SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs10044 | snp | A/G | | | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075501 | CTAAAGCTCTGTAAA[A/G]AAAAAAATATAATAA | 55827 |
rs10693 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056108 | TGGTGCTTTGGAAAG[C/T]GTGAAAGCTGCTAGT | 55827 |
rs149912 | snp | A/T | 0.491629 | 0.0641526 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988565 | AAACTACTGTGCTCT[A/T]AATAATGTATGTCAG | 55827 |
rs169309 | snp | A/G | 0.197703 | 0.244469 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064031 | TGAGAAAGAGAGGGG[A/G]AAAAAAAAAAAAAAA | 55827 |
rs169310 | snp | A/C | 0.249038 | 0.249998 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034741 | AGGTTTAGAACTTCA[A/C]GTAAACACACAAATA | 55827 |
rs172088 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064076 | AAAAAAAAAAAATCC[A/C]CCAGAAACTTTTCAG | 55827 |
rs172113 | snp | A/G | 0.489837 | 0.0705577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011738 | ATCCCAGCACTTTGG[A/G]AGGCCGAGGTGGGTG | 55827 |
rs175752 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977262 | gaaggaaagaaaagg[A/G]aaCTGAAATTGTTTT | 55827 |
rs175753 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977246 | aaCTGAAATTGTTTT[C/T]TATCAACAAACTCTC | 55827 |
rs175754 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977155 | gagctttgagaggca[A/G]aggcaggcagatcac | 55827 |
rs175755 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977141 | agaggcaggcagatc[A/C]cctgaggtcgggagt | 55827 |
rs175756 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977046 | ggagtggtggtatgc[A/C]cctataatcccagct | 55827 |
rs182141 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033075 | ACGAAATTATAATCA[C/T]GAGGTTCTAAAAGAT | 55827 |
rs183230 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040658 | CACGTCTTTTCCATT[C/T]TCATGTTTCTGTACA | 55827 |
rs185702 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977233 | TTCTATCAACAAACT[C/T]TCATGTAAAAAAAAA | 55827 |
rs188033 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977170 | atgcctgtaatccca[A/G]agctttgagaggcag | 55827 |
rs191847 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049763 | caggttcacgccatt[C/T]tcctgcctcagcctc | 55827 |
rs191852 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976988 | tgaacccaggaggca[A/G]aggttgtggtgagcc | 55827 |
rs201533 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168047012 | AGGCTAATTATAACA[C/G]TTAATACCAAGCCTG | 55827 |
rs201534 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | DCAF6 | GRCh38.p7 | 1:168057598 | GTATCTAGCACATAA[C/T]AGGTTTATTGAAGTA | 55827 |
rs201535 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056893 | AGTGAAAAACTAAAG[A/G]GAAATAAAAGCTTCT | 55827 |
rs201536 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033606 | TTTCAggccgggcgc[A/G]gtggctcacacctgt | 55827 |
rs201537 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030352 | TAGTCATCCTGTATG[C/T]GGCATCTCAGAGGCT | 55827 |
rs201538 | snp | A/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027883 | GACAACCAGGGAGCT[A/G]CATTAATGAATGAAG | 55827 |
rs201539 | snp | C/T | 0.493748 | 0.0555599 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026169 | TGATTACAAATGTGA[C/T]AAATGCAATGAGGAA | 55827 |
rs201540 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023645 | AATAAGTAACGCGTT[C/T]ATTTCATCAGGCTCT | 55827 |
rs201541 | snp | A/T | 0.491157 | 0.065903 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023106 | GTGAGAGAGCTTAGT[A/T]TATGCATTGCAATAA | 55827 |
rs202238 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984258 | CAGAAGTGCTTCTTC[G/T]GTAACATTCTTACAC | 55827 |
rs202239 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984010 | ttactgttttttaca[A/C/G]ctaccatagtcgcaa | 55827 |
rs202240 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982741 | tctttctcaagtcca[A/G]tgtctagaatggcgt | 55827 |
rs202241 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965741 | aagcagttctcctgt[C/T]gggaggctgaggcct | 55827 |
rs202242 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965854 | tggtcaggctggtct[C/T]gaacctctgacatca | 55827 |
rs202243 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969403 | AGCTGGGATAACATA[C/T]GAGTTCTAATTAGGT | 55827 |
rs202244 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972874 | AAATTTTAATTAGTT[G/T]ATTTAATAAGGGAAT | 55827 |
rs202245 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971378 | ATCCTCAACACTTAA[C/T]ATTATTTATTTACCT | 55827 |
rs202246 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970731 | ACCATGAGTCAAATA[C/T]TACCTGTTTTTATAG | 55827 |
rs202247 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000918 | ttatataatgatgac[A/G]gttgtacctctttat | 55827 |
rs202248 | snp | A/G | 0.434253 | 0.168969 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002785 | TGGTAGTTGTTATCA[A/G]ATTAGTCTCCAAAAA | 55827 |
rs202249 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008208 | tcctaacctcaagca[G/T]tccatccgcctcggc | 55827 |
rs202250 | snp | C/G | 0.348574 | 0.229746 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008513 | TCTCCTAATTAATCT[C/G]CCTGTACCTACTGTT | 55827 |
rs202251 | snp | C/G | 0.378174 | 0.214642 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009452 | tctttctttctttct[C/G]tctctctctcttcct | 55827 |
rs202252 | snp | C/T | 0.314787 | 0.241459 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010980 | TATGATTTAGAGAAG[C/T]TGGTAACTTTGAAGT | 55827 |
rs202253 | snp | G/T | 0.476746 | 0.10529 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017227 | AATAAAACATTTTTG[G/T]TTTTTTTTTTGCTGT | 55827 |
rs202254 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018393 | TATTTTTGGTTGTTC[A/G]CTCTTTGTCATCAGT | 55827 |
rs202255 | snp | A/G | 0.429837 | 0.173662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019415 | CATATAAAGGCCCCC[A/G]TAAGGTTGATAGCAT | 55827 |
rs202256 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996008 | ataaggactatgttc[C/T]gtataagtagaacaa | 55827 |
rs202257 | snp | A/G | 0.488606 | 0.0746142 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995478 | TGAGGTCAGGAGTTC[A/G]AGACCAACCTGGCCA | 55827 |
rs202258 | snp | C/T | 0.491421 | 0.0649309 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995444 | TAGCACTTTGGGAGG[C/T]CGAGGCGAGTGGATC | 55827 |
rs202259 | snp | A/G | 0.489318 | 0.0722982 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992834 | AAGGATATTGCATAC[A/G]TTGCATACTAATGTA | 55827 |
rs202260 | snp | G/T | 0.485933 | 0.0826777 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986929 | AAAAAAGGtttttat[G/T]gtagtaaaatacata | 55827 |
rs202261 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985692 | tttgggctactatta[C/T]tctgcttaccacaAT | 55827 |
rs202262 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022012 | AGGGCTACAGTAAAA[C/G]AGAAACATAGGTAAT | 55827 |
rs202263 | snp | C/T | 0.432063 | 0.171327 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021844 | GGTATTTTAAGATTG[C/T]CCTTAGCTGGATAGC | 55827 |
rs202264 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021375 | AAAAATGTGACTCAC[A/G]GTGAAATAAATATTG | 55827 |
rs202265 | snp | C/G | 0.490563 | 0.0680388 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020993 | TCCTTTTTGGTTTTA[C/G]TCTGCCATAGACATT | 55827 |
rs202266 | snp | G/T | 0.489492 | 0.0717183 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960545 | ctgacctcgtgatct[G/T]cctgtcttggcctcc | 55827 |
rs202267 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959957 | tcatctgagtttttt[C/T]cctatgttatcttct | 55827 |
rs202268 | snp | A/G | 0.484421 | 0.0868729 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958101 | cactatgaggaaggc[A/G]aaaagacaacccata | 55827 |
rs202269 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957101 | aaattaaaaaaaaaA[A/T]AAATGTCCACTTATA | 55827 |
rs202270 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955730 | attccactccttcta[G/T]tcaatcttataatag | 55827 |
rs202271 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953719 | cccagctactcggga[A/G]gctgcagcggagaac | 55827 |
rs202272 | snp | A/G | 0.31721 | 0.240796 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953615 | agaccccatatcaaa[A/G]aaTAATAATAATAAT | 55827 |
rs202273 | snp | A/G | 0.484491 | 0.0866827 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950725 | GAAGGCTGAATTTAC[A/G]ACAAAGAACAATAAT | 55827 |
rs202274 | snp | C/G | 0.305934 | 0.243663 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950253 | TCTCATTGAGTTATA[C/G]GAGTTAAGAAACAAA | 55827 |
rs203248 | snp | G/T | 0.0618563 | 0.164627 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963324 | tcaaagggattactg[G/T]tatagttggattaat | 55827 |
rs203255 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980200 | taaataaataaataa[A/G]taaataaataaattc | 55827 |
rs203787 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936547 | AGATGACGACCACCC[C/T]GGGGACTGAGGCTGG | 55827 |
rs203788 | snp | G/T | 0 | 0 | synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937001 | CCGCTCACCCAGGTA[G/T]CGACTCCGCAGCCGG | 55827 |
rs203789 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940382 | CTCACCCTGCCCCCC[A/G]CCTCCCACCAAAAAA | 55827 |
rs203790 | snp | A/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941485 | CACAGGTTGCCACAT[A/G]AATGTACTTTTATCA | 55827 |
rs203791 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943661 | atgaggaggtgggag[C/G]atgatgagaaattcg | 55827 |
rs203792 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945861 | tgatttggttttcat[C/T]ttgaatcattattgg | 55827 |
rs369851 | snp | C/G | 0.249603 | 0.25 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065228 | AATAGAAAATCCCCC[C/G]TAAGAAGAGGGACTT | 55827 |
rs369914 | snp | A/T | 0.203267 | 0.245593 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065018 | GAAATAATTCACAGA[A/T]AAAAGAAATTGTCTT | 55827 |
rs370952 | snp | C/T | 0.249603 | 0.25 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065525 | CAAAGATTTATGCTA[C/T]TCTTACATTTTTTTA | 55827 |
rs380095 | snp | C/G | 0.178144 | 0.239451 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065866 | CTATCTGACTAGGCA[C/G]CAGTAGAGTCAATTA | 55827 |
rs380682 | snp | C/T | 0.236724 | 0.249647 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037104 | GAGATTCTCCCCCCC[C/T]TTTTTTTTTTTTTTT | 55827 |
rs380753 | snp | G/T | 0.4582 | 0.138394 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066035 | ATTGTATATCCAAAT[G/T]GAACATCCAGTCATT | 55827 |
rs381095 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054052 | AGTATCTGAAATAAG[C/T]GAGGGAGATGGGTTG | 55827 |
rs399096 | snp | A/G | 0.000447616 | 0.0149535 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065787 | TGACTGATGAGTCAT[A/G]CAAATAATTTCTAGC | 55827 |
rs399273 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067497 | GCTCCCTGTCTGCCT[A/G]GTGAACTATTCTCAG | 55827 |
rs410215 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052974 | TCCAAGTATGGCAAT[A/G]TAGACAGCATGACCA | 55827 |
rs413168 | snp | C/G | 0.492137 | 0.0622048 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036551 | TCTGTTTCATCTATT[C/G]CAGAAGCCTAAAGAC | 55827 |
rs417427 | snp | G/T | 0.288646 | 0.246995 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045294 | TTTGTTTGAAGTCAT[G/T]GAAGGGAATCTCTCC | 55827 |
rs428694 | snp | C/G | 0.434109 | 0.169127 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002742 | AGAAGTGGAATGGCG[C/G]AGTCACTGGATAAGT | 55827 |
rs430565 | snp | C/T | 0.211516 | 0.24702 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055006 | tatttttagtagaga[C/T]ggggtttTTAACTTG | 55827 |
rs433173 | snp | G/T | 0.288646 | 0.246995 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045295 | TTGTTTGAAGTCATT[G/T]AAGGGAATCTCTCCA | 55827 |
rs433385 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990425 | GACAGTATGAGAGAT[C/T]TGTCATAGGTAGATT | 55827 |
rs435486 | snp | A/T | 0.0659589 | 0.169201 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072295 | AGGGAGAATCAGTCT[A/T]AAAAAAAAAAAAAAA | 55827 |
rs435847 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049549 | ctataggcgtgagcc[A/C]ccgcgcctggccATA | 55827 |
rs436256 | snp | G/T | 0.434687 | 0.168495 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002741 | TAGAAGTGGAATGGC[G/T]CAGTCACTGGATAAG | 55827 |
rs438806 | snp | A/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041894 | ATACATGTTTGTCGC[A/G]CACACACACACACAC | 55827 |
rs445995 | snp | A/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002045 | TAAATTGTCAATAAT[A/G]AGTAAATTGTCAATA | 55827 |
rs463206 | snp | C/T | 0.00350262 | 0.0417018 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953001 | ATATCTTCAGCAAGG[C/T]GGATCTTCAGCAAGG | 55827 |
rs593632 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049363 | ttttcccccttcagt[C/T]tcccaagtagctggg | 55827 |
rs598535 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071092 | gatcaAGGGTATATA[A/C]ATATTAGGTCTATTC | 55827 |
rs624006 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049357 | aagcgatcttcctcc[C/T]tcagtctcccaagta | 55827 |
rs671608 | snp | A/C | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938272 | TCTCATACACACACA[A/C]ACACACACACACCCC | 55827 |
rs675686 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050046 | AGTAATTTAGGTTTT[C/T]TTTTGAGTTTAGAAA | 55827 |
rs675689 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050044 | TAATTTAGGTTTTTT[C/T]TTGAGTTTAGAAACA | 55827 |
rs718885 | snp | A/G | 0.285257 | 0.247501 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985421 | aagtccccttcctct[A/G]tcttcaaacccagca | 55827 |
rs1050297 | snp | G/T | 0.45795 | 0.138769 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055963 | CTGAGTAACCCTTCA[G/T]AACTAGATGAACTTA | 55827 |
rs1060041 | snp | C/T | 0.356189 | 0.226327 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168004738 | GCTATCTTCTCCAGA[C/T]AGTGAACAAAGGCAG | 55827 |
rs1803756 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168056205 | CAGTGGGAATCAGCA[A/G]TTTTGCACAGGAAGC | 55827 |
rs1846416 | snp | C/T | 0.283947 | 0.247685 | upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167936173 | GGCGGGCAGCTCGGC[C/T]TGCGCAAGCGCGCTG | 55827 |
rs2272911 | snp | C/T | 0.284733 | 0.247575 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967064 | TACTTTTATGTGTTA[C/T]CTTAATATATTATCT | 55827 |
rs2294493 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996470 | ATCAGCATCTCTGGC[A/G]TGACCTATCCCCCTT | 55827 |
rs2745556 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064051 | TCTCTTTCTCACATT[G/T]GCTGTCTACCTGAAA | 55827 |
rs2902568 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990212 | gtacaaaattttttt[A/T]aaaaaattagcctgg | 55827 |
rs3180857 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040488 | cagtggaggtggttt[A/T]aaaaaaaaaaaagtg | 55827 |
rs3209912 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168055391 | AGTGAAGCAACAGCT[G/T]TGCAGCAAAATAATA | 55827 |
rs3209913 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168055389 | TGAAGCAACAGCTTT[A/G]CAGCAAAATAATAAA | 55827 |
rs3209917 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168055368 | AAATAATAAAATACT[C/T]CTTCGTTaaaaaaaa | 55827 |
rs3220655 | microsatellite | (CA)31/33/34/35/36 | 0.612362 | 0.154174 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985186 | tttaagccacGTGTA[(CA)31/33/34/35/36]CGTGGTTTGGCTATG | 55827 |
rs3767463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003216 | AAATGTAAGAAGAAC[C/T]GATTTTCATTTTAAA | 55827 |
rs3767464 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006272 | TGACAATCATTTGAA[C/T]TATTGAAGAAGAAAA | 55827 |
rs3767465 | snp | A/G | 0.029116 | 0.117091 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020293 | CAGGGTTACAATATT[A/G]CTGAGTAGAAAAACC | 55827 |
rs3767466 | snp | C/G | 0.230603 | 0.249246 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020879 | AAGGAGTTGTGTGTT[C/G]CCAAGATTACAAATA | 55827 |
rs3767469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028160 | AGTTTTCCTTTTTAT[C/T]TCTCTACTATAAGAG | 55827 |
rs3767471 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037582 | CTCTTTTTTTTTGGC[A/G]GGTGGGGAAGGTAGC | 55827 |
rs3767472 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052643 | TTATCACAGATGTTT[A/G]TATCTACTGCCCGTT | 55827 |
rs3767473 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054915 | tctgcctgctgggtt[C/G]aagcaattctcctgc | 55827 |
rs3831959 | in-del | -/G | 0.489837 | 0.0705577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016089 | CCTTTCCTTGCATAT[-/G]GGTGGTATTCAACAT | 55827 |
rs3961453 | snp | C/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055709 | ATATTGTGAAAAAGA[C/T]GCATATTATATTTAT | 55827 |
rs3977718 | snp | C/T | 0.408163 | 0.193609 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055804 | TCCCCATCGGTAATA[C/T]TAAAAGTTTCTATTC | 55827 |
