G | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459359 | AAATTCAGTAGTAGT[A/G]CATTAAAAGAAATAG | 80067 |
rs112059279 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434030 | CTAAGTGCAGGGCGC[A/G]CACACGGGGCGGAGA | 80067 |
rs112062518 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432408 | CTCTCCCTTGGTGAC[A/G]ACTTGGTGGTGAAAT | 80067 |
rs112128400 | snp | A/C | 0.0755793 | 0.179102 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460162 | ACCCCATCTCTACTA[A/C]AAATACAAAAATTAG | 80067 |
rs112219335 | snp | C/T | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478651 | ACATATAAACCATTG[C/T]GTAAATTCTAAATCC | 80067 |
rs112263625 | snp | A/T | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487655 | CTCAAACTCCTGACC[A/T]CAAGTGATCCACTCA | 80067 |
rs112384852 | in-del | -/T | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461793 | CCCAAAAAGTTCCCC[-/T]GTGCTCTTCGCAGTA | 80067 |
rs112399226 | snp | C/T | 0.176861 | 0.239062 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489737 | GCTCACTGCGAGCTC[C/T]GCCTCCCAGGTTCAC | 80067 |
rs112420356 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487534 | ATTCAAGAGATTCTC[A/G]TGCCTCAGCCTCCCA | 80067 |
rs112420917 | snp | A/C | 0.392881 | 0.205147 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467749 | AAAAAAAAAAAAAAA[A/C]AAAAAGTTGTACGTG | 80067 |
rs112468571 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444143 | GGCTGTGAAAAACTA[A/G]GTTTGGGACATTCTG | 80067 |
rs112471541 | snp | C/T | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437199 | GCTCCTAGGTTTTTT[C/T]CTAAAGGGTTTATAG | 80067 |
rs112519318 | snp | A/G | 0.00148533 | 0.0272114 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483462 | GTTTCTGCATTCTCA[A/G]AGCATCAATGCAGCA | 80067 |
rs112546863 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489776 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 80067 |
rs112604249 | snp | A/T | 0.175897 | 0.238765 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491117 | GAGGATCATGAGGTC[A/T]GGAGTTCGAGACCAG | 80067 |
rs112606482 | snp | G/T | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468584 | TATTAAATGTACTTT[G/T]TCATTTCTTACCATC | 80067 |
rs112682130 | snp | C/T | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448642 | CAAATTGTTCATGGC[C/T]AAGCAGTTTCATTTT | 80067 |
rs112686269 | snp | C/T | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446269 | ATCTAGGAGAGTGGC[C/T]AGGTGCGGTGGCTCA | 80067 |
rs112712598 | snp | C/T | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479685 | ATGTGTTTAGTCCTG[C/T]CCAGGAATCAGCAAA | 80067 |
rs112721895 | in-del | -/T | 0.343477 | 0.231866 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476150 | TTCTCTCTGCTGTTC[-/T]TTTTTTTTTTGCATT | 80067 |
rs112783448 | snp | A/G | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453015 | TTTCATAATATGAAA[A/G]TGTCTGTATAACTAC | 80067 |
rs112860953 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432638 | TACAAAGCACTCTAC[C/T]GTATGCTGTAAATAA | 80067 |
rs112892042 | in-del | -/TTCT | 0.226484 | 0.248892 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486999 | AGCTACGAGGTATAA[-/TTCT]TTGTATGGACATACG | 80067 |
rs112955444 | snp | A/G | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461615 | GAAAAGAATCATACC[A/G]TAAGTGCTCTTTTAT | 80067 |
rs112971058 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435026 | GCTTTGAAAATTTAA[A/C]ATCTAACTTAAAGCC | 80067 |
rs112994547 | snp | G/T | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443185 | AATTCAACAGAGATA[G/T]TCTTAGTAAATGTTC | 80067 |
rs113044466 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433532 | GAAAGTTTAGTGTGC[C/T]GGGAACTTTGAACAT | 80067 |
rs113112720 | in-del | -/CT | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443720 | TAAATATCATAGTGA[-/CT]CTTGCATCTTTAAAG | 80067 |
rs113154418 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438202 | ATTTGTGGTTTAATA[C/T]CACTATGACCCAAGA | 80067 |
rs113204019 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171467736 | CTGTCTCAAAAAAAA[A/C]AAAAAAAAAAAAAAA | 80067 |
rs113208637 | snp | C/T | 0.120674 | 0.21395 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489940 | ACAGGCGTGAGCTGC[C/T]GTGCCCAGCCCTAAT | 80067 |
rs113212658 | snp | C/G | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462794 | AAGATTGGAAACAAT[C/G]TATACATTGGTAAGT | 80067 |
rs113215140 | snp | A/T | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449866 | AATAAACTTCTCTTC[A/T]TTCTTTTAAAAGATA | 80067 |
rs113259802 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460622 | TGCCACCTCCACCTC[C/T]TGGGCTCAAGTGATC | 80067 |
rs113353859 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448877 | TGAAACCTGTGGCCC[A/G]TGAAATTTCAAGCCT | 80067 |
rs113417445 | snp | A/G | 0.030665 | 0.119967 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440226 | TCTTCAAACTTTTGT[A/G]TTTTGCCTGTTAGCA | 80067 |
rs113478476 | snp | A/G | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477492 | TTTTAGCCATTAAAA[A/G]CTTTAATAAAGTATT | 80067 |
rs113506865 | snp | C/T | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452737 | CCAAAGGGCTGGAAT[C/T]ATAGGCGTGAGCTAC | 80067 |
rs113618728 | in-del | -/C | 0.000216947 | 0.0104128 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481134 | GTGAGATAATTGTAA[-/C]CCTAAGAGACTTTTA | 80067 |
rs113619289 | snp | A/G | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457529 | CTATCCAGGGGCTGG[A/G]CACCTCTAATTAACT | 80067 |
rs113646183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438462 | TTGAAATCTCTATAA[C/T]AGTGAGTGGATTTAT | 80067 |
rs113678114 | snp | C/G | 0.095934 | 0.196885 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489951 | CTGCCGTGCCCAGCC[C/G]TAATTTCCTAGTTTT | 80067 |
rs113790650 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442786 | TTGGGAGGCTGAGGC[A/G]GGACAATTACATGAG | 80067 |
rs113836968 | snp | C/G | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487747 | AGAAAGAGAGAGAGA[C/G]ACTTACTATGTTATG | 80067 |
rs113840857 | in-del | -/T | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479513 | AGCAGCCATTTTTGC[-/T]TTATTTAAAAAACCA | 80067 |
rs113860053 | snp | A/C | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437605 | ATTTCTTTAATAGAT[A/C]CAGACTTATTCAAGT | 80067 |
rs113864498 | snp | C/T | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478986 | CATGAGATTAAAAAA[C/T]AAAATATTTTAGCCT | 80067 |
rs113878229 | snp | C/T | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171436832 | CAGGCTGGAGTGCAA[C/T]GGCGTGATCTCGGCT | 80067 |
rs113928683 | snp | A/C | 0.5 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171490389 | AAATGCAGTGTGTTC[A/C]AAATAATTGTAAAAG | 80067 |
rs113940733 | snp | C/T | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438828 | TGTAACACCAAACTC[C/T]TGGACTGAAGCAATC | 80067 |
rs114074462 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461650 | CACTTGTTAAGAAAT[C/G]AACTCTATTGAGGTA | 80067 |
rs114097492 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | DCAF17 | GRCh38.p7 | 2:171447322 | TTCACTTTTTGGCCT[A/C]AGCAGATACTAGATT | 80067 |
rs114268267 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171489447 | AGGACATATAGCTGA[C/T]GATATTACCTGCTAC | 80067 |
rs114419034 | snp | A/G | 0.000494323 | 0.0157136 | missense, nc-transcript-variant, synonymous-codon | DCAF17 | GRCh38.p7 | 2:171468962 | CATCCTTGGCACTAC[A/G]TCGTCACACCTAATA | 80067 |
rs114513165 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475410 | TCTGTTTTGCTGACA[C/T]CTATAACCCCAGCAC | 80067 |
rs114519296 | snp | C/G/T | 0.00557306 | 0.0524926 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482955 | GAAAGACAGTAAGGA[C/G/T]TTGTGGGCAGTGTAA | 80067 |
rs114530159 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446573 | AAAAATCTAGGAGAG[A/T]CAACTAAGAAAAATA | 80067 |
rs114606322 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489255 | GTACTAGTCTCACTT[C/G]TGACACCAATTTGTA | 80067 |
rs114656724 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471088 | GTATATCAAGCATGC[C/T]TGTCACATACTCTCC | 80067 |
rs114671516 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171447190 | TCAATTATATGTAGT[C/T]ATACAAAAAAAAAAC | 80067 |
rs114770484 | snp | A/T | 0.031825 | 0.122064 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467988 | AAACTAAAAATTAAA[A/T]TCTCAAGTTAGAGGG | 80067 |
rs114785890 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440795 | CTGGAAAGCTGTAAT[A/T]GTCAGTATCCACCTT | 80067 |
rs114807440 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440401 | CCAACATGGCAAAAC[C/G]CCATCTCTACAAAAA | 80067 |
rs114854121 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466412 | CCCCTTTTTTTCACA[A/G]TGTAGGAAGTGGAAG | 80067 |
rs114982618 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436030 | ACCACTAGTCTGTTT[G/T]CTGTCTGTAGATTCA | 80067 |
rs114982703 | snp | A/G | 0.0314385 | 0.121371 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171477007 | TTTCTATATAAGACT[A/G]TAATATGCTAATATA | 80067 |
rs115005655 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438592 | ATTGACACCTTTTTC[A/G]TTATCTTATGCCCAC | 80067 |
rs115034842 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480418 | TAAAACTTCATGTGT[C/T]TTCCTGAGACATGTT | 80067 |
rs115037143 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462447 | AAATATAAATGACTT[C/T]TAATTAGGGGAGTGC | 80067 |
rs115048187 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475256 | CCCTTGTTAGATTTG[C/T]TTGCCCATCATATTT | 80067 |
rs115174779 | snp | A/G | 0.0774956 | 0.18126 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439696 | ACTTTGGGAGGACTA[A/G]GTGGGCAGATCACTT | 80067 |
rs115226206 | snp | A/T | 0.0414363 | 0.137845 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467989 | AACTAAAAATTAAAT[A/T]CTCAAGTTAGAGGGT | 80067 |
rs115242634 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489346 | ACATTTCTGTAATAG[A/G]AAAGTATATGAAATG | 80067 |
rs115260785 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467200 | TAAATACAGGAAAAT[G/T]TTTTGGAGATTTGCC | 80067 |
rs115396774 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449295 | TTACAGGCGTGAGCC[A/G]TCGTGCCCAGCTGTC | 80067 |
rs115493043 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465311 | GATGTGTTCAAAGGC[A/G]ATTTGAAATCATTTT | 80067 |
rs115589695 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456797 | GACTGTGGTTGTTGT[A/G]TAGGAATGCTAGCAA | 80067 |
rs115676571 | snp | A/G | 0.000186237 | 0.009648 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481644 | TTTTAAAAATCTTAT[A/G]TATGTATTTATATGT | 80067 |
rs115798465 | snp | A/C | 0.000372926 | 0.01365 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481791 | CTAATGTAAAAGATT[A/C]CAAGCAAACCTTAAG | 80067 |
