SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs114879636 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001449 | TCAGTGAACTTGGCA[A/G]TTGATCATTCACTGG | 55827 |
rs114883970 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020604 | TAAACTACCATTGGA[C/G]CATATATTCAGGTTT | 55827 |
rs114902296 | snp | G/T | 0.0212758 | 0.100922 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019588 | CTGCTCAGAGTGACA[G/T]CACCCTGTGGAGTCT | 55827 |
rs114922140 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005146 | TATGTCTATATTAAA[A/G]TGATTATGAAAATAT | 55827 |
rs114970675 | snp | C/T | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025026 | ACAATGAAGAATAAT[C/T]AAGGCAAAATACAAC | 55827 |
rs114972287 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006669 | ATTGTCCATTGGGTG[A/T]ATGTAGTAGATGGAA | 55827 |
rs115006992 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019471 | ACATGTATCAGATGA[A/C]TGTCCTAAACAGGTA | 55827 |
rs115015863 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066025 | TGAACTTTTTATTGT[A/G]TATCCAAATGGAACA | 55827 |
rs115025363 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940388 | GGTGGGAGGCGGGGG[A/G]CAGGGTGAGGCAGGG | 55827 |
rs115058304 | snp | A/G | 0.000115408 | 0.00759543 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168004726 | TTCTACTCCTTTGCT[A/G]TCTTCTCCAGACAGT | 55827 |
rs115113304 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990985 | ATTGAGTATATTTAT[C/T]TTGATTTCACATAGG | 55827 |
rs115132069 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002152 | ATAGAAAACTAAGGC[G/T]CAAGATGGTTAAAAA | 55827 |
rs115151729 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997330 | TTTTAAGAATAGTTC[A/G]TATGAAGGATGAAGC | 55827 |
rs115171490 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974296 | CTTTATCTGCAACAA[A/G]TTATACAAATATTAA | 55827 |
rs115214496 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970696 | CCAATGATTCATTAT[A/T]TAGGAAAAAAAGCTT | 55827 |
rs115220686 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983011 | TCTCTATTCTGTTTC[A/G]TTGGCCTGTGTGTCT | 55827 |
rs115222049 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051711 | AAAATATAATAGATG[C/T]ATGGAAATTTCTGGT | 55827 |
rs115244694 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040693 | GAGCTGGCATCTTCT[A/G]AAGAATCTTATCTAA | 55827 |
rs115252715 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973086 | GTGTGTAGTTAGCTA[C/T]TTGGTAAACCACCCT | 55827 |
rs115260205 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996185 | ATAATTTCTTTCATT[A/T]TTTTCCCCCTTCTTT | 55827 |
rs115270655 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990673 | AATTGTCACATAAAT[A/T]TGAGTTTCTTGGATT | 55827 |
rs115277456 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959337 | TAAAGTTGCCATAAA[C/T]GTTTGTGGGCAGGTG | 55827 |
rs115295501 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942004 | ATTTGGTGTAGTGAG[C/T]CTTCCTAATTGTAGC | 55827 |
rs115311406 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988496 | AAACTTACAAAAGGC[C/T]TGAGAAATCATTCAG | 55827 |
rs115319343 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988430 | ACTTGGTGTCCCAAA[A/G]TGCTGAGATTACAGG | 55827 |
rs115320696 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028458 | AGTTGACAGTGCCAT[C/G]GAGTTTGAAACTTAC | 55827 |
rs115348578 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045971 | TAAAATCCTAGTTTA[C/T]AAAGGAGTGAGATTC | 55827 |
rs115356785 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960174 | CAAAGGTCCGATGAT[C/T]GTGTTTATGTGGGTC | 55827 |
rs115361097 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014885 | GCTTTCCTGAGTTGC[A/C]ATATATAAAATAACC | 55827 |
rs115395532 | snp | C/T | 0.040671 | 0.13668 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061898 | TGAGGTCTAGCAGCT[C/T]CTCTTCTAGGTATAT | 55827 |
rs115447175 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957447 | ATTTCATTCCTTTTT[A/G]TGATTGAATAAATAT | 55827 |
rs115449347 | snp | A/T | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967560 | CTTCTGTTTTAGAAA[A/T]ATGACTAAATAGTTA | 55827 |
rs115458032 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965941 | CGCCCGGCCTTCCCT[A/G]GAGTTTTTAACATTC | 55827 |
rs115469907 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074203 | AGTCCCTTCAGTGTA[C/G]TGTTCTTGGTGCTGT | 55827 |
rs115486373 | snp | A/C | 0.0333695 | 0.124785 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961665 | TTTCTTGTCTTACTG[A/C]ATTAGCTAGGACTTA | 55827 |
rs115500630 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017251 | TTGCTGTATATAAAC[A/G]TCTAGCAAACATGTT | 55827 |
rs115506969 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063858 | TGCCAATGGGATTTC[A/C]GTATTACATTATTAA | 55827 |
rs115508774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944898 | AGTTGATTTTTATGT[A/G]TTAGTGAGAGATAAG | 55827 |
rs115549576 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949623 | AACCAATGTAAACCT[G/T]AAGCTCATACTGCTT | 55827 |
rs115556973 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019844 | GCAGGCTCTAAACAA[C/T]ACCAGATTTCCCACA | 55827 |
rs115595668 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939403 | TTTTTTTGTGTGTGG[C/T]GATAAAATGACTTTA | 55827 |
rs115685338 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953136 | ATCTAATATATAGTC[C/T]ATATTTTCTTTGTTT | 55827 |
rs115689553 | snp | A/G | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033133 | CACAGCGTGTGCATT[A/G]CAAAAAATAGTTACT | 55827 |
rs115700732 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014220 | TAAAATAGCTCTTGT[C/T]GAGGTCATCAATGAC | 55827 |
rs115712172 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964235 | TGCAAAGTAGGTCTG[C/T]TGGCAACAAATTCCC | 55827 |
rs115720978 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984374 | TAATTATAAGAAATA[C/G]ATACATGTTTTAATA | 55827 |
rs115749020 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990085 | GGAGAAAGGTTTTAT[A/G]AGTAAAAAGTATAAA | 55827 |
rs115751470 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958085 | ATATTTCCCTTCATT[C/T]TATGGGTTGTCTTTT | 55827 |
rs115859007 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958910 | AAAGTCCATAGTTTA[A/C]AATAGGGCTCACTCT | 55827 |
rs115860742 | snp | A/G | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949362 | GTGAATAGCCTTGGA[A/G]TATATAACAATTCTA | 55827 |
rs115881225 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983049 | GTACCAGTACTATGC[C/T]GTTTTGGTTACTGTA | 55827 |
rs115885665 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065485 | TCTAAGCCAGTTTTT[A/T]AAAAAATGTAAGAAT | 55827 |
rs115893613 | snp | A/C | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936422 | GTGAGCGAGAGACTA[A/C]AGAATTGAGTAGCTT | 55827 |
rs115901801 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940669 | TATCCCATATATATA[C/T]GGTTTTGTAAAGATA | 55827 |
rs115906613 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964575 | CTTACTGGATCTATG[A/G]TTTGGTTTCTCACAT | 55827 |
rs115990438 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037256 | GATATAAGTCCTTCA[C/T]TGCAATAGAAAGTAG | 55827 |
rs115991365 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016782 | CTATAGTAGGTATAA[A/T]AAGTTATTTAGGAAC | 55827 |
rs116025282 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967609 | CTTAAACATTCAACA[C/T]ATCATTTAAAGTTCC | 55827 |
rs116026359 | snp | A/G | 0.0402882 | 0.136092 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167996977 | AGTAACTTTCTATGT[A/G]TATTTTGCTTTTTCA | 55827 |
rs116036262 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020288 | TTGCCCAGGGTTACA[A/G]TATTACTGAGTAGAA | 55827 |
rs116038177 | snp | C/T | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945570 | AATCTCGGCTTACTA[C/T]AACCTCCGGCTCCCA | 55827 |
rs116045381 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067233 | GTATACTTTCACTCA[C/T]TGAATAGGCATTTAT | 55827 |
rs116047178 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012968 | TTTGGTAACTCAATA[G/T]AGAGGGTTGACACTC | 55827 |
rs116048893 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001792 | AAAGCACAGATGGAG[A/G]AATTAGGCTTAAATA | 55827 |
rs116064922 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016534 | AAGTACTCCACAGTC[C/T]CATGTTCTTATTATG | 55827 |
rs116140231 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997550 | ATGCAAAGATTTTTT[C/T]CTATTCATGTTACTA | 55827 |
rs116150926 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058264 | TTTTGGTATTAACAG[C/T]GCTGCTTTGAGCATT | 55827 |
rs116185029 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016321 | TGCTTTATGGCTCCT[A/G]GCTCTTCTTCTTCTT | 55827 |
rs116214470 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050710 | TTCTGTTTCCTTAAT[C/T]TCTTCATATACATTT | 55827 |
rs116216125 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961075 | TCATTCAATTTATAC[C/G]TAAGTGTTTCATGTT | 55827 |
rs116223143 | snp | A/T | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036372 | ATCTGAGAAATTCAG[A/T]CTTACACTTCTCTCA | 55827 |
rs116233090 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000334 | AATATGAGAATTACT[A/G]AAATGTGACACAAAC | 55827 |
rs116250480 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983068 | TTGGTTACTGTAGCC[C/T]TAAAGTATGGTTTGC | 55827 |
rs116250729 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026758 | TTGGATATCCACGTG[A/G]AGAGATCTCATAGAT | 55827 |
rs116316010 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997329 | GTTTTAAGAATAGTT[C/T]GTATGAAGGATGAAG | 55827 |
rs116322917 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962126 | AGTGTGGTCTGTCTT[A/G]GTAAATGTTTCATGT | 55827 |
rs116331567 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167939063 | GTGGTTTTCTAAGTA[C/T]TTGAAAATACTTTTT | 55827 |
rs116459507 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994689 | CAGCTGTAGAAAAAT[G/T]TTTGCTTTAACCTGT | 55827 |
rs116461989 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071838 | CTGACTTCCACTCAG[A/T]CCACCTTTTTTTCTA | 55827 |
rs116472455 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992616 | TCATTTTGCAAGGTT[A/T]TACAGCTTTGTGGGA | 55827 |
rs116543893 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030338 | ATAGCATATTGCAGA[G/T]CCTCTGAGATGCCAC | 55827 |
rs116544532 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037620 | ACTCTATTAATTTGT[C/G]TAGGCTTTCTTGATT | 55827 |
rs116549253 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956052 | ATTACAGGTATGAGC[C/T]GCTGTGCTTAGCTAA | 55827 |
rs116556792 | snp | A/T | 0.030665 | 0.119967 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938513 | CTTCTGTGCATTTGT[A/T]GTAGGATAAGTACCT | 55827 |
rs116559002 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977489 | ATAGGTAACCTGTTT[A/C]TTTTCCTTGACTACT | 55827 |
rs116559787 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020169 | TGTCTGAATATTTTA[C/T]ATGGATTATCTCATT | 55827 |
rs116625183 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034044 | AAGTGATAATTTTGG[C/T]TACCAGAACTCTTAA | 55827 |
rs116630188 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951131 | CCTCTCATAAGCAGG[C/T]AGAAATCTTTTTGTT | 55827 |
rs116642314 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021937 | AACATTTGCTAAGAA[C/T]TAGAGCACAGGATAT | 55827 |
rs116696121 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008445 | TCAGCAAGTTCTTTT[C/G]TTCCTGTATCTAAAC | 55827 |
rs116732894 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | DCAF6 | GRCh38.p7 | 1:168057417 | AATAGTAAAATACAA[A/G]GTCAGGAGTCTAGGT | 55827 |
rs116733878 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983544 | CAAGTGCCTTGGAAA[C/T]TTACAACTCTGCCTT | 55827 |
rs116798411 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042943 | TTTTTTGGTCTACCT[C/T]TCTAGTTGTAAAATA | 55827 |
rs116804234 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956695 | AAATAGAGGTTTCTT[C/T]GGTGCTGTAAATTTT | 55827 |
rs116823587 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943829 | TCCACGTTGCTGTAT[A/G]TGTCATGATTTCATT | 55827 |
rs117000515 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003096 | AACCAAAATCTTACT[A/G]TAATGACTTCTGAAA | 55827 |
rs117253811 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002700 | ATATAGGTATACTTA[A/T]GCAAATATATCTTAG | 55827 |
rs117475307 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038781 | GAAAATGCAAAAGAT[A/G]ATACTAATAATAATA | 55827 |
rs117506283 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019949 | TAGTTAATAAATTAG[A/T]TATATTAGTCTGGTT | 55827 |
rs117560141 | snp | A/T | 0.0387552 | 0.1337 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987252 | TTCAGATAACTTTTT[A/T]TCTGAAGTTAAGTTA | 55827 |
rs117626621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970948 | TACCCTATTATGGCA[C/T]AGGTGAAAGAGAAGG | 55827 |
rs117645438 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022020 | TGTTTCTCTTTTACT[A/G]TAGCCCTACTGGAAC | 55827 |
rs117678565 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965239 | AAAGAGCCTATACGT[C/T]TGAACTGTGGGCTTC | 55827 |
rs117876264 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965660 | TGAGACAGAGTCTTG[C/T]TCTGTCGCGTAGGCT | 55827 |
rs117917149 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998178 | CAGATCTTTTGGTTT[C/T]CCAGTGCATGTAAAA | 55827 |
rs118036657 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043619 | ACAATTACATGAAAT[C/T]TAATGTCTAGCACAG | 55827 |
rs137863197 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955563 | CTTCCTGAACTCTCA[C/T]ATTCATTCAAGTAGC | 55827 |
rs137882219 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025292 | TCCCAGATTTTTTAC[A/T]TCAGTGCCTGGGTAG | 55827 |
rs137901174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983502 | TTCCAGTCTTTGTCA[A/G]AGGGGCCTGTGTGTT | 55827 |
rs137942309 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021234 | AATAAATGTTTGAAG[A/T]TAAGATTTCTTGGAG | 55827 |
rs137968136 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066063 | ATTTTTAGTCTTCAC[A/G]TAGCTGAATTAATTT | 55827 |
rs138091563 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015729 | TAATCAAATTCTTAT[C/T]ATTTTCTATTTTATT | 55827 |
rs138105548 | in-del | -/AATA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168015317 | TTTAGAGCTCTTCTC[-/AATA]AATTCTGAGTTGTTT | 55827 |
rs138106371 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052510 | TGGAAACTTCTAATT[A/G]TAAGGCAGTATTTTC | 55827 |
rs138113663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978078 | ATTCATCCATGTTGT[A/G]TGTAACTATAATTTG | 55827 |
rs138116371 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971547 | TGGATACTTTTGGAC[G/T]GAGCTTCAAGTTTTG | 55827 |
rs138134552 | snp | C/T | 0.00165437 | 0.0287132 | synonymous-codon, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167951813 | AGGAAGAAGAGAATT[C/T]ATCCAAAGATTAAAA | 55827 |
rs138142223 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986308 | ATTGTACCATTTTAT[A/C]CTCCCATCAGCAATG | 55827 |
rs138158820 | in-del | -/A | 0.0333695 | 0.124785 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956242 | ACTATAATTCCATTT[-/A]ATTTAGTAAAAATAA | 55827 |
rs138202115 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048334 | ATATTATACAAGTGT[A/T]TACTTAATTTGATCT | 55827 |
rs138204713 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049431 | GTTGTTGTTGTTGTT[G/T]TTTTTTTTTTTTTTT | 55827 |
rs138236578 | in-del | -/TTCT | 0.0356815 | 0.128715 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964143 | CTCCTTCAGTGCTCC[-/TTCT]TTCTTTATGTAGATA | 55827 |
rs138241562 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001300 | CTGCCTGGAAAAAAA[A/G]AAGTTAAAAATGTAA | 55827 |
rs138243810 | in-del | -/TCTAT | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969612 | AATAAGTGTGTATCA[-/TCTAT]CAGCTGAAAAAGAAG | 55827 |
rs138248125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966895 | GTGGGTCTCTTAGAT[C/T]ACTTAGGGAAACAAG | 55827 |
rs138263364 | snp | A/G | 0.000436906 | 0.0147737 | missense | DCAF6 | GRCh38.p7 | 1:168004559 | CAATCAGATATTTCA[A/G]CTCTTCCTACGGTCC | 55827 |
rs138270916 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041766 | AATGTATACACTAAG[C/T]GTTTTATTCATGCCT | 55827 |
rs138318449 | in-del | -/T | 0.0893983 | 0.191591 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050958 | TATGTTCCTTCATAA[-/T]TTTTTTTTTATGATG | 55827 |
rs138321307 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042494 | TTACCCTGTCCTTCT[A/G]CAGAACTATGATGCT | 55827 |
rs138398953 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020148 | AAATGACCCATTCCT[A/G]TGTGCTGTCTGAATA | 55827 |
rs138400025 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991710 | TGCCTTCTCCCCTAG[C/T]TCATGGTGGTTGCTG | 55827 |
rs138412743 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943156 | CCTTGTGATCTGCCC[A/G]CCTTGGCCTACCAAA | 55827 |
rs138427386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026026 | GCTGTTCCCTCTACC[A/G]AAACTACTTTTTTGT | 55827 |
rs138475087 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993573 | TGACCAACATGGAGA[A/T]ACCCCGTCTTTACTA | 55827 |
rs138486290 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007725 | TTCGTGTTTCTTGTT[C/G]TATCTCCTTCTGAAT | 55827 |
rs138490924 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935487 | GTTTGGGTTGGAGTC[C/G]TGCGTAAGGGAGCGG | 55827 |
rs138501587 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995848 | AATATTTATTGGGTG[C/G]CTACTATACACCAAG | 55827 |
rs138534958 | snp | A/G | 0.113685 | 0.209567 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939661 | TCAGCTCCTTGGGAG[A/G]CTGAGGCAGGAGAAT | 55827 |
rs138546313 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952856 | AAACAGAGCTCTTTT[C/T]AATTTTTATTATAAA | 55827 |
rs138550377 | snp | A/C | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036373 | TCTGAGAAATTCAGT[A/C]TTACACTTCTCTCAC | 55827 |
rs138593814 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060825 | ACCTGGGAGGCAGAG[A/G]TTGCAGTGAGCTGAG | 55827 |
rs138632512 | in-del | -/GTATCTGGC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167978018 | TTTGTTGTTGTTTTT[-/GTATCTGGC]TTTTTTTGCTGAGCA | 55827 |
rs138653430 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981159 | TAATCTGCCCGTCTC[C/T]GCCTCCAAAGTGCTG | 55827 |
rs138673343 | in-del | -/T | 0.0333695 | 0.124785 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005390 | TCTGTTAAAATGCTA[-/T]TTTTTTTCTCAGTAT | 55827 |
rs138674790 | in-del | -/CGCACA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041893 | AATACATGTTTGTCG[-/CGCACA]CACACACACACACAC | 55827 |
rs138677391 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937953 | AAAGTGTTTGTTGCT[C/T]TCATTTGTTTTTGAT | 55827 |
rs138744694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958156 | ATTTTGGTGAAGTCT[A/G]ATTTCTTTTTGCTGT | 55827 |
rs138771849 | snp | C/T | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954535 | TCGGCTCACTGCAAG[C/T]TCCGCCTCCCGGATT | 55827 |
rs138812460 | snp | G/T | 0.0333695 | 0.124785 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008112 | GTAGCTGGGATTACA[G/T]GTTCCTGCCACCACA | 55827 |
rs138815900 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052364 | AAAAGCTGAAACACT[A/G]AAGTAGAGATTATCA | 55827 |
rs138818852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059509 | CTTTGTCCTTTGGTT[A/G]ATTTTATAATCAACT | 55827 |
rs138819017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012169 | TTTATAGCAGGCAGA[A/T]AAAGTGCCACCAAAT | 55827 |
rs138821548 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977437 | CTTCCATTGTTGAAG[C/T]TGCAAAGTCAGACAT | 55827 |
rs138830172 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967259 | AGTTCTTGAGGTACT[A/G]AGAAAATTAAAATGG | 55827 |
rs138832533 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011692 | GGTTAGAAACAAGTG[A/G]AGAGACCAGGTGTGG | 55827 |
rs138855103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014843 | ATTTCCTCGAGGTGT[C/T]TGTTCAAGTGGTGCC | 55827 |
rs138890139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000695 | CTGATACCTGCTACA[A/G]TATGAATAAACCTTG | 55827 |
rs138905267 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988265 | TTCTGGGCTCGAGTA[A/G]TCTTCCTGCCTTAGC | 55827 |
rs138913911 | in-del | -/TTTTTTAT | 0.159292 | 0.232964 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954441 | GTGCTTAAATTTTTA[-/TTTTTTAT]TTTTTTATTTTTTTA | 55827 |
rs138948724 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045907 | ATTATTAGTGCTATC[A/G]TATCTTATTGTAAGT | 55827 |
rs139026909 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971133 | TCTTTCTGAGATCAC[C/G]TGCTTTCTCGGGTAT | 55827 |
rs139032648 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941659 | GAAAATTGTTCTAGA[A/T]GGTGTGTAGTTCTTG | 55827 |
rs139102633 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953127 | TCGGTATTAATCTAA[C/T]ATATAGTCCATATTT | 55827 |
rs139105556 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064292 | TTTTGTAGTTTTTAC[A/G]ATCTACAAGTTTCTA | 55827 |
rs139118311 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053380 | ATCTCCCTGCATGAT[A/G]TGGGTTTTTGCTTTC | 55827 |
rs139143256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003725 | GAGAGCTCTAATAGA[C/T]TTATATACATTCATA | 55827 |
rs139170636 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017432 | GGAAAGAAGTATACA[C/T]TGTAGATGTTGGAAA | 55827 |
rs139202721 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049876 | TAGCCAGGATGATCT[C/T]GATCTCCTGACCTCG | 55827 |
rs139207525 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979652 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCAGATCA | 55827 |
rs139231779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030209 | GAGAGTGGGCCTTCA[C/T]TCCCTCCAGTTGAGG | 55827 |
rs139240197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959565 | CCTTGCCAGTATTTG[A/G]TGTTGTCAGTGTTCT | 55827 |
rs139268768 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959870 | AATTTTAATGAAGTC[A/G]GTCTTATCAATGATT | 55827 |
rs139276016 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035987 | GAATTGCTGGAACCC[A/G]GGAGGCGGAGCTTGC | 55827 |
rs139280557 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963673 | ACCTCAAGTGATCCA[C/T]CCACCTTGGCCTCCC | 55827 |
rs139281402 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032561 | GAGATAGTTAAACTT[C/T]ATTATTTTTTCAGAA | 55827 |
rs139283821 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068747 | TTAGGATATATTATC[A/G]TGCATATTCTTTAAT | 55827 |
rs139331954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965334 | GTTATGTATTTTCCT[C/T]CCCCAATGCGGAAGG | 55827 |
rs139373056 | snp | C/T | 6.60186e-05 | 0.00574499 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167987521 | ACCCAATGACCCTTA[C/T]ACTTTTCTCTCTTGT | 55827 |
rs139393023 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061506 | GCAGTATAATGGTGA[C/T]ATCTTTCATGTGGTT | 55827 |
rs139412260 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018341 | AATGAGCTGTATAAA[A/G]TAGGTATTAGAAGAT | 55827 |
rs139414177 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951309 | GCCGGGCGTGGTGGC[C/T]CACACCTGTAATCCT | 55827 |
rs139435890 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009390 | CTTCCTTCCTTCCTT[C/T]CTTTCTTTCTTTCTC | 55827 |
rs139515957 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013581 | AAACCAATTCCTCCT[C/G]TGATACACTGGAACT | 55827 |
rs139560022 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042945 | TTTTGGTCTACCTTT[C/T]TAGTTGTAAAATATA | 55827 |
rs139583115 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039594 | TTTCTTAATATATAA[A/T]ATAGTTGTATAATAT | 55827 |
rs139668542 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053708 | GTTTACTGGGGTCTG[A/G]TCATGTAGGCACCTC | 55827 |
rs139688445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038285 | TATGACAAGGACAAC[C/G]TAATATAAGTTTTAT | 55827 |
rs139707829 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993698 | AGGTTGTGGTGAGCC[A/G]AAATCACGCCATCGC | 55827 |
rs139738177 | snp | A/G/T | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968648 | CAGGACTCTGGTGCT[A/G/T]TGGTGTTGGGGAAAC | 55827 |
rs139779448 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972270 | ATAGATTTGGTTTCA[A/G]CAATTAAAGAACAAA | 55827 |
rs139811354 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949364 | GAATAGCCTTGGAAT[A/G]TATAACAATTCTAAA | 55827 |
rs139851098 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981371 | TACTTTATGGATTCA[G/T]TTTTTTCCTCAACTT | 55827 |
rs139859129 | in-del | -/A | 0.0333695 | 0.124785 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008487 | TCTTTTCATCTCACC[-/A]TCATTTCTTGTCTCC | 55827 |
rs139871396 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983858 | AGGATGGGGTTGAAT[A/G]TGGTCAGATTCATGT | 55827 |
rs139871460 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945004 | AGTGTATGTTCTTGT[C/T]GGCTTTGTCAAACAT | 55827 |
rs139909081 | snp | G/T | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995152 | CTTGAAATACATGGG[G/T]AAGTAAAGTTATAGT | 55827 |
rs139992607 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981850 | ACATGTGAGTGCATG[C/T]GTCTTTTTGGTAGAA | 55827 |
rs140021384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965145 | AAGTAATGGTATAAA[C/T]AGGTCCTTAGGAATT | 55827 |
rs140060354 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997399 | CACAGCTGCCACATT[A/G]AGCTTTGTTCTGGTT | 55827 |
rs140068460 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040699 | GCATCTTCTGAAGAA[A/T]CTTATCTAAACTTTT | 55827 |
rs140122746 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013895 | CAAGTGTGCATCACC[A/G]TGCCTGGCTAATTTT | 55827 |
rs140157351 | snp | A/C | 0.0399052 | 0.1355 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984982 | TGAAAGGCATGTCTC[A/C]CATGACAGCAGACAA | 55827 |
rs140202403 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988846 | AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA | 55827 |
rs140206944 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058578 | TTTTTTGTTTGTTTG[A/T]TTGTTTGTTTTGAGA | 55827 |
rs140282832 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049902 | CCTCGTGATCCGCCT[A/G]CCTCAGCCTCCCAAA | 55827 |
rs140334920 | snp | C/T | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961203 | TGTATCCTATTACTT[C/T]GCTACAATCACTTAT | 55827 |
rs140369690 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995557 | TGGTGGCAGGCGCCT[A/G]TAATCCCAGCTACTT | 55827 |
rs140373542 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025003 | ATATGTTTATTACAG[A/C]GGTATTAACAATGAA | 55827 |
rs140374328 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168074108 | TACATTATGTCATTG[C/G]TTTGACATTGGATTA | 55827 |
rs140405173 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957873 | TTTTGGTTTTTATTT[A/C/T]TCTGATGACTAATGA | 55827 |
rs140411490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059536 | AACTTTTTCAGTTCT[A/G]CAAATAAGTCATCAG | 55827 |
rs140435572 | snp | C/G | 0.046775 | 0.145601 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011725 | GCTCATGCCTGTAAT[C/G]CCAGCACTTTGGAAG | 55827 |
rs140439456 | in-del | -/TGTG | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938272 | GGGTGTGTGTGTGTT[-/TGTG]TGTGTGTGTATGAGA | 55827 |
rs140466531 | snp | C/T | 6.60164e-05 | 0.0057449 | missense | DCAF6 | GRCh38.p7 | 1:168065743 | CCACATCCGTTTGAC[C/T]CAAGTAAGATATCTT | 55827 |
rs140500191 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954043 | ACTGAGTCTCACTCC[A/G]TCTTCCAGGCTGGAG | 55827 |
rs140538505 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007189 | CATTGTGATAGAAGC[A/G]GAAAGCTCCTATCAA | 55827 |
rs140581779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005055 | ATAGTGTTTTGACAT[A/G]GTTTAATGTGCCTGA | 55827 |
rs140623896 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939899 | TAAACATTACGATTG[C/T]CTATCTACAGGGTTG | 55827 |
rs140658846 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935094 | CTCAAGGTCACAACT[A/G]TAAGTGGTAGAAGAG | 55827 |
rs140678533 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942059 | TATCATTGTTTTAAT[G/T]TGCATTTCTCTTTTT | 55827 |
rs140691275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067009 | CTGAGTTCTTTGGAG[A/C]TCTGGATTTCTTCTG | 55827 |
rs140691986 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | DCAF6 | GRCh38.p7 | 1:168047718 | TGTGTGTGTGTGTAT[A/G]TATATATAAAAGATG | 55827 |
rs140698633 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971182 | ATTTAAAATTCATTC[G/T]TCAAATCTCAGCTCT | 55827 |
rs140717937 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976559 | TGTTTCTTGCTTCTA[A/C]GATAGACATTCATTT | 55827 |
rs140737439 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943193 | GGATTACAGGCGTGA[C/G]CCACCGCGCCTGGCC | 55827 |
rs140737781 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051415 | CCTTATAAATAGTTT[A/G]GAAATAGTGTCACAT | 55827 |
rs140740178 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953664 | GGAGTGAGTGGTGCA[A/G]TCTTGGCTCACTGCA | 55827 |
rs140822421 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168029185 | TCCAGTTTGTTTAAC[G/T]TAGAATTGTCTTATC | 55827 |
rs140861073 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033590 | CCAAAGTGCTGGGAT[C/T]ACAGGTGTGAGCCAC | 55827 |
rs140867815 | snp | A/G | 0.040671 | 0.13668 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961521 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCT | 55827 |
rs140905828 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020092 | ATTATTTTTCATTCA[A/G]TACCATATGTCTGAA | 55827 |
rs140916263 | in-del | -/TTC | 0.0599851 | 0.162463 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010806 | ATCTCTTTCAGTTAT[-/TTC]TTAAGTTAAGCCTAG | 55827 |
rs140973207 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027970 | GCACATTGTTATTAA[C/T]TGTATCCTATTATAA | 55827 |
rs140985069 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071591 | GTGAGCCAAAATTGC[A/G]CCACTACACTCCAGC | 55827 |
rs140988432 | in-del | -/CTTC/TC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009461 | TTTCTGTCTCTCTCT[-/CTTC/TC]CTTCCTTCCTCCCTC | 55827 |
rs140990750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985787 | GAAAAGTGCTGGCAT[C/T]GTGTATTTGTGCAAC | 55827 |
rs141009321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038732 | CTTTCCAGATGATGC[C/T]GGTGCTGCTCATCCT | 55827 |
rs141011750 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014520 | CATCCAAATTTATAT[A/C]TCTGAATTGTAGACT | 55827 |
rs141032990 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045558 | ACTTAGCTCTCAGAT[A/T]ATCTTGTAGATATCC | 55827 |
rs141034177 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970252 | TTTTTAAAGAAATGA[C/T]GATCCCTTTGATGTA | 55827 |
rs141036819 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955870 | GGCTCAAGCTATCTT[C/G]CCACCTCAGCCTCCT | 55827 |
rs141073015 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986562 | TTTTCCATGGAGTGG[G/T]GATGGTTTTGGGTTT | 55827 |
rs141109546 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965888 | GATCCACCCGCTTTG[G/T]CCTCCCAAAGTGCTG | 55827 |
rs141112909 | in-del | -/AG | 0.079617 | 0.182947 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031201 | TAGAAAGAAGAGGAC[-/AG]AGTAAGAGAGCTAAA | 55827 |
rs141127179 | in-del | -/CTT | 0.227959 | 0.249026 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973757 | ATATTCCCCACTCAC[-/CTT]CTCTCTATTGTATAT | 55827 |
rs141127612 | snp | A/C | 1.64893e-05 | 0.0028713 | missense | DCAF6 | GRCh38.p7 | 1:168063734 | TAAAAATGGTTTATA[A/C]AGGCCATCGCAACTC | 55827 |
rs141154760 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052987 | TACATTGCCATACTT[A/G]GAGTGTCACTGAATA | 55827 |
rs141159142 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069488 | TCTGTTGAGATAACT[A/T]CTTACTGTAAGAACT | 55827 |
rs141177213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029662 | CATTTTTCAGATGAG[A/G]AAACTGAGGCAAAGG | 55827 |
rs141191160 | snp | C/G/T | 1.6476e-05 | 0.00287014 | missense | DCAF6 | GRCh38.p7 | 1:167991270 | CCAATACCATATTAC[C/G/T]TTGCTGTTGGTTGTT | 55827 |
rs141250338 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948903 | GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTAC | 55827 |
rs141268419 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049354 | CTCAAGCGATCTTCC[C/T]CCCTCAGTCTCCCAA | 55827 |
rs141277303 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006298 | GAAAAAATATCTTTG[A/G]TGGTCATGTGATGAT | 55827 |
rs141279187 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963057 | CTGAGGTCTGGAGTT[C/T]GAGACCAGCCTGGGC | 55827 |
rs141284222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957161 | CATCTTAAGTGTTCA[A/G]TTCGGTGGTTTTTAG | 55827 |
rs141382124 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007744 | CTCCTTCTGAATATT[A/G]TAATCAAACCCCTTA | 55827 |
rs141385841 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983033 | TGTGTGTCTTGTTTT[C/T]GTACCAGTACTATGC | 55827 |
rs141386398 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054409 | ATAACCTATTAATCT[A/G]TAAGTGAATTAATTC | 55827 |
rs141425112 | in-del | -/A | 0.0119091 | 0.0762411 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962440 | GACCTCTTTATCGTT[-/A]ATGAAATACCCTTCT | 55827 |
rs141431074 | snp | C/G/T | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942180 | AAGAGATTCTCCTGC[C/G/T]TCAGCCTGCCAAGTA | 55827 |
rs141531616 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982274 | TTGAGACGGAGTCTC[A/G]CTTCATCGCCAGGCT | 55827 |
rs141550329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996548 | CCTACAGCCCTATAG[C/T]TATACAGCATTCAAA | 55827 |
rs141556772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020309 | CTGAGTAGAAAAACC[A/G]CATTTGAACCCAGGA | 55827 |
rs141583609 | in-del | -/AAACA | 0.114036 | 0.209795 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989080 | GCGAGACTCCATCTC[-/AAACA]AAAACAAAACAAAAC | 55827 |
rs141598071 | in-del | -/A | 0.0475351 | 0.146656 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990332 | TGATCACACCACTGT[-/A]TAAGCCTGGGCAACA | 55827 |
rs141604879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019751 | AAGGGTGTAAAACAT[C/T]GGTGATTATTTTTGA | 55827 |
rs141636255 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013035 | AAATTTGACATATAT[A/G]GCCTCTCTCATAGAT | 55827 |
rs141642235 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009842 | TATAAAAATTTATAA[-/C]TTTTCTTTTACTATG | 55827 |
rs141677063 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017250 | TTTGCTGTATATAAA[C/T]GTCTAGCAAACATGT | 55827 |
rs141678868 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065338 | TTTTTTATAGATAGG[A/G]GATCTCACTATATTG | 55827 |
rs141680305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070642 | TGGATAGAGATTAAG[C/T]GTCTACATTTTTAAA | 55827 |
rs141683052 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949596 | TCCCTATGAGACTTG[G/T]ATTACAGGAAGAACC | 55827 |
rs141692383 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022863 | ACTGCTTGGGAATCA[C/T]ACCACAGTACTTACT | 55827 |
rs141705281 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955625 | TCTATGTAAATAATC[A/G]AGTCATCTGAGAATT | 55827 |
rs141746483 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008375 | ATTTGCTTATTTGAA[A/T]AACCTGTGAGTTTTT | 55827 |
rs141759138 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064260 | AATAAGAATAGACCA[A/G]AAAGATCTCTAAGAT | 55827 |
rs141812470 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167952641 | TGACTCCTCCGCATA[C/T]GTTCCTTCACATGTT | 55827 |
rs141817117 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167955240 | TTGCCATGAATATTC[A/G]TGTTGCGTCTTTGTA | 55827 |
rs141859624 | in-del | -/C | 0.0614824 | 0.164198 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968347 | ACTGAAAAGAAGAGA[-/C]CCCCCCCGTGCTGAG | 55827 |
rs141946693 | snp | A/G | | | intron-variant, downstream-variant-500B | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998961 | CTTAATAAGGCATCT[A/G]GAATGGTCAATCCTT | 55827 |
rs141970859 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042373 | GTCACAGAATACTTA[C/T]TGAAAATTATTTCTT | 55827 |
rs141979238 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964446 | CCTCTATAGATAATG[C/T]TTTTTCCTCCAGCTT | 55827 |
rs141997465 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003362 | ACAAAATACTTTCTG[A/G]TTCCAGTTAATTTCA | 55827 |
rs142023876 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041430 | TTTCTGCCTGTGATA[A/G]CATGCATAGGAAAGC | 55827 |
rs142071612 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979525 | TCATATTGTAGCATA[A/T]GTCAGAATTTATTTC | 55827 |
rs142078564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965211 | CAGGCCTATGATTAG[A/G]TGTCTGTCACTTAAA | 55827 |
rs142114912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044807 | GAGGAATTAGACATC[A/G]TATTAGAATGTGTTT | 55827 |
rs142116743 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995744 | ATACATAGAATAAAT[G/T]AATAATCTGTCTTAT | 55827 |
rs142196156 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940625 | AGTGCTTTTGGAAAT[C/G]AGTGATTTATTAGCC | 55827 |
rs142213724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040419 | GAAGAACAGTTAAAA[A/G]GCTATGGCAGTAAGA | 55827 |
rs142328126 | snp | C/T | 0.000961682 | 0.021907 | missense | DCAF6 | GRCh38.p7 | 1:167993421 | TTAAAACTCCTTCTG[C/T]GGAAGAGAGAAGAGA | 55827 |
rs142337092 | snp | A/G | 0.00122337 | 0.024702 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951776 | TTGTGTGATTTATTT[A/G]ATTTGTTCTTTCTTT | 55827 |
rs142342970 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031510 | TTTTAGAGCAGGAGA[C/T]GAAAAAATGGAAATG | 55827 |
rs142369065 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989595 | GACTTAAAAACATTA[C/G]TGAGGGGCCGGGCGC | 55827 |
rs142374644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983596 | CAGAGCCTCAAGGTC[A/G]GCCAGAGATGTTAGA | 55827 |
rs142381787 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059345 | AAAACAGATTTGTTT[C/T]TAGGCTCTTTTGTTT | 55827 |
rs142405612 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168050905 | AGATTTAATATCAGA[C/G]GAACAACAATAGGTG | 55827 |
rs142408415 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021267 | TTTATAGTTTTCTTA[C/T]GGCTCTTAAATTGTT | 55827 |
rs142416798 | snp | A/G/T | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951234 | AATGAAGAAATGTAC[A/G/T]AGTGTTTATTGTGGT | 55827 |
rs142432852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948483 | CAACATTTCTTGCCC[C/T]AACCATCTCTATAAG | 55827 |
rs142472894 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168061202 | TGTCAGCTTTTCTGG[G/T]AGTTTCTAACTGTAT | 55827 |
rs142476546 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168062206 | AGGCAAAATTAATTC[A/G]TGATATCAGAAGTCA | 55827 |
rs142477093 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984666 | ACATTTTCACAAATA[G/T]GAAATGAGTAAAAAT | 55827 |
rs142492003 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168025449 | AGGTTAGTATTGAGT[A/G]GCTTTGGCAGAAGCT | 55827 |
rs142498195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981253 | TTCAGTTTGTAGGTT[C/T]AGATCTTTAATCCGT | 55827 |
rs142498935 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944481 | TAACCAACATTGTCT[C/G]TCTTTTTAATAAAAG | 55827 |
rs142557483 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006967 | TGACCACAAATTTCA[A/G]TGGGTGCTCAACACT | 55827 |
rs142690749 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998725 | TTGCTCATCCATAAG[C/G]AGCAACTCCTTATCT | 55827 |
rs142724601 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961281 | AGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 55827 |
rs142733157 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958878 | ATGAGCCTACATTAA[A/T]ACATCATAATCCATC | 55827 |
rs142767917 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058868 | AGCCACTGCACCCGG[A/T]CCTGATCTGGTTTTC | 55827 |
rs142783720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002024 | TTCTGTTTGGGAACC[A/G]AAGAGTAAATTGTCA | 55827 |
rs142816105 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015228 | GATTATGTAAATCTT[C/T]TTGAACTTAAAAAAT | 55827 |
rs142817166 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972109 | GATCCAGCTGCCTTG[A/G]CCTCCCAAAGTGCTG | 55827 |
rs142846667 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042539 | GTTTGAACAGCAGAT[C/G]AGAACTGGAAGTGAT | 55827 |
rs142854521 | in-del | -/T | 0.0763149 | 0.179815 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937746 | TCGTTTTGCATAACA[-/T]TTTTTTTTTTGAGGA | 55827 |
rs142867161 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072212 | TGAGGCAGGAGAATC[A/G]CCTGAACCCAGGAGG | 55827 |
rs142886792 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048593 | GCATGAGAAGGAAAT[A/G]TCTTAGAAAATGAAG | 55827 |
rs142887118 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167996735 | CTGTGCTCTAACCAC[A/G]TCTACTTGCTTAGTA | 55827 |
rs142889486 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956862 | TTCTTAGTTTTCCAA[C/T]GTATCTTTATGTTAA | 55827 |
rs142891503 | snp | A/G | 0.000287043 | 0.0119766 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168066438 | ATTAGAAGAGTCAAG[A/G]ATTTTTAACCGAAAA | 55827 |
rs142931976 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981788 | CACCATTGATGGGCA[C/T]CTAGGTTGATTCTGT | 55827 |
rs142989949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021442 | ACCAATTTATCTGTT[C/T]TTTAAAAACAACATA | 55827 |
rs143007077 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071749 | TCTCAGGGACTCCCT[A/G]TTGCTCTTAAAGTAA | 55827 |
rs143027430 | snp | G/T | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167936210 | GGCCCGCCCCGAGGC[G/T]CGGGCGGGGTCGAGC | 55827 |
rs143066637 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168075055 | CTGCCTCCTCACTCC[C/T]CTTTGCAGCACCTGA | 55827 |
rs143069307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977953 | TTTTCTAATACCCCT[C/G]TTTTTCTGTTTTTGA | 55827 |
rs143079192 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969422 | TTCTAATTAGGTTAG[C/G]ATTATGTTCTGATTT | 55827 |
rs143093548 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958113 | TTTTGCCTTCCTCAT[A/G]GTGTCCTTTAATGTA | 55827 |
rs143117975 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024859 | GGTGAATTTCTGATC[G/T]TAAATTACTCCTTAT | 55827 |
rs143132333 | snp | C/T | 0.000347938 | 0.0131851 | synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936942 | TCCTACCCACACCTG[C/T]TGTGGGACGTGAGGA | 55827 |
rs143135477 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982881 | ATTCTTCTACATATG[G/T]TTGGCCAGTGATCCC | 55827 |
rs143220905 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945022 | CTTTGTCAAACATCA[G/T]TTGGCTGCAAGTATG | 55827 |
rs143230699 | snp | A/G | 0.00183783 | 0.0302579 | upstream-variant-2KB, missense, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935774 | AATTTCTCGGGCAGC[A/G]TCAGCTCCACTTTAT | 55827 |
rs143237035 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035993 | CTGGAACCCGGGAGG[C/T]GGAGCTTGCAGTGGG | 55827 |
rs143243452 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980378 | GTAATTCCATTTTTA[A/G]GTTTTTGAGGACCCT | 55827 |
rs143257340 | in-del | -/AAAG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168011978 | CCTCTGTCTCAGAAA[-/AAAG]AAAGAAAGAAAGAAA | 55827 |
rs143327343 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996475 | CATCTCTGGCATGAC[C/G]TATCCCCCTTTGTAG | 55827 |
rs143357975 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959609 | TCTAATAGATATGTA[A/G]TACATTTCCCTGATA | 55827 |
rs143371376 | in-del | -/TG | 0.171704 | 0.237423 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994067 | AGTATTTTTGTAATT[-/TG]TGTTATAATTAATAG | 55827 |
rs143383868 | in-del | -/CAG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024242 | AAAAAAAAAAAAGAA[-/CAG]AAAAAAGGCAGGTGA | 55827 |
rs143386421 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042281 | GCATTTCTATGAACT[G/T]AATTTAAATCTCAGT | 55827 |
rs143391227 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998232 | TCTGTTAAGTGTGCA[A/G]TAGCATTATATCTTA | 55827 |
rs143392091 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942355 | AAGCATGAGCCGCTG[C/T]GCCTGGCCTTTAATT | 55827 |
rs143397385 | snp | A/C/T | 0.013097 | 0.0799021 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957642 | ATTATCTTGGCTGTA[A/C/T]ACCTAGTTGCAGAAT | 55827 |
rs143429586 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992385 | AGATGGACATAGATT[A/T]TTGAGATGGGAATAC | 55827 |
rs143503059 | in-del | -/A | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039086 | TGTTTACCATTTTTT[-/A]ACCAAATAAGGCTTT | 55827 |
rs143531272 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063210 | CTGCTATTATATATT[A/G]CCTTTAGTTTCTTTT | 55827 |
rs143556392 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952374 | AGGTGCCTGCCACCA[C/T]GCCTGGCTAATTTTT | 55827 |
rs143576569 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052478 | TTCATTTTATTTCTT[A/T]TGTAGAGATTATCTG | 55827 |
rs143602099 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981067 | GCATGCCACCACGCC[C/T]GGCTAATTTTTTGTA | 55827 |
rs143617727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986270 | CAGCTTTAATAGATA[C/T]TGATACATAGTTTTC | 55827 |
rs143749667 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964423 | TGGATGTAATTCTTA[C/T]CTTTGCTCCTCTATA | 55827 |
rs143767312 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052605 | AACTTCTGCTTAAGA[C/T]AGACAAAATTAGAAA | 55827 |
rs143775268 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978156 | TGATTTATCTGTTCT[A/G]TGCTGTTGGAAGTTT | 55827 |
rs143798431 | snp | A/G | 0.000396059 | 0.0140667 | missense | DCAF6 | GRCh38.p7 | 1:168044609 | AAGAATCATCAGAGG[A/G]TGTGACAAAATATCA | 55827 |
rs143808833 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001174 | TTGTGGTGGCACATG[A/C]ACCAACTACTCAGGA | 55827 |
rs143812711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975937 | TTGTGTTAAACTGGT[A/G]TACTTTTTCCATCAT | 55827 |
rs143909616 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016287 | CTATTGAAAGTTTGC[A/G]TATGCTGAAATGAAT | 55827 |
rs143932253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014209 | TATTATTTAACTAAA[A/G]TAGCTCTTGTCGAGG | 55827 |
rs143999777 | snp | G/T | 0.00473271 | 0.0484144 | missense | DCAF6 | GRCh38.p7 | 1:167993261 | ACTACTGGAATGGTT[G/T]CCCGTTTTATTCCTT | 55827 |
rs144008662 | snp | C/T | 0.00136004 | 0.0260417 | intron-variant | DCAF6 | GRCh38.p7 | 1:168075350 | TATTTCTCTTTGCGA[C/T]TCTCTTATCTGTGTT | 55827 |
rs144013262 | in-del | -/T | 0.0240643 | 0.107019 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983446 | GTTGTCAGCTAAGGG[-/T]TTAGATAGAGATTTC | 55827 |
rs144017072 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979895 | CTGTCTCAAAATAAA[C/T]AAACAGGCTGGGCGC | 55827 |
rs144102039 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989774 | TAATCCCAGCTACTC[C/T]GGAGGCTGAGGCTGG | 55827 |
rs144102125 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039659 | CAATATATTAATTAT[C/T]CATAATTAATATATT | 55827 |
rs144121890 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004303 | GTGTATAAACAAGTT[G/T]TATGTAATAGGAAAG | 55827 |
rs144124077 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978647 | TCCTATTCTGTGGTT[A/G]TATTTTCACTCTCCT | 55827 |
rs144125208 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071121 | TCTCCCTGCTTCTAC[C/T]TCTCTTGTCCTCATA | 55827 |
rs144141339 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993578 | AACATGGAGAAACCC[C/T]GTCTTTACTAAAAAC | 55827 |
rs144208748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031268 | AAAGATTTTGCCAGC[A/G]AAGAGCTGGTAAAGG | 55827 |
rs144218623 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005060 | GTTTTGACATAGTTT[A/G]ATGTGCCTGACTTAA | 55827 |
rs144240906 | in-del | -/TTTTGAAATC | 0.17138 | 0.237316 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015486 | TTTGTTCTATGTTCA[-/TTTTGAAATC]TTTTGCTTATGGAGG | 55827 |
rs144273925 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048809 | TGACCATTTAAAATA[C/T]TAACATTTAAAAATG | 55827 |
rs144278097 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972052 | GTGGAGATGGGGTTT[C/T]GCCATGTTGGGCAGG | 55827 |
rs144288650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994486 | TTTCACAGTTACATA[C/T]TAGTGATTTATAACA | 55827 |
rs144297241 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045374 | AGAAACTTTACAGTT[G/T]ACTGTAAATGATTTT | 55827 |
rs144315466 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026325 | AGTAAATGAATTCTT[C/T]AAGCAATTATTTAAG | 55827 |
rs144336225 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050256 | CCATATACCTACTCT[A/G]GACCATGGAGCATAG | 55827 |
rs144389560 | in-del | -/AAAAG | 0.0185938 | 0.0946107 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068952 | TGAATAATTTATAAC[-/AAAAG]AAAAGGTCTAGTATC | 55827 |
rs144411535 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056959 | ATTTATTCAAAATTC[A/G]CCAGCTATAATTCTA | 55827 |
rs144537259 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980066 | TGTGCCTATAGTCCC[A/G]GTTACTTGGGAGGCT | 55827 |
rs144588042 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067565 | AAGCATGAGAGGGTA[A/G]ATGAACCATCAGTGT | 55827 |
rs144598517 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944089 | CCTTGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA | 55827 |
rs144607016 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986627 | TTCTCATAAGGAGTG[C/T]ACAACCTGTGAGAAA | 55827 |
rs144622238 | in-del | -/ATAAATAAATAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939762 | GGGAAACTCTGCGTC[-/ATAAATAAATAA]ATAAATAAATAAATA | 55827 |
rs144624606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022166 | AACTTACTAACTTCT[C/G]ATGAGTGCTCTTTCC | 55827 |
rs144631081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064878 | GTCATTATAACTATT[C/G]CAGTATATCATATGC | 55827 |
rs144635426 | snp | C/G/T | 0.000186742 | 0.00966127 | missense, synonymous-codon | DCAF6 | GRCh38.p7 | 1:168043094 | TCAGGAGGAATCTTT[C/G/T]GTCCCACAGAGCTCA | 55827 |
rs144640667 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953693 | CAACCTCCGTCTCCC[A/G]GGTTCAAGCAGTTCT | 55827 |
rs144652192 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072019 | GAAAAGTCTTCCCTG[C/G]TAGTGCGGTGGCTCA | 55827 |
rs144703806 | snp | C/T | 0.000676194 | 0.018375 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168045048 | AGATCAGACTAGCAC[C/T]GAGAGTGCTACCAAT | 55827 |
rs144704213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956145 | GTTGAGGATGTTCTC[C/T]TCTATTACTAACTTG | 55827 |
rs144704671 | snp | A/G | 0.000115736 | 0.00760622 | missense | DCAF6 | GRCh38.p7 | 1:168044662 | CCAGTTGAGAACCAT[A/G]TCAATATAAGTGAGT | 55827 |
rs144725303 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008281 | GCCTATTGTTGTACG[C/T]CATAAATCTACATGT | 55827 |
rs144729327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939141 | CTTTACCCTTAGTAG[A/G]CCTTTACACTGTTAT | 55827 |
rs144765682 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066313 | ATACATATATGCATA[A/C]TATAAGCATATCCTG | 55827 |
rs144780485 | snp | C/T | 1.65345e-05 | 0.00287524 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167991206 | TTATGTTTTGTAGGA[C/T]ATTTTAATTAACTGT | 55827 |
rs144786329 | snp | C/T | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953173 | GTCTTTTTATTGTTA[C/T]TTGTTCAAAAGATGA | 55827 |
rs144811769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021305 | GGCATAATGAAATGT[A/G]TAACAAATCCAAATG | 55827 |
rs144868778 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069542 | ACTTCCTCAGAGAGA[A/G]TGGGGAATGGAGACA | 55827 |
rs144869376 | snp | A/C/G | 0.0185938 | 0.0946107 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995587 | TGGGAGGTTGAGGCA[A/C/G]GAGAATTGCTTGAAC | 55827 |
rs144870781 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991694 | TGGAAGCTCTGTTCG[A/G]TGCCTTCTCCCCTAG | 55827 |
rs144872925 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952703 | CACCCTCTTTTCTCT[C/T]CAGCTCAAAATGACC | 55827 |
rs144879741 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955888 | ACCTCAGCCTCCTGA[A/G]TTAGCTGGGACCATA | 55827 |
rs144887393 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074183 | AACAATTAAAAGGGA[C/T]ATATAGTCCCTTCAG | 55827 |
rs144892077 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167947344 | TTGACCTTTTGTGGG[-/T]TTTTTTTTTTCAGTC | 55827 |
rs144919338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026984 | CAGGAATGATGAGAG[A/G]AGTACGCAGGGCAGA | 55827 |
rs144938178 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942051 | TAGAAATATATCATT[A/G]TTTTAATTTGCATTT | 55827 |
rs144957746 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009611 | TTTCTTTCCCTCTTT[C/T]CTTCTTACACTTTGT | 55827 |
rs145000325 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069487 | CTCTGTTGAGATAAC[A/T]TCTTACTGTAAGAAC | 55827 |
rs145000921 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041097 | ACGGGCATGTTTAAT[A/G]GAACCTACTTCATAG | 55827 |
rs145005617 | in-del | -/CTTA | 0.0295035 | 0.117819 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054621 | ACTTTTTTCTAGACT[-/CTTA]CTTATAGGATTCAAT | 55827 |
rs145026376 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023788 | AAAAAGGCTATTTAG[C/T]GTTAGCGCAAATGTT | 55827 |
rs145030657 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954320 | TTCAAGGTCTTACAC[A/G]AATGTTTTCTAGTAT | 55827 |
rs145041786 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043556 | AATACCTGAAGTGCC[A/T]CTTAAGGGATTTTTC | 55827 |
rs145047753 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969085 | CCAAGTTATTTAAAC[G/T]TTCCTTAGCCTTTTT | 55827 |
rs145156053 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967109 | GTTACTTATTTTAAT[A/G]TTAAGAATAGTGTGG | 55827 |
rs145158701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011436 | TTTTTTAAAGATAGC[A/G]TATGATGTGGTCTGT | 55827 |
rs145176379 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970891 | TTTTAATTATATATA[G/T]CATAGAGACTCCCCA | 55827 |
rs145189179 | snp | A/G | 0.00138964 | 0.0263228 | missense | DCAF6 | GRCh38.p7 | 1:168045209 | CAGGTGCAAGGTATC[A/G]AGCAGGACCTGGTGA | 55827 |
rs145205107 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070415 | AAAATGGACTTGGAT[C/T]AAATAAGCACATGGT | 55827 |
rs145213378 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019142 | CAACCTCCACCTCCC[C/G]GGTTCAAGTGATTCT | 55827 |
rs145218949 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057952 | TTTGTCCATCTGCCT[A/C]CCACGCCAGTGGTAA | 55827 |
rs145245480 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025100 | TTAAAGGATTTTTTT[C/T]CTAAGGATATATGGA | 55827 |
rs145256445 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955514 | TACATTTCCTGCCCC[A/G]TTAATTTTTAGATAT | 55827 |
rs145272870 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972491 | ACTGATATGATTTAT[A/G]TTTTTAAAAGATAGC | 55827 |
rs145295686 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049890 | TCGATCTCCTGACCT[C/T]GTGATCCGCCTGCCT | 55827 |
rs145351069 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061596 | ATAATTTATTTAACC[G/T]ATTCTTTCTATATGA | 55827 |
rs145383858 | snp | C/T | 5.06308e-05 | 0.00503119 | missense | DCAF6 | GRCh38.p7 | 1:168045200 | TCCTGATCCCAGGTG[C/T]AAGGTATCGAGCAGG | 55827 |
rs145457574 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033732 | TTATGTGGTCATTGC[A/T]GTGCTTCTGAAGCAT | 55827 |
rs145462305 | in-del | -/CTGTC | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948322 | TTAACTAGCAGTCAT[-/CTGTC]CTGTGCCAAGGATGA | 55827 |
rs145499471 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974295 | CCTTTATCTGCAACA[A/G]ATTATACAAATATTA | 55827 |
rs145520499 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050475 | TTTGCTCATTTGTTA[C/T]ATAGTCTTGTGGTTA | 55827 |
rs145551721 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028229 | TTATATTATTAAAAC[G/T]TAACAAATTTTTCCT | 55827 |
rs145611009 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951402 | CCACATGATGAAATC[C/T]TGTCTCTACTAAAAA | 55827 |
rs145612917 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988936 | ATACAAAAAATTAGC[C/T]GGGCGTGGTGGCAGG | 55827 |
rs145662996 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048303 | AGCTGGGGTAGAGAA[A/G]TGGTCCTAAAATTAA | 55827 |
rs145702271 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953392 | ATTATTATTATTGAT[A/C]GTGCTTACTATCTGG | 55827 |
rs145727131 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058724 | CAGGTGCATGCCACC[A/G]CACCCGGCTAATTTT | 55827 |
rs145749410 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952218 | TTTTGTTTTTGTTTT[C/T]GAGACAGAGTCTTGC | 55827 |
rs145830582 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053566 | TCAGACACAGTGGAA[A/G]AATCCAGGCTCAGTG | 55827 |
rs145863917 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995810 | AACTTTGATGATAGT[A/G]TTCAGACAAACTTAA | 55827 |
rs145881271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051507 | TTAAAGTGAACCTCA[A/G]TGACATCAGTCACCT | 55827 |
rs145885100 | in-del | -/T | 0.0678174 | 0.1712 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994995 | AAATATACTTTGAGA[-/T]TTTTTATCCTTGCAG | 55827 |
rs145893059 | in-del | -/TTTC | 0.0236746 | 0.106192 | intron-variant | DCAF6 | GRCh38.p7 | 1:168057847 | TCATACTTGGCTCCT[-/TTTC]TTTCTTTCTTTAGAT | 55827 |
rs145893785 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976678 | AAAGGAACTTGGAAC[A/T]TACCTTGTTCCATTT | 55827 |
rs145897286 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999441 | TTGAAGGCAGGCATC[A/T]GCTTCTCCTCTCTAG | 55827 |
rs145898206 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009847 | AAAATTTATAATTTT[-/C]TTTTACTATGATAAG | 55827 |
rs145913651 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935398 | TCGAAAAGAGAAAGA[A/G]AATGAGTGTTTCATG | 55827 |
rs145929950 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944732 | TGAATAATTTGCAGA[A/T]ATTTTCTGTCATTCA | 55827 |
rs145937348 | snp | C/T | 0.000217848 | 0.0104344 | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168022996 | GTTTCAGATTCTCCT[C/T]CTTCTGTGGTTAACA | 55827 |
rs145940992 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949345 | TCAGTGAGGTTTATA[C/T]AGTGAATAGCCTTGG | 55827 |
rs145964607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981266 | TTTAGATCTTTAATC[C/T]GTTTTGAATTAATTT | 55827 |
rs145975507 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056549 | TTTTTGAATGGAATA[A/T]TTTAATTACAGAATA | 55827 |
rs146011118 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042732 | AGGAGACAATGTAGT[G/T]CACTTAAAATTCAAT | 55827 |
rs146047694 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059460 | GCAAGACCCTTCCTT[C/G]TCTTTATTCATTTTT | 55827 |
rs146049067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002224 | AGAAATCACATATAC[A/G]TGATTTCAAAGTTGC | 55827 |
rs146052431 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011955 | TCCAGCCTGGGCGAC[A/G]GAGTGAGCCTCTGTC | 55827 |
rs146059344 | in-del | -/ATTC | 0.0236746 | 0.106192 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066674 | CTTACTAATTATAAT[-/ATTC]ATCATCGGTAACACC | 55827 |
rs146084520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167996910 | CTATTTAAAATCACG[A/G]CCTTTAACTGATACT | 55827 |
rs146108577 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168057646 | ATAATGATAACACAA[C/T]GCCTACCCTCCTTGA | 55827 |
rs146136233 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060894 | TGATTTGAGCTGCCA[C/T]GTAAATTCTTGTTGC | 55827 |
rs146172946 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021035 | TTTAATACTTTCTGT[C/G]TTAACATAGCTTTAA | 55827 |
rs146175237 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953010 | AGATCCGCCTTGCTG[A/G]AGATATATTATTTTA | 55827 |
rs146206461 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065890 | TCAATTACAGCTGAA[C/T]TTGCACTTCAAACAC | 55827 |
rs146206970 | snp | A/C/T | 0.0284018 | 0.116123 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017327 | AATAAAATGTCCCTA[A/C/T]GTATATAATTATTTT | 55827 |
rs146209716 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950583 | AAAACAAATTGGCTT[C/T]AAGAGGCTCTTGATT | 55827 |
rs146290530 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042376 | ACAGAATACTTATTG[A/G]AAATTATTTCTTTAA | 55827 |
rs146323296 | in-del | -/T | 0.0134861 | 0.0810011 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051261 | AGAATGCAATTTATG[-/T]TTTTTTAAATTTGAT | 55827 |
rs146327587 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965310 | AACAGGTTAGTAGAT[G/T]AGGCTGGAGTTATGT | 55827 |
rs146339127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039013 | TAGCTGTGTAATAGT[C/T]CATCAAGTAGATGTT | 55827 |
rs146367867 | snp | A/G | 0.00019924 | 0.00997898 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168003955 | AAGTGAGGTTGCACA[A/G]AGCAATAGAGGACGA | 55827 |
rs146431276 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028425 | TTTCTATTCCTTACA[A/G]TGATTCCATTAAGTG | 55827 |
rs146468052 | in-del | -/A | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987982 | TCAAATAGCAGTTAT[-/A]AAAGCTTGTGGTAGT | 55827 |
rs146472180 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990376 | TCAAAAAGAAAAAAA[A/T]ATATGAATACTATAT | 55827 |
rs146472284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039972 | TAAAGTACTTAAAAC[A/C]CCTGCCTTATTGGAA | 55827 |
rs146517316 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014579 | CACTTGGATGTCTAT[G/T]CATTCTTTCCCCCAA | 55827 |
rs146520790 | snp | A/C/G | 0.000889487 | 0.0210711 | missense, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936921 | AGAGCCATGTCTCGG[A/C/G]GTGGCTCCTACCCAC | 55827 |
rs146521475 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033089 | CATGATTATAATTTC[A/G]TAGTGGAAATGTACA | 55827 |
rs146595176 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942164 | TCTGCCTGCTGGGTT[C/T]AAGAGATTCTCCTGC | 55827 |
rs146619486 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013812 | GTGCAATGGTGCAGT[C/T]GTGGCTTACTGCAGC | 55827 |
rs146620440 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167946020 | GGAGTGCAATGGCAC[A/G]ATCTCAGCTCACTGC | 55827 |
rs146621541 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952068 | TTTTCTAATATTATC[A/G]AAAGGCTTCCATCTC | 55827 |
rs146639548 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054109 | CAATTCTAACATATA[C/G]AACTTTTTTATTGAT | 55827 |
rs146674557 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069756 | AACAACAAAAAATAA[A/G]CCTGGAATGTAAACA | 55827 |
rs146679768 | snp | C/G | 0.00119737 | 0.0244387 | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168076125 | TAACAGCCTGTTGAT[C/G]GCAAGCCTTACTGAT | 55827 |
rs146712248 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028104 | TAATGTCCATCATGC[A/G]TCTTGTTTAGTTTCA | 55827 |
rs146714788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957680 | TCATATGGTAAACTG[A/G]TATCTCACTTTTTGA | 55827 |
rs146738889 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031966 | CCATAAATTCTAAAT[A/G]CTGGTAGGAATGTGG | 55827 |
rs146739595 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961073 | TTTCATTCAATTTAT[A/G]CCTAAGTGTTTCATG | 55827 |
rs146761071 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073292 | AATTGCCAACCAGAG[A/G]TTTGTATAAGTGTTA | 55827 |
rs146782783 | in-del | -/A | 0.00953873 | 0.0683987 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944654 | TAATAGGATTGTTAG[-/A]TTTTTTTGGTTGTTG | 55827 |
rs146834576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976433 | GCCAAGACTGCGCTA[C/T]TGTACTCCAACCTGG | 55827 |
rs146885417 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014224 | ATAGCTCTTGTCGAG[G/T]TCATCAATGACTTCC | 55827 |
rs146895084 | snp | A/G | 0.000528358 | 0.016245 | missense, intron-variant, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167966642 | AGGTTAATACAATCT[A/G]TTGGAATGACACTGG | 55827 |
rs146960674 | in-del | -/AATAA | 0.0337553 | 0.125452 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940694 | AAGATAAACATTGTT[-/AATAA]AATAAACTTATTTCA | 55827 |
rs146965130 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965915 | GCTGGGATTATAGAC[A/G]TGAGCCACCGCGCCC | 55827 |
rs146974042 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015569 | GAAATATATGTATCT[A/C]ATTCATCGTAGTTAA | 55827 |
rs147049846 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168055171 | ACAGTAACTTTGATT[C/T]TTATAGAAAAGTTTT | 55827 |
rs147060520 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980777 | CAAATATTTTCACCC[A/G]TTCCATGGATTGTCT | 55827 |
rs147080084 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036255 | GCATGTAGATATCTA[C/T]AACTGTCTCTTAAAT | 55827 |
rs147089194 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041581 | CCATAGCTTTGGTTT[C/T]ACCACATGGCTGTTT | 55827 |
rs147093322 | in-del | -/TA | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043432 | GAATTAGTCTTTATC[-/TA]ATTTTTATACCTAGC | 55827 |
rs147150856 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049897 | CCTGACCTCGTGATC[C/T]GCCTGCCTCAGCCTC | 55827 |
rs147184811 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939790 | ATAAATAAATAAAGT[A/G]TGGTACACTTATAAA | 55827 |
rs147194663 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943928 | ACTGCAAGTTCCGCC[A/T]CCGAGGTTCACGCCA | 55827 |
rs147213569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052637 | ATAAAATTATCACAG[A/G]TGTTTATATCTACTG | 55827 |
rs147258329 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989141 | TCAGTTTTTTTGTTA[C/T]GTATTTGTATATACA | 55827 |
rs147291552 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955815 | TCCCAGATTGGAGTG[C/T]AGTGGCACAATCATA | 55827 |
rs147301417 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959068 | GAACTCCTGATGACC[A/G]CTGATCTTTTTATAG | 55827 |
rs147321913 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993681 | TTGAACCCGGGAGGC[A/G]GAGGTTGTGGTGAGC | 55827 |
rs147330942 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071296 | CAGGTATGGCACTTA[C/T]AATAAAACTTAATAT | 55827 |
rs147406238 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977971 | TTTCTGTTTTTGAAC[A/G]TTATATAAATGGAAA | 55827 |
rs147425187 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012246 | TTGTAGAGGCAGGAT[A/G]TGAGGTTAGAACCAG | 55827 |
rs147527057 | in-del | -/C | 0.079617 | 0.182947 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036445 | ATAAACAGCAAAACA[-/C]TTTATAAAATATTAA | 55827 |
rs147550773 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043612 | TTATATGACAATTAC[A/G]TGAAATTTAATGTCT | 55827 |
rs147552147 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969122 | ATATTAAGAAAGTCA[G/T]TATGTCTAAAGTCCT | 55827 |
rs147593591 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041280 | GTGTTTATCTTTTTC[G/T]TATTGCGTTATTAGA | 55827 |
rs147656425 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985294 | CTTACTGTTCTGGAA[G/T]TCAGAAGTCTGAAAT | 55827 |
rs147678973 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951541 | GATCATGCCACTGCA[C/T]TCCAGCCTGGGCAAC | 55827 |
rs147697996 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058947 | AAGAGTTCTTAATGC[A/G]TTTTTGATACTAATC | 55827 |
rs147698580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982638 | TGTTGATAGTTTCTT[C/T]TGCTGTGCAGAGCTT | 55827 |
rs147741049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953648 | CTCTGTCACCAAGGC[C/T]GGAGTGAGTGGTGCA | 55827 |
rs147782361 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965881 | ATCAGGTGATCCACC[C/T]GCTTTGGCCTCCCAA | 55827 |
rs147803878 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999983 | GGCTTTCAACATGCT[A/T]TCCTCACTTAGCTTA | 55827 |
rs147844797 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968625 | GTAGGTGGGCCCTGG[G/T]GAAACTGCAGGACTC | 55827 |
rs147863815 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022220 | ATACCAGTGTTTTTC[A/T]AACAGTAGAAACCGC | 55827 |
rs147870716 | snp | A/G/T | 0.000186827 | 0.00966337 | missense | DCAF6 | GRCh38.p7 | 1:168043095 | CAGGAGGAATCTTTC[A/G/T]TCCCACAGAGCTCAG | 55827 |
rs147888321 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982265 | CTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTTCAT | 55827 |
rs147896090 | in-del | -/ATTT | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003743 | ATATACATTCATACA[-/ATTT]ATTTAGGAAATTTGA | 55827 |
rs147906958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019387 | TATGTTGTTTGCTAC[C/T]TAAAAATGTCCTCAT | 55827 |
rs147907503 | snp | C/G | 0.000626773 | 0.0176916 | missense | DCAF6 | GRCh38.p7 | 1:168045049 | GATCAGACTAGCACT[C/G]AGAGTGCTACCAATG | 55827 |
rs147951786 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984867 | CATGCTGCTAATAAA[A/G]GTATACCCGAGACTG | 55827 |
rs148010469 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070449 | CACAAAGTACCTCTC[A/G]GCTCATCCATTACTC | 55827 |
rs148012547 | snp | C/T | 0.00019787 | 0.00994463 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167993344 | TGGTCAAGAGATTCT[C/T]GTTAGTTACTCTTCA | 55827 |
rs148032714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020047 | GTTTAAACATAATAC[A/G]CTCCAGATGTTTCAG | 55827 |
rs148037823 | in-del | -/A | 0.0681886 | 0.171594 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006273 | ACAATCATTTGAATT[-/A]ATTGAAGAAGAAAAA | 55827 |
rs148041936 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008337 | CTACCCTTCCTGTTC[C/T]GTAATTGGCTCCTTC | 55827 |
rs148062410 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063290 | TGGATAAAATTTGTT[A/G]TATTTGTAGTAAAAT | 55827 |
rs148096138 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976807 | GCATATTTACTAATA[C/T]CTTTGGTTTACCTTT | 55827 |
rs148171609 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964428 | GTAATTCTTATCTTT[A/G]CTCCTCTATAGATAA | 55827 |
rs148178916 | in-del | -/T | 0.0185938 | 0.0946107 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059005 | TTTTCTATTTTATGA[-/T]TTTTTTTCACTGTTT | 55827 |
rs148211991 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168075109 | TCCAAAGAACACTGT[C/T]TGACAACCACTGCAG | 55827 |
rs148222549 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029436 | TACCTTGTGGCAAGT[A/C]CTGGGATAGGTACTA | 55827 |
rs148226733 | snp | A/G | 0.000285702 | 0.0119486 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168063687 | GAAAGAAATGGAAGA[A/G]TTGGATACTTTGAAC | 55827 |
rs148233862 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983002 | TTTCTGGGTTCTCTA[A/T]TCTGTTTCATTGGCC | 55827 |
rs148254205 | snp | C/T | 0.040671 | 0.13668 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972075 | TGGGCAGGCTGGTCT[C/T]GAACTCCTGACTTCA | 55827 |
rs148277230 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024927 | TTCTTGAGAAAGAAA[A/G]AATGAATGAATGAAT | 55827 |
rs148310205 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942580 | TCTTTTATAGTTCAT[A/G]CTTTTTATGTCCTAT | 55827 |
rs148317167 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049059 | CGTAAGGCAAGAACA[C/T]GGAACAGTAAATGGG | 55827 |
rs148356659 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975288 | CTGTAAGCAAACAGA[C/T]GTTTACCTTTAAAGA | 55827 |
rs148369208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042297 | AATTTAAATCTCAGT[C/T]AGATTGTTATACATG | 55827 |
rs148371314 | in-del | -/AGTC | 0.0248432 | 0.108648 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072399 | TCTTCCCTCTCACTT[-/AGTC]ATTCTTGTTCATTGC | 55827 |
rs148379154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996510 | TTTTGCTAGCTTTCT[A/G]ACCAGTCTTCCTGCT | 55827 |
rs148411635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944287 | AAACATACTGGTGCA[C/T]ATATCTTTTAGATAT | 55827 |
rs148418100 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050757 | CCTTGCTTAATGCCC[A/G]AAGTCACAAAGGGAA | 55827 |
rs148473282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043405 | TAAATGGATGAGATA[C/T]AAATGTTAGTTTGAA | 55827 |
rs148482890 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168044943 | ATTGGATTCCAACTC[A/G]GGAGAAAGAAATGAC | 55827 |
rs148505939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956210 | CAAGTGTCTTTTTTT[C/T]TTCCTGGGAAATGTC | 55827 |
rs148534815 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994440 | CTCTTCATATATGGA[C/T]AGCAATCCCTTTCTG | 55827 |
rs148546650 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072166 | GCTGGGTGTGGTGGC[A/G]CGTGCCTGTAGTCCC | 55827 |
rs148551684 | in-del | -/CT | 0.168135 | 0.236216 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942290 | GCTGGTCTCGAACTC[-/CT]GACCTCAGGTGATTG | 55827 |
rs148555804 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021401 | TTTTTCTTGTTTTTT[A/T]AAAGAGTTTAATTTG | 55827 |
rs148558689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953272 | AAAGCTTACCTTCTC[A/G]TTTTATTTAGCTCTC | 55827 |
rs148597576 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066627 | GATAAAAGGATGTCT[A/G]TAATACTAGGGAGGT | 55827 |
rs148610056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016769 | TATTATATAAATACT[A/G]TAGTAGGTATAATAA | 55827 |
rs148618445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978768 | CTGGGTTCAAGGAAT[C/T]GTCTTGCCTCCCAAG | 55827 |
rs148651781 | in-del | -/A | 0.0279526 | 0.114869 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957276 | ATTTCCCCTCTATTT[-/A]AGCAGTTAGCAATCA | 55827 |
rs148693087 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965831 | GTAGAGACGGGGTTT[C/T]GCCATATTGGTCAGG | 55827 |
rs148702458 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040213 | AGAGAGAAAACCAGT[A/G]CAAAGACTCTGAAGC | 55827 |
rs148715030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989184 | TAGGGAAGCATTGAA[C/T]TAAACTCAGAAATAA | 55827 |
rs148744677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031351 | GTCTTGTGATCAAGA[A/G]AAATTTTCAAATACG | 55827 |
rs148766357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061171 | CCTCCCAGTCAGAAA[C/T]AGAGTGAACTAAACA | 55827 |
rs148778863 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950980 | TAGTTGGTACTTACT[A/G]TTGCTGTTTGCCATC | 55827 |
rs148817406 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991942 | TAACTAACTACATCT[A/G]TAAAGGTCACATTCT | 55827 |
rs148842529 | snp | A/G | 0.00295914 | 0.0383512 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975058 | TATATGTAAGTATGT[A/G]TATTTTTGATTAAGT | 55827 |
rs148860537 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034415 | ACTTGGGAGGCTGAG[A/G]CAGGAGATTCACTTG | 55827 |
rs148872436 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986138 | ATATTTGGGTTGTTT[C/T]AAGTGTTTGGCTAAT | 55827 |
rs148881800 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063023 | TTCATGCCATTCTCC[C/T]GCCTCAGCCTCCCGA | 55827 |
rs148884987 | snp | A/G | 8.25948e-05 | 0.00642577 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167993383 | ATATCTTTTTGACCC[A/G]AAAGATGATACAGCA | 55827 |
rs148923476 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058783 | CATGTTAGTCAGGCT[A/G]GTCTTGAACTCCTAA | 55827 |
rs148998563 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014446 | CATTTGACTGCCTCA[A/G]GATTCAGTTCTTAGA | 55827 |
rs149000352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948082 | TATTTAGAATTGTTA[C/T]ATATTCTTGCTGAAT | 55827 |
rs149028534 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958018 | TGTTGAGTTGTGTTT[C/G]TATATTCTGGGACTC | 55827 |
rs149067870 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074231 | TGTTGACCTAGGATC[C/T]AGTGGGAGCATTTAA | 55827 |
rs149080368 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023852 | TTAAATATATTGTGA[C/G]AAAGTGTGATAAGTA | 55827 |
rs149125468 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013789 | CTTCCTCTGTTGCCC[A/G]GGCTGGAGTGCAATG | 55827 |
rs149209367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980325 | GTTTCCAGTTTTTTC[A/G]GATCTGTACCCAGAA | 55827 |
rs149229675 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042153 | AAAAAGTCCATGATC[A/G]TTTGTATTGTTTATT | 55827 |
rs149233167 | in-del | -/TA | 0.252421 | 0.249988 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022670 | GGGCAAGGAGTCTTG[-/TA]TGTAGTGAACTAGAT | 55827 |
rs149259351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983991 | ACTTACAGTGGCTGC[A/G]AAGTTACTGTTTTTT | 55827 |
rs149312855 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981177 | CTCCAAAGTGCTGGG[C/T]TTACAGGCATGAGCC | 55827 |
rs149365447 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052383 | TAGAGATTATCATGA[A/G]CTGATAAACAATGGT | 55827 |
rs149386525 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038805 | AATAATAATTAAAAT[C/T]AGTGCAAAAATATAA | 55827 |
rs149388597 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008217 | CAAGCAGTCCATCCG[C/T]CTCGGCCTCCCAAAA | 55827 |
rs149390365 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938503 | ATTCTACAAGCTTCT[C/G]TGCATTTGTTGTAGG | 55827 |
rs149398295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964411 | CTGAGGAGATGTTGG[A/G]TGTAATTCTTATCTT | 55827 |
rs149408478 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066128 | GAAATTGCCCACATA[C/T]CTCATAAAAGAACAA | 55827 |
rs149410717 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988555 | GTGATTTTTCCTGAC[A/T]TACATTATTAAGAGC | 55827 |
rs149441571 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000855 | AGAGGGATGAGTGGG[A/G]AGTGGCTGATGATGG | 55827 |
rs149461170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060479 | GGGTGAGCCACCGTG[C/T]CTGGCCTAGAGCATA | 55827 |
rs149472711 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953131 | TATTAATCTAATATA[A/T]AGTCCATATTTTCTT | 55827 |
rs149523505 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016196 | ATATATTTGGAGAGG[A/G]GCAAATATTTATTAC | 55827 |
rs149526123 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949066 | CATACTTTGTGGCAG[G/T]CACTGTATTAGGTAT | 55827 |
rs149567403 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031244 | AAAATCAGAAAAATT[C/G]TAAAATTAAAAGATT | 55827 |
rs149578142 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011951 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGCCTC | 55827 |
rs149600761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971917 | CTGCAGTGCAGTGGC[A/G]TATTCTCAGCTCACT | 55827 |
rs149618487 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026304 | ATAATATTCGTTAAA[C/T]GAGTGAGTAAATGAA | 55827 |
rs149653383 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966978 | TTAATAATTGGTACA[A/G]GTGACATTATTTCAA | 55827 |
rs149701057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974127 | TGCATTTCCCTTATG[A/G]ATGATCCAAGTTGAG | 55827 |
rs149722016 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028074 | TAAAGTGAAATTCTG[G/T]TTGAATAAGCACAGT | 55827 |
rs149752196 | snp | C/G/T | 0.00207725 | 0.0321607 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042980 | TCCTAAAAGATCATA[C/G/T]TGATTAACTTCTTGG | 55827 |
rs149754496 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968549 | GTAGTATGCTACAAA[A/G]TGTCTAGGGACGTGG | 55827 |
rs149756774 | snp | A/G | 9.89805e-05 | 0.00703423 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167993359 | CGTTAGTTACTCTTC[A/G]GATTACATATATCTT | 55827 |
rs149785081 | in-del | -/T | 0.0599851 | 0.162463 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038693 | GGTTTGGAGTGGGGG[-/T]CTGAGAATTTGCATT | 55827 |
rs149788696 | in-del | -/AACAAC | 0.172026 | 0.237529 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993756 | CTCCGTCTCAGAAAA[-/AACAAC]AACAACAACAACAAC | 55827 |
rs149797355 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985788 | AAAAGTGCTGGCATC[A/G]TGTATTTGTGCAACT | 55827 |
rs149861697 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167946198 | TGACCTCAGGTGATC[A/T]GGCCACCTCAGCCTC | 55827 |
rs149931414 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069132 | CTAATTATTTCACAG[C/T]TTTATCCTCATTTAC | 55827 |
rs149937051 | snp | C/T | 5.12869e-05 | 0.00506368 | missense | DCAF6 | GRCh38.p7 | 1:168043054 | CAAGTTCTAGAGGAA[C/T]TGGGAGCCATTGCAA | 55827 |
rs149966372 | in-del | -/CT | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026083 | CTCACTGAGATGTTA[-/CT]CTCAAAAATAATATA | 55827 |
rs149966666 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004090 | TACCATGTTTTACAT[C/G]TGTAATAATCACAAG | 55827 |
rs150007823 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023100 | ATAGCTTTATTGCAA[C/T]GCATATACTAAGCTC | 55827 |
rs150013434 | in-del | -/T | 0.0240643 | 0.107019 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019759 | AAACATTGGTGATTA[-/T]TTTTTGAAAAAGGGC | 55827 |
rs150059156 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018435 | ATTCCAATAGAAAGT[A/C]TATAAAAGTAGCACT | 55827 |
rs150091905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961881 | AACTACTTTGTTGCA[C/T]CTCACAGATTTTAAT | 55827 |
rs150132496 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981153 | CTCAGGTAATCTGCC[C/T]GTCTCCGCCTCCAAA | 55827 |
rs150163669 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020129 | GCAAGTAATGATAAA[C/T]ATTAAATGACCCATT | 55827 |
rs150184784 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052086 | AGGGTTGGTCACCAT[G/T]TTGGCCAGGCTGGTC | 55827 |
rs150186106 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977307 | TTCTTCCTTTTCTTT[C/G]CTTTGTGAAAAATGT | 55827 |
rs150195695 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937929 | CCAGTTTTGCCACTT[G/T]CTAGTTAAAAAGTGT | 55827 |
rs150236193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045817 | TATGTGATCACAAGG[A/G]TATATTTTCTTTTGT | 55827 |
rs150256569 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029865 | GGCACCTGTAGTTCC[A/G]GCTACTTGGGAGGCT | 55827 |
rs150369718 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059685 | GGGTCTTGCTGTGTC[A/G]CCTAGGCTGGATTGC | 55827 |
rs150373677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983323 | GGAAAAACATTGTTG[C/T]TGTTTGTTGTTGTCA | 55827 |
rs150374729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957918 | CTATGTGCATATGAA[A/G]GTATGAGTCATTTAC | 55827 |
rs150428384 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954222 | TGTTGGCTAGGCTGG[C/T]CTCGAACTCCTGACC | 55827 |
rs150437171 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943112 | GATGGGGTTTCACCG[C/T]GTTAGCCAGGATGGT | 55827 |
rs150447937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007490 | CAACCCCCATCTGCT[C/T]TTCAACCCCCTTTTC | 55827 |
rs150459061 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966791 | AGAAATGAAGAAACT[C/G]TGAACAGTCATAGAA | 55827 |
rs150466667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071006 | AAGCCTGTTATCCTA[C/T]TGAGATCACAATCAC | 55827 |
rs150470162 | in-del | -/ATA | 0.0236746 | 0.106192 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941056 | ATTACCAGGTTCTTC[-/ATA]ATATGTTGCCAAGTT | 55827 |
rs150490314 | snp | A/G | 1.73072e-05 | 0.00294165 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168004546 | AGGTGGAACAAGTCA[A/G]TCAGATATTTCAACT | 55827 |
rs150522814 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973167 | TACGTTAATTACTCT[C/G]TCTGTTTCATGACAT | 55827 |
rs150529062 | snp | C/T | 0.00365044 | 0.0425663 | upstream-variant-2KB, missense, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935786 | AGCATCAGCTCCACT[C/T]TATCGAGGAGCCGGT | 55827 |
rs150530302 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025791 | CTTCAAGATGTAAAT[A/G]TAATCATGTGATTCA | 55827 |
rs150562997 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968023 | GGCATGAGCCACCAC[A/G]CCCAGCCCAAATTTC | 55827 |
rs150616514 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965012 | ATTCCTGGTCTTACA[A/G]TTCCAACAGTCCTGC | 55827 |
rs150627306 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037246 | AATGAAAAAAGATAT[A/G]AGTCCTTCATTGCAA | 55827 |
rs150698211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021537 | CGAATAGATTAGGGA[A/G]CTGATTGAAATGCTA | 55827 |
rs150699452 | in-del | -/CT | 0.0693013 | 0.172766 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073533 | CTCTTTATTGTGTGC[-/CT]CTGAGTGTAAAAGTC | 55827 |
rs150706289 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052988 | ACATTGCCATACTTG[A/G]AGTGTCACTGAATAC | 55827 |
rs150717646 | snp | C/T | | | missense | DCAF6 | GRCh38.p7 | 1:168044590 | TTACTTACAGAAGCT[C/T]CTGAAGAATCATCAG | 55827 |
rs150718654 | in-del | -/TC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009402 | CTTTCTTTCTTTCTT[-/TC]TCTCTCTCTCTTTTG | 55827 |
rs150719044 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941536 | GGATTCTCTAGGTGT[A/T]TATATAAACCTTACT | 55827 |
rs150740345 | snp | A/C/T | 3.38291e-05 | 0.00411262 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987468 | AAATGTTCGTATGAT[A/C/T]ATCTGCACTTTTCTT | 55827 |
rs150784529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003714 | TAAAATGTGATGAGA[A/G]CTCTAATAGATTTAT | 55827 |
rs150805154 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949045 | TCAGCAAACGTATAT[C/T]GAATGCATACTTTGT | 55827 |
rs150807998 | snp | A/G | 1.65853e-05 | 0.00287964 | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168023036 | GATCCATGTCACTTG[A/G]CGAGCAACAGGGTGC | 55827 |
rs150836904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996595 | TAAGTTAAATCATGC[C/T]GCTCTTCTCATCAAC | 55827 |
rs150890634 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167942234 | CATGCCCAGCTAATG[A/T]TGTATTTTTAGTAGA | 55827 |
rs150900896 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959749 | TTTTAAGAGTTCTTT[A/G]TTTATTTTAGATAAC | 55827 |
rs150910974 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061407 | AAATTGTTAGTCACA[A/G]TTTAATGTCCATCTT | 55827 |
rs150942455 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998842 | GCAGTGACTTCCTCT[A/G]CTGAAGTCTTCTACC | 55827 |
rs150993504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072523 | CCTTGTTTGTTGTCT[A/G]TCTTCCTCCTTAGAA | 55827 |
rs151002295 | in-del | -/CTAAA | 0.0185938 | 0.0946107 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068587 | AGGGTAGCTTAACTT[-/CTAAA]CTAGGATTTCTGTGA | 55827 |
rs151003767 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961367 | TCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 55827 |
rs151024257 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014512 | TAAAATGACATCCAA[A/G]TTTATATCTCTGAAT | 55827 |
rs151057930 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957128 | ATTTAGATGTGCTCA[A/C]ATACTATAAAACTGA | 55827 |
rs151069488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027746 | TGGTTACTGAAGAAA[C/T]TTTTTTCTTTGAATA | 55827 |
rs151079311 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981849 | AACATGTGAGTGCAT[A/G]TGTCTTTTTGGTAGA | 55827 |
rs151091097 | in-del | -/T | 0.0966517 | 0.197444 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997507 | TGGAATTTATGGGGA[-/T]TTTTTTTTTCTGTCT | 55827 |
rs151099453 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045462 | CCATATCTCTAGCAC[G/T]GAGGCTTGCTTCTGA | 55827 |
rs151099951 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969986 | TTCACCATGTTGGCC[A/G]GGCTGGTCTCGAACT | 55827 |
rs151151815 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040662 | TCTTTTCCATTCTCA[A/T]GTTTCTGTACACAAG | 55827 |
rs151160318 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961564 | GTTTTTAAAATTTTA[-/T]TTTTCCATATAGATG | 55827 |
rs151213744 | in-del | -/GAT | 0.0322114 | 0.122752 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943501 | TGTAATGCTATTTTA[-/GAT]GATATTTTTATTTAT | 55827 |
rs151277736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067620 | CAAAAGTAGCTTAAT[C/G]AAACTAAACGGTTAG | 55827 |
rs151289852 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018229 | TAATCCCAGATGGAA[C/T]ATTATCTATTTAGTT | 55827 |
rs151291974 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951297 | AAATAACTACAGGCC[C/G/T]GGCGTGGTGGCTCAC | 55827 |
rs151299337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051308 | AACTTTTTGTTATTC[A/G]TATATGCTCCTTTTC | 55827 |
rs151312426 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167934720 | TACAGATTTTAACTA[C/T]GTAGGAGAATAAAAG | 55827 |
rs180695471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063216 | TTATATATTACCTTT[A/G]GTTTCTTTTCATTTC | 55827 |
rs180696682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013587 | ATTCCTCCTCTGATA[C/T]ACTGGAACTTATCTC | 55827 |
rs180701971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032994 | GAACAGTATTTAAAT[A/G]TATAAAATACTCAGC | 55827 |
rs180708133 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053394 | TATGGGTTTTTGCTT[G/T]CTTTCTCTGCTTCCT | 55827 |
rs180721079 | snp | A/G | | | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075529 | TAGTGCAATTTTAAG[A/G]TTATGGTTTTTGGAG | 55827 |
rs180800159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976447 | ACTGTACTCCAACCT[A/G]GGCGACAGAGTGAGA | 55827 |
rs180804607 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960659 | CTGTTACTGATTTTA[A/G]TTTAATTCCATTGTG | 55827 |
rs180807902 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995450 | TTTGGGAGGTCGAGG[C/T]GAGTGGATCACCTGA | 55827 |
rs180823299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023941 | GGCAGATAGCTGGAC[A/G]TGGTGGCACACGCCT | 55827 |
rs180836732 | snp | A/G/T | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940996 | AATGGATAATTTTGC[A/G/T]TGTCGATTACTCTTT | 55827 |
rs180841465 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167949115 | TAAAGCAGTGTTCTT[A/C]TGGAGTTTATAACCT | 55827 |
rs180845185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985995 | CTTTTGTGTCTGGCT[G/T]TTTTCACACAGAAGG | 55827 |
rs180849590 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003026 | GCACACTTGAAAATA[A/G/T]AATTAATCTATGAAT | 55827 |
