| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs370297758 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171460277 | GCAGTGAGCCGAGAT[C/T]GTGCCACTGCACTCT | 80067 |
| rs370405068 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435909 | CATTCACAGATACAT[G/T]TAATCACTACCACAG | 80067 |
| rs370438709 | snp | A/G | 1.65756e-05 | 0.00287881 | missense, intron-variant | DCAF17 | GRCh38.p7 | 2:171458465 | GGCATTCCTTGTAAT[A/G]TTAAAATCACAGGTA | 80067 |
| rs370439514 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171441348 | TGCGCACTTGGAGTT[A/G]AGGAAACACTGACCT | 80067 |
| rs370669812 | snp | A/G | | | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447564 | AGATGGGGTTTCGCC[A/G]TGTTGGCCAGGCTGG | 80067 |
| rs370737715 | snp | A/G | 1.85228e-05 | 0.0030432 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435043 | TCTAACTTAAAGCCT[A/G]AGAGTTCTTTCCTGA | 80067 |
| rs370751081 | in-del | -/AT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438172 | TGGGATTTTCCAGTT[-/AT]CATTGTTTTATTGAT | 80067 |
| rs370768341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479672 | AGAACCGAGCTTCAT[A/G]TGTTTAGTCCTGTCC | 80067 |
| rs370890403 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171450873 | GGTGAGGATTCTGAG[C/T]CCCAGAGAAGCTAAG | 80067 |
| rs370984688 | snp | A/T | 1.65037e-05 | 0.00287256 | synonymous-codon, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480103 | AGCTGTTACTCAAAT[A/T]GATGCTGAAGGAAAA | 80067 |
| rs371057430 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455759 | TTGCATTTCTCTAAT[A/G]ATCAGTGATGTTGAG | 80067 |
| rs371179981 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171434246 | GCCGGGCTGCCTCAC[A/G]AGGCACTAGGAACTA | 80067 |
| rs371218367 | in-del | -/ATT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444811 | CTGTACGCTAAATTT[-/ATT]GTTAATTTTTTTTTC | 80067 |
| rs371230892 | snp | A/G/T | 0.000149493 | 0.00864456 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171453167 | ACCTTGCAGTGTTCC[A/G/T]AGTTCTACCTTTTTC | 80067 |
| rs371234289 | snp | A/C | 1.65831e-05 | 0.00287945 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448777 | GCAACTACGGGAAAA[A/C]TCCTTGAGAAAATAT | 80067 |
| rs371241862 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171477527 | AGCCGGGCATGGTGG[C/T]TCACACCTGTAATCT | 80067 |
| rs371316750 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171440690 | TTGTTTGTTGTAGCC[A/G]TAGGTATTAGAGGTT | 80067 |
| rs371324447 | snp | A/G | 1.6563e-05 | 0.00287771 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457950 | CTTTTCTCAGGTGAT[A/G]TCTGTCTTTCCCCCC | 80067 |
| rs371616391 | snp | A/G/T | 6.65563e-05 | 0.00576841 | intron-variant, missense, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473921 | AATCTGACTGGATCT[A/G/T]TTTCCATCCTGATGC | 80067 |
| rs371650850 | in-del | C/TA | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171473567 | GTGCCTATAAAGCAT[C/TA]AAACGCAGTTCCTGA | 80067 |
| rs371655701 | snp | A/G | 6.97289e-05 | 0.0059042 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477955 | CATGTAATAGAACTT[A/G]TCATATCTTTTTATT | 80067 |
| rs371677535 | snp | A/C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171462957 | GGAGTTTTAACTGGG[A/C/G]ATAGTGGCTCATGCC | 80067 |
| rs371697332 | in-del | -/A | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171473567 | TGCCTATAAAGCATC[-/A]AAACGCAGTTCCTGA | 80067 |
| rs371862241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488912 | CATTATGTCTGGACA[A/G]CAGGCAAAAACCAAG | 80067 |
| rs371919091 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171473524 | TTTTCAGTACTTCCT[C/T]TGAGTGTTATTAAGA | 80067 |
| rs371942932 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432338 | ATGAAGATGAGATGG[A/G]TAAGAGTCTAAAGGA | 80067 |
| rs372031833 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171440933 | ACAGACGGGTGGCAC[C/T]TCCAGGCTGTTTTCG | 80067 |
| rs372035434 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171489511 | AATTTTGCTCTGTTA[C/T]AGGGAATTTTATACT | 80067 |
| rs372044313 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171458770 | CAAAATGAGTTGCAG[C/G]AAATGATACCATCTT | 80067 |
| rs372046405 | snp | A/G | | | synonymous-codon, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480172 | ACTTAAAAGCATTCC[A/G]CTAGTGGAGTCATGG | 80067 |
| rs372085272 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489281 | TTGTACTGTCAAACA[A/G]GAAAGTGATATAAAG | 80067 |
| rs372158032 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486502 | GGAGAGATGTGGTTT[C/T]ACCATGTTGGCAAGG | 80067 |
| rs372199991 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171463190 | GAGTGAGACTGCGCC[A/G]CTGCACTCCAGCCTG | 80067 |
| rs372309837 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433473 | GGCCCCACCCTTAAG[A/G]GACTTAGAGCATGGC | 80067 |
| rs372362818 | snp | G/T | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433501 | GGCGGTGGGACACAT[G/T]TGGTGCAAGCTTGCT | 80067 |
| rs372384100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479780 | CTGTGGAGAATTTCA[A/G]TTATACTTTGAGATC | 80067 |
| rs372408217 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439337 | TACTTGAATATTCTG[C/T]TCTACTTTTTCTTTC | 80067 |
| rs372481846 | snp | A/G | 1.65641e-05 | 0.00287781 | missense, intron-variant | DCAF17 | GRCh38.p7 | 2:171458409 | TAGGGTGTGCATGCA[A/G]ATGGGGTGGGACTAC | 80067 |
| rs372482315 | snp | C/G | | | intron-variant, missense, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469407 | CCACGGCTTGTTGCT[C/G]TTTGCCTTCCAGAGC | 80067 |
| rs372539451 | in-del | -/T/TT/TTT | 0.220592 | 0.265148 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448667 | ATTTTTATATCTCTC[-/T/TT/TTT]TTTTTTTTTTTAGGG | 80067 |
| rs372547092 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171449494 | CAAGAACTGTTATTT[C/T]AACTATTAGTTTTAT | 80067 |
| rs372569766 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171447178 | ATAATGTGTTATTCA[A/G]TTATATGTAGTCATA | 80067 |
| rs372573107 | snp | A/C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171465785 | CCACTGTGCCCAGCC[A/C/G]CATTTTCTATTTCAT | 80067 |
| rs372580982 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487290 | TTTTTAATTTTAGAC[A/T]TTCTAATAGGTAGTA | 80067 |
| rs372613347 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486825 | TGGCTGCTTTCATTC[A/C]GTACAGTTATTTGGA | 80067 |
| rs372935297 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171488753 | AGTTTGTCTTGGTCT[A/G]CCCTACCAGCTGGAC | 80067 |
| rs372970736 | snp | C/T | | | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447651 | ACAGGCGTGAGCCAC[C/T]GCACCTAGCCACTTC | 80067 |
| rs373071355 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469506 | CTTAAGTTATTTATG[A/G]CAGAGTAGGTAGAAA | 80067 |
| rs373291150 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438978 | ACCTCAAGTAGTCCT[C/G]CCACCTCAGCCTCTG | 80067 |
| rs373344754 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484682 | TGTGTAACCCAAACC[-/C]TTTCCAAAATTTAGA | 80067 |
| rs373359005 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437066 | GGCATGAGCCACCGC[A/G]TCCAGCCACAGAGAG | 80067 |
| rs373424695 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171463989 | TATAAACACAATAGA[C/T]TTGTGGATTTTTTAT | 80067 |
| rs373435062 | snp | A/G | 3.29576e-05 | 0.00405928 | missense, nc-transcript-variant, synonymous-codon | DCAF17 | GRCh38.p7 | 2:171468890 | CCTGTCTCTACAGAC[A/G]TGCCACCACTGCTCT | 80067 |
| rs373466341 | snp | A/G | 1.66059e-05 | 0.00288144 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171449932 | TTAAGTCAGCTCAGA[A/G]CAGAGGCTCAGCAGT | 80067 |
| rs373670282 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171441180 | CTCCACACTCTGTTG[C/G]AAATAAAATTAGTTT | 80067 |
| rs373722641 | snp | G/T | 0.000185856 | 0.00963813 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434388 | TCCGCGCTCTGGCGG[G/T]GCAAGCGGCTCTGCT | 80067 |
| rs373752576 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171457156 | GTCAGAGTAAACAAT[A/G]CTTATCCTTCTAAGA | 80067 |
| rs373833929 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483406 | AGGTACAGACGTTAC[A/G]CTGAAAAGAGGTGCA | 80067 |
| rs373863503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473249 | TGTGCATGATTATGG[A/C]AGAGTTATATAATGG | 80067 |
| rs373914686 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171456688 | ATCTCCTTGTAGAGA[C/T]CTTTCACTTCCTCTG | 80067 |
| rs373929284 | snp | A/G | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475497 | GGGGCTGGGCTTGGT[A/G]GTTTAGGCCTATAAT | 80067 |
| rs373997425 | snp | A/G | 0.000116222 | 0.00762217 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448684 | TTTTTTTTTTAGGGA[A/G]ATATACTTCCCAATT | 80067 |
| rs374035044 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171451017 | ATATGGACTGGCAGG[G/T]GAAGTTTATATAGAA | 80067 |
| rs374119806 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171479357 | CACTGATCTGCTTTC[C/T]GTGCAAGGTTTCTGG | 80067 |
| rs374148699 | snp | A/G | 0.000101698 | 0.00713014 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478117 | CCAGTGTGTCCTTGC[A/G]TTGTGAATTTCATAT | 80067 |
| rs374188707 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171434822 | GTCACATGTGATGGG[A/G]AGGAGGATACAAGCC | 80067 |
| rs374205599 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171472179 | TCTATACTTTTGGTT[C/T]TTTTGTTTGTTTTGT | 80067 |
| rs374209485 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171461612 | CAAGAAAAGAATCAT[A/G]CCATAAGTGCTCTTT | 80067 |
| rs374222088 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437055 | CTGGGATTACAGGCA[C/T]GAGCCACCGCGTCCA | 80067 |
| rs374234095 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171473552 | AGATTAAATGAAACA[A/G]TGCCTATAAAGCATC | 80067 |
| rs374256774 | snp | C/T | 2.14885e-05 | 0.00327777 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453230 | TAAGAACTCATTTCT[C/T]ATTTAATTGCAATAT | 80067 |
| rs374323832 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433863 | CAACATGCGGCTGAA[A/G]GGAAAGCCGCGGGGC | 80067 |
| rs374357109 | snp | C/T | 0.00129009 | 0.025365 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435060 | GAGTTCTTTCCTGAA[C/T]GGAAATTCTTTATGT | 80067 |
| rs374359784 | snp | A/G | 5.01735e-05 | 0.00500842 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458491 | AGGTATGGCTACTCT[A/G]TAGTATTTTTTCACC | 80067 |
| rs374429249 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446962 | GAAGGGTCAAGACTG[A/C]AATGTATTGTCTTTA | 80067 |
| rs374463582 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479705 | GAATCAGCAAACACA[C/T]TTGTGAGAGGCAGCA | 80067 |
| rs374467773 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480147 | TCCACTGTAATGAAT[A/G]TGGAACTTTACTTAA | 80067 |
| rs374570811 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452902 | TTTTTGTCTGTATAT[A/G]TGCGCATGTGTGTCT | 80067 |
| rs374646610 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439512 | ATTTCTTTTTTTTCC[-/T]TTTTTTTTTTTTTTT | 80067 |
| rs374716482 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171450643 | TTCTTTATACACCGG[A/G]ACACCTAGAAAAAGC | 80067 |
| rs374757935 | snp | A/G | | | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448713 | TTCATCAGATTATAA[A/G]TCCTCACTCATAGCA | 80067 |
| rs374778213 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171489167 | CTACCCTGGTATTCC[G/T]GGATCATATTTTCTT | 80067 |
| rs374810983 | in-del | -/TTTG | 0.00132038 | 0.0256602 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484121 | AAAAGGTACTTTCCC[-/TTTG]TTTGTGGTGATAATC | 80067 |
| rs374823854 | snp | A/G | 1.67503e-05 | 0.00289393 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453099 | ACTTTTGAGAGCTGC[A/G]TGTAATTGTAGTCTT | 80067 |
| rs374877117 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171458641 | TAATGAATAAGCTTC[A/G]AGGAAAATCTGTCAG | 80067 |
| rs374882763 | snp | A/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433564 | CAGGCAGGGCTAGTT[A/T]ACAAAGTATATCTTT | 80067 |
| rs375112740 | in-del | -/TT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171463221 | GGCGATGGAGCGAGA[-/TT]TTAAAAAAAAAAAAA | 80067 |
| rs375191229 | snp | A/G | 4.96142e-05 | 0.00498043 | synonymous-codon, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481084 | ATGTGACACTGGGGA[A/G]GAAGAAGAAACCATA | 80067 |
| rs375260354 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443035 | AGTAATTTGGGAGTA[A/G]AAAAAAAAACCATAA | 80067 |
| rs375272479 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469672 | ACACAATCTCTTCCC[C/T]CAAGTTATACTCTTA | 80067 |
| rs375308118 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432527 | ATTTCATTTAAGCCA[A/C]AGAAAACCCAGTTAT | 80067 |
| rs375412538 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171457960 | GTGATATCTGTCTTT[A/C]CCCCCGCCAGATTTT | 80067 |
| rs375426959 | snp | A/T | 5.00496e-05 | 0.00500223 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435093 | TTTAGGAAAGTACTA[A/T]ATTTAAGAATGTCTG | 80067 |
| rs375509459 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463274 | TTGCACTGGTATAGG[A/G]TAATTTCCAGGATGT | 80067 |
| rs375644386 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435912 | TCACAGATACATGTA[A/G]TCACTACCACAGTTA | 80067 |
| rs375645836 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471028 | GAAGCAATCCCCTGT[A/C/G]GTTTCCAAGGAATTA | 80067 |
| rs375662120 | snp | C/G | 0.000230696 | 0.0107375 | missense, nc-transcript-variant | DCAF17 | GRCh38.p7 | 2:171468918 | TCTTTGAGGTGTCAT[C/G]CCTGGAGAATGCTTT | 80067 |
| rs375679028 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462832 | GTATTATTATATCAT[C/T]GTATACAAAAGATTG | 80067 |
| rs375752562 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465846 | TTTAATCCTGTTACT[C/G]TCATCAGTAACCATT | 80067 |
| rs375763123 | snp | C/T | 6.63097e-05 | 0.00575764 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448753 | CATAATTGGCTACTT[C/T]GTATATCAGCAACTA | 80067 |
| rs375769963 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441447 | GGGCCTCAGTATCCT[C/G]AGCTGTGCTACATCC | 80067 |
| rs375801946 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171441642 | TTGGAAAACAGGGAG[C/T]CTCGTACTCTTGGCT | 80067 |
| rs375879310 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487164 | AGTTCTAGTTGCTTC[A/T]TATCTTTGCCAGCAC | 80067 |
| rs375912637 | in-del | -/AT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455039 | GTTATATAGATAAAC[-/AT]GTGTCATGGGGGTTT | 80067 |
| rs376025348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456094 | TCTTTGCCCATGCCT[A/G]TGTCCAGAATGATAT | 80067 |
| rs376150622 | snp | A/G | 4.96849e-05 | 0.00498397 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457966 | TCTGTCTTTCCCCCC[A/G]CCAGATTTTTGGGAA | 80067 |
| rs376182176 | snp | A/G | 1.67478e-05 | 0.00289372 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458493 | GTATGGCTACTCTAT[A/G]GTATTTTTTCACCTT | 80067 |
| rs376303254 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452380 | GCTATCCTTTTCAAG[C/T]AGAAGAGTCACTCAA | 80067 |
| rs376359964 | in-del | -/AAACA | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486791 | TATATAAATGAAATA[-/AAACA]GTAAGTATTTTTATT | 80067 |
| rs376365737 | in-del | -/A | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433618 | TATCTTAGGCCGTCC[-/A]ATAAGAATGTAAGCA | 80067 |
| rs376416867 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171446318 | TTTGGGAGGCCGAGG[C/T]GGGCAGATCACGAGA | 80067 |
| rs376418592 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466727 | CATCTGTTTGTACTG[-/T]TTTTTTTTTTTTTTT | 80067 |
| rs376429479 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486507 | GATGTGGTTTCACCA[C/T]GTTGGCAAGGCTGGT | 80067 |
| rs376448571 | snp | A/G | | | utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171490929 | GAGGCCAAGAAGATC[A/G]GAATTAATGCAAGCT | 80067 |
| rs376463360 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171445608 | TCAAGAAAATATTTC[A/G]AACGTATTATATTTG | 80067 |
| rs376756357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486417 | CGGGTTCAAGTGATC[C/T]TCCCACTTCAGCCTC | 80067 |
| rs376845783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437749 | AACGTCCATGAGATC[A/G]GTAGTGATAGCCACT | 80067 |
| rs376880442 | snp | A/G | 4.99097e-05 | 0.00499524 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458122 | TTAGCATGAGTTTTC[A/G]ACTAAAGTATGATTT | 80067 |
| rs376895547 | in-del | -/TC | | | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447695 | TATCTAGAAACAGAG[-/TC]TTGCTGTGTTGCCTA | 80067 |
| rs376977508 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171456928 | TGTCGTTTGAAAAGA[A/G]GGATAGTTTGACTTC | 80067 |
| rs377077804 | snp | A/G/T | 0.00046393 | 0.0152245 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458098 | AAACTGAAATTTGTC[A/G/T]TGTTACTATTAGCAT | 80067 |
| rs377137480 | snp | C/G | 2.27311e-05 | 0.00337121 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473828 | AATCATTTGATTTTC[C/G]CTTAATCTTTGTCTT | 80067 |
| rs377182072 | snp | C/T | 0.0200587 | 0.0981172 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434365 | AAGGGAGTGCTTCTT[C/T]CCTTCTCTCCGCGCT | 80067 |
| rs377364475 | snp | C/T | 6.6589e-05 | 0.00576975 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171449952 | GGCTCAGCAGTGGCC[C/T]GGCAGGTATACATAT | 80067 |
| rs377564415 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433796 | AAACTAAGAGTGAAT[A/G]GGAAGCCAGCATCTT | 80067 |
| rs377736393 | snp | C/T | 8.29717e-05 | 0.00644042 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448688 | TTTTTTAGGGAGATA[C/T]ACTTCCCAATTCATC | 80067 |
| rs386652700 | multinucleotide-polymorphism | CTG/GTT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171440834 | GTTTTGGAGGCAGCA[CTG/GTT]TGCCCTGTGACCTGA | 80067 |
| rs386652701 | multinucleotide-polymorphism | AA/TT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171467988 | AAACTAAAAATTAAA[AA/TT]CTCAAGTTAGAGGGT | 80067 |
| rs386652702 | multinucleotide-polymorphism | CA/TG | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171471939 | AGAATTGATTGAGGC[CA/TG]AGAGGTCAAGGCTCC | 80067 |
| rs397761720 | in-del | -/A | | | intron-variant, upstream-variant-2KB | METTL8, DCAF17 | GRCh38.p7 | 2:171432238 | GTCAAAAAAAAAAAA[-/A]TCCTGTGTCACAAGT | 80067 |
| rs397868310 | in-del | -/A | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171467754 | AAAAAAAAAAAAAAA[-/A]GTTGTACGTGGATTT | 80067 |
| rs397868903 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171461857 | TGATCTGCTTTTTTT[-/T]CACAGTAGATTAAAT | 80067 |
| rs398071435 | in-del | -/CTC | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486730 | TCCCAAGACAACCTC[-/CTC]GGATCTGTTTCTGTA | 80067 |
| rs398080810 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171461856 | GTGATCTGCTTTTTT[-/T]TCACAGTAGATTAAA | 80067 |
| rs398104970 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171445144 | CTATTTTTTTTTTTT[-/T]GAGACGGTCTCTCTT | 80067 |
| rs398104971 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171477463 | AATAATTTTTTTTTT[-/T]GCCCATTCTGGCATT | 80067 |
| rs527260140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472167 | TGGATTAGCACGTCT[A/G]TACTTTTGGTTTTTT | 80067 |
| rs527336371 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457519 | GCATGAAAGACTATC[C/G]AGGGGCTGGGCACCT | 80067 |
| rs527440085 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487186 | TGCCAGCACTTGATA[A/T]GGCCAATCTTTTTAA | 80067 |
| rs527476950 | snp | C/G | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432480 | GAAAGAGAAATGAGA[C/G]AGTTGATGAATTCAA | 80067 |
| rs527559301 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471402 | AGCTGATAATAAGCT[G/T]CCCAGTATTTCACAC | 80067 |
| rs527562606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480331 | GGTTTTGTCCTATAT[A/G]CAGGACAAAAGAGTA | 80067 |
| rs527577790 | snp | A/G | 0.000186968 | 0.00966691 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434300 | CCGGCCGGCCGCGCG[A/G]TACCGGAGCGTCGCA | 80067 |
| rs527674333 | snp | C/T | | | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491233 | CTGAGGCAGGAGAAT[C/T]GCTTGAACTCGGGCA | 80067 |
| rs527738123 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439118 | ATATAGTTAAGGTGC[G/T]TTTTTTTCATCTGGC | 80067 |
| rs527779083 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448527 | CCACAATCTTATCTT[G/T]CCTTGTCTTAATTCT | 80067 |
| rs527782481 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440452 | TGGTGGCACACACCT[C/G]TAGTCCCAGCTACCA | 80067 |
| rs527797321 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437290 | AGGTATCCAACTCCA[-/T]TTTTTTTTAACATGC | 80067 |
| rs527869750 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478314 | AATAATTTGAAAACA[C/G]GATTAGCTTATTGTT | 80067 |
| rs528033439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470097 | GGCACAATCAGAGCT[C/T]ACTGCAGCCTCAACC | 80067 |
| rs528057967 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171488276 | CCAATAATTTAGCAA[-/T]TTTTTTTTGCCATAT | 80067 |
| rs528058690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439670 | GCGGAGGCTCACACC[C/T]GTAATCTCACACTTT | 80067 |
| rs528061045 | snp | C/T | | | intron-variant, missense, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469406 | TCCACGGCTTGTTGC[C/T]CTTTGCCTTCCAGAG | 80067 |
| rs528072209 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171442113 | GTGTTTTATCCACAG[A/G]TTATAATCGCATATG | 80067 |
| rs528087089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439020 | AGACACGAGCCACCA[C/G]AACACTTTAGGTATT | 80067 |
| rs528094869 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491382 | GCAATAATGAGAGAA[A/G]GCCTCTGGCAGCACT | 80067 |
| rs528096266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446980 | TGTATTGTCTTTACT[A/G]TCAAGAACTCTACTT | 80067 |
| rs528157673 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | METTL8, DCAF17 | GRCh38.p7 | 2:171432221 | CTCCAGTGGCAAAGC[A/C]ACGTCAAAAAAAAAA | 80067 |
| rs528375128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446528 | TCCAGCCTGGGTGAC[A/G]GAGCAAGACTCTGTC | 80067 |
| rs528551847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460584 | TGCCCAGAGTGGAGT[A/G]CAGTGGAGAGATCAC | 80067 |
| rs528618185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489910 | CCTGCCTCAGCCTCC[C/T]GAAGTGCTGGGATTA | 80067 |
| rs528625147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467942 | ATCATCTTCCTAAGA[C/T]AAGCCCCTTTACTAA | 80067 |
| rs528664287 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171437515 | ATTTCTTCTTTAAAT[A/G]CTTGGTGGAATTAAC | 80067 |
| rs528667092 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437206 | GGTTTTTTTCTAAAG[G/T]GTTTATAGTTTTAGC | 80067 |
| rs528752626 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474760 | GCATTCTCTTTCTCT[C/G]ATACATACACACCAT | 80067 |
| rs528766825 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437873 | AATTTTACTACTTTC[G/T]GAGCTAATTTTTGTT | 80067 |
| rs528800956 | snp | A/C | 0.000399281 | 0.0141238 | missense | DCAF17 | GRCh38.p7 | 2:171490756 | TTTTCAGATTGCCCA[A/C]GGCAGAATTCACCTT | 80067 |
| rs528802776 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444258 | ATGATGATTATCAAG[A/C]CATTTCCCCAAATTC | 80067 |
| rs529003704 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171451016 | AATATGGACTGGCAG[A/G]TGAAGTTTATATAGA | 80067 |
| rs529038429 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487609 | TGTATTTCTAGTAGA[C/G]ATGGGGTTTCACCAT | 80067 |
| rs529100311 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171449365 | AGTTTAAATAAACTT[A/T]AAAAAAAAAATTCCC | 80067 |
| rs529218349 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461522 | ATTATAGTCCTCTTA[-/C]ATGGGGTTAACTGTT | 80067 |
| rs529221113 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473591 | TTCCTGACACAAAGT[A/T]GATGCTTGAGATATG | 80067 |
| rs529221637 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434387 | CTCCGCGCTCTGGCG[C/G]TGCAAGCGGCTCTGC | 80067 |
| rs529244488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442605 | AAGAAAAGCGCCAGG[C/T]GAAGTGGCTCACACC | 80067 |
| rs529280678 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450441 | GTAGATTTTTTTTTT[C/G]TGAAGCGTGCTATTT | 80067 |
| rs529296010 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441687 | TGGAGTTTCCATCTT[A/G]CTGAGCTGGGATTGG | 80067 |
| rs529368169 | snp | A/T | 1.66718e-05 | 0.00288715 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481130 | AAAGAGTGAGATAAT[A/T]GTAACCTAAGAGACT | 80067 |
| rs529657436 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479457 | TCCCAGTCCTGTTCT[G/T]TGGGTTGGATTTCAT | 80067 |
| rs529717676 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472007 | GCAACAGAGTGAGAC[C/T]CTGTCTCAAAAAATA | 80067 |
| rs529762295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437737 | TATTATTGTTTTAAC[A/G]TCCATGAGATCGGTA | 80067 |
| rs529845532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471299 | AAAAATGTAAGCAGC[C/T]GAACTTAAGATTTCA | 80067 |
| rs529919202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478614 | GTATTTATGAAATCA[A/C]CTGATAGTGATCATG | 80067 |
| rs529977321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486395 | GCTCACTGCAACCTC[C/T]GCCTCTCGGGTTCAA | 80067 |
| rs530006747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440872 | CTGATGGATCTAAGA[A/G]TAATTATGGATTTTC | 80067 |
| rs530008703 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433393 | CAGTCAGGTGCGATC[A/G]CTGGCTTTCTTTGAG | 80067 |
| rs530128726 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465683 | AGAGGTGGGGTTTTG[A/C]CACCTTGGCCAGGCT | 80067 |
| rs530170664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454902 | AAAAAAAAAGTTTGA[A/C]TTGCACAAGTCCTCT | 80067 |
| rs530173007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462989 | GTAATCTGAGCACTT[C/T]GGGAAGCGAGGCAAG | 80067 |
| rs530215099 | in-del | -/GAGACT | 0.00199481 | 0.0315187 | intron-variant, cds-indel | DCAF17 | GRCh38.p7 | 2:171474106 | TTGGGTGCTTCCTCA[-/GAGACT]GGCATACAGAACACC | 80067 |
| rs530266268 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488061 | TAATACCTGCTCTGA[A/C]CTAGTTAATGCCTTG | 80067 |
| rs530291555 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, synonymous-codon, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469396 | GTTCTGCTTCTCCAC[A/G]GCTTGTTGCTCTTTG | 80067 |
| rs530300646 | in-del | -/TT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439385 | CCCCAGCTTGGGAAG[-/TT]TCTGTTGACCTATCT | 80067 |
| rs530362467 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171462870 | TCTATACATTGGTAA[A/G]TGGCATTAGTATTAT | 80067 |
| rs530410030 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446841 | AAATAGAAAATATTA[A/C/T]GAAATTTTAATAAGA | 80067 |
| rs530440435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445742 | AGCTGGAGTCCAGTG[A/G]CACAATCACAGCTCA | 80067 |
| rs530469431 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171472457 | GTGCTAGGATTACAG[A/G]CGTAAGCCACTGCCC | 80067 |
| rs530470443 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171490971 | GAGGTAAATGAAAAA[A/C]AACTTGGATCCTGGG | 80067 |
| rs530498334 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484661 | GTTCTTGCAGACATA[C/T]ACACCTGTGTAACCC | 80067 |
| rs530542649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453570 | AAAATATTTCATTTT[A/C]ATTGCAAGATATAGG | 80067 |
| rs530659365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446416 | CCAGGTGTGGTGGCA[C/T]GCACCTGTAATCCCA | 80067 |
| rs530660406 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491267 | GAGGTTGCAGTGAGC[C/T]GAGATCATGCCACTG | 80067 |
| rs530669267 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452900 | GATTTTTGTCTGTAT[A/G]TATGCGCATGTGTGT | 80067 |
| rs530700982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467896 | TTAATAAAGTATGCA[C/T]TTCTGTATATAACAT | 80067 |
| rs530746388 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171468198 | TTGGTGCTTTTTAGC[A/T]CCAAGAGAAATTTAT | 80067 |
| rs530867060 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460513 | TGGTATGATAGTGGG[C/T]AAATTATTATTATTA | 80067 |
| rs530991098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467408 | GGGAAGTCAAAAGTT[C/T]GGCTGGGCACAGTGG | 80067 |
| rs531077606 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475019 | TCAAATGCTTTAACC[-/T]TTTAATGGCTTTTCA | 80067 |
| rs531086312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489873 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 80067 |
| rs531146531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442894 | AAAAGGAACAAAATA[A/G]AATTAAACATTTATG | 80067 |
| rs531211176 | snp | A/G | 0.000186411 | 0.00965249 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482087 | TATTTCTTCTTTGTT[A/G]GGAAAGATCTAAATA | 80067 |
| rs531224572 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436127 | CTTTGCGTGTTTTCA[A/G]GGTTCATCCATGTTG | 80067 |
| rs531259006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458975 | TCTATAAATATAGTA[A/G]AAATGTTCTATATTT | 80067 |
| rs531367078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435001 | AAAATAATATAGGTG[A/G]CATTATGTTGCTTTG | 80067 |
| rs531388737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450701 | CAGAGTCTGTTGTAG[C/T]TCTTTCTCATTTTTA | 80067 |
| rs531465100 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465107 | GGAGGCTGAGGCAGG[A/T]GAATCGCATGAACCC | 80067 |
| rs531465211 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472772 | GATACCTAGAACATA[C/G]TAGCCTATCAATATA | 80067 |
| rs531473523 | snp | C/G | 1.66724e-05 | 0.0028872 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458124 | AGCATGAGTTTTCGA[C/G]TAAAGTATGATTTTT | 80067 |
| rs531533696 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434328 | GCACTGTCAGCGGCC[A/G]GAGAGCCTGGGGCAG | 80067 |
| rs531589144 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451325 | ACTTAACTGCATGCC[C/T]TTTATTGGAATCTCC | 80067 |
| rs531716641 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440930 | AGGACAGACGGGTGG[A/C]ACTTCCAGGCTGTTT | 80067 |
| rs531722372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449372 | ATAAACTTAAAAAAA[A/G]AAATTCCCTGTATTC | 80067 |
| rs531748790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487373 | CACATTTTCATGTTT[A/G]TTTGTTGTGTGTATA | 80067 |
| rs531787582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463184 | TGCGGTGAGTGAGAC[C/T]GCGCCACTGCACTCC | 80067 |
| rs531949458 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455917 | CTGGATATTAGACCT[G/T]TGTCAGAGGTATGGA | 80067 |
| rs531982758 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456742 | ATTCTTTTTAGGACA[A/G]CTGTGAATGAGAGTT | 80067 |
| rs532070538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463985 | CATATATAAACACAA[C/T]AGACTTGTGGATTTT | 80067 |
| rs532096002 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433286 | AGTAGCCCCGGTAGG[A/C]AATTATTATTTTTTC | 80067 |
| rs532120598 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171463552 | TGTATTACCTATGTG[A/T]CAAAGTGGTTCTGTG | 80067 |
| rs532134720 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477667 | CATGGTGGTGTATGC[C/T]TGTAGCCCCAGCTAC | 80067 |
| rs532171313 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491182 | AAATACAAAAATTAG[C/T]CAGGCACATGCCTGT | 80067 |
| rs532209602 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470292 | ATATCAGAAGAATTT[C/G]CTTTTTTTTTTGAGG | 80067 |
| rs532248145 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478477 | ATGTTTGTTAATGTC[C/T]GTAGTCCAGAGGAAG | 80067 |
| rs532351603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468654 | CGGGCCACATATACC[C/T]CCTGAAAACAGATAC | 80067 |
| rs532354463 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454748 | CTAAAAATATAAAAA[C/T]TAGCCACGGGTGGTA | 80067 |
| rs532361047 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446561 | AAAAGAAAAAAAAAA[A/C]ATCTAGGAGAGTCAA | 80067 |
| rs532456595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453825 | CTCCTACTGGTCTTT[A/G]ATTCAGCACCTGAAG | 80067 |
| rs532540667 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461473 | AAATTTAAAAATTGG[A/G]AAATAAAGATAAGCA | 80067 |
| rs532619445 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171490816 | TCAGAGCAACATGAC[A/G]TACATGAAGTACTGT | 80067 |
| rs532718904 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464387 | CTGGTGGTTGTTCAC[A/G]ATCTTTGGTGTTTCT | 80067 |
| rs532782179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451927 | TCACCTGATAATGTT[A/G]ATAAAATCTTGTCAG | 80067 |
| rs532795086 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171458916 | ACAGAACTTCCCAGT[A/G]TACTTAAAGAGTGCC | 80067 |
| rs532854674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445621 | TCGAACGTATTATAT[C/T]TGCTGCTTCAAATTA | 80067 |
| rs532886693 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484399 | AAACATACAGTAAAA[C/T]TGAAAGAATTTTATA | 80067 |
| rs532889914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445050 | GAGTATGGGGGAAGA[C/T]GACAGATTTCTTAAT | 80067 |
| rs532891919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452744 | GCTGGAATTATAGGC[A/G]TGAGCTACCTGATCC | 80067 |
| rs532958848 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171473325 | AAATATTGGAAAAGG[G/T]CAGGTGCAGTGGCTT | 80067 |
| rs533032181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459841 | AGATGCCTTGGACAA[A/G]CTGAATTAGGCAGTT | 80067 |
| rs533128332 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466552 | CCACAAGACATGGAA[G/T]CAGCTACTCTGAGAA | 80067 |
| rs533141352 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474492 | TTTGCTTTCATGTTC[G/T]TCCTTCTCTACCCAG | 80067 |
| rs533146558 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435882 | AAGTGTACAGTTCAA[A/T]AATATTTAATGCATT | 80067 |
| rs533211237 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171479663 | TTAGGTTTCAGAACC[A/G]AGCTTCATGTGTTTA | 80067 |
| rs533336462 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482527 | CAAGACCAGTAAGAG[G/T]CCAGTGAAAGTACTA | 80067 |
| rs533375170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443891 | AGTTATATAAGCAGC[A/G]TAAGCTAATGTATAA | 80067 |
| rs533423154 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171488401 | CCGTTTTTGAATCCT[A/G]TTCTAAACACCACTT | 80067 |
| rs533510209 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481810 | GCAAACCTTAAGTGA[A/G]ATTGTTTTCTGATTT | 80067 |
| rs533525154 | snp | A/C | 3.36078e-05 | 0.00409912 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453080 | AACAGTGTGTTTCTG[A/C]AGTACTTTTGAGAGC | 80067 |
| rs533535391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464432 | ATAACTCCAAATTCT[C/G]CCTCTCACTTTTCCA | 80067 |
| rs533581220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449807 | ATAGTTTACTTATAA[A/G]ATATAATATTTTGGT | 80067 |
| rs533731575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478777 | AGGTTAGAGGTGGCC[C/T]AGTATGTAGCTGTTC | 80067 |
| rs533738998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469764 | AAAGTGAGTTAAGGG[C/G]GGAGTTCCATTTTTA | 80067 |
| rs533754425 | snp | A/G | 0.000557569 | 0.0166875 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483758 | ATAACCACATGAAGT[A/G]TGAACTGCCATTATC | 80067 |
| rs533759311 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486444 | CCTCCAGAGTAGCTG[G/T]GAGTATAGGCACCAC | 80067 |
| rs533825166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448889 | CCCATGAAATTTCAA[A/G]CCTTTTTTCCCTGTC | 80067 |
| rs534060306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171485902 | TTTCCTCATTATAAC[C/T]TGAGTCCTATAGAAG | 80067 |
| rs534060640 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463271 | TTTTTGCACTGGTAT[A/G]GGATAATTTCCAGGA | 80067 |
| rs534109627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461705 | CCCATTTTAACTGTA[C/T]AGTTTGAGTTTTGTC | 80067 |
| rs534181213 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455004 | AAGTTCAGGGGTACA[C/T]GTGCATTATGTGCAG | 80067 |
| rs534185775 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446782 | ATGTAACATTTTTTA[A/T]CAATCCTTTAATCTC | 80067 |
| rs534266970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454140 | GCACCACTACACTCC[A/G]GCCTGGGTGACAGAG | 80067 |
| rs534394499 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481423 | CCAATTGTTGAGGAG[G/T]TAAGTCATTGATGGG | 80067 |
| rs534424697 | snp | C/T | 0.00221324 | 0.0331922 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453089 | TTTCTGAAGTACTTT[C/T]GAGAGCTGCGTGTAA | 80067 |
| rs534430537 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464119 | TTAGAGAATTTCCTC[A/G]CTTTCTAGAACAATA | 80067 |