rs115859470 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467613 | ATACTTAGGAGGCTG[A/T]GTAATACTTAGGAGG | 80067 |
rs115869663 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483075 | ATGGTTGTTAACAAG[A/G]TAGATGGTAAAAAGA | 80067 |
rs116027708 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469691 | GTTATACTCTTAAAG[A/G]AAACATGTAGAAAAA | 80067 |
rs116041957 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439693 | CACACTTTGGGAGGA[C/T]TAGGTGGGCAGATCA | 80067 |
rs116043944 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473425 | GCCTGGGCAACATAG[C/T]GAGACTCTATCTCTA | 80067 |
rs116148396 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440343 | CACTTTTGGAGGCCA[A/G]CGTCTGGGGTTGCTT | 80067 |
rs116198705 | snp | A/G | 0.00557542 | 0.0525036 | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485521 | GGGTTCTAAGGGCAC[A/G]TGTTCCACCGTTTCA | 80067 |
rs116305732 | snp | C/T | 0.0785177 | 0.181917 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487509 | GCTCATTCCAGCCTC[C/T]GCCTCCCGGATTCAA | 80067 |
rs116360378 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438947 | CTGTGTTGCCCAAGC[A/T]GATCTCATACTCCTG | 80067 |
rs116512816 | snp | A/G | 0.0232847 | 0.105357 | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469558 | AAATTTCTACCCTTC[A/G]AATTCATTTTTATTT | 80067 |
rs116632851 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440443 | AGCTGGGCATGGTGG[C/T]ACACACCTGTAGTCC | 80067 |
rs116741835 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460822 | ATTACAGGCATGAGC[C/T]ACTGTGCCCAGCTGA | 80067 |
rs116772362 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171485739 | TCACTAACTGTAGTA[G/T]TCTAGGCCGGATATG | 80067 |
rs116795973 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466758 | CTATTTTGAATTCCT[A/G]TGTCCTCTATATTGA | 80067 |
rs116868307 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443899 | AAGCAGCATAAGCTA[A/G]TGTATAATTATCTTA | 80067 |
rs116916821 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461802 | TTCCCCTGTGCTCTT[C/T]GCAGTAAATTCCTCT | 80067 |
rs117102922 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456739 | TTTATTCTTTTTAGG[A/G]CAACTGTGAATGAGA | 80067 |
rs117150300 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489958 | GCCCAGCCCTAATTT[C/G]CTAGTTTTAATATCC | 80067 |
rs117209863 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440923 | TGCTATGAGGACAGA[C/T]GGGTGGCACTTCCAG | 80067 |
rs117212671 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486020 | AACCCACTGAGATTA[A/G]CAGACAATAGCAAGG | 80067 |
rs117406597 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446767 | AAAATTGCATTGTGA[A/G]TGTAACATTTTTTAT | 80067 |
rs117486204 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439843 | CAAGGCAGAAGAATT[C/G]CTTGAATCTGGGAGG | 80067 |
rs117496992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489176 | TATTCCTGGATCATA[G/T]TTTCTTCTACAGTTT | 80067 |
rs117574700 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474502 | TGTTCTTCCTTCTCT[A/G]CCCAGACTTTAATTG | 80067 |
rs117983003 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473100 | ATTAGAGTTCAACAT[A/T]TGACTTATCCAAGAT | 80067 |
rs118030053 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433773 | ACTCAATCCCAGTTT[G/T]GAGGGTGAAACTAAG | 80067 |
rs137914244 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447583 | TGGCCAGGCTGGTCT[C/T]GATCTCCTGACATCG | 80067 |
rs138020138 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489369 | ATGAAATGTACAGAG[A/T]TGATCCCAAAAATGA | 80067 |
rs138041470 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441450 | CCTCAGTATCCTCAG[A/C]TGTGCTACATCCAAG | 80067 |
rs138120900 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475291 | TGCACCCACTGTGTC[A/G]TCTTCCTTTGTAGCA | 80067 |
rs138141219 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462172 | CAGTGTGGGGAAGAC[A/C]TTTTTAAGTATGGCA | 80067 |
rs138157431 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486062 | TGAGATCAGCAATAG[C/T]CTGTAATATTTGTCT | 80067 |
rs138268520 | snp | A/G | 9.93789e-05 | 0.00704837 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457933 | AGGATTGGACTTCCA[A/G]TCTTTTCTCAGGTGA | 80067 |
rs138362232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480442 | ACATGTTGTCTCTTT[C/T]CCTACCCTAGTCTTT | 80067 |
rs138589111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171485553 | ATGACTACTGGAGCT[A/G]GACAAAATGGCACTG | 80067 |
rs138657121 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453436 | TCATATTGGATACCT[A/G]TGGTCATTAACAAAC | 80067 |
rs138703610 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448177 | CACTCTGTCACCCAG[G/T]CTGGAGTGCAGTGGC | 80067 |
rs138741477 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442476 | GGCTGAGGCAGGAGA[A/C]TCGCTTGAACCTGGG | 80067 |
rs138943827 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465189 | GGTGACAGAGTGAAA[C/T]TCTGTCTCAAAAAGG | 80067 |
rs138997216 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461862 | TGCTTTTTTTTCACA[A/G]TAGATTAAATTTATA | 80067 |
rs139029345 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473700 | AATGTTCAGAATTTC[G/T]CAAATTTGCATGTCC | 80067 |
rs139050633 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476680 | GTTTAACAGAATCTC[C/T]GAATTTGAAGGAGTT | 80067 |
rs139061039 | snp | A/G | 1.6601e-05 | 0.00288101 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171478057 | ACCTTCTGGATGATG[A/G]CCCAGAACAAGAGGT | 80067 |
rs139116642 | snp | A/T | 0.00067929 | 0.0184169 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481240 | TCTTGTGTTGACTTC[A/T]GATGACTATGACTTC | 80067 |
rs139157873 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456041 | ATTTGTCAATTTTTG[C/T]TTCTGTTGCAATTGC | 80067 |
rs139175361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467073 | ATATTTGATATGTTT[A/G]TGCCTGTCTCTTCTT | 80067 |
rs139266433 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450200 | GGATGCAAAGGCATA[A/G]GAATGATACAATTTA | 80067 |
rs139273240 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463498 | CAAAGGAAGACTTAG[-/T]TTTCATTATATCTTC | 80067 |
rs139529937 | snp | A/C | 0.000371678 | 0.0136272 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483227 | GCCAGACATTAATGT[A/C]TTCCTGCCCTACCTA | 80067 |
rs139548496 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459973 | GTTATTTTGAAATGG[A/G]TTATTTTGGACAGAG | 80067 |
rs139652603 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476401 | CTTAGTTTCTATTTA[A/G]GTATAGATTTAATTG | 80067 |
rs139655160 | in-del | -/T/TT/TTT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171448665 | TCATTTTTATATCTC[-/T/TT/TTT]TCTTTTTTTTTTTAG | 80067 |
rs139657518 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467910 | ACTTCTGTATATAAC[A/G]TGTGACTCTTACACG | 80067 |
rs139711618 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477503 | AAAAACTTTAATAAA[G/T]TATTTTTGAGCCGGG | 80067 |
rs139799465 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463922 | AGAGCAAGGAGTTGG[G/T]ATAATAGTCACTTTT | 80067 |
rs139809189 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433248 | ATGCAGACGTGGGGA[A/G]AAGGGGCAAGATCCA | 80067 |
rs139816205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437751 | CGTCCATGAGATCGG[C/T]AGTGATAGCCACTCT | 80067 |
rs139908156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487381 | CATGTTTATTTGTTG[C/T]GTGTATATCTTTTTG | 80067 |
rs140018349 | snp | A/G | 0.030278 | 0.119257 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455535 | TATATACCCAGTAAT[A/G]GGATTGCAGGGTTAA | 80067 |
rs140025362 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458595 | AACTCAATTCATTTT[A/G]CTCCTATACATCATG | 80067 |
rs140072790 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439248 | ATTATTACTTCAAAT[A/C]TTTATTTTTCTCTTT | 80067 |
rs140074872 | snp | A/G | 0.0471551 | 0.14613 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491208 | CCTGTAGTCCCAGCT[A/G]CCCAGGAGGCTGAGG | 80067 |
rs140304084 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469718 | AAAATAAGATGCAAT[A/G]TATTAAGTACAGTGA | 80067 |
rs140422102 | snp | A/G | 3.2975e-05 | 0.00406035 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481019 | GACTTGGTGCTACAC[A/G]TAGAGCAGAAACCCA | 80067 |
rs140452570 | snp | A/G | 0.030665 | 0.119967 | intron-variant | DCAF17 | GRCh38.p7 | 2:171447127 | CTGAAATTTATAATT[A/G]TGAGTTTTTTGTATT | 80067 |
rs140470891 | in-del | -/AAAAC | 0.0387552 | 0.1337 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486790 | GTATATAAATGAAAT[-/AAAAC]AGTAAGTATTTTTAT | 80067 |
rs140489809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488387 | TCTCAAGTAGACAAC[C/T]GTTTTTGAATCCTAT | 80067 |
rs140524090 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440598 | TACAAATTTAAGATA[A/G]TATTGGATAAAAAGA | 80067 |
rs140638817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472224 | TTACTCTGTTGCCCA[A/G]GCTGGAGTGCAGTGG | 80067 |
rs140661531 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464641 | GGGAACACAAGTCAA[A/C]TCACAACAGAGACCC | 80067 |
rs140723880 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452563 | GGCTGAAGTGCTCCT[C/G]TCACGTCACCCTCCT | 80067 |
rs140740017 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465541 | CAGGCTGGAGTGCAG[C/T]GGCGCGATCTCAGCT | 80067 |
rs140913375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449709 | AATAGGGATATGTCC[A/G]TATGGGGATATAGAG | 80067 |
rs141015767 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485311 | AGTTGATACTCAGAT[A/T]GTTTCTACTTGTGGT | 80067 |
rs141049881 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445657 | ATAGGCAAGTTATAA[A/G]TAGTATATTTTTTAA | 80067 |
rs141076055 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457603 | ATTGATCCTTGGAAG[A/C]GTATGAATAGTAGAT | 80067 |
rs141121608 | snp | G/T | 0.000149233 | 0.00863679 | synonymous-codon, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171478016 | CACTGTTACAGCTTC[G/T]GGACGGGTGGTAAAA | 80067 |
rs141153405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489471 | CTGCTACACACAGTG[A/G]TGTTCATCCAGGCAT | 80067 |
rs141154458 | in-del | -/T | 0.134802 | 0.221877 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473565 | GTGCCTATAAAGCAT[-/T]CAAACGCAGTTCCTG | 80067 |
rs141207248 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486918 | TATGGATATGTCTAC[A/G]GTTTGTTTATACTGT | 80067 |
rs141305830 | in-del | -/G | 0.3512 | 0.228601 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466951 | CAACTCATGCCTTTT[-/G]TCCCTTTTTCTATTG | 80067 |
rs141311430 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450748 | CTGTTTCTCACTAGT[A/G]TCCTTGATTGCAAAA | 80067 |
rs141357604 | snp | A/G | 0.0091503 | 0.067098 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465059 | AAAATTTAGCCAGGC[A/G]TGGTGGTGTGCACTT | 80067 |