rs180864597 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044326 | CCTCCCAAAATAACA[A/G]TATGACAATAAAAAG | 55827 |
rs180873188 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966856 | CTGAGGTTTATTGTA[C/T]AATTTAGAGGTTCTT | 55827 |
rs180986223 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038927 | AATATACTGTATTCT[A/C]CCCTGCATTTGTTTG | 55827 |
rs180989714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989621 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 55827 |
rs180994285 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963829 | TTTAATTATTTGCCC[C/T]AAAGTTTTCACTATA | 55827 |
rs181009358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059328 | ATTACAAAGATTTAT[A/G]TAAAACAGATTTGTT | 55827 |
rs181009500 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017703 | TACATAATAATTAAA[C/T]GCAGTTTTGTATATG | 55827 |
rs181022078 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999899 | TAAAAGTTCCTTCCA[G/T]AACTTTTCCTTTGCA | 55827 |
rs181032415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981201 | ATGAGCCACCGCTCC[C/T]GGCCTCCCCCATGTT | 55827 |
rs181126843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953899 | CCACTGTTCCTGGCC[C/T]AACATTTTTTTCAAG | 55827 |
rs181149709 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970254 | TTTAAAGAAATGACG[A/G]TCCCTTTGATGTATG | 55827 |
rs181153242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945216 | TGGGGCTTCTTTTTG[A/G]TTCCATATGAATTTT | 55827 |
rs181165348 | snp | G/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936732 | GGCGAGCTCCGGCCC[G/T]GGTGCGGCCGGGCTT | 55827 |
rs181257634 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054305 | GGACTCTGCAGAGTC[C/T]CGAGCTGGCACAGGA | 55827 |
rs181285683 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949715 | ATCCAAGAAAGGTAG[C/T]AGTCCAATTGGTTAC | 55827 |
rs181295051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986319 | TTATACTCCCATCAG[C/T]AATGTGTTCCGTAAC | 55827 |
rs181295267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967183 | TTGAAATTTAGTCTT[C/T]TAGAAAATTTACATT | 55827 |
rs181347256 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003358 | AGAGACAAAATACTT[A/T]CTGGTTCCAGTTAAT | 55827 |
rs181444371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069582 | CAGAAAGTAGACAGC[A/G]TATAGCGTTTTTCTA | 55827 |
rs181446375 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063848 | CTTCATATATTGCCA[A/G]TGGGATTTCAGTATT | 55827 |
rs181460752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000939 | ACCTCTTTATGAATA[C/T]ACACCACTGAATTGT | 55827 |
rs181463755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168047476 | TTTAAAAATTAAATA[C/T]TATTTAATATTCTGT | 55827 |
rs181473525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060456 | CTCCCAAGTAGCTGG[G/T]ATTACTGGGGTGAGC | 55827 |
rs181485727 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024496 | GAAAACTTCTTTTGT[A/G]CTTCTGATCTTAAAT | 55827 |
rs181504782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018288 | AAACACCATTCTAAG[A/G]CACCAAATGATATCA | 55827 |
rs181575893 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007666 | ATGATATCATATTTG[C/T]CTATTTACTCTTATT | 55827 |
rs181579812 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027152 | TTGTAGTTTGAGATA[A/C/T]GATGTAGTGGAAGCA | 55827 |
rs181641487 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039730 | ATGATCATGTTATCT[C/G]TTACTATAATATATG | 55827 |
rs181682474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987171 | ACATAAAAATTAAGC[C/T]TTGAATAGTTTGAAC | 55827 |
rs181685720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004290 | TATATAAAATTCTGT[A/G]TATAAACAAGTTTTA | 55827 |
rs181695231 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024940 | AAGAATGAATGAATG[A/C]ATTGGTAAATTAATT | 55827 |
rs181719039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954071 | GAGTGGAGTGGCACA[A/G]TCTCAGCTCACTGCA | 55827 |
rs181743503 | snp | A/G | 0.00013423 | 0.00819129 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044888 | GTTACATACAACTTT[A/G]TTTTCTGACAGCACA | 55827 |
rs181751940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064636 | AACCAATTTATATTT[A/C]TTGCATTTTATTGCC | 55827 |
rs181764945 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940845 | TCAAGGGAGTTATTT[A/G]TTATAATGTATAAAA | 55827 |
rs181775330 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959661 | TTCATATGCTCGTTT[G/T]CAATCTGTGTATCTT | 55827 |
rs181824351 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032740 | ATGTTCCACAGCTTA[C/T]CTAACTACTATAGTT | 55827 |
rs181851177 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937387 | TTTCCCCGCTCAGCC[G/T]AAGAACCTAAGTTGT | 55827 |
rs181852730 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074668 | GTGGAGGAGGGAGTT[A/C]ATAATTCTGCAGATA | 55827 |
rs181860845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967642 | TTAAGAATAGGAATA[C/T]GTATATTTCCTAGCT | 55827 |
rs181864303 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994905 | TTTTGGAATTCCTAC[A/G]AGATACAAAACTATA | 55827 |
rs181871987 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970776 | GATCCTATGATTTTG[C/T]GGGAACATTAATTTA | 55827 |
rs181883631 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937793 | AGTCAACTAAAAAGT[C/T]TGGTTTCTTAAAAAT | 55827 |
rs181885026 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167980849 | TGGCTTTGTTAACTG[G/T]GATTTTGTTGTTATA | 55827 |
rs181886279 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167963706 | AGTGCTGGGATTACA[A/G]GTGTGAGTCACCATG | 55827 |
rs181896373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999663 | TAAACTGCATGAACC[A/C]ACCTCTGTTAGCTTC | 55827 |
rs181908576 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943803 | ACCTAAGATAATGAC[C/T]TCTAGTTCCATCCAC | 55827 |
rs181943689 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016911 | TCTAATTTGATTATT[C/T]GGAACTAATTTATAT | 55827 |
rs181950704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037353 | TTCAAGAGAAGTTTA[G/T]TTTTAGTATTAAATC | 55827 |
rs181958043 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058980 | CTATCGTGTATTAGT[A/G]TACAAATATTTTTTC | 55827 |
rs182092074 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052893 | GTTTATGATATAAAG[A/G]AGAAACAAACCCAGC | 55827 |
rs182101289 | snp | A/T | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997627 | CAAGTTTTTATCAAA[A/T]CCTGTTTAATTTTCA | 55827 |
rs182102592 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014995 | CAAACACATATGTTC[A/C]ACATCATGTGTGCCT | 55827 |
rs182110446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035480 | AAACAACCTGGAGTT[A/G]AAGAAACCAGGTTCT | 55827 |
rs182112607 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950192 | GTTTCCAATACTTTA[A/G]TATTTTAATGTGTTT | 55827 |
rs182118048 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975265 | TTGTAATTGCTTGAG[C/G]AACCATGCTGTAAGC | 55827 |
rs182130977 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962438 | ACTGACCTCTTTATC[A/G]TTATGAAATACCCTT | 55827 |
rs182131307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012636 | CTAGCAGAACTGTTA[C/T]TTAGTCTGTTATGTC | 55827 |
rs182162223 | snp | A/C | 0.0414363 | 0.137845 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056298 | AGAGCGGGTCCAGTG[A/C]GTAGCGTACGGACGG | 55827 |
rs182164947 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167934691 | CAACTTTCCTAATGA[C/T]ACCAACTACAGAATA | 55827 |
rs182184255 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048152 | GGGTTGTGAAGCTCT[G/T]TTGTAACAATCATAC | 55827 |
rs182207424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971809 | GCATTGATCCAAGGA[A/G]AGCACAACTAAGAAG | 55827 |
rs182218156 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008093 | TCCTGCCTCAGCCTC[C/T]CAAGTAGCTGGGATT | 55827 |
rs182281317 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972376 | AAATTAGAGAGTGGT[A/G]CAAAATGAAGTTCAA | 55827 |
rs182295643 | snp | A/G | 0.00245456 | 0.0349465 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991356 | TAAGAAGATAATATT[A/G]GAGAAAATATAGGAC | 55827 |
rs182298834 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008401 | TTTTTCTTGATTCCT[G/T]CCTTTTCCTCAAGTC | 55827 |
rs182316946 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955006 | AGAATTTTAAATAAA[C/T]GGAATCATTGACTAT | 55827 |
rs182320642 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938501 | TCATTCTACAAGCTT[C/T]TGTGCATTTGTTGTA | 55827 |
rs182348333 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025289 | AACTCCCAGATTTTT[C/T]ACATCAGTGCCTGGG | 55827 |
rs182350187 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028565 | GTATGAAAAATATCA[A/G]TGTTAATTTTCCACT | 55827 |
rs182356368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048980 | GCCTCTACTGGCAAA[A/G]ATCCAGACTTTGAAA | 55827 |
rs182365343 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065333 | TTTTTTTTTTTATAG[A/G]TAGGGGATCTCACTA | 55827 |
rs182386078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987674 | TTAAAATTGGTTATA[A/G]TTAAAGTTATAATTA | 55827 |
rs182416635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954554 | GCCTCCCGGATTCAC[A/G]CCAGTCTCCTGCCTC | 55827 |
rs182439023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027775 | TAACTGTATACACAG[C/T]ATTAAACTGGTTGAG | 55827 |
rs182464684 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070034 | TCCTGCAGAAAATTA[A/G]TTCTCTTTCCAGTTG | 55827 |
rs182468338 | snp | A/G/T | 0.00159649 | 0.0282165 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025470 | GGCAGAAGCTGCACC[A/G/T]TAGTAGACTATCAGA | 55827 |
rs182472367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990495 | GGCATTTCTAATGGT[A/G]CTAATGACTTAGTGA | 55827 |
rs182543329 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951599 | ACAAACAAAAAACTG[C/T]GTGAGGTAGAGGTAT | 55827 |
rs182579754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968438 | CTGTGATGTCATGCT[A/G]GTGTAACTTGTTGCG | 55827 |
rs182583382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033521 | ACGGGGTTTCACCTT[A/G]TTAGCCAGGATGGTC | 55827 |
rs182587476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988219 | AGGCCGGAGTGCAGT[A/G]GTGCAATCCTAGCTC | 55827 |
rs182593580 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005856 | GTATACATTTTATCC[A/C]TAATAATAAGCTAAA | 55827 |
rs182595807 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935047 | TCATTCTCATAGACC[C/G]CGTATTACACAAACA | 55827 |
rs182608738 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951997 | TTACATTAAAATATA[A/T]AATTATATTTTGAAT | 55827 |
rs182612230 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045385 | AGTTTACTGTAAATG[A/C]TTTTACGTATTATAT | 55827 |
rs182643323 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942558 | TTATGTCTTTTTCTT[A/G]ACAGGTTCTTTTATA | 55827 |
rs182647165 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005062 | TTTGACATAGTTTAA[A/T]GTGCCTGACTTAAAT | 55827 |
rs182683694 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965780 | GCTGGGATTACAGGC[G/T]CATGCCACCATGGCC | 55827 |
rs182720091 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029579 | AAACATTGCTTGGAG[C/T]AATTTTTTATATGTT | 55827 |
rs182726347 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041286 | ATCTTTTTCTTATTG[C/T]GTTATTAGAGCTATT | 55827 |
rs182728411 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050027 | TGATTGGTAGCTCTT[A/G]CTGTTTCTAAACTCA | 55827 |
rs182764058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001957 | AGGGCAAGAATGAGG[A/G]CAGCAGGATGGAATA | 55827 |
rs182770271 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071462 | AAAAAATAAAAAAAA[G/T]TATAAATACAAAAAT | 55827 |
rs182771207 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070742 | AGGCATTTCTGACAT[C/G]CCTAGAAGCTTTGAG | 55827 |
rs182817391 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968289 | TAAAATACAGAAATA[A/G]CAGATACTATGAACC | 55827 |
rs182904799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067411 | AAGCCCACAGAGAGG[A/G]ACAGCTGTTTGTAAA | 55827 |
rs182921227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045627 | TTTTCTGCTTTTCTA[C/T]TGACCCTGGATTAAG | 55827 |
rs182970670 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167946596 | GGATGTTGAATTTTA[C/T]TAAATTCTTTTTTCG | 55827 |
rs182995816 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964140 | TTCCTCCTTCAGTGC[G/T]CCTTCTTTCTTTATG | 55827 |
rs183002679 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945586 | AACCTCCGGCTCCCA[A/G]GTTCAAGCACTTCTC | 55827 |
rs183014536 | snp | A/T | 0.0352966 | 0.128072 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941742 | AGGAGATTAAAAAAA[A/T]TTTTTTTTAAACACT | 55827 |
rs183014618 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061650 | TCTCAATTACAGTTG[G/T]GCAGTGAAAAAAAGT | 55827 |
rs183017759 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982266 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTTCATC | 55827 |
rs183023801 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983185 | TTTAGAATAGTTTTT[C/T]CTAATTCTGTGAAAA | 55827 |
rs183027900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025745 | ATCCACTCAGGCTAT[A/T]GTCTATTCTCTACCG | 55827 |
rs183035046 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046011 | TATTTCACATTTTAT[A/T]TGCTCAATATATTGC | 55827 |
rs183043902 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020808 | GTATTTATGAATAGT[G/T]GTTAAAAAAACATGT | 55827 |
rs183057501 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013833 | TTACTGCAGCCTTGA[C/T]CTCCCTGGCTCAAGT | 55827 |
rs183102539 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977341 | TTTTTTTTAAATGCC[A/G]GTTCTTCAAAGATAG | 55827 |
rs183123670 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962358 | GTTTTTATCTCACAT[A/G]TTTCGATGCTCTGTT | 55827 |
rs183131100 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942278 | CATGTTGGTCAGGCT[C/G]GTCTCGAACTCCTGA | 55827 |
rs183143849 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977912 | AGCTCCCTTTATTCT[A/G]AATTCTAACACTGGA | 55827 |
rs183222647 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065901 | TGAACTTGCACTTCA[A/T]ACACACCTGTAATCT | 55827 |
rs183253966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955969 | TCTCATTATGTTGCC[C/T]GTCTGGTCTTGAACT | 55827 |
rs183308236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040351 | GGAGGATATTTAAAA[A/G]GAAAAGGTTATTTCT | 55827 |
rs183315926 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168061146 | GACCTCTCTATCCTT[C/T]CCATTCTCACCTCCC | 55827 |
rs183353479 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961052 | CTCATAGAAATCTTA[C/T]ACATATTTCATTCAA | 55827 |
rs183365996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996374 | TTTCTTCTGGTCCCC[A/G]TAGCTTGTGCCTAAA | 55827 |
rs183419619 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982562 | ATTCTGGATATTAAA[C/T]CTTCGTCAGGTGCAT | 55827 |
rs183448567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018703 | GGAAATACACCACAA[C/T]TCATTTAGGAAATAC | 55827 |
rs183452742 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973472 | TGATGACTTCTGTTT[C/G]AATCGGTTGTTGTAA | 55827 |
rs183466102 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009159 | GCCTGCCACCATGCC[C/T]GGCTAATTTTTTATA | 55827 |
rs183477872 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965161 | AGGTCCTTAGGAATT[A/T]ACTGGTAAAGTGTAG | 55827 |
rs183497312 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017314 | CAATAGAAAGAAAAA[C/T]AAAATGTCCCTACGT | 55827 |
rs183510245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038276 | AAAAAGAATTATGAC[A/G]AGGACAACCTAATAT | 55827 |
rs183514749 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059042 | TGTTTTTTGATGAAC[C/T]ATTTTTAATTTTCAC | 55827 |
rs183533210 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999748 | ATTTAGCGCCTTGCT[C/T]TGGGTTAGGCTTTAG | 55827 |
rs183607433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953015 | CGCCTTGCTGAAGAT[A/G]TATTATTTTACCTTC | 55827 |
rs183620935 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997011 | CATGTGTTGTTTGCT[C/T]CATCGGGCTGTAAAT | 55827 |
rs183632899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938877 | GGAAATGGAATTTGT[A/G]TATTGGGTCTAGGGG | 55827 |
rs183636155 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034983 | TAGTTTAGAATATGC[A/G]TTTTATCACAAAGAG | 55827 |
rs183646367 | snp | C/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936550 | GCCTCAGTCCCCAGG[C/G]TGGTCGTCATCTCGC | 55827 |
rs183758185 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050652 | TAAAAGATAAAAGGG[A/T]TTAAGTGCAATGTCT | 55827 |
rs183784270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073101 | GAATCGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 55827 |
rs183814940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055055 | GTATTCAGAATTATA[A/G]TGAGCATTTCCAATG | 55827 |
rs183822311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051254 | TTTGTTGAAGAATGC[A/G]ATTTATGTTTTTTAA | 55827 |
rs183841337 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014650 | GTTACTTGTTTTTCC[C/T]GTTACCTAGGCCAAA | 55827 |
rs183931508 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994174 | TACTATTTCTAAAAC[A/C]TTATCCCTAACAGTG | 55827 |
rs183934542 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949116 | AAAGCAGTGTTCTTA[C/T]GGAGTTTATAACCTA | 55827 |
rs183946836 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011633 | TTCCTTAAATGGGAT[A/G]AAGGTCTAGTCTAGT | 55827 |
rs183953767 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031232 | AACATCTCAAGAAAA[A/G]TCAGAAAAATTCTAA | 55827 |
rs183957046 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957752 | CATTTCTGACAGCAA[C/G]ATACAGGGTTCCAGT | 55827 |
rs183958543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939997 | ACTGCTAAATAGTAA[A/G]ATTGGGATAGAACAA | 55827 |
rs183959729 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945901 | ACACTACTAATTTTT[A/G]TATGTTGATTTTGTA | 55827 |
rs183964062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973914 | TAGAAATAGATTTGC[C/G]TAGTCAAAGAGTAAG | 55827 |
rs183997959 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072098 | GTCAGGAGATTGAGA[C/T]CAGCCTGGCCAACAT | 55827 |
rs183999901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030066 | ACCCAAGAGGTCTGG[C/T]TCTGGCATCCGTGAT | 55827 |
rs184078837 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006822 | TACATGTCCTCCCTC[A/T]TTTTTACTGATATCA | 55827 |
rs184081812 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058132 | TATCTTACTGTGATT[C/T]ATCCATGTTACATGT | 55827 |
rs184087885 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027060 | ACAGGTTAGTAATGC[C/G]ATGTAAATCAATGAT | 55827 |
rs184096328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953943 | TTGTTCTCTGCTTTC[A/G]TACTTCATTGGTGAT | 55827 |
rs184103919 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937067 | GAGTGGGGGAGGGGG[C/T]ACGCTGCCGGGTCTG | 55827 |
rs184114928 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970398 | GCTCACGCTTATAAT[C/G]CCAGCACTTTGGGAG | 55827 |
rs184116384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993579 | ACATGGAGAAACCCC[A/G]TCTTTACTAAAAACA | 55827 |
rs184128887 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989549 | AGTAATGTTCTGAGA[G/T]TAGTAATTGAACAAA | 55827 |
rs184151007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046716 | ATGCAGATGAGGTTA[A/G]CAAGCTTAGCACAAT | 55827 |
rs184175134 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985112 | CATGATTCAGTTACC[G/T]CCCACTGGGTCCCTC | 55827 |
rs184175230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965931 | TGAGCCACCGCGCCC[A/G]GCCTTCCCTGGAGTT | 55827 |
rs184187462 | snp | C/T | 0.000399281 | 0.0141238 | stop-gained | DCAF6 | GRCh38.p7 | 1:168002485 | CTTATTTTTTAGTTG[C/T]GACAACCACCAGTTA | 55827 |
rs184198892 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026221 | TTAATATCTACCTTT[C/T]TGCATATTCTCTAAA | 55827 |
rs184204639 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068124 | GCCTCAAAATTTGAC[C/G]TTTGTTTTTCTGCCA | 55827 |
rs184208395 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | DCAF6 | GRCh38.p7 | 1:167947788 | GTTTTGTGGCTTAAC[A/G]TATGGTCTGTCTTGG | 55827 |
rs184234380 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021100 | TGTAGAGATGACAGC[A/G]TTCTATATCTTTCAT | 55827 |
rs184269329 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969697 | TACTTAATTGTCCTG[A/G]CTTAGCAAAAAAAGC | 55827 |
rs184328536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006685 | ATGTAGTAGATGGAA[A/G]TGTCAGCTTAGGACC | 55827 |
rs184356648 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046464 | TCTTAACTATGAAAG[G/T]GTATGTTTCTTTCTT | 55827 |
rs184374099 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003244 | AAATTATAAGACTAT[A/C]GAATAGAGTTGTCAC | 55827 |
rs184391930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044490 | GCCATTATATATGAG[A/G]GACTTGAGGAGCTGC | 55827 |
rs184400413 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052207 | ACTTTCTGATTAATT[G/T]TATGACAATAAAATG | 55827 |
rs184421527 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073836 | TAAAAACAATGTAAT[G/T]TTTTTTATACTAATA | 55827 |
rs184467210 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980578 | TACTGAAGTTGAGCT[C/G/T]CTTTTCATATGCTTC | 55827 |
rs184469248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006368 | TATAGGAAGTAAGGA[A/G]ATATTTTTAACTGGG | 55827 |
rs184478672 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167999069 | TTTCTTAAATAAGAC[C/T]TGAAGGTTGAAATTA | 55827 |
rs184480556 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063366 | TAAAAACCAGTTTGC[C/T]GCATGCTATTGCCTT | 55827 |
rs184505062 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966902 | TCTTAGATTACTTAG[A/G]GAAACAAGATTTTAT | 55827 |
rs184507442 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963377 | TTCTGCTTTTTGTCT[G/T]TGTTCCTTGTTCCTA | 55827 |
rs184509314 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943742 | TGTTTAGAACACACT[G/T]ATGAGTCAGAACATC | 55827 |
rs184516522 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024102 | CATGCCTGTAGTCCC[A/C]GCTAATAGGGAGGCT | 55827 |
rs184619167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022662 | GTTTGAGAAGGGCAA[A/G]GAGTCTTGTGTAGTG | 55827 |
rs184627847 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043773 | GCTATCTGGTAAGCA[A/G]ATGTCCAGTAAGGAA | 55827 |
rs184655260 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168002852 | AATGCCCATTACCCC[A/G]TAGTACGTTGGGTAT | 55827 |
rs184655621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986167 | ATATAAATAGTGCTG[C/T]TGTGAACATTCTAGT | 55827 |
rs184683352 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063004 | GCAAGCTCCGCCTCC[C/T]GGGTTCATGCCATTC | 55827 |
rs184696310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015534 | TTTCCATTTGGTTTA[A/G]TTACTTAAATATTCC | 55827 |
rs184800198 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036708 | TTCTGTAAGCTAAAG[G/T]TCTATTAATTCAGTT | 55827 |
rs184820002 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998590 | ATCAACTAAGTTTAT[A/G]TAGTACTCTATAATA | 55827 |
rs184831387 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943225 | AAATTTGGTCTTTTT[A/T]AAAAAAATTTATAGT | 55827 |
rs184849034 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069260 | CTTACTCCCCTTTGA[C/T]CTATAAATTTCACTT | 55827 |
rs184940294 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972153 | TGAGCCGCCATGCCT[C/G]GCCCAGCTATCAAAA | 55827 |
rs184946974 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963012 | CATCTGTAATCCTAG[C/G]ACTTTGGGAGGCCAA | 55827 |
rs184958423 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937859 | TGTATACTCTTCATT[A/G]CTCTTTCTTTCTATT | 55827 |
rs184971366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954655 | GACGGTGTTTCACTG[C/T]GTTAGCCAGGATGGT | 55827 |
rs184975415 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167980855 | TGTTAACTGTGATTT[G/T]GTTGTTATATCTAAT | 55827 |
rs184997323 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959129 | ATATAATTGGAATCA[C/T]ATAGTATGTAGCCTT | 55827 |
rs185000276 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938993 | TAAATAATATTTTAG[A/G]TATGATAATATATAC | 55827 |
rs185025452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032218 | TGGCTTGCATAGTAT[C/T]ACTTCTGTTTTATAA | 55827 |
rs185055320 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994712 | TAACCTGTTTAAGCT[G/T]CTTTCCTCAACATGT | 55827 |
rs185066622 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168062467 | TCCTCTCAGTAATGC[C/G]TGTTTTCCTGAACTC | 55827 |
rs185084372 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013641 | TTCCTGTGGTTTTCC[A/G]CTTTTTTTTAAGCAT | 55827 |
rs185088381 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033476 | GCCCGCCACCGCGCC[C/T]GGCTAATTTTTTGTA | 55827 |
rs185088762 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940414 | CAGGGTTTTGCTCTG[G/T]CTCCCAGGCTGGTGT | 55827 |
rs185098332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053818 | TGCAGTTTACGCAAG[C/T]TGGCCCCGCAGGGTT | 55827 |
rs185106843 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976534 | TTTTACTTTTTGTCC[A/T]TTGTGTTTCTGTTTC | 55827 |
rs185126550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995945 | CACAGCTTAGTGGAA[A/G]TAGAGGTACAAGTAA | 55827 |
rs185145822 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075611 | ATGAATTTGGGAGAT[G/T]GTATAAAACAAAACT | 55827 |
rs185162230 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974517 | ATTTCAAAAGTCAGT[C/T]AAAGTAGTTCGTTGT | 55827 |
rs185167673 | snp | A/G | 0.000455529 | 0.015085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043012 | GGAATCACTTATCTT[A/G]TTTTGATGATAGGAG | 55827 |
rs185173559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012272 | ACCAGGTGGACCTTT[A/G]TTGCGTCAACTGTAG | 55827 |
rs185202961 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037087 | TAGAAGAGAGGTTCT[A/G]TGAGATTCTCCCCCC | 55827 |
rs185287770 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935782 | GGGCAGCATCAGCTC[C/T]ACTTTATCGAGGAGC | 55827 |
rs185290936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071305 | CACTTATAATAAAAC[C/T]TAATATATAAAAACA | 55827 |
rs185314050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016528 | CAGCAAAAGTACTCC[A/C]CAGTCTCATGTTCTT | 55827 |
rs185326557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058452 | CTTGTTGTCACATAT[C/T]TTGATTTTTCTAATT | 55827 |
rs185344381 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969339 | TTTTTATCAGTTTAC[A/G]AACAGTGGCTAGGTT | 55827 |
rs185438990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049346 | CTCCTGGGCTCAAGC[A/G]ATCTTCCTCCCTCAG | 55827 |
rs185461453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992927 | TTTGGAAGATGACTT[C/T]GTGTGATTGTATTTA | 55827 |
rs185470289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952665 | ACATGTTGGTTGCAC[A/G]AAGACCCTGTCTTGG | 55827 |
rs185475729 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989142 | CAGTTTTTTTGTTAC[A/G]TATTTGTATATACAC | 55827 |
rs185497758 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985942 | TAGTTTGGGCCTTTT[A/T]ACGATTTTATAAAAA | 55827 |
rs185620387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948606 | ACCATTAAAAATGAG[C/G]AATAGCTGTATATTT | 55827 |
rs185638560 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168074711 | ATGTCCAGGAAAAGT[G/T]TCACCAAGGGTATAA | 55827 |
rs185811922 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990561 | CTAAAGATGTTCATT[A/T]TTCATGAGTATGGGA | 55827 |
rs185826072 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044728 | AAAAAGCCTTAATCT[A/T]TGTTAATCTCTCTAT | 55827 |
rs185839695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963752 | GTTTTAATTGAGCAT[G/T]TCATATAGTTTTTTT | 55827 |
rs185899866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943815 | GACCTCTAGTTCCAT[C/T]CACGTTGCTGTATAT | 55827 |
rs185957850 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004151 | AATAAAAGATATTGG[A/T]TATAATTTGTCCCTT | 55827 |
rs185963791 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024674 | CCGGATGTGGTGGCC[C/T]GTGCCTGTAATCCTA | 55827 |
rs185973806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949828 | TTTTATTAAGGTACT[A/G]TTCTTATTTTGTGGT | 55827 |
rs185990358 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986742 | GCTCACCTGCTGCTC[A/G]CTACCTGCTTTGCTG | 55827 |
rs185993950 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967214 | TAAAACTTTTAAAGA[C/T]AAAAACAGCCAAATG | 55827 |
rs186039166 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045466 | ATCTCTAGCACTGAG[A/G]CTTGCTTCTGAATTT | 55827 |
rs186095513 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000964 | AATTGTATAATTTAA[A/T]ATTATGAATATTATG | 55827 |
rs186101900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168047707 | TTATATATATATGTG[A/T]GTGTGTGTATATATA | 55827 |
rs186112307 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018655 | TTTAAAAATATTTTC[A/G]CTTGTTAGTTTTTTA | 55827 |
rs186116460 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960824 | ATGTGTTGGCTAGCC[C/T]GAGTCTTTGGCATCT | 55827 |
rs186125343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941314 | TCATAACAACCATAG[A/G]CACTATGATAGCTCT | 55827 |
rs186126080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069602 | GCGTTTTTCTAAGCC[C/T]TAGAGGAGAGAAAGT | 55827 |
rs186128184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945687 | GTGTATTTTTAGTAG[A/G]GACAGGGTTTCACCA | 55827 |
rs186136994 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964223 | TTTGTAATTTCTTGC[A/G]AAGTAGGTCTGCTGG | 55827 |
rs186139102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982469 | GATGGTTTTGATCTC[C/G]TGACCTCATGATCTG | 55827 |
rs186139309 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027228 | GGTAGAGACTTTGTT[A/G]TGTCTCTTTTCATAA | 55827 |
rs186169353 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975395 | CCAACATGCTTATCA[A/G]ATTTTTGTAGGATAG | 55827 |
rs186173501 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995267 | TTAGCCAAAAGATAT[G/T]TATATAATCAGAGTG | 55827 |
rs186179082 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065386 | CTCCTCAGCTCAGGC[A/G]GTCCTCCTGCCTTGG | 55827 |
rs186197046 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960309 | TTTATTTATTTATTT[A/T]TTTTTTTGAGATGGA | 55827 |
rs186206891 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940852 | AGTTATTTATTATAA[A/T]GTATAAAATGTGTAA | 55827 |
rs186262218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945221 | CTTCTTTTTGGTTCC[A/G]TATGAATTTTAGGAT | 55827 |
rs186266438 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981587 | ATCTTTATGTCCACA[A/G]GTATCCAGTGTGTAG | 55827 |
rs186309285 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168059433 | TTTTAGTAAATCTTA[A/G]TGGCGGCTAAGGCAA | 55827 |
rs186331712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018149 | ACCTTGAAACCACTT[C/T]GTAGAAATAATCACC | 55827 |
rs186412558 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065222 | AAAGCAAAGTCCCTC[A/T]TCTTAGGGGGGATTT | 55827 |
rs186416760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963941 | AATCTTCCATCTTAT[A/G]CCTTGTACTATTTCT | 55827 |
rs186439061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025186 | CACATACAATAATTT[C/T]CATAGCATTACATTT | 55827 |
rs186494123 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168063897 | TTATCTCTTTATCCA[A/G]CATGGTTCTTTTAGC | 55827 |
rs186499848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033899 | GGGATTTTTTCCCCA[C/G]TATATTGTGTGTGTG | 55827 |
rs186522560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000489 | AGGTACTATGTTTCA[A/G]TTCTTTTGGGTAGTT | 55827 |
rs186544510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038987 | CTTAGTTTTAATAAA[C/T]ATTATTTTACTAGCT | 55827 |
rs186590505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962297 | AGGGAATTGAAGTCT[C/T]CAGGTATCATACTAG | 55827 |
rs186608055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996630 | TAAGTGGCTCCCTGT[C/T]GGACCTAAAGCAAAA | 55827 |
rs186660809 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968348 | ACTGAAAAGAAGAGA[C/G]CCCCCCGTGCTGAGT | 55827 |
rs186681905 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167934755 | TTTTCGGGTAGCACT[C/T]CAGTCTTTCAATTTA | 55827 |
rs186696862 | snp | G/T | 0.000127029 | 0.00796859 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951770 | CAGTATTTGTGTGAT[G/T]TATTTAATTTGTTCT | 55827 |
rs186705781 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168014206 | CCTTATTATTTAACT[A/G]AAATAGCTCTTGTCG | 55827 |
rs186777038 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039768 | ATATAGTTATGTATT[G/T]TCTTAATATGTAATG | 55827 |
rs186795464 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007732 | TTCTTGTTCTATCTC[C/G]TTCTGAATATTATAA | 55827 |
rs186840115 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035986 | AGAATTGCTGGAACC[C/T]GGGAGGCGGAGCTTG | 55827 |
rs186844169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977818 | GAAAAGTACCTAAAT[C/T]CTAAGTATATGGCTT | 55827 |
rs186850433 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056472 | TCGGCCACCCGCGCC[A/G]GGAGGCGGGGCGGGG | 55827 |
rs186860593 | snp | A/C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941843 | GAACACTTTTAAATA[A/C/G]ATATCTATTGTGGGA | 55827 |
rs186879273 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015249 | CTTAAAAAATTTTTT[A/T]AAATGACAATTCTAA | 55827 |
rs186928711 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955435 | CTCACCAGCATTTGG[C/T]GTGGTCAGTTTTTTT | 55827 |
rs186937704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937519 | TTTTTGCGGCGCTGA[A/G]CCAAAACCTAAAAGT | 55827 |
rs186944078 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971456 | TCTGTATATTCGATA[C/T]CTCAGACAGGGTTAT | 55827 |
rs186989072 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972592 | CAGGTAAGAGGGAAA[G/T]ATGACTCAGGCACAG | 55827 |
rs187002774 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990317 | AGGTTACAATGAGCT[A/G]TGATCACACCACTGT | 55827 |
rs187013340 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167946617 | TCTTTTTTCGCGTCT[A/G]TTAAGATGATCATAT | 55827 |
rs187047847 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060964 | TTAGCAACACAGTTA[C/T]TTCCTCTGCTACCTA | 55827 |
rs187100024 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950755 | CTTTCATTACAGCTT[C/G]TGAATAAACATGCTT | 55827 |
rs187107911 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025514 | AATAAGACCTCTGAG[C/G]AGAAATGTTCTAATG | 55827 |
rs187113861 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045766 | CAGCAATAAAAAATT[G/T]AATTGCCAACATGTT | 55827 |
rs187115279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012941 | GATGGAGATTTATGT[C/T]TTCATAAAACATTTG | 55827 |
rs187137801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066199 | ATGGTATTAAAATTA[C/T]GTTCTAGGATAACAT | 55827 |
rs187138274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954414 | TTACTTTTGTGAATT[A/G]CCCCTAGATTTGTGC | 55827 |
rs187146839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968785 | TTTTTACTGGCAAAG[C/T]TTAACATCATGCCAA | 55827 |
rs187151237 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988756 | ATTATTTTATATATT[A/T]GAAACAGAAATAAAA | 55827 |
rs187163396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987172 | CATAAAAATTAAGCT[C/T]TGAATAGTTTGAACA | 55827 |
rs187173417 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052899 | GATATAAAGAAGAAA[C/T]AAACCCAGCTTCCTT | 55827 |
rs187261677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952318 | CGCCTCCCGGGTTCA[C/T]GTCATTCTCCTGCCT | 55827 |
rs187282857 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967922 | TTTTGGTAGAGACAG[C/G]GTTTCACCATGTTGG | 55827 |
rs187315804 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070079 | TGTGCTAATGTAGCA[A/G]TGGTTGGTTAGTTAA | 55827 |
rs187350214 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027892 | TTAATGCAGCTCCCT[C/G]GTTGTCTCAATAGTT | 55827 |
rs187422904 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022389 | TAACGCTAAAGAAAC[C/T]TGAGCCTTTACATAG | 55827 |
rs187433888 | snp | A/G | 0.000537863 | 0.0163903 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043178 | TTGTTATAAAATTGC[A/G]GCATTGGATGTTTAT | 55827 |
rs187438761 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168062583 | ACTGAGCATCTTTTA[C/T]ATATTTGTTAACTGT | 55827 |
rs187446242 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985548 | ACCCTTGTAATTATA[C/T]TGGGCCTCTGTGGAT | 55827 |
rs187449645 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966262 | GGAAGCTTGTTTTTT[G/T]AATACATCAACTATT | 55827 |
rs187458373 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071687 | ATGGGCTATAGTCTG[C/G]TACCACCTTTTTAAA | 55827 |
rs187461288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050141 | AGTTTTTAATTATAG[C/G]CTCAGTTAGGATGAT | 55827 |
rs187496966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965709 | TTGGCTCACTGAAAC[C/T]TCCACCTCTTGGGTT | 55827 |
rs187573321 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067601 | GAACCCTAGAGTACA[C/T]GCACAAAAGTAGCTT | 55827 |
rs187573559 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046240 | TTATTGTAAGAATTT[A/T]AAAAAAATCTATCAG | 55827 |
rs187595896 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942572 | TAACAGGTTCTTTTA[G/T]AGTTCATACTTTTTA | 55827 |
rs187605835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005258 | TTTGATATGGTCTTT[C/T]GTCAACAACATATAA | 55827 |
rs187608810 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979451 | ATTTTAGATACCTCA[G/T]ATAATTGTAATCATG | 55827 |
rs187614387 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168048260 | TCCCTCCATGCTGCC[A/G]TTTGCAAAGCCCAGT | 55827 |
rs187734878 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | DCAF6 | GRCh38.p7 | 1:167946477 | ATGCTTTCATCTTTT[A/C]CCTATTCAGTATGAT | 55827 |
rs187824938 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061993 | TTAGTAATCAAAAAT[A/G]TCGACAACCCAATGT | 55827 |
rs187860777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014733 | CTTTAAAATGTATTG[C/T]ACATTCCTATATGCT | 55827 |
rs187873019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962368 | CACATATTTCGATGC[C/T]CTGTTGTTAAGCACA | 55827 |
rs187875317 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988008 | GTAGTTGTCTTTTTT[C/T]CTCCTGTCTTTTAAA | 55827 |
rs187876865 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942357 | GCATGAGCCGCTGCG[C/T]CTGGCCTTTAATTTG | 55827 |
rs187883171 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977989 | ATATAAATGGAAATA[C/T]GGCTTTTTGTGTCTT | 55827 |
rs187887419 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962863 | GGGAGGCTGAGGCAG[A/G]AGAATTGCTTGAACC | 55827 |
rs187941766 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983531 | TTTGGGTTGCCTTCA[A/G]GTGCCTTGGAAATTT | 55827 |
rs187942915 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025295 | CAGATTTTTTACATC[A/T]GTGCCTGGGTAGGGT | 55827 |
rs187997281 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040462 | GGTGGTGGCTTAGAC[A/G]AGGATGGGAGCAGTG | 55827 |
rs187998863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993588 | AACCCCGTCTTTACT[A/G]AAAACACAAAATTAG | 55827 |
rs188004537 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061299 | TTTTTAAGTAAGTCT[A/G]TATAGCTTAAAGTAT | 55827 |
rs188016684 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957407 | AATGTTTTCAAGGTT[A/C]ATCCATGTTGTAGTA | 55827 |
rs188024883 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001168 | AGCTGGTTGTGGTGG[C/T]ACATGCACCAACTAC | 55827 |
rs188026533 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939265 | TTAAAAAATGACTTT[A/C]CCTCCCAGTTTTATT | 55827 |
rs188039519 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019332 | GGATTACAGGTGTGA[A/G]CCACCATGCCCAGCC | 55827 |
rs188039654 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973580 | TTCTCTGTCCCTAGC[A/C]CCTTAAACATTTTTT | 55827 |
rs188089550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017328 | ATAAAATGTCCCTAC[A/G]TATATAATTATTTTT | 55827 |
rs188094386 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042139 | GTTTTTGTCATGGCA[A/G]AAAGTCCATGATCGT | 55827 |
rs188097574 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168038788 | CAAAAGATAATACTA[A/T]TAATAATAATTAAAA | 55827 |
rs188103944 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168059229 | GTGTAACTTTTCCCT[C/G]CCCCATTTAGATAGC | 55827 |
rs188154428 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036716 | GCTAAAGGTCTATTA[A/G]TTCAGTTATTTATCA | 55827 |
rs188188354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938691 | GTTTTGCATGGATAC[A/C]TTTATAATTTGGTCC | 55827 |
rs188227132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002054 | AATAATGAGTAAATT[A/G]TCAATAATAAATAAA | 55827 |
rs188248883 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935211 | ACTGGACCTATGGGA[C/T]GAGAAATGACACTGA | 55827 |
rs188254245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965794 | CGCATGCCACCATGG[C/T]CGGCTAATTTTTGTA | 55827 |
rs188299864 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936706 | TGGTTAGTCTAAGAA[A/G]GAGAGTATGAGGCGA | 55827 |
rs188361370 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953374 | TATCTTTCTCCTTAC[A/G]TTATTATTATTATTG | 55827 |
rs188378591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989558 | CTGAGATTAGTAATT[A/G]AACAAAGTATAAGGT | 55827 |
rs188378873 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969710 | TGGCTTAGCAAAAAA[A/C]GCTTGATGTTTTCAA | 55827 |
rs188382364 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015576 | ATGTATCTAATTCAT[C/T]GTAGTTAAATAGAAG | 55827 |
rs188396084 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973145 | TATTTATCTTGTTTA[A/G]AGGCTTTACGTTAAT | 55827 |
rs188418115 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938892 | GTATTGGGTCTAGGG[A/G]AATTGAAGGGTTCAC | 55827 |
rs188452915 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009179 | AATTTTTTATACTTT[C/T]AGTAGAGACAGGGTT | 55827 |
rs188453880 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058396 | TAAATATAATATCTA[A/T]CAATATTTTTTAAAA | 55827 |
rs188486679 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051633 | GAAACATATAGCAAC[A/T]ATCAGAAATGTAAAG | 55827 |
rs188513380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073768 | CATTCCTGAGCCCTA[C/T]TTAAGTAGAATAGCA | 55827 |
rs188515421 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949324 | GTTTTGTTCTGGACT[A/G]TCTTCTCAGTGAGGT | 55827 |
rs188523300 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011833 | AATAAATTTGTTGTG[C/T]GTGGTGGCATGTGCC | 55827 |
rs188527531 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031672 | TATCTACAAAATGAG[A/T]GTGTTATTTATGATA | 55827 |
rs188608034 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055065 | TTATAATGAGCATTT[A/C]CAATGAACCATAAAT | 55827 |
rs188612389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025882 | TGGCTTACAAAACCT[A/G]CATGACTTGATTTCT | 55827 |
rs188644432 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974093 | AAGTGAGAATTGATA[C/T]CTCAGCATAATTTCA | 55827 |
rs188671171 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943254 | GTTATCCTGGCTATT[C/T]TGAACCCTTTCTATT | 55827 |
rs188672389 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956388 | ATGTTTTTAAGTATC[C/T]GTAGAATCTGTAGTG | 55827 |
rs188682339 | snp | C/G | 4.97113e-05 | 0.00498529 | missense | DCAF6 | GRCh38.p7 | 1:167993412 | CACGAGAACTTAAAA[C/G]TCCTTCTGCGGAAGA | 55827 |
rs188732336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952759 | ACATGACTTCTGCCT[C/T]TTCCCAGAGTTTTTA | 55827 |
rs188748027 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029702 | AATCATGTCTAAGGC[C/T]GGGCGTGGTGGCTCA | 55827 |
rs188749482 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989283 | TTTGTTATTGCAAAC[G/T]CTCTTAAACTATTTT | 55827 |
rs188787597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970613 | TCTGGATGACAGCAA[A/G]AGCTGATATCTTAAA | 55827 |
rs188828693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168047288 | AATAGCCTCATTGAC[C/T]CAAGGAAACCCAGAT | 55827 |
rs188851105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990104 | AAAAAGTATAAAATA[C/T]AGAAGTCAGTTAATT | 55827 |
rs188864726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006923 | TCTTAGTCTACAGTG[A/G]AATCACTGAATGATA | 55827 |
rs188867293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027081 | AATCAATGATACCAA[C/G]TCCCAGAAAGTCTGA | 55827 |
rs188886280 | snp | A/G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168006471 | ACTATTGAGAAAAAT[A/G/T]ATTTGGTGTTAGATG | 55827 |
rs188896516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030716 | TTCAGAATTTTCTTA[C/T]GTAGATAGTTTAGTA | 55827 |
rs188953549 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948529 | AGTCTAGTAAAGGAG[A/T]TAGGTATGTGAATAA | 55827 |
rs189009113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969431 | GGTTAGGATTATGTT[C/T]TGATTTTCATTGGCT | 55827 |
rs189023893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035170 | CTGCAGTTGGGCCAA[C/G]TGCGGTGGCTCACAC | 55827 |
rs189051947 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167936043 | GGTTGAGGGGGCGGA[A/G]GCTGCCGACTGCCAG | 55827 |
rs189098976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046522 | GCCATGGCACTTTTT[C/T]TGTAGATATGAAGCA | 55827 |
rs189137610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016892 | GAGTTTGGGCTTTGA[A/G]AGTTCTAATTTGATT | 55827 |
rs189143894 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037150 | ACCCAGACTCGACTC[A/G]AACTCCTGGGCTTAA | 55827 |
rs189159761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980774 | TCACAAATATTTTCA[C/T]CCGTTCCATGGATTG | 55827 |
rs189163741 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011352 | TGATCTCCTGAGCTC[A/G]TGATCCACCCGCCTT | 55827 |
rs189164136 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167963649 | GGCCAGGCTGGTCTC[A/T]AATTCCTGACCTCAA | 55827 |
rs189169824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999233 | CAATAGTGGGCTTCA[A/G]ATAGTCAGTAAAACA | 55827 |
rs189184853 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982997 | CTTTATTTCTGGGTT[C/T]TCTATTCTGTTTCAT | 55827 |
rs189232076 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006699 | AATGTCAGCTTAGGA[A/C]CATGATTTCTATTAT | 55827 |
rs189233905 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168051097 | TTTCCACAAACTATA[C/T]TTAGCTGCATGCACT | 55827 |
rs189238313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981140 | TCAGACTCCTGAGCT[C/T]AGGTAATCTGCCCGT | 55827 |
rs189265372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944387 | ATTCTTGGAGAAATC[G/T]CCATACTGTTTTCCA | 55827 |
rs189297265 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943744 | TTTAGAACACACTTA[C/T]GAGTCAGAACATCAT | 55827 |
rs189325119 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069800 | GACCAACAAAATGTT[C/T]TTGTGATCTTCTTTG | 55827 |
rs189371287 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068218 | TTGAATAGACTTAAG[A/G]CAGAAATATAGACAT | 55827 |
rs189386007 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024385 | GTCAATAGTAATGCA[G/T]AAATTAAATATTGCT | 55827 |
rs189418237 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986210 | ATGCCCCATGCAGGC[A/G]TTTATTTTTAGTGGA | 55827 |
rs189437603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960593 | AGGCACTTTATAGTA[A/G]GTCTTGAAGTTGGGT | 55827 |
rs189445813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940894 | GCAGCCAGTGACAAT[A/T]TTTTAGTGGAGATTG | 55827 |
rs189452794 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063544 | TTTCCTAGACTTACT[A/G]TATTTTCATAAGTTT | 55827 |
rs189472020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063132 | TTTTTACCTAAAGTA[C/G]TCTGTTTTTGGAACA | 55827 |
rs189496452 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976430 | TCAGCCAAGACTGCG[A/C]TACTGTACTCCAACC | 55827 |
rs189502310 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022674 | CAAGGAGTCTTGTGT[A/C]GTGAACTAGATACCC | 55827 |
rs189511051 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995298 | AATGAGGCTGAGTCA[C/T]GAACATTTTTTTTTC | 55827 |
rs189513028 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043958 | CAGTTTTAAGTTTAG[A/G]TTTCGGGAAGGTTAG | 55827 |
rs189517301 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013354 | CGTAACAAGAAATTA[C/G]TACCTGGCGTTATTG | 55827 |
rs189517677 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963817 | TTTTTTAAACTTTTT[A/C]ATTATTTGCCCTAAA | 55827 |
rs189523895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026347 | TTATTTAAGAGCTGT[A/G]GGGATTACTTCAGCT | 55827 |
rs189527823 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999851 | CTGTTTCGTTTTCTT[A/C/G]TCATTCATATGTCCA | 55827 |
rs189541535 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957966 | ATGTCTATTTAAATC[C/G]TTTACCTATTTTTAA | 55827 |
rs189601329 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168031262 | AAATTAAAAGATTTT[C/G]CCAGCGAAGAGCTGG | 55827 |
rs189653466 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972190 | ACTTCCCAAGTACAC[A/G]TAAATATTTTTAATC | 55827 |
rs189658339 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003297 | TTTAATTTGAAAATA[A/C/T]CCTTGGAAAAACTTG | 55827 |
rs189660291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990766 | TTTGAAAGTAATTTT[C/T]ATTTTTTCCTTTTTA | 55827 |
rs189662186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008279 | CGGCCTATTGTTGTA[C/T]GTCATAAATCTACAT | 55827 |
rs189677945 | snp | A/G | 1.6588e-05 | 0.00287988 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044556 | CCTCATGGATACCAA[A/G]GGATGACTGTAATTT | 55827 |
rs189703972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937069 | GTGGGGGAGGGGGCA[C/T]GCTGCCGGGTCTGTT | 55827 |
rs189709980 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998666 | GGAGTTGCTTCTTAC[C/G]GATGAGCAAAGAAAG | 55827 |
rs189732286 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963169 | CTCGGGAGGCTGAGG[C/T]GGGAGAATCGCTTGA | 55827 |
rs189765410 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938447 | ACTCAACCTTTCTTC[G/T]TTAAGTAGACGTTCG | 55827 |
rs189774003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954712 | CCGCCTCTGCCTCCC[A/G]AAGTGCTGGGATTAC | 55827 |
rs189804026 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940271 | CAAGATTCACCTGGG[C/T]CAACAGAGTGTTGTT | 55827 |
rs189826422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041017 | GGCAATAGAACATGC[G/T]AAGAGCTTGGACTGA | 55827 |
rs189911607 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167934809 | GTCTTAGGCTTGAAA[A/C]AGACCTCAGAATATA | 55827 |
rs189925434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052781 | TGGTAGTCATCCCCT[A/G]TTCTTCATTCTACTT | 55827 |
rs189932189 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995968 | ACAAGTAAATAAATA[C/T]GTAAAACTTAATATA | 55827 |
rs189947734 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953964 | CATTGGTGATCTGAG[A/T]GGATACAGGATTCTA | 55827 |
rs189955806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980070 | CCTATAGTCCCAGTT[A/G]CTTGGGAGGCTGAGG | 55827 |
rs189985552 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013704 | CATCAGAATACAGAC[A/G]TGTGTATTAGCTCCC | 55827 |
rs189991610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988066 | AAAGAAATAATAAGA[C/T]AGCATGCTATCAACA | 55827 |
rs189993347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968434 | GTCTCTGTGATGTCA[C/T]GCTAGTGTAACTTGT | 55827 |
rs189999502 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033489 | CCCGGCTAATTTTTT[G/T]TATTTTTTTAGTAGA | 55827 |
rs190003698 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168075987 | GAATCACATAGAAGG[A/G]CTTCCTTCATTTCTC | 55827 |
rs190007726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054274 | GCCACAATGGTACAA[A/G]CCTTCTTGCTGGCAA | 55827 |
rs190047146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975159 | ATTGACAATATCTAG[A/G]TGTCAGCAGAGCATT | 55827 |
rs190061881 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012384 | GGGTTTGTAGTTTGA[A/G]GAGATGACAAAGTAC | 55827 |
rs190063985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940797 | CTAAATTAAAAGATA[A/G]TAATTGATAAAAAAG | 55827 |
rs190134603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009109 | GTTCACGCCATTCTC[C/T]TGCCTCAGCCTCCCA | 55827 |
rs190140572 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028880 | TGTATTAATAAGAAT[A/G]TAAGTTCAGTATTCC | 55827 |
rs190145984 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074637 | ATTATGAAGTTCATA[C/T]AAGATATTCTAGAAT | 55827 |
rs190147062 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049856 | GATACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 55827 |
rs190150831 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071433 | ACATGGCAAAACCCC[A/G]TCTCTATAAAAATAA | 55827 |
rs190172597 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032641 | TTTGGTATAATGAAG[G/T]GGGAATTAGAATATC | 55827 |
rs190207510 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058524 | ATTTACAAATAAGAT[G/T]ATGCATCTCATGTTT | 55827 |
rs190262978 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027721 | ATTTTTTTAAAAATT[A/T]TAGTGGACTTGGTTA | 55827 |
rs190266994 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993145 | CATTAAGTCACATGT[A/G]ATAATTCAGATTAAG | 55827 |
rs190295181 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994873 | TAATACGTTTTAAAG[A/G/T]TTACTAATAACAGTG | 55827 |
rs190334935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959630 | TTCCCTGATAACATA[A/G]GATGTGGATTATCTT | 55827 |
rs190409040 | snp | A/G | 3.49321e-05 | 0.00417909 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168075390 | GTTGGAGGGTGACAG[A/G]TCAGAAGGCTCTGGT | 55827 |
rs190423728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964016 | GTATATGTGCTAGAT[A/G]TAAGCATAGATGATC | 55827 |
rs190427767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945577 | GCTTACTACAACCTC[C/T]GGCTCCCAGGTTCAA | 55827 |
rs190450164 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168008022 | GTCACCCAGGCTGGA[A/G]TGCAGTGCACAATCT | 55827 |
rs190487700 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966793 | AAATGAAGAAACTGT[C/G]AACAGTCATAGAATG | 55827 |
rs190521179 | snp | C/G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168048020 | CAATTTAGCTGACTT[C/G/T]TATTCTAAAGAGAGA | 55827 |
rs190538748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044840 | GAGCTCCTAAGTTAG[A/G]TTAAATAATTAGTAT | 55827 |
rs190541903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032985 | CAACATTTTGAACAG[C/T]ATTTAAATATATAAA | 55827 |
rs190564898 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003009 | CTGGGAGCTTTAAGA[C/T]AGCACACTTGAAAAT | 55827 |
rs190569750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004248 | TCCTATTTTAAGCCT[C/T]TTTTTAATGCACTCT | 55827 |
rs190583134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024873 | CTTAAATTACTCCTT[A/G]TGGACCTTAGATGAC | 55827 |
rs190684043 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983108 | ATGTGATACCTCTGG[C/G]TTTGTTCTTTTTGCT | 55827 |
rs190687409 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950013 | TATCTATTTAACCAC[A/G]ATGTGTTATGCCTCT | 55827 |
rs190698207 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048791 | TTATGGTAGGTACTT[A/C]TATGACCATTTAAAA | 55827 |
rs190702555 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942142 | ATGATCTTGGCTTAC[C/T]GCAACCTCTGCCTGC | 55827 |
rs190706017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020150 | ATGACCCATTCCTAT[A/G]TGCTGTCTGAATATT | 55827 |
rs190710856 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967297 | GAAGAAAAAAATTAC[C/T]ATAAGCTAATAAACT | 55827 |
rs190749435 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985965 | TATAAAAATGGGAAT[C/T]ATACTGTGCCTTCTC | 55827 |
rs190855442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964229 | ATTTCTTGCAAAGTA[C/G]GTCTGCTGGCAACAA | 55827 |
rs190885667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039850 | TTTGTGTTTATGTAT[A/G]TGTGTATTTTATATT | 55827 |
rs190892020 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060979 | TTTCCTCTGCTACCT[A/G]TAACTCTACTTTCTT | 55827 |
rs190917830 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001039 | GATGTGGTGGCTCAT[G/T]CCTGTAATCCCAACA | 55827 |
rs190936821 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028309 | TAACAACAGCAAAAA[A/G]AATATGTAATTGTTG | 55827 |
rs190952185 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001565 | AATATAGAATTTTCT[C/G/T]AAGAAGCTTAAGTAA | 55827 |
rs190961148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070539 | GTGATTTTTAATGAA[A/G]GAGCCTCTTAAAATC | 55827 |
rs190991797 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960825 | TGTGTTGGCTAGCCC[A/G]AGTCTTTGGCATCTC | 55827 |
rs191036412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025364 | AATAGAAATCAGGTG[G/T]TTCTTTATCTTTTTG | 55827 |
rs191043006 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055301 | AGAACCTAGATCTTC[A/G]ATCTTTGAATTGAAA | 55827 |
rs191083752 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035212 | GCACTTTGAGAGGCC[A/T]AGGCAGACGGATTGC | 55827 |
rs191231856 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977333 | AATGTCTTTTTTTTT[A/T]AAATGCCAGTTCTTC | 55827 |
rs191265276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941517 | TATACACAACGAAAA[C/T]AAAGGATTCTCTAGG | 55827 |
rs191285928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045471 | TAGCACTGAGGCTTG[C/T]TTCTGAATTTACAGA | 55827 |
rs191322042 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005346 | GCTTATCTTCTTGAT[A/T]CTTGATGCTAGTGAA | 55827 |
rs191333550 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957520 | ATATACCACATTTAA[A/T]CTGTTCATCAGTTGT | 55827 |
rs191339432 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939902 | ACATTACGATTGTCT[A/G]TCTACAGGGTTGTAG | 55827 |
rs191341345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973782 | GTATATCTGTTATGG[A/G]GATATACTGTAGTTT | 55827 |
rs191352337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039184 | AACTATATCTAGATT[A/G]AAAGATATTGCCAAA | 55827 |
rs191377675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938738 | AGTTTAAGTACTTGT[A/G]TATAGTTCTATATTT | 55827 |
rs191405647 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993705 | GGTGAGCCGAAATCA[C/T]GCCATCGCACTCCAG | 55827 |
rs191411566 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168011518 | GCCTATGTAGAATTA[C/T]TATAGCTAAATTGAG | 55827 |
rs191422341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031095 | GAGCTCAGAAAAGAT[A/G]TCAGAGCTCAAGAAA | 55827 |
rs191449061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059691 | TGCTGTGTCGCCTAG[A/G]CTGGATTGCAGTGGC | 55827 |
rs191493338 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014501 | TTTAGGGGACTTAAA[A/G]TGACATCCAAATTTA | 55827 |
rs191551350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036377 | AGAAATTCAGTCTTA[C/T]ACTTCTCTCACATCT | 55827 |
rs191557017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006712 | GACCATGATTTCTAT[A/T]ATTTCCCTGCATAGA | 55827 |
rs191557526 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055047 | GAACAGTGGTATTCA[C/G]AATTATAATGAGCAT | 55827 |
rs191561052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168057066 | CATTTCATTCCTGGT[C/T]CTCTCCTAATCTTTG | 55827 |
rs191565373 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168026636 | GTGTCTTGATAGGGT[A/G]ATAATGAACCATCAG | 55827 |
rs191581602 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018184 | TTTTTAGTGGGCTCA[A/C]ATGGGAAGGGGCCTG | 55827 |
rs191581687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955553 | ATTCTGGAAACTTCC[G/T]GAACTCTCATATTCA | 55827 |
rs191626942 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982134 | ATTAGTGGATGTGGA[A/G]CATTTTATTTTGTGT | 55827 |
rs191713298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965930 | GTGAGCCACCGCGCC[C/T]GGCCTTCCCTGGAGT | 55827 |
rs191717034 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984788 | TGCAAAATTGGTTCA[A/G]TTGAAGCAAAGGACA | 55827 |
rs191739807 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167996904 | ACCATCCTATTTAAA[A/G]TCACGGCCTTTAACT | 55827 |
rs191753130 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034523 | ATGGAAAGGATGGAG[A/T]GGGGGAGGAAAAGTC | 55827 |
rs191762262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962349 | GTTCTGTCAGTTTTT[A/G]TCTCACATATTTCGA | 55827 |
rs191796726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990404 | TATAAATAATCAATA[A/G]TTATAGACAGTATGA | 55827 |
rs191832499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954454 | TATTTTTTATTTTTT[C/T]ATTTTTTTATTTTTT | 55827 |
rs191832940 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168073784 | TTAAGTAGAATAGCA[A/G]CTTCATGTTTTGTTC | 55827 |
rs191845023 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032084 | TGGGTTAAAATTATT[A/C/G]TAATTGACATAGAGT | 55827 |
rs191849545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051648 | AATCAGAAATGTAAA[A/G]TTTGTAGAGTTCCTA | 55827 |
rs191858740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167947378 | ATTTCATTTAGTTCT[A/G]CTCTGATCTTTATTT | 55827 |
rs191987266 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968932 | ATCTGCTTCTTGGTA[A/T]TATTGCAATGTGAAA | 55827 |
rs192003702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989101 | AACAAAACAAAACAA[A/G]AAAACCTTTAAACAT | 55827 |
rs192004048 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963240 | CTTCACTTCAGCCTG[C/G]GCAAAAGCGTGAAAC | 55827 |
rs192009638 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943462 | ATTTTTTGGTGTTAG[G/T]TTTATCCTTAAATAT | 55827 |
rs192042645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066655 | GGTAAAATCTAAATA[A/G]TAGCTTACTAATTAT | 55827 |
rs192077131 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025539 | CTAATGGTGGAAAAT[A/G]TATCTAATTAATTAA | 55827 |
rs192088035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045787 | CCAACATGTTTTTAT[A/G]GTTTTTCTATATTTT | 55827 |
rs192104421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005010 | TCAATTTATATAAAA[C/T]AATTGTTTTAAAAGT | 55827 |
rs192115413 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937612 | TTGACCGCTTAAAGG[G/T]GGTGTAGGGTTTCAC | 55827 |
rs192117865 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167934653 | AGAGAGCTGGTTCAT[A/G]ATCAGATAATGGGGG | 55827 |
rs192127777 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968132 | TAGTAGCAACCGTGT[A/G]TTGGTGATTGTATCA | 55827 |
rs192129390 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971639 | TCAAAATAAACTGGT[A/G]ATCAGCAGAATGACA | 55827 |
rs192228123 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022661 | AGTTTGAGAAGGGCA[A/G]GGAGTCTTGTGTAGT | 55827 |
rs192247534 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062745 | AGAAGTTTTATTTTA[A/G]TAGTTAAATCAGTTT | 55827 |
rs192271847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051145 | AAAGAAATTTCCTGT[A/G]TGCAGACTGATGTTC | 55827 |
rs192360894 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966375 | CTTTCTTAAAACATT[A/T]TGAGATTTTTTTGCT | 55827 |
rs192364919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985753 | CAAGTAAATTTTTAA[A/G]AAGTATAAAACACCT | 55827 |
rs192366945 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168002840 | TGAAAGTATAAGAAT[A/G]CCCATTACCCCATAG | 55827 |
rs192460296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069119 | TATCAGGCTTATACT[A/G]ATTATTTCACAGCTT | 55827 |
rs192469796 | snp | A/G | 0.000667665 | 0.0182589 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987455 | GAGCCGTCTGTTTAA[A/G]TGTTCGTATGATTAT | 55827 |
rs192483264 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025242 | AATTTACATATGATA[C/T]GGGATATAAGAGGAA | 55827 |
rs192510282 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951121 | TTGTTTTTCTCCTCT[C/G]ATAAGCAGGCAGAAA | 55827 |
rs192552340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014886 | CTTTCCTGAGTTGCC[A/G]TATATAAAATAACCC | 55827 |
rs192579674 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998505 | TTGTAACGGTGTTTG[A/G]TAGCTTCTTACACAC | 55827 |
rs192623351 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962934 | GCACGCCAGCCTGGC[A/G]ATGAAGCGAGACTCC | 55827 |
rs192658715 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942372 | CCTGGCCTTTAATTT[G/T]CATTTCTCTAGTGGT | 55827 |
rs192664338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978681 | GGTGGGGGAGGGTGC[A/G]GTTTGTGTGTTTTGA | 55827 |
rs192666425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965760 | AGGCTGAGGCCTCCC[A/G]AGTAGCTGGGATTAC | 55827 |
rs192668716 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962411 | ATTGGGAAACTATGT[G/T]GTCTTGGGGAAACTG | 55827 |
rs192707730 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072482 | ATTGTCTTATTACAG[A/C]TTAGAGGAGAAAAAT | 55827 |
rs192712391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042317 | TGTTATACATGTCCT[C/G]TTTCTCATTCAGTCC | 55827 |
rs192729719 | snp | A/G | 6.60186e-05 | 0.00574499 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002467 | ACATAGAATTTACCC[A/G]TTCTTATTTTTTAGT | 55827 |
rs192730273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974382 | TTAATTGGATGTAGG[A/G]ACTTCTGCTGTGTCT | 55827 |
rs192842612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979622 | CTGTGTGCTGTGGCT[C/T]ATGCCTGTGATCCCA | 55827 |
rs192849823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015504 | TGAAATCTTTTGCTT[A/G]TGGAGGACTTTTTAT | 55827 |
rs192851516 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942746 | TTCATTTCTTTGCAT[A/T]TTAATGTGCAATTGA | 55827 |
rs192874487 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952571 | CTAACACCATACTCT[C/T]TTGGTTTTCTTCCTA | 55827 |
rs192886114 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058427 | ATCGTGTTTATTCAC[A/G]TCACTGATTCTTGTT | 55827 |
rs192900759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015675 | GTATTCCTCTATGAG[A/G]CATGTGTTTTGTTTA | 55827 |
rs192915029 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168020960 | ATGGGAGGAACAGCA[A/G]ATGCCTCAGAAATAC | 55827 |
rs192917928 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994562 | ATAAGTTAAAGTAGT[C/T]GTATATATTGAAAAG | 55827 |
rs192922073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168062441 | TTTATGTGTAAAAAC[C/T]GCTTTCAAACTCCTC | 55827 |
rs192935374 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958710 | ACAGTCAATATTTAA[C/T]GCTTTATTTTGAATT | 55827 |
rs192961345 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071790 | TCTTACTCTGGCCTT[A/C]AAGGTCCTACATGAC | 55827 |
rs193035843 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029873 | TAGTTCCAGCTACTT[A/G]GGAGGCTGAGGTGGG | 55827 |
rs193044724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956688 | TTTTCTAAAATAGAG[A/G]TTTCTTTGGTGCTGT | 55827 |
rs193050023 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993508 | TAATCCCAGCGCTTT[C/G]GGAGGCCGAGGTGGG | 55827 |
rs193083730 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935263 | GCATGCAGTTTGGGG[A/G]AGGGCTCAGTCTGCA | 55827 |
rs193088709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036923 | TATTTTCAAATAGCA[A/G]TTCTGTAGGACAGGA | 55827 |
rs193097139 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006576 | GTAAGGACTTAATTT[A/G]TTTCTGTTTTTGTTT | 55827 |
rs193105492 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969558 | TTTTACAGAATAAAT[A/T]GTTTATTTCTTGTTT | 55827 |
rs193142916 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167936197 | GCCCGCCATGATTGG[C/T]CCGCCCCGAGGCGCG | 55827 |
rs193152495 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998953 | CAAAAGTTCTTAATA[A/C]GGCATCTAGAATGGT | 55827 |
rs193219166 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010304 | TTTTCACTCATGTAT[A/T]TATGGGTGAATATGG | 55827 |
rs193222300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050268 | TCTGGACCATGGAGC[A/G]TAGCCCTCACTTTTA | 55827 |
rs193225819 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948598 | ATTACACAACCATTA[A/C]AAATGAGCAATAGCT | 55827 |
rs193227719 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973280 | AACATTTTTGGTGAG[A/C]ATTCTCAGGTGATAT | 55827 |
rs193257108 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025884 | GCTTACAAAACCTAC[A/T]TGACTTGATTTCTGT | 55827 |
rs193262458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952765 | CTTCTGCCTCTTCCC[A/G]GAGTTTTTATATCCA | 55827 |
rs193265371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989333 | ATTTAGTTGTGTTTT[C/T]CTAAACAAAACCCCC | 55827 |
rs193270603 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068068 | CTCTGAGAAGCAAAT[G/T]GCAAGTAAAAGCTAA | 55827 |
rs199524585 | in-del | -/A | 0.0360663 | 0.129354 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011160 | TCTTGCTCTGTCACC[-/A]GGCTGGAGTGCAGTG | 55827 |
rs199557349 | snp | A/G | 0.000399281 | 0.0141238 | missense | DCAF6 | GRCh38.p7 | 1:168038454 | ACAGAAGGAACAACT[A/G]CAAGCACAATAAAAC | 55827 |
rs199573600 | in-del | -/CCTT | 0.478437 | 0.10157 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009346 | TTTCCTTCCTTCCTC[-/CCTT]CCTTCCTTCCTTCCT | 55827 |
rs199583522 | snp | C/T | 0.000150909 | 0.00868515 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168068372 | GGTTATAACTCGAAA[C/T]GAACTCATGCTGGAA | 55827 |
rs199586898 | snp | C/T | 0.00199798 | 0.0315436 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167987599 | CTGCACAAAAGAAGA[C/T]TGTAAAGATGTAAGA | 55827 |
rs199597681 | snp | A/G | 0.000813794 | 0.0201553 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966769 | AGAGAAAAAAAATCA[A/G]GAAGGCAGAAATGAA | 55827 |
rs199627667 | snp | A/G | 0.440057 | 0.162414 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072326 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGTCTTC | 55827 |
rs199631459 | snp | C/T | 0.000181715 | 0.00953018 | missense | DCAF6 | GRCh38.p7 | 1:168004683 | CAGCTCAGGCTCATT[C/T]GACATCATCTCCCAC | 55827 |
rs199698110 | in-del | -/C | 0.0248432 | 0.108648 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031997 | AACCAAGCACAGTTT[-/C]AATCTAAATGTATCG | 55827 |
rs199713023 | snp | A/G | | | missense | DCAF6 | GRCh38.p7 | 1:168002560 | GCAAGGCCGGAGAGT[A/G]AACGAGAACGAGATG | 55827 |
rs199718334 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168045295 | TGTTTGAAGTCATTG[-/T]AAGGGAATCTCTCCA | 55827 |
rs199742968 | in-del | -/CTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964142 | CCTCCTTCAGTGCTC[-/CTT]CTTTCTTTATGTAGA | 55827 |
rs199784267 | snp | C/T | 9.95157e-05 | 0.00705322 | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168023027 | AACAGCTCGGATCCA[C/T]GTCACTTGACGAGCA | 55827 |
rs199784937 | in-del | -/A | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997645 | TGTTTAATTTTCAGG[-/A]AAAAAAAATCAATGA | 55827 |
rs199795203 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015562 | TCCTAGAGAAATATA[C/T]GTATCTAATTCATCG | 55827 |
rs199798598 | in-del | -/TCTG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948321 | CTTAACTAGCAGTCA[-/TCTG]TCCTGTGCCAAGGAT | 55827 |
rs199814913 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007962 | GTTATTGTTGTACAT[C/T]TTTTTTTTTTTTTTT | 55827 |
rs199835245 | in-del | -/TTTC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168039366 | AGTAAGGTTGAACTT[-/TTTC]TTTATTTAATGGTCA | 55827 |
rs199881227 | snp | A/G | 0.00199792 | 0.0315431 | missense | DCAF6 | GRCh38.p7 | 1:168043066 | GAATTGGGAGCCATT[A/G]CAAATCTGAGGGTCA | 55827 |
rs199899920 | in-del | -/A | 0.0387552 | 0.1337 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978599 | GAGTTTTTGAAAAAA[-/A]TATCTTCTGCATATG | 55827 |
rs199918829 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168055364 | TTTTTTTTTTTTAAC[A/G]AAGAAGTATTTTATT | 55827 |
rs200026976 | snp | A/C | 2.14756e-05 | 0.00327679 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975051 | TATGATATATATGTA[A/C]GTATGTATATTTTTG | 55827 |
rs200095163 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167978831 | TGGGTAATTTTTTTT[A/T]TTTTTTGTAGAGACG | 55827 |
rs200104830 | snp | A/G | 0.00299551 | 0.0385848 | intron-variant, synonymous-codon | DCAF6 | GRCh38.p7 | 1:168015890 | TGCACATACCCAGCA[A/G]CAGCCTTCCACTTCT | 55827 |
rs200128752 | in-del | -/TCTTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168015749 | TCTATTTTATTACTG[-/TCTTT]TCACCTTTCTTTTCC | 55827 |
rs200134915 | in-del | -/TC | 0.0333695 | 0.124785 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998167 | AGCAAGTCACACAGA[-/TC]TTTTGGTTTCCCAGT | 55827 |
rs200142639 | in-del | -/AA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975784 | CTCCAACTCCTGAGT[-/AA]TCATACAATCCTCCC | 55827 |
rs200149585 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961411 | CCACACCCGGCTAAT[G/T]TTTTGTATTTTTAGT | 55827 |
rs200169844 | in-del | -/T | 0.0433635 | 0.140717 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026712 | TGTGAGTTTTTTTTT[-/T]AATGTTAAGTTTGAA | 55827 |
rs200189322 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009345 | CTTTCCTTCCTTCCT[C/T]CCTTCCTTCCTTCCT | 55827 |
rs200224937 | in-del | -/T | 0.0322114 | 0.122752 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041832 | ATATACCACCTTAGC[-/T]TTTTTTTTGCCAAAA | 55827 |
rs200226971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000811 | TCCACAGAGACAGGA[A/G]GTAGATTAGTGGTTG | 55827 |
rs200233772 | in-del | -/TT | 0.00557542 | 0.0525036 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941834 | ACTAGGGTCGAACAC[-/TT]TTAAATAGATATCTA | 55827 |
rs200253166 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009853 | ATAATTTTCTTTTAC[-/T]TATGATAAGCTCTCT | 55827 |
rs200261747 | in-del | -/AT | 0.0256215 | 0.110247 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995960 | TAGAGGTACAAGTAA[-/AT]ATAAATATGTAAAAC | 55827 |
rs200264933 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017225 | TAATAAAACATTTTT[-/G]GTTTTTTTTTTTGCT | 55827 |
rs200278520 | in-del | -/TTAG | 0.0146672 | 0.084371 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993960 | AATTATAATTAGCAA[-/TTAG]TTACTAATTACTAAT | 55827 |
rs200282567 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937197 | AGCCCCCTGTGCATG[A/C/T]TGCCAGCCGCCGCCC | 55827 |
rs200283219 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022789 | TTCTCAACTCATTCT[C/G]AAAGTTACTAAATGC | 55827 |
rs200291600 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995682 | AAAACTCAGTCTCAG[-/A]AAAAAAAAAAAAAAG | 55827 |
rs200292246 | snp | G/T | 0.0696718 | 0.173152 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049437 | GTTGTTGTTGTTTTT[G/T]TTTTTTTTTTTTTTT | 55827 |
rs200333727 | in-del | -/GGG | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073201 | AAGAAAAAGAAAAAC[-/GGG]AGTATACATAGAAGT | 55827 |
rs200358185 | snp | A/C/G/T | 5.12635e-05 | 0.00506256 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168043109 | CGTCCCACAGAGCTC[A/C/G/T]GTGCAACCACCAGAA | 55827 |
rs200388847 | snp | A/C/T | 3.31764e-05 | 0.00407275 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168044901 | TTATTTTCTGACAGC[A/C/T]CAATCAGATAAGTTC | 55827 |
rs200401545 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168033305 | TTTCTGAAAAGGATC[-/TTTTTTTTTTTTT]TTTTTTTTTGAGACG | 55827 |
rs200434209 | snp | A/C | 0.000848056 | 0.0205745 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066489 | TTTATTGTACTTACT[A/C]TAGACCATATTTCAA | 55827 |
rs200439229 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167996163 | TTCTATTTCCTTACC[A/G]CCTCTAATAATTTCT | 55827 |
rs200439862 | snp | G/T | 0.00498754 | 0.049688 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050943 | AATGAGGTAATTCAG[G/T]ATGTTCCTTCATAAT | 55827 |
rs200444622 | snp | A/C/T | 3.35261e-05 | 0.00409413 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993452 | AGAGGTAGGTTTACT[A/C/T]AAAACCATGTCCTTT | 55827 |
rs200464935 | in-del | -/C | 0.0298908 | 0.118541 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979937 | CCCATCATCCCAGCA[-/C]TTTGGGAGGCTGAGG | 55827 |
rs200513174 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945336 | CATTTTAATGATATT[C/T]TTCTGAATATCCAGT | 55827 |
rs200521057 | in-del | -/G | 0.0142736 | 0.0832652 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940509 | AGCCTCCTGGAATTT[-/G]TTTTTTTTTTTAAAG | 55827 |
rs200523695 | in-del | -/A | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997644 | TGTTTAATTTTCAGG[-/A]AAAAAAAAATCAATG | 55827 |
rs200621093 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167958854 | TGAGTGGTACATTTG[C/T]TGTATTTCATGAGCC | 55827 |
rs200625438 | snp | C/T | 2.17219e-05 | 0.00329552 | synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936968 | GAGGAAAAGGTCCCT[C/T]GGGCTGGAGGACCCG | 55827 |
rs200694842 | snp | A/G | | | missense | DCAF6 | GRCh38.p7 | 1:168003974 | AATAGAGGACGAGGA[A/G]GATCTCGACCCAGAG | 55827 |
rs200704335 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064019 | CATTGCTTTTGTTTT[-/G]TTTTTTTTTTTCCCC | 55827 |
rs200715274 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168029994 | CAAAAAAAAAAAAAA[C/T]AAAAGAAACATGTCT | 55827 |
rs200744444 | in-del | -/TG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009451 | CTCTTTCTTTCTTTC[-/TG]TCTCTCTCTCTTCCT | 55827 |
rs200790575 | snp | C/T | 0.00199797 | 0.0315435 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004464 | TGTGTTTTCTGAGCA[C/T]ATCTGTTTAGAGTTG | 55827 |
rs200843977 | snp | C/T | 3.30557e-05 | 0.00406531 | missense | DCAF6 | GRCh38.p7 | 1:167993264 | ACTGGAATGGTTGCC[C/T]GTTTTATTCCTTCCC | 55827 |
rs200850392 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168023964 | ACACGCCTGTAATCC[A/C]AGCTACTTGGGAGGC | 55827 |
rs200895023 | in-del | -/AAAG | 0.0103295 | 0.0711199 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045357 | CATTCATATAAACTT[-/AAAG]AAACTTTACAGTTTA | 55827 |
rs200898615 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167994220 | GGCTTTAGAAAAAAA[A/T]ATTTTAAATTATTTT | 55827 |
rs200923785 | in-del | -/TT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972350 | ATTCTTTGAACAATT[-/TT]ATTCATTAATAAATT | 55827 |
rs200925439 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005385 | TACGTTCTGTTAAAA[-/A]TGCTATTTTTTTCTC | 55827 |
rs200948191 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011362 | AGCTCGTGATCCACC[C/T]GCCTTGGCCTCCCAA | 55827 |
rs200954948 | snp | C/T | 1.65272e-05 | 0.0028746 | synonymous-codon, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974949 | AATATTTTATACCAA[C/T]GTTGAGCAAGATGCA | 55827 |
rs200967132 | in-del | -/CGCACACA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041893 | AATACATGTTTGTCG[-/CGCACACA]CACACACACACACAC | 55827 |
rs201077407 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168065511 | AGAATTAAAACAAAT[-/A]AAAAAATGTAAGAGT | 55827 |
rs201085062 | snp | A/G | 0.00199792 | 0.0315431 | missense, intron-variant, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167966690 | GCTCAGATGACACCA[A/G]ATTAGTAATTAGTAA | 55827 |
rs201119096 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168056494 | GGGGCGGGGAGGGGC[C/T]CAGGCTTAAGTTTTT | 55827 |
rs201155129 | in-del | -/TG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168002742 | GAAGTGGAATGGCGC[-/TG]AGTCACTGGATAAGT | 55827 |
rs201164669 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986227 | TTATTTTTAGTGGAA[C/G]TGCTGGGTTATAGGA | 55827 |
rs201170790 | snp | G/T | 1.66626e-05 | 0.00288635 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038504 | GTAAGTTAATATTTT[G/T]GTAAAGATGTTCTTA | 55827 |
rs201171039 | in-del | -/A | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993951 | GTTATTACTAATTAT[-/A]ATTAGCAATTAGTTA | 55827 |
rs201178684 | snp | C/T | 1.69908e-05 | 0.00291463 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168043097 | GGAGGAATCTTTCGT[C/T]CCACAGAGCTCAGTG | 55827 |
rs201207426 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009382 | CTTCCTTCCTTCCTT[C/T]CTTCCTTTCTTTCTT | 55827 |
rs201286301 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037101 | ATGAGATTCTCCCCC[-/T]CCCTTTTTTTTTTTT | 55827 |
rs201286396 | in-del | -/AAG | 0.0130921 | 0.0798413 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008657 | GAAATACAACTACAA[-/AAG]AAAAAAAAATCAAAC | 55827 |
rs201294070 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168014936 | CACTATCCCCTTTAC[A/C]TTACCCTGCCAATTT | 55827 |
rs201322254 | snp | A/G | 8.25593e-05 | 0.0064244 | missense | DCAF6 | GRCh38.p7 | 1:168045077 | ATGAAAATAACACCA[A/G]TCCTGAGCCTCAGTT | 55827 |
rs201324090 | snp | A/G | | | missense | DCAF6 | GRCh38.p7 | 1:168002567 | CGGAGAGTGAACGAG[A/G]ACGAGATGGTAACTA | 55827 |
rs201378959 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167991722 | TAGCTCATGGTGGTT[A/C]CTGCCAATCCTTGGC | 55827 |
rs201382199 | in-del | -/ATTG | 0.0221141 | 0.102801 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073964 | ATTTTATAAATATGT[-/ATTG]AATACATATTTATAA | 55827 |
rs201409873 | snp | A/G | 1.80156e-05 | 0.00300124 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974806 | TAATAAGTTACCATT[A/G]ACTGCTTTCTTTGTG | 55827 |
rs201412865 | in-del | -/TAATA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168039746 | TTACTATAATATATG[-/TAATA]TAATATAGTTATGTA | 55827 |
rs201450110 | in-del | -/ATA | 0.00914312 | 0.0669923 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994031 | TAATAATTTGTAATT[-/ATA]ATTAGTAATGACAAA | 55827 |
rs201480453 | in-del | -/T | 0.0402882 | 0.136092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031994 | TGGAACCAAGCACAG[-/T]TTCAATCTAAATGTA | 55827 |
rs201541841 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168006265 | TTAAATGTGACAATC[A/G]TTTGAATTATTGAAG | 55827 |
rs201549898 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058084 | GATGTCATACTGTAT[A/G]CAAGACTGGGACTCT | 55827 |
rs201563029 | in-del | -/CC | 0.039522 | 0.134904 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963524 | AGCTCACTGCTACCT[-/CC]CCGCCTCCCAGGTTC | 55827 |
rs201580904 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995157 | ATACATGGGTAAGTA[-/T]AAGTTATAGTCAAAC | 55827 |
rs201606118 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974213 | GGTACCTTGCCCATT[-/A]AAAAAAAAATCAGGT | 55827 |
rs201612004 | in-del | -/T | 0.077417 | 0.180873 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943846 | TCATGATTTCATTCA[-/T]TTTTTTTTTTGAGAT | 55827 |
rs201615768 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168033010 | AGCATTTTTTTTTTT[-/T]ACTATGGTTATCACA | 55827 |
rs201620238 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168002740 | TAGAAGTGGAATGGC[-/T]GCAGTCACTGGATAA | 55827 |
rs201641031 | snp | A/C/G | 8.47054e-05 | 0.00650741 | missense | DCAF6 | GRCh38.p7 | 1:168043069 | TTGGGAGCCATTGCA[A/C/G]ATCTGAGGGTCAGGA | 55827 |
rs201683584 | snp | A/C | 8.32161e-05 | 0.00644989 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038497 | ATGAATGGTAAGTTA[A/C]TATTTTTGTAAAGAT | 55827 |
rs201688980 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938282 | TGTGTTTGTGTGTGT[C/T]TGAGAGAGACACCTG | 55827 |
rs201699377 | in-del | -/ATATTAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168039686 | TATTAATATATTAAT[-/ATATTAA]ATATTTAATTGTATA | 55827 |
rs201706480 | in-del | -/ATTAATAT | 0.00597247 | 0.0543191 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039664 | TATTAATTATTCATA[-/ATTAATAT]ATTAATATATTAATA | 55827 |
rs201756029 | snp | A/G | 3.35413e-05 | 0.00409506 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044707 | AATTGCTTTGTATGG[A/G]AAAATAAAAAGCCTT | 55827 |
rs201802007 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168008273 | TGCACCCGGCCTATT[G/T]TTGTACGTCATAAAT | 55827 |
rs201815206 | snp | A/C | 0.000115686 | 0.00760459 | missense | DCAF6 | GRCh38.p7 | 1:168045106 | TTCCAAACAGAAGCC[A/C]CTGGGCCTTCAGCTC | 55827 |
rs201857344 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064036 | TTTTTTTTTTCCCCC[-/T]CTCTTTCTCACATTT | 55827 |
rs201913080 | snp | A/G | 0.000627208 | 0.0176978 | missense | DCAF6 | GRCh38.p7 | 1:168044627 | TGACAAAATATCAGG[A/G]AGGAGTATCTGCAGA | 55827 |
rs201922591 | snp | A/G/T | 3.36526e-05 | 0.00410188 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991166 | TTTCACCTCTGCTGT[A/G/T]TAACTATATGTAATT | 55827 |
rs201936206 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167960563 | TGTCTTGGCCTCCCA[A/G]AGTGGTGGGATTACA | 55827 |
rs202004365 | in-del | -/TAT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036711 | TGTAAGCTAAAGGTC[-/TAT]TAATTCAGTTATTTA | 55827 |
rs202065715 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935699 | AGGAAGCGAGAAGGA[A/G]GGTCTCGATAAGGAG | 55827 |
rs202075843 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995303 | GCTGAGTCATGAACA[-/T]TTTTTTTTTCTGGGA | 55827 |
rs202077282 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943288 | ATAAAAATTTTAGAA[A/G]TAGCTTGTCAATTTC | 55827 |
rs202085958 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028004 | AATTTTCAGTGTTCT[-/C]CAAATTTGGAGTTGT | 55827 |
rs202111993 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049434 | GTTGTTGTTGTTGTT[G/T]TTTTTTTTTTTTTTT | 55827 |
rs202187604 | snp | A/G | 0.000131876 | 0.00811915 | missense | DCAF6 | GRCh38.p7 | 1:168044939 | AGCCATTGGATTCCA[A/G]CTCAGGAGAAAGAAA | 55827 |
rs202191716 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962709 | CCCTGTAATCCCAGC[A/C]CTTTGGGAGGTCGAG | 55827 |
rs202226756 | in-del | -/TACAAAAAA | 0.0240643 | 0.107019 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988913 | GTGAAACCCTGTCTC[-/TACAAAAAA]TACAAAAAATTAGCC | 55827 |
rs207460582 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167979192 | GTTTTTTGTGTTAAC[A/G]TAATTTATTTTTTAG | 55827 |
rs367545192 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938132 | AATGAAGCAAAAATC[C/T]CTTTGATCCCTCCCA | 55827 |
rs367552627 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972601 | GGGAAAGATGACTCA[A/G]GCACAGATAATGACA | 55827 |
rs367555228 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167951054 | TTATCTCTTTTTCCT[G/T]CTTTATTTTTCTGCA | 55827 |
rs367577811 | snp | A/C/T | 7.03351e-05 | 0.00592986 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951903 | GAAGGGATTTGATAC[A/C/T]AAGTGTTTAAGTGTT | 55827 |
rs367578427 | snp | C/T | 1.75151e-05 | 0.00295927 | missense | DCAF6 | GRCh38.p7 | 1:168075400 | GACAGATCAGAAGGC[C/T]CTGGTCAAGAGAATG | 55827 |
rs367588117 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167987789 | CATATAGTTTATAAT[C/T]AGAAATTGAAAAATG | 55827 |
rs367597180 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966455 | TGGCCGGAGACAATT[A/C]TTCTTCTTCTACTGT | 55827 |
rs367603056 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167946980 | ACATTTGGTAGAATT[C/T]GGCTGTGAAGCCATC | 55827 |
rs367610595 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975789 | AACTCCTGAGTTCAT[A/G]CAATCCTCCCACCTT | 55827 |
rs367680902 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168006296 | AAGAAAAAATATCTT[C/T]GGTGGTCATGTGATG | 55827 |
rs367699323 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961303 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAA | 55827 |
rs367702995 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997179 | TTCACATACTCAGAA[A/C]GTCAAATTTGAGATT | 55827 |
rs367709208 | snp | C/T | 5.09446e-05 | 0.00504675 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966766 | ATGAGAGAAAAAAAA[C/T]CAAGAAGGCAGAAAT | 55827 |
rs367735112 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009445 | CTCTCTCTCTTTCTT[C/T]CTTTCTGTCTCTCTC | 55827 |
rs367746432 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954777 | TTTTTAAGAGCTTTA[-/T]TGAGATATGATCAGC | 55827 |
rs367748107 | snp | A/G | 6.60458e-05 | 0.00574618 | missense | DCAF6 | GRCh38.p7 | 1:168044629 | ACAAAATATCAGGAA[A/G]GAGTATCTGCAGAAA | 55827 |
rs367750492 | in-del | -/TCT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167973759 | ATTCCCCACTCACCT[-/TCT]CTCTATTGTATATCT | 55827 |
rs367760226 | in-del | -/CT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168027480 | TATTTGAATATATCT[-/CT]GACTAATGATTATTT | 55827 |
rs367798220 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058260 | TAGTTTTTGGTATTA[A/C]CAGTGCTGCTTTGAG | 55827 |
rs367811501 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168032349 | TCCTAGAAGCAGCAT[A/C]TCCACTTTGAATCCA | 55827 |
rs367853220 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040887 | TTCAACATTCATTGT[-/A]AAAAAAAAAAAAAAA | 55827 |
rs367930800 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046211 | CTATAAAATAGGGTT[A/G]TGATTATCTAAAATT | 55827 |
rs367941513 | snp | A/T | 0.0126979 | 0.078662 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935064 | GTATTACACAAACAG[A/T]GATCTAGGCTTTTGC | 55827 |
rs367944117 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168051114 | TAGCTGCATGCACTG[C/T]ATGGGGATAGAATGA | 55827 |
rs367973474 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058913 | AATTGAGTTGTTTTT[A/C]TTTTCCTTATTGATT | 55827 |
rs368013464 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040629 | TTAAGATGACAGTAG[A/G]TCATCGTACTTATCA | 55827 |
rs368043289 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988808 | CCTTTAGGCTGGGTG[C/T]GGTGGCTCATGCCTC | 55827 |
rs368070889 | multinucleotide-polymorphism | CA/GG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168065228 | AAGTCCCTCTTCTTA[CA/GG]GGGGATTTTCTATTA | 55827 |