| rs534464831 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171471561 | TAATTTCAGTGGTTA[C/T]AATCAATCAACATAT | 80067 |
| rs534540269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445229 | TCCCAGGCTCAAGCA[A/G]TTCTCCTGCCTCAGC | 80067 |
| rs534543416 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171489796 | AGCTGGGACTACAGG[C/T]GCCCGCCACCATGCC | 80067 |
| rs534654728 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171475802 | AAGTGTCTGCCTTTA[-/T]TTTTTTATGCTTCGT | 80067 |
| rs534678763 | in-del | -/A | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470475 | GATGTCATGGCCATC[-/A]GGGGACAATGTGTCT | 80067 |
| rs534790743 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171461014 | TTTCAGTGTTTATTT[A/C]ATACTGTAGAGACTT | 80067 |
| rs534805761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171490350 | GAAAGACTCGCTAAA[A/G]TCAGGTCACTAGAAA | 80067 |
| rs534905893 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489648 | CATAATTTCCTAGTT[G/T]TTTTTTTTTTTTTTT | 80067 |
| rs534906173 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481390 | AAAATGCTGGGAACA[G/T]AAAAGGACAGGTTAA | 80067 |
| rs534948496 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491043 | TAAAAATAACAATTC[C/T]TGAGGCCAGGCGCGG | 80067 |
| rs534948599 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483486 | TGCAGCAAGCTTATT[A/G]TTCCTCAATTTTTTA | 80067 |
| rs534954157 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445857 | CCAGCTAATTTTTGT[A/T]TTTTTTGTAGAGGTG | 80067 |
| rs535172332 | snp | A/G | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474284 | GAAAGAAGAGTATTT[A/G]TCTTTGTTCTGAAAG | 80067 |
| rs535205979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488938 | CCAAGCCTATTCTGA[A/G]CAAAAGGGGGCATGT | 80067 |
| rs535234459 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443029 | CTGAAAAGTAATTTG[G/T]GAGTAAAAAAAAAAA | 80067 |
| rs535322644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458285 | GACATTTTCTTTGTC[A/G]TATACATGTGAATTT | 80067 |
| rs535396727 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171445084 | GAAAGTTTTTAATAC[A/G]CTAGTATAAAACACC | 80067 |
| rs535462898 | in-del | -/T | 0.208779 | 0.246578 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489646 | AGCATAATTTCCTAG[-/T]TTTTTTTTTTTTTTT | 80067 |
| rs535465731 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434035 | TGCAGGGCGCACACA[C/T]GGGGCGGAGACCTGG | 80067 |
| rs535518598 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171480443 | CATGTTGTCTCTTTC[C/T]CTACCCTAGTCTTTG | 80067 |
| rs535527907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464620 | GGACTTTAACATATC[C/T]TTTGAGGGAACACAA | 80067 |
| rs535543581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435409 | AAAGCAAAACTACAG[C/T]GCAGGCAAAACCACA | 80067 |
| rs535742583 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433599 | TAGAGACATCGACGA[A/G]GAATATCTTAGGCCG | 80067 |
| rs535795872 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479831 | TATCAAATCTGTAGG[A/T]TACTGCTTAACTCTT | 80067 |
| rs536007093 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455375 | TATTCCCTGGTGTAT[A/T]TGTACAACATTTTCG | 80067 |
| rs536066406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448124 | GCAATATGAATGTCT[A/G]TTCTAGCAGAGAACC | 80067 |
| rs536073936 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171485029 | ACTGTTATGAATAAA[A/G]CTGCTATGAACATTC | 80067 |
| rs536179404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440569 | ACAGAGCGAGACAGT[A/G]TCTCAAAAAATTTTA | 80067 |
| rs536185720 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486528 | CAAGGCTGGTCTCGA[A/T]CTCCTGACCTCAACT | 80067 |
| rs536236377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462704 | AGCAACTTCAGTACT[A/G]GGAATTTATCCCAGA | 80067 |
| rs536239314 | snp | C/G | 0.00199481 | 0.0315187 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491071 | CGGTGGCTCATGCCT[C/G]TAATCCCAACACTTT | 80067 |
| rs536251339 | in-del | -/TCTCTTAG | 0.00993419 | 0.0697739 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451395 | GAGAGATGCTATCTC[-/TCTCTTAG]TCTCTTAGTAATACT | 80067 |
| rs536286669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486494 | TATTTTTAGGAGAGA[G/T]GTGGTTTCACCATGT | 80067 |
| rs536293122 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456210 | TGTAAGGAAGGGGTC[A/G]AGTTTCAATTTTCTG | 80067 |
| rs536449935 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464632 | ATCTTTTGAGGGAAC[A/T]CAAGTCAACTCACAA | 80067 |
| rs536507350 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171453208 | ATTCTAGAGATCAAC[A/G]AAAAGGTAAGAACTC | 80067 |
| rs536557023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477777 | GGCAAGATCGCACCA[C/T]GGCACTCCAGCCTAG | 80067 |
| rs536557848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469146 | ATTTGTATTAACAAT[C/T]TGCAAACAATTTAAA | 80067 |
| rs536596866 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483443 | ATTGCACTCCTGGAT[C/G]TAAGTTTCTGCATTC | 80067 |
| rs536598117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460820 | GGATTACAGGCATGA[A/G]CCACTGTGCCCAGCT | 80067 |
| rs536623497 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437946 | AGTTTCCTAAGGTAG[A/G]AACTTAGATTACGAT | 80067 |
| rs536721271 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467660 | GCTTGAACCCAGGAG[A/G]TGAAGGTTGCAGTGA | 80067 |
| rs536762383 | in-del | -/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171442427 | AAATTAGCTGGGCAT[-/G]GTAGCATGCACCTGT | 80067 |
| rs536785773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446703 | GCAGGATAACAGTGT[A/G]GAGACTGCTAAGTTG | 80067 |
| rs536872322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451599 | TGTTTTGTTTTGAGA[C/T]GGAGTCTCGCTTTGT | 80067 |
| rs536900467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445186 | CTGCAGTGCAGTGGC[A/G]TGATCTCCACTCACT | 80067 |
| rs536943063 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436673 | TCCTTACATATTTTA[C/G]ATACAAGTCCCTTAT | 80067 |
| rs536982323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444379 | AAATTCAAAACTTTT[C/T]GAATGCCGACATGAC | 80067 |
| rs537066061 | snp | C/T | 0.000557258 | 0.0166829 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482645 | TCAGAATAGGATGTC[C/T]TAAGACTTCAGTCAT | 80067 |
| rs537111291 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459258 | CAGAGGTTGTGGTGA[C/G]CCAAGATCATGCCAT | 80067 |
| rs537123658 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171475735 | AGCGCTGTACTCCAG[C/G]CTGGGTAATGGAGTA | 80067 |
| rs537189202 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483979 | ATACTAGATATGTAG[G/T]AAAGTGCTTAATAAT | 80067 |
| rs537344929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444505 | ATATGAAACATAAAT[A/G]AATTTTGTGTTTAGA | 80067 |
| rs537382523 | snp | C/T | 0.00015319 | 0.00875052 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481247 | TTGACTTCAGATGAC[C/T]ATGACTTCTTTTTTA | 80067 |
| rs537392111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452048 | GTTTAAGGAACACAG[A/G]AGGAGTCTGATTTAC | 80067 |
| rs537420856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457524 | AAAGACTATCCAGGG[A/G]CTGGGCACCTCTAAT | 80067 |
| rs537547793 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171471206 | CCTTTTATCACAATT[G/T]TATCACTGTGACATT | 80067 |
| rs537583175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450026 | TCTGCAGATTTGTTA[C/T]GAAAAATCTAATGAT | 80067 |
| rs537635799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463468 | AAAACTTGATAAATC[A/G]GAAGAGATACAGATC | 80067 |
| rs537637925 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471793 | GCCTAGGCAGGCAGA[C/T]GGCTTGAGCCCAGGA | 80067 |
| rs537657779 | snp | A/G | 0.000798403 | 0.0199641 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434618 | TGTGCAGCCGGCTGA[A/G]TCGCCGGGCGCTGGG | 80067 |
| rs537667321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488206 | GACACTCTACCTGCC[A/G]AGATAATATGCATCT | 80067 |
| rs537750481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472440 | TGCCTCGGCCTCCCA[A/G]AGTGCTAGGATTACA | 80067 |
| rs537772678 | snp | C/T | 3.41047e-05 | 0.00412931 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435199 | CAGGTAACTTTTTAT[C/T]GATAATTTTGCTGTA | 80067 |
| rs537824995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449112 | CTACCAGGTTCAAGC[A/G]ATTCTCCTGACTCAG | 80067 |
| rs537869170 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432780 | GTACTGTAAGTACTC[A/G]CTTAATGTCATCAAC | 80067 |
| rs537894508 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441944 | CTTATCATGTCATTA[G/T]CACACCTAGGAAAAT | 80067 |
| rs538108073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457135 | AAAAGTCATGAACTA[A/G]TCAATGTCAGAGTAA | 80067 |
| rs538320871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454250 | AGAATTAAAACAGAT[G/T]GGCTACTTTATTATA | 80067 |
| rs538355806 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171489361 | AAAAGTATATGAAAT[A/G]TACAGAGATGATCCC | 80067 |
| rs538364762 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433535 | AGTTTAGTGTGCTGG[C/G]AACTTTGAACATACA | 80067 |
| rs538620294 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171437841 | TTGTTGATTTTCTCT[A/C]TTGATTTTTGGTTTT | 80067 |
| rs538826790 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491459 | CCACAGATGCAGCTG[C/G]AATTGTGCTGAAAGA | 80067 |
| rs538850846 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454765 | AGCCACGGGTGGTAG[C/T]GCACACCTGTAGTCC | 80067 |
| rs538868578 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483409 | TACAGACGTTACGCT[G/T]AAAAGAGGTGCATTC | 80067 |
| rs538959870 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439071 | CTTATGCTCTCTGAA[A/G]AGAAATCCAAATTAA | 80067 |
| rs538989418 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465146 | GAGGTTGCAGTGAGC[C/T]GAGATTGCGCCACTG | 80067 |
| rs539003683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460670 | CAAGTAGCTGGGACT[A/G]CAGGTGCATGCCACC | 80067 |
| rs539010847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452440 | CCTGTAAAGGAGTCA[A/G]CACAACACTACTTTC | 80067 |
| rs539060650 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444242 | AATAATACTAATAGG[A/T]ATGATGATTATCAAG | 80067 |
| rs539085185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445995 | GCCAAAAACTTTTAA[A/G]TCTTCATGAAACAAC | 80067 |
| rs539178611 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445324 | GACACGGGGTTTCAC[A/C]ATGTTGGCCAGGCTG | 80067 |
| rs539187113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436317 | GGGCATTTATTTTCA[C/T]TTCTCCTAGATTATA | 80067 |
| rs539235134 | in-del | -/AG | 0.000186237 | 0.009648 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484557 | TGCAGATTATTAACT[-/AG]AGTTTAGTATTTATT | 80067 |
| rs539237511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458555 | TAATTATAGTCATCC[A/G]AATGTTTTTCTCATT | 80067 |
| rs539432257 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435639 | CTCATCCACAACTGT[C/T]CAACATGAGGGGGGA | 80067 |
| rs539515187 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465751 | TGGCCTCCCAAGGTG[C/G]TGGGATTACAGACAT | 80067 |
| rs539617957 | snp | C/T | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474726 | TTTCATCAATGTACA[C/T]ACATTTAAACACTTA | 80067 |
| rs539713047 | snp | C/T | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171477323 | ACTTTTCTTTTAGTG[C/T]ATAAATTAAGACCAC | 80067 |
| rs539743471 | snp | A/G | 0.00199203 | 0.0314968 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434550 | CCACTCGGCGGCCCA[A/G]CCTACCCAGGGCCCG | 80067 |
| rs539779986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441746 | CACCACAGACTCACT[A/G]TTCTTACTGAGCAGT | 80067 |
| rs539834426 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472371 | TTTAGTAGAAACAGG[G/T]TTTCATCTTGTTGGC | 80067 |
| rs539862955 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480596 | TGTCTGATATTTCAA[A/C]TATTATAGAATGTCA | 80067 |
| rs539925894 | snp | C/T | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171477428 | GTCAGGTGAATGAGG[C/T]AGCTAATCTATAATC | 80067 |
| rs539926325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465266 | TTCTTTTCTCCTTAG[C/T]GTACAGCCCAGTAAG | 80067 |
| rs539945692 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171449309 | CATCGTGCCCAGCTG[A/T]CATTTATCTTTGTAT | 80067 |
| rs540037677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441242 | ATGGCCTGCTTCTCC[C/T]CTCCTGCACAGTTTT | 80067 |
| rs540049401 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483609 | CAAATTAAGGCACTT[C/G]ACATTCTTCCACCAA | 80067 |
| rs540152787 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434070 | GGCAGCACCGCGCCC[C/T]CAGGGCTCTGCCCAG | 80067 |
| rs540170514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479980 | AAATACAGAAATAAG[C/T]CTACCTGAATAACTG | 80067 |
| rs540187884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476162 | TTCTTTTTTTTTTTG[C/T]ATTTGAGACTTTGAG | 80067 |
| rs540242814 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484242 | CATCTTTTAGAATCC[C/G]AGGGAGCTAATTTCT | 80067 |
| rs540255807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450924 | TGTTGGTAACCTTGG[C/T]TCAAACTCAGGCAGT | 80067 |
| rs540276952 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171433108 | AACCAACCCTTGGAC[A/G]CGACGACATTCCATC | 80067 |
| rs540288434 | snp | C/G | 0.000185787 | 0.00963634 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482591 | CAGCTGCAATGCTGT[C/G]TAAAAGTAGAGTGTT | 80067 |
| rs540305230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486158 | AATTTTAGTTTCATA[A/G]AGAATTTTGGCTACA | 80067 |
| rs540345118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171477113 | GTTTTAGCCCCATGT[A/G]CATTTCAGATTTAAA | 80067 |
| rs540385119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468645 | ACTCACCTGCGGGCC[A/G]CATATACCTCCTGAA | 80067 |
| rs540416017 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462147 | AAAACTTGGGAGAAT[A/C]TTTTTATCTCAGTGT | 80067 |
| rs540447781 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445557 | TAAGTTAGTGTCCAT[C/G]TTTTCCAAGACTCTG | 80067 |
| rs540450815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469242 | CATTTGAAAATTCTT[A/G]TAGCAACAAGAATTT | 80067 |
| rs540455444 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | DCAF17 | GRCh38.p7 | 2:171490793 | AGTGGACAGGAAGCA[A/G]GGAGGACTCAGAGCA | 80067 |
| rs540501078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455465 | AGTGCTGCAGTGAAC[A/G]TATATGTGCATGTGT | 80067 |
| rs540557265 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171448995 | TCTGAGTATAGAGAC[C/T]CTCTATCATTTGTCT | 80067 |
| rs540607648 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438903 | CTATTTTTAAAACAA[-/T]TTTTTTAGAGATAGG | 80067 |
| rs540610334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437898 | TTTGTTATTTCTTTG[C/T]TTACTTTGGATTTAA | 80067 |
| rs540692431 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452724 | CTGCCTTAGCCTCCC[A/T]AAGGGCTGGAATTAT | 80067 |
| rs540874070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438639 | TTCCTTGCCAAATTC[A/G]ACTTTGTCTGAAATT | 80067 |
| rs541103391 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171440668 | AGTAGGAGTTCGGCT[A/G]TGATTATTGTTTGTT | 80067 |
| rs541223174 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482977 | GCAGTGTAACAAACA[C/G]GAGAGCTATGCCCCA | 80067 |
| rs541243124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171436902 | GCCTCAGCCTCCCGA[A/G]TAGCTGGGACTACAG | 80067 |
| rs541263855 | snp | A/T | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432593 | ATTCATGAATTACCA[A/T]ATTAACTATTGTAGC | 80067 |
| rs541383817 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457324 | TCCAAGGTAATTGGA[C/T]ATCTTCCTCTATTCC | 80067 |
| rs541383956 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171472268 | TACTGCAAGCTCTGC[C/G]TCCTGGGTTCAAGCC | 80067 |
| rs541390428 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171442869 | TGGAGTGTGAGAAAC[A/T]GTCTCAAAAAAAAGG | 80067 |
| rs541420635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488290 | AATTTTTTTTGCCAT[A/G]TAGCATTTACCAGCA | 80067 |
| rs541431186 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487643 | GGCCAAGCTGGTCTC[A/T]AACTCCTGACCTCAA | 80067 |
| rs541476501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444537 | TTGGGTCCCATCCCC[A/G]AGATACCTCATTATG | 80067 |
| rs541563210 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464645 | ACACAAGTCAACTCA[C/G]AACAGAGACCCAGAT | 80067 |
| rs541572600 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171462465 | ATTAGGGGAGTGCAA[A/C]GCTCAATGTCACTGA | 80067 |
| rs541600259 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486317 | TTGACGTGCAGTAAA[A/C]ACTTTTTTTTGAGAC | 80067 |
| rs541691886 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487125 | TGGCTGTACCACTTC[A/G]TATTCCCATTATCAG | 80067 |
| rs541718643 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466030 | TCTAAATTAAAAAAA[A/T]TTTTTTTATTTTTAG | 80067 |
| rs541750069 | snp | A/G | 8.28041e-05 | 0.00643391 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171457983 | CAGATTTTTGGGAAC[A/G]TTACAGATGCTACCT | 80067 |
| rs541803582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449208 | AGCTGAGGTTTCCCT[A/G]TGTTGGCCAGGCTGG | 80067 |
| rs541804471 | snp | C/G | 3.41495e-05 | 0.00413202 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480228 | TACAAAGTTGTAAAC[C/G]TTTCCTTTATAGGTG | 80067 |
| rs541812629 | in-del | -/TTGTTGTTGTTGTTATTG | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448354 | CTGTTATTGTTGTTA[-/TTGTTGTTGTTGTTATTG]TTGTTATCACAGAGG | 80067 |
| rs541816086 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171437016 | CAGCTTCAGGTGATC[C/T]GGCCACCTCGGCCTC | 80067 |
| rs541891871 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456506 | TTTGGTTCCATAGGA[A/T]TTCTAAAATAGTTTT | 80067 |
| rs541926993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472060 | ATAGAAAGCACTTAC[A/G]ATATAACCCCAGCCT | 80067 |
| rs541928890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455670 | CCACAACCTTGCCAG[C/T]ATCTGTTATTTTTTG | 80067 |
| rs541979057 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444387 | AACTTTTTGAATGCC[A/G]ACATGACGCCACAAG | 80067 |
| rs541992811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448411 | ATGACTAACATTTGT[A/G]AATACTTAATAAAAT | 80067 |
| rs542014019 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477453 | ATAATCTTTTAAATA[A/C]TTTTTTTTTTGCCCA | 80067 |
| rs542114598 | snp | A/G | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475211 | TATGGCCCAGCTTCA[A/G]TGTCACTTTTCCACA | 80067 |
| rs542149184 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432990 | TATACATACATTTAA[G/T]GAAGATTAATAAAAA | 80067 |
| rs542245455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446460 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG | 80067 |
| rs542277063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439476 | TCTTCATTTCTCTTA[C/T]GGTGTTTTTTGATTT | 80067 |
| rs542292070 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171488265 | AAAAGAAAATTACCA[A/G]TAATTTAGCAATTTT | 80067 |
| rs542314932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447437 | ACGATCTCAGCTCAC[C/T]GCAACCTCCACCTCC | 80067 |
| rs542527502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453571 | AAATATTTCATTTTA[A/C]TTGCAAGATATAGGT | 80067 |
| rs542529090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478204 | AGTTGGGTGGGGTTG[C/T]GCATGCTATTTCAAC | 80067 |
| rs542580604 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171459313 | GCGAAACTCCATCTC[A/G]AAAAAAAAGAAAAGA | 80067 |
| rs542589096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454429 | AGCTGGGACTACAGG[C/T]GCCTGCCACCACACC | 80067 |
| rs542617286 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171490662 | AGTATGTGTGAGATG[A/G]GTTGGGAAGAATTTA | 80067 |
| rs542728508 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438369 | GTTTGATCCAGTTGA[-/CT]GATGGTACCTTTCAG | 80067 |
| rs542840789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451796 | GGCCAGCATGGTCTC[A/G]ATCTCTTGACCTCCC | 80067 |
| rs542880694 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489905 | ATCCGCCTGCCTCAG[A/C]CTCCCGAAGTGCTGG | 80067 |
| rs543009717 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466376 | TTTTAATTAATCATA[A/T]TATTTGTTTTCTTTT | 80067 |
| rs543124117 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466995 | TTTTATTGCTTAAAA[G/T]ACCTTTATATATTAA | 80067 |
| rs543136730 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484206 | TTTCTTCTCCTTCTT[A/T]CCATGTTTACTTATA | 80067 |
| rs543313879 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462347 | GGGCAATTTCCTTAA[-/T]ATGTGAAGGGTTCTA | 80067 |
| rs543380542 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481603 | TGTGAGAACATTATT[G/T]TGAGCCCAAAATGTG | 80067 |
| rs543402469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474215 | TGCAAGTAAAAGGGA[A/G]TTACAGACTGGCCCT | 80067 |
| rs543437696 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457862 | AATGCTAGGCGGCAG[G/T]GTTATCATAGTGACA | 80067 |
| rs543512244 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458985 | TAGTAAAAATGTTCT[A/G]TATTTAGCTTATGAA | 80067 |
| rs543701650 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436747 | CTTTTTACTTTCCTG[A/G]TGTTATTGTTTGAAA | 80067 |
| rs543776027 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171479887 | TAGGCATATAAACAG[A/G]TACATTTCTACCTAT | 80067 |
| rs543927389 | snp | G/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434147 | CTCCGCGGGCCGGAG[G/T]AGGCGGGGCCGCGGC | 80067 |
| rs544000774 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441120 | TCCCATTTGCCTTTC[A/G]TCACAAACTCCACAG | 80067 |
| rs544067815 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452883 | AAATGTTTACTTTTA[C/T]GGATTTTTGTCTGTA | 80067 |
| rs544072566 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460946 | TGTAAAAAAAAATAA[A/T]TCAATGATTTTTGTA | 80067 |
| rs544137502 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464968 | TGGGAGGCCAAGGCA[G/T]GTGGATCACTTGAGG | 80067 |
| rs544185320 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486934 | GTTTGTTTATACTGT[A/G]GCCTTTCGATGGACA | 80067 |
| rs544311698 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171469850 | TCACTGTGTCATCCA[C/T]GCTGGAGTACAGTGG | 80067 |
| rs544322305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479317 | CAAGATGTACCTTCC[C/T]GTGGTCTATTCCTGG | 80067 |
| rs544336519 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433708 | CAATTATCGCAAAAC[C/T]AGTCAGTGTCCCCGC | 80067 |
| rs544389543 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462315 | CAGGAGACATAGTTA[C/G]AAATCATACTGTAAT | 80067 |
| rs544460029 | in-del | -/TA | 0.0483228 | 0.147737 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464854 | AACTTTATCCTACTA[-/TA]TATATATATGATAGT | 80067 |
| rs544468117 | snp | A/G | 0.000199302 | 0.00998056 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484476 | TTATTTTCCTATCCA[A/G]CGTACTTTTTGATGG | 80067 |
| rs544477043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440340 | CAGCACTTTTGGAGG[A/C]CAACGTCTGGGGTTG | 80067 |
| rs544477314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448345 | ATTTTAAGAGCTGTT[A/G]TTGTTGTTATTGTTA | 80067 |
| rs544545158 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439413 | ATCTTCAAACTCACT[G/T]ATTCTGTCCTTGGCT | 80067 |
| rs544666489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462951 | GAAGGAGGAGTTTTA[A/G]CTGGGCATAGTGGCT | 80067 |
| rs544669884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446336 | GCAGATCACGAGATC[A/G]GGTGTTCAAGACCAG | 80067 |
| rs544901449 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484202 | ATATTTTCTTCTCCT[C/T]CTTACCATGTTTACT | 80067 |
| rs544916220 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485456 | ATGGGATACATTGCT[C/T]ATCAAAGAACCCTGA | 80067 |
| rs545061800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489834 | TTTTTTGTATTTTTA[A/G]TACAGACGGGGTTTC | 80067 |
| rs545106801 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171462024 | GTTAATATATTATGA[A/G]TATTTCCATCTAGAT | 80067 |
| rs545128647 | snp | C/T | | | intron-variant, upstream-variant-2KB | METTL8, DCAF17 | GRCh38.p7 | 2:171432197 | GGGTAGGTCTCCAGC[C/T]GCGGAGGTCTCCAGT | 80067 |
| rs545198408 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483123 | GATAGCAAAGAATGT[C/G]GGGAATTTGGATACC | 80067 |
| rs545262031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458940 | GAGTGCCAAATCACA[A/G]AAAGAAAATTATATA | 80067 |
| rs545278792 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482359 | TTATATTAAAATCTT[C/T]CCATTTTTTTTTTCA | 80067 |
| rs545333554 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467858 | GTATAGCTCTAAGTA[C/G]TACATTGTCCTTATG | 80067 |
| rs545393430 | snp | A/G | 0.000554888 | 0.0166474 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481494 | TGTTTGTTAAGGCTA[A/G]GAAAGACAGGGAGAG | 80067 |
| rs545423176 | in-del | -/A | 0.27278 | 0.24896 | intron-variant, upstream-variant-2KB | METTL8, DCAF17 | GRCh38.p7 | 2:171432226 | TGGCAAAGCAACGTC[-/A]AAAAAAAAAAAATCC | 80067 |
| rs545524020 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171453408 | CTGCATGTTTTTATG[A/C]CTCTCAGGTGGATCA | 80067 |
| rs545542679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487861 | CACTGCACCCGGCCA[A/G]AGACACAAATACTAA | 80067 |
| rs545574290 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450187 | AGCTAAGCCTTGAGG[A/T]TGCAAAGGCATAAGA | 80067 |
| rs545584750 | in-del | -/T | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436635 | TGCCCACTTGTAAAT[-/T]TTTTTTTTTTTTTTT | 80067 |
| rs545680857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451721 | GCTGGGACTACAGGC[A/G]TGCACCACCAGGCCC | 80067 |
| rs545683663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459463 | TCACATGAGTAAACT[A/G]AAAGAGAAAATTTTC | 80067 |
| rs545730842 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476231 | TAAACAGATTTCTGT[-/G]GGTGGTGAGCAAATT | 80067 |
| rs545730956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171434937 | AAAGTTGGTCACCTC[A/G]TTAAGCCAAAACATG | 80067 |
| rs545753413 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488349 | CAATTAAGTATTTTT[A/T]ATTTTCTCTTAAAAG | 80067 |
| rs545782469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456652 | GGAGTGTTTTTCCAT[C/T]TGTTTGTGTCATCTT | 80067 |
| rs545867807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464777 | ACTTCCAAATTTAGC[C/T]GTTCTTTTTTGATTA | 80067 |
| rs545893671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457286 | TGGCAAAGTAATAAA[C/G]TGTTTCTATTTATTC | 80067 |
| rs545959064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441572 | GCAGCTGGGGACTGG[A/G]TGAGAAATGCTGTCA | 80067 |
| rs546120602 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434301 | CGGCCGGCCGCGCGG[C/T]ACCGGAGCGTCGCAC | 80067 |
| rs546204414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463834 | AGCTTTAACTCATCA[A/G]CTAGAGATAAACTGT | 80067 |
| rs546383560 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171473469 | AAACAACATACACCA[A/G]AAAAAATTGGGCAAA | 80067 |
| rs546417932 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432307 | AAATGGTGAGGCCCT[A/T]AATTACTTAGGTGAA | 80067 |
| rs546458357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478330 | GATTAGCTTATTGTT[C/T]TGTTTTATTTTGTAT | 80067 |
| rs546491870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471005 | TTTGGTATTTGTGAG[A/G]GGTCCTGGAAGCAAT | 80067 |
| rs546582830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476691 | TCTCCGAATTTGAAG[A/G]AGTTCATGGACATTT | 80067 |
| rs546672144 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171476252 | TGAGCAAATTATTTT[A/C]TTTTCTTTTAATAGG | 80067 |
| rs546693558 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477520 | ATTTTTGAGCCGGGC[A/G]TGGTGGCTCACACCT | 80067 |
| rs546718315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467476 | GGCGGATCGCTTGTG[A/G]CCAGGAGTTTGAGAC | 80067 |
| rs546776106 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483312 | CTTAACAGGTACTAG[G/T]GACAGGTACAAAACA | 80067 |
| rs546826435 | in-del | -/T | 0.402277 | 0.198272 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477453 | TAATCTTTTAAATAA[-/T]TTTTTTTTTTGCCCA | 80067 |
| rs546836512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439028 | GCCACCAGAACACTT[C/T]AGGTATTTATGTCTC | 80067 |
| rs546842001 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453067 | TTCAACTAATGAAAA[A/C]AGTGTGTTTCTGAAG | 80067 |
| rs546863765 | snp | C/T | 0.000743494 | 0.0192664 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483780 | GCCATTATCTTTCCC[C/T]TTTGTACAAATGAGG | 80067 |
| rs546878583 | in-del | -/CTC | 0.000626392 | 0.0176863 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449860 | CAAATAAATAAACTT[-/CTC]TTCATTCTTTTAAAA | 80067 |
| rs546917416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446534 | CTGGGTGACAGAGCA[A/G]GACTCTGTCTCAAAA | 80067 |
| rs546924513 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467982 | CCTCATAAACTAAAA[A/T]TTAAATTCTCAAGTT | 80067 |
| rs546955387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474818 | TACAAAATATTTTTT[A/C]AATCTGCCTGTTTCT | 80067 |
| rs547052388 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489679 | TTTTTTGAAACAGAG[G/T]CTTGCTGTGTCACCC | 80067 |
| rs547054118 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171479731 | CAGCAGTTGAATACT[C/T]TTTTAAATTTAGAGA | 80067 |
| rs547139570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436244 | AGACATTGGTGTTTC[C/T]ACCTTTTAGCTATTA | 80067 |
| rs547149974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437282 | GTATAAGGTAGGTAT[A/C]CAACTCCATTTTTTT | 80067 |
| rs547221291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489929 | GTGCTGGGATTACAG[A/G]CGTGAGCTGCCGTGC | 80067 |
| rs547229928 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465724 | ACCTGACCTCAGGCA[A/G]TCTACCCACTTTGGC | 80067 |
| rs547306608 | snp | A/G | 1.65638e-05 | 0.00287778 | missense, intron-variant | DCAF17 | GRCh38.p7 | 2:171458414 | TGTGCATGCAGATGG[A/G]GTGGGACTACTGGAA | 80067 |
| rs547425322 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171467395 | TAGTTAAGTTTTGGG[A/G]AAGTCAAAAGTTTGG | 80067 |
| rs547443043 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433600 | AGAGACATCGACGAG[A/G]AATATCTTAGGCCGT | 80067 |
| rs547737458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441715 | TGGGAAGGAAGGGAC[C/T]ATGCCCTGGTTCAGA | 80067 |
| rs547797988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480561 | AGCATGCGGGATTCC[C/T]AGGTACTCTTGTATA | 80067 |
| rs547798075 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488675 | GAATCCAGTGTAGAC[G/T]TGAAGAAGTCCTTCG | 80067 |
| rs547829286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471300 | AAAATGTAAGCAGCC[A/G]AACTTAAGATTTCAG | 80067 |
| rs547860315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488006 | TATCAGAAATACTTC[A/G]TATCTAAAGTAGTAT | 80067 |
| rs547873154 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466854 | AATTCCAACTCTAAT[A/T]GTATGTTTTTCTTTT | 80067 |
| rs547884737 | snp | A/G | 3.35706e-05 | 0.00409685 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481150 | CCTAAGAGACTTTTA[A/G]CCAAACACCCCAGCA | 80067 |
| rs547885748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479586 | TATGATGGGTTATCC[A/G]TCCTTCTAGAAATGA | 80067 |
| rs547897132 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433488 | GGACTTAGAGCATGG[C/T]GGTGGGACACATGTG | 80067 |
| rs547967533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486400 | CTGCAACCTCTGCCT[C/G]TCGGGTTCAAGTGAT | 80067 |
| rs547996978 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434071 | GCAGCACCGCGCCCC[C/T]AGGGCTCTGCCCAGC | 80067 |
| rs548001768 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457474 | TTAAATATTGTTACT[G/T]GGGATTGAAGAACAT | 80067 |
| rs548027989 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171485876 | GTGCCAAAGTTTGCA[G/T]GTTCAGTTCCTTTCC | 80067 |
| rs548040918 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465058 | AAAAATTTAGCCAGG[C/T]GTGGTGGTGTGCACT | 80067 |
| rs548168260 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454912 | TTTGAATTGCACAAG[C/T]CCTCTTTTTCTTCTT | 80067 |
| rs548320769 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464556 | ACTTGATTATATCTG[A/T]AAAGATCCTATTTGC | 80067 |
| rs548508621 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439990 | AGGCGTTGCTTTGTT[G/T]CCCAGGCTAGAGTGC | 80067 |
| rs548552704 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433421 | GAGCACCTATGAACA[A/T]GAGGTAGCATGCCCA | 80067 |
| rs548554440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438098 | ATTTTTAAATTTCTC[C/T]TGGGACTTCTTTGAC | 80067 |
| rs548635850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439805 | TGGTGGCACACACCC[A/G]TAATCCCAGCTACTC | 80067 |
| rs548644452 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466155 | AGGCGTGAGCCACCA[C/T]ACCTGGGCAAATTTT | 80067 |
| rs548684828 | snp | A/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483980 | TACTAGATATGTAGG[A/G/T]AAGTGCTTAATAATC | 80067 |
| rs548714528 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171462368 | AAGGGTTCTATAGAT[C/T]AATAAGAAAAGGAGT | 80067 |
| rs548783917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171475802 | GAAGTGTCTGCCTTT[A/G]TTTTTTATGCTTCGT | 80067 |
| rs548980756 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491268 | AGGTTGCAGTGAGCC[A/G]AGATCATGCCACTGT | 80067 |
| rs549018643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445206 | CTCCACTCACTGCAA[C/T]CTCTGCCTCCCAGGC | 80067 |
| rs549045934 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171490985 | AAAACTTGGATCCTG[A/G]GCTCAGATTTCTTCA | 80067 |
| rs549058894 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171454859 | CCAGGATTGTGCCAC[A/G]GCAACAGAGCAAAAC | 80067 |
| rs549071606 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433413 | CTTTCTTTGAGCACC[C/T]ATGAACAAGAGGTAG | 80067 |
| rs549116176 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482993 | GAGAGCTATGCCCCA[A/G]CTAAAAGGAGCAGCT | 80067 |
| rs549151463 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473785 | GTACCTTTGACCTAC[A/T]GATCTATCACTTGGG | 80067 |
| rs549232032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460094 | CTTTGGGAGGCTGAG[A/G]CGGGTGGATCACGAG | 80067 |
| rs549268222 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452905 | TTGTCTGTATATATG[C/T]GCATGTGTGTCTGAA | 80067 |
| rs549315318 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474641 | AAAATGTATATACCA[A/G]CCTCAACCTCTCATC | 80067 |
| rs549352660 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466715 | TTCTTTTTAAGTACA[C/T]CTGTTTGTACTGTTT | 80067 |
| rs549364274 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483271 | CCTGATATTTTAATT[C/T]GAGACTCTAGCTACA | 80067 |
| rs549506154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458261 | TAAACAGAAAGGCCA[C/T]TGGAAAAAGACATTT | 80067 |
| rs549522285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472229 | CTGTTGCCCAGGCTG[A/G]AGTGCAGTGGCACGA | 80067 |
| rs549586389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443925 | TCTTAGTGTTTAAGA[A/G]ATCATTCCACTCAAT | 80067 |
| rs549586409 | snp | C/T | 1.71849e-05 | 0.00293124 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435208 | TTTTATTGATAATTT[C/T]GCTGTAATTCACCTC | 80067 |
| rs549618622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450739 | CTACTTCAGCTGTTT[C/G]TCACTAGTGTCCTTG | 80067 |
| rs549683571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465109 | AGGCTGAGGCAGGAG[A/G]ATCGCATGAACCCGG | 80067 |
| rs549824244 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466714 | TTTCTTTTTAAGTAC[A/G]TCTGTTTGTACTGTT | 80067 |
| rs549875768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442920 | TTATGATCACATCTC[A/G]ACTAATCAGAGAAGT | 80067 |
| rs549908851 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434017 | GAGGGAGGGATCCCT[A/C]AGTGCAGGGCGCACA | 80067 |
| rs550175967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448608 | ATATTTAGCTATTTT[C/T]TTTGGACATTGATTA | 80067 |
| rs550217470 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479799 | TACTTTGAGATCTAC[A/C]TAGACTTGGTTTTGT | 80067 |
| rs550218844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456763 | AATGAGAGTTTGTTC[A/G]TTATTTAACTCTTGG | 80067 |
| rs550309951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486336 | TTTTTTTGAGACAGA[A/C]TCTCGCTCTGTCACC | 80067 |