rs141383439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480858 | CTCTTTCTAGCAACT[A/G]TTTTCTTCTAAGTGT | 80067 |
rs141488689 | in-del | -/A | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171451042 | TAGAACTCTAGCATT[-/A]TAAAAAAAAAAAAAA | 80067 |
rs141498116 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479358 | ACTGATCTGCTTTCC[A/G]TGCAAGGTTTCTGGA | 80067 |
rs141503270 | snp | A/T | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437845 | TGATTTTCTCTATTG[A/T]TTTTTGGTTTTCAAT | 80067 |
rs141563827 | snp | A/G | 0.000185856 | 0.00963813 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484933 | TCTTTTTATTGCTGA[A/G]TATTCTTTCGTATGA | 80067 |
rs141675528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457804 | TTACTGTTCACTCCT[A/G]ATAACACCCTAGCCT | 80067 |
rs141721824 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475457 | CACAGAGTAGATGCT[A/C]AGTATTTGTTGAATA | 80067 |
rs141747523 | snp | A/G | 0.00597247 | 0.0543191 | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485194 | CGATTTTACATGCTT[A/G]CAGCAATGTAGGAGA | 80067 |
rs141826455 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466326 | GTTAAAATTGTCTTT[C/T]AAAGTATTATTTGAC | 80067 |
rs141894211 | in-del | -/A | 0.0244538 | 0.107838 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442017 | TTCCTGCTTTAACTT[-/A]AAAAAAAAATTAAAT | 80067 |
rs141990877 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455316 | TCTGGCTCCATCCAC[A/G]TCCCTGCAAAGGACA | 80067 |
rs142043787 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469484 | ACTTTGAATTTTTAA[A/G]GATATTCTTAAGTTA | 80067 |
rs142118361 | in-del | -/TTA | 0.0130921 | 0.0798413 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444809 | GGCTGTACGCTAAAT[-/TTA]TTGTTAATTTTTTTT | 80067 |
rs142315519 | snp | A/T | 0.0281384 | 0.115228 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481302 | GGACTTCATTTTTTT[A/T]AAAGGTTTTTTAGAA | 80067 |
rs142320900 | snp | G/T | 0.00588837 | 0.0539399 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435034 | AATTTAAAATCTAAC[G/T]TAAAGCCTAAGAGTT | 80067 |
rs142353487 | snp | A/C/G | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439907 | TGCACTCCAGCCTGG[A/C/G]TAACAGAGCGAGACT | 80067 |
rs142460755 | snp | A/C | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484656 | ACTGAGTTCTTGCAG[A/C]CATATACACCTGTGT | 80067 |
rs142462938 | snp | C/T | 0.00363176 | 0.0424581 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449973 | GTATACATATTTAAA[C/T]ATTCAATAAAATGAA | 80067 |
rs142513867 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441596 | GCTGTCATCCCACCC[C/T]TCCTAGGAAGATAGC | 80067 |
rs142546653 | in-del | -/T | 0.0770237 | 0.180497 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443832 | TTAAAATTAGATAGA[-/T]TTTTTTTAGATCCTG | 80067 |
rs142566843 | in-del | -/A | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171470893 | ATTGGAAATATTCAG[-/A]AAAAAAAAGGATGGT | 80067 |
rs142641856 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486307 | TAAAGTATAATTGAC[G/T]TGCAGTAAACACTTT | 80067 |
rs142735693 | snp | C/T | 0.000626504 | 0.0176878 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480977 | GTTTTGTTACAGACA[C/T]ATAGCCATGAAGTCT | 80067 |
rs142740199 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448178 | ACTCTGTCACCCAGG[C/T]TGGAGTGCAGTGGCA | 80067 |
rs142774320 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453971 | GTAATATTAGTTACC[A/G]TTCATTGCTTATTTT | 80067 |
rs142869317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459546 | CTTATCATGTTGAAC[A/G]CATTCCTCTTATTTA | 80067 |
rs142873393 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446927 | TATTTGAGATCAAGG[A/G]ACAATGGTGTGACCA | 80067 |
rs143073006 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460574 | CTCACTCTGTTGCCC[A/G]GAGTGGAGTGCAGTG | 80067 |
rs143146748 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480615 | TATAGAATGTCAAAG[G/T]TGTAAGGAACAATAG | 80067 |
rs143149937 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474388 | ACACAACTCCCACAA[A/T]CTGACCTCTCCTTCC | 80067 |
rs143237458 | in-del | -/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171459170 | AAATTAGCCAGGCGT[-/G]GGTGGCACATGCCTG | 80067 |
rs143250983 | snp | A/G | 0.000542005 | 0.0164532 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472902 | GACTTCTGTAAAGCC[A/G]GTGAAGTTAATATAT | 80067 |
rs143281019 | snp | G/T | 0.0256215 | 0.110247 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433664 | CCTATAAAGAAAAAA[G/T]AATGGAGGCGAGAGG | 80067 |
rs143349057 | in-del | -/TCTC/TTCT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487000 | GCTACGAGGTATAAT[-/TCTC/TTCT]TGTATGGACATACGC | 80067 |
rs143566585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436256 | TTCTACCTTTTAGCT[A/G]TTATAAATAATGCTG | 80067 |
rs143604314 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451777 | GACGGGGTTTCACCA[C/T]GTTGGCCAGCATGGT | 80067 |
rs143704920 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455597 | CCACCACACTGTCTT[C/T]CATAATGGTCAGACT | 80067 |
rs143724083 | in-del | -/GTTTT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171468710 | GGTTCCGACTGGCTG[-/GTTTT]TTTCTTTTCTTACAA | 80067 |
rs143796647 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465626 | CTGGGACTACAGGCA[A/C]ACACCACCACACCTG | 80067 |
rs143808941 | in-del | -/A | 0.138546 | 0.223781 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467222 | AGATTTGCCACAATT[-/A]AAAAAAAAATCACAG | 80067 |
rs143963337 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448085 | ATCTAAAGGAAACAA[A/G]TCCTGTGGTAAAGGA | 80067 |
rs144040719 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF17 | GRCh38.p7 | 2:171470653 | ATTGGTCACCTCCCA[A/G]TGAGTGGACATCATT | 80067 |
rs144043690 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476719 | TTTAGTGATCACTTA[C/T]TAGTATTGTAGACTA | 80067 |
rs144095736 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468702 | CCTAATTTAGGTTCC[C/G]ACTGGCTGTTTCTTT | 80067 |
rs144129951 | in-del | -/TAA | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444212 | TCTCAGAGCCTTTAC[-/TAA]TAATAATAATACAAT | 80067 |
rs144138827 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432680 | TCAGCAAAAGCTCGA[G/T]CCCTGAAGGAAATTC | 80067 |
rs144262489 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462486 | ATGTCACTGATAAGA[C/G]AAATGTAAATTAAAA | 80067 |
rs144376053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463320 | AAAAAAAAAAAAATC[A/G]GTGCAAAACTGTGTA | 80067 |
rs144456180 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443141 | ATTTTCATTTTAAAT[A/G]TCAGAACAATAGTTT | 80067 |
rs144505060 | snp | C/T | 0.00478085 | 0.0486577 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491054 | ATTCTTGAGGCCAGG[C/T]GCGGTGGCTCATGCC | 80067 |
rs144521403 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460095 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCACGAGG | 80067 |
rs144579350 | in-del | -/AGAG | 0.097727 | 0.198275 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487736 | GCACTTAAAATAGAA[-/AGAG]AGAGAGAGACTTACT | 80067 |
rs144791050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487472 | TTTGTCACCCAGGCT[A/G]GAGTGCGGTGGCTCA | 80067 |
rs144812292 | snp | G/T | 0.030278 | 0.119257 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446951 | GTGACCAATATGAAG[G/T]GTCAAGACTGAAATG | 80067 |
rs144849696 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454635 | GGTGCAGTGGCTCAC[A/G]CCTGTAATTTCAGCA | 80067 |
rs144883256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, missense | DCAF17 | GRCh38.p7 | 2:171460437 | TTTAGAAAGAAGACT[G/T]GATTTGGGATCAGAA | 80067 |
rs144909477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442095 | GTTATTTAATGTCCA[A/G]TGGTGTTTTATCCAC | 80067 |
rs144992352 | snp | C/G | 0.0759472 | 0.179459 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456831 | TTGCATATTGATTTT[C/G]TATCCTGAGACTTTG | 80067 |
rs145127110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465102 | ACTCGGGAGGCTGAG[A/G]CAGGAGAATCGCATG | 80067 |
rs145173372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461803 | TCCCCTGTGCTCTTC[A/G]CAGTAAATTCCTCTC | 80067 |
rs145216821 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487980 | GAAGGATCATATACT[A/G]AATAAAATTATATCA | 80067 |
rs145296894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464344 | CTGAAGGCTCTAGGG[A/G]AGAATCCTTTCTTAC | 80067 |
rs145303166 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171468064 | TGGTGTTTCCTAAAG[A/G]CTGCTTGAAATGAAT | 80067 |
rs145373123 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483659 | CAGTTCTTTTTTTAA[A/G]TAATATATTTATTGA | 80067 |
rs145388254 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472389 | TCATCTTGTTGGCCA[C/T]GCTAGTCTCAAACTC | 80067 |
rs145482561 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171488748 | CCCAGAGTTTGTCTT[A/G]GTCTGCCCTACCAGC | 80067 |
rs145497108 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465022 | CCAACATGGTGAAAC[C/T]CTGTCTCTACTAAAA | 80067 |
rs145524184 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445325 | ACACGGGGTTTCACC[A/C]TGTTGGCCAGGCTGG | 80067 |
rs145576851 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486043 | TAGCAAGGAAAGGGA[A/G]GATTGAGATCAGCAA | 80067 |
rs145659145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487610 | GTATTTCTAGTAGAG[A/G]TGGGGTTTCACCATG | 80067 |
rs145669607 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439718 | AGATCACTTGAGGCT[A/G]GGAGTTCGACACCAG | 80067 |
rs145671454 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491434 | TAGGGCATAACACGG[A/G]TGAGGAACACCACAG | 80067 |
rs145804939 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171445133 | CTATTTTTTTTTTTT[-/T]GAGACGGTCTCTCTT | 80067 |
rs145934835 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483197 | AGTGTCACACAGCTG[C/T]TCATTCTGCCACCTG | 80067 |
rs145952646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486352 | TCTCGCTCTGTCACC[C/T]AGGCTGGAGTGCAGC | 80067 |
rs145953985 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171433101 | AGGTGGGAACCAACC[C/T]TTGGACACGACGACA | 80067 |
rs145955312 | snp | C/T | 4.94776e-05 | 0.00497357 | synonymous-codon, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480058 | CAAAATTGTGGACTA[C/T]GAAGATGAGTTAGAT | 80067 |
rs146017405 | in-del | -/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171463759 | ATTTGCAGAATGGCA[-/G]GTTTTTAAAACTCTG | 80067 |
rs146018819 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171437713 | CTAGACTTATTCATA[A/G]TATTTCTTTATTATT | 80067 |
rs146075009 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455390 | ATGTACAACATTTTC[A/G]TTACCCAGTCTATCA | 80067 |
rs146132754 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457522 | TGAAAGACTATCCAG[A/G]GGCTGGGCACCTCTA | 80067 |