rs3977719 | snp | C/T | 0.244898 | 0.249948 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056007 | AGCCAACCATCTTCA[C/T]AACAAGATTTGTTTA | 55827 |
rs3977720 | snp | A/G | 0.277778 | 0.248452 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056024 | ACAAGATTTGTTTAC[A/G]AGTCCTGGATTTTCT | 55827 |
rs3977721 | snp | C/G | 0.126004 | 0.217083 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056162 | TGTCCCAACTTCAGG[C/G]AGACTACAATAAACA | 55827 |
rs3977722 | snp | A/G | 0.247576 | 0.249988 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056171 | TTCAGGGAGACTACA[A/G]TAAACAACATCTCCC | 55827 |
rs3977723 | snp | C/T | 0.471768 | 0.115407 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056300 | AGCGGGTCCAGTGCG[C/T]AGCGTACGGACGGCG | 55827 |
rs4656564 | snp | C/T | 0.284733 | 0.247575 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959754 | agagttctttattta[C/T]tttagataacattac | 55827 |
rs4656565 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977864 | AGCAAATCTATTCAT[A/G]TAACTACCACCTAGC | 55827 |
rs4657727 | snp | C/T | 0.279991 | 0.248195 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996003 | TATGTATAAGGACTA[C/T]GTTCTGTATAAGTAG | 55827 |
rs5778563 | in-del | -/T | 0.413083 | 0.189483 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940506 | CTCAGCCTCCTGGAA[-/T]TTTTTTTTTTTTTTA | 55827 |
rs5778564 | in-del | -/A/AA | 0.496874 | 0.0394129 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050066 | TCTGAAAAAAAAAAA[-/A/AA]CAAGCATCTAAGAAA | 55827 |
rs6656479 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167999254 | cagtaaaacatgctg[G/T]aaagagatgtgccct | 55827 |
rs6657295 | snp | A/G | 0.196562 | 0.244222 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056204 | CGCTTCCTGTGCAAA[A/G]TTGCTGATTCCCACT | 55827 |
rs6657523 | snp | C/G | 0.0402882 | 0.136092 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938463 | TTAAGTAGACGTTCG[C/G]CCTTACAGCATTTTA | 55827 |
rs6658314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997025 | tccatcgggctgtaa[A/G]ttctgtgacattggg | 55827 |
rs6660416 | snp | A/G | 0.00577454 | 0.0534221 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002608 | AGCTTTTCTTTGTAT[A/G]TGGtattttaaaatt | 55827 |
rs6662158 | snp | C/G | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020991 | ACAATGTCTATGGCA[C/G]AGTAAAACCAAAAAG | 55827 |
rs6668938 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053060 | CTTAAGTCAGCGTAT[A/C]TTTACATACTCTGAG | 55827 |
rs6669166 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983949 | ttgaggatagggcat[C/T]tgggggagtctcaaa | 55827 |
rs6672946 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018685 | AAAAGTATATCTTTT[C/G]TAGGAAATACACCAC | 55827 |
rs6672997 | snp | A/G | 0.114036 | 0.209795 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988457 | cagggatgagccacT[A/G]TGTTTGACTTTTAAT | 55827 |
rs6676447 | snp | G/T | 0.302686 | 0.244385 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954506 | cacccaggctggagt[G/T]cagtggcacaatctc | 55827 |
rs6683293 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956599 | tgagtcttctgcaga[C/T]tttgggtttcatttg | 55827 |
rs6686464 | snp | C/G | 0.279726 | 0.248226 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967923 | tttggtagagacagg[C/G]tttcaccatgttggc | 55827 |
rs6687064 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045847 | TGGGAGTTAAAATAA[A/G]TTTTTAAAGTATACT | 55827 |
rs6697439 | snp | G/T | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032520 | TTTTCTATACAAGTC[G/T]AGTAAGTTGGAGTGC | 55827 |
rs6697465 | snp | A/T | 0.17138 | 0.237316 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988831 | catgcctctaatccc[A/T]gcactttgggaggcc | 55827 |
rs6700210 | snp | A/G | 0.473081 | 0.112848 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019291 | CTGACCTTGTGATCC[A/G]CCCACTGCAGCCACC | 55827 |
rs7414183 | snp | G/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961097 | tttcatgttttggag[G/T]gctaatgtaatggta | 55827 |
rs7416833 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970495 | tgtctctacaaaaaa[A/T]ttaaaagctggatgt | 55827 |
rs7514793 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005696 | CTGTCACTTTATTCT[C/T]ACATCTCTGGAAACT | 55827 |
rs7517933 | snp | C/T | 0.17138 | 0.237316 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976657 | ATTTCTACTCTTCTC[C/T]TGAATAAAGGAACTT | 55827 |
rs7520120 | snp | G/T | 0.172028 | 0.23753 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982415 | cccagctaatatttt[G/T]tatttctagtagaga | 55827 |
rs7520219 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982533 | ggcatgacatttttt[A/T]aagttctttgtggat | 55827 |
rs7520232 | snp | C/T | 0.295854 | 0.245759 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042757 | TTCAATAGAGAGACA[C/T]GTAGAAATACATACT | 55827 |
rs7521894 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004399 | CAAATGGGCCAAATC[A/G]CCAGTAGTTATTATC | 55827 |
rs7523124 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013272 | TGAGTGAGTATGATG[G/T]TATGAGTTATTAAAT | 55827 |
rs7523437 | snp | A/G | 0.296109 | 0.245711 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060127 | tgtatatgattatgt[A/G]tccAGCTACATTCCT | 55827 |
rs7523800 | snp | C/T | 0.171704 | 0.237423 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962903 | gagggttgtagtaag[C/T]ggagatagcaccact | 55827 |
rs7526546 | snp | C/G | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023602 | TTCAATGTGGGAAAG[C/G]TATAGAATCAATCTC | 55827 |
rs7530635 | snp | A/C | 0.114036 | 0.209795 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982381 | tgagtagctgggact[A/C]taggcgcatgcaacc | 55827 |
rs7531376 | snp | A/G | 0.225893 | 0.248835 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990141 | TATATTTTAATAGCA[A/G]TGATTACAATTAAAA | 55827 |
rs7535138 | snp | G/T | 0.284733 | 0.247575 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962224 | ggtaattgatggttt[G/T]gagtttaactgtgtc | 55827 |
rs7535741 | snp | C/T | 0.375 | 0.216506 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056339 | CAGCTGCCAGGGCCT[C/T]GGCGGGCAGGGCGCG | 55827 |
rs7535844 | snp | A/C | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056426 | TCGCAGCGCCATGTT[A/C]GCAGGGGTGCGGGGG | 55827 |
rs7535915 | snp | A/G | 0.32 | 0.24 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056390 | CAGGGTGCAGAGCAG[A/G]GCCCGCACGCTCCGC | 55827 |
rs7535984 | snp | C/T | 0.226188 | 0.248863 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963129 | gccaagcatagtggc[C/T]ggcaggcacctgtaa | 55827 |
rs7536129 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026664 | cagccaagatagaga[C/T]tttaggaggaacagc | 55827 |
rs7538251 | snp | C/G | 0.283158 | 0.247791 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032514 | TTTGCCTTTTCTATA[C/G]AAGTCTAGTAAGTTG | 55827 |
rs7538581 | snp | A/G | 0.284995 | 0.247539 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010109 | ACACCTAGAAGAGAG[A/G]TGCTGTGATTAGCTG | 55827 |
rs7539141 | snp | A/T | 0.226188 | 0.248863 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990213 | tacaaaatttttttt[A/T]aaaaattagcctggt | 55827 |
rs7539823 | snp | A/G | 0.17138 | 0.237316 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967892 | tgtgccaccatgctc[A/G]gctaatttttatgtt | 55827 |
rs7541567 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973335 | TATTCCCTTATTGGA[A/G]ATGTTGTTTGATCCC | 55827 |
rs7542368 | snp | A/C | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968358 | agagacccccccgtg[A/C]tgagtgctgagattt | 55827 |
rs7543994 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030761 | GCAGAGGCCAGGACT[G/T]GTGTCTTAAATCTTT | 55827 |
rs7550901 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976450 | gtactccaacctggg[C/T]gacagagtgagactg | 55827 |
rs7553070 | snp | C/T | 0.171057 | 0.237209 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982392 | gactataggcgcatg[C/T]aaccacgcccagcta | 55827 |
rs9651032 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944084 | cccgaccttgtgatc[C/T]gcccgcctcggcctc | 55827 |
rs9651040 | snp | G/T | 0.0869089 | 0.189476 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007722 | ttgttcgtgtttctt[G/T]ttctatctccttctg | 55827 |
rs9730237 | snp | C/T | 0.097727 | 0.198275 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979957 | ggaggctgaggaggg[C/T]ggatcacgaggtcaa | 55827 |
rs9943195 | snp | C/T | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935965 | GCCTCTCGCCTGGAG[C/T]ACCCTTCCCGCGGCT | 55827 |
rs9970931 | snp | A/G | 0.040671 | 0.13668 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037766 | GTCAGGAAGAGAAAC[A/G]GAAATATACCAAAAT | 55827 |
rs10047060 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043232 | CTGTATTTTGTTTCT[C/T]GTTTTTAATAAATTA | 55827 |
rs10047108 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042845 | TTTCAAGAGTAAAGT[A/G]TGTTATGATAGTCAT | 55827 |
rs10399591 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168056403 | AGGGCCCGCACGCTC[C/G]GCACCACTCGCAGCG | 55827 |
rs10489203 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972234 | TTTATCTGCAGTATC[A/G]TACATACCCATATTG | 55827 |
rs10489204 | snp | G/T | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995800 | TTTATACTGAAACTT[G/T]GATGATAGTATTCAG | 55827 |
rs10489205 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996147 | CAATTTGTGGAGGCC[C/T]TTCTATTTCCTTACC | 55827 |
rs10489206 | snp | C/T | 0.252702 | 0.249985 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071994 | TCTTAGCTCCAATAT[C/T]ACCTCCTTAGAAAAG | 55827 |
rs10668446 | in-del | -/AAA | 0.491263 | 0.0655142 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950173 | TTTTAAAATTTTGAC[-/AAA]AAAGTTTCCAATACT | 55827 |
rs10800333 | snp | C/T | 0.226188 | 0.248863 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965343 | TTTCCTTCCCCAATG[C/T]GGAAGGCTGGAATTG | 55827 |
rs10918799 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167956335 | TTTTATGTAAATTAT[G/T]GAATTTATTGACATA | 55827 |
rs10918800 | snp | C/T | 0.226484 | 0.248892 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964756 | TTGTTCTTTTTGCTT[C/T]TCAGTTTTGTACGTT | 55827 |
rs10918801 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965184 | AAGTGTAGGAGGAGA[A/G]GAAGTGTTCTACAGG | 55827 |
rs10918802 | snp | G/T | 0.227074 | 0.248947 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966201 | tttatttgttgttag[G/T]atggagtggcaactg | 55827 |
rs10918803 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966906 | AGATTACTTAGGGAA[A/T]CAAGATTTTATTCAG | 55827 |
rs10918804 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967742 | ttttttttttttttg[G/T]ggcaaggtctcactc | 55827 |
rs10918805 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985243 | TGTGTGTGTGCGTGC[A/G]CGTGTGCACGTGGCT | 55827 |
rs10918806 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988705 | CTTGCTAACTAAACC[A/G]GTTACCAACTGGTTA | 55827 |
rs10918807 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990128 | GTTAATTTTTTGTTA[C/T]ATTTTAATAGCAGTG | 55827 |
rs10918808 | snp | C/T | 0.226188 | 0.248863 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001679 | gaacctttagcatgc[C/T]gtggcaaagagccaa | 55827 |
rs10918809 | snp | A/G | 0.226484 | 0.248892 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007127 | CAATGAAAAGTACTC[A/G]TTTTCCTACTGTCAA | 55827 |
rs10918810 | snp | A/G | 0.138886 | 0.22395 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020633 | TTTTAGTTTGTGATT[A/G]TATTCTCTAGAAGGT | 55827 |
rs10918811 | snp | C/T | 0.138886 | 0.22395 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023312 | AAATTATAATGGATA[C/T]AAACTATATCCATTT | 55827 |
rs10918812 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034237 | AAAAGAAACCTCAGC[A/G]GGCACAGTGGCCCAT | 55827 |
rs10918813 | snp | C/T | 0.138886 | 0.22395 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039349 | GTATTTAATTGATTA[C/T]TAGTAAGGTTGAACT | 55827 |
rs10918814 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040700 | CATCTTCTGAAGAAT[C/T]TTATCTAAACTTTTT | 55827 |
rs10918815 | snp | A/G | 0.138546 | 0.223781 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051845 | TAAGGTATATTTGAA[A/G]TAACTTTTTCAAATT | 55827 |
rs10918816 | snp | C/G | 0.0644693 | 0.167566 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053864 | agagcaatgtaacat[C/G]ccaaaagtcaagttc | 55827 |
rs10918817 | snp | A/T | 0.138886 | 0.22395 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060175 | AATTGGCCCGTAGAT[A/T]TTTTGAGTTTTGGTT | 55827 |
rs10918818 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | DCAF6 | GRCh38.p7 | 1:168062972 | gctggagtgcagtgg[C/T]gcgatctcggctcac | 55827 |
rs10918819 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072465 | CTTTAATTTCTTTAT[C/T]TATTGTCTTATTACA | 55827 |
rs10918820 | snp | A/T | 0.0648419 | 0.167978 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072722 | TTCTTTTAAAGAAAG[A/T]AAATAAATTCTTTGT | 55827 |
rs11295033 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064016 | TAATCATTGCTTTTG[-/T]TTTTTTTTTTTTTTC | 55827 |
rs11295034 | in-del | -/T | 0.49995 | 0.00499176 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064099 | TTTTTTTTTTTTTTT[-/T]AGCTTGTATTAGCAT | 55827 |
rs11305260 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168031996 | GAACCAAGCACAGTT[-/T]CAATCTAAATGTATC | 55827 |
rs11322208 | in-del | -/A | 0.284995 | 0.247539 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984561 | CTTAATAAAGTCATC[-/A]AAGCTAAGTCAATAA | 55827 |
rs11369573 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049432 | TGTTGTTGTTGTTGT[-/T]TTTTTTTTTTTTTTT | 55827 |
rs11553557 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935868 | CAGCCACGCTCCCAC[A/C]CGGCTGCCAACGATC | 55827 |
rs11558510 | snp | A/G | 0.214541 | 0.247473 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936749 | GTGCGGCCGGGCTTC[A/G]GGGGCCCAGGCGCCG | 55827 |
rs11558511 | snp | C/T | 0.371083 | 0.218721 | missense | DCAF6 | GRCh38.p7 | 1:168044612 | AATCATCAGAGGATG[C/T]GACAAAATATCAGGA | 55827 |
rs11578006 | snp | C/T | 0.17138 | 0.237316 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959799 | cttttgaaagtattt[C/T]ccctgtcttgtcttc | 55827 |
rs11581302 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168061398 | TTATTTTAAAAATTG[G/T]TAGTCACAATTTAAT | 55827 |
rs11581963 | snp | A/G | 0.114036 | 0.209795 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984934 | agttctgtgtacctg[A/G]gaggcctcacaatca | 55827 |
rs11581997 | snp | G/T | 0.172028 | 0.23753 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985140 | ctcccacaacacgtg[G/T]caattcaagataaga | 55827 |
rs11583998 | snp | A/T | 0.17138 | 0.237316 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007216 | TCAAAAGCTAGTCAA[A/T]GTAGTTGCTATCCCT | 55827 |
rs11584428 | snp | C/T | 0.172351 | 0.237636 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007646 | actttcctttcttgg[C/T]atctatgatatcata | 55827 |
rs11584693 | snp | C/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053127 | TCATTTGGGTCACCT[C/G]ATCTTTCAACATCAT | 55827 |
rs11585320 | snp | A/G | 0.159292 | 0.232964 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944935 | attgcattcttctgc[A/G]tatggatatctaatt | 55827 |
rs11586950 | snp | A/G | 0.214843 | 0.247516 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944730 | gatgaataatttgca[A/G]atattttctgtcatt | 55827 |
rs11587594 | snp | A/T | 0.283158 | 0.247791 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019942 | TTATAAGTAGTTAAT[A/T]AATTAGATATATTAG | 55827 |
rs11588503 | snp | C/T | 0.159292 | 0.232964 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945590 | tccggctcccaggtt[C/T]aagcacttctcctgc | 55827 |
rs11588522 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945775 | aaagtgctgggatta[C/T]aggcgtgagccacca | 55827 |
rs11588575 | snp | C/T | 0.159951 | 0.233219 | intron-variant | DCAF6 | GRCh38.p7 | 1:167946081 | cctgcctcagcctcc[C/T]gagtagctgggatta | 55827 |
rs11589242 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941926 | tcttccaaagtaatt[A/C]taccatactgcattc | 55827 |
rs11590536 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009386 | CTTCCTTCCTTCCTT[C/T]CTTTCTTTCTTTCTT | 55827 |
rs11799577 | snp | C/G | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039334 | ttaaaaatactttta[C/G]tatttaattgattat | 55827 |
rs11800280 | snp | G/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978574 | tcttattttattttg[G/T]tattattaatttata | 55827 |
rs11800943 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168055458 | AAATTAAGATAGTGG[G/T]GTTCCTCATCTGACA | 55827 |
rs11802003 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168055450 | GTATCGCAAAATTAA[A/G]ATAGTGGTGTTCCTC | 55827 |