rs368071764 | snp | A/G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064360 | TTTGAGATGACTAGT[A/G/T]TAACTGTTACTCTGA | 55827 |
rs368073749 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168015425 | TGTGTATAAATCAGA[G/T]GAGTTAACTGATTGT | 55827 |
rs368098945 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168027853 | CAATTTGATAGAAGT[A/G]TGTTTAGCCTGAATC | 55827 |
rs368157823 | in-del | -/TGATTGTTTATAACA/TTTTTTCACTTTTGATTGATTGTTTATAACA/TTTTTTCACTTTTGATTGTTTGTTTATAACA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009843 | ATAAAAATTTATAAT[lengthTooLong]TTTCTTTTACTATGA | 55827 |
rs368191039 | snp | G/T | 4.08388e-05 | 0.0045186 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937055 | GGTCGCCGCCTAGAG[G/T]GGGGGAGGGGGCACG | 55827 |
rs368193640 | snp | C/G | 1.65151e-05 | 0.00287355 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167993278 | CCGTTTTATTCCTTC[C/G]CATCTTAATAATAAG | 55827 |
rs368203047 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971550 | ATACTTTTGGACTGA[A/G]CTTCAAGTTTTGGGA | 55827 |
rs368222117 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025677 | ATAGAGACTGCCCAC[C/G]ACCATTTGTCTCTCC | 55827 |
rs368231938 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167984366 | AAAGGCATTAATTAT[A/G]AGAAATAGATACATG | 55827 |
rs368270987 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005409 | TTTTCTCAGTATTAT[A/G]AGTCTTTATGGTCAA | 55827 |
rs368274983 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167988643 | CAAAATATGTTTTTA[A/C]TGAAAGTTACAAAAA | 55827 |
rs368292905 | snp | G/T | 0.000153988 | 0.00877327 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004487 | TAGAGTTGTTGGTTT[G/T]AGAAAATATTTAAAA | 55827 |
rs368300074 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168063233 | TTTCTTTTCATTTCT[C/T]TTTATGTGTTTTCTT | 55827 |
rs368362439 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041083 | TTTCTCCCTTGAAAA[C/T]GGGCATGTTTAATAG | 55827 |
rs368376489 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168022993 | TTTGTTTCAGATTCT[C/G]CTTCTTCTGTGGTTA | 55827 |
rs368387867 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035726 | TATTACCAATATTTG[A/G]CATGTTTTGTAATAT | 55827 |
rs368422144 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072025 | TCTTCCCTGGTAGTG[C/T]GGTGGCTCATGCCTG | 55827 |
rs368438878 | in-del | -/GTCA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072400 | CTTCCCTCTCACTTA[-/GTCA]TTCTTGTTCATTGCC | 55827 |
rs368518237 | in-del | -/CT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009413 | TCTTTCTCTCTCTCT[-/CT]TTTGTTTCTTTCTGT | 55827 |
rs368550113 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168027608 | CTTCACCATTTTCCA[A/G]GTGCCCAAATCATTT | 55827 |
rs368554519 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168076343 | GCGTTGGTCTTGCTG[C/T]CTGAGGGATGGCAGA | 55827 |
rs368558173 | snp | A/G | | | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168076151 | CTGATAGCATGGTCA[A/G]TTAACACATATTTTG | 55827 |
rs368564689 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962846 | TATAATCCCAGTTAC[C/T]TGGGAGGCTGAGGCA | 55827 |
rs368602018 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952269 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCAAGCT | 55827 |
rs368615097 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054137 | GATAAAGCTAGATAA[C/T]GCTAACATACTAATA | 55827 |
rs368669077 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987183 | AGCTTTGAATAGTTT[A/G]AACAAGCTACCTAGG | 55827 |
rs368673629 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167966184 | TTACAGTTTGTTAAC[A/T]TTTTATTTGTTGTTA | 55827 |
rs368678222 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978373 | TTCTGATCTTTGCCA[A/G]CAGTTGGTATTTTCA | 55827 |
rs368734933 | snp | A/G | 0.00237315 | 0.0343649 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935707 | AGAAGGAAGGTCTCG[A/G]TAAGGAGCCATTCAG | 55827 |
rs368749102 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168008998 | TCTCCTTCCTTCCTT[C/T]CTTTCTTTTTCTTCT | 55827 |
rs368752646 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982188 | GGCGAAGTGTCTGTT[C/T]ATGTCCTTTGCTCAT | 55827 |
rs368765823 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167969694 | TTTTACTTAATTGTC[C/T]TGGCTTAGCAAAAAA | 55827 |
rs368823756 | snp | C/T | 1.65875e-05 | 0.00287984 | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168023032 | CTCGGATCCATGTCA[C/T]TTGACGAGCAACAGG | 55827 |
rs368901629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045898 | ACTATTTCTATTATT[A/G]GTGCTATCATATCTT | 55827 |
rs368936998 | in-del | -/AAGAT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040616 | CTTAATACATAATTT[-/AAGAT]GACAGTAGGTCATCG | 55827 |
rs368937156 | in-del | -/CTTCTTTGGCATGTGCACATTC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167983630 | GGGCCTTCTTGGGTC[-/CTTCTTTGGCATGTGCACATTC]TTATATATGTGCATA | 55827 |
rs368952074 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168018285 | CTAAAACACCATTCT[A/G]AGGCACCAAATGATA | 55827 |
rs368986637 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944522 | TAGGATAAGGTGATA[C/T]CTCATTGTGAATTTG | 55827 |
rs369013894 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167949896 | ACTAAAAGGGTAGTG[G/T]ATGTTTTTGCTAGTT | 55827 |
rs369024246 | snp | A/G | 4.94882e-05 | 0.0049741 | missense | DCAF6 | GRCh38.p7 | 1:168063727 | CCGCTAGTAAAAATG[A/G]TTTATAAAGGCCATC | 55827 |
rs369044688 | snp | A/C/T | 6.16242e-05 | 0.00555058 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975043 | TATGATTATATGATA[A/C/T]ATATGTAAGTATGTA | 55827 |
rs369050344 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167980869 | TTGTTGTTATATCTA[A/G]TAAATCATTGTAAAA | 55827 |
rs369068482 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012804 | TATTTAAAAAGCACC[A/G]GAAATATTGAATAAA | 55827 |
rs369082564 | snp | C/T | 4.95152e-05 | 0.00497545 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002466 | TACATAGAATTTACC[C/T]GTTCTTATTTTTTAG | 55827 |
rs369082616 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968931 | TATCTGCTTCTTGGT[A/G]TTATTGCAATGTGAA | 55827 |
rs369105281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072167 | CTGGGTGTGGTGGCG[C/T]GTGCCTGTAGTCCCA | 55827 |
rs369105952 | snp | A/T | 0.00066361 | 0.0182034 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066360 | GCTTCATATTAATAT[A/T]TAAATTTTATTTCTA | 55827 |
rs369106333 | snp | G/T | 2.67476e-05 | 0.00365692 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937015 | GATACCTGGGTGAGC[G/T]GGGGCCCCGGGGCGG | 55827 |
rs369110984 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048879 | GCATTTGGCGGAGAT[C/G]TAGCCCAAGAGCCAT | 55827 |
rs369113107 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168026263 | AATAATTTCCTCTAT[A/G]CCTAAAATCATACAT | 55827 |
rs369118959 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167999096 | ATTACTCTTTGATCT[A/G]TGGGATACAATGAAA | 55827 |
rs369135708 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975374 | CTTGCTTGTGTAAAG[G/T]CATAGCCAACATGCT | 55827 |
rs369159879 | snp | A/G | 0.000148411 | 0.00861298 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168002496 | GTTGCGACAACCACC[A/G]GTTAAGCGTTTGAGA | 55827 |
rs369182275 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167984916 | AGGTTTATTGGACTT[-/A]ACAGTTCTGTGTACC | 55827 |
rs369196603 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948054 | TAGTACTCCAGTGTC[A/G]GGTGCAAATATGTAT | 55827 |
rs369232908 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009490 | TCCCTCCCTTCCTTC[-/A]CTTCTTCCCTCCCTT | 55827 |
rs369237362 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035963 | GCTACTCTGGAGGCT[C/G]AGGCAGGAGAATTGC | 55827 |
rs369247764 | in-del | -/AT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168033036 | TACTATGGTTATCAC[-/AT]GTGTTTTTGTATGTC | 55827 |
rs369263808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950050 | GTTCTAATGTGCAAA[C/T]GTCATATAGAAGAGT | 55827 |
rs369297247 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017716 | AATGCAGTTTTGTAT[A/G]TGGACATTAATTGAT | 55827 |
rs369299958 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985117 | TTCAGTTACCTCCCA[C/G]TGGGTCCCTCCCACA | 55827 |
rs369306474 | in-del | -/AAAAAAAAAAAAAAAAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072295 | AGGGAGAATCAGTCT[-/AAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAG | 55827 |
rs369331069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066150 | AAAGAACAATGAATA[A/G]GTGACTTCAACAATG | 55827 |
rs369365164 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007953 | TATGTTTTTGTTATT[G/T]TTGTACATCTTTTTT | 55827 |
rs369378256 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962171 | TGTATATTCTGCTGT[C/T]GTTGAATGAAGTAGT | 55827 |
rs369388952 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964860 | CATTGTTCCTTTCTG[-/T]TACATTGTTTTTGAT | 55827 |
rs369467496 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963248 | CAGCCTGGGCAAAAG[C/T]GTGAAACTCTGTCTC | 55827 |
rs369473335 | snp | C/T | 1.65072e-05 | 0.00287286 | missense | DCAF6 | GRCh38.p7 | 1:168065714 | CTGATAATCATGTGG[C/T]AAACTGCCTGCAGCC | 55827 |
rs369493272 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001920 | TTTTATTTTCTCTGA[A/G]GTAGGAGGAAAAATT | 55827 |
rs369499777 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168042777 | AAATACATACTAGAT[A/T]ATGAAAGGATCCAAA | 55827 |
rs369502712 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954814 | TATTTAAAGTGTACT[A/G]TTTGATATGTTTAAC | 55827 |
rs369504346 | snp | A/G | 9.91015e-05 | 0.00703853 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168045084 | TAACACCAATCCTGA[A/G]CCTCAGTTCCAAACA | 55827 |
rs369550095 | snp | C/T | | | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075652 | TTTTAAAACTTTTTG[C/T]CGTGTATGAGGAGTG | 55827 |
rs369582005 | in-del | -/CTC | 0.00676609 | 0.0577691 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015314 | TTTTTTAGAGCTCTT[-/CTC]AATAAATTCTGAGTT | 55827 |
rs369584766 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944932 | TCAATTGCATTCTTC[C/T]GCATATGGATATCTA | 55827 |
rs369658760 | in-del | -/TC | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009429 | TTTTGTTTCTTTCTG[-/TC]TCTCTCTCTTTCTTT | 55827 |
rs369669818 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168068661 | TACATTTGTCGTAAA[A/G]TGGTCAAAATGAAAA | 55827 |
rs369685468 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043962 | TTTAAGTTTAGATTT[C/T]GGGAAGGTTAGTAAA | 55827 |
rs369697861 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167963995 | AGCACTCATAAGCAT[A/G]TTTTTGTATATGTGC | 55827 |
rs369706016 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942809 | CTTTGTTGAAAATCA[A/G]TTGACCATAAATGTT | 55827 |
rs369718530 | in-del | -/ACAT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168053291 | GACAGTGTAATACAT[-/ACAT]GCATACAGAAATAAA | 55827 |
rs369776001 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029484 | ACACTACTGTCTTCT[C/G]TACTGGGAGCATTGA | 55827 |
rs369778479 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168031297 | GGAGATTGAGAAGAA[C/G]CAACTAGAGAGGTGG | 55827 |
rs369791899 | in-del | -/C | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936546 | ACCAGCCTCAGTCCC[-/C]AGGGTGGTCGTCATC | 55827 |
rs369834393 | in-del | -/TTACAGGTGCC | 0.226188 | 0.248863 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963577 | CCTGAGTAGCTGGGA[-/TTACAGGTGCC]TGCCACCACACCCAG | 55827 |
rs369878293 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985849 | GTACTCAGCATCTAG[A/T]ACAAGAAACAGCCCC | 55827 |
rs369888965 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985245 | TGTGTGTGCGTGCGC[A/C/G]TGTGCACGTGGCTTA | 55827 |
rs369892561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943819 | TCTAGTTCCATCCAC[A/G]TTGCTGTATATGTCA | 55827 |
rs369918453 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937582 | TCCCAGTTCCACTCT[C/G]CTCTTCAGTTCGTTT | 55827 |
rs369920853 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989610 | CTGAGGGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 55827 |
rs369951469 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024043 | AATATAGCGAGACCC[C/T]GTCTCTTAAAAAAAA | 55827 |
rs369957691 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982026 | TTCTCTGCGGCCTCA[C/T]CAGCAACTTTTGTTT | 55827 |
rs369988779 | in-del | -/TTTG | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058565 | CTCCTGATCTGGTTT[-/TTTG]TTTGTTTGTTTGTTT | 55827 |
rs369995569 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035062 | AACCTGATAGGTTGT[A/G]TATGACCAAGCAAAC | 55827 |
rs369997354 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167989176 | TATGCAAATAGGGAA[A/G]CATTGAACTAAACTC | 55827 |
rs370002372 | in-del | -/T | 0.359364 | 0.22481 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054819 | AACATACGGGTTTGG[-/T]TTTTTTTTTTTTTTT | 55827 |
rs370039386 | snp | A/G | 1.70072e-05 | 0.00291605 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168043100 | GGAATCTTTCGTCCC[A/G]CAGAGCTCAGTGCAA | 55827 |
rs370126282 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049542 | TGGGGGACTATAGGC[A/G]TGAGCCACCGCGCCT | 55827 |
rs370148100 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003319 | AAAAACTTGTTTACT[G/T]GCAGGAGGAAAAGGA | 55827 |
rs370155257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960590 | TACAGGCACTTTATA[A/G]TAAGTCTTGAAGTTG | 55827 |
rs370231009 | snp | A/G | 0.000432943 | 0.0147066 | missense | DCAF6 | GRCh38.p7 | 1:168063623 | GTAATTCATATAGAC[A/G]CTCTGCTGTTGCCCG | 55827 |
rs370241807 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168045450 | AGTCTTCATTCTCCA[C/T]ATCTCTAGCACTGAG | 55827 |
rs370244393 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056453 | GGGGTCGCAGCGCTA[A/C/T]GCCTCGGCCACCCGC | 55827 |
rs370282731 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167979610 | CATTTATCTAGGCTG[G/T]GTGCTGTGGCTCATG | 55827 |
rs370286423 | snp | A/C/G | 6.65796e-05 | 0.00576942 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991190 | TGTAATTGGTATTAT[A/C/G]TTATGTTTTGTAGGA | 55827 |
rs370291307 | snp | A/G | 0.000299865 | 0.012241 | missense | DCAF6 | GRCh38.p7 | 1:168003969 | AAAGCAATAGAGGAC[A/G]AGGAAGATCTCGACC | 55827 |
rs370317925 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013563 | TTTTTATGCACCTAT[G/T]CAAAACCAATTCCTC | 55827 |
rs370324913 | snp | A/C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168063552 | ACTTACTATATTTTC[A/C/T]TAAGTTTCTCATTAT | 55827 |
rs370328260 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167999608 | AGGACTTGCTGCTTT[A/G]CCTTGTACTTTTATG | 55827 |
rs370330569 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168014996 | AAACACATATGTTCA[A/G]CATCATGTGTGCCTG | 55827 |
rs370331379 | snp | A/G | 3.29603e-05 | 0.00405944 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167991236 | TCGACGTGCTGCCAC[A/G]TCTGTTGCTATTTGC | 55827 |
rs370335406 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167969284 | TACTCTTTTAGGCTC[A/C]TAGAATGTAATCTTC | 55827 |
rs370399845 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961311 | GCAGTGGCGCGATCT[C/T]GGCTCAATGCAAGCT | 55827 |
rs370404308 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938407 | ATTATTACATAGTAG[C/G]TAACATTATGAAGTA | 55827 |
rs370431797 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168003294 | ACTTTTAATTTGAAA[A/G]TACCCTTGGAAAAAC | 55827 |
rs370447027 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168031733 | AGGAGAATATACCTG[A/C]GGAAACAGTCATGAA | 55827 |
rs370456367 | snp | A/G | 0.000101537 | 0.00712446 | missense | DCAF6 | GRCh38.p7 | 1:168004644 | CTGAACAATTTCTTC[A/G]GCCTTCTACATCCTC | 55827 |
rs370460088 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050130 | TAGTCTTGAATAGTT[G/T]TTAATTATAGCCTCA | 55827 |
rs370460448 | snp | G/T | 1.80338e-05 | 0.00300276 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068468 | TATCCGAGCTGGTAG[G/T]AACTTTAAGTATACT | 55827 |
rs370467772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024751 | GGAGGTTACAGTGAG[C/T]CGAGATTGCGCCATT | 55827 |
rs370468059 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989402 | AGTCTTTCCTTAGTA[A/G]AACTTTTCCTTTATG | 55827 |
rs370515138 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013064 | ATTTCTTTTGAAGTG[C/T]GAAGTGACAAACTTT | 55827 |
rs370531728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035394 | TGAGGATGCAGCGAG[C/G]CATGATTTCGCCACT | 55827 |
rs370551187 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030788 | CTTTTGTAAAACAAA[C/T]ACACTGTTTTTACTT | 55827 |
rs370555123 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992964 | ATTTTCCTTGATTAA[C/T]TCATTTCAACAAAGC | 55827 |
rs370557684 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986803 | TGGGTCTTTGGGACA[C/T]AGGGAGAGAAGAACT | 55827 |
rs370570817 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943952 | CACGCCATTCTCCTG[C/T]CTCAGCCTCCCAAGT | 55827 |
rs370571548 | in-del | -/ATTA | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978579 | TTTTATTTTGTTATT[-/ATTA]ATTTATAGGAGTTTT | 55827 |
rs370573025 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167952354 | TCCTGGGTAGCTGGG[A/T]CTACAGGTGCCTGCC | 55827 |
rs370599559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984021 | TACAACTACCATAGT[C/T]GCAAGGCTGCTGTTG | 55827 |
rs370610100 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938974 | TACAGGGAGTTCTTT[A/G]TCTTAAATAATATTT | 55827 |
rs370630507 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075746 | AAGAATAATTTTCAT[C/T]ATAGTGAAAATGTTG | 55827 |
rs370659710 | in-del | -/AACTA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168068590 | GTAGCTTAACTTCTA[-/AACTA]GGATTTCTGTGAATG | 55827 |
rs370678424 | in-del | -/AAAAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072294 | agggagaatcagtct[-/AAAAA]aaaaaaaaaaaaaaa | 55827 |
rs370689907 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061294 | AACACTTTTTAAGTA[A/C]GTCTATATAGCTTAA | 55827 |
rs370699264 | snp | A/G | 1.65935e-05 | 0.00288036 | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168023020 | GTTAACAAACAGCTC[A/G]GATCCATGTCACTTG | 55827 |
rs370705581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965612 | ACCATACCCCCACCG[C/T]ATGACTGGGTTCCCT | 55827 |
rs370707163 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058162 | TAGCTCTTGCCCAAT[A/C]ATTTTTACTGCTATC | 55827 |
rs370763073 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168011111 | CTCAGACCATCAGAA[-/T]TTTTTTTTTTTTTTT | 55827 |
rs370801908 | in-del | -/TA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168010263 | AAAAAATTGTCTCAT[-/TA]TATATATATATATTT | 55827 |
rs370812742 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954640 | GGTATTTTTAGTAGA[C/G]ACGGTGTTTCACTGT | 55827 |
rs370816683 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167965418 | AGTGGGTAGGCTGTG[C/G]TGAAATAGCTTTTCT | 55827 |
rs370824617 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965926 | AGACGTGAGCCACCG[C/T]GCCCGGCCTTCCCTG | 55827 |
rs370826741 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997352 | GGATGAAGCCCTCTC[C/T]TTTTGGGAGTGATTA | 55827 |
rs370885588 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168076057 | AGTGGCACCAGCCCC[C/G]CTCACAGTTGAAGAT | 55827 |
rs370889459 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974231 | AAAAAAATCAGGTCT[C/T]GTCAGTTATTTTTCC | 55827 |
rs370926316 | snp | C/G | 0.00014259 | 0.00844243 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951781 | TGATTTATTTAATTT[C/G]TTCTTTCTTTTTAAA | 55827 |
rs370940214 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | DCAF6 | GRCh38.p7 | 1:168057934 | TCTACCTGTTCACCC[C/T]ATTTTGTCCATCTGC | 55827 |
rs370972180 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998188 | GGTTTCCCAGTGCAT[A/G]TAAAAGTTATGTTTA | 55827 |
rs370982183 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955187 | CACCTGTCAGTGGAC[A/T]TTGGGTTGTATCCAG | 55827 |
rs371005449 | in-del | -/CTGT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167947873 | ATGTTTTGTAAATGT[-/CTGT]TAAGTTCATTTGGTC | 55827 |
rs371069651 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070476 | ACTCCAGAAGGCTTC[A/C/G]TAGGAAGTCCAGGGA | 55827 |
rs371072672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048641 | AGATATTTTTAAATG[A/G]AATGCTCTTCTCATT | 55827 |
rs371086151 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009191 | TTTTAGTAGAGACAG[C/G]GTTTCACCGTGTTGG | 55827 |
rs371091382 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052924 | TTCCTTGCCTGGTAT[A/G]TAGGGCACTTCATAT | 55827 |
rs371128278 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168027326 | ATGTTTATAGAGTAA[-/A]CAGATTGTGTGTTCA | 55827 |
rs371147051 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064015 | GTAATCATTGCTTTT[G/T]TTTTTTTTTTTTTTT | 55827 |
rs371193317 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968009 | GTGTTGGGATTACAG[A/G]CATGAGCCACCACGC | 55827 |
rs371304934 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954840 | TTAACACATGTAAAC[A/T]TACACAAAGTCATCA | 55827 |
rs371337853 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168008523 | AATCTGCCTGTACCT[A/G]CTGTTGTTCCATTAT | 55827 |
rs371352033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026323 | TGAGTAAATGAATTC[C/T]TTAAGCAATTATTTA | 55827 |
rs371352526 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988440 | CCAAAGTGCTGAGAT[G/T]ACAGGGATGAGCCAC | 55827 |
rs371355971 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054214 | AATTAATAAAAGAAA[C/T]GCATTTTTTACAGTT | 55827 |
rs371366575 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168069651 | TGAAAGAAGACCCAT[A/G]TGTTTGTAATTAAAA | 55827 |
rs371382901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055865 | AACTCTGCTGGCTTG[C/T]GTTATTTCATACTAG | 55827 |
rs371435176 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168006666 | GGAATTGTCCATTGG[G/T]TGAATGTAGTAGATG | 55827 |
rs371443162 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168006290 | TTGAAGAAGAAAAAA[C/T]ATCTTTGGTGGTCAT | 55827 |
rs371459266 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167942106 | GTTTCGCTCTTGTCG[C/T]CCAGGCTGGAGTGCA | 55827 |
rs371517707 | snp | C/T | 1.651e-05 | 0.0028731 | missense | DCAF6 | GRCh38.p7 | 1:168044600 | AAGCTCCTGAAGAAT[C/T]ATCAGAGGATGTGAC | 55827 |
rs371524406 | snp | C/T | 8.29346e-05 | 0.00643898 | intron-variant, synonymous-codon | DCAF6 | GRCh38.p7 | 1:168023037 | ATCCATGTCACTTGA[C/T]GAGCAACAGGGTGCG | 55827 |
rs371549538 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168031611 | TCTCCTAAACTGTCT[-/T]ACCTCATTTGTTTTC | 55827 |
rs371557591 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969606 | TATTTAAATAAGTGT[A/G]TATCATCTATCAGCT | 55827 |
rs371569588 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009477 | CTTCCTTCCTCCCTC[C/T]CTCCCTTCCTTCACT | 55827 |
rs371589283 | snp | C/T | 8.55278e-05 | 0.00653885 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044856 | TTAAATAATTAGTAT[C/T]GCCCACATTACCACC | 55827 |
rs371592075 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168048872 | AAAATCGGCATTTGG[C/T]GGAGATCTAGCCCAA | 55827 |
rs371594321 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168063022 | GTTCATGCCATTCTC[C/G]TGCCTCAGCCTCCCG | 55827 |
rs371597403 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055107 | AATTTATTCTTTTAA[C/T]ATCTTTTTTCTTATT | 55827 |
rs371597865 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028386 | TCTGAGTTTTAGGTT[A/T]TGGCCATGATTGAAA | 55827 |
rs371598030 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035290 | TTTCTACAAAAGTTA[-/A]CTACAAATTAGCCAG | 55827 |
rs371614334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006363 | TTATTTATAGGAAGT[A/G]AGGAAATATTTTTAA | 55827 |
rs371720331 | snp | A/T | 0.000397542 | 0.014093 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966589 | GCATATTTTCTTTTA[A/T]GTCCAATTTGCTTAT | 55827 |
rs371723765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058428 | TCGTGTTTATTCACA[C/T]CACTGATTCTTGTTG | 55827 |
rs371737621 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168010238 | TTAAGGTAACTTACA[A/G]AAATACTTTAAAAAA | 55827 |
rs371742109 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941129 | TTGCCTCTTTTTTTA[A/G]CCATTGGGGAAAAGT | 55827 |
rs371742507 | in-del | -/AATT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036715 | AGCTAAAGGTCTATT[-/AATT]CAGTTATTTATCAGA | 55827 |
rs371753497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966829 | TTATATTAGAATATC[C/T]TCCCTATTTTGCTGA | 55827 |
rs371754101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035425 | GCACTCCAACCTGGA[C/T]GACGGAGTGAGACTC | 55827 |
rs371854963 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971142 | GATCACCTGCTTTCT[C/T]GGGTATCTCCCATCT | 55827 |
rs371881262 | snp | A/C | 0.000307953 | 0.0124049 | synonymous-codon, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974877 | AAACATATTTAGTGC[A/C]AAGTTCTTACCTTGT | 55827 |
rs371887009 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984487 | ATATCCTTGGAAATA[A/T]ATGCTTCCAATGATT | 55827 |
rs371930763 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167947835 | TGATGAAAATATTGT[A/G]TATTCTGCAGTTGTT | 55827 |
rs371933696 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167942351 | TTACAAGCATGAGCC[A/G]CTGCGCCTGGCCTTT | 55827 |
rs371943166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942626 | TAATCCAAGGTAACA[A/G]AGATTTTTACTTTTT | 55827 |
rs371949456 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167953680 | TCTTGGCTCACTGCA[A/G]CCTCCGTCTCCCGGG | 55827 |
rs371950432 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040635 | TGACAGTAGGTCATC[A/G]TACTTATCACGTCTT | 55827 |
rs371997173 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168027942 | AAATTGTAGGGAAAT[A/G]AATGTATAACATGCA | 55827 |
rs372023431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059302 | GTGATCTGCTATCCC[A/G]CCTATGTCATATTAC | 55827 |
rs372070991 | snp | C/G | 1.72832e-05 | 0.00293961 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991384 | GACTGTCAGTTCAAA[C/G]AGTAAATCTCTATGA | 55827 |
rs372082854 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959496 | GTCCTTCAAAGTGAC[A/T]GTACAATTTTGCATT | 55827 |
rs372107371 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167960937 | ACAAGTTGGGAATAA[C/T]TGACATCTTGAAAAT | 55827 |
rs372111255 | snp | A/G/T | 5.63019e-05 | 0.0053055 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022937 | GATCATGACATTGCT[A/G/T]TGCAGTTTTCTGCTG | 55827 |
rs372121154 | snp | A/C | 1.64849e-05 | 0.00287092 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168045003 | AGAAGAATCTGCTTC[A/C]TCTGAAAAAGCCAAG | 55827 |
rs372129636 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937268 | GTACTGGCTTGTAAA[G/T]GTGTTGGGGTCGCTG | 55827 |
rs372130980 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167978136 | TTATATGAATATACC[A/G]CAATTGATTTATCTG | 55827 |
rs372136339 | snp | A/T | 2.19744e-05 | 0.00331462 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042975 | AAAAATCCTAAAAGA[A/T]CATATTGATTAACTT | 55827 |
rs372142933 | snp | A/G | 0.0126979 | 0.078662 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935212 | CTGGACCTATGGGAT[A/G]AGAAATGACACTGAC | 55827 |
rs372162574 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986890 | GAAGTGGATACAGGC[A/G]TATCTAAAATATTGT | 55827 |
rs372173095 | snp | A/T | 1.77439e-05 | 0.00297853 | missense | DCAF6 | GRCh38.p7 | 1:168075412 | GGCTCTGGTCAAGAG[A/T]ATGAAAATGAGGATG | 55827 |
rs372187324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962203 | TATAAATGTCCGTTA[C/T]ATTCAGGTAATTGAT | 55827 |
rs372197188 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046766 | TTTCCAAAATCAAAC[G/T]GATAATTTCCAAAAC | 55827 |
rs372254321 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968205 | GAAAGTGTAATAAAA[-/A]GAATTACTACCTATA | 55827 |
rs372264746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962548 | TGTATTAGTATGATA[C/T]ATTTTTCTCAATCCA | 55827 |
rs372281066 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168032689 | ACATCGTTATACAAT[A/G]GAAAACTCATTAGGT | 55827 |
rs372284274 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064036 | TTTTTTTTTTCCCCC[C/T]CTCTTTCTCACATTT | 55827 |
rs372291616 | snp | A/G | 1.65034e-05 | 0.00287253 | missense | DCAF6 | GRCh38.p7 | 1:167993366 | TACTCTTCAGATTAC[A/G]TATATCTTTTTGACC | 55827 |
rs372314164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041287 | TCTTTTTCTTATTGC[A/G]TTATTAGAGCTATTT | 55827 |
rs372324215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041154 | ATGCAGAGAAAGTAC[A/G]TAGCACTTACTAGCA | 55827 |
rs372342042 | in-del | -/AGATGG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948160 | TTTTTAACTGTTTTT[-/AGATGG]TTTTTTCTCTTGCCA | 55827 |
rs372356161 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168018022 | AGTATAGAAAGAATT[G/T]CTGCATTACATTGTT | 55827 |
rs372381859 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971981 | GTGCCTTAGCCTCCC[A/G]AGTAGCTGGGACTAC | 55827 |
rs372429514 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071361 | GTAATCTCAGCACTT[C/T]GGGAGGCTGAGGCAG | 55827 |
rs372463685 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072326 | AAAAAAAAAAAAAAA[-/G]AAAAGAAAAGTCTTC | 55827 |
rs372464813 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034522 | TATGGAAAGGATGGA[G/T]TGGGGGAGGAAAAGT | 55827 |
rs372481187 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040099 | AAGTGATTGGGAAAC[C/G]TAGGCATCATTGAGA | 55827 |
rs372486648 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009495 | CCCTTCCTTCACTTC[C/T]TCCCTCCCTTCCTTC | 55827 |
rs372491807 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168066763 | TAAAGAATCACACAC[-/A]AAAAAAATCTGTCCT | 55827 |
rs372506722 | snp | A/C/G | 0.000164787 | 0.00907568 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063772 | ATGGTACCAAATGTT[A/C/G]ATGGCATTTTTTGGT | 55827 |
rs372528720 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168045536 | TTATTTATGAAGTCA[A/G]GGTTATACTTAGCTC | 55827 |
rs372582835 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968536 | TTTCTCATCAGAGGT[A/G]GTATGCTACAAAATG | 55827 |
rs372600187 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036177 | TGGTGGGGAACCTGT[A/G]TAAATGTTTTCTGCT | 55827 |
rs372607216 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167990879 | TTTAATTGGTTTATA[A/G]GGAAAGTCTACAATA | 55827 |
rs372609102 | in-del | -/TTTA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168003748 | CATTCATACAATTTA[-/TTTA]GGAAATTTGATTTTT | 55827 |
rs372615689 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975197 | ATGTATCTTGATAGG[C/T]TTCTGGATAAAGTTA | 55827 |
rs372622460 | in-del | -/TG | 0.0166325 | 0.0896639 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962061 | TCTAAGAGTAGACAC[-/TG]TTTGATTTTTATTCT | 55827 |
rs372638961 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954206 | AGACGGGGTTTCGCC[A/G]TGTTGGCTAGGCTGG | 55827 |
rs372639666 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943898 | GGCTGTAGTGCAGTG[A/G]TGAGATCTCGGCTTA | 55827 |
rs372697375 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972483 | AAACATGTACTGATA[C/T]GATTTATATTTTTAA | 55827 |
rs372701526 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943802 | AACCTAAGATAATGA[C/T]CTCTAGTTCCATCCA | 55827 |
rs372731612 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168018722 | TTTAGGAAATACACC[A/G]TAACTTGTTTTCTAG | 55827 |
rs372737753 | snp | C/T | 3.30158e-05 | 0.00406286 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168065718 | TAATCATGTGGTAAA[C/T]TGCCTGCAGCCACAT | 55827 |
rs372760188 | snp | A/G | 0.000157987 | 0.00888643 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935691 | CATTTTAGAGGAAGC[A/G]AGAAGGAAGGTCTCG | 55827 |
rs372796215 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168033304 | ATTTCTGAAAAGGAT[-/C]TTTTTTTTTTTTTTT | 55827 |
rs372817543 | snp | A/C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034272 | GTAATCCCAACACTT[A/C/T]GGAGTGCTGAGGAAG | 55827 |
rs372838927 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001163 | AAAACAGCTGGTTGT[A/G]GTGGCACATGCACCA | 55827 |
rs372876478 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049877 | AGCCAGGATGATCTC[A/G]ATCTCCTGACCTCGT | 55827 |
rs372884574 | snp | A/G | 0.000155988 | 0.00883004 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937041 | GGCGGAGGCGCTGAG[A/G]TCGCCGCCTAGAGTG | 55827 |
rs372896984 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062913 | TATATATTAATATTC[-/T]TTTTTTTTTTTTTTT | 55827 |
rs372911024 | snp | C/T | 0.000518135 | 0.0160872 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987444 | AATGTTTTTCAGAGC[C/T]GTCTGTTTAAATGTT | 55827 |
rs372929706 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167947897 | TCATTTGGTCTAAAG[G/T]CCAGTTTAAGTCCAG | 55827 |
rs372931123 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050817 | TGATGATAAAAAGGG[-/T]GTCCTTAATGCTTTA | 55827 |
rs372933381 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168066258 | ATTAACAGTTAAATA[C/T]ATAGTGTACAATTGC | 55827 |
rs372938801 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168043130 | ACCACCAGAAGGAGA[C/T]AGTGAAACAAGTAAG | 55827 |
rs373032010 | in-del | -/CA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070958 | CTGGATCTTAGCACA[-/CA]GATAGTTATCATTTC | 55827 |
rs373037531 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167947354 | TGTGGGTTTTTTTTT[-/T]CAGTCCATATTTCAT | 55827 |
rs373062559 | in-del | -/TTTC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009469 | TCTCTCTCTTCCTTC[-/TTTC]CTCCCTCCCTCCCTT | 55827 |
rs373079620 | in-del | -/A | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970636 | TCTTAAAAAAAAAAA[-/A]TTATTATCATAAGCC | 55827 |
rs373094452 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167965244 | GCCTATACGTCTGAA[C/G]TGTGGGCTTCACAAG | 55827 |
rs373099936 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995599 | GCAGGAGAATTGCTT[C/G]AACCCAAGAGAAGGA | 55827 |
rs373104896 | in-del | A/TT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995158 | ATACATGGGTAAGTA[A/TT]AGTTATAGTCAAACT | 55827 |
rs373132820 | snp | A/G | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997706 | AAAGAGTGACCCACA[A/G]GATGGGAGAAAATGT | 55827 |
rs373138905 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168028600 | ATCATTTTATATAAG[C/G]TGACTGTCTTTGATG | 55827 |
rs373141831 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013645 | TGTGGTTTTCCGCTT[C/T]TTTTTAAGCATCATC | 55827 |
rs373151714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023494 | CTTATCTGGTAGCCA[A/G]ATTCCTGGTAGCTTT | 55827 |
rs373156543 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167951100 | TTATAGCACTTACAC[C/T]GATTATTGTTTTTCT | 55827 |
rs373170863 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167981539 | TCCCTTTCTCCCTCC[C/T]TGCTCTACTAGTTCA | 55827 |
rs373195034 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037721 | ATGAAATTGCTGTTT[C/T]CACAATTAAACAAAT | 55827 |
rs373217139 | in-del | -/T | 0.0150606 | 0.0854603 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974677 | TATATGGGATTCTGA[-/T]TTTTTTAAATTATAA | 55827 |
rs373235517 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030196 | GTGTGGAACATAGGA[G/T]AGTGGGCCTTCATTC | 55827 |
rs373253662 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937265 | AAGGTACTGGCTTGT[A/G]AAGGTGTTGGGGTCG | 55827 |
rs373273815 | snp | A/C/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985923 | GGCTCTTAAAAGTAC[A/C/T]GGTTAGTTTGGGCCT | 55827 |
rs373291485 | snp | A/C | 4.3517e-05 | 0.0046644 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042983 | TAAAAGATCATATTG[A/C]TTAACTTCTTGGTGG | 55827 |
rs373366246 | snp | A/G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070394 | TGTGCATATTCAGGA[A/G/T]AGTTAAAAATGGACT | 55827 |
rs373380903 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168029979 | AGCAAGACTCCGTCT[A/C]AAAAAAAAAAAAAAG | 55827 |
rs373382999 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058793 | AGGCTGGTCTTGAAC[C/T]CCTAAACCTCAAGTG | 55827 |
rs373384047 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982284 | GTCTCGCTTCATCGC[C/G]AGGCTGGAGTGCAGT | 55827 |
rs373391367 | snp | C/T | 0.000153988 | 0.00877327 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935718 | CTCGATAAGGAGCCA[C/T]TCAGGGTCCATTACC | 55827 |
rs373426381 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019235 | TTGTATTTTTGGTAG[A/C]GATGGGATTTCACCG | 55827 |
rs373444136 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168031024 | TATTGAGTTTGAGTT[A/G]TCTGTATGAGATACC | 55827 |
rs373525115 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168003338 | GGAGGAAAAGGAGTG[A/C]GGGAAGAGACAAAAT | 55827 |
rs373556141 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168018636 | AAAAAATTAGAATAT[A/G]TCATTTAAAAATATT | 55827 |
rs373576258 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168053847 | TTGTGTCCCAGGCAG[A/G]CAGAGCAATGTAACA | 55827 |
rs373589048 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168061953 | TCACCAAACAACATA[C/T]ACAAATGTGGATAGT | 55827 |
rs373622265 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057958 | CATCTGCCTACCACG[A/C]CAGTGGTAACCAGTG | 55827 |
rs373634061 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009441 | CTGTCTCTCTCTCTT[C/T]CTTTCTTTCTGTCTC | 55827 |
rs373649432 | snp | A/G | 3.32784e-05 | 0.00407898 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966727 | CAGCAGAAAGGTAAA[A/G]TAGTTTAAAAAATCT | 55827 |
rs373653573 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168003109 | CTATAATGACTTCTG[A/G]AACATCTCTTGTGAT | 55827 |
rs373660631 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167993088 | CTGCAGAGGAAGAAC[C/T]TCTACTGGAAATAAA | 55827 |
rs373685438 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168065254 | CTATTACTTACTGCC[A/G]TCTTACCCTTGCTGA | 55827 |
rs373721697 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007947 | TGACAGTATGTTTTT[G/T]TTATTGTTGTACATC | 55827 |
rs373747207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070141 | TTAGATAAGGTGTTT[C/T]ATAATATAAAAATTC | 55827 |
rs373757656 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019820 | CAGCACTTACCCGAT[C/G]CTGTGCAAGCAGGCT | 55827 |
rs373766337 | snp | A/G/T | 0.00147164 | 0.0270885 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044852 | TAGGTTAAATAATTA[A/G/T]TATTGCCCACATTAC | 55827 |
rs373768949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058067 | GAACTTTATATAAAA[A/G]TGATGTCATACTGTA | 55827 |
rs373776357 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032216 | TTTGGCTTGCATAGT[A/T]TCACTTCTGTTTTAT | 55827 |
rs373785515 | snp | A/C | 0.000173596 | 0.00931493 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066362 | TTCATATTAATATAT[A/C]AATTTTATTTCTAGT | 55827 |
rs373794205 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009781 | TTTTCTTCTTGCTGA[A/T]ATTTTATTCTCTTCT | 55827 |
rs373872789 | snp | C/T | 3.84512e-05 | 0.00438453 | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075445 | GAATAATAAACTCTT[C/T]TTGGCAAGCACTTAA | 55827 |
rs373909573 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954645 | TTTTAGTAGAGACGG[C/T]GTTTCACTGTGTTAG | 55827 |
rs373921890 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031330 | GGCGACATAGAACAG[C/T]GTGGTGTCTTGTGAT | 55827 |
rs373935220 | snp | C/T | 0.000100705 | 0.00709523 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004809 | GTGAGGATAAGTATG[C/T]TGTGGTTCATCTAAT | 55827 |
rs374083779 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938353 | CACATTTTGGAGATC[C/T]TTCCATGGCAGTAAA | 55827 |
rs374086980 | snp | A/C/G | 1.6522e-05 | 0.00287414 | missense | DCAF6 | GRCh38.p7 | 1:167991325 | ATCGGCGAATGCTGG[A/C/G]CACAAGAGCTACAGG | 55827 |
rs374089917 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964629 | ATTATTATTTCAGAT[A/G]TTCTGTTCTTTTCTC | 55827 |
rs374095350 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167942881 | GTCTTTATACCGAGG[A/C]TTGAAATCAGCTAGT | 55827 |
rs374110101 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071792 | TTACTCTGGCCTTCA[A/G]GGTCCTACATGACAT | 55827 |
rs374143164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051255 | TTGTTGAAGAATGCA[A/G]TTTATGTTTTTTAAA | 55827 |
rs374155148 | snp | C/T | 9.88777e-05 | 0.00703058 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063792 | CATTTTTTGGTGAAA[C/T]TGCAGTTTCATGCTC | 55827 |
rs374181629 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168016455 | TGTCATTATTTGAAA[A/T]TTTTCAATATTTGCT | 55827 |
rs374198720 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967292 | TCAATGAAGAAAAAA[-/A]TTACCATAAGCTAAT | 55827 |
rs374221378 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167988536 | CCCAGACAAGTAATT[C/T]CAAGTGATTTTTCCT | 55827 |
rs374273871 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966154 | CTCTGAAGGATCCAA[A/G]ATCAGTTATTGATTT | 55827 |
rs374288746 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939501 | GGCGCGGTGGCTTAC[A/G]CCTGGAATCCCAGCA | 55827 |
rs374309309 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167969938 | TGTGCCACCACGCCC[C/G]GCTAGTTTTTGTATT | 55827 |
rs374335718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938532 | GGATAAGTACCTAGA[A/G]TGGTGATTAATCATT | 55827 |
rs374340044 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035650 | AAGGCTGATGAATTC[A/G]TTAACAACTTAAATG | 55827 |
rs374343151 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167984076 | AAGTGGCTCAAGGCT[C/T]ACTATTCTTTCTGAG | 55827 |
rs374344283 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961231 | TATTAGTTCCAGGAG[C/G]GTTTTATTTTGTTTT | 55827 |
rs374345815 | snp | A/C | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998365 | CTTACCTTAATGTTG[A/C]TCACTGCTGACTGAT | 55827 |
rs374350864 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168011922 | AGGTTGCAGTGAGCC[A/G]AGATCACTCCATTGC | 55827 |
rs374355019 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937883 | TTCTATTTGGAGATA[C/T]GGCAAACAACATCAT | 55827 |
rs374365981 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937228 | TTGCTGGGTTTTTCT[C/T]GGAGGGCCGGGCCGT | 55827 |
rs374465104 | snp | A/G | 1.7221e-05 | 0.00293432 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993472 | CCATGTCCTTTGGCC[A/G]GGCGCGGTGGCTCAC | 55827 |
rs374489717 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168056493 | CGGGGCGGGGAGGGG[A/C]CCAGGCTTAAGTTTT | 55827 |
rs374501188 | snp | A/G | 3.30115e-05 | 0.00406259 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168044604 | TCCTGAAGAATCATC[A/G]GAGGATGTGACAAAA | 55827 |
rs374506029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008689 | CTCCTCACTGTGGAC[A/G]TATAAGAATTTATAT | 55827 |
rs374506657 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024221 | GACCCCCATCTCTTT[-/A]AAAAAAAAAAAAAAA | 55827 |
rs374517332 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167960424 | CTGCCTCAGACTCCC[A/G]AGTAGCTGGGATTAC | 55827 |
rs374535779 | snp | A/G | 6.63845e-05 | 0.00576089 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003858 | TCACTGATAAGACCT[A/G]TATTGTAATAGGAGA | 55827 |
rs374589231 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168061508 | AGTATAATGGTGATA[C/T]CTTTCATGTGGTTTA | 55827 |
rs374590951 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005574 | CTTTGGTTCTTCTAA[C/G]GAAGAATTTTACTCA | 55827 |
rs374598083 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167984716 | TATACTTATTTAGGT[A/T]GAATATACTTTTTAT | 55827 |
rs374602156 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059935 | TTATAGGTGTGAACT[A/G/T]CTGCACTCAGCCTAG | 55827 |
rs374602996 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962685 | TTTAGGCTGGGTGCG[A/G]TGGCTCACCCCTGTA | 55827 |
rs374605312 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941811 | TCATGTACATCTTGG[A/C]CAAAATAACTAGGGT | 55827 |
rs374618997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067119 | GTGGGTTCTCATATA[C/T]TATTTCTTATGAAAA | 55827 |
rs374626983 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972593 | AGGTAAGAGGGAAAG[A/G]TGACTCAGGCACAGA | 55827 |
rs374637702 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035146 | TTGGAATATATACTG[G/T]CACTAATACTGCAGT | 55827 |
rs374639696 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168006256 | ATGTAAGTATTAAAT[G/T]TGACAATCATTTGAA | 55827 |
rs374653778 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168006293 | AAGAAGAAAAAATAT[C/T]TTTGGTGGTCATGTG | 55827 |
rs374661904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985098 | GAAAGACCTGCCCAC[A/G]TGATTCAGTTACCTC | 55827 |
rs374710534 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969617 | GTGTGTATCATCTAT[C/T]AGCTGAAAAAGAAGT | 55827 |
rs374765934 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168042551 | GATCAGAACTGGAAG[-/T]GATCCACAGGGAGCA | 55827 |
rs374773402 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168073842 | CAATGTAATTTTTTT[A/T]ATACTAATATCCCTT | 55827 |
rs374785748 | snp | C/G | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167936063 | CCGACTGCCAGCCCC[C/G]GGTCCGCCTCCGGCC | 55827 |
rs374788739 | in-del | -/GTGTGTGTG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985203 | TGTGTGTGTGTGTGT[-/GTGTGTGTG]GTGTGTGTGTGTGTG | 55827 |
rs374815296 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050754 | ATTCCTTGCTTAATG[C/G]CCGAAGTCACAAAGG | 55827 |
rs374823089 | snp | A/G | 3.95617e-05 | 0.00444739 | intron-variant | DCAF6 | GRCh38.p7 | 1:168075348 | AGTATTTCTCTTTGC[A/G]ATTCTCTTATCTGTG | 55827 |
rs374831352 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168004439 | ATATATTTGTGTGTG[A/T]AAATATAAATGTGTT | 55827 |
rs374928690 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986807 | TCTTTGGGACATAGG[A/G]AGAGAAGAACTTATT | 55827 |
rs374946661 | snp | C/T | 3.56182e-05 | 0.00421994 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975027 | TGAGGTATGGTATTA[C/T]TATGATTATATGATA | 55827 |
rs374991592 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167949790 | ATGTGAGTTTATTTT[A/T]ATTTTAATTTGAGGA | 55827 |
rs375003579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056707 | CTGAGAAGACTTGCA[A/G]CAAGAAACCTCTTTA | 55827 |
rs375022471 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168042860 | GTGTTATGATAGTCA[C/T]CTTGATTTGTTTGAA | 55827 |
rs375037741 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168057656 | CACAACGCCTACCCT[A/C]CTTGAGCTCTCAGTT | 55827 |
rs375039546 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001891 | TAGAATTCAGCTGAA[A/G]AAAATGATGTTATTT | 55827 |
rs375047477 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168002961 | CATAAAATGTTTTCT[A/G]TCAAGTGCCTTTGAT | 55827 |
rs375048997 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167981063 | AGGCGCATGCCACCA[C/T]GCCCGGCTAATTTTT | 55827 |
rs375074409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990310 | GAGTTTGAGGTTACA[A/G]TGAGCTGTGATCACA | 55827 |
rs375125464 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167978295 | AGAGATAAAGCCAAA[C/T]AGTTTTCCAAAGTGT | 55827 |
rs375201472 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065083 | GAAAGTTCAGCAACA[A/T]ATATGTAAATTGCCA | 55827 |
rs375216379 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032246 | TAAAGCCAGATTTGC[A/G]CTAGTGTAAGCACTC | 55827 |
rs375220783 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168028354 | AACTTTTGAGAGGAT[A/G]TAAGAAAGTAATTTT | 55827 |
rs375265058 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005186 | TTTCACTTTGCTTAT[A/G]TTCTTGATTATTTCC | 55827 |
rs375341166 | snp | A/C | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936855 | AACGGGTGTCCCCTC[A/C]CCCTCCTCCCCTCCC | 55827 |
rs375365717 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977210 | TGCCTGGGCCACAGT[G/T]TTTTTTTTTTTTTTT | 55827 |
rs375372242 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168023308 | AACAAAATTATAATG[C/G]ATACAAACTATATCC | 55827 |
rs375374045 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167956655 | GGAAGCTGAGGTCAT[C/T]GATATGAGACCGTTG | 55827 |
rs375376046 | snp | A/C/G | 3.31753e-05 | 0.00407269 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168045162 | TGCTCTTCAGGACAC[A/C/G]GATGACAGTGATGAT | 55827 |
rs375392202 | snp | C/G | 0.000153988 | 0.00877328 | missense | DCAF6 | GRCh38.p7 | 1:168002491 | TTTTAGTTGCGACAA[C/G]CACCAGTTAAGCGTT | 55827 |
rs375414743 | in-del | -/AGAGTAGTTA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168025056 | TATAGCCTACTATAT[-/AGAGTAGTTA]TAGACTACTGTATAT | 55827 |
rs375415461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952004 | AAAATATAAAATTAT[A/T]TTTTGAATCTAGAAG | 55827 |
rs375429942 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167981810 | TGATTCTGTGTCTTT[C/G]TTATTGTGAATAGTG | 55827 |
rs375454350 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001066 | AACACTTTGGGAGGC[A/T]GAAGTGGGAGGATTG | 55827 |
rs375510312 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049431 | GTTGTTGTTGTTGTT[-/G]TTTTTTTTTTTTTTT | 55827 |
rs375511404 | snp | C/T | 1.6517e-05 | 0.00287372 | synonymous-codon, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974898 | CTTACCTTGTACAAA[C/T]GATAAACAGATTGTA | 55827 |
rs375520394 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167958146 | AAAGTTTTTAATTTT[A/G]GTGAAGTCTAATTTC | 55827 |
rs375542668 | snp | A/G | 0.000407512 | 0.0142685 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004005 | GTAATTTTTAATGTT[A/G]ATTAAAGTCATCAGA | 55827 |
rs375591797 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168063537 | TTATGTATTTCCTAG[A/G]CTTACTATATTTTCA | 55827 |
rs375600784 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942792 | AAAGACTACTTTTTT[C/G]CCTTTGTTGAAAATC | 55827 |
rs375603904 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025874 | CCATACCTTGGCTTA[C/T]AAAACCTACATGACT | 55827 |
rs375629127 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167992180 | CACTCACTATAGGAT[A/C]AAAGTACTTCCAAAA | 55827 |
rs375648019 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168033121 | ATTAAATCATTTCAC[A/T]GCGTGTGCATTACAA | 55827 |
rs375656740 | snp | A/C/T | 3.34746e-05 | 0.00409101 | missense | DCAF6 | GRCh38.p7 | 1:168045193 | GACCCAGTCCTGATC[A/C/T]CAGGTGCAAGGTATC | 55827 |
rs375711919 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017564 | TGTGAAGTAAGATGC[C/T]GTCTTTCCAACTCTT | 55827 |
rs375743099 | snp | G/T | 5.07833e-05 | 0.00503876 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168043073 | GAGCCATTGCAAATC[G/T]GAGGGTCAGGAGGAA | 55827 |
rs375804277 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073183 | TCGGTCTCAAAAAAA[A/G]AAGAAGAAAAAGAAA | 55827 |
rs375816671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989940 | TCAACAGAGTACCTT[C/T]AGGATATGTTTGGGG | 55827 |
rs375823426 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942510 | ATAACAGTCCTTAAT[C/T]AGATATGTACTTTAC | 55827 |
rs375861995 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167952654 | TATGTTCCTTCACAT[A/G]TTGGTTGCACGAAGA | 55827 |
rs375882321 | snp | A/G | 3.31044e-05 | 0.0040683 | missense | DCAF6 | GRCh38.p7 | 1:168038377 | AATTTTCAGATAACA[A/G]TAATGAAAAGCTGAG | 55827 |
rs375888056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026520 | CCTAAGGCAATAGTG[A/G]TGAGAAGTGGGAATG | 55827 |
rs375895068 | snp | A/T | 1.89023e-05 | 0.00307422 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043144 | ACAGTGAAACAAGTA[A/T]GGTGTTATTTTGCTT | 55827 |
rs375913837 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168043662 | AGTAGATGTTCAATA[A/G]ATGCTTGATTAATGA | 55827 |
rs375920232 | snp | A/G | 5.03242e-05 | 0.00501593 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991174 | CTGCTGTATAACTAT[A/G]TGTAATTGGTATTAT | 55827 |
rs375927038 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973870 | ATTTTTTTTGGTCTT[A/C]TTGGAAGCATATCTT | 55827 |
rs375929598 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972048 | TTTAGTGGAGATGGG[G/T]TTTCGCCATGTTGGG | 55827 |
rs375999580 | snp | A/G | 9.50977e-05 | 0.00689491 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935706 | GAGAAGGAAGGTCTC[A/G]ATAAGGAGCCATTCA | 55827 |
rs376060918 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168055507 | CTCTTCACTTCCAGT[G/T]ATTTCCAATGGAAAG | 55827 |
rs376069520 | snp | A/C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943555 | ATTTATGGGTACATA[A/C/T]GCAGTTTTGTTACAT | 55827 |
rs376078144 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938234 | TGCATTCTTACAAGT[A/G]CATATGTACATGTAC | 55827 |
rs376080572 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063786 | TCATGGCATTTTTTG[A/G]TGAAATTGCAGTTTC | 55827 |
rs376095159 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167969187 | ATGTTTTAAAACATT[G/T]TTGTCTATTAATTTA | 55827 |
rs376106564 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167969275 | GTTATGACTTACTCT[G/T]TTAGGCTCATAGAAT | 55827 |
rs376143850 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168038007 | AAATTAGTTCTTATT[A/G]ATGCTCAAGCAACTG | 55827 |
rs376155398 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167991746 | CCTTGGCATCCCCTT[A/G]GTATAGATGAATCAC | 55827 |
rs376156386 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013786 | GGTCTTCCTCTGTTG[C/G]CCGGGCTGGAGTGCA | 55827 |
rs376187500 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071717 | AACACAAATTAGATA[C/G]CACCCCCTCTTAAAA | 55827 |
rs376209264 | snp | A/G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037217 | TTAATGTGTGCTCCA[A/G/T]CATCTTCAAGAGGAA | 55827 |
rs376217442 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167960075 | TTTATTTTTATTTTT[A/C]TTTTTTTTGCATGTG | 55827 |
rs376217535 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036043 | CTCCAGTCTGGGGAA[C/G]AAAAAGAGCCTCCAT | 55827 |
rs376246485 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167994657 | AAAAGTAGAAATAAG[A/G]TATCTTTGACAGTAC | 55827 |
rs376247764 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954611 | GCACCCACCACCAAG[C/T]GCGGCTAATTTTTGG | 55827 |
rs376253430 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986108 | GATAACAATTTAATC[A/C]CAGTTTATTGTTGGA | 55827 |
rs376255164 | snp | A/G | 5.02424e-05 | 0.00501185 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991178 | TGTATAACTATATGT[A/G]ATTGGTATTATGTTA | 55827 |
rs376263682 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009481 | CTTCCTCCCTCCCTC[C/T]CTTCCTTCACTTCTT | 55827 |
rs376271341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972195 | CCAAGTACACATAAA[C/T]ATTTTTAATCAGCCT | 55827 |
rs376283008 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984794 | ATTGGTTCAATTGAA[A/G]CAAAGGACATTAATA | 55827 |
rs376291700 | snp | C/T | 0.000145381 | 0.00852462 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068336 | TTATGATCTTTGATA[C/T]GATTTTTAACTTGCC | 55827 |
rs376444066 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986852 | AGAGAGCCTCAACTT[A/G]CAATATTGTCATTGC | 55827 |
rs376453303 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935504 | GCGTAAGGGAGCGGA[C/T]GTCACATAGGTGGGG | 55827 |
rs376516958 | snp | A/G | 1.65056e-05 | 0.00287272 | missense | DCAF6 | GRCh38.p7 | 1:168045070 | GCTACCAATGAAAAT[A/G]ACACCAATCCTGAGC | 55827 |
rs376528213 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168006872 | TATGAAAATTTGCTA[C/T]GCTCCATCTCTGGTT | 55827 |
rs376537520 | in-del | -/TTTGTT | 0.030665 | 0.119967 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952198 | TCATACTTTTTTTTG[-/TTTGTT]TTTGTTTTTGTTTTT | 55827 |
rs376543081 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168060176 | ATTGGCCCGTAGATA[C/T]TTTGAGTTTTGGTTT | 55827 |
rs376569719 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168065154 | GCAGTTAATAATTAA[A/G]CACCTATTGTATCCC | 55827 |
rs376606497 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013221 | AATGAATACTACCCT[A/G]TTGGTACTGGATCAT | 55827 |
rs376608875 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167983904 | AGCTTTTCCAGGGAA[C/T]TTAAGGACAGATTAA | 55827 |
rs376615323 | snp | C/T | 0.000153988 | 0.00877328 | missense | DCAF6 | GRCh38.p7 | 1:168004566 | ATATTTCAACTCTTC[C/T]TACGGTCCCATCAAG | 55827 |
rs376620847 | snp | C/T | 6.15593e-05 | 0.0055476 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066359 | GGCTTCATATTAATA[C/T]ATAAATTTTATTTCT | 55827 |
rs376625019 | snp | C/G | 0.000312614 | 0.0124984 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935830 | CAGGCCTCGGGCACC[C/G]GCGGCCGACATCGCC | 55827 |
rs376691026 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168047493 | ATTTAATATTCTGTA[C/T]ACTCATTTGAGTATT | 55827 |
rs376773027 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007950 | CAGTATGTTTTTGTT[A/T]TTGTTGTACATCTTT | 55827 |
rs376777392 | in-del | -/TGAC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034863 | TGCTGATCCAACCTC[-/TGAC]AGAGAAGTTGGGAAC | 55827 |
rs376798419 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953775 | GGCTAATTTTTGTGT[C/G]TTTAGTAGAGACTGA | 55827 |
rs376911165 | snp | A/T | 0.000100497 | 0.00708792 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044890 | TACATACAACTTTAT[A/T]TTCTGACAGCACAAT | 55827 |
rs376917656 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986008 | CTTTTTTCACACAGA[A/G]GGTTTGTGAGATTCA | 55827 |
rs376938187 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168028380 | ATTTTGTCTGAGTTT[-/T]AGGTTTTGGCCATGA | 55827 |
rs376969219 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059578 | AGTTGTAATAAATCT[C/G]TAAAATAAATTTGGG | 55827 |
rs376977688 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168069589 | TAGACAGCGTATAGC[A/G]TTTTTCTAAGCCCTA | 55827 |
rs376978295 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168011550 | TTTGTAGAAAAATTG[C/T]TGGAGAAGAACTCTG | 55827 |
rs376980185 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989274 | GTACTAAATTTTGTT[A/G]TTGCAAACTCTCTTA | 55827 |
rs376982929 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967298 | AAGAAAAAAATTACC[A/G]TAAGCTAATAAACTC | 55827 |
rs376987488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025912 | TGTATCTCTAATCTC[A/G]TCTCAGGCCACTATC | 55827 |
rs376990663 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948245 | TTGCCATGGTGGAGA[A/C]CTTTTTACACTGTAT | 55827 |
rs376990780 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007482 | TATTAACCAACCCCC[-/C]ATCTGCTTTTCAACC | 55827 |
rs377059922 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167955015 | AATAAACGGAATCAT[G/T]GACTATGTATCCTTT | 55827 |
rs377073714 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938510 | AAGCTTCTGTGCATT[C/T]GTTGTAGGATAAGTA | 55827 |
rs377089126 | snp | A/G | 3.29902e-05 | 0.00406128 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168002553 | ACCCAGAGCAAGGCC[A/G]GAGAGTGAACGAGAA | 55827 |
rs377100493 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167990815 | AAATACTGATCATTT[A/T]AAAAATCTGTATTTT | 55827 |
rs377110281 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016033 | AGGTGCTTCCCTTTT[C/G]CCATTCAAAAAGAGA | 55827 |
rs377116302 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971370 | CTTTTTGCATCCTCA[A/G]CACTTAACATTATTT | 55827 |
rs377118494 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167952928 | GTAATTATCAAGATT[C/T]TGCCATATTTTCTTT | 55827 |
rs377137944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008744 | GCCTCATCTCATTCA[A/G]TTTTCTCAGTACTTG | 55827 |
rs377174807 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168056770 | CTTTATCATAAGCCT[A/T]TTTTGTGGAATACCT | 55827 |
rs377206568 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059977 | AATATCTTTCAGTAA[C/T]ATTTTATTTTTCTGT | 55827 |
rs377207678 | in-del | -/TACAGGTGCCT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167963578 | CTGAGTAGCTGGGAT[-/TACAGGTGCCT]GCCACCACACCCAGC | 55827 |
rs377214029 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035811 | CTCATGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 55827 |
rs377218325 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949164 | CAGAGTAGAGTCAGA[A/G]TTATAAGAGGCAGCT | 55827 |
rs377239715 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961571 | AAAATTTTATTTTCC[A/G]TATAGATGATCTTGT | 55827 |
rs377241854 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991009 | ACATAGGCTGAATGT[A/G]TTAGAAATATTTCTA | 55827 |
rs377260259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981650 | GGTTTTCTGTTCCTG[C/T]GTTAATTTGCTTAGG | 55827 |
rs377269222 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937367 | TTTGCTCTTTTCCAG[C/G]GCGCTTTCCCCGCTC | 55827 |
rs377275632 | snp | A/G | 0.000155988 | 0.00883003 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937051 | CTGAGGTCGCCGCCT[A/G]GAGTGGGGGAGGGGG | 55827 |
rs377288430 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035829 | GCACTTTGGGAGGCC[A/G]AAGTGGGTGAATCAC | 55827 |
rs377290868 | snp | A/G | | | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075628 | TATAAAACAAAACTA[A/G]CAGAATGTTTTTAAA | 55827 |
rs377298301 | snp | A/G | 0.00045082 | 0.0150069 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068337 | TATGATCTTTGATAC[A/G]ATTTTTAACTTGCCT | 55827 |
rs377301314 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168056207 | TTCCTGTGCAAAATT[A/G]CTGATTCCCACTGTT | 55827 |
rs377320466 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070311 | GATATCTAGTTATTT[A/G]ATGGGTCAGTTAGTC | 55827 |
rs377337336 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945662 | ATGCCCAGCTAATTT[G/T]TGTGTGTGTGTGTAT | 55827 |
rs377345617 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056352 | CTCGGCGGGCAGGGC[A/G]CGGCGGGTGACGGGA | 55827 |
rs377349337 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030680 | TGAGGAGGAATCCAG[A/G]GTATAAGTTGCAGTA | 55827 |
rs377350754 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998647 | GTTCACAGCATCTTC[A/G]CTAGGAGTTGCTTCT | 55827 |
rs377364957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030530 | ATTAGAGACTGAATC[A/G]CTTACGAAGTTCTCC | 55827 |
rs377370442 | in-del | -/CCTGT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948326 | CTAGCAGTCATCTGT[-/CCTGT]GCCAAGGATGAAATA | 55827 |
rs377462543 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064015 | GTAATCATTGCTTTT[-/G]TTTTTTTTTTTTTTT | 55827 |
rs377473336 | snp | C/T | 1.65795e-05 | 0.00287914 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003867 | AGACCTATATTGTAA[C/T]AGGAGAGCAGAGTCC | 55827 |
rs377515992 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168073090 | GCGAGACAGGAGAAT[C/T]GCTTGAACCCGGGAG | 55827 |
rs377541138 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168016298 | TTGCATATGCTGAAA[C/T]GAATCTATGCTTTAT | 55827 |
rs377569891 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051080 | ATTGTAAAGCAGGTC[A/G]CTTTCCACAAACTAT | 55827 |
rs377645768 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167963454 | TTTTTTTTTTTTTCC[C/T]TTTTGAGATGGAGTC | 55827 |
rs377654407 | in-del | -/AAATCTTTTG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168015491 | TCTATGTTCATTTTG[-/AAATCTTTTG]CTTATGGAGGACTTT | 55827 |
rs377688864 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063233 | TTTCTTTTCATTTCT[-/C]TTTATGTGTTTTCTT | 55827 |
rs377711572 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003663 | TCAAGAAACCTTACC[A/T]TACACATGGAAAGTC | 55827 |
rs377714455 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982398 | AGGCGCATGCAACCA[C/T]GCCCAGCTAATATTT | 55827 |
rs377757853 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167981960 | CCAAATTGTTTTCCA[C/T]AGTGGCTGAACGAAT | 55827 |
rs377759048 | in-del | CC/TTCTGT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009472 | TCTCTCTTCCTTCCT[CC/TTCTGT]CTCCCTCCCTTCCTT | 55827 |
rs377761374 | snp | A/G/T | 0.00080357 | 0.0200287 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987461 | TCTGTTTAAATGTTC[A/G/T]TATGATTATCTGCAC | 55827 |
rs377766249 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943582 | ACATGCATAGATTAT[A/G]CTGCAGTCAAGTGAG | 55827 |
rs386368644 | in-del | -/GTGT | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938278 | GTGTGTGTTTGTGTG[-/GTGT]TGTATGAGAGAGACA | 55827 |
rs386368645 | in-del | -/AAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167950174 | TTTAAAATTTTGACA[-/AAA]AAGTTTCCAATACTT | 55827 |
rs386368646 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970632 | GATATCTTAAAAAAA[-/A]AAAATTATTATCATA | 55827 |
rs386636522 | multinucleotide-polymorphism | AA/TC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975785 | CTCCAACTCCTGAGT[AA/TC]ATACAATCCTCCCAC | 55827 |
rs386636523 | multinucleotide-polymorphism | GC/TG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168002741 | TAGAAGTGGAATGGC[GC/TG]AGTCACTGGATAAGT | 55827 |
rs386636524 | multinucleotide-polymorphism | CAC/GAG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168020991 | ACAATGTCTATGGCA[CAC/GAG]TAAAACCAAAAAGGA | 55827 |
rs386636525 | multinucleotide-polymorphism | AA/TC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036372 | ATCTGAGAAATTCAG[AA/TC]TTACACTTCTCTCAC | 55827 |
rs386636526 | multinucleotide-polymorphism | GT/TG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168045294 | TTTGTTTGAAGTCAT[GT/TG]AAGGGAATCTCTCCA | 55827 |
rs386636527 | multinucleotide-polymorphism | AT/TG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049412 | TGCACTCTGCTAATT[AT/TG]TTGTTGTTGTTGTTG | 55827 |
rs386636528 | in-del | AT/TGTTG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049412 | TGCACTCTGCTAATT[AT/TGTTG]TTGTTGTTGTTGTTG | 55827 |
rs397691818 | in-del | -/T | 0.375 | 0.216506 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064030 | GTTTTTTTTTTTTTT[-/T]CCCCCTCTCTTTCTC | 55827 |
rs397719066 | in-del | -/ACAC | 0.5 | 0 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938281 | AGGTGTCTCTCTCAT[-/ACAC]ACACACACAAACACA | 55827 |
rs397773988 | in-del | -/T | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050077 | TTTCTTAGATGCTTG[-/T]TTTTTTTTTTTCAGA | 55827 |
rs397779102 | in-del | -/AAA | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950176 | TAAAATTTTGACAAA[-/AAA]GTTTCCAATACTTTA | 55827 |
rs397806985 | in-del | -/A | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029993 | CAAAAAAAAAAAAAA[-/A]GAAAAGAAACATGTC | 55827 |
rs397832250 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041904 | ATACATGTTTGTCGc[A/G]cacacacacacacac | 55827 |
rs397840690 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168016091 | TTTCCTTGCATATGG[-/G]TGGTATTCAACATCA | 55827 |
rs397941895 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168051044 | CTCCCTTTGGACTTA[-/A]CTGAATTCTAAGTGC | 55827 |
rs397956578 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167942408 | TGTTGAGTATCTTTT[-/T]GTGGCTTTTGTTTTT | 55827 |
rs397981858 | in-del | -/A | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944015 | CTCTACTGAAAATAC[-/A]AAAAAAAAGTTAGTC | 55827 |
rs397981859 | in-del | -/A | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963451 | TCCATCTCAAAAGGG[-/A]AAAAAAAAAAAAACA | 55827 |
rs397981860 | in-del | -/A | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976920 | GCGAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 55827 |
rs398039786 | in-del | -/A | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940520 | TGATAATTATTCTTT[-/A]AAAAAAAAAAAAAAT | 55827 |
rs398049687 | in-del | -/A | 0.5 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984563 | TAATAAAGTCATCAA[-/A]GCTAAGTCAATAAAT | 55827 |
rs398074395 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944014 | TGACTAACTTTTTTT[-/T]TGTATTTTCAGTAGA | 55827 |
rs527257325 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954941 | ATCACCCTCAACCCC[A/T]GTCAACCAATGATCT | 55827 |
rs527277697 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052174 | CAGGCTTGAGCCACC[G/T]CATCTGGCCTAGTTA | 55827 |
rs527291951 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954482 | TTTTGAGATGGAGTC[A/T]CGCTGTGCCACCCAG | 55827 |
rs527326045 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168011744 | GCACTTTGGAAGGCC[A/G]AGGTGGGTGGATTAC | 55827 |
rs527347570 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037717 | TAAAATGAAATTGCT[C/G]TTTCCACAATTAAAC | 55827 |
rs527378551 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168016797 | TAAGTTATTTAGGAA[C/T]AAGAATGTCTAGGTT | 55827 |
rs527412825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024525 | ATTATTCCTTATGGG[G/T]CCAGGCGTGGTGGCC | 55827 |
rs527460879 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066883 | TCTTAAAAAGGAAAT[A/G]GAACTTTGTTTTTCA | 55827 |
rs527507603 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966879 | AGGTTCTTAGGTACA[G/T]GTGGGTCTCTTAGAT | 55827 |
rs527518461 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975131 | GTGTATGCACATTTG[A/C]TGCATATAAATTATT | 55827 |
rs527533738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051351 | AACTAAAAATGTACT[G/T]GAATCTAAATCTGTG | 55827 |
rs527571835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009656 | TCTGTATGCTTGGGA[A/G]GCCCTTGTCCTGGCT | 55827 |
rs527597114 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009362 | CTTCCTTCCTTCCTT[C/T]CTTCCTTCCTTCCTT | 55827 |
rs527650724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029817 | AACCCCGTCTCTATG[A/G]AAAACACAAAAAATT | 55827 |
rs527666853 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168004022 | TTAAAGTCATCAGAA[A/G]GCTGGCAAAAACTAC | 55827 |
rs527674065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981141 | CAGACTCCTGAGCTC[A/G]GGTAATCTGCCCGTC | 55827 |
rs527734349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981521 | AGTGTTTCACCCCTT[C/T]CTTCCCTTTCTCCCT | 55827 |
rs527764164 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167934633 | TAGTAACCAGTTCAG[A/T]CTCCAGAGAGCTGGT | 55827 |
rs527768739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, stop-gained | DCAF6 | GRCh38.p7 | 1:168015933 | CATGAGGGCTCTTCA[C/T]AGGACCCTCATGCTT | 55827 |
rs527769012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023952 | GGACGTGGTGGCACA[C/T]GCCTGTAATCCCAGC | 55827 |
rs527799808 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064843 | TTTGATGTTTCATTC[A/G]TGTGCATTCATTTAA | 55827 |
rs527810287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030401 | GGACAAAGTGACTTT[C/T]TGGACATTTTTAGGT | 55827 |
rs527869804 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971679 | ACTAGACCACCTTAA[C/T]GTATAGTAATCATTG | 55827 |
rs527873550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049846 | ATTTTTAGTAGATAC[A/G]GGGTTTCACCGTGTT | 55827 |
rs527889518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959550 | CCTGATGCTCCACAT[C/G]CTTGCCAGTATTTGA | 55827 |
rs527912439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050428 | CAAAGAGAAAGAACT[A/G]GACTCCTAGGGAGTT | 55827 |
rs527940358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035715 | GATTAAATGAATATT[A/G]CCAATATTTGACATG | 55827 |
rs527948411 | snp | A/G | 2.36902e-05 | 0.00344159 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043188 | ATTGCAGCATTGGAT[A/G]TTTATCTACTTTCCT | 55827 |
rs527979006 | snp | C/T | 0.000123545 | 0.00785858 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993487 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 55827 |
rs527981808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939221 | AGCAAAATCCACATT[A/G]GTAATGTTTGAATTA | 55827 |
rs527984422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167946082 | CTGCCTCAGCCTCCC[G/T]AGTAGCTGGGATTAC | 55827 |
rs528038493 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968668 | GTTGGGGAAACTGCC[C/T]GTGCTGGAAGACCCT | 55827 |
rs528060986 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167950252 | CTTTGTTTCTTAACT[A/C]GTATAACTCAATGAG | 55827 |
rs528088046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972323 | CAACTATACATACAT[A/G]ACACGAATAATAATT | 55827 |
rs528096642 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065391 | CAGCTCAGGCAGTCC[G/T]CCTGCCTTGGCCTCC | 55827 |
rs528192581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007252 | GCTTCTCAAAGATTT[C/T]GCCCCTTCTCTTGCA | 55827 |
rs528210749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966045 | CACAGAGGTTTCTGC[C/T]CATGAGTCTGTGCTC | 55827 |
rs528219026 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167979059 | TCCCAAAGTTATGAA[A/G]ATATTCTTCTACTTT | 55827 |
rs528228488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937940 | ACTTGCTAGTTAAAA[A/G]GTGTTTGTTGCTCTC | 55827 |
rs528241695 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168006835 | TCATTTTTACTGATA[A/T]CAAAGAAACGGACAA | 55827 |
rs528260252 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027529 | GTTTTTCATACTTTT[A/G]ACAAAACACGAATGC | 55827 |
rs528266973 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042086 | GTACTCTCTTTTTTT[A/T]AAAAAGTCAATTTGA | 55827 |
rs528279347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008798 | CTACTGATTTCTTTC[A/G]GTTATCAGAGAATTT | 55827 |
rs528279431 | in-del | -/GG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976239 | CTGGGAGGCTGAGGT[-/GG]GGGCGGATCACTTGA | 55827 |
rs528320659 | in-del | -/T | 0.0893983 | 0.191591 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050957 | TATGTTCCTTCATAA[-/T]TTTTTTTTTTATGAT | 55827 |
rs528322857 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034895 | ACATTTAAATAGTTA[C/T]AATTTTTTTTCAAAT | 55827 |
rs528368905 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072895 | GAAATATTCTAACAG[A/C]ATAAAAGGAACCTTT | 55827 |
rs528406445 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037681 | GATAGATGTGTATTA[C/T]AGACATCATCTATAG | 55827 |
rs528435820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951150 | AATCTTTTTGTTTTA[C/T]TTTACCACCGTAAAA | 55827 |
rs528451479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957905 | GTTGAGCATCTTTCT[A/G]TGTGCATATGAAGGT | 55827 |
rs528454411 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168047262 | TTAGATCTGTCACAA[A/C]GTTGGTTCCCAATAG | 55827 |
rs528455477 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168014561 | GTCCCTACCTAATTT[C/T]TCCACTTGGATGTCT | 55827 |
rs528474443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055661 | ATAATTTCATGAATT[C/G]TGAACACTAGAGCCT | 55827 |
rs528475346 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977076 | CTGGCTAATTTTGTA[-/T]TTTTTTTAGGAGAGA | 55827 |
rs528488869 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964862 | TTGTTCCTTTCTGTT[A/C]CATTGTTTTTGATTG | 55827 |
rs528528612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006353 | TACTCATAAATTATT[G/T]ATAGGAAGTAAGGAA | 55827 |
rs528538083 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041250 | TCTTTCAGATACTTT[G/T]CCCAGTTTTCTATGG | 55827 |
rs528560444 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991886 | GTTAGGGTGAGGTGG[A/G]CCCTGGATTAGGTGG | 55827 |
rs528570962 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168045904 | TCTATTATTAGTGCT[A/G]TCATATCTTATTGTA | 55827 |
rs528573167 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987196 | TTGAACAAGCTACCT[-/A]GGGGAGAATCATTCT | 55827 |
rs528597616 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989493 | CTACTAAAAACTTAG[A/C]ATTATGAAAGGCATT | 55827 |
rs528651287 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168016993 | CTGTGGTAACAAAAG[C/T]ACATTTTATATGTGG | 55827 |
rs528720235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977715 | TTTGTAGTCTGGGGA[A/G]ATTCTGATTAGCCAT | 55827 |
rs528759828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005498 | TATCTACAGTTTACT[C/T]GGTACTTTAAACTAT | 55827 |
rs528762602 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013477 | GAAATTCTCTATGCT[C/T]CTACCACCAAATCTC | 55827 |
rs528798558 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012847 | TTATCACAACTAAAT[C/G]TTGATTTTTTTCAAG | 55827 |
rs528902740 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167946247 | AGGCATGAGCTACCG[C/T]GCCTGGCAAATCTAA | 55827 |
rs528902851 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973874 | TTTTTGGTCTTATTG[G/T]AAGCATATCTTTGGG | 55827 |
rs528945170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015653 | TTTTATCAGTAATTT[A/G]TTTATAGTATTCCTC | 55827 |
rs528989097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000555 | ACAGAAACTTGTACA[C/T]ATGCTTAATTCAGCA | 55827 |
rs529000211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960423 | CCTGCCTCAGACTCC[C/T]GAGTAGCTGGGATTA | 55827 |
rs529012867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938970 | TACATACAGGGAGTT[C/T]TTTATCTTAAATAAT | 55827 |
rs529017001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072039 | GCGGTGGCTCATGCC[C/T]GTAATCCCAGCACTT | 55827 |
rs529027069 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033607 | CAGGTGTGAGCCACC[A/G]CGCCCGGCCTGAAAA | 55827 |
rs529059473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072246 | AGGTTGTAGTGAGCC[A/G]AGATCGCACCACTGC | 55827 |
rs529066720 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036712 | GTAAGCTAAAGGTCT[A/G]TTAATTCAGTTATTT | 55827 |
rs529091356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980358 | AGAGATTGCTGGATC[A/G]TATGGTAATTCCATT | 55827 |
rs529106723 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979859 | GCCACTGCACTCCAG[C/G/T]GTGGGTGACAGAGTG | 55827 |
rs529161074 | snp | C/T | 3.31972e-05 | 0.004074 | intron-variant, synonymous-codon | DCAF6 | GRCh38.p7 | 1:168023019 | GGTTAACAAACAGCT[C/T]GGATCCATGTCACTT | 55827 |
rs529173628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966993 | AGTGACATTATTTCA[A/G]TAACATTTTTTGGGG | 55827 |
rs529208936 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070665 | TTTTTAAAAAGCAAC[C/T]AAAGTTAATCTCATG | 55827 |
rs529242541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944139 | GAGCCACCACGCCCA[A/G]CCTGATTTCATTCTT | 55827 |
rs529244673 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970310 | AAAAAATGATACTCT[G/T]TCTCATTTCCAGCTT | 55827 |
rs529276286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048915 | GCAAATACCTGCTCT[A/G]TAGTAATCAGTGTTA | 55827 |
rs529282598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951640 | AAACTAAGTCTTAGG[C/T]GGAGGTTAAATTGCC | 55827 |
rs529316871 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958528 | TTGCCAGTGCCACAC[A/C]GTCTTGATTACTGTA | 55827 |
rs529329172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999507 | AAGGCTGTTTCATTT[A/G]CATTGGAAATCTGTC | 55827 |
rs529336881 | snp | A/G | 0.000399281 | 0.0141238 | missense | DCAF6 | GRCh38.p7 | 1:167993390 | TTTGACCCGAAAGAT[A/G]ATACAGCACGAGAAC | 55827 |
rs529347644 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035477 | ACAAAACAACCTGGA[G/T]TTGAAGAAACCAGGT | 55827 |
rs529348270 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991924 | TCCAGTATGACCTCA[C/G]TGTAACTAACTACAT | 55827 |
rs529365092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945524 | TGAGACGGAGTCTCA[C/T]TCTGTCACCCAGGCT | 55827 |
rs529398528 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013712 | TACAGACGTGTGTAT[G/T]AGCTCCCAAACTAAA | 55827 |
rs529410302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992821 | GTTGTATCATCTTAA[A/G]GATATTGCATACGTT | 55827 |
rs529422906 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948952 | CCACCACGCACAGCA[A/G]TCACCATGTGTTATT | 55827 |
rs529476259 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055725 | GCATATTATATTTAT[A/C]TATAATCATTAGAAA | 55827 |
rs529500834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982304 | TGGAGTGCAGTGGTG[C/T]GATCTCGGCTCACAG | 55827 |
rs529512964 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971892 | ACAGAGTCTTGCTCT[A/G]TCGCCCAGGCTGCAG | 55827 |
rs529521037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007118 | TTTCATTCACAATGA[A/G]AAGTACTCGTTTTCC | 55827 |
rs529539907 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998857 | ACTGAAGTCTTCTAC[C/G]CCTCAAAGTGATCCA | 55827 |
rs529542620 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056139 | AACTCATCTTGTTTG[A/T]TCAATTTTGTCCCAA | 55827 |
rs529558848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014374 | ATCATTCAGTTCTCC[A/G]GCTCTCTCTCTGGCT | 55827 |
rs529575623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006459 | CAAGACATTATCACT[A/G]TTGAGAAAAATGATT | 55827 |
rs529637601 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058474 | TTTCTAATTGATTTG[A/G]TAAACAATAATATGG | 55827 |
rs529672189 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937119 | GGTGGGGGCGCCCGG[A/T]GACTCTGGGGTGTTG | 55827 |
rs529713899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970751 | TGTTTTTATAGTTTG[A/G]TTATTTTTAGATCCT | 55827 |
rs529715212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070688 | ATCTCATGAATAATG[C/T]ACTAAAGACTGCTAG | 55827 |
rs529721091 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035942 | GGTGGGTGCCTATAA[-/C]CCCCAGCTACTCTGG | 55827 |
rs529746653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978593 | TATTAATTTATAGGA[A/G]TTTTTGAAAAAATAT | 55827 |
rs529821905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949958 | GACGATGCAATAAAT[C/T]TTATCTCCAAAGTCA | 55827 |
rs529831750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937746 | TTCGTTTTGCATAAC[A/G]TTTTTTTTTTGAGGA | 55827 |
rs529836002 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167953030 | ATATTATTTTACCTT[C/T]ATATGTAAGCCTAAA | 55827 |
rs529853209 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168062861 | GTAATATGGAGTCCA[C/T]AAAGAAGATGCTATT | 55827 |
rs529857398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071414 | TTCAAGACCAGCCTC[A/G]CCAACATGGCAAAAC | 55827 |
rs529890435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167996897 | CTACTTCACCATCCT[A/G]TTTAAAATCACGGCC | 55827 |
rs529924096 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167955319 | AATGGGTCATATGGT[A/C]GGTACCTGCTTAACT | 55827 |
rs529963758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033025 | ATTTTTTTTTTTACT[A/G]TGGTTATCACATGTG | 55827 |
rs530012568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943455 | GATTTGTATTTTTTG[A/G]TGTTAGGTTTATCCT | 55827 |
rs530020028 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041013 | ATGAGGCAATAGAAC[A/G]TGCTAAGAGCTTGGA | 55827 |
rs530024366 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969900 | TCCTGCCTCAGCCTT[A/C]CAAATAGCTGAGGCT | 55827 |
rs530050271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943021 | ACACCATTCTCCTGC[C/T]TCAGCCTCCCGAGTA | 55827 |
rs530057592 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061470 | TCTATGAATTATTCT[G/T]TAGCCTGTGTTTTAG | 55827 |
rs530059137 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969239 | TGGGCCTGGCTGGCT[C/G]TTTGAAGCTGGATCT | 55827 |
rs530064245 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168014442 | TAAACATTTGACTGC[C/T]TCAAGATTCAGTTCT | 55827 |
rs530068449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011208 | TGCAACCTCTGCCCC[C/T]GGGTTCAAGTGATTC | 55827 |
rs530068612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019283 | TTGATCTCCTGACCT[C/T]GTGATCCACCCACTG | 55827 |
rs530091718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053868 | CAATGTAACATGCCA[A/G]AAGTCAAGTTCTCAG | 55827 |
rs530113426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004425 | TTATCACTGAAATTA[C/T]ATATTTGTGTGTGTA | 55827 |
rs530120145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053056 | CTGCCTTAAGTCAGC[A/G]TATCTTTACATACTC | 55827 |
rs530138108 | in-del | -/AAGTTG | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051391 | CTGATTTTTGCAAGA[-/AAGTTG]TTTCCTTATAAATAG | 55827 |
rs530181165 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963605 | CAGCTAATTTTTGTG[A/T]TTTAGTAGAGATGGG | 55827 |
rs530198719 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075687 | AAAATGCAAAGTGCA[A/G]TATTTTCCCTAACCT | 55827 |
rs530203025 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017905 | AGTGGTGATAGTGCC[A/G]GTAAAACATATTTCT | 55827 |
rs530204441 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057139 | TAAGGTATTTTAATA[A/T]TACCTATAATATCAG | 55827 |
rs530228587 | snp | G/T | 6.66411e-05 | 0.00577201 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003824 | TGTATTAATGAAAGA[G/T]TCTGACTTATTACTA | 55827 |
rs530230878 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011835 | TAAATTTGTTGTGCG[G/T]GGTGGCATGTGCCTG | 55827 |
rs530239589 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168020569 | TCAAATAAGCTGACC[A/T]ACCATATTACATGTT | 55827 |
rs530313185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975790 | ACTCCTGAGTTCATA[C/T]AATCCTCCCACCTTG | 55827 |
rs530345856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989257 | CTTAGAGTAAGTGGT[A/G]GGTACTAAATTTTGT | 55827 |
rs530352507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025439 | GCTATGTAAGAGGTT[A/G]GTATTGAGTGGCTTT | 55827 |
rs530369400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068751 | GATATATTATCGTGC[A/G]TATTCTTTAATGGTA | 55827 |
rs530398816 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071439 | CAAAACCCCGTCTCT[A/G]TAAAAATAAAAAATA | 55827 |
rs530405408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971929 | GGCGTATTCTCAGCT[C/T]ACTGCAACCTCCACC | 55827 |
rs530405883 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954545 | GCAAGCTCCGCCTCC[C/T]GGATTCACGCCAGTC | 55827 |
rs530408185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018388 | TTATTTATTTTTGGT[G/T]GTTCACTCTTTGTCA | 55827 |
rs530530905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063538 | TATGTATTTCCTAGA[C/T]TTACTATATTTTCAT | 55827 |
rs530538370 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071884 | GCCATACTGGCCTCT[C/T]TTCCTCAAACTCATC | 55827 |
rs530557845 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167952664 | CACATGTTGGTTGCA[C/T]GAAGACCCTGTCTTG | 55827 |
rs530583889 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167979506 | CTGATTTCACTTAGC[A/G]TGATCATATTGTAGC | 55827 |
rs530586603 | in-del | -/AAA | 0.00411521 | 0.0451738 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065511 | AGAATTAAAACAAAT[-/AAA]AAAATGTAAGAGTAG | 55827 |
rs530592099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943539 | CTTTTTATTTGTACA[A/G]ATTTATGGGTACATA | 55827 |
rs530611694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040520 | TGGGATTCTAGATAT[A/G]TATTTGAAGGTGCAG | 55827 |
rs530616579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984789 | GCAAAATTGGTTCAA[C/T]TGAAGCAAAGGACAT | 55827 |
rs530624833 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167950523 | ACTTATATGTTCATC[C/G]TTTACCTAGCCATCT | 55827 |
rs530672153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972262 | TTGGCTGTATAGATT[C/T]GGTTTCAACAATTAA | 55827 |
rs530676335 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985238 | TGTGGTGTGTGTGTG[C/T]GTGCGCGTGTGCACG | 55827 |
rs530742788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009060 | CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 55827 |
rs530750120 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937349 | AGAGCAAAAGTTAGC[G/T]CTTTTGCTCTTTTCC | 55827 |
rs530755451 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033572 | TCCACCCGCCTCGGC[C/T]TCCCAAAGTGCTGGG | 55827 |
rs530757442 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998648 | TTCACAGCATCTTCA[A/C]TAGGAGTTGCTTCTT | 55827 |
rs530793045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054022 | AAGGAGCAGAAACAG[C/T]AAGATACTCTCTAGC | 55827 |
rs530793806 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034067 | ACTCTTAACCAGTTA[G/T]TAATGTTGTTGATAT | 55827 |
rs530797338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956532 | CTCATTAATTGTCTC[C/T]GTTGTTTTTCTGTTT | 55827 |
rs530815155 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168042830 | TATTTTTGAATTTTT[C/T]TTCAAGAGTAAAGTG | 55827 |
rs530821822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027402 | AATTTTAACCTTTAC[C/T]AAGATTCTTGTTCTC | 55827 |
rs530830521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963770 | ATATAGTTTTTTTTT[C/T]CTCCTTCCTTAGTAT | 55827 |
rs530848415 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167958841 | AACATCTTCCACCTG[A/G]GTGGTACATTTGCTG | 55827 |
rs530863835 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046858 | AATGAGCTAATGTCT[G/T]ATTTTTCTACATTTA | 55827 |
rs530880191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997696 | ATAAAAATAAAAAGA[A/G]TGACCCACAGGATGG | 55827 |
rs530901270 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052975 | GGTCATGCTGTCTAC[A/G]TTGCCATACTTGGAG | 55827 |
rs530916253 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964254 | CAACAAATTCCCTCA[A/T]TGTTAATTTATCTGA | 55827 |
rs530935220 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985211 | TGTGTGTGTGTGTGT[C/G]GTGTGTGTGTGTGTG | 55827 |
rs530937699 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017418 | AAAACTGTCTAACAG[A/G]AAAGAAGTATACATT | 55827 |
rs530954012 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970590 | GCGTTCCACCACTAC[A/C]CTCCAAGTCTGGATG | 55827 |
rs530957734 | snp | G/T | 0.0314385 | 0.121371 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957364 | ATACAATATTGGCTG[G/T]TAATGTAAGGGTTCT | 55827 |
rs530967986 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168018196 | TCAAATGGGAAGGGG[A/C]CTGATGCTGGTTTAG | 55827 |