| rs550313377 | snp | A/C | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469696 | ACTCTTAAAGGAAAC[A/C]TGTAGAAAAATAAGA | 80067 |
| rs550324713 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433287 | GTAGCCCCGGTAGGA[A/T]ATTATTATTTTTTCT | 80067 |
| rs550395679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463990 | ATAAACACAATAGAC[C/T]TGTGGATTTTTTATT | 80067 |
| rs550441690 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171437415 | ACACTTTTGGATTTA[C/T]TTCCGGACGTTCAAG | 80067 |
| rs550461974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448104 | TGTGGTAAAGGAAAA[A/G]GGGGGCAATATGAAT | 80067 |
| rs550595793 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468666 | ACCTCCTGAAAACAG[A/T]TACCTAGAAAGTTGA | 80067 |
| rs550661528 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171479262 | GTGATTGAGGGAAAC[A/G]TGCTATGCCTGTCTT | 80067 |
| rs550704035 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171446555 | TGTCTCAAAAGAAAA[A/G]AAAAAAATCTAGGAG | 80067 |
| rs550734481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460736 | AGATGGTGTTTCACT[A/G]TGTTGCTCAATTTGG | 80067 |
| rs550770853 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454764 | TAGCCACGGGTGGTA[G/T]TGCACACCTGTAGTC | 80067 |
| rs550776802 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439076 | GCTCTCTGAAGAGAA[A/G]TCCAAATTAATTCTT | 80067 |
| rs550778606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171447069 | AACACTGTTTTCCTG[A/G]GTTTGTTTTGGGTAT | 80067 |
| rs550808832 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432429 | GTGGTGAAATAAAGG[C/T]CACAAGAAAGAAGAC | 80067 |
| rs550819523 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171485778 | GCAAATTAGTATATT[A/C]AAATTTTAGAGGTGC | 80067 |
| rs550947160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445081 | TGAGAAAGTTTTTAA[C/T]ACACTAGTATAAAAC | 80067 |
| rs550952423 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461518 | AAACATTATAGTCCT[C/T]TTACATGGGGTTAAC | 80067 |
| rs550953804 | snp | C/T | 1.66023e-05 | 0.00288113 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171449927 | TGCAGTTAAGTCAGC[C/T]CAGAACAGAGGCTCA | 80067 |
| rs551029145 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437959 | AGAAACTTAGATTAC[G/T]ATTTGAAGTCTTTCT | 80067 |
| rs551232988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437389 | CCTTGTCAAAAATCA[A/G]TTGACCATAGACACT | 80067 |
| rs551234155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451997 | CAACAAGTAGTAGCT[C/T]TTAGTTGGGGTATAT | 80067 |
| rs551324817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466581 | AATTTTTAGGCCTTT[C/T]TCATTGAGAATATTA | 80067 |
| rs551578164 | in-del | -/AT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455719 | TCTGACTGGTGTGAA[-/AT]ATGGTACCTCATTGT | 80067 |
| rs551601332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467283 | AATTAAGAAAAAGGT[A/G]CATGATGAGTGCATC | 80067 |
| rs551665679 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459852 | ACAAACTGAATTAGG[C/T]AGTTGTATGAAAATT | 80067 |
| rs551697665 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171451631 | GCCAGGCTAGAGTGT[C/G]GTGGTGAGCTCTCAG | 80067 |
| rs551788116 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481991 | GAAAAGTGGATAAAG[A/C]GTCCCAGAAGAAGTT | 80067 |
| rs551794459 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472184 | ACTTTTGGTTTTTTT[G/T]TTTGTTTTGTTTTGA | 80067 |
| rs551802113 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481219 | CTCCAGTATTTTCCA[A/G]AAAAGTCTTGTGTTG | 80067 |
| rs551838634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465067 | GCCAGGCGTGGTGGT[A/G]TGCACTTGTAATCCC | 80067 |
| rs551979370 | snp | A/G | 3.31609e-05 | 0.00407177 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458112 | CATGTTACTATTAGC[A/G]TGAGTTTTCGACTAA | 80067 |
| rs551994956 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441769 | TGAGCAGTAGTAGGT[G/T]TTCTTGAATAAATGT | 80067 |
| rs552031635 | snp | C/G | 4.98004e-05 | 0.00498976 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171449916 | CAAGAAGTCATTGCA[C/G]TTAAGTCAGCTCAGA | 80067 |
| rs552065111 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433953 | GCACCTGGCCAGAAC[C/T]TCCCAGGGCGAAGGT | 80067 |
| rs552078259 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471478 | AACAATCTCCTAAAA[A/T]GATATGTATAGTATG | 80067 |
| rs552107381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442855 | ATTGCACTCCAGCCT[A/G]GAGTGTGAGAAACTG | 80067 |
| rs552158631 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439701 | GGGAGGACTAGGTGG[A/G]CAGATCACTTGAGGC | 80067 |
| rs552186608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464488 | AATCTCTTTCTCCTT[A/G]TAAGGACACCAGTCA | 80067 |
| rs552191433 | snp | C/T | 0.00835141 | 0.0640778 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491056 | TCTTGAGGCCAGGCG[C/T]GGTGGCTCATGCCTG | 80067 |
| rs552259441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448541 | TTCCTTGTCTTAATT[C/T]TCTAGTTGGGCATTT | 80067 |
| rs552357150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440925 | CTATGAGGACAGACG[A/G]GTGGCACTTCCAGGC | 80067 |
| rs552359713 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432651 | ACCGTATGCTGTAAA[A/T]AAGTCATGAAAAATC | 80067 |
| rs552364687 | snp | C/T | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475598 | AGTGAGACTTCGTCT[C/T]TACAAAAAATAAAAA | 80067 |
| rs552389517 | in-del | -/AAA | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443034 | AAGTAATTTGGGAGT[-/AAA]AAAAAAAACCATAAA | 80067 |
| rs552411783 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470434 | GCAGGTCAGCATAGC[A/G]TTGGGTCCATTTGTC | 80067 |
| rs552441166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470235 | GCTGTGTTTCCCTGG[A/G]TAGTCTCAAACTCCT | 80067 |
| rs552607309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463172 | GGAGACAGAGGTTGC[A/G]GTGAGTGAGACTGCG | 80067 |
| rs552622322 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171454313 | TTTTTGAGACAGAGT[C/T]TTGCTCTGTCACCCA | 80067 |
| rs552646421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440490 | TGAGGTGGGAGGATC[A/G]CTTGAGCCCAGGAGG | 80067 |
| rs552659232 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472006 | TGCAACAGAGTGAGA[A/C]CCTGTCTCAAAAAAT | 80067 |
| rs552769867 | snp | C/T | 1.64789e-05 | 0.0028704 | synonymous-codon, nc-transcript-variant, missense | DCAF17 | GRCh38.p7 | 2:171468904 | CATGCCACCACTGCT[C/T]TTTGAGGTGTCATCC | 80067 |
| rs552834335 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171442771 | TGTAGTCCCAGTTAC[G/T]TGGGAGGCTGAGGCA | 80067 |
| rs552908569 | snp | A/G | | | intron-variant, synonymous-codon, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469453 | TCTGGTGGTCACAGT[A/G]TAGGTAAATTGAAGC | 80067 |
| rs552997031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438278 | TTTTATGGCTCAGAA[C/T]GTGGTCTACCTTGGT | 80067 |
| rs553054579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171475851 | CTGGATCTATTTAAT[A/G]TAAGGAAGATGAAAG | 80067 |
| rs553124977 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437540 | ATTAACCATTGAAAG[C/G]ATCTGGGCTTGGCAC | 80067 |
| rs553144343 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489797 | GCTGGGACTACAGGC[G/T]CCCGCCACCATGCCT | 80067 |
| rs553179661 | snp | A/G | 0.000185925 | 0.00963993 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483494 | GCTTATTGTTCCTCA[A/G]TTTTTTACAATATTT | 80067 |
| rs553199100 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482186 | TGTTTCTTTGTGCTT[C/T]CTGTTTGAGAAATTC | 80067 |
| rs553207698 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444557 | ACCTCATTATGCATA[A/T]GCAAATATCCCCAAA | 80067 |
| rs553254539 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466031 | CTAAATTAAAAAAAA[A/T]TTTTTTATTTTTAGT | 80067 |
| rs553290006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475201 | ATTCATATTTTATGG[C/T]CCAGCTTCAATGTCA | 80067 |
| rs553291279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473370 | AGCACTTTAAGAGGC[C/T]AAGGTGAGAGGATCA | 80067 |
| rs553327446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480783 | CTTTTTATTCTCTAT[A/G]TTTTGTAGAATGCCT | 80067 |
| rs553382751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450754 | CTCACTAGTGTCCTT[C/G]ATTGCAAAACAGGCA | 80067 |
| rs553390785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488300 | GCCATATAGCATTTA[C/T]CAGCAAATGCTCTGT | 80067 |
| rs553441289 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171456080 | TTTTCATCATGAAAT[C/G]TTTGCCCATGCCTAT | 80067 |
| rs553474811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488960 | GGGGCATGTGGTCAC[A/C]CTAGCTAGAGCTAAT | 80067 |
| rs553481368 | in-del | -/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171434997 | TTTTAAAATAATATA[-/G]GTGACATTATGTTGC | 80067 |
| rs553547741 | snp | A/C | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474809 | TTATTTTGCTACAAA[A/C]TATTTTTTAAATCTG | 80067 |
| rs553605267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466765 | GAATTCCTATGTCCT[C/T]TATATTGAATTTCAT | 80067 |
| rs553663312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450163 | TGTATTTTCTCACTC[A/G]TAAGTGAGAGCTAAG | 80067 |
| rs553680509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458830 | TCGATGAAATTTACC[C/T]CCTCTCTAAGAAAGG | 80067 |
| rs553844924 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471937 | AGAGAATTGATTGAG[G/T]CCAAGAGGTCAAGGC | 80067 |
| rs553882769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449253 | CCTCAAGTGATCTGC[C/T]CACCTCAGCCTCCTA | 80067 |
| rs553952238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464640 | AGGGAACACAAGTCA[A/G]CTCACAACAGAGACC | 80067 |
| rs554006456 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434038 | AGGGCGCACACACGG[G/T]GCGGAGACCTGGAGG | 80067 |
| rs554021068 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171463601 | ATGTTCAGAACTTGA[C/T]CTATATGCCATTTTA | 80067 |
| rs554256533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479833 | TCAAATCTGTAGGAT[A/G]CTGCTTAACTCTTGA | 80067 |
| rs554370577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440118 | ACAGTCACATACCAT[C/T]GCACCTGGCTTAATC | 80067 |
| rs554423280 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171489841 | TATTTTTAGTACAGA[C/T]GGGGTTTCACCATGT | 80067 |
| rs554435887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479170 | TATAAATTTTTATGT[C/T]TTAGGGTGGTAAAGG | 80067 |
| rs554465329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487478 | ACCCAGGCTGGAGTG[C/T]GGTGGCTCAATCTCA | 80067 |
| rs554485915 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461079 | TCTTAAGGTCTATAC[A/T]AATAGTATTTATTTT | 80067 |
| rs554530382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486578 | TCCAAAGTAAACTGC[A/G]TGTATTTAAAGTACA | 80067 |
| rs554578435 | snp | A/G | 0.00597247 | 0.0543191 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491079 | CATGCCTGTAATCCC[A/G]ACACTTTGGGAGGCC | 80067 |
| rs554603193 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171485041 | AAAGCTGCTATGAAC[A/T]TTCTTAGACAATTCT | 80067 |
| rs554638208 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439749 | CCTGGCCAACATGGC[A/G]AAACCCCATCTCTAC | 80067 |
| rs554684015 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443255 | AACAACGTCCAGGTA[C/T]GTATATGTATATAAA | 80067 |
| rs554714031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469221 | CCCATAATTTTAAAA[C/T]GTTAACATTTGAAAA | 80067 |
| rs554722494 | in-del | -/T | 0.0298928 | 0.118545 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443832 | TAAAATTAGATAGAT[-/T]TTTTTTTAGATCCTG | 80067 |
| rs554723042 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456103 | ATGCCTATGTCCAGA[A/T]TGATATTGCCTAGGT | 80067 |
| rs554752609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171477036 | TATTTGCCTTTGAGT[C/G]TAGCAGAAAACAACA | 80067 |
| rs554760110 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464698 | GATATCTTTACTTTT[A/G]GGTCCTTTAAATGAA | 80067 |
| rs554778073 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473800 | GATCTATCACTTGGG[-/T]TTAGATTTGTAAAAT | 80067 |
| rs554785149 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468231 | TACAGTGTCAGTCTT[A/C]AAAAGAAACTGACTG | 80067 |
| rs554820519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452642 | TATTTTTTGTATAAA[C/T]GAGGTCTCACTATTT | 80067 |
| rs554830342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459085 | GAGGCTGAGGCGGGC[A/G]GATCACTTGAGGTTG | 80067 |
| rs554900224 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171445123 | AGTAACCTAATTCCT[A/G]TTCTCACTATTTTTT | 80067 |
| rs554974149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446255 | CTCTTATAAGAAATA[C/T]CTAGGAGAGTGGCCA | 80067 |
| rs554993459 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438523 | GCCACATTGTGTTTT[C/G]ATACTCTGTTGTTAG | 80067 |
| rs555023452 | snp | A/G | 0.153997 | 0.230832 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467728 | GAGCGAGACTGTCTC[A/G]AAAAAAAAAAAAAAA | 80067 |
| rs555071998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474223 | AAAGGGAATTACAGA[C/G]TGGCCCTTTCTCATC | 80067 |
| rs555075493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468342 | TGTGACAGGCCCTTT[C/T]CTAAGTGGTTACATT | 80067 |
| rs555101975 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439170 | ACTTTTGATTTTCTG[A/C]AGTTTGAATATGCTT | 80067 |
| rs555214723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437419 | TTTTGGATTTATTTC[C/T]GGACGTTCAAGTCTG | 80067 |
| rs555253518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436718 | CAAATACTTTCTCCC[A/G]TTGTGTAGATTGTCT | 80067 |
| rs555309774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474895 | GCCAAGGCTACAGTA[A/G]TAGCCCACTCCAGGG | 80067 |
| rs555557787 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450747 | GCTGTTTCTCACTAG[G/T]GTCCTTGATTGCAAA | 80067 |
| rs555570887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451616 | GAGTCTCGCTTTGTT[A/G]CCAGGCTAGAGTGTC | 80067 |
| rs555648311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472474 | GTAAGCCACTGCCCC[C/T]GGCCGATTAACACTT | 80067 |
| rs555659349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171490253 | CCAGTTATGTGTGTT[A/G]TTATAATTATATATT | 80067 |
| rs555678442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475338 | TAAATTATTTTTGTG[A/G]TCTTCTGCTTAAATA | 80067 |
| rs555720199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489752 | TGCCTCCCAGGTTCA[C/T]GCCATTCTCCTGCCT | 80067 |
| rs555729249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480701 | CTCGTAAATGATCAC[A/G]CAGTGAGATAGATAA | 80067 |
| rs555752961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458640 | ATAATGAATAAGCTT[C/T]GAGGAAAATCTGTCA | 80067 |
| rs555764158 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171448545 | TTGTCTTAATTCTCT[A/G]GTTGGGCATTTAATC | 80067 |
| rs555897425 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464566 | ATCTGTAAAGATCCT[A/G]TTTGCAAATAAAGTC | 80067 |
| rs555918350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459300 | CTGGGCAACAAGAGC[A/G]AAACTCCATCTCAAA | 80067 |
| rs555983484 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471806 | GATGGCTTGAGCCCA[A/G]GAGTTCAAGATCAGC | 80067 |
| rs555985454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463489 | GATACAGATCAAAGG[A/G]AGACTTAGTTTTCAT | 80067 |
| rs556018297 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171485792 | TCAAATTTTAGAGGT[A/G]CACAAAATTTCAGAA | 80067 |
| rs556077580 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465358 | ACCAGCATGACCTAA[G/T]TAGATTCATTTGTTT | 80067 |
| rs556120131 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450071 | GCATGCTGTAAAAGA[G/T]AGGATTCACGGCAAC | 80067 |
| rs556174287 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171456917 | ATACAGGATCATGTC[A/G]TTTGAAAAGAGGGAT | 80067 |
| rs556210490 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171458162 | GTGAGATGCTTTTAG[A/C]GTAAGGCACTTCTGT | 80067 |
| rs556252318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479114 | AGGCAAAAAGGAAAT[A/G]ACGTAAAAGTACATT | 80067 |
| rs556269367 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434664 | CGCAGGCGTGGTGCA[A/G]AGGACCAACCTGGGC | 80067 |
| rs556273300 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171456632 | TTCTTCCTAACCATG[A/G]ACATGGAGTGTTTTT | 80067 |
| rs556282420 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456390 | CAGTACCATGCTGTT[G/T]TGGTTACTGTAGCCC | 80067 |
| rs556292920 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171490136 | TAAAATATTGCACAA[A/G]CCAAACAAAATTAAC | 80067 |
| rs556306122 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434151 | GCGGGCCGGAGGAGG[C/G]GGGGCCGCGGCAGGC | 80067 |
| rs556334670 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483937 | AGGCATGTTATTTTA[G/T]CCCAATTTAGCATAC | 80067 |
| rs556403631 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481915 | TCTTGTTTAGGCAAT[A/G]TTTGCATACTTATGC | 80067 |
| rs556414428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440561 | CCTGAGCAACAGAGC[A/G]AGACAGTGTCTCAAA | 80067 |
| rs556450333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440026 | CTTTTCACAGGTATG[A/G]TAATAGTGCACTGTA | 80067 |
| rs556712418 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476136 | GGACACATAGCTGCT[G/T]CTCTCTGCTGTTCTT | 80067 |
| rs556892870 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171437226 | ATAGTTTTAGCTCAT[A/G]TTTAGGTGGTTGATC | 80067 |
| rs556905701 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171460302 | CACTCTAGCCTGGGC[C/G]ATTGAGCGAGATTCC | 80067 |
| rs557077848 | snp | A/G | 1.66043e-05 | 0.00288129 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171453142 | GGCATTCAACAACAT[A/G]TTTTGCTGTACCTTG | 80067 |
| rs557112123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462635 | CAACAATTTGTCAAT[A/C]TGACAGTTTGTTAAT | 80067 |
| rs557162290 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484187 | ATATTAATCATTTTT[A/G]TATTTTCTTCTCCTT | 80067 |
| rs557163159 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171475972 | AGTTTGAACTTAAGA[A/T]AACAAGGCCCACGAA | 80067 |
| rs557179037 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474835 | ATCTGCCTGTTTCTG[C/T]CCTTGGCCACTGTCT | 80067 |
| rs557380578 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491064 | CCAGGCGCGGTGGCT[C/T]ATGCCTGTAATCCCA | 80067 |
| rs557386554 | in-del | -/AACTC | 0.0119091 | 0.0762411 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464809 | ATTTGTATTTCTCTT[-/AACTC]ATACTGAGCTTCTTG | 80067 |
| rs557412009 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171448061 | TGCATTTTGCCAGTT[C/T]TGACTTCCATCTAAA | 80067 |
| rs557414648 | snp | C/T | 3.51377e-05 | 0.00419137 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473990 | AGTGAGTAATCTCAT[C/T]AGCACTTGAAAGTTA | 80067 |
| rs557497811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446107 | AAAAAAAAAATCTTA[C/T]AGCCAGTATTTTAAG | 80067 |
| rs557538919 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171471262 | ACTCCCCACCTGTTA[G/T]TCAGAAGAGTAGATA | 80067 |
| rs557553711 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171451711 | CTCCTGAGTAGCTGG[A/G]ACTACAGGCGTGCAC | 80067 |
| rs557567549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450197 | TGAGGATGCAAAGGC[A/G]TAAGAATGATACAAT | 80067 |
| rs557602002 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444304 | TTCCTTGTTTAAGGA[A/G]TATTTCTAAGTACAG | 80067 |
| rs557654316 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460193 | CTAGGCACGGTGGCA[A/G]GCACCTGTAATCCCA | 80067 |
| rs557721212 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489215 | CTCCCTCAAATTAAC[C/T]TAGCCGTTAAGGTCT | 80067 |
| rs557740051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435667 | GGAAGGAAAGCCACA[A/G]TGCATCCCCATATAC | 80067 |
| rs557741620 | snp | A/G | 0.000299965 | 0.0122431 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478076 | AGAACAAGAGGTATT[A/G]CTTTGGCCAGAGATG | 80067 |
| rs557827863 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465284 | ACAGCCCAGTAAGTA[A/T]ACACATGGAGTGATG | 80067 |
| rs557882558 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455042 | ATATAGATAAACATG[C/T]GTCATGGGGGTTTGT | 80067 |
| rs557969150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458568 | CCAAATGTTTTTCTC[A/G]TTTATTTAAAAAACT | 80067 |
| rs558011410 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452847 | ATTCAAAATATAAAT[G/T]CATGGTATTTTATTG | 80067 |
| rs558110059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487514 | TTCCAGCCTCCGCCT[C/T]CCGGATTCAAGAGAT | 80067 |
| rs558214306 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443246 | TTTTTGGAAAACAAC[A/G]TCCAGGTACGTATAT | 80067 |
| rs558253684 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465759 | CAAGGTGCTGGGATT[A/G]CAGACATGGGCCACT | 80067 |
| rs558293396 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470578 | GGCCCAGCCCAGTGA[C/T]GTTCTCTTTTATAAA | 80067 |
| rs558352470 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171477891 | GTGGATGTGGGAGAA[G/T]GGTTGGTAAGTTTTA | 80067 |
| rs558379842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478838 | GGACCATACAAACCT[A/G]TTGAGAACAAAGAAG | 80067 |
| rs558413527 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171458734 | TCACTTTACTTTTCT[C/G]ATCCTTGATTTCCTT | 80067 |
| rs558420029 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171472491 | GCCGATTAACACTTC[C/T]GTACTTTCGATTTTA | 80067 |
| rs558455849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480608 | CAACTATTATAGAAT[A/G]TCAAAGTTGTAAGGA | 80067 |
| rs558474116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471963 | AAGGCTCCAGTGAGC[C/T]GAGATCACACCACTG | 80067 |
| rs558497757 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171445426 | CACCATGCCCGGTCC[A/G]TATTCTCACTTATTT | 80067 |
| rs558583535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448313 | AGAGGACTCTTAATC[A/G]CTATGCTATATACAT | 80067 |
| rs558629141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440664 | TCTGAGTAGGAGTTC[A/G]GCTATGATTATTGTT | 80067 |
| rs558656819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441243 | TGGCCTGCTTCTCCC[C/G]TCCTGCACAGTTTTT | 80067 |
| rs558671317 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435625 | GTTTAACAGTCAGCC[C/T]CATCCACAACTGTCC | 80067 |
| rs558672427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439976 | AAAAACAAGAAATGA[A/G]GCGTTGCTTTGTTGC | 80067 |
| rs558679662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454143 | CCACTACACTCCAGC[C/G]TGGGTGACAGAGTTA | 80067 |
| rs558689227 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171465154 | AGTGAGCCGAGATTG[C/T]GCCACTGCACTCCAG | 80067 |
| rs558760770 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453291 | TTAATTATTTATGAG[A/T]TATTTGATTGGAAAT | 80067 |
| rs558763801 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469776 | GGGGGGAGTTCCATT[G/T]TTATTTTGTATTGCT | 80067 |
| rs558823030 | in-del | -/TAGCTTGTTGTTGGGTGCTTCC | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474081 | ATTAATGGAAATAAT[-/TAGCTTGTTGTTGGGTGCTTCC]TCAGAGACTGGCATA | 80067 |
| rs558883439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451887 | ATTCTATACGTTATC[A/G]TATGTTAATGTTTTA | 80067 |
| rs559044308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452739 | AAAGGGCTGGAATTA[C/T]AGGCGTGAGCTACCT | 80067 |
| rs559047356 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460408 | AAGAATTGACCTGGA[G/T]TTTTATCCCTTTTTT | 80067 |
| rs559176507 | snp | C/T | 0.000942892 | 0.0216923 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481256 | GATGACTATGACTTC[C/T]TTTTTAAACTCTTGC | 80067 |
| rs559254880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466497 | CATCCTTGCTTTCTC[A/G]AAACAACAGATTGTC | 80067 |
| rs559294724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473616 | GATATGGTATCTCTT[A/G]GGTTATTAACTCCTG | 80067 |
| rs559347711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459781 | AGTTCAAGTAAGTTA[C/T]TCATGAAGTTCAAAA | 80067 |
| rs559419889 | snp | A/C | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474701 | CCTGATACCTTCTTA[A/C]CAATTTGTCTTTCAT | 80067 |
| rs559441907 | snp | C/T | 1.65715e-05 | 0.00287845 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435136 | CAGGTCACCTATAGC[C/T]TATGAGAGAGGAAGA | 80067 |
| rs559529466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442781 | GTTACTTGGGAGGCT[A/G]AGGCAGGACAATTAC | 80067 |
| rs559562563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474488 | TTAGTTTGCTTTCAT[A/G]TTCTTCCTTCTCTAC | 80067 |
| rs559634416 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446092 | AGGGTTAATAAACTT[-/A]AAAAAAAAATCTTAT | 80067 |
| rs559653501 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443830 | TTTTAAAATTAGATA[A/G]ATTTTTTTTAGATCC | 80067 |
| rs559813030 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488689 | CTTGAAGAAGTCCTT[C/G]GGCCTCACTGCCACA | 80067 |
| rs559813785 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435823 | GAGCTTTTTTTATAG[C/G]CTTTATTAGGATATA | 80067 |
| rs559825523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451003 | TTGAAATTTCTGTAA[C/T]ATGGACTGGCAGGTG | 80067 |
| rs559841645 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465217 | AGGAAAAAAAAAAAA[A/T]AGTATGGGGTGAAGG | 80067 |
| rs559868985 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472162 | CTATATGGATTAGCA[C/T]GTCTATACTTTTGGT | 80067 |
| rs559965972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487658 | AAACTCCTGACCTCA[A/G]GTGATCCACTCACCT | 80067 |
| rs559966266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479592 | GGGTTATCCGTCCTT[C/G]TAGAAATGACTGTGT | 80067 |
| rs560036514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457516 | CATGCATGAAAGACT[A/G]TCCAGGGGCTGGGCA | 80067 |
| rs560037343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, missense, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469395 | GGTTCTGCTTCTCCA[C/T]GGCTTGTTGCTCTTT | 80067 |
| rs560066295 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450531 | ATTTATATCAAGAAA[C/T]TTTTTGTTTCTATTG | 80067 |
| rs560080976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463814 | GGCATTTTTCTAGAA[A/C]TAAAAGCTTTAACTC | 80067 |
| rs560115340 | snp | C/T | | | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485179 | CCCCAAAGGATTGTA[C/T]GATTTTACATGCTTG | 80067 |
| rs560117192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463102 | CAGGTGTGGTGGCGA[G/T]CACCTGTGATCCCAG | 80067 |
| rs560178345 | in-del | -/T | 0.453158 | 0.145695 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482669 | CAGTCATGTCAGAGA[-/T]TTTTTTTTTTAGGTG | 80067 |
| rs560180113 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472596 | TGTTCACTTGGATAT[A/C]TGGTGCATGGGTCAA | 80067 |
| rs560191426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456544 | TCTGTGAAGAACATC[A/C]GTGGTAGTTTAATGG | 80067 |
| rs560219922 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434290 | GAGAGCGGCTCCGGC[C/T]GGCCGCGCGGTACCG | 80067 |
| rs560230950 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171449453 | AGGCTAGTCTGTTTC[A/G]GTTAAATTGTCTGCT | 80067 |
| rs560341112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | METTL8, DCAF17 | GRCh38.p7 | 2:171432200 | TAGGTCTCCAGCTGC[A/G]GAGGTCTCCAGTGGC | 80067 |
| rs560378979 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453556 | TGAAAAGTTGCAACA[A/G]AATATTTCATTTTAA | 80067 |
| rs560469533 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433879 | GGAAAGCCGCGGGGC[G/T]TACCTTTAGCACGGG | 80067 |
| rs560750679 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477465 | ATAATTTTTTTTTTG[C/T]CCATTCTGGCATTTT | 80067 |
| rs560865625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469496 | TAAGGATATTCTTAA[C/G]TTATTTATGGCAGAG | 80067 |
| rs560893561 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491346 | AGAAAAGAAAAAAAG[A/G]AGTCACTGAATGTGT | 80067 |
| rs560929511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468607 | TTACCATCATAAACA[C/T]CTTTAGCCCAGTTTC | 80067 |
| rs560982558 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483607 | GACAAATTAAGGCAC[C/T]TCACATTCTTCCACC | 80067 |
| rs561028337 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461363 | ACCCAGGAGGCAGAG[A/G]TTGCAGTGAGCCGAG | 80067 |
| rs561142552 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453666 | CAGTTTTGGGTTTTA[A/T]TGTTGTTCCCATTTG | 80067 |
| rs561149943 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435963 | CTTCAAAACAGAACC[A/G]TGTACCTTTAAGCAG | 80067 |
| rs561216195 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476128 | CACTCTCTGGACACA[A/T]AGCTGCTTCTCTCTG | 80067 |
| rs561245876 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483272 | CTGATATTTTAATTC[A/G]AGACTCTAGCTACAT | 80067 |
| rs561246125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171490685 | AGAATTTATGATTCC[C/T]CAGCTCTTATCTGCC | 80067 |
| rs561258160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489906 | TCCGCCTGCCTCAGC[C/T]TCCCGAAGTGCTGGG | 80067 |
| rs561349447 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472402 | CACGCTAGTCTCAAA[C/T]TCCTGACCTCAAGTG | 80067 |
| rs561353653 | in-del | -/A | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433478 | ACCCTTAAGGGACTT[-/A]AGAGCATGGCGGTGG | 80067 |
| rs561418749 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469557 | GAAATTTCTACCCTT[C/T]GAATTCATTTTTATT | 80067 |
| rs561424358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467924 | CATGTGACTCTTACA[C/T]GAATCATCTTCCTAA | 80067 |
| rs561426821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459600 | TTTTAGGTGAAATGC[C/T]AAAGGATTTTCTAAT | 80067 |
| rs561464300 | in-del | -/AG | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470282 | CCCTCTTGATATATC[-/AG]AAGAATTTGCTTTTT | 80067 |
| rs561530297 | snp | C/T | | | utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171490897 | CTTGGTAGCAGTGGC[C/T]GGAACAAGAGAATAG | 80067 |
| rs561572203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451832 | CCTGGGATTTACAGG[C/T]GTGAACCACCACTCC | 80067 |
| rs561578559 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487584 | GTGCACCATCATGCC[C/T]AGCTAATTTTGTATT | 80067 |
| rs561581338 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437157 | ATATCTAAGAATCCA[C/T]TGCAAAATTTGAGGT | 80067 |
| rs561610173 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451239 | ATTTGTTGGCTACTT[C/G]TACTTACTTTTTATC | 80067 |
| rs561860473 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472853 | TAGGAAATATGGCAT[C/G]ATTTCATTTTACATT | 80067 |
| rs561860874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442599 | GAAAGAAAGAAAAGC[A/G]CCAGGCGAAGTGGCT | 80067 |
| rs562068823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450413 | AAATATTTTAAAAAA[A/G]AAAAGTTGATAGGTA | 80067 |
| rs562224841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457439 | ATAATAGAAAAATAT[A/G]CAATTAGAGAGATTT | 80067 |
| rs562446314 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171446461 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 80067 |
| rs562494018 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433289 | AGCCCCGGTAGGAAA[C/T]TATTATTTTTTCTCA | 80067 |
| rs562503998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440866 | AATTCTCTGATGGAT[C/T]TAAGAATAATTATGG | 80067 |
| rs562561033 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471286 | GTAGATAACTAAAAA[A/T]AATGTAAGCAGCCGA | 80067 |
| rs562583654 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455603 | CACTGTCTTCCATAA[A/T]GGTCAGACTAATTTC | 80067 |
| rs562621312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462964 | TAACTGGGCATAGTG[G/T]CTCATGCCTGTAATC | 80067 |
| rs562667641 | snp | C/T | | | missense | DCAF17 | GRCh38.p7 | 2:171490780 | TCACCTTGACATCAG[C/T]GGACAGGAAGCAAGG | 80067 |
| rs562680439 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485530 | GGGCACGTGTTCCAC[C/T]GTTTCACATGACTAC | 80067 |
| rs562741876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439437 | CTTGGCTGCATCCAG[C/T]TTACTGATAACTGTT | 80067 |
| rs562745014 | in-del | -/A | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171478979 | CTGTATCATGAGATT[-/A]AAAAAACAAAATATT | 80067 |
| rs562777402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438849 | TGAAGCAATCCGACC[A/G]TCTCAGCCTCCCAAG | 80067 |
| rs562823924 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448354 | GCTGTTATTGTTGTT[A/T]TTGTTATCACAGAGG | 80067 |
| rs562904612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445737 | GCCTAAGCTGGAGTC[C/T]AGTGGCACAATCACA | 80067 |
| rs562907751 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433414 | TTTCTTTGAGCACCT[A/G]TGAACAAGAGGTAGC | 80067 |
| rs562975130 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487635 | ACCATGTTGGCCAAG[C/G]TGGTCTCAAACTCCT | 80067 |
| rs563032683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171477288 | TAAAAATCACATACC[A/G]TACTTTAACTCCAGA | 80067 |
| rs563067231 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446371 | ACCAACATAGTGAAA[C/G]CCCGTCTCTACTAAA | 80067 |
| rs563182452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461214 | CTTTAGGAGGCTGAC[A/G]CGGGCAGATCACTTG | 80067 |
| rs563343046 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452875 | TTGCTAAGAAATGTT[A/G/T]ACTTTTATGGATTTT | 80067 |
| rs563442393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467886 | ATGAAGATGCTTAAT[A/G]AAGTATGCACTTCTG | 80067 |
| rs563477835 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467390 | ATTAGTAGTTAAGTT[G/T]TGGGGAAGTCAAAAG | 80067 |
| rs563502790 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466646 | ACATTAGAGTTGTGG[A/G]CAGAGTAATAGTGCT | 80067 |
| rs563545725 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488583 | AAAGAGCAAAACCAG[G/T]GAGAAGTAAAGGAAT | 80067 |
| rs563570005 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436063 | TATTCTGTACTTTTC[A/G]TATAAATGGAATCAT | 80067 |
| rs563582079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | DCAF17 | GRCh38.p7 | 2:171460472 | AGTCTGCTGACTAGT[A/G]AGGGTGACACTCTGC | 80067 |
| rs563600482 | snp | A/G | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475274 | GCCCATCATATTTTC[A/G]TTGCACCCACTGTGT | 80067 |
| rs563672232 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437063 | ACAGGCATGAGCCAC[C/T]GCGTCCAGCCACAGA | 80067 |
| rs563710970 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444689 | TAAGAAATGCACTTA[G/T]GAAATACTACAACAG | 80067 |
| rs563734605 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489850 | TACAGACGGGGTTTC[A/G]CCATGTTAGCCAGGA | 80067 |
| rs563816056 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443368 | TTTTATATGAATTAT[A/G]TGATCAGAAAAAAAT | 80067 |
| rs563821948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489448 | GGACATATAGCTGAC[A/G]ATATTACCTGCTACA | 80067 |
| rs563884404 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171468701 | GCCTAATTTAGGTTC[C/T]GACTGGCTGTTTCTT | 80067 |
| rs563895625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465546 | TGGAGTGCAGTGGCG[C/T]GATCTCAGCTGACTG | 80067 |
| rs563994911 | snp | A/T | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475507 | TTGGTGGTTTAGGCC[A/T]ATAATCCTGCACTTT | 80067 |
| rs563995326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443903 | AGCATAAGCTAATGT[A/G]TAATTATCTTAGTGT | 80067 |
| rs564120655 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434315 | GTACCGGAGCGTCGC[A/C]CTGTCAGCGGCCAGA | 80067 |
| rs564181497 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant, frameshift-variant | DCAF17 | GRCh38.p7 | 2:171460440 | AGAAAGAAGACTGGA[-/T]TTGGGATCAGAATTT | 80067 |
| rs564264742 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449298 | CAGGCGTGAGCCATC[A/G]TGCCCAGCTGTCATT | 80067 |
| rs564361141 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480907 | CATAGGTACTGTGAC[A/T]TTTTAGTAACACAGT | 80067 |
| rs564412407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171434980 | AGGAAGGATGCAAAA[A/C]GTTTTAAAATAATAT | 80067 |
| rs564678896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470269 | CTCAAGTGATCCTCC[C/T]TCTTGATATATCAGA | 80067 |
| rs564711572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479302 | TGCCAGGCATTCAGC[C/G]AAGATGTACCTTCCT | 80067 |
| rs564722538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440270 | TTTTGGTTGAGGGCT[A/G]TATATGATATGATAT | 80067 |
| rs564845982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486306 | TTAAAGTATAATTGA[C/T]GTGCAGTAAACACTT | 80067 |