rs146140606 | snp | A/G | 0.00165593 | 0.0287267 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458100 | ACTGAAATTTGTCAT[A/G]TTACTATTAGCATGA | 80067 |
rs146196653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476625 | AGCTGATCATTACCT[A/G]CTTCAGTGGCACCTG | 80067 |
rs146258833 | snp | C/T | 0.000749681 | 0.0193463 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481129 | AAAAGAGTGAGATAA[C/T]TGTAACCTAAGAGAC | 80067 |
rs146298324 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171441072 | AGCCAGCCTACAATT[C/T]AGCCTGTATCTCCGC | 80067 |
rs146310976 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462155 | GGAGAATCTTTTTAT[C/G]TCAGTGTGGGGAAGA | 80067 |
rs146337106 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459152 | CCATCTCTACTAAAA[A/T]TACAAATTAGCCAGG | 80067 |
rs146435269 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440345 | CTTTTGGAGGCCAAC[A/G]TCTGGGGTTGCTTGA | 80067 |
rs146445235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171477361 | ATTATGGGGAGAACA[A/G]TTTCAAAAACAGATC | 80067 |
rs146543312 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450538 | TCAAGAAACTTTTTG[C/T]TTCTATTGGTGACTT | 80067 |
rs146556466 | snp | A/C | 0.00370966 | 0.0429077 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435068 | TCCTGAACGGAAATT[A/C]TTTATGTCTTTTAGG | 80067 |
rs146569710 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446940 | GGGACAATGGTGTGA[C/T]CAATATGAAGGGTCA | 80067 |
rs146645275 | in-del | -/CCT | 0.406123 | 0.195258 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486726 | CACTTCCCAAGACAA[-/CCT]CCTCGGATCTGTTTC | 80067 |
rs146683580 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477879 | GAGGAAAGAATTGTG[A/G]ATGTGGGAGAAGGGT | 80067 |
rs146734823 | snp | C/T | 1.65688e-05 | 0.00287821 | synonymous-codon, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480166 | AACTTTACTTAAAAG[C/T]ATTCCACTAGTGGAG | 80067 |
rs146737671 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451649 | GGTGAGCTCTCAGCT[C/G]ACTGCATCCTCTGCC | 80067 |
rs146745875 | snp | C/T | 6.59283e-05 | 0.00574106 | synonymous-codon, nc-transcript-variant, missense | DCAF17 | GRCh38.p7 | 2:171468964 | TCCTTGGCACTACAT[C/T]GTCACACCTAATAAG | 80067 |
rs146802661 | snp | C/T | 0.021333 | 0.101051 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455785 | TTGAGCTTTTTTTCA[C/T]GTGCTTGTTGGCCAC | 80067 |
rs146850238 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471964 | AGGCTCCAGTGAGCC[A/G]AGATCACACCACTGC | 80067 |
rs146946978 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454345 | GCTGCAGTGCAGTGG[C/T]GCAATCTCTGCCCAC | 80067 |
rs146963549 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457636 | AATATTCATTTAGAA[C/T]GACATGGCCTTGGTG | 80067 |
rs147052415 | snp | A/G | 0.0260105 | 0.111035 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474721 | TTGTCTTTCATCAAT[A/G]TACATACATTTAAAC | 80067 |
rs147068576 | snp | A/G | 0.000131978 | 0.0081223 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480086 | GATTTGCTTTCTGTG[A/G]TAGCTGTTACTCAAA | 80067 |
rs147113116 | snp | C/T | 0.000371678 | 0.0136272 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434374 | CTTCTTCCCTTCTCT[C/T]CGCGCTCTGGCGGTG | 80067 |
rs147295073 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445607 | TTCAAGAAAATATTT[C/T]GAACGTATTATATTT | 80067 |
rs147311745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448327 | CGCTATGCTATATAC[A/G]TGATTTTAAGAGCTG | 80067 |
rs147401363 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463715 | TCTATAACTATTAGT[G/T]ATCCTTGCCTGAATC | 80067 |
rs147416458 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467455 | GCACTTTGGGAGGCC[A/G]AGGCAGGCGGATCGC | 80067 |
rs147685213 | snp | C/T | 0.000181565 | 0.00952624 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481070 | GTTTACCAGATGATA[C/T]GTGACACTGGGGAAG | 80067 |
rs147733426 | in-del | -/T | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436791 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTTTTGC | 80067 |
rs147774209 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457523 | GAAAGACTATCCAGG[A/G]GCTGGGCACCTCTAA | 80067 |
rs147879973 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171478380 | GTATATTTTCTAGGG[A/C]AATCTCTTAAGGGAA | 80067 |
rs147950025 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484699 | TTCCAAAATTTAGAC[C/T]ATTGCAATCATCTTC | 80067 |
rs147999088 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457671 | CCAGTGTCTATGAGG[A/G]ATGGAATTTGTTATT | 80067 |
rs148017437 | snp | A/G | 0.0130921 | 0.0798413 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491067 | GGCGCGGTGGCTCAT[A/G]CCTGTAATCCCAACA | 80067 |
rs148033562 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171436868 | CAGTCTCCACCTTCC[A/G]GGTTCAGGTGATTCT | 80067 |
rs148052925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452289 | ATTCCCTTCAAAACT[C/G]TATTGGAGAAGTACA | 80067 |
rs148088011 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465648 | CCACACCTGGCTAAT[A/T]GTTTTTTTGTATTCT | 80067 |
rs148190437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486601 | AAAGTACACAATTTG[A/G]TAAGTTTTGCCATGA | 80067 |
rs148234281 | in-del | -/CC | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439510 | GTATTTCTTTTTTTT[-/CC]TTTTTTTTTTTTTTT | 80067 |
rs148245880 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480768 | CCTGGGTCCAGAGTT[A/C]TTTTTATTCTCTATA | 80067 |
rs148401399 | snp | G/T | 1.66852e-05 | 0.0028883 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171443532 | TCCCAGTGTTGCATC[G/T]GAGCCAAGAAAACTT | 80067 |
rs148433321 | in-del | -/TA | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464852 | AAAACTTTATCCTAC[-/TA]TATATATATATGATA | 80067 |
rs148542951 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459304 | GCAACAAGAGCGAAA[C/T]TCCATCTCAAAAAAA | 80067 |
rs148595487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455162 | ACCCTCCGATAGGCC[C/T]GAGTGTGTGTTGTTC | 80067 |
rs148617910 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, missense, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469380 | GTGGAATGTGTTGTT[C/G]GTTCTGCTTCTCCAC | 80067 |
rs148670567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462507 | TAAATTAAAATTATT[A/G]TAAGATAACATCTCT | 80067 |
rs148758818 | snp | A/G | 0.000372162 | 0.0136361 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483837 | GCCCAGGGTCCCACA[A/G]CTAGTCAGTGCAGAG | 80067 |
rs148869116 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF17 | GRCh38.p7 | 2:171485603 | CATTATAATAAAAGC[A/G]GAAAGGTGACTTTTT | 80067 |
rs148918960 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446256 | TCTTATAAGAAATAT[C/G]TAGGAGAGTGGCCAG | 80067 |
rs149124414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457160 | GAGTAAACAATACTT[A/G]TCCTTCTAAGAGATG | 80067 |
rs149213719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472849 | CTAGTAGGAAATATG[A/G]CATCATTTCATTTTA | 80067 |
rs149238425 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171490475 | TATATGCTACCTCCT[C/T]GGTAAGGAGTGAAAT | 80067 |
rs149318384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476563 | AGGTAAGGTTCTTCA[A/G]AGTAACTTTCATTAA | 80067 |
rs149373029 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436234 | ATCAGTTGTTAGACA[C/T]TGGTGTTTCTACCTT | 80067 |
rs149444945 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | DCAF17 | GRCh38.p7 | 2:171447830 | AAGAAGAAAACTTTG[C/T]TTCTCTTTTTCTTCC | 80067 |
rs149584945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480553 | CATATCTAAGCATGC[A/G]GGATTCCCAGGTACT | 80067 |
rs149591222 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462321 | ACATAGTTACAAATC[A/C]TACTGTAATGGGGCA | 80067 |
rs149597381 | in-del | -/CCACCCT | 0.390277 | 0.206936 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455131 | ATCCTTTCCCTCCTC[-/CCACCCT]CCACCCTCCACCCTC | 80067 |
rs149650431 | snp | A/G | 0.00135735 | 0.026016 | missense, nc-transcript-variant | DCAF17 | GRCh38.p7 | 2:171458067 | AGCTTCCAAACCATC[A/G]CTGAACAGGTAGAGA | 80067 |
rs149691298 | snp | A/G/T | 0.00319106 | 0.0398404 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483561 | CTATTTACTATTTGT[A/G/T]CTACCTAGTGAGGAG | 80067 |
rs149692963 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465021 | GCCAACATGGTGAAA[C/T]CCTGTCTCTACTAAA | 80067 |
rs149851281 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445868 | TTGTATTTTTTGTAG[A/C]GGTGGGGTTTTGTCA | 80067 |
rs149898652 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438920 | TTTTTAGAGATAGGG[G/T]TCTCAGTCGTGCTGT | 80067 |
rs149921837 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456375 | TTTCTGTTCTTGTAC[C/T]AGTACCATGCTGTTT | 80067 |
rs149975124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450493 | AATTACCCAGGATTT[A/C]CTAGATTTTATAAAG | 80067 |
rs150095386 | snp | A/C | 0.000929784 | 0.0215413 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171453165 | GTACCTTGCAGTGTT[A/C]CGAGTTCTACCTTTT | 80067 |
rs150187836 | snp | A/G | 0.000181298 | 0.00951926 | missense, nc-transcript-variant, synonymous-codon | DCAF17 | GRCh38.p7 | 2:171468965 | CCTTGGCACTACATC[A/G]TCACACCTAATAAGA | 80067 |
rs150216826 | snp | C/T | 0.00318978 | 0.0398085 | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485474 | CAAAGAACCCTGATT[C/T]CTTTAATGGAGATCA | 80067 |
rs150267939 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478277 | CTTAAAGTTTTATTT[G/T]CAGAAAAGTTGATAG | 80067 |
rs150373361 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF17 | GRCh38.p7 | 2:171447195 | TATATGTAGTCATAC[A/C]AAAAAAAAACACTAG | 80067 |
rs150426998 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440663 | ATCTGAGTAGGAGTT[C/T]GGCTATGATTATTGT | 80067 |
rs150464431 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171457867 | TAGGCGGCAGTGTTA[C/T]CATAGTGACATGAAT | 80067 |
rs150488527 | snp | G/T | 0.0741063 | 0.177655 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472243 | GGAGTGCAGTGGCAC[G/T]ATCTCGGCTTACTGC | 80067 |
rs150593509 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475585 | GCCTGGGCAACATAG[C/T]GAGACTTCGTCTCTA | 80067 |
rs150645534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466937 | TCTCTTATAATTTAC[C/T]AACTCATGCCTTTTT | 80067 |
rs150733487 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487151 | ATCAGTATATGAGAG[G/T]TCTAGTTGCTTCATA | 80067 |
rs150748690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438188 | TCATTGTTTTATTGA[C/T]TTGTGGTTTAATACC | 80067 |
rs150775557 | in-del | -/TCA | 0.132409 | 0.220618 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433302 | AATTATTATTTTTTC[-/TCA]TCAAGTTATACAAAA | 80067 |
rs150802374 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432637 | ATACAAAGCACTCTA[C/T]CGTATGCTGTAAATA | 80067 |