rs530974965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012654 | AGTCTGTTATGTCTG[A/G]TTGAATTTTTTAATT | 55827 |
rs530976851 | snp | G/T | 1.73249e-05 | 0.00294315 | missense | DCAF6 | GRCh38.p7 | 1:168004628 | GAAGTAGATACTCCA[G/T]CTGAACAATTTCTTC | 55827 |
rs531036145 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037195 | ACTGAGCCCCGCTGA[C/G]ATTCTCTTAATGTGT | 55827 |
rs531038442 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005314 | TATTTACATGAAAAA[G/T]AATTATTTTACCAAA | 55827 |
rs531107880 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976853 | ACATTTTCCATGTTG[A/T]ATCATTTTGTACTGA | 55827 |
rs531146642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976505 | TAAAGTCTACCTTTC[A/G]AATTACTTGAGTATT | 55827 |
rs531148543 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983774 | TCTTGTTTCCCTCAC[A/C]TAGTATTACTGCCTC | 55827 |
rs531201034 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045610 | TGGTTTTAATGTTAA[G/T]TTTTTCTGCTTTTCT | 55827 |
rs531202905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989301 | CTTAAACTATTTTAG[C/T]GTTTCAGTGTAGTAA | 55827 |
rs531218486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011912 | CAGTAGGCAGAGGTT[A/G]CAGTGAGCCGAGATC | 55827 |
rs531221189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019817 | AATCAGCACTTACCC[A/G]ATCCTGTGCAAGCAG | 55827 |
rs531235311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038547 | GATTGTATTAGATTT[G/T]AATTTTTAACACTTC | 55827 |
rs531242619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996189 | TTTCTTTCATTTTTT[C/T]CCCCCTTCTTTCTTT | 55827 |
rs531272013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032263 | TAGTGTAAGCACTCA[A/G]TTTTTAGAATGAAAT | 55827 |
rs531274924 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070429 | TCAAATAAGCACATG[G/T]TAGCCACAAAGTACC | 55827 |
rs531303902 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167936107 | AGGGAGGAGCCATGG[C/G]AACAGGTGCCAAAAT | 55827 |
rs531306785 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168063345 | TGTTTTTATAAAATA[A/G]CCCTTTAAAAACCAG | 55827 |
rs531308324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032917 | ATTCTCCAGGGGTAT[C/T]CCAGCTTAAAGTCTG | 55827 |
rs531348765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948737 | GCTCACTGCAGCCTC[C/T]GCCTCCCAGGTTCAA | 55827 |
rs531368981 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938962 | TGTATGTATACATAC[A/C]GGGAGTTCTTTATCT | 55827 |
rs531383670 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065852 | AAGAATAATCCAAAC[C/T]ATCTGACTAGGCAGC | 55827 |
rs531431807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025498 | AGAAATGTAGCTTTG[C/T]AATAAGACCTCTGAG | 55827 |
rs531450825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009797 | ATTTTATTCTCTTCT[A/G]TATAACCCTGTTTAT | 55827 |
rs531460558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052908 | AAGAAACAAACCCAG[C/T]TTCCTTGCCTGGTAT | 55827 |
rs531473207 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003465 | TAAGGCTATTTTGTG[G/T]CTGTACTTGATTATA | 55827 |
rs531511736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010850 | TTTAGTTCATGATTT[A/G]TAAATTATTCTCATG | 55827 |
rs531518968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962090 | TCTTTTAAATTTGAT[A/G]AAGTGTATTTTAAGG | 55827 |
rs531545913 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962730 | GGAGGTCGAGGTGGG[C/T]GATCACCTGAGGTCA | 55827 |
rs531550757 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052239 | AATTTGCTTCAGAGT[G/T]TTTTGATATCCTGAT | 55827 |
rs531576114 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942307 | GACCTCAGGTGATTG[A/C]CCTGCTTCGGCCTCC | 55827 |
rs531586851 | snp | C/G | 3.30573e-05 | 0.00406541 | missense | DCAF6 | GRCh38.p7 | 1:168045107 | TCCAAACAGAAGCCA[C/G]TGGGCCTTCAGCTCA | 55827 |
rs531590251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982355 | CAAGCGATTCTCCTG[C/T]CTCAGCCTCCTGAGT | 55827 |
rs531682051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962610 | TAAAATGGATTTCTT[A/G]TAAACAACATATATT | 55827 |
rs531691557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024035 | GCCTGGTCAATATAG[C/T]GAGACCCCGTCTCTT | 55827 |
rs531695609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074420 | TAGTGATTTTATGCT[A/G]TTGCCTTCTTCACAA | 55827 |
rs531732724 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940228 | ATTTATGATTAAAAG[A/G]TATGTTTACTTAGAG | 55827 |
rs531742921 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168029021 | CTTAGTTACTTGGAA[C/T]GAGGTAACTAATTTC | 55827 |
rs531801226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051158 | GTGTGCAGACTGATG[C/T]TCACTTCAAATATGT | 55827 |
rs531851455 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001859 | AGTTAGAAAGTTGTA[C/G]ATGTAGATTTAATTT | 55827 |
rs531852321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988166 | AATTAAATTAATTAA[C/T]TAATTTTTTTTGAGA | 55827 |
rs531864122 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935307 | AGCAGCTGAAGAAAG[A/T]GACCTTTACTCCAAA | 55827 |
rs531907351 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940757 | TTTCCTTTTGGACAG[A/T]CACTCCTACAACTTT | 55827 |
rs531908092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167946246 | CAGGCATGAGCTACC[A/G]CGCCTGGCAAATCTA | 55827 |
rs531925033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043265 | TTTGCTTCTATAGTC[C/T]AGCTGTTAAACTGAT | 55827 |
rs531966166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994000 | TAATTACTAATTATA[A/G]TTAGTAATTAGTTAC | 55827 |
rs532008243 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039624 | TTTGTTAATATATAA[G/T]TATACCAATTGTTTA | 55827 |
rs532040087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030455 | GAGGGAAGCTAATGA[A/G]GTGTTTAAATTAGGG | 55827 |
rs532044450 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032961 | GTATTTGGATATTTA[C/G]ATCTATACCAACATT | 55827 |
rs532071041 | snp | A/G | 0.000816493 | 0.0201886 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026712 | GAAGAAAGTATGTGA[A/G]TTTTTTTTTAATGTT | 55827 |
rs532095489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942969 | TGGAGTGCAGTGGCT[C/T]GATCTTGGCTCACTA | 55827 |
rs532097807 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167981942 | AAGTTCTTTGAGAAA[G/T]CTCCAAATTGTTTTC | 55827 |
rs532099415 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054133 | TATTGATAAAGCTAG[A/G]TAACGCTAACATACT | 55827 |
rs532123128 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936685 | GTTGCTGATCTTTGG[A/C]TGTTCTGGTTAGTCT | 55827 |
rs532173594 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957302 | AATCACTAATACTTT[-/C]TGTCTCTACCAATGT | 55827 |
rs532196151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976932 | TTTTGAGACGGAGTT[C/T]CGCTCTTGTTGCCCA | 55827 |
rs532218659 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048865 | CATTTCAAAAATCGG[C/G]ATTTGGCGGAGATCT | 55827 |
rs532247406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167996699 | TGGTCCTAATTATTA[C/T]TTCTACTGTTTTCTT | 55827 |
rs532284271 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996333 | TACCCCATTATTGGG[C/T]TTCTTTGTTGAATTC | 55827 |
rs532286023 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168063297 | AATTTGTTATATTTG[C/T]AGTAAAATTGCACAT | 55827 |
rs532323730 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959430 | CTTTGGATAAATACC[A/G]AGGAGCATGCTGTAT | 55827 |
rs532367808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045661 | GTGTGTTAGTAGTTC[A/T]GTTTTTGGGAACACT | 55827 |
rs532394095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038692 | AGGTTTGGAGTGGGG[A/G]TCTGAGAATTTGCAT | 55827 |
rs532405602 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046113 | AAGAGCATGATGATG[G/T]GTTTGAATACTGGTT | 55827 |
rs532410248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989430 | ATGTATAAAAGTGAA[A/G]TGAAGCAGAGAGTAT | 55827 |
rs532413102 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068659 | ACTACATTTGTCGTA[A/T]AATGGTCAAAATGAA | 55827 |
rs532436416 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949817 | AGGAGGCTCAGTTTT[A/T]TTAAGGTACTGTTCT | 55827 |
rs532474183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949291 | TTTCTGAACATCTTC[A/G]GAGCAGAGGCACTAG | 55827 |
rs532488106 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988895 | ACCAGCCTGGTCAAC[A/G]TAGTGAAACCCTGTC | 55827 |
rs532490488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956036 | AAAGCAAAGTGCTGG[A/G]ATTACAGGTATGAGC | 55827 |
rs532490573 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986459 | GTTTGAATACCTTTC[A/G]TATATACAGTGTTTC | 55827 |
rs532491527 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017659 | GAGGGTAGGTTTTAA[A/T]TGAGTAACAATTATA | 55827 |
rs532506637 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067630 | TTAATCAAACTAAAC[C/G]GTTAGGTGAGGGTAA | 55827 |
rs532507186 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025350 | TTGAGTAGCTTGGAA[A/G]TAGAAATCAGGTGGT | 55827 |
rs532548102 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060847 | TGAGCTGAGACCCCG[A/C]CACTGCACTCCAGCC | 55827 |
rs532562870 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022892 | CTTCTATTCCGCAGC[C/T]TTATACATTTGTTTC | 55827 |
rs532591382 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044838 | GTGAGCTCCTAAGTT[A/C]GGTTAAATAATTAGT | 55827 |
rs532595240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988779 | AAATAAAACAAAAAG[C/T]AGAAATTGAAAAACC | 55827 |
rs532645921 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167956654 | TGGAAGCTGAGGTCA[C/T]TGATATGAGACCGTT | 55827 |
rs532654623 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010009 | ACTAGATAGGGTATA[G/T]TTAGCTTTATTTTAG | 55827 |
rs532670934 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935358 | CCCATCCAGCTCTGC[C/T]TAGAGTGGGTTAATA | 55827 |
rs532700180 | snp | A/G/T | 5.66228e-05 | 0.0053206 | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075439 | GATGAGGAATAATAA[A/G/T]CTCTTTTTGGCAAGC | 55827 |
rs532709085 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167990702 | TTATTACCATCTTTT[C/T]GTAGCTGGCGCTGTT | 55827 |
rs532720827 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030682 | AGGAGGAATCCAGAG[G/T]ATAAGTTGCAGTAAC | 55827 |
rs532734004 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037121 | TTTTTTTTTTTTTTT[G/T]GAGATGAGGTCTCAC | 55827 |
rs532734792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953724 | CCGCTGCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 55827 |
rs532748507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050650 | TTTAAAAGATAAAAG[A/G]GATTAAGTGCAATGT | 55827 |
rs532847533 | in-del | -/AGGGCTTTGA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057735 | TTGACAGGGCTTTGC[-/AGGGCTTTGA]GAGTATTAAGGACCC | 55827 |
rs532847695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024921 | TTTCTGTTCTTGAGA[A/G]AGAAAGAATGAATGA | 55827 |
rs532852938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167947520 | TGCTGTGTTCTTCTT[A/G]GCACTGCTTTTGCTG | 55827 |
rs532853470 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167934848 | TAGCCCCTAGCAAAT[A/G]AGTATTATTACAACT | 55827 |
rs532854865 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070099 | TGGTTAGTTAATAGC[C/T]ACTACCATCCTTCTT | 55827 |
rs532887027 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031318 | AGAGAGGTGGATGGC[A/G]ACATAGAACAGCGTG | 55827 |
rs532914577 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168033569 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 55827 |
rs532915098 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967358 | ATTAAATAATTTTCT[A/G]ACTCTCAAGTAACTT | 55827 |
rs532923328 | in-del | -/T | 0.292266 | 0.246401 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977209 | GTGCCTGGGCCACAG[-/T]TTTTTTTTTTTTTTT | 55827 |
rs532964128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972056 | AGATGGGGTTTCGCC[A/G]TGTTGGGCAGGCTGG | 55827 |
rs533033823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994756 | TTTTTTATTTTATAA[C/T]GTCCTGTGTTATTCA | 55827 |
rs533035406 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168029144 | ATGCTCGTGTGTTCT[A/G]CTCTTCTGCTGATCA | 55827 |
rs533062152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016493 | TCCTCTATACGTAAT[C/G]AACTTTCTGATGTGT | 55827 |
rs533125114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066684 | ATAATATTCATCATC[A/G]GTAACACCAGATTAG | 55827 |
rs533139717 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973982 | TCCACTGGTATTACC[C/G]TTTAGCATTCCTACC | 55827 |
rs533166219 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991427 | AAAATTTCTTGTTTG[-/T]TTATAAAATTTCAGA | 55827 |
rs533183290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981082 | CGGCTAATTTTTTGT[A/G]TTTTAGTAGAGATGG | 55827 |
rs533238469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036108 | ACTTTGTAGTAGATA[C/T]TGTAGGAAGAAAGTT | 55827 |
rs533262180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022286 | TTAAAAAGATAAGAA[C/T]GAAGCTGTTCTATTT | 55827 |
rs533282456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029002 | TTCTTAGAACTAGTT[A/G]TCACTTAGTTACTTG | 55827 |
rs533301792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072620 | ACAGTGCCTACCACA[C/T]AGTAGTTGCTTAACA | 55827 |
rs533315827 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168038211 | AATATAAAAGAGTAT[A/T]TCCACAACACATGCC | 55827 |
rs533390589 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168063324 | ACATGAATTTTGTCT[C/G]TATTATGTTTTTATA | 55827 |
rs533393234 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035638 | CTAGTTTTACACAAG[A/G]CTGATGAATTCATTA | 55827 |
rs533416174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042310 | GTCAGATTGTTATAC[A/G]TGTCCTCTTTCTCAT | 55827 |
rs533423875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980404 | ACCCTCCATACTATT[C/T]TCCATAGCAGCTCCA | 55827 |
rs533432479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992849 | GTTGCATACTAATGT[A/G]TGTAGTATGCTAATA | 55827 |
rs533453404 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941634 | CTAATGAGTCTCAGC[C/T]TGAGGTTTGGAAAAT | 55827 |
rs533473316 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168021399 | CATTTTTCTTGTTTT[G/T]TTAAAGAGTTTAATT | 55827 |
rs533485536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959403 | GTATGTGTGGACATA[C/T]GTTTTCAGCTCCTTT | 55827 |
rs533539471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055212 | TGAAAGTAGAGATAT[A/G]GAAATGTAATAATTG | 55827 |
rs533549937 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056248 | TTTCTGTTGTTACCC[A/T]TTCGTGTTTCTCTGT | 55827 |
rs533564399 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168059114 | TTTACAAAATTCTTA[C/T]CTGGAATTTTAAAAT | 55827 |
rs533587832 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056656 | TGTGTATACCTCTTT[A/G]TGAGATTCACAAGAA | 55827 |
rs533624656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049720 | GAGTGCAGTGGGGCA[A/G]TCTTGGCTCACTGCA | 55827 |
rs533658220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952917 | ACCTAGACTTAGTAA[G/T]TATCAAGATTTTGCC | 55827 |
rs533671041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074634 | ATCATTATGAAGTTC[A/G]TATAAGATATTCTAG | 55827 |
rs533674458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941105 | ATGAAGATTAGTAAC[C/T]TCTGACTTTTGCCTC | 55827 |
rs533695759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952451 | GTGTTGATCTGACCT[C/T]GTGATCCTCCTGCCT | 55827 |
rs533705297 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168059492 | GAAGGATCTTGGCTA[G/T]TCTTTGTCCTTTGGT | 55827 |
rs533715656 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050059 | GAGAAAACCTAAATT[A/G]CTCTCTGAAAAAAAA | 55827 |
rs533724780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058160 | TGTAGCTCTTGCCCA[A/G]TCATTTTTACTGCTA | 55827 |
rs533740545 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167994460 | ATCCCTTTCTGTCCC[A/G]ATTGTGCCTCTTTCA | 55827 |
rs533754169 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964512 | GTTTGAAAAATGCTT[A/G]CCTAGCTGTAGTTCT | 55827 |
rs533756403 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030045 | AGCGTTAGAAACGTG[A/T]CTCAAACCCAAGAGG | 55827 |
rs533763048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050734 | TACATTTAGTTGACT[A/G]ACATATTCCTTGCTT | 55827 |
rs533770459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036485 | TGAAAAAACTAGCCC[A/G]AACTCAGTCTCTCAG | 55827 |
rs533778294 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967067 | TTTTATGTGTTACCT[C/T]AATATATTATCTTAA | 55827 |
rs533792166 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935542 | CTGACTTGAGATACG[C/T]TGGCTTAGGAAGAGA | 55827 |
rs533812241 | snp | C/T | 0.000115465 | 0.00759731 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167987536 | CACTTTTCTCTCTTG[C/T]GGTGAAGATGGAACT | 55827 |
rs533832092 | snp | G/T | 7.31328e-05 | 0.00604657 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068334 | CTTTATGATCTTTGA[G/T]ACGATTTTTAACTTG | 55827 |
rs533857755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974777 | TTATATTAAAAATGA[A/G]TATTTCTAGGAAATA | 55827 |
rs533861528 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001302 | GCCTGGAAAAAAAAA[A/C]GTTAAAAATGTAAAC | 55827 |
rs533878023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988365 | TAGGAGGTCTTGCCA[C/T]ATTGCCTAGGCTGGT | 55827 |
rs533880342 | snp | G/T | 0.031825 | 0.122064 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945811 | GGCCTTTTTTTTTTT[G/T]TTATTTGTAGCTATT | 55827 |
rs533895782 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022505 | CTTATAAACCATTTT[C/T]TTTGTATAAGATCTT | 55827 |
rs533896525 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168031724 | TTCCAGTAAAGGAGA[A/G]TATACCTGAGGAAAC | 55827 |
rs533909829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023658 | ATGAACGCGTTACTT[A/G]TTTATCAGGCTTTAT | 55827 |
rs533941533 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029209 | TCTTATCATAAAAAT[A/T]ACTGACATTTATTGA | 55827 |
rs534059570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994317 | AGATCAACAGTGCTA[A/G]CACTTGCAGAAAAGG | 55827 |
rs534112654 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168055515 | TTCCAGTTATTTCCA[A/G]TGGAAAGATCATTAA | 55827 |
rs534117828 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034457 | TTGAGACCACAGTGA[A/G]CTATGAAGGTGCCAC | 55827 |
rs534152183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072812 | GAAATTTTTTTCTTA[C/T]CTACCTTCCCTCCCT | 55827 |
rs534203187 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065572 | TTGAATTTTTAAATA[A/T]TTTTTTTTAACCCTT | 55827 |
rs534220498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972832 | GAGATTTGTTCAAAG[C/G]AACGGGCCCCCAATT | 55827 |
rs534289149 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008226 | CATCCGCCTCGGCCT[A/C]CCAAAATGCTGGGAT | 55827 |
rs534303006 | in-del | -/TAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017208 | TACAATAATGACATT[-/TAA]TAATAAAACATTTTT | 55827 |
rs534340211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965237 | TTAAAGAGCCTATAC[A/G]TCTGAACTGTGGGCT | 55827 |
rs534342724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168057104 | TGTTTTTTCCACCCT[A/G]AAAAGTCTTTGTTCT | 55827 |
rs534345819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957660 | CTAGTTGCAGAATTG[C/G]TAGGTCATATGGTAA | 55827 |
rs534355217 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032623 | TTTGGTTTTTAAAAA[A/G]TATTTGGTATAATGA | 55827 |
rs534358091 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938220 | CAGACCTTTTTGTTT[G/T]CATTCTTACAAGTAC | 55827 |
rs534389329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999829 | TGTTTCCATATCAGT[A/G]ATAAGGCTGTTTCGT | 55827 |
rs534429676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035253 | GAGTTAAAGACCAGC[C/T]TGGGCAACATGGCAA | 55827 |
rs534475069 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940611 | ACTAGGTGTAGAGTA[A/G]TGCTTTTGGAAATCA | 55827 |
rs534476281 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972835 | ATTTGTTCAAAGGAA[C/T]GGGCCCCCAATTTTT | 55827 |
rs534476304 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071031 | AATCACTTATTAAAT[C/G/T]GTTCACAGATTGACT | 55827 |
rs534489647 | in-del | -/TCTT | 0.0119091 | 0.0762411 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037200 | GCCCCGCTGAGATTC[-/TCTT]AATGTGTGCTCCAAC | 55827 |
rs534508460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971233 | CATTTCCTGGACACA[C/T]GTAGCCACTCCTTCA | 55827 |
rs534528325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072194 | CCCAGCTACTTGGGA[A/G]GCTGAGGCAGGAGAA | 55827 |
rs534588812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055932 | TTTATGTATTTCTCA[C/T]ATGCTTCTTCACTCA | 55827 |
rs534632041 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167969852 | CACGATCTCGGCCCA[C/T]TGCAAACTCTGCCTC | 55827 |
rs534638208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013106 | ATAATGCTTTATTTT[A/G]TATTGCTAAAAGCAT | 55827 |
rs534651928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055175 | TAACTTTGATTCTTA[C/T]AGAAAAGTTTTATAG | 55827 |
rs534666705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943172 | CCTTGGCCTACCAAA[A/G]TGCTGGGATTACAGG | 55827 |
rs534732347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033115 | GTACAGATTAAATCA[C/T]TTCACAGCGTGTGCA | 55827 |
rs534755920 | snp | A/G | 1.75459e-05 | 0.00296186 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951908 | GATTTGATACTAAGT[A/G]TTTAAGTGTTTGATG | 55827 |
rs534755993 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167955578 | ATTCATTCAAGTAGC[-/T]TTTTTTTTTTCCTTA | 55827 |
rs534757616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049262 | TGTTTTATTTTTTTG[A/G]GACAGGGTCTTGCCC | 55827 |
rs534758507 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167951342 | CACTTTGGGAGGCCA[A/G]TGCGGGTGGATCAGT | 55827 |
rs534759279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041683 | TTAAATATATTTACT[C/T]GGTTGCTGTGTCTTT | 55827 |
rs534856935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004127 | ATTGTGTGGTGTGAA[A/G]TAGTAGAGAATAAAA | 55827 |
rs534861122 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007651 | CCTTTCTTGGTATCT[A/G]TGATATCATATTTGC | 55827 |
rs534861893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053469 | ACGGCCTCCCCACAC[A/G]GTTGATTGCTTGCTA | 55827 |
rs534898606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054092 | ATATGTTGAAATGAC[A/G]GCAATTCTAACATAT | 55827 |
rs534920886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963179 | TGAGGCGGGAGAATC[A/G]CTTGAACTCAGGAGG | 55827 |
rs534942564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020792 | AGGAGTTCTAGGTAT[C/T]GTATTTATGAATAGT | 55827 |
rs534964035 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168075270 | CACACATAGTGGTGA[A/G]CTGATTTTTAATGCG | 55827 |
rs534983825 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951334 | AATCCTAGCACTTTG[C/G]GAGGCCAATGCGGGT | 55827 |
rs535011415 | in-del | -/CA | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070954 | ACCTCTGGATCTTAG[-/CA]CACAGATAGTTATCA | 55827 |
rs535027446 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050330 | AGCATTTATTCAGTC[A/G]TCATTGTAACCATGA | 55827 |
rs535055930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990235 | TAGCCTGGTATGGTG[A/G]TGTGCACCTGTAGTC | 55827 |
rs535081116 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037040 | TTTCTGTATTTGAAG[C/T]CTTGTTAATTGTCCT | 55827 |
rs535100657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958912 | AGTCCATAGTTTACA[A/G]TAGGGCTCACTCTTG | 55827 |
rs535114245 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168042042 | ACACCCATATGAATA[C/T]ACAGTTTTAGTTAAA | 55827 |
rs535125415 | snp | A/G | 3.29979e-05 | 0.00406175 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167991314 | ACGAATATATGATCG[A/G]CGAATGCTGGGCACA | 55827 |
rs535141474 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167996015 | CTATGTTCTGTATAA[A/G]TAGAACAAAGTAGGG | 55827 |
rs535146970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986246 | TGGGTTATAGGAGAA[A/G]CATATGATCAGCTTT | 55827 |
rs535153782 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980757 | TTTTTTAGATACATG[G/T]TTCACAAATATTTTC | 55827 |
rs535173146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993528 | GCCGAGGTGGGTGGA[C/T]CACCTGCGGTTGGGA | 55827 |
rs535175635 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168043894 | TTAACTACTTGTTCA[C/T]GATAGTTTAGATTTT | 55827 |
rs535175973 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011981 | CTGTCTCAGAAAAAA[G/T]AAAGAAAGAAAGAAA | 55827 |
rs535240460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953048 | ATGTAAGCCTAAAAA[A/G]CGATTGACATTTTCT | 55827 |
rs535252603 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046431 | GAGGATAGCTTGCAG[C/T]TCAGGGGAACTGCCT | 55827 |
rs535263150 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055056 | TATTCAGAATTATAA[-/T]GAGCATTTCCAATGA | 55827 |
rs535264425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965285 | CACCTCCTATTCCCA[A/G]CTGAGGTGGAACAGG | 55827 |
rs535295755 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055980 | GAAGGGTTACTCAGT[C/G]TCATCTTGATCAGCC | 55827 |
rs535301507 | in-del | -/AT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167969400 | ATAAGCTGGGATAAC[-/AT]ATGAGTTCTAATTAG | 55827 |
rs535311411 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997002 | TTTTCATTTCATGTG[G/T]TGTTTGCTCCATCGG | 55827 |
rs535324587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958149 | GTTTTTAATTTTGGT[A/G]AAGTCTAATTTCTTT | 55827 |
rs535360191 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168025879 | CCTTGGCTTACAAAA[C/T]CTACATGACTTGATT | 55827 |
rs535367211 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956669 | TTGATATGAGACCGT[G/T]GTCTTTTCTAAAATA | 55827 |
rs535369413 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167999214 | TTTTCTGAGCAGTAG[G/T]TCTCAATAGTGGGCT | 55827 |
rs535413130 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943878 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGTAGTGC | 55827 |
rs535423818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048670 | TTAACTACAGCAAGT[C/T]TATGTAAATGTAACT | 55827 |
rs535458516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042492 | TATTACCCTGTCCTT[C/G]TACAGAACTATGATG | 55827 |
rs535483945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034212 | GTATATTAAGTAGGA[A/G]CTTCATATAAAAAGA | 55827 |
rs535493663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948754 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTACCTCA | 55827 |
rs535497269 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035326 | ATGGCATGTGCCTAT[A/T]GTCCCAGCTACTCAG | 55827 |
rs535497353 | snp | C/G | 4.22672e-05 | 0.00459694 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042995 | TTGATTAACTTCTTG[C/G]TGGAATCACTTATCT | 55827 |
rs535544585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071201 | TAATTTTTTTGTTAA[C/T]GGCCAGATATGGTTT | 55827 |
rs535545584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993087 | ACTGCAGAGGAAGAA[A/C]CTCTACTGGAAATAA | 55827 |
rs535581492 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071567 | TTAACTTGGGAGGTA[C/G]AGGTTGCAGTGAGCC | 55827 |
rs535585654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938004 | TGAAATCTCATTACA[A/G]CCAACAGTTCTGGTT | 55827 |
rs535586182 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972714 | AATGAAAAAAGGTTC[C/T]TTAGTTTTTGACTTG | 55827 |
rs535704012 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040703 | CTTCTGAAGAATCTT[A/G]TCTAAACTTTTTGGG | 55827 |
rs535722043 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997076 | CATTGTTGTTTTCCA[A/G]TACCTGTAATAGTAC | 55827 |
rs535783543 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056320 | TACGGACGGCGCCCA[C/G]CCCCAGCTGCCAGGG | 55827 |
rs535794047 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071695 | TAGTCTGCTACCACC[G/T]TTTTAAAACACAAAT | 55827 |
rs535819258 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009369 | CCTTCCTTCCTTCCT[C/T]CCTTCCTTCCTTCCT | 55827 |
rs535894659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984971 | AAGGTGAAAGGTGAA[A/G]GGCATGTCTCACATG | 55827 |
rs535902217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969509 | ATCTGAAAACATGGT[A/G]TTAGCAGTCCAAAGT | 55827 |
rs535911383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978966 | TTGATGAAGAAAAGT[A/G]TTTAATGTTGTCTAA | 55827 |
rs535950282 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004879 | AAGATACTAAATCAC[A/G]TCAACTTCTTGTTGG | 55827 |
rs535956077 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168047015 | CTAATTATAACACTT[A/G]ATACCAAGCCTGCTT | 55827 |
rs535960054 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985331 | TACTGGGCTAAAATC[A/G]AAGTGTTGGCAAGTG | 55827 |
rs535979772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027648 | TTTAATTTTCCATAG[C/T]ATTTTCATAGATTTC | 55827 |
rs535998447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005592 | AGAATTTTACTCAAT[A/G]TAGAGCCAGAATTAT | 55827 |
rs536002890 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168074061 | TTGTATTCAATACCT[A/G]TTTGTATAATTAAGG | 55827 |
rs536016347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035412 | TGATTTCGCCACTGC[A/G]CTCCAACCTGGACGA | 55827 |
rs536046494 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050789 | CAAAAGTTTTTTTTT[A/G]AATTGAGATGATTGA | 55827 |
rs536074429 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956809 | TTATTTTGTAATTTC[G/T]TCTTTGACCATCTGT | 55827 |
rs536083930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032512 | AATTTGCCTTTTCTA[C/T]ACAAGTCTAGTAAGT | 55827 |
rs536096146 | in-del | -/AAC | 0.00922044 | 0.0672696 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993761 | CTCAGAAAAAACAAC[-/AAC]AACAACAACAACAAC | 55827 |
rs536110343 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997616 | TTAAGTGTCACCAAG[C/T]TTTTATCAAAACCTG | 55827 |
rs536135552 | snp | A/G | 1.69097e-05 | 0.00290768 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991365 | AATATTAGAGAAAAT[A/G]TAGGACTGTCAGTTC | 55827 |
rs536140366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018960 | TTGCTGTAATTTACA[A/G]AGACCATGTAAGGAT | 55827 |
rs536146058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983429 | CTGTTCTTGGTTAGC[C/T]TAGTTGTCAGCTAAG | 55827 |
rs536180285 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168012747 | TTTAATCCAAGGAGA[A/G]AAAAGCCACCATACA | 55827 |
rs536190556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025702 | CTCTCCTAGATTAAT[A/G]GAATAATCCCTTTAC | 55827 |
rs536202531 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168047430 | AATCCAGATTTGAAA[C/T]CACTCTGGGATCACA | 55827 |
rs536240585 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970188 | AAAATAATCACTTGG[A/C/G]TACCAAAGGAATGAT | 55827 |
rs536247946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963285 | AAAACCAAAATAATA[A/G]TTTTTAATTTAGACT | 55827 |
rs536363384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995862 | GCCTACTATACACCA[A/G]GTCCTCTACTTAACT | 55827 |
rs536391351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948854 | ATGGGGTTTTGACAT[A/G]TTGATCAGGCTGGTC | 55827 |
rs536422844 | snp | A/T | 8.77925e-05 | 0.00662484 | upstream-variant-2KB, missense, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935777 | TTCTCGGGCAGCATC[A/T]GCTCCACTTTATCGA | 55827 |
rs536431598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962381 | GCTCTGTTGTTAAGC[A/G]CATACATGTTAGGGA | 55827 |
rs536452443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067879 | TTGGTACTTAAGGCT[C/T]AGTTTCTTGTTAACC | 55827 |
rs536456177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941967 | TATATGAGAGTTCCA[A/G]TTGCTCCACATTCTC | 55827 |
rs536480881 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975353 | CTTTACCCTTTTAAA[C/T]AATCGCTTGCTTGTG | 55827 |
rs536508632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968535 | GTTTCTCATCAGAGG[C/T]AGTATGCTACAAAAT | 55827 |
rs536540401 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050602 | TAAGCCAGTGCAGTT[G/T]CCCATACTGTGACAG | 55827 |
rs536546755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026225 | TATCTACCTTTTTGC[A/G]TATTCTCTAAATATT | 55827 |
rs536574189 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030971 | AAGCATGGGCGGGGA[C/T]GTGTAGGGGTAGGTG | 55827 |
rs536575514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069205 | CAAGTCACACAACTG[A/C]TAAATATTAAAGCCA | 55827 |
rs536582938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015442 | AGTTAACTGATTGTT[C/T]TCAATTTCTGTTTCT | 55827 |
rs536582954 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167983550 | CCTTGGAAATTTACA[A/G]CTCTGCCTTAGCTTT | 55827 |
rs536656596 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940104 | AAGCTTTGTAATTGA[-/T]TTTACTTAAACTGAT | 55827 |
rs536659925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045343 | CTCTAAGAGTGTCTC[A/G]TTCATATAAACTTAA | 55827 |
rs536696599 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038157 | GAATCAAAGGGAGTC[A/G]TGTACACAAAGCTAG | 55827 |
rs536697769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951273 | TGTGCTAAGCCCTTT[C/T]TGTCCTTAAAATAAC | 55827 |
rs536729267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996455 | ACCCTGATCCGAGCT[A/G]TCAGCATCTCTGGCA | 55827 |
rs536769833 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005836 | GTTACATAACTGTTA[A/T]CACTGTATACATTTT | 55827 |
rs536773627 | snp | C/T | | | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168076107 | TCCCAAAAATTTGAC[C/T]ATTAACAGCCTGTTG | 55827 |
rs536806917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016919 | GATTATTTGGAACTA[A/G]TTTATATATTGGTAG | 55827 |
rs536817705 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948494 | GCCCCAACCATCTCT[A/G]TAAGTAATAATTCTC | 55827 |
rs536839528 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977193 | ACAGGCATGAACCAC[C/T]GTGCCTGGGCCACAG | 55827 |
rs536937299 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167973746 | AAAGCACAACAGATA[C/T]TCCCCACTCACCTCT | 55827 |
rs536945445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070155 | TTATAATATAAAAAT[A/T]CTCTTTCATTTCTTT | 55827 |
rs536977877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019492 | TAAACAGGTATGGCA[C/G]AGGCATTCAGCATAT | 55827 |
rs536994644 | in-del | -/A | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997507 | ATGGAATTTATGGGG[-/A]TTTTTTTTTCTGTCT | 55827 |
rs537013765 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949450 | TTGTTGTTCAGTTTA[A/T]TAATGTCTCCTTAGG | 55827 |
rs537070659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038836 | ACATTTTGGGACTTT[C/T]TGCAGTCGTGGTCCT | 55827 |
rs537148718 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026264 | ATAATTTCCTCTATG[C/G]CTAAAATCATACATC | 55827 |
rs537185880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957591 | AATGCTGCTGTGAAC[A/G]TTTGTGTACAAATTT | 55827 |
rs537189619 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055816 | ATACTAAAAGTTTCT[A/G]TTCTAAGTCTTCTAT | 55827 |
rs537196157 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950038 | GCCTCTATACATGTT[C/G]TAATGTGCAAACGTC | 55827 |
rs537211789 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026311 | TCGTTAAACGAGTGA[G/T]TAAATGAATTCTTTA | 55827 |
rs537221041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060297 | CCATCCTCCCACCTC[A/G]GCCTCCCAAATAGCA | 55827 |
rs537224842 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936858 | GGGTGTCCCCTCCCC[C/T]TCCTCCCCTCCCCCA | 55827 |
rs537236359 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033062 | TATGTCTTTGAGCAT[C/G]TTTTAGAACCTCATG | 55827 |
rs537261614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943129 | TTAGCCAGGATGGTC[G/T]CGATCTCCTGACCTT | 55827 |
rs537342893 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007200 | AAGCAGAAAGCTCCT[A/G]TCAAAAGCTAGTCAA | 55827 |
rs537360668 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954743 | AGGCGTGAGCCACCG[C/T]ACCCGGCAAATTTTT | 55827 |
rs537375335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026903 | CTAGAAAAAGAGGGT[A/G]GTGTGAGAAGAGTAG | 55827 |
rs537379501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168062122 | GGTGAATCTTACAAA[C/T]ATAATTCTGAGCTAA | 55827 |
rs537385085 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046214 | TAAAATAGGGTTATG[A/T]TTATCTAAAATTATT | 55827 |
rs537389808 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070789 | GTAATGGTTTGCATG[G/T]ATCATTCTAGACTCC | 55827 |
rs537407026 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167956197 | TGCTGGATTTTGCCA[A/G]GTGTCTTTTTTTTTT | 55827 |
rs537419989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031511 | TTTAGAGCAGGAGAC[A/G]AAAAAATGGAAATGA | 55827 |
rs537421374 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995615 | AACCCAAGAGAAGGA[A/G]GTTGCATGAGCCGAG | 55827 |
rs537452823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941198 | TTTCAGTGAAAGCTG[A/G]AAAATGTATGATTTT | 55827 |
rs537452883 | snp | C/G | 0.000200418 | 0.0100084 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991183 | AACTATATGTAATTG[C/G]TATTATGTTATGTTT | 55827 |
rs537469880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046387 | ACTCTAGGGATAAAG[A/G]CTGAAAGAAGACAGG | 55827 |
rs537503097 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030018 | CATGTCTAAGGTTGC[A/T]CACAGCTAGTAAGCG | 55827 |
rs537522861 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990207 | TATTTGTACAAAATT[A/T]TTTTTAAAAAATTAG | 55827 |
rs537531917 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936368 | CAGTGCCTAAAGATG[A/G]TGCCGCACAATTCTC | 55827 |
rs537538667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017911 | GATAGTGCCAGTAAA[A/G]CATATTTCTGTTGTC | 55827 |
rs537544684 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168075830 | AGAAACTGGTTGTTT[C/T]AAGATACCCTGAATT | 55827 |
rs537546586 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067201 | CTAACACTGACTGTT[A/C]GTAGCACAATTCCCA | 55827 |
rs537547053 | in-del | -/ATAA/ATAAATAA/ATAAATAAATAA/ATAAATAAATAAATAA | 0.109717 | 0.214152 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939774 | GTCATAAATAAATAA[lengthTooLong]ATAAATAAATAAAGT | 55827 |
rs537559594 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167996932 | ACTGATACTACCTAT[A/C]CCCTTTTCTACTTTA | 55827 |
rs537566616 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050675 | CAATGTCTTCCTTCT[A/G]TTCTAGCTTCAATGA | 55827 |
rs537577093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025081 | GTATATAACTACTCT[A/G]TAATTAAAGGATTTT | 55827 |
rs537578886 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068002 | CTGTATTTCGTCACT[A/G]AAGTTATCAGTTCTC | 55827 |
rs537588935 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954185 | TAATTTTTGAATTTC[C/T]AGTAGAGACGGGGTT | 55827 |
rs537619057 | in-del | -/AAATACAA | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071466 | AATAAAAAAAATTAT[-/AAATACAA]AAATACAAAAATTAG | 55827 |
rs537622145 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051495 | TTGAGTAGATCTTTA[A/T]AGTGAACCTCAATGA | 55827 |
rs537624791 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168012803 | TTATTTAAAAAGCAC[C/T]GGAAATATTGAATAA | 55827 |
rs537701939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037245 | GAATGAAAAAAGATA[C/T]AAGTCCTTCATTGCA | 55827 |
rs537727761 | snp | C/T | 0.000228168 | 0.0106786 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004041 | GGCAAAAACTACTTA[C/T]TGAAGCCAGTTTTTA | 55827 |
rs537756897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995048 | TTGATGAAGAAGGGT[A/T]TGATGGCTAATAAAA | 55827 |
rs537794806 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045397 | ATGATTTTACGTATT[A/T]TATTCTTTGAGCACT | 55827 |
rs537799619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167947983 | TTGAATTTTCACACT[A/G]TTGTGTTGCAGTGTA | 55827 |
rs537808764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016110 | TATTCAACATCACGT[A/G]TTAGGGGGACAGATT | 55827 |
rs537815715 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168021202 | GATTTGTACATTTCA[C/T]GGTATTTTTTAGAAA | 55827 |
rs537817327 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024421 | TACTTGGTGTGAAAT[A/G]TATGTAATTTAAACT | 55827 |
rs537822717 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941754 | AAATTTTTTTTTAAA[C/T]ACTGCTGATGGCTCC | 55827 |
rs537858175 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961245 | GGGTTTTATTTTGTT[C/T]TGTTTTGTTTGTTTT | 55827 |
rs537873983 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982145 | TGGAGCATTTTATTT[G/T]GTGTTCGTTGGCTCC | 55827 |
rs537874759 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168021983 | ATTCTTATTGGTTGG[C/G]GAGAGTTGCGCTTAT | 55827 |
rs537878506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988963 | CAGGTGCCTGTAATC[A/C]CAGCTACTCGGGAGG | 55827 |
rs537896236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976099 | TCTGATATATTTGGA[A/T]TTGTTTCTATCCCTT | 55827 |
rs537934454 | snp | C/T | 0.128976 | 0.218754 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009374 | CTTCCTTCCTTCCTT[C/T]CTTCCTTCCTTCCTT | 55827 |
rs537969738 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062328 | GTGCTGATTATATGG[A/G]CCTGTTTTGTTTGCA | 55827 |
rs537973577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008815 | TTATCAGAGAATTTC[C/T]GTGCCAAATTCTGCC | 55827 |
rs537974116 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019261 | CACCGTGTCAGCCAG[G/T]ATGGTCTTGATCTCC | 55827 |
rs538000016 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168051334 | TTTTCCTTGAGCTCA[A/G]TAACTAAAAATGTAC | 55827 |
rs538033402 | in-del | -/T | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167934933 | TTCAGTTTCTTACAG[-/T]TTTTTTTTTTCAACC | 55827 |
rs538059527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961335 | GCAAGCTCCGCCTCC[C/T]GGGTTCATGCCATTC | 55827 |
rs538070390 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937314 | GGAGACTTGCGGAAC[C/T]TCCAGGAGCTGCCGC | 55827 |
rs538082336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986855 | GAGCCTCAACTTACA[A/G]TATTGTCATTGCTAA | 55827 |
rs538089499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994387 | AGACTAAATGTGTAT[A/G]TCCATGGATCAATAG | 55827 |
rs538117680 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981154 | TCAGGTAATCTGCCC[A/G]TCTCCGCCTCCAAAG | 55827 |
rs538144373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015479 | GTATCATTTTGTTCT[A/G]TGTTCATTTTGAAAT | 55827 |
rs538145552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987793 | TAGTTTATAATCAGA[A/G]ATTGAAAAATGTAAA | 55827 |
rs538154220 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023435 | CACAGTGATATTCTA[A/T]ATTACTAGATTGCTT | 55827 |
rs538182618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073681 | AACTTTGAGATAGGC[C/T]GTTACTGCTTCATCA | 55827 |
rs538213933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168057377 | TTGGAGTTATCTCCA[A/G]GATTCCAGATTTTCT | 55827 |
rs538221919 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960175 | AAAGGTCCGATGATC[C/G]TGTTTATGTGGGTCT | 55827 |
rs538246497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058328 | CGTATATACCAAGGA[A/T]TGGACCATTTACAAA | 55827 |
rs538331458 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168047714 | TATATGTGTGTGTGT[A/G]TATATATATATAAAA | 55827 |
rs538349553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011379 | CCTTGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 55827 |
rs538388623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061200 | CATGTCAGCTTTTCT[A/G]GGAGTTTCTAACTGT | 55827 |
rs538416049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939500 | GGGCGCGGTGGCTTA[C/T]GCCTGGAATCCCAGC | 55827 |
rs538430189 | snp | G/T | 0.0023933 | 0.0345097 | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168076334 | AAGAAGGAGGCGTTG[G/T]TCTTGCTGTCTGAGG | 55827 |
rs538432423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035816 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCCGAA | 55827 |
rs538438121 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168023649 | CCTGATGAAATGAAC[A/G]CGTTACTTATTTATC | 55827 |
rs538452983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938836 | CCATATACCTGCTTT[C/T]CCCCCTCCTACTCCA | 55827 |
rs538478694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037806 | TATATTTTAGAAAAT[A/G]TCAAAGCACTATAAA | 55827 |
rs538490640 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168065304 | AAAGAAGCTAGAAGA[C/T]AGATTTTTGTCAGTT | 55827 |
rs538529426 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072941 | TTATTTACAAAAGCA[A/G]TTTGACATTGCTACT | 55827 |
rs538558522 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989026 | CGGAGGTTGCAGTGA[A/G]CCGAGATCACACCAC | 55827 |
rs538573562 | snp | C/G | 1.6552e-05 | 0.00287676 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065770 | TCTTTTCTAGGACGA[C/G]GGCTAGAAATTATTT | 55827 |
rs538577104 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022605 | TCATGCTTCGAATCC[G/T]CCAAGGCAGGATGAA | 55827 |
rs538580323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015593 | TAGTTAAATAGAAGC[A/G]TTTGGTTGTATATGT | 55827 |
rs538586683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941850 | TTTAAATAGATATCT[A/G]TTGTGGGATTGCTGA | 55827 |
rs538594690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068110 | AAATGTTTTAAGTAG[C/T]CTCAAAATTTGACCT | 55827 |
rs538596433 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017992 | CTATGATTTGGAAAC[C/G/T]AAGAAATTTTAAAAA | 55827 |
rs538611098 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009405 | TCTTTCTTTCTTTCT[C/T]TCTCTCTCTTTTGTT | 55827 |
rs538625058 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032371 | TTGAATCCAGATATG[C/T]TTCCTTATACAAATA | 55827 |
rs538626565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976567 | GCTTCTAAGATAGAC[A/G]TTCATTTTTGTTATT | 55827 |
rs538665871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983275 | GTCATTTTAACGATA[C/T]TGATTCTTCCAATCC | 55827 |
rs538741377 | snp | A/G | 0.00180715 | 0.0300051 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050983 | ATGATGGATTTGCCA[A/G]GTCTTCTTTTGCCAC | 55827 |
rs538746898 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003364 | AAAATACTTTCTGGT[G/T]CCAGTTAATTTCAAA | 55827 |
rs538762515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002303 | GTGGATATTTATCCT[C/T]AGAATGAATGCTTTA | 55827 |
rs538766767 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945448 | TCTGGTTAAATATAT[G/T]CCTAGTTTGTGTGTG | 55827 |
rs538821591 | snp | A/G | 2.6254e-05 | 0.00362302 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045261 | AACATGAACTGTAAA[A/G]AATGTATTTCACAAG | 55827 |
rs538836212 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974683 | GGATTCTGATTTTTT[A/T]AAATTATAATAGCTT | 55827 |
rs538955143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016796 | ATAAGTTATTTAGGA[A/G]CAAGAATGTCTAGGT | 55827 |
rs538972427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957820 | TTAAAAAATTATTAT[A/G]ATCATCCTAGTGGAT | 55827 |
rs538976673 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167988539 | AGACAAGTAATTCCA[A/G]GTGATTTTTCCTGAC | 55827 |
rs539009500 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945770 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC | 55827 |
rs539037966 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001250 | TGAGCTAGGATGGGA[C/T]CACTGCAATCCAGTC | 55827 |
rs539121774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980750 | TTAACCCTTTTTTAG[A/G]TACATGGTTCACAAA | 55827 |
rs539147025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940276 | TTCACCTGGGCCAAC[A/G]GAGTGTTGTTTTAGA | 55827 |
rs539148695 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167994682 | CAGTACACAGCTGTA[G/T]AAAAATGTTTGCTTT | 55827 |
rs539169243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994099 | TAAATAATTACTAGC[A/G]TCTATTCTTAATAAT | 55827 |
rs539173073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167946423 | ATATTGAAGAGTGGT[A/G]AAAGTAGGCATCCTT | 55827 |
rs539174448 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954546 | CAAGCTCCGCCTCCC[A/G]GATTCACGCCAGTCT | 55827 |
rs539184676 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052333 | AAAGTACCATGATGC[C/T]TTAATTGAGTTTTAG | 55827 |
rs539211659 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024753 | AGGTTACAGTGAGCC[A/G]AGATTGCGCCATTGC | 55827 |
rs539216439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015318 | TTAGAGCTCTTCTCA[A/G]TAAATTCTGAGTTGT | 55827 |
rs539239897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029956 | CTGCGCTCCAGCCTG[A/G]GTGACAGAGCAAGAC | 55827 |
rs539298402 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168059930 | TGGGATTATAGGTGT[A/G]AACTGCTGCACTCAG | 55827 |
rs539325485 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061416 | GTCACAATTTAATGT[A/C]CATCTTTCCAAACCC | 55827 |
rs539349398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016210 | GGGCAAATATTTATT[A/C]CTTTTAAAGCTGATG | 55827 |
rs539361012 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072040 | CGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 55827 |
rs539362492 | in-del | -/TT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168063889 | ATCTTCAGTTATCTC[-/TT]TATCCAACATGGTTC | 55827 |
rs539402531 | snp | A/T | 3.42185e-05 | 0.00413619 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168043052 | ATCAAGTTCTAGAGG[A/T]ATTGGGAGCCATTGC | 55827 |
rs539484708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985964 | TTATAAAAATGGGAA[C/T]CATACTGTGCCTTCT | 55827 |
rs539545962 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939576 | AGACCGGCCTGGCCA[A/G]CATGGTGAAACCCTG | 55827 |
rs539566124 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967831 | TGCCTCCTGCGTTCA[A/G]GCGATTCTCCTGCCT | 55827 |
rs539572627 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167992312 | CATTCATATATTCAC[A/G]TATTTTATATTGTTA | 55827 |
rs539583548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029418 | GATACGTAAATGCCT[A/G]CCTACCTTGTGGCAA | 55827 |
rs539634703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965835 | AGACGGGGTTTCGCC[A/G]TATTGGTCAGGCTGG | 55827 |
rs539692470 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991430 | AATTTCTTGTTTGTT[A/T]TAAAATTTCAGAAAA | 55827 |
rs539729925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000616 | TTTGTTCGTCAACCA[A/G]TTGACGAATGGATGA | 55827 |
rs539793442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073130 | GCAGTGAGCCAAGAT[C/G]GCGCCACTGCACTCC | 55827 |
rs539840128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979908 | AATAAACAGGCTGGG[C/T]GCAGTGGCTCACACC | 55827 |
rs539859015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029545 | CATAAGACACTTAAT[A/G]CCACATTTTCTTTGT | 55827 |
rs539877088 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979080 | CTTCTACTTTAATTT[A/C]ATTGCTTTGTCTTTA | 55827 |
rs539914305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014585 | GATGTCTATTCATTC[C/T]TTCCCCCAACACTAC | 55827 |
rs539917224 | in-del | -/AAAAATA | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071441 | AAACCCCGTCTCTAT[-/AAAAATA]AAAAATAAAAAAAAT | 55827 |
rs539921883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032020 | ATGTATCGAAATCAC[A/G]TATTTAAGTTCAATT | 55827 |
rs539952194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021539 | AATAGATTAGGGAAC[C/T]GATTGAAATGCTATT | 55827 |
rs539965108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066604 | ATTTTAAGAAAAAGA[A/G]AAATTAAGATAAAAG | 55827 |
rs539981833 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961996 | TTGTGTGTATTTTGG[A/G]ATTTTCCAGTTATCT | 55827 |
rs540007537 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048514 | TGATTTTTAAAAAAA[A/T]ATTTACATTCTTATA | 55827 |
rs540016872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042605 | CAGGCTTTTGTTCAA[A/G]TACTAATTTTAAAGT | 55827 |
rs540021106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945515 | TTTCTTTTTTGAGAC[A/G]GAGTCTCACTCTGTC | 55827 |
rs540042454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958033 | GTATATTCTGGGACT[C/T]TTGTCATGGGACTCT | 55827 |
rs540043441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041363 | TGTTGCAAATATTTT[C/T]CCCAATTTGGTGTTT | 55827 |
rs540057353 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944687 | TCGTTTGAGTTCCTT[G/T]TGTAGTCTGGATATT | 55827 |
rs540098716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985493 | ATCATCTTGTCTCCT[C/T]CTCTGACTCTGACTC | 55827 |
rs540106862 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036017 | CAGTGGGCCGAGATC[A/G]CGCCATTGCACTCCA | 55827 |
rs540152088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072418 | ATTCTTGTTCATTGC[C/G]TTATTTTCCTCAAGT | 55827 |
rs540180079 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938961 | GTGTATGTATACATA[C/G]AGGGAGTTCTTTATC | 55827 |
rs540191663 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995525 | TCTCTACTGAAAATA[C/T]AAAAATTAGCTGGGC | 55827 |
rs540210005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022819 | CTTGCCTGGAATAAC[A/G]TATCTTAAGCACATG | 55827 |
rs540232962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048873 | AAATCGGCATTTGGC[A/G]GAGATCTAGCCCAAG | 55827 |
rs540234780 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014233 | GTCGAGGTCATCAAT[A/G]ACTTCCATCATACAA | 55827 |
rs540236616 | snp | A/T | 1.65121e-05 | 0.00287329 | missense | DCAF6 | GRCh38.p7 | 1:168044628 | GACAAAATATCAGGA[A/T]GGAGTATCTGCAGAA | 55827 |
rs540263370 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168061730 | GTTAAATTGCTGAGT[C/G]AAAGCTTATATTACT | 55827 |
rs540267179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973116 | TAAATCTCTGACAGC[A/G]TTAAAGAACATGATA | 55827 |
rs540310744 | in-del | -/CCTT | 0.00676609 | 0.0577691 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009502 | TTCACTTCTTCCCTC[-/CCTT]CCTTCCTTCCTTCTT | 55827 |
rs540321768 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167989294 | AAACTCTCTTAAACT[A/G]TTTTAGTGTTTCAGT | 55827 |
rs540331266 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959282 | TCCATTCACTTGCTG[A/G]AGGACATCTTGGGTG | 55827 |
rs540382198 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986371 | GATATTATAAGTCTT[C/T]TCATTTTGGCCATTC | 55827 |
rs540446504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027832 | CCTGAATTTTTAACA[A/G]AATCACAATTTGATA | 55827 |
rs540510911 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062867 | TGGAGTCCATAAAGA[A/G]GATGCTATTTGAAGG | 55827 |
rs540532688 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007012 | CCTCACACTGTTGCT[C/G]TCCAGCTGTACAAAA | 55827 |
rs540551941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986557 | ACAATTTTTCCATGG[A/G]GTGGGGATGGTTTTG | 55827 |
rs540557908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063315 | TAAAATTGCACATGA[A/G]TTTTGTCTGTATTAT | 55827 |
rs540573439 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979374 | TATCAACAGCTCTCC[C/T]TTCTTCCTTATCCTA | 55827 |
rs540581097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998452 | GTGAAGTTTCTGCAT[C/T]GATAGACTCTTCCTT | 55827 |
rs540584319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056101 | AGAGTTCACTAGCAG[C/T]TTTCACACTTTCCAA | 55827 |
rs540606023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013488 | TGCTCCTACCACCAA[A/G]TCTCACTATTGACAT | 55827 |
rs540619756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958463 | CCATAAATAGAAGAG[C/T]TTATTTCTGAACTCT | 55827 |
rs540665794 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965537 | ATTTTAATCTGAAAT[G/T]TATTGTGAAAATCTG | 55827 |
rs540709907 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168033287 | GAGAGGTCTCTAGTA[A/G]CATTTCTGAAAAGGA | 55827 |
rs540722196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992618 | ATTTTGCAAGGTTAT[A/G]CAGCTTTGTGGGATT | 55827 |
rs540744343 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991543 | TTAAAAAGTTGTAAC[A/T]TTTGATGTATTAGTT | 55827 |
rs540772167 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070069 | AAAATCTATTTGTGC[A/T]AATGTAGCAATGGTT | 55827 |
rs540781383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071342 | GGTACAGTGGCTCAC[A/G]CCTGTAATCTCAGCA | 55827 |
rs540813162 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937077 | GGGGGCACGCTGCCG[G/T]GTCTGTTGGAGGTGG | 55827 |
rs540829251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937692 | GTTAAGCTTTCTAAA[A/T]ACAACCTTCAGTACT | 55827 |
rs540833483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004403 | TGGGCCAAATCACCA[A/G]TAGTTATTATCACTG | 55827 |
rs540863599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978515 | TATTCTTAATGAAAT[A/G]TGTAGTCAAATCTCT | 55827 |
rs540868162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956259 | TTTAGTAAAAATAAA[C/T]TATTCAGGGTATCTA | 55827 |
rs540899939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964930 | CTGCTGACATTGCCC[A/G]TCTCTTCTTACATGC | 55827 |
rs540905288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963575 | CCTCCTGAGTAGCTG[A/G]GATGCCACCACACCC | 55827 |
rs540919944 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997365 | TCCTTTTGGGAGTGA[A/T]TAGTTGTTTGAGAAT | 55827 |
rs540919971 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968218 | AAAGAATTACTACCT[A/C]TATCAGGAGATTGGA | 55827 |
rs540951782 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064218 | AGATTGACAAGTGAA[A/T]ATTTGTTTTAGTGAC | 55827 |
rs540993221 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939508 | TGGCTTACGCCTGGA[A/G]TCCCAGCACTTTGGG | 55827 |
rs541004325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168047813 | CATTATTTTCTAGCT[C/T]TTTACCAAAAATTTG | 55827 |
rs541012265 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943401 | CTGTGGTTCTGGTTT[G/T]TCTCCGTGTATTAAG | 55827 |
rs541015268 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168028096 | AAGCACAGTAATGTC[C/G]ATCATGCATCTTGTT | 55827 |
rs541071028 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167936016 | GAAAAGCTGCGGCCC[C/G]CGCCCCGCGAAGGTT | 55827 |
rs541072228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033896 | AAAGGGATTTTTTCC[C/G]CACTATATTGTGTGT | 55827 |
rs541073581 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976444 | GCTACTGTACTCCAA[C/T]CTGGGCGACAGAGTG | 55827 |
rs541138507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976785 | TGTTGTTTGTTTAGA[C/T]TTACCTGCATATTTA | 55827 |
rs541139562 | in-del | -/CTGA | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034862 | TTGCTGATCCAACCT[-/CTGA]CAGAGAAGTTGGGAA | 55827 |
rs541140383 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034776 | GGTTTTAAATAAAAA[G/T]CTACCTTTTAAGTAA | 55827 |
rs541147287 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167991400 | AGTAAATCTCTATGA[C/T]ATTTTCAGTTTTAAA | 55827 |
rs541154421 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945452 | GTTAAATATATTCCT[A/C]GTTTGTGTGTGTGTG | 55827 |
rs541205928 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945649 | AGTGCGCACCACTAT[-/G]CCCAGCTAATTTTTG | 55827 |
rs541222722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054424 | ATAAGTGAATTAATT[C/T]ATTCTTGAGAGTGGA | 55827 |
rs541249120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948525 | AACTAGTCTAGTAAA[A/G]GAGATAGGTATGTGA | 55827 |
rs541276751 | snp | C/G | 1.65266e-05 | 0.00287455 | missense | DCAF6 | GRCh38.p7 | 1:168038415 | CCAGGGACAGGTGAA[C/G]CAGTTTTAAGTTTGC | 55827 |
rs541313497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032082 | CTTGGGTTAAAATTA[C/T]TATAATTGACATAGA | 55827 |
rs541340188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983050 | TACCAGTACTATGCT[G/T]TTTTGGTTACTGTAG | 55827 |
rs541347734 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961396 | TACAGGTGCCCACCA[C/G]CACACCCGGCTAATT | 55827 |
rs541377474 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046657 | AGTTCTATTTCTTTC[A/C]ATACCCAGAGGGAGT | 55827 |
rs541444083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027316 | AAAACTGAGCATGTT[C/T]ATAGAGTAAACAGAT | 55827 |
rs541446383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944479 | GATAACCAACATTGT[C/T]TGTCTTTTTAATAAA | 55827 |
rs541454165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983611 | AGCCAGAGATGTTAG[A/C]GTAGGGCCTTCTTGG | 55827 |
rs541494602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979505 | ACTGATTTCACTTAG[C/T]ATGATCATATTGTAG | 55827 |
rs541505608 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168065357 | CTCACTATATTGCCC[A/G]GGCTGGTCTCAAACT | 55827 |
rs541533689 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985676 | ATAGGATGTAGATAT[C/T]TTTGGGCTACTATTA | 55827 |
rs541563496 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948977 | GTTATTGAGTGGTAA[C/T]ACAGATTCCAGAACA | 55827 |
rs541594026 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975100 | TAGATGCATGTGTGT[A/T]CATGTACAGATGTGT | 55827 |
rs541627924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955393 | ATTCCCAGTGTTAGT[A/G]TGTAGAAATTCCAGT | 55827 |
rs541630005 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046770 | CAAAATCAAACTGAT[A/C]ATTTCCAAAACCCAG | 55827 |
rs541688277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989665 | AGGCGGGCAGATCAC[C/T]TGAGGTTAGGAGTTC | 55827 |
rs541721400 | in-del | -/AA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001334 | TTAAAGGGAGCGGTC[-/AA]GAGTGATAGGTGCCA | 55827 |
rs541775115 | in-del | -/CTTT | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073311 | TATAAGTGTTAACTG[-/CTTT]CTTTGCAGCCTTACT | 55827 |
rs541781626 | snp | C/G/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070334 | AGTTAGTCAACCACT[C/G/T]TTTTTCTCTCCTATC | 55827 |
rs541789389 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167965221 | ATTAGGTGTCTGTCA[C/G]TTAAAGAGCCTATAC | 55827 |
rs541827480 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041776 | CTAAGCGTTTTATTC[A/G]TGCCTGAATCATAGC | 55827 |
rs541827527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034015 | CAACATAGTTTTCCT[A/G]TACTATGATGCCAAA | 55827 |
rs541831648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937752 | TTGCATAACATTTTT[G/T]TTTTGAGGATTCTAG | 55827 |
rs541832530 | snp | G/T | 0.00306534 | 0.0390291 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937030 | GGGGGCCCCGGGGCG[G/T]AGGCGCTGAGGTCGC | 55827 |
rs541864224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034539 | GGGGGAGGAAAAGTC[C/T]GTAACTAGAGAAAAA | 55827 |
rs541875650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964233 | CTTGCAAAGTAGGTC[C/T]GCTGGCAACAAATTC | 55827 |
rs541952574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005250 | ATGGTGGATTTGATA[C/T]GGTCTTTTGTCAACA | 55827 |
rs541953629 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027925 | ACTTTTTTTAAGAAA[C/G]AAAATTGTAGGGAAA | 55827 |
rs541991736 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054543 | CATGCAAACCATAGC[A/T]CATAGCTTTTACTAT | 55827 |
rs541993142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938381 | AAAAATAGATTGATT[C/G]TGTCTTTTAAATTAT | 55827 |
rs542007489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006071 | TATAAGTTTTTAGGA[A/G]AACTTAGCAAGAAGA | 55827 |
rs542041073 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942152 | CTTACCGCAACCTCT[C/G]CCTGCTGGGTTCAAG | 55827 |
rs542066270 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951435 | CAAAAGTTAGCTGGG[C/T]GTGGTGCTGTGTGCC | 55827 |
rs542071757 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033203 | AAATACATAACAGTT[A/C]AAGGAAACTGCTTTC | 55827 |
rs542088932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991677 | TTATGATTGGTTTCT[A/G]CTGGAAGCTCTGTTC | 55827 |
rs542200869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970411 | ATCCCAGCACTTTGG[A/G]AGGCCCGAGGTGGGA | 55827 |
rs542253748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955531 | TAATTTTTAGATATT[C/T]ATCTGTATTCTGGAA | 55827 |
rs542336262 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168003627 | GAATAGGCAAAGATG[A/G]AGGAGAGGTGAGCCC | 55827 |
rs542342049 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013232 | CCCTATTGGTACTGG[A/G]TCATTTTCTAGGAAG | 55827 |
rs542374775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012618 | CTTTAAAATTTCAAG[C/T]TGCTAGCAGAACTGT | 55827 |
rs542380516 | snp | A/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936823 | CGCGGATGGTGCCGG[A/T]GCGGCTCGGGTGTTG | 55827 |
rs542401453 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000644 | TGAACAGAATAGGGT[A/G]TCTTGCTAAAATGGG | 55827 |
rs542429983 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004872 | ATTTTGAAAGATACT[A/G]AATCACATCAACTTC | 55827 |
rs542433135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949707 | TTGCTAGCATCCAAG[A/G]AAGGTAGCAGTCCAA | 55827 |
rs542457158 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037527 | ATAAAATGAAAAATA[C/T]GTAAAGCTCTGTTTA | 55827 |
rs542468250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024735 | CTTGAACCTGGGAGG[C/T]GGAGGTTACAGTGAG | 55827 |
rs542485461 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989735 | TAAAAATACAAAATA[G/T]CCAGGCGTGGTGGCA | 55827 |
rs542492192 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168069514 | GAACTGCATAAGCAG[G/T]GAATTAAATATCACT | 55827 |
rs542501200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975570 | CTTTTATTTATGATA[C/T]AGGGTCACACTGTCA | 55827 |
rs542511617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984138 | TGGATTGTTCTAATC[C/T]CTTGGTTAAATTTCA | 55827 |
rs542512292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010653 | AAAATGTGATTATAA[A/G]ATTATATGTTTAAAA | 55827 |
rs542551015 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009748 | TTCATAACTACCCTA[C/G]GTAAAGTCCTCTTTC | 55827 |
rs542558543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032765 | ATAGTTAATTAATGT[A/G]TGATTATAAAGTTAT | 55827 |
rs542567381 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995437 | GTAATCCTAGCACTT[C/T]GGGAGGTCGAGGCGA | 55827 |
rs542582047 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060655 | CCAGCACTTTGGGAA[C/G]CTGAGGTGGGTGGAT | 55827 |
rs542613470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053496 | GCTACAAAGACTCAA[A/G]AGAATCAAAGGCACT | 55827 |
rs542678077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962516 | ATTAATGTAACTACT[C/T]CTGTTTTCTTTTGAT | 55827 |
rs542691228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996616 | TCTCATCAACATTCT[A/G]AGTGGCTCCCTGTCG | 55827 |
rs542718534 | snp | C/G/T | 0.00239393 | 0.0345281 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061138 | GAATATTTGACCTCT[C/G/T]TATCCTTCCCATTCT | 55827 |
rs542750494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045964 | TTAATCTTAAAATCC[C/T]AGTTTACAAAGGAGT | 55827 |
rs542788941 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071668 | CAGTGGGCTGTATTT[G/T]CCTATGGGCTATAGT | 55827 |
rs542801945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031113 | AGAGCTCAAGAAAGA[A/C]ATTTGGGAGATTTTT | 55827 |
rs542807219 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960933 | TAGAACAAGTTGGGA[A/G]TAATTGACATCTTGA | 55827 |
rs542814114 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009178 | TAATTTTTTATACTT[A/T]TAGTAGAGACAGGGT | 55827 |
rs542844090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960375 | GCGATCTCAGCTCAC[A/G]GCAGCCTCCACCTCC | 55827 |
rs542851798 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935223 | GGATGAGAAATGACA[C/T]TGACTCAAGCCTGGA | 55827 |
rs542857450 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051143 | GAAAAGAAATTTCCT[G/T]TGTGCAGACTGATGT | 55827 |
rs542899471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059719 | GGCATGATCATGGCT[C/T]ACTGCAGTTTTGACC | 55827 |
rs542908525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954268 | AAAGTGCTGGGATTA[C/T]AGGTGTGAGCCACTG | 55827 |
rs542912632 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014494 | CTTACTCTTTAGGGG[A/C]CTTAAAATGACATCC | 55827 |
rs542912870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968841 | ACTCAGTTCCATTGC[A/G]TAATCTATAAAAGTG | 55827 |
rs542915588 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034020 | TAGTTTTCCTATACT[A/G]TGATGCCAAAGTGAT | 55827 |
rs542976623 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040634 | ATGACAGTAGGTCAT[C/T]GTACTTATCACGTCT | 55827 |
rs542989533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948208 | ACTCTTCACTTTGAC[C/T]TCAGACAGTCTGATT | 55827 |
rs542991806 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030420 | ACATTTTTAGGTTTC[A/G/T]CATTTTTATTTTAAG | 55827 |
rs543020893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046067 | TGTCAACTGAAAAAT[A/G]TAATGAAAGATTAAT | 55827 |
rs543049073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048570 | TTTCACTTTTGGGCT[A/G]AGATCAAGCATGAGA | 55827 |
rs543049732 | in-del | -/TC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964910 | TTCTTAGGATTTCCG[-/TC]TCTCTGCTGACATTG | 55827 |
rs543059506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039571 | TTAGTTAATATATTG[A/G]TATAGTATTTCTTAA | 55827 |
rs543114321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981537 | CTTCCCTTTCTCCCT[C/G]CCTGCTCTACTAGTT | 55827 |
rs543135691 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036295 | AAGGAAAGTTTTCAT[A/G]TATCATTTAAATTCC | 55827 |
rs543160129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032920 | CTCCAGGGGTATCCC[A/G]GCTTAAAGTCTGAAC | 55827 |
rs543176316 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989806 | GAATCTCTTGAACCC[A/C]GGAGGTGGAGGTTGC | 55827 |
rs543189680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941374 | GATGAATCAAGTTAT[A/C]AGTGCTTAGAAGGTT | 55827 |
rs543241316 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962814 | ACAAAAATTAGCCAC[A/G/T]CATGGTGGCACATGC | 55827 |
rs543309492 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004350 | AGAATATGTTGTAGA[A/T]AAGTTTTTATCCCTC | 55827 |
rs543322027 | in-del | -/AAAG | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011977 | CCTCTGTCTCAGAAA[-/AAAG]AAAGAAAGAAAGAAA | 55827 |
rs543340128 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003559 | TTGGCTGGGTACTCT[G/T]AGAACTAAAAATTTA | 55827 |
rs543375182 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049962 | ACCCAGGCTGTATAA[-/T]TTTTTTTTTTTTTTA | 55827 |
rs543412743 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046613 | TAATCTTGAGCATTC[A/T]TAGTATATATTTTAG | 55827 |
rs543418147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949777 | TAATAGCATTCAGAT[A/G]TGAGTTTATTTTAAT | 55827 |
rs543491077 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046516 | ACTTTGCCATGGCAC[-/T]TTTTTTTGTAGATAT | 55827 |
rs543535388 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168076275 | ACTGTTCACTAGGTG[G/T]AAATGGATCATCATA | 55827 |
rs543561246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069373 | TTCTTTTCTTCTGTG[A/G]CTACTCCATCCACAC | 55827 |
rs543572284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068563 | TATATTTTTTAATAT[C/T]ACAAAATGAGGGTAG | 55827 |
rs543622343 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051894 | CTTTTTTTTTTTTTT[C/T]CCCCAAGATGTAGCC | 55827 |
rs543625889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954353 | ACTTCAGCTGGTAAG[A/G]CTGTTGCCAGCCTAA | 55827 |
rs543627696 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961600 | GTTATCTACAAAGAC[C/T]GTTTTATTTCTTTTC | 55827 |
rs543647800 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025760 | AGTCTATTCTCTACC[G/T]GCAGCCAGAGTGAAA | 55827 |
rs543663719 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044734 | CCTTAATCTATGTTA[A/T]TCTCTCTATAGTTAG | 55827 |
rs543696301 | snp | A/C | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167934904 | TCTAGATCTTTAATA[A/C]AGGGATTGGAATCTT | 55827 |
rs543733020 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167981057 | GATTACAGGCGCATG[A/C]CACCACGCCCGGCTA | 55827 |
rs543782112 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995454 | GGAGGTCGAGGCGAG[C/T]GGATCACCTGAGGTC | 55827 |
rs543801281 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935320 | AGTGACCTTTACTCC[A/G]AACCCTACAGTGCGA | 55827 |
rs543819481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031937 | CAAAGGTCAAATGGC[C/T]ACCACATTTCAACCC | 55827 |
rs543821562 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038245 | AAACTTTAAATGAAA[A/C]CCATAACAGATGTGA | 55827 |
rs543833604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016462 | ATTTGAAAATTTTCA[A/G]TATTTGCTTTCTTAT | 55827 |
rs543855724 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967421 | CCACAGAATGTTTCC[G/T]TTACAAGGATGGTTT | 55827 |
rs543872472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023795 | CTATTTAGTGTTAGC[A/G]CAAATGTTTTACTAT | 55827 |
rs543895185 | snp | C/T | 6.91085e-05 | 0.00587788 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974845 | GTTTTGACAACAATT[C/T]GTTCAGGGCACCGAG | 55827 |
rs543967566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044134 | GCAAATACATATTTG[C/T]CTTGTACTGAGGGGA | 55827 |
rs543971771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167947442 | CTTGGTTTTCTGGTT[C/T]CTCGAGGTGCGTTCT | 55827 |
rs543984795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029587 | CTTGGAGCAATTTTT[C/T]ATATGTTAATTTACT | 55827 |
rs543984994 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036070 | CCATCTCAAAAAAAA[G/T]AAAAACAAAACAAAA | 55827 |
rs544040272 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951419 | GTCTCTACTAAAAAT[A/G]CAAAAGTTAGCTGGG | 55827 |
rs544056995 | snp | A/G | 1.67953e-05 | 0.00289782 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991172 | CTCTGCTGTATAACT[A/G]TATGTAATTGGTATT | 55827 |
rs544065710 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057684 | GTTCAGTGGGATACA[C/G]AGACACATATACATA | 55827 |
rs544079475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945938 | AAGTTTACTGAATTC[A/G]TTTACCAAATCTAAG | 55827 |
rs544103840 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168016057 | AAAGAGAGCTAATGC[A/G]CTTGCAGCTTACCCC | 55827 |
rs544130675 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978499 | GTTGGTTATTTGGAT[A/G]TATTCTTAATGAAAT | 55827 |
rs544158210 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022388 | GTAACGCTAAAGAAA[C/G]TTGAGCCTTTACATA | 55827 |
rs544172123 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037496 | TATTTTAATGTTTCC[C/T]AAACTGTTGTTCATC | 55827 |
rs544202425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074035 | AGATCAGTAAGGAAT[A/T]GAATACTTATTTGTA | 55827 |
rs544224213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966809 | AACAGTCATAGAATG[C/G]GCATTTATATTAGAA | 55827 |
rs544249270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968216 | AAAAAGAATTACTAC[C/T]TATATCAGGAGATTG | 55827 |
rs544282896 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168056624 | AATGTGGTCACAAAA[G/T]TTGGGAAATACTACA | 55827 |
rs544289450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050229 | AAGTGTTATTTTCAT[A/G]GAAATTTGGTTCCAT | 55827 |
rs544321067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009556 | TCTCCTCTTTCTCCT[C/T]TTTCTCCTTTCCCAT | 55827 |
rs544321589 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168020216 | ATTATGTAGTAGATA[C/T]TGTGATTATCCTCAT | 55827 |
rs544330634 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954904 | CTAAAAGTTTGCCCA[C/T]GTGCCCTCTCATTCC | 55827 |
rs544355717 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009227 | ATGGTCTCAATCTCC[A/T]GACCTTGTGATCCGC | 55827 |
rs544370907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014415 | ACTCTTTCTAGAGGT[C/T]CTTTTTCCTCTTAAA | 55827 |
rs544382868 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168014081 | GACAATGATTATCCA[A/G]TTTATCTGTTCTCCA | 55827 |
rs544391651 | in-del | -/TGTGGCAACC | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941487 | ATAAAAGTACATTTA[-/TGTGGCAACC]TGTGATATACACAAC | 55827 |
rs544448772 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168053099 | CAGAAAAGACCTCCT[A/G]TCACTATCACCATCA | 55827 |
rs544466849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987094 | ACAGTTGTCTTAAAC[A/G]TTACCAGAGAAGAAA | 55827 |
rs544471892 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972897 | AAGGGAATGCTTTTC[A/T]ATTTATGAGTGACTG | 55827 |
rs544480850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073169 | CGATAGAGCGAGACT[C/T]GGTCTCAAAAAAAAA | 55827 |
rs544489576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981267 | TTAGATCTTTAATCC[A/G]TTTTGAATTAATTTT | 55827 |
rs544535041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014824 | CCATGTGGTTTACTC[A/G]CTTATTTCCTCGAGG | 55827 |
rs544539898 | snp | A/G | 4.98004e-05 | 0.00498976 | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168023045 | CACTTGACGAGCAAC[A/G]GGGTGCGTGCAACAG | 55827 |
rs544540397 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168047925 | ATCTTGAACAACTGT[A/G]AAAAAGTATACTTTT | 55827 |
rs544542169 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940564 | CTGTAGGTTTAAATG[A/T]TTAAATGTAATAGTT | 55827 |
rs544621295 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062715 | ACAAAATTATTAAGT[A/G]ATATGTGTTAGGAGA | 55827 |
rs544634272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959363 | AGGTGTTGGTGTGCA[C/T]ATACGTTTACGTTCG | 55827 |
rs544678669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017264 | ACGTCTAGCAAACAT[A/G]TTTTGAAGGTTAAAA | 55827 |
rs544683478 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037785 | ATATACCAAAATATA[A/G]CAAAGTATATTTTAG | 55827 |
rs544703953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986588 | GGTTTAAAACTGTTA[C/T]ACCTCAGATCACCAG | 55827 |
rs544715811 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935510 | GGGAGCGGATGTCAC[A/G]TAGGTGGGGAAGGGA | 55827 |
rs544716799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982106 | TTGTGGTTTTGATTT[A/G]CATTTCTCTGAGATT | 55827 |
rs544732167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945560 | GCAGTGGCACAATCT[C/T]GGCTTACTACAACCT | 55827 |
rs544735877 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969063 | TGGTTTTTTTTTACC[A/T]TTCTGACCAAGTTAT | 55827 |
rs544737701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954916 | CCATGTGCCCTCTCA[C/T]TCCTTACACATCACC | 55827 |
rs544744972 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060996 | AACTCTACTTTCTTA[A/G]CAAAAGAGTTTTTTC | 55827 |
rs544778508 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064351 | AGAAAAGTTTTTGAG[A/T]TGACTAGTGTAACTG | 55827 |
rs544783011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030965 | GGGATGAAGCATGGG[C/T]GGGGACGTGTAGGGG | 55827 |
rs544842936 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167934604 | CATTCCATTATCAAA[C/T]TGGAAATCAGATTTA | 55827 |
rs544873210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958671 | TTTCATTGTAAAATA[C/T]CAGAACATTGTGTTT | 55827 |
rs544913462 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981403 | TATTTTAGATTCGAG[C/G]GGTACATGTGCAGGT | 55827 |
rs544919236 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065286 | GAATGCCTATCATAA[C/T]TTAAAGAAGCTAGAA | 55827 |
rs544951504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993714 | AAATCACGCCATCGC[A/G]CTCCAGCCTGGGCAA | 55827 |
rs544985567 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939168 | TTATTCAGCTCTTCT[A/G]TACTACAGTGCTAAT | 55827 |
rs545003427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067399 | ATAGTGTTTTGGAAG[C/T]CCACAGAGAGGAACA | 55827 |
rs545040252 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962450 | ATCGTTATGAAATAC[C/G]CTTCTTTTTCCCTGA | 55827 |
rs545084215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060476 | CTGGGGTGAGCCACC[A/G]TGCCTGGCCTAGAGC | 55827 |
rs545099501 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052821 | CATCACCTCTTACCT[C/G]GTGTACTGAGGGAGT | 55827 |
rs545113745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994502 | TAGTGATTTATAACA[C/G]TAACCTTAGGTATAT | 55827 |
rs545119339 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010561 | AACCACGTTCTATAT[A/G]CCTCGCCCAGAATTT | 55827 |
rs545147457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987905 | TATATACTGTCTAAT[A/G]TAAAAACCTGAAGAA | 55827 |
rs545222218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973630 | CAATCACTGATGTTA[C/T]TCTTTTTGATACTCA | 55827 |
rs545227871 | snp | C/G | 5.9363e-05 | 0.00544775 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045231 | ACCTGGTGATAGGTT[C/G]GTAAATTTTTAATTA | 55827 |
rs545242401 | in-del | -/T | 0.111765 | 0.208305 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033011 | ATAAAATACTCAGCA[-/T]TTTTTTTTTTACTAT | 55827 |
rs545280663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066780 | AAAAAATCTGTCCTT[C/T]TAAGAAAATAATTTT | 55827 |
rs545298304 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975407 | TCAAATTTTTGTAGG[A/T]TAGAAGGGACTCCAG | 55827 |
rs545313705 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074970 | ACATAGTATTTAATT[A/T]AAAAAAATCTTTTTA | 55827 |
rs545316061 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935172 | TCAACAATTTCATAA[A/G]TAAGGATAGACTTAA | 55827 |
rs545324309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016513 | TTCTGATGTGTAGGG[C/T]AGCAAAAGTACTCCA | 55827 |
rs545330050 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960305 | ATTATTTATTTATTT[A/T]TTTATTTTTTTGAGA | 55827 |
rs545396583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954202 | GTAGAGACGGGGTTT[C/T]GCCGTGTTGGCTAGG | 55827 |
rs545396808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036124 | TGTAGGAAGAAAGTT[G/T]TAATTATCATTAACC | 55827 |
rs545401361 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945369 | TCATGGGATGTTTTT[A/C]CATTTGTGTCATGTA | 55827 |
rs545407965 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008370 | GGTCCATTTGCTTAT[A/T]TGAATAACCTGTGAG | 55827 |
rs545431378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979571 | GAAGATTCCGTTGTA[C/T]GTATATACCACATTT | 55827 |
rs545433583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953532 | TATCAACAGGAATGC[C/T]TGAAACAGATGTGGC | 55827 |
rs545456469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973047 | CAATGGCCTAACAAA[C/T]GAAGTAACTAATGGC | 55827 |
rs545465890 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035329 | GCATGTGCCTATAGT[C/G]CCAGCTACTCAGGAG | 55827 |
rs545548127 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017868 | TTTTCCTTCATACTT[C/T]GGTATCTTTAGAGTA | 55827 |
rs545552633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007769 | CCCTTAGTTTGGGCT[C/T]TCTTCTCTTCTCTTT | 55827 |
rs545567969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048812 | CCATTTAAAATATTA[A/G]CATTTAAAAATGTAA | 55827 |
rs545573259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959450 | GCATGCTGTATTGTG[C/T]ATGTTTAGTTTTTAT | 55827 |
rs545602087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073060 | ACGCTCCTGTAGTCC[C/T]AGCTACTCGGGAGGG | 55827 |
rs545609313 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036525 | TCATCCAATCATCCA[A/G]TCTTTAGCTGTCTGT | 55827 |
rs545691732 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070746 | ATTTCTGACATCCCT[A/G]GAAGCTTTGAGAGGC | 55827 |
rs545694115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958219 | CTTGCTTAATCACTG[A/G]TCGTGAAGATTTATA | 55827 |
rs545713796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168057562 | ATTGCTGGATAATCA[A/G]TTTTTTACCTATTAT | 55827 |
rs545735730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944537 | TCTCATTGTGAATTT[C/G]ATTTGCATTTCTCTT | 55827 |
rs545744093 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970540 | GTAGTCCCAGTTACT[C/T]GGGAGGGAGTGGCAG | 55827 |
rs545750607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050273 | ACCATGGAGCATAGC[C/T]CTCACTTTTAAAGCC | 55827 |
rs545764275 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939760 | AGAGGGAAACTCTGC[A/G]TCATAAATAAATAAA | 55827 |
rs545789665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938425 | ACATTATGAAGTACC[A/G]TAGGGTACTCAACCT | 55827 |
rs545794435 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167989609 | ACTGAGGGGCCGGGC[A/G]CGGTGGCTCACGCCT | 55827 |
rs545799679 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060320 | AATAGCAGGGACTAC[-/A]AGGTGTGTGTGTACC | 55827 |
rs545829725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028014 | GTTCTCCAAATTTGG[A/G]GTTGTGTGTAAACAC | 55827 |
rs545867315 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072259 | CCGAGATCGCACCAC[A/T]GCACTCCAGCCTGGT | 55827 |
rs545891621 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055557 | CAAATCCAGGTATGG[A/T]TACATGCAAGTTACA | 55827 |
rs545903320 | in-del | -/AT | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964799 | TCCTCAAGGTCAGAG[-/AT]TGTTTCCTCAATTGT | 55827 |
rs545921806 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969965 | ATTTTTTGTAGAGTT[-/G]GGGGTTTCACCATGT | 55827 |
rs545930165 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056047 | GATTTTCTGCAAGAG[C/T]TTCATTAATTTCAGT | 55827 |
rs545944343 | in-del | -/CGACATCGCCGCCGA | | | upstream-variant-2KB, cds-indel, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935836 | TCGGGCACCGGCGGC[-/CGACATCGCCGCCGA]GGGATCGTTGGCAGC | 55827 |
rs545971657 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033434 | CATTCTCCTGCCTCA[G/T]CCTCCCGAGTAGCTG | 55827 |
rs545973042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999377 | GCTTCTGCTTAATGT[C/T]ACCACTGCATAAGCC | 55827 |
rs545978618 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996021 | TCTGTATAAGTAGAA[A/C]AAAGTAGGGAATAAT | 55827 |
rs545989673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042069 | TAAATAATATTATAT[A/G]TGTACTCTCTTTTTT | 55827 |
rs546008441 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033793 | GAGACCACTCTAAGC[C/T]GCTGATGTCATCAGT | 55827 |
rs546055090 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985744 | AAAGTTTTCCAAGTA[A/C]ATTTTTAAAAAGTAT | 55827 |
rs546093686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992558 | GCTTAATTATTGTTT[C/T]TCAACAGGTGGACAC | 55827 |
rs546108961 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168062599 | ATATTTGTTAACTGT[G/T]ATGAGATCTGTTTTT | 55827 |
rs546139612 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050779 | AAAGGGAAACAAAAG[-/T]TTTTTTTTTAAATTG | 55827 |
rs546140042 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065392 | AGCTCAGGCAGTCCT[A/C]CTGCCTTGGCCTCCC | 55827 |
rs546144432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970607 | TCCAAGTCTGGATGA[C/T]AGCAAGAGCTGATAT | 55827 |
rs546145036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013363 | AAATTAGTACCTGGC[A/G]TTATTGATTTCTGAA | 55827 |
rs546247530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971595 | ATGATTAAGAAGGAA[A/G]GAGATGCCAACTTTG | 55827 |
rs546293536 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000180 | GTGAAGCAGTCAGAA[C/T]ACACATAACATTTGT | 55827 |
rs546342887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937037 | CCGGGGCGGAGGCGC[C/T]GAGGTCGCCGCCTAG | 55827 |
rs546371820 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938473 | GTTCGCCCTTACAGC[A/G]TTTTAATGAACATCA | 55827 |
rs546408886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937946 | TAGTTAAAAAGTGTT[C/T]GTTGCTCTCATTTGT | 55827 |
rs546409456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049849 | TTTAGTAGATACGGG[A/G]TTTCACCGTGTTAGC | 55827 |
rs546413934 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008003 | TTAAAGACAGTCTCA[C/T]TCTGTCACCCAGGCT | 55827 |
rs546495898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071261 | AATGCAAAAACAGCC[A/G]TAGACCATATGTAAA | 55827 |
rs546509025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972053 | TGGAGATGGGGTTTC[A/G]CCATGTTGGGCAGGC | 55827 |
rs546531664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977575 | GTCTTGATGTGCATT[A/G]TTTTTTATTTTTTAT | 55827 |
rs546544130 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168065162 | TAATTAAGCACCTAT[A/T]GTATCCCAAGTACCA | 55827 |
rs546548807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021630 | AAGGATAAGTAAAAG[C/T]TGTTATTCAAATAAT | 55827 |
rs546549271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007312 | TCTTTTGGCCTTAAC[A/G]TGCTCTTATTATCTC | 55827 |
rs546557740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048254 | TAAAGTTCCCTCCAT[A/G]CTGCCATTTGCAAAG | 55827 |
rs546595882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979677 | AGATCACTTGAGGTT[A/G]GGAGTTCAAGACCAG | 55827 |
rs546645400 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952579 | ATACTCTCTTGGTTT[A/T]CTTCCTATTTCAATC | 55827 |
rs546671411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951605 | AAAAAACTGCGTGAG[A/G]TAGAGGTATTCTAAT | 55827 |
rs546760622 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000225 | GTCTTATATGGATGC[A/G]GTTTGTGGCTCCCCA | 55827 |
rs546802548 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019886 | GACAGTCACATGGCA[G/T]CACTTCTCAGATGGA | 55827 |
rs546887546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064927 | AAATTAAGTATGTTT[G/T]TATCTTTCTCAATTG | 55827 |
rs546888098 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011988 | AGAAAAAAGAAAGAA[A/G]GAAAGAAAGAAACAA | 55827 |