| rs565016238 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171437276 | TATAGGGTATAAGGT[A/G]GGTATCCAACTCCAT | 80067 |
| rs565022695 | snp | A/G | | | intron-variant, upstream-variant-2KB | METTL8, DCAF17 | GRCh38.p7 | 2:171432218 | GGTCTCCAGTGGCAA[A/G]GCAACGTCAAAAAAA | 80067 |
| rs565065854 | snp | C/T | 0.000928764 | 0.0215295 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482484 | TGTATCTAAATAGTC[C/T]CACTCAGTAAACTTA | 80067 |
| rs565134241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446319 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACGAGAT | 80067 |
| rs565191054 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484273 | GGTCCCTGTGTTGCT[A/G]TCAAATCTGTATCTT | 80067 |
| rs565197695 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171447029 | GTTAATTTCAGCTTC[A/G]TAGAGATTTCTGACC | 80067 |
| rs565231911 | in-del | -/ATT | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438652 | TCGACTTTGTCTGAA[-/ATT]AGTATAGCTACTCCA | 80067 |
| rs565242724 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171461236 | GATCACTTGAGGTCA[A/G]GAGTGCAAGACCAGC | 80067 |
| rs565352365 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171462165 | TTTATCTCAGTGTGG[A/G]GAAGACCTTTTTAAG | 80067 |
| rs565366563 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461463 | AAATAAAATAAAATT[A/T]AAAAATTGGGAAATA | 80067 |
| rs565373821 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461352 | GAATTGCTTGAACCC[A/C]GGAGGCAGAGGTTGC | 80067 |
| rs565430048 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482189 | TTCTTTGTGCTTCCT[C/G]TTTGAGAAATTCAGT | 80067 |
| rs565456627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438663 | TGAAATTAGTATAGC[G/T]ACTCCAGCTTTCTTT | 80067 |
| rs565504510 | snp | A/C | 0.000399281 | 0.0141238 | missense | DCAF17 | GRCh38.p7 | 2:171490809 | GGAGGACTCAGAGCA[A/C]CATGACGTACATGAA | 80067 |
| rs565583463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443163 | CAATAGTTTTTGATC[C/T]TGATGGAATTCAACA | 80067 |
| rs565629539 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489930 | TGCTGGGATTACAGG[C/T]GTGAGCTGCCGTGCC | 80067 |
| rs565667994 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171460935 | TCATTTGTCATTGTA[A/G]AAAAAAATAATTCAA | 80067 |
| rs565773827 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489684 | TGAAACAGAGTCTTG[C/T]TGTGTCACCCAGGCT | 80067 |
| rs565877766 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465748 | CTTTGGCCTCCCAAG[G/T]TGCTGGGATTACAGA | 80067 |
| rs566075362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472303 | TCCTGCCTCAGCCTC[C/T]TGAGTAGCTGGGATT | 80067 |
| rs566095351 | snp | A/C | 0.00266109 | 0.0363794 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434593 | ATGGGCCCGACCCGG[A/C]AGCCCAACGTGTGCA | 80067 |
| rs566098911 | snp | A/G | 0.000389029 | 0.0139414 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434519 | GCGGCTGCCCAGCAC[A/G]GGAGTGTGGGGCGCG | 80067 |
| rs566100145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441149 | AGATTTTGTTAGTGC[C/T]CCTAGGCCTTAACTT | 80067 |
| rs566107784 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480590 | TACATTTGTCTGATA[G/T]TTCAACTATTATAGA | 80067 |
| rs566193671 | snp | A/G | 0.000252634 | 0.0112362 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481155 | GAGACTTTTAGCCAA[A/G]CACCCCAGCAGCTGC | 80067 |
| rs566237798 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449736 | AGAGGAAATTTTTTT[A/T]GCTATTTATTTTTTA | 80067 |
| rs566345467 | in-del | -/C | 0.00018596 | 0.00964082 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484680 | CCTGTGTAACCCAAA[-/C]CCTTTCCAAAATTTA | 80067 |
| rs566356306 | snp | A/T | 0.081446 | 0.184634 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463225 | ATGGAGCGAGATTTT[A/T]AAAAAAAAAAAAAAA | 80067 |
| rs566438639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464355 | AGGGAAGAATCCTTT[C/T]TTACCCCTTCTCGCT | 80067 |
| rs566448282 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455310 | ATGGCCTCTGGCTCC[A/G]TCCACGTCCCTGCAA | 80067 |
| rs566450407 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456145 | GTTTTTATAGTTTTG[C/G]GTTTTAGATTTAAGT | 80067 |
| rs566474935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471348 | TCTCTATTAAACTGA[A/G]CTTTAAAATCTAACA | 80067 |
| rs566531136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171454937 | CTTCTTTTACTTTTT[A/C]TTTCTTTTTTTAAAG | 80067 |
| rs566558838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456869 | TGCTTATCAGTTTAA[A/G]AAGCTTTTGGATTAG | 80067 |
| rs566616418 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF17 | GRCh38.p7 | 2:171485901 | CTTTCCTCATTATAA[A/C]CTGAGTCCTATAGAA | 80067 |
| rs566626735 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433444 | CATGCCCAAGTCCAC[C/G]TGGGAGATACAGCGG | 80067 |
| rs566697586 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461697 | AAAATGCACCCATTT[A/T]AACTGTACAGTTTGA | 80067 |
| rs566724506 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171447166 | ATTTAGTGGTGTATA[A/C/G]TGTGTTATTCAATTA | 80067 |
| rs566727657 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445035 | TCCATTTTCATTGGG[A/G]AGTATGGGGGAAGAC | 80067 |
| rs566819227 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452326 | TGTTTTACATTTCAC[A/G]GTGGCAAGAAATTGG | 80067 |
| rs566963506 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468808 | GATGTTGCATGCAAA[G/T]AAAGGTTGAATTCAG | 80067 |
| rs567179720 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171485669 | ATAACAGGTGAAATC[A/G]GGTGAATTTTTTTTC | 80067 |
| rs567201727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437532 | TTGGTGGAATTAACC[A/G]TTGAAAGCATCTGGG | 80067 |
| rs567248500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476681 | TTTAACAGAATCTCC[A/G]AATTTGAAGGAGTTC | 80067 |
| rs567261343 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486318 | TGACGTGCAGTAAAC[A/T]CTTTTTTTTGAGACA | 80067 |
| rs567330302 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483898 | GAACTTGTGCCAAAT[C/T]TCCTCCAAAGTTCTC | 80067 |
| rs567354606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468280 | TAAAGTTAACTTGTC[G/T]GATGATAATAGTGGT | 80067 |
| rs567391438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171475815 | TTATTTTTTATGCTT[C/T]GTAGTAATCAGTCTA | 80067 |
| rs567421835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445226 | GCCTCCCAGGCTCAA[A/G]CAATTCTCCTGCCTC | 80067 |
| rs567432616 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452993 | TGCAATCTAGATAGA[G/T]GGTTGTTTTCATAAT | 80067 |
| rs567678064 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466735 | TTGTACTGTTTTTTT[C/T]TTTTTTTCTATTTTG | 80067 |
| rs567805062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488923 | GACAACAGGCAAAAA[C/T]CAAGCCTATTCTGAG | 80067 |
| rs567828953 | in-del | -/ATT | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435003 | AATAATATAGGTGAC[-/ATT]ATGTTGCTTTGAAAA | 80067 |
| rs567854403 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171473141 | ATGTCTGAGGCTTTA[A/G]GTTTGTTTACATGTT | 80067 |
| rs567899805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473789 | CTTTGACCTACTGAT[C/T]TATCACTTGGGTTAG | 80067 |
| rs567913500 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464702 | TCTTTACTTTTAGGT[A/C]CTTTAAATGAACAGA | 80067 |
| rs567960772 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482123 | CTTGACTTTTAATAA[A/T]CATTCTTTAGAATGT | 80067 |
| rs567961274 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171450851 | ACTTTTATCATCCCA[C/T]TTTACAGGTGAGGAT | 80067 |
| rs568095705 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439840 | GGCCAAGGCAGAAGA[A/C]TTGCTTGAATCTGGG | 80067 |
| rs568119132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442285 | GAAAAGGGGCTGGGC[A/G]CAGTGGCTCACGCCT | 80067 |
| rs568129129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442983 | GATATAGCATTCAAT[A/G]TTGGCAGAAGTATAA | 80067 |
| rs568412550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171471880 | ATTAGCCAAGTGTGG[G/T]GGTGCACACCTGTGG | 80067 |
| rs568473548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479817 | GACTTGGTTTTGTTT[A/G]TCAAATCTGTAGGAT | 80067 |
| rs568524207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448120 | GGGGGCAATATGAAT[A/G]TCTATTCTAGCAGAG | 80067 |
| rs568539517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480552 | CCATATCTAAGCATG[C/T]GGGATTCCCAGGTAC | 80067 |
| rs568577543 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487978 | CAGAAGGATCATATA[A/C]TGAATAAAATTATAT | 80067 |
| rs568712419 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448661 | CAGTTTCATTTTTAT[A/C]TCTCTCTTTTTTTTT | 80067 |
| rs568871544 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171489450 | ACATATAGCTGACGA[C/T]ATTACCTGCTACACA | 80067 |
| rs568917322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461520 | ACATTATAGTCCTCT[C/T]ACATGGGGTTAACTG | 80067 |
| rs568965389 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463217 | CCTGGGCGATGGAGC[A/G]AGATTTTAAAAAAAA | 80067 |
| rs569108215 | snp | A/G | 0.000928419 | 0.0215255 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483079 | TTGTTAACAAGATAG[A/G]TGGTAAAAAGATGCC | 80067 |
| rs569112947 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439089 | AAATCCAAATTAATT[A/C]TTATTGTTCCCCTAT | 80067 |
| rs569124184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453970 | AGTAATATTAGTTAC[C/T]GTTCATTGCTTATTT | 80067 |
| rs569143715 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171449683 | AAAGATTAAAATTAT[C/G]TATGTATTTAAATAG | 80067 |
| rs569269640 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484629 | AAATGTACAAATCTT[A/C]AGTATAAATTTACTG | 80067 |
| rs569350621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446674 | GGTTCTTTTTAGGTT[C/T]CCAGGGGAAAAGAGC | 80067 |
| rs569351632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445149 | TTTTTTTTTTTGAGA[C/T]GGTCTCTCTTTGTTG | 80067 |
| rs569365698 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474836 | TCTGCCTGTTTCTGC[C/T]CTTGGCCACTGTCTT | 80067 |
| rs569368314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171475720 | GTGAGCTATGATTGT[A/G]GCGCTGTACTCCAGC | 80067 |
| rs569527272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460817 | CTGGGATTACAGGCA[C/T]GAGCCACTGTGCCCA | 80067 |
| rs569592254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444319 | ATATTTCTAAGTACA[A/G]GTTGAGCATCCCTAA | 80067 |
| rs569647129 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483942 | TGTTATTTTATCCCA[A/G]TTTAGCATACCAACA | 80067 |
| rs569741110 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483423 | TGAAAAGAGGTGCAT[C/T]CTGCATTGCACTCCT | 80067 |
| rs569741194 | in-del | -/TAGC | 0.00438332 | 0.0466095 | intron-variant | DCAF17 | GRCh38.p7 | 2:171442971 | TTCACATCAAAGATA[-/TAGC]TAGCATTCAATATTG | 80067 |
| rs569798338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451578 | GCAAGAATTTTTGTT[C/T]TGTTTTGTTTTGTTT | 80067 |
| rs569813251 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441480 | GGTAGATCCTCCATC[C/G]CATGAATAGGGGCTG | 80067 |
| rs569829713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452013 | TTAGTTGGGGTATAT[A/C]AACTGTACTTTTCCT | 80067 |
| rs569837138 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171459248 | ACCTAGGAGGCAGAG[C/G]TTGTGGTGAGCCAAG | 80067 |
| rs569982209 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482050 | CCAGAGAAAATTTTT[G/T]GCTTACTTATGGAAC | 80067 |
| rs570009200 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171467932 | TCTTACACGAATCAT[A/C]TTCCTAAGACAAGCC | 80067 |
| rs570110822 | snp | A/G | 0.000376081 | 0.0137076 | synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434604 | CCGGAAGCCCAACGT[A/G]TGCAGCCGGCTGAGT | 80067 |
| rs570156060 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466592 | CTTTTTCATTGAGAA[G/T]ATTAGAGATCAAAAT | 80067 |
| rs570192863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473767 | TAATATTTTTTCTTC[C/T]GTGTACCTTTGACCT | 80067 |
| rs570194607 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171465815 | TTGCTTTCTGTTTTT[A/C]TTTTTTATTATTTCC | 80067 |
| rs570247437 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444749 | GTCCTTTAGGAAAAA[C/T]GGAACTCATAATATG | 80067 |
| rs570309863 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171442637 | GTCATCCCAACACTT[C/T]GGGAGGCTGAGGCAG | 80067 |
| rs570310881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171441900 | CTCTTCATGCCCTCA[G/T]GCTGGAAGTGGAAAT | 80067 |
| rs570329676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171470646 | TGGTTTGATTGGTCA[C/T]CTCCCAGTGAGTGGA | 80067 |
| rs570361743 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457072 | TGGTTTTCAAGGGGA[A/G]TGACAAGATGTCTTT | 80067 |
| rs570407510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472219 | GGGTTTTACTCTGTT[A/G]CCCAGGCTGGAGTGC | 80067 |
| rs570572964 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171470808 | TCATACACAAACACA[C/T]GCACACGTACAGATA | 80067 |
| rs570607958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452101 | AAATTTATCCCTTTG[A/G]AAGGGAGAATCTTTT | 80067 |
| rs570661340 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433982 | GTCGGGGCCGAGAAG[C/T]TTGTGAGTACCGGGG | 80067 |
| rs570795368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171447306 | TCTTCATTCTTTTCT[A/G]TTCACTTTTTGGCCT | 80067 |
| rs570823292 | snp | A/G | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171477322 | TACTTTTCTTTTAGT[A/G]TATAAATTAAGACCA | 80067 |
| rs570919658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487316 | TAGTAGCATCTCAAT[A/G]TGGTTTAAATTTACA | 80067 |
| rs570927632 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455155 | ACCCTCCACCCTCCG[A/G]TAGGCCCGAGTGTGT | 80067 |
| rs570933938 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171472677 | TTATTTTTTGTTTAT[A/G]TTTCTGCCTCCCCCT | 80067 |
| rs571107792 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455871 | GGGTTGTTTTTTTTT[C/T]TTGTAAATTTGTTGA | 80067 |
| rs571203985 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477455 | ATCTTTTAAATAATT[-/G]TTTTTTTTGCCCATT | 80067 |
| rs571316654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461743 | TACATCCATGAAATC[A/G]CCACTACAGTCAAGA | 80067 |
| rs571398618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477658 | TTAGCCAGGCATGGT[A/G]GTGTATGCCTGTAGC | 80067 |
| rs571424135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446535 | TGGGTGACAGAGCAA[A/G]ACTCTGTCTCAAAAG | 80067 |
| rs571444202 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484884 | TAATGTTTTTGAGAT[G/T]TATTCATGTTGTTGC | 80067 |
| rs571456378 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491452 | AGGAACACCACAGAT[A/G]CAGCTGGAATTGTGC | 80067 |
| rs571521701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460640 | GGCTCAAGTGATCAT[C/T]CTACATTAGCCTCCC | 80067 |
| rs571537121 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483368 | AATGCAAGCCCAGGT[A/G]AAGCAGGGTAGCTTC | 80067 |
| rs571639144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171452437 | TTTCCTGTAAAGGAG[G/T]CAGCACAACACTACT | 80067 |
| rs571640785 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474822 | AAATATTTTTTAAAT[C/G]TGCCTGTTTCTGCCC | 80067 |
| rs571675645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480821 | TAATAATCTGCATAT[C/T]CACAAATAATGAAAA | 80067 |
| rs571765992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473392 | AGAGGATCACTTGAG[A/G]CCAGGAGTTTGATAC | 80067 |
| rs571781472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437340 | CACCATTTATTAGAA[A/G]GACTTTTCTTTCTTC | 80067 |
| rs571812082 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455746 | TTGTGGTTTTGATTT[A/G]CATTTCTCTAATGAT | 80067 |
| rs571876266 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171485991 | CATGCTGTGAACACT[-/A]AGCTCTCAGATAGAA | 80067 |
| rs571903626 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435465 | TTAGTCTACTTATAC[C/G]ACAGTCAAGAAATCC | 80067 |
| rs571905094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467504 | GACCAGCCTGGCCAA[C/T]GTAGTGAAACCCTGT | 80067 |
| rs571916717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449271 | CCTCAGCCTCCTAAA[G/T]TTCTGGGATTACAGG | 80067 |
| rs572052207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171434932 | TTCTAAAAGTTGGTC[A/G]CCTCATTAAGCCAAA | 80067 |
| rs572203710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457268 | ACAACAGAAATGAAC[A/G]TGTGGCAAAGTAATA | 80067 |
| rs572261839 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433613 | AGGAATATCTTAGGC[C/T]GTCCAATAAGAATGT | 80067 |
| rs572264674 | in-del | -/ACTG | 0.0109574 | 0.0732026 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484421 | AATTTTATAGTAAAT[-/ACTG]ACCACGGGGATTCTA | 80067 |
| rs572285582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171488328 | TGTAACAAATGTTTT[A/G]TGGCTCAATTAAGTA | 80067 |
| rs572368408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463830 | TAAAAGCTTTAACTC[A/G]TCAGCTAGAGATAAA | 80067 |
| rs572486473 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171489792 | GAGTAGCTGGGACTA[C/T]AGGCGCCCGCCACCA | 80067 |
| rs572643872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440621 | TAAAAAGAATTAAAT[A/G]GGCCTTTAGAGTGAG | 80067 |
| rs572730711 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171448971 | TCCCCTCATGACTAC[A/G]TTTAGAGGTCTGAGT | 80067 |
| rs572821788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479176 | TTTTTATGTCTTAGG[A/G]TGGTAAAGGCAGAAA | 80067 |
| rs572828426 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478348 | TTTTATTTTGTATTG[-/T]TTTGTTTTGTTGATG | 80067 |
| rs572833350 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440214 | GTTTGTTTTGTTTCT[A/T]CAAACTTTTGTATTT | 80067 |
| rs572867368 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484229 | TACTTATATCATCCA[C/T]CTTTTAGAATCCCAG | 80067 |
| rs572887262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171455448 | TCTTTGCTCTTGTGA[A/G]CAGTGCTGCAGTGAA | 80067 |
| rs572975282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469228 | TTTTAAAACGTTAAC[A/G]TTTGAAAATTCTTAT | 80067 |
| rs573018907 | in-del | -/TA | 0.00122775 | 0.024746 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464853 | AAAACTTTATCCTAC[-/TA]TATATATATGATAGT | 80067 |
| rs573074710 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453282 | TGTCATTATTTAATT[A/G]TTTATGAGATATTTG | 80067 |
| rs573085776 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171442864 | CAGCCTGGAGTGTGA[A/G]AAACTGTCTCAAAAA | 80067 |
| rs573111040 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF17 | GRCh38.p7 | 2:171460830 | CATGAGCCACTGTGC[C/T]CAGCTGATAGTGGGC | 80067 |
| rs573150188 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439270 | TTTCTCTTTTTCTTC[C/T]TTCTGGTATTCCCAT | 80067 |
| rs573179913 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491086 | GTAATCCCAACACTT[G/T]GGGAGGCCAGGGTGG | 80067 |
| rs573210362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171462065 | GTGGCCTTGTGAAAA[C/T]AACAAAGTTGTAATC | 80067 |
| rs573215399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171477102 | ATGGGTAGCCAGTTT[C/T]AGCCCCATGTACATT | 80067 |
| rs573442682 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171446079 | GTGTAAGACTTCAAG[C/G]GTTAATAAACTTAAA | 80067 |
| rs573504634 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435768 | TGACCTCTTTTAAAG[C/T]ATATTCTAAACATAC | 80067 |
| rs573578284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474930 | AGGATCACTCTTGCG[C/T]TGTCTGTTTTCTTCT | 80067 |
| rs573578488 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171456136 | TCTTCCAGGGTTTTT[A/G]TAGTTTTGGGTTTTA | 80067 |
| rs573612522 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171453684 | TTGTTCCCATTTGTT[A/C]TTGACTTGTGGAGCA | 80067 |
| rs573689440 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467741 | TCAAAAAAAAAAAAA[A/C]AAAAAAAAAAAAAGT | 80067 |
| rs573741884 | in-del | -/ACATATGTAGAT | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467301 | TGATGAGTGCATCAA[-/ACATATGTAGAT]ACTAGTTTATGTGTT | 80067 |
| rs573804203 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481769 | AATATTTGTGTTTCT[A/G]TATAGGCTAATGTAA | 80067 |
| rs573845224 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489761 | GGTTCACGCCATTCT[C/T]CTGCCTCAGCCTCCT | 80067 |
| rs573867592 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171478646 | TTTAAACATATAAAC[A/C]ATTGTGTAAATTCTA | 80067 |
| rs573985993 | snp | A/G | 0.00074474 | 0.0192825 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482967 | GGAGTTGTGGGCAGT[A/G]TAACAAACAGGAGAG | 80067 |
| rs574039636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451647 | GTGGTGAGCTCTCAG[C/T]TCACTGCATCCTCTG | 80067 |
| rs574062680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443673 | CTAGAAGAACCAGTT[A/G]TTATTAACATATTGC | 80067 |
| rs574098032 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171454591 | GCCTGGCCAGCACTC[A/C]TTATTTTAAAATATG | 80067 |
| rs574289172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473329 | ATTGGAAAAGGTCAG[C/G]TGCAGTGGCTTACGC | 80067 |
| rs574305542 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171464594 | GTCACATTTACCAGT[A/C]CTGGGGGTTAGGACT | 80067 |
| rs574454856 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434165 | GCGGGGCCGCGGCAG[A/G]CAGAGGCAGGGCCGG | 80067 |
| rs574531711 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433583 | AAGTATATCTTTTAC[G/T]TAGAGACATCGACGA | 80067 |
| rs574544058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171463503 | GAAGACTTAGTTTTC[A/G]TTATATCTTCTGATA | 80067 |
| rs574561736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171456459 | GCTTTGTTCTTTTTG[C/T]TTAGGATTGCCTTGG | 80067 |
| rs574665826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449181 | CCCAGCTACTTTTTG[C/T]ATTTTTGGTAGAGCT | 80067 |
| rs574671781 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448399 | TCTACTGTTATTATG[A/T]CTAACATTTGTGAAT | 80067 |
| rs574698972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171439459 | ATAACTGTTAAAGGC[A/G]TTCTTCATTTCTCTT | 80067 |
| rs574734682 | in-del | -/T | 0.3512 | 0.228601 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445132 | TTCCTATTCTCACTA[-/T]TTTTTTTTTTTTGAG | 80067 |
| rs574751343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171479116 | GCAAAAAGGAAATAA[C/T]GTAAAAGTACATTTT | 80067 |
| rs574772608 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432958 | TTCTAATATTAAACA[C/T]TGAAATAAATGGGAG | 80067 |
| rs574806943 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469528 | AGGTAGAAATGGTAC[A/G]TGGTAAAACAATGGA | 80067 |
| rs574838124 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443348 | ACTATTTTAATCTTG[-/T]TTTTTTTTATATGAA | 80067 |
| rs575154541 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458671 | GTTATTCATTGAACC[-/A]AAGGCCTGGGGATGC | 80067 |
| rs575163001 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171479371 | CCGTGCAAGGTTTCT[A/G]GAGTCTCAGGTTTTC | 80067 |
| rs575172582 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171486526 | GGCAAGGCTGGTCTC[C/G]AACTCCTGACCTCAA | 80067 |
| rs575322611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171475984 | AGAAAACAAGGCCCA[C/T]GAAGAGTGTATGGCC | 80067 |
| rs575449531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467636 | TTAGGAGGCTGAGGC[A/G]TGAGAATTGCTTGAA | 80067 |
| rs575553821 | in-del | -/TCACTTGAGC | 0.00199481 | 0.0315187 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477704 | GCTGAGCTGGGAGGA[-/TCACTTGAGC]TCACTTGAGCCTGGG | 80067 |
| rs575563180 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171461216 | TTAGGAGGCTGACGC[A/G]GGCAGATCACTTGAG | 80067 |
| rs575563191 | snp | A/G | 0.000182048 | 0.00953892 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469054 | GTGATCAGACTTTTT[A/G]TTAGCAAATTTGTAT | 80067 |
| rs575635525 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484197 | TTTTTATATTTTCTT[C/T]TCCTTCTTACCATGT | 80067 |
| rs575648917 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468403 | ATCTTAAGCAAGATA[G/T]ATGTATACCTGAGTA | 80067 |
| rs575673492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446143 | TGATTATACTTACGA[A/G]AGGAACATTGTTTGT | 80067 |
| rs575708651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445345 | GGCCAGGCTGGTCTC[A/G]AACTCTTGACCTCAA | 80067 |
| rs575771971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474198 | TTATTTGATGGATGA[C/T]ATGCAAGTAAAAGGG | 80067 |
| rs575783194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438480 | TGAGTGGATTTATCT[A/G]TTTCTCCTTGCATTT | 80067 |
| rs575797618 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171473419 | ATACCAGCCTGGGCA[A/G]CATAGCGAGACTCTA | 80067 |
| rs575798043 | in-del | -/AGAA | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171458251 | GTGGGGAAGATAAAC[-/AGAA]AGGCCATTGGAAAAA | 80067 |
| rs575908808 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435671 | GGAAAGCCACAATGC[A/C]TCCCCATATACTCAT | 80067 |
| rs576105333 | snp | A/G | | | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435138 | GGTCACCTATAGCCT[A/G]TGAGAGAGGAAGAAT | 80067 |
| rs576169953 | snp | A/G | 0.000374392 | 0.0136768 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484085 | AAAATGTAGTTCTTC[A/G]TTCAATGGTTAGCAG | 80067 |
| rs576242592 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489731 | ATCTCGGCTCACTGC[A/G]AGCTCTGCCTCCCAG | 80067 |
| rs576288416 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171454004 | GCCATGCACTTTGAA[A/T]ATTTTACAACATTGT | 80067 |
| rs576332901 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489216 | TCCCTCAAATTAACC[G/T]AGCCGTTAAGGTCTG | 80067 |
| rs576350801 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482024 | ACTAGCTTGGGAGTT[-/A]ACCTGATTAACCAGA | 80067 |
| rs576437854 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171490151 | GCCAAACAAAATTAA[C/T]CTGCAAGCTCATGAC | 80067 |
| rs576523247 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171438505 | GCATTTCTATCCGTG[-/T]TTGCCACATTGTGTT | 80067 |
| rs576555512 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171460953 | AAAAATAATTCAATG[A/G]TTTTTGTATGTTTGA | 80067 |
| rs576625229 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434117 | CAGAGAAGCGCGCCC[A/G]CAAGACAGCGCAGCC | 80067 |
| rs576671866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480611 | CTATTATAGAATGTC[A/G]AAGTTGTAAGGAACA | 80067 |
| rs576687266 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171440207 | TTCTGATGTTTGTTT[A/T]GTTTCTTCAAACTTT | 80067 |
| rs576712443 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171460855 | GTGGGCAAGTTATTT[A/C]ACCTCTCTGGGCCTC | 80067 |
| rs576806047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171477167 | TCTTTTGCTGATTTC[C/T]GCTTCTTTTCTGAGT | 80067 |
| rs576855947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171487533 | GATTCAAGAGATTCT[C/T]GTGCCTCAGCCTCCC | 80067 |
| rs576872873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171440775 | TTGTTCCTGGGCTTA[C/T]GTTCCTGGAAAGCTG | 80067 |
| rs576882160 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469819 | TGTTGGTTAGTTTGT[G/T]TTTCAAGACAGGATC | 80067 |
| rs576965808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469363 | TGCTTCTGAAATTGC[C/T]GGTGGAATGTGTTGT | 80067 |
| rs577033676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171446329 | GAGGCGGGCAGATCA[C/T]GAGATCGGGTGTTCA | 80067 |
| rs577128524 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432734 | CCAATGTTTACTAAA[C/T]ACTTAAACTGTGACC | 80067 |
| rs577199486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447641 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCACC | 80067 |
| rs577214130 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171469200 | AGAAAACATTTGTGT[A/G]TATCACCCATAATTT | 80067 |
| rs577314171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453381 | ACATTTGCCTAATAT[C/T]CCTTCATCTTTCTGC | 80067 |
| rs577325921 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491124 | ATGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 80067 |
| rs577440375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171445522 | GAATTGTTATTAACA[C/T]ACTGATATGAAACTA | 80067 |
| rs577450934 | snp | A/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485431 | CAGCTTGAATTATTC[A/T]TTCTCAAACATGGGA | 80067 |
| rs577520268 | snp | A/G | 0.0123806 | 0.0776981 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484819 | ATTTACCTGTTCTAA[A/G]CTTCATATGAGTGAA | 80067 |
| rs577585891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468324 | CTGTAATAAAGCTTT[C/T]ATTGTGACAGGCCCT | 80067 |
| rs577622393 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171478336 | CTTATTGTTTTGTTT[C/T]ATTTTGTATTGTTTT | 80067 |
| rs577680366 | snp | A/G | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475594 | ACATAGTGAGACTTC[A/G]TCTCTACAAAAAATA | 80067 |
| rs577809288 | snp | G/T | 0 | 0 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437566 | GGCACTTTCTGTTTT[G/T]GTAGGTTGTTCATTA | 80067 |
| rs577824211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171467837 | CCATTTGTGTTTTTT[C/T]CCCATGTATAGCTCT | 80067 |
| rs577966690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171475914 | TTAAACTGTGGTTCC[A/G]CTTCAGTAAGCCTTA | 80067 |
| rs578020682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171490422 | TGAGAGATGTCTTAG[C/G]TTGGGTGCTCCCAAA | 80067 |
| rs578039786 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171437027 | GATCCGGCCACCTCG[G/T]CCTCCCAAAGTGCTG | 80067 |
| rs578052553 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF17 | GRCh38.p7 | 2:171444561 | CATTATGCATATGCA[A/G]ATATCCCCAAATCCA | 80067 |
| rs578075663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451717 | AGTAGCTGGGACTAC[A/G]GGCGTGCACCACCAG | 80067 |
| rs578081394 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171489820 | CCATGCCTGGCTGAT[A/T]TTTTGTATTTTTAGT | 80067 |
| rs578139248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466051 | TTATTTTTAGTAGAG[A/G]TGAGGTTTTGCCATG | 80067 |
| rs578168490 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435854 | TTCACATACCATATA[-/T]TTTACCCATTTAAAG | 80067 |
| rs578212376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171466776 | TCCTCTATATTGAAT[C/T]TCATATTCTTTATAT | 80067 |
| rs578222676 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458864 | TTTCCAAGAAAAAAT[G/T]TTTACCATGACATCT | 80067 |
| rs578249070 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF17 | GRCh38.p7 | 2:171451034 | AAGTTTATATAGAAC[C/T]CTAGCATTAAAAAAA | 80067 |
| rs587780328 | snp | C/T | 0.00020118 | 0.0100274 | DCAF17 | 2 | allele_origin=T(germline)/C(germline) | 2:171477981 | TTATTTCTTTCCATA[C/T]GATAGAATGAAAATG | 80067 |
| rs745324970 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171479684 | CATGTGTTTAGTCCT[A/G]TCCAGGAATCAGCAA | 80067 |
| rs745329682 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171465296 | GTATACACATGGAGT[A/G]ATGTGTTCAAAGGCG | 80067 |
| rs745350604 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171478818 | ACACAAAAAAGTATT[A/G]TTTTGGACCATACAA | 80067 |
| rs745369769 | snp | A/G | 1.72237e-05 | 0.00293455 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435209 | TTTATTGATAATTTT[A/G]CTGTAATTCACCTCA | 80067 |
| rs745422590 | snp | G/T | 1.65704e-05 | 0.00287836 | missense, intron-variant | DCAF17 | GRCh38.p7 | 2:171458459 | CCTTTTGGCATTCCT[G/T]GTAATATTAAAATCA | 80067 |
| rs745431606 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171478575 | AATACATTTTTATCC[C/G]CTTCCTTTAAAAAGG | 80067 |
| rs745437821 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444604 | TCTGAAACACTTCTA[A/G]TCCCAAGTGTTTCAG | 80067 |
| rs745454200 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171454721 | GGCCAACATGGTGAA[A/G]CCCCGTCTCTACTAA | 80067 |
| rs745500589 | snp | G/T | 0.000185822 | 0.00963724 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483266 | CTTTACCTGATATTT[G/T]AATTCGAGACTCTAG | 80067 |
| rs745526404 | snp | C/T | 0.000558191 | 0.0166968 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482837 | TACTTCTGGTCTAGA[C/T]ATAACTTACCACTAA | 80067 |
| rs745543375 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171457765 | CGCACTTCCATTAGT[A/G]CTCCAGTATGAGAAT | 80067 |
| rs745604419 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171456916 | GATACAGGATCATGT[C/T]GTTTGAAAAGAGGGA | 80067 |
| rs745661005 | in-del | -/T | 0.00487052 | 0.0491074 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482362 | ATTAAAATCTTTCCA[-/T]TTTTTTTTTTCAGTT | 80067 |
| rs745696181 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438644 | TGCCAAATTCGACTT[C/T]GTCTGAAATTAGTAT | 80067 |
| rs745701144 | snp | A/G | 1.83451e-05 | 0.00302857 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449847 | AAGGAAACTGACCCA[A/G]ATAAATAAACTTCTC | 80067 |
| rs745767198 | snp | A/G | 1.64879e-05 | 0.00287118 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481023 | TGGTGCTACACATAG[A/G]GCAGAAACCCAACAG | 80067 |
| rs745776305 | snp | A/G | 1.66496e-05 | 0.00288522 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458342 | TAAATAGGTGCTAAA[A/G]CCACCATTTTTGTTT | 80067 |
| rs745783336 | snp | A/C | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470102 | AATCAGAGCTCACTG[A/C]AGCCTCAACCTCCTG | 80067 |
| rs745784916 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483580 | CCTAGTGAGGAGATA[C/G]CGCTCTGTTTAGACA | 80067 |
| rs745818094 | snp | A/T | 1.68878e-05 | 0.00290579 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480212 | AGTAGAGTCCGTGGG[A/T]TACAAAGTTGTAAAC | 80067 |
| rs745846051 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436542 | ATTTTCCTGATGACT[A/G]GTGATGTCAGGCATC | 80067 |
| rs746007838 | snp | C/G | 4.68e-05 | 0.00483713 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481244 | GTGTTGACTTCAGAT[C/G]ACTATGACTTCTTTT | 80067 |
| rs746074897 | snp | A/G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171473688 | TTTCTGAATTTAAAT[A/G/T]TTCAGAATTTCTCAA | 80067 |
| rs746101734 | snp | C/T | 0.000185408 | 0.00962652 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481523 | AGACAAAAGTAAACA[C/T]GCAGAAAGAAATCTT | 80067 |
| rs746101867 | snp | C/G | 1.648e-05 | 0.0028705 | synonymous-codon, nc-transcript-variant, missense | DCAF17 | GRCh38.p7 | 2:171468919 | CTTTGAGGTGTCATC[C/G]CTGGAGAATGCTTTT | 80067 |
| rs746126854 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171436996 | TCAGGCTGGTCTCGA[A/G]CGCCCAGCTTCAGGT | 80067 |
| rs746126862 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171440030 | TCACAGGTATGATAA[C/T]AGTGCACTGTAGCCC | 80067 |
| rs746163364 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487356 | TGACCAATAATGATA[A/C]GCACATTTTCATGTT | 80067 |
| rs746203651 | in-del | -/T | 0.000136855 | 0.00827096 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481295 | ATGGTGAGGACTTCA[-/T]TTTTTTTAAAGGTTT | 80067 |
| rs746225963 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439199 | TTCCCAGATTTGGGG[C/T]TTGGTATCTGTCAGT | 80067 |
| rs746303463 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171451427 | CTCTCTTTATACTCT[C/T]ACTACCTTGCTTTTA | 80067 |
| rs746364079 | snp | G/T | 1.65743e-05 | 0.00287869 | synonymous-codon, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171478022 | TACAGCTTCTGGACG[G/T]GTGGTAAAAAAAAGT | 80067 |
| rs746475473 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171451712 | TCCTGAGTAGCTGGG[A/T]CTACAGGCGTGCACC | 80067 |
| rs746564010 | snp | C/T | 3.32474e-05 | 0.00407708 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171443596 | ATAGAGGATGCTTTA[C/T]TATGGGAATGCCCAG | 80067 |
| rs746565766 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171480676 | GTGGAGAACCTGGGA[A/G]GTTTGGCACCTCGTA | 80067 |
| rs746573605 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466607 | TATTAGAGATCAAAA[C/T]TGGGGCTCTTGGGTT | 80067 |
| rs746610463 | snp | G/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171433081 | TCCCCTCAGCTCAGG[G/T]TGCAAGGTGGGAACC | 80067 |
| rs746620356 | snp | C/G | 1.66037e-05 | 0.00288125 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171478059 | CTTCTGGATGATGAC[C/G]CAGAACAAGAGGTAT | 80067 |
| rs746656019 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433747 | CAAGGACAAGCCTCC[A/G]GGAAAGAGTAACTCA | 80067 |
| rs746656482 | snp | A/T | 1.75881e-05 | 0.00296543 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477936 | ACAGTTTTACCTTTG[A/T]CTGCATGTAATAGAA | 80067 |