rs150892636 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450080 | AAAAGATAGGATTCA[C/T]GGCAACCTGGATGGG | 80067 |
rs150941246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464555 | AACTTGATTATATCT[A/G]TAAAGATCCTATTTG | 80067 |
rs150947926 | in-del | -/C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477460 | TTAAATAATTTTTTT[-/C/T]TTTGCCCATTCTGGC | 80067 |
rs150994631 | snp | C/T | 0.021333 | 0.101051 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459566 | CCTCTTATTTATAAC[C/T]AACCAATAAGCATTA | 80067 |
rs151139278 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469679 | CTCTTCCCTCAAGTT[A/T]TACTCTTAAAGGAAA | 80067 |
rs151242438 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440517 | GAGGTCAAGGCTGCT[C/T]GAGCCGTCAGCATGC | 80067 |
rs151265174 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488277 | CCAATAATTTAGCAA[A/T]TTTTTTTGCCATATA | 80067 |
rs180806832 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489460 | GACGATATTACCTGC[A/T]ACACACAGTGATGTT | 80067 |
rs180809674 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446705 | AGGATAACAGTGTGG[A/G]GACTGCTAAGTTGAG | 80067 |
rs180822496 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466803 | ATATATTAAATTTCA[C/T]ATTCTCTATAACATA | 80067 |
rs180978563 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450793 | TCTGAGTTCTTTACC[C/T]GTATTTACTAATTTG | 80067 |
rs181004285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471973 | TGAGCCGAGATCACA[C/T]CACTGCACTCCAGCC | 80067 |
rs181080251 | snp | C/T | 0.000185822 | 0.00963724 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171485013 | TTTCTGCTTGTTTTT[C/T]ACTGTTATGAATAAA | 80067 |
rs181208680 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467595 | AATACTTAGGAGGTT[G/T]TAATACTTAGGAGGC | 80067 |
rs181220862 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171447199 | TGTAGTCATACAAAA[A/C]AAAAACACTAGCATA | 80067 |
rs181286044 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171476019 | GCCAGGTTTTACAAT[A/G]TAAGCATTTAAAAAT | 80067 |
rs181358896 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435800 | TCAGTTTGCATTTTT[A/T]AAAAAATGAGCTTTT | 80067 |
rs181473020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456639 | TAACCATGAACATGG[A/G]GTGTTTTTCCATTTG | 80067 |
rs181523297 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441557 | CAGCCCCAGCAATAG[A/G]CAGCTGGGGACTGGA | 80067 |
rs181547829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | DCAF17 | GRCh38.p7 | 2:171460433 | TTTTTTTAGAAAGAA[A/G]ACTGGATTTGGGATC | 80067 |
rs181652730 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472593 | TTCTGTTCACTTGGA[A/T]ATCTGGTGCATGGGT | 80067 |
rs181668017 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482250 | TCCGATGTAACCTCA[A/G]AAGAATAACTGGTAA | 80067 |
rs181670862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451142 | GTATTCCCATACATG[C/T]TGGGTCTGTGAACTC | 80067 |
rs181723930 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436484 | CACATTCTTGTCAAC[A/G]CTTGATGTGTGACTC | 80067 |
rs181728507 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457453 | TGCAATTAGAGAGAT[A/T]TGGTTTTAAATATTG | 80067 |
rs181730322 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446183 | TTTTAAATATGGAGA[A/G]GTTTAATCCTTTACC | 80067 |
rs181734704 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488609 | GGAATTCCCAACCCC[C/T]ACCTCATCTAAAACC | 80067 |
rs181735689 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465455 | GTATATAGTTGAAAG[G/T]TTGAAACCGAATAAA | 80067 |
rs181936672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461373 | CAGAGGTTGCAGTGA[A/G]CCGAGATCGTGCCAC | 80067 |
rs181938173 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484491 | GCGTACTTTTTGATG[A/G]ATTTCAAAATAAATT | 80067 |
rs181987214 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441987 | TTCAGGATCATTTAA[C/T]GTCAAGTTTATAACT | 80067 |
rs182148543 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457692 | ATTTGTTATTAATAG[A/T]TATTGACAATGCTAT | 80067 |
rs182152990 | snp | C/T | 8.35122e-05 | 0.00646136 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478083 | GAGGTATTGCTTTGG[C/T]CAGAGATGACAAACC | 80067 |
rs182168830 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171477168 | CTTTTGCTGATTTCC[A/G]CTTCTTTTCTGAGTT | 80067 |
rs182216670 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171470856 | CCGTGGGTTCCACAT[C/G]TGTGGATTCAACCAA | 80067 |
rs182233059 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438078 | ATTTTCATTTAGTTC[A/G]GAATATTTTTAAATT | 80067 |
rs182384534 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473445 | CTCTATCTCTATTTA[A/C]AAAAAAACAAACAAC | 80067 |
rs182402251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453796 | ATTCTTGGTGCATAG[C/T]TATTTATTGAGCTCT | 80067 |
rs182423435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171447835 | GAAAACTTTGCTTCT[C/G]TTTTTCTTCCTGCCT | 80067 |
rs182481451 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171449699 | TATGTATTTAAATAG[A/G]GATATGTCCATATGG | 80067 |
rs182700407 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468468 | TCACATTTGAAGGCA[A/T]TATTAGACCTAATTA | 80067 |
rs182757225 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171462687 | GTGTACTCCTTGAAC[C/G]CAGCAACTTCAGTAC | 80067 |
rs182770006 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442875 | GTGAGAAACTGTCTC[A/C]AAAAAAAGGAACAAA | 80067 |
rs182771210 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462003 | TAGCCTAACCCACTT[A/T]TTGATGTTAATATAT | 80067 |
rs182783435 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171485834 | TTTATACTCTTTTTG[A/G]CTCTCAATTCAAGTG | 80067 |
rs182973247 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459227 | TGAGGCAGGAGAATA[A/T]CTTAGACCTAGGAGG | 80067 |
rs182975162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171490396 | GTGTGTTCAAAATAA[C/T]TGTAAAAGATTGAGA | 80067 |
rs182984922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479313 | CAGCCAAGATGTACC[G/T]TCCTGTGGTCTATTC | 80067 |
rs182985268 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439780 | TAAAAAAACAAAAAT[G/T]AGCTGGGCATGGTGG | 80067 |
rs183031320 | snp | C/T | | | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171457987 | TTTTTGGGAACGTTA[C/T]AGATGCTACCTTGTC | 80067 |
rs183035771 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442296 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 80067 |
rs183045010 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439576 | ATCTTTTCTTGCATG[G/T]TGTCCACTTTTCCCA | 80067 |
rs183048169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478567 | ACTGAAGTAATACAT[C/T]TTTATCCCCTTCCTT | 80067 |
rs183196943 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486517 | CACCATGTTGGCAAG[A/G]CTGGTCTCGAACTCC | 80067 |
rs183272802 | snp | A/G | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462897 | TTATTATATCACCAT[A/G]TAGCTGTATCACAAA | 80067 |
rs183312348 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458772 | AAATGAGTTGCAGCA[A/G]ATGATACCATCTTAG | 80067 |
rs183324172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454539 | TCTGCTCACCTCAGC[C/G]TCCCAAAGTGCTGGG | 80067 |
rs183464591 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481193 | CCATTTTATTATCTG[A/C]ATGGCACATTCTCCA | 80067 |
rs183473333 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171449737 | GAGGAAATTTTTTTA[A/G]CTATTTATTTTTTAA | 80067 |
rs183521978 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459755 | AATGACAAATTATAA[A/G]AACTACTGGGAGTTC | 80067 |
rs183564622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473781 | CCGTGTACCTTTGAC[C/T]TACTGATCTATCACT | 80067 |
rs183626391 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468196 | TCTTGGTGCTTTTTA[G/T]CACCAAGAGAAATTT | 80067 |
rs183668114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171475667 | CCTCAGGAGTCTGGG[A/G]CAGGAGGATCAGCTG | 80067 |
rs183737696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456026 | GTTTAAGTAGATCCT[A/G]TTTGTCAATTTTTGC | 80067 |
rs183749904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435293 | GTGAAATAGAATGAA[A/G]AAAATGGGTCCGAAA | 80067 |
rs183836178 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447501 | AAGTAGCTGGGATTA[A/T]AGGCAAGCACCGCAA | 80067 |
rs183914118 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443356 | AATCTTGTTTTTTTT[A/T]ATATGAATTATGTGA | 80067 |
rs183918378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472979 | TTTGTGTACACATGT[A/G]ATAACATATCAGATG | 80067 |
rs184060479 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451564 | TAAATTGCTAAAGAG[A/C]AAGAATTTTTGTTTT | 80067 |
rs184132913 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469720 | AATAAGATGCAATGT[A/T]TTAAGTACAGTGATT | 80067 |
rs184208846 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448422 | TTGTGAATACTTAAT[A/T]AAATAATTAATTCAT | 80067 |
rs184269251 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171471375 | AACATTTGAGCAAAT[A/G]AAAACAATAGAAGCT | 80067 |
rs184356597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440926 | TATGAGGACAGACGG[A/G]TGGCACTTCCAGGCT | 80067 |
rs184364173 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465156 | TGAGCCGAGATTGCG[C/G]CACTGCACTCCAGCC | 80067 |
rs184366121 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487890 | AACAGACTCAAATTA[C/T]TTTCTTCCCAGGACT | 80067 |
rs184425948 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445297 | GCCCCACTAATTTTT[A/G]TATTTTTAGTAGACA | 80067 |
rs184489253 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464012 | TTTTTTATTTGTCCA[A/G]TATTATATAGTAATA | 80067 |
rs184582512 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444195 | CTATTGATAGAATTA[C/G]TTCTCAGAGCCTTTA | 80067 |
rs184607257 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487742 | AAAATAGAAAGAGAG[A/G]GAGAGACTTACTATG | 80067 |
rs184670633 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171434838 | AGGAGGATACAAGCC[C/G]GGAATCTGGGATAGG | 80067 |
rs184680866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455637 | TGACACAAACAGTGT[A/G]TAAGTGTTTCCTTTT | 80067 |
rs184698577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441350 | CGCACTTGGAGTTGA[A/G]GAAACACTGACCTCA | 80067 |
rs184741043 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481568 | AAACTTTGCTTAAGG[A/C]TGAGAAATGAGATGT | 80067 |
rs184848610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460272 | AGGTTGCAGTGAGCC[A/G]AGATCGTGCCACTGC | 80067 |
rs184907632 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488839 | CCCCTCTGGAGTGAT[A/T]ATATAATTTATTGTC | 80067 |
rs185157481 | snp | C/T | 0.000186341 | 0.00965069 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484639 | ATCTTAAGTATAAAT[C/T]TACTGAGTTCTTGCA | 80067 |