rs546891399 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167953037 | TTTACCTTCATATGT[A/G]AGCCTAAAAAGCGAT | 55827 |
rs546905868 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168042633 | AGTAGCCTGGAATAA[C/G]AGAGTCTAGAAGGGC | 55827 |
rs546943259 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054029 | AGAAACAGCAAGATA[C/T]TCTCTAGCAACCCAT | 55827 |
rs546980056 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168018634 | TTAAAAAATTAGAAT[A/G]TATCATTTAAAAATA | 55827 |
rs547008683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055723 | ACGCATATTATATTT[A/G]TCTATAATCATTAGA | 55827 |
rs547046083 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167960453 | ACAGGCACGCGCCAC[C/T]ATTCCCAGCTTATTT | 55827 |
rs547064235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985252 | GCGTGCGCGTGTGCA[C/T]GTGGCTTAAAGTAAC | 55827 |
rs547082077 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071480 | TAAATACAAAAATAC[A/G]AAAATTAGCTGGACG | 55827 |
rs547097157 | in-del | -/AA | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983979 | CTTGTTTTGTGACTT[-/AA]ACAGTGGCTGCGAAG | 55827 |
rs547111439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034149 | TAAAATAGTTACTTA[C/T]CTAAGTAATCTTATT | 55827 |
rs547121778 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168062824 | TTAAGAGAGTAAAAT[A/C]TGCTTCATTAGTTCT | 55827 |
rs547133176 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020472 | CAGTAATTGACCATG[-/A]AGACATGCTGAGCTT | 55827 |
rs547136418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991911 | AGGTGGGCCCTAATC[C/T]AGTATGACCTCACTG | 55827 |
rs547138908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026737 | AATGTTAAGTTTGAA[A/G]TGTCTTTGGATATCC | 55827 |
rs547139634 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024661 | AAACAAAAATTAGCC[A/G]GATGTGGTGGCCCGT | 55827 |
rs547143950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012894 | CATGTACTGAGATCT[C/T]GCTGTTTGCCACTTC | 55827 |
rs547188717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061701 | AGTTTTTCTGTAATA[C/T]ACATTTTTTAAAAGT | 55827 |
rs547213174 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168020766 | AATATTTGAAAATAT[C/T]TATGTAAGATAGGAG | 55827 |
rs547241816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957481 | ATTGTACACATATAC[C/T]ACATTTAATATTTCA | 55827 |
rs547264297 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054921 | TGCTGGGTTCAAGCA[A/C]TTCTCCTGCCTCAGC | 55827 |
rs547309301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998166 | AAGCAAGTCACACAG[A/G]TCTTTTGGTTTCCCA | 55827 |
rs547325546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964402 | ACATGATTTCTGAGG[A/G]GATGTTGGATGTAAT | 55827 |
rs547356242 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054672 | AAAATTTATAATTTA[A/C]ATGTAAATTTCAGCT | 55827 |
rs547357224 | in-del | -/GAA | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006277 | ATCATTTGAATTATT[-/GAA]GAAGAAAAAATATCT | 55827 |
rs547435311 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942984 | CGATCTTGGCTCACT[A/G]CAAGCTCCGCCTCCT | 55827 |
rs547489537 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976956 | TTGCCCAGGCTGAAG[G/T]GCAATGGCATGATCT | 55827 |
rs547491747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069884 | TGTTCAATAACAGCA[A/G]GTAACCCTTAAAATT | 55827 |
rs547518505 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167994512 | TAACAGTAACCTTAG[C/G]TATATTTTACAAAAT | 55827 |
rs547523528 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034573 | AAGCTTATTGTTTTC[A/T]GTTCATCATCTGTAA | 55827 |
rs547548159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955074 | TTACTTAGAATAATT[A/G]TTTTGGGATTCATGT | 55827 |
rs547577531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045684 | GGAACACTGTTTTTC[C/T]TTGATTTCTACTAAA | 55827 |
rs547608776 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949321 | GTCGTTTTGTTCTGG[A/T]CTATCTTCTCAGTGA | 55827 |
rs547614911 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046135 | ATACTGGTTTCACCA[A/C]TTACCAGCAGTGTTT | 55827 |
rs547671402 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942298 | CGAACTCCTGACCTC[A/C]GGTGATTGACCTGCT | 55827 |
rs547697131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030683 | GGAGGAATCCAGAGT[A/G]TAAGTTGCAGTAACA | 55827 |
rs547705552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975300 | AGACGTTTACCTTTA[A/G]AGATACCTCTGTTAT | 55827 |
rs547710024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039644 | CCAATTGTTTAATGA[A/C]AATATATTAATTATT | 55827 |
rs547788793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067746 | TTCTCTTCCTCTCAT[A/G]CTCTTTCTTTCATCC | 55827 |
rs547822357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017691 | AACTTTATCTTATAC[A/G]TAATAATTAAATGCA | 55827 |
rs547837805 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168073087 | AGGGCGAGACAGGAG[A/T]ATCGCTTGAACCCGG | 55827 |
rs547923843 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071328 | TAAAAACAGAGCCAG[A/G]TACAGTGGCTCACGC | 55827 |
rs547925522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943198 | ACAGGCGTGAGCCAC[C/T]GCGCCTGGCCGAAAT | 55827 |
rs547944400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971894 | AGAGTCTTGCTCTGT[C/T]GCCCAGGCTGCAGTG | 55827 |
rs547945454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037660 | AAAAAAGATTTCATA[A/C]ATTGAGATAGATGTG | 55827 |
rs547946270 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168059334 | AAGATTTATATAAAA[C/T]AGATTTGTTTCTAGG | 55827 |
rs547957208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031322 | AGGTGGATGGCGACA[C/T]AGAACAGCGTGGTGT | 55827 |
rs547964571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071420 | ACCAGCCTCGCCAAC[A/G]TGGCAAAACCCCGTC | 55827 |
rs547996035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024109 | GTAGTCCCAGCTAAT[A/T]GGGAGGCTAAGGCAG | 55827 |
rs548024757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020577 | GCTGACCAACCATAT[C/T]ACATGTTACAATAAA | 55827 |
rs548064254 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984729 | GTTGAATATACTTTT[A/T]ATATATTTTTTGCAG | 55827 |
rs548101549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983993 | TTACAGTGGCTGCGA[A/G]GTTACTGTTTTTTAC | 55827 |
rs548113535 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935375 | AGAGTGGGTTAATAT[A/G]CCACAATTCGAAAAG | 55827 |
rs548122932 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971935 | TTCTCAGCTCACTGC[A/G]ACCTCCACCTCCCGG | 55827 |
rs548138406 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061486 | TAGCCTGTGTTTTAG[A/G]TTAAGCAGTATAATG | 55827 |
rs548166371 | snp | C/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977039 | CCTGAGTAGCTGGGA[C/T]TATAGGTGCATACCA | 55827 |
rs548187881 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026825 | TGATCTGAGGTAGAA[A/T]TAAAGGTAAGGAATC | 55827 |
rs548206674 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963029 | CTTTGGGAGGCCAAG[A/G]CGGGTGGATCACCTG | 55827 |
rs548210459 | in-del | -/TCTC | 0.00341311 | 0.0411692 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991391 | AGTTCAAAGAGTAAA[-/TCTC]TATGACATTTTCAGT | 55827 |
rs548231831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937151 | GTGGGGCCTTGGTTG[C/T]CGAATTCCGTGCCGG | 55827 |
rs548251976 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168023755 | CTGAAAAGGCTGGAG[A/T]TAGGAAGACTAAAAA | 55827 |
rs548256120 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070720 | CTAGTGGCCACTTGA[A/G]ATGGAAAGGCATTTC | 55827 |
rs548262683 | snp | A/G | 1.6552e-05 | 0.00287676 | missense | DCAF6 | GRCh38.p7 | 1:168003885 | GAGAGCAGAGTCCCA[A/G]TGTGTCATTGATGCA | 55827 |
rs548293813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168062941 | TTTTGAGACAGAGTC[A/T]CGCTCTGTCACCCAG | 55827 |
rs548300508 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168067494 | AGTCTGAGAATAGTT[C/T]ACCAGGCAGACAGGG | 55827 |
rs548311932 | in-del | -/AAG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168021508 | ATGAGAAGGCATCTT[-/AAG]AAAGTAAAGCACGAA | 55827 |
rs548321362 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168066776 | CACAAAAAAATCTGT[A/C]CTTTTAAGAAAATAA | 55827 |
rs548343145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943111 | AGATGGGGTTTCACC[A/G]CGTTAGCCAGGATGG | 55827 |
rs548357867 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167936066 | ACTGCCAGCCCCCGG[A/T]CCGCCTCCGGCCCCC | 55827 |
rs548379755 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949961 | GATGCAATAAATTTT[A/T]TCTCCAAAGTCATGT | 55827 |
rs548398942 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935429 | GTGGCCCCAGACAGT[G/T]TGGTGGCCGCAGAAG | 55827 |
rs548423591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067902 | TGTTAACCCTTGCCC[A/G]AAAATTTATTTTCCA | 55827 |
rs548454053 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937397 | CAGCCGAAGAACCTA[A/G]GTTGTTGCCCACCCT | 55827 |
rs548459034 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168031419 | CAAAAAAATTATCCC[C/G]TAAGTTAGGCAATGT | 55827 |
rs548538118 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037183 | GTTCCTCCCACCACT[A/G]AGCCCCGCTGAGATT | 55827 |
rs548541483 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975841 | TATAGATGTGAGCCA[A/C]TGTACTAGCCTCCAG | 55827 |
rs548542436 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936801 | GCTGCGCCCTGGAGG[C/T]CCGGCGCGCGGATGG | 55827 |
rs548546778 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033538 | TAGCCAGGATGGTCT[C/G]GATCTTCTGACCTCA | 55827 |
rs548572835 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011901 | CTGCATGAACCCAGT[A/C]GGCAGAGGTTGCAGT | 55827 |
rs548573766 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037742 | TTAAACAAATTCCTT[G/T]CAAGATTAGTCAGGA | 55827 |
rs548659653 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053964 | CCTTACCTTTATTTA[A/C]TAATACATTGTAAGG | 55827 |
rs548661467 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940274 | GATTCACCTGGGCCA[A/G]CAGAGTGTTGTTTTA | 55827 |
rs548696416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046288 | TGGCTCATGTTAATA[A/G]CACTAATTAAATGAT | 55827 |
rs548723314 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968528 | AGGAGAGGTTTCTCA[A/T]CAGAGGTAGTATGCT | 55827 |
rs548738629 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167947916 | GTTTAAGTCCAGTGT[A/T]TCTTTGCTGATTCTT | 55827 |
rs548742321 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009370 | CTTCCTTCCTTCCTT[C/T]CTTCCTTCCTTCCTT | 55827 |
rs548783715 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972770 | GCCATTGAGATGGAG[A/G]ACACTGGAAGAGGGG | 55827 |
rs548857693 | in-del | -/TTCTC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009310 | GCCATTTTCTTTTCT[-/TTCTC]TTCTCTTCTCTTCTT | 55827 |
rs548868962 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976453 | CTCCAACCTGGGCGA[C/G]AGAGTGAGACTGTGT | 55827 |
rs548916224 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167946435 | GGTGAAAGTAGGCAT[C/T]CTTGTTTTCTTCCAG | 55827 |
rs548997717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954945 | CCCTCAACCCCAGTC[A/C]ACCAATGATCTCTAT | 55827 |
rs549002296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994991 | TTTATAAATATACTT[C/T]GAGATTTTTATCCTT | 55827 |
rs549039360 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002159 | ACTAAGGCTCAAGAT[A/G]GTTAAAAATATCTTC | 55827 |
rs549105759 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168067376 | CTGTGTCAGTCAGAG[G/T]TATACACATAGTGTT | 55827 |
rs549140632 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024381 | ATATGTCAATAGTAA[C/T]GCAGAAATTAAATAT | 55827 |
rs549216372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974181 | CATTTGTATATCTGC[A/G]TGTATACTGTCTGTT | 55827 |
rs549242984 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167950051 | TTCTAATGTGCAAAC[A/G]TCATATAGAAGAGTT | 55827 |
rs549244130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967826 | ACCTCTGCCTCCTGC[A/G]TTCAAGCGATTCTCC | 55827 |
rs549246947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987263 | TTTTATCTGAAGTTA[A/G]GTTAATGCTAATCTT | 55827 |
rs549285588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986821 | GGAGAGAAGAACTTA[C/T]TGAGGCAGGGTTTAT | 55827 |
rs549287697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993850 | TAAAGGCCAAAAAAA[A/G]AAATTAATTTTCAAG | 55827 |
rs549305720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961293 | TGTCGCCCAGGCTGG[A/G]GTGCAGTGGCGCGAT | 55827 |
rs549375184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032300 | CCTCACAGTTATCTG[C/T]AGGGTAGATAGATCT | 55827 |
rs549393313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031580 | TAACTGGAAGGAGAA[A/G]TTGTTAAAGGGAGTG | 55827 |
rs549418088 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025506 | AGCTTTGTAATAAGA[A/C]CTCTGAGCAGAAATG | 55827 |
rs549422562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940071 | ACCATAGCATGTGCC[C/T]TTTCAATGTTAATAT | 55827 |
rs549425657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975148 | GCATATAAATTATTG[A/G]CAATATCTAGGTGTC | 55827 |
rs549441217 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168011539 | CTAAATTGAGCTTTG[C/T]AGAAAAATTGCTGGA | 55827 |
rs549447400 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073655 | AAAGAAATTTGAGTA[A/G]GAAGCCTGCCAACTT | 55827 |
rs549450769 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168033594 | AGTGCTGGGATTACA[G/T]GTGTGAGCCACCGCG | 55827 |
rs549482573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066215 | GTTCTAGGATAACAT[A/T]TAGCAAATTGTCAAA | 55827 |
rs549484501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074313 | GACAGTGGGACTGAA[C/T]TGTTTTCCTTATGCT | 55827 |
rs549501397 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023976 | TCCCAGCTACTTGGG[A/C]GGCTGGGGCGGGAGG | 55827 |
rs549530195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002927 | AATGAAAACTCAGCC[C/T]AAGGGTTTTATATTA | 55827 |
rs549530699 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941755 | AATTTTTTTTTAAAC[A/G]CTGCTGATGGCTCCA | 55827 |
rs549554223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988622 | ATGAAATAAGAAAGT[A/G]CTATTCAAAATATGT | 55827 |
rs549558496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035769 | CCTGAGAGATTAAAT[A/G]AGAACTCTGTAGGCC | 55827 |
rs549567051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002287 | TAGGCTGTCAACATC[A/G]GTGGATATTTATCCT | 55827 |
rs549569296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009825 | TATTTTGTGAAAAGC[A/G]ATTATAAAAATTTAT | 55827 |
rs549610195 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030033 | ACACAGCTAGTAAGC[A/G]TTAGAAACGTGTCTC | 55827 |
rs549611500 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029210 | CTTATCATAAAAATA[A/C]CTGACATTTATTGAG | 55827 |
rs549613829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167946097 | GAGTAGCTGGGATTA[C/T]AGGCATGTGCCACCA | 55827 |
rs549627057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068888 | TGTGAGGTGCAGTGC[C/T]ACAGATACATAAAAA | 55827 |
rs549634309 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980498 | TACAATTTTTTTTTA[C/G]TGGGCATTCCAGTGG | 55827 |
rs549636527 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168063916 | GGTTCTTTTAGCCCT[A/C]TAATATATTGTGAAA | 55827 |
rs549673424 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168065931 | TGCTTTTTGCACAAA[A/G]TAAAAGAAAATAGGT | 55827 |
rs549723815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038563 | AATTTTTAACACTTC[A/G]TCATCTTTATGTTTT | 55827 |
rs549730227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942185 | ATTCTCCTGCCTCAG[A/C]CTGCCAAGTAGCTGG | 55827 |
rs549749495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982790 | GGATTCTTATAGTTC[A/G]AGGTCTTACATTTAA | 55827 |
rs549795167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989011 | CTTGATCCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 55827 |
rs549800934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975232 | ATAAGATGCAAGTAA[C/T]AGTACTCTAAGATGG | 55827 |
rs549825032 | in-del | -/TAAAG | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052363 | GAAAAGCTGAAACAC[-/TAAAG]TAGAGATTATCATGA | 55827 |
rs549835732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995774 | TTTGTAATTCTGACA[C/T]ATTTTGGTGTTTTAT | 55827 |
rs549842322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037780 | CGGAAATATACCAAA[A/T]TATAACAAAGTATAT | 55827 |
rs549856743 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939292 | TATTGGGGTATAATT[C/G]ACAATTAAAAATTGT | 55827 |
rs549869491 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167981205 | GCCACCGCTCCCGGC[A/C]TCCCCCATGTTTTCT | 55827 |
rs549886645 | in-del | -/A | 0.0612266 | 0.163904 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065513 | AATTAAAACAAATAA[-/A]AAAATGTAAGAGTAG | 55827 |
rs549888868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016771 | TTATATAAATACTAT[A/G]GTAGGTATAATAAGT | 55827 |
rs549889719 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167936135 | AATAATCACCTCACC[A/C]AGTCTGCGCTGCGCC | 55827 |
rs549889909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983802 | CTCAAGCAACTGTGA[C/T]GTTAAATCATTGCTG | 55827 |
rs549905020 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009393 | CCTTCCTTCCTTTCT[C/T]TCTTTCTTTCTCTCT | 55827 |
rs549914862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983224 | GGTAGTTTGATAGGA[A/G]TAGCATTGAATCTGT | 55827 |
rs549923673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024041 | TCAATATAGCGAGAC[C/T]CCGTCTCTTAAAAAA | 55827 |
rs549952621 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067031 | TTTCTTCTGGGATGG[G/T]AGAGGGAAGGTGGAT | 55827 |
rs549963861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052276 | TTTTTATCACAAGTA[C/T]GCAAAGCTGGTTTCT | 55827 |
rs549973343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962111 | TATTTTAAGGCCTCA[A/G]GTGTGGTCTGTCTTG | 55827 |
rs549989828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954984 | TATAAATCAGTTTGC[A/G]TTTTCTAGAATTTTA | 55827 |
rs550026827 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941741 | AAGGAGATTAAAAAA[A/T]TTTTTTTTTAAACAC | 55827 |
rs550038056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996258 | TTTTCCCTTATTTTT[A/C]TATCCTTTTTTCTTT | 55827 |
rs550050981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955569 | GAACTCTCATATTCA[C/T]TCAAGTAGCTTTTTT | 55827 |
rs550100368 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945005 | GTGTATGTTCTTGTC[A/G]GCTTTGTCAAACATC | 55827 |
rs550117035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168057814 | ATTCTTGGTTTGTGA[C/T]ACATTATCATTGTTA | 55827 |
rs550120563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167946287 | TGGGGAGTCTTTAGG[C/T]TTTTCTAGATATAAG | 55827 |
rs550153739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960501 | AGATGGGGTGGTCTC[A/G]AACCACCAGCCAGGC | 55827 |
rs550186665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959657 | TCTTTTCATATGCTC[A/G]TTTGCAATCTGTGTA | 55827 |
rs550213598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968412 | TGGCTCACTGGATGG[C/G]AGGGAAGTCTCTGTG | 55827 |
rs550244646 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168043192 | CAGCATTGGATGTTT[A/G]TCTACTTTCCTGTTC | 55827 |
rs550264941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961342 | CCGCCTCCCGGGTTC[A/G]TGCCATTCTTCTGCC | 55827 |
rs550305811 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168038593 | TGTTTTGCTATAAGG[C/T]ATTGGTTTTCAAACT | 55827 |
rs550323292 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167950602 | AGGCTCTTGATTTTG[A/T]CATGGAATGGCAAGA | 55827 |
rs550369041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036344 | TAAGAAGTCTTAACT[A/G]TAACCAAGGTGGATC | 55827 |
rs550378808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028898 | AGTTCAGTATTCCCC[A/T]CACTGGAATACATCC | 55827 |
rs550389259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029896 | GAGGTGGGAGAATGG[C/T]GTGAACCCAGGAAGC | 55827 |
rs550398191 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050624 | CTGTGACAGGATTGG[G/T]TTCTGATTTATTTAA | 55827 |
rs550402039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994041 | TAATTATAATTAGTA[A/G]TGACAAAAATAGTAT | 55827 |
rs550404650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023471 | ATGATACTTGGTTTT[A/G]TGTCTCACTTATCTG | 55827 |
rs550417213 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950453 | AGTTTAGAAACCATA[A/G]AGCATCTCCCTCCCC | 55827 |
rs550436791 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043328 | CAGTTAAAATGAGGA[G/T]ACACAGTGAAGCACA | 55827 |
rs550485566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056935 | ACAGTAAAGAATTTC[G/T]TTCTACAGATTTATT | 55827 |
rs550527362 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167946052 | AGCTCTGCCTCCCGG[A/G]TTCAAGTGATTCTCC | 55827 |
rs550565803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966169 | GATCAGTTATTGATT[C/T]TACAGTTTGTTAACT | 55827 |
rs550566222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008505 | ATTTCTTGTCTCCTA[A/G]TTAATCTGCCTGTAC | 55827 |
rs550604360 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973186 | GTTTCATGACATTGA[A/C]ATGTCAGGCTAGTTA | 55827 |
rs550605748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945721 | TGGCCAGGATGGTCT[C/T]GATCTCTTGACCTTG | 55827 |
rs550642731 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017496 | GTTCACGGATTTGAA[C/T]TGAAGCAAGCTCTTT | 55827 |
rs550663640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992830 | TCTTAAGGATATTGC[A/G]TACGTTGCATACTAA | 55827 |
rs550677893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993556 | GGAGTTTGCAACCAG[C/G]CTGACCAACATGGAG | 55827 |
rs550729717 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001092 | GATTGCTTGAGGCCA[C/G]GAGTTCAAGACCAAC | 55827 |
rs550732935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006460 | AAGACATTATCACTA[C/T]TGAGAAAAATGATTT | 55827 |
rs550769982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021535 | CACGAATAGATTAGG[A/G]AACTGATTGAAATGC | 55827 |
rs550771479 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013744 | CCACAAACTTCTCTT[G/T]ATTATTATTATTATT | 55827 |
rs550772871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014566 | TACCTAATTTCTCCA[C/T]TTGGATGTCTATTCA | 55827 |
rs550832699 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046531 | CTTTTTTTGTAGATA[A/C/T]GAAGCAAGAATTTCC | 55827 |
rs550835936 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009103 | TCCTGGGTTCACGCC[A/G]TTCTCCTGCCTCAGC | 55827 |
rs550896357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041290 | TTTTCTTATTGCGTT[A/G]TTAGAGCTATTTATT | 55827 |
rs550927076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051298 | AACAATTACCAACTT[C/T]TTGTTATTCGTATAT | 55827 |
rs550929327 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995630 | GGTTGCATGAGCCGA[C/G]ATCACGCCATTGCAC | 55827 |
rs550956118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985357 | AAGTGTGTATTCCTT[C/T]TGGTCTTGCCTTTTC | 55827 |
rs550957706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167946431 | GAGTGGTGAAAGTAG[A/G]CATCCTTGTTTTCTT | 55827 |
rs550966688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944226 | CATCCATTGATGGAC[A/G]CTTAGGTTGATTCCA | 55827 |
rs550990019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999523 | CATTGGAAATCTGTC[A/G]TTTAGGGTAGCCACT | 55827 |
rs550996898 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021298 | AAATGAGGGCATAAT[A/G]AAATGTATAACAAAT | 55827 |
rs551009480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028189 | AGGAAAAATTCTCTT[C/T]TGACATATATTTATT | 55827 |
rs551020827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167947643 | TTGTCATTCAGGAGC[A/G]TGTTGTTTAATTGTT | 55827 |
rs551038280 | snp | G/T | 0.0399052 | 0.1355 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985212 | GTGTGTGTGTGTGTG[G/T]TGTGTGTGTGTGTGG | 55827 |
rs551060802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072064 | GCACTTTGGGAGGCC[A/G]AGGCGGGTAGATCAC | 55827 |
rs551078242 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167950267 | CGTATAACTCAATGA[C/G]ATTACCAATCCTTTG | 55827 |
rs551080727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979893 | CTCTGTCTCAAAATA[A/G]ATAAACAGGCTGGGC | 55827 |
rs551157749 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971605 | AGGAAAGAGATGCCA[A/C/G]CTTTGGCCAGCTATT | 55827 |
rs551189627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957985 | ACCTATTTTTAATTG[A/G]ATTGTTTGTCTTTTT | 55827 |
rs551203183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976341 | GGGTGTGGTGGTGCA[C/T]GCCTGTAATACCAGC | 55827 |
rs551211038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951641 | AACTAAGTCTTAGGC[A/G]GAGGTTAAATTGCCC | 55827 |
rs551226835 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037147 | CTCACCCAGACTCGA[A/C/T]TCGAACTCCTGGGCT | 55827 |
rs551243121 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066144 | CTCATAAAAGAACAA[A/T]GAATAAGTGACTTCA | 55827 |
rs551250104 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048362 | TCTGTACTTTATATG[A/T]AGAACTATATAGTGG | 55827 |
rs551265611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015770 | CACCTTTCTTTTCCT[A/G]TTTGTGTCAGAATTT | 55827 |
rs551292820 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998929 | GTTATTTTGACCTCC[C/T]ACGAATCACAAAAGT | 55827 |
rs551316340 | in-del | -/AAT | 0.00557542 | 0.0525036 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988056 | TCTTTTTTAAAAAGA[-/AAT]AATAAGATAGCATGC | 55827 |
rs551338908 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017874 | TTCATACTTTGGTAT[C/G]TTTAGAGTATCAATT | 55827 |
rs551350382 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029130 | TTTTTTTGTTGCATA[A/T]GCTCGTGTGTTCTAC | 55827 |
rs551358246 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009317 | TCTTTTCTTTCTCTT[C/G]TCTTCTCTTCTTCTT | 55827 |
rs551400311 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001285 | GAAGAGTGTGAGACC[C/G]TGCCTGGAAAAAAAA | 55827 |
rs551413731 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022373 | TCCTTTCCCTACCAG[G/T]TAACGCTAAAGAAAC | 55827 |
rs551425419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008613 | AACTTTGCTGTTTAA[A/G]TCCCTTCAGAAGTTC | 55827 |
rs551437630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986665 | CCATAGTGTCTATGC[C/T]CCTGTGAGAATCTAA | 55827 |
rs551448626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049356 | CAAGCGATCTTCCTC[C/T]CTCAGTCTCCCAAGT | 55827 |
rs551464934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939185 | ACTACAGTGCTAATC[C/T]TGGCTTTGCATTCAG | 55827 |
rs551551604 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992557 | GGCTTAATTATTGTT[G/T]CTCAACAGGTGGACA | 55827 |
rs551559503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007204 | AGAAAGCTCCTATCA[A/G]AAGCTAGTCAATGTA | 55827 |
rs551568106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015415 | CTTAAATTTTTGTGT[A/G]TAAATCAGATGAGTT | 55827 |
rs551600367 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966227 | AACTGCTAAGCTTCT[A/T]ACGTGTGGAACTGGA | 55827 |
rs551608029 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168014612 | CTACTTGTTTCTCCA[C/T]TGTTCCCTGCCGTAA | 55827 |
rs551617566 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037682 | ATAGATGTGTATTAT[A/G]GACATCATCTATAGG | 55827 |
rs551681949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058865 | ATGAGCCACTGCACC[C/T]GGTCCTGATCTGGTT | 55827 |
rs551683609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000396 | GCACCAATAGTCTTA[C/T]TCAATGCAGGGTTGC | 55827 |
rs551722284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958735 | TGAATTTTTTTAGAG[C/T]AGTTTTAGGTTCATA | 55827 |
rs551756542 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951345 | TTTGGGAGGCCAATG[C/T]GGGTGGATCAGTTGA | 55827 |
rs551824190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042895 | TGTTTACAAATGCTA[C/T]TAAAATTATAAATCC | 55827 |
rs551829926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981091 | TTTTGTATTTTAGTA[C/G]AGATGGGGTTTCACC | 55827 |
rs551892099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006596 | TGTTTTTGTTTTTTG[C/T]CCAATCTCTTTTGCA | 55827 |
rs551919483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980442 | ACATGCCTACCAGCT[G/T]TGTGCAAGGGTGCCA | 55827 |
rs551927328 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982750 | AGTCCAATGTCTAGA[A/C]TGGCGTTTCCTATAT | 55827 |
rs551959474 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049679 | TTTTTTTTTGGAGAC[A/G]GAGTCTCGCTCCCTC | 55827 |
rs551960483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965689 | CTGGGTGCAGTGACA[C/T]GATCTTGGCTCACTG | 55827 |
rs551968609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049204 | AGCAAAAAAATAGTA[C/T]GTGTATCTTTTAGTG | 55827 |
rs551977186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064662 | TTGCCTAAAAGTTAG[C/T]ATGAAAATAATTAGA | 55827 |
rs552020903 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064030 | GTTTTTTTTTTTTTT[C/T]CCCCCTCTCTTTCTC | 55827 |
rs552024161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014488 | TCATCCCTTACTCTT[C/T]AGGGGACTTAAAATG | 55827 |
rs552074808 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978682 | GTGGGGGAGGGTGCG[C/G]TTTGTGTGTTTTGAG | 55827 |
rs552090260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035220 | AGAGGCCAAGGCAGA[C/T]GGATTGCTTGAGCCC | 55827 |
rs552101128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049783 | GCCTCAGCCTCCCAA[A/G]TAGCTGGGACTACAG | 55827 |
rs552114337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054695 | TTTCAGCTTCACCCT[A/G]TCTGAATAATCACAG | 55827 |
rs552165940 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020670 | CAGAGAGGTAGAGTA[C/G]AATATGCCAGTAACT | 55827 |
rs552169062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070847 | GCCCTGCTTAAAATT[C/T]TCCTTTGCCCACACA | 55827 |
rs552201653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985242 | GTGTGTGTGTGCGTG[C/T]GCGTGTGCACGTGGC | 55827 |
rs552208317 | in-del | -/TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT | 0.49931 | 0.0185575 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967714 | TAAATTTCCTGTATC[lengthTooLong]TTTTTTTTTTTTTTT | 55827 |
rs552232408 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937903 | AACAACATCATAAAA[A/T]TTTTTTCTTTCCAGT | 55827 |
rs552250362 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058412 | CAATATTTTTTAAAA[A/C]TCGTGTTTATTCACA | 55827 |
rs552260380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965210 | ACAGGCCTATGATTA[A/G]GTGTCTGTCACTTAA | 55827 |
rs552290772 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055819 | CTAAAAGTTTCTATT[C/G]TAAGTCTTCTATCCA | 55827 |
rs552295677 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012773 | ATACAAGCAGCTTTC[A/C]AAGCAGATAAATTCT | 55827 |
rs552311195 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054297 | GCTGGCAAGGACTCT[G/T]CAGAGTCCCGAGCTG | 55827 |
rs552329462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048548 | TGGTTAAATAAATGA[C/T]CCAGGTTTTCACTTT | 55827 |
rs552329569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056272 | TCTCTGTGAATTTAC[A/G]CACCGAGAGCAGAGC | 55827 |
rs552374516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033580 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 55827 |
rs552389691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168039878 | ATTAAAATATTTGAT[C/T]AAGTAGGATCTTAAA | 55827 |
rs552411445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034109 | TTCTGAGGAGTAACA[A/T]CATCAACAATTGATA | 55827 |
rs552451437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027466 | TTTAATAAGTTTCCT[A/G]TTTGAATATATCTCT | 55827 |
rs552460939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071452 | CTATAAAAATAAAAA[A/G]TAAAAAAAATTATAA | 55827 |
rs552498619 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936650 | CTCCTCCTGTTGGAG[C/G]GGGGCTGAGGGAGGA | 55827 |
rs552520826 | in-del | -/TTC | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950243 | ATTTGAATACTTTGT[-/TTC]TTAACTCGTATAACT | 55827 |
rs552539088 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168010480 | AAATCAGTTGATGGA[-/T]TTTTTTTTTTGCTTT | 55827 |
rs552543807 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969402 | AAGCTGGGATAACAT[A/T]TGAGTTCTAATTAGG | 55827 |
rs552573233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005488 | TCAGCAGATGTATCT[A/G]CAGTTTACTCGGTAC | 55827 |
rs552580317 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168020967 | GAACAGCAAATGCCT[C/T]AGAAATACACAATGT | 55827 |
rs552606905 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963162 | CCAGCTACTCGGGAG[A/G]CTGAGGCGGGAGAAT | 55827 |
rs552618914 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167990996 | TTATTTTGATTTCAC[A/G]TAGGCTGAATGTATT | 55827 |
rs552628179 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991107 | AATTAGGAGTTCTGA[A/G]AATGGTTATTCTAAT | 55827 |
rs552635597 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962265 | TTCTGCCTGCTAGGT[C/T]TGTCTGTTTCTGATA | 55827 |
rs552644920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992928 | TTGGAAGATGACTTC[A/G]TGTGATTGTATTTAT | 55827 |
rs552645136 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985644 | GTATAAGGTAAAGTA[A/T]TCGTAGGTTCTAACA | 55827 |
rs552663712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167999107 | ATCTATGGGATACAA[C/T]GAAAATGTTAATCTC | 55827 |
rs552676905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040586 | TTAAAAATTGTGATG[C/T]TTGTGGCCCTTTTTC | 55827 |
rs552681901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992410 | GAATACCAGATGAGA[C/T]CTTTCTTTTCGGAAC | 55827 |
rs552682290 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168047576 | CTTCCTGAAGAGTAA[C/T]AGAAGAACGATAAAA | 55827 |
rs552778427 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167955685 | ATTCCTTTTATTTCG[-/T]TTTCTTGACTTATTT | 55827 |
rs552800380 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963782 | TTTTCTCCTTCCTTA[G/T]TATTTATTAGTTACA | 55827 |
rs552836899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969996 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGAGCTCA | 55827 |
rs552839485 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966555 | TAAAAATTTTGTACC[A/G]CCAGGTGAGTGAAAG | 55827 |
rs552842085 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976925 | TTTTTTTTTTTGAGA[C/T]GGAGTTTCGCTCTTG | 55827 |
rs552947267 | snp | A/G | 4.21381e-05 | 0.00458991 | synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936992 | GGACCCGTCCCGGCT[A/G]CGGAGTCGATACCTG | 55827 |
rs552983531 | snp | G/T | | | missense | DCAF6 | GRCh38.p7 | 1:168044983 | GATCGCTCTTGTGGG[G/T]TTCCAGAAGAATCTG | 55827 |
rs552986390 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943190 | CTGGGATTACAGGCG[G/T]GAGCCACCGCGCCTG | 55827 |
rs553009179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055961 | CATAAGTTCATCTAG[C/T]TCTGAAGGGTTACTC | 55827 |
rs553010665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937493 | GCTCCAGACAGAATC[C/T]GTGTAAACTGTTTTT | 55827 |
rs553021221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070198 | AAAAAGACAATTTCT[A/G]GTTGGTTTAGTCAGC | 55827 |
rs553031149 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970388 | CAAGTGTGTGGCTCA[C/G]GCTTATAATCCCAGC | 55827 |
rs553055333 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027103 | AAGTCTGATAAATCA[-/T]TTTTTTAAATTTGGC | 55827 |
rs553063310 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034493 | TACCGTGGGTGATAG[A/G]GCAAGACCCTGTCTA | 55827 |
rs553095780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041749 | AATATTTTAATTACT[A/G]TAATGTATACACTAA | 55827 |
rs553104748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045934 | AAGTTCTGTCCTCTT[C/T]CAGAGAACCTAGTTT | 55827 |
rs553130206 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979446 | TGACTATTTTAGATA[-/C]CTCATATAATTGTAA | 55827 |
rs553134491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042409 | ATTGGCCTCGTATTC[C/T]GCTATAGCTAGAAAT | 55827 |
rs553141233 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000029 | TGATTTAAAGTGAAA[A/G]GCATATGACTCTTCC | 55827 |
rs553142598 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167952319 | GCCTCCCGGGTTCAC[A/G]TCATTCTCCTGCCTC | 55827 |
rs553152154 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026990 | TGATGAGAGAAGTAC[A/G]CAGGGCAGAAAGAAT | 55827 |
rs553179828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063097 | TTTGTATTTTTAGTA[C/G]AGATGGGGTTTCATT | 55827 |
rs553185809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013187 | GCAGTATGCCACTGA[A/G]CATCACCATTTGTTT | 55827 |
rs553216539 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055202 | ATAGCTACTATGAAA[A/G]TAGAGATATAGAAAT | 55827 |
rs553224612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020061 | CGCTCCAGATGTTTC[A/G]GAACAGCTTTGTACC | 55827 |
rs553280497 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040061 | TATGTTAGAAGGACA[A/G]TGGAGGAAAATAGAG | 55827 |
rs553288397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984100 | TTCTGAGATCCAGTT[A/G]TTTGTCTTGAATAAA | 55827 |
rs553327214 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026457 | AAACACCAAGAACAC[G/T]TAAGAGGCCATTGCT | 55827 |
rs553328352 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167957294 | CAGTTAGCAATCACT[A/G]ATACTTTCTGTCTCT | 55827 |
rs553337615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018786 | CTTAGCAATTTTTTT[C/T]AACCAAAAAGAAATG | 55827 |
rs553353133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013870 | CCTACCTCAGCCTCC[C/T]GAGGGGCCACAAGTG | 55827 |
rs553365212 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950125 | CACCATTTTCTCCAG[A/C]CTGAAGTGGCTAGAG | 55827 |
rs553369627 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034329 | AGACCAGCCTGGACA[A/G]CATAGTGAGACTCCA | 55827 |
rs553369865 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052686 | CATTAGGGACTGTCT[C/T]ACAATGGGGAATGTG | 55827 |
rs553374742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025613 | TTTTAAAGTACTAGG[A/G]ACTTCACATTGCAGG | 55827 |
rs553447053 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976573 | AAGATAGACATTCAT[G/T]TTTGTTATTCTGGAG | 55827 |
rs553517917 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989037 | GTGAGCCGAGATCAC[A/G]CCACTGCACTCCAGC | 55827 |
rs553528994 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935660 | GAGGCAGTTGTCAGA[A/G]GGCCTCTAAAAGGTC | 55827 |
rs553530408 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168043309 | AAAAGATGGGGACCT[G/T]AAGCAGTTAAAATGA | 55827 |
rs553545812 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001965 | AATGAGGGCAGCAGG[A/G]TGGAATAGATAGCCT | 55827 |
rs553576563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955970 | CTCATTATGTTGCCC[A/G]TCTGGTCTTGAACTC | 55827 |
rs553606612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962487 | TTCTTGCTTTGAACT[C/G]TGGTCTGTCTGAAAT | 55827 |
rs553631084 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954396 | ATTATATAATAACTT[C/T]AATTACTTTTGTGAA | 55827 |
rs553670202 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056736 | TAAGCTTTGTTTGGT[A/G]TATCATTTTCCACAC | 55827 |
rs553699190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990248 | TGGTGTGCACCTGTA[A/G]TCCTAGCCACTTGAG | 55827 |
rs553700129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984109 | CCAGTTATTTGTCTT[G/T]AATAAATGTTTCTTG | 55827 |
rs553720807 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002329 | CTTTAAAAGACTGAC[A/G]CTTATACCAGTGTCT | 55827 |
rs553736155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989728 | TCTCTACTAAAAATA[C/T]AAAATAGCCAGGCGT | 55827 |
rs553759208 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001704 | AGCCAAGAGAGAGAA[A/C]ATGGATGTAGGTATA | 55827 |
rs553760439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968807 | TCATGCCAACTGGCA[A/G]AGGAAAAATATTTGA | 55827 |
rs553807138 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061233 | CTAACTTAAAAATGT[A/T]TGTGGAGATTCCTTT | 55827 |
rs553848049 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053476 | CCCCACACAGTTGAT[G/T]GCTTGCTACAAAGAC | 55827 |
rs553866900 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992061 | AACAGTGACTTGGGT[A/G]TGTATTAATGTGTAG | 55827 |
rs553880700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011411 | GTGAGCCACTGCGCC[C/T]GACCCAGAATTTTTT | 55827 |
rs553896542 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038014 | TTCTTATTGATGCTC[A/C]AGCAACTGAGGAATT | 55827 |
rs553906113 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974685 | ATTCTGATTTTTTTA[A/C]ATTATAATAGCTTGC | 55827 |
rs553929281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031697 | ATGATAGGCAGACTT[C/G]ATTTTTTTTTTTTCC | 55827 |
rs553940049 | in-del | -/TC | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028159 | TAGTTTTCCTTTTTA[-/TC]TCTCTACTATAAGAG | 55827 |
rs553949972 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168026342 | AGCAATTATTTAAGA[G/T]CTGTAGGGATTACTT | 55827 |
rs553959085 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168021668 | TTTTGTCAAAATCTA[A/G]TAAGAGAAAAATACA | 55827 |
rs554003030 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037315 | TATTTGCTTTTATGA[A/C]ATTGTGATTGTCTTT | 55827 |
rs554040638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948812 | GCCCATCACCACACC[C/T]GGCTAATTTTTGTAT | 55827 |
rs554046456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941327 | AGACACTATGATAGC[C/T]CTACTGTGGGTTTCA | 55827 |
rs554065404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967107 | AAGTTACTTATTTTA[A/G]TGTTAAGAATAGTGT | 55827 |
rs554065953 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982895 | GGTTGGCCAGTGATC[C/T]CAGCACCATTTATTT | 55827 |
rs554072576 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168076010 | CATTTCTCCTTCCAC[A/G]GTACAGCTGACCCTT | 55827 |
rs554101493 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976256 | GGCGGATCACTTGAG[C/G]CCAGGAATTTGAGAC | 55827 |
rs554109903 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066537 | TCCCTAAGAAAAATT[A/T]AAAGTTATTAGTTGC | 55827 |
rs554150930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960849 | GCATCTCTTATAAAC[C/T]TTAGAATCAGTTTGT | 55827 |
rs554155615 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030484 | GGAGTATGGCTATGG[C/G]CTGATACTCTGAATG | 55827 |
rs554159495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168011662 | GTCTAGTCAGATAGA[C/T]ATAGGCCATTTATAG | 55827 |
rs554162581 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044002 | CAGGTAATTTCAGCT[C/G]TAAGGGATAGTCTAA | 55827 |
rs554182692 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961508 | TGCCTCCCAAAATGC[G/T]GGGATTACAGGCGTG | 55827 |
rs554218578 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052710 | GAATGTGTTCTACTA[C/T]AATCTGCTAAGATTC | 55827 |
rs554283051 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948203 | GATTCACTCTTCACT[A/T]TGACTTCAGACAGTC | 55827 |
rs554284448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004991 | TAACAAATAGCAGGA[A/G]TCTTCAATTTATATA | 55827 |
rs554285793 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019485 | AATGTCCTAAACAGG[C/T]ATGGCAGAGGCATTC | 55827 |
rs554304574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983431 | GTTCTTGGTTAGCTT[A/G]GTTGTCAGCTAAGGG | 55827 |
rs554308177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970199 | TTGGGTACCAAAGGA[A/G]TGATTGTTAAAAGAC | 55827 |
rs554310187 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961966 | TTCTTCTTTGACCGA[C/T]GTGTTATTTTGAACT | 55827 |
rs554318400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053559 | AAAAAGATCAGACAC[A/G]GTGGAAGAATCCAGG | 55827 |
rs554418790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976344 | TGTGGTGGTGCACGC[C/T]TGTAATACCAGCTAC | 55827 |
rs554461510 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168076198 | TATTCTATACTCTTA[C/G]AATAAAGTAAGCTAC | 55827 |
rs554524263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051092 | GTCGCTTTCCACAAA[C/T]TATATTTAGCTGCAT | 55827 |
rs554617837 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986293 | TAGTTTTCCATTGCA[A/G]TTGTACCATTTTATA | 55827 |
rs554636214 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054178 | TCATTTCCTGTTGCT[C/T]ATGATAGAAATCTTC | 55827 |
rs554641666 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989560 | GAGATTAGTAATTGA[A/G]CAAAGTATAAGGTTA | 55827 |
rs554644956 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951300 | TAACTACAGGCCGGG[C/T]GTGGTGGCTCACACC | 55827 |
rs554649449 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061966 | TACACAAATGTGGAT[A/G]GTAGCCTAATATTAG | 55827 |
rs554668092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956832 | CCATCTGTTATTTCT[A/G]TGGCCATCTGTTATT | 55827 |
rs554680751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989120 | ACCTTTAAACATACA[C/G]TTTAATCAGTTTTTT | 55827 |
rs554704877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956058 | GGTATGAGCCGCTGT[C/G]CTTAGCTAAGAACAT | 55827 |
rs554732946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031781 | GATTTTGGCAGGACT[C/T]ATGTGCCACATGGCG | 55827 |
rs554735315 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168069574 | GTATTCCACAGAAAG[C/T]AGACAGCGTATAGCG | 55827 |
rs554735628 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168023102 | AGCTTTATTGCAATG[A/C]ATATACTAAGCTCTC | 55827 |
rs554742426 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025708 | TAGATTAATGGAATA[A/T]TCCCTTTACTAGTCT | 55827 |
rs554784902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968128 | ATGGTAGTAGCAACC[A/G]TGTATTGGTGATTGT | 55827 |
rs554796551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051626 | TGAACATGAAACATA[C/T]AGCAACAATCAGAAA | 55827 |
rs554803779 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986777 | CTTCCTAACAGGCTA[C/T]GGACCAGTACTGGGT | 55827 |
rs554828162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060246 | AATACATGGCATGAT[C/T]TTAGCTCACTGCATC | 55827 |
rs554833773 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168055101 | GAATTTAATTTATTC[C/T]TTTAATATCTTTTTT | 55827 |
rs554861802 | in-del | -/TTTTTTTTTTTTT | 0.368733 | 0.220005 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055332 | AAAATCAGGCTTAAG[-/TTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 55827 |
rs554863243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976618 | TTTCACAAGAATATC[A/G]AACAAAGCCAAATAT | 55827 |
rs554872540 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069226 | ATTAAAGCCAGAATT[C/T]GAAATTAGCTTCCAA | 55827 |
rs554895537 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167950976 | AAATAGTTGGTACTT[-/A]ACTATTGCTGTTTGC | 55827 |
rs554910196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070083 | CTAATGTAGCAATGG[C/T]TGGTTAGTTAATAGC | 55827 |
rs554921534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995911 | CCAGACAAAGACATG[A/G]TCTCTTACTTAAGGA | 55827 |
rs554976311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073988 | ATATTTATAAAATAA[A/G]TGAACAAAATAAGAT | 55827 |
rs554978612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955227 | ATTACAAATAAAGTT[G/T]CCATGAATATTCGTG | 55827 |
rs555013594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066624 | TAAGATAAAAGGATG[C/T]CTATAATACTAGGGA | 55827 |
rs555055400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067162 | GCTAAAAATGTTAGT[A/G]AGTTGGAAAACCACT | 55827 |
rs555082412 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069527 | AGTGAATTAAATATC[A/G]CTTCCTCAGAGAGAG | 55827 |
rs555097489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038216 | AAAAGAGTATTTCCA[C/T]AACACATGCCTTCAA | 55827 |
rs555185663 | snp | C/T | 0.341685 | 0.232581 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009484 | CCTCCCTCCCTCCCT[C/T]CCTTCACTTCTTCCC | 55827 |
rs555222406 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017069 | GGGATAAATCATAAA[C/G]TTTATTTTTAATTCA | 55827 |
rs555272151 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057171 | TAATTTGTGCCATTC[C/T]ACCTATGTGTAATGG | 55827 |
rs555284603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000756 | CACGAAAGGCCATGT[A/G]TTGTATGATTATTTA | 55827 |
rs555323523 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015443 | GTTAACTGATTGTTT[A/T]CAATTTCTGTTTCTT | 55827 |
rs555336370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030721 | AATTTTCTTATGTAG[A/G]TAGTTTAGTAATAAA | 55827 |
rs555347285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010314 | TGTATATATGGGTGA[A/G]TATGGGTATGAAAAT | 55827 |
rs555362471 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022538 | TGTTAGCTCCTTGTT[C/G]AGCCCACAGTACAGC | 55827 |
rs555380314 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968099 | CAAAAATGTACTCCA[A/G]CTTTTAATTTTTTAT | 55827 |
rs555397892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024368 | TATTAGATGACTCAT[A/G]TGTCAATAGTAATGC | 55827 |
rs555417902 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941584 | TTTTTTTTCATATTG[G/T]TACAACTGTTGGTGT | 55827 |
rs555420025 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975358 | CCCTTTTAAACAATC[A/G]CTTGCTTGTGTAAAG | 55827 |
rs555457269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016399 | TTTAGAATTATAGTA[C/T]TATTTGGCCATACTA | 55827 |
rs555513439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001378 | ATAAGCTCTGAAAGA[C/T]GCTGTTTGAGTTGGC | 55827 |
rs555531733 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974164 | TTACTATTTTTAAGG[A/G]CCATTTGTATATCTG | 55827 |
rs555541734 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974316 | ACAAATATTAAAATA[C/T]CAATTTTAAACTTTA | 55827 |
rs555562401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168057341 | GACTGTTTCTGCTTC[A/G]TGTAACTTCATACTT | 55827 |
rs555596615 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021667 | GTTTTGTCAAAATCT[A/T]GTAAGAGAAAAATAC | 55827 |
rs555625642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008265 | TGAGCCACTGCACCC[A/G]GCCTATTGTTGTACG | 55827 |
rs555648196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035293 | TCTACAAAAGTTACT[A/G]CAAATTAGCCAGGTG | 55827 |
rs555666532 | in-del | -/CA | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939373 | ACATATCCATCATGT[-/CA]CATAATTACCATCTT | 55827 |
rs555676681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028407 | ATGATTGAAACAAGT[C/T]GCTTTCTATTCCTTA | 55827 |
rs555697780 | snp | A/G | 6.61113e-05 | 0.00574903 | missense | DCAF6 | GRCh38.p7 | 1:167987571 | GGTGGTTTGATACAC[A/G]CATCAAAACTAGCTG | 55827 |
rs555710768 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168039941 | TATTCTAGACATTGG[A/C]AATACATCAGTGAAA | 55827 |
rs555734261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986996 | ATTTCGTTGACATTA[A/G]GTATATTCATGTTGT | 55827 |
rs555736302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994333 | CACTTGCAGAAAAGG[C/T]GATTAAAATAATAGA | 55827 |
rs555756373 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935107 | CTATAAGTGGTAGAA[A/G]AGAATGATATCCAGG | 55827 |
rs555773968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973476 | GACTTCTGTTTGAAT[C/T]GGTTGTTGTAATGTC | 55827 |
rs555783912 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019269 | CAGCCAGGATGGTCT[C/T]GATCTCCTGACCTTG | 55827 |
rs555838656 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965882 | TCAGGTGATCCACCC[A/G]CTTTGGCCTCCCAAA | 55827 |
rs555845018 | snp | G/T | 0.000198985 | 0.00997261 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065586 | AATTTTTTTTAACCC[G/T]TAGATAAAAGAAGCC | 55827 |
rs555856615 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060350 | CACCATGCCCAGCTA[A/T]TTTTTTTCATCTTTT | 55827 |
rs555861272 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007589 | TTACTAGATTTTTCG[A/G]CCCGGTTGCATTTAA | 55827 |
rs555888523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979415 | ACCATCATTCTACTT[C/T]CTGTTTCTAAGAATT | 55827 |
rs555901500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036636 | TGGACAAATGACTAG[C/T]AAACAGCAAGTTTTT | 55827 |
rs555913018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024448 | AACTATATTCTTAGA[A/G]AAATATTCAGAAACT | 55827 |
rs555919304 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035490 | GAGTTGAAGAAACCA[-/G]GTTCTTCATTGTGTT | 55827 |
rs555927208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067226 | TTCCCATGTATACTT[C/T]CACTCATTGAATAGG | 55827 |
rs555958382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027889 | TCATTAATGCAGCTC[C/T]CTGGTTGTCTCAATA | 55827 |
rs555970084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961601 | TTATCTACAAAGACC[A/G]TTTTATTTCTTTTCC | 55827 |
rs555978654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071752 | CAGGGACTCCCTATT[G/T]CTCTTAAAGTAAAAC | 55827 |
rs556031019 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938277 | GTGTGTGTGTTTGTG[G/T]GTGTATGAGAGAGAC | 55827 |
rs556032616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945036 | AGTTGGCTGCAAGTA[C/T]GCGGCTTTATTTCTG | 55827 |
rs556040508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030234 | TTGAGGGCCAAATAA[A/G]GCATCCCTGAGGAAG | 55827 |
rs556047990 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024777 | CCATTGCACTCCAGC[C/T]TGGGCAGCAGAGTGA | 55827 |
rs556076240 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940588 | AATAGTTTCTCAAAT[G/T]ACTGTATACTAGGTG | 55827 |
rs556113641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000887 | TTGTTTCTGGGATGA[C/T]GAAAACGGTCTGGAA | 55827 |
rs556114976 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167946659 | TTCATTCTGTTGATA[G/T]GATGTATCACATTTA | 55827 |
rs556133870 | in-del | -/TAAGA | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040615 | TCTTAATACATAATT[-/TAAGA]TGACAGTAGGTCATC | 55827 |
rs556151606 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940876 | TGTGTAAATTATGAT[G/T]AGGCAGCCAGTGACA | 55827 |
rs556167212 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168075944 | TTCTAGATTTAACAA[C/T]CTTTTCCTTTTTTGC | 55827 |
rs556188504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074784 | GGCAAAAGTATCCCA[A/G]GCAGAGGAATAGCAA | 55827 |
rs556202068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068017 | AAAGTTATCAGTTCT[C/T]CTATAGGGAAAACAA | 55827 |
rs556211969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968685 | TGCTGGAAGACCCTG[A/G]CACTGGAAAACCTGT | 55827 |
rs556245094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009604 | CTTTTCTTTTCTTTC[C/T]CTCTTTCCTTCTTAC | 55827 |
rs556277100 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001639 | TATGAAGTTGAAATA[A/T]TGTTTTTTTTCTTAA | 55827 |
rs556289317 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980641 | TCCTTTGCTTTTTTT[A/T]AATCTGCATTATTTT | 55827 |
rs556315116 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948057 | TACTCCAGTGTCGGG[G/T]GCAAATATGTATTTA | 55827 |
rs556318405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976114 | TTTGTTTCTATCCCT[G/T]TGTTTTCTACTTTTT | 55827 |
rs556318456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938112 | GTTTATAAAAACTCA[A/G]TAAAAATGAAGCAAA | 55827 |
rs556350209 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935511 | GGAGCGGATGTCACA[C/T]AGGTGGGGAAGGGAG | 55827 |
rs556368076 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995178 | ATAGTCAAACTGTGA[-/T]TGTTACATAATGAAA | 55827 |
rs556376425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941235 | GAAAAATGACGGTCA[A/G]TTGTGACAAACGTAA | 55827 |
rs556407211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043933 | CATGATAGAGGGGCA[A/G]AAAAATGCTCAGTTT | 55827 |
rs556440878 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167965029 | TCCAACAGTCCTGCT[A/G]TGTTTGGTTCTGATG | 55827 |
rs556485732 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982156 | ATTTTGTGTTCGTTG[C/G]CTCCTTGTATGCCTT | 55827 |
rs556521108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073033 | ACAAAAAAATCAGCC[A/G]GGTGTGGTGGCACGC | 55827 |
rs556524395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981301 | ATATGTAGGGTAAGG[A/G]TCTAAGTTCATTCTT | 55827 |
rs556539542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016124 | TGTTAGGGGGACAGA[C/T]TGGCAGCAGCATCTG | 55827 |
rs556602839 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973608 | TTTTAATTCAGTGTT[G/T]TATAGTCAATCACTG | 55827 |
rs556627625 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168003204 | TGATTTCACAGAAAA[C/T]GTAAGAAGAACCGAT | 55827 |
rs556642457 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058329 | GTATATACCAAGGAA[A/T]GGACCATTTACAAAA | 55827 |
rs556649114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993112 | AAATAAACGTGATGG[C/T]TTTTATTTGTATTGC | 55827 |
rs556658964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954054 | CTCCGTCTTCCAGGC[C/T]GGAGTGGAGTGGCAC | 55827 |
rs556675669 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945315 | GGCTGCTTTGTACAG[A/T]ATGGTCATTTTAATG | 55827 |
rs556684094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999969 | TTTTGGCCTGTCTTG[A/G]CTTTCAACATGCTTT | 55827 |
rs556736978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938852 | CCCCCTCCTACTCCA[A/G]CTCCCTAATGGAAAT | 55827 |
rs556786336 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056001 | TTGATCAGCCAACCA[C/T]CTTCATAACAAGATT | 55827 |
rs556789640 | in-del | -/TAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168069065 | GTATTAGCTATCATT[-/TAA]TAATAATAATAGGTA | 55827 |
rs556800700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958936 | ACTCTTGGTTTCAGG[C/T]ATCTTATGAGTTTGG | 55827 |
rs556823571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056332 | CCACCCCCAGCTGCC[A/G]GGGCCTCGGCGGGCA | 55827 |
rs556824290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029316 | TAATTTTACTAATGA[A/G]GAAACTGAGACTCCA | 55827 |
rs556828369 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071610 | CTACACTCCAGCCTG[A/G]GTGACAGATTGAGAC | 55827 |
rs556860349 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948500 | ACCATCTCTATAAGT[A/G]ATAATTCTCAACTAG | 55827 |
rs556919764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992481 | TCTAATAATAATTGA[A/G]GAGTCCAGTCTATTT | 55827 |
rs556950353 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937594 | TCTGCTCTTCAGTTC[C/G]TTTTGACCGCTTAAA | 55827 |
rs556973557 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167955220 | GAGGACTATTACAAA[C/T]AAAGTTGCCATGAAT | 55827 |
rs557058867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028500 | GTTGTGCATCTGCAG[A/G]CACTAATTTTCTGTT | 55827 |
rs557091503 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035327 | TGGCATGTGCCTATA[C/G]TCCCAGCTACTCAGG | 55827 |
rs557093155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040116 | AGGCATCATTGAGAA[A/G]GTGACATTTGGGCAA | 55827 |
rs557151370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972076 | GGGCAGGCTGGTCTC[A/G]AACTCCTGACTTCAG | 55827 |
rs557173374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006803 | ATGTAAATGTTTATC[C/G]CTTTACATGTCCTCC | 55827 |
rs557183345 | snp | A/T | 0.00303725 | 0.038851 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937031 | GGGGCCCCGGGGCGG[A/T]GGCGCTGAGGTCGCC | 55827 |
rs557199534 | in-del | -/TA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168010262 | AAAAAATTGTCTCAT[-/TA]TATATATATATATAT | 55827 |
rs557204223 | snp | A/C | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935222 | GGGATGAGAAATGAC[A/C]CTGACTCAAGCCTGG | 55827 |
rs557231051 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168047490 | ATTATTTAATATTCT[A/G]TACACTCATTTGAGT | 55827 |
rs557240102 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168012875 | AAGTTTTAGAGCATC[A/T]CTACATGTACTGAGA | 55827 |
rs557245744 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041787 | ATTCATGCCTGAATC[A/G]TAGCTTTCTCAATGG | 55827 |
rs557267207 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961278 | AACAGAGTCTTGCTC[C/T]GTCGCCCAGGCTGGA | 55827 |
rs557281135 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009394 | CTTCCTTCCTTTCTT[C/T]CTTTCTTTCTCTCTC | 55827 |
rs557315047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020139 | ATAAACATTAAATGA[C/T]CCATTCCTATGTGCT | 55827 |
rs557317558 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982836 | TGAGTTAATTTTTAT[A/G]TATGGTGAAATGTAG | 55827 |
rs557328277 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071814 | ACATGACATACATTC[G/T]GCCAACCTCTGACTT | 55827 |
rs557334695 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007519 | TCCTCTGAAACTTTT[A/G]ATCAAAGTCACTAGT | 55827 |
rs557353515 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978316 | TCCAAAGTGTAGTAA[A/C]GACTTACATTCCCAC | 55827 |
rs557353725 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027094 | AACTCCCAGAAAGTC[A/T]GATAAATCATTTTTT | 55827 |
rs557366956 | snp | A/C | | | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075459 | TTTTGGCAAGCACTT[A/C]AATGTTCTGAAATTT | 55827 |
rs557404859 | snp | A/C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991420 | TCAGTTTTAAAATTT[A/C/T]TTGTTTGTTATAAAA | 55827 |
rs557431075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073911 | TTAAATTCCTTACTG[A/G]TCTATAAAGGTCTAT | 55827 |
rs557437610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986966 | TTGACATTTAAACTA[C/T]TGTTTTGAGAGTACA | 55827 |
rs557462306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939589 | CAACATGGTGAAACC[C/T]TGGTCTTTACTAAAA | 55827 |
rs557514268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978991 | GTCTAATATGTTGGT[C/G]TGCTCCTTTATGATT | 55827 |
rs557523945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943229 | TTGGTCTTTTTTAAA[A/C]AAATTTATAGTTATC | 55827 |
rs557546316 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040719 | CTAAACTTTTTGGGC[-/T]TTTTTTTTTTTTTAG | 55827 |
rs557572635 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167951537 | CTGAGATCATGCCAC[G/T]GCACTCCAGCCTGGG | 55827 |
rs557604345 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953163 | GTTTTAAAATGTCTT[C/T]TTATTGTTATTTGTT | 55827 |
rs557616187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969988 | CACCATGTTGGCCAG[A/G]CTGGTCTCGAACTCC | 55827 |
rs557684189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007587 | CCTTACTAGATTTTT[C/T]GACCCGGTTGCATTT | 55827 |
rs557717074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959193 | ATTTAGGTTTCCTCT[A/G]TCTTTTCATAGCTTC | 55827 |
rs557724016 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984189 | TTGAAATTTTGTAGT[A/G]TTGTCAGTGCTTTTA | 55827 |
rs557739591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986389 | ATTTTGGCCATTCGG[A/G]TATGGTATAGCTGTA | 55827 |
rs557789058 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167942079 | TTTCTCTTTTTTTGT[C/T]TTTGAGACGGAGTTT | 55827 |
rs557810834 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056051 | TTCTGCAAGAGCTTC[A/T]TTAATTTCAGTTACT | 55827 |
rs557825605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981195 | ACAGGCATGAGCCAC[C/T]GCTCCCGGCCTCCCC | 55827 |
rs557835893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065867 | TATCTGACTAGGCAG[C/G]AGTAGAGTCAATTAC | 55827 |
rs557843182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056417 | CCGCACCACTCGCAG[C/T]GCCATGTTCGCAGGG | 55827 |
rs557846778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022733 | GTGCCTCTGGTATAC[C/G]AATTTGATAAAAGGT | 55827 |
rs557848744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029989 | CGTCTCAAAAAAAAA[A/G]AAAAGAAAAGAAACA | 55827 |
rs557862362 | snp | A/G | 0.000406201 | 0.0142455 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987469 | AATGTTCGTATGATT[A/G]TCTGCACTTTTCTTT | 55827 |
rs557889226 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168051701 | AATAAGCCAAAAAAT[A/G]TAATAGATGTATGGA | 55827 |
rs557917552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014624 | CCATTGTTCCCTGCC[A/G]TAATAAATTGGTTAC | 55827 |
rs557929451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027101 | AGAAAGTCTGATAAA[C/T]CATTTTTTAAATTTG | 55827 |
rs557951639 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065226 | CAAAGTCCCTCTTCT[A/T]AGGGGGGATTTTCTA | 55827 |
rs557955889 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965837 | ACGGGGTTTCGCCAT[A/T]TTGGTCAGGCTGGTC | 55827 |
rs557992809 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027811 | CTGGTGTCTTTGCTT[A/C]TTTATCCTGAATTTT | 55827 |
rs558022500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042564 | AGTGATCCACAGGGA[A/G]CAGTTCAAAAGACCA | 55827 |
rs558036577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992094 | TATATTTATTCCTGC[G/T]TACCTTAAAGTGCTG | 55827 |
rs558061319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035386 | TGGGAAATTGAGGAT[A/G]CAGCGAGCCATGATT | 55827 |
rs558069230 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034443 | TTGAGCCCAGAAGTT[A/T]GAGACCACAGTGAGC | 55827 |
rs558107295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005847 | GTTAACACTGTATAC[A/G]TTTTATCCATAATAA | 55827 |
rs558115951 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009638 | TTGTTCTTAGTGTTA[C/T]TCTCTGTATGCTTGG | 55827 |
rs558125465 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000643 | ATGAACAGAATAGGG[C/T]ATCTTGCTAAAATGG | 55827 |
rs558137478 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979913 | ACAGGCTGGGCGCAG[C/T]GGCTCACACCCATCA | 55827 |
rs558177570 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168044098 | CCATCCGTCCATGAT[A/G]GTGTTTGTACAATTT | 55827 |
rs558205849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004369 | TTTTTATCCCTCTTG[A/G]CTGGCCTATTTTGTC | 55827 |
rs558214720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958285 | TTCTGTTTAGATATT[G/T]GATCTATTTTCAGTT | 55827 |
rs558268536 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167980776 | ACAAATATTTTCACC[C/T]GTTCCATGGATTGTC | 55827 |
rs558268923 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024251 | AAAGAACAGAAAAAA[A/G]GCAGGTGATTGCCTT | 55827 |
rs558273224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998322 | ATCTGAACCTCAGTA[A/G]GTTGTATTCTTTTTG | 55827 |
rs558281646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013067 | TCTTTTGAAGTGTGA[A/G]GTGACAAACTTTATG | 55827 |
rs558294694 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033831 | AATAACCATAATTAC[C/T]GAGCAATATAGAATC | 55827 |
rs558305438 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972608 | ATGACTCAGGCACAG[A/T]TAATGACATTGGAGT | 55827 |
rs558307190 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167951357 | ATGCGGGTGGATCAG[G/T]TGAGGTGAGGAGTTT | 55827 |
rs558318647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964497 | CTTTGATTTTCTTTA[A/G]TTTGAAAAATGCTTG | 55827 |
rs558325072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937627 | TGGTGTAGGGTTTCA[C/T]GTTCCTCTTCCCACC | 55827 |
rs558401541 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040263 | TGTTCAAGGATCTTA[A/G]GAAGACCAGTGTAGC | 55827 |
rs558428110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071748 | TTCTCAGGGACTCCC[C/T]ATTGCTCTTAAAGTA | 55827 |
rs558428384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969659 | CTGTCTTTAATGGGT[C/T]GTAGTTTTATTTCAT | 55827 |
rs558439991 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007842 | CTTTTAATATCTCCT[A/G]TAAATTCATGACTCA | 55827 |
rs558447530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970267 | CGATCCCTTTGATGT[A/G]TGATTTCCAATAGAA | 55827 |
rs558491577 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936895 | GGTCTCCCCTCCCAC[A/C]CGGCTCAGGCAGAGC | 55827 |
rs558497720 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019164 | AGTGATTCTCTTGCC[C/T]CAGCCTCCCAAGTAG | 55827 |
rs558517922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978462 | CTGATACTACTGAGG[C/T]TGAGCATCTCTTCAA | 55827 |
rs558556775 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949482 | ATAAAGGTCGGGCAG[G/T]TTTGCTTGATAAAAG | 55827 |
rs558561000 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168061821 | ATACAGCCACTTTGG[-/A]AAAACCACAAATAGA | 55827 |
rs558592291 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013561 | GGTTTTTATGCACCT[A/G]TTCAAAACCAATTCC | 55827 |
rs558634367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956917 | GGTCAGAGAACATAC[C/T]TTCAATGACTTGTAG | 55827 |
rs558642771 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168027585 | TATGTTTATGTCACA[A/G]AATATTTCTTCACCA | 55827 |
rs558658697 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168051034 | ACAGTTAATACTCCC[-/T]TTTGGACTTACTGAA | 55827 |
rs558693494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950555 | ACCAGTTAAATAACA[C/T]GGAGAAAGAAGTAAA | 55827 |
rs558706272 | snp | A/G | 0.00266687 | 0.0364187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019543 | CTTTTTTTCCATTTC[A/G]GGTCCCCTGAAGTCA | 55827 |
rs558759689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070156 | TATAATATAAAAATT[C/G]TCTTTCATTTCTTTT | 55827 |
rs558769724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012308 | TTTGTTGTTCTTCTG[C/T]CTCACTGGAATTAAG | 55827 |
rs558793342 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042078 | TATATATGTACTCTC[-/T]TTTTTTTTAAAAAGT | 55827 |
rs558795774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168062127 | ATCTTACAAACATAA[C/T]TCTGAGCTAAAGAAG | 55827 |
rs558797266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949040 | CTGATTCAGCAAACG[C/T]ATATTGAATGCATAC | 55827 |
rs558802020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964032 | TAAGCATAGATGATC[A/G]AATACATTGTTGCTG | 55827 |
rs558822166 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168047868 | ACTTTTATCTAAATC[A/G]GTTATTATAATTCTT | 55827 |
rs558873843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038864 | CCTAGGTAGGTGTAT[A/G]TGTATGATTTTTGTT | 55827 |
rs558897349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991584 | GCCATAACAAATGAC[C/T]ACAAACTGGGTATCT | 55827 |
rs558913847 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167978800 | AGCTGAGACTACAGG[A/C]ATGCACTACTGCACC | 55827 |
rs558964114 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936417 | GACTCGTGAGCGAGA[A/G]ACTACAGAATTGAGT | 55827 |
rs558975181 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168008793 | ATGTACTACTGATTT[A/C]TTTCGGTTATCAGAG | 55827 |
rs558992651 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996515 | CTAGCTTTCTAACCA[C/G]TCTTCCTGCTTTCAC | 55827 |
rs559056114 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025786 | TGAAACTTCAAGATG[A/T]AAATATAATCATGTG | 55827 |
rs559058288 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985181 | ATCATAGCCAAACCA[C/T]GTCGTGTGTGTGTGT | 55827 |
rs559093364 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032565 | TAGTTAAACTTTATT[A/G]TTTTTTCAGAATATT | 55827 |
rs559108973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167996867 | CTTTGCTTATGTAAC[C/T]TTCTTGGTGAAGCCC | 55827 |
rs559153520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027224 | AAAAGGTAGAGACTT[C/T]GTTATGTCTCTTTTC | 55827 |
rs559177563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033898 | AGGGATTTTTTCCCC[A/G]CTATATTGTGTGTGT | 55827 |
rs559179778 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978524 | TGAAATGTGTAGTCA[A/C]ATCTCTTGCCTATTT | 55827 |
rs559208470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010503 | TTTGCTTTACCCTTT[A/G]TATTCTTGAATTTTA | 55827 |
rs559208945 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060242 | CTGGAATACATGGCA[C/T]GATCTTAGCTCACTG | 55827 |
rs559258420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033499 | TTTTTGTATTTTTTT[A/G]GTAGAGACGGGGTTT | 55827 |
rs559272020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072251 | GTAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC | 55827 |
rs559274711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984624 | TTCATAAGTAAACTG[C/T]TGACTTGATTAGATG | 55827 |
rs559275724 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969133 | GTCATTATGTCTAAA[G/T]TCCTTTCTAATATTA | 55827 |
rs559298459 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041371 | ATATTTTTCCCAATT[A/T]GGTGTTTGTTTTTCA | 55827 |
rs559329893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054432 | ATTAATTCATTCTTG[A/C]GAGTGGAGCCCTCAT | 55827 |
rs559336801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004075 | CTATCATGTAAATTA[C/T]ACCATGTTTTACATC | 55827 |
rs559348900 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041056 | AGTTTTTGAATCTCT[C/G]TAAATCTCAGTTTTC | 55827 |
rs559351064 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950680 | AGGCAGATACAATTT[C/T]ATGAGAGATCTCATC | 55827 |
rs559364529 | in-del | -/AA | 0.00036513 | 0.0135067 | intron-variant, splice-donor-variant | DCAF6 | GRCh38.p7 | 1:168050935 | ATAGAATAATGAGGT[-/AA]AATTCAGTATGTTCC | 55827 |
rs559377355 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936824 | GCGGATGGTGCCGGT[A/G]CGGCTCGGGTGTTGA | 55827 |
rs559379037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937117 | TCGGTGGGGGCGCCC[A/G]GAGACTCTGGGGTGT | 55827 |
rs559400117 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963589 | GGGATGCCACCACAC[C/T]CAGCTAATTTTTGTG | 55827 |
rs559405838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026754 | GTCTTTGGATATCCA[C/T]GTGGAGAGATCTCAT | 55827 |
rs559434422 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977782 | TTTAAAAATTTTAAA[A/T]TTGAAATATAGAACA | 55827 |
rs559437114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969820 | CTTGCTCTGTTGCCC[A/G]GGCTGGAGTGCAGTG | 55827 |
rs559441961 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976799 | ATTTACCTGCATATT[G/T]ACTAATACCTTTGGT | 55827 |
rs559442295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937706 | AAACAACCTTCAGTA[C/T]TTGGGGGAACAGTAT | 55827 |
rs559486775 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168048940 | GTGTTATAGAGAGAA[A/G]TCAAACTATAGTCTG | 55827 |
rs559525301 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060938 | CATTTATAGCTCTTA[A/C/T]GTCCTTTGGCTTAGC | 55827 |
rs559525474 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168014551 | TTTGTATTCAGTCCC[C/T]ACCTAATTTCTCCAC | 55827 |
rs559525525 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936500 | AGTGGCCCGAATGCA[G/T]TCTTCCAGGGTGAGG | 55827 |
rs559540838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956359 | TGACATAAAATTGTT[C/T]ATAATATTCCCTTAT | 55827 |
rs559561355 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072852 | ACTCAGTGTCTCTTC[A/G]TATCATTATCTTCCC | 55827 |
rs559568213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941633 | ACTAATGAGTCTCAG[C/T]TTGAGGTTTGGAAAA | 55827 |
rs559571924 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961530 | ACAGGCGTGAGCCAC[G/T]GTGCCTGGCCTCCAG | 55827 |
rs559599874 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949945 | TATGAGATGTCTGGA[C/T]GATGCAATAAATTTT | 55827 |
rs559603551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168062351 | TGTTTGCAAAAATTC[A/G]TTGAGCTTTTTACCT | 55827 |
rs559633788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046139 | TGGTTTCACCACTTA[C/T]CAGCAGTGTTTTTTC | 55827 |
rs559647430 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988717 | ACCAGTTACCAACTG[G/T]TTAACATGCTTTAGG | 55827 |
rs559670023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046669 | TTCCATACCCAGAGG[G/T]AGTTCCTTAGAATGT | 55827 |
rs559704688 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040401 | TGCCATCAGTAGAAA[A/C]CAGAAGAACAGTTAA | 55827 |
rs559723379 | in-del | -/T | 0.00953873 | 0.0683987 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961088 | CCTAAGTGTTTCATG[-/T]TTTTGGAGTGCTAAT | 55827 |
rs559762198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052173 | ACAGGCTTGAGCCAC[C/T]GCATCTGGCCTAGTT | 55827 |
rs559777042 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019225 | GGCTAATTTTTTGTA[A/T]TTTTGGTAGAGATGG | 55827 |
rs559791726 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983622 | TTAGAGTAGGGCCTT[C/G]TTGGGTCCTTCTTTG | 55827 |
rs559817349 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025835 | TTTTAATTACTTCCC[A/G]TAGCCTTTCAAAAGA | 55827 |
rs559818749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018376 | AACAGTGGTTTTTTA[C/T]TTATTTTTGGTTGTT | 55827 |
rs559824681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032728 | TTTTATTTTCACATG[C/T]TCCACAGCTTATCTA | 55827 |
rs559853033 | snp | A/C/G | 0.000297636 | 0.0121956 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168038441 | TTTGCACTACAGCAC[A/C/G]GAAGGAACAACTACA | 55827 |
rs559914476 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168016355 | CTTTGAATGTTAGCC[A/G]ATATTCCTAAAACCT | 55827 |
rs559917464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002136 | TATATTTATCATCAC[A/G]ATAGAAAACTAAGGC | 55827 |
rs559929328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976273 | CAGGAATTTGAGACC[A/G]GCCTGGCCAACATGG | 55827 |
rs559957007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989206 | CAGAAATAAGCTTAA[A/G]TATCACGTTATTAGG | 55827 |
rs559966144 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167980753 | ACCCTTTTTTAGATA[A/C]ATGGTTCACAAATAT | 55827 |
rs559971510 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167936028 | CCCGCGCCCCGCGAA[C/G]GTTGAGGGGGCGGAG | 55827 |
rs560008921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037661 | AAAAAGATTTCATAC[A/G]TTGAGATAGATGTGT | 55827 |
rs560029296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983058 | CTATGCTGTTTTGGT[C/T]ACTGTAGCCTTAAAG | 55827 |
rs560034836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003327 | GTTTACTTGCAGGAG[A/G]AAAAGGAGTGAGGGA | 55827 |
rs560114027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009637 | TTTGTTCTTAGTGTT[A/G]TTCTCTGTATGCTTG | 55827 |
rs560121287 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168003842 | TGACTTATTACTAAA[C/T]TCACTGATAAGACCT | 55827 |
rs560121331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993744 | ACAAAAGTGAAACTC[C/T]GTCTCAGAAAAAACA | 55827 |
rs560124901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066822 | TTCTCCAAAAGCCTA[G/T]CAATTTTTCCATTTT | 55827 |
rs560144839 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009324 | TTTCTCTTCTCTTCT[C/G]TTCTTCTTTCCTTCC | 55827 |
rs560162047 | snp | C/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968243 | ATTGGAGTAGTAAAG[C/G]CTTGGCTGCTAAAAA | 55827 |
rs560196700 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954939 | ACATCACCCTCAACC[C/T]CAGTCAACCAATGAT | 55827 |
rs560222910 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995909 | GACCAGACAAAGACA[C/T]GATCTCTTACTTAAG | 55827 |
rs560243655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036147 | CATTAACCATCTTAG[A/G]AAGCTTCTTGCCTTT | 55827 |
rs560295735 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000407 | CTTATTCAATGCAGG[C/G]TTGCCACTAAATTTG | 55827 |
rs560329759 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936442 | TTGAGTAGCTTCTCT[C/G]TCTACTCGTCTTTTA | 55827 |
rs560330745 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167934607 | TCCATTATCAAACTG[A/G]AAATCAGATTTAGTA | 55827 |
rs560351134 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167990535 | TAGGTAATTTTGAAT[G/T]TTTTACATTTCTAAA | 55827 |
rs560391159 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029762 | GAGGTGGGCGAATCA[C/T]GAGGTCAGGAGATCG | 55827 |
rs560405921 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059690 | TTGCTGTGTCGCCTA[C/G]GCTGGATTGCAGTGG | 55827 |
rs560425194 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074971 | CATAGTATTTAATTT[A/T]AAAAAATCTTTTTAC | 55827 |
rs560435768 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959400 | GGTGTATGTGTGGAC[A/G]TACGTTTTCAGCTCC | 55827 |
rs560439997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959514 | ACAATTTTGCATTCC[C/T]ACCAGCAATGAATAT | 55827 |
rs560448808 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168061957 | CAAACAACATACACA[A/C]ATGTGGATAGTAGCC | 55827 |
rs560457508 | snp | A/G | 3.47996e-05 | 0.00417116 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993481 | TTGGCCGGGCGCGGT[A/G]GCTCACGCCTGTAAT | 55827 |
rs560458754 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167984965 | TGGTGGAAGGTGAAA[A/G]GTGAAAGGCATGTCT | 55827 |
rs560468329 | in-del | -/AT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986458 | GTTTGAATACCTTTC[-/AT]ATATATACAGTGTTT | 55827 |
rs560469953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967696 | TTTTCTCTCCTGATT[C/G]TCTTAAATTTCCTGT | 55827 |
rs560470239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975451 | CAGATTCCTAAAGGA[C/T]ATTAATGAGCTTAAG | 55827 |
rs560530689 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073378 | ATTCTGAGAAGTTGG[G/T]CTTACATTCTGGAAG | 55827 |
rs560545031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940642 | GTGATTTATTAGCCA[C/G]ACAGATTTTATTATC | 55827 |
rs560561287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974116 | TAATTTCAATTTGCA[C/T]TTCCCTTATGAATGA | 55827 |
rs560578219 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939940 | TATTTTTCTGATACA[G/T]TTTCATTATTTGTAT | 55827 |
rs560630736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981405 | TTTTAGATTCGAGGG[A/G]TACATGTGCAGGTTT | 55827 |
rs560667646 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987931 | AAGAATTTATATAAA[A/T]GTATCTCATTTACTC | 55827 |
rs560709137 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049790 | CCTCCCAAGTAGCTG[A/G]GACTACAGGCGCCTG | 55827 |
rs560735089 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062975 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 55827 |
rs560740498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018178 | CCTACATTTTTAGTG[C/G]GCTCAAATGGGAAGG | 55827 |
rs560740948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009751 | ATAACTACCCTAGGT[A/G]AAGTCCTCTTTCCTT | 55827 |
rs560745858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050401 | GAAAATTGCAGAGAG[A/G]AAAGATGTACTCAAA | 55827 |
rs560753765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945580 | TACTACAACCTCCGG[C/G]TCCCAGGTTCAAGCA | 55827 |
rs560771553 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022713 | ATATATCTACCTTGC[A/G]CCTTGTGCCTCTGGT | 55827 |
rs560788577 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953000 | ACCTTGCTGAAGATC[C/T]GCCTTGCTGAAGATA | 55827 |
rs560790144 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167955141 | TGAGGAGCATTTATT[A/G]TATGGATAAATCATA | 55827 |
rs560803253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010750 | TAAAAAATATTTCAA[A/G]ATAACTATGAATATT | 55827 |
rs560813863 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976734 | AGTTATATTCTGTTT[C/T]CTCTCATGAATTAGA | 55827 |
rs560822451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953581 | TGATGAGACAAAGAG[C/T]ATATTATGTGTTAGA | 55827 |
rs560921106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981538 | TTCCCTTTCTCCCTC[C/G]CTGCTCTACTAGTTC | 55827 |
rs560950977 | in-del | -/TA | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020745 | TATTCTAATGGTTAT[-/TA]TGTTAATATTTGAAA | 55827 |
rs560956430 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167984647 | ATTAGATGGAATACT[A/G]ATTACATTTTCACAA | 55827 |
rs560957907 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988108 | ATTTAGCCCACTTTC[C/G]TAAAGATAATATCTC | 55827 |
rs560976710 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002787 | GTAGTTGTTATCAGA[G/T]TAGTCTCCAAAAAAG | 55827 |
rs561043168 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949097 | TTGGAATACATGGGT[A/C]AATAAAGCAGTGTTC | 55827 |
rs561043201 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167958507 | TTGATCTGTATGTGT[C/T]TGTTTTTGCCAGTGC | 55827 |
rs561055458 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168014301 | CTAGCAGCATTTCAC[A/G]CAACTGCTTACTCCA | 55827 |
rs561077381 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024696 | GTAATCCTAGCTACT[A/C]AGGAGGCTGAGGGAG | 55827 |
rs561081026 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982333 | AGCAACCTCCTCTTC[A/C]TGCTTTCAAGCGATT | 55827 |
rs561087273 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968355 | AGAAGAGACCCCCCC[A/G/T]TGCTGAGTGCTGAGA | 55827 |
rs561129540 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982345 | TTCCTGCTTTCAAGC[A/G]ATTCTCCTGCCTCAG | 55827 |
rs561136377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060766 | ATGTGGTGGAGGCCT[A/G]TAGTCCCAGGTACTT | 55827 |
rs561144336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954950 | AACCCCAGTCAACCA[A/G]TGATCTCTATTCTGT | 55827 |
rs561167198 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030446 | TTAAGAACAGAGGGA[A/T]GCTAATGAAGTGTTT | 55827 |
rs561181379 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962060 | GTCTAAGAGTAGACA[C/G]TGTTTGATTTTTATT | 55827 |
rs561188493 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961012 | TTAATTCTTTGATTT[A/C]TTTTACCAGAGTTTT | 55827 |
rs561208091 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061376 | GAAGTATATAATTGT[C/T]ACATAATTATTTTAA | 55827 |
rs561224269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037367 | ATTTTTAGTATTAAA[C/T]CAGTCCTTGAACTGG | 55827 |
rs561230553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023986 | TTGGGAGGCTGGGGC[A/G]GGAGGATCACTTGAA | 55827 |
rs561247701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052905 | AAGAAGAAACAAACC[C/T]AGCTTCCTTGCCTGG | 55827 |
rs561251027 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975151 | TATAAATTATTGACA[A/G]TATCTAGGTGTCAGC | 55827 |
rs561254691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941418 | TAGCATGGAGCTTAT[A/G]TTACAAGTATGCTTT | 55827 |
rs561293463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940718 | AACTTATTTCAATAC[A/G]TTGCTTGTTTCTACT | 55827 |
rs561299275 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966142 | GTGTCCTTACCTCTC[C/T]GAAGGATCCAAGATC | 55827 |
rs561301543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993899 | ACAAAAAACATGAGA[C/T]ATACTTGAAAGAATA | 55827 |
rs561301691 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168053113 | TATCACTATCACCAT[C/T]ATTTGGGTCACCTCA | 55827 |
rs561303539 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969788 | TATTTTTTATTATTC[-/T]TTTTTTGAGATAGAG | 55827 |
rs561338187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001069 | ACTTTGGGAGGCAGA[A/G]GTGGGAGGATTGCTT | 55827 |
rs561341302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073132 | AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG | 55827 |
rs561354951 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040252 | CAGACCTAGTATGTT[C/T]AAGGATCTTAAGAAG | 55827 |
rs561389902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168075284 | AACTGATTTTTAATG[C/T]GTTTTAAATAAAAGG | 55827 |
rs561422426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975578 | TATGATACAGGGTCA[A/C]ACTGTCACTCACACT | 55827 |
rs561548093 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044081 | AGGAAGAAGCAGTGG[C/G]CCCATCCGTCCATGA | 55827 |
rs561589961 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037003 | TATCAGCTTGACTCT[G/T]GTGGAATACTTTTCT | 55827 |
rs561639253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050529 | TTAATTATTTATTTT[C/T]CAAAGAGCTCCTCAG | 55827 |
rs561670011 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168063436 | ACTAAAATACTTTGT[C/T]GTAGTAACTCAACTA | 55827 |
rs561673344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994603 | AATTACTTTCACAAG[A/G]CTACTAGAAGATAAT | 55827 |
rs561679138 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168027455 | AAAGTAGTACATTTA[A/G]TAAGTTTCCTATTTG | 55827 |
rs561831516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042152 | CAAAAAGTCCATGAT[C/G]GTTTGTATTGTTTAT | 55827 |
rs561834501 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058556 | TCAGCCTGATCTCCT[A/G]ATCTGGTTTTTTGTT | 55827 |
rs561840274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028872 | AAGCTTGCTGTATTA[A/G]TAAGAATATAAGTTC | 55827 |
rs561867141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035048 | TCCTGAGAAAATGTA[A/G]CCTGATAGGTTGTAT | 55827 |
rs561868831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042647 | ACAGAGTCTAGAAGG[A/G]CATATGATAAAAATC | 55827 |
rs561869888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980349 | CCCAGAAGTAGAGAT[G/T]GCTGGATCATATGGT | 55827 |
rs561877453 | snp | C/T | 1.65181e-05 | 0.00287381 | missense | DCAF6 | GRCh38.p7 | 1:167993382 | TATATCTTTTTGACC[C/T]GAAAGATGATACAGC | 55827 |
rs561919821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999454 | TCAGCTTCTCCTCTC[C/T]AGCTGTGAAAGTCCT | 55827 |
rs561946985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945518 | CTTTTTTGAGACGGA[C/G]TCTCACTCTGTCACC | 55827 |
rs562002504 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014300 | ACTAGCAGCATTTCA[C/T]ACAACTGCTTACTCC | 55827 |
rs562013703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980827 | ATGTAGTTCCACTTG[C/T]CTGTTATGGCTTTGT | 55827 |
rs562015855 | snp | A/C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936278 | GTTGGAGAAGGGAAA[A/C/G]TGAAGCTGCGCTGGT | 55827 |
rs562044842 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168010552 | ACCATTTGAAACCAC[A/G]TTCTATATACCTCGC | 55827 |