| rs746673241 | snp | C/T | 0.000557569 | 0.0166875 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483774 | TGAACTGCCATTATC[C/T]TTCCCCTTTGTACAA | 80067 |
| rs746704673 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171445767 | AGCTCACTGCAGCCT[C/T]TACCTCCTGGGCTCA | 80067 |
| rs746838445 | snp | A/C | 4.95634e-05 | 0.00497788 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481076 | CAGATGATATGTGAC[A/C]CTGGGGAAGAAGAAG | 80067 |
| rs746865242 | snp | C/T | 4.96915e-05 | 0.0049843 | synonymous-codon, nc-transcript-variant | DCAF17 | GRCh38.p7 | 2:171458066 | TAGCTTCCAAACCAT[C/T]GCTGAACAGGTAGAG | 80067 |
| rs746899310 | snp | G/T | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | DCAF17 | GRCh38.p7 | 2:171468903 | ACATGCCACCACTGC[G/T]CTTTGAGGTGTCATC | 80067 |
| rs746903038 | snp | G/T | 1.80133e-05 | 0.00300105 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435235 | CCTCACTGTTGATCT[G/T]AACTATAATTTGTAT | 80067 |
| rs746956061 | snp | A/T | 1.67013e-05 | 0.0028897 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458488 | CACAGGTATGGCTAC[A/T]CTATAGTATTTTTTC | 80067 |
| rs746959346 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171472154 | TATGCATACTATATG[A/G]ATTAGCACGTCTATA | 80067 |
| rs746994978 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455040 | TTATATAGATAAACA[G/T]GTGTCATGGGGGTTT | 80067 |
| rs747014569 | snp | A/C | 0.000185995 | 0.00964172 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482861 | CCACTAAGAAACCCC[A/C]AGTATGTCACCACTG | 80067 |
| rs747064360 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171448382 | AGGTAGCATCATTGT[C/G]TTCTACTGTTATTAT | 80067 |
| rs747141943 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452456 | CACAACACTACTTTC[A/G]TTATATATTTATTTA | 80067 |
| rs747147998 | in-del | -/AG | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481502 | AAGGCTAGGAAAGAC[-/AG]GGAGAGACAAAAGTA | 80067 |
| rs747152291 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464103 | ACACACTCCAGTAAT[C/T]TTAGAGAATTTCCTC | 80067 |
| rs747162256 | snp | A/C | | | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447590 | GCTGGTCTCGATCTC[A/C]TGACATCGTGATCCA | 80067 |
| rs747162352 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171463141 | GAGGCTGAGGCACGA[A/G]AATCACTTGAACCCA | 80067 |
| rs747173001 | snp | C/T | 0.000185856 | 0.00963813 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482248 | TATCCGATGTAACCT[C/T]AAAAGAATAACTGGT | 80067 |
| rs747184081 | snp | A/G | 3.31614e-05 | 0.00407181 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448770 | TATATCAGCAACTAC[A/G]GGAAAAATCCTTGAG | 80067 |
| rs747209139 | snp | C/G | 0.000185891 | 0.00963903 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484815 | TTAAATTTACCTGTT[C/G]TAAACTTCATATGAG | 80067 |
| rs747211504 | in-del | -/TTCAT | 0.000186064 | 0.00964351 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484912 | TGCATGTGTCAGTGA[-/TTCAT]TTCTTTTTATTGCTG | 80067 |
| rs747241616 | snp | A/G | 1.75228e-05 | 0.00295991 | intron-variant, missense, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473866 | TTTTTCCAACTTCAG[A/G]CAAAAAATGGGATCC | 80067 |
| rs747326851 | in-del | -/TGT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171437495 | TGATCACTGCTGCTG[-/TGT]TGTTATTTCTTCTTT | 80067 |
| rs747334764 | snp | A/G | 1.65614e-05 | 0.00287757 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171457981 | GCCAGATTTTTGGGA[A/G]CGTTACAGATGCTAC | 80067 |
| rs747343455 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171440994 | ATAGTCAGCTTTTGA[A/G]ATTTGTTCTAACCCC | 80067 |
| rs747356771 | snp | G/T | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475026 | CTTTAACCTTTTAAT[G/T]GCTTTTCATTGCTCT | 80067 |
| rs747394245 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171469262 | ACAAGAATTTTATAG[-/T]TTTTTTTAATCTCAC | 80067 |
| rs747418796 | snp | C/G | 0.000163492 | 0.00903988 | synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434646 | GGGCTGCTTCTCGCG[C/G]GACGCAGGCGTGGTG | 80067 |
| rs747441331 | snp | C/T | 0.000371816 | 0.0136297 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481625 | CAAAATGTGTCATCA[C/T]AGTTTTTAAAAATCT | 80067 |
| rs747460553 | snp | A/G | 2.97703e-05 | 0.00385801 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453255 | CAATATTTTATTGAC[A/G]ATAAGTTGTAATGTC | 80067 |
| rs747472144 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452697 | TCAGACTCCTAGCCT[C/G]AAGCGATCCTCCTGC | 80067 |
| rs747595294 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171488813 | TCTGTAGAAAGTCTT[C/G]AGTGCCTCTGCCCCT | 80067 |
| rs747597774 | in-del | -/TC | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171441380 | GATCTTCCCACCTTG[-/TC]TCTCTCTCTCAGTGT | 80067 |
| rs747625728 | in-del | -/CATATTTAAACATT | 0.000150395 | 0.00867034 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449963 | GGCCCGGCAGGTATA[-/CATATTTAAACATT]CAATAAAATGAAGAC | 80067 |
| rs747653193 | in-del | -/AGTATTCCC | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455358 | TTTTTGTGGCTGCAT[-/AGTATTCCC]TGGTGTATATGTACA | 80067 |
| rs747674263 | snp | A/G | 0.000186133 | 0.0096453 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484567 | TAACTAGAGTTTAGT[A/G]TTTATTTAGTTTTTA | 80067 |
| rs747756077 | snp | A/G | 1.65605e-05 | 0.0028775 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171457986 | ATTTTTGGGAACGTT[A/G]CAGATGCTACCTTGT | 80067 |
| rs747760427 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452794 | GAGCACGATAACTAC[A/C]TTATCTTTTTATTAG | 80067 |
| rs747811042 | snp | A/G/T | 3.30149e-05 | 0.00406283 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480025 | CCCTCTATTTTATCT[A/G/T]TCTATCCCAAAGACT | 80067 |
| rs747837854 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171447768 | CACTCTCTCAAAGTG[C/T]TGGGATTACAGGTGG | 80067 |
| rs747869004 | snp | C/T | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474869 | TCTTGGCCAGGTCAC[C/T]GTCATCACTAGCCAA | 80067 |
| rs747934448 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171447210 | AAAAAAAAAACACTA[A/G]CATACAAACAAAAAT | 80067 |
| rs747944118 | snp | A/G | 9.8868e-05 | 0.00703024 | missense, nc-transcript-variant, synonymous-codon | DCAF17 | GRCh38.p7 | 2:171468911 | CCACTGCTCTTTGAG[A/G]TGTCATCCCTGGAGA | 80067 |
| rs747954198 | in-del | -/CCTCCAC | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455135 | TTTCCCTCCTCCCAC[-/CCTCCAC]CCTCCACCCTCCGAT | 80067 |
| rs747990360 | snp | G/T | | | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480050 | AAGACTTTCAAAATT[G/T]TGGACTATGAAGATG | 80067 |
| rs748029308 | snp | A/T | 5.20359e-05 | 0.00510051 | splice-acceptor-variant | DCAF17 | GRCh38.p7 | 2:171448679 | TCTCTTTTTTTTTTT[A/T]GGGAGATATACTTCC | 80067 |
| rs748100010 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171440947 | CTTCCAGGCTGTTTT[A/C]GTCTTGGACCAGAAA | 80067 |
| rs748120696 | snp | A/T | 3.30524e-05 | 0.00406511 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469042 | CCTGGTAAATGAGTG[A/T]TCAGACTTTTTATTA | 80067 |
| rs748137212 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434270 | GGAACTACATTTCCC[C/G]GTGAGAGAGCGGCTC | 80067 |
| rs748223074 | snp | A/G | | | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485502 | TCATAGTTGGGAACA[A/G]CCTGGGTTCTAAGGG | 80067 |
| rs748226282 | snp | C/T | 1.66153e-05 | 0.00288225 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448799 | AGAAAATATATCTTG[C/T]ACCTTATTGCAAATT | 80067 |
| rs748228250 | snp | A/G | 0.00611728 | 0.0549656 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483705 | TAGTCACTGTGATAC[A/G]GTATAAGTAAAGTGG | 80067 |
| rs748257732 | snp | G/T | 3.37439e-05 | 0.00410741 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449871 | ACTTCTCTTCATTCT[G/T]TTAAAAGATACTTGA | 80067 |
| rs748309174 | snp | G/T | 0.000537384 | 0.016383 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474003 | ATTAGCACTTGAAAG[G/T]TAAGAGCAGCTTTTG | 80067 |
| rs748324448 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464998 | GTCAGGAGTTCAAGA[C/T]TAGCCTGGCCAACAT | 80067 |
| rs748397501 | in-del | -/TTA | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436308 | TTTTTATGTGGGCAT[-/TTA]TTTTCACTTCTCCTA | 80067 |
| rs748498879 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171463445 | TGGAATATCTGAAAG[A/G]ACACATAAAAACTTG | 80067 |
| rs748563436 | snp | C/T | 1.66646e-05 | 0.00288652 | intron-variant, missense, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473896 | CAAGAAATGGATTGT[C/T]GTTCTCTAGAATCTG | 80067 |
| rs748586810 | snp | A/C | 0.00111848 | 0.0236218 | missense, upstream-variant-2KB, splice-donor-variant, nc-transcript-variant, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434672 | TGGTGCAGAGGACCA[A/C]CCTGGGCATCCTGCG | 80067 |
| rs748613463 | snp | C/T | | | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491310 | GGCAACAGAGTGAGA[C/T]TTCATCTCAAAAAAA | 80067 |
| rs748632737 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171441144 | TCCACAGATTTTGTT[A/G]GTGCTCCTAGGCCTT | 80067 |
| rs748634846 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466619 | AAATTGGGGCTCTTG[C/G]GTTCACAGGGCACAT | 80067 |
| rs748647626 | in-del | -/AAT | 1.74199e-05 | 0.00295121 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443490 | GTCTTGGTTATCAAG[-/AAT]AATAATAATCATTTA | 80067 |
| rs748651947 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171490134 | CTTAAAATATTGCAC[A/T]AGCCAAACAAAATTA | 80067 |
| rs748671292 | snp | A/G | 0.000185891 | 0.00963903 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482332 | AAATATGGAATTTTT[A/G]GCTTGGATGATTTAT | 80067 |
| rs748768583 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171476805 | GTACTTAAACTTTGG[C/T]ACCTTGATGGTGTTT | 80067 |
| rs748802684 | snp | A/G | 3.33767e-05 | 0.004085 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480196 | GTCATGGGATGTGGT[A/G]AGTAGAGTCCGTGGG | 80067 |
| rs748865569 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171456848 | ATCCTGAGACTTTGC[C/T]GATGTTGCTTATCAG | 80067 |
| rs748881265 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171490271 | ATAATTATATATTTA[C/T]GACTTTAACCCATGA | 80067 |
| rs748887234 | snp | G/T | 1.65616e-05 | 0.00287759 | missense, nc-transcript-variant | DCAF17 | GRCh38.p7 | 2:171458044 | GCTCAGGACTGGTCA[G/T]ACTCTATAGCTTCCA | 80067 |
| rs748899036 | snp | A/G | 1.65718e-05 | 0.00287848 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435133 | TTCCAGGTCACCTAT[A/G]GCCTATGAGAGAGGA | 80067 |
| rs748910614 | snp | A/T | 0.000185822 | 0.00963724 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482441 | CCTGGTGCTAGACAT[A/T]GCCCCATACTTTCAA | 80067 |
| rs748981663 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171470649 | TTTGATTGGTCACCT[C/G]CCAGTGAGTGGACAT | 80067 |
| rs748993508 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171451765 | ATTTTTACTAGAGAC[A/G]GGGTTTCACCATGTT | 80067 |
| rs749020238 | in-del | -/TCT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171448666 | TCATTTTTATATCTC[-/TCT]TTTTTTTTTTAGGGA | 80067 |
| rs749064558 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436274 | ATAAATAATGCTGCT[A/G]TAAACATTTCCATGT | 80067 |
| rs749100873 | snp | A/G | 1.65784e-05 | 0.00287905 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448756 | AATTGGCTACTTCGT[A/G]TATCAGCAACTACGG | 80067 |
| rs749171538 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436755 | TTTCCTGATGTTATT[A/G]TTTGAAACAGAGAGG | 80067 |
| rs749189434 | snp | A/G | 0.000389712 | 0.0139536 | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485087 | CTTTATTTCTCTTGG[A/G]TAAATACCTGGGGAT | 80067 |
| rs749237410 | snp | G/T | | | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481043 | AAACCCAACAGAGTC[G/T]TCAGCTGCTATGTTT | 80067 |
| rs749242448 | snp | A/C | 0.000136212 | 0.00825151 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484717 | TGCAATCATCTTCAG[A/C]AAGTTTCCTAAATCC | 80067 |
| rs749277004 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171458238 | CTTTAAAGCAGGGGT[A/G]GGGAAGATAAACAGA | 80067 |
| rs749369756 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171472198 | TGTTTGTTTTGTTTT[A/G]AGACAGGGTTTTACT | 80067 |
| rs749386315 | snp | C/G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439098 | TTAATTCTTATTGTT[C/G/T]CCCTATATAGTTAAG | 80067 |
| rs749410667 | snp | A/G | 0.000188342 | 0.00970234 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434281 | TCCCGGTGAGAGAGC[A/G]GCTCCGGCCGGCCGC | 80067 |
| rs749434549 | snp | C/G | 1.67722e-05 | 0.00289583 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453094 | GAAGTACTTTTGAGA[C/G]CTGCGTGTAATTGTA | 80067 |
| rs749478142 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171451237 | CTATTTGTTGGCTAC[G/T]TCTACTTACTTTTTA | 80067 |
| rs749530940 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438112 | CCTGGGACTTCTTTG[A/G]CCCATGTGTTATTTA | 80067 |
| rs749541080 | snp | C/T | 1.65627e-05 | 0.00287769 | synonymous-codon, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481096 | GGAAGAAGAAGAAAC[C/T]ATAAACAGAAGCTGT | 80067 |
| rs749618871 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466283 | CCTTCTTCTTTGATA[A/T]ATAGTAAAGTTATTT | 80067 |
| rs749706689 | snp | A/T | 1.71375e-05 | 0.00292719 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435204 | AACTTTTTATTGATA[A/T]TTTTGCTGTAATTCA | 80067 |
| rs749716370 | snp | A/G | 0.000187073 | 0.00966962 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482760 | GAACTCGTCTATTCT[A/G]AAAGGCATTTGAGAA | 80067 |
| rs749731033 | in-del | -/CAA | 4.98558e-05 | 0.00499254 | cds-indel, nc-transcript-variant | DCAF17 | GRCh38.p7 | 2:171453133 | TTCTAGGCAGGCATT[-/CAA]CAACATGTTTTGCTG | 80067 |
| rs749751184 | snp | A/G | 1.66713e-05 | 0.0028871 | intron-variant, missense, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171476948 | AACAGGGAGAACCAT[A/G]AAGTAAGTCAAGAGT | 80067 |
| rs749770451 | snp | A/C | 0.000185822 | 0.00963724 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483244 | TCCTGCCCTACCTAA[A/C]CCCCCTCTTTACCTG | 80067 |
| rs749778256 | in-del | -/GAA | 1.65337e-05 | 0.00287517 | cds-indel, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481082 | ATATGTGACACTGGG[-/GAA]GAAGAAGAAACCATA | 80067 |
| rs749798415 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171478315 | ATAATTTGAAAACAC[A/G]ATTAGCTTATTGTTT | 80067 |
| rs749808092 | snp | A/G | 1.88329e-05 | 0.00306857 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474019 | TAAGAGCAGCTTTTG[A/G]TAGCATTTATTGGCA | 80067 |
| rs749932237 | snp | A/G | 0.000166293 | 0.00911694 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481328 | TAGAATACTGTTCCA[A/G]GAAGTTTAGTGTTTT | 80067 |
| rs749985794 | snp | C/G | 5.21399e-05 | 0.00510561 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481174 | CCCAGCAGCTGCGTC[C/G]AATCCATTTTATTAT | 80067 |
| rs749990174 | snp | G/T | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | DCAF17 | GRCh38.p7 | 2:171468976 | CATCGTCACACCTAA[G/T]AAGAAGAAACAGAAA | 80067 |
| rs750015343 | snp | G/T | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474225 | AGGGAATTACAGACT[G/T]GCCCTTTCTCATCAG | 80067 |
| rs750021840 | snp | A/G | 0.000196676 | 0.00991461 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484478 | ATTTTCCTATCCAGC[A/G]TACTTTTTGATGGAT | 80067 |
| rs750038271 | snp | A/G | 1.66092e-05 | 0.00288172 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171443583 | CAAATCAGAAAAAAT[A/G]GAGGATGCTTTATTA | 80067 |
| rs750231739 | snp | A/G | 1.69879e-05 | 0.00291439 | intron-variant | DCAF17 | GRCh38.p7 | 2:171450000 | TGAAGACTCTTTTTC[A/G]TAGGAATTTGTCTGC | 80067 |
| rs750277215 | snp | A/T | 1.65803e-05 | 0.00287922 | intron-variant, missense, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171476898 | AAAATAATAGTTCTC[A/T]GCATCAGATCTCTGA | 80067 |
| rs750279227 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466139 | GCAGTGTTGGGATTA[C/T]AGGCGTGAGCCACCA | 80067 |
| rs750280987 | snp | A/T | | | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485203 | ATGCTTGCAGCAATG[A/T]AGGAGACTTCCACTT | 80067 |
| rs750300966 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171450933 | CCTTGGCTCAAACTC[A/G]GGCAGTTTAGCTCTA | 80067 |
| rs750319630 | snp | A/T | 1.66037e-05 | 0.00288125 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171453143 | GCATTCAACAACATG[A/T]TTTGCTGTACCTTGC | 80067 |
| rs750326729 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171468048 | GCCCAAACAGACCAT[A/G]TGGTGTTTCCTAAAG | 80067 |
| rs750345263 | in-del | -/ATATT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443800 | GTATTAAAAATACTA[-/ATATT]ATGAATGTGTTTTTA | 80067 |
| rs750345667 | in-del | -/A | 1.65485e-05 | 0.00287645 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469053 | GTGATCAGACTTTTT[-/A]ATTAGCAAATTTGTA | 80067 |
| rs750388815 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171450148 | TGGAAAACCAGACAT[G/T]GTATTTTCTCACTCA | 80067 |
| rs750394711 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171465927 | CAAATTTATGTTTGC[A/G]TACTTTAAATATTTA | 80067 |
| rs750449902 | snp | C/T | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171475995 | CCCACGAAGAGTGTA[C/T]GGCCTTTTGCCAGGT | 80067 |
| rs750492583 | snp | A/C | 1.65729e-05 | 0.00287857 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458097 | AAAACTGAAATTTGT[A/C]ATGTTACTATTAGCA | 80067 |
| rs750556163 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171489440 | TCTCACAAGGACATA[C/T]AGCTGACGATATTAC | 80067 |
| rs750580321 | snp | G/T | 1.68275e-05 | 0.0029006 | stop-gained, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435083 | CTTTATGTCTTTTAG[G/T]AAAGTACTAAATTTA | 80067 |
| rs750612132 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171440912 | AGCATTTTTCGTGCT[A/G]TGAGGACAGACGGGT | 80067 |
| rs750627144 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171488226 | AATATGCATCTATAA[A/G]TTGACCTCTTAAATG | 80067 |
| rs750634308 | snp | A/G | 0.000186689 | 0.00965969 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482163 | GCAACCCAAGTAAAG[A/G]GAGAAAATGTTTCTT | 80067 |
| rs750701779 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171453644 | TATGTAAATTTTCCA[A/G]TTCATTCAGTTTTGG | 80067 |
| rs750734384 | snp | C/T | | | intron-variant, stop-lost, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469454 | CTGGTGGTCACAGTG[C/T]AGGTAAATTGAAGCA | 80067 |
| rs750778801 | snp | A/T | 3.31592e-05 | 0.00407167 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448723 | TATAAGTCCTCACTC[A/T]TAGCACTGACTGCTC | 80067 |
| rs750787386 | snp | A/G | 0.000300978 | 0.0122637 | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447487 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTATA | 80067 |
| rs750862065 | snp | A/G | 0.000213881 | 0.010339 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171434249 | GGGCTGCCTCACGAG[A/G]CACTAGGAACTACAT | 80067 |
| rs750945995 | snp | A/G | 0.000710985 | 0.0188411 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484430 | GTAAATACTGACCAC[A/G]GGGATTCTACATCTT | 80067 |
| rs750950347 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171480589 | ATACATTTGTCTGAT[A/G]TTTCAACTATTATAG | 80067 |
| rs750993361 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171449157 | GGGATTTTGGGTGTG[C/T]ACCCCATGCCCAGCT | 80067 |
| rs751025778 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171434897 | TTTTACGCTTCTTAT[A/G]TCTTACCTGGAAACA | 80067 |
| rs751026272 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482035 | GAGTTACCTGATTAA[C/T]CAGAGAAAATTTTTG | 80067 |
| rs751056490 | snp | C/T | 1.69499e-05 | 0.00291112 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448641 | GCAAATTGTTCATGG[C/T]CAAGCAGTTTCATTT | 80067 |
| rs751109190 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171447913 | AGCTATCCTCTCCCT[A/T]TTCTAGGATAATTCA | 80067 |
| rs751111716 | snp | C/T | 1.64955e-05 | 0.00287184 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171469024 | TGCCCTAAAAGACAA[C/T]TCCCTGGTAAATGAG | 80067 |
| rs751143227 | in-del | -/TT | 0.000175042 | 0.00935364 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448668 | ATTTTTATATCTCTC[-/TT]TTTTTTTTTAGGGAG | 80067 |
| rs751154514 | snp | A/G | 1.65787e-05 | 0.00287907 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448739 | TAGCACTGACTGCTC[A/G]TAATTGGCTACTTCG | 80067 |
| rs751186320 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171461624 | CATACCATAAGTGCT[C/T]TTTTATAACTCACTT | 80067 |
| rs751199219 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171462199 | GGCACAAAACCCAAA[C/G]CCATAAAAGAAGAGA | 80067 |
| rs751222714 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171459817 | ATTTTAAAAATTACT[C/T]AAGTTTTTAGATGCC | 80067 |
| rs751224010 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435970 | ACAGAACCATGTACC[C/T]TTAAGCAGTCACCTC | 80067 |
| rs751320777 | in-del | -/A | 1.68593e-05 | 0.00290334 | intron-variant, splice-acceptor-variant | DCAF17 | GRCh38.p7 | 2:171476857 | CCTTTTTCCCTTCTC[-/A]AGAGTTTTGAAGCTA | 80067 |
| rs751325533 | in-del | -/A | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435654 | CCAACATGAGGGGGG[-/A]AGGAAAGCCACAATG | 80067 |
| rs751396025 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171470815 | CAAACACACGCACAC[A/G]TACAGATACAGCCGG | 80067 |
| rs751441467 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487756 | GAGAGAGACTTACTA[C/T]GTTATGTTGCCCAGG | 80067 |
| rs751442905 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439764 | GAAACCCCATCTCTA[C/T]TAAAAAAACAAAAAT | 80067 |
| rs751468818 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171473078 | GTATTAGATCATTTC[C/T]TCAGATATTAGAGTT | 80067 |
| rs751484603 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452098 | TAAAAATTTATCCCT[C/T]TGGAAGGGAGAATCT | 80067 |
| rs751559399 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171463222 | GCGATGGAGCGAGAT[-/T]TTAAAAAAAAAAAAA | 80067 |
| rs751569721 | snp | G/T | 1.66504e-05 | 0.0028853 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435174 | TTGACAATTATCGGC[G/T]CTGTGTCAGCAGGTA | 80067 |
| rs751624341 | snp | G/T | 1.6566e-05 | 0.00287797 | stop-gained, intron-variant | DCAF17 | GRCh38.p7 | 2:171458394 | AACAGAAACTTGACT[G/T]AGGGTGTGCATGCAG | 80067 |
| rs751687518 | snp | G/T | 1.73812e-05 | 0.00294793 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473984 | AAGTCAAGTGAGTAA[G/T]CTCATTAGCACTTGA | 80067 |
| rs751732245 | snp | C/T | | | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171478020 | GTTACAGCTTCTGGA[C/T]GGGTGGTAAAAAAAA | 80067 |
| rs751763677 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443926 | CTTAGTGTTTAAGAG[A/C]TCATTCCACTCAATA | 80067 |
| rs751818892 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432650 | TACCGTATGCTGTAA[A/G]TAAGTCATGAAAAAT | 80067 |
| rs751821846 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171490744 | ATCTCTCCTGAATTT[G/T]CAGATTGCCCAAGGC | 80067 |
| rs751853690 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171441702 | GCTGAGCTGGGATTG[A/G]GAAGGAAGGGACTAT | 80067 |
| rs751927562 | snp | A/G | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470414 | AGATCACCTTTTACC[A/G]TGTTGCAGGTCAGCA | 80067 |
| rs751971793 | snp | A/G | 1.65081e-05 | 0.00287293 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480117 | TAGATGCTGAAGGAA[A/G]AGCTCACCTGGATTT | 80067 |
| rs752019061 | snp | C/G/T | 3.30471e-05 | 0.00406481 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480005 | TAACTGGATTTTGCC[C/G/T]CTTTCCCTCTATTTT | 80067 |
| rs752065485 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483181 | CTTCCCAGCTCGCCA[C/G]AGTGTCACACAGCTG | 80067 |
| rs752103736 | snp | A/G | 1.72621e-05 | 0.00293781 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481171 | CACCCCAGCAGCTGC[A/G]TCCAATCCATTTTAT | 80067 |
| rs752132163 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435892 | TTCAATAATATTTAA[C/T]GCATTCACAGATACA | 80067 |
| rs752153207 | snp | C/G | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470531 | GTTCCCTTCCATTTC[C/G]CCAAGTACTTATCAC | 80067 |
| rs752201590 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484796 | CATTCTTTTATATCA[A/G]AGGTTAAATTTACCT | 80067 |
| rs752234683 | snp | A/T | 3.51327e-05 | 0.00419108 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448854 | TTCAAGATTTTATTT[A/T]AAAAATTTGAAACCT | 80067 |
| rs752272195 | in-del | -/ATGTA | 1.64776e-05 | 0.00287028 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477940 | TTTACCTTTGACTGC[-/ATGTA]ATGTAATAGAACTTG | 80067 |
| rs752287637 | snp | C/G | 1.66715e-05 | 0.00288712 | intron-variant, missense, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473932 | ATCTATTTCCATCCT[C/G]ATGCTTCTGGTAGAA | 80067 |
| rs752305487 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171440126 | ATACCATCGCACCTG[C/G]CTTAATCATTGTTAT | 80067 |
| rs752339872 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436064 | ATTCTGTACTTTTCA[C/T]ATAAATGGAATCATA | 80067 |
| rs752354273 | snp | G/T | 3.30781e-05 | 0.00406669 | stop-gained, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480149 | CACTGTAATGAATAT[G/T]GAACTTTACTTAAAA | 80067 |
| rs752396778 | in-del | -/TAA | 0.000186445 | 0.00965339 | utr-variant-3-prime, nc-transcript-variant, cds-indel, intron-variant | DCAF17 | GRCh38.p7 | 2:171483988 | ATGTAGGAAAGTGCT[-/TAA]TAATCGTTTTTTACT | 80067 |
| rs752404121 | snp | A/G | 0.00018596 | 0.00964082 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171485024 | TTTTTACTGTTATGA[A/G]TAAAGCTGCTATGAA | 80067 |
| rs752407824 | snp | G/T | 1.83296e-05 | 0.00302729 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435052 | AAGCCTAAGAGTTCT[G/T]TCCTGAACGGAAATT | 80067 |
| rs752528088 | snp | C/T | 0.000264445 | 0.0114958 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472962 | GGATATAAGGTAATA[C/T]ATTTGTGTACACATG | 80067 |
| rs752565445 | snp | C/G | 4.2277e-05 | 0.00459747 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434602 | ACCCGGAAGCCCAAC[C/G]TGTGCAGCCGGCTGA | 80067 |
| rs752718186 | snp | A/G | 1.65756e-05 | 0.00287881 | intron-variant, missense, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171476904 | ATAGTTCTCAGCATC[A/G]GATCTCTGAAGATTT | 80067 |
| rs752749215 | snp | A/C | 1.66518e-05 | 0.00288542 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171443543 | CATCTGAGCCAAGAA[A/C]ACTTTATGAAATGCC | 80067 |
| rs752790262 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171451081 | TTCCTTTAATTTTAC[C/G]TTGTTTAGATAACTA | 80067 |
| rs752806217 | snp | C/T | 1.68038e-05 | 0.00289855 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453085 | TGTGTTTCTGAAGTA[C/T]TTTTGAGAGCTGCGT | 80067 |
| rs752912991 | snp | C/T | 3.3284e-05 | 0.00407932 | synonymous-codon, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171477995 | ATGATAGAATGAAAA[C/T]GTACTCACTGTTACA | 80067 |
| rs752938211 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171446756 | ATAAGATTTTTAAAA[C/T]TGCATTGTGAATGTA | 80067 |
| rs752975201 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171479174 | AATTTTTATGTCTTA[G/T]GGTGGTAAAGGCAGA | 80067 |
| rs753000759 | in-del | -/AC | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444542 | TCCCATCCCCAAGAT[-/AC]CTCATTATGCATATG | 80067 |
| rs753063138 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171478155 | TCCCCATATCCTGGG[G/T]TAGAGGTTGGGGTTG | 80067 |
| rs753106369 | snp | A/G | 1.65638e-05 | 0.00287778 | missense, intron-variant | DCAF17 | GRCh38.p7 | 2:171458406 | ACTTAGGGTGTGCAT[A/G]CAGATGGGGTGGGAC | 80067 |
| rs753155468 | snp | A/G | | | synonymous-codon | DCAF17 | GRCh38.p7 | 2:171490790 | ATCAGTGGACAGGAA[A/G]CAAGGAGGACTCAGA | 80067 |
| rs753188924 | snp | A/G | 1.69818e-05 | 0.00291387 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435197 | AGCAGGTAACTTTTT[A/G]TTGATAATTTTGCTG | 80067 |
| rs753197965 | snp | C/G/T | 5.16519e-05 | 0.0050817 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458517 | TCACCTTAAAAAAAT[C/G/T]AAGTGGTCATATAAA | 80067 |
| rs753207674 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171471489 | AAAAAGATATGTATA[A/G]TATGTGCATATTTTG | 80067 |
| rs753262810 | snp | C/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171433088 | AGCTCAGGGTGCAAG[C/G]TGGGAACCAACCCTT | 80067 |
| rs753362621 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171472499 | ACACTTCTGTACTTT[C/G]GATTTTACTGTCTCT | 80067 |
| rs753380867 | snp | A/T | 0.000135738 | 0.00823715 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481162 | TTAGCCAAACACCCC[A/T]GCAGCTGCGTCCAAT | 80067 |
| rs753423974 | snp | A/G | 1.67947e-05 | 0.00289777 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449978 | CATATTTAAACATTC[A/G]ATAAAATGAAGACTC | 80067 |
| rs753441928 | snp | C/T | | | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485065 | CAATTCTTTTGTGAA[C/T]ATGTGTCTTTATTTC | 80067 |
| rs753477159 | snp | C/T | 1.65638e-05 | 0.00287778 | synonymous-codon, intron-variant | DCAF17 | GRCh38.p7 | 2:171458425 | ATGGGGTGGGACTAC[C/T]GGAACTGTAGGAGAG | 80067 |
| rs753532618 | snp | A/G | 1.64885e-05 | 0.00287123 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481001 | GAAGTCTACTTTGAC[A/G]GAGACTTGGTGCTAC | 80067 |
| rs753552945 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171437614 | ATAGATACAGACTTA[C/T]TCAAGTTATCTAATT | 80067 |
| rs753657865 | snp | A/G | 1.8995e-05 | 0.00308174 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449835 | GGTTTTAAGTATAAG[A/G]AAACTGACCCAAATA | 80067 |
| rs753679131 | snp | C/T | 0.000117601 | 0.00766723 | intron-variant, synonymous-codon, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473955 | TGGTAGAATAATACA[C/T]GTTGGTCCAAATCAA | 80067 |
| rs753686429 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464648 | CAAGTCAACTCACAA[C/G]AGAGACCCAGATCTA | 80067 |
| rs753722250 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171490398 | GTGTTCAAAATAATT[A/G]TAAAAGATTGAGAGA | 80067 |
| rs753734153 | snp | C/T | 0.000185787 | 0.00963634 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482609 | AAAGTAGAGTGTTCA[C/T]TCTCCATTTCCAAGA | 80067 |
| rs753755740 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171477922 | CCAAATTTGTTAATA[C/T]AGTTTTACCTTTGAC | 80067 |
| rs753773215 | snp | A/G | | | intron-variant, missense, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171476883 | AGCTAACTGAAATAG[A/G]AAATAATAGTTCTCA | 80067 |
| rs753776237 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171477757 | AGATTGTGCCACTAC[A/T]GTGAGGCAAGATCGC | 80067 |
| rs753786023 | in-del | -/CT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171488560 | CTCTGATCTGTCTGC[-/CT]CTCTTTAAAGAGCAA | 80067 |
| rs753818890 | in-del | -/TCTT | 0.000214176 | 0.0103461 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448666 | TCATTTTTATATCTC[-/TCTT]TTTTTTTTTAGGGAG | 80067 |
| rs753872183 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487983 | GGATCATATACTGAA[C/T]AAAATTATATCAGAA | 80067 |
| rs753906990 | snp | A/T | 1.66405e-05 | 0.00288443 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171453177 | GTTCCGAGTTCTACC[A/T]TTTTCACTTGTAGGG | 80067 |
| rs753909220 | snp | C/G/T | 8.43027e-05 | 0.00649192 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478111 | ACCAAACCAGTGTGT[C/G/T]CTTGCATTGTGAATT | 80067 |
| rs753962914 | snp | A/G | 1.65866e-05 | 0.00287976 | synonymous-codon, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171478010 | TGTACTCACTGTTAC[A/G]GCTTCTGGACGGGTG | 80067 |
| rs753997812 | snp | C/T | 1.65619e-05 | 0.00287762 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457957 | CAGGTGATATCTGTC[C/T]TTCCCCCCGCCAGAT | 80067 |
| rs754018356 | in-del | -/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438859 | CGACCATCTCAGCCT[-/C]CCAAGTAGCTAGGAC | 80067 |
| rs754027837 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171469165 | AAACAATTTAAAATA[C/T]AGAAGAATACAGACA | 80067 |
| rs754100450 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171450811 | ATTTACTAATTTGAT[C/T]TTCAGCACACTCCTT | 80067 |
| rs754106293 | snp | C/G | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434113 | AGCACAGAGAAGCGC[C/G]CCCGCAAGACAGCGC | 80067 |
| rs754191203 | snp | A/G | 1.7678e-05 | 0.00297299 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458526 | AAAAATTAAGTGGTC[A/G]TATAAATAGTTATTA | 80067 |
| rs754215351 | in-del | -/TGAGGTA | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171461659 | AGAAATCAACTCTAT[-/TGAGGTA]TAATTTACATGTAAT | 80067 |
| rs754236793 | snp | C/T | 1.66366e-05 | 0.0028841 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171443550 | GCCAAGAAAACTTTA[C/T]GAAATGCCAAAATGT | 80067 |
| rs754237291 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171459645 | ATAAGAATTTTTTCT[A/G]TCATTTTTCCTTAAC | 80067 |
| rs754245126 | snp | A/T | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433497 | GCATGGCGGTGGGAC[A/T]CATGTGGTGCAAGCT | 80067 |
| rs754320297 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486082 | AATATTTGTCTGATA[C/T]TCTCCTTTAATTCTT | 80067 |
| rs754327552 | snp | A/G | 0.000185856 | 0.00963813 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483636 | CCAATTGAAAGTTTT[A/G]TATCTTACAGTTCTT | 80067 |
| rs754334454 | snp | C/T | 0.000133645 | 0.00817342 | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447433 | TGGCACGATCTCAGC[C/T]CACCGCAACCTCCAC | 80067 |
| rs754378119 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444419 | GGAAAATTTTACACC[C/T]GCCCTCATGTGACAG | 80067 |
| rs754407685 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435953 | ATTTTCATCACTTCA[A/G]AACAGAACCATGTAC | 80067 |
| rs754454595 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171459935 | TTAAGAATTTTAAAA[C/T]TGTAGGCTGCAGTGG | 80067 |
| rs754514206 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482157 | ATAAAGGCAACCCAA[G/T]TAAAGGGAGAAAATG | 80067 |
| rs754536332 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436145 | TTCATCCATGTTGTC[A/C]CATGCATCAGAATTC | 80067 |
| rs754553993 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171434919 | CTGGAAACAATTATT[C/G]TAAAAGTTGGTCACC | 80067 |
| rs754605742 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171480702 | TCGTAAATGATCACA[C/T]AGTGAGATAGATAAT | 80067 |
| rs754618329 | in-del | -/AAATAATAGT | 1.66293e-05 | 0.00288346 | intron-variant, frameshift-variant, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171476884 | GCTAACTGAAATAGA[-/AAATAATAGT]TCTCAGCATCAGATC | 80067 |
| rs754648178 | snp | C/T | 3.31554e-05 | 0.00407144 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448744 | CTGACTGCTCATAAT[C/T]GGCTACTTCGTATAT | 80067 |
| rs754663663 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171447046 | AGAGATTTCTGACCA[A/C]ATTAAGGAACACTGT | 80067 |
| rs754667938 | snp | G/T | 0.00222717 | 0.033296 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484994 | GTTGATGGACACTGG[G/T]CTCTTTCTGCTTGTT | 80067 |
| rs754675602 | snp | A/G | 7.87216e-05 | 0.00627332 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481194 | CATTTTATTATCTGC[A/G]TGGCACATTCTCCAG | 80067 |
| rs754753735 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171461025 | ATTTCATACTGTAGA[A/G]ACTTAAATCCCATTC | 80067 |
| rs754795856 | snp | C/G | 0.000138227 | 0.00831229 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434255 | CCTCACGAGGCACTA[C/G]GAACTACATTTCCCG | 80067 |
| rs754834566 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171446375 | ACATAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 80067 |
| rs754841506 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171459451 | TAGCTATAAAGATCA[C/T]ATGAGTAAACTAAAA | 80067 |
| rs754897640 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439819 | CATAATCCCAGCTAC[G/T]CCAGAGGCCAAGGCA | 80067 |
| rs754915518 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171473102 | TAGAGTTCAACATTT[C/G]ACTTATCCAAGATTC | 80067 |
| rs754977913 | snp | A/T | 0.000184451 | 0.00960163 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481474 | TAAAGGATGGTATGG[A/T]ATTTTGTTTGTTAAG | 80067 |
| rs755028977 | snp | A/G | 0.0020467 | 0.0319243 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482682 | GATTTTTTTTTTTAG[A/G]TGATTATTGAGTTTC | 80067 |
| rs755038147 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464854 | AAACTTTATCCTACT[A/G]TATATATATGATAGT | 80067 |
| rs755136582 | snp | A/G | 1.65784e-05 | 0.00287905 | intron-variant, synonymous-codon, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171476899 | AAATAATAGTTCTCA[A/G]CATCAGATCTCTGAA | 80067 |