rs11803758 | snp | A/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984042 | gctgctgttgactta[A/G]ggaaaataccacaag | 55827 |
rs11803859 | snp | A/G | 0.149665 | 0.228982 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059436 | tagtaaatcttaatg[A/G]cggctaaggcaagac | 55827 |
rs12032727 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935696 | TAGAGGAAGCGAGAA[A/G]GAAGGTCTCGATAAG | 55827 |
rs12038687 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941824 | ggacaaaataactag[A/G]gtcgaacacttttaa | 55827 |
rs12041771 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937540 | ACCTAAAAGTGATAG[C/T]TGAGCTCTCCCCACC | 55827 |
rs12059034 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977753 | ctgctTATTAGACCT[C/T]ATTCCATCCACtatt | 55827 |
rs12059225 | snp | C/T | 0.0220355 | 0.102626 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043169 | TTGCTTTTGTTGTTA[C/T]AAAATTGCAGCATTG | 55827 |
rs12059506 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017835 | AGAATGTGCGTTTCT[C/T]ATATGTAAGAAGCAT | 55827 |
rs12059592 | snp | G/T | 0.227178 | 0.249228 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975405 | tatcaaatttttgta[G/T]gatagaagggactcc | 55827 |
rs12066564 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967825 | aacctctgcctcctg[C/T]gttcaagcgattctc | 55827 |
rs12067868 | snp | A/C/G | 0.076741 | 0.181921 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056943 | GAATTTCTTTCTACA[A/C/G]ATTTATTCAAAATTC | 55827 |
rs12069228 | snp | A/G | 0.138546 | 0.223781 | intron-variant | DCAF6 | GRCh38.p7 | 1:168057727 | TAATTGCATTGACAG[A/G]GCTTTGCAGGGCTTT | 55827 |
rs12069575 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969937 | gtgtgccaccacgcc[C/T]ggctagtttttgtat | 55827 |
rs12069749 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964311 | tgaaggataattttg[C/T]ggggtacagtattct | 55827 |
rs12071982 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976827 | GGTTTACCTTTCCTT[C/T]TTCCCATCACACATT | 55827 |
rs12073071 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048099 | AGCTTGTAATTAGTC[C/T]TATGATTTTGGAGAG | 55827 |
rs12073929 | snp | C/G | 0.226779 | 0.248919 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973115 | CTAAATCTCTGACAG[C/G]GTTAAAGAACATGAT | 55827 |
rs12075119 | snp | A/T | 0.0678174 | 0.1712 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167934728 | TTAACTATGTAGGAG[A/T]ATAAAAGCCACTTTT | 55827 |
rs12075574 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049349 | ctgggctcaagcgat[C/T]ttcctccctcagtct | 55827 |
rs12077027 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006679 | GGGTGAATGTAGTAG[A/G]TGGAAATGTCAGCTT | 55827 |
rs12077181 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940672 | CCCATATATATACGG[G/T]TTTGTAAAGATAAAC | 55827 |
rs12078030 | snp | A/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064204 | TATACCCATTTTTAA[A/G]ATTGACAAGTGAAAA | 55827 |
rs12078041 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064273 | CAGAAAGATCTCTAA[A/G]ATCTTTTGTAGTTTT | 55827 |
rs12078184 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056679 | cacaagaacctgtag[C/T]gtaataaagcctctg | 55827 |
rs12078574 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007888 | gcaatctgatcttct[A/G]ccctgaattccagac | 55827 |
rs12079036 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064337 | TTAATTACTTAATAA[A/G]AAAAGTTTTTGAGAT | 55827 |
rs12079038 | snp | A/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064350 | AAGAAAAGTTTTTGA[A/G]ATGACTAGTGTAACT | 55827 |
rs12079077 | snp | A/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064426 | TACATTGCATCATCA[A/G]AAGGTATCTACAGAA | 55827 |
rs12079829 | snp | A/G | 0.0678174 | 0.1712 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935011 | GAGCATTTACAAAGA[A/G]TCAAGCACATATGTT | 55827 |
rs12079918 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073767 | CCATTCCTGAGCCCT[A/G]CTTAAGTAGAATAGC | 55827 |
rs12080570 | snp | C/T | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982961 | aactttgtcgaagat[C/T]agatgactgtaggtg | 55827 |
rs12082923 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950569 | ATGGAGAAAGAAGTA[A/G]AACAAATTGGCTTCA | 55827 |
rs12083089 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011139 | ttttttttttttgag[A/G]tggagtcttgctctg | 55827 |
rs12084077 | snp | C/T | 0.137867 | 0.223442 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060842 | tgcagtgagctgaga[C/T]cccgccactgcactc | 55827 |
rs12084187 | snp | C/T | 0.226188 | 0.248863 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011276 | acatgccaccatgtc[C/T]ggctaattttttttg | 55827 |
rs12084894 | snp | A/C | 0.0648419 | 0.167978 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027476 | TTCCTATTTGAATAT[A/C]TCTCTGACTAATGAT | 55827 |
rs12084920 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027535 | CATACTTTTAACAAA[A/G]CACGAATGCTTTTTA | 55827 |
rs12086685 | snp | G/T | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958037 | attctgggactcttg[G/T]catgggactcttatc | 55827 |
rs12088982 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011834 | ataaatttgttgtgc[A/G]tggtggcatgtgcct | 55827 |
rs12089243 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069647 | AAATTGAAAGAAGAC[C/T]CATATGTTTGTAATT | 55827 |
rs12089554 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014540 | aattgtagacttttg[C/T]attcagtccctacct | 55827 |
rs12090041 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940254 | TAGAGCTCCCAAATC[C/T]ACAAGATTCACCTGG | 55827 |
rs12090518 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966372 | aaactttcttaaaac[A/G]ttatgagattttttt | 55827 |
rs12093434 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967995 | ctcatcctcccaaag[C/T]gttgggattacaggc | 55827 |
rs12093872 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073167 | ggcgatagagcgaga[C/T]tcggtctcaaaaaaa | 55827 |
rs12093927 | snp | C/T | 0.226188 | 0.248863 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008289 | ttgtacgtcataaat[C/T]tacatgttcaaacta | 55827 |
rs12094142 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963919 | gtgtgagtacaaagt[A/G]attttaaatcttcca | 55827 |
rs12095210 | snp | G/T | 0.226188 | 0.248863 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963822 | taaactttttaatta[G/T]ttgccctaaagtttt | 55827 |
rs12095271 | snp | C/G | 0.227369 | 0.248974 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966445 | attttatgtgtggcc[C/G]gagacaattcttctt | 55827 |
rs12096322 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970089 | agccCCCTTTTCTTA[C/T]AATAGAGAAGATTTC | 55827 |
rs12096452 | snp | G/T | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964359 | ttttgtttccgttac[G/T]gctttaaatatttca | 55827 |
rs12096539 | snp | C/T | 0.226188 | 0.248863 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009605 | ttttcttttctttcc[C/T]tctttccttcttACA | 55827 |
rs12117741 | snp | A/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964523 | gcttgcctagctgta[A/G]ttctttttgtattta | 55827 |
rs12121305 | snp | A/C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168043713 | TCTTATAAATGTGTA[A/C/G]GTACCTTAGTATAAC | 55827 |
rs12121926 | snp | C/T | 0 | 0 | missense, intron-variant, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167966672 | GAGAATATATTTTAT[C/T]TGGCTCAGATGACAC | 55827 |
rs12122010 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167966923 | AAGATTTTATTCAGC[C/T]TTGGGATCTAGAAAA | 55827 |
rs12128133 | snp | A/C/T | 0.00152941 | 0.0276109 | missense, synonymous-codon | DCAF6 | GRCh38.p7 | 1:168043106 | TTTCGTCCCACAGAG[A/C/T]TCAGTGCAACCACCA | 55827 |
rs12134132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950095 | CTTACTTTATCTTCT[A/G]TTCTTAGGTTCTGCC | 55827 |
rs12134997 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167950554 | TACCAGTTAAATAAC[A/G]TGGAGAAAGAAGTAA | 55827 |
rs12136645 | snp | A/G | 0.136166 | 0.22258 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944064 | agccaggatggcctc[A/G]atcccccgaccttgt | 55827 |
rs12142728 | snp | A/C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072293 | agagggagaatcagt[A/C/T]taaaaaaaaaaaaaa | 55827 |
rs12145186 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967915 | tttatgtttttggta[A/G]agacagggtttcacc | 55827 |
rs12145187 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967917 | tatgtttttggtaga[A/G]acagggtttcaccat | 55827 |
rs12239051 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952310 | gcaagctccgcctcc[C/T]gggttcacgtcattc | 55827 |
rs12239460 | snp | C/T | 0.040671 | 0.13668 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977526 | tttgtttttctttgc[C/T]gggtttttttcttat | 55827 |
rs12240018 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952452 | tgttgatctgacctc[A/G]tgatcctcctgcctc | 55827 |
rs12404574 | snp | A/G | 0.328382 | 0.237395 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991997 | TGGGGAGACTCTGCT[A/G]TTTTTCAATCAAGAA | 55827 |
rs12405126 | snp | A/G | 0.021333 | 0.101051 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985207 | tgtgtgtgtgtgtgt[A/G]tgtggtgtgtgtgtg | 55827 |
rs12405837 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940643 | TGATTTATTAGCCAC[A/G]CAGATTTTATTATCC | 55827 |
rs12407660 | snp | C/T | 0.284995 | 0.247539 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985125 | CCTCCCACTGGGTCC[C/T]TCCCACAACACGTGG | 55827 |
rs12408205 | snp | A/G | 0.279991 | 0.248195 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013094 | TATGGCTGTATAATA[A/G]TGCTTTATTTTATAT | 55827 |
rs12408720 | snp | A/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030055 | acgtgtctcaaaccc[A/T]agaggtctggctctg | 55827 |
rs12409275 | snp | C/T | 0.000100451 | 0.00708628 | intron-variant | DCAF6 | GRCh38.p7 | 1:168075347 | AAGTATTTCTCTTTG[C/T]GATTCTCTTATCTGT | 55827 |
rs12564175 | snp | C/T | 0.00952359 | 0.0683454 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040691 | AGGAGCTGGCATCTT[C/T]TGAAGAATCTTATCT | 55827 |
rs12724587 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072325 | aaaaaaaaaaaaaaa[A/G]gaaaagaaaagtctt | 55827 |
rs12727036 | snp | A/G | 0.279461 | 0.248258 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002909 | CTATTAGATATTAAG[A/G]GAAATGAAAACTCAG | 55827 |
rs12727995 | snp | A/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959991 | aggtttatagttttg[A/T]gtttatatttaggtc | 55827 |
rs12728655 | snp | G/T | 0.284733 | 0.247575 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954488 | gatggagtctcgctg[G/T]gccacccaggctgga | 55827 |
rs12728880 | snp | C/T | 0.334182 | 0.235401 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007559 | cagtttaaaggatat[C/T]tctctgttagtacct | 55827 |
rs12730926 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167978941 | ggatttcagCCTAAA[A/G]tggtgtcttttgatg | 55827 |
rs12731280 | snp | G/T | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935652 | TGCCTCTAGAGGCAG[G/T]TGTCAGAGGGCCTCT | 55827 |
rs12736786 | snp | C/G | 0.463559 | 0.129972 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019045 | ATGATAATGTACTCT[C/G]TCTTTTTTTTTTTTC | 55827 |
rs12741312 | snp | G/T | 0.00961516 | 0.0686668 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990046 | TTTGTATTTATATGT[G/T]TACTTTATTTTTGAG | 55827 |
rs12741521 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054487 | cacctctcagtactg[C/G]cacattggggattaa | 55827 |
rs12742247 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967711 | GTCTTAAATTTCCTG[G/T]ATCtttttttttttt | 55827 |
rs12742249 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967715 | TAAATTTCCTGTATC[C/T]ttttttttttttttt | 55827 |
rs12744717 | snp | G/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956057 | aggtatgagccgctg[G/T]gcttagctaagaaca | 55827 |
rs12744853 | snp | C/G | 3.55739e-05 | 0.00421731 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935711 | GGAAGGTCTCGATAA[C/G]GAGCCATTCAGGGTC | 55827 |
rs12746154 | snp | C/T | | | upstream-variant-2KB, missense, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935820 | AGGTGGCCCGCAGGC[C/T]TCGGGCACCGGCGGC | 55827 |
rs12755146 | snp | G/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017923 | AAAACATATTTCTGT[G/T]GTCTTCTCACCTATT | 55827 |
rs12760393 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968319 | cgccactaaccctgg[A/G]actgagataaaccac | 55827 |
rs16859971 | snp | C/T | 0.00339586 | 0.0410658 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993464 | ACTCAAAACCATGTC[C/T]TTTGGCCGGGCGCGG | 55827 |
rs16859989 | snp | A/G | 0.114036 | 0.209795 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013444 | TTTGGTAGTTTGTAT[A/G]ATTTCATGCTAGTGT | 55827 |
rs16859999 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023357 | ATCTGTCATAAAATT[A/G]TGTAGAACTGTGGGT | 55827 |
rs16860012 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038231 | CAACACATGCCTTCA[A/G]ACTTTAAATGAAACC | 55827 |
rs16860019 | snp | C/T | 0.138886 | 0.22395 | intron-variant | DCAF6 | GRCh38.p7 | 1:168047584 | AGAGTAACAGAAGAA[C/T]GATAAAATTCTTATC | 55827 |
rs16860031 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067042 | ATGGGAGAGGGAAGG[C/T]GGATAATAGGAAGGC | 55827 |
rs16865517 | snp | A/G | 0.4712 | 0.116493 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055439 | CTATCTTAATTTTGC[A/G]ATACACTGCATTTGC | 55827 |
rs16865519 | snp | C/T | 0.1958 | 0.244054 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055440 | ACTATCTTAATTTTG[C/T]GATACACTGCATTTG | 55827 |
rs16865525 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168056361 | CAGGGCGCGGCGGGT[A/G]ACGGGACCGCGCGCA | 55827 |
rs17485889 | snp | G/T | 0.292008 | 0.246445 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049602 | ATATGCCCTTGGAAT[G/T]AAAAGAGTGTGGTTG | 55827 |
rs17557135 | snp | A/G | 0.284995 | 0.247539 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016650 | AGTTCATGATGCTCA[A/G]TAAACATTTGTTAAA | 55827 |
rs17557162 | snp | A/T | 0.286042 | 0.247388 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016712 | AATAATTTGTCAACT[A/T]AGTTATTTCAAGATG | 55827 |
rs28407455 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058866 | TGAGCCACTGCACCC[A/G]GTCCTGATCTGGTTT | 55827 |
rs28527241 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989166 | TATACACAGATATGC[A/G]AATAGGGAAGCATTG | 55827 |
rs28574636 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064790 | AGTAGCAGCTGCAGT[A/T]AAAATTTTTTAAAAT | 55827 |
rs28602715 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988260 | CAATCTTCTGGGCTC[A/G]AGTAATCTTCCTGCC | 55827 |
rs28666412 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019482 | ATGAATGTCCTAAAC[A/G]GGTATGGCAGAGGCA | 55827 |
rs28691278 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074604 | ATGCAAACGACTATT[A/G]CTGTAATTAGGATCA | 55827 |
rs28757774 | snp | C/G | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984073 | TTAAAGTGGCTCAAG[C/G]CTCACTATTCTTTCT | 55827 |
rs28796400 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964842 | TAATACGCCCATCAG[A/G]GGCATTGTTCCTTTC | 55827 |
rs28818922 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167946057 | TGCCTCCCGGGTTCA[A/G]GTGATTCTCCTGCCT | 55827 |
rs33966059 | in-del | -/G/GT/GTGT/GTGTGT/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985184 | TAGCCAAACCACGTC[-/G/GT/GTGT/GTGTGT/T]GTGTGTGTGTGTGTG | 55827 |
rs34101871 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167980885 | AAATCATTGTAAAAT[-/C]CCAATGTCATGAAGC | 55827 |
rs34122837 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168067150 | TGAGAATCCATTGCT[-/A]AAAATGTTAGTAAGT | 55827 |
rs34138271 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071959 | AACTTTGCCCCCAGG[-/T]ACTTCACATACAATT | 55827 |
rs34174891 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974602 | TGTTTTATTTTCATG[-/A]ATACTGTTCCTGTTG | 55827 |
rs34207014 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168060770 | GTGGAGGCCTGTAGT[-/C]CCCAGGTACTTGGGA | 55827 |
rs34285031 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940514 | CCTGGAATTTTTTTT[-/T]TTTTTTAAAGAATAA | 55827 |
rs34338954 | in-del | -/TGTA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985207 | GTGTGTGTGTGTGTG[-/TGTA]TGTGGTGTGTGTGTG | 55827 |
rs34350582 | in-del | -/TTAA | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935368 | TCTGCCTAGAGTGGG[-/TTAA]TATGCCACAATTCGA | 55827 |
rs34416997 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168061657 | TACAGTTGTGCAGTG[-/A]AAAAAAGTTTATGTA | 55827 |
rs34431578 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167955380 | GTACCGTTTAACATT[-/C]CCCAGTGTTAGTATG | 55827 |
rs34458694 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168056342 | TGCCAGGGCCTCGGC[-/A]GGGCAGGGCGCGGCG | 55827 |