rs562107808 | snp | A/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958495 | AATTCCATTACATTG[A/G]TCTGTATGTGTTTGT | 55827 |
rs562179991 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952790 | TATCCAACTTTCTAC[G/T]TAACATGTCCAGTTG | 55827 |
rs562192674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049571 | CTGGCCATATACTGG[A/G]TTAAGAAACGTAAAT | 55827 |
rs562211704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992656 | TTTAGCATTCCTGGG[C/T]CCCCAGGGCACAAAG | 55827 |
rs562231648 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954385 | TACTTTTTGTTATTA[C/T]ATAATAACTTTAATT | 55827 |
rs562243433 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049302 | GGCTGGAGTGCAGTG[G/T]TATGATCATAGCTCA | 55827 |
rs562251630 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056122 | CACTTTCCAAAGCAC[C/G]AAACTCATCTTGTTT | 55827 |
rs562304996 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071783 | CCAGACTTCTTACTC[G/T]GGCCTTCAAGGTCCT | 55827 |
rs562321258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033035 | TTACTATGGTTATCA[C/G]ATGTGTTTTTGTATG | 55827 |
rs562343638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064279 | GATCTCTAAGATCTT[C/T]TGTAGTTTTTACGAT | 55827 |
rs562367575 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065499 | TTAAAAAATGTAAGA[A/G]TTAAAACAAATAAAA | 55827 |
rs562376720 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055724 | CGCATATTATATTTA[G/T]CTATAATCATTAGAA | 55827 |
rs562421639 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972193 | TCCCAAGTACACATA[A/C]ATATTTTTAATCAGC | 55827 |
rs562443790 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168057928 | CTTAAATCTACCTGT[G/T]CACCCTATTTTGTCC | 55827 |
rs562457724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009240 | CCTGACCTTGTGATC[C/T]GCCCTCCTCGGCCTC | 55827 |
rs562459140 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044201 | AAAGGGTTAAGAACC[A/T]TTTATCCATAGGAAA | 55827 |
rs562523490 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002001 | AAGTCATAAAGGGTC[G/T]CAATAGATTCTGTTT | 55827 |
rs562531224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016488 | CTTATTCCTCTATAC[A/G]TAATCAACTTTCTGA | 55827 |
rs562556771 | snp | G/T | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167936143 | CCTCACCAAGTCTGC[G/T]CTGCGCCCTGCTGGC | 55827 |
rs562571758 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073170 | GATAGAGCGAGACTC[A/G]GTCTCAAAAAAAAAA | 55827 |
rs562617197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028929 | ATAAATAGTATATTT[C/T]AAATTCTAGTGAAAT | 55827 |
rs562631160 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035502 | CCAGGTTCTTCATTG[A/T]GTTGTCTTTCTGCCA | 55827 |
rs562638106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966824 | GGCATTTATATTAGA[A/C]TATCCTCCCTATTTT | 55827 |
rs562642049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023077 | AGATGCGCTATGCCC[A/G]TCCATCCATAGCTTT | 55827 |
rs562651926 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939879 | TTTTAAAAGACTTCA[A/G]TATTTAAACATTACG | 55827 |
rs562675469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980386 | ATTTTTAAGTTTTTG[A/G]GGACCCTCCATACTA | 55827 |
rs562691324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042793 | ATGAAAGGATCCAAA[C/T]AGTGAAGAAGCAGTC | 55827 |
rs562731429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007158 | TAATTTCCCAGCTTT[C/T]CAACATCTGTACTCA | 55827 |
rs562733009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939893 | AATATTTAAACATTA[C/T]GATTGTCTATCTACA | 55827 |
rs562768510 | snp | A/C | 1.6507e-05 | 0.00287284 | synonymous-codon, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974934 | CTCTGGAGATGGAGT[A/C]ATATTTTATACCAAC | 55827 |
rs562770757 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074102 | TACACATACATTATG[G/T]CATTGGTTTGACATT | 55827 |
rs562773062 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167989837 | ACTGCACTCCAACCT[A/G]GCGACAGAGCAAAAT | 55827 |
rs562778752 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962230 | TGATGGTTTTGAGTT[G/T]AACTGTGTCCTTACT | 55827 |
rs562805219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973951 | CGTAGTTTTGTGAGA[C/T]ATTGCTAAATTCCCT | 55827 |
rs562805845 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066671 | TAGCTTACTAATTAT[A/C]ATATTCATCATCGGT | 55827 |
rs562850999 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945569 | CAATCTCGGCTTACT[A/G]CAACCTCCGGCTCCC | 55827 |
rs562851160 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970542 | AGTCCCAGTTACTCG[A/G]GAGGGAGTGGCAGGA | 55827 |
rs562903055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965666 | AGAGTCTTGCTCTGT[C/T]GCGTAGGCTGGGTGC | 55827 |
rs562908869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978622 | ATCTTCTGCATATGA[A/G]CCTATCTTTTCCTAT | 55827 |
rs562918438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952909 | TACTTGTGACCTAGA[C/G]TTAGTAATTATCAAG | 55827 |
rs562967046 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945963 | TCTAAGGGTTTTTTT[G/T]TTTTTTTTTTTGAGA | 55827 |
rs562985680 | snp | A/G | 3.42062e-05 | 0.00413545 | missense | DCAF6 | GRCh38.p7 | 1:168043110 | GTCCCACAGAGCTCA[A/G]TGCAACCACCAGAAG | 55827 |
rs563106174 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000620 | TCGTCAACCAATTGA[-/C]CGAATGGATGAACAG | 55827 |
rs563115282 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056246 | ATTTTCTGTTGTTAC[C/G]CATTCGTGTTTCTCT | 55827 |
rs563115519 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065327 | TGTCAGTTTTTTTTT[A/T]TATAGATAGGGGATC | 55827 |
rs563126596 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167996032 | AGAACAAAGTAGGGA[A/G]TAATTAATCTTGAGT | 55827 |
rs563152880 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999629 | TACTTTTATGTTACA[G/T]AAAGACAGCTTCTTT | 55827 |
rs563160188 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072223 | AATCGCCTGAACCCA[C/G]GAGGTGGAGGTTGTA | 55827 |
rs563160881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952436 | GTGTTAGCCAGGATG[G/T]TGTTGATCTGACCTC | 55827 |
rs563160946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959393 | GTGTGCAGGTGTATG[C/T]GTGGACATACGTTTT | 55827 |
rs563182996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957759 | GACAGCAACATACAG[A/G]GTTCCAGTTTCTTGA | 55827 |
rs563197576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958705 | AAATGACAGTCAATA[C/T]TTAACGCTTTATTTT | 55827 |
rs563235857 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034565 | AAAAAATTAAGCTTA[C/T]TGTTTTCAGTTCATC | 55827 |
rs563236789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972246 | ATCATACATACCCAT[A/G]TTGGCTGTATAGATT | 55827 |
rs563300884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937791 | CGAGTCAACTAAAAA[A/G]TTTGGTTTCTTAAAA | 55827 |
rs563324851 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975616 | AGTGGCATGACCATG[A/G]CTCTCTGCAGCTTCA | 55827 |
rs563326778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071432 | AACATGGCAAAACCC[C/T]GTCTCTATAAAAATA | 55827 |
rs563374428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027956 | TAAATGTATAACATG[C/T]ACATTGTTATTAATT | 55827 |
rs563376403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064623 | TATTAATAGAAGTAA[C/T]CAATTTATATTTCTT | 55827 |
rs563384866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048101 | CTTGTAATTAGTCCT[A/G]TGATTTTGGAGAGTT | 55827 |
rs563403464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943931 | GCAAGTTCCGCCTCC[A/G]AGGTTCACGCCATTC | 55827 |
rs563423327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041153 | CATGCAGAGAAAGTA[C/T]GTAGCACTTACTAGC | 55827 |
rs563437757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951500 | GAATTGCTTGAACTT[C/G]GGAGGCAGAGGTTGC | 55827 |
rs563452981 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055411 | GTTGCTTCACTGTAT[A/T]AAAATAGCACCAGCA | 55827 |
rs563472641 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991686 | GTTTCTACTGGAAGC[A/T]CTGTTCGATGCCTTC | 55827 |
rs563484919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970583 | AGCCCAGGCGTTCCA[A/C]CACTACACTCCAAGT | 55827 |
rs563491792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006234 | GCTAAATTCCTTTCA[A/G]TATTTAATGTAAGTA | 55827 |
rs563523947 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040487 | GCAGTGGAGGTGGTT[A/T]AAAAAAAAAAAAAGT | 55827 |
rs563531883 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936535 | CCGCAGCACACACCA[A/G]CCTCAGTCCCCAGGG | 55827 |
rs563568591 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167936075 | CCCCGGTCCGCCTCC[C/G]GCCCCCGGCAGGAGA | 55827 |
rs563616144 | in-del | -/AAAA | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036087 | AAAACAAAACAAAAC[-/AAAA]AAACTTTGTAGTAGA | 55827 |
rs563621985 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982152 | TTTTATTTTGTGTTC[G/T]TTGGCTCCTTGTATG | 55827 |
rs563688793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045626 | TTTTTCTGCTTTTCT[A/G]TTGACCCTGGATTAA | 55827 |
rs563695084 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972275 | TTTGGTTTCAACAAT[G/T]AAAGAACAAATTCTA | 55827 |
rs563729502 | snp | C/T | 0.000100012 | 0.00707077 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002596 | TATACTTTGGTCAGC[C/T]TTTCTTTGTATATGG | 55827 |
rs563775539 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054582 | TGTGTGTTTTAAAGC[A/C]CTTAAAATGTTTATT | 55827 |
rs563796435 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167978506 | ATTTGGATGTATTCT[G/T]AATGAAATGTGTAGT | 55827 |
rs563814800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046816 | TCTATAATTAAGCTT[A/G]TACATTTATGGCCTT | 55827 |
rs563873975 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989742 | ACAAAATAGCCAGGC[A/G]TGGTGGCACATGCCT | 55827 |
rs563874061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983138 | TTAAGATTGCTTTGG[C/T]TGTTCAGGCTCTTTT | 55827 |
rs563973037 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019292 | TGACCTTGTGATCCA[C/T]CCACTGCAGCCACCC | 55827 |
rs563974185 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167950070 | TATAGAAGAGTTCTT[A/G]CTAAAACAGCTTACT | 55827 |
rs563983860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952262 | CTGGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT | 55827 |
rs563988068 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944076 | CTCGATCCCCCGACC[C/T]TGTGATCTGCCCGCC | 55827 |
rs564026547 | in-del | -/G | 0.00993419 | 0.0697739 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963068 | GTTCGAGACCAGCCT[-/G]GGGCAACATGGTGAA | 55827 |
rs564030047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056680 | ACAAGAACCTGTAGC[A/G]TAATAAAGCCTCTGA | 55827 |
rs564046853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976824 | TTTGGTTTACCTTTC[C/T]TTCTTCCCATCACAC | 55827 |
rs564051565 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944606 | GGGTGTATGCTTTTG[A/T]AAAATGTCTATTCAT | 55827 |
rs564070172 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021986 | CTTATTGGTTGGGGA[A/C/G]AGTTGCGCTTATTAC | 55827 |
rs564077584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980324 | CGTTTCCAGTTTTTT[C/T]GGATCTGTACCCAGA | 55827 |
rs564080950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042075 | ATATTATATATGTAC[C/T]CTCTTTTTTTTAAAA | 55827 |
rs564103249 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021350 | TTCACAGATTTTTAG[G/T]AGAGTTTCCCAATAT | 55827 |
rs564105218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028582 | GTTAATTTTCCACTA[C/T]GTATCATTTTATATA | 55827 |
rs564105468 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168033376 | TGCGGACTGCAGTGG[C/T]GCAATCTCGGCTCAC | 55827 |
rs564136383 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064706 | AAAGAGAAGATAAGT[A/T]AATTTAACAGTAGCT | 55827 |
rs564182244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055592 | TATATAAGGCTTAAG[A/G]ATAACAATGTTATCT | 55827 |
rs564223510 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951555 | ACTCCAGCCTGGGCA[A/C]CAGAGTGAGACTGTG | 55827 |
rs564243694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992575 | CAACAGGTGGACACA[A/G]TTGACATTTTGAGCA | 55827 |
rs564260852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034111 | CTGAGGAGTAACAAC[A/G]TCAACAATTGATATT | 55827 |
rs564282060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964836 | GTCTACTAATACGCC[C/T]ATCAGAGGCATTGTT | 55827 |
rs564314289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991792 | CTCTCTTTACATGCA[A/G]TTTTCCCTGTGTGTG | 55827 |
rs564343931 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028032 | TGTGTGTAAACACAT[G/T]GATGGCCTTTCTGTG | 55827 |
rs564459235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006340 | TATGCAGTACTTTTA[C/T]TCATAAATTATTTAT | 55827 |
rs564495262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005490 | AGCAGATGTATCTAC[A/C]GTTTACTCGGTACTT | 55827 |
rs564553447 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976679 | AAGGAACTTGGAACA[C/T]ACCTTGTTCCATTTT | 55827 |
rs564555488 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167996671 | TATGGTGGCTTCAAG[A/T]TCTTATATTATCTGG | 55827 |
rs564606655 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982250 | TAATTTTTTAAGTTC[-/T]TTTTTTTTTTGAGAC | 55827 |
rs564610446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025956 | AGCTCTTGCCAAATA[A/G]ACTTACTTTCATTTC | 55827 |
rs564616048 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998715 | ACCACTTTCTTTGCT[A/C]ATCCATAAGGAGCAA | 55827 |
rs564619890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041227 | CAGTTCTCATCTTTT[A/G]TAAATTGTCTTTCAG | 55827 |
rs564625447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063285 | AACATTGGATAAAAT[C/T]TGTTATATTTGTAGT | 55827 |
rs564628736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032935 | AGCTTAAAGTCTGAA[C/T]GTCCTTATTAGTATT | 55827 |
rs564638458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977639 | ATTGGCATCTTGAAA[A/C]ATGTAAGAAATTTTC | 55827 |
rs564666021 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033465 | GGACTACAGGCGCCC[C/G]CCACCGCGCCCGGCT | 55827 |
rs564676927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976929 | TTTTTTTGAGACGGA[A/G]TTTCGCTCTTGTTGC | 55827 |
rs564679887 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941481 | TCCATGATAAAAGTA[A/C]ATTTATGTGGCAACC | 55827 |
rs564700219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019867 | TTCCCACAGTGTCCA[C/T]AATGACAGTCACATG | 55827 |
rs564765541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168062746 | GAAGTTTTATTTTAA[C/T]AGTTAAATCAGTTTT | 55827 |
rs564781398 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975202 | TCTTGATAGGCTTCT[G/T]GATAAAGTTAAGAAA | 55827 |
rs564795825 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964354 | CTTTGTTTTGTTTCC[A/G]TTACTGCTTTAAATA | 55827 |
rs564797254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943376 | ATGTTTACAATATGA[A/C]TCTTCTCATCTGTGG | 55827 |
rs564813650 | in-del | -/AGGTGGGCCCTGGATT | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991880 | AATCCAGTTAGGGTG[-/AGGTGGGCCCTGGATT]AGGTGGGCCCTAATC | 55827 |
rs564882316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996290 | TATCATCTCTCTTTT[C/T]TTCTTTTTGACAGTT | 55827 |
rs564902540 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983048 | CGTACCAGTACTATG[C/G]TGTTTTGGTTACTGT | 55827 |
rs564917674 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949804 | TAATTTTAATTTGAG[G/T]AGGCTCAGTTTTATT | 55827 |
rs564964940 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936651 | TCCTCCTGTTGGAGG[G/T]GGGCTGAGGGAGGAG | 55827 |
rs564976385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061378 | AGTATATAATTGTTA[C/T]ATAATTATTTTAAAA | 55827 |
rs564995129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052892 | TGTTTATGATATAAA[A/G]AAGAAACAAACCCAG | 55827 |
rs564999403 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167984497 | AAATATATGCTTCCA[A/G]TGATTTCATTTATAG | 55827 |
rs564999456 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942865 | ATTGATCTAGCTTCA[C/T]GTCTTTATACCGAGG | 55827 |
rs565035926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983844 | TGACAAGCACCCTTA[A/G]GATGGGGTTGAATAT | 55827 |
rs565048477 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962837 | GCACATGCCTATAAT[C/G]CCAGTTACTTGGGAG | 55827 |
rs565057400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963527 | CTCACTGCTACCTCC[A/G]CCTCCCAGGTTCAAG | 55827 |
rs565071631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976432 | AGCCAAGACTGCGCT[A/G]CTGTACTCCAACCTG | 55827 |
rs565086766 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168008993 | TCTTTTCTCCTTCCT[G/T]CCTTTCTTTCTTTTT | 55827 |
rs565110450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010983 | GATTTAGAGAAGCTG[A/G]TAACTTTGAAGTGGA | 55827 |
rs565129308 | snp | C/T | 0.00280586 | 0.0373504 | upstream-variant-2KB, missense, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935813 | CGGTGGTAGGTGGCC[C/T]GCAGGCCTCGGGCAC | 55827 |
rs565129358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017372 | TTAGCAGATTACAAA[C/G]TTAGTATTAAAATGA | 55827 |
rs565142428 | in-del | -/T | 0.0853583 | 0.188131 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033011 | TAAAATACTCAGCAT[-/T]TTTTTTTTTTACTAT | 55827 |
rs565154863 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049398 | CAGGTGCATGTTGCT[A/G]CACTCTGCTAATTTG | 55827 |
rs565164162 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956199 | CTGGATTTTGCCAAG[C/T]GTCTTTTTTTTTTCC | 55827 |
rs565168775 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986827 | AAGAACTTATTGAGG[A/C]AGGGTTTATAGAGAG | 55827 |
rs565183009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167947452 | TGGTTCCTCGAGGTG[C/T]GTTCTTAGATTATTA | 55827 |
rs565186749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954747 | GTGAGCCACCGCACC[C/T]GGCAAATTTTTGTAT | 55827 |
rs565197661 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955572 | CTCTCATATTCATTC[A/C]AGTAGCTTTTTTTTT | 55827 |
rs565198348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046106 | CATAGTCAAGAGCAT[G/T]ATGATGGGTTTGAAT | 55827 |
rs565204640 | in-del | -/TT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985323 | TAAGGTGTACTGGGC[-/TT]TAAAATCGAAGTGTT | 55827 |
rs565207126 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944896 | GAGTTGATTTTTATG[-/T]TATTAGTGAGAGATA | 55827 |
rs565269833 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034560 | TAGAGAAAAAATTAA[A/G]CTTATTGTTTTCAGT | 55827 |
rs565307608 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168076279 | TTCACTAGGTGGAAA[C/T]GGATCATCATAAAGG | 55827 |
rs565313463 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935330 | ACTCCAAACCCTACA[A/G]TGCGACAAACCACCC | 55827 |
rs565316282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024887 | TATGGACCTTAGATG[A/C]CCTGTATTACTATAA | 55827 |
rs565340417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018250 | CTATTTAGTTGCTGA[C/T]ATTTCTTGGCAATTG | 55827 |
rs565344235 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068655 | ATGAACTACATTTGT[C/T]GTAAAATGGTCAAAA | 55827 |
rs565353667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994747 | CACTTTGGCTTTTTT[A/G]TTTTATAATGTCCTG | 55827 |
rs565363114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017942 | TTCTCACCTATTTAA[A/G]TGTTTTAGCTATAAG | 55827 |
rs565375057 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969070 | TTTTTACCATTCTGA[C/T]CAAGTTATTTAAACT | 55827 |
rs565378307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018898 | CAGGTCATTTGACTG[C/T]TTTATGCCTCAGTTT | 55827 |
rs565403465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012000 | GAAAGAAAGAAAGAA[A/G]CAAGTGGAAATATTA | 55827 |
rs565405440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019925 | ATCTATGTGTTTGAT[A/G]TTTATAAGTAGTTAA | 55827 |
rs565409652 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976040 | TCCAGTCTCACAGTT[G/T]TGGGGTTTTACTGGA | 55827 |
rs565443072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019440 | TAGCATTCAGGGTTT[C/T]GAATGAGCTATATGT | 55827 |
rs565497406 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002643 | TTTTAACTTCCAGTT[G/T]CTTCACTATTATAAA | 55827 |
rs565505045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976986 | TTGGCTCACCACAAC[C/T]TCTGCCTCCTGGGTT | 55827 |
rs565535612 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168002756 | GCAGTCACTGGATAA[A/G]TACCTTTTAATTTTG | 55827 |
rs565545127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941487 | ATAAAAGTACATTTA[G/T]GTGGCAACCTGTGAT | 55827 |
rs565550723 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983990 | GACTTACAGTGGCTG[C/G/T]GAAGTTACTGTTTTT | 55827 |
rs565563798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989046 | GATCACACCACTGCA[C/T]TCCAGCTCGGGTGAC | 55827 |
rs565574337 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972828 | TCTAGAGATTTGTTC[A/G]AAGGAACGGGCCCCC | 55827 |
rs565612668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988768 | ATTTGAAACAGAAAT[A/G]AAACAAAAAGTAGAA | 55827 |
rs565647740 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167946860 | TTGTGTCCTTCTTTG[A/G]TTTTGTTATCAGGGC | 55827 |
rs565663221 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069175 | ACAAAGTAGGTTATT[A/T]GTAATAACTTAGCCC | 55827 |
rs565670952 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976593 | TTATTCTGGAGGTTA[A/C]CCCAGCTACTTTCAC | 55827 |
rs565684610 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990094 | TTTTATAAGTAAAAA[C/G]TATAAAATATAGAAG | 55827 |
rs565698019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069998 | ACTCTTATCTAGTGG[A/G]TGGCTCTTCCTCAGT | 55827 |
rs565704184 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936746 | CGGGTGCGGCCGGGC[C/T]TCAGGGGCCCAGGCG | 55827 |
rs565726130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061889 | TGCACATACTGAGGT[C/T]TAGCAGCTCCTCTTC | 55827 |
rs565737849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070662 | ACATTTTTAAAAAGC[A/G]ACCAAAGTTAATCTC | 55827 |
rs565768957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963861 | ATGTACAACAAATCT[A/C]AGTCCACTTTATTTC | 55827 |
rs565771050 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970733 | CATGAGTCAAATACT[A/T]CCTGTTTTTATAGTT | 55827 |
rs565796968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995851 | ATTTATTGGGTGCCT[A/G]CTATACACCAAGTCC | 55827 |
rs565798162 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034432 | AGGAGATTCACTTGA[G/T]CCCAGAAGTTTGAGA | 55827 |
rs565807887 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970116 | TTTCCTGAAATAATG[G/T]ATATGTAGAAAGCTT | 55827 |
rs565809184 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978003 | ATGGCTTTTTGTGTC[-/TT]TGTTGTTGTTTTTGT | 55827 |
rs565896401 | in-del | -/TGAGAT | 0.0119091 | 0.0762411 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037192 | ACCACTGAGCCCCGC[-/TGAGAT]TCTCTTAATGTGTGC | 55827 |
rs565917640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074618 | TACTGTAATTAGGAT[C/T]ATCATTATGAAGTTC | 55827 |
rs565924609 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168068995 | GCAGAATATATTTAT[C/T]AAACAAAAGAGTTTT | 55827 |
rs565929376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038742 | GATGCCGGTGCTGCT[C/T]ATCCTAGAATATTTC | 55827 |
rs565945736 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942999 | ACAAGCTCCGCCTCC[G/T]GGGTTCACACCATTC | 55827 |
rs565945814 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936255 | TCTCCCCATGCCCTC[G/T]AGGCCATGTTGGAGA | 55827 |
rs565947432 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032487 | ATTGGTTTAAAAACT[A/G]TGGTTGAGAAATTTG | 55827 |
rs565956839 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075663 | TTTGCCGTGTATGAG[G/T]AGTGCTAGAAAATGC | 55827 |
rs565993994 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067821 | TGCTCATGGTTACAT[A/G]TTGCATCTCTGGGTG | 55827 |
rs566001300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003790 | GCTTTCATTTTAAAG[C/T]CCTTCAAATCTAGGT | 55827 |
rs566009833 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053027 | GACTATTGGAGTTCT[C/G]TGAATACATTATGCT | 55827 |
rs566013416 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983395 | ATCTGCATTCTTTTT[C/G]AGGTGTAGGCACTGG | 55827 |
rs566024851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968534 | GGTTTCTCATCAGAG[A/G]TAGTATGCTACAAAA | 55827 |
rs566064442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060196 | AGTTTTGGTTTTTGT[A/T]GTTGTTTTAAGAGTT | 55827 |
rs566099104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010178 | GACTGTCTAGACCAC[A/G]TAGGACTGAGTAGAT | 55827 |
rs566154664 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948827 | CGGCTAATTTTTGTA[A/T]TTTTAGTAGAGATGG | 55827 |
rs566158285 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950088 | AAAACAGCTTACTTT[A/G]TCTTCTATTCTTAGG | 55827 |
rs566169679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167946438 | GAAAGTAGGCATCCT[C/T]GTTTTCTTCCAGTTC | 55827 |
rs566175645 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044447 | ACAGTATAAGGAAGG[G/T]TATGCATAGGTTATA | 55827 |
rs566187463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038096 | TTAATACTTTTTGAT[G/T]CCCCTAATGACTAAA | 55827 |
rs566231353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961520 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGTGCC | 55827 |
rs566249611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040035 | ACATAATTAATAAGT[A/G]TACCATATAGTATGT | 55827 |
rs566308583 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168003584 | AATTTAGGTTGAGGT[A/G]GGAAGTGGGAGGTTT | 55827 |
rs566319779 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024143 | GATTGCTAGAGCACA[A/G]GAGTTCAAGGATCCA | 55827 |
rs566328909 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050737 | ATTTAGTTGACTGAC[A/G]TATTCCTTGCTTAAT | 55827 |
rs566361582 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168015879 | CAAGAGCTAGCTGCA[A/C]ATACCCAGCAACAGC | 55827 |
rs566361699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049954 | GCCACCGCACCCAGG[C/G]TGTATAATTTTTTTT | 55827 |
rs566384930 | snp | A/G | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954474 | TTTTATTTTTTTGAG[A/G]TGGAGTCTCGCTGTG | 55827 |
rs566390700 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036482 | AAATGAAAAAACTAG[C/G]CCGAACTCAGTCTCT | 55827 |
rs566410397 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069330 | CTGGATGATCTAATC[-/T]TCAAACTATTCTAGC | 55827 |
rs566435466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043527 | ATCTAAACAAGTTAC[A/G]AGTGAATCTATTTAA | 55827 |
rs566485136 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054082 | TTGTAAAGATATATG[C/T]TGAAATGACAGCAAT | 55827 |
rs566498305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994197 | TAACAGTGAATTATT[A/C]GGGATAAGGCTTTAG | 55827 |
rs566571213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029190 | TTTGTTTAACTTAGA[A/G]TTGTCTTATCATAAA | 55827 |
rs566583858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008218 | AAGCAGTCCATCCGC[C/T]TCGGCCTCCCAAAAT | 55827 |
rs566601664 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167963368 | GTTAACTGTTTCTGC[C/T]TTTTGTCTTTGTTCC | 55827 |
rs566611636 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988328 | ACTATGCTCAACTAA[-/T]TTTTTTTTTATTTGT | 55827 |
rs566626799 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966860 | GGTTTATTGTATAAT[G/T]TAGAGGTTCTTAGGT | 55827 |
rs566643231 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046541 | AGATATGAAGCAAGA[A/G]TTTCCCATGTTTATA | 55827 |
rs566654045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008688 | ACTCCTCACTGTGGA[C/T]GTATAAGAATTTATA | 55827 |
rs566670536 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000650 | GAATAGGGTATCTTG[A/C]TAAAATGGGGTATTA | 55827 |
rs566671157 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953168 | AAAATGTCTTTTTAT[A/T]GTTATTTGTTCAAAA | 55827 |
rs566685928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022004 | TTGCGCTTATTACCT[A/G]TGTTTCTCTTTTACT | 55827 |
rs566706580 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992875 | TAATAAGTATTAGCT[C/T]TTTGTAAAAATTTGT | 55827 |
rs566718717 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167988522 | TTCAGTCTTTTGACC[C/T]CAGACAAGTAATTCC | 55827 |
rs566739585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953856 | TGCCCGCCTTGGCCT[C/T]CAAAAGTGCTGGGAT | 55827 |
rs566747360 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992258 | GGCCAGGATTACACA[C/G]ACACACACACACACA | 55827 |
rs566775946 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960638 | TGGGATTCTCCACTT[A/G]TCTTTCTGTTACTGA | 55827 |
rs566780918 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985568 | CCTCTGTGGATAATT[C/T]AGGATAATCTCCTTA | 55827 |
rs566805252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028380 | ATTTTGTCTGAGTTT[C/T]AGGTTTTGGCCATGA | 55827 |
rs566823193 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015433 | AATCAGATGAGTTAA[A/C]TGATTGTTTTCAATT | 55827 |
rs566828864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980458 | TGTGCAAGGGTGCCA[A/G]CTTCTCCATTTCCTT | 55827 |
rs566838392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972661 | TATTTTGGCATGGCT[C/T]TGCTGGTGGATTTGA | 55827 |
rs566858825 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072179 | GCGCGTGCCTGTAGT[C/G]CCAGCTACTTGGGAG | 55827 |
rs566873698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030752 | TAGCAGTCTGCAGAG[C/G]CCAGGACTTGTGTCT | 55827 |
rs566895914 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072732 | GAAAGTAAATAAATT[A/C]TTTGTAAAGGGTAGC | 55827 |
rs566904480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939218 | AGCAGCAAAATCCAC[A/G]TTGGTAATGTTTGAA | 55827 |
rs566923337 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046581 | TAATCAAACATCTTC[G/T]CTTTACCTGTACACA | 55827 |
rs566958080 | in-del | -/TCTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168016267 | TAGAGCCTGCATTGA[-/TCTT]TCTATTGAAAGTTTG | 55827 |
rs566965999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941160 | TAGTGAAATATTTGT[A/G]TTTTGTTTCTTTAGT | 55827 |
rs566972342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037744 | AAACAAATTCCTTGC[A/G]AGATTAGTCAGGAAG | 55827 |
rs567028474 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935085 | AGGCTTTTGCTCAAG[A/G]TCACAACTATAAGTG | 55827 |
rs567035017 | snp | G/T | 0 | 0 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035221 | GAGGCCAAGGCAGAC[G/T]GATTGCTTGAGCCCA | 55827 |
rs567039186 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938625 | TTTCTTTTAGAATTT[A/G]TTTGCGGAGAAAGAA | 55827 |
rs567074825 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167979096 | ATTGCTTTGTCTTTA[A/G]CATTTAGATCTGTAA | 55827 |
rs567109544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944311 | TAGATATATTAATTT[C/T]TTTTCTTTTTGTAAA | 55827 |
rs567112611 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168018743 | TGTTTTCTAGACTTT[C/T]AGGAAATATGCAGGA | 55827 |
rs567154822 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009373 | CCTTCCTTCCTTCCT[C/T]CCTTCCTTCCTTCCT | 55827 |
rs567171906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035681 | AACAAATTCTATCAA[C/T]TATAATCAATCATTT | 55827 |
rs567194034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945018 | TCGGCTTTGTCAAAC[A/G]TCAGTTGGCTGCAAG | 55827 |
rs567236314 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037185 | TCCTCCCACCACTGA[G/T]CCCCGCTGAGATTCT | 55827 |
rs567307645 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075758 | CATCATAGTGAAAAT[G/T]TTGGTTCAAATAAAT | 55827 |
rs567373795 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167988027 | CTGTCTTTTAAACCA[A/G]TAATTACATGTTATC | 55827 |
rs567399083 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167979958 | GAGGCTGAGGAGGGC[A/G]GATCACGAGGTCAAG | 55827 |
rs567442550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002208 | TGATACAGGTGGGAT[G/T]AGAAATCACATATAC | 55827 |
rs567460490 | snp | G/T | 1.64803e-05 | 0.00287052 | missense | DCAF6 | GRCh38.p7 | 1:168044968 | AATGACCTCAATCTT[G/T]ATCGCTCTTGTGGGG | 55827 |
rs567489011 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051457 | ATATAAGCCTCAAGC[A/C]CTTCTCTATTTGGGA | 55827 |
rs567496009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986831 | ACTTATTGAGGCAGG[G/T]TTTATAGAGAGCCTC | 55827 |
rs567497748 | in-del | -/GTT | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006511 | AAGGTTATGACTGTA[-/GTT]GTTCTGATAACAGCT | 55827 |
rs567505198 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995012 | TTTTATCCTTGCAGT[C/G]TATTTATTTGAATTA | 55827 |
rs567558120 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996609 | CCGCTCTTCTCATCA[A/G]CATTCTAAGTGGCTC | 55827 |
rs567563912 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973510 | AAACAGTGATTTTTA[A/T]ATTGTCATTTCTTCT | 55827 |
rs567623069 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021489 | CCAACTGTGAAATGG[A/T]TAAATGAGAAGGCAT | 55827 |
rs567640487 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960199 | TGGGTCTGTTTCTGG[G/T]CTCTGAATTCTGTTT | 55827 |
rs567642800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073679 | CCAACTTTGAGATAG[A/G]CCGTTACTGCTTCAT | 55827 |
rs567644113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167967832 | GCCTCCTGCGTTCAA[A/G]CGATTCTCCTGCCTC | 55827 |
rs567657462 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013074 | AAGTGTGAAGTGACA[A/G]ACTTTATGGCTGTAT | 55827 |
rs567657651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987274 | GTTAAGTTAATGCTA[A/G]TCTTCAAAGTACTGA | 55827 |
rs567691959 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066280 | TACAATTGCTGTTCA[A/C]GGTTAGTTTTGCTAT | 55827 |
rs567720945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066985 | GCCTGTTAAAACAGT[A/G]TTTTCAGCCTGAGTT | 55827 |
rs567760701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960718 | ATTCTTTTAAATTTG[C/T]TAAAGTGTATTTTAA | 55827 |
rs567783677 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985543 | GTAAGACCCTTGTAA[G/T]TATATTGGGCCTCTG | 55827 |
rs567891538 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945655 | CACCACTATGCCCAG[A/C]TAATTTTTGTGTGTG | 55827 |
rs567896868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071559 | GAGTCACTTTAACTT[A/G]GGAGGTAGAGGTTGC | 55827 |
rs567906569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035785 | AGAACTCTGTAGGCC[A/G]GGCATGGTGGCTCAT | 55827 |
rs567926027 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029869 | CCTGTAGTTCCAGCT[A/G]CTTGGGAGGCTGAGG | 55827 |
rs567928179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940138 | TTATCTCCTTTCTTC[C/T]CATCAAAGAAAATTA | 55827 |
rs567944742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036259 | GTAGATATCTATAAC[C/T]GTCTCTTAAATTTTC | 55827 |
rs567951520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999885 | GAGTAGCACTTTTCT[A/G]AAAGTTCCTTCCAGA | 55827 |
rs567961733 | snp | A/C/T | 0.0111196 | 0.0737302 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056318 | CGTACGGACGGCGCC[A/C/T]ACCCCCAGCTGCCAG | 55827 |
rs567965373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939496 | GGCCGGGCGCGGTGG[C/T]TTACGCCTGGAATCC | 55827 |
rs567994223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007434 | GAGTTGTTGATAGAT[A/G]CTCTCTCCATTTTCT | 55827 |
rs568039411 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965266 | CTTCACAAGGGATTA[G/T]CAGCACCTCCTATTC | 55827 |
rs568054368 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008016 | CACTCTGTCACCCAG[A/G]CTGGAGTGCAGTGCA | 55827 |
rs568054406 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068238 | AATATAGACATCAGA[C/T]GCATAAAGAATGAAG | 55827 |
rs568076280 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054265 | GGTTGAAGGGCCACA[A/G]TGGTACAAGCCTTCT | 55827 |
rs568077083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952608 | TCCATTGACTTGCTA[C/T]ATCTTCTCTGTCTCA | 55827 |
rs568078423 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167994306 | AGCAGCAAGAAAGAT[C/G]AACAGTGCTAACACT | 55827 |
rs568123273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953026 | AGATATATTATTTTA[C/T]CTTCATATGTAAGCC | 55827 |
rs568137203 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042486 | AGAAAATATTACCCT[G/T]TCCTTCTACAGAACT | 55827 |
rs568158886 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943784 | TGTGTGCCTGGTTTG[G/T]TTAACCTAAGATAAT | 55827 |
rs568171980 | snp | A/G | 0.000194993 | 0.00987211 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042987 | AGATCATATTGATTA[A/G]CTTCTTGGTGGAATC | 55827 |
rs568174521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978842 | TTTTATTTTTTGTAG[A/G]GACGGGGCCTTGCTA | 55827 |
rs568215212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944135 | GGGTGAGCCACCACG[C/T]CCAGCCTGATTTCAT | 55827 |
rs568219342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937506 | TCCGTGTAAACTGTT[G/T]TTGCGGCGCTGAGCC | 55827 |
rs568219826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167979847 | AGCTGAGATCATGCC[A/C]CTGCACTCCAGCGTG | 55827 |
rs568287311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028122 | TTGTTTAGTTTCAAC[A/G]GTATGTTTTAATGGG | 55827 |
rs568302687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020858 | ATAGGAAAATAATCC[G/T]TCCCAAAGGAGTTGT | 55827 |
rs568352967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046529 | CACTTTTTTTGTAGA[C/T]ATGAAGCAAGAATTT | 55827 |
rs568369188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013885 | CGAGGGGCCACAAGT[A/G]TGCATCACCATGCCT | 55827 |
rs568369855 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972559 | GGAAGTAGGAGATAG[C/G]AGGCCATTGAAATAA | 55827 |
rs568386271 | in-del | -/TAGTCTGATT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071135 | CTTCTCTTGTCCTCA[-/TAGTCTGATT]TTCACACAGCAGCCA | 55827 |
rs568389092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168047387 | CCCACTTCATGCATA[C/T]ACTCTTGAATTCATA | 55827 |
rs568445221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034198 | TTATTTCTAAGATTG[C/T]ATATTAAGTAGGAAC | 55827 |
rs568450308 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991921 | TAATCCAGTATGACC[G/T]CACTGTAACTAACTA | 55827 |
rs568485083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951613 | GCGTGAGGTAGAGGT[A/G]TTCTAATGAGGAAAC | 55827 |
rs568488592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033707 | CCTTTACAGTCTTTT[A/G]TCTTGATGTTTATGT | 55827 |
rs568552633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005576 | TTGGTTCTTCTAAGG[A/G]AGAATTTTACTCAAT | 55827 |
rs568590977 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940290 | CAGAGTGTTGTTTTA[G/T]ACTAGCATGGATTTA | 55827 |
rs568597450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054926 | GGTTCAAGCAATTCT[C/T]CTGCCTCAGCCTCCC | 55827 |
rs568606066 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168029763 | AGGTGGGCGAATCAC[A/G]AGGTCAGGAGATCGA | 55827 |
rs568610046 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168003240 | TTTTAAATTATAAGA[C/T]TATAGAATAGAGTTG | 55827 |
rs568630909 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937580 | TCTCCCAGTTCCACT[C/T]TGCTCTTCAGTTCGT | 55827 |
rs568667724 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004874 | TTTGAAAGATACTAA[A/G]TCACATCAACTTCTT | 55827 |
rs568673348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050642 | CTGATTTATTTAAAA[A/G]ATAAAAGGGATTAAG | 55827 |
rs568691037 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968176 | CAAAGAAACCACACA[C/G]TAATTTCAATAGGGA | 55827 |
rs568698672 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065160 | AATAATTAAGCACCT[A/G/T]TTGTATCCCAAGTAC | 55827 |
rs568743221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056343 | TGCCAGGGCCTCGGC[A/G]GGCAGGGCGCGGCGG | 55827 |
rs568766367 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054935 | AATTCTCCTGCCTCA[C/G]CCTCCCAAGTAGCTG | 55827 |
rs568777867 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167988803 | AAAAACCTTTAGGCT[G/T]GGTGCGGTGGCTCAT | 55827 |
rs568799959 | snp | A/G | 1.73942e-05 | 0.00294903 | missense | DCAF6 | GRCh38.p7 | 1:168043035 | GATAGGAGCAGTATA[A/G]CATCAAGTTCTAGAG | 55827 |
rs568814582 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986884 | AAATTAGAAGTGGAT[A/C]CAGGCATATCTAAAA | 55827 |
rs568842882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939563 | GGTCAGGAGTTTGAG[A/G]CCGGCCTGGCCAACA | 55827 |
rs568845938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958962 | TTTGGACAAATGTAT[A/G]GTGATATATATCCAC | 55827 |
rs568850010 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058611 | GAGTCTTGCTGTCAC[A/C]AGGCTGGAGTGCAGT | 55827 |
rs568862778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035203 | GTACTCCCAGCACTT[C/T]GAGAGGCCAAGGCAG | 55827 |
rs568878081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945766 | TGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 55827 |
rs568899892 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000592 | ATAATAGCCAACAAG[G/T]GGAATAAGTTTGTTC | 55827 |
rs568911619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043389 | GTTGTTCATCATACT[A/G]TAAATGGATGAGATA | 55827 |
rs568950944 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035902 | ACCCCATCTCTCCTA[A/G]AATACAAAAATTAGC | 55827 |
rs568966728 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972599 | GAGGGAAAGATGACT[A/C/G]AGGCACAGATAATGA | 55827 |
rs568974464 | in-del | -/ATAAATAAATAA | 0.00506861 | 0.050086 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939763 | GGGAAACTCTGCGTC[-/ATAAATAAATAA]ATAAATAAATAAAGT | 55827 |
rs569021646 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072533 | TGTCTATCTTCCTCC[G/T]TAGAAAGTAAGCTTA | 55827 |
rs569058460 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065453 | GCGCCCAGCATCAAT[G/T]TTTAATTTTACTATT | 55827 |
rs569070161 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168007540 | AGTCACTAGTGACAT[A/T]CACCAGTTTAAAGGA | 55827 |
rs569134984 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168006517 | ATGACTGTAGTTGTT[A/C]TGATAACAGCTTTTT | 55827 |
rs569135081 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167934588 | ATCCAGATGTTCAAT[A/T]CATTCCATTATCAAA | 55827 |
rs569139327 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008168 | AGAGATGGGGTTCCC[C/G/T]ATGTTGGTCAGGCTG | 55827 |
rs569202641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938046 | TAAGAAAAGTTAGCA[C/T]GCAATTTTTTAATTC | 55827 |
rs569311943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977882 | ACTACCACCTAGCAC[A/G]TTAAGTATCCCAAAA | 55827 |
rs569342819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938530 | TAGGATAAGTACCTA[C/G]AGTGGTGATTAATCA | 55827 |
rs569343690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998943 | CCACGAATCACAAAA[C/G]TTCTTAATAAGGCAT | 55827 |
rs569376148 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005820 | ATAAAAGCCAGAGTC[A/G]GTTACATAACTGTTA | 55827 |
rs569379955 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167966209 | TTGTTAGTATGGAGT[A/G]GCAACTGCTAAGCTT | 55827 |
rs569388490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048507 | AGAGTAATGATTTTT[A/T]AAAAAATATTTACAT | 55827 |
rs569413447 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013036 | AATTTGACATATATG[G/T]CCTCTCTCATAGATT | 55827 |
rs569433753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944231 | ATTGATGGACACTTA[C/G]GTTGATTCCATATCT | 55827 |
rs569487682 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991058 | AGTTAAAAGAAAGCC[A/G]TATTGTTTTTCCGCT | 55827 |
rs569493029 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983998 | GTGGCTGCGAAGTTA[C/T]TGTTTTTTACAACTA | 55827 |
rs569493084 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030583 | GTGATAAAAGTAAGG[C/T]AGGAGAGATGTGAAG | 55827 |
rs569542334 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972315 | GAAATTACCAACTAT[A/G]CATACATAACACGAA | 55827 |
rs569579742 | in-del | -/TCTT | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937861 | TATACTCTTCATTAC[-/TCTT]TCTTTCTATTTGGAG | 55827 |
rs569589053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020016 | CCAAAGCAAAACAGT[A/G]ATGAGTCTTTTAGAA | 55827 |
rs569617337 | in-del | -/AAC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167993755 | CTCCGTCTCAGAAAA[-/AAC]AACAACAACAACAAC | 55827 |
rs569654665 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168025773 | CCGGCAGCCAGAGTG[A/T]AACTTCAAGATGTAA | 55827 |
rs569657964 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940997 | ATGGATAATTTTGCG[G/T]GTCGATTACTCTTTA | 55827 |
rs569662546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977148 | ACCTCAGGTGATCTG[C/T]CTGCCTCTGCCTCTC | 55827 |
rs569675202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955843 | ATAGCTCACTATAGC[C/G]TCGACCTCCTGGGCT | 55827 |
rs569690117 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167969330 | GAAACTGGATTTTTA[C/T]CAGTTTACAAACAGT | 55827 |
rs569728891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965164 | TCCTTAGGAATTTAC[C/T]GGTAAAGTGTAGGAG | 55827 |
rs569732356 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052689 | TAGGGACTGTCTTAC[-/A]ATGGGGAATGTGTTC | 55827 |
rs569735298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063532 | TGTGTTTATGTATTT[C/T]CTAGACTTACTATAT | 55827 |
rs569755598 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168069842 | TATTAAATTATAATA[A/G]CACTGTAACTTTTTT | 55827 |
rs569767923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957557 | TTTGGGTTGTTTCCA[C/T]TTTTTGGCAATTATG | 55827 |
rs569768189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055796 | TTTTTTTTTCCCCAT[C/T]GGTAATACTAAAAGT | 55827 |
rs569817214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033036 | TACTATGGTTATCAC[A/G]TGTGTTTTTGTATGT | 55827 |
rs569825738 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026857 | TTAGTTTATAGATAG[A/C]AGTTGAAACCATGGG | 55827 |
rs569838286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956507 | TCTTCTCCAAGAACC[A/G]ACCTCTGGTCTCATT | 55827 |
rs569849459 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998213 | TGTTTATACTGTACC[A/G]TAGTCTGTTAAGTGT | 55827 |
rs569857158 | in-del | -/TTC | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966453 | TGTGGCCGGAGACAA[-/TTC]TTCTTCTTCTACTGT | 55827 |
rs569884809 | in-del | -/C | 0.0333695 | 0.124785 | intron-variant | DCAF6 | GRCh38.p7 | 1:168008892 | CCCACCCCCTCCCCT[-/C]CCCCCTCCCTCCCTC | 55827 |
rs569908132 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067996 | ATTTAACTGTATTTC[A/G]TCACTAAAGTTATCA | 55827 |
rs569909167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019487 | TGTCCTAAACAGGTA[G/T]GGCAGAGGCATTCAG | 55827 |
rs569943875 | in-del | -/A | 0.223819 | 0.248625 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024805 | TGAGACTCTGTATCC[-/A]AAAAAAAAAAAAAAA | 55827 |
rs569944640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068828 | TGCTAAGAAATGAAA[C/T]ATACCTCAGTTTGCT | 55827 |
rs569953783 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033564 | CCTCATGATCCACCC[A/G]CCTCGGCCTCCCAAA | 55827 |
rs569971881 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953723 | TCCGCTGCAGCCTCC[C/T]GAGTAGCTGGGATTA | 55827 |
rs569974742 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936803 | TGCGCCCTGGAGGCC[C/G]GGCGCGCGGATGGTG | 55827 |
rs569991416 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054018 | CACAAAGGAGCAGAA[A/C]CAGCAAGATACTCTC | 55827 |
rs569999001 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167994863 | CAATGCCTATTAATA[C/T]GTTTTAAAGGTTACT | 55827 |
rs570029064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046373 | TTACAGTAAGAATGA[C/T]TCTAGGGATAAAGAC | 55827 |
rs570041817 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007253 | CTTCTCAAAGATTTC[A/G]CCCCTTCTCTTGCAT | 55827 |
rs570045619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976757 | GAATTAGATGTTATT[A/G]GTTTACTGTTAGTGT | 55827 |
rs570080172 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009287 | ACAGGCGTGAGCCAC[C/T]GTGCCCTGCCATTTT | 55827 |
rs570118494 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942363 | GCCGCTGCGCCTGGC[C/G]TTTAATTTGCATTTC | 55827 |
rs570124978 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976493 | AAAAAATAAAAATAA[A/G]GTCTACCTTTCGAAT | 55827 |
rs570141210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038822 | GTGCAAAAATATAAA[C/T]ATTTTGGGACTTTTT | 55827 |
rs570253204 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018398 | TTGGTTGTTCACTCT[C/T]TGTCATCAGTCTTAT | 55827 |
rs570270912 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017887 | ATCTTTAGAGTATCA[A/C]TTAGTGGTGATAGTG | 55827 |
rs570290312 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167969328 | AAGAAACTGGATTTT[C/T]ATCAGTTTACAAACA | 55827 |
rs570330931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053302 | ACATACATGCATACA[A/G]AAATAAAAGTTGGCA | 55827 |
rs570347423 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997206 | GATTGTTTTTAATTT[G/T]AAGATTTTATTCTAT | 55827 |
rs570364479 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010319 | ATATGGGTGAATATG[G/T]GTATGAAAATAATTA | 55827 |
rs570385052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013813 | TGCAATGGTGCAGTC[A/G]TGGCTTACTGCAGCC | 55827 |
rs570388902 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937947 | AGTTAAAAAGTGTTT[A/G]TTGCTCTCATTTGTT | 55827 |
rs570391630 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072027 | TTCCCTGGTAGTGCG[A/G]TGGCTCATGCCTGTA | 55827 |
rs570407388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972016 | ATGCGCCACCATACC[C/T]GGCTAATTTTTGTAT | 55827 |
rs570456865 | in-del | -/AAG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967494 | ACTGATTGTAATAAA[-/AAG]AAAGTGTGTGATGTT | 55827 |
rs570484759 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167994669 | AAGGTATCTTTGACA[C/G]TACACAGCTGTAGAA | 55827 |
rs570493623 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968965 | TACTTCATTAATATT[G/T]AGGTCTTTGAATGAA | 55827 |
rs570519727 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036018 | AGTGGGCCGAGATCG[C/T]GCCATTGCACTCCAG | 55827 |
rs570523235 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958853 | CTGAGTGGTACATTT[G/T]CTGTATTTCATGAGC | 55827 |
rs570528395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056277 | GTGAATTTACGCACC[A/G]AGAGCAGAGCGGGTC | 55827 |
rs570534285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048564 | CCAGGTTTTCACTTT[A/T]GGGCTGAGATCAAGC | 55827 |
rs570540717 | snp | A/G | 1.69919e-05 | 0.00291473 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167951847 | GAAGCAACCCTTAAT[A/G]TGCATGATGGTTGTG | 55827 |
rs570560695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984819 | TTAATAGATTGAAGT[C/T]TGGTAAATTAAAAAT | 55827 |
rs570566983 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168049222 | GTATCTTTTAGTGAT[G/T]TTATATACTGTATTT | 55827 |
rs570633289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943168 | CCCGCCTTGGCCTAC[C/T]AAAGTGCTGGGATTA | 55827 |
rs570647056 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024673 | GCCGGATGTGGTGGC[A/C]CGTGCCTGTAATCCT | 55827 |
rs570685871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063012 | CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 55827 |
rs570704400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026978 | ACCAAACAGGAATGA[C/T]GAGAGAAGTACGCAG | 55827 |
rs570718129 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964563 | TTGTTCTCTGAGCTT[A/C]CTGGATCTATGGTTT | 55827 |
rs570730637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020762 | TGTTAATATTTGAAA[A/G]TATTTATGTAAGATA | 55827 |
rs570747345 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954483 | TTTGAGATGGAGTCT[C/T]GCTGTGCCACCCAGG | 55827 |
rs570764276 | in-del | -/ACAA | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935056 | TAGACCGCGTATTAC[-/ACAA]ACAGAGATCTAGGCT | 55827 |
rs570776158 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037968 | GCCCTTGTATCTTAC[A/G]TCTCAGTGTTTCTGA | 55827 |
rs570776833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054078 | ATACTTGTAAAGATA[C/T]ATGTTGAAATGACAG | 55827 |
rs570807723 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034674 | TTGATGTATATTCAT[A/G]GTAATGCTCAATAAA | 55827 |
rs570835681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040645 | TCATCGTACTTATCA[C/T]GTCTTTTCCATTCTC | 55827 |
rs570841255 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168073100 | AGAATCGCTTGAACC[C/G]GGGAGGCGGAGGTTG | 55827 |
rs570863558 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168032308 | TTATCTGTAGGGTAG[A/G/T]TAGATCTTCTCTGTT | 55827 |
rs570971100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984031 | ATAGTCGCAAGGCTG[C/T]TGTTGACTTAGGGAA | 55827 |
rs570983997 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167950493 | GCCCCCATAATTATC[C/T]ATAATTTTTTTTTAA | 55827 |
rs571001967 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071386 | AGGCAGGTGAATCAC[C/T]TGAGGTCAGGAATTC | 55827 |
rs571026567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970002 | GGCTGGTCTCGAACT[C/T]CTGAGCTCAAATGAT | 55827 |
rs571033564 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168045892 | TGGAAAACTATTTCT[A/G]TTATTAGTGCTATCA | 55827 |
rs571051838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956667 | CATTGATATGAGACC[A/G]TTGTCTTTTCTAAAA | 55827 |
rs571062721 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168068030 | CTCCTATAGGGAAAA[C/G]AAGGAGCCAACAAAG | 55827 |
rs571070510 | in-del | -/G | 0.00953873 | 0.0683987 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978701 | TGTGTTTTGAGAGAT[-/G]GGGGTCTCACTTTTT | 55827 |
rs571105373 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976404 | AACAACCTGGGAGGC[A/G]GAGGTTGCAGTCAGC | 55827 |
rs571134011 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940731 | ACATTGCTTGTTTCT[A/G]CTCATATTTCTTTCC | 55827 |
rs571156927 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955962 | GGTGGGGTCTCATTA[A/T]GTTGCCCGTCTGGTC | 55827 |
rs571174127 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943200 | AGGCGTGAGCCACCG[C/T]GCCTGGCCGAAATTT | 55827 |
rs571199053 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942238 | CCCAGCTAATGTTGT[A/G]TTTTTAGTAGACATG | 55827 |
rs571228094 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982841 | TAATTTTTATATATG[C/G]TGAAATGTAGGGGGG | 55827 |
rs571231426 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167976130 | TGTTTTCTACTTTTT[A/T]AAAAAAGTTTCCAAT | 55827 |
rs571271250 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022271 | TAGAAACCCAGCATA[C/T]TAAAAAGATAAGAAC | 55827 |
rs571272990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168069082 | AATAATAATAGGTAC[C/T]ATTTATAAAGTAACT | 55827 |
rs571365289 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002292 | TGTCAACATCAGTGG[A/C]TATTTATCCTCAGAA | 55827 |
rs571373686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995164 | GGGTAAGTAAAGTTA[C/T]AGTCAAACTGTGATT | 55827 |
rs571424021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954989 | ATCAGTTTGCATTTT[C/T]TAGAATTTTAAATAA | 55827 |
rs571428221 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948078 | TATGTATTTAGAATT[G/T]TTATATATTCTTGCT | 55827 |
rs571468423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038581 | ATCTTTATGTTTTGT[C/T]TTGCTATAAGGTATT | 55827 |
rs571523826 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168068239 | ATATAGACATCAGAC[A/G]CATAAAGAATGAAGT | 55827 |
rs571561743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989012 | TTGATCCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 55827 |
rs571611255 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009835 | AAAGCAATTATAAAA[A/C]TTTATAATTTTCTTT | 55827 |
rs571630883 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954630 | GCTAATTTTTGGTAT[A/T]TTTAGTAGAGACGGT | 55827 |
rs571650852 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044503 | AGGGACTTGAGGAGC[C/T]GCAGATTTTGGTATT | 55827 |
rs571672920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014726 | CTTTTACCTTTAAAA[G/T]GTATTGCACATTCCT | 55827 |
rs571690549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993706 | GTGAGCCGAAATCAC[A/G]CCATCGCACTCCAGC | 55827 |
rs571698416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059319 | CTATGTCATATTACA[A/G]AGATTTATATAAAAC | 55827 |
rs571703171 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167956053 | TTACAGGTATGAGCC[A/G]CTGTGCTTAGCTAAG | 55827 |
rs571738062 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945205 | GCTTTGGCTATTGGG[C/G]CTTCTTTTTGGTTCC | 55827 |
rs571738780 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051534 | ACCTACTGAAAACCT[G/T]TTTTGCTGACAAAAT | 55827 |
rs571763645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954541 | CACTGCAAGCTCCGC[C/T]TCCCGGATTCACGCC | 55827 |
rs571765156 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168012645 | CTGTTATTTAGTCTG[C/T]TATGTCTGGTTGAAT | 55827 |
rs571768149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045496 | TACAGATCAAGAGAA[A/G]AGAATGTTAAGAATG | 55827 |
rs571773763 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168052305 | CTGGTTTTATAATGA[A/C]AATTGCAACTATAAA | 55827 |
rs571863174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024718 | CTGAGGGAGGAGAAT[C/T]GCTTGAACCTGGGAG | 55827 |
rs571863923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074550 | AAAAAGAAGTAACTC[C/G]TGCCCTCCAGGAACT | 55827 |
rs571908372 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167969513 | GAAAACATGGTATTA[A/G]CAGTCCAAAGTGTAA | 55827 |
rs571918146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029911 | CGTGAACCCAGGAAG[C/T]GGAGCTTGCAGTGAG | 55827 |
rs571954688 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071786 | GACTTCTTACTCTGG[C/T]CTTCAAGGTCCTACA | 55827 |
rs571981462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030553 | AGTTCTCCTGGTAAT[A/G]GAGATTTTGATCTGG | 55827 |
rs571990204 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168018116 | TAATACCTAATTCCT[G/T]TAGGAAAGTTAGATC | 55827 |
rs571990948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168060571 | CATTTACTAATGCAG[C/T]CTTAATTTTGTCCAT | 55827 |
rs572006990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168053495 | TGCTACAAAGACTCA[A/G]AAGAATCAAAGGCAC | 55827 |
rs572009413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004225 | GTAAAGTAGAAGAAT[C/G]TGAGGTTTCCTATTT | 55827 |
rs572016143 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033263 | TTTTCTGAGCCAATG[C/T]ACTATCCTGAGAGGT | 55827 |
rs572036659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167962505 | GTCTGTCTGAAATTA[A/C]TGTAACTACTCCTGT | 55827 |
rs572049986 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010584 | CAGAATTTGAAGATA[C/T]TTTGATTTTTATATA | 55827 |
rs572069818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968810 | TGCCAACTGGCAAAG[A/G]AAAAATATTTGAAGG | 55827 |
rs572098071 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995299 | ATGAGGCTGAGTCAT[C/G]AACATTTTTTTTTCT | 55827 |
rs572099309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031740 | TATACCTGAGGAAAC[A/G]GTCATGAAAAGAAAT | 55827 |
rs572099484 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949067 | ATACTTTGTGGCAGG[C/G]ACTGTATTAGGTATT | 55827 |
rs572134794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996099 | TTGTTGTATGATTTT[A/G]TCTTATGTTTCCATA | 55827 |
rs572180603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975489 | CTGAATTAAATAAGG[C/T]GGAATAAATTTAAGA | 55827 |
rs572180804 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941599 | TTACAACTGTTGGTG[A/T]TGAACTGGTAGAGTA | 55827 |
rs572200743 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938844 | CTGCTTTTCCCCCTC[C/G]TACTCCAACTCCCTA | 55827 |
rs572240367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168075070 | CCTTTGCAGCACCTG[A/G]TGTACCTCCTTAGAA | 55827 |
rs572278585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067432 | TGTTTGTAAATGGGG[C/T]AGATAGGATGGAGAG | 55827 |
rs572301418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954614 | CCCACCACCAAGCGC[A/G]GCTAATTTTTGGTAT | 55827 |
rs572306879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974726 | TAATCTTTCACTGAG[A/G]TGAGAATGTTAATGA | 55827 |
rs572376256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002380 | TAATTTGCATACTCA[A/G]GAAGTAGGGAGATGG | 55827 |
rs572382546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036810 | GGAATGGGTTATTAG[G/T]TTATTTCCAGGAGTT | 55827 |
rs572408677 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167968340 | GATAAACCACTGAAA[A/T]GAAGAGACCCCCCCG | 55827 |
rs572425868 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167947211 | TCTGTGGAATCAGTT[G/T]TAATGTCTCCTTTTT | 55827 |
rs572469949 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044044 | TGCACATAGAGTTCA[A/T]GAAGCTCAATTCCTG | 55827 |
rs572475740 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037328 | GAAATTGTGATTGTC[G/T]TTGTTATTTTTCAAG | 55827 |
rs572488721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167981897 | GGATATATACCCAGG[A/G]TTGGGATTGCTGGGT | 55827 |
rs572493514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031096 | AGCTCAGAAAAGATA[C/T]CAGAGCTCAAGAAAG | 55827 |
rs572508540 | snp | A/G | 1.65097e-05 | 0.00287308 | missense | DCAF6 | GRCh38.p7 | 1:168044621 | AGGATGTGACAAAAT[A/G]TCAGGAAGGAGTATC | 55827 |
rs572509450 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033888 | ACAAGTTAAAAGGGA[-/T]TTTTTCCCCACTATA | 55827 |
rs572543234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167939599 | AAACCCTGGTCTTTA[C/G]TAAAAATACAAAAAT | 55827 |
rs572548649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941365 | CTAAAATAGGATGAA[C/T]CAAGTTATAAGTGCT | 55827 |
rs572583473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066566 | GCTAACATGAAACAA[A/G]TTAATGCAGTTAAGG | 55827 |
rs572590188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167940659 | CAGATTTTATTATCC[C/T]ATATATATACGGTTT | 55827 |
rs572590324 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948207 | CACTCTTCACTTTGA[A/C]TTCAGACAGTCTGAT | 55827 |
rs572625028 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042335 | TCTCATTCAGTCCTC[-/TT]GTTACACATATGCCA | 55827 |
rs572640573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973769 | TCACCTCTCTATTGT[A/G]TATCTGTTATGGGGA | 55827 |
rs572664452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001755 | CAAGCAAGATACTCA[A/G]GGAGTTGAAGGAATG | 55827 |
rs572695507 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035939 | TGGTGGTGGGTGCCT[A/G]TAACCCCAGCTACTC | 55827 |
rs572718196 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016294 | AAGTTTGCATATGCT[A/G]AAATGAATCTATGCT | 55827 |
rs572723369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960894 | TAATTTGCTGAGATT[G/T]TGATAGGAATTGCAT | 55827 |
rs572734037 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042604 | CCAGGCTTTTGTTCA[A/C]ATACTAATTTTAAAG | 55827 |
rs572738528 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051115 | AGCTGCATGCACTGC[A/C]TGGGGATAGAATGAA | 55827 |
rs572777233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938925 | ACTATATTAGAAAGC[C/T]TGAATTACAGTTTTT | 55827 |
rs572777342 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945779 | TGCTGGGATTACAGG[C/G]GTGAGCCACCACACC | 55827 |
rs572780620 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013339 | ATAAATAGAAACCAT[C/T]GTAACAAGAAATTAG | 55827 |
rs572785750 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937433 | TCAATCTCCAGAGGG[G/T]TTAGGTGTCGGCTGC | 55827 |
rs572814106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945457 | ATATATTCCTAGTTT[A/G]TGTGTGTGTGTATGT | 55827 |
rs572820727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167986968 | GACATTTAAACTATT[A/G]TTTTGAGAGTACATT | 55827 |
rs572895403 | in-del | -/A | 0.289683 | 0.24683 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970625 | AAGAGCTGATATCTT[-/A]AAAAAAAAAAATTAT | 55827 |
rs572896614 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967035 | ATAAATAAAGTATGA[A/G]TTAATGAGAAAATTA | 55827 |
rs572896684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010566 | CGTTCTATATACCTC[A/G]CCCAGAATTTGAAGA | 55827 |
rs572915013 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003125 | AACATCTCTTGTGAT[C/G]AAAAGCATATTCCCC | 55827 |
rs572939312 | in-del | -/TTAA | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:168047611 | TATCCTTCAAGAAAC[-/TTAA]TTATTTATGAATAAG | 55827 |
rs572960597 | snp | A/C | | | missense | DCAF6 | GRCh38.p7 | 1:168045136 | CATGAAGAAACATCC[A/C]CCAGGGACTCTGCTC | 55827 |
rs572992541 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022786 | AGTTTCTCAACTCAT[C/T]CTCAAAGTTACTAAA | 55827 |
rs573045291 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DCAF6 | GRCh38.p7 | 1:168028634 | GTGAAACATTCATCT[A/G]TAGGAGACTAGTGGA | 55827 |
rs573108923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000098 | ACTGGCCTAATTTCA[A/G]TATTATTGTTGTGTC | 55827 |
rs573122868 | in-del | -/CTA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052791 | CCCCTATTCTTCATT[-/CTA]CTTTTATTACCTCAT | 55827 |
rs573134536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993582 | TGGAGAAACCCCGTC[C/T]TTACTAAAAACACAA | 55827 |
rs573137069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064206 | TACCCATTTTTAAGA[C/T]TGACAAGTGAAAATT | 55827 |
rs573161869 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017129 | AGAGGCCTCTGATTT[G/T]TTTTTTTCCTATGGG | 55827 |
rs573176183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056089 | ATAAAGGAGAATAGA[A/G]TTCACTAGCAGCTTT | 55827 |
rs573238780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965440 | AGCTTTTCTTAAGGG[C/T]AGATCTTGTTAAGAA | 55827 |
rs573246230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056431 | GCGCCATGTTCGCAG[A/G]GGTGCGGGGGTCGCA | 55827 |
rs573277370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972179 | CAAAAATTATAACTT[C/T]CCAAGTACACATAAA | 55827 |
rs573280934 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167959265 | AGATGTACCACAGTT[A/T]GTCCATTCACTTGCT | 55827 |
rs573286393 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958336 | TAGGGGTCCAAGGTG[G/T]TTTTTTTTGTTTTTT | 55827 |
rs573288778 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168044864 | TTAGTATTGCCCACA[G/T]TACCACCTGTTACAT | 55827 |
rs573347548 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999421 | CCAGCATGTCCTTCG[A/G]AGCTTTGAAGGCAGG | 55827 |
rs573356323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168067174 | AGTAAGTTGGAAAAC[C/T]ACTACTCTAGACTAA | 55827 |
rs573396113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937662 | GAAAACACACTTGGC[A/G]TTTACAGTTTCGTAG | 55827 |
rs573420125 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036091 | CAAAACAAAACAAAA[A/C]AACTTTGTAGTAGAT | 55827 |
rs573455637 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056788 | TTGTGGAATACCTAC[A/C]AAAATCCCAAGTTTT | 55827 |
rs573483065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938156 | CCTCCCATTCAATTT[C/T]ACTCCGCCACCCTTA | 55827 |
rs573537285 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036047 | AGTCTGGGGAACAAA[A/G]AGAGCCTCCATCTCA | 55827 |
rs573562168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168074022 | AATAGACCTTTATAG[A/G]TCAGTAAGGAATTGA | 55827 |
rs573566321 | snp | A/G | 1.7586e-05 | 0.00296524 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974830 | CTTTGTGTGTTTTAG[A/G]TTTTGACAACAATTC | 55827 |
rs573573517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036548 | CTGTCTGTTTCATCT[A/G]TTGCAGAAGCCTAAA | 55827 |
rs573669412 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168015026 | GTGTATTCGCAAATG[G/T]CTTTTTCTCTCAGAA | 55827 |
rs573736730 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015444 | TTAACTGATTGTTTT[C/T]AATTTCTGTTTCTTT | 55827 |
rs573744386 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167994345 | AGGCGATTAAAATAA[A/T]AGAAAATATGATGAT | 55827 |
rs573757107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009211 | CACCGTGTTGGCCAC[A/G]ATGGTCTCAATCTCC | 55827 |
rs573794255 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168016415 | TATTTGGCCATACTA[A/G]CATGCTGACTAAATT | 55827 |
rs573827582 | snp | C/T | | | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974969 | AGCAAGATGCAGAAA[C/T]CAACAGACAATGCCA | 55827 |
rs573872019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987042 | ATTAAAATTTTTCTA[A/G]GAGGTGAGTTATGCA | 55827 |
rs573876617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029581 | ACATTGCTTGGAGCA[A/G]TTTTTTATATGTTAA | 55827 |
rs573909372 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961328 | GCTCAATGCAAGCTC[C/T]GCCTCCCGGGTTCAT | 55827 |
rs573936617 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980944 | TTTTTTTGAGCTCTG[G/T]CACCCAGGCTGGAGT | 55827 |
rs573940437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056474 | GGCCACCCGCGCCGG[A/G]AGGCGGGGCGGGGAG | 55827 |
rs573971335 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014809 | TCTTCCTCCAGGTAT[C/G]CATGTGGTTTACTCG | 55827 |
rs574007070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168057353 | TTCATGTAACTTCAT[A/G]CTTTAACCTTGGAGT | 55827 |
rs574044045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050166 | GATGATCTAACAATT[C/T]TTTCCCTAAAGAGTG | 55827 |
rs574048053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000793 | ATGTTTAGAAAAGGC[A/G]TATCCACAGAGACAG | 55827 |
rs574051701 | snp | C/T | | | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167993296 | TCTTAATAATAAGTC[C/T]TGCAGAGTGACATCT | 55827 |
rs574055811 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168000306 | TAGGTAGGATAATAA[G/T]GAATAAGTTTGAAAT | 55827 |
rs574056896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966427 | TATTGTTAGTGTTAG[C/T]GTATTTTATGTGTGG | 55827 |
rs574080111 | snp | A/T | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935494 | TTGGAGTCGTGCGTA[A/T]GGGAGCGGATGTCAC | 55827 |
rs574082110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992426 | CTTTCTTTTCGGAAC[C/T]GTGATAGCTTTTATT | 55827 |
rs574086422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952801 | CTACTTAACATGTCC[A/G]GTTGCATGTCTAATA | 55827 |
rs574100961 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021117 | TCTATATCTTTCATT[A/T]ATAGTTTTTTCCCCG | 55827 |
rs574147785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985647 | TAAGGTAAAGTATTC[A/G]TAGGTTCTAACAAAT | 55827 |
rs574257120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964671 | GTATTCACATTATAC[A/G]TGAGTTATGCCTTTT | 55827 |
rs574282024 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012377 | AAGAATAGGGTTTGT[A/G]GTTTGAGGAGATGAC | 55827 |
rs574290524 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168021773 | TTTAAATGTACAAAT[A/G]CAAGCAATCAAATCC | 55827 |
rs574300971 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072219 | GGAGAATCGCCTGAA[C/G/T]CCAGGAGGTGGAGGT | 55827 |
rs574301285 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:168064291 | CTTTTGTAGTTTTTA[C/T]GATCTACAAGTTTCT | 55827 |
rs574318671 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031125 | AGAAATTTGGGAGAT[A/T]TTTGCATACAGATGT | 55827 |
rs574325461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938748 | CTTGTATATAGTTCT[A/G]TATTTTAGTGTTTTC | 55827 |
rs574338052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065279 | TGCTGATGAATGCCT[A/G]TCATAATTTAAAGAA | 55827 |
rs574371277 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961982 | GTGTTATTTTGAACT[C/T]GTGTGTATTTTGGGA | 55827 |
rs574410853 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167958556 | TAGTTTTGTAATAAG[-/T]TTTTTCTAGTTTTAT | 55827 |
rs574418767 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957693 | TGATATCTCACTTTT[G/T]GAGGAGGTATCAAAA | 55827 |
rs574440356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943927 | TACTGCAAGTTCCGC[C/T]TCCGAGGTTCACGCC | 55827 |
rs574478407 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167992909 | CTTAATTTGGGGGGA[A/C]CTTTTGGAAGATGAC | 55827 |
rs574491851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944390 | CTTGGAGAAATCTCC[A/G]TACTGTTTTCCATAG | 55827 |
rs574509123 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168070267 | ATAAAGTGCCCAAGA[G/T]TTAACATTTCTGCTG | 55827 |
rs574517169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167995490 | TTCAAGACCAACCTG[A/G]CCAACATGGTGAAAC | 55827 |
rs574545991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168062386 | ATTTTCAACTTTCCC[A/G]TATATGTGTTATATT | 55827 |
rs574564024 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938378 | AGTAAAAATAGATTG[A/T]TTCTGTCTTTTAAAT | 55827 |
rs574565427 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168054470 | TCACCTTTTAAAGAC[A/C]CCACCTCTCAGTACT | 55827 |
rs574587122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167971324 | TGTGCTTAGATGGCA[A/G]CTTCTTTGAGATAAT | 55827 |
rs574596153 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035325 | GATGGCATGTGCCTA[C/T]AGTCCCAGCTACTCA | 55827 |
rs574606447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168048030 | GACTTTTATTCTAAA[A/G]AGAGAAAGTTTAAGA | 55827 |
rs574608550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998477 | TTCCTTTCATAAAAG[A/G]TGTATTTGTAGCTTG | 55827 |
rs574612483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005241 | ATACTCTCTATGGTG[G/T]ATTTGATATGGTCTT | 55827 |
rs574634898 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055966 | GTTCATCTAGTTCTG[A/G]AGGGTTACTCAGTGT | 55827 |
rs574641698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970394 | TGTGGCTCACGCTTA[C/T]AATCCCAGCACTTTG | 55827 |
rs574650916 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168005972 | AATTAAAAGCAGAAG[A/T]AGTTAAAAGTTTGTT | 55827 |
rs574672879 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168016672 | TTTGTTAAAAGAATT[A/G]ATGAAAGATATATTA | 55827 |
rs574692879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045935 | AGTTCTGTCCTCTTT[C/T]AGAGAACCTAGTTTT | 55827 |
rs574696105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026481 | CATTGCTATAGTCCA[C/T]CTAAGAGATTATGAG | 55827 |
rs574718024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977372 | TTTTGCTGGGCATGG[A/G]TTTCATTTGATAGTT | 55827 |
rs574728030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013193 | TGCCACTGAGCATCA[C/T]CATTTGTTTGTCAAT | 55827 |
rs574764490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040092 | CAGGTAAAAGTGATT[A/G]GGAAACCTAGGCATC | 55827 |
rs574770734 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167936516 | TCTTCCAGGGTGAGG[A/G]CAGCCGCAGCACACA | 55827 |
rs574810707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942602 | ATGTCCTATCTAAGA[A/G]TCTTTACCTAATCCA | 55827 |
rs574813740 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061640 | TTCCAATCTGTCTCA[A/G]TTACAGTTGTGCAGT | 55827 |
rs574864106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167977899 | TAAGTATCCCAAAAG[C/T]TCCCTTTATTCTGAA | 55827 |
rs574884044 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064909 | CTTTGATTCTGCTTC[A/G]TAAAATTAAGTATGT | 55827 |
rs574890335 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949633 | AACCTGAAGCTCATA[C/T]TGCTTGCCATACATG | 55827 |
rs574925940 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168006874 | TGAAAATTTGCTACG[C/T]TCCATCTCTGGTTGA | 55827 |
rs574963218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012445 | TTGAATTTTTATCAT[C/T]GTTGTTTTTAAAATT | 55827 |
rs574986521 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935523 | ACATAGGTGGGGAAG[A/G]GAGCTGACTTGAGAT | 55827 |
rs575001546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019644 | AGCCCCACTGGAGCA[C/T]GGAGCCAGCCTAGAG | 55827 |
rs575027442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167983626 | AGTAGGGCCTTCTTG[A/G]GTCCTTCTTTGGCAT | 55827 |
rs575039881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980072 | TATAGTCCCAGTTAC[C/T]TGGGAGGCTGAGGCA | 55827 |
rs575041211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033193 | ATACCTAATTAAATA[C/T]ATAACAGTTCAAGGA | 55827 |
rs575065126 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167958192 | TGGGCTGTTGGTGCC[A/G]TATTTAAGAAACTTG | 55827 |
rs575066286 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168025858 | TCAAAAGAACCCAAA[C/T]CCATACCTTGGCTTA | 55827 |
rs575074563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989729 | CTCTACTAAAAATAC[A/G]AAATAGCCAGGCGTG | 55827 |
rs575089345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056023 | AACAAGATTTGTTTA[A/C]AAGTCCTGGATTTTC | 55827 |
rs575093906 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950171 | AGGTTTTAAAATTTT[C/G]ACAAAGTTTCCAATA | 55827 |
rs575137864 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990273 | CTTGAGAGGCTGAGA[C/T]AGGAGGATCACCTGA | 55827 |
rs575138831 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167945365 | GTGATCATGGGATGT[G/T]TTTCCATTTGTGTCA | 55827 |
rs575150509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167985718 | ACAATAATAGTAAAC[A/C]TTTTAAGACAAAAGT | 55827 |
rs575188976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167952155 | TCTTAGAAACTAGAC[A/C]TATCACTCAAACATA | 55827 |
rs575199045 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062210 | AAAATTAATTCATGA[C/T]ATCAGAAGTCAGAAT | 55827 |
rs575237173 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022153 | AGTTAAGAATTAAAA[C/G]TTACTAACTTCTGAT | 55827 |
rs575251181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063272 | GAAGAGGGGAAAGAA[C/T]ATTGGATAAAATTTG | 55827 |
rs575286474 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167984515 | ATTTCATTTATAGAC[A/C]GTAGTATACAAAGCA | 55827 |
rs575288713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168055446 | CAGTGTATCGCAAAA[C/T]TAAGATAGTGGTGTT | 55827 |
rs575294083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168072252 | TAGTGAGCCGAGATC[A/G]CACCACTGCACTCCA | 55827 |
rs575296456 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167960374 | CGCGATCTCAGCTCA[C/T]GGCAGCCTCCACCTC | 55827 |
rs575321133 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938876 | TGGAAATGGAATTTG[G/T]GTATTGGGTCTAGGG | 55827 |
rs575351453 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035328 | GGCATGTGCCTATAG[A/T]CCCAGCTACTCAGGA | 55827 |
rs575359883 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168056521 | TTTTAATAATAAATT[A/C]ACACTCAATTTATTT | 55827 |
rs575395982 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168029394 | TGTCTGTACTTCATT[A/C]ATTCAACTGATACGT | 55827 |
rs575405741 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167965323 | ATTAGGCTGGAGTTA[C/T]GTATTTTCCTTCCCC | 55827 |
rs575415389 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041899 | TGTTTGTCGCGCACA[C/G]ACACACACACACACA | 55827 |
rs575448243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167944485 | CAACATTGTCTGTCT[C/T]TTTAATAAAAGACAT | 55827 |
rs575472541 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033420 | TCCCGGGTTCACGCC[A/G]TTCTCCTGCCTCAGC | 55827 |
rs575475819 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168047872 | TTATCTAAATCGGTT[A/G]TTATAATTCTTAACT | 55827 |
rs575505856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167999253 | TCAGTAAAACATGCT[A/G]TAAAGAGATGTGCCC | 55827 |
rs575509342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033774 | ATGGTAATTTGCCTC[C/T]ATAGAGACCACTCTA | 55827 |
rs575518128 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168027095 | ACTCCCAGAAAGTCT[A/G]ATAAATCATTTTTTA | 55827 |
rs575527517 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071255 | CATTGTAATGCAAAA[A/C]CAGCCATAGACCATA | 55827 |
rs575553925 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937033 | GGCCCCGGGGCGGAG[G/T]CGCTGAGGTCGCCGC | 55827 |
rs575554294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168026529 | ATAGTGGTGAGAAGT[A/G]GGAATGGACAGATTT | 55827 |
rs575607646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168071671 | TGGGCTGTATTTGCC[C/T]ATGGGCTATAGTCTG | 55827 |
rs575614313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168034707 | ATAGTTATTAATATG[A/G]TAGCTTTCTACATAA | 55827 |
rs575661774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168013297 | TTAAATCTTAACTAC[C/T]AATTGGGTAATTGAA | 55827 |
rs575666796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014178 | CTTAAACCTGCTGCT[A/G]TCAGATTTTGGTCCT | 55827 |
rs575692743 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964801 | CTCAAGGTCAGAGAT[C/T]GTTTCCTCAATTGTG | 55827 |
rs575705406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168020931 | AGGATTTCTTCATAA[A/G]ATTAATCTTCAAGAT | 55827 |
rs575706831 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943270 | TGAACCCTTTCTATT[G/T]CCATAAAAATTTTAG | 55827 |
rs575726338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167978339 | ATTCCCACCAACAGC[A/G]TGTAAGAGGTCCTGT | 55827 |
rs575738279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972089 | TCGAACTCCTGACTT[C/T]AGGTGATCCAGCTGC | 55827 |
rs575785493 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991424 | TTTTAAAATTTCTTG[C/T]TTGTTATAAAATTTC | 55827 |
rs575835133 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040726 | TTTTTGGGCTTTTTT[G/T]TTTTTTAGAGAAAAT | 55827 |
rs575878146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937602 | TCAGTTCGTTTTGAC[C/T]GCTTAAAGGTGGTGT | 55827 |
rs575878674 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168060513 | TTTAAATGAACATTT[A/T]TGCTTTGATACAGTT | 55827 |
rs575901169 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167984257 | GCAGAAGTGCTTCTT[A/C]TGTAACATTCTTACA | 55827 |
rs575909579 | in-del | -/G | 0.0126979 | 0.078662 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043982 | GGTTAGTAAAATGCA[-/G]GGATCAGGTAATTTC | 55827 |
rs575943052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168073107 | CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG | 55827 |
rs575966760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963961 | GTACTATTTCTGTTA[C/T]TCATTTCACTTATTT | 55827 |
rs575980214 | in-del | -/ATAT | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168041735 | CTACTCAGTACCATA[-/ATAT]TTTAATTACTATAAT | 55827 |
rs576020397 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168046575 | AGAGATTAATCAAAC[A/T]TCTTCTCTTTACCTG | 55827 |
rs576022563 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997259 | ACCAGTTCTTTGGCT[A/G]TGTAATATAAAAATT | 55827 |
rs576051086 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167950415 | CATGTTACTGAATTT[C/G]TCTAGGTTGTTTTAT | 55827 |
rs576057655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040166 | GAAGGAGTGAGCCAC[A/G]TATTTATATCTAGGG | 55827 |
rs576059052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988740 | GCTTTAGGGGAAAAA[G/T]ATTATTTTATATATT | 55827 |
rs576066783 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168061592 | TGCCATAATTTATTT[A/G]ACCTATTCTTTCTAT | 55827 |
rs576076824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956072 | TGCTTAGCTAAGAAC[A/G]TTGTCTCTTTCTATT | 55827 |
rs576113798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167963362 | ATATTTGTTAACTGT[G/T]TCTGCTTTTTGTCTT | 55827 |
rs576123554 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167949751 | AAATAGGCCAGACTC[G/T]TCACAGCTTTTAATA | 55827 |
rs576161679 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167965060 | CTGGCTTTATCCCTT[C/G]AAATTGTATTTTTGC | 55827 |
rs576167292 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986905 | ATATCTAAAATATTG[C/T]ACTTCATTAAAAAAG | 55827 |
rs576203774 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961598 | TTGTTATCTACAAAG[A/T]CCGTTTTATTTCTTT | 55827 |
rs576217981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168059462 | AAGACCCTTCCTTCT[C/T]TTTATTCATTTTTAG | 55827 |
rs576241461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167956861 | TTTCTTAGTTTTCCA[A/G]CGTATCTTTATGTTA | 55827 |
rs576241695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961026 | TCTTTTACCAGAGTT[C/T]TATAATTTTCCTCAT | 55827 |
rs576324410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167992480 | ATCTAATAATAATTG[A/G]GGAGTCCAGTCTATT | 55827 |
rs576327054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955230 | ACAAATAAAGTTGCC[A/G]TGAATATTCGTGTTG | 55827 |
rs576335856 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974100 | AATTGATATCTCAGC[A/G]TAATTTCAATTTGCA | 55827 |
rs576343030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941430 | TATGTTACAAGTATG[C/T]TTTAGGTCAGTGTTT | 55827 |
rs576350477 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936287 | GGGAAAGTGAAGCTG[A/C]GCTGGTTCTACTGCC | 55827 |
rs576354981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061365 | TTATGAAAGTAGAAG[C/T]ATATAATTGTTACAT | 55827 |
rs576364123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954694 | CCTGACCTCATGATC[C/T]GCCCGCCTCTGCCTC | 55827 |
rs576465272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997349 | GAAGGATGAAGCCCT[C/T]TCCTTTTGGGAGTGA | 55827 |
rs576480708 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942039 | ATGGTAGGCGTGTAG[A/T]AATATATCATTGTTT | 55827 |
rs576491789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991522 | TTGGGATGATACTTT[G/T]GCAGTTTAAAAAGTT | 55827 |
rs576519926 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971045 | TTTTCTTGATTTGGC[C/T]TCAGCCAGCTACTTA | 55827 |
rs576581335 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000493 | ACTATGTTTCAATTC[C/T]TTTGGGTAGTTCTCC | 55827 |
rs576594519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167970305 | ATTTGAAAAAATGAT[A/G]CTCTTTCTCATTTCC | 55827 |
rs576633863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168031882 | CGTTTATGAATAGAG[A/G]TATATAAAACTACTG | 55827 |
rs576668628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167948228 | ACAGTCTGATTATAA[C/T]GTTGCCATGGTGGAG | 55827 |
rs576714487 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070692 | CATGAATAATGCACT[A/G]AAGACTGCTAGTCTA | 55827 |
rs576749804 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009527 | TTCCTTCTTTCCTCC[A/C]TCCCTTCTTTCCTTC | 55827 |
rs576772840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167990523 | TGATACATTATATAG[A/G]TAATTTTGAATTTTT | 55827 |
rs576778198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003139 | TCAAAAGCATATTCC[C/T]CAATATATGAGCTAC | 55827 |
rs576803615 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040323 | TAGTAGATAAGGTCA[C/G]CCAGGAAATTGAGGA | 55827 |
rs576810787 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168037397 | GTATCAAGGAAAAAG[A/T]TATCTCACAGAAGAG | 55827 |
rs576833506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168040847 | TGTCAGAAAAGCAGT[C/T]AGCATTTTTTATTAT | 55827 |
rs576843332 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167969993 | TGTTGGCCAGGCTGG[C/T]CTCGAACTCCTGAGC | 55827 |
rs576847780 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168032597 | CACCATATGTTTTAT[G/T]TCGACCTTACTTTGG | 55827 |
rs576871631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168033832 | ATAACCATAATTACT[A/G]AGCAATATAGAATCG | 55827 |
rs576906220 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040904 | AAAAAAAAAAAAAAA[-/C]CAAACAGGCAGAACT | 55827 |
rs576947293 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF6 | GRCh38.p7 | 1:168047748 | GTGTATACTGAGGTA[A/G]TTAGAAAGTGATTAG | 55827 |
rs576955229 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168061395 | TAATTATTTTAAAAA[C/T]TGTTAGTCACAATTT | 55827 |
rs576978156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167955381 | GTACCGTTTAACATT[C/T]CCAGTGTTAGTATGT | 55827 |
rs576987879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168062149 | CTAAAGAAGCTAGAC[A/G]TAAAAAAAATGTATT | 55827 |
rs576989123 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943875 | ATGGAGTCTCACTCT[G/T]TCGCCCAGGCTGTAG | 55827 |
rs577028789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167943385 | ATATGAATCTTCTCA[C/T]CTGTGGTTCTGGTTT | 55827 |
rs577030735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951365 | GGATCAGTTGAGGTG[A/G]GGAGTTTGAGACCAG | 55827 |
rs577055929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167957016 | TGTACACTTAAAAAA[C/T]GTATATTTTGCTGTT | 55827 |
rs577064741 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167996933 | CTGATACTACCTATC[A/C]CCTTTTCTACTTTAT | 55827 |
rs577072146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168012369 | AAGAAAACAAGAATA[A/G]GGTTTGTAGTTTGAG | 55827 |
rs577094137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167964092 | CTCAATTAAGAATAA[A/G]TAAAATGAAAGTTTG | 55827 |
rs577095682 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989604 | ACATTACTGAGGGGC[A/C]GGGCGCGGTGGCTCA | 55827 |
rs577133365 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962198 | TAGTCTATAAATGTC[C/T]GTTATATTCAGGTAA | 55827 |
rs577133518 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167992237 | CACATTTTTTCAGTA[A/C]AGGAAGGCCAGGATT | 55827 |
rs577153504 | snp | C/T | 0.000775254 | 0.019673 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019550 | TCCATTTCAGGTCCC[C/T]TGAAGTCATGGGTTG | 55827 |
rs577185531 | snp | C/G | | | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168076002 | ACTTCCTTCATTTCT[C/G]CTTCCACGGTACAGC | 55827 |
rs577207194 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935921 | CGAAGGGGAGCTAGT[C/T]ACTTTTCCTGCCACG | 55827 |
rs577250542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019175 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGATTACA | 55827 |
rs577278961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051951 | AGTGGCGCAGTCCCA[A/G]CCCACTACAACCTCT | 55827 |
rs577308956 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168032005 | ACAGTTTCAATCTAA[A/G]TGTATCGAAATCACA | 55827 |
rs577310077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167954830 | TTTGATATGTTTAAC[A/G]CATGTAAACATACAC | 55827 |
rs577374481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030290 | TGAGCCTGAATAAGT[C/T]AGGTGAAGGAGCATG | 55827 |
rs577374829 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168026607 | TTAGAAATGAATGAG[A/G]GTATGATAACCAGGT | 55827 |
rs577443643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942071 | AATTTGCATTTCTCT[C/T]TTTTTGTTTTTGAGA | 55827 |
rs577481116 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168065078 | TTTTGGAAAGTTCAG[C/T]AACATATATGTAAAT | 55827 |
rs577498650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168024502 | TTCTTTTGTACTTCT[C/G]ATCTTAAATTATTCC | 55827 |
rs577505128 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:167989257 | CTTAGAGTAAGTGGT[-/G]GGTACTAAATTTTGT | 55827 |
rs577512387 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167996011 | AGGACTATGTTCTGT[A/G]TAAGTAGAACAAAGT | 55827 |
rs577533160 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036252 | ATAGCATGTAGATAT[A/C]TATAACTGTCTCTTA | 55827 |
rs577536078 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023869 | AAGTGTGATAAGTAA[A/T]CTTAGTTAAGTCTTT | 55827 |
rs577536475 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:168030953 | AGCCCTGGAAAAGGG[A/G]TGAAGCATGGGCGGG | 55827 |
rs577609899 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168001651 | ATATTGTTTTTTTTC[G/T]TAAAAATGATAAGAA | 55827 |
rs577610958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168017256 | GTATATAAACGTCTA[C/G]CAAACATGTTTTGAA | 55827 |
rs577632449 | in-del | -/C | 0.00874735 | 0.0655527 | intron-variant | DCAF6 | GRCh38.p7 | 1:168035983 | GGAGAATTGCTGGAA[-/C]CCCGGGAGGCGGAGC | 55827 |
rs577634278 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF6 | GRCh38.p7 | 1:168010551 | GACCATTTGAAACCA[C/T]GTTCTATATACCTCG | 55827 |
rs577651331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009058 | GGCTGGAGTGCAGTG[A/G]CGTGATCTCGGCTCA | 55827 |
rs577696149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167961618 | TTTATTTCTTTTCCA[A/G]TCTTCATACTTTTCC | 55827 |
rs577744664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167988520 | CATTCAGTCTTTTGA[A/C]CCCAGACAAGTAATT | 55827 |
rs577786320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002688 | ACATTCTTATACATA[C/T]AGGTATACTTATGCA | 55827 |
rs577789726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987868 | TAAAATATATTTATG[A/G]AAATTCAAATAATTT | 55827 |
rs577797085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167973610 | TTAATTCAGTGTTTT[A/G]TAGTCAATCACTGAT | 55827 |
rs577821824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167972980 | AAGTGGAGGTAAATC[A/G]TAAATTTTTAAGAGT | 55827 |
rs577834346 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167980729 | TTTCTTTATATATTC[A/C]AAATATTAACCCTTT | 55827 |
rs577845707 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935162 | TAGAGCTTGTTCAAC[A/G]ATTTCATAAATAAGG | 55827 |
rs577884531 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167941304 | ATATAAGTAATCATA[A/G]CAACCATAGACACTA | 55827 |
rs577954042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993711 | CCGAAATCACGCCAT[C/T]GCACTCCAGCCTGGG | 55827 |
rs577976627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167960211 | TGGGCTCTGAATTCT[A/G]TTTAGTTATCTGTTT | 55827 |
rs577982450 | snp | A/G | 8.38592e-05 | 0.00647476 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043165 | TATTTTGCTTTTGTT[A/G]TTATAAAATTGCAGC | 55827 |
rs578031518 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF6 | GRCh38.p7 | 1:167982214 | CTCATTTTTTAAGGG[A/G]GTTATTTGGTTTTTG | 55827 |
rs578032884 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF6 | GRCh38.p7 | 1:167942104 | GAGTTTCGCTCTTGT[C/T]GCCCAGGCTGGAGTG | 55827 |
rs578049794 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167953458 | TCTACACTTTTGCCC[A/C]CCTGCCTTGGCATAT | 55827 |
rs578053598 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168036699 | TTAATACATTTCTGT[A/C]AGCTAAAGGTCTATT | 55827 |
rs578063450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168058415 | TATTTTTTAAAAATC[A/G]TGTTTATTCACATCA | 55827 |
rs578091059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF6 | GRCh38.p7 | 1:168051016 | CTAACCACCTTTCCT[A/G]TTAACAGTTAATACT | 55827 |
rs578109025 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009853 | TATAATTTTCTTTTA[C/G]TATGATAAGCTCTCT | 55827 |
rs578133952 | in-del | -/TTCT | 0.0209421 | 0.100162 | intron-variant | DCAF6 | GRCh38.p7 | 1:168009466 | GTCTCTCTCTCTTCC[-/TTCT]TTCCTCCCTCCCTCC | 55827 |
rs578142239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168014846 | TCCTCGAGGTGTTTG[A/T]TCAAGTGGTGCCTTA | 55827 |
rs578143080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167946663 | TTCTGTTGATATGAT[A/G]TATCACATTTATTGA | 55827 |
rs578145714 | in-del | -/TTACT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959766 | TTATTTTAGATAACA[-/TTACT]TTATCAGATGTGTCT | 55827 |
rs578157559 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022669 | AAGGGCAAGGAGTCT[G/T]GTGTAGTGAACTAGA | 55827 |
rs578168692 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF6 | GRCh38.p7 | 1:167946013 | CCAGGCTGGAGTGCA[A/G]TGGCACAATCTCAGC | 55827 |
rs578218781 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007902 | TACCCTGAATTCCAG[A/G]CCCTTATGCCTGATG | 55827 |
rs578227859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966466 | AATTCTTCTTCTTCT[A/G]CTGTGGCCAAGGGAA | 55827 |
rs578238378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF6 | GRCh38.p7 | 1:168057503 | ATGTTTCTTCCAAAT[A/G]GAATAATAATTGATA | 55827 |
rs745327676 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168014027 | TACAGGTGTGAGTCA[C/T]GGTGCCCTTCCTGCC | 55827 |
rs745332249 | snp | C/G | 1.69642e-05 | 0.00291236 | synonymous-codon, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167951840 | AAAACTTGAAGCAAC[C/G]CTTAATGTGCATGAT | 55827 |
rs745394186 | snp | C/T | 1.84283e-05 | 0.00303542 | intron-variant | DCAF6 | GRCh38.p7 | 1:168075359 | TTGCGATTCTCTTAT[C/T]TGTGTTTCCAGACCG | 55827 |
rs745395404 | snp | C/T | 1.68618e-05 | 0.00290356 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044712 | CTTTGTATGGGAAAA[C/T]AAAAAGCCTTAATCT | 55827 |
rs745396019 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970262 | AATGACGATCCCTTT[A/G]ATGTATGATTTCCAA | 55827 |
rs745419731 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167999508 | AGGCTGTTTCATTTG[C/T]ATTGGAAATCTGTCG | 55827 |
rs745441333 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050102 | AAGAAAGCTTCCTGA[A/G]TAAGTCCTCACATAG | 55827 |
rs745447512 | snp | A/C/G | 3.46064e-05 | 0.0041596 | missense | DCAF6 | GRCh38.p7 | 1:168004545 | AAGGTGGAACAAGTC[A/C/G]ATCAGATATTTCAAC | 55827 |
rs745468135 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040040 | ATTAATAAGTGTACC[A/G]TATAGTATGTTAGAA | 55827 |
rs745476337 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974689 | TGATTTTTTTAAATT[A/C]TAATAGCTTGCAGTC | 55827 |
rs745509780 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167981561 | ACTAGTTCACAGTTT[C/T]TGTTGTTGCCATCTT | 55827 |
rs745526552 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168065411 | CCTTGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 55827 |
rs745545431 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168028058 | CTGTGCTAATTATGC[A/G]TAAAGTGAAATTCTG | 55827 |
rs745553873 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168048486 | CAGAACAGTTCCTTG[C/T]AATACAGAGTAATGA | 55827 |
rs745568985 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168068997 | AGAATATATTTATCA[A/G]ACAAAAGAGTTTTAC | 55827 |
rs745578537 | snp | C/T | 1.66346e-05 | 0.00288393 | missense | DCAF6 | GRCh38.p7 | 1:168004659 | AGCCTTCTACATCCT[C/T]TACAATGTCAGCTCA | 55827 |
rs745586932 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167949657 | ATACATGAGTAGTAA[A/T]TTTTTTTGCCTCTGA | 55827 |
rs745596240 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168006456 | TATCAAGACATTATC[A/G]CTATTGAGAAAAATG | 55827 |
rs745611974 | snp | C/G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167991779 | TTAATCTCTGCCACT[C/G/T]TCTTTACATGCAATT | 55827 |
rs745674858 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024325 | ATTAGCACTAAAGCC[A/G]TAAGATTTGGTTGAC | 55827 |
rs745692629 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995957 | GAAGTAGAGGTACAA[A/G]TAAATAAATATGTAA | 55827 |
rs745695399 | in-del | -/TAC | 1.94437e-05 | 0.00311793 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068480 | TAGGAACTTTAAGTA[-/TAC]TACTAAAACCATTTT | 55827 |
rs745699952 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167993133 | TTTGTATTGCTACAT[A/T]AAGTCACATGTAATA | 55827 |
rs745712683 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168026653 | TAATGAACCATCAGC[A/C]AAGATAGAGACTTTA | 55827 |
rs745724831 | snp | C/T | 1.67933e-05 | 0.00289765 | missense | DCAF6 | GRCh38.p7 | 1:168065665 | ATTTTCATCTGGGAT[C/T]GGCACACTGCTGAGC | 55827 |
rs745739170 | in-del | -/AC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995855 | TTGGGTGCCTACTAT[-/AC]ACACCAAGTCCTCTA | 55827 |
rs745793010 | snp | C/T | 8.79314e-05 | 0.00663008 | upstream-variant-2KB, missense, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935762 | TACAACGGCCTCAAT[C/T]TCTCGGGCAGCATCA | 55827 |
rs745849322 | snp | A/G | 3.46554e-05 | 0.00416251 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168043037 | TAGGAGCAGTATAGC[A/G]TCAAGTTCTAGAGGA | 55827 |
rs745857752 | snp | C/T | 0.000118015 | 0.00768073 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935859 | CCGCCGAGGGATCGT[C/T]GGCAGCCGGGTGGGA | 55827 |
rs745864954 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962731 | GAGGTCGAGGTGGGC[A/G]ATCACCTGAGGTCAG | 55827 |
rs745886341 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167996038 | AAGTAGGGAATAATT[A/T]ATCTTGAGTAAAGCC | 55827 |
rs745891652 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168059435 | TTAGTAAATCTTAAT[-/G]GCGGCTAAGGCAAGA | 55827 |
rs745917973 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168060259 | ATCTTAGCTCACTGC[A/G]TCCTGTAACTACTGG | 55827 |
rs745918094 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168044387 | GCAACCGCTTACATA[A/G]CATTTACATTGCATT | 55827 |
rs745926034 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168048051 | AAGTTTAAGAGATTT[G/T]GCTTCTTAAGAACAT | 55827 |
rs745956288 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167983316 | AATAAATGGAAAAAC[A/G]TTGTTGCTGTTTGTT | 55827 |
rs745985560 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167983685 | TCTAAATTCCCAGAA[A/G]TGTTTTGTTGCTTTT | 55827 |
rs746032366 | snp | C/T | 3.29919e-05 | 0.00406138 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002479 | CCCGTTCTTATTTTT[C/T]AGTTGCGACAACCAC | 55827 |
rs746134480 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168004181 | TCTGGTGCCATTGGA[C/T]CTAGTGCGTATCTTT | 55827 |
rs746159036 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167966521 | TTAAATACTTTTTAA[C/T]GTATAACCTCATTAG | 55827 |
rs746163583 | snp | A/G | 7.23262e-05 | 0.00601314 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974803 | AAATAATAAGTTACC[A/G]TTAACTGCTTTCTTT | 55827 |
rs746176313 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072090 | ATCACGAGGTCAGGA[A/G]ATTGAGACCAGCCTG | 55827 |
rs746183273 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167988476 | TTGACTTTTAATACT[A/G]TTTTAAACTTACAAA | 55827 |
rs746194078 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168021550 | GAACTGATTGAAATG[C/T]TATTGTTCCCACTTT | 55827 |
rs746196043 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037221 | TGTGTGCTCCAACAT[C/T]TTCAAGAGGAATGAA | 55827 |
rs746215430 | snp | A/G | 1.6501e-05 | 0.00287232 | synonymous-codon, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974913 | TGATAAACAGATTGT[A/G]TCCTGCTCTGGAGAT | 55827 |
rs746238084 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167946164 | GTTTCACCATGTTGG[A/C]CAGCTGGTCTTGAAC | 55827 |
rs746256345 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940607 | GTATACTAGGTGTAG[A/G]GTAGTGCTTTTGGAA | 55827 |
rs746261234 | snp | G/T | 1.75542e-05 | 0.00296256 | stop-gained | DCAF6 | GRCh38.p7 | 1:168045214 | GCAAGGTATCGAGCA[G/T]GACCTGGTGATAGGT | 55827 |
rs746277415 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977007 | CTCCTGGGTTCAAGT[A/G]ATTCTCCTGTCAGCC | 55827 |
rs746296638 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062697 | TTAAATAAATTCAAA[A/C]TGACAAAATTATTAA | 55827 |
rs746312697 | snp | A/C | 1.86124e-05 | 0.00305055 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022947 | TTGCTGTGCAGTTTT[A/C]TGCTGCTTACTTTTA | 55827 |
rs746329187 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167993174 | AGAGTTTTAAAAAAT[A/G]TTTTTCTTTAAAACA | 55827 |
rs746372636 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000499 | TTTCAATTCTTTTGG[A/G]TAGTTCTCCTGTATA | 55827 |
rs746392127 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035992 | GCTGGAACCCGGGAG[A/G]CGGAGCTTGCAGTGG | 55827 |
rs746399810 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168073035 | AAAAAAATCAGCCGG[G/T]TGTGGTGGCACGCTC | 55827 |
rs746432682 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058355 | CAAAATAATTTAAAA[C/T]TGTTTTCCAAAGTGG | 55827 |
rs746450901 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | DCAF6 | GRCh38.p7 | 1:167991274 | TACCATATTACCTTG[C/T]TGTTGGTTGTTCTGA | 55827 |
rs746475534 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000839 | TTGCCAGGAGCTGAG[C/T]AGAGGGATGAGTGGG | 55827 |
rs746487225 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168067196 | CTAGACTAACACTGA[C/G]TGTTCGTAGCACAAT | 55827 |
rs746499915 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050430 | AAGAGAAAGAACTGG[A/G]CTCCTAGGGAGTTAA | 55827 |
rs746502256 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036153 | CCATCTTAGAAAGCT[G/T]CTTGCCTTTGGTGGG | 55827 |
rs746539199 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168016584 | TAGTAAAAATTGTCA[C/T]TCTTTTTTTCTCAAT | 55827 |
rs746540848 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945027 | TCAAACATCAGTTGG[C/T]TGCAAGTATGCGGCT | 55827 |
rs746564630 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037361 | AAGTTTATTTTTAGT[A/G]TTAAATCAGTCCTTG | 55827 |
rs746579186 | snp | C/G | | | missense | DCAF6 | GRCh38.p7 | 1:168065692 | GAGCATTTGATGCTT[C/G]TGGAAGCTGATAATC | 55827 |
rs746603818 | snp | A/G | 1.65021e-05 | 0.00287241 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167987557 | AGATGGAACTGTTAG[A/G]TGGTTTGATACACGC | 55827 |
rs746603968 | snp | A/G | 1.64895e-05 | 0.00287132 | missense | DCAF6 | GRCh38.p7 | 1:168004757 | GAACAAAGGCAGTCT[A/G]TTGAGGCATCTGGAC | 55827 |
rs746637606 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970431 | CCGAGGTGGGAAGAT[C/T]GCTTGAGGCCAGGAG | 55827 |
rs746661276 | in-del | -/T | 3.50911e-05 | 0.00418859 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951908 | ATTTGATACTAAGTG[-/T]TTTAAGTGTTTGATG | 55827 |
rs746677714 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168015232 | ATGTAAATCTTTTTG[A/C]ACTTAAAAAATTTTT | 55827 |
rs746705183 | snp | C/G | 1.65754e-05 | 0.00287879 | missense | DCAF6 | GRCh38.p7 | 1:168065685 | CACTGCTGAGCATTT[C/G]ATGCTTCTGGAAGCT | 55827 |
rs746715349 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168043282 | GCTGTTAAACTGATA[C/G]ATAGCAAATCCAAAA | 55827 |
rs746724506 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976975 | ATGGCATGATCTTGG[C/T]TCACCACAACCTCTG | 55827 |
rs746727435 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971802 | TCATAATGCATTGAT[C/G]CAAGGAAAGCACAAC | 55827 |
rs746729556 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167958424 | ATTGAATGGTCTTGG[A/G]TCTCTTGTCAAAAAA | 55827 |
rs746769749 | snp | C/T | 0.000103268 | 0.00718495 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936863 | TCCCCTCCCCCTCCT[C/T]CCCTCCCCCACGCGG | 55827 |
rs746772620 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168028290 | CTTATTTTATTTTAA[A/G]AAATAACAACAGCAA | 55827 |
rs746777537 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | DCAF6 | GRCh38.p7 | 1:167991256 | TTGCTATTTGCCCAC[C/T]AATACCATATTACCT | 55827 |
rs746783088 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168031499 | CATAGGCCAGATTTT[A/C]GAGCAGGAGACGAAA | 55827 |
rs746786686 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168042775 | AGAAATACATACTAG[A/G]TAATGAAAGGATCCA | 55827 |
rs746801998 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938732 | TTGGACAGTTTAAGT[A/G]CTTGTATATAGTTCT | 55827 |
rs746812267 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001027 | TAAAATGGATCAGAT[A/G]TGGTGGCTCATGCCT | 55827 |
rs746886704 | snp | A/G | 1.71905e-05 | 0.00293172 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168043115 | ACAGAGCTCAGTGCA[A/G]CCACCAGAAGGAGAC | 55827 |
rs746892287 | in-del | -/TC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009403 | TTCTTTCTTTCTTTC[-/TC]TCTCTCTCTCTTTTG | 55827 |
rs746900310 | in-del | -/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936675 | GGAGGAGACTGTTGC[-/T]GATCTTTGGATGTTC | 55827 |
rs746933419 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964203 | CTTTTCTTTAAAGAA[C/T]TCCTTTTGTAATTTC | 55827 |
rs746939898 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936665 | GGGGGCTGAGGGAGG[A/G]GACTGTTGCTGATCT | 55827 |
rs746942825 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007488 | ACCAACCCCCATCTG[C/G]TTTTCAACCCCCTTT | 55827 |
rs746962901 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024802 | AGTGAGACTCTGTAT[-/C]CCAAAAAAAAAAAAA | 55827 |
rs746963503 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168020078 | ACAGCTTTGTACCAT[-/A]TATTTTTCATTCAAT | 55827 |
rs746977411 | snp | A/G | 1.64925e-05 | 0.00287158 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168002547 | TACTGGACCCAGAGC[A/G]AGGCCGGAGAGTGAA | 55827 |
rs747009221 | snp | C/T | 1.65356e-05 | 0.00287533 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044579 | TGTAATTTGGTTTAC[C/T]TACAGAAGCTCCTGA | 55827 |
rs747021200 | snp | A/C | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167934791 | CATTTTCTAGTTTGC[A/C]AAGTCTTAGGCTTGA | 55827 |
rs747030498 | snp | A/G/T | 0.000124462 | 0.00788777 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974819 | TTAACTGCTTTCTTT[A/G/T]TGTGTTTTAGGTTTT | 55827 |
rs747065782 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046482 | ATGTTTCTTTCTTTA[A/G]TCATATTTGGGAAAT | 55827 |
rs747082953 | snp | G/T | 3.31752e-05 | 0.00407265 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003863 | GATAAGACCTATATT[G/T]TAATAGGAGAGCAGA | 55827 |
rs747094628 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167942856 | CCACATTCCATTGAT[C/T]TAGCTTCATGTCTTT | 55827 |
rs747138510 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986202 | GTTTTTACATGCCCC[A/T]TGCAGGCGTTTATTT | 55827 |
rs747163510 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967891 | GTGTGCCACCATGCT[C/T]GGCTAATTTTTATGT | 55827 |
rs747167055 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019108 | AGCTGGAGTGCAGTG[A/G]TGCTATCTTGGCTCA | 55827 |
rs747191406 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050778 | ACAAAGGGAAACAAA[A/G]GTTTTTTTTTAAATT | 55827 |
rs747207803 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964327 | GGGGTACAGTATTCT[A/G]GGTTGGTTTTGCTTT | 55827 |
rs747221943 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167953003 | TTGCTGAAGATCCGC[C/T]TTGCTGAAGATATAT | 55827 |
rs747244133 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168069506 | TACTGTAAGAACTGC[A/G]TAAGCAGTGAATTAA | 55827 |
rs747245027 | snp | A/C | 1.70327e-05 | 0.00291823 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063604 | ATTTTTGTTTTTTTA[A/C]TATGTAATTCATATA | 55827 |
rs747252677 | snp | A/G | 1.81622e-05 | 0.00301343 | missense | DCAF6 | GRCh38.p7 | 1:168045220 | TATCGAGCAGGACCT[A/G]GTGATAGGTTGGTAA | 55827 |
rs747253676 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168031418 | CCAAAAAAATTATCC[C/T]CTAAGTTAGGCAATG | 55827 |
rs747288938 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941946 | ATACTGCATTCCCAC[C/T]AGCAGTATATGAGAG | 55827 |
rs747313841 | in-del | -/CTTTATTTTAGTCTTTAGATTATA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168010014 | ATAGGGTATATTTAG[-/CTTTATTTTAGTCTTTAGATTATA]CTTTTAGCCCCAGTC | 55827 |
rs747337217 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007569 | GATATTTCTCTGTTA[A/G]TACCTTACTAGATTT | 55827 |
rs747356996 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024298 | GTTCCTTTCAAAAAC[A/G]TTTTTTAAAAAATTA | 55827 |
rs747360905 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168074394 | ACATCCTAGTTCCAT[C/T]TCAGTGATGGTAGTG | 55827 |
rs747367665 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945780 | GCTGGGATTACAGGC[A/G]TGAGCCACCACACCC | 55827 |
rs747390024 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168073098 | GGAGAATCGCTTGAA[C/T]CCGGGAGGCGGAGGT | 55827 |
rs747392514 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168038664 | CATATTACTGGACCC[A/C]ACTCTCAGAATTAGG | 55827 |
rs747431050 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167946378 | GTTTCATTCTCTTGC[C/T]TGATTGCTCTGGTTA | 55827 |
rs747446894 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167996217 | TTTGGTTCATTCTTT[A/T]GTCTTAATTTTTTTT | 55827 |
rs747452786 | in-del | -/CT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971273 | CTGTCTTGTGGATAA[-/CT]CTATTATTATATTGT | 55827 |
rs747460982 | snp | A/G | 2.22008e-05 | 0.00333165 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993202 | ACATTATTAATTTTA[A/G]ATAACTTCTTGTTTC | 55827 |
rs747493293 | snp | A/G | 1.65345e-05 | 0.00287524 | missense | DCAF6 | GRCh38.p7 | 1:168038437 | TAAGTTTGCACTACA[A/G]CACAGAAGGAACAAC | 55827 |
rs747509366 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167989630 | GCTCACGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 55827 |
rs747512853 | snp | G/T | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167934769 | TTCAGTCTTTCAATT[G/T]ACAACACATTTTCTA | 55827 |
rs747526756 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022771 | TGGAAATAGAAGAAT[A/G]GTTTCTCAACTCATT | 55827 |
rs747568809 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168060700 | AGTCCAAGACCAGCC[C/T]GGTCAATATGGTGAA | 55827 |
rs747570707 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168032586 | TCAGAATATTTCACC[A/G]TATGTTTTATTTCGA | 55827 |
rs747616202 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968709 | AACCTGTGCATGGTT[G/T]CAGGAGCTCCCATTA | 55827 |
rs747638535 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167990110 | TATAAAATATAGAAG[A/T]CAGTTAATTTTTTGT | 55827 |
rs747640018 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037571 | ATATCCATGTACTCT[A/T]TTTTTTTGGCAGGTG | 55827 |
rs747645638 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167991150 | AATATTTTAAATATA[A/C]TTTCACCTCTGCTGT | 55827 |
rs747661098 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167991185 | CTATATGTAATTGGT[A/G]TTATGTTATGTTTTG | 55827 |
rs747670255 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024579 | TGGAGGCCAAGGCAG[A/G]CAGATCACCTGAGGT | 55827 |
rs747704216 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | DCAF6 | GRCh38.p7 | 1:167991267 | CCACCAATACCATAT[C/T]ACCTTGCTGTTGGTT | 55827 |
rs747723379 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167987020 | TGTTGTATAACCATT[-/A]ACCACAATTAAAATT | 55827 |
rs747729413 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168051451 | GATGATATATAAGCC[C/T]CAAGCACTTCTCTAT | 55827 |
rs747755505 | snp | A/G | 0.000107099 | 0.00731696 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066335 | CATATCCTGAATTGC[A/G]TGTTTCTAGGCTTCA | 55827 |
rs747796586 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168047515 | TTGAGTATTTAGCCT[A/G]TGTTGGTCCTACATG | 55827 |
rs747818426 | in-del | -/GTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168033807 | CTGCTGATGTCATCA[-/GTT]GTTCTTAATAACCAT | 55827 |
rs747833725 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168038823 | TGCAAAAATATAAAC[A/G]TTTTGGGACTTTTTG | 55827 |
rs747838962 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168016734 | TTCAAGATGGGTAAT[A/C]GATACTGTAAATCCT | 55827 |
rs747852910 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167946901 | TTATAGAATAAGTTA[A/G]GGAGAGGCCTGTCCT | 55827 |
rs747854156 | in-del | -/TG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945904 | CTACTAATTTTTGTA[-/TG]TTGATTTTGTATCTT | 55827 |
rs747865303 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961246 | GGTTTTATTTTGTTT[C/T]GTTTTGTTTGTTTTG | 55827 |
rs747878751 | snp | A/G | 0.000133975 | 0.00818348 | synonymous-codon, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936935 | GGGTGGCTCCTACCC[A/G]CACCTGTTGTGGGAC | 55827 |
rs747879449 | snp | A/G | 1.75108e-05 | 0.0029589 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066480 | AGTAAGATTTTTATT[A/G]TACTTACTATAGACC | 55827 |
rs747888827 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954416 | ACTTTTGTGAATTAC[C/T]CCTAGATTTGTGCTT | 55827 |
rs747897025 | snp | A/C/G | 5.49032e-05 | 0.00523919 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937019 | CCTGGGTGAGCGGGG[A/C/G]CCCCGGGGCGGAGGC | 55827 |
rs747961658 | snp | A/G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168045392 | TGTAAATGATTTTAC[A/G/T]TATTATATTCTTTGA | 55827 |
rs748019228 | snp | C/T | 1.65496e-05 | 0.00287655 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168003886 | AGAGCAGAGTCCCAA[C/T]GTGTCATTGATGCAG | 55827 |
rs748052348 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168067468 | CACAGAAGAAATAAG[A/G]ATTGGACAGAAGTCT | 55827 |
rs748069135 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977663 | AATTTTCAGTCAGTA[A/G]GTCTTTGGTTTACTA | 55827 |
rs748090998 | snp | C/G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030076 | TCTGGCTCTGGCATC[C/G/T]GTGATCATAACCACT | 55827 |
rs748094622 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001291 | TGTGAGACCCTGCCT[A/G]GAAAAAAAAAAGTTA | 55827 |
rs748099536 | snp | A/T | 1.65269e-05 | 0.00287457 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974948 | TAATATTTTATACCA[A/T]CGTTGAGCAAGATGC | 55827 |
rs748119322 | in-del | -/A/AA | 5.08365e-05 | 0.00504144 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966757 | GTAATTTAATGAGAG[-/A/AA]AAAAAAAATCAAGAA | 55827 |
rs748119678 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939157 | CCTTTACACTGTTAT[G/T]CAGCTCTTCTATACT | 55827 |
rs748138049 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071195 | GTCAGTTAATTTTTT[G/T]GTTAATGGCCAGATA | 55827 |
rs748143217 | in-del | -/TTG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168012727 | CTTCTGAGCCTGATT[-/TTG]TTTTTAATCCAAGGA | 55827 |
rs748150100 | snp | A/G | 1.74306e-05 | 0.00295211 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004502 | TAGAAAATATTTAAA[A/G]TTTGAATTTGCCTTA | 55827 |
rs748263366 | snp | C/T | 1.64904e-05 | 0.00287139 | missense | DCAF6 | GRCh38.p7 | 1:168063626 | ATTCATATAGACGCT[C/T]TGCTGTTGCCCGTAT | 55827 |
rs748264090 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167999672 | TGAACCAACCTCTGT[A/T]AGCTTCAGACTTTTA | 55827 |
rs748290013 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168006550 | TTATTCTGGAGTTCA[A/G]CGTTTCAGGAGTAAG | 55827 |
rs748294635 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937185 | CTCCCCCAGTCAAGC[C/T]CCCTGTGCATGCTGC | 55827 |
rs748296532 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019314 | CAGCCACCCAAAGTT[C/G]TGGGATTACAGGTGT | 55827 |
rs748312142 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168045917 | TATCATATCTTATTG[-/T]TAAGTTCTGTCCTCT | 55827 |
rs748316865 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | DCAF6 | GRCh38.p7 | 1:168063758 | GCAACTCCAGGACAA[C/T]GGTACCAAATGTTCA | 55827 |
rs748332329 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034540 | GGGGAGGAAAAGTCC[A/G]TAACTAGAGAAAAAA | 55827 |
rs748337461 | snp | C/T | 0.0004669 | 0.0152719 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023067 | GTGCAACAGGAGATG[C/T]GCTATGCCCATCCAT | 55827 |
rs748360354 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986273 | CTTTAATAGATATTG[A/T]TACATAGTTTTCCAT | 55827 |
rs748362023 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168025091 | ACTCTATAATTAAAG[C/G]ATTTTTTTTCTAAGG | 55827 |
rs748375177 | snp | G/T | 1.6552e-05 | 0.00287676 | missense | DCAF6 | GRCh38.p7 | 1:168038458 | AAGGAACAACTACAA[G/T]CACAATAAAACTGAA | 55827 |
rs748379648 | snp | A/C | 1.78401e-05 | 0.00298659 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935710 | AGGAAGGTCTCGATA[A/C]GGAGCCATTCAGGGT | 55827 |
rs748389537 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962460 | AATACCCTTCTTTTT[A/C]CCTGATAATTTTTCT | 55827 |
rs748413206 | in-del | -/CGCG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041891 | GAAATACATGTTTGT[-/CGCG]CACACACACACACAC | 55827 |
rs748428757 | snp | C/T | 1.64906e-05 | 0.00287142 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167993323 | ATCTCTGTGTTACAG[C/T]GAAGATGGTCAAGAG | 55827 |
rs748466645 | snp | A/T | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997050 | ATTGGGGATTTTTTG[A/T]GTGTTTTGTCCATTG | 55827 |
rs748477521 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985658 | ATTCGTAGGTTCTAA[C/T]AAATAGGATGTAGAT | 55827 |
rs748497002 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168012486 | TATTTATTGTATTCA[A/G]TTTTCAGTTTGGGTC | 55827 |
rs748522149 | in-del | -/TATT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167987860 | TGTACATTTAAAATA[-/TATT]TATGAAAATTCAAAT | 55827 |
rs748551016 | snp | C/T | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935932 | TAGTCACTTTTCCTG[C/T]CACGACGACTCGCGT | 55827 |
rs748556637 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998183 | CTTTTGGTTTCCCAG[G/T]GCATGTAAAAGTTAT | 55827 |
rs748608605 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168011185 | GCAGTGGCGCGACCT[C/T]GGCTCACTGCAACCT | 55827 |
rs748632421 | snp | C/T | 1.69893e-05 | 0.00291451 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167951850 | GCAACCCTTAATGTG[C/T]ATGATGGTTGTGTAA | 55827 |
rs748640034 | snp | A/G | 1.66134e-05 | 0.00288208 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167993428 | TCCTTCTGCGGAAGA[A/G]AGAAGAGAAGAGGTA | 55827 |
rs748641731 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167980105 | AGAATCACTTGAACA[C/T]GGGAGGCAGAGGTTG | 55827 |
rs748671404 | in-del | -/GAG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168067558 | TGTGCCAAAGCATGA[-/GAG]GGTAAATGAACCATC | 55827 |
rs748687203 | snp | A/G | 1.77037e-05 | 0.00297515 | missense | DCAF6 | GRCh38.p7 | 1:168075374 | CTGTGTTTCCAGACC[A/G]GTTGGAGGGTGACAG | 55827 |
rs748706067 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937479 | CTCAGGGACTTCACG[C/T]TCCAGACAGAATCCG | 55827 |
rs748706633 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167980916 | TTTTCTCTGAATTTT[-/C]TTTTTTTTTTTTTTT | 55827 |
rs748713628 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046637 | ATTTTAGGCAAGTAA[A/G]ACTTAGTTCTATTTC | 55827 |
rs748722296 | snp | C/G | 1.65176e-05 | 0.00287376 | missense, intron-variant, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167966654 | TCTGTTGGAATGACA[C/G]TGGAGAATATATTTT | 55827 |
rs748730585 | in-del | -/TC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167946172 | ATGTTGGCCAGCTGG[-/TC]TTGAACTACTGACCT | 55827 |
rs748736603 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167992846 | TACGTTGCATACTAA[A/T]GTATGTAGTATGCTA | 55827 |
rs748742223 | snp | C/T | 1.65141e-05 | 0.00287346 | missense | DCAF6 | GRCh38.p7 | 1:168044918 | AATCAGATAAGTTCA[C/T]AGCCAAGCCATTGGA | 55827 |
rs748770330 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168026297 | GTGGTAAATAATATT[C/T]GTTAAACGAGTGAGT | 55827 |
rs748774862 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167980338 | TCGGATCTGTACCCA[G/T]AAGTAGAGATTGCTG | 55827 |
rs748781948 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167981379 | GGATTCATTTTTTTC[C/T]TCAACTTTTATTTTA | 55827 |
rs748787337 | snp | C/T | 2.19272e-05 | 0.00331106 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936964 | ACGTGAGGAAAAGGT[C/T]CCTCGGGCTGGAGGA | 55827 |
rs748789159 | snp | C/T | | | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168076009 | TCATTTCTCCTTCCA[C/T]GGTACAGCTGACCCT | 55827 |
rs748792905 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167987116 | GAGAAGAAAATTTGC[C/T]TACGTATTTATTGTA | 55827 |
rs748815679 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041118 | TACTTCATAGGTTTA[C/G]TATGAAGATTTAATG | 55827 |
rs748816059 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168067607 | TAGAGTACATGCACA[A/G]AAGTAGCTTAATCAA | 55827 |
rs748827787 | snp | C/T | 3.5643e-05 | 0.0042214 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066495 | GTACTTACTATAGAC[C/T]ATATTTCAATTTGTT | 55827 |
rs748862783 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968044 | CCCAAATTTCTTGTA[C/T]CTTTAAGTCTTTTAA | 55827 |
rs748864022 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948398 | CCCCAAGTAAGAACT[A/T]AGGCTCTGAGAAAAT | 55827 |
rs748880860 | snp | C/T | 1.67694e-05 | 0.00289558 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168068411 | AAACACCATTACAGT[C/T]CCAGCCTCTTTCATG | 55827 |
rs748889182 | in-del | -/TC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167991393 | TTCAAAGAGTAAATC[-/TC]TATGACATTTTCAGT | 55827 |
rs748908390 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968957 | GTGAAATTTACTTCA[C/T]TAATATTTAGGTCTT | 55827 |
rs748918859 | in-del | -/TAAT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168025544 | GGTGGAAAATATATC[-/TAAT]TAATTAAATCCTGAG | 55827 |
rs748942762 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962651 | TTTTTGATCCACTCT[G/T]ACAGTCTCTGTCTTA | 55827 |
rs748964332 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024999 | TTTTATATGTTTATT[A/G]CAGAGGTATTAACAA | 55827 |
rs748992913 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168018944 | ATTTAGATAGTGTAG[C/T]TTGCTGTAATTTACA | 55827 |
rs749026499 | snp | A/T | 4.98774e-05 | 0.00499362 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044690 | AGTTGCTCCCTTTAG[A/T]TAATTGCTTTGTATG | 55827 |
rs749030276 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167993622 | AGCGTGGTGGCACAT[A/G]CCTGTAATCCCAGCT | 55827 |
rs749064105 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961306 | GGAGTGCAGTGGCGC[G/T]ATCTCGGCTCAATGC | 55827 |
rs749075535 | snp | C/T | 1.73246e-05 | 0.00294312 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004513 | TAAAATTTGAATTTG[C/T]CTTAACATGTGTTTT | 55827 |
rs749128244 | snp | C/G | | | missense | DCAF6 | GRCh38.p7 | 1:168004550 | GGAACAAGTCAATCA[C/G]ATATTTCAACTCTTC | 55827 |
rs749162405 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168067851 | GTTCACGAGTATTCA[A/G]GTAATCCTATTCTTG | 55827 |
rs749188174 | in-del | -/ACCCG | 1.764e-05 | 0.00296979 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993489 | CGCGGTGGCTCACGC[-/ACCCG]CTGTAATCCCAGCGC | 55827 |
rs749211357 | in-del | -/T | 1.71793e-05 | 0.00293076 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068351 | GATTTTTAACTTGCC[-/T]TTGTAGGTTATAACT | 55827 |
rs749224117 | snp | C/G/T | 3.29969e-05 | 0.00406172 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167987530 | CCCTTACACTTTTCT[C/G/T]TCTTGTGGTGAAGAT | 55827 |
rs749229416 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982789 | AGGATTCTTATAGTT[C/T]GAGGTCTTACATTTA | 55827 |
rs749229561 | snp | A/G | 3.29582e-05 | 0.00405931 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063773 | TGGTACCAAATGTTC[A/G]TGGCATTTTTTGGTG | 55827 |
rs749255770 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017322 | AGAAAAATAAAATGT[C/T]CCTACGTATATAATT | 55827 |
rs749299050 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057316 | CTAGTACTTTTAAAA[C/T]GGGTTTATAGACTGT | 55827 |
rs749345528 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072905 | AACAGAATAAAAGGA[A/T]CCTTTCTACAAATGT | 55827 |
rs749353269 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167950675 | AGTATAGGCAGATAC[A/C]ATTTTATGAGAGATC | 55827 |
rs749386826 | in-del | -/ATAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167960842 | TCTTTGGCATCTCTT[-/ATAA]ATAAACTTTAGAATC | 55827 |
rs749416135 | snp | C/T | 0.000221558 | 0.0105228 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168065607 | AAAAGAAGCCAATTT[C/T]TGGGGTGCTAACTTT | 55827 |
rs749421326 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995054 | AAGAAGGGTATGATG[A/G]CTAATAAAATGATTT | 55827 |
rs749439776 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071872 | CACTACATTTTAGCC[A/G]TACTGGCCTCTCTTC | 55827 |
rs749459860 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049431 | TTGTTGTTGTTGTTG[-/T]TTTTTTTTTTTTTTT | 55827 |
rs749462500 | snp | G/T | 1.64811e-05 | 0.00287059 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042996 | TGATTAACTTCTTGG[G/T]GGAATCACTTATCTT | 55827 |
rs749474809 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001545 | GAAGGAGGAGTGGTA[A/G]ATTGAATATAGAATT | 55827 |
rs749480130 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168021137 | TTTTTTCCCCGTGAC[G/T]TATTCTTTCTTAAAT | 55827 |
rs749489280 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976286 | CCGGCCTGGCCAACA[C/T]GGTGAAACCCTGTCT | 55827 |
rs749537504 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964252 | GGCAACAAATTCCCT[A/C]AATGTTAATTTATCT | 55827 |
rs749545155 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058696 | GCCTTAGCCTCCCAG[A/G]TAGCTGGGATTACAG | 55827 |
rs749561231 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062350 | TTGTTTGCAAAAATT[C/T]ATTGAGCTTTTTACC | 55827 |
rs749565512 | in-del | -/TTCA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168027869 | TGTTTAGCCTGAATC[-/TTCA]TTCATTAATGCAGCT | 55827 |
rs749569969 | snp | C/T | 1.65389e-05 | 0.00287562 | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167966692 | TCAGATGACACCAAA[C/T]TAGTAATTAGTAATC | 55827 |
rs749586768 | in-del | -/C | 0.000339533 | 0.013025 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966766 | TGAGAGAAAAAAAAT[-/C]CAAGAAGGCAGAAAT | 55827 |
rs749594782 | in-del | -/AT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948346 | GCCAAGGATGAAATA[-/AT]TTTGTGTTTTGTCTC | 55827 |
rs749597806 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986318 | TTTATACTCCCATCA[A/G]CAATGTGTTCCGTAA | 55827 |
rs749602799 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057616 | TGTGCTAGATACTCT[-/A]GGTGGGTGCTGGTGA | 55827 |
rs749610316 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167999406 | CCCCTAACAAGAGAA[A/C]CAGCATGTCCTTCGA | 55827 |
rs749635416 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034733 | CATAAAGCTATTTGT[A/G]TGTTTACTTGAAGTT | 55827 |
rs749646909 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022915 | TTTGTTTCTTAAGCT[C/T]AGAGATGATCATGAC | 55827 |
rs749674581 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035881 | CAGCCTGGCTAACAT[A/G]GTGAAACCCCATCTC | 55827 |
rs749719878 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168020241 | CCTCATTTTACAGAT[A/G]GAGAAACTGAGACTT | 55827 |
rs749724505 | snp | C/T | 1.64999e-05 | 0.00287222 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168045057 | TAGCACTGAGAGTGC[C/T]ACCAATGAAAATAAC | 55827 |
rs749754257 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998284 | ATTTAAAAATACTTC[A/G]TTGCTAAAAAGTGCT | 55827 |
rs749758867 | snp | G/T | 1.85269e-05 | 0.00304354 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974787 | AATGAATATTTCTAG[G/T]AAATAATAAGTTACC | 55827 |
rs749767800 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024239 | AAAAAAAAAAAAAAA[A/G]AACAGAAAAAAGGCA | 55827 |
rs749786136 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167988189 | TTTTGAGACAAGGTC[C/T]CACTGTGTCATCTCA | 55827 |
rs749810830 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013808 | TGGAGTGCAATGGTG[C/T]AGTCGTGGCTTACTG | 55827 |
rs749823369 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049552 | TAGGCGTGAGCCACC[A/G]CGCCTGGCCATATAC | 55827 |
rs749834996 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167979322 | CACACTTTAATTAGC[A/G]TAGAATTTTTTTTTT | 55827 |
rs749857445 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168029636 | TATGTAGTTGGTGCT[A/G]TTATTACCCCCATTT | 55827 |
rs749864251 | snp | C/T | 3.30426e-05 | 0.0040645 | missense | DCAF6 | GRCh38.p7 | 1:168004781 | TCTGGACACCACACA[C/T]ATCATCAGTCTGGTG | 55827 |
rs749890037 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168043712 | TTCTTATAAATGTGT[A/G]GGTACCTTAGTATAA | 55827 |
rs749894234 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939999 | TGCTAAATAGTAAAA[C/T]TGGGATAGAACAAAT | 55827 |
rs749913884 | snp | C/T | 1.65754e-05 | 0.00287879 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167993416 | AGAACTTAAAACTCC[C/T]TCTGCGGAAGAGAGA | 55827 |
rs749923949 | snp | A/T | 1.69539e-05 | 0.00291147 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168043091 | GGGTCAGGAGGAATC[A/T]TTCGTCCCACAGAGC | 55827 |
rs749946946 | in-del | -/TT | | | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168075850 | TACCCTGAATTTGAC[-/TT]TTTATTTAATGCCTT | 55827 |
rs749953064 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167983176 | CATGTGAATTTTAGA[A/G]TAGTTTTTTCTAATT | 55827 |
rs749997121 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030535 | AGACTGAATCACTTA[C/T]GAAGTTCTCCTGGTA | 55827 |
rs750027861 | snp | A/G | 1.65241e-05 | 0.00287433 | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075470 | ACTTAAATGTTCTGA[A/G]ATTTGTATAAGACAT | 55827 |
rs750046667 | snp | C/G | 4.95651e-05 | 0.00497796 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966617 | TATATTTCTTTTTTG[C/G]TTTCTCTTTAGGTTA | 55827 |
rs750058521 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000896 | GGATGATGAAAACGG[C/T]CTGGAATTATATAAT | 55827 |
rs750060435 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167994412 | CAATAGAAGTTTTAC[G/T]TATTACCATTTACTC | 55827 |
rs750080713 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030584 | TGATAAAAGTAAGGT[A/G]GGAGAGATGTGAAGA | 55827 |
rs750088510 | snp | A/C | 1.67882e-05 | 0.00289721 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966750 | AAAAATCTGTAATTT[A/C]ATGAGAGAAAAAAAA | 55827 |
rs750149895 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167965823 | TATTTTTAGTAGAGA[C/T]GGGGTTTCGCCATAT | 55827 |
rs750158437 | snp | A/G | 1.64942e-05 | 0.00287173 | missense | DCAF6 | GRCh38.p7 | 1:168045043 | ACTTCAGATCAGACT[A/G]GCACTGAGAGTGCTA | 55827 |
rs750170351 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168026820 | CAAAGTGATCTGAGG[G/T]AGAAATAAAGGTAAG | 55827 |
rs750213293 | snp | A/G | 1.64863e-05 | 0.00287104 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168004744 | TTCTCCAGACAGTGA[A/G]CAAAGGCAGTCTGTT | 55827 |
rs750242684 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976592 | GTTATTCTGGAGGTT[A/G]CCCCAGCTACTTTCA | 55827 |
rs750296880 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057954 | TGTCCATCTGCCTAC[C/T]ACGCCAGTGGTAACC | 55827 |
rs750335634 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057475 | CTTCAGATTTACTCT[C/T]TTCCTCCATTAAATG | 55827 |
rs750382616 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072479 | TTTATTGTCTTATTA[A/C]AGATTAGAGGAGAAA | 55827 |
rs750389346 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035741 | ACATGTTTTGTAATA[A/T]GTAGATTATATTCCT | 55827 |
rs750396803 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944333 | TTTTGTAAAAATCTA[A/G]TAGTGGGATTGCTAG | 55827 |
rs750454705 | in-del | -/ATTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005118 | AAAATATCTTTCTAG[-/ATTT]ATTTGGTTTTATGTC | 55827 |
rs750457636 | snp | A/G | 1.65181e-05 | 0.00287381 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167991323 | TGATCGGCGAATGCT[A/G]GGCACAAGAGCTACA | 55827 |
rs750459192 | snp | A/G | 1.65586e-05 | 0.00287733 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936907 | CACCCGGCTCAGGCA[A/G]AGCCATGTCTCGGGG | 55827 |
rs750477813 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167980878 | TATCTAATAAATCAT[C/T]GTAAAATCCAATGTC | 55827 |
rs750492982 | snp | A/G | | | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075594 | TTGGAATGATTGTGT[A/G]CATGAATTTGGGAGA | 55827 |
rs750500517 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040371 | AGGTTATTTCTGGTT[A/G]TTGTGTTGAGCATAT | 55827 |
rs750508464 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168012019 | GTGGAAATATTAGGT[C/T]AATGGCCATTTTTGG | 55827 |
rs750521609 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040946 | AGTATACAGACTTTT[C/T]CATCTATATCAGGAT | 55827 |
rs750535345 | snp | A/G/T | 3.38801e-05 | 0.00411571 | missense | DCAF6 | GRCh38.p7 | 1:168066412 | GATTATGACATAAAG[A/G/T]TCTGGTCACCATTAG | 55827 |
rs750553471 | snp | A/C | 3.31796e-05 | 0.00407292 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044555 | CCCTCATGGATACCA[A/C]GGGATGACTGTAATT | 55827 |
rs750565473 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037854 | TCAGGTGCAGACTGT[G/T]ATTCCTCCCTAAATT | 55827 |
rs750596038 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167973014 | GTCTGCTGAATGTTA[C/G]TAATGCACAGCCAAA | 55827 |
rs750611972 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046335 | CAAGATAGTCTATGA[A/G]GCCACTTTAATTTTT | 55827 |
rs750658900 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945564 | TGGCACAATCTCGGC[G/T]TACTACAACCTCCGG | 55827 |
rs750718341 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168066857 | ACAGCTATTTTTCCA[C/T]TTTGAGTTTTTCTTA | 55827 |
rs750724509 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935677 | GCCTCTAAAAGGTCC[A/G]TTTTAGAGGAAGCGA | 55827 |
rs750731550 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970675 | GCTTTTTAAAATTTT[A/T]AAACACCAATGATTC | 55827 |
rs750755058 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001659 | TTTTTTCTTAAAAAT[A/G]ATAAGAACCTTTAGC | 55827 |
rs750778714 | snp | A/G | 1.71767e-05 | 0.00293054 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004027 | GTCATCAGAAAGCTG[A/G]CAAAAACTACTTATT | 55827 |
rs750808072 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168065150 | TTTAGCAGTTAATAA[G/T]TAAGCACCTATTGTA | 55827 |
rs750844502 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167994264 | CTTGATAGCAAAATG[-/T]TTATCTTAACTTTGT | 55827 |
rs750863985 | snp | C/T | 0.000373297 | 0.0136568 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063590 | GAATATTTTTATTTA[C/T]TTTTGTTTTTTTAAT | 55827 |
rs750868535 | snp | A/C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168067142 | TATGAAAATGAGAAT[A/C/T]CATTGCTAAAAATGT | 55827 |
rs750874408 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168038121 | ACTAAATATGGTTCT[A/C]AATGTGTGTGATTTC | 55827 |
rs750877433 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168028775 | TATCACCAAATTGAA[A/C]TTTCATTTTAGTACT | 55827 |
rs750907595 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971574 | TTTGGGAGTGTTGTA[C/T]GTGACATGATTAAGA | 55827 |
rs750908967 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168020773 | GAAAATATTTATGTA[A/G]GATAGGAGTTCTAGG | 55827 |
rs750922643 | snp | A/G | 1.68858e-05 | 0.00290561 | synonymous-codon, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974991 | ACAATGCCAATTTAC[A/G]TGTCATTATGGAACT | 55827 |
rs750930142 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052014 | GCCTCCTGAGTATCT[A/G]GGATTACAGGCGCCC | 55827 |
rs750979321 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167956884 | TTATGTTAATGATTT[C/T]TGATTTAATTCCATT | 55827 |
rs750982053 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972921 | GTGACTGATGAAGCA[C/G]TGAGGCTCCTGCTTT | 55827 |
rs751022802 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168032199 | ATTGCACTTTGTTTC[A/G]TTTTGGCTTGCATAG | 55827 |
rs751083015 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167973010 | TAATGTCTGCTGAAT[A/G]TTACTAATGCACAGC | 55827 |
rs751083301 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168047376 | CTGGAACTGATCCCA[C/T]TTCATGCATATACTC | 55827 |
rs751113476 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167942143 | TGATCTTGGCTTACC[A/G]CAACCTCTGCCTGCT | 55827 |
rs751118325 | snp | G/T | 1.71959e-05 | 0.00293217 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974846 | TTTTGACAACAATTC[G/T]TTCAGGGCACCGAGC | 55827 |
rs751122562 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168018084 | ATAGAACTCATGGGA[A/C]TATTCTGTGAAATCA | 55827 |
rs751163250 | snp | C/G | 1.67186e-05 | 0.0028912 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168045189 | TGATGACCCAGTCCT[C/G]ATCCCAGGTGCAAGG | 55827 |
rs751180148 | in-del | -/A | 4.45286e-05 | 0.00471829 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987641 | ATACAAATGATGCAG[-/A]AAAAATTAAGGTTAT | 55827 |
rs751233369 | snp | A/G | 3.41233e-05 | 0.00413043 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045274 | AAAAATGTATTTCAC[A/G]AGGATTTGTTTGAAG | 55827 |
rs751235539 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167984685 | ATGAGTAAAAATTCT[A/C]ATTTTCCTTGAAATG | 55827 |
rs751235724 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005131 | AGATTTATTTGGTTT[A/T]ATGTCTATATTAAAG | 55827 |
rs751257358 | in-del | -/AG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037973 | TGTATCTTACATCTC[-/AG]TGTTTCTGAAAGAGC | 55827 |
rs751283034 | snp | A/G | 3.68168e-05 | 0.00429034 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068499 | ACTAAAACCATTTTT[A/G]TATTTGAAAATATAT | 55827 |
rs751292439 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058448 | GATTCTTGTTGTCAC[A/G]TATCTTGATTTTTCT | 55827 |
rs751309305 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167953685 | GCTCACTGCAACCTC[C/T]GTCTCCCGGGTTCAA | 55827 |
rs751321770 | snp | A/G | 0.000158265 | 0.00889425 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019585 | CTCCTGCTCAGAGTG[A/G]CAGCACCCTGTGGAG | 55827 |
rs751363577 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935318 | AAAGTGACCTTTACT[C/T]CAAACCCTACAGTGC | 55827 |
rs751372053 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167966082 | GCCAAGACTCCTTGT[A/G]TTTACCTGTTCATCT | 55827 |
rs751380512 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072802 | CTTCCATTGGGAAAT[G/T]TTTTTCTTATCTACC | 55827 |
rs751400131 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938641 | TTTGCGGAGAAAGAA[C/T]TTAATTTTAGCTTAA | 55827 |
rs751434646 | snp | A/T | 1.68545e-05 | 0.00290292 | missense | DCAF6 | GRCh38.p7 | 1:168066431 | GGTCACCATTAGAAG[A/T]GTCAAGGATTTTTAA | 55827 |
rs751436107 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009800 | TTATTCTCTTCTATA[C/T]AACCCTGTTTATTTT | 55827 |
rs751467532 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167989112 | ACAAAAAAACCTTTA[A/T]ACATACAGTTTAATC | 55827 |
rs751467799 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168027706 | AATGTTACTAATAAA[-/T]TTTTTTTAAAAATTT | 55827 |
rs751478008 | in-del | -/GT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985213 | GTGTGTGTGTGTGGT[-/GT]GTGTGTGTGTGTGGT | 55827 |
rs751485109 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071041 | TAAATCGTTCACAGA[-/T]TGACTCCCTCAGTAA | 55827 |
rs751501475 | snp | A/G | 1.66045e-05 | 0.00288132 | missense | DCAF6 | GRCh38.p7 | 1:167991336 | CTGGGCACAAGAGCT[A/G]CAGGTAAGAAGATAA | 55827 |
rs751547930 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168059768 | CTCCCACCTCAGCTT[A/C]CTGAGTAGCTGGGAC | 55827 |
rs751570903 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167978268 | GTCATAGAATATATA[C/T]TTGGTTATTTTAGAG | 55827 |
rs751578163 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997967 | ATCACTTCATACCCA[C/T]TAGGATGACTAAAAT | 55827 |
rs751582527 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013594 | CTCTGATACACTGGA[A/G]CTTATCTCCTTTAGT | 55827 |
rs751591039 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167989605 | CATTACTGAGGGGCC[A/G]GGCGCGGTGGCTCAC | 55827 |
rs751610828 | snp | A/T | 3.30497e-05 | 0.00406494 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168044652 | TGCAGAAAACCCAGT[A/T]GAGAACCATATCAAT | 55827 |
rs751671191 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937170 | ATTCCGTGCCGGTGC[C/T]TCCCCCAGTCAAGCC | 55827 |
rs751677220 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049007 | GAAACAATGAAATAA[A/T]ATGAATCTCCACATA | 55827 |
rs751691113 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168015577 | TGTATCTAATTCATC[A/G]TAGTTAAATAGAAGC | 55827 |
rs751721398 | in-del | -/AA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168061685 | GTATTTACATATTTT[-/AA]GTTTTTCTGTAATAT | 55827 |
rs751734893 | snp | A/G | 3.86817e-05 | 0.00439765 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975037 | TATTATTATGATTAT[A/G]TGATATATATGTAAG | 55827 |
rs751745359 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034476 | TGAAGGTGCCACCAC[A/G]CTACCGTGGGTGATA | 55827 |
rs751758843 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167949946 | ATGAGATGTCTGGAC[A/G]ATGCAATAAATTTTA | 55827 |
rs751761453 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168065009 | AAAATACAAAAGACA[A/G]TTTCTTTTATCTGTG | 55827 |
rs751774524 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168012231 | AAAATACTGTATGTA[G/T]TGTAGAGGCAGGATG | 55827 |
rs751803527 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168027412 | TTTACCAAGATTCTT[A/G]TTCTCAGTTTTACCA | 55827 |
rs751808308 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005715 | TCTCTGGAAACTGAT[G/T]CCAGATTACCAAATA | 55827 |
rs751809715 | snp | G/T | 1.7704e-05 | 0.00297518 | missense | DCAF6 | GRCh38.p7 | 1:168004586 | GTCCCATCAAGTCCT[G/T]ATTTGGAAGTGAGTG | 55827 |
rs751836095 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948109 | GAATTGGTCTCTTTA[A/G]TATTATATAACGACT | 55827 |
rs751863389 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168047724 | TGTGTGTATATATAT[A/G]TAAAAGATGTGTATA | 55827 |
rs751908496 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167991039 | AGTAGAAATCCGAAA[A/G]AAAAGTTAAAAGAAA | 55827 |
rs751917219 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168025883 | GGCTTACAAAACCTA[C/G]ATGACTTGATTTCTG | 55827 |
rs751938652 | snp | G/T | 1.67008e-05 | 0.00288965 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987480 | GATTATCTGCACTTT[G/T]CTTTTCATCTTCAGA | 55827 |
rs751940717 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168038573 | ACTTCGTCATCTTTA[C/T]GTTTTGTTTTGCTAT | 55827 |
rs751957796 | snp | G/T | 1.69063e-05 | 0.00290738 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065579 | TTTAAATAATTTTTT[G/T]TAACCCTTAGATAAA | 55827 |
rs751961480 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168053275 | TGTAAGCACCTTTAA[G/T]GACAGTGTAATACAT | 55827 |
rs751985814 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167973297 | TTCTCAGGTGATATT[A/G]TGGTACATGATGTTA | 55827 |
rs751988217 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070448 | CCACAAAGTACCTCT[C/T]GGCTCATCCATTACT | 55827 |
rs751994875 | in-del | -/AAAG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168011981 | TGTCTCAGAAAAAAG[-/AAAG]AAAGAAAGAAAGAAA | 55827 |
rs751998241 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167992425 | TCTTTCTTTTCGGAA[C/G]TGTGATAGCTTTTAT | 55827 |
rs752004373 | snp | A/G | 1.83954e-05 | 0.00303271 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935701 | GAAGCGAGAAGGAAG[A/G]TCTCGATAAGGAGCC | 55827 |
rs752020599 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974230 | AAAAAAAATCAGGTC[G/T]TGTCAGTTATTTTTC | 55827 |
rs752021344 | snp | C/T | | | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075782 | AATAAATTTCTACAC[C/T]TGCCATTTGCATGTT | 55827 |
rs752056536 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041560 | CCCATAAAGTATAAC[G/T]TGAAGCCATAGCTTT | 55827 |
rs752074482 | snp | A/G | 0.000131458 | 0.00810627 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042979 | ATCCTAAAAGATCAT[A/G]TTGATTAACTTCTTG | 55827 |
rs752116620 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168023226 | TTTTTGGCCTATACA[A/G]ATTATTTTCTATGTA | 55827 |
rs752154814 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167947875 | GTTTTGTAAATGTCT[C/G]TTAAGTTCATTTGGT | 55827 |
rs752162659 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962429 | CTTGGGGAAACTGAC[C/G]TCTTTATCGTTATGA | 55827 |
rs752171575 | snp | A/C | 0.000182399 | 0.00954809 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050936 | ATAGAATAATGAGGT[A/C]ATTCAGTATGTTCCT | 55827 |
rs752283767 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005913 | CACTCAGTTGACATA[A/G]CATTTTAATTTATGG | 55827 |
rs752293371 | snp | A/G | 1.66222e-05 | 0.00288285 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038360 | TCAAATGTTTTAAAC[A/G]CAATTTTCAGATAAC | 55827 |
rs752295885 | in-del | -/TT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064081 | AAGTTTCTGGTGGAT[-/TT]TTTTTTTTTTTTTTT | 55827 |
rs752296176 | snp | A/C | 1.6585e-05 | 0.00287962 | missense | DCAF6 | GRCh38.p7 | 1:168063703 | TTGGATACTTTGAAC[A/C]TTAGAAGGCCGCTAG | 55827 |
rs752330890 | in-del | -/T | 0.00147565 | 0.0271228 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065573 | TGAATTTTTAAATAA[-/T]TTTTTTTAACCCTTA | 55827 |
rs752337879 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040797 | CTAAAAACTGACCAT[A/G]AATTATATTCTCATT | 55827 |
rs752339473 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054758 | TTTCTTTTCTAAGAA[C/G]TACTAAGCTAATATA | 55827 |
rs752384697 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167957352 | ATAAATGGAACCATA[A/C]AATATTGGCTGTTAA | 55827 |
rs752417831 | snp | C/T | 1.65384e-05 | 0.00287557 | missense | DCAF6 | GRCh38.p7 | 1:167993256 | GAGGGACTACTGGAA[C/T]GGTTGCCCGTTTTAT | 55827 |
rs752420047 | snp | A/G | | | missense | DCAF6 | GRCh38.p7 | 1:168045130 | TCAGCTCATGAAGAA[A/G]CATCCACCAGGGACT | 55827 |
rs752448825 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037103 | GAGATTCTCCCCCCC[-/T]CTTTTTTTTTTTTTT | 55827 |
rs752463092 | snp | A/G | 1.66813e-05 | 0.00288797 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168068387 | CGAACTCATGCTGGA[A/G]GAAACTAGAAACACC | 55827 |
rs752515964 | snp | C/T | 4.97624e-05 | 0.00498786 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044682 | TATAAGTGAGTTGCT[C/T]CCTTTAGATAATTGC | 55827 |
rs752566899 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168010092 | GTTTCCAAAATTTGG[C/T]AACACCTAGAAGAGA | 55827 |
rs752568867 | snp | A/T | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997690 | AAATAAATAAAAATA[A/T]AAAGAGTGACCCACA | 55827 |
rs752602819 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167979716 | ACAAGATGAAACCGT[A/G]CCTCTATTGAAACTA | 55827 |
rs752620833 | snp | C/T | 4.0863e-05 | 0.00451994 | intron-variant | DCAF6 | GRCh38.p7 | 1:168075345 | AAAAGTATTTCTCTT[C/T]GCGATTCTCTTATCT | 55827 |
rs752628993 | in-del | -/TCTCTCTTTTG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009408 | TTCTTTCTTTCTCTC[-/TCTCTCTTTTG]TTTCTTTCTGTCTCT | 55827 |
rs752696778 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030919 | ACAACTAAGTGAATG[A/G]CTATTTTCTTAAATA | 55827 |
rs752697126 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064419 | CCTCATATACATTGC[A/G]TCATCAGAAGGTATC | 55827 |
rs752697699 | snp | G/T | 1.64808e-05 | 0.00287057 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168044976 | CAATCTTGATCGCTC[G/T]TGTGGGGTTCCAGAA | 55827 |
rs752716942 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046049 | AAGATACCCTAAAGT[A/G]TCTGTCAACTGAAAA | 55827 |
rs752747972 | snp | A/C | 3.49907e-05 | 0.0041826 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168004618 | AACTGCAATGGAAGT[A/C]GATACTCCAGCTGAA | 55827 |
rs752769673 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036489 | AAAACTAGCCCGAAC[C/T]CAGTCTCTCAGTTTC | 55827 |
rs752775171 | in-del | -/AAAGAAAGCAGTT | 1.66942e-05 | 0.00288909 | frameshift-variant, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974977 | CAGAAACCAACAGAC[-/AAAGAAAGCAGTT]AATGCCAATTTACGT | 55827 |
rs752782463 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035798 | CCGGGCATGGTGGCT[C/T]ATGCCTGTAATCCCA | 55827 |
rs752786686 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168061264 | TTCTTTGATAGCATA[A/G]AAAAAAGTTTTGAAA | 55827 |
rs752797276 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167988125 | AAAGATAATATCTCT[A/G]CTATCAGTTTCTTAT | 55827 |
rs752808656 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049345 | ACTCCTGGGCTCAAG[C/T]GATCTTCCTCCCTCA | 55827 |
rs752831249 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944499 | TTTTTAATAAAAGAC[A/G]TTCTGACTAGGATAA | 55827 |
rs752832437 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959290 | CTTGCTGAAGGACAT[C/G]TTGGGTGCTTCCAAA | 55827 |
rs752872727 | snp | C/T | 4.94809e-05 | 0.00497373 | missense | DCAF6 | GRCh38.p7 | 1:168004707 | CTCCCACAGAAAGCC[C/T]TCATTCTACTCCTTT | 55827 |
rs752874636 | snp | A/G | 0.000181643 | 0.00952829 | missense | DCAF6 | GRCh38.p7 | 1:167987511 | TTATGACTGTACCCA[A/G]TGACCCTTACACTTT | 55827 |
rs752903482 | snp | A/G | | | intron-variant, downstream-variant-500B | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167999222 | GCAGTAGGTCTCAAT[A/G]GTGGGCTTCAAATAG | 55827 |
rs752925883 | snp | G/T | 5.42476e-05 | 0.00520777 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987652 | GCAGAAAAAATTAAG[G/T]TTATAATTAAAATTG | 55827 |
rs752932603 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017972 | GATGTTCAAAGGAGA[C/T]ATTACTATGATTTGG | 55827 |
rs752948690 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167990093 | GTTTTATAAGTAAAA[A/G]GTATAAAATATAGAA | 55827 |
rs752954109 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168014679 | AAAACTTTGGGATCA[C/T]TCTGCATCCAAACTA | 55827 |
rs753022328 | snp | C/G | 1.65932e-05 | 0.00288034 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065585 | TAATTTTTTTTAACC[C/G]TTAGATAAAAGAAGC | 55827 |
rs753024228 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168015967 | GTTATTAATGTCAAG[G/T]GTCCTTAAGCAGCTG | 55827 |
rs753025228 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982170 | GGCTCCTTGTATGCC[C/T]TTGGCGAAGTGTCTG | 55827 |
rs753029225 | snp | C/T | 7.63271e-05 | 0.0061772 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936888 | ACGCGGTGGTCTCCC[C/T]TCCCACCCGGCTCAG | 55827 |
rs753043678 | snp | G/T | 3.83318e-05 | 0.00437772 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935833 | GCCTCGGGCACCGGC[G/T]GCCGACATCGCCGCC | 55827 |
rs753047468 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013703 | CCATCAGAATACAGA[C/T]GTGTGTATTAGCTCC | 55827 |
rs753058560 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938426 | CATTATGAAGTACCA[C/T]AGGGTACTCAACCTT | 55827 |
rs753070664 | snp | G/T | 2.17228e-05 | 0.0032956 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042984 | AAAAGATCATATTGA[G/T]TAACTTCTTGGTGGA | 55827 |
rs753077604 | snp | A/C | 3.30126e-05 | 0.00406266 | missense | DCAF6 | GRCh38.p7 | 1:168065746 | CATCCGTTTGACCCA[A/C]GTAAGATATCTTTTC | 55827 |
rs753106040 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041892 | AAATACATGTTTGTC[G/T]CGCACACACACACAC | 55827 |
rs753148120 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168029145 | TGCTCGTGTGTTCTA[C/T]TCTTCTGCTGATCAA | 55827 |
rs753199254 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168074723 | AGTTTCACCAAGGGT[A/G]TAATAGTTGTATTGA | 55827 |
rs753207636 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167963195 | CTTGAACTCAGGAGG[C/T]GGAGGTTGTAGTGAG | 55827 |
rs753226513 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168063870 | TTCAGTATTACATTA[G/T]TAAATCTTCAGTTAT | 55827 |
rs753240397 | in-del | -/TCA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167957525 | CCACATTTAATCTGT[-/TCA]TCAGTTGTTGGATAT | 55827 |
rs753281418 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974109 | CTCAGCATAATTTCA[A/G]TTTGCATTTCCCTTA | 55827 |
rs753287420 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168006891 | CCATCTCTGGTTGAA[C/G]CTAATTGTCTGCCTT | 55827 |
rs753317067 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168026556 | ATTTTAAAAATAGTT[C/G]AAAGGTTGAATTCAT | 55827 |
rs753318675 | snp | A/G | 1.65263e-05 | 0.00287452 | missense | DCAF6 | GRCh38.p7 | 1:168038406 | AGCCCCAAACCAGGG[A/G]CAGGTGAACCAGTTT | 55827 |
rs753413764 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997236 | TAAATAATTGCTGAG[G/T]TTGTAAAACCAGTTC | 55827 |
rs753425349 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168020597 | GTTACAATAAACTAC[A/C]ATTGGACCATATATT | 55827 |
rs753443654 | snp | A/G | 1.67744e-05 | 0.00289602 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038530 | TCTTAGCCATTTTGT[A/G]GGATTGTATTAGATT | 55827 |
rs753451377 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168027763 | TTTTTCTTTGAATAA[C/G]TGTATACACAGTATT | 55827 |
rs753470435 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168042104 | AAAGTCAATTTGACT[C/T]CTGCAGTCAGCCTAA | 55827 |
rs753483406 | snp | A/G | 1.65247e-05 | 0.00287438 | missense | DCAF6 | GRCh38.p7 | 1:167993265 | CTGGAATGGTTGCCC[A/G]TTTTATTCCTTCCCA | 55827 |
rs753496627 | snp | A/G | 1.65405e-05 | 0.00287576 | missense | DCAF6 | GRCh38.p7 | 1:167993400 | AAGATGATACAGCAC[A/G]AGAACTTAAAACTCC | 55827 |
rs753514497 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975989 | TCCTCATGTTTTTGT[A/G]TGTACTTATATATAT | 55827 |
rs753517402 | snp | C/T | 1.65252e-05 | 0.00287443 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966612 | TTGCTTATATTTCTT[C/T]TTTGCTTTCTCTTTA | 55827 |
rs753544060 | snp | A/G | 4.98409e-05 | 0.00499179 | splice-acceptor-variant | DCAF6 | GRCh38.p7 | 1:168044899 | CTTTATTTTCTGACA[A/G]CACAATCAGATAAGT | 55827 |
rs753561908 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057761 | AGTATTAAGGACCCC[C/T]AATCTAACCTGAGGA | 55827 |
rs753590536 | snp | A/G | 1.71047e-05 | 0.00292439 | synonymous-codon, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167951810 | AACAGGAAGAAGAGA[A/G]TTTATCCAAAGATTA | 55827 |
rs753600626 | snp | C/T | | | intron-variant, downstream-variant-500B | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998817 | TTCTTTTGTTGTTTT[C/T]ACCTCATCTGCAGTG | 55827 |
rs753618603 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986031 | GAGATTCATTTATGT[G/T]GCTGAGAATAGTAAT | 55827 |
rs753622282 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035661 | ATTCATTAACAACTT[A/C]AATGAACAAATTCTA | 55827 |
rs753677046 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168047497 | AATATTCTGTACACT[C/T]ATTTGAGTATTTAGC | 55827 |
rs753701285 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997800 | AACAATAAAAAGACA[A/G]ATATCCAAACTTAAA | 55827 |
rs753705423 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986626 | CTTCTCATAAGGAGT[A/G]CACAACCTGTGAGAA | 55827 |
rs753706778 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071489 | AAATACAAAAATTAG[C/G]TGGACGTGATGGTGC | 55827 |
rs753711637 | snp | A/G | 3.49699e-05 | 0.00418136 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974836 | GTGTTTTAGGTTTTG[A/G]CAACAATTCGTTCAG | 55827 |
rs753733109 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968291 | AAATACAGAAATAAC[A/G]GATACTATGAACCGC | 55827 |
rs753737116 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167953840 | CTGGCCTCAGGTGAT[C/T]TGCCCGCCTTGGCCT | 55827 |
rs753820992 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167955900 | TGAGTTAGCTGGGAC[C/T]ATAGGTGCATGCCAC | 55827 |
rs753842818 | snp | C/T | 0.000197668 | 0.00993955 | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168015813 | GAGATAGCTTTGCTT[C/T]GTAAGCGCCTGCAAC | 55827 |
rs753843473 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037489 | CCCTATGTATTTTAA[C/T]GTTTCCCAAACTGTT | 55827 |
rs753887234 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167989464 | GAAAAACTGGTAACT[A/C]GAGTAATCCTTAACT | 55827 |
rs753909721 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022424 | GTTTTAATATGCACA[A/G]TATACTGTAGAGTTT | 55827 |
rs753939481 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167978332 | GACTTACATTCCCAC[C/G]AACAGCATGTAAGAG | 55827 |
rs753940627 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168060122 | TAACTTGTATATGAT[C/T]ATGTATCCAGCTACA | 55827 |
rs753949218 | snp | A/C | 1.65201e-05 | 0.00287398 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065756 | ACCCAAGTAAGATAT[A/C]TTTTCTAGGACGAGG | 55827 |
rs753967366 | snp | A/G | 1.68601e-05 | 0.00290341 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168066426 | GATCTGGTCACCATT[A/G]GAAGAGTCAAGGATT | 55827 |
rs753997614 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167969833 | CCAGGCTGGAGTGCA[A/G]TGGCACGATCTCGGC | 55827 |
rs754022376 | snp | A/T | 1.65061e-05 | 0.00287277 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167991215 | GTAGGATATTTTAAT[A/T]AACTGTCGACGTGCT | 55827 |
rs754024630 | snp | A/G | 2.05143e-05 | 0.00320261 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935851 | CGACATCGCCGCCGA[A/G]GGATCGTTGGCAGCC | 55827 |
rs754046451 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168075092 | TCCTTAGAAACCTAG[A/G]CTCCAAAGAACACTG | 55827 |
rs754074932 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959347 | ATAAACGTTTGTGGG[C/T]AGGTGTTGGTGTGCA | 55827 |
rs754087400 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167994940 | TTCCTCATAATTTCA[C/G]GTGTAGAGGGCTGTA | 55827 |
rs754104265 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037989 | GTGTTTCTGAAAGAG[C/G]CAAAATTAGTTCTTA | 55827 |
rs754114376 | snp | C/G | 0.000181505 | 0.00952467 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936897 | TCTCCCCTCCCACCC[C/G]GCTCAGGCAGAGCCA | 55827 |
rs754155661 | snp | C/T | 1.81375e-05 | 0.00301138 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168066384 | ATTTCTAGTTTTAGC[C/T]TCATCTGGCATAGAT | 55827 |
rs754164857 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945647 | CAAGTGCGCACCACT[A/G]TGCCCAGCTAATTTT | 55827 |
rs754170848 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971433 | TCTTAGTAAAACGAG[C/T]GTATAAATCTGTATA | 55827 |
rs754179165 | snp | C/T | 3.40194e-05 | 0.00412414 | missense | DCAF6 | GRCh38.p7 | 1:168043099 | AGGAATCTTTCGTCC[C/T]ACAGAGCTCAGTGCA | 55827 |
rs754179762 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168065360 | ACTATATTGCCCAGG[A/C]TGGTCTCAAACTCCT | 55827 |
rs754283834 | snp | A/G | 0.000909008 | 0.0212997 | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168050931 | AGGTGATAGAATAAT[A/G]AGGTAATTCAGTATG | 55827 |
rs754315525 | in-del | -/A | 2.19546e-05 | 0.00331313 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042983 | TAAAAGATCATATTG[-/A]TTAACTTCTTGGTGG | 55827 |
rs754329922 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168066602 | AAATTTTAAGAAAAA[G/T]AAAAATTAAGATAAA | 55827 |
rs754348789 | in-del | -/AA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024220 | GACCCCCATCTCTTT[-/AA]AAAAAAAAAAAAAAA | 55827 |
rs754349991 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982295 | TCGCCAGGCTGGAGT[A/G]CAGTGGTGCGATCTC | 55827 |
rs754351060 | snp | A/G | 1.66638e-05 | 0.00288645 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003821 | TTTTGTATTAATGAA[A/G]GATTCTGACTTATTA | 55827 |
rs754366442 | in-del | -/TGTTTAAA | 1.71861e-05 | 0.00293134 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987448 | TTTTTCAGAGCCGTC[-/TGTTTAAA]TGTTCGTATGATTAT | 55827 |
rs754382234 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939890 | TTCAATATTTAAACA[C/T]TACGATTGTCTATCT | 55827 |
rs754404105 | snp | A/C | 3.40032e-05 | 0.00412316 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004009 | TTTTTAATGTTAATT[A/C]AAGTCATCAGAAAGC | 55827 |
rs754458571 | snp | A/G | 1.6498e-05 | 0.00287206 | missense | DCAF6 | GRCh38.p7 | 1:168045053 | AGACTAGCACTGAGA[A/G]TGCTACCAATGAAAA | 55827 |
rs754460269 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167973034 | GCACAGCCAAAGCCA[A/G]TGGCCTAACAAACGA | 55827 |
rs754473396 | snp | C/T | 1.69441e-05 | 0.00291063 | synonymous-codon, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974856 | AATTCGTTCAGGGCA[C/T]CGAGCAAACATATTT | 55827 |
rs754491128 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001808 | AATTAGGCTTAAATA[C/G]AATAAATGATACACC | 55827 |
rs754516053 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168004177 | CCCTTCTGGTGCCAT[C/T]GGACCTAGTGCGTAT | 55827 |
rs754540272 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168047439 | TTGAAACCACTCTGG[A/G]ATCACATTTAGTTCC | 55827 |
rs754585469 | in-del | -/CTC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964648 | TGTTCTTTTCTCCTT[-/CTC]CTCTGGTATTCACAT | 55827 |
rs754589200 | in-del | -/TTATG | 1.66864e-05 | 0.00288841 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991186 | TATATGTAATTGGTA[-/TTATG]TTATGTTTTGTAGGA | 55827 |
rs754625017 | in-del | -/CG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041893 | AATACATGTTTGTCG[-/CG]CACACACACACACAC | 55827 |
rs754629831 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971810 | CATTGATCCAAGGAA[A/G]GCACAACTAAGAAGA | 55827 |
rs754633976 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168045364 | ATAAACTTAAAGAAA[C/T]TTTACAGTTTACTGT | 55827 |
rs754658471 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168032299 | GCCTCACAGTTATCT[C/G]TAGGGTAGATAGATC | 55827 |
rs754667762 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941538 | ATTCTCTAGGTGTAT[A/G]TATAAACCTTACTAG | 55827 |
rs754675886 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052372 | AAACACTAAAGTAGA[A/G]ATTATCATGAACTGA | 55827 |
rs754699090 | snp | A/G | 4.97698e-05 | 0.00498823 | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168023021 | TTAACAAACAGCTCG[A/G]ATCCATGTCACTTGA | 55827 |
rs754699999 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995770 | CTTATTTGTAATTCT[G/T]ACACATTTTGGTGTT | 55827 |
rs754717069 | snp | A/G | 1.64762e-05 | 0.00287016 | missense | DCAF6 | GRCh38.p7 | 1:167991258 | GCTATTTGCCCACCA[A/G]TACCATATTACCTTG | 55827 |
rs754719139 | in-del | -/AAAT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167980181 | GAGACTCCATCTCAG[-/AAAT]AAATAAATAAATAAA | 55827 |
rs754741883 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167951465 | CTGTGATCCCAGCCA[C/T]TTGGGAAGCTGAGGA | 55827 |
rs754785790 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167983480 | AAATGCCTTGAACCA[A/G]TAAGCCTTCCAGTCT | 55827 |
rs754841555 | snp | A/C | 1.66277e-05 | 0.00288333 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167991338 | GGGCACAAGAGCTAC[A/C]GGTAAGAAGATAATA | 55827 |
rs754844004 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058490 | TAAACAATAATATGG[C/T]CTTGATGTTCATTGC | 55827 |
rs754845179 | snp | G/T | 1.66804e-05 | 0.00288789 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168068384 | AAACGAACTCATGCT[G/T]GAAGAAACTAGAAAC | 55827 |
rs754845180 | in-del | -/TTAC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168061741 | GAGTCAAAGCTTATA[-/TTAC]TTAATTTCTCTTCAA | 55827 |
rs754873419 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938724 | TATCTCAGTTGGACA[A/G]TTTAAGTACTTGTAT | 55827 |
rs754878888 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022165 | AAACTTACTAACTTC[G/T]GATGAGTGCTCTTTC | 55827 |
rs754889771 | snp | A/G | 1.65097e-05 | 0.00287308 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168044598 | AGAAGCTCCTGAAGA[A/G]TCATCAGAGGATGTG | 55827 |
rs754916003 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167978287 | GTTATTTTAGAGATA[A/G]AGCCAAATAGTTTTC | 55827 |
rs754941627 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168060923 | GCATAATTTTTTTCT[C/T]ATTTATAGCTCTTAT | 55827 |
rs754952309 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167956106 | TATGATGTCATCAGT[A/T]TTTTCATGGATGCTT | 55827 |
rs754963290 | snp | A/G | 2.45679e-05 | 0.00350476 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167937007 | GCGGAGTCGATACCT[A/G]GGTGAGCGGGGGCCC | 55827 |
rs754966537 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168047742 | AAAGATGTGTATACT[A/G]AGGTAATTAGAAAGT | 55827 |
rs755035062 | in-del | -/TTATT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168023228 | TTTGGCCTATACAGA[-/TTATT]TTCTATGTAAGCTCA | 55827 |
rs755062399 | snp | A/G | 1.74494e-05 | 0.00295371 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004490 | AGTTGTTGGTTTTAG[A/G]AAATATTTAAAATTT | 55827 |
rs755078734 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943873 | AGATGGAGTCTCACT[C/T]TGTCGCCCAGGCTGT | 55827 |
rs755082324 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964246 | TCTGCTGGCAACAAA[-/T]TCCCTCAATGTTAAT | 55827 |
rs755102366 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034482 | TGCCACCACGCTACC[A/G]TGGGTGATAGAGCAA | 55827 |
rs755113040 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167957840 | TCCTAGTGGATGTGA[A/C]GTGGTAATTTGTTGT | 55827 |
rs755147531 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986814 | GACATAGGGAGAGAA[G/T]AACTTATTGAGGCAG | 55827 |
rs755153368 | in-del | -/AAAC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962958 | AGACTCCATCTCAAA[-/AAAC]AAACAAACAAAAATG | 55827 |
rs755170315 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167987292 | TTCAAAGTACTGAAT[C/T]ATATTAATTCAACAA | 55827 |
rs755188934 | snp | A/T | 3.53407e-05 | 0.00420346 | missense | DCAF6 | GRCh38.p7 | 1:168004589 | CCATCAAGTCCTGAT[A/T]TGGAAGTGAGTGAAA | 55827 |
rs755203634 | snp | A/G | 4.96184e-05 | 0.00498063 | missense | DCAF6 | GRCh38.p7 | 1:167987500 | TCATCTTCAGATTAT[A/G]ACTGTACCCAATGAC | 55827 |
rs755215881 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013618 | CTTTAGTTTACTCAG[A/G]GACATCATTCCTGTG | 55827 |
rs755217777 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997988 | TGACTAAAATAAAAA[A/C]GACAGACAATAACAA | 55827 |
rs755270607 | snp | A/G | | | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168075890 | GACCCACAGTTTTCC[A/G]ATCTCTCCTGTAGCA | 55827 |
rs755272053 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013200 | GAGCATCACCATTTG[A/T]TTGTCAATGAATACT | 55827 |
rs755281066 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948851 | GAGATGGGGTTTTGA[C/T]ATGTTGATCAGGCTG | 55827 |
rs755348752 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168038762 | TAGAATATTTCTTCT[A/G]ATAGAAAATGCAAAA | 55827 |
rs755358152 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168025886 | TTACAAAACCTACAT[C/G]ACTTGATTTCTGTAT | 55827 |
rs755372990 | in-del | -/A | | | intron-variant, nc-transcript-variant | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998678 | TACGGATGAGCAAAG[-/A]AAGTGGTTTGCGCCT | 55827 |
rs755402589 | snp | A/T | 0.000164312 | 0.00906249 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065580 | TTAAATAATTTTTTT[A/T]AACCCTTAGATAAAA | 55827 |
rs755416171 | in-del | -/TCT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168016324 | TTTATGGCTCCTAGC[-/TCT]TCTTCTTCTTCCTCT | 55827 |
rs755464947 | snp | A/C | 3.3024e-05 | 0.00406336 | missense | DCAF6 | GRCh38.p7 | 1:167993282 | TTTATTCCTTCCCAT[A/C]TTAATAATAAGTCCT | 55827 |
rs755477766 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024454 | ATTCTTAGAGAAATA[C/T]TCAGAAACTAATTTT | 55827 |
rs755500707 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062353 | TTTGCAAAAATTCAT[C/T]GAGCTTTTTACCTTA | 55827 |
rs755514792 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168067441 | ATGGGGTAGATAGGA[C/T]GGAGAGGTCTTCACA | 55827 |
rs755521485 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167996939 | CTACCTATCCCCTTT[G/T]CTACTTTATTTCTCT | 55827 |
rs755579052 | snp | A/T | 0.00010568 | 0.00726836 | intron-variant | DCAF6 | GRCh38.p7 | 1:168050967 | TCATAATTTTTTTTT[A/T]ATGATGGATTTGCCA | 55827 |
rs755591463 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005963 | AGATTTGGGAATTAA[A/G]AGCAGAAGTAGTTAA | 55827 |
rs755632177 | in-del | -/TACTATAGACCATATTTCAA | 1.75912e-05 | 0.00296569 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066484 | GATTTTTATTGTACT[-/TACTATAGACCATATTTCAA]TACTATAGACCATAT | 55827 |
rs755643079 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168023324 | ATACAAACTATATCC[A/G]TTTTTTAAATTCTAG | 55827 |
rs755723070 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054776 | CTAAGCTAATATAAG[A/G]AAAATGTATACATAG | 55827 |
rs755750426 | in-del | -/TG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985304 | TGGAAGTCAGAAGTC[-/TG]AAATAAGGTGTACTG | 55827 |
rs755767443 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072884 | GTTTCCTGAAGAAAT[-/A]ATTCTAACAGAATAA | 55827 |
rs755789175 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961040 | TTTATAATTTTCCTC[A/C]TAGAAATCTTATACA | 55827 |
rs755789290 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019661 | GAGCCAGCCTAGAGA[A/G]GGTCAGGTAGGAACT | 55827 |
rs755797989 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974528 | CAGTCAAAGTAGTTC[A/G]TTGTTATTTATTGAG | 55827 |
rs755808688 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167953759 | ACCCACCACCACACC[C/T]GGCTAATTTTTGTGT | 55827 |
rs755823075 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046091 | GATTAATTTACCACT[C/T]ATAGTCAAGAGCATG | 55827 |
rs755851650 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168032502 | GTGGTTGAGAAATTT[C/G]CCTTTTCTATACAAG | 55827 |
rs755881342 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167957369 | ATATTGGCTGTTAAT[A/G]TAAGGGTTCTTTCAC | 55827 |
rs755886931 | snp | C/T | 4.99804e-05 | 0.00499877 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168068393 | CATGCTGGAAGAAAC[C/T]AGAAACACCATTACA | 55827 |
rs755894714 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167942311 | TCAGGTGATTGACCT[C/G]CTTCGGCCTCCCAAA | 55827 |
rs755937819 | snp | A/C/T | 3.31941e-05 | 0.00407383 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044684 | TAAGTGAGTTGCTCC[A/C/T]TTTAGATAATTGCTT | 55827 |
rs755942571 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997728 | AGAAAATGTTTTGCA[C/G]ATCATGTGTCTGGTT | 55827 |
rs755943265 | in-del | -/TATTAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986955 | CATATAAAGTTTGAC[-/TATTAA]ATTTAAACTATTGTT | 55827 |
rs755989271 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168069035 | CACTGATTTCATAAA[C/T]GTCCCCATACGTTTG | 55827 |
rs756012977 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049646 | ATAATCTGCATATAA[-/T]TTTTTTTTTTTTTTT | 55827 |
rs756018322 | snp | C/T | 1.76918e-05 | 0.00297415 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951785 | TTATTTAATTTGTTC[C/T]TTCTTTTTAAACAGG | 55827 |
rs756031259 | snp | A/T | 1.73915e-05 | 0.0029488 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004507 | AATATTTAAAATTTG[A/T]ATTTGCCTTAACATG | 55827 |
rs756081187 | snp | A/C | 3.48402e-05 | 0.00417359 | missense | DCAF6 | GRCh38.p7 | 1:168004623 | CAATGGAAGTAGATA[A/C]TCCAGCTGAACAATT | 55827 |
rs756092017 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944511 | GACATTCTGACTAGG[A/G]TAAGGTGATATCTCA | 55827 |
rs756120023 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030933 | GGCTATTTTCTTAAA[C/T]AGGTAGCCCTGGAAA | 55827 |
rs756153943 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168031137 | GATTTTTGCATACAG[A/T]TGTTAACTGAAGCCA | 55827 |
rs756156739 | in-del | -/TTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064080 | AAAGTTTCTGGTGGA[-/TTT]TTTTTTTTTTTTTTT | 55827 |
rs756205104 | snp | A/C | 1.65102e-05 | 0.00287312 | missense | DCAF6 | GRCh38.p7 | 1:167987515 | GACTGTACCCAATGA[A/C]CCTTACACTTTTCTC | 55827 |
rs756207861 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036494 | TAGCCCGAACTCAGT[C/T]TCTCAGTTTCCTTAA | 55827 |
rs756224509 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939173 | CAGCTCTTCTATACT[A/G]CAGTGCTAATCCTGG | 55827 |
rs756243690 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168061868 | ATCTATTAAAGCAGA[A/T]CATTATGCACATACT | 55827 |
rs756252780 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945616 | CCTGCCTGAGCCTCC[A/G]GAGTAGCTGGGACTA | 55827 |
rs756258272 | snp | C/T | 3.38409e-05 | 0.00411331 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991154 | TTTTAAATATAATTT[C/T]ACCTCTGCTGTATAA | 55827 |
rs756306426 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000243 | TTGTGGCTCCCCAAA[A/G]CAATTACAATAGTAA | 55827 |
rs756306815 | snp | C/T | 3.96424e-05 | 0.00445193 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935844 | CGGCGGCCGACATCG[C/T]CGCCGAGGGATCGTT | 55827 |
rs756331912 | in-del | -/ATG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057612 | GTTATGTGCTAGATA[-/ATG]CTCTGGTGGGTGCTG | 55827 |
rs756333000 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035828 | AGCACTTTGGGAGGC[C/T]GAAGTGGGTGAATCA | 55827 |
rs756343925 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167987022 | GTTGTATAACCATTA[A/C]CACAATTAAAATTTT | 55827 |
rs756403877 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167957922 | GTGCATATGAAGGTA[C/T]GAGTCATTTACATAC | 55827 |
rs756405386 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938451 | AACCTTTCTTCTTTA[A/C]GTAGACGTTCGCCCT | 55827 |
rs756447466 | snp | A/C | 3.32375e-05 | 0.00407647 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167993432 | TCTGCGGAAGAGAGA[A/C]GAGAAGAGGTAGGTT | 55827 |
rs756505107 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168014685 | TTGGGATCACTCTGC[A/G]TCCAAACTATCAGCA | 55827 |
rs756505910 | snp | G/T | 0.000247694 | 0.0111259 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065753 | TTGACCCAAGTAAGA[G/T]ATCTTTTCTAGGACG | 55827 |
rs756569567 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167999255 | AGTAAAACATGCTGT[A/T]AAGAGATGTGCCCTC | 55827 |
rs756603326 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937525 | CGGCGCTGAGCCAAA[A/G]CCTAAAAGTGATAGC | 55827 |
rs756609309 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168074822 | TCCTGAAAACTTGAA[C/G]GAGCATACTGTACTC | 55827 |
rs756614679 | in-del | -/CA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041892 | AATACATGTTTGTCG[-/CA]CGCACACACACACAC | 55827 |
rs756628773 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013367 | TAGTACCTGGCGTTA[C/T]TGATTTCTGAAACAG | 55827 |
rs756637001 | snp | C/G | 6.61135e-05 | 0.00574912 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002431 | TGCTTTAAGAGTTGA[C/G]AGTAGATGAGTTTTA | 55827 |
rs756639140 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168048084 | AAAGAATCACTTACC[A/G]GCTTGTAATTAGTCC | 55827 |
rs756690962 | snp | A/G | 1.70816e-05 | 0.00292242 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966773 | AAAAAAAATCAAGAA[A/G]GCAGAAATGAAGAAA | 55827 |
rs756722299 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168027509 | TTTCAGCATATTTTA[A/C]ATTTGTTTTTCATAC | 55827 |
rs756726733 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167994137 | TAATAATAAATCACT[A/G]ATTTATTATTGGTAT | 55827 |
rs756734534 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167950222 | TTAATTGCTGTCATA[C/T]TGTTAATTTGAATAC | 55827 |
rs756762795 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167981399 | CTTTTATTTTAGATT[C/T]GAGGGGTACATGTGC | 55827 |
rs756764935 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071415 | TCAAGACCAGCCTCG[C/T]CAACATGGCAAAACC | 55827 |
rs756818996 | snp | C/T | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167936190 | CCGAGCTGCCCGCCA[C/T]GATTGGCCCGCCCCG | 55827 |
rs756835892 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168006323 | GATGATTATTGAAAC[A/C]TTATGCAGTACTTTT | 55827 |
rs756838383 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168055007 | ATTTTTAGTAGAGAC[A/G]GGGTTTTTAACTTGA | 55827 |
rs756878517 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168023809 | CGCAAATGTTTTACT[A/G]TCTCACCTCAGAATT | 55827 |
rs756908961 | in-del | -/CCCAGGCTGGAGTAGAGTGGTTCAAT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167963481 | AGTCTCACTCTGCCA[-/CCCAGGCTGGAGTAGAGTGGTTCAAT]CTCAGCTCACTGCTA | 55827 |
rs756910789 | in-del | -/TC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167953614 | AATTATTATTATTAT[-/TC]TTTGATATGGGGTCT | 55827 |
rs756923966 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167992889 | TTTTTGTAAAAATTT[A/G]TTATCTTAATTTGGG | 55827 |
rs756939357 | snp | A/C | 3.79025e-05 | 0.00435314 | intron-variant | DCAF6 | GRCh38.p7 | 1:168075354 | TCTCTTTGCGATTCT[A/C]TTATCTGTGTTTCCA | 55827 |
rs756955020 | snp | C/G/T | 3.30476e-05 | 0.00406484 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966614 | GCTTATATTTCTTTT[C/G/T]TGCTTTCTCTTTAGG | 55827 |
rs756967884 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167963761 | GAGCATTTCATATAG[G/T]TTTTTTTTTCTCCTT | 55827 |