| rs755189449 | snp | C/G | 0.000371471 | 0.0136234 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483094 | ATGGTAAAAAGATGC[C/G]AGAAGATACAGAAGA | 80067 |
| rs755232804 | snp | A/C | 3.61533e-05 | 0.00425151 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449850 | GAAACTGACCCAAAT[A/C]AATAAACTTCTCTTC | 80067 |
| rs755288625 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171476419 | ATAGATTTAATTGCT[A/G]ATTGAATTTCTTTTT | 80067 |
| rs755304811 | snp | C/T | 1.65611e-05 | 0.00287755 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171457982 | CCAGATTTTTGGGAA[C/T]GTTACAGATGCTACC | 80067 |
| rs755308861 | snp | A/G | | | missense | DCAF17 | GRCh38.p7 | 2:171490761 | AGATTGCCCAAGGCA[A/G]AATTCACCTTGACAT | 80067 |
| rs755330994 | snp | A/T | 1.65119e-05 | 0.00287327 | synonymous-codon, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480121 | TGCTGAAGGAAAAGC[A/T]CACCTGGATTTCCAC | 80067 |
| rs755358041 | snp | A/G | 5.03495e-05 | 0.00501719 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477980 | TTTATTTCTTTCCAT[A/G]TGATAGAATGAAAAT | 80067 |
| rs755376555 | in-del | -/TCTT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171451415 | TTAGTAATACTTCTC[-/TCTT]TATACTCTTACTACC | 80067 |
| rs755391973 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171454259 | ACAGATTGGCTACTT[C/T]ATTATAGCAGTCATT | 80067 |
| rs755419401 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171456741 | TATTCTTTTTAGGAC[A/G]ACTGTGAATGAGAGT | 80067 |
| rs755463686 | snp | C/T | 1.65773e-05 | 0.00287895 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458107 | TTTGTCATGTTACTA[C/T]TAGCATGAGTTTTCG | 80067 |
| rs755473775 | snp | C/T | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470441 | AGCATAGCGTTGGGT[C/T]CATTTGTCCACTTCC | 80067 |
| rs755643591 | snp | A/T | 1.78115e-05 | 0.0029842 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448860 | ATTTTATTTTAAAAA[A/T]TTGAAACCTGTGGCC | 80067 |
| rs755652507 | snp | G/T | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470562 | ATGGCTGCTCCTATT[G/T]GGCCCAGCCCAGTGA | 80067 |
| rs755674655 | in-del | -/A | 1.64743e-05 | 0.00287 | frameshift-variant, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171478028 | TTCTGGACGGGTGGT[-/A]AAAAAAAGTTTTAAC | 80067 |
| rs755729484 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171437437 | ACGTTCAAGTCTGTT[C/T]CACTGATCTGTATGT | 80067 |
| rs755732492 | snp | A/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469788 | ATTTTTATTTTGTAT[A/T]GCTGATTATGTTTTT | 80067 |
| rs755750047 | in-del | -/GT | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483183 | TCCCAGCTCGCCAGA[-/GT]GTCACACAGCTGCTC | 80067 |
| rs755775466 | snp | A/G | 1.64904e-05 | 0.00287139 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480989 | ACATATAGCCATGAA[A/G]TCTACTTTGACAGAG | 80067 |
| rs755782376 | snp | A/T | 0.000142197 | 0.00843079 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482508 | AAACTTACATCTTGA[A/T]AAACAAGACCAGTAA | 80067 |
| rs755806887 | snp | C/G | 1.65312e-05 | 0.00287495 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469044 | TGGTAAATGAGTGAT[C/G]AGACTTTTTATTAGC | 80067 |
| rs755819632 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436194 | TATTGCATTGTATCA[A/G]TTACCACATTTTACG | 80067 |
| rs755882378 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171462615 | TTGGGACCCTTTATG[A/G]CCCCCAACAATTTGT | 80067 |
| rs755912021 | snp | G/T | 0.000373622 | 0.0136628 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482143 | CTTTAGAATGTTAAA[G/T]AAAGGCAACCCAAGT | 80067 |
| rs755984087 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171448669 | TTTTTATATCTCTCT[C/T]TTTTTTTTTAGGGAG | 80067 |
| rs755987789 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487601 | GCTAATTTTGTATTT[C/T]TAGTAGAGATGGGGT | 80067 |
| rs755997846 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171447288 | ATATATAAAATAACT[A/C]TGTCTTCATTCTTTT | 80067 |
| rs756012008 | in-del | -/ATCT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171473787 | ACCTTTGACCTACTG[-/ATCT]ATCACTTGGGTTAGA | 80067 |
| rs756046104 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171461127 | TTTCTTAGTGCAAAA[C/G]CAGTTCCTTTGCATT | 80067 |
| rs756053962 | snp | A/C/G | 4.97338e-05 | 0.00498646 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448754 | ATAATTGGCTACTTC[A/C/G]TATATCAGCAACTAC | 80067 |
| rs756103858 | snp | A/T | 0.000102025 | 0.00714158 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472975 | TACATTTGTGTACAC[A/T]TGTGATAACATATCA | 80067 |
| rs756121328 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439059 | TCTCTGCTTGCTCTT[A/G]TGCTCTCTGAAGAGA | 80067 |
| rs756127137 | snp | A/G | 1.65693e-05 | 0.00287826 | intron-variant, missense, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171476921 | ATCTCTGAAGATTTT[A/G]TCATTTTGGCCAACA | 80067 |
| rs756134446 | snp | C/T | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474720 | TTTGTCTTTCATCAA[C/T]GTACATACATTTAAA | 80067 |
| rs756157349 | snp | A/G | | | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485516 | AACCTGGGTTCTAAG[A/G]GCACGTGTTCCACCG | 80067 |
| rs756259473 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466203 | TGGTAGAAGAAATAT[A/G]TCAAGTTAATTATCC | 80067 |
| rs756304520 | snp | C/T | | | intron-variant, upstream-variant-2KB | METTL8, DCAF17 | GRCh38.p7 | 2:171432205 | CTCCAGCTGCGGAGG[C/T]CTCCAGTGGCAAAGC | 80067 |
| rs756356358 | snp | A/G | 1.6599e-05 | 0.00288084 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171478005 | GAAAATGTACTCACT[A/G]TTACAGCTTCTGGAC | 80067 |
| rs756388098 | snp | A/T | 1.67897e-05 | 0.00289733 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453086 | GTGTTTCTGAAGTAC[A/T]TTTGAGAGCTGCGTG | 80067 |
| rs756479437 | snp | A/G | 1.65726e-05 | 0.00287855 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435122 | TGGACAACTCATTCC[A/G]GGTCACCTATAGCCT | 80067 |
| rs756491426 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171479213 | GTGGATTAGAGAGCA[C/G]TTTGACCAAACATAG | 80067 |
| rs756526335 | in-del | -/CAT | 1.6609e-05 | 0.0028817 | cds-indel, nc-transcript-variant | DCAF17 | GRCh38.p7 | 2:171453139 | GCAGGCATTCAACAA[-/CAT]GTTTTGCTGTACCTT | 80067 |
| rs756551332 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444214 | TCAGAGCCTTTACTA[A/C]TAATAATAATACAAT | 80067 |
| rs756576521 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171442385 | AACATGGTGAAACCC[G/T]GTCTCTACTAAAAAT | 80067 |
| rs756579625 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171478265 | ATTGTAATTATTCTT[A/G]AAGTTTTATTTGCAG | 80067 |
| rs756605585 | snp | C/T | 0.000185822 | 0.00963724 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483203 | ACACAGCTGCTCATT[C/T]TGCCACCTGCCAGAC | 80067 |
| rs756611433 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171457616 | AGAGTATGAATAGTA[G/T]ATTAAATATTCATTT | 80067 |
| rs756655038 | snp | A/G | 1.6649e-05 | 0.00288518 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171443544 | ATCTGAGCCAAGAAA[A/G]CTTTATGAAATGCCA | 80067 |
| rs756656686 | snp | C/T | 0.000373134 | 0.0136539 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482705 | TGAGTTTCTCCTTCT[C/T]CTTTAAGTCATCACC | 80067 |
| rs756663758 | snp | C/T | 1.64874e-05 | 0.00287113 | synonymous-codon, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481018 | AGACTTGGTGCTACA[C/T]ATAGAGCAGAAACCC | 80067 |
| rs756669598 | snp | A/G | | | utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171490820 | AGCAACATGACGTAC[A/G]TGAAGTACTGTTGGC | 80067 |
| rs756817915 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171457725 | AGCAGATGAATGCTG[A/G]TGCATTATTCTGAGG | 80067 |
| rs756909925 | snp | C/G | 1.64825e-05 | 0.00287071 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468848 | AGTCCAGAGCCCCCA[C/G]AACAGTGCAGCTAAT | 80067 |
| rs756915171 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171470725 | GGATCTAGTGAAATC[C/T]TGCACAGTTCACATT | 80067 |
| rs756931601 | snp | A/G | 1.65787e-05 | 0.00287907 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448761 | GCTACTTCGTATATC[A/G]GCAACTACGGGAAAA | 80067 |
| rs756943541 | snp | C/T | 1.71399e-05 | 0.0029274 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435205 | ACTTTTTATTGATAA[C/T]TTTGCTGTAATTCAC | 80067 |
| rs756960086 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171437673 | TCTTTCAAGGAATTC[A/G]TCTAAGTTATCCAAA | 80067 |
| rs756963461 | snp | C/T | 1.72204e-05 | 0.00293427 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481170 | ACACCCCAGCAGCTG[C/T]GTCCAATCCATTTTA | 80067 |
| rs757025041 | snp | C/G | | | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485165 | CTGCCAGACCTTTTC[C/G]CCAAAGGATTGTACG | 80067 |
| rs757047969 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171449870 | AACTTCTCTTCATTC[C/T]TTTAAAAGATACTTG | 80067 |
| rs757133526 | in-del | -/T | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435807 | GCATTTTTAAAAAAA[-/T]GAGCTTTTTTTATAG | 80067 |
| rs757217428 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171448234 | CCTCCCAGTCTCAAG[C/T]GATCCTCTTGCCTCA | 80067 |
| rs757257068 | snp | G/T | 1.68533e-05 | 0.00290282 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171453194 | TTTCACTTGTAGGGA[G/T]TCTAGAGATCAACAA | 80067 |
| rs757286307 | snp | C/T | 1.88319e-05 | 0.00306848 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449840 | TAAGTATAAGGAAAC[C/T]GACCCAAATAAATAA | 80067 |
| rs757330160 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171488120 | ACCTTGGATCACCAC[A/G]GAAGTGATGAAACTT | 80067 |
| rs757358425 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171448924 | TTCTAATCCATTACC[A/G]GATCTCAATTAATAA | 80067 |
| rs757473806 | in-del | -/CAATT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452830 | TTATTGTTCAAACTC[-/CAATT]CAAAATATAAATGCA | 80067 |
| rs757489748 | snp | C/G/T | 9.93664e-05 | 0.007048 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457965 | ATCTGTCTTTCCCCC[C/G/T]GCCAGATTTTTGGGA | 80067 |
| rs757543988 | snp | A/G | 0.000185031 | 0.00961672 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481497 | TTGTTAAGGCTAGGA[A/G]AGACAGGGAGAGACA | 80067 |
| rs757589748 | snp | C/T | 0.000185891 | 0.00963903 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483248 | GCCCTACCTAAACCC[C/T]CTCTTTACCTGATAT | 80067 |
| rs757635706 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171467434 | AGTGGCTCACCTGTA[A/G]TCCAAGCACTTTGGG | 80067 |
| rs757639715 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171451244 | TTGGCTACTTCTACT[G/T]ACTTTTTATCATGGT | 80067 |
| rs757659996 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432602 | TTACCAAATTAACTA[C/T]TGTAGCACTCTCTAA | 80067 |
| rs757667631 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171480559 | TAAGCATGCGGGATT[C/G]CCAGGTACTCTTGTA | 80067 |
| rs757681376 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171479282 | ATGCCTGTCTTTAAA[C/G]TTGATGCCAGGCATT | 80067 |
| rs757682033 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435843 | ATTAGGATATAATTC[A/G]CATACCATATATTTA | 80067 |
| rs757732239 | in-del | -/T | 0.000186411 | 0.00965249 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484530 | TGATATACTTCCCCC[-/T]AGTACTTCAACTGCA | 80067 |
| rs757742700 | snp | A/G | 0.00018596 | 0.00964082 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483684 | TATTGAGCACTTTCT[A/G]TCTACTAGTCACTGT | 80067 |
| rs757747726 | snp | C/G | 3.31708e-05 | 0.00407238 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171478012 | TACTCACTGTTACAG[C/G]TTCTGGACGGGTGGT | 80067 |
| rs757751652 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171445351 | GCTGGTCTCGAACTC[G/T]TGACCTCAAGTGATC | 80067 |
| rs757760166 | snp | A/T | 1.6615e-05 | 0.00288223 | stop-gained, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171443565 | TGAAATGCCAAAATG[A/T]TCCAAATCAGAAAAA | 80067 |
| rs757796903 | snp | C/T | 1.67635e-05 | 0.00289507 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171476957 | AACCATAAAGTAAGT[C/T]AAGAGTACTTTAAAA | 80067 |
| rs757839826 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant, synonymous-codon | DCAF17 | GRCh38.p7 | 2:171468893 | GTCTCTACAGACATG[C/T]CACCACTGCTCTTTG | 80067 |
| rs757870957 | snp | C/T | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171469912 | CTGGGTTCAAGTGAT[C/T]CTCCTGCCACAACCT | 80067 |
| rs757915049 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171454858 | GCCAGGATTGTGCCA[C/T]GGCAACAGAGCAAAA | 80067 |
| rs757945899 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171458135 | CGACTAAAGTATGAT[-/T]TTTTTTTTTTAGTGA | 80067 |
| rs758012127 | snp | A/G | 1.66128e-05 | 0.00288204 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171443586 | ATCAGAAAAAATAGA[A/G]GATGCTTTATTATGG | 80067 |
| rs758039475 | snp | C/T | 0.000733003 | 0.0191302 | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447512 | ATTATAGGCAAGCAC[C/T]GCAACGCCCAGCTAA | 80067 |
| rs758069459 | in-del | -/T | 0.00380661 | 0.0434605 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448668 | ATTTTTATATCTCTC[-/T]TTTTTTTTTTAGGGA | 80067 |
| rs758118215 | snp | G/T | 0.000185925 | 0.00963993 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483759 | TAACCACATGAAGTA[G/T]GAACTGCCATTATCT | 80067 |
| rs758118536 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466301 | AGTAAAGTTATTTTG[C/T]ATGCTTTATGTTAAA | 80067 |
| rs758219406 | in-del | -/A | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171468169 | TGATAAAAGAAGATG[-/A]CTAAAAATTTCTCTT | 80067 |
| rs758228171 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438814 | CAATCATAGCTCACT[A/G]TAACACCAAACTCCT | 80067 |
| rs758302316 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486648 | AAGATAAAGGACATA[C/G]CCATTACCCAAAAAG | 80067 |
| rs758303905 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171472000 | AGCCTGTGCAACAGA[A/G]TGAGACCCTGTCTCA | 80067 |
| rs758318127 | snp | A/G | 1.77313e-05 | 0.00297747 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481180 | AGCTGCGTCCAATCC[A/G]TTTTATTATCTGCAT | 80067 |
| rs758336940 | snp | C/T | 1.68063e-05 | 0.00289877 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453076 | TGAAAACAGTGTGTT[C/T]CTGAAGTACTTTTGA | 80067 |
| rs758371635 | snp | C/T | 0.000272183 | 0.0116626 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171434207 | CTCCCCGCCGCCTGA[C/T]GGGAATTGTAGTTCC | 80067 |
| rs758412198 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171462907 | ACCATATAGCTGTAT[C/T]ACAAATTTAATTGCT | 80067 |
| rs758502229 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171476307 | TCCAAACCCCCAAAT[C/G]TTTAAATATAACCAA | 80067 |
| rs758537916 | snp | C/T | 0.000185753 | 0.00963545 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482614 | AGAGTGTTCATTCTC[C/T]ATTTCCAAGAGTGTT | 80067 |
| rs758543435 | snp | C/G | 0.000176289 | 0.00938688 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434626 | CGGCTGAGTCGCCGG[C/G]CGCTGGGCTGCTTCT | 80067 |
| rs758568654 | in-del | -/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439773 | TCTCTACTAAAAAAA[-/C]AAAAATTAGCTGGGC | 80067 |
| rs758636084 | snp | A/C/G | 3.34645e-05 | 0.0040904 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435089 | GTCTTTTAGGAAAGT[A/C/G]CTAAATTTAAGAATG | 80067 |
| rs758677778 | snp | C/T | 1.87317e-05 | 0.00306031 | intron-variant | DCAF17 | GRCh38.p7 | 2:171473857 | TTTAATACTTTTTTC[C/T]AACTTCAGGCAAAAA | 80067 |
| rs758713057 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171488368 | TTCTCTTAAAAGGGT[A/G]TGTTCTCAAGTAGAC | 80067 |
| rs758732684 | snp | A/G | 0.000371747 | 0.0136285 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482217 | AGTTGCTTCCATTTC[A/G]CATGTTCTGCACATT | 80067 |
| rs758733497 | snp | A/C | 1.65729e-05 | 0.00287857 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171478032 | GGACGGGTGGTAAAA[A/C]AAAGTTTTAACCTTC | 80067 |
| rs758748448 | in-del | -/T | 0.000744463 | 0.0192789 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484585 | TATTTAGTTTTTAAA[-/T]TTTTTTGATTTAAGA | 80067 |
| rs758757734 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171437703 | ACTTGTGAGCCTAGA[C/T]TTATTCATAATATTT | 80067 |
| rs758764028 | in-del | -/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444118 | GTGTCAGAGGAGTTA[-/G]GGGGAATTGGGCTGT | 80067 |
| rs758777886 | snp | A/G | 0.000593648 | 0.0172183 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484441 | CCACGGGGATTCTAC[A/G]TCTTACTCTACTTGT | 80067 |
| rs758811597 | snp | G/T | 3.31225e-05 | 0.00406941 | splice-acceptor-variant | DCAF17 | GRCh38.p7 | 2:171457970 | TCTTTCCCCCCGCCA[G/T]ATTTTTGGGAACGTT | 80067 |
| rs758911517 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481853 | GCTCTTAATGTATCT[A/G]AGGATGTTCTCATCT | 80067 |
| rs758916081 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171434813 | CTTTATAGGGTCACA[C/T]GTGATGGGGAGGAGG | 80067 |
| rs759014517 | in-del | -/GTG | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171450357 | ATGTGACCCAACACC[-/GTG]ACCTGTTCCTCAAAA | 80067 |
| rs759079300 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171449412 | TATTTTCTATGTAAG[A/G]TGCTCTTTATGGTAG | 80067 |
| rs759155559 | snp | C/G | 1.72392e-05 | 0.00293586 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448844 | GAATTTATTATTCAA[C/G]ATTTTATTTTAAAAA | 80067 |
| rs759165085 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464054 | TAATGATGTTCAAAT[C/T]GTCCTGAATTTGGCC | 80067 |
| rs759180619 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171461887 | TTTATATTTTCTGGA[A/G]TTTTATATTAATGAA | 80067 |
| rs759192537 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171490384 | CTGTCAAATGCAGTG[C/T]GTTCAAAATAATTGT | 80067 |
| rs759316028 | snp | C/G | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171475680 | GGGCAGGAGGATCAG[C/G]TGAGCCCAGGAGTTC | 80067 |
| rs759321882 | in-del | -/AG | 0.000185891 | 0.00963903 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483180 | GCTTCCCAGCTCGCC[-/AG]AGTGTCACACAGCTG | 80067 |
| rs759375695 | snp | C/G | 0.000186133 | 0.0096453 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482065 | GGCTTACTTATGGAA[C/G]AAGCATTATTTCTTC | 80067 |
| rs759392662 | snp | A/G | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480057 | TCAAAATTGTGGACT[A/G]TGAAGATGAGTTAGA | 80067 |
| rs759404029 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171489312 | TAATATAAAAACACT[A/G]ACAGACAGAGGATGG | 80067 |
| rs759440827 | snp | C/T | 1.6563e-05 | 0.00287771 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457951 | TTTTCTCAGGTGATA[C/T]CTGTCTTTCCCCCCG | 80067 |
| rs759469596 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171480470 | TTTGATTTTCTTTCA[A/G]TTGTAAATTTGGAAA | 80067 |
| rs759528673 | snp | C/G | 0.000190132 | 0.00974833 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434595 | GGGCCCGACCCGGAA[C/G]CCCAACGTGTGCAGC | 80067 |
| rs759651629 | in-del | -/C | 8.28102e-05 | 0.00643415 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457959 | GTGATATCTGTCTTT[-/C]CCCCCCGCCAGATTT | 80067 |
| rs759684052 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171479142 | ATTTTAATAATCAAA[C/T]GTAATAAATCCATAT | 80067 |
| rs759690253 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443947 | CCACTCAATATACTG[A/G]AACAGTAACAAAGTA | 80067 |
| rs759690510 | snp | C/T | 1.68142e-05 | 0.00289945 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443516 | ATTTATTTTTCTTTT[C/T]TCCCAGTGTTGCATC | 80067 |
| rs759704034 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444994 | AAAAGTAACTGTTGT[A/G]CCTTTAGCAATTTAA | 80067 |
| rs759755757 | snp | A/T | 1.6998e-05 | 0.00291525 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458508 | AGTATTTTTTCACCT[A/T]AAAAAAATTAAGTGG | 80067 |
| rs759757822 | snp | C/G | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432701 | AAGGAAATTCAGCAG[C/G]GTTAAAAAGAGATAT | 80067 |
| rs759763006 | snp | A/G | 5.07198e-05 | 0.00503561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443634 | ATTTGTTTTTAGAGC[A/G]TTTGTTTCTAAAGCA | 80067 |
| rs759776218 | snp | G/T | | | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435183 | ATCGGCGCTGTGTCA[G/T]CAGGTAACTTTTTAT | 80067 |
| rs759779779 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171457437 | GAATAATAGAAAAAT[A/G]TGCAATTAGAGAGAT | 80067 |
| rs759786120 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171442829 | AGGTTGAAGTGAGCT[A/G]AGATCATGCCATTGC | 80067 |
| rs759805004 | snp | C/T | | | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491431 | CAATAGGGCATAACA[C/T]GGGTGAGGAACACCA | 80067 |
| rs759826689 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481373 | GGTGGTAATGCAAAT[A/G]TAAAATGCTGGGAAC | 80067 |
| rs759843593 | in-del | -/TAAAAACTTTAA | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171477487 | TGGCATTTTAGCCAT[-/TAAAAACTTTAA]TAAAGTATTTTTGAG | 80067 |
| rs759888827 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438501 | CCTTGCATTTCTATC[C/T]GTGTTTGCCACATTG | 80067 |
| rs759922443 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464452 | CACTTTTCCATGGCC[-/T]TTTCTCCCTCTGTGT | 80067 |
| rs759948524 | snp | C/T | 1.66418e-05 | 0.00288455 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171449950 | GAGGCTCAGCAGTGG[C/T]CCGGCAGGTATACAT | 80067 |
| rs760034253 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484454 | ACATCTTACTCTACT[C/T]GTTTTATTATTTTCC | 80067 |
| rs760059288 | snp | A/G | 3.31279e-05 | 0.00406975 | synonymous-codon, intron-variant | DCAF17 | GRCh38.p7 | 2:171458398 | GAAACTTGACTTAGG[A/G]TGTGCATGCAGATGG | 80067 |
| rs760173945 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486215 | GCAAAGGTGGTAAAT[C/G]CAATAAAAAGATGTC | 80067 |
| rs760207728 | snp | A/C | 3.32452e-05 | 0.00407695 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171453130 | TCCTTCTAGGCAGGC[A/C]TTCAACAACATGTTT | 80067 |
| rs760217085 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438614 | TATGCCCACTTAATC[C/T]CTGGTAATGTTCCTT | 80067 |
| rs760235908 | in-del | -/AGTT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171488039 | CTAAATTATGTCTAA[-/AGTT]AGTTAATACCTGCTC | 80067 |
| rs760296557 | snp | G/T | 1.75078e-05 | 0.00295864 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476832 | GTTTTGAAGTCTTAG[G/T]TTCTCAGAATCCTTT | 80067 |
| rs760313083 | in-del | -/ACTT | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432780 | GTACTGTAAGTACTC[-/ACTT]AATGTCATCAACAGA | 80067 |
| rs760384569 | snp | C/T | 3.34275e-05 | 0.00408811 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449963 | GGCCCGGCAGGTATA[C/T]ATATTTAAACATTCA | 80067 |
| rs760427034 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171450944 | CTCAGGCAGTTTAGC[-/T]TCTAGAGTCCCTGCT | 80067 |
| rs760504028 | snp | A/G | 1.66824e-05 | 0.00288806 | intron-variant, missense, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473935 | TATTTCCATCCTGAT[A/G]CTTCTGGTAGAATAA | 80067 |
| rs760524776 | snp | C/T | 1.6577e-05 | 0.00287893 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458369 | GTTTTGTTTTGTTTT[C/T]AGTTCATGCAACAGA | 80067 |
| rs760538522 | snp | C/G | 1.65921e-05 | 0.00288024 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435161 | GGAAGAATATATTTT[C/G]ACAATTATCGGCGCT | 80067 |
| rs760540591 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171441635 | TGGAAGCTTGGAAAA[C/T]AGGGAGCCTCGTACT | 80067 |
| rs760582684 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443187 | TTCAACAGAGATATT[A/C]TTAGTAAATGTTCAG | 80067 |
| rs760651198 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435434 | ACCACAGATTGTTCA[A/G]AGTACTGTTTAGTGT | 80067 |
| rs760659792 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171489355 | TAATAGAAAAGTATA[C/T]GAAATGTACAGAGAT | 80067 |
| rs760665138 | snp | C/T | 0.000186306 | 0.00964979 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482932 | CAGGCAGGAAATATA[C/T]CTCATGTGAAAGACA | 80067 |
| rs760680285 | in-del | -/T | 9.91269e-05 | 0.00703943 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469040 | TCCCTGGTAAATGAG[-/T]GATCAGACTTTTTAT | 80067 |
| rs760686279 | snp | C/T | 0.000185891 | 0.00963903 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483545 | CAAAACAAATCCTAT[C/T]CTATTTACTATTTGT | 80067 |
| rs760726025 | snp | G/T | 0.000185822 | 0.00963724 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482561 | AAAGAAACCAATGTT[G/T]TGTGAGTTTCAAAGC | 80067 |
| rs760780121 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435457 | TTTAGTGTTTAGTCT[A/G]CTTATACCACAGTCA | 80067 |
| rs760860274 | snp | A/G | 5.02753e-05 | 0.00501349 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478099 | CAGAGATGACAAACC[A/G]AACCAGTGTGTCCTT | 80067 |
| rs760911781 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171445176 | GTTGCCCAGGCTGCA[C/G]TGCAGTGGCGTGATC | 80067 |
| rs760915283 | snp | A/G | 0.000378286 | 0.0137477 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484128 | ACTTTCCCTTTGTTT[A/G]TGGTGATAATCAGTA | 80067 |
| rs760978794 | snp | C/T | 1.65864e-05 | 0.00287974 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448700 | ATATACTTCCCAATT[C/T]ATCAGATTATAAGTC | 80067 |
| rs761101140 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439396 | GAAGTTTCTGTTGAC[C/G]TATCTTCAAACTCAC | 80067 |
| rs761204520 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171467915 | TGTATATAACATGTG[A/T]CTCTTACACGAATCA | 80067 |
| rs761229686 | snp | A/G | 3.29625e-05 | 0.00405958 | stop-gained, nc-transcript-variant, missense | DCAF17 | GRCh38.p7 | 2:171468955 | TGGAGGCCATCCTTG[A/G]CACTACATCGTCACA | 80067 |
| rs761236782 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171472459 | GCTAGGATTACAGGC[G/T]TAAGCCACTGCCCCC | 80067 |
| rs761267211 | snp | G/T | 9.19583e-05 | 0.00678017 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481273 | TTTTAAACTCTTGCT[G/T]TAAAAGATGGTGAGG | 80067 |
| rs761324965 | snp | A/G | 0.000189915 | 0.00974278 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434497 | GCCTCGAAATTCGAA[A/G]GCAGCGGCGGCTGCC | 80067 |
| rs761471487 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443000 | TGGCAGAAGTATAAA[C/T]TTACTCAACCTTTCT | 80067 |
| rs761523874 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486402 | GCAACCTCTGCCTCT[C/T]GGGTTCAAGTGATCC | 80067 |
| rs761537068 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438752 | CTTTTTTTTTCCCCC[C/T]CAAAGTCAGGGTCTG | 80067 |
| rs761646871 | snp | A/G | 1.73054e-05 | 0.00294149 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443494 | TTGGTTATCAAGAAT[A/G]ATAATCATTTATTTT | 80067 |
| rs761811966 | snp | A/C | 1.68187e-05 | 0.00289984 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477978 | TTTTTATTTCTTTCC[A/C]TATGATAGAATGAAA | 80067 |
| rs761814031 | snp | C/T | 1.65545e-05 | 0.00287697 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449991 | TCAATAAAATGAAGA[C/T]TCTTTTTCATAGGAA | 80067 |
| rs761867442 | snp | C/G/T | 3.3172e-05 | 0.00407248 | intron-variant, missense, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171476895 | TAGAAAATAATAGTT[C/G/T]TCAGCATCAGATCTC | 80067 |
| rs761994628 | snp | A/G | 3.314e-05 | 0.00407049 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458091 | GTAGAGAAAACTGAA[A/G]TTTGTCATGTTACTA | 80067 |
| rs762022365 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481643 | TTTTTAAAAATCTTA[C/T]ATATGTATTTATATG | 80067 |
| rs762023221 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435680 | CAATGCATCCCCATA[C/T]ACTCATTACCCAGAT | 80067 |
| rs762028964 | snp | C/G | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470281 | TCCCTCTTGATATAT[C/G]AGAAGAATTTGCTTT | 80067 |
| rs762066440 | snp | A/G | 1.69965e-05 | 0.00291513 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480222 | GTGGGATACAAAGTT[A/G]TAAACCTTTCCTTTA | 80067 |
| rs762115556 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434115 | CACAGAGAAGCGCGC[C/T]CGCAAGACAGCGCAG | 80067 |
| rs762118586 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171469295 | ATCTCCCAGCAAGGA[A/G]TCTCATGTAAAACCT | 80067 |
| rs762232315 | snp | A/G | 0.00186081 | 0.0304457 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481680 | GTATTTGTATATAGT[A/G]TCAGGAATTGGTTCT | 80067 |
| rs762234249 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171461353 | AATTGCTTGAACCCA[A/G]GAGGCAGAGGTTGCA | 80067 |
| rs762344074 | snp | C/T | 1.65814e-05 | 0.00287931 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448720 | GATTATAAGTCCTCA[C/T]TCATAGCACTGACTG | 80067 |
| rs762364516 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171460422 | AGTTTTATCCCTTTT[C/T]TTAGAAAGAAGACTG | 80067 |
| rs762387316 | snp | G/T | 0.000180391 | 0.00949543 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481402 | ACAGAAAAGGACAGG[G/T]TAATTCCAATTGTTG | 80067 |
| rs762399244 | snp | A/G | 1.66059e-05 | 0.00288144 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469073 | GCAAATTTGTATCAA[A/G]TTCTTTATTTTCTAC | 80067 |
| rs762407022 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171434978 | GGAGGAAGGATGCAA[A/G]AAGTTTTAAAATAAT | 80067 |
| rs762513366 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171462091 | TAATCCTATCTCACT[C/T]TTAAATAATAGATGG | 80067 |
| rs762563231 | snp | A/G | 0.000575374 | 0.0169516 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472894 | AATTAAATGACTTCT[A/G]TAAAGCCAGTGAAGT | 80067 |
| rs762585568 | snp | G/T | 0.000187143 | 0.00967143 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484079 | TGACAGAAAATGTAG[G/T]TCTTCATTCAATGGT | 80067 |
| rs762600826 | snp | A/C | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475517 | AGGCCTATAATCCTG[A/C]ACTTTGGGAGGCCGA | 80067 |
| rs762602818 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171460589 | AGAGTGGAGTGCAGT[A/G]GAGAGATCACAGCTC | 80067 |
| rs762608997 | snp | A/G | 0.00019393 | 0.00984517 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434578 | CCGGCCCGCGCCTCC[A/G]TGGGCCCGACCCGGA | 80067 |
| rs762694451 | snp | C/T | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474235 | AGACTGGCCCTTTCT[C/T]ATCAGGTCTTAGTTA | 80067 |
| rs762697120 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452913 | ATATATGCGCATGTG[C/T]GTCTGAAGGGCTGAA | 80067 |
| rs762751087 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487621 | AGAGATGGGGTTTCA[C/T]CATGTTGGCCAAGCT | 80067 |
| rs762753576 | snp | C/T | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470433 | TGCAGGTCAGCATAG[C/T]GTTGGGTCCATTTGT | 80067 |
| rs762776852 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452005 | AGTAGCTCTTAGTTG[A/G]GGTATATAAACTGTA | 80067 |
| rs762819110 | snp | A/G | 1.67326e-05 | 0.00289241 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478091 | GCTTTGGCCAGAGAT[A/G]ACAAACCAAACCAGT | 80067 |
| rs762849211 | in-del | -/AAATT | 0.000664231 | 0.0182119 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472873 | CATTTTACATTAGAG[-/AAATT]AAATTAAATGACTTC | 80067 |
| rs762855426 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171468780 | AGTAATTTTTCATTA[A/C]TAGAAATTTATAGAT | 80067 |
| rs762875945 | snp | G/T | 5.02668e-05 | 0.00501307 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477982 | TATTTCTTTCCATAT[G/T]ATAGAATGAAAATGT | 80067 |
| rs762884850 | snp | C/G | | | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491194 | TAGCCAGGCACATGC[C/G]TGTAGTCCCAGCTAC | 80067 |
| rs762950773 | snp | C/G | 3.31274e-05 | 0.00406972 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457935 | GATTGGACTTCCAGT[C/G]TTTTCTCAGGTGATA | 80067 |
| rs762965505 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171477804 | CTAGGCGACAGAATG[A/C]GACCCTGTCTCAAAA | 80067 |
| rs762992963 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433906 | CGGGACGCTGCTTTG[G/T]GGGGATCGCCCTCGA | 80067 |
| rs762999248 | snp | A/G | 1.66015e-05 | 0.00288105 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171453150 | ACAACATGTTTTGCT[A/G]TACCTTGCAGTGTTC | 80067 |
| rs763014009 | snp | G/T | 0.00137999 | 0.0262314 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480937 | TAGTGAATATGGCTG[G/T]GTGAAAAGGACTCCA | 80067 |
| rs763030484 | in-del | -/ATGT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455801 | GTGCTTGTTGGCCAC[-/ATGT]ATGCCATCTTTTTAG | 80067 |
| rs763066284 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171480918 | TGACATTTTAGTAAC[A/G]CAGTAGTGAATATGG | 80067 |
| rs763076918 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443415 | GAGGAAAGCAAATAA[A/G]TTGTGCCTTGGTATT | 80067 |
| rs763098025 | snp | C/G | 3.314e-05 | 0.00407049 | missense, intron-variant | DCAF17 | GRCh38.p7 | 2:171458381 | TTTTAGTTCATGCAA[C/G]AGAAACTTGACTTAG | 80067 |
| rs763126868 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171490702 | AGCTCTTATCTGCCA[C/G]TCCTCAAAGATTCAC | 80067 |
| rs763163216 | snp | A/T | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470302 | AATTTGCTTTTTTTT[A/T]TGAGGCAGGTTCAGC | 80067 |
| rs763203959 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171437304 | CATTTTTTTTAACAT[A/G]CAGCTATACATTTGT | 80067 |
| rs763211883 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171456201 | TGCGTATGGTGTAAG[A/G]AAGGGGTCGAGTTTC | 80067 |
| rs763225391 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171470953 | TTATATGCAAATACT[A/G]CACCATTTTATATAA | 80067 |
| rs763251767 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171456297 | TTTGTCAAGTTTGTC[A/G]AAGATCAGATAGTTA | 80067 |
| rs763285402 | snp | C/T | 1.65789e-05 | 0.0028791 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448727 | AGTCCTCACTCATAG[C/T]ACTGACTGCTCATAA | 80067 |
| rs763293564 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171448935 | TACCAGATCTCAATT[A/G]ATAAACCTATTTTCT | 80067 |
| rs763298523 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432351 | GGATAAGAGTCTAAA[A/G]GACTTGGTTGTGGGT | 80067 |
| rs763346182 | in-del | -/A | 1.68898e-05 | 0.00290596 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448660 | CAGTTTCATTTTTAT[-/A]ATCTCTCTTTTTTTT | 80067 |
| rs763367236 | in-del | -/AGCTACT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171471900 | CACACCTGTGGTCCC[-/AGCTACT]TGGGAGGCTGAGGTG | 80067 |
| rs763441128 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435777 | TTAAAGCATATTCTA[A/G]ACATACATCAGTTTG | 80067 |
| rs763459534 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171442437 | GGCATGGTAGCATGC[A/G]CCTGTAATCCCAGCT | 80067 |
| rs763494857 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486298 | TAGACTTATTAAAGT[A/G]TAATTGACGTGCAGT | 80067 |
| rs763521117 | snp | C/T | 1.67902e-05 | 0.00289738 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448825 | AAATTCAGGTATTTA[C/T]TGTGAATTTATTATT | 80067 |
| rs763527140 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171447771 | TCTCTCAAAGTGCTG[G/T]GATTACAGGTGGGGA | 80067 |
| rs763640307 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171465197 | AGTGAAACTCTGTCT[C/G]AAAAAGGAAAAAAAA | 80067 |
| rs763645572 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171471845 | CATGGTGAAACCCTG[A/C]CTCCACAAAAAATAC | 80067 |
| rs763660064 | snp | A/G | 3.81098e-05 | 0.00436502 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449830 | ATTTTGGTTTTAAGT[A/G]TAAGGAAACTGACCC | 80067 |
| rs763672996 | in-del | -/A | 0.00160282 | 0.0282638 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484322 | TCAAACAAGGGACAT[-/A]ACAATAGAAAGATAA | 80067 |
| rs763703917 | snp | A/C | 5.20793e-05 | 0.00510264 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476838 | AAGTCTTAGGTTCTC[A/C]GAATCCTTTTTCCCT | 80067 |
| rs763716716 | snp | C/G | 1.64901e-05 | 0.00287137 | synonymous-codon, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480991 | ATATAGCCATGAAGT[C/G]TACTTTGACAGAGAC | 80067 |
| rs763724456 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171467366 | AAGGCTTCTGGTCAA[C/T]AGTAGGCTATTAGTA | 80067 |
| rs763726200 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438621 | ACTTAATCCCTGGTA[A/G]TGTTCCTTGCCAAAT | 80067 |
| rs763726394 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171440450 | CATGGTGGCACACAC[C/G]TGTAGTCCCAGCTAC | 80067 |
| rs763776425 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171450832 | CACACTCCTTTCAGT[A/G]GATACTTTTATCATC | 80067 |
| rs763821953 | snp | A/G | 1.65979e-05 | 0.00288074 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435164 | AGAATATATTTTGAC[A/G]ATTATCGGCGCTGTG | 80067 |