rs34512553 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168033238 | ATATTTCAGCTTATT[-/G]CTGAATTTTTTTTCT | 55827 |
rs34555735 | in-del | -/A | 0.356811 | 0.226034 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029979 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAG | 55827 |
rs34613671 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168015094 | TTTTATTTATCCCTA[-/G]GAGCCTAAAACAATG | 55827 |
rs34645801 | snp | C/G | 0.227074 | 0.248947 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969291 | TTAGGCTCATAGAAT[C/G]TAATCTTCAGCCAAG | 55827 |
rs34662814 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167994637 | TTATTATTTATAAAA[-/G]GGGGAAAAGTAGAAA | 55827 |
rs34716266 | in-del | -/T/TT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948134 | CGACTTTCTTAGTCC[-/T/TT]TTTTTTTTTTTTTTT | 55827 |
rs34734675 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167973135 | AAGAACATGATATTT[A/G]TCTTGTTTAAAGGCT | 55827 |
rs34740332 | in-del | -/C | | | intron-variant, frameshift-variant | DCAF6 | GRCh38.p7 | 1:168015882 | AGCTAGCTGCACATA[-/C]CCCAGCAACAGCCTT | 55827 |
rs34742843 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168002995 | ATAAGAATCAACCCT[-/G]GGGAGCTTTAAGATA | 55827 |
rs34774552 | snp | A/G | 0.291235 | 0.246576 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063007 | AGCTCCGCCTCCCGG[A/G]TTCATGCCATTCTCC | 55827 |
rs34790693 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167963899 | CTATAATGATTCACA[-/G]GGGAGTGTGAGTACA | 55827 |
rs34875817 | in-del | -/CAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167993757 | CCGTCTCAGAAAAAA[-/CAA]CAACAACAACAACAA | 55827 |
rs34951489 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167987337 | TTTCTATCTGTATTG[G/T]ACCATTCTGAATCAT | 55827 |
rs34954529 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952175 | CTCAAACATATCCTC[-/T]TTTTTTTTCATACTT | 55827 |
rs34996604 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168073205 | AAAAAGAAAAACAGT[-/A]TACATAGAAGTGATT | 55827 |
rs35002079 | in-del | -/CTT/T/TTC | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973758 | TATTCCCCACTCACC[-/CTT/T/TTC]TCTCTATTGTATATC | 55827 |
rs35006395 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168065106 | ATTGCCATTATACTG[-/C]CCCAAAACCCAGAAA | 55827 |
rs35042830 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168055747 | CATTAGAAAGTTAAA[-/G]GGCATTTTCTTTCAT | 55827 |
rs35049141 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167969528 | CAGTCCAAAGTGTAA[-/T]TTTAAAATTTTCAGT | 55827 |
rs35063054 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168028795 | TTTTAGTACTATTAT[-/G]CTAATATTATTTTAA | 55827 |
rs35113990 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167987193 | AGTTTGAACAAGCTA[-/C]CTAGGGGAGAATCAT | 55827 |
rs35151685 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952230 | TTTTGAGACAGAGTC[-/T]TGCTCTGTTGCCCAG | 55827 |
rs35160460 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050143 | TTTTTAATTATAGCC[C/T]CAGTTAGGATGATCT | 55827 |
rs35185748 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007962 | TTATTGTTGTACATC[-/T]TTTTTTTTTTTTTTT | 55827 |
rs35224558 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167953113 | ATTGACTGTTTTTTC[-/G]GGTATTAATCTAATA | 55827 |
rs35286371 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168055781 | CAGTGTTAACAGTAG[-/T]TTTTTTTTCCCCATC | 55827 |
rs35293301 | snp | A/C | 0.000972193 | 0.0220262 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168063738 | AATGGTTTATAAAGG[A/C]CATCGCAACTCCAGG | 55827 |
rs35303544 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071251 | CTGCCATTGTAATGC[-/A]AAAACAGCCATAGAC | 55827 |
rs35325315 | in-del | -/TG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985212 | TGTGTGTGTGTGTGG[-/TG]TGTGTGTGTGTGTGG | 55827 |
rs35337691 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057465 | TTGTACATCCTTCAG[-/C]ATTTACTCTTTTCCT | 55827 |
rs35366916 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970626 | AAGAGCTGATATCTT[-/A]AAAAAAAAAAATTAT | 55827 |
rs35384469 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940214 | ATTTCCCAGATGTTA[-/T]TTATGATTAAAAGAT | 55827 |
rs35476943 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168003575 | AGAACTAAAAATTTA[G/T]GTTGAGGTAGGAAGT | 55827 |
rs35480806 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168074343 | TAACCTTAATATTTT[-/G]CCATGTTACTATGTG | 55827 |
rs35483063 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964204 | TTTCTTTAAAGAACT[-/C]CCTTTTGTAATTTCT | 55827 |
rs35493310 | in-del | -/A | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937952 | AAAGTGTTTGTTGCT[-/A]CTCATTTGTTTTTGA | 55827 |
rs35502759 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168066477 | GAAGTAAGATTTTTA[-/C]TTGTACTTACTATAG | 55827 |
rs35636377 | snp | A/C | 0.0259695 | 0.110952 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168066420 | CATAAAGATCTGGTC[A/C]CCATTAGAAGAGTCA | 55827 |
rs35674173 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168025987 | TTTACATCCCTTGTA[-/C]CAGGCTGTACATCTC | 55827 |
rs35696094 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040459 | GGTGGTGGTGGCTTA[A/G]ACAAGGATGGGAGCA | 55827 |
rs35819242 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050137 | GAATAGTTTTTAATT[A/C]TAGCCTCAGTTAGGA | 55827 |
rs35926942 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970347 | GATTAGTCAGATTTT[-/C]CTTTTTAAAGATTAT | 55827 |
rs35936928 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052656 | TTATATCTACTGCCC[A/G]TTATGACTAGTCTTC | 55827 |
rs35937677 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970408 | TAATCCCAGCACTTT[-/G]GGGAGGCCCGAGGTG | 55827 |
rs35938548 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022686 | GTAGTGAACTAGATA[-/C]CCCCATTTCTAATAT | 55827 |
rs35974686 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167969969 | TTTGTAGAGTTGGGG[-/T]TTTCACCATGTTGGC | 55827 |
rs35978091 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168042138 | AGTTTTTGTCATGGC[-/A]AAAAGTCCATGATCG | 55827 |
rs35980143 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167988654 | TTTACTGAAAGTTAC[-/A]AAAAAAAAAGGTACT | 55827 |
rs36040455 | snp | G/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960998 | AGCTCTTCATTTATT[G/T]AATTCTTTGATTTCT | 55827 |
rs36063643 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168012214 | TCCAGAGTCCAGGAC[-/A]AAAAATACTGTATGT | 55827 |
rs36116558 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995090 | TTATTCTGGTTAAAA[-/C]ACATGAAATCTGCTC | 55827 |
rs41270741 | snp | A/G | 0.114036 | 0.209795 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969044 | CAAATATAGATTTAT[A/G]TGTTGGTTTTTTTTT | 55827 |
rs41270743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023541 | TACGAACCCAGAGGT[A/G]AGCTCAAAAGCTGTC | 55827 |
rs41271645 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043217 | CTGTTCCCTTCGATG[C/T]TGTATTTTGTTTCTT | 55827 |
rs41271647 | snp | A/T | 0.130733 | 0.219717 | missense | DCAF6 | GRCh38.p7 | 1:168044966 | GAAATGACCTCAATC[A/T]TGATCGCTCTTGTGG | 55827 |
rs41322644 | snp | C/T | 0.114036 | 0.209795 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971667 | TACGTTAAGGTGGTC[C/T]AGTTGTAACATCTGT | 55827 |
rs41428546 | snp | A/T | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971137 | GGAGATACCCGAGAA[A/T]GCAGGTGATCTCAGA | 55827 |
rs55637346 | snp | G/T | 0.0648419 | 0.167978 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049413 | GCACTCTGCTAATTT[G/T]TTGTTGTTGTTGTTG | 55827 |
rs55675849 | snp | A/G/T | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943827 | CATCCACGTTGCTGT[A/G/T]TATGTCATGATTTCA | 55827 |
rs55683538 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024991 | ATGTGTTATTTTATA[C/T]GTTTATTACAGAGGT | 55827 |
rs55872845 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071898 | TCTTCCTCAAACTCA[C/T]CAAGCTTAGTAGCAC | 55827 |
rs55968152 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167988838 | CTAATCCCAGCACTT[G/T]GGGAGGCCGAGGCAG | 55827 |
rs56081546 | snp | A/C | 0.227074 | 0.248947 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960418 | ATTCTCCTGCCTCAG[A/C]CTCCCGAGTAGCTGG | 55827 |
rs56104264 | snp | A/G | 0.0060929 | 0.0548573 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004012 | TTAATGTTAATTAAA[A/G]TCATCAGAAAGCTGG | 55827 |
rs56118659 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970069 | AGGCGTGAACCATTG[C/T]GCCTAGCCCCCTTTT | 55827 |
rs56180735 | snp | A/T | 0.227369 | 0.248974 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999710 | GCTCCCTTACCTCTA[A/T]CAGTTTTCATAGCTT | 55827 |
rs56203811 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168026148 | TTCCTTTGTGACTTG[G/T]TATTTTTCCTCATTG | 55827 |
rs56223678 | snp | A/T | 0.0729998 | 0.176553 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980340 | GGATCTGTACCCAGA[A/T]GTAGAGATTGCTGGA | 55827 |
rs56237744 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975371 | TCGCTTGCTTGTGTA[A/C]AGTCATAGCCAACAT | 55827 |
rs56358061 | snp | G/T | 0.0678174 | 0.1712 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998174 | CACACAGATCTTTTG[G/T]TTTCCCAGTGCATGT | 55827 |
rs56684519 | in-del | -/GCACACACAC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041894 | ATACATGTTTGTCGC[-/GCACACACAC]ACACACACACACACA | 55827 |
rs56692073 | in-del | -/TA | 0.0471551 | 0.14613 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072352 | CTTCCCTGGTCACTC[-/TA]AATCTAAAGTTGTTT | 55827 |
rs56745269 | snp | A/C | 0.0685596 | 0.171987 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975786 | TCCAACTCCTGAGTT[A/C]ATACAATCCTCCCAC | 55827 |
rs56843139 | snp | A/G | 0.079617 | 0.182947 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042502 | TCCTTCTACAGAACT[A/G]TGATGCTCAGTCACC | 55827 |
rs56870396 | snp | A/T | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975785 | CTCCAACTCCTGAGT[A/T]CATACAATCCTCCCA | 55827 |
rs56962532 | snp | A/G | 0.079617 | 0.182947 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025250 | TATGATATGGGATAT[A/G]AGAGGAAGAGAAAAA | 55827 |
rs56983339 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943913 | GTGAGATCTCGGCTT[A/C]CTGCAAGTTCCGCCT | 55827 |
rs57170545 | in-del | -/A | 0.0652144 | 0.168387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051043 | ACTCCCTTTGGACTT[-/A]ACTGAATTCTAAGTG | 55827 |
rs57484294 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052441 | CTGTAGAGTGAATGA[A/G]GTGAGACTCATTCTT | 55827 |
rs57607860 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061646 | TCTGTCTCAATTACA[A/G]TTGTGCAGTGAAAAA | 55827 |
rs57651050 | in-del | -/TTTTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049448 | TTTTTTTTTTTTTTT[-/TTTTT]AGAAGAGACAGTCTC | 55827 |
rs57738266 | in-del | -/G | 0.0988009 | 0.199095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019176 | GCCTCAGCCTCCCAA[-/G]TAGCTGGGATTACAG | 55827 |
rs57775588 | snp | A/T | 0.0652144 | 0.168387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049412 | TGCACTCTGCTAATT[A/T]GTTGTTGTTGTTGTT | 55827 |
rs57935937 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025813 | TGTGATTCATCTGCC[C/T]AAAACATTTTAATTA | 55827 |
rs57936134 | snp | A/G | 0.17138 | 0.237316 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001780 | GGAATGAAATAAAAA[A/G]CACAGATGGAGAAAT | 55827 |
rs58001729 | in-del | -/T | 0.17654 | 0.238964 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963761 | GAGCATTTCATATAG[-/T]TTTTTTTTTTCTCCT | 55827 |
rs58065965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948589 | GGTTTAATGATTACA[C/T]AACCATTAAAAATGA | 55827 |
rs58082401 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070180 | TTCTTTTTGCCAGCA[A/G]TCAAAAAGACAATTT | 55827 |
rs58308587 | in-del | -/GAT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943504 | AATGCTATTTTAGAT[-/GAT]ATTTTTATTTATTTT | 55827 |
rs58478609 | in-del | -/AAG | 0.114036 | 0.209795 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940810 | TAGTAATTGATAAAA[-/AAG]TAATTTTAAGGTACT | 55827 |
rs58545386 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064030 | TTTTTTTTTTTTTTT[-/T]CCCCCTCTCTTTCTC | 55827 |
rs58620558 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167956068 | GCTGTGCTTAGCTAA[G/T]AACATTGTCTCTTTC | 55827 |
rs58678963 | in-del | -/T | 0.158962 | 0.232835 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942404 | ATGATGTTGAGTATC[-/T]CTTTTGTGGCTTTTG | 55827 |
rs58731723 | snp | G/T | 0.0689305 | 0.172377 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066970 | TTAAGATTTTTTTAA[G/T]CCTGTTAAAACAGTA | 55827 |
rs58954501 | in-del | -/AT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022671 | GGCAAGGAGTCTTGT[-/AT]GTAGTGAACTAGATA | 55827 |
rs58973738 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939855 | TTTTCCTAAGGAAAT[A/G]GATTCCTTTTTTAAA | 55827 |
rs58989856 | snp | C/T | 0.21875 | 0.248039 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952511 | GTGAGCCACTGTGCC[C/T]GTCCCATATCCTCTT | 55827 |
rs59135639 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040500 | TTTAAAAAAAAAAAA[-/A]GTGATGGGATTCTAG | 55827 |
rs59261808 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951074 | ATTTTTCTGCATAGC[A/G]CTATACTAACTTATA | 55827 |
rs59489094 | snp | C/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037105 | AGATTCTCCCCCCCC[C/T]TTTTTTTTTTTTTTT | 55827 |
rs59573567 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059760 | AGGCGATCCTCCCAC[C/T]TCAGCTTCCTGAGTA | 55827 |
rs59674650 | in-del | -/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072323 | AAAAAAAAAAAAAAA[-/G]GAAAAGAAAAGTCTT | 55827 |
rs59960933 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040903 | AAAAAAAAAAAAAAA[-/A]CCAAACAGGCAGAAC | 55827 |
rs60001959 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975742 | TGTTGTTGTGGAGAC[A/G]GGGTTTTGCTATGTT | 55827 |
rs60024821 | snp | A/G | 0.114036 | 0.209795 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983271 | AATGGTCATTTTAAC[A/G]ATATTGATTCTTCCA | 55827 |
rs60056673 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951546 | TGCCACTGCACTCCA[G/T]CCTGGGCAACAGAGT | 55827 |
rs60135464 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037121 | TTTTTTTTTTTTTTT[-/T]GAGATGAGGTCTCAC | 55827 |
rs60142550 | snp | C/T | 0.114036 | 0.209795 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004410 | AATCACCAGTAGTTA[C/T]TATCACTGAAATTAT | 55827 |
rs60163725 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168029987 | TCCGTCTCAAAAAAA[-/A]AAAAAAAGAAAAGAA | 55827 |
rs60292161 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976194 | CCTTTGGAGGCCAGA[C/T]GTGGTGGCTCACACC | 55827 |
rs60343684 | snp | C/G | 0.0325976 | 0.123435 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952984 | ACCTTGCTGAAGATC[C/G]ACCTTGCTGAAGATC | 55827 |
rs60640035 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064888 | CTATTCCAGTATATC[A/G]TATGCCTTTGATTCT | 55827 |
rs60739127 | snp | C/T | 0.17138 | 0.237316 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989852 | GGCGACAGAGCAAAA[C/T]TCTATCTCAAAAAAA | 55827 |
rs60756950 | in-del | -/TTTCACTTTTGATTGATTGTTTATAACATTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009846 | AAAATTTATAATTTT[lengthTooLong]CTTTTACTATGATAA | 55827 |
rs60775715 | snp | A/T | 0.0689305 | 0.172377 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034884 | AGAAGTTGGGAACAT[A/T]TAAATAGTTACAATT | 55827 |
rs60872248 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944007 | CCACACCTGACTAAC[-/T]TTTTTTTTGTATTTT | 55827 |
rs60990671 | in-del | -/TGT | 0.159292 | 0.232964 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942232 | ACCATGCCCAGCTAA[-/TGT]TTGTATTTTTAGTAG | 55827 |
rs61141688 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168051267 | CAATTTATGTTTTTT[-/T]AAATTTGATTGGGAT | 55827 |
rs61212424 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028791 | TTTCATTTTAGTACT[A/G]TTATCTAATATTATT | 55827 |
rs61238731 | snp | G/T | 0.0596104 | 0.162024 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944294 | CTGGTGCACATATCT[G/T]TTAGATATATTAATT | 55827 |
rs61423719 | snp | A/G | 0.172351 | 0.237636 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003086 | ATTGGTCTGTAACCA[A/G]AATCTTACTATAATG | 55827 |
rs61458635 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976266 | TTGAGGCCAGGAATT[C/T]GAGACCGGCCTGGCC | 55827 |
rs61587457 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167953676 | GCAATCTTGGCTCAC[C/T]GCAACCTCCGTCTCC | 55827 |
rs61636395 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040715 | CTTATCTAAACTTTT[G/T]GGGCTTTTTTTTTTT | 55827 |
rs61643149 | snp | G/T | 0.0693013 | 0.172766 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059130 | CTGGAATTTTAAAAT[G/T]TATCTGAATTTCCTT | 55827 |