rs185316084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470504 | CTTCTAGTTTTCTTT[C/T]GTAGGAGCATTGTTC | 80067 |
rs185405017 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171458229 | ACAAGTAACCTTTAA[A/G]GCAGGGGTGGGGAAG | 80067 |
rs185407539 | snp | C/T | 0.000183764 | 0.00958374 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478084 | AGGTATTGCTTTGGC[C/T]AGAGATGACAAACCA | 80067 |
rs185449170 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450914 | AGCATCATAGTGTTG[G/T]TAACCTTGGCTCAAA | 80067 |
rs185461305 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472249 | CAGTGGCACGATCTC[C/G]GCTTACTGCAAGCTC | 80067 |
rs185544070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446286 | GGTGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 80067 |
rs185629344 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489931 | GCTGGGATTACAGGC[A/G]TGAGCTGCCGTGCCC | 80067 |
rs185685655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465544 | GCTGGAGTGCAGTGG[C/T]GCGATCTCAGCTGAC | 80067 |
rs185718285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171447212 | AAAAAAAACACTAGC[A/G]TACAAACAAAAATTA | 80067 |
rs185799264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461718 | TACAGTTTGAGTTTT[A/G]TCAAATGTATACATC | 80067 |
rs185897611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442084 | AATATTATTGAGTTA[C/T]TTAATGTCCAATGGT | 80067 |
rs186007384 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466807 | ATTAAATTTCACATT[C/G]TCTATAACATACCTA | 80067 |
rs186143382 | snp | A/G | 0.00259643 | 0.0359371 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483417 | TTACGCTGAAAAGAG[A/G]TGCATTCTGCATTGC | 80067 |
rs186147885 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489612 | GCCTCAGTTTTTACT[A/G]TGAGACTACATAAGA | 80067 |
rs186154026 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171446835 | AATGTTAAATAGAAA[A/G]TATTATGAAATTTTA | 80067 |
rs186159279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460540 | ATTATTATTATTATT[A/G]TTAATTTTGAGACAG | 80067 |
rs186225334 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441587 | ATGAGAAATGCTGTC[A/C]TCCCACCCCTCCTAG | 80067 |
rs186268256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171485773 | TGATAGCAAATTAGT[A/G]TATTCAAATTTTAGA | 80067 |
rs186272240 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171442533 | GGTGCCATTGCTCTC[C/T]AGCCTGGGAGACAGA | 80067 |
rs186359489 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477727 | AGCCTGGGAGGCAGA[A/G]GATGCAGTGAGCCAA | 80067 |
rs186369094 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457581 | AAAGAACATTTTAGC[A/T]TAAAGAATTGATCCT | 80067 |
rs186416511 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462379 | AGATCAATAAGAAAA[A/G]GAGTGATAACACAAT | 80067 |
rs186423127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437073 | GCCACCGCGTCCAGC[C/T]ACAGAGAGGTTAATT | 80067 |
rs186542881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457172 | CTTATCCTTCTAAGA[A/G]ATGACAAAAAATACA | 80067 |
rs186558607 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473296 | GGAGTCAGATCTGCT[C/G]TTTAGTAGGTTGAAA | 80067 |
rs186625570 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432553 | GTTATCTTTTCTGGG[C/T]TCCAGTTTTCTCAGT | 80067 |
rs186634127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451715 | TGAGTAGCTGGGACT[A/G]CAGGCGTGCACCACC | 80067 |
rs186769288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436209 | ATTACCACATTTTAC[A/G]TATCCGTTTATCAGT | 80067 |
rs186810008 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476688 | GAATCTCCGAATTTG[A/T]AGGAGTTCATGGACA | 80067 |
rs186853315 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472640 | TACAGTGGCACAATC[A/G]TAGCTCACAATAACT | 80067 |
rs186874042 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF17 | GRCh38.p7 | 2:171447918 | TCCTCTCCCTTTTCT[A/G]GGATAATTCACTGGT | 80067 |
rs187024317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451418 | GTAATACTTCTCTCT[C/T]TATACTCTTACTACC | 80067 |
rs187093964 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473572 | TATAAAGCATCAAAC[A/G]CAGTTCCTGACACAA | 80067 |
rs187099970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444478 | TATCTTCAGGCTACA[C/T]GTATAAGATAGATAT | 80067 |
rs187109737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453872 | ATCTTGAGGATCTAC[C/T]GATCTTTATAAGCAA | 80067 |
rs187330915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171469916 | GTTCAAGTGATCCTC[C/T]TGCCACAACCTCCTG | 80067 |
rs187338503 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448585 | TGGTTTATTTATTTG[G/T]CATTTGAATATTTAG | 80067 |
rs187371240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486098 | TCTCCTTTAATTCTT[C/T]GTTTTCATGAATACA | 80067 |
rs187444896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462813 | ACATTGGTAAGTGAC[A/G]TTAGTATTATTATAT | 80067 |
rs187461664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443251 | GGAAAACAACGTCCA[A/G]GTACGTATATGTATA | 80067 |
rs187569045 | snp | C/T | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171470036 | TATTTTATATTTATT[C/T]ATTTAGAGACAGAGT | 80067 |
rs187600867 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, missense, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171469332 | AGTGGGAATCACCAA[A/T]GGAATGTGTTCACAT | 80067 |
rs187696536 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459349 | ACTATTACTCAAATT[A/C]AGTAGTAGTACATTA | 80067 |
rs187702299 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479962 | ATAGAATACTTAAAC[A/T]ATAAATACAGAAATA | 80067 |
rs187710089 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440084 | CTCCTCCCTCAGCCT[A/C]CTGAGTATAGCTGGA | 80067 |
rs187833131 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487808 | CAAGCAATTCTCCCA[A/C]CTCAGTCTCCCGAAG | 80067 |
rs188129842 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464849 | TAATAAAACTTTATC[A/C]TACTATATATATATG | 80067 |
rs188150171 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459080 | TTTGGGAGGCTGAGG[C/T]GGGCGGATCACTTGA | 80067 |
rs188173618 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433485 | AAGGGACTTAGAGCA[C/T]GGCGGTGGGACACAT | 80067 |
rs188188790 | snp | C/T | 0.000106604 | 0.00730005 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481281 | TCTTGCTGTAAAAGA[C/T]GGTGAGGACTTCATT | 80067 |
rs188197065 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471932 | AGGTGAGAGAATTGA[C/T]TGAGGCCAAGAGGTC | 80067 |
rs188204936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450227 | TTTACTCTGGAGACT[C/T]GGGTGAAAGGGTGGG | 80067 |
rs188426964 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439722 | CACTTGAGGCTAGGA[C/G]TTCGACACCAGCCTG | 80067 |
rs188432713 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478932 | AGCATAATTCATTAA[C/G/T]GGGGGAGAGGTGGTG | 80067 |
rs188434527 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171475960 | ACCACCCATATTAGT[A/C/T]TGAACTTAAGAAAAC | 80067 |
rs188460268 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434040 | GGCGCACACACGGGG[A/C]GGAGACCTGGAGGCG | 80067 |
rs188679288 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447612 | CGTGATCCAGCCACC[G/T]CAGCCTCCCAAAGTG | 80067 |
rs188679937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455059 | TCATGGGGGTTTGTT[A/G]TACAGATTATTTCAT | 80067 |
rs188705639 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171490889 | AGAACAGTCTTGGTA[G/T]CAGTGGCTGGAACAA | 80067 |
rs188936358 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463100 | GTCAGGTGTGGTGGC[A/G]AGCACCTGTGATCCC | 80067 |
rs189080965 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445787 | TCCTGGGCTCAGGTG[A/T]TCCTTCCACCTTGGC | 80067 |
rs189116896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465408 | GGGTTTGCTGTTTTC[C/G]TTTTGAGTTTATTCT | 80067 |
rs189118813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488466 | CTTTTCAAGTTTTAC[C/G]TGTTAGAGCAACAAG | 80067 |
rs189196385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441004 | TTTGAGATTTGTTCT[A/G]ACCCCAAGAGGGCTC | 80067 |
rs189208029 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443726 | TCATAGTGACTCTTG[C/T]ATCTTTAAAGCAATC | 80067 |
rs189237757 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486941 | TATACTGTGGCCTTT[C/T]GATGGACATTTCAGT | 80067 |
rs189327037 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441742 | CAGACACCACAGACT[C/T]ACTATTCTTACTGAG | 80067 |
rs189360107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461075 | TCAATCTTAAGGTCT[A/G]TACAAATAGTATTTA | 80067 |
rs189368440 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483995 | AAAGTGCTTAATAAT[C/T]GTTTTTTACTGATGA | 80067 |
rs189426365 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456179 | TAATCCATCTTGAGT[G/T]AATTTTTGCGTATGG | 80067 |
rs189464285 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460096 | TTGGGAGGCTGAGGC[A/G]GGTGGATCACGAGGT | 80067 |
rs189496195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455803 | GCTTGTTGGCCACAT[A/G]TATGCCATCTTTTTA | 80067 |
rs189511106 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474631 | TGAGAACTCCAAAAT[G/T]TATATACCAGCCTCA | 80067 |
rs189513364 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171434894 | TAGTTTTACGCTTCT[C/T]ATGTCTTACCTGGAA | 80067 |
rs189704042 | snp | C/G/T | 0.01469 | 0.0846354 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460301 | GCACTCTAGCCTGGG[C/G/T]GATTGAGCGAGATTC | 80067 |
rs189719374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435454 | CTGTTTAGTGTTTAG[C/T]CTACTTATACCACAG | 80067 |
rs189803218 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432881 | TAAACAAAAGTTAAG[C/T]TCCTATAACATATTT | 80067 |
rs189826325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473350 | TGGCTTACGCATGTA[C/G]TCCTAGCACTTTAAG | 80067 |
rs189836615 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453283 | GTCATTATTTAATTA[C/T]TTATGAGATATTTGA | 80067 |
rs189942415 | snp | C/G/T | 3.55286e-05 | 0.00421465 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476810 | TAAACTTTGGCACCT[C/G/T]GATGGTGTTTTGAAG | 80067 |
rs189949476 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481862 | GTATCTAAGGATGTT[C/G]TCATCTCACCATTCT | 80067 |
rs189989482 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466969 | CCTTTTTCTATTGGG[G/T]TGTTTATATTTTTTA | 80067 |
rs190005769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171447008 | CTTTCAGTTTTTTCT[C/T]GGACAGTTAATTTCA | 80067 |
rs190013277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436481 | TTCCACATTCTTGTC[A/G]ACACTTGATGTGTGA | 80067 |
rs190024697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441483 | AGATCCTCCATCCCA[C/T]GAATAGGGGCTGGGT | 80067 |