| rs763886128 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171442844 | AAGATCATGCCATTG[C/T]ACTCCAGCCTGGAGT | 80067 |
| rs763977173 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171477561 | CACTTTGGAAGGCCA[A/G]GGCAGACAGATTGCT | 80067 |
| rs764017376 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452113 | TTGGAAGGGAGAATC[-/T]TTTGGGCTTTAAGCA | 80067 |
| rs764097264 | snp | C/G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452316 | TACAAGAGATTGTTT[C/G/T]ACATTTCACAGTGGC | 80067 |
| rs764124723 | snp | C/T | 1.65894e-05 | 0.00288 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171478009 | ATGTACTCACTGTTA[C/T]AGCTTCTGGACGGGT | 80067 |
| rs764126945 | snp | A/G | 0.000189663 | 0.00973631 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484131 | TTCCCTTTGTTTGTG[A/G]TGATAATCAGTATTA | 80067 |
| rs764182538 | snp | C/T | 1.68026e-05 | 0.00289845 | intron-variant, missense, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473953 | TCTGGTAGAATAATA[C/T]ATGTTGGTCCAAATC | 80067 |
| rs764357943 | snp | A/C | 1.67801e-05 | 0.00289651 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478104 | ATGACAAACCAAACC[A/C]GTGTGTCCTTGCATT | 80067 |
| rs764380652 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486784 | TAGAATTGTATATAA[A/G]TGAAATAGTAAGTAT | 80067 |
| rs764382253 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171456933 | TTTGAAAAGAGGGAT[A/G]GTTTGACTTCCTTTC | 80067 |
| rs764436474 | snp | C/T | | | intron-variant, upstream-variant-2KB | METTL8, DCAF17 | GRCh38.p7 | 2:171432240 | TCAAAAAAAAAAAAT[C/T]CTGTGTCACAAGTAA | 80067 |
| rs764451791 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171445251 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGACTACA | 80067 |
| rs764458836 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171480508 | TAAAATAAGAGAATA[C/T]GGTAATCCCCACAAT | 80067 |
| rs764470218 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171459612 | TGCCAAAGGATTTTC[A/T]AATATATGCAGAATA | 80067 |
| rs764491015 | in-del | -/ACAGG | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171480331 | GGTTTTGTCCTATAT[-/ACAGG]ACAAAAGAGTACTTC | 80067 |
| rs764509776 | snp | C/G | 5.23565e-05 | 0.0051162 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458523 | TAAAAAAATTAAGTG[C/G]TCATATAAATAGTTA | 80067 |
| rs764555678 | snp | C/T | 1.64811e-05 | 0.00287059 | synonymous-codon, nc-transcript-variant, missense | DCAF17 | GRCh38.p7 | 2:171468961 | CCATCCTTGGCACTA[C/T]ATCGTCACACCTAAT | 80067 |
| rs764604646 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171448666 | CATTTTTATATCTCT[-/T]CTTTTTTTTTTTAGG | 80067 |
| rs764627740 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171457660 | CTTGGTGTATGCCAG[A/T]GTCTATGAGGAATGG | 80067 |
| rs764689728 | snp | G/T | 0.000534331 | 0.0163365 | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447409 | TTCTGTCGCCAGGCT[G/T]GAGTGCAGTGGCACG | 80067 |
| rs764744666 | snp | C/T | 3.32784e-05 | 0.00407898 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171443548 | GAGCCAAGAAAACTT[C/T]ATGAAATGCCAAAAT | 80067 |
| rs764769215 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443117 | TAATGGGACCCTTTT[C/T]ATCCAGTAATTTTCA | 80067 |
| rs764851574 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438767 | CCAAAGTCAGGGTCT[A/G]GCTGTGTCTCCCAGG | 80067 |
| rs764855236 | snp | A/G | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474052 | TTTATTTTTGCCAGC[A/G]AACTAGTGAGCCAAT | 80067 |
| rs764892006 | in-del | -/TATA | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433570 | GGCTAGTTAACAAAG[-/TATA]TATATCTTTTACTTA | 80067 |
| rs764928097 | snp | A/T | 0.000150026 | 0.00865971 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481303 | GACTTCATTTTTTTT[A/T]AAGGTTTTTTAGAAT | 80067 |
| rs764957607 | snp | C/T | 0.000372093 | 0.0136348 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482986 | CAAACAGGAGAGCTA[C/T]GCCCCAACTAAAAGG | 80067 |
| rs765024071 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171488564 | ATCTGTCTGCCTCTC[-/T]TTTAAAGAGCAAAAC | 80067 |
| rs765113317 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171465857 | TACTCTCATCAGTAA[C/T]CATTGTTTTTAGATT | 80067 |
| rs765172251 | in-del | -/TT | 1.65362e-05 | 0.00287538 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469049 | AATGAGTGATCAGAC[-/TT]TTTATTAGCAAATTT | 80067 |
| rs765263586 | snp | A/C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171478933 | GCATAATTCATTAAG[A/C/G]GGGGAGAGGTGGTGG | 80067 |
| rs765317190 | snp | A/T | 5.06752e-05 | 0.00503339 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449995 | TAAAATGAAGACTCT[A/T]TTTCATAGGAATTTG | 80067 |
| rs765320898 | snp | A/T | 1.64988e-05 | 0.00287213 | synonymous-codon, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480088 | TTTGCTTTCTGTGGT[A/T]GCTGTTACTCAAATA | 80067 |
| rs765494093 | snp | A/G | 0.000149141 | 0.00863414 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458095 | AGAAAACTGAAATTT[A/G]TCATGTTACTATTAG | 80067 |
| rs765511733 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171453603 | TAAAACTTGCTTTAT[G/T]ATATATAACAAGCCT | 80067 |
| rs765590570 | snp | A/C | 0.000145783 | 0.00853641 | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447481 | TTCTCCTGCCTCAGC[A/C]TCCCAAGTAGCTGGG | 80067 |
| rs765592834 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171480574 | CCCAGGTACTCTTGT[A/G]TACATTTGTCTGATA | 80067 |
| rs765620580 | snp | G/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171434193 | CGGGCAAGCCCTCGC[G/T]CCCCGCCGCCTGACG | 80067 |
| rs765706124 | snp | C/T | 1.65806e-05 | 0.00287924 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448722 | TTATAAGTCCTCACT[C/T]ATAGCACTGACTGCT | 80067 |
| rs765728248 | snp | A/G | | | intron-variant, stop-gained | DCAF17 | GRCh38.p7 | 2:171460443 | AAGAAGACTGGATTT[A/G]GGATCAGAATTTTAG | 80067 |
| rs765730468 | snp | C/T | 0.00033206 | 0.012881 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484324 | CAAACAAGGGACATA[C/T]AATAGAAAGATAAGA | 80067 |
| rs765837085 | snp | C/T | 3.29734e-05 | 0.00406025 | missense, nc-transcript-variant | DCAF17 | GRCh38.p7 | 2:171468999 | AACAGAAAGGAGTTT[C/T]CCATATTTGTGCCCT | 80067 |
| rs765891154 | snp | C/G | 0.000366166 | 0.0135259 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481441 | AGTCATTGATGGGGT[C/G]GGTCATTGATGAGTT | 80067 |
| rs765908978 | snp | A/G | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474346 | TTTGAAGTAAATCTT[A/G]TTTTATTTTGATTGG | 80067 |
| rs765919954 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486987 | CTACTACAAATGAAG[C/T]TACGAGGTATAATTG | 80067 |
| rs766009927 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171459714 | TGTCATTGTTCAAAA[G/T]GAAAAAAATATTATT | 80067 |
| rs766017408 | snp | C/T | 1.65784e-05 | 0.00287905 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448734 | ACTCATAGCACTGAC[C/T]GCTCATAATTGGCTA | 80067 |
| rs766067561 | in-del | -/T | 0.000649773 | 0.0180129 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472996 | TAACATATCAGATGG[-/T]TTTTTTCTTTATTTT | 80067 |
| rs766081770 | snp | A/T | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171475659 | TCTTAGCTCCTCAGG[A/T]GTCTGGGGCAGGAGG | 80067 |
| rs766094319 | snp | A/T | 1.6741e-05 | 0.00289314 | intron-variant | DCAF17 | GRCh38.p7 | 2:171477983 | ATTTCTTTCCATATG[A/T]TAGAATGAAAATGTA | 80067 |
| rs766109409 | in-del | -/ATTTCTCTTGGTGCTTTTT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171468176 | AGAAGATGACTAAAA[-/ATTTCTCTTGGTGCTTTTT]AGCACCAAGAGAAAT | 80067 |
| rs766154346 | snp | A/G | 6.69478e-05 | 0.00578528 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478092 | CTTTGGCCAGAGATG[A/G]CAAACCAAACCAGTG | 80067 |
| rs766276441 | in-del | -/T | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436774 | AAACAGAGAGGTTAA[-/T]TTTTTTTTTTTTTTT | 80067 |
| rs766277189 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486655 | AGGACATACCCATTA[C/T]CCAAAAAGTTTTTTT | 80067 |
| rs766281663 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452090 | TAGTTCAATAAAAAT[G/T]TATCCCTTTGGAAGG | 80067 |
| rs766299946 | in-del | -/T | 0.453158 | 0.145695 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482668 | CAGTCATGTCAGAGA[-/T]TTTTTTTTTTTAGGT | 80067 |
| rs766413776 | snp | C/T | 0.000192548 | 0.00981005 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434585 | GCGCCTCCATGGGCC[C/T]GACCCGGAAGCCCAA | 80067 |
| rs766434466 | snp | A/G | 1.65688e-05 | 0.00287821 | missense, intron-variant | DCAF17 | GRCh38.p7 | 2:171458382 | TTTAGTTCATGCAAC[A/G]GAAACTTGACTTAGG | 80067 |
| rs766445970 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171490720 | CTCAAAGATTCACCC[C/T]AGAACATAATCTCTC | 80067 |
| rs766469563 | snp | C/G | | | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491217 | CCAGCTACCCAGGAG[C/G]CTGAGGCAGGAGAAT | 80067 |
| rs766487991 | snp | G/T | 1.65056e-05 | 0.00287272 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480946 | TGGCTGTGTGAAAAG[G/T]ACTCCATATGATTGT | 80067 |
| rs766497476 | snp | A/C | 1.72222e-05 | 0.00293442 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443497 | GTTATCAAGAATAAT[A/C]ATCATTTATTTTTCT | 80067 |
| rs766502544 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171454075 | CTCAGAAGGCTGAGG[A/C]AGGAGAATGGTTTGA | 80067 |
| rs766579099 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171471017 | GAGGGGTCCTGGAAG[A/C]AATCCCCTGTGGTTT | 80067 |
| rs766629618 | snp | C/T | 1.66377e-05 | 0.00288419 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435173 | TTTGACAATTATCGG[C/T]GCTGTGTCAGCAGGT | 80067 |
| rs766686423 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171441694 | TCCATCTTGCTGAGC[A/T]GGGATTGGGAAGGAA | 80067 |
| rs766747678 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432639 | ACAAAGCACTCTACC[A/G]TATGCTGTAAATAAG | 80067 |
| rs766763268 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435845 | TAGGATATAATTCAC[A/G]TACCATATATTTACC | 80067 |
| rs766820600 | snp | A/C/G | 0.000371557 | 0.0136259 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484979 | TTTTTTTATCTTTCT[A/C/G]TTGATGGACACTGGG | 80067 |
| rs766836121 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483121 | AAGATAGCAAAGAAT[A/G]TGGGGAATTTGGATA | 80067 |
| rs766852319 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171447785 | GGGATTACAGGTGGG[C/G]ACCACGATGCCCTTT | 80067 |
| rs766858148 | snp | A/G | 1.65072e-05 | 0.00287286 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480113 | CAAATAGATGCTGAA[A/G]GAAAAGCTCACCTGG | 80067 |
| rs766897062 | snp | A/C | 1.66663e-05 | 0.00288667 | intron-variant, missense, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473929 | TGGATCTATTTCCAT[A/C]CTGATGCTTCTGGTA | 80067 |
| rs766924280 | snp | C/T | 0.000185925 | 0.00963993 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481864 | ATCTAAGGATGTTCT[C/T]ATCTCACCATTCTAC | 80067 |
| rs766946153 | snp | A/T | 0.000185856 | 0.00963813 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482519 | TTGAAAAACAAGACC[A/T]GTAAGAGGCCAGTGA | 80067 |
| rs766972994 | snp | C/T | 1.65778e-05 | 0.002879 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448747 | ACTGCTCATAATTGG[C/T]TACTTCGTATATCAG | 80067 |
| rs766988676 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482151 | GTTAAATAAAGGCAA[-/C]CCCAAGTAAAGGGAG | 80067 |
| rs767060033 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435964 | TTCAAAACAGAACCA[G/T]GTACCTTTAAGCAGT | 80067 |
| rs767063938 | snp | A/C | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473994 | AGTAATCTCATTAGC[A/C]CTTGAAAGTTAAGAG | 80067 |
| rs767066254 | snp | C/G | 9.98552e-05 | 0.00706524 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472956 | GCTTCTGGATATAAG[C/G]TAATACATTTGTGTA | 80067 |
| rs767115585 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171462557 | AAAGTTAGAACTTTC[A/G]ATACAATATGGTTGG | 80067 |
| rs767123945 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171437969 | ATTACGATTTGAAGT[C/G]TTTCTCCTTTTCTGC | 80067 |
| rs767141523 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171449414 | TTTTCTATGTAAGAT[A/G]CTCTTTATGGTAGAT | 80067 |
| rs767165065 | snp | A/G | 2.13322e-05 | 0.00326583 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434600 | CGACCCGGAAGCCCA[A/G]CGTGTGCAGCCGGCT | 80067 |
| rs767201556 | snp | A/C | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171475773 | GTCTCTTAAAAAATA[A/C]AAAATAACAAAGGGA | 80067 |
| rs767217834 | snp | A/C | 1.65627e-05 | 0.00287769 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457956 | TCAGGTGATATCTGT[A/C]TTTCCCCCCGCCAGA | 80067 |
| rs767229444 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171447967 | AACCAGGTCCATTTT[C/G]TGTACTTTGGCTGTC | 80067 |
| rs767230951 | in-del | -/TAGA | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443824 | ATGTGTTTTTAAAAT[-/TAGA]TAGATTTTTTTTAGA | 80067 |
| rs767232889 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171446417 | CAGGTGTGGTGGCAC[A/G]CACCTGTAATCCCAG | 80067 |
| rs767331075 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171448319 | CTCTTAATCGCTATG[C/G]TATATACATGATTTT | 80067 |
| rs767339694 | in-del | -/GTTACGCTGAAA | 0.000371678 | 0.0136272 | utr-variant-3-prime, nc-transcript-variant, cds-indel, intron-variant | DCAF17 | GRCh38.p7 | 2:171483401 | TCAGCAGGTACAGAC[-/GTTACGCTGAAA]AGAGGTGCATTCTGC | 80067 |
| rs767450484 | snp | G/T | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474459 | TGAATATTTTCCTAT[G/T]TCATCTATCTTTTTT | 80067 |
| rs767498072 | snp | C/T | 1.67139e-05 | 0.00289079 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435180 | ATTATCGGCGCTGTG[C/T]CAGCAGGTAACTTTT | 80067 |
| rs767508320 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466000 | TCTATACCTTATAAT[C/T]TTACTTAACATGTAT | 80067 |
| rs767557924 | snp | C/T | 0.000185718 | 0.00963455 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483101 | AAAGATGCCAGAAGA[C/T]ACAGAAGATAGCAAA | 80067 |
| rs767659250 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435285 | AGTGCCTAGTGAAAT[A/G]GAATGAAAAAAATGG | 80067 |
| rs767709440 | snp | A/T | 1.70339e-05 | 0.00291833 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458513 | TTTTTCACCTTAAAA[A/T]AATTAAGTGGTCATA | 80067 |
| rs767849361 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444122 | CAGAGGAGTTAGGGG[G/T]AATTGGGCTGTGAAA | 80067 |
| rs767904274 | snp | C/T | | | downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171491453 | GGAACACCACAGATG[C/T]AGCTGGAATTGTGCT | 80067 |
| rs767959697 | snp | C/T | 4.95037e-05 | 0.00497488 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480953 | GTGAAAAGGACTCCA[C/T]ATGATTGTGTTTTGT | 80067 |
| rs767979485 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484114 | AGTCATTAAAAGGTA[C/T]TTTCCCTTTGTTTGT | 80067 |
| rs767994103 | snp | C/G | | | missense | DCAF17 | GRCh38.p7 | 2:171490779 | TTCACCTTGACATCA[C/G]TGGACAGGAAGCAAG | 80067 |
| rs768050246 | in-del | -/G | 0.00110254 | 0.0234532 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434721 | GACCGCCAGCCGGCC[-/G]GGGCGGGACGGAGGG | 80067 |
| rs768059186 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484616 | TTTACCTGCAATAAA[A/G]TGTACAAATCTTAAG | 80067 |
| rs768078861 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171451733 | GGCGTGCACCACCAG[C/G]CCCAGCTAATTTTTG | 80067 |
| rs768175146 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466641 | AGGGCACATTAGAGT[G/T]GTGGGCAGAGTAATA | 80067 |
| rs768187940 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171468560 | TGTTCAATAAATGTC[C/T]GCTACTTTTATTAAA | 80067 |
| rs768194770 | snp | C/G | 3.31296e-05 | 0.00406985 | missense, intron-variant | DCAF17 | GRCh38.p7 | 2:171458403 | TTGACTTAGGGTGTG[C/G]ATGCAGATGGGGTGG | 80067 |
| rs768221012 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439411 | CTATCTTCAAACTCA[C/T]TGATTCTGTCCTTGG | 80067 |
| rs768361114 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483425 | AAAAGAGGTGCATTC[G/T]GCATTGCACTCCTGG | 80067 |
| rs768382294 | snp | C/G | 1.67036e-05 | 0.0028899 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458489 | ACAGGTATGGCTACT[C/G]TATAGTATTTTTTCA | 80067 |
| rs768397399 | snp | C/T | 1.66067e-05 | 0.00288151 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171453139 | GCAGGCATTCAACAA[C/T]ATGTTTTGCTGTACC | 80067 |
| rs768442815 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443256 | ACAACGTCCAGGTAC[A/G]TATATGTATATAAAC | 80067 |
| rs768449754 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171478911 | GTACTAAAATTTCCA[A/G]AAGGTAGCATAATTC | 80067 |
| rs768464200 | snp | G/T | 1.66477e-05 | 0.00288506 | splice-donor-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171478072 | ACCCAGAACAAGAGG[G/T]ATTGCTTTGGCCAGA | 80067 |
| rs768468372 | snp | A/G | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469596 | AAAAATGGCTTAGGC[A/G]TTGATTTGTCATTTA | 80067 |
| rs768515730 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452678 | GTGAGTGGCCAGGCT[G/T]GTCTCAGACTCCTAG | 80067 |
| rs768549033 | snp | A/T | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436688 | GATACAAGTCCCTTA[A/T]CAGATATATGATTTC | 80067 |
| rs768558594 | snp | A/G | 9.97573e-05 | 0.00706178 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171443598 | AGAGGATGCTTTATT[A/G]TGGGAATGCCCAGTG | 80067 |
| rs768565338 | snp | A/G | 3.47705e-05 | 0.00416942 | intron-variant, synonymous-codon, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473868 | TTTCCAACTTCAGGC[A/G]AAAAATGGGATCCAA | 80067 |
| rs768613603 | snp | C/G | 1.7494e-05 | 0.00295748 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443482 | ACAAATACTGTCTTG[C/G]TTATCAAGAATAATA | 80067 |
| rs768693296 | in-del | -/T | 0.00487052 | 0.0491074 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482363 | ATTAAAATCTTTCCA[-/T]TTTTTTTTTCAGTTT | 80067 |
| rs768720066 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464232 | TCCTAGAGAGCAACA[A/C]TACAAACTGGGCAGC | 80067 |
| rs768768460 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171457253 | TGCTTATTACAGTCT[A/G]CAACAGAAATGAACA | 80067 |
| rs768800288 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435644 | CCACAACTGTCCAAC[A/G]TGAGGGGGGAAGGAA | 80067 |
| rs768818183 | in-del | -/TTTCT | 0.00018596 | 0.00964082 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484915 | TGTGTCAGTGATTCA[-/TTTCT]TTTCTTTTTATTGCT | 80067 |
| rs768832107 | snp | A/G | | | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447592 | TGGTCTCGATCTCCT[A/G]ACATCGTGATCCAGC | 80067 |
| rs768839208 | snp | A/C | 0.000928936 | 0.0215315 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434394 | CTCTGGCGGTGCAAG[A/C]GGCTCTGCTTTCCCT | 80067 |
| rs768860063 | snp | C/T | 9.18991e-05 | 0.00677799 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481274 | TTTAAACTCTTGCTG[C/T]AAAAGATGGTGAGGA | 80067 |
| rs768866544 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482909 | CAGGGTCCAAATGCC[A/G]TCCAGGCCAGGCAGG | 80067 |
| rs768910751 | snp | C/G | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475284 | TTTTCATTGCACCCA[C/G]TGTGTCGTCTTCCTT | 80067 |
| rs768928357 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171461405 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 80067 |
| rs769033929 | snp | A/G | 1.65825e-05 | 0.00287941 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448775 | CAGCAACTACGGGAA[A/G]AATCCTTGAGAAAAT | 80067 |
| rs769038472 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171489100 | TTGAAACAATTTTCC[A/C]TTTTTATCTACAAGC | 80067 |
| rs769039613 | snp | A/G | 0.000185856 | 0.00963813 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482265 | AAAGAATAACTGGTA[A/G]TAAGGGAAGGAAACA | 80067 |
| rs769153707 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171473780 | TCCGTGTACCTTTGA[C/G]CTACTGATCTATCAC | 80067 |
| rs769204619 | snp | G/T | 1.65756e-05 | 0.00287881 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469065 | TTTTATTAGCAAATT[G/T]GTATCAAGTTCTTTA | 80067 |
| rs769209137 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171440296 | GATATATTGGATAGG[A/C]CAGGCACAGTGGCTT | 80067 |
| rs769229427 | snp | G/T | 1.89878e-05 | 0.00308116 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434657 | CGCGCGACGCAGGCG[G/T]GGTGCAGAGGACCAA | 80067 |
| rs769245425 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487480 | CCAGGCTGGAGTGCG[A/G]TGGCTCAATCTCAGC | 80067 |
| rs769277345 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171440208 | TCTGATGTTTGTTTT[C/G]TTTCTTCAAACTTTT | 80067 |
| rs769280254 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171441169 | GGCCTTAACTTCTCC[A/T]CACTCTGTTGCAAAT | 80067 |
| rs769316511 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171454197 | ATAAAAAATAAAAAG[C/T]AGCTACCTAAATCCT | 80067 |
| rs769442902 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171488994 | AGTAACCAGGAAATC[A/G]TAAATCTGCCCATTT | 80067 |
| rs769529754 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171447790 | TACAGGTGGGGACCA[C/T]GATGCCCTTTTAGTC | 80067 |
| rs769583422 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466767 | ATTCCTATGTCCTCT[A/G]TATTGAATTTCATAT | 80067 |
| rs769595023 | snp | A/T | 0.000283086 | 0.0118938 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483461 | AGTTTCTGCATTCTC[A/T]GAGCATCAATGCAGC | 80067 |
| rs769602895 | snp | A/G | 1.65603e-05 | 0.00287747 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171458007 | GCTACCTTGTCTCAT[A/G]GAATACTGATTGTGA | 80067 |
| rs769636178 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171480952 | TGTGAAAAGGACTCC[A/T]TATGATTGTGTTTTG | 80067 |
| rs769736759 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433638 | GAATGTAAGCATTTC[A/G]TATTTTATTCCCTAT | 80067 |
| rs769852582 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171441981 | CAATTCTTCAGGATC[A/T]TTTAATGTCAAGTTT | 80067 |
| rs769909783 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438058 | TGTTGATACGTTGTA[G/T]GTGCATTTTCATTTA | 80067 |
| rs769952651 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482985 | ACAAACAGGAGAGCT[A/G]TGCCCCAACTAAAAG | 80067 |
| rs769993723 | snp | C/T | 1.70772e-05 | 0.00292204 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448836 | TTTACTGTGAATTTA[C/T]TATTCAAGATTTTAT | 80067 |
| rs770003540 | snp | A/T | 0.000431034 | 0.0146742 | splice-acceptor-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171458370 | TTTTGTTTTGTTTTT[A/T]GTTCATGCAACAGAA | 80067 |
| rs770050161 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171450228 | TTACTCTGGAGACTC[G/T]GGTGAAAGGGTGGGA | 80067 |
| rs770078005 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464761 | ATTAGCTCATTTTCA[C/T]ACTTCCAAATTTAGC | 80067 |
| rs770099902 | snp | G/T | 0.000185891 | 0.00963903 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482365 | TAAAATCTTTCCATT[G/T]TTTTTTTCAGTTTTG | 80067 |
| rs770190404 | snp | A/G | 1.8435e-05 | 0.00303598 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474012 | TGAAAGTTAAGAGCA[A/G]CTTTTGGTAGCATTT | 80067 |
| rs770193682 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483593 | TACCGCTCTGTTTAG[A/G]CAAATTAAGGCACTT | 80067 |
| rs770323650 | snp | A/T | 1.67312e-05 | 0.00289229 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448821 | TTGCAAATTCAGGTA[A/T]TTACTGTGAATTTAT | 80067 |
| rs770373151 | snp | C/T | 1.66479e-05 | 0.00288508 | intron-variant, synonymous-codon, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473901 | AATGGATTGTTGTTC[C/T]CTAGAATCTGACTGG | 80067 |
| rs770375570 | in-del | -/A | 1.66246e-05 | 0.00288305 | frameshift-variant, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171443559 | ACTTTATGAAATGCC[-/A]AAATGTTCCAAATCA | 80067 |
| rs770413753 | snp | A/G | 1.67214e-05 | 0.00289144 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458126 | CATGAGTTTTCGACT[A/G]AAGTATGATTTTTTT | 80067 |
| rs770432686 | in-del | -/T | 3.35582e-05 | 0.00409609 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449974 | ATACATATTTAAACA[-/T]TTCAATAAAATGAAG | 80067 |
| rs770443968 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171490272 | TAATTATATATTTAT[A/G]ACTTTAACCCATGAA | 80067 |
| rs770506183 | snp | A/C | 1.86059e-05 | 0.00305001 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435037 | TTAAAATCTAACTTA[A/C]AGCCTAAGAGTTCTT | 80067 |
| rs770541391 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171441454 | AGTATCCTCAGCTGT[A/G]CTACATCCAAGGTAG | 80067 |
| rs770588377 | in-del | AGCTTGTTGTTGGGTGCTTCCTCAGAGACT/CA | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474082 | TTAATGGAAATAATT[lengthTooLong]GGCATACAGAACACC | 80067 |
| rs770660920 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171489250 | TCTTTGTACTAGTCT[C/T]ACTTCTGACACCAAT | 80067 |
| rs770670358 | snp | A/G | 0.000185856 | 0.00963813 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484719 | CAATCATCTTCAGAA[A/G]GTTTCCTAAATCCCT | 80067 |
| rs770671472 | snp | C/G | 0.000185822 | 0.00963724 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482460 | CCATACTTTCAATTA[C/G]ACACTAGCTGTATCT | 80067 |
| rs770720263 | in-del | -/AA | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171460323 | GCGAGATTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 80067 |
| rs770724186 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171468800 | AATTTATAGATGTTG[C/T]ATGCAAAGAAAGGTT | 80067 |
| rs770768880 | snp | C/G | 1.65614e-05 | 0.00287757 | missense, nc-transcript-variant | DCAF17 | GRCh38.p7 | 2:171458046 | TCAGGACTGGTCAGA[C/G]TCTATAGCTTCCAAA | 80067 |
| rs770773053 | snp | G/T | 3.32121e-05 | 0.00407492 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435166 | AATATATTTTGACAA[G/T]TATCGGCGCTGTGTC | 80067 |
| rs770811882 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481237 | AAGTCTTGTGTTGAC[G/T]TCAGATGACTATGAC | 80067 |
| rs770819824 | snp | A/G | 1.64936e-05 | 0.00287168 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480044 | ATCCCAAAGACTTTC[A/G]AAATTGTGGACTATG | 80067 |
| rs770896326 | snp | C/T | 0.000252247 | 0.0112276 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480206 | GTGGTGAGTAGAGTC[C/T]GTGGGATACAAAGTT | 80067 |
| rs770938548 | in-del | -/GTTGACT | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438363 | ATTCTGTTTGATCCA[-/GTTGACT]GTTGACTGATGGTAC | 80067 |
| rs771088921 | snp | C/T | 1.66092e-05 | 0.00288172 | synonymous-codon, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481111 | CATAAACAGAAGCTG[C/T]TAAAAAGAGTGAGAT | 80067 |
| rs771100235 | snp | C/T | 1.68992e-05 | 0.00290677 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458503 | TCTATAGTATTTTTT[C/T]ACCTTAAAAAAATTA | 80067 |
| rs771163706 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171472214 | AGACAGGGTTTTACT[C/G]TGTTGCCCAGGCTGG | 80067 |
| rs771178201 | snp | A/G | 1.64795e-05 | 0.00287045 | synonymous-codon, nc-transcript-variant, missense | DCAF17 | GRCh38.p7 | 2:171468913 | ACTGCTCTTTGAGGT[A/G]TCATCCCTGGAGAAT | 80067 |
| rs771200708 | in-del | -/TC | 0.00349867 | 0.0416785 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448662 | AGTTTCATTTTTATA[-/TC]TCTCTTTTTTTTTTT | 80067 |
| rs771202185 | snp | A/G | 0.000186272 | 0.0096489 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482816 | TGCTGGGGGTAGATG[A/G]TGGAATACTTCTGGT | 80067 |
| rs771231052 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171450458 | GAAGCGTGCTATTTA[A/G]AGAGATTTTTCTCTT | 80067 |
| rs771234717 | snp | G/T | 1.77713e-05 | 0.00298083 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476809 | TTAAACTTTGGCACC[G/T]TGATGGTGTTTTGAA | 80067 |
| rs771287652 | snp | A/T | 1.66402e-05 | 0.00288441 | intron-variant, missense, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473917 | CTAGAATCTGACTGG[A/T]TCTATTTCCATCCTG | 80067 |
| rs771324052 | snp | G/T | 1.66305e-05 | 0.00288357 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481224 | GTATTTTCCAAAAAA[G/T]TCTTGTGTTGACTTC | 80067 |
| rs771364237 | in-del | -/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171437898 | TTTGTTATTTCTTTG[-/C]TTACTTTGGATTTAA | 80067 |
| rs771414175 | snp | C/T | 1.67643e-05 | 0.00289515 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453096 | AGTACTTTTGAGAGC[C/T]GCGTGTAATTGTAGT | 80067 |
| rs771484449 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171465298 | ATACACATGGAGTGA[A/T]GTGTTCAAAGGCGAT | 80067 |
| rs771507295 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444794 | TTTTAAAGGATAAGA[A/G]GCTGTACGCTAAATT | 80067 |
| rs771548032 | snp | A/T | 1.72997e-05 | 0.00294101 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435215 | GATAATTTTGCTGTA[A/T]TTCACCTCACTGTTG | 80067 |
| rs771565382 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452413 | TTTCATTGATGATAT[G/T]ATTTCTAATTTCCTG | 80067 |
| rs771570661 | snp | A/G | 0.000186029 | 0.00964261 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482853 | ATAACTTACCACTAA[A/G]AAACCCCCAGTATGT | 80067 |
| rs771572216 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171478654 | TATAAACCATTGTGT[A/G]AATTCTAAATCCATT | 80067 |
| rs771613535 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171479748 | TTTAAATTTAGAGAA[G/T]CTCTGATTTGCTGTC | 80067 |
| rs771617030 | in-del | -/AA | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487868 | CCCGGCCAAAGACAC[-/AA]ATACTAACAGACTCA | 80067 |
| rs771617054 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444622 | CCAAGTGTTTCAGTA[G/T]GAGAAGGGATAATCG | 80067 |
| rs771617372 | snp | C/T | 1.76027e-05 | 0.00296665 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171476988 | TCCTTTATATATCAT[C/T]GTCTTTCTATATAAG | 80067 |
| rs771705192 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171465312 | TGTGTTCAAAGGCGA[-/T]TTTGAAATCATTTTT | 80067 |
| rs771801869 | snp | A/G | 1.77382e-05 | 0.00297805 | intron-variant | DCAF17 | GRCh38.p7 | 2:171476811 | AAACTTTGGCACCTT[A/G]ATGGTGTTTTGAAGT | 80067 |
| rs771802943 | snp | C/G | 1.69335e-05 | 0.00290972 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480215 | AGAGTCCGTGGGATA[C/G]AAAGTTGTAAACCTT | 80067 |
| rs771837471 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171490526 | GGTCAGCAGAGTGAA[G/T]CAGATCCAGAAGGAA | 80067 |
| rs771883446 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438695 | GTTTAGTGTTTACAC[A/T]TTGTATCTTTTGCCA | 80067 |
| rs771886950 | snp | C/T | 1.65795e-05 | 0.00287914 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435153 | ATGAGAGAGGAAGAA[C/T]ATATTTTGACAATTA | 80067 |
| rs771932346 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171476492 | AGAAATAAAAATGCA[A/C]ATATCTGCTTTAATT | 80067 |
| rs771991023 | snp | G/T | | | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447406 | GTCTTCTGTCGCCAG[G/T]CTGGAGTGCAGTGGC | 80067 |
| rs772064673 | in-del | -/A | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171460933 | ATCATTTGTCATTGT[-/A]AAAAAAAAATAATTC | 80067 |
| rs772068575 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171488690 | TTGAAGAAGTCCTTC[A/G]GCCTCACTGCCACAC | 80067 |
| rs772109023 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171470833 | CAGATACAGCCGGCC[G/T]TCTATATCCGTGGGT | 80067 |
| rs772132845 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433961 | CCAGAACCTCCCAGG[A/G]CGAAGGTCGGGGCCG | 80067 |
| rs772187578 | in-del | -/T | 0.000136855 | 0.00827096 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481294 | ATGGTGAGGACTTCA[-/T]TTTTTTTTAAAGGTT | 80067 |
| rs772200605 | snp | A/G | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470163 | TGAGCATCTGGGACT[A/G]TAGGAGCGCACCACC | 80067 |
| rs772200637 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483581 | CTAGTGAGGAGATAC[C/T]GCTCTGTTTAGACAA | 80067 |
| rs772220298 | snp | A/G | 1.72234e-05 | 0.00293452 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443656 | TCTAAAGCATTTTTA[A/G]CCTAGAAGAACCAGT | 80067 |
| rs772225477 | snp | A/G | 1.648e-05 | 0.0028705 | synonymous-codon, nc-transcript-variant, stop-gained | DCAF17 | GRCh38.p7 | 2:171468922 | TGAGGTGTCATCCCT[A/G]GAGAATGCTTTTCAG | 80067 |
| rs772226605 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171446428 | GCACGCACCTGTAAT[C/T]CCAGATACTCGGGAG | 80067 |
| rs772229487 | snp | C/G | 0.000185753 | 0.00963545 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481546 | GAAATCTTATATCCT[C/G]TATACCAAACTTTGC | 80067 |
| rs772284112 | in-del | -/C | 8.28102e-05 | 0.00643415 | intron-variant | DCAF17 | GRCh38.p7 | 2:171457960 | GTGATATCTGTCTTT[-/C]CCCCCGCCAGATTTT | 80067 |
| rs772322764 | snp | A/C | 1.65921e-05 | 0.00288024 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448693 | TAGGGAGATATACTT[A/C]CCAATTCATCAGATT | 80067 |
| rs772336689 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487386 | TTATTTGTTGTGTGT[A/G]TATCTTTTTGATGAC | 80067 |
| rs772346331 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171473734 | TTTGGCCCTCAAATA[G/T]ATTCCACTTTAACTG | 80067 |
| rs772362676 | snp | C/T | 9.99567e-05 | 0.00706883 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453118 | AATTGTAGTCTTTCC[C/T]TCTAGGCAGGCATTC | 80067 |
| rs772459391 | snp | A/C | 1.65605e-05 | 0.0028775 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469059 | CAGACTTTTTATTAG[A/C]AAATTTGTATCAAGT | 80067 |
| rs772557046 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171472729 | CAAGGATTATGTTTA[A/G]TTGATGTGAGGTATG | 80067 |
| rs772591456 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439238 | ATTCTCAGCCATTAT[A/T]ACTTCAAATATTTAT | 80067 |
| rs772669685 | snp | C/T | 2.17749e-05 | 0.00329954 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453232 | AGAACTCATTTCTTA[C/T]TTAATTGCAATATTT | 80067 |
| rs772679666 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171451558 | ATAATTTAAATTGCT[A/G]AAGAGCAAGAATTTT | 80067 |
| rs772741400 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171445671 | AATAGTATATTTTTT[A/G]AAACTTAAATTTTTT | 80067 |
| rs772758863 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486871 | CATGTATCAATAGAT[A/C]ATTCCTTTTTATTGT | 80067 |
| rs772797259 | snp | C/T | 0.000186098 | 0.00964441 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481749 | TTGGCTTGATGTTCA[C/T]ATTGAATATTTGTGT | 80067 |
| rs772824611 | snp | A/G | 1.65611e-05 | 0.00287755 | missense, nc-transcript-variant | DCAF17 | GRCh38.p7 | 2:171458040 | TACAGCTCAGGACTG[A/G]TCAGACTCTATAGCT | 80067 |
| rs772878506 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171440300 | TATTGGATAGGCCAG[C/G]CACAGTGGCTTACTC | 80067 |
| rs772919379 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171489195 | CTTCTACAGTTTATC[G/T]ATGTCTCCCTCAAAT | 80067 |
| rs772985920 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171451971 | TGGACTGTTTTCCTA[C/T]AGTCTCCAGCCAACA | 80067 |
| rs772988219 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171468672 | TGAAAACAGATACCT[A/G]GAAAGTTGATTCAGC | 80067 |
| rs773066148 | snp | A/G | 0.000603682 | 0.0173631 | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434724 | CGCCAGCCGGCCGGG[A/G]CGGGACGGAGGGCCG | 80067 |
| rs773077955 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466936 | TTCTCTTATAATTTA[C/G]CAACTCATGCCTTTT | 80067 |
| rs773138723 | snp | G/T | 1.6722e-05 | 0.00289149 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478090 | TGCTTTGGCCAGAGA[G/T]GACAAACCAAACCAG | 80067 |
| rs773169533 | in-del | -/CTTCTTATGTCTTACCTGGAAA | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | METTL8, DCAF17 | GRCh38.p7 | 2:171434889 | GCTTTTAGTTTTACG[-/CTTCTTATGTCTTACCTGGAAA]CAATTATTCTAAAAG | 80067 |
| rs773232927 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171480373 | TTCCTCCCCTGGGCA[C/G]TAGGGGATCCTTACC | 80067 |
| rs773244943 | snp | A/G | 1.65449e-05 | 0.00287614 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481088 | GACACTGGGGAAGAA[A/G]AAGAAACCATAAACA | 80067 |
| rs773252920 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171470890 | TGGATTGGAAATATT[A/C]AGAAAAAAAAAGGAT | 80067 |
| rs773329397 | snp | C/G | 1.7634e-05 | 0.00296929 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480244 | TTTCCTTTATAGGTG[C/G]CATTTATTAGAACAG | 80067 |
| rs773360559 | snp | C/G | 3.31499e-05 | 0.0040711 | missense, intron-variant | DCAF17 | GRCh38.p7 | 2:171458374 | GTTTTGTTTTTAGTT[C/G]ATGCAACAGAAACTT | 80067 |
| rs773362482 | snp | A/G | 0.000116207 | 0.00762167 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171449924 | CATTGCAGTTAAGTC[A/G]GCTCAGAACAGAGGC | 80067 |