rs61745202 | snp | C/T | 0.0117505 | 0.0757442 | missense | DCAF6 | GRCh38.p7 | 1:168044900 | TTTATTTTCTGACAG[C/T]ACAATCAGATAAGTT | 55827 |
rs61807023 | snp | A/G | 0.170733 | 0.237101 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943908 | CAGTGGTGAGATCTC[A/G]GCTTACTGCAAGTTC | 55827 |
rs61807024 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944028 | TTTGTATTTTCAGTA[G/T]AGACAGGGTTTCACA | 55827 |
rs61807025 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944136 | GGTGAGCCACCACGC[C/T]CAGCCTGATTTCATT | 55827 |
rs61807026 | snp | A/G | 0.247621 | 0.249989 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951077 | TTTCTGCATAGCACT[A/G]TACTAACTTATAGCA | 55827 |
rs61807027 | snp | A/C | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963898 | CACTATAATGATTCA[A/C]AGGGAGTGTGAGTAC | 55827 |
rs61807028 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965667 | GAGTCTTGCTCTGTC[A/G]CGTAGGCTGGGTGCA | 55827 |
rs61807029 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976302 | GGTGAAACCCTGTCT[A/C]TACTAAAAATACAGG | 55827 |
rs61807030 | snp | A/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989877 | AAAAAAAAAAAAAAT[A/T]ACTGAGAAGAATGAG | 55827 |
rs61807031 | snp | A/C | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992284 | ACACACACACACACA[A/C]ACACCGAATGCACAT | 55827 |
rs61807032 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009448 | TCTCTCTTTCTTTCT[G/T]TCTGTCTCTCTCTCT | 55827 |
rs61807033 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009460 | TCTTTCTGTCTCTCT[C/T]TCTTCCTTCCTCCCT | 55827 |
rs61807034 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009461 | CTTTCTGTCTCTCTC[C/T]CTTCCTTCCTCCCTC | 55827 |
rs61807035 | snp | C/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051898 | TTTTTTTTTTTTCCC[C/T]AAGATGTAGCCTTGC | 55827 |
rs61807037 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168055751 | AGAAAGTTAAAGGGC[A/G]TTTTCTTTCATTAGC | 55827 |
rs61809575 | snp | C/G | 0.46865 | 0.121211 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073967 | TTATAAATATGTATT[C/G]AATACATATTTATAA | 55827 |
rs61809576 | snp | G/T | 0.158962 | 0.232835 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074500 | CAGTAAACCTTCATT[G/T]AACATCCTATACTAG | 55827 |
rs66468162 | in-del | -/TAAT | 0.375 | 0.216506 | intron-variant | DCAF6 | GRCh38.p7 | 1:168047614 | TCTCTTATTCATAAA[-/TAAT]TAAGTTTCTTGAAGG | 55827 |
rs66514173 | in-del | -/GTGC | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041894 | TGTGTGTGTGTGTGT[-/GTGC]GCGACAAACATGTAT | 55827 |
rs66750894 | in-del | -/TAATC | 0.0655868 | 0.168795 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035684 | AAATTCTATCAACTA[-/TAATC]AATCATTTTATGATT | 55827 |
rs66923770 | in-del | -/A | 0.0689305 | 0.172377 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063962 | CAAGAAAACTCTACT[-/A]AAAAAATGCAGATTA | 55827 |
rs66950781 | snp | A/C | 0.29175 | 0.246489 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049541 | CTGGGGGACTATAGG[A/C]GTGAGCCACCGCGCC | 55827 |
rs67172910 | in-del | -/GTGT/TGTG | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938273 | TGTGTTTGTGTGTGT[-/GTGT/TGTG]ATGAGAGAGACACCT | 55827 |
rs67600256 | snp | C/T | 0.284733 | 0.247575 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003119 | TTCTGAAACATCTCT[C/T]GTGATCAAAAGCATA | 55827 |
rs71100917 | in-del | -/A | 0.206642 | 0.246211 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963438 | GGAAAAAAAAAAAAA[-/A]CAGAAACAAAAAAAA | 55827 |
rs71100920 | in-del | -/A | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980935 | TGGGTGACAGAGCTC[-/A]AAAAAAAAAAAAAAA | 55827 |
rs71100921 | in-del | -/A | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007989 | AGTGAGACTGTCTTT[-/A]AAAAAAAAAAAAAAA | 55827 |
rs71100923 | in-del | -/AGGA | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009471 | GGAAGGGAGGGAGGG[-/AGGA]AGGAAGGAAGAGAGA | 55827 |
rs71100924 | in-del | -/A | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054834 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55827 |
rs71299099 | in-del | -/A | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049452 | GAGACTGTCTCTTCT[-/A]AAAAAAAAAAAAAAA | 55827 |
rs71572475 | in-del | -/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980916 | TTTCTCTGAATTTTC[-/T]TTTTTTTTTTTTTTT | 55827 |
rs71572476 | in-del | -/C | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009394 | TTCCTTCCTTTCTTT[-/C]CTTTCTTTCTCTCTC | 55827 |
rs71572478 | in-del | -/A | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056801 | CAAAAATCCCAAGTT[-/A]TTAGAAATGCTCTGC | 55827 |
rs71572479 | in-del | A/GT | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056804 | AAAATCCCAAGTTTT[A/GT]GAAATGCTCTGCTTC | 55827 |
rs71572480 | in-del | -/A | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056805 | AATCCCAAGTTTTAG[-/A]AAATGCTCTGCTTCT | 55827 |
rs71587022 | in-del | AGCAGAGCA/TGCGTCT | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056809 | TTAGAATAATCCAGA[AGCAGAGCA/TGCGTCT]TTTCTAAAACTTGGG | 55827 |
rs71632333 | snp | A/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943213 | CGCGCCTGGCCGAAA[A/T]TTGGTCTTTTTTAAA | 55827 |
rs71632334 | snp | A/G | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993676 | ATCGCTTGAACCCGG[A/G]AGGCGGAGGTTGTGG | 55827 |
rs71632335 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017796 | CAAAATTAGCCTCCT[A/G]GATTTTAATTTATTA | 55827 |
rs71632336 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043426 | TTAGTTTGAATTAGT[C/T]TTTATCATTTTTATA | 55827 |
rs71632337 | snp | C/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049403 | GCATGTTGCTGCACT[C/T]TGCTAATTTGTTGTT | 55827 |
rs71632338 | snp | G/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068102 | AAATTCTTAAATGTT[G/T]TAAGTAGCCTCAAAA | 55827 |
rs71675981 | in-del | -/TG | 0.00835141 | 0.0640778 | intron-variant | DCAF6 | GRCh38.p7 | 1:168075216 | CAAAGCTAATAATAC[-/TG]TGTTTTCTTTACTCT | 55827 |
rs71868296 | in-del | -/CAT | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939365 | GTTAATTAACATATC[-/CAT]CATGTCACATAATTA | 55827 |
rs72312672 | in-del | -/CG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041891 | GAAATACATGTTTGT[-/CG]CGCACACACACACAC | 55827 |
rs72517005 | in-del | -/CGCA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041893 | AATACATGTTTGTCG[-/CGCA]CACACACACACACAC | 55827 |
rs72699717 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948557 | TAAATAACTTACAAA[A/G]TTGTAATTTATTTAA | 55827 |
rs72699719 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957278 | TTTCCCCTCTATTTA[A/G]CAGTTAGCAATCACT | 55827 |
rs72699723 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979235 | AAATCCAAAACAGCA[C/T]ACAAACAAAAGAAAG | 55827 |
rs72699727 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996034 | AACAAAGTAGGGAAT[A/G]ATTAATCTTGAGTAA | 55827 |
rs72699729 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000449 | AGTATCTGTGAAATT[C/T]AGTGAAGCAAAGTGC | 55827 |
rs72699731 | snp | C/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009472 | TCTCTCTTCCTTCCT[C/T]CCTCCCTCCCTTCCT | 55827 |
rs72699740 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | DCAF6 | GRCh38.p7 | 1:168062815 | AATCATTTCTTAAGA[A/G]AGTAAAATCTGCTTC | 55827 |
rs72699741 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074645 | GTTCATATAAGATAT[A/T]CTAGAATGTGGAGGA | 55827 |
rs73024126 | snp | G/T | 0.0535932 | 0.154675 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167936519 | TCCAGGGTGAGGGCA[G/T]CCGCAGCACACACCA | 55827 |
rs73024128 | snp | G/T | 0.0479149 | 0.147179 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938102 | AATACATTTTGTTTA[G/T]AAAAACTCAATAAAA | 55827 |
rs73024130 | snp | A/G | 0.0923359 | 0.194016 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938523 | TTTGTTGTAGGATAA[A/G]TACCTAGAGTGGTGA | 55827 |
rs73024131 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938966 | TGTATACATACAGGG[A/C]GTTCTTTATCTTAAA | 55827 |
rs73024135 | snp | C/G | 0.159292 | 0.232964 | intron-variant | DCAF6 | GRCh38.p7 | 1:167947049 | TACTGATTAATTCTT[C/G]CTGCTCATTATTGGT | 55827 |
rs73024136 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | DCAF6 | GRCh38.p7 | 1:167947960 | TGTCTAATGCTGTAA[A/G]TGGGGTGTTGAATTT | 55827 |
rs73024137 | snp | C/T | 0.143959 | 0.226396 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948943 | AGGTGTGAGCCACCA[C/T]GCACAGCAATCACCA | 55827 |
rs73024138 | snp | A/C | 0.247337 | 0.249986 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951388 | GAGACCAGCCTGGCC[A/C]ACATGATGAAATCCT | 55827 |
rs73024140 | snp | G/T | 0.143284 | 0.226079 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951952 | CTCCCAGAAAGGATT[G/T]TGACTATAATAAAAT | 55827 |
rs73024143 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952707 | CTCTTTTCTCTCCAG[C/T]TCAAAATGACCCTAT | 55827 |
rs73026103 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953232 | TATGCCTTATACCTA[A/G]AATTCTCTTCTCTCA | 55827 |
rs73026108 | snp | C/G | 0.159292 | 0.232964 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954302 | CCCACCCACTCTGTA[C/G]TTTTCAAGGTCTTAC | 55827 |
rs73026111 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960762 | GTCTGTCTTGGTAAA[C/T]GTTCCATGTAAGCTT | 55827 |
rs73026119 | snp | A/T | 0.0923359 | 0.194016 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964660 | CTTCTCCTCTGGTAT[A/T]CACATTATACATGAG | 55827 |
rs73026124 | snp | C/T | 0.143284 | 0.226079 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968271 | AAAGTAAAAAGGTCT[C/T]TATAAAATACAGAAA | 55827 |
rs73026125 | snp | C/G | 0.226779 | 0.248919 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968473 | CCCCTCTGGAACTTG[C/G]TGGAACACCTCTCTC | 55827 |
rs73026130 | snp | A/G | 0.172351 | 0.237636 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969459 | GCTTTTAGCTTCTGA[A/G]TTCATATATAGAGGA | 55827 |
rs73026133 | snp | C/T | 0.172674 | 0.237741 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974293 | GTCCTTTATCTGCAA[C/T]AAATTATACAAATAT | 55827 |
rs73026135 | snp | A/G | 0.114036 | 0.209795 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975632 | CTCTCTGCAGCTTCA[A/G]ACTCCCAGGCTCAAG | 55827 |
rs73026136 | snp | C/G | 0.172028 | 0.23753 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975767 | TATGTTGCCAGGGCT[C/G]GTCTCCAACTCCTGA | 55827 |
rs73026142 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981152 | GCTCAGGTAATCTGC[A/C]CGTCTCCGCCTCCAA | 55827 |
rs73026148 | snp | A/G | 0.172351 | 0.237636 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987861 | GTACATTTAAAATAT[A/G]TTTATGAAAATTCAA | 55827 |
rs73026149 | snp | A/G | 0.17138 | 0.237316 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996432 | ACCACCACCCTTGCT[A/G]CATTACCACCCTGAT | 55827 |
rs73026150 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996579 | GTGATCCTTAGAAAC[A/G]TAAGTTAAATCATGC | 55827 |
rs73026152 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998299 | ATTGCTAAAAAGTGC[C/T]AACAATCATCTGAAC | 55827 |
rs73026155 | snp | G/T | 0.0599851 | 0.162463 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000024 | GCTTTTGATTTAAAG[G/T]GAAAGGCATATGACT | 55827 |
rs73026156 | snp | A/G | 0.17138 | 0.237316 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000894 | TGGGATGATGAAAAC[A/G]GTCTGGAATTATATA | 55827 |
rs73026167 | snp | A/T | 0.229723 | 0.249176 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008388 | AATAACCTGTGAGTT[A/T]TTCTTGATTCCTTCC | 55827 |
rs73026169 | snp | C/T | 0.226484 | 0.248892 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010360 | TGAGTGAGTTGAATA[C/T]GCAAAATGAATGCCC | 55827 |
rs73026173 | snp | A/T | 0.114036 | 0.209795 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010999 | TAACTTTGAAGTGGA[A/T]GGGGATATCAGTATA | 55827 |
rs73026177 | snp | A/G | 0.114036 | 0.209795 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015679 | TCCTCTATGAGACAT[A/G]TGTTTTGTTTATATC | 55827 |
rs73026184 | snp | A/T | 0.100231 | 0.200173 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019352 | CATGCCCAGCCAATA[A/T]TGTACTATCTTAATT | 55827 |
rs73026187 | snp | G/T | 0.0414363 | 0.137845 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020053 | ACATAATACGCTCCA[G/T]ATGTTTCAGAACAGC | 55827 |
rs73026196 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027611 | CACCATTTTCCAGGT[C/G]CCCAAATCATTTTAT | 55827 |
rs73026198 | snp | G/T | 0.0689305 | 0.172377 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027813 | GGTGTCTTTGCTTAT[G/T]TATCCTGAATTTTTA | 55827 |
rs73026200 | snp | A/T | 0.0689305 | 0.172377 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028352 | TTAACTTTTGAGAGG[A/T]TATAAGAAAGTAATT | 55827 |
rs73028104 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036149 | TTAACCATCTTAGAA[A/G]GCTTCTTGCCTTTGG | 55827 |
rs73028106 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041198 | CTGAGAAGGCCCTCA[C/T]TGATTGTTAGCTACA | 55827 |
rs73028108 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041320 | TTATTATAGAATTAA[A/G]TGAGGATTATACCAT | 55827 |
rs73028112 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045797 | TTTATAGTTTTTCTA[C/T]ATTTTATGTGATCAC | 55827 |
rs73028184 | snp | C/T | 0.0221141 | 0.102801 | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168075989 | ATCACATAGAAGGAC[C/T]TCCTTCATTTCTCCT | 55827 |
rs74120570 | snp | A/G | 0.0322114 | 0.122752 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935466 | AGGCTCAAATCTGGA[A/G]ATCAGGTTTGGGTTG | 55827 |
rs74120571 | snp | A/G | 0.0681886 | 0.171594 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938400 | CTTTTAAATTATTAC[A/G]TAGTAGGTAACATTA | 55827 |
rs74120572 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948944 | GGTGTGAGCCACCAC[G/T]CACAGCAATCACCAT | 55827 |
rs74120581 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968354 | AAGAAGAGACCCCCC[C/T]GTGCTGAGTGCTGAG | 55827 |
rs74120583 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968744 | TAGGAAGCAAACTCC[A/G]TTTTCCTGCATTATT | 55827 |
rs74120587 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976803 | ACCTGCATATTTACT[A/G]ATACCTTTGGTTTAC | 55827 |
rs74120590 | snp | G/T | 0.0681886 | 0.171594 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998457 | GTTTCTGCATCGATA[G/T]ACTCTTCCTTTCATA | 55827 |
rs74120591 | snp | C/T | 0.0681886 | 0.171594 | intron-variant, downstream-variant-500B | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167999159 | CCTTGGATGACCAGG[C/T]GCATTGTCAATGCCC | 55827 |
rs74120593 | snp | A/C/G | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004463 | ATGTGTTTTCTGAGC[A/C/G]TATCTGTTTAGAGTT | 55827 |
rs74120594 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006844 | CTGATATCAAAGAAA[C/G]GGACAATGGGAATAT | 55827 |
rs74120596 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014096 | ATTTATCTGTTCTCC[A/G]CTAATAGCAAGAGTT | 55827 |
rs74120598 | snp | G/T | 0.0685596 | 0.171987 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014854 | GTGTTTGTTCAAGTG[G/T]TGCCTTATGAGAGAA | 55827 |
rs74120600 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014985 | CCACGTGACACAAAC[A/G]CATATGTTCAACATC | 55827 |
rs74120601 | snp | C/T | 0.00832676 | 0.0639847 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019551 | CCATTTCAGGTCCCC[C/T]GAAGTCATGGGTTGC | 55827 |
rs74122606 | snp | A/T | 0.138886 | 0.22395 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037300 | AAAAAATCCTAAGTA[A/T]ATTTGCTTTTATGAA | 55827 |
rs74122608 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:168062831 | AGTAAAATCTGCTTC[A/G]TTAGTTCTAAATTCG | 55827 |
rs74122611 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067082 | GGCCTTTCCTCCCCA[A/C]CTTCAACCAGGGTTT | 55827 |
rs74122612 | snp | A/T | 0.0659589 | 0.169201 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069857 | ACACTGTAACTTTTT[A/T]AAAATATATTTTGTT | 55827 |
rs74122614 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073958 | TCATTTATTTTATAA[A/G]TATGTATTGAATACA | 55827 |
rs74332183 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937566 | CCACCCCCGCGCGCT[A/C]TCCCAGTTCCACTCT | 55827 |
rs74388891 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040314 | AGAGAAGAGTAGTAG[A/G]TAAGGTCAGCCAGGA | 55827 |
rs74477863 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982759 | TCTAGAATGGCGTTT[C/T]CTATATTTTCTTTTA | 55827 |
rs74516268 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168028580 | ATGTTAATTTTCCAC[A/T]ATGTATCATTTTATA | 55827 |
rs74525769 | snp | A/G | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074793 | ATCCCAAGCAGAGGA[A/G]TAGCAAGTGTAATTC | 55827 |
rs74539245 | snp | A/G | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995684 | AACTCAGTCTCAGAA[A/G]AAAAAAAAAAAAGCT | 55827 |