rs190208458 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450968 | CCCTGCTCTTATGCA[C/G]TGTAGTAAGCTGCCC | 80067 |
rs190216698 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472273 | CAAGCTCTGCCTCCT[A/G]GGTTCAAGCCATTCT | 80067 |
rs190254451 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448957 | CTATTTTCTTTTTCT[C/T]CCCTCATGACTACAT | 80067 |
rs190274353 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457250 | GTTTGCTTATTACAG[G/T]CTACAACAGAAATGA | 80067 |
rs190449572 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447454 | CAACCTCCACCTCCC[A/G]GGTTCAAGTGATTCT | 80067 |
rs190459502 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468042 | CCACCTGCCCAAACA[A/G]ACCATGTGGTGTTTC | 80067 |
rs190483033 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171490154 | AAACAAAATTAACCT[G/T]CAAGCTCATGACTTC | 80067 |
rs190485579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466272 | ACAGGTGTAGCCCTT[C/T]TTCTTTGATAAATAG | 80067 |
rs190507277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171470755 | TCTGGACATTTAACA[C/T]GTATTCTTTTTTATA | 80067 |
rs190705104 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462851 | TACAAAAGATTGGAA[A/G]CAATCTATACATTGG | 80067 |
rs190729839 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486486 | TATTTTTGTATTTTT[A/G]GGAGAGATGTGGTTT | 80067 |
rs190747754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442148 | TGCCTTCATTCTTGT[C/G]AAACTGTTTGGTTTA | 80067 |
rs190749922 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484889 | TTTTTGAGATTTATT[C/G]ATGTTGTTGCATGTG | 80067 |
rs190751591 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489101 | TGAAACAATTTTCCA[G/T]TTTTATCTACAAGCC | 80067 |
rs190753413 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446501 | CAGTGAGCAGAGATC[A/G]TGCCACTGCACTCCA | 80067 |
rs190992008 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489726 | GCGCAATCTCGGCTC[A/G]CTGCGAGCTCTGCCT | 80067 |
rs191001101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458265 | CAGAAAGGCCATTGG[A/C]AAAAGACATTTTCTT | 80067 |
rs191002047 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171461955 | CTCAGGATATTATAT[A/T]TGAGATTCGTTTCAT | 80067 |
rs191143152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437748 | TAACGTCCATGAGAT[C/T]GGTAGTGATAGCCAC | 80067 |
rs191161483 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477883 | AAAGAATTGTGGATG[C/T]GGGAGAAGGGTTGGT | 80067 |
rs191173932 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457599 | AAGAATTGATCCTTG[G/T]AAGAGTATGAATAGT | 80067 |
rs191183094 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455858 | CCACTTTTTAATGGG[G/T]TTGTTTTTTTTTCTT | 80067 |
rs191195257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475173 | TTTCCCCTACCTGTT[C/T]TGCCTAATTTCTATT | 80067 |
rs191203387 | snp | A/G | 6.669e-05 | 0.00577413 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435094 | TTAGGAAAGTACTAA[A/G]TTTAAGAATGTCTGG | 80067 |
rs191247827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478095 | TGGCCAGAGATGACA[A/G]ACCAAACCAGTGTGT | 80067 |
rs191310154 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438751 | CCTTTTTTTTTCCCC[A/C]CCAAAGTCAGGGTCT | 80067 |
rs191311527 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462671 | TCAAAATTTTAAATG[C/T]GTGTACTCCTTGAAC | 80067 |
rs191560700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171485828 | TATTTATTTATACTC[C/T]TTTTGACTCTCAATT | 80067 |
rs191622572 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448016 | TTCATTTGAGCTTAG[G/T]TTAGAACCACAGTGA | 80067 |
rs191638505 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469527 | TAGGTAGAAATGGTA[C/T]GTGGTAAAACAATGG | 80067 |
rs191831717 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445260 | CTCCCAAGTAGCTGG[A/G]ACTACAGGCACCCAG | 80067 |
rs191856241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464885 | CTTAAAATTGCAGTA[A/C]CAGTGTTACTACTAA | 80067 |
rs191860942 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487810 | AGCAATTCTCCCACC[A/T]CAGTCTCCCGAAGTG | 80067 |
rs191867181 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451488 | ATAGTATAAAAAAGC[A/G]AAACATTTTGCTACT | 80067 |
rs192017058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468350 | GCCCTTTCCTAAGTG[A/G]TTACATTCATTGGGA | 80067 |
rs192056873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171469961 | TAGAAAAATCACTCA[A/G]GCTTTAATTGTTGAT | 80067 |
rs192086208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439766 | AACCCCATCTCTACT[A/G]AAAAAACAAAAATTA | 80067 |
rs192096175 | snp | C/T | 0.000245791 | 0.0110831 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472931 | ATCCAAGTTGATGTT[C/T]GTTCCCAGTGCTTCT | 80067 |
rs192225128 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487234 | TATATATATATTACA[C/T]ATATGAAATTGTTTT | 80067 |
rs192296332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443994 | TTTTACGTTATTTTA[C/T]GTGTTAGGAAAATAA | 80067 |
rs192321411 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443335 | TATGGTATTGTAAAC[C/T]ATTTTAATCTTGTTT | 80067 |
rs192349308 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491055 | TTCTTGAGGCCAGGC[A/G]CGGTGGCTCATGCCT | 80067 |
rs192434357 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447726 | AGGCTGATATCGAAC[A/T]CCTGGGCTCAGGTAA | 80067 |
rs192554805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460186 | AAATTAGCTAGGCAC[A/G]GTGGCAGGCACCTGT | 80067 |
rs192556210 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171459704 | AAATGAATGATGTCA[A/T]TGTTCAAAAGGAAAA | 80067 |
rs192572147 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440911 | CAGCATTTTTCGTGC[C/T]ATGAGGACAGACGGG | 80067 |
rs192590459 | snp | A/G | 1.64955e-05 | 0.00287184 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481053 | GAGTCTTCAGCTGCT[A/G]TGTTTACCAGATGAT | 80067 |
rs192707882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463145 | CTGAGGCACGAGAAT[C/T]ACTTGAACCCAGGAG | 80067 |
rs192770132 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433636 | AAGAATGTAAGCATT[C/T]CATATTTTATTCCCT | 80067 |
rs192793810 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481564 | TACCAAACTTTGCTT[A/G]AGGATGAGAAATGAG | 80067 |
rs192828646 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441091 | CTGTATCTCCGCTGA[A/G]TCTACCAGTCTCCTC | 80067 |
rs192861143 | snp | C/T | 0.328382 | 0.237395 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448667 | CATTTTTATATCTCT[C/T]TTTTTTTTTTTAGGG | 80067 |
rs192898478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478981 | TGTATCATGAGATTA[A/G]AAAACAAAATATTTT | 80067 |
rs192946735 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454039 | TATATATTTAATTAA[C/G]TTAAGCAGCAGTCCC | 80067 |
rs193025083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455546 | TAATGGGATTGCAGG[A/G]TTAAATGGTATTTCT | 80067 |
rs193118469 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459168 | TACAAATTAGCCAGG[C/T]GTGGTGGCACATGCC | 80067 |
rs193213973 | snp | A/G | 0.000893256 | 0.0211147 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171434235 | TCCTGGGAGAAGCCG[A/G]GCTGCCTCACGAGGC | 80067 |
rs193214847 | snp | C/T | 0.000186959 | 0.00966667 | intron-variant, synonymous-codon, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473967 | ACATGTTGGTCCAAA[C/T]CAAGTCAAGTGAGTA | 80067 |
rs199565983 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455137 | TCCCTCCTCCCACCC[C/T]CCACCCTCCACCCTC | 80067 |
rs199570871 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438370 | TTTGATCCAGTTGAC[A/T]GATGGTACCTTTCAG | 80067 |
rs199572740 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486182 | GGCTACACTTTTTTT[C/T]TCAGAAAAACCAACT | 80067 |
rs199614195 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438929 | ATAGGGGTCTCAGTC[G/T]TGCTGTGTTGCCCAA | 80067 |
rs199695390 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171450430 | AAGTTGATAGGTAGA[-/T]TTTTTTTTTTCTGAA | 80067 |
rs199742600 | snp | C/T | 0.000380905 | 0.0137952 | synonymous-codon, intron-variant | DCAF17 | GRCh38.p7 | 2:171458431 | TGGGACTACTGGAAC[C/T]GTAGGAGAGGCTCCT | 80067 |
rs199761860 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468879 | GAATTCCTTTTCCTG[G/T]CTCTACAGACATGCC | 80067 |
rs199780746 | snp | A/G | 3.02952e-05 | 0.00389188 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453259 | ATTTTATTGACAATA[A/G]GTTGTAATGTCATTA | 80067 |
rs199782196 | in-del | -/TATT | 0.0414363 | 0.137845 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467335 | TATGTGTTAATTGAC[-/TATT]TATGTTATTGGTAAG | 80067 |
rs199808149 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443283 | AAACCAGAAGGAAAT[A/G]AACCAAAATGTTAAT | 80067 |
rs199942138 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435541 | TTGTGTTTTGGAAGT[A/G]CTTGCCTTTTTTTTT | 80067 |
rs200152531 | snp | C/G/T | 6.79698e-05 | 0.00582932 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478119 | AGTGTGTCCTTGCAT[C/G/T]GTGAATTTCATATTA | 80067 |
rs200189652 | snp | A/G | 0.000811856 | 0.0201313 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435148 | AGCCTATGAGAGAGG[A/G]AGAATATATTTTGAC | 80067 |
rs200234183 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468781 | GTAATTTTTCATTAA[G/T]AGAAATTTATAGATG | 80067 |
rs200237165 | snp | C/G | 5.21626e-05 | 0.00510672 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477957 | TGTAATAGAACTTGT[C/G]ATATCTTTTTATTTC | 80067 |
rs200268904 | in-del | -/AG | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461491 | ATAAAGATAAGCAAA[-/AG]AGAAAATGTAAAACA | 80067 |
rs200300830 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466728 | CATCTGTTTGTACTG[-/T]TTTTTTTTTTTTTTC | 80067 |
rs200380164 | snp | A/G | 0.000166011 | 0.00910922 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435165 | GAATATATTTTGACA[A/G]TTATCGGCGCTGTGT | 80067 |
rs200433540 | snp | A/G | 0.00199798 | 0.0315436 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449964 | GCCCGGCAGGTATAC[A/G]TATTTAAACATTCAA | 80067 |
rs200459384 | snp | A/G | 5.18829e-05 | 0.00509301 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448845 | AATTTATTATTCAAG[A/G]TTTTATTTTAAAAAT | 80067 |
rs200562186 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487002 | CTACGAGGTATAATT[C/G]TATGGACATACGCTT | 80067 |
rs200583745 | in-del | -/TT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466728 | CATCTGTTTGTACTG[-/TT]TTTTTTTTTTTTTCT | 80067 |
rs200593970 | in-del | -/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171467735 | CTGTCTCAAAAAAAA[-/C]AAAAAAAAAAAAAAA | 80067 |
rs200621819 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451961 | TTCTATATTCTGGAC[-/T]GTTTTCCTACAGTCT | 80067 |
rs200642784 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171479228 | GTTTGACCAAACATA[G/T]GTGAAGAATTAGTGC | 80067 |