| rs773462698 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171437047 | CCAAAGTGCTGGGAT[C/T]ACAGGCATGAGCCAC | 80067 |
| rs773482982 | in-del | -/A | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171467727 | GAGCGAGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 80067 |
| rs773494648 | in-del | -/A | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171441991 | GGATCATTTAATGTC[-/A]AGTTTATAACTTCCT | 80067 |
| rs773519447 | snp | C/T | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470298 | GAAGAATTTGCTTTT[C/T]TTTTTGAGGCAGGTT | 80067 |
| rs773523341 | snp | C/T | | | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447721 | TGCCTAGGCTGATAT[C/T]GAACTCCTGGGCTCA | 80067 |
| rs773543654 | snp | C/T | 0.000557465 | 0.016686 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484942 | TGCTGAGTATTCTTT[C/T]GTATGAATATATCAC | 80067 |
| rs773544733 | snp | C/T | 1.6636e-05 | 0.00288405 | intron-variant, synonymous-codon, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473910 | TTGTTCTCTAGAATC[C/T]GACTGGATCTATTTC | 80067 |
| rs773555321 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483869 | TGGGAAACATAACCA[C/G]ATTTGTTCGGCATGA | 80067 |
| rs773586902 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464792 | CGTTCTTTTTTGATT[A/G]TATTTGTATTTCTCT | 80067 |
| rs773597984 | snp | A/G | 0.000306357 | 0.0123727 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472866 | ATCATTTCATTTTAC[A/G]TTAGAGAAATTAAAT | 80067 |
| rs773600080 | snp | A/G | 0.000185787 | 0.00963634 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482439 | GCCCTGGTGCTAGAC[A/G]TTGCCCCATACTTTC | 80067 |
| rs773607342 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483042 | CCAGTTGCAACAGTA[G/T]GTGGGAATGTAGGCT | 80067 |
| rs773660075 | snp | G/T | 1.67733e-05 | 0.00289592 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448822 | TGCAAATTCAGGTAT[G/T]TACTGTGAATTTATT | 80067 |
| rs773703472 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171463628 | TTTACAAATGAACCA[C/T]AATTTACTTAACCAG | 80067 |
| rs773743596 | in-del | -/TA | 0.000320662 | 0.0126581 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448658 | AAGCAGTTTCATTTT[-/TA]TATCTCTCTTTTTTT | 80067 |
| rs773752168 | snp | A/G | 1.66949e-05 | 0.00288915 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458325 | TCTCTCCAGATATCA[A/G]ATAAATAGGTGCTAA | 80067 |
| rs773914315 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171449822 | AATATAATATTTTGG[-/T]TTTAAGTATAAGGAA | 80067 |
| rs773966484 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464044 | TTATTATTCTTAATG[A/T]TGTTCAAATTGTCCT | 80067 |
| rs773967537 | snp | A/G | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171477147 | AGTTGACTATCTTGA[A/G]TTTGTCTTTTGCTGA | 80067 |
| rs773991916 | snp | A/T | 0.000186168 | 0.0096462 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482836 | ATACTTCTGGTCTAG[A/T]TATAACTTACCACTA | 80067 |
| rs773997525 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171489302 | TGATATAAAGTAATA[C/T]AAAAACACTAACAGA | 80067 |
| rs774025973 | in-del | -/TACTTTCACT | 0.000147918 | 0.00859867 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482681 | GATTTTTTTTTTTAG[-/TACTTTCACT]GTGATTATTGAGTTT | 80067 |
| rs774050739 | snp | A/C | 1.67475e-05 | 0.00289369 | intron-variant | DCAF17 | GRCh38.p7 | 2:171478096 | GGCCAGAGATGACAA[A/C]CCAAACCAGTGTGTC | 80067 |
| rs774054317 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171490343 | AACTTTGGAAAGACT[C/T]GCTAAAATCAGGTCA | 80067 |
| rs774097348 | snp | G/T | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171470077 | TGCCTAGCCTAGAGT[G/T]CAGTGGCACAATCAG | 80067 |
| rs774136261 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443383 | GTGATCAGAAAAAAA[-/T]ATTAATATTTAGTTA | 80067 |
| rs774169442 | snp | C/G | 0.000371816 | 0.0136297 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484764 | CCTCCCCACCCCTCA[C/G]GTATAACTACTGTTC | 80067 |
| rs774240323 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171436960 | TGTATTTTTGGTAGA[C/G]ACCGGGTTTCTCCAT | 80067 |
| rs774256835 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171456495 | TCAGCCTCTGTTTTG[A/G]TTCCATAGGAATTCT | 80067 |
| rs774288683 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171453004 | TAGATGGTTGTTTTC[A/G]TAATATGAAAATGTC | 80067 |
| rs774291784 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444896 | TTCTCTGAATACTTA[C/T]TGTCTGTTCACTGAA | 80067 |
| rs774374740 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171468801 | ATTTATAGATGTTGC[A/C]TGCAAAGAAAGGTTG | 80067 |
| rs774389075 | snp | C/G | 6.68003e-05 | 0.0057789 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435179 | AATTATCGGCGCTGT[C/G]TCAGCAGGTAACTTT | 80067 |
| rs774474650 | snp | C/T | 0.000118917 | 0.00771002 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458507 | TAGTATTTTTTCACC[C/T]TAAAAAAATTAAGTG | 80067 |
| rs774507646 | in-del | -/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171457930 | CAGAGGATTGGACTT[-/C]CAGTCTTTTCTCAGG | 80067 |
| rs774529161 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486487 | ATTTTTGTATTTTTA[A/G]GAGAGATGTGGTTTC | 80067 |
| rs774566117 | snp | A/T | 1.68315e-05 | 0.00290094 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443515 | CATTTATTTTTCTTT[A/T]TTCCCAGTGTTGCAT | 80067 |
| rs774610171 | snp | A/G | 6.65048e-05 | 0.00576611 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481117 | CAGAAGCTGTTAAAA[A/G]GAGTGAGATAATTGT | 80067 |
| rs774619253 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171458753 | CTTGATTTCCTTATC[C/T]GCAAAATGAGTTGCA | 80067 |
| rs774654813 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171437372 | TTGCAAGGCCTTGCC[A/G]CCCTTGTCAAAAATC | 80067 |
| rs774655886 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171457410 | TTAAGCTGCTGAATT[A/G]TATAAAAATAAGAAT | 80067 |
| rs774669776 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171485797 | TTTTAGAGGTGCACA[A/G]AATTTCAGAAGTATT | 80067 |
| rs774670596 | in-del | -/G | 1.67186e-05 | 0.0028912 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453263 | TATTGACAATAAGTT[-/G]TAATGTCATTATTTA | 80067 |
| rs774674106 | snp | C/G | 4.98202e-05 | 0.00499075 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171449933 | TAAGTCAGCTCAGAA[C/G]AGAGGCTCAGCAGTG | 80067 |
| rs774729157 | snp | A/G | 1.70761e-05 | 0.00292194 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448838 | TACTGTGAATTTATT[A/G]TTCAAGATTTTATTT | 80067 |
| rs774736126 | snp | A/C/G | 0.000185925 | 0.00963993 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483924 | TTCTCAAAAGGCAAG[A/C/G]CATGTTATTTTATCC | 80067 |
| rs774879338 | snp | A/C | 3.49107e-05 | 0.00417782 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435221 | TTTGCTGTAATTCAC[A/C]TCACTGTTGATCTTA | 80067 |
| rs774910948 | snp | C/T | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474051 | CTTTATTTTTGCCAG[C/T]GAACTAGTGAGCCAA | 80067 |
| rs774945136 | snp | G/T | 3.30077e-05 | 0.00406236 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480949 | CTGTGTGAAAAGGAC[G/T]CCATATGATTGTGTT | 80067 |
| rs775034680 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464196 | CATTTTATTAGAGAA[C/T]GTCATTAGAGACTCT | 80067 |
| rs775130915 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443085 | TTTTTTTAAATCCAC[C/T]AGTTTTCATTCTAAA | 80067 |
| rs775140323 | snp | A/G | 1.89521e-05 | 0.00307826 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171476999 | TCATTGTCTTTCTAT[A/G]TAAGACTATAATATG | 80067 |
| rs775188242 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171476630 | ATCATTACCTACTTC[A/G]GTGGCACCTGTTGTC | 80067 |
| rs775236367 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171478727 | GAAACATTAGAGTGG[C/G]CTTCCAAGGACAGTT | 80067 |
| rs775246401 | snp | C/T | 3.31549e-05 | 0.0040714 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458366 | TTTGTTTTGTTTTGT[C/T]TTTAGTTCATGCAAC | 80067 |
| rs775291842 | snp | A/G | 1.65663e-05 | 0.002878 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458084 | TGAACAGGTAGAGAA[A/G]ACTGAAATTTGTCAT | 80067 |
| rs775326585 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171490527 | GTCAGCAGAGTGAAG[C/G]AGATCCAGAAGGAAA | 80067 |
| rs775395103 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435413 | CAAAACTACAGTGCA[C/G]GCAAAACCACAGATT | 80067 |
| rs775480389 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171479410 | GACACAGTTCTGGGA[C/T]TTTTCTCTCTTTACC | 80067 |
| rs775497773 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171457174 | TATCCTTCTAAGAGA[A/T]GACAAAAAATACAAC | 80067 |
| rs775511787 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171446439 | TAATCCCAGATACTC[A/G]GGAGGCTGAGGCAGG | 80067 |
| rs775518305 | snp | A/G | 0.000185856 | 0.00963813 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482520 | TGAAAAACAAGACCA[A/G]TAAGAGGCCAGTGAA | 80067 |
| rs775523364 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455501 | ATATTTATAATAGAA[C/G]GATTTATATCCCTTT | 80067 |
| rs775568340 | snp | A/G | 1.65811e-05 | 0.00287929 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435154 | TGAGAGAGGAAGAAT[A/G]TATTTTGACAATTAT | 80067 |
| rs775577850 | in-del | -/TTTTG | 4.98401e-05 | 0.00499175 | intron-variant | DCAF17 | GRCh38.p7 | 2:171458350 | TGCTAAAGCCACCAT[-/TTTTG]TTTTGTTTTGTTTTT | 80067 |
| rs775629782 | snp | C/T | 0.000436205 | 0.0147619 | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447525 | ACCGCAACGCCCAGC[C/T]AATTTTTGTATTTTT | 80067 |
| rs775631025 | in-del | -/AGGG | 0.000185048 | 0.00961716 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481502 | AAGGCTAGGAAAGAC[-/AGGG]AGAGACAAAAGTAAA | 80067 |
| rs775685832 | snp | A/G | 1.65669e-05 | 0.00287805 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469062 | ACTTTTTATTAGCAA[A/G]TTTGTATCAAGTTCT | 80067 |
| rs775777831 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171480494 | TTGGAAAAATTTTTT[A/G]AAATAAGAGAATACG | 80067 |
| rs775802780 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171458886 | ATGACATCTGAACAT[A/C]GAGCTTAGACACAGA | 80067 |
| rs775865142 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486196 | TCTCAGAAAAACCAA[C/T]TTTGCAAAGGTGGTA | 80067 |
| rs775888786 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171472417 | CTCCTGACCTCAAGT[A/G]ATCCACCTGCCTCGG | 80067 |
| rs775915730 | snp | A/C | 1.67091e-05 | 0.00289038 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481138 | AGATAATTGTAACCT[A/C]AGAGACTTTTAGCCA | 80067 |
| rs775916885 | snp | A/G | 1.6588e-05 | 0.00287988 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448697 | GAGATATACTTCCCA[A/G]TTCATCAGATTATAA | 80067 |
| rs775942372 | snp | C/T | 1.6654e-05 | 0.00288561 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453120 | TTGTAGTCTTTCCTT[C/T]TAGGCAGGCATTCAA | 80067 |
| rs775977014 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487396 | TGTGTATATCTTTTT[C/G]ATGACATAGTGAAAT | 80067 |
| rs775985887 | snp | A/G | 4.98144e-05 | 0.00499047 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171453140 | CAGGCATTCAACAAC[A/G]TGTTTTGCTGTACCT | 80067 |
| rs775989796 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452784 | CAAATGATATGAGCA[C/T]GATAACTACATTATC | 80067 |
| rs776039653 | snp | A/G | 0.000185856 | 0.00963813 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434386 | TCTCCGCGCTCTGGC[A/G]GTGCAAGCGGCTCTG | 80067 |
| rs776187710 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171439458 | GATAACTGTTAAAGG[C/T]GTTCTTCATTTCTCT | 80067 |
| rs776253926 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452715 | GCGATCCTCCTGCCT[C/T]AGCCTCCCAAAGGGC | 80067 |
| rs776344051 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171486357 | CTCTGTCACCCAGGC[C/T]GGAGTGCAGCAGCAC | 80067 |
| rs776380751 | snp | A/G | 1.7429e-05 | 0.00295199 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443489 | CTGTCTTGGTTATCA[A/G]GAATAATAATCATTT | 80067 |
| rs776564383 | snp | G/T | 0.000186237 | 0.009648 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482965 | AAGGAGTTGTGGGCA[G/T]TGTAACAAACAGGAG | 80067 |
| rs776612803 | in-del | -/ACCCTCC | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171455133 | CCTTTCCCTCCTCCC[-/ACCCTCC]ACCCTCCACCCTCCG | 80067 |
| rs776654201 | snp | A/G | 0.000185684 | 0.00963366 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483441 | GCATTGCACTCCTGG[A/G]TCTAAGTTTCTGCAT | 80067 |
| rs776729717 | snp | A/G | 0.000380084 | 0.0137803 | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485060 | TTAGACAATTCTTTT[A/G]TGAACATGTGTCTTT | 80067 |
| rs776773436 | snp | A/G | 1.64947e-05 | 0.00287177 | synonymous-codon, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480076 | AGATGAGTTAGATTT[A/G]CTTTCTGTGGTAGCT | 80067 |
| rs776791418 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435666 | GGGAAGGAAAGCCAC[A/G]ATGCATCCCCATATA | 80067 |
| rs776817151 | snp | C/T | | | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171470180 | AGGAGCGCACCACCA[C/T]GCCTGGCTACTTTTT | 80067 |
| rs776839643 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171448962 | TTCTTTTTCTCCCCT[C/T]ATGACTACATTTAGA | 80067 |
| rs776847935 | snp | C/T | 0.000372578 | 0.0136437 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481664 | TATTTATATGTGTTT[C/T]GTATTTGTATATAGT | 80067 |
| rs776877044 | snp | A/G | 3.31664e-05 | 0.00407211 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448709 | CCAATTCATCAGATT[A/G]TAAGTCCTCACTCAT | 80067 |
| rs776883898 | snp | C/T | | | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447672 | TAGCCACTTCTTTTT[C/T]TCCTTTTTATCTAGA | 80067 |
| rs776939642 | snp | A/T | 1.65844e-05 | 0.00287957 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469068 | TATTAGCAAATTTGT[A/T]TCAAGTTCTTTATTT | 80067 |
| rs776985449 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171476852 | CAGAATCCTTTTTCC[C/G]TTCTCAGAGTTTTGA | 80067 |
| rs777044067 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171440224 | TTTCTTCAAACTTTT[C/G]TATTTTGCCTGTTAG | 80067 |
| rs777053231 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171461486 | GGGAAATAAAGATAA[A/G]CAAAAGAGAAAATGT | 80067 |
| rs777096255 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171489149 | CCAAGGGTGGTCCTA[C/T]TGCTACCCTGGTATT | 80067 |
| rs777131474 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464240 | AGCAACACTACAAAC[C/T]GGGCAGCTTTAAACA | 80067 |
| rs777147076 | in-del | -/GTTT | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171469813 | GTTTTTTGTTGGTTA[-/GTTT]GTTTTTCAAGACAGG | 80067 |
| rs777176864 | snp | A/G | 1.6504e-05 | 0.00287258 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480029 | CTATTTTATCTATCT[A/G]TCCCAAAGACTTTCA | 80067 |
| rs777209074 | in-del | -/TC | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171465947 | TTAAATATTTAATCT[-/TC]TTTCTTACATCAAAT | 80067 |
| rs777221977 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171470643 | TCTTGGTTTGATTGG[C/T]CACCTCCCAGTGAGT | 80067 |
| rs777239060 | in-del | -/G | 3.6324e-05 | 0.00426154 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435057 | TAAGAGTTCTTTCCT[-/G]AACGGAAATTCTTTA | 80067 |
| rs777310967 | snp | G/T | 3.32011e-05 | 0.00407424 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480177 | AAAGCATTCCACTAG[G/T]GGAGTCATGGGATGT | 80067 |
| rs777311799 | snp | A/G | 0.000371402 | 0.0136222 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483426 | AAAGAGGTGCATTCT[A/G]CATTGCACTCCTGGA | 80067 |
| rs777339992 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171454204 | ATAAAAAGCAGCTAC[C/G]TAAATCCTAAAGGTG | 80067 |
| rs777356827 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171478130 | GCATTGTGAATTTCA[A/T]ATTAATACTTCCCCA | 80067 |
| rs777361744 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171438223 | GACCCAAGAGCATAC[-/T]TTTATATTAGTTCTA | 80067 |
| rs777371472 | snp | A/C | 0.000386772 | 0.013901 | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485080 | CATGTGTCTTTATTT[A/C]TCTTGGGTAAATACC | 80067 |
| rs777390466 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171490208 | ATCCCTAGCAAGGGC[C/G]AAGTATGTTTATTTC | 80067 |
| rs777396496 | snp | A/G | 0.000205952 | 0.0101456 | intron-variant | DCAF17 | GRCh38.p7 | 2:171472983 | TGTACACATGTGATA[A/G]CATATCAGATGGTTT | 80067 |
| rs777533878 | snp | A/C | | | intron-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171447400 | GATGGAGTCTTCTGT[A/C]GCCAGGCTGGAGTGC | 80067 |
| rs777550757 | snp | A/G | | | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171449957 | AGCAGTGGCCCGGCA[A/G]GTATACATATTTAAA | 80067 |
| rs777591762 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482559 | AGAAAGAAACCAATG[C/T]TGTGTGAGTTTCAAA | 80067 |
| rs777591799 | snp | A/G | 1.66026e-05 | 0.00288115 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448685 | TTTTTTTTTAGGGAG[A/G]TATACTTCCCAATTC | 80067 |
| rs777645107 | snp | C/T | 8.27068e-05 | 0.00643013 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469051 | TGAGTGATCAGACTT[C/T]TTATTAGCAAATTTG | 80067 |
| rs777749413 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171458732 | ATTCACTTTACTTTT[C/G]TGATCCTTGATTTCC | 80067 |
| rs777823275 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171460106 | GAGGCGGGTGGATCA[C/T]GAGGTCAGGAGTTCG | 80067 |
| rs777850235 | snp | A/G | 3.31549e-05 | 0.0040714 | intron-variant, missense, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171476930 | GATTTTGTCATTTTG[A/G]CCAACAGGGAGAACC | 80067 |
| rs777896355 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171450339 | ACCACTAAAGAACTT[A/G]CTCATGTGACCCAAC | 80067 |
| rs777915318 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436616 | AATGTTTGGTTAGAT[A/G]TTTTGCCCACTTGTA | 80067 |
| rs777923617 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171462721 | GAATTTATCCCAGAT[A/G]TATTCACTTGTACAG | 80067 |
| rs777986542 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171465027 | ATGGTGAAACCCTGT[C/T]TCTACTAAAAATAGA | 80067 |
| rs778092477 | snp | A/G | 0.000186759 | 0.0096615 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482734 | CCTTCCTTTTATGAA[A/G]TGATAGTAAGGAACT | 80067 |
| rs778114154 | snp | C/T | 1.66396e-05 | 0.00288436 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171453176 | TGTTCCGAGTTCTAC[C/T]TTTTTCACTTGTAGG | 80067 |
| rs778189945 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466252 | AGAAAAAATCATATT[G/T]TATTACAGGTGTAGC | 80067 |
| rs778207174 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444394 | TGAATGCCGACATGA[C/T]GCCACAAGTGGAAAA | 80067 |
| rs778234568 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171433474 | GCCCCACCCTTAAGG[A/G]ACTTAGAGCATGGCG | 80067 |
| rs778241115 | snp | A/G | 5.12037e-05 | 0.00505957 | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171435201 | GGTAACTTTTTATTG[A/G]TAATTTTGCTGTAAT | 80067 |
| rs778276293 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171479249 | GAATTAGTGCATAGT[C/G]ATTGAGGGAAACATG | 80067 |
| rs778294502 | snp | C/T | 1.65721e-05 | 0.0028785 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435128 | ACTCATTCCAGGTCA[C/T]CTATAGCCTATGAGA | 80067 |
| rs778321442 | snp | C/T | 3.74497e-05 | 0.00432706 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474016 | AGTTAAGAGCAGCTT[C/T]TGGTAGCATTTATTG | 80067 |
| rs778352408 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171478815 | AACACACAAAAAAGT[A/G]TTATTTTGGACCATA | 80067 |
| rs778369413 | snp | C/G | | | utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171490852 | TGGCAGGTTGTGCCA[C/G]CAGGGAGTTCAGAGT | 80067 |
| rs778370006 | in-del | -/GAA | 1.68269e-05 | 0.00290055 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449986 | AACATTCAATAAAAT[-/GAA]GACTCTTTTTCATAG | 80067 |
| rs778411344 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444519 | TGAATTTTGTGTTTA[G/T]ACTTGGGTCCCATCC | 80067 |
| rs778451530 | snp | C/T | 1.65669e-05 | 0.00287805 | missense, intron-variant | DCAF17 | GRCh38.p7 | 2:171458445 | CTGTAGGAGAGGCTC[C/T]TTTTGGCATTCCTTG | 80067 |
| rs778488574 | in-del | -/AG | 1.64904e-05 | 0.00287139 | frameshift-variant, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481037 | GAGCAGAAACCCAAC[-/AG]AGTCTTCAGCTGCTA | 80067 |
| rs778489822 | snp | A/C | 1.64811e-05 | 0.00287059 | intron-variant | DCAF17 | GRCh38.p7 | 2:171468861 | CAGAACAGTGCAGCT[A/C]ATGAATTCCTTTTCC | 80067 |
| rs778717106 | snp | C/T | | | | | GRCh38.p7 | 2:171463138 | CAGGAGGCTGAGGCA[C/T]GAGAATCACTTGAAC | 80067 |
| rs778753121 | snp | C/T | | | | | GRCh38.p7 | 2:171448361 | TTGTTGTTATTGTTA[C/T]CACAGAGGTAGCATC | 80067 |
| rs778762140 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171470813 | CACAAACACACGCAC[A/G]CGTACAGATACAGCC | 80067 |
| rs778769146 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171449986 | AACATTCAATAAAAT[A/G]AAGACTCTTTTTCAT | 80067 |
| rs778815572 | snp | C/G | 1.85259e-05 | 0.00304345 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449845 | ATAAGGAAACTGACC[C/G]AAATAAATAAACTTC | 80067 |
| rs778868652 | snp | C/T | 1.65817e-05 | 0.00287933 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448769 | GTATATCAGCAACTA[C/T]GGGAAAAATCCTTGA | 80067 |
| rs778920494 | snp | C/T | 0.000186445 | 0.00965339 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434309 | CGCGCGGTACCGGAG[C/T]GTCGCACTGTCAGCG | 80067 |
| rs778932293 | snp | A/G | 0.00315544 | 0.039595 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483543 | AACAAAACAAATCCT[A/G]TCCTATTTACTATTT | 80067 |
| rs778959225 | snp | G/T | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171474745 | TTTAAACACTTACAG[G/T]CATTCTCTTTCTCTC | 80067 |
| rs778975572 | snp | C/T | 3.3938e-05 | 0.0041192 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171453197 | CACTTGTAGGGATTC[C/T]AGAGATCAACAAAAA | 80067 |
| rs778988552 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171488158 | ACAAAATTCATAAAA[A/G]TAACAGTCGGTGAAA | 80067 |
| rs778994056 | in-del | -/CTC | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436320 | CATTTATTTTCACTT[-/CTC]CTAGATTATACCTAG | 80067 |
| rs779024389 | snp | C/G | 0.000559649 | 0.0167186 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482699 | GATTATTGAGTTTCT[C/G]CTTCTCCTTTAAGTC | 80067 |
| rs779045227 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171488188 | AGTGAAATTCATACT[C/T]AGGACACTCTACCTG | 80067 |
| rs779135584 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487319 | TAGCATCTCAATGTG[A/G]TTTAAATTTACATTT | 80067 |
| rs779151739 | snp | G/T | 2.02173e-05 | 0.00317935 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434612 | CCAACGTGTGCAGCC[G/T]GCTGAGTCGCCGGGC | 80067 |
| rs779152661 | snp | C/G | 8.30585e-05 | 0.00644379 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171443568 | AATGCCAAAATGTTC[C/G]AAATCAGAAAAAATA | 80067 |
| rs779164442 | in-del | -/CTT | 5.51937e-05 | 0.00525298 | utr-variant-3-prime, nc-transcript-variant, cds-indel, intron-variant | DCAF17 | GRCh38.p7 | 2:171481252 | TTCAGATGACTATGA[-/CTT]CTTTTTTAAACTCTT | 80067 |
| rs779174983 | snp | C/T | 0.000557465 | 0.016686 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483263 | CCTCTTTACCTGATA[C/T]TTTAATTCGAGACTC | 80067 |
| rs779200425 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171490659 | AACAGTATGTGTGAG[A/T]TGGGTTGGGAAGAAT | 80067 |
| rs779206254 | snp | C/G | 0.000185408 | 0.00962652 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481511 | AAAGACAGGGAGAGA[C/G]AAAAGTAAACATGCA | 80067 |
| rs779227349 | snp | A/T | 1.69086e-05 | 0.00290758 | intron-variant, downstream-variant-500B | DCAF17 | GRCh38.p7 | 2:171476963 | AAAGTAAGTCAAGAG[A/T]ACTTTAAAATCCTTT | 80067 |
| rs779368643 | snp | C/G | | | upstream-variant-2KB, intron-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171432629 | CTAAAAATATACAAA[C/G]CACTCTACCGTATGC | 80067 |
| rs779410799 | in-del | -/TAAC | 0.000186272 | 0.0096489 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484552 | TCAACTGCAGATTAT[-/TAAC]TAGAGTTTAGTATTT | 80067 |
| rs779420870 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171466434 | AAGTGGAAGCCCTTT[C/T]GCTGGCTCTCCTACT | 80067 |
| rs779434873 | snp | G/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171433040 | CCTAATTATTCCAGT[G/T]CAGGGTCGAGGGTGG | 80067 |
| rs779459945 | snp | C/T | 6.7068e-05 | 0.00579046 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453098 | TACTTTTGAGAGCTG[C/T]GTGTAATTGTAGTCT | 80067 |
| rs779493587 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171479505 | CAAGTATAAGCAGCC[A/G]TTTTTGCTTTATTTA | 80067 |
| rs779520723 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171445728 | CACTCTGTTGCCTAA[A/G]CTGGAGTCCAGTGGC | 80067 |
| rs779536134 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171472351 | TGCCCACTAATTTTT[A/G]TATTTTTAGTAGAAA | 80067 |
| rs779537657 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171480653 | TTTATCCAGGTCTTG[A/T]TTTATCAGTGGAGAA | 80067 |
| rs779556352 | snp | A/C | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant, stop-gained | DCAF17 | GRCh38.p7 | 2:171468902 | GACATGCCACCACTG[A/C]TCTTTGAGGTGTCAT | 80067 |
| rs779579578 | snp | A/C | 1.66239e-05 | 0.00288299 | missense, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171443595 | AATAGAGGATGCTTT[A/C]TTATGGGAATGCCCA | 80067 |
| rs779626012 | snp | A/G | | | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171475310 | TCCTTTGTAGCACTT[A/G]GGGCAACTTAAATAA | 80067 |
| rs779673462 | in-del | -/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171454693 | TTGAGGTTAGGAGAT[-/C]CAATACCAGCCTGGC | 80067 |
| rs779786259 | snp | A/G | 0.000185891 | 0.00963903 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171483760 | AACCACATGAAGTAT[A/G]AACTGCCATTATCTT | 80067 |
| rs779792580 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444632 | CAGTAGGAGAAGGGA[C/T]AATCGACCTGTATTT | 80067 |
| rs779834748 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171461980 | TTTCATGTTGTTGCA[G/T]GTATCTATAGCCTAA | 80067 |
| rs779881241 | snp | A/T | | | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485438 | AATTATTCTTTCTCA[A/T]ACATGGGATACATTG | 80067 |
| rs779974974 | snp | A/G | 0.000185925 | 0.00963993 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482238 | TCTGCACATTTATCC[A/G]ATGTAACCTCAAAAG | 80067 |
| rs779984525 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171472976 | ACATTTGTGTACACA[A/T]GTGATAACATATCAG | 80067 |
| rs780029249 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171467087 | TATGCCTGTCTCTTC[-/T]TTTTCCTCAAGATTT | 80067 |
| rs780033111 | snp | A/G | 1.86135e-05 | 0.00305064 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481188 | CCAATCCATTTTATT[A/G]TCTGCATGGCACATT | 80067 |
| rs780036993 | snp | C/T | 3.31713e-05 | 0.00407242 | synonymous-codon, intron-variant | DCAF17 | GRCh38.p7 | 2:171458473 | TTGTAATATTAAAAT[C/T]ACAGGTATGGCTACT | 80067 |
| rs780089738 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171462997 | AGCACTTTGGGAAGC[A/G]AGGCAAGTGGATCAC | 80067 |
| rs780114312 | snp | G/T | 5.82745e-05 | 0.00539758 | synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434628 | GCTGAGTCGCCGGGC[G/T]CTGGGCTGCTTCTCG | 80067 |
| rs780179665 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171461281 | GAAACCCCGTCTCTA[C/T]CAAAAATACAAAAAA | 80067 |
| rs780212623 | snp | A/G | 0.000185787 | 0.00963634 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481584 | TGAGAAATGAGATGT[A/G]TTATGTGAGAACATT | 80067 |
| rs780249144 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171488477 | TTACCTGTTAGAGCA[A/G]CAAGACTAGTTAAAG | 80067 |
| rs780253154 | snp | A/C | 2.34601e-05 | 0.00342484 | intron-variant | DCAF17 | GRCh38.p7 | 2:171453241 | TTCTTATTTAATTGC[A/C]ATATTTTATTGACAA | 80067 |
| rs780292085 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171453898 | AGCAAACAAGTTGAA[C/T]GTATTAAAATTTTAC | 80067 |
| rs780343535 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171489799 | TGGGACTACAGGCGC[C/T]CGCCACCATGCCTGG | 80067 |
| rs780485735 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171440954 | GCTGTTTTCGTCTTG[G/T]ACCAGAAACCAGAAT | 80067 |
| rs780493577 | snp | A/C | 1.76639e-05 | 0.00297181 | intron-variant, splice-acceptor-variant | DCAF17 | GRCh38.p7 | 2:171473864 | CTTTTTTCCAACTTC[A/C]GGCAAAAAATGGGAT | 80067 |
| rs780566273 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171452603 | GGACTACAGGCATGC[A/G]CCACCATGTCCAGCT | 80067 |
| rs780589850 | snp | C/G | 0.000514933 | 0.0160375 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484452 | CTACATCTTACTCTA[C/G]TTGTTTTATTATTTT | 80067 |
| rs780590311 | in-del | -/A | 1.68303e-05 | 0.00290084 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449874 | TCTCTTCATTCTTTT[-/A]AAAGATACTTGAGCT | 80067 |
| rs780662008 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171434981 | GGAAGGATGCAAAAA[A/G]TTTTAAAATAATATA | 80067 |
| rs780693396 | snp | A/C | 6.53203e-05 | 0.00571453 | intron-variant | DCAF17 | GRCh38.p7 | 2:171448663 | GTTTCATTTTTATAT[A/C]TCTCTTTTTTTTTTT | 80067 |
| rs780733984 | snp | C/T | 0.000186306 | 0.00964979 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171484549 | ACTTCAACTGCAGAT[C/T]ATTAACTAGAGTTTA | 80067 |
| rs780757035 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482395 | GGCTTGATGCCATGT[A/T]AAGAATGATGTGAAT | 80067 |
| rs780759044 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171468577 | CTACTTTTATTAAAT[A/G]TACTTTGTCATTTCT | 80067 |
| rs780849058 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171480725 | TAGATAATAGCAGCG[C/T]TGGCAATAGAATCTG | 80067 |
| rs780861777 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171446366 | GCCTGACCAACATAG[C/T]GAAACCCCGTCTCTA | 80067 |
| rs780929146 | in-del | -/TCAGATC | 3.31485e-05 | 0.00407102 | intron-variant, frameshift-variant, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171476902 | TAATAGTTCTCAGCA[-/TCAGATC]TCTGAAGATTTTGTC | 80067 |
| rs781010136 | snp | A/G | 6.59141e-05 | 0.00574045 | synonymous-codon, nc-transcript-variant, missense | DCAF17 | GRCh38.p7 | 2:171468910 | ACCACTGCTCTTTGA[A/G]GTGTCATCCCTGGAG | 80067 |
| rs781040231 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171473127 | AGATTCTGTGACCCA[C/T]GTCTGAGGCTTTAGG | 80067 |
| rs781040668 | in-del | -/AG | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171487738 | ACTTAAAATAGAAAG[-/AG]AGAGAGAGACTTACT | 80067 |
| rs781042836 | snp | C/T | 0.000192178 | 0.00980062 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434264 | GCACTAGGAACTACA[C/T]TTCCCGGTGAGAGAG | 80067 |
| rs781052412 | in-del | -/TGAG | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171462021 | GATGTTAATATATTA[-/TGAG]TATTTCCATCTAGAT | 80067 |
| rs781056426 | snp | C/T | 1.65255e-05 | 0.00287445 | intron-variant | DCAF17 | GRCh38.p7 | 2:171469040 | TCCCTGGTAAATGAG[C/T]GATCAGACTTTTTAT | 80067 |
| rs781062036 | snp | A/C | 1.65173e-05 | 0.00287374 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480016 | TGCCCCTTTCCCTCT[A/C]TTTTATCTATCTATC | 80067 |
| rs781065193 | snp | C/T | 2.13614e-05 | 0.00326806 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171481200 | ATTATCTGCATGGCA[C/T]ATTCTCCAGTATTTT | 80067 |
| rs781101492 | snp | G/T | 3.55252e-05 | 0.00421442 | intron-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171473997 | AATCTCATTAGCACT[G/T]GAAAGTTAAGAGCAG | 80067 |
| rs781121289 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171461063 | CAAATTTGTTTTTCA[A/G]TCTTAAGGTCTATAC | 80067 |
| rs781164465 | snp | A/G/T | 5.02158e-05 | 0.00501057 | intron-variant | DCAF17 | GRCh38.p7 | 2:171443619 | ATGCCCAGTGGTAAG[A/G/T]TTTGTTTTTAGAGCG | 80067 |
| rs781234378 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171459478 | AAAAGAGAAAATTTT[A/C]TTTATTATCCTAATA | 80067 |
| rs781256751 | snp | C/T | | | downstream-variant-500B, intron-variant | DCAF17 | GRCh38.p7 | 2:171485246 | CTCCAGCATGTGTGG[C/T]TGTTAGTCTTCTTTA | 80067 |
| rs781276466 | snp | C/T | 0.000558815 | 0.0167061 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482689 | TTTTTTAGGTGATTA[C/T]TGAGTTTCTCCTTCT | 80067 |
| rs781361408 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171468531 | TATCTAACCCAGAGT[A/C]TTTACATAGTAGATG | 80067 |
| rs781363432 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171441674 | CACCAGTCTGGAGTG[A/G]AGTTTCCATCTTGCT | 80067 |
| rs781372214 | snp | A/G | 0.00127166 | 0.0251836 | synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434658 | GCGCGACGCAGGCGT[A/G]GTGCAGAGGACCAAC | 80067 |
| rs781410825 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171476500 | AAATGCAAATATCTG[C/T]TTTAATTGTTAGAGC | 80067 |
| rs781413185 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171442003 | GTCAAGTTTATAACT[C/T]CCTGCTTTAACTTAA | 80067 |
| rs781438514 | snp | A/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171464900 | CCAGTGTTACTACTA[A/G]GAACTAAAGTATGGG | 80067 |
| rs781453185 | snp | A/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444607 | GAAACACTTCTAGTC[A/C]CAAGTGTTTCAGTAG | 80067 |
| rs781502861 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171456746 | TTTTTAGGACAACTG[A/T]GAATGAGAGTTTGTT | 80067 |
| rs781538668 | snp | A/G | | | intron-variant, missense, nc-transcript-variant, utr-variant-3-prime | DCAF17 | GRCh38.p7 | 2:171476901 | ATAATAGTTCTCAGC[A/G]TCAGATCTCTGAAGA | 80067 |
| rs781622815 | snp | C/T | 3.43654e-05 | 0.00414506 | intron-variant | DCAF17 | GRCh38.p7 | 2:171449863 | ATAAATAAACTTCTC[C/T]TCATTCTTTTAAAAG | 80067 |
| rs781660960 | snp | A/T | 0.000169782 | 0.00921207 | intron-variant | DCAF17 | GRCh38.p7 | 2:171480221 | CGTGGGATACAAAGT[A/T]GTAAACCTTTCCTTT | 80067 |
| rs781676498 | snp | A/G | 0.000185856 | 0.00963813 | utr-variant-3-prime, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171482269 | AATAACTGGTAATAA[A/G]GGAAGGAAACAGCAG | 80067 |
| rs781702276 | snp | C/T | 1.65236e-05 | 0.00287429 | missense, nc-transcript-variant, intron-variant | DCAF17 | GRCh38.p7 | 2:171480137 | CACCTGGATTTCCAC[C/T]GTAATGAATATGGAA | 80067 |
| rs781716250 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171441832 | TGCAGAGACTTTAAA[-/T]AGTTGTCCTTTTATG | 80067 |
| rs781741762 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171490020 | TGGAGTCCATTTCTA[C/T]GAGTCCAATGTTGCC | 80067 |
| rs781747388 | snp | C/G | 1.66327e-05 | 0.00288376 | missense, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | DCAF17, METTL8 | GRCh38.p7 | 2:171435100 | AAGTACTAAATTTAA[C/G]AATGTCTGGACAACT | 80067 |
| rs786205638 | in-del | -/TTAAAAGATACTTGAGCTGGGACACTCCTCAAGAAGTCATTGCAGTTA | | | intron-variant, splice-acceptor-variant | DCAF17 | GRCh38.p7 | 2:171449872 | CTTCTCTTCATTCTT[lengthTooLong]AGTCAGCTCAGAACA | 80067 |
| rs796145384 | in-del | -/C | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171444257 | ATGATGATTATCAAG[-/C]CCATTTCCCCAAATT | 80067 |
| rs796204980 | in-del | -/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171458145 | TATGATTTTTTTTTT[-/T]AGTGAGATGCTTTTA | 80067 |
| rs796230923 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF17, METTL8 | GRCh38.p7 | 2:171436338 | CTAGATTATACCTAG[G/T]AATGGAATTGGTAGG | 80067 |
| rs796246351 | snp | A/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171443350 | TATTTTAATCTTGTT[A/T]TTTTTTATATGAATT | 80067 |
| rs796247151 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171462100 | CTCACTCTTAAATAA[C/T]AGATGGATCAAAGAC | 80067 |
| rs796310774 | snp | C/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171461893 | TTTTCTGGAGTTTTA[C/T]ATTAATGAAATCACA | 80067 |
| rs796391886 | snp | C/G | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171437432 | TCCGGACGTTCAAGT[C/G]TGTTCCACTGATCTG | 80067 |
| rs796783579 | in-del | -/A | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171473625 | TCTCTTGGGTTATTA[-/A]CTCCTGTTTGTGAGA | 80067 |
| rs796850239 | snp | G/T | | | intron-variant | DCAF17 | GRCh38.p7 | 2:171471324 | ATTTCAGAAAATGTT[G/T]CATAGCTTTCTCTAT | 80067 |
| rs796932573 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | DCAF17, METTL8 | GRCh38.p7 | 2:171434765 | GCGGCCGAGCCTCCT[C/G]CGGGGATGCGGTTTT | 80067 |
| rs797045038 | in-del | -/C | | | frameshift-variant, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171448795 | CTTGAGAAAATATAT[-/C]TTGCACCTTATTGCA | 80067 |
| rs863224865 | in-del | -/A | | | frameshift-variant, nc-transcript-variant, utr-variant-5-prime | DCAF17 | GRCh38.p7 | 2:171443581 | CCAAATCAGAAAAAA[-/A]TAGAGGATGCTTTAT | 80067 |