rs756984740 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019816 | AAATCAGCACTTACC[C/T]GATCCTGTGCAAGCA | 55827 |
rs756987334 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070875 | ACATGTTCTTAGGGT[A/G]GAGTCCAAATGTGTT | 55827 |
rs757039496 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019175 | GCCTCAGCCTCCCAA[-/G]GTAGCTGGGATTACA | 55827 |
rs757069898 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961140 | ATTCAAATTCCACTT[C/G]TTCATTTCTGGTATT | 55827 |
rs757079968 | snp | C/T | 2.19099e-05 | 0.00330975 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975053 | TGATATATATGTAAG[C/T]ATGTATATTTTTGAT | 55827 |
rs757082471 | snp | C/T | 6.72314e-05 | 0.00579752 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168004648 | ACAATTTCTTCAGCC[C/T]TCTACATCCTCTACA | 55827 |
rs757124643 | snp | A/G | 3.29707e-05 | 0.00406008 | missense | DCAF6 | GRCh38.p7 | 1:168045013 | GCTTCATCTGAAAAA[A/G]CCAAGGAACCAGAAA | 55827 |
rs757132060 | snp | C/T | 1.64866e-05 | 0.00287106 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168004732 | TCCTTTGCTATCTTC[C/T]CCAGACAGTGAACAA | 55827 |
rs757135760 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168053583 | ATCCAGGCTCAGTGT[G/T]CCAAAGTTCTCCCTT | 55827 |
rs757169898 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962683 | TTTTTAGGCTGGGTG[C/T]GGTGGCTCACCCCTG | 55827 |
rs757170569 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167983115 | CCTCTGGCTTTGTTC[-/T]TTTTTGCTTAAGATT | 55827 |
rs757171593 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976059 | GGTTTTACTGGAGAT[A/T]TATGAATTTACATTT | 55827 |
rs757171763 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050093 | CAAGCATCTAAGAAA[A/G]CTTCCTGAATAAGTC | 55827 |
rs757173112 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167955901 | GAGTTAGCTGGGACC[A/G]TAGGTGCATGCCACC | 55827 |
rs757173301 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167942693 | TAGGTCTGTGAACAA[G/T]TTCGAGTTAAGTTTT | 55827 |
rs757179631 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071590 | AGTGAGCCAAAATTG[C/T]GCCACTACACTCCAG | 55827 |
rs757214015 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009655 | CTCTGTATGCTTGGG[A/G]AGCCCTTGTCCTGGC | 55827 |
rs757229400 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986088 | AGTACTTTATTTTAG[C/G]AATAGATAACAATTT | 55827 |
rs757233888 | snp | C/T | 1.93609e-05 | 0.00311128 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168065631 | TAACTTTGTAATGAG[C/T]GGTTCTGACTGTGGC | 55827 |
rs757256703 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037716 | TTAAAATGAAATTGC[C/T]GTTTCCACAATTAAA | 55827 |
rs757264526 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168008458 | TTGTTCCTGTATCTA[A/C]ACTATAACCTGGGTC | 55827 |
rs757291801 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168038104 | TTTTGATTCCCCTAA[C/T]GACTAAATATGGTTC | 55827 |
rs757338856 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167947494 | TTCTCCTTTTTGATG[C/T]AGGAATTTATTGCTG | 55827 |
rs757362257 | snp | C/T | 1.65482e-05 | 0.00287643 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065767 | ATATCTTTTCTAGGA[C/T]GAGGGCTAGAAATTA | 55827 |
rs757373217 | snp | C/T | 0.00011782 | 0.00767439 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935856 | TCGCCGCCGAGGGAT[C/T]GTTGGCAGCCGGGTG | 55827 |
rs757382904 | snp | A/G | 3.29761e-05 | 0.00406041 | missense | DCAF6 | GRCh38.p7 | 1:167991223 | TTTTAATTAACTGTC[A/G]ACGTGCTGCCACGTC | 55827 |
rs757416180 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036564 | TTGCAGAAGCCTAAA[C/G]ACAGCAGTGATGAAA | 55827 |
rs757431513 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167989475 | AACTAGAGTAATCCT[G/T]AACTACTAAAAACTT | 55827 |
rs757440858 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168073032 | AACAAAAAAATCAGC[C/T]GGGTGTGGTGGCACG | 55827 |
rs757455634 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022598 | TTTCGTTTCATGCTT[C/T]GAATCCTCCAAGGCA | 55827 |
rs757463143 | snp | G/T | 4.97104e-05 | 0.00498525 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936903 | CTCCCACCCGGCTCA[G/T]GCAGAGCCATGTCTC | 55827 |
rs757536137 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062413 | TATTTAGTAAAAAGT[G/T]TACAATATCTTTTTT | 55827 |
rs757556732 | in-del | -/AAACA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167989084 | ACTCCATCTCAAACA[-/AAACA]AAACAAAACAAAACA | 55827 |
rs757580947 | snp | A/T | 1.84391e-05 | 0.00303632 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974790 | GAATATTTCTAGGAA[A/T]TAATAAGTTACCATT | 55827 |
rs757595710 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971457 | CTGTATATTCGATAC[C/T]TCAGACAGGGTTATG | 55827 |
rs757622063 | in-del | -/G | 3.42217e-05 | 0.00413638 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987461 | TCTGTTTAAATGTTC[-/G]TATGATTATCTGCAC | 55827 |
rs757650514 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019103 | GCCCAAGCTGGAGTG[C/T]AGTGGTGCTATCTTG | 55827 |
rs757737989 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959373 | GTGCACATACGTTTA[C/T]GTTCGTGTGCAGGTG | 55827 |
rs757738098 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944707 | GTCTGGATATTAGTC[C/T]CCTGTTGGATGAATA | 55827 |
rs757776848 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168029298 | CAATGAGGTGAATTA[C/T]CTTAATTTTACTAAT | 55827 |
rs757818522 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168016417 | TTTGGCCATACTAGC[A/G]TGCTGACTAAATTAT | 55827 |
rs757828716 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954060 | CTTCCAGGCTGGAGT[A/G]GAGTGGCACAATCTC | 55827 |
rs757838275 | snp | A/T | 1.65146e-05 | 0.0028735 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974900 | TACCTTGTACAAATG[A/T]TAAACAGATTGTATC | 55827 |
rs757855464 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940115 | TTGATTTTACTTAAA[C/T]TGATTAATTATCTCC | 55827 |
rs757860067 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167983221 | GTTGGTAGTTTGATA[A/G]GAATAGCATTGAATC | 55827 |
rs757865155 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941310 | GTAATCATAACAACC[A/G]TAGACACTATGATAG | 55827 |
rs757867920 | snp | A/G | 3.56436e-05 | 0.00422144 | missense | DCAF6 | GRCh38.p7 | 1:168075371 | TATCTGTGTTTCCAG[A/G]CCGGTTGGAGGGTGA | 55827 |
rs757912664 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168015150 | AATATCTCTTTGCAG[A/G]ATTTAATGTTATTTT | 55827 |
rs757920140 | in-del | -/TG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945662 | TGCCCAGCTAATTTT[-/TG]TGTGTGTGTGTGTAT | 55827 |
rs757950040 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971621 | CTTTGGCCAGCTATT[C/T]AGTCAAAATAAACTG | 55827 |
rs757952182 | snp | A/G | 6.60622e-05 | 0.00574689 | missense, intron-variant, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167966638 | CTTTAGGTTAATACA[A/G]TCTGTTGGAATGACA | 55827 |
rs757954151 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168043746 | AGTTTAAAATTAAGT[A/T]TGTGTAAGACAGCTA | 55827 |
rs757972511 | snp | G/T | | | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168076122 | CATTAACAGCCTGTT[G/T]ATCGCAAGCCTTACT | 55827 |
rs757978549 | snp | A/C | 1.68462e-05 | 0.00290221 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966760 | AATTTAATGAGAGAA[A/C]AAAAATCAAGAAGGC | 55827 |
rs758064450 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982351 | CTTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCT | 55827 |
rs758065005 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168002701 | TATAGGTATACTTAT[A/G]CAAATATATCTTAGG | 55827 |
rs758104123 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007234 | AGTTGCTATCCCTTT[C/T]CAGCTTCTCAAAGAT | 55827 |
rs758105651 | snp | A/G | 4.94858e-05 | 0.00497398 | missense | DCAF6 | GRCh38.p7 | 1:168045046 | TCAGATCAGACTAGC[A/G]CTGAGAGTGCTACCA | 55827 |
rs758108801 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168029755 | GGAGGCTGAGGTGGG[C/T]GAATCACGAGGTCAG | 55827 |
rs758129569 | in-del | -/TT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168033304 | TTTCTGAAAAGGATC[-/TT]TTTTTTTTTTTTTTT | 55827 |
rs758135981 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168056817 | TTAGAAATGCTCTGC[C/T]TCTGGATTATTCTAA | 55827 |
rs758152890 | in-del | -/ATATA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000905 | AAACGGTCTGGAATT[-/ATATA]ATGATGACGGTTGTA | 55827 |
rs758190304 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167994429 | ATTACCATTTACTCT[C/T]CATATATGGACAGCA | 55827 |
rs758213205 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936474 | CCCTAGCGACTTAAG[A/G]ATCTGGTTAGAGTGG | 55827 |
rs758214370 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167963940 | AAATCTTCCATCTTA[C/T]ACCTTGTACTATTTC | 55827 |
rs758228451 | snp | C/G | 3.29734e-05 | 0.00406025 | missense | DCAF6 | GRCh38.p7 | 1:168004745 | TCTCCAGACAGTGAA[C/G]AAAGGCAGTCTGTTG | 55827 |
rs758238954 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168026870 | AGCAGTTGAAACCAT[G/T]GGAGTGGATGAGATT | 55827 |
rs758242808 | in-del | -/A | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998045 | AACCCTCAAAAAATT[-/A]AGAGTTATTATATGA | 55827 |
rs758263884 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | DCAF6 | GRCh38.p7 | 1:167991253 | CTGTTGCTATTTGCC[C/T]ACCAATACCATATTA | 55827 |
rs758275966 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168053484 | AGTTGATTGCTTGCT[A/G]CAAAGACTCAAAAGA | 55827 |
rs758279257 | in-del | -/ATAAGCACTC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167963977 | TCATTTCACTTATTT[-/ATAAGCACTC]ATAAGCATATTTTTG | 55827 |
rs758282807 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168008215 | CTCAAGCAGTCCATC[C/T]GCCTCGGCCTCCCAA | 55827 |
rs758290359 | snp | C/G | 0.000201935 | 0.0100462 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936911 | CGGCTCAGGCAGAGC[C/G]ATGTCTCGGGGTGGC | 55827 |
rs758303444 | snp | A/G | 0.000215198 | 0.0103708 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065772 | TTTTCTAGGACGAGG[A/G]CTAGAAATTATTTGT | 55827 |
rs758308188 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964779 | TGTACGTTTTTATTG[A/C]TATATCCTCAAGGTC | 55827 |
rs758308196 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167950408 | ATGAAAACATGTTAC[G/T]GAATTTCTCTAGGTT | 55827 |
rs758328145 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058207 | TGACTAAACCACAGT[A/T]TATCCATTTTCCTGT | 55827 |
rs758330322 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168042531 | CCTGCCATGTTTGAA[C/G]AGCAGATCAGAACTG | 55827 |
rs758353088 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019876 | TGTCCATAATGACAG[C/T]CACATGGCAGCACTT | 55827 |
rs758357751 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967833 | CCTCCTGCGTTCAAG[C/T]GATTCTCCTGCCTCA | 55827 |
rs758358225 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976123 | ATCCCTTTGTTTTCT[A/G]CTTTTTAAAAAAAGT | 55827 |
rs758382790 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167996740 | CTCTAACCACATCTA[C/T]TTGCTTAGTAACTCA | 55827 |
rs758405227 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168012518 | TGTTGACAAAAGCTA[A/G]TTCTCCAAGCATTTA | 55827 |
rs758414317 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009349 | CCTTCCTTCCTCCCT[C/T]CCTTCCTTCCTTCCT | 55827 |
rs758440158 | snp | A/G | | | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075654 | TTAAAACTTTTTGCC[A/G]TGTATGAGGAGTGCT | 55827 |
rs758449400 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168012100 | CAGTCCCAGGAGAAA[A/C]AATGCACAAGGATCA | 55827 |
rs758459276 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985509 | CTCTGACTCTGACTC[G/T]CCTGCCTTGTTTTGC | 55827 |
rs758489214 | snp | G/T | | | missense | DCAF6 | GRCh38.p7 | 1:168066382 | TTATTTCTAGTTTTA[G/T]CCTCATCTGGCATAG | 55827 |
rs758496764 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062281 | TACTTAGGAGACTTC[A/G]GGAATTCTGGTTATA | 55827 |
rs758508324 | in-del | -/TAAAAAGAAAG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967490 | GCTGACTGATTGTAA[-/TAAAAAGAAAG]TGTGTGATGTTCTTT | 55827 |
rs758545042 | snp | A/C/G | 6.30541e-05 | 0.0056146 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936999 | TCCCGGCTGCGGAGT[A/C/G]GATACCTGGGTGAGC | 55827 |
rs758555399 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168023985 | CTTGGGAGGCTGGGG[C/T]GGGAGGATCACTTGA | 55827 |
rs758567432 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997907 | TAAGGAGATACTCAA[C/T]GTTATTAGTCCTCAG | 55827 |
rs758588776 | snp | A/G | 1.71761e-05 | 0.00293049 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004030 | ATCAGAAAGCTGGCA[A/G]AAACTACTTATTGAA | 55827 |
rs758589522 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168060296 | GCCATCCTCCCACCT[C/T]GGCCTCCCAAATAGC | 55827 |
rs758635021 | snp | C/T | 1.65954e-05 | 0.00288053 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003859 | CACTGATAAGACCTA[C/T]ATTGTAATAGGAGAG | 55827 |
rs758639835 | in-del | -/GTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168012446 | TGAATTTTTATCATC[-/GTT]GTTTTTAAAATTCAA | 55827 |
rs758645461 | in-del | -/TAC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974749 | TTAATGAGAATGTAT[-/TAC]TACTGGCTATGATTA | 55827 |
rs758653644 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167966576 | TGAGTGAAAGATGGC[A/G]TATTTTCTTTTATGT | 55827 |
rs758665226 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935681 | CTAAAAGGTCCATTT[C/T]AGAGGAAGCGAGAAG | 55827 |
rs758680029 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168038005 | CAAAATTAGTTCTTA[C/T]TGATGCTCAAGCAAC | 55827 |
rs758682984 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971154 | TCTCGGGTATCTCCC[A/G]TCTACTTGGTAAATT | 55827 |
rs758692201 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046336 | AAGATAGTCTATGAG[A/G]CCACTTTAATTTTTA | 55827 |
rs758736718 | snp | C/T | 1.6501e-05 | 0.00287232 | synonymous-codon, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974919 | ACAGATTGTATCCTG[C/T]TCTGGAGATGGAGTA | 55827 |
rs758742672 | in-del | -/TTTTTG | 0.00025208 | 0.0112239 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063590 | GAATATTTTTATTTA[-/TTTTTG]TTTTTTTAATATGTA | 55827 |
rs758758330 | snp | A/T | 1.86253e-05 | 0.0030516 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063594 | ATTTTTATTTATTTT[A/T]GTTTTTTTAATATGT | 55827 |
rs758814405 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168066920 | GTATATAGCAGAACA[A/G]ATGAGTGAAGAATCT | 55827 |
rs758821135 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167947579 | TACATTTTCATTTGT[G/T]TCAAAAACATTTTTT | 55827 |
rs758857581 | snp | C/T | 1.73845e-05 | 0.00294821 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975019 | ACTACTTATGAGGTA[C/T]GGTATTATTATGATT | 55827 |
rs758860004 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167978845 | TATTTTTTGTAGAGA[C/T]GGGGCCTTGCTATCT | 55827 |
rs758874115 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168068285 | TGGCTGATTGTTTAC[A/G]GTTTGCCTGATCTTC | 55827 |
rs758882323 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968632 | GGCCCTGGTGAAACT[G/T]CAGGACTCTGGTGCT | 55827 |
rs758883529 | snp | A/G | 1.65908e-05 | 0.00288012 | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168023038 | TCCATGTCACTTGAC[A/G]AGCAACAGGGTGCGT | 55827 |
rs758894787 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167990744 | ACTCAGTATTTTCAG[C/T]CTTATATTTGAAAGT | 55827 |
rs758898038 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972957 | CTGAAATTATAAATA[A/G]ACCTCTTAAGTGGAG | 55827 |
rs758899349 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167960292 | AAAATTTTTATTATT[-/T]ATTTATTTATTTATT | 55827 |
rs758904464 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167955264 | CTTTGTATGAACATA[C/T]GCTTTTATTCTTTTT | 55827 |
rs758905074 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000566 | TACATATGCTTAATT[C/T]AGCATTATTCATAAT | 55827 |
rs759026901 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034150 | AAAATAGTTACTTAT[C/T]TAAGTAATCTTATTT | 55827 |
rs759075283 | snp | A/C | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998626 | TTTTGTTGTCATTTC[A/C]GCAGTGTTCACAGCA | 55827 |
rs759114970 | snp | C/T | 3.34683e-05 | 0.0040906 | missense | DCAF6 | GRCh38.p7 | 1:168003977 | AGAGGACGAGGAAGA[C/T]CTCGACCCAGAGGTA | 55827 |
rs759116782 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019547 | TTTTCCATTTCAGGT[A/C]CCCTGAAGTCATGGG | 55827 |
rs759152451 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005373 | TGAAAATAACCTCTA[C/T]GTTCTGTTAAAATGC | 55827 |
rs759166225 | snp | A/G | 1.65638e-05 | 0.00287778 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974960 | CCAACGTTGAGCAAG[A/G]TGCAGAAACCAACAG | 55827 |
rs759167790 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167946738 | CTTGATCATGGTGTA[G/T]TATCTTTTTGATTTG | 55827 |
rs759246517 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168033797 | CCACTCTAAGCTGCT[A/G]ATGTCATCAGTTGTT | 55827 |
rs759260166 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070277 | CAAGAGTTAACATTT[C/T]TGCTGCCCTTATCTT | 55827 |
rs759267481 | snp | A/C | 0.000118691 | 0.0077027 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038327 | AATGTCATCTTTTTA[A/C]TGGTTTCAGAGACTT | 55827 |
rs759268313 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997578 | CTAGGTATGGTTTCC[A/G]GAAGAAATCAGAAAA | 55827 |
rs759280063 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167979658 | TTGGGAGGCCGAGGT[A/G]GGCAGATCACTTGAG | 55827 |
rs759281088 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036530 | CAATCATCCAATCTT[C/T]AGCTGTCTGTTTCAT | 55827 |
rs759312565 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037941 | AGTTTTTGCCAAACC[A/G]CTTTTCACAGAGCCC | 55827 |
rs759321134 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168065992 | AGTTTTACAAGCTGT[-/A]AAGAGGTTTGGTGTG | 55827 |
rs759350397 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040172 | GTGAGCCACGTATTT[A/G]TATCTAGGGGAAGAG | 55827 |
rs759352060 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168075045 | TCTCACACAGCTGCC[C/T]CCTCACTCCCCTTTG | 55827 |
rs759355025 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167993893 | CAGAAAACAAAAAAC[A/G]TGAGACATACTTGAA | 55827 |
rs759368104 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167980492 | AACACTTACAATTTT[G/T]TTTTAGTGGGCATTC | 55827 |
rs759371584 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167947374 | CCATATTTCATTTAG[C/T]TCTGCTCTGATCTTT | 55827 |
rs759376930 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009855 | TAATTTTCTTTTACT[A/G]TGATAAGCTCTCTTG | 55827 |
rs759395666 | snp | A/G | 1.648e-05 | 0.0028705 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063791 | GCATTTTTTGGTGAA[A/G]TTGCAGTTTCATGCT | 55827 |
rs759416159 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967305 | AAATTACCATAAGCT[A/G]ATAAACTCCCTCACT | 55827 |
rs759447471 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935360 | CATCCAGCTCTGCCT[A/G]GAGTGGGTTAATATG | 55827 |
rs759464691 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168011748 | TTTGGAAGGCCGAGG[C/T]GGGTGGATTACCTGA | 55827 |
rs759477011 | snp | C/T | 9.9749e-05 | 0.00706148 | missense | DCAF6 | GRCh38.p7 | 1:167993235 | TTTTAGGGAATTATG[C/T]AGGTCGAGGGACTAC | 55827 |
rs759522166 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168061120 | TAAGTATGTCTCTTT[C/T]GAGAATATTTGACCT | 55827 |
rs759549667 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940630 | TTTTGGAAATCAGTG[A/G]TTTATTAGCCACACA | 55827 |
rs759585689 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948481 | TCCAACATTTCTTGC[C/T]CCAACCATCTCTATA | 55827 |
rs759601372 | snp | C/T | 0.000313694 | 0.0125199 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167993377 | TTACATATATCTTTT[C/T]GACCCGAAAGATGAT | 55827 |
rs759610738 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168027454 | AAAAGTAGTACATTT[A/G]ATAAGTTTCCTATTT | 55827 |
rs759616523 | snp | A/G | 2.24338e-05 | 0.00334909 | intron-variant | DCAF6 | GRCh38.p7 | 1:168075330 | ATAATTGTAATTACT[A/G]AAAGTATTTCTCTTT | 55827 |
rs759621559 | snp | C/T | 1.70545e-05 | 0.0029201 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044868 | TATTGCCCACATTAC[C/T]ACCTGTTACATACAA | 55827 |
rs759674503 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000027 | TTTGATTTAAAGTGA[A/G]AGGCATATGACTCTT | 55827 |
rs759726214 | snp | A/G | | | missense | DCAF6 | GRCh38.p7 | 1:168043034 | TGATAGGAGCAGTAT[A/G]GCATCAAGTTCTAGA | 55827 |
rs759731322 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970886 | TTATATTTTAATTAT[A/G]TATAGCATAGAGACT | 55827 |
rs759732603 | in-del | -/ATATAAGCAAATT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167966772 | AAAAAAAATCAAGAA[-/ATATAAGCAAATT]GGCAGAAATGAAGAA | 55827 |
rs759746198 | snp | A/G/T | 6.59243e-05 | 0.00574094 | missense | DCAF6 | GRCh38.p7 | 1:168044972 | ACCTCAATCTTGATC[A/G/T]CTCTTGTGGGGTTCC | 55827 |
rs759778424 | snp | C/G | 1.65444e-05 | 0.00287609 | missense, intron-variant, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167966702 | CCAAATTAGTAATTA[C/G]TAATCCTTACAGCAG | 55827 |
rs759801607 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995123 | TCATTTTGTTACTGC[C/T]ATGCAAATTTCCCCT | 55827 |
rs759803247 | snp | A/G | 4.94923e-05 | 0.0049743 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168004699 | GACATCATCTCCCAC[A/G]GAAAGCCCTCATTCT | 55827 |
rs759827834 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168029046 | AATTTCTTCCTATCC[C/G]CAACTACTAGGTCTT | 55827 |
rs759838122 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167963078 | CAGCCTGGGCAACAT[A/G]GTGAAACCCTGGCTC | 55827 |
rs759859607 | in-del | -/T | 1.73869e-05 | 0.00294842 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004038 | GCTGGCAAAAACTAC[-/T]TATTGAAGCCAGTTT | 55827 |
rs759868124 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167993609 | ACAAAATTAGCTGAG[C/T]GTGGTGGCACATGCC | 55827 |
rs759871519 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939630 | TAGCCGGGAGTGGTG[G/T]CGTACGCCTGTAGTC | 55827 |
rs759921884 | snp | A/T | 1.70243e-05 | 0.00291751 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004826 | GTGGTTCATCTAATG[A/T]TTTTTGATAGTGAAA | 55827 |
rs759957620 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944588 | TTTTTCATATACCTG[-/T]TTGGGTGTATGCTTT | 55827 |
rs759973087 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168003406 | GCTTACAGTAAATGA[-/T]TGTTGAAAATAAATT | 55827 |
rs759973651 | snp | A/G | 1.74324e-05 | 0.00295227 | missense | DCAF6 | GRCh38.p7 | 1:167987606 | AAAGAAGATTGTAAA[A/G]ATGTAAGAATTAAAT | 55827 |
rs759974362 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041767 | ATGTATACACTAAGC[A/G]TTTTATTCATGCCTG | 55827 |
rs759991231 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000312 | GGATAATAATGAATA[A/G]GTTTGAAATATGAGA | 55827 |
rs760007465 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168026280 | CTAAAATCATACATC[A/G]TGTGGTAAATAATAT | 55827 |
rs760052595 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168020355 | TTTTTGTGATTTACC[G/T]GTTAGACTATAATTG | 55827 |
rs760058327 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975925 | GTTTCCCATTTTTTG[G/T]GTTAAACTGGTATAC | 55827 |
rs760077800 | snp | C/G | 0.000104915 | 0.007242 | upstream-variant-2KB, missense, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935829 | GCAGGCCTCGGGCAC[C/G]GGCGGCCGACATCGC | 55827 |
rs760090675 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944093 | GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 55827 |
rs760095083 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054811 | AATTAAAAGAACATA[C/T]GGGTTTGGTTTTTTT | 55827 |
rs760102282 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005869 | CCATAATAATAAGCT[A/G]AAGCTGAGCTACAGA | 55827 |
rs760189815 | snp | A/G | 1.65288e-05 | 0.00287474 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168063714 | GAACATTAGAAGGCC[A/G]CTAGTAAAAATGGTT | 55827 |
rs760210937 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049948 | GCATGAGCCACCGCA[-/C]CCAGGCTGTATAATT | 55827 |
rs760243028 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168006863 | CAATGGGAATATGAA[A/G]ATTTGCTACGCTCCA | 55827 |
rs760272843 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035404 | GCGAGCCATGATTTC[A/G]CCACTGCACTCCAAC | 55827 |
rs760275833 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976451 | TACTCCAACCTGGGC[A/G]ACAGAGTGAGACTGT | 55827 |
rs760296164 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167957292 | AGCAGTTAGCAATCA[C/T]TAATACTTTCTGTCT | 55827 |
rs760308477 | snp | A/C | 1.64849e-05 | 0.00287092 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063810 | CAGTTTCATGCTCTG[A/C]GTGTTTTTCCATAAT | 55827 |
rs760310041 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944252 | TTCCATATCTTTGCT[G/T]TTGTGAATAGTGCTG | 55827 |
rs760312876 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034315 | AGGCCAGGAGTTCAA[A/G]ACCAGCCTGGACAAC | 55827 |
rs760353815 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943469 | GGTGTTAGGTTTATC[C/T]TTAAATATTTCATAT | 55827 |
rs760363470 | snp | C/T | 1.67237e-05 | 0.00289164 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038521 | TAAAGATGTTCTTAG[C/T]CATTTTGTAGGATTG | 55827 |
rs760405150 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167999746 | AGATTTAGCGCCTTG[C/T]TCTGGGTTAGGCTTT | 55827 |
rs760405512 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986584 | TTTGGGTTTAAAACT[C/G]TTATACCTCAGATCA | 55827 |
rs760447088 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040321 | AGTAGTAGATAAGGT[C/T]AGCCAGGAAATTGAG | 55827 |
rs760457148 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959595 | TCTATTTTGGCCATT[-/C]TAATAGATATGTAGT | 55827 |
rs760486058 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168043061 | TAGAGGAATTGGGAG[C/T]CATTGCAAATCTGAG | 55827 |
rs760503615 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168063560 | TATTTTCATAAGTTT[A/C]TCATTATTCTTTGTG | 55827 |
rs760522291 | snp | A/G | 1.65542e-05 | 0.00287695 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966594 | TTTTCTTTTATGTCC[A/G]ATTTGCTTATATTTC | 55827 |
rs760533166 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041368 | CAAATATTTTTCCCA[A/G]TTTGGTGTTTGTTTT | 55827 |
rs760535104 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037218 | TAATGTGTGCTCCAA[C/T]ATCTTCAAGAGGAAT | 55827 |
rs760593528 | snp | G/T | | | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168076293 | ATGGATCATCATAAA[G/T]GTCTTCACTGTTGAG | 55827 |
rs760598765 | snp | C/T | 1.73809e-05 | 0.0029479 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993477 | TCCTTTGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 55827 |
rs760603733 | snp | A/T | | | intron-variant, downstream-variant-500B | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998750 | TTATCTGTTAGTTTT[A/T]TCATGAGATTGCAAC | 55827 |
rs760625045 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168066138 | ACATATCTCATAAAA[A/G]AACAATGAATAAGTG | 55827 |
rs760635580 | in-del | -/AGA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034491 | GCTACCGTGGGTGAT[-/AGA]GCAAGACCCTGTCTA | 55827 |
rs760646456 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972345 | ATAATAATTCTTTGA[A/G]CAATTATTCATTAAT | 55827 |
rs760647899 | snp | A/G | 1.83491e-05 | 0.0030289 | missense | DCAF6 | GRCh38.p7 | 1:168075430 | GAAAATGAGGATGAG[A/G]AATAATAAACTCTTT | 55827 |
rs760656971 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167949422 | CTGAGAGCCTCTTGA[A/G]CCAAGGACAAATTTG | 55827 |
rs760672350 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168047344 | TAGAAGAGAGATAAT[C/T]AGTGACAACAAACAG | 55827 |
rs760695969 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064663 | TGCCTAAAAGTTAGC[A/G]TGAAAATAATTAGAG | 55827 |
rs760704742 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050773 | AAGTCACAAAGGGAA[A/G]CAAAAGTTTTTTTTT | 55827 |
rs760704950 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168067914 | CCCAAAAATTTATTT[C/T]CCAAGACTACTCTGC | 55827 |
rs760705596 | snp | A/C | 1.64817e-05 | 0.00287064 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168044988 | CTCTTGTGGGGTTCC[A/C]GAAGAATCTGCTTCA | 55827 |
rs760710783 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064423 | ATATACATTGCATCA[G/T]CAGAAGGTATCTACA | 55827 |
rs760750835 | snp | A/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938051 | AAAGTTAGCATGCAA[A/T]TTTTTAATTCTTTTT | 55827 |
rs760763828 | snp | A/G | 4.94735e-05 | 0.00497336 | missense | DCAF6 | GRCh38.p7 | 1:168004715 | GAAAGCCCTCATTCT[A/G]CTCCTTTGCTATCTT | 55827 |
rs760775834 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001389 | AAGATGCTGTTTGAG[C/T]TGGCAATTGATTATT | 55827 |
rs760783481 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959333 | TGAGTAAAGTTGCCA[C/T]AAACGTTTGTGGGCA | 55827 |
rs760792720 | snp | A/G | | | missense | DCAF6 | GRCh38.p7 | 1:168066401 | CATCTGGCATAGATT[A/G]TGACATAAAGATCTG | 55827 |
rs760814000 | in-del | -/TAT | 8.76125e-05 | 0.00661805 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975022 | ACTTATGAGGTATGG[-/TAT]TATTATGATTATATG | 55827 |
rs760832266 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168048386 | ATAGTGGACCTCATC[A/C]GTTTTTGTTCCAAAT | 55827 |
rs760856046 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940892 | AGGCAGCCAGTGACA[A/G]TTTTTTAGTGGAGAT | 55827 |
rs760866920 | in-del | -/TGTAT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168067260 | TTATAAAACAGTTGA[-/TGTAT]TGTATACATAATGCT | 55827 |
rs760884879 | snp | A/T | 0.000205023 | 0.0101227 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015769 | TCACCTTTCTTTTCC[A/T]ATTTGTGTCAGAATT | 55827 |
rs760896852 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168051631 | ATGAAACATATAGCA[A/G]CAATCAGAAATGTAA | 55827 |
rs760906002 | in-del | -/CTT | 0.000201823 | 0.0100434 | intron-variant, cds-indel | DCAF6 | GRCh38.p7 | 1:168022994 | TTGTTTCAGATTCTC[-/CTT]CTTCTGTGGTTAACA | 55827 |
rs760907447 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995228 | ATTTTAAGTGGGCCA[A/G]CTAGTTTTGATACCA | 55827 |
rs760913802 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168059072 | CATTAAATTTTATCA[A/G]TCTTTTATGCTTGTC | 55827 |
rs760939923 | snp | A/G | 1.65373e-05 | 0.00287548 | missense | DCAF6 | GRCh38.p7 | 1:167991205 | GTTATGTTTTGTAGG[A/G]TATTTTAATTAACTG | 55827 |
rs760971924 | snp | A/T | | | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168015838 | TGCAACAACTGAGGC[A/T]TAAGAAGGCTGAGCA | 55827 |
rs761009992 | snp | C/T | 1.71296e-05 | 0.00292652 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022983 | AAATCTCATTTTTGT[C/T]TCAGATTCTCCTTCT | 55827 |
rs761023158 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168018465 | TGTTGGGACTTAAAC[A/C]TGAAACAAGGAGCGA | 55827 |
rs761052144 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167952031 | GAAGAGTGTATGCAA[G/T]ATTTTTTAAAGTGCA | 55827 |
rs761062262 | snp | A/C | 0.000148328 | 0.00861056 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167991300 | TCTGACAGCTCAGTA[A/C]GAATATATGATCGGC | 55827 |
rs761073184 | in-del | -/ATTA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940118 | ATTTTACTTAAACTG[-/ATTA]ATTATCTCCTTTCTT | 55827 |
rs761093625 | in-del | -/ATGA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046106 | ATAGTCAAGAGCATG[-/ATGA]ATGATGGGTTTGAAT | 55827 |
rs761101834 | in-del | -/GTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167981503 | GCATAGTACCCAGTA[-/GTT]AGTGTTTCACCCCTT | 55827 |
rs761102883 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168029146 | GCTCGTGTGTTCTAC[C/T]CTTCTGCTGATCAAA | 55827 |
rs761131035 | snp | C/T | 0.000136607 | 0.00826348 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002609 | GCTTTTCTTTGTATA[C/T]GGTATTTTAAAATTA | 55827 |
rs761131701 | snp | A/G | 2.44424e-05 | 0.0034958 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066369 | TAATATATAAATTTT[A/G]TTTCTAGTTTTAGCC | 55827 |
rs761136754 | snp | C/T | 7.00452e-05 | 0.00591757 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936892 | GGTGGTCTCCCCTCC[C/T]ACCCGGCTCAGGCAG | 55827 |
rs761182029 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057943 | TCACCCTATTTTGTC[C/T]ATCTGCCTACCACGC | 55827 |
rs761220950 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974387 | TGGATGTAGGGACTT[C/T]TGCTGTGTCTTATGT | 55827 |
rs761225329 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940995 | AAATGGATAATTTTG[C/T]GTGTCGATTACTCTT | 55827 |
rs761241439 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967308 | TTACCATAAGCTAAT[A/G]AACTCCCTCACTAGA | 55827 |
rs761258313 | snp | C/G | 1.91834e-05 | 0.00309698 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068313 | TTCAAGGAAAAAATA[C/G]AGTTACTTTATGATC | 55827 |
rs761258320 | snp | A/G/T | 9.40689e-05 | 0.00685752 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043186 | AAATTGCAGCATTGG[A/G/T]TGTTTATCTACTTTC | 55827 |
rs761311383 | snp | A/G | 1.65064e-05 | 0.00287279 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168044613 | ATCATCAGAGGATGT[A/G]ACAAAATATCAGGAA | 55827 |
rs761326222 | snp | C/T | 1.68292e-05 | 0.00290075 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038535 | GCCATTTTGTAGGAT[C/T]GTATTAGATTTTAAT | 55827 |
rs761346075 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964669 | TGGTATTCACATTAT[A/C]CATGAGTTATGCCTT | 55827 |
rs761366753 | snp | C/G | 1.77555e-05 | 0.0029795 | upstream-variant-2KB, missense, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935811 | GCCGGTGGTAGGTGG[C/G]CCGCAGGCCTCGGGC | 55827 |
rs761394587 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168021939 | CATTTGCTAAGAACT[A/G]GAGCACAGGATATTA | 55827 |
rs761396161 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938405 | AAATTATTACATAGT[A/G]GGTAACATTATGAAG | 55827 |
rs761404188 | snp | G/T | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935069 | ACACAAACAGAGATC[G/T]AGGCTTTTGCTCAAG | 55827 |
rs761407957 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030175 | AAGGGGAAATAGCAG[G/T]GTTCAGTGTGGAACA | 55827 |
rs761461503 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168020599 | TACAATAAACTACCA[C/T]TGGACCATATATTCA | 55827 |
rs761486106 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167965140 | ATTAAAAGTAATGGT[A/G]TAAATAGGTCCTTAG | 55827 |
rs761536250 | snp | A/G | 1.70542e-05 | 0.00292007 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936875 | CCTCCCCTCCCCCAC[A/G]CGGTGGTCTCCCCTC | 55827 |
rs761545752 | snp | C/T | 3.34163e-05 | 0.00408742 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966740 | AAGTAGTTTAAAAAA[C/T]CTGTAATTTAATGAG | 55827 |
rs761550263 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976543 | TTGTCCATTGTGTTT[C/G]TGTTTCTTGCTTCTA | 55827 |
rs761585540 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168015309 | CTCACTTTTTTAGAG[C/T]TCTTCTCAATAAATT | 55827 |
rs761598229 | in-del | -/AC/ACACACACACACAC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167992252 | AGGAAGGCCAGGATT[-/AC/ACACACACACACAC]ACACACACACACACA | 55827 |
rs761602453 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970658 | TCATAAGCCTTTATA[A/G]GGCTTTTTAAAATTT | 55827 |
rs761628731 | snp | A/G | 1.65105e-05 | 0.00287315 | missense | DCAF6 | GRCh38.p7 | 1:168002573 | GTGAACGAGAACGAG[A/G]TGGTAACTATACTTT | 55827 |
rs761631491 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167999951 | TGGTGCAAGAGGCCT[A/G]GCTTTTGGCCTGTCT | 55827 |
rs761639724 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167969384 | CATGATATACAATTC[A/G]ATAAGCTGGGATAAC | 55827 |
rs761685364 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035683 | CAAATTCTATCAACT[A/G]TAATCAATCATTTTA | 55827 |
rs761721179 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167987757 | TAAATTTTTGTTTTG[C/G]TAAAATATTTAATAA | 55827 |
rs761756929 | in-del | -/TA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975995 | GTTTTTGTATGTACT[-/TA]TATATATATAGCTAG | 55827 |
rs761758809 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954715 | CCTCTGCCTCCCAAA[-/G]TGCTGGGATTACAGG | 55827 |
rs761816060 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938901 | CTAGGGGAATTGAAG[G/T]GTTCACTGACTATAT | 55827 |
rs761830393 | snp | A/G | 1.65583e-05 | 0.00287731 | missense | DCAF6 | GRCh38.p7 | 1:168045143 | AAACATCCACCAGGG[A/G]CTCTGCTCTTCAGGA | 55827 |
rs761844181 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167992017 | TCAATCAAGAAAACA[A/G]TGGTAAATGTGGTAG | 55827 |
rs761854089 | snp | C/G | 0.000122212 | 0.00781608 | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168015874 | GGCAGCAAGAGCTAG[C/G]TGCACATACCCAGCA | 55827 |
rs761857288 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167955263 | TCTTTGTATGAACAT[A/G]TGCTTTTATTCTTTT | 55827 |
rs761858846 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168066653 | GAGGTAAAATCTAAA[C/T]AGTAGCTTACTAATT | 55827 |
rs761876903 | snp | G/T | 1.64993e-05 | 0.00287218 | missense | DCAF6 | GRCh38.p7 | 1:167991313 | TACGAATATATGATC[G/T]GCGAATGCTGGGCAC | 55827 |
rs761911088 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167990377 | CAAAAAGAAAAAAAA[A/C]TATGAATACTATATA | 55827 |
rs761919856 | snp | A/C | 8.89102e-05 | 0.00666687 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168066387 | TCTAGTTTTAGCCTC[A/C]TCTGGCATAGATTAT | 55827 |
rs761923328 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070060 | AGTTGCACAAAAATC[C/T]ATTTGTGCTAATGTA | 55827 |
rs761925958 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167960560 | TCCTGTCTTGGCCTC[C/G]CAAAGTGGTGGGATT | 55827 |
rs762006375 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948633 | ATTTATTGTCATTGA[A/G]ATACATTCACCATGT | 55827 |
rs762035265 | snp | C/T | 1.654e-05 | 0.00287571 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936987 | CTGGAGGACCCGTCC[C/T]GGCTGCGGAGTCGAT | 55827 |
rs762077084 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167973894 | ATATCTTTGGGGTAA[A/C]TTCCTAGAAATAGAT | 55827 |
rs762095708 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167942073 | TTTGCATTTCTCTTT[C/T]TTTGTTTTTGAGACG | 55827 |
rs762121588 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167984252 | CCATTGCAGAAGTGC[C/T]TCTTCTGTAACATTC | 55827 |
rs762122649 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168075095 | TTAGAAACCTAGACT[C/G]CAAAGAACACTGTTT | 55827 |
rs762133688 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995092 | TATTCTGGTTAAAAA[C/T]ATGAAATCTGCTCTG | 55827 |
rs762143158 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070261 | GATAGAATAAAGTGC[A/C]CAAGAGTTAACATTT | 55827 |
rs762153897 | snp | C/T | 0.000391486 | 0.0139853 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993221 | ACTTCTTGTTTCTTT[C/T]TTAGGGAATTATGCA | 55827 |
rs762241506 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168016428 | TAGCATGCTGACTAA[A/G]TTATTTCCTTCTGTC | 55827 |
rs762250476 | in-del | -/C | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938229 | TTGTTTGCATTCTTA[-/C]AAGTACATATGTACA | 55827 |
rs762254270 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167960209 | TCTGGGCTCTGAATT[C/T]TGTTTAGTTATCTGT | 55827 |
rs762273716 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982019 | TTCCTTTTTCTCTGC[A/G]GCCTCACCAGCAACT | 55827 |
rs762284966 | in-del | -/GGTG/GGTGTG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985183 | ATAGCCAAACCACGT[-/GGTG/GGTGTG]CGTGTGTGTGTGTGT | 55827 |
rs762289983 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167953134 | TAATCTAATATATAG[C/T]CCATATTTTCTTTGT | 55827 |
rs762309601 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167996347 | GCTTCTTTGTTGAAT[G/T]CATTCTTTCATTTTC | 55827 |
rs762332776 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167996449 | ATTACCACCCTGATC[C/T]GAGCTATCAGCATCT | 55827 |
rs762333476 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017829 | AATAGAAGAATGTGC[A/G]TTTCTCATATGTAAG | 55827 |
rs762342207 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167984315 | AAATTGTGAGGAAAG[A/G]TTCCTAAATGATTCA | 55827 |
rs762412009 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168060922 | TGCATAATTTTTTTC[C/T]CATTTATAGCTCTTA | 55827 |
rs762448136 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941255 | GACAAACGTAAGATA[C/T]ACTGATAATTCCTTA | 55827 |
rs762462208 | snp | C/G | 1.67736e-05 | 0.00289595 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974982 | AACCAACAGACAATG[C/G]CAATTTACGTGTCAT | 55827 |
rs762475614 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944280 | CTGCAGTAAACATAC[G/T]GGTGCACATATCTTT | 55827 |
rs762482334 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167952433 | ACTGTGTTAGCCAGG[A/G]TGGTGTTGATCTGAC | 55827 |
rs762489281 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168011572 | AGAACTCTGTTGTGC[A/G]CCATATCAAAGCAAA | 55827 |
rs762498492 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167979565 | GCAGGAGAAGATTCC[A/G]TTGTATGTATATACC | 55827 |
rs762530857 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009785 | CTTCTTGCTGAAATT[G/T]TATTCTCTTCTATAT | 55827 |
rs762542603 | snp | C/G | 2.2757e-05 | 0.00337313 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043180 | GTTATAAAATTGCAG[C/G]ATTGGATGTTTATCT | 55827 |
rs762547885 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005129 | CTAGATTTATTTGGT[C/T]TTATGTCTATATTAA | 55827 |
rs762567512 | snp | G/T | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935239 | TGACTCAAGCCTGGA[G/T]GAAGTAAAGCATGCA | 55827 |
rs762567797 | snp | A/G | 1.6577e-05 | 0.00287893 | missense | DCAF6 | GRCh38.p7 | 1:168003938 | AGATGGTTTGAAGAA[A/G]CAAGTGAGGTTGCAC | 55827 |
rs762638253 | in-del | -/TCTCA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941979 | CCAATTGCTCCACAT[-/TCTCA]TCAGCATTTGGTGTA | 55827 |
rs762650151 | snp | A/G | 0.000103936 | 0.00720812 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974842 | TAGGTTTTGACAACA[A/G]TTCGTTCAGGGCACC | 55827 |
rs762654037 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967666 | CCTAGCTGCCTCCCA[A/G]CTCACATGATACATT | 55827 |
rs762667307 | snp | A/G | 4.69032e-05 | 0.00484246 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045251 | ATTTTTAATTAACAT[A/G]AACTGTAAAAAATGT | 55827 |
rs762703198 | snp | C/T | 1.65351e-05 | 0.00287528 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974951 | TATTTTATACCAACG[C/T]TGAGCAAGATGCAGA | 55827 |
rs762719018 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030631 | AAGATGTAGAATAAA[C/T]AGGACTTGGTGGTAG | 55827 |
rs762739889 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167965639 | CCTGGAGTTTTTTTC[-/T]TTTTTTGAGACAGAG | 55827 |
rs762742078 | snp | A/C/T | 1.70232e-05 | 0.00291741 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991374 | GAAAATATAGGACTG[A/C/T]CAGTTCAAAGAGTAA | 55827 |
rs762759284 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017427 | TAACAGGAAAGAAGT[A/C]TACATTGTAGATGTT | 55827 |
rs762775542 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168051532 | TCACCTACTGAAAAC[C/T]TGTTTTGCTGACAAA | 55827 |
rs762788277 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959195 | TTAGGTTTCCTCTAT[C/T]TTTTCATAGCTTCTA | 55827 |
rs762805621 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167987952 | TCATTTACTCATGGA[A/T]ACAGCTTTGACTTAT | 55827 |
rs762820579 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022061 | CAGTGTCTTGCTTAG[A/G]TTACTAGATCCCCAG | 55827 |
rs762832560 | snp | C/T | | | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168045171 | GGACACAGATGACAG[C/T]GATGATGACCCAGTC | 55827 |
rs762901475 | in-del | -/ATAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968326 | AACCCTGGGACTGAG[-/ATAA]ACCACTGAAAAGAAG | 55827 |
rs762909491 | in-del | -/CCTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009505 | CTTCTTCCCTCCCTT[-/CCTT]CCTTCCTTCCTTCTT | 55827 |
rs762909910 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168023198 | CAATAGGTGGTATTG[C/T]ACATAAAAGGTCTTT | 55827 |
rs762947635 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168073475 | TCAGAAGCCACTGTC[A/C]CTTATTCTGTGACCT | 55827 |
rs762978498 | snp | A/G | 1.66189e-05 | 0.00288256 | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168023012 | CTTCTGTGGTTAACA[A/G]ACAGCTCGGATCCAT | 55827 |
rs762981218 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167981971 | TCCATAGTGGCTGAA[C/T]GAATTTACATTCCCA | 55827 |
rs763005371 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037693 | TTATAGACATCATCT[A/G]TAGGCTCTTAAAATG | 55827 |
rs763015632 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036329 | AGGCTTCTCATAACT[G/T]AAGAAGTCTTAACTA | 55827 |
rs763026973 | snp | A/G | 1.70667e-05 | 0.00292114 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068354 | TTTTTAACTTGCCTT[A/G]TAGGTTATAACTCGA | 55827 |
rs763028204 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041035 | GAGCTTGGACTGAAA[C/T]TGACAAGTTTTTGAA | 55827 |
rs763032007 | snp | A/G | 1.6686e-05 | 0.00288838 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023073 | CAGGAGATGCGCTAT[A/G]CCCATCCATCCATAG | 55827 |
rs763059136 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948782 | TCAGCCTCCCGAGTA[A/G]CTGGGACTACAGGTG | 55827 |
rs763084772 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168044089 | GCAGTGGGCCCATCC[A/G]TCCATGATAGTGTTT | 55827 |
rs763088111 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168028444 | TTCCATTAAGTGGAA[C/G]TTGACAGTGCCATCG | 55827 |
rs763134297 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938187 | GAAATAATATTTTCT[A/G]TTTTCTGAATATTCT | 55827 |
rs763153779 | snp | A/G | 1.98194e-05 | 0.00314791 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068481 | AGGAACTTTAAGTAT[A/G]CTACTAAAACCATTT | 55827 |
rs763156521 | snp | A/T | 1.67192e-05 | 0.00289125 | missense | DCAF6 | GRCh38.p7 | 1:167993228 | GTTTCTTTTTTAGGG[A/T]ATTATGCAGGTCGAG | 55827 |
rs763174822 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062914 | TATATATTAATATTC[-/T]TTTTTTTTTTTTTTT | 55827 |
rs763210862 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962933 | TGCACGCCAGCCTGG[C/T]GATGAAGCGAGACTC | 55827 |
rs763213593 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168073608 | TTTTCTTAACTCTCT[A/G]TTATCCCATCTTCTT | 55827 |
rs763235831 | snp | C/T | | | missense | DCAF6 | GRCh38.p7 | 1:168063728 | CGCTAGTAAAAATGG[C/T]TTATAAAGGCCATCG | 55827 |
rs763243782 | snp | C/G | 1.72121e-05 | 0.00293356 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951886 | AGTTAATTCTCAACT[C/G]TGAAGGGATTTGATA | 55827 |
rs763244772 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974056 | GTCTGTTGTCAAGCT[C/T]TTGAATTTTTGCCAG | 55827 |
rs763258552 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961917 | TTGTTTTGATTTCAT[G/T]GAATTCAGAATCTTT | 55827 |
rs763276316 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167992141 | CTGAATTTGAATCTA[A/T]TATAAACTAATGCTC | 55827 |
rs763278652 | snp | A/G | 6.84463e-05 | 0.00584965 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044854 | GGTTAAATAATTAGT[A/G]TTGCCCACATTACCA | 55827 |
rs763300492 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167949695 | GTTTGGTGTCTTTTG[C/T]TAGCATCCAAGAAAG | 55827 |
rs763301220 | snp | C/T | 1.65255e-05 | 0.00287445 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168004681 | GTCAGCTCAGGCTCA[C/T]TCGACATCATCTCCC | 55827 |
rs763338585 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975548 | AAAAAATGTACAACT[C/G]AGTTCTCTTTTATTT | 55827 |
rs763374460 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168053174 | TGGCCCATATATTCC[C/T]TAATCAAAAATATGG | 55827 |
rs763383520 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022831 | AACATATCTTAAGCA[C/T]ATGGCCCTGCTTACT | 55827 |
rs763390688 | in-del | -/TTAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052334 | AAGTACCATGATGCT[-/TTAA]TTGAGTTTTAGAAAA | 55827 |
rs763392802 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034042 | CAAAGTGATAATTTT[A/G]GCTACCAGAACTCTT | 55827 |
rs763398475 | snp | A/G | 1.76182e-05 | 0.00296796 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168004576 | TCTTCCTACGGTCCC[A/G]TCAAGTCCTGATTTG | 55827 |
rs763441410 | in-del | -/TCTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948001 | GTGTTGCAGTGTATC[-/TCTT]TCTTTAGGTCTAGTA | 55827 |
rs763449345 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054607 | TTTATTTTTTAATAA[C/T]TTTTTTCTAGACTCT | 55827 |
rs763471529 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005509 | TACTCGGTACTTTAA[A/T]CTATATACATGTAAT | 55827 |
rs763481978 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167942110 | CGCTCTTGTCGCCCA[G/T]GCTGGAGTGCAATGG | 55827 |
rs763524312 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962942 | GCCTGGCGATGAAGC[A/G]AGACTCCATCTCAAA | 55827 |
rs763534837 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954772 | TTGTATTTTTAAGAG[C/T]TTTATTGAGATATGA | 55827 |
rs763550090 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168023443 | TATTCTATATTACTA[A/G]ATTGCTTTAGTAATG | 55827 |
rs763581508 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964626 | GTCATTATTATTTCA[G/T]ATATTCTGTTCTTTT | 55827 |
rs763591110 | snp | A/C/G | 4.95465e-05 | 0.00497707 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168063717 | CATTAGAAGGCCGCT[A/C/G]GTAAAAATGGTTTAT | 55827 |
rs763604306 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009765 | TAAAGTCCTCTTTCC[-/T]TTTTCTTCTTGCTGA | 55827 |
rs763606844 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168026504 | ATTATGAGGGATCCA[A/G]CCTAAGGCAATAGTG | 55827 |
rs763626206 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943244 | AAAATTTATAGTTAT[C/T]CTGGCTATTCTGAAC | 55827 |
rs763628772 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057758 | GAGAGTATTAAGGAC[C/T]CCTAATCTAACCTGA | 55827 |
rs763636959 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052888 | CCATTGTTTATGATA[A/T]AAAGAAGAAACAAAC | 55827 |
rs763644360 | in-del | -/ACACACAC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167992253 | AGGAAGGCCAGGATT[-/ACACACAC]ACACACACACACACA | 55827 |
rs763646045 | snp | C/T | 1.65332e-05 | 0.00287512 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168038388 | AACAATAATGAAAAG[C/T]TGAGCCCCAAACCAG | 55827 |
rs763675160 | snp | A/G | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167936035 | CCCGCGAAGGTTGAG[A/G]GGGCGGAGGCTGCCG | 55827 |
rs763679362 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976467 | ACAGAGTGAGACTGT[C/G]TCTCAAAAATAAAAA | 55827 |
rs763701461 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019671 | AGAGAGGGTCAGGTA[A/G]GAACTGTTTTTTCAC | 55827 |
rs763720471 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072406 | TCTCACTTAGTCATT[A/C]TTGTTCATTGCCTTA | 55827 |
rs763734493 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054978 | TGTGCCACCATGCCC[A/G]GCTAGTTTTTTGTAT | 55827 |
rs763750077 | in-del | -/TTTTGAAATC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168015485 | TTTGTTCTATGTTCA[-/TTTTGAAATC]TTTTGAAATCTTTTG | 55827 |
rs763770872 | snp | A/T | 1.67601e-05 | 0.00289478 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038526 | ATGTTCTTAGCCATT[A/T]TGTAGGATTGTATTA | 55827 |
rs763788204 | snp | A/C | | | intron-variant, downstream-variant-500B | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998804 | CTTCTAATTCTAGTT[A/C]TTTTGTTGTTTTCAC | 55827 |
rs763812012 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944277 | GTGCTGCAGTAAACA[C/T]ACTGGTGCACATATC | 55827 |
rs763812816 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168042044 | ACCCATATGAATATA[C/T]AGTTTTAGTTAAATA | 55827 |
rs763813379 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034385 | GCATGGTGACACACA[C/G]CTGCAATCCTAGCTA | 55827 |
rs763861200 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168020582 | CCAACCATATTACAT[G/T]TTACAATAAACTACC | 55827 |
rs763862456 | snp | G/T | 1.74005e-05 | 0.00294957 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993478 | CCTTTGGCCGGGCGC[G/T]GTGGCTCACGCCTGT | 55827 |
rs763869565 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054998 | GTTTTTTGTATTTTT[A/G]GTAGAGACGGGGTTT | 55827 |
rs763873818 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975948 | TGGTATACTTTTTCC[A/G]TCATTTGAATTCCAG | 55827 |
rs763894032 | snp | A/G | 1.65315e-05 | 0.00287498 | missense | DCAF6 | GRCh38.p7 | 1:167993393 | GACCCGAAAGATGAT[A/G]CAGCACGAGAACTTA | 55827 |
rs763906699 | in-del | -/TAAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167994084 | TGTTATAATTAATAG[-/TAAA]TAATTACTAGCGTCT | 55827 |
rs763917577 | snp | A/T | 1.66643e-05 | 0.0028865 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966734 | AAGGTAAAGTAGTTT[A/T]AAAAATCTGTAATTT | 55827 |
rs763934112 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167957609 | TGTGTACAAATTTTT[C/G]TGTGTTGTAAGTTTT | 55827 |
rs763951286 | snp | C/T | 1.65318e-05 | 0.002875 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966609 | AATTTGCTTATATTT[C/T]TTTTTTGCTTTCTCT | 55827 |
rs763968446 | snp | A/T | 3.29679e-05 | 0.00405991 | missense | DCAF6 | GRCh38.p7 | 1:168044995 | GGGGTTCCAGAAGAA[A/T]CTGCTTCATCTGAAA | 55827 |
rs763974355 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985970 | AAATGGGAATCATAC[C/T]GTGCCTTCTCTTTTG | 55827 |
rs764019740 | snp | C/T | 1.64898e-05 | 0.00287135 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168004720 | CCCTCATTCTACTCC[C/T]TTGCTATCTTCTCCA | 55827 |
rs764024822 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167947310 | TTTTTATCTCTTTGA[C/G]GAACCAGCTTTTCAT | 55827 |
rs764028349 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037400 | TCAAGGAAAAAGATA[C/T]CTCACAGAAGAGTTT | 55827 |
rs764029048 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167980870 | TGTTGTTATATCTAA[C/T]AAATCATTGTAAAAT | 55827 |
rs764037924 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168066171 | TTCAACAATGAATCT[C/G]AGTGACTTCAACATG | 55827 |
rs764049107 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168011991 | AAAAAGAAAGAAAGA[A/G]AGAAAGAAACAAGTG | 55827 |
rs764074554 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168067377 | TGTGTCAGTCAGAGG[-/T]ATACACATAGTGTTT | 55827 |
rs764091838 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168051702 | ATAAGCCAAAAAATA[C/T]AATAGATGTATGGAA | 55827 |
rs764145800 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972539 | GGTAGAGTTTGAACT[A/G]GATTGGAAGTAGGAG | 55827 |
rs764153679 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167989417 | AAACTTTTCCTTTAT[A/G]TATAAAAGTGAAATG | 55827 |
rs764178146 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050887 | TATTGTGTTCCCTTC[A/G]CTAGATTTAATATCA | 55827 |
rs764220841 | snp | C/G | 6.75584e-05 | 0.0058116 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991157 | TAAATATAATTTCAC[C/G]TCTGCTGTATAACTA | 55827 |
rs764233971 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167969668 | ATGGGTCGTAGTTTT[A/G]TTTCATTAAGTTTTA | 55827 |
rs764239851 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945638 | CTGGGACTACAAGTG[C/T]GCACCACTATGCCCA | 55827 |
rs764258202 | in-del | -/ATTG | 4.36719e-05 | 0.00467269 | intron-variant | DCAF6 | GRCh38.p7 | 1:168042979 | ATCCTAAAAGATCAT[-/ATTG]ATTAACTTCTTGGTG | 55827 |
rs764259610 | in-del | -/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936648 | CCTCCTCCTGTTGGA[-/G]GGGGGGCTGAGGGAG | 55827 |
rs764295531 | snp | C/T | 0.000188875 | 0.00971607 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015775 | TTCTTTTCCTATTTG[C/T]GTCAGAATTTTTAAG | 55827 |
rs764298238 | snp | C/T | 1.83149e-05 | 0.00302607 | missense | DCAF6 | GRCh38.p7 | 1:168066383 | TATTTCTAGTTTTAG[C/T]CTCATCTGGCATAGA | 55827 |
rs764313970 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971379 | TCCTCAACACTTAAC[A/G]TTATTTATTTACCTC | 55827 |
rs764327740 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167947413 | TCTTCTGCTAGTTTT[A/G]GGTTTGGTTTTTTCT | 55827 |
rs764330694 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168018993 | GTTAAGGCAATACAG[C/T]ATATATGAAGTTACC | 55827 |
rs764388269 | in-del | -/AATTA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167988155 | GCTTTAATACAATTA[-/AATTA]AATTAATTAATTAAT | 55827 |
rs764397763 | snp | C/T | 1.65165e-05 | 0.00287367 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065755 | GACCCAAGTAAGATA[C/T]CTTTTCTAGGACGAG | 55827 |
rs764416977 | snp | C/G | 6.28082e-05 | 0.00560358 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936896 | GTCTCCCCTCCCACC[C/G]GGCTCAGGCAGAGCC | 55827 |
rs764418661 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046175 | AATTACTTAATGACT[A/C]TTAAAGATTCAGTTT | 55827 |
rs764434084 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959338 | AAAGTTGCCATAAAC[A/G]TTTGTGGGCAGGTGT | 55827 |
rs764436453 | in-del | -/AAAT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001361 | TGCCATAAACATGTC[-/AAAT]AAGCTCTGAAAGATG | 55827 |
rs764490764 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941199 | TTCAGTGAAAGCTGA[A/G]AAATGTATGATTTTA | 55827 |
rs764491192 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168044763 | AGAGGCCATGTTCAA[G/T]TGTATTGTGGAAGTT | 55827 |
rs764505682 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935078 | GAGATCTAGGCTTTT[A/G]CTCAAGGTCACAACT | 55827 |
rs764507123 | snp | G/T | 2.12136e-05 | 0.00325674 | synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936983 | CGGGCTGGAGGACCC[G/T]TCCCGGCTGCGGAGT | 55827 |
rs764509208 | in-del | -/GT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167953877 | GTGCTGGGATTGCAG[-/GT]GTAAGCCACTGTTCC | 55827 |
rs764563052 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030398 | GCAGGACAAAGTGAC[C/T]TTTTGGACATTTTTA | 55827 |
rs764647027 | snp | C/T | | | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168045135 | TCATGAAGAAACATC[C/T]ACCAGGGACTCTGCT | 55827 |
rs764660277 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168074960 | AATGCCTGGAACATA[A/G]TATTTAATTTAAAAA | 55827 |
rs764662810 | snp | A/T | 1.79586e-05 | 0.0029965 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002620 | TATATGGTATTTTAA[A/T]ATTAATATTTTAACT | 55827 |
rs764684413 | in-del | -/TGTCT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959803 | TGAAAGTATTTCCCC[-/TGTCT]TGTCTTCTTGTTTTC | 55827 |
rs764714610 | snp | A/T | 1.69298e-05 | 0.0029094 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168043079 | TTGCAAATCTGAGGG[A/T]CAGGAGGAATCTTTC | 55827 |
rs764719095 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995464 | GCGAGTGGATCACCT[A/G]AGGTCAGGAGTTCAA | 55827 |
rs764730608 | snp | A/G | 3.30136e-05 | 0.00406273 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168044619 | AGAGGATGTGACAAA[A/G]TATCAGGAAGGAGTA | 55827 |
rs764736643 | in-del | -/T | 2.37268e-05 | 0.00344424 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975067 | TATGTATATTTTTGA[-/T]TTAAGTACATACATG | 55827 |
rs764741603 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168073406 | AAGAGGTGACTATGC[A/G]TCAGTTAAATGAATT | 55827 |
rs764762478 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168002262 | CTCTTTAGGTTGAAG[A/C]TATTAGATATAGGCT | 55827 |
rs764777880 | snp | C/T | 3.41705e-05 | 0.00413329 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044862 | AATTAGTATTGCCCA[C/T]ATTACCACCTGTTAC | 55827 |
rs764787359 | snp | C/T | 1.65726e-05 | 0.00287855 | missense | DCAF6 | GRCh38.p7 | 1:167993414 | CGAGAACTTAAAACT[C/T]CTTCTGCGGAAGAGA | 55827 |
rs764798813 | in-del | -/AAG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940809 | TAGTAATTGATAAAA[-/AAG]AAGTAATTTTAAGGT | 55827 |
rs764803271 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975048 | TTATATGATATATAT[A/G]TAAGTATGTATATTT | 55827 |
rs764810377 | snp | C/T | 3.57283e-05 | 0.00422645 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935812 | CCGGTGGTAGGTGGC[C/T]CGCAGGCCTCGGGCA | 55827 |
rs764840250 | snp | C/G/T | 5.29828e-05 | 0.00514675 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993488 | GGCGCGGTGGCTCAC[C/G/T]CCTGTAATCCCAGCG | 55827 |
rs764901294 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168021945 | CTAAGAACTAGAGCA[A/C]AGGATATTAGAAACT | 55827 |
rs764914223 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976561 | TTTCTTGCTTCTAAG[A/G]TAGACATTCATTTTT | 55827 |
rs764955220 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167991663 | AAATCAGGATGTCTT[-/A]ATGATTGGTTTCTAC | 55827 |
rs764962389 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936274 | CCATGTTGGAGAAGG[A/G]AAAGTGAAGCTGCGC | 55827 |
rs764963031 | snp | C/G | 3.34359e-05 | 0.00408862 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966741 | AGTAGTTTAAAAAAT[C/G]TGTAATTTAATGAGA | 55827 |
rs764969154 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944331 | CTTTTTGTAAAAATC[C/T]AGTAGTGGGATTGCT | 55827 |
rs764972889 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168026784 | TAGATGGTTGGATGG[C/T]TATATGATGCTGGAA | 55827 |
rs764987317 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007889 | CAATCTGATCTTCTA[C/T]CCTGAATTCCAGACC | 55827 |
rs764996249 | snp | A/G | 2.0005e-05 | 0.00316261 | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075455 | CTCTTTTTGGCAAGC[A/G]CTTAAATGTTCTGAA | 55827 |
rs765000263 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964691 | TTATGCCTTTTGTAG[C/T]TGTCCCACATTCCTT | 55827 |
rs765010027 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168043624 | TACATGAAATTTAAT[A/G]TCTAGCACAGAGACT | 55827 |
rs765010948 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036369 | TGGATCTGAGAAATT[-/C]AGTCTTACACTTCTC | 55827 |
rs765027560 | in-del | -/AT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034793 | TACCTTTTAAGTAAC[-/AT]ATCTGTGCATTATGT | 55827 |
rs765061489 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168056002 | TGATCAGCCAACCAT[C/T]TTCATAACAAGATTT | 55827 |
rs765062003 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945492 | GTTTATAATTTCTTT[C/T]TTCTTTTTTTCTTTT | 55827 |
rs765074199 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986661 | TTCACCATAGTGTCT[A/G]TGCTCCTGTGAGAAT | 55827 |
rs765117966 | snp | A/T | 0.00116054 | 0.0240608 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015992 | CAGCTGATAGAATTG[A/T]TTTTTAATACTGCTA | 55827 |
rs765119034 | snp | C/T | 1.6489e-05 | 0.00287128 | missense | DCAF6 | GRCh38.p7 | 1:168045029 | CCAAGGAACCAGAAA[C/T]TTCAGATCAGACTAG | 55827 |
rs765121279 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072475 | TTTATTTATTGTCTT[A/C]TTACAGATTAGAGGA | 55827 |
rs765137150 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036306 | TCATATATCATTTAA[A/G]TTCCACAAGGCTTCT | 55827 |
rs765147504 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168048967 | TCTGTGGTAAAATGC[C/T]TCTACTGGCAAAAAT | 55827 |
rs765173203 | snp | C/T | 1.64811e-05 | 0.00287059 | missense | DCAF6 | GRCh38.p7 | 1:167991235 | GTCGACGTGCTGCCA[C/T]GTCTGTTGCTATTTG | 55827 |
rs765174645 | in-del | -/GCACTCCA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168011936 | CGAGATCACTCCATT[-/GCACTCCA]GCCTGGGCGACAGAG | 55827 |
rs765175577 | snp | A/G | | | intron-variant, downstream-variant-500B | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998971 | CATCTAGAATGGTCA[A/G]TCCTTTCTAGGTTTT | 55827 |
rs765176243 | snp | A/C | 3.31406e-05 | 0.00407053 | missense | DCAF6 | GRCh38.p7 | 1:168045155 | GGGACTCTGCTCTTC[A/C]GGACACAGATGACAG | 55827 |
rs765230471 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167957760 | ACAGCAACATACAGG[C/G]TTCCAGTTTCTTGAC | 55827 |
rs765245812 | in-del | -/ATAAATAAATAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939766 | AACTCTGCGTCATAA[-/ATAAATAAATAA]ATAAATAAATAAATA | 55827 |
rs765263631 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986712 | ACAGGAGGTGGAGCT[C/G]AGGTGGTAATGCTCG | 55827 |
rs765300528 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167950514 | TTTTTTTTAACTTAT[A/G]TGTTCATCCTTTACC | 55827 |
rs765300814 | snp | A/T | 2.13778e-05 | 0.00326932 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045241 | AGGTTGGTAAATTTT[A/T]AATTAACATGAACTG | 55827 |
rs765327569 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168038109 | ATTCCCCTAATGACT[A/G]AATATGGTTCTCAAT | 55827 |
rs765331278 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035684 | AAATTCTATCAACTA[C/T]AATCAATCATTTTAT | 55827 |
rs765338137 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939100 | ATCGAAACTTGAAAA[-/T]GTTTGCAAAGAACTA | 55827 |
rs765343035 | in-del | -/AT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967559 | CCTTCTGTTTTAGAA[-/AT]ATGACTAAATAGTTA | 55827 |
rs765351867 | snp | G/T | 1.66796e-05 | 0.00288782 | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168023002 | GATTCTCCTTCTTCT[G/T]TGGTTAACAAACAGC | 55827 |
rs765366190 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948678 | TTTTTTTGAGGTGGA[A/G]TCTCACTCTGTTGCC | 55827 |
rs765382509 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167947570 | TGTTGTGTTTACATT[C/T]TCATTTGTTTCAAAA | 55827 |
rs765387617 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961678 | TGCATTAGCTAGGAC[A/T]TAAAGTATGGTGTTG | 55827 |
rs765393339 | snp | G/T | 1.65405e-05 | 0.00287576 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936988 | TGGAGGACCCGTCCC[G/T]GCTGCGGAGTCGATA | 55827 |
rs765398426 | snp | A/G | 1.73519e-05 | 0.00294545 | missense | DCAF6 | GRCh38.p7 | 1:168066394 | TTAGCCTCATCTGGC[A/G]TAGATTATGACATAA | 55827 |
rs765409926 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037839 | CCACCCTCTTCTCCA[A/T]CAGGTGCAGACTGTG | 55827 |
rs765413251 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167990388 | AAAAATATGAATACT[A/G]TATAAATAATCAATA | 55827 |
rs765424181 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972892 | TTAATAAGGGAATGC[C/T]TTTCAATTTATGAGT | 55827 |
rs765449501 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936533 | AGCCGCAGCACACAC[C/T]AGCCTCAGTCCCCAG | 55827 |
rs765465592 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167946662 | ATTCTGTTGATATGA[C/T]GTATCACATTTATTG | 55827 |
rs765476583 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995129 | TGTTACTGCTATGCA[A/G]ATTTCCCCTTGAAAT | 55827 |
rs765496247 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168066760 | ACAATAAAGAATCAC[A/T]CACAAAAAAATCTGT | 55827 |
rs765506133 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168023940 | AGGCAGATAGCTGGA[C/T]GTGGTGGCACACGCC | 55827 |
rs765520758 | snp | C/T | 1.66114e-05 | 0.00288192 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044542 | TTTTAGAACTAATCC[C/T]TCATGGATACCAAGG | 55827 |
rs765523788 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167950562 | AAATAACATGGAGAA[A/G]GAAGTAAAACAAATT | 55827 |
rs765562513 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168020407 | TAATTCTGGTGTCAA[-/G]GGGGCTAAAGAATTT | 55827 |
rs765569155 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167947508 | GTAGGAATTTATTGC[G/T]GTGTTCTTCTTAGCA | 55827 |
rs765584559 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167942091 | TGTTTTTGAGACGGA[A/G]TTTCGCTCTTGTCGC | 55827 |
rs765628535 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030491 | GGCTATGGCCTGATA[A/C]TCTGAATGGAGTATG | 55827 |
rs765664868 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941264 | AAGATATACTGATAA[G/T]TCCTTAAGGCAGGAC | 55827 |
rs765678087 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167996356 | TTGAATTCATTCTTT[C/T]ATTTTCTTCTGGTCC | 55827 |
rs765679677 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167983144 | TTGCTTTGGCTGTTC[A/C]GGCTCTTTTTTGGTT | 55827 |
rs765697756 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971473 | TCAGACAGGGTTATG[A/G]GTCAGGTTTGAAAGG | 55827 |
rs765699093 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167960724 | TTAAATTTGTTAAAG[C/T]GTATTTTAAGGCCTC | 55827 |
rs765720764 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049230 | TAGTGATTTTATATA[C/T]TGTATTTATTTCATT | 55827 |
rs765744799 | snp | A/G | 4.55259e-05 | 0.00477084 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043181 | TTATAAAATTGCAGC[A/G]TTGGATGTTTATCTA | 55827 |
rs765746377 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052006 | CCGCCTCAGCCTCCT[G/T]AGTATCTGGGATTAC | 55827 |
rs765758219 | snp | A/G | 3.42777e-05 | 0.00413977 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004026 | AGTCATCAGAAAGCT[A/G]GCAAAAACTACTTAT | 55827 |
rs765808967 | snp | C/T | 0.000158751 | 0.00890788 | missense | DCAF6 | GRCh38.p7 | 1:168004569 | TTTCAACTCTTCCTA[C/T]GGTCCCATCAAGTCC | 55827 |
rs765811124 | snp | C/T | 3.37496e-05 | 0.00410775 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974990 | GACAATGCCAATTTA[C/T]GTGTCATTATGGAAC | 55827 |
rs765812646 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046891 | TAGTAGAACATGATA[C/T]GGAGGTCATAATTGA | 55827 |
rs765820514 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168032033 | ACATATTTAAGTTCA[A/G]TTCACACTTCTATGT | 55827 |
rs765829965 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168031964 | ACCCATAAATTCTAA[A/G]TACTGGTAGGAATGT | 55827 |
rs765832210 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168068227 | CTTAAGGCAGAAATA[C/T]AGACATCAGACGCAT | 55827 |
rs765856852 | snp | C/T | 0.000935891 | 0.0216118 | intron-variant, nc-transcript-variant | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998702 | TGCGCCTCAAGAAAC[C/T]ACTTTCTTTGCTCAT | 55827 |
rs765866923 | in-del | -/CTC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167956142 | CAGGTTGAGGATGTT[-/CTC]CTCTATTACTAACTT | 55827 |
rs765871433 | snp | C/T | 1.68681e-05 | 0.00290409 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002603 | TGGTCAGCTTTTCTT[C/T]GTATATGGTATTTTA | 55827 |
rs765902671 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168016530 | GCAAAAGTACTCCAC[A/G]GTCTCATGTTCTTAT | 55827 |
rs765943458 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941504 | TGGCAACCTGTGATA[C/T]ACACAACGAAAATAA | 55827 |
rs765973083 | snp | C/T | 3.33e-05 | 0.00408031 | missense | DCAF6 | GRCh38.p7 | 1:168045181 | GACAGTGATGATGAC[C/T]CAGTCCTGATCCCAG | 55827 |
rs766028833 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037804 | AGTATATTTTAGAAA[A/G]TATCAAAGCACTATA | 55827 |
rs766044789 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005130 | TAGATTTATTTGGTT[C/T]TATGTCTATATTAAA | 55827 |
rs766051409 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167947214 | GTGGAATCAGTTGTA[A/T]TGTCTCCTTTTTCAT | 55827 |
rs766065672 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167978189 | AGAACATTGTTTTAC[A/G]TGTCTTTTCAGTACA | 55827 |
rs766080377 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967234 | ACAGCCAAATGACTG[C/T]GGTGTGAATAGTTCT | 55827 |
rs766098944 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167996457 | CCTGATCCGAGCTAT[C/G]AGCATCTCTGGCATG | 55827 |
rs766128549 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019385 | AGTATGTTGTTTGCT[A/G]CTTAAAAATGTCCTC | 55827 |
rs766137493 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167988828 | GCTCATGCCTCTAAT[-/C]CCAGCACTTTGGGAG | 55827 |
rs766142535 | snp | A/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938575 | ATAGCTGGAGTCTGG[A/T]TTTTAAAACTATTTA | 55827 |
rs766153391 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167965965 | AACATTCAGACTTAA[A/C]GCTTTCTGAACCTCC | 55827 |
rs766180586 | in-del | -/TC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168015324 | CTCTTCTCAATAAAT[-/TC]TGAGTTGTTTCTAAA | 55827 |
rs766195564 | in-del | -/TTTTA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168032713 | ATTAGGTAAACAGTG[-/TTTTA]TTTTCACATGTTCCA | 55827 |
rs766199911 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935302 | CCAGCAGCAGCTGAA[A/G]AAAGTGACCTTTACT | 55827 |
rs766203863 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072796 | CACAGGCTTCCATTG[A/G]GAAATTTTTTTCTTA | 55827 |
rs766223107 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168056871 | TTCCTTAGAAACCTG[C/G]ACTAGGAGAAGCTTT | 55827 |
rs766246555 | in-del | -/TGGAATACA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168060228 | TTTTGTTACCCAGGC[-/TGGAATACA]TGGCATGATCTTAGC | 55827 |
rs766249000 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001242 | GCTTACAGTGAGCTA[G/T]GATGGGACCACTGCA | 55827 |
rs766273803 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168059643 | TCTACATTTATTTAG[A/G]CCTTTTTTTCTTTTT | 55827 |
rs766288283 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168073553 | AGTGTAAAAGTCTAA[A/C]CTCTACTGCAAACTC | 55827 |
rs766309972 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036488 | AAAAACTAGCCCGAA[C/G]TCAGTCTCTCAGTTT | 55827 |
rs766316940 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938365 | ATCTTTCCATGGCAG[G/T]AAAAATAGATTGATT | 55827 |
rs766335196 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167989028 | GAGGTTGCAGTGAGC[C/T]GAGATCACACCACTG | 55827 |
rs766343706 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968349 | CTGAAAAGAAGAGAC[C/T]CCCCCGTGCTGAGTG | 55827 |
rs766387161 | snp | C/T | 1.68026e-05 | 0.00289845 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023094 | CCATCCATAGCTTTA[C/T]TGCAATGCATATACT | 55827 |
rs766387347 | snp | A/C | 1.65373e-05 | 0.00287548 | missense | DCAF6 | GRCh38.p7 | 1:167991327 | CGGCGAATGCTGGGC[A/C]CAAGAGCTACAGGTA | 55827 |
rs766401019 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041442 | ATAGCATGCATAGGA[A/C]AGCCTTGTTATTCCT | 55827 |
rs766445617 | snp | A/G | 1.68046e-05 | 0.00289862 | missense | DCAF6 | GRCh38.p7 | 1:168068368 | TGTAGGTTATAACTC[A/G]AAACGAACTCATGCT | 55827 |
rs766484284 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022106 | AAGGAGAAGCTTGGG[A/C]CTAAAAATGTTGCTA | 55827 |
rs766498819 | snp | C/T | 1.65187e-05 | 0.00287386 | missense | DCAF6 | GRCh38.p7 | 1:168044647 | GTATCTGCAGAAAAC[C/T]CAGTTGAGAACCATA | 55827 |
rs766511714 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167949905 | GTAGTGGATGTTTTT[A/G]CTAGTTTGCTCTAGA | 55827 |
rs766516732 | snp | A/G/T | 3.32708e-05 | 0.00407854 | missense | DCAF6 | GRCh38.p7 | 1:167993234 | TTTTTAGGGAATTAT[A/G/T]CAGGTCGAGGGACTA | 55827 |
rs766536271 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948495 | CCCCAACCATCTCTA[C/T]AAGTAATAATTCTCA | 55827 |
rs766538223 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167981051 | AGCTGGGATTACAGG[C/T]GCATGCCACCACGCC | 55827 |
rs766543278 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982018 | ATTCCTTTTTCTCTG[C/T]GGCCTCACCAGCAAC | 55827 |
rs766546936 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167969444 | TTCTGATTTTCATTG[C/G]CTTTTAGCTTCTGAG | 55827 |
rs766549181 | snp | C/T | 3.67546e-05 | 0.00428672 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951752 | TCTGTGTTATATTTT[C/T]CTCAGTATTTGTGTG | 55827 |
rs766560918 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070236 | TTGCTTCTCTTATAC[-/A]AAAATACTAGATAGA | 55827 |
rs766561132 | in-del | -/TG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167950866 | TTGCAGTATTTAAAC[-/TG]TTCTGCTATTGATGG | 55827 |
rs766571320 | snp | A/G | 0.000148318 | 0.00861028 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168063756 | TCGCAACTCCAGGAC[A/G]ATGGTACCAAATGTT | 55827 |
rs766572428 | in-del | -/GT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985211 | GTGTGTGTGTGTGTG[-/GT]GTGTGTGTGTGTGTG | 55827 |
rs766593524 | snp | A/G | 1.76577e-05 | 0.00297129 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168004579 | TCCTACGGTCCCATC[A/G]AGTCCTGATTTGGAA | 55827 |
rs766604928 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168044110 | GATAGTGTTTGTACA[A/G]TTTTGTGTGCAAATA | 55827 |
rs766647225 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976056 | TGGGGTTTTACTGGA[A/G]ATTTATGAATTTACA | 55827 |
rs766657389 | snp | A/T | 1.71852e-05 | 0.00293127 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004032 | CAGAAAGCTGGCAAA[A/T]ACTACTTATTGAAGC | 55827 |
rs766692775 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168073682 | ACTTTGAGATAGGCC[A/G]TTACTGCTTCATCAT | 55827 |
rs766697389 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961964 | ATTTCTTCTTTGACC[C/G]ATGTGTTATTTTGAA | 55827 |
rs766730589 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985853 | TCAGCATCTAGAACA[A/G]GAAACAGCCCCCCAT | 55827 |
rs766738676 | in-del | -/AGA | 9.55566e-05 | 0.00691153 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935692 | ATTTTAGAGGAAGCG[-/AGA]AGGAAGGTCTCGATA | 55827 |
rs766757110 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168018010 | GAAATTTTAAAAAGT[A/G]TAGAAAGAATTTCTG | 55827 |
rs766775427 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054328 | GCACAGGAAATCACA[C/T]GATGAGAAGGCTAAG | 55827 |
rs766785370 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167963018 | TAATCCTAGCACTTT[G/T]GGAGGCCAAGGCGGG | 55827 |
rs766850893 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167990809 | TTGCTCAAATACTGA[C/T]CATTTTAAAAATCTG | 55827 |
rs766875900 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167973915 | GAAATAGATTTGCCT[-/A]AGTCAAAGAGTAAGC | 55827 |
rs766886491 | snp | A/G | 1.6643e-05 | 0.00288465 | missense | DCAF6 | GRCh38.p7 | 1:167987588 | ATCAAAACTAGCTGC[A/G]CAAAAGAAGATTGTA | 55827 |
rs766891565 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974222 | GCCCATTAAAAAAAA[A/G]TCAGGTCTTGTCAGT | 55827 |
rs766921793 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986558 | CAATTTTTCCATGGA[A/G]TGGGGATGGTTTTGG | 55827 |
rs766935555 | snp | A/T | 9.67165e-05 | 0.00695334 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065573 | TGAATTTTTAAATAA[A/T]TTTTTTTAACCCTTA | 55827 |
rs766976450 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168053271 | AGAATGTAAGCACCT[C/T]TAAGGACAGTGTAAT | 55827 |
rs766984842 | snp | G/T | 0.000182598 | 0.00955332 | intron-variant, splice-donor-variant | DCAF6 | GRCh38.p7 | 1:168050935 | GATAGAATAATGAGG[G/T]AATTCAGTATGTTCC | 55827 |
rs766986972 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049551 | ATAGGCGTGAGCCAC[C/T]GCGCCTGGCCATATA | 55827 |
rs767000590 | snp | C/T | 1.65463e-05 | 0.00287626 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974887 | AGTGCAAAGTTCTTA[C/T]CTTGTACAAATGATA | 55827 |
rs767007303 | snp | A/C | 1.66942e-05 | 0.00288909 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974977 | GCAGAAACCAACAGA[A/C]AATGCCAATTTACGT | 55827 |
rs767082765 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168047020 | TATAACACTTAATAC[C/T]AAGCCTGCTTTATAG | 55827 |
rs767103381 | snp | A/T | 1.65902e-05 | 0.00288008 | intron-variant, synonymous-codon | DCAF6 | GRCh38.p7 | 1:168023022 | TAACAAACAGCTCGG[A/T]TCCATGTCACTTGAC | 55827 |
rs767177062 | snp | C/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936286 | AGGGAAAGTGAAGCT[C/G]CGCTGGTTCTACTGC | 55827 |
rs767187961 | snp | A/C | 1.66699e-05 | 0.00288698 | missense | DCAF6 | GRCh38.p7 | 1:168063695 | TGGAAGAATTGGATA[A/C]TTTGAACATTAGAAG | 55827 |
rs767229108 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997606 | AAATTCACTGTTAAG[G/T]GTCACCAAGTTTTTA | 55827 |
rs767256121 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070367 | GTGTCCTGCAGTCCA[A/G]ATACAATAATGTGTG | 55827 |
rs767281011 | snp | A/C | 6.6589e-05 | 0.00576975 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038357 | TTTTCAAATGTTTTA[A/C]ACACAATTTTCAGAT | 55827 |
rs767285590 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167953710 | GTTCAAGCAGTTCTC[C/T]GCTGCAGCCTCCCGA | 55827 |
rs767287989 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944468 | TTTTTTCACATGATA[A/G]CCAACATTGTCTGTC | 55827 |
rs767292399 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982386 | AGCTGGGACTATAGG[C/T]GCATGCAACCACGCC | 55827 |
rs767294502 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167942193 | GCCTCAGCCTGCCAA[A/G]TAGCTGGGATATGGG | 55827 |
rs767332265 | snp | C/T | 1.65162e-05 | 0.00287365 | missense | DCAF6 | GRCh38.p7 | 1:167993381 | ATATATCTTTTTGAC[C/T]CGAAAGATGATACAG | 55827 |
rs767356538 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168060054 | TGCTGTTATAAATGC[A/G]TTCCTTTTAAAATTT | 55827 |
rs767369922 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968142 | CGTGTATTGGTGATT[A/G]TATCAGTCGGGTTCT | 55827 |
rs767375473 | snp | A/G | 2.23681e-05 | 0.00334418 | intron-variant | DCAF6 | GRCh38.p7 | 1:168075331 | TAATTGTAATTACTA[A/G]AAGTATTTCTCTTTG | 55827 |
rs767381427 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968138 | CAACCGTGTATTGGT[A/G]ATTGTATCAGTCGGG | 55827 |
rs767383292 | in-del | -/AT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034138 | TATTTCTTAATTAAA[-/AT]AGTTACTTATCTAAG | 55827 |
rs767384331 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167978322 | GTGTAGTAACGACTT[A/G]CATTCCCACCAACAG | 55827 |
rs767408995 | in-del | -/AGA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005967 | TTGGGAATTAAAAGC[-/AGA]AGTAGTTAAAAGTTT | 55827 |
rs767409390 | snp | A/C/G | 4.96471e-05 | 0.00498208 | missense | DCAF6 | GRCh38.p7 | 1:167993249 | GCAGGTCGAGGGACT[A/C/G]CTGGAATGGTTGCCC | 55827 |
rs767409889 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168025471 | GCAGAAGCTGCACCG[C/T]AGTAGACTATCAGAA | 55827 |
rs767417113 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167996477 | TCTCTGGCATGACCT[A/G]TCCCCCTTTGTAGTT | 55827 |
rs767420544 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168061223 | CTAACTGTATCTAAC[G/T]TAAAAATGTATGTGG | 55827 |
rs767421631 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168011825 | TCTACCAAAATAAAT[G/T]TGTTGTGCGTGGTGG | 55827 |
rs767427243 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168063909 | CCAACATGGTTCTTT[G/T]AGCCCTATAATATAT | 55827 |
rs767429668 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168075072 | TTTGCAGCACCTGAT[A/G]TACCTCCTTAGAAAC | 55827 |
rs767475854 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167979713 | ACAACAAGATGAAAC[C/T]GTGCCTCTATTGAAA | 55827 |
rs767503488 | snp | A/C | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935384 | TAATATGCCACAATT[A/C]GAAAAGAGAAAGAGA | 55827 |
rs767514748 | snp | C/T | 1.68889e-05 | 0.00290588 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044881 | ACCACCTGTTACATA[C/T]AACTTTATTTTCTGA | 55827 |
rs767517350 | snp | A/G | 1.79499e-05 | 0.00299577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951777 | TGTGTGATTTATTTA[A/G]TTTGTTCTTTCTTTT | 55827 |
rs767564978 | snp | A/G | 1.82274e-05 | 0.00301883 | missense | DCAF6 | GRCh38.p7 | 1:168075425 | AGAATGAAAATGAGG[A/G]TGAGGAATAATAAAC | 55827 |
rs767580509 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000106 | AATTTCAATATTATT[A/G]TTGTGTCTCAAGAAA | 55827 |
rs767640865 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939654 | TGTAGTCTCAGCTCC[C/T]TGGGAGGCTGAGGCA | 55827 |
rs767641505 | snp | G/T | 3.5256e-05 | 0.00419842 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168004606 | GGAAGTGAGTGAAAC[G/T]GCAATGGAAGTAGAT | 55827 |
rs767685003 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970976 | AGGAAGCCCAGAGAT[A/G]GTCTTGCAATATCTT | 55827 |
rs767686056 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168014618 | GTTTCTCCATTGTTC[A/C]CTGCCGTAATAAATT | 55827 |
rs767690828 | snp | C/T | 1.64939e-05 | 0.0028717 | missense | DCAF6 | GRCh38.p7 | 1:168004706 | TCTCCCACAGAAAGC[C/T]CTCATTCTACTCCTT | 55827 |
rs767700275 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049314 | GTGGTATGATCATAG[C/T]TCACTGCAACCTCAT | 55827 |
rs767706136 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959257 | CATTCTGTAGATGTA[A/C]CACAGTTTGTCCATT | 55827 |
rs767722723 | snp | A/G | 2.08875e-05 | 0.00323161 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987634 | AATTTTTATACAAAT[A/G]ATGCAGAAAAAATTA | 55827 |
rs767727033 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962712 | GTAATCCCAGCACTT[-/G]TGGGAGGTCGAGGTG | 55827 |
rs767736142 | in-del | -/T | 1.78452e-05 | 0.00298702 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974815 | CCATTAACTGCTTTC[-/T]TTTGTGTGTTTTAGG | 55827 |
rs767738868 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013649 | GTTTTCCGCTTTTTT[G/T]TAAGCATCATCTTTC | 55827 |
rs767757087 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050756 | TCCTTGCTTAATGCC[C/T]GAAGTCACAAAGGGA | 55827 |
rs767769096 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017869 | TTTCCTTCATACTTT[G/T]GTATCTTTAGAGTAT | 55827 |
rs767781077 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982161 | GTGTTCGTTGGCTCC[C/T]TGTATGCCTTTGGCG | 55827 |
rs767792808 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168066192 | CTTCAACATGGTATT[A/C]AAATTACGTTCTAGG | 55827 |
rs767834168 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167978680 | TGGTGGGGGAGGGTG[C/T]GGTTTGTGTGTTTTG | 55827 |
rs767840585 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167950029 | ATGTGTTATGCCTCT[A/G]TACATGTTCTAATGT | 55827 |
rs767862619 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005887 | GCTGAGCTACAGAAT[C/G]AAGGTTTTCACACTC | 55827 |
rs767924586 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017226 | AATAAAACATTTTTG[-/G]TTTTTTTTTTTGCTG | 55827 |
rs767925052 | snp | C/T | 4.9769e-05 | 0.00498819 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991197 | GGTATTATGTTATGT[C/T]TTGTAGGATATTTTA | 55827 |
rs767939695 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168027472 | AAGTTTCCTATTTGA[A/G]TATATCTCTGACTAA | 55827 |
rs767946825 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962267 | CTGCCTGCTAGGTCT[A/G]TCTGTTTCTGATAGA | 55827 |
rs767952068 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167992526 | AGGGGAAACAGTAAT[A/G]TAATATGAAATAATA | 55827 |
rs767966921 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168020374 | AGACTATAATTGTCT[A/G]TTTTTTCTACAGTGG | 55827 |
rs767986060 | snp | A/C | 7.14413e-05 | 0.00597625 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065584 | ATAATTTTTTTTAAC[A/C]CTTAGATAAAAGAAG | 55827 |
rs768001209 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945146 | AATATAATTTGAAGT[G/T]AGATAATGTGATGCC | 55827 |
rs768005205 | snp | C/T | 1.65778e-05 | 0.002879 | missense | DCAF6 | GRCh38.p7 | 1:168004668 | CATCCTCTACAATGT[C/T]AGCTCAGGCTCATTC | 55827 |
rs768013301 | snp | C/T | 7.81647e-05 | 0.0062511 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936887 | CACGCGGTGGTCTCC[C/T]CTCCCACCCGGCTCA | 55827 |
rs768016465 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054627 | TTCTAGACTCTTACT[A/T]ATAGGATTCAATTGG | 55827 |
rs768052439 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168021850 | CAGCTAAGGGCAATC[G/T]TAAAATACCTACTTT | 55827 |
rs768061922 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070859 | ATTCTCCTTTGCCCA[C/G]ACATGTTCTTAGGGT | 55827 |
rs768085023 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168021574 | CCACTTTCTTTTTTG[-/T]GTACTAAAGATTTAA | 55827 |
rs768111266 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168006850 | TCAAAGAAACGGACA[A/C]TGGGAATATGAAAAT | 55827 |
rs768134227 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168015257 | ATTTTTTAAAATGAC[A/C]ATTCTAACATGAAAT | 55827 |
rs768169376 | in-del | -/TTTT | 1.65726e-05 | 0.00287855 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966584 | AGATGGCATATTTTC[-/TTTT]ATGTCCAATTTGCTT | 55827 |
rs768169832 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938197 | TTTCTGTTTTCTGAA[C/T]ATTCTTCCAGACCTT | 55827 |
rs768215355 | snp | C/G | 1.64931e-05 | 0.00287163 | missense | DCAF6 | GRCh38.p7 | 1:168004760 | CAAAGGCAGTCTGTT[C/G]AGGCATCTGGACACC | 55827 |
rs768215387 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037478 | CCATTTGTATTCCCT[A/G]TGTATTTTAATGTTT | 55827 |
rs768226437 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000845 | GGAGCTGAGCAGAGG[A/G]ATGAGTGGGGAGTGG | 55827 |
rs768229406 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058599 | TGTTTTGAGATGGAG[G/T]CTTGCTGTCACCAGG | 55827 |
rs768248653 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036231 | GTGTAATATATTCCT[A/G]TAGTCATAGCATGTA | 55827 |
rs768250244 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167946575 | CTAAGGGTTTTTCTT[A/G]TGAAGGGATGTTGAA | 55827 |
rs768286663 | snp | A/G | 1.65195e-05 | 0.00287393 | missense | DCAF6 | GRCh38.p7 | 1:167987567 | GTTAGGTGGTTTGAT[A/G]CACGCATCAAAACTA | 55827 |
rs768294990 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167999843 | TAATAAGGCTGTTTC[A/G]TTTTCTTATCATTCA | 55827 |
rs768309632 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050823 | TAAAAAGGGTGTCCT[C/T]AATGCTTTAAATATT | 55827 |
rs768315366 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050560 | CTTTGAGGAGCATGT[A/G]CGTGTTCCAGAGGAT | 55827 |
rs768330714 | snp | G/T | 1.6563e-05 | 0.00287771 | missense | DCAF6 | GRCh38.p7 | 1:168065688 | TGCTGAGCATTTGAT[G/T]CTTCTGGAAGCTGAT | 55827 |
rs768343971 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977664 | ATTTTCAGTCAGTAG[A/G]TCTTTGGTTTACTAC | 55827 |
rs768384349 | snp | A/C | 1.65891e-05 | 0.00287998 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065788 | CTAGAAATTATTTGT[A/C]TGACTCATCAGTCAT | 55827 |
rs768393171 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167952635 | CTCAGCTGACTCCTC[C/T]GCATATGTTCCTTCA | 55827 |
rs768454233 | snp | C/T | 1.74909e-05 | 0.00295722 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936866 | CCTCCCCCTCCTCCC[