rs74567038 | snp | A/C | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073175 | AGCGAGACTCGGTCT[A/C]AAAAAAAAAAGAAGA | 55827 |
rs74577863 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008446 | CAGCAAGTTCTTTTG[A/T]TCCTGTATCTAAACT | 55827 |
rs74647325 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035784 | AAGAACTCTGTAGGC[C/G]GGGCATGGTGGCTCA | 55827 |
rs74648809 | snp | A/G | 0.079617 | 0.182947 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074593 | TGCAGGAAGACATGC[A/G]AACGACTATTACTGT | 55827 |
rs74653733 | snp | A/T | 0.0356815 | 0.128715 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008534 | ACCTACTGTTGTTCC[A/T]TTATAATGTATTCTC | 55827 |
rs74654016 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994864 | AATGCCTATTAATAC[A/G]TTTTAAAGGTTACTA | 55827 |
rs74665461 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028581 | TGTTAATTTTCCACT[A/G]TGTATCATTTTATAT | 55827 |
rs74679963 | snp | G/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049668 | TTTTTTTTTTTTTTT[G/T]TTTTGGAGACGGAGT | 55827 |
rs74691232 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025208 | ATTACATTTAATATT[A/G]TATTCAATTTAAGTT | 55827 |
rs74725546 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037149 | CACCCAGACTCGACT[C/G]GAACTCCTGGGCTTA | 55827 |
rs74746493 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943727 | CTGTGTGAACACGTT[C/T]GTTTAGAACACACTT | 55827 |
rs74781565 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063374 | AGTTTGCCGCATGCT[A/G]TTGCCTTTACTTTTC | 55827 |
rs74794756 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071243 | ACTCAACTCTGCCAT[G/T]GTAATGCAAAAACAG | 55827 |
rs74824308 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976617 | CTTTCACAAGAATAT[C/T]GAACAAAGCCAAATA | 55827 |
rs74824792 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057551 | ATTGCTTTGAAATTG[C/T]TGGATAATCAATTTT | 55827 |
rs74898737 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046633 | ATATATTTTAGGCAA[A/G]TAAGACTTAGTTCTA | 55827 |
rs74898895 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054138 | ATAAAGCTAGATAAC[A/G]CTAACATACTAATAG | 55827 |
rs74932916 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053577 | GGAAGAATCCAGGCT[C/T]AGTGTTCCAAAGTTC | 55827 |
rs74960990 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943334 | GATTTTGTGTTGAAT[C/T]TATATATTATTTCAG | 55827 |
rs74997562 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955168 | CATAATGTTTATCTC[G/T]GTTCACCTGTCAGTG | 55827 |
rs75089467 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980599 | CATATGCTTCTTGGC[C/T]ATCTGTGTATCTTCT | 55827 |
rs75094526 | snp | C/T | 0.113334 | 0.209338 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936285 | AAGGGAAAGTGAAGC[C/T]GCGCTGGTTCTACTG | 55827 |
rs75134051 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034392 | GACACACACCTGCAA[C/T]CCTAGCTACTTGGGA | 55827 |
rs75150848 | snp | G/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054835 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCACT | 55827 |
rs75217028 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986776 | ACTTCCTAACAGGCT[A/G]CGGACCAGTACTGGG | 55827 |
rs75235967 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019210 | TGTGCCACTATGCCC[A/G]GCTAATTTTTTGTAT | 55827 |
rs75249474 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023128 | CTCTCTCACACCTTT[C/T]GTAGCATTTCATTTT | 55827 |
rs75290899 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971263 | ATCTGTGTTCCTGTC[G/T]TGTGGATAACTCTAT | 55827 |
rs75393090 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997516 | ATGGGGATTTTTTTT[C/T]CTGTCTCCTTTGCTC | 55827 |
rs75405077 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023225 | CTTTTTGGCCTATAC[A/G]GATTATTTTCTATGT | 55827 |
rs75530273 | in-del | -/TT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948148 | CCTTTTTTTTTTTTT[-/TT]AACTGTTTTTAGATG | 55827 |
rs75532563 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965597 | AAAAACACCCTCTGC[A/G]CCATACCCCCACCGC | 55827 |
rs75541034 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976224 | CTGTAATCTGAGCAC[A/T]CTGGGAGGCTGAGGT | 55827 |
rs75559713 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989183 | ATAGGGAAGCATTGA[A/T]CTAAACTCAGAAATA | 55827 |
rs75576994 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962362 | TTATCTCACATATTT[C/T]GATGCTCTGTTGTTA | 55827 |
rs75624889 | snp | C/T | 0.0352966 | 0.128072 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938018 | AACCAACAGTTCTGG[C/T]TTGTAAATTATTTAA | 55827 |
rs75626335 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007111 | TCTAACCTTTCATTC[A/G]CAATGAAAAGTACTC | 55827 |
rs75699156 | snp | A/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067012 | AGTTCTTTGGAGCTC[A/T]GGATTTCTTCTGGGA | 55827 |
rs75780280 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048862 | GTTCATTTCAAAAAT[C/T]GGCATTTGGCGGAGA | 55827 |
rs75886886 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962057 | GTGGTCTAAGAGTAG[A/G]CACTGTTTGATTTTT | 55827 |
rs75889027 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051587 | GGCATATATCTGTTA[C/T]TTACCATCAGTTTCT | 55827 |
rs75899813 | snp | A/G | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972498 | TGATTTATATTTTTA[A/G]AAGATAGCTCTGGCT | 55827 |
rs75912580 | snp | A/G | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024236 | AAAAAAAAAAAAAAA[A/G]AAGAACAGAAAAAAG | 55827 |
rs75928605 | snp | A/C | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020307 | TACTGAGTAGAAAAA[A/C]CACATTTGAACCCAG | 55827 |
rs75974334 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022205 | ATGCTGCCTGCCTTA[A/T]TACCAGTGTTTTTCA | 55827 |
rs75988885 | snp | A/C | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000579 | TTCAGCATTATTCAT[A/C]ATAGCCAACAAGTGG | 55827 |
rs76002838 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029602 | TATATGTTAATTTAC[G/T]TAATCCTTACCACAA | 55827 |
rs76023228 | snp | C/G | 0.0253447 | 0.109681 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044541 | ATTTTAGAACTAATC[C/G]CTCATGGATACCAAG | 55827 |
rs76024048 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063274 | AGAGGGGAAAGAACA[C/T]TGGATAAAATTTGTT | 55827 |
rs76082508 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960350 | CTTGCCCAGGCTGGA[A/G]TGCAATGGCGCGATC | 55827 |
rs76107581 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073040 | AATCAGCCGGGTGTG[A/G]TGGCACGCTCCTGTA | 55827 |
rs76151783 | snp | A/G | 0.0644444 | 0.167538 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041002 | TTTGGCAACAGATGA[A/G]GCAATAGAACATGCT | 55827 |
rs76173240 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021956 | AGCACAGGATATTAG[A/G]AACTGGGAATTATTC | 55827 |
rs76178208 | in-del | -/AAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024820 | AAAAAAAAAAAAAAA[-/AAA]GATTATTCCTTATGG | 55827 |
rs76189857 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958140 | TGTACAAAAGTTTTT[A/G]ATTTTGGTGAAGTCT | 55827 |
rs76219034 | snp | A/C | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073176 | GCGAGACTCGGTCTC[A/C]AAAAAAAAAGAAGAA | 55827 |
rs76236379 | snp | A/G | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995681 | CAAAACTCAGTCTCA[A/G]AAAAAAAAAAAAAAA | 55827 |
rs76246537 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029223 | TAACTGACATTTATT[A/G]AGTTTTTTGTGACTA | 55827 |
rs76289410 | snp | C/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073001 | GCTAACATGGTGAAA[C/T]CCCATCTCTACTAAA | 55827 |
rs76328380 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957536 | CTGTTCATCAGTTGT[G/T]GGATATTTGGGTTGT | 55827 |
rs76397675 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032452 | TGGATTCCCTGACCT[A/G]TGAACATGGAAAATT | 55827 |
rs76401243 | snp | A/T | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021647 | GTTATTCAAATAATG[A/T]TCATGTTTTGTCAAA | 55827 |
rs76439828 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044476 | TATGCAAATATTATG[C/G]CATTATATATGAGGG | 55827 |
rs76460027 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027096 | CTCCCAGAAAGTCTG[A/T]TAAATCATTTTTTAA | 55827 |
rs76486243 | snp | A/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065329 | TCAGTTTTTTTTTTT[A/T]TAGATAGGGGATCTC | 55827 |
rs76532604 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984840 | AATTAAAAATTATGT[A/G]TAGTTCATTTTCATG | 55827 |
rs76533012 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980062 | GGCATGTGCCTATAG[C/T]CCCAGTTACTTGGGA | 55827 |
rs76570666 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957844 | AGTGGATGTGAAGTG[A/G]TAATTTGTTGTGATT | 55827 |
rs76574213 | in-del | -/T | 0.0360663 | 0.129354 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000781 | TATTTATATGAAATG[-/T]TTAGAAAAGGCATAT | 55827 |
rs76581670 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048180 | TACCATTTGGTTCCT[A/G]GAGTCCAAGGATACA | 55827 |
rs76636756 | snp | G/T | 0.0607341 | 0.163335 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943425 | TATTAAGCATTCTTT[G/T]ATTCTCTCAGCAGTG | 55827 |
rs76667324 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023900 | AAGAATGATTTAACA[C/T]GATATTCACTTTCTC | 55827 |
rs76684450 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074346 | ACCTTAATATTTTCC[A/G]TGTTACTATGTGGAA | 55827 |
rs76704788 | snp | G/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054834 | GTTTTTTTTTTTTTT[G/T]GAGACGGAGTCTCAC | 55827 |
rs76740085 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067440 | AATGGGGTAGATAGG[A/G]TGGAGAGGTCTTCAC | 55827 |
rs76765947 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952687 | CTGTCTTGGTATCTC[C/T]CACCCTCTTTTCTCT | 55827 |
rs76773546 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033720 | TTATCTTGATGTTTA[C/T]GTGGTCATTGCTGTG | 55827 |
rs76803782 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046463 | TTCTTAACTATGAAA[C/G]GGTATGTTTCTTTCT | 55827 |
rs76820695 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978703 | GTGTTTTGAGAGATG[C/G]GGTCTCACTTTTTCA | 55827 |
rs76831300 | snp | A/C/G | 0.00557542 | 0.0525036 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021552 | ACTGATTGAAATGCT[A/C/G]TTGTTCCCACTTTCT | 55827 |
rs76864596 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029256 | ACTGTGTTAAGAATT[G/T]AACATGCATCATCTA | 55827 |
rs76865585 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063396 | TTACTTTTCATCCAG[A/T]ACCAAATTTCTAAGT | 55827 |
rs76869885 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986987 | TGAGAGTACATTTCG[C/T]TGACATTAAGTATAT | 55827 |
rs76950971 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045524 | ATGACCCACAGGTTA[G/T]TTATGAAGTCAAGGT | 55827 |
rs76960979 | snp | A/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029115 | TTAAACCCTATTTAA[A/T]TTTTTTGTTGCATAT | 55827 |
rs77009797 | snp | A/C | 0.079617 | 0.182947 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048159 | GAAGCTCTGTTGTAA[A/C]AATCATACCATTTGG | 55827 |
rs77017864 | snp | C/T | 0.0228947 | 0.104514 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997430 | ATTCCCTGTCACACA[C/T]TTACGTCTTCCTGTG | 55827 |
rs77019564 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957503 | AATATTTCATTGTAC[A/G]GATATACCACATTTA | 55827 |
rs77024813 | snp | A/C | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025434 | GAGTTGCTATGTAAG[A/C]GGTTAGTATTGAGTG | 55827 |
rs77040559 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952672 | GGTTGCACGAAGACC[C/T]TGTCTTGGTATCTCC | 55827 |
rs77064095 | snp | A/G | 0.0165908 | 0.0895552 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168065736 | CCTGCAGCCACATCC[A/G]TTTGACCCAAGTAAG | 55827 |
rs77066357 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957965 | AATGTCTATTTAAAT[C/T]CTTTACCTATTTTTA | 55827 |
rs77074077 | snp | A/C | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040903 | AAAAAAAAAAAAAAA[A/C]CCAAACAGGCAGAAC | 55827 |
rs77118249 | snp | A/G | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031586 | GAAGGAGAAGTTGTT[A/G]AAGGGAGTGTTCTCC | 55827 |
rs77120784 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064939 | TTTGTATCTTTCTCA[A/G]TTGTGTTAGCTTATA | 55827 |
rs77153427 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049124 | TTCTCTAATCATGGT[A/G]TTTAAAAAAATAAAA | 55827 |
rs77187510 | snp | G/T | 0.253544 | 0.249975 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064020 | CATTGCTTTTGTTTT[G/T]TTTTTTTTTTCCCCC | 55827 |
rs77188947 | snp | C/G/T | 0.0275041 | 0.113998 | upstream-variant-2KB, missense, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935790 | TCAGCTCCACTTTAT[C/G/T]GAGGAGCCGGTGGTA | 55827 |
rs77204294 | snp | C/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990529 | ATTATATAGGTAATT[C/T]TGAATTTTTTACATT | 55827 |
rs77214543 | snp | A/G | 0.0209421 | 0.100162 | intron-variant, downstream-variant-500B | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998954 | AAAAGTTCTTAATAA[A/G]GCATCTAGAATGGTC | 55827 |
rs77230007 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016107 | TGGTATTCAACATCA[C/T]GTGTTAGGGGGACAG | 55827 |
rs77309368 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168056245 | CATTTTCTGTTGTTA[C/G]CCATTCGTGTTTCTC | 55827 |
rs77419003 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005525 | CTATATACATGTAAT[C/T]ATAAAAACCAATAAG | 55827 |
rs77468436 | snp | A/C | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024808 | GACTCTGTATCCAAA[A/C]AAAAAAAAAAAAAAG | 55827 |
rs77506234 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956403 | TGTAGAATCTGTAGT[A/G]TATGTTACTGTGTTT | 55827 |
rs77527066 | snp | C/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955579 | ATTCATTCAAGTAGC[C/T]TTTTTTTTTCCTTAA | 55827 |
rs77536885 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074115 | TGTCATTGGTTTGAC[A/C]TTGGATTAGAGTTGG | 55827 |
rs77581874 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065241 | TAGGGGGGATTTTCT[A/G]TTACTTACTGCCATC | 55827 |
rs77647203 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015183 | TACTTTTCATCTGTG[A/G]TCACTTCAGATAAAG | 55827 |
rs77650481 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985828 | TTCACAAAGTAAAAT[A/G]TATATGTACTCAGCA | 55827 |
rs77682570 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955807 | CCTCTGTTTCCCAGA[C/T]TGGAGTGCAGTGGCA | 55827 |
rs77752211 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017486 | TTTGTAACTAGTTCA[C/T]GGATTTGAATTGAAG | 55827 |
rs77809346 | snp | G/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966402 | ATTTTTTTTTTTTTA[G/T]CTCATCAGCTATTGT | 55827 |
rs77831531 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000359 | ACAAACATAAAATGA[C/G]CACATGCTATTGGAA | 55827 |
rs77835254 | snp | A/C | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984513 | TGATTTCATTTATAG[A/C]CAGTAGTATACAAAG | 55827 |
rs77869144 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973470 | ATTGATGACTTCTGT[G/T]TGAATCGGTTGTTGT | 55827 |
rs77873310 | in-del | -/CTTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037104 | GAGATTCTCCCCCCC[-/CTTT]TTTTTTTTTTTTTTG | 55827 |
rs77881627 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033308 | CTGAAAAGGATCTTT[C/T]TTTTTTTTTTTTTTT | 55827 |
rs77901992 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072840 | CCTCTGCAGCAAACT[C/T]AGTGTCTCTTCATAT | 55827 |
rs77959584 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961042 | TATAATTTTCCTCAT[A/G]GAAATCTTATACATA | 55827 |
rs77980796 | snp | A/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007984 | TTTTTTTTTTTTTTT[A/T]TTTTTAAAGACAGTC | 55827 |
rs78074750 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985683 | GTAGATATCTTTGGG[C/T]TACTATTATTCTGCT | 55827 |
rs78077359 | snp | A/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989875 | CAAAAAAAAAAAAAA[A/T]TTACTGAGAAGAATG | 55827 |
rs78086423 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955770 | TTGTCTTGTTCTGAT[A/C]TTAGAAGGAAAACAG | 55827 |
rs78091068 | snp | C/G | 0.114036 | 0.209795 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985539 | CTCAGTAAGACCCTT[C/G]TAATTATATTGGGCC | 55827 |
rs78101811 | snp | G/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967741 | TTTTTTTTTTTTTTT[G/T]TGGCAAGGTCTCACT | 55827 |
rs78140993 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996617 | CTCATCAACATTCTA[A/G]GTGGCTCCCTGTCGG | 55827 |
rs78153720 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988209 | GTGTCATCTCAGGCC[A/G]GAGTGCAGTGGTGCA | 55827 |
rs78173670 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978609 | TTTTTGAAAAAATAT[C/T]TTCTGCATATGAGCC | 55827 |
rs78198165 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996622 | CAACATTCTAAGTGG[C/T]TCCCTGTCGGACCTA | 55827 |