rs200707008 | snp | C/T | 3.31219e-05 | 0.00406938 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171457973 | TTCCCCCCGCCAGAT[C/T]TTTGGGAACGTTACA | 80067 |
rs200749196 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171458134 | ATGATTTTTTTTTTT[-/T]AGTGAGATGCTTTTA | 80067 |
rs200751522 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466594 | TTTTCATTGAGAATA[A/T]TAGAGATCAAAATTG | 80067 |
rs200756917 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471280 | GAAGAGTAGATAACT[-/A]AAAAAAAATGTAAGC | 80067 |
rs201028876 | snp | A/G | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470579 | GCCCAGCCCAGTGAC[A/G]TTCTCTTTTATAAAG | 80067 |
rs201054185 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487004 | ACGAGGTATAATTGT[A/T]TGGACATACGCTTTA | 80067 |
rs201088582 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171460544 | TTATTATTATTATTA[A/T]TTTTGAGACAGGGTC | 80067 |
rs201095236 | snp | A/C | 3.52466e-05 | 0.00419787 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476827 | ATGGTGTTTTGAAGT[A/C]TTAGGTTCTCAGAAT | 80067 |
rs201193654 | in-del | -/A | 0.0197687 | 0.0974348 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437034 | CCACCTCGGCCTCCC[-/A]AAGTGCTGGGATTAC | 80067 |
rs201206877 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171440518 | AGGTCAAGGCTGCTC[A/G]AGCCGTCAGCATGCC | 80067 |
rs201242074 | in-del | -/GCTTTTACCTTCAATA | 0.0197687 | 0.0974348 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463780 | TAAAACTCTGTTACT[-/GCTTTTACCTTCAATA]GCTGGCATTTTTCTA | 80067 |
rs201280317 | snp | A/T | 3.31691e-05 | 0.00407228 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448706 | TTCCCAATTCATCAG[A/T]TTATAAGTCCTCACT | 80067 |
rs201337674 | snp | A/T | 1.73492e-05 | 0.00294522 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473983 | CAAGTCAAGTGAGTA[A/T]TCTCATTAGCACTTG | 80067 |
rs201346228 | snp | A/G | 0.00119259 | 0.02439 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435140 | TCACCTATAGCCTAT[A/G]AGAGAGGAAGAATAT | 80067 |
rs201355335 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171458135 | TCGACTAAAGTATGA[A/T]TTTTTTTTTTAGTGA | 80067 |
rs201370556 | in-del | -/A | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171463222 | CGATGGAGCGAGATT[-/A]TTAAAAAAAAAAAAA | 80067 |
rs201445013 | in-del | -/CT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486167 | TCATAAAGAATTTTG[-/CT]GCTACACTTTTTTTC | 80067 |
rs201494527 | in-del | -/C | 0.000987474 | 0.0221982 | DCAF17 | 2 | allele_origin=C(germline)/(germline) | 2:171448667 | CATTTTTATATCTCT[-/C]TTTTTTTTTTTAGGG | 80067 |
rs201495882 | snp | A/C | 0.134802 | 0.221877 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473567 | GTGCCTATAAAGCAT[A/C]AAACGCAGTTCCTGA | 80067 |
rs201520226 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171451689 | CAAGCAATTCTCCTG[A/C]CTCAGCCTCCTGAGT | 80067 |
rs201547812 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438738 | TAATCTATCTGTGCC[-/T]TTTTTTTTCCCCCCC | 80067 |
rs201551934 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171454946 | CTTTTTCTTTCTTTT[C/T]TTAAAGCTTTTCTTT | 80067 |
rs201574888 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171442972 | TTCACATCAAAGATA[C/T]AGCATTCAATATTGG | 80067 |
rs201596030 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438909 | TTAAAACAATTTTTT[G/T]AGAGATAGGGGTCTC | 80067 |
rs201612035 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452235 | AGCAGAGACTGGCTG[G/T]GATGGGGCAGACAGC | 80067 |
rs201627555 | snp | G/T | | | intron-variant, upstream-variant-2KB | METTL8, DCAF17 | GRCh38.p7 | 2:171432226 | GTGGCAAAGCAACGT[G/T]AAAAAAAAAAAATCC | 80067 |
rs201630526 | snp | A/T | 1.65677e-05 | 0.00287812 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469063 | CTTTTTATTAGCAAA[A/T]TTGTATCAAGTTCTT | 80067 |
rs201975084 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171459043 | GGCCAGGCATGGTGG[A/C]TCATGCCCGTAATCC | 80067 |
rs202002271 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171476761 | TACCTCAGTGTTACT[A/G]TAATTTTTATTTGTT | 80067 |
rs202068099 | snp | C/T | 3.29853e-05 | 0.00406098 | synonymous-codon, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480049 | AAAGACTTTCAAAAT[C/T]GTGGACTATGAAGAT | 80067 |
rs202090752 | in-del | -/TA | 0.0150606 | 0.0854603 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438171 | TTGGGATTTTCCAGT[-/TA]TCATTGTTTTATTGA | 80067 |
rs202131890 | snp | A/C/T | 0.00018578 | 0.00963637 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443633 | GATTTGTTTTTAGAG[A/C/T]GTTTGTTTCTAAAGC | 80067 |
rs202152236 | snp | A/C | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475546 | GAAGCAGGAGGATCC[A/C]CTGAAACCAGCAGTT | 80067 |
rs202194361 | in-del | -/T | 0.490563 | 0.0680388 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436634 | TTGCCCACTTGTAAA[-/T]TTTTTTTTTTTTTTT | 80067 |
rs202231211 | snp | A/G | 0.000549419 | 0.0165652 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171449953 | GCTCAGCAGTGGCCC[A/G]GCAGGTATACATATT | 80067 |
rs202231834 | in-del | -/TG | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478880 | CTCTGCATATAAAAC[-/TG]TATTCCAGAAAGATG | 80067 |
rs267599007 | snp | C/T | | | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480983 | TTACAGACATATAGC[C/T]ATGAAGTCTACTTTG | 80067 |
rs367570156 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171442278 | AAAAAATGAAAAGGG[A/G]CTGGGCGCAGTGGCT | 80067 |
rs367574996 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171478238 | TGCAAACCCATCATC[C/T]TCTCTTTTCATATTG | 80067 |
rs367741251 | snp | A/G | 1.6563e-05 | 0.00287771 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457947 | AGTCTTTTCTCAGGT[A/G]ATATCTGTCTTTCCC | 80067 |
rs367808593 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467463 | GGAGGCCGAGGCAGG[C/T]GGATCGCTTGTGGCC | 80067 |
rs368065483 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486493 | GTATTTTTAGGAGAG[A/T]TGTGGTTTCACCATG | 80067 |
rs368080589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478711 | GGACCATTTTTAGGT[A/G]GAAACATTAGAGTGG | 80067 |
rs368122415 | multinucleotide-polymorphism | AA/TT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171463224 | CGATGGAGCGAGATT[AA/TT]AAAAAAAAAAAAAAA | 80067 |
rs368128908 | snp | A/G/T | 3.72476e-05 | 0.0043154 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435039 | AAAATCTAACTTAAA[A/G/T]CCTAAGAGTTCTTTC | 80067 |
rs368249337 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483573 | TGTGCTACCTAGTGA[A/G]GAGATACCGCTCTGT | 80067 |
rs368324500 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440098 | TCCTGAGTATAGCTG[G/T]AACTACAGTCACATA | 80067 |
rs368372459 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171471495 | ATATGTATAGTATGT[A/G]CATATTTTGTATTAA | 80067 |
rs368385629 | snp | A/G | 0.000169986 | 0.00921759 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435061 | AGTTCTTTCCTGAAC[A/G]GAAATTCTTTATGTC | 80067 |
rs368454581 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443126 | CCTTTTTATCCAGTA[A/C]TTTTCATTTTAAATA | 80067 |
rs368493049 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469039 | TTCCCTGGTAAATGA[A/G]TGATCAGACTTTTTA | 80067 |
rs368608347 | snp | A/G | 1.73564e-05 | 0.00294583 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171476983 | TAAAATCCTTTATAT[A/G]TCATTGTCTTTCTAT | 80067 |
rs368631365 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171462556 | GAAAGTTAGAACTTT[C/T]GATACAATATGGTTG | 80067 |
rs368707741 | snp | A/G | 0.000100954 | 0.007104 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480207 | TGGTGAGTAGAGTCC[A/G]TGGGATACAAAGTTG | 80067 |
rs368727688 | snp | C/G/T | 0.00220867 | 0.0331601 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458121 | ATTAGCATGAGTTTT[C/G/T]GACTAAAGTATGATT | 80067 |
rs368766432 | in-del | -/TTA | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438653 | CGACTTTGTCTGAAA[-/TTA]GTATAGCTACTCCAG | 80067 |
rs368787265 | snp | A/G/T | 6.62552e-05 | 0.00575533 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457921 | GTGAACATTCAGAGG[A/G/T]TTGGACTTCCAGTCT | 80067 |
rs368831169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465547 | GGAGTGCAGTGGCGC[A/G]ATCTCAGCTGACTGC | 80067 |
rs369075736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171490344 | ACTTTGGAAAGACTC[A/G]CTAAAATCAGGTCAC | 80067 |
rs369160925 | in-del | -/ACCCTCC | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455147 | CACCCTCCACCCTCC[-/ACCCTCC]GATAGGCCCGAGTGT | 80067 |
rs369164414 | snp | A/C | 8.31926e-05 | 0.00644898 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458344 | AATAGGTGCTAAAGC[A/C]ACCATTTTTGTTTTG | 80067 |
rs369174398 | snp | A/G | 1.65616e-05 | 0.00287759 | missense, nc-transcript-variant | DCAF17 | GRCh38.p7 | 2:171458050 | GACTGGTCAGACTCT[A/G]TAGCTTCCAAACCAT | 80067 |
rs369221870 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171456527 | AAATAGTTTTTTCTA[A/G]TTCTGTGAAGAACAT | 80067 |
rs369440846 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171441097 | CTCCGCTGAGTCTAC[C/T]AGTCTCCTCCCATTT | 80067 |
rs369447743 | snp | C/T | 0.00606303 | 0.0547244 | synonymous-codon, upstream-variant-2KB, missense, utr-variant-5-prime, nc-transcript-variant, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434679 | GAGGACCAACCTGGG[C/T]ATCCTGCGGGCGCTG | 80067 |
rs369500669 | in-del | -/T | | | intron-variant, frameshift-variant | DCAF17 | GRCh38.p7 | 2:171460442 | AAAGAAGACTGGATT[-/T]GGGATCAGAATTTTA | 80067 |
rs369667535 | snp | G/T | | | utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171490944 | GGAATTAATGCAAGC[G/T]GTTTGATAAAAGAGG | 80067 |
rs369859810 | snp | C/G | 3.47621e-05 | 0.00416891 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443661 | AGCATTTTTAGCCTA[C/G]AAGAACCAGTTATTA | 80067 |
rs369891642 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452459 | AACACTACTTTCATT[A/G]TATATTTATTTATTT | 80067 |
rs370000017 | in-del | -/TTAT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171467338 | GTGTTAATTGACTAT[-/TTAT]GTTATTGGTAAGGCT | 80067 |
rs370019169 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171441526 | CCCCACCTCTTGACT[A/G]TACTGACCCAATACT | 80067 |
rs370048164 | snp | A/G | 1.64806e-05 | 0.00287054 | synonymous-codon, nc-transcript-variant, missense | DCAF17 | GRCh38.p7 | 2:171468937 | GGAGAATGCTTTTCA[A/G]ATTGGAGGCCATCCT | 80067 |
rs370107436 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171490028 | ATTTCTACGAGTCCA[A/G]TGTTGCCAGGTCTTG | 80067 |
rs370150751 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481990 | AGAAAAGTGGATAAA[C/G]AGTCCCAGAAGAAGT | 80067 |
rs370205436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488889 | AAGTGAAAGGAGATA[C/T]CAATAATCATTATGT | 80067 |