rs78226387 | snp | C/T | 0.079617 | 0.182947 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053381 | TCTCCCTGCATGATA[C/T]GGGTTTTTGCTTTCT | 55827 |
rs78255075 | snp | A/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007985 | TTTTTTTTTTTTTTT[A/T]TTTTAAAGACAGTCT | 55827 |
rs78258385 | snp | A/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040931 | AACTTAAAAAAAAAA[A/G]GTATACAGACTTTTT | 55827 |
rs78278411 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015591 | CGTAGTTAAATAGAA[A/G]CATTTGGTTGTATAT | 55827 |
rs78281347 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031455 | TGATTGAGCCCATTA[A/G]TAGAACACTTTCACT | 55827 |
rs78286591 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071803 | TTCAAGGTCCTACAT[A/G]ACATACATTCTGCCA | 55827 |
rs78335090 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018961 | TGCTGTAATTTACAG[A/C]GACCATGTAAGGATG | 55827 |
rs78357988 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992866 | GTAGTATGCTAATAA[A/G]TATTAGCTTTTTGTA | 55827 |
rs78380986 | snp | A/C | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966409 | TCCTTTTAGCTCATC[A/C]GTTATTGCTAGCATT | 55827 |
rs78397276 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944384 | TTAATTCTTGGAGAA[A/G]TCTCCATACTGTTTT | 55827 |
rs78404359 | snp | A/G | 0.079617 | 0.182947 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034450 | CAGAAGTTTGAGACC[A/G]CAGTGAGCTATGAAG | 55827 |
rs78536146 | snp | A/G | 0.0360663 | 0.129354 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997786 | AACACTTACAGTGCA[A/G]CAATAAAAAGACAAA | 55827 |
rs78537384 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012223 | CCAGGACAAAAATAC[C/T]GTATGTATTGTAGAG | 55827 |
rs78539716 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044088 | AGCAGTGGGCCCATC[C/T]GTCCATGATAGTGTT | 55827 |
rs78541645 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026974 | TGAGACCAAACAGGA[A/G]TGATGAGAGAAGTAC | 55827 |
rs78545244 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058024 | AAACAAAACATAAAC[A/G]TATAAACATAAAGTT | 55827 |
rs78553015 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970376 | ATAATCATAGGCCAA[A/G]TGTGTGGCTCACGCT | 55827 |
rs78554176 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940192 | GTTGTGGGAATGAAG[A/G]TGAATAATTTCCCAG | 55827 |
rs78572274 | snp | A/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937571 | CCCGCGCGCTCTCCC[A/T]GTTCCACTCTGCTCT | 55827 |
rs78595126 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040785 | ACTTTTCCTTCTCTA[A/G]AAACTGACCATGAAT | 55827 |
rs78668329 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967124 | GTTAAGAATAGTGTG[A/G]GTAAAGCTGCCAACT | 55827 |
rs78725506 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168028579 | AATGTTAATTTTCCA[C/G]TATGTATCATTTTAT | 55827 |
rs78732575 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059384 | AATTTGCCTGTCTCT[C/G]TGTCAGTATCATACT | 55827 |
rs78740771 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986631 | CATAAGGAGTGCACA[A/G]CCTGTGAGAAACAGT | 55827 |
rs78754160 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | DCAF6 | GRCh38.p7 | 1:167947303 | TCAATTTTTTTTATC[C/T]CTTTGAGGAACCAGC | 55827 |
rs78761138 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053716 | GGGTCTGGTCATGTA[A/G]GCACCTCTGCCTGTG | 55827 |
rs78813840 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958891 | AATACATCATAATCC[A/G]TCCAAAGTCCATAGT | 55827 |
rs78841916 | snp | A/T | 0.095934 | 0.196885 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944633 | TCATGTGTTTTGCCT[A/T]CTTTTTAATAGGATT | 55827 |
rs78848096 | snp | C/T | 0.154329 | 0.23097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982784 | CTTTTAGGATTCTTA[C/T]AGTTCGAGGTCTTAC | 55827 |
rs78858219 | snp | C/T | 0.0352966 | 0.128072 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938570 | TGAACATAGCTGGAG[C/T]CTGGTTTTTAAAACT | 55827 |
rs78875217 | snp | G/T | 0.0799831 | 0.183287 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066066 | TTTAGTCTTCACATA[G/T]CTGAATTAATTTATC | 55827 |
rs78887699 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964811 | GAGATTGTTTCCTCA[A/G]TTGTGTCTAGTCTAC | 55827 |
rs78896011 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006873 | ATGAAAATTTGCTAC[A/G]CTCCATCTCTGGTTG | 55827 |
rs78905342 | snp | G/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943856 | CATTCATTTTTTTTT[G/T]GAGATGGAGTCTCAC | 55827 |
rs79003547 | snp | A/G | 0.079617 | 0.182947 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068817 | TAAATGTGACATGCT[A/G]AGAAATGAAACATAC | 55827 |
rs79013925 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976225 | TGTAATCTGAGCACT[C/T]TGGGAGGCTGAGGTG | 55827 |
rs79037544 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954958 | TCAACCAATGATCTC[C/T]ATTCTGTCACTATAA | 55827 |
rs79069945 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054380 | TTATAAAGCCACCAG[G/T]CCCCACTGACCTGAT | 55827 |
rs79169041 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026485 | GCTATAGTCCACCTA[A/C]GAGATTATGAGGGAT | 55827 |
rs79176981 | snp | A/C/T | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017933 | TCTGTTGTCTTCTCA[A/C/T]CTATTTAAGTGTTTT | 55827 |
rs79196711 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039466 | TTGAGAAAAGCAAGT[C/T]ATGTAAGCTTTTTAT | 55827 |
rs79205594 | snp | A/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065328 | GTCAGTTTTTTTTTT[A/T]ATAGATAGGGGATCT | 55827 |
rs79209999 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981180 | CAAAGTGCTGGGCTT[A/G]CAGGCATGAGCCACC | 55827 |
rs79213826 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937572 | CCGCGCGCTCTCCCA[G/T]TTCCACTCTGCTCTT | 55827 |
rs79292211 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051904 | TTTTTTCCCCAAGAT[A/G]TAGCCTTGCTCTGTT | 55827 |
rs79303586 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973312 | GTGGTACATGATGTT[A/G]TATAATTTATTCCCT | 55827 |
rs79316144 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067157 | CCATTGCTAAAAATG[C/T]TAGTAAGTTGGAAAA | 55827 |
rs79325119 | snp | A/T | 0.0352966 | 0.128072 | intron-variant | DCAF6 | GRCh38.p7 | 1:167947047 | ATTACTGATTAATTC[A/T]TGCTGCTCATTATTG | 55827 |
rs79326714 | snp | G/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007986 | TTTTTTTTTTTTTTT[G/T]TTTAAAGACAGTCTC | 55827 |
rs79443313 | snp | C/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037097 | GTTCTATGAGATTCT[C/T]CCCCCCCTTTTTTTT | 55827 |
rs79498844 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031777 | AAAGGATTTTGGCAG[C/G]ACTCATGTGCCACAT | 55827 |
rs79517104 | snp | A/C | 0.0792508 | 0.182605 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020558 | TTCTAAACACTTCAA[A/C]TAAGCTGACCAACCA | 55827 |
rs79542640 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995194 | TGTTACATAATGAAA[A/G]AGTTGGAAGTCCATA | 55827 |
rs79560088 | snp | A/G | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988663 | AGTTACAAAAAAAAA[A/G]GGTACTACTGTTAAT | 55827 |
rs79571613 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065440 | GGTGTGAGCCACTGC[A/G]CCCAGCATCAATTTT | 55827 |
rs79572862 | in-del | -/TTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037119 | CTTTTTTTTTTTTTT[-/TTT]GAGATGAGGTCTCAC | 55827 |
rs79605788 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981854 | GTGAGTGCATGTGTC[C/T]TTTTGGTAGAACAAT | 55827 |
rs79618120 | snp | C/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945800 | CCACCACACCCGGCC[C/T]TTTTTTTTTTGTTAT | 55827 |
rs79639536 | snp | A/G | 0.0176736 | 0.092328 | intron-variant, nc-transcript-variant | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998720 | TTTCTTTGCTCATCC[A/G]TAAGGAGCAACTCCT | 55827 |
rs79646836 | snp | A/G | 0.079617 | 0.182947 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073402 | CTGGAAGAGGTGACT[A/G]TGCATCAGTTAAATG | 55827 |
rs79654583 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937569 | CCCCCGCGCGCTCTC[A/C]CAGTTCCACTCTGCT | 55827 |
rs79674562 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068701 | CACGTAAAAACTCTT[A/G]TCAGCTGCTGTTTTC | 55827 |
rs79683534 | snp | G/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017225 | ATAATAAAACATTTT[G/T]GTTTTTTTTTTTGCT | 55827 |
rs79741161 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045782 | AATTGCCAACATGTT[C/T]TTATAGTTTTTCTAT | 55827 |
rs79745968 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995578 | CCAGCTACTTGGGAG[A/G]TTGAGGCAGGAGAAT | 55827 |
rs79747918 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044473 | TTATATGCAAATATT[A/G]TGCCATTATATATGA | 55827 |
rs79823681 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955239 | GTTGCCATGAATATT[C/T]GTGTTGCGTCTTTGT | 55827 |
rs79831185 | snp | A/G | 0.079617 | 0.182947 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065229 | AGTCCCTCTTCTTAG[A/G]GGGGATTTTCTATTA | 55827 |
rs79832054 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938268 | TGCTGGGGTGTGTGT[G/T]TGTTTGTGTGTGTAT | 55827 |
rs79847605 | snp | A/C | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024807 | AGACTCTGTATCCAA[A/C]AAAAAAAAAAAAAAA | 55827 |
rs79896575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991510 | GTTTATGACCCTTTG[G/T]GATGATACTTTTGCA | 55827 |
rs79903199 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986067 | GTTCATTATTACTGA[A/T]GATTTAGTACTTTAT | 55827 |
rs79908764 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023681 | GGCTTTATTACTAGC[A/G]ATCAAATATAGCACA | 55827 |
rs79921722 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000296 | ATCACCATAATAGGT[A/G]GGATAATAATGAATA | 55827 |
rs79931917 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948235 | GATTATAATGTTGCC[A/G]TGGTGGAGACCTTTT | 55827 |
rs79986816 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044299 | ATGCCCATGGATTCC[A/G]TGGAAATACTCCCTC | 55827 |
rs80038380 | snp | A/G | 0.079617 | 0.182947 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044067 | AATTCCTGGGCTTCA[A/G]GAAGAAGCAGTGGGC | 55827 |
rs80043524 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020943 | TAAAATTAATCTTCA[A/G]GATGGGAGGAACAGC | 55827 |
rs80084446 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980071 | CTATAGTCCCAGTTA[C/T]TTGGGAGGCTGAGGC | 55827 |
rs80086442 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943289 | TAAAAATTTTAGAAC[C/T]AGCTTGTCAATTTCT | 55827 |
rs80103548 | snp | A/T | 0.021333 | 0.101051 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027218 | GGGGGAAAAAGGTAG[A/T]GACTTTGTTATGTCT | 55827 |
rs80109837 | snp | G/T | 0.0364509 | 0.129988 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025154 | GATTTTATAGCCAGA[G/T]TTATATTCTAGTTAA | 55827 |
rs80111856 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964790 | ATTGATATATCCTCA[A/G]GGTCAGAGATTGTTT | 55827 |
rs80116045 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063931 | ATAATATATTGTGAA[A/G]GATCATTATTTTTTA | 55827 |
rs80119861 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040795 | CTCTAAAAACTGACC[A/G]TGAATTATATTCTCA | 55827 |
rs80130471 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973765 | CCACTCACCTCTCTA[C/T]TGTATATCTGTTATG | 55827 |
rs80131352 | snp | G/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168062927 | TCTTTTTTTTTTTTT[G/T]TTGAGACAGAGTCTC | 55827 |
rs80171614 | snp | G/T | 0.114036 | 0.209795 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985528 | GCCTTGTTTTGCTCA[G/T]TAAGACCCTTGTAAT | 55827 |
rs80303561 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999389 | TGTCACCACTGCATA[A/G]GCCCCTAACAAGAGA | 55827 |
rs80338468 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949224 | CACAATGGTAAGTTC[A/G]TCCATAACAAGTGTG | 55827 |
rs111242307 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981196 | CAGGCATGAGCCACC[A/G]CTCCCGGCCTCCCCC | 55827 |
rs111248539 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000509 | TTTGGGTAGTTCTCC[C/T]GTATACCCAAGAGAA | 55827 |
rs111268600 | snp | C/G | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016131 | GGGACAGATTGGCAG[C/G]AGCATCTGCCAGAGA | 55827 |
rs111288350 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011240 | CCTGCCTCAGCCTCC[C/T]GAGTAACTGGGACTA | 55827 |
rs111293393 | snp | A/G | 8.25689e-05 | 0.00642477 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002454 | GAGTTTTAGACTTAC[A/G]TAGAATTTACCCGTT | 55827 |
rs111342825 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967847 | GCGATTCTCCTGCCT[C/T]AGCCTCCCAAGGATC | 55827 |
rs111359344 | snp | A/G | 0.00344023 | 0.0413314 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063811 | AGTTTCATGCTCTGA[A/G]TGTTTTTCCATAATG | 55827 |
rs111359998 | snp | C/G/T | 0.0387552 | 0.1337 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987219 | ATCATTCTTCCCTAG[C/G/T]TGTTAGAAGTTTATA | 55827 |
rs111370829 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011903 | GCATGAACCCAGTAG[A/G]CAGAGGTTGCAGTGA | 55827 |
rs111385664 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020882 | GAGTTGTGTGTTCCC[A/G]AGATTACAAATAGAA | 55827 |
rs111408192 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071454 | ATAAAAATAAAAAAT[-/A]AAAAAAATTATAAAT | 55827 |
rs111431245 | snp | A/C | 0.225893 | 0.248835 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980987 | TCGTGGCTCACTGCA[A/C]CCTCTGCCTCCCAGG | 55827 |
rs111444726 | snp | A/T | 0.0596104 | 0.162024 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977001 | CTCTGCCTCCTGGGT[A/T]CAAGTAATTCTCCTG | 55827 |
rs111492034 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939675 | GGCTGAGGCAGGAGA[A/G]TAGCTTGAACTTGGG | 55827 |
rs111499358 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966090 | TCCTTGTGTTTACCT[A/G]TTCATCTCTGCAATC | 55827 |
rs111518874 | in-del | -/ATTA | 0.079617 | 0.182947 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036712 | GTAAGCTAAAGGTCT[-/ATTA]ATTCAGTTATTTATC | 55827 |
rs111523265 | snp | C/T | 0.171704 | 0.237423 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963529 | CACTGCTACCTCCGC[C/T]TCCCAGGTTCAAGTG | 55827 |
rs111603041 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952420 | GAGACAGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 55827 |
rs111603458 | snp | G/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942742 | AAGTTTCATTTCTTT[G/T]CATATTAATGTGCAA | 55827 |
rs111613698 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013851 | CCCTGGCTCAAGTGA[C/T]CCTCCTACCTCAGCC | 55827 |
rs111624453 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960688 | TGGTCTAAGAGTAGA[C/G]ACTGTATGATTTTTA | 55827 |
rs111631754 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944753 | CTGTCATTCAACAGG[A/G]TTGGTTGTCTCTTCA | 55827 |
rs111644929 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979566 | CAGGAGAAGATTCCG[C/T]TGTATGTATATACCA | 55827 |
rs111654785 | snp | C/T | 0.021333 | 0.101051 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993515 | AGCGCTTTGGGAGGC[C/T]GAGGTGGGTGGATCA | 55827 |
rs111666242 | snp | A/G | 0.114036 | 0.209795 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982290 | CTTCATCGCCAGGCT[A/G]GAGTGCAGTGGTGCG | 55827 |
rs111671669 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167946515 | ACAGGTTTATCATAT[A/G]TGGCCTTTATTATTT | 55827 |
rs111673721 | snp | C/T | 0.159622 | 0.233092 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954204 | AGAGACGGGGTTTCG[C/T]CGTGTTGGCTAGGCT | 55827 |
rs111682768 | snp | C/T | 0.079617 | 0.182947 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070174 | TTTCATTTCTTTTTG[C/T]CAGCAATCAAAAAGA | 55827 |
rs111710153 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967999 | TCCTCCCAAAGTGTT[A/G]GGATTACAGGCATGA | 55827 |
rs111788379 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941447 | TTAGGTCAGTGTTTT[C/T]AAAATGTTTTAAAAA | 55827 |
rs111800889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964436 | TATCTTTGCTCCTCT[A/G]TAGATAATGTTTTTT | 55827 |
rs111815066 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994526 | GGTATATTTTACAAA[A/G]TAAATATAAGTGGGA | 55827 |
rs111819792 | in-del | -/AGGCG | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059744 | TGACCTCCTAGGCTC[-/AGGCG]AGGCGATCCTCCCAC | 55827 |
rs111860870 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000101 | GGCCTAATTTCAATA[C/T]TATTGTTGTGTCTCA | 55827 |
rs111963033 | snp | C/T | 0.5 | 0 | stop-gained | DCAF6 | GRCh38.p7 | 1:168003968 | CAAAGCAATAGAGGA[C/T]GAGGAAGATCTCGAC | 55827 |
rs112004625 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060287 | TGGGCTCAAGCCATC[C/T]TCCCACCTCGGCCTC | 55827 |
rs112018318 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991640 | AAATTTCTGGAGGCT[C/T]AGTGTCTGAAATCAG | 55827 |
rs112024454 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030690 | TCCAGAGTATAAGTT[G/T]CAGTAACAACTTCAG | 55827 |
rs112062215 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948217 | TTTGACTTCAGACAG[C/T]CTGATTATAATGTTG | 55827 |
rs112081369 | snp | C/G/T | 0.0408687 | 0.138038 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020050 | TAAACATAATACGCT[C/G/T]CAGATGTTTCAGAAC | 55827 |
rs112159049 | snp | G/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037414 | ATCTCACAGAAGAGT[G/T]TTCTTTCTGCAAGCA | 55827 |
rs112164030 | snp | A/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012569 | ATGTTTGTGATATCT[A/T]TTTAAAGGATGTAAT | 55827 |
rs112195940 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005867 | ATCCATAATAATAAG[C/T]TAAAGCTGAGCTACA | 55827 |
rs112235141 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049603 | TATGCCCTTGGAATG[A/G]AAAGAGTGTGGTTGA | 55827 |
rs112239909 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941948 | ACTGCATTCCCACCA[G/T]CAGTATATGAGAGTT | 55827 |
rs112252909 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167987359 | CTGAATCATAGTATG[A/G]GTAAGCCATGAGTAA | 55827 |
rs112255691 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032808 | ACAGCAGAGAAAAAT[A/G]TTGGGCATGGTGGTT | 55827 |
rs112271647 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997186 | ACTCAGAAAGTCAAA[C/T]TTGAGATTGTTTTTA | 55827 |
rs112277977 | in-del | -/ATAC | 0.0209421 | 0.100162 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053285 | TTTAAGGACAGTGTA[-/ATAC]ATACATGCATACAGA | 55827 |
rs112314786 | snp | C/T | 0.00190263 | 0.0307846 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168045225 | AGCAGGACCTGGTGA[C/T]AGGTTGGTAAATTTT | 55827 |
rs112331438 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049932 | AGTGCTGGGATTACC[A/G]GCATGAGCCACCGCA | 55827 |
rs112374553 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980058 | TGGTGGCATGTGCCT[A/G]TAGTCCCAGTTACTT | 55827 |
rs112461068 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966213 | TAGTATGGAGTGGCA[A/G]CTGCTAAGCTTCTTA | 55827 |
rs112481290 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054822 | CATACGGGTTTGGTT[G/T]TTTTTTTTTTTTGAG | 55827 |
rs112481640 | snp | A/G | 0.079617 | 0.182947 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072134 | AATCCCATCTGTACT[A/G]AAAAATACAAAAATT | 55827 |
rs112484352 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027392 | ATTATTTCAAAATTT[G/T]AACCTTTACCAAGAT | 55827 |
rs112505025 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014471 | CTTAGACCTCTTCTG[G/T]GTCATCCCTTACTCT | 55827 |
rs112524290 | in-del | -/AATTA | 0.230017 | 0.2492 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988150 | CTTATGCTTTAATAC[-/AATTA]AATTAAATTAATTAA | 55827 |
rs112544469 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000381 | CTATTGGAAAAAATA[A/G/T]CACCAATAGTCTTAT | 55827 |
rs112570281 | snp | G/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967971 | CCTGACCTCAAGTGA[G/T]CTGCCCACCTCATCC | 55827 |
rs112573826 | snp | A/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072932 | ATGTAAACCTTATTT[A/T]CAAAAGCAATTTGAC | 55827 |
rs112576185 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053016 | TACATTCAGAGGACT[A/G]TTGGAGTTCTCTGAA | 55827 |
rs112580171 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046622 | GCATTCTTAGTATAT[A/G]TTTTAGGCAAGTAAG | 55827 |
rs112650545 | snp | A/C | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001978 | GGATGGAATAGATAG[A/C]CTGAGGCAAGTCATA | 55827 |
rs112665573 | snp | A/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024304 | TTCAAAAACATTTTT[A/T]AAAAAATTAGCACTA | 55827 |
rs112698635 | snp | A/G | 0.5 | 0 | missense | DCAF6 | GRCh38.p7 | 1:168004541 | TTTGAAGGTGGAACA[A/G]GTCAATCAGATATTT | 55827 |
rs112751562 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011026 | TATATATAAAATTCA[C/T]CTTTAGGGCTCATAT | 55827 |
rs112801602 | snp | G/T | 0.5 | 0 | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168076186 | TTTTATGTGTTATAT[G/T]CTATACTCTTACAAT | 55827 |
rs112804999 | snp | A/G | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060306 | CACCTCGGCCTCCCA[A/G]ATAGCAGGGACTACA | 55827 |
rs112809110 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994559 | AAGATAAGTTAAAGT[A/G]GTTGTATATATTGAA | 55827 |
rs112837846 | snp | C/G/T | 0.0670745 | 0.170406 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037102 | ATGAGATTCTCCCCC[C/G/T]CCTTTTTTTTTTTTT | 55827 |
rs112843871 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011789 | TTGAGACCAGCCTGG[A/G]CAACATGGTGAAACT | 55827 |
rs112893768 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942117 | GTCGCCCAGGCTGGA[A/G]TGCAATGGCATGATC | 55827 |
rs112900094 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948777 | CTACCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 55827 |
rs112902410 | snp | C/G | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939640 | TGGTGGCGTACGCCT[C/G]TAGTCTCAGCTCCTT | 55827 |
rs112906965 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069396 | ATCCACACTGGCCCT[C/T]TTTGATTTTTGGGGA | 55827 |
rs112911679 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986881 | GCTAAATTAGAAGTG[A/G]ATACAGGCATATCTA | 55827 |
rs112940637 | snp | C/G/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167946292 | AGTCTTTAGGTTTTT[C/G/T]TAGATATAAGATCAT | 55827 |
rs112949638 | snp | A/C | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031483 | ACTAGAGTGATAGAG[A/C]CATAGGCCAGATTTT | 55827 |
rs112953607 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168039676 | ATAATTAATATATTA[A/G]TATATTAATATATTA | 55827 |
rs112979588 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019313 | GCAGCCACCCAAAGT[G/T]CTGGGATTACAGGTG | 55827 |
rs112989876 | snp | A/G | 0.279991 | 0.248195 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993745 | CAAAAGTGAAACTCC[A/G]TCTCAGAAAAAACAA | 55827 |
rs113062613 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961987 | ATTTTGAACTTGTGT[A/G]TATTTTGGGATTTTC | 55827 |
rs113066698 | snp | A/G | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025933 | GGCCACTATCCCATC[A/G]TTCACTAAGCTCTTG | 55827 |
rs113068805 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046411 | AGACAGGCAAAAATC[C/G]TGAAGAGGATAGCTT | 55827 |
rs113070317 | snp | C/G | 0.144296 | 0.226554 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948805 | TACAGGTGCCCATCA[C/G]CACACCCGGCTAATT | 55827 |
rs113097116 | snp | C/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042735 | AGACAATGTAGTTCA[C/T]TTAAAATTCAATAGA | 55827 |
rs113151068 | snp | A/G | 0.0051068 | 0.0502725 | missense | DCAF6 | GRCh38.p7 | 1:168044638 | CAGGAAGGAGTATCT[A/G]CAGAAAACCCAGTTG | 55827 |
rs113160934 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979218 | TTTAGAAAATTAAAT[C/T]AAAATCCAAAACAGC | 55827 |
rs113187924 | snp | C/T | 0.16976 | 0.236773 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008852 | TGCCCTGCCCTCCCC[C/T]GCCCCACCCCGCCTC | 55827 |
rs113203752 | in-del | -/AA | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063554 | TTACTATATTTTCAT[-/AA]GTTTCTCATTATTCT | 55827 |
rs113220041 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056223 | CTGATTCCCACTGTT[C/T]CAATGCCATTTTCTG | 55827 |
rs113250402 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983707 | GTTGCTTTTCAAATT[C/T]TACTATTAATGTCTA | 55827 |
rs113254574 | snp | C/G | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993873 | TTTTCAAGGCACTTA[C/G]AGTTCAGAAAACAAA | 55827 |
rs113324639 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019869 | CCCACAGTGTCCATA[A/G]TGACAGTCACATGGC | 55827 |
rs113373212 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940366 | TCAATGTAGGATTCT[C/T]TTTTTTGGTGGGAGG | 55827 |
rs113395630 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949048 | GCAAACGTATATTGA[A/G]TGCATACTTTGTGGC | 55827 |
rs113459149 | snp | G/T | 0.079617 | 0.182947 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060819 | GCTTGAACCTGGGAG[G/T]CAGAGGTTGCAGTGA | 55827 |
rs113474849 | in-del | -/TG | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953105 | TTTAATAATATTGAC[-/TG]TTTTTTCGGTATTAA | 55827 |
rs113536440 | snp | A/G | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966309 | ACACACGGCCCGTGG[A/G]CTGCATGAGGCCCAG | 55827 |
rs113553641 | snp | A/C/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997891 | AATGGCAATAAGTAC[A/C/G]TAAGGAGATACTCAA | 55827 |
rs113566973 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054149 | TAACGCTAACATACT[A/G]ATAGTATCTTAGTTC | 55827 |
rs113567309 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068839 | GAAACATACCTCAGT[C/T]TGCTTTTTGAATATT | 55827 |
rs113589711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986583 | TTTTGGGTTTAAAAC[C/T]GTTATACCTCAGATC | 55827 |
rs113629117 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017871 | TCCTTCATACTTTGG[C/T]ATCTTTAGAGTATCA | 55827 |
rs113638866 | in-del | -/A | 0.137187 | 0.223099 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024050 | GAGACCCCGTCTCTT[-/A]AAAAAAAAAAAAATT | 55827 |
rs113677573 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943514 | TAGATGATATTTTTA[C/T]TTATTTTTACTTTTT | 55827 |
rs113679621 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960741 | TATTTTAAGGCCTCA[A/G]ATATGGTCTGTCTTG | 55827 |
rs113696915 | snp | A/G | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993752 | GAAACTCCGTCTCAG[A/G]AAAAACAACAACAAC | 55827 |
rs113763879 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058668 | CTGCCTCCCAGGTTC[A/G]AGTGATTCTCCTGCC | 55827 |
rs113770603 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994096 | TAGTAAATAATTACT[A/G]GCGTCTATTCTTAAT | 55827 |
rs113822420 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011327 | TTCACCATGTTGGCC[A/G]GGATGGTCTTGATCT | 55827 |
rs113841757 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026604 | AAGTTAGAAATGAAT[G/T]AGAGTATGATAACCA | 55827 |
rs113848261 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013661 | TTTTTAAGCATCATC[C/T]TTCTCTCTCCTTCAG | 55827 |
rs113860874 | in-del | -/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019215 | ACTATGCCCGGCTAA[-/T]TTTTTTGTATTTTTG | 55827 |
rs113873712 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045402 | TTTACGTATTATATT[C/T]TTTGAGCACTGTGCA | 55827 |
rs113887506 | snp | C/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959605 | CCATTCTAATAGATA[C/T]GTAGTACATTTCCCT | 55827 |
rs113898939 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025184 | ATCACATACAATAAT[C/T]TTCATAGCATTACAT | 55827 |
rs113942949 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980485 | CCTTGCCAACACTTA[C/T]AATTTTTTTTTAGTG | 55827 |
rs113943976 | in-del | -/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957102 | ATAAGTGGACATTTA[-/T]TTTTTTTTTAATTTA | 55827 |
rs113980518 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985960 | GATTTTATAAAAATG[A/G]GAATCATACTGTGCC | 55827 |
rs113981354 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001077 | AGGCAGAAGTGGGAG[A/G]ATTGCTTGAGGCCAG | 55827 |
rs114021049 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959311 | TGCTTCCAAAAATTG[G/T]CAGTTATGAGTAAAG | 55827 |
rs114024286 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039798 | GAATTATATGTTGAT[A/G]TGTGATATTACTTTT | 55827 |
rs114063955 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013764 | TTATTATTATTATTT[C/T]TTGGTGGGTCTTCCT | 55827 |
rs114065251 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034112 | TGAGGAGTAACAACA[C/T]CAACAATTGATATTT | 55827 |
rs114067869 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168057694 | ATACACAGACACATA[C/T]ACATAGTTACAATAC | 55827 |
rs114087018 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986435 | AATTTATATTTCCTC[A/G]ATGGCTGAGTTTGAA | 55827 |
rs114094645 | snp | C/G | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975237 | ATGCAAGTAATAGTA[C/G]TCTAAGATGGGTTTG | 55827 |
rs114101251 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018013 | ATTTTAAAAAGTATA[A/G]AAAGAATTTCTGCAT | 55827 |
rs114101507 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039019 | TGTAATAGTCCATCA[A/G]GTAGATGTTCTATAG | 55827 |
rs114134571 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935420 | TGTTTCATGGTGGCC[C/T]CAGACAGTTTGGTGG | 55827 |
rs114192610 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030852 | GGTACTGTTGGAGAT[C/T]AACAGGTGACTTTTT | 55827 |
rs114203853 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024973 | CAAACTAAGGAATTA[A/C]GCATGTGTTATTTTA | 55827 |
rs114207848 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046892 | AGTAGAACATGATAC[A/G]GAGGTCATAATTGAA | 55827 |
rs114208770 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941888 | GGTAAGTATGTTTAA[C/T]TTTATAAAAAACTTC | 55827 |
rs114209044 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984377 | TTATAAGAAATAGAT[A/G]CATGTTTTAATAATT | 55827 |
rs114210274 | snp | A/G | 0.00435278 | 0.0464483 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987445 | ATGTTTTTCAGAGCC[A/G]TCTGTTTAAATGTTC | 55827 |
rs114217863 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988251 | CTGCAGCCTCAATCT[G/T]CTGGGCTCGAGTAAT | 55827 |
rs114258209 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051191 | TATGGCAAAGTAACT[A/G]TAATCTGAAATGATG | 55827 |
rs114306523 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067121 | GGGTTCTCATATACT[A/G]TTTCTTATGAAAATG | 55827 |
rs114320524 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949510 | AAGATTTAGGTTCCC[C/T]AAGTTCAAGATTCCT | 55827 |
rs114349314 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021943 | TGCTAAGAACTAGAG[C/T]ACAGGATATTAGAAA | 55827 |
rs114352374 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071486 | CAAAAATACAAAAAT[C/T]AGCTGGACGTGATGG | 55827 |
rs114353298 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972970 | TAAACCTCTTAAGTG[A/G]AGGTAAATCATAAAT | 55827 |
rs114362113 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072872 | ATTATCTTCCCCAGT[C/T]TCCTGAAGAAATATT | 55827 |
rs114366852 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061355 | CATCTTTTTATTATG[A/G]AAGTAGAAGTATATA | 55827 |
rs114379553 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937449 | TTAGGTGTCGGCTGC[A/G]ACGCGTTGACCACCC | 55827 |
rs114380339 | snp | C/T | 0.0275645 | 0.114116 | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168076227 | ACAGAAAAAGTGTTA[C/T]TAAGAAAATCATAAG | 55827 |
rs114380644 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983645 | CTTCTTTGGCATGTG[C/T]ACATTCTTATATATG | 55827 |
rs114382142 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048229 | TGCCCACCTAAAAGG[A/T]TGTATGTCTTAAAGT | 55827 |
rs114386721 | snp | A/C/T | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005128 | TCTAGATTTATTTGG[A/C/T]TTTATGTCTATATTA | 55827 |
rs114387368 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052217 | TAATTGTATGACAAT[A/G]AAATGGAATTTGCTT | 55827 |
rs114395322 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965742 | AGCAGTTCTCCTGTC[A/G]GGAGGCTGAGGCCTC | 55827 |
rs114403535 | snp | A/T | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005947 | AATAAAATATTTTGG[A/T]AGATTTGGGAATTAA | 55827 |
rs114441489 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957144 | ATACTATAAAACTGA[C/T]GCATCTTAAGTGTTC | 55827 |
rs114529053 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997434 | CCTGTCACACACTTA[C/T]GTCTTCCTGTGTAGA | 55827 |
rs114545588 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949093 | GTATTTGGAATACAT[C/G]GGTCAATAAAGCAGT | 55827 |
rs114573675 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955363 | TTGTTTTCCAGTATC[A/G]TTGTACCGTTTAACA | 55827 |
rs114583974 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019715 | TTTACCAATTGGAAA[A/C]AAGTAATTTTTATAC | 55827 |
rs114585189 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979035 | TCCTGGTTAAGAAAT[A/C]TTTTCCTATCCCAAA | 55827 |
rs114596703 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | DCAF6 | GRCh38.p7 | 1:167947216 | GGAATCAGTTGTAAT[G/T]TCTCCTTTTTCATTT | 55827 |
rs114644930 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975344 | TGTACTAGGCTTTAC[C/T]CTTTTAAACAATCGC | 55827 |
rs114673055 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993140 | TGCTACATTAAGTCA[C/T]ATGTAATAATTCAGA | 55827 |
rs114713430 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059784 | CTGAGTAGCTGGGAC[C/T]ACAGATGTGTGCCAC | 55827 |
rs114751730 | snp | C/G/T | 0.0162516 | 0.088765 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065439 | AGGTGTGAGCCACTG[C/G/T]GCCCAGCATCAATTT | 55827 |
rs114796522 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957418 | GGTTAATCCATGTTG[C/T]AGTATGTGTCAGTAT | 55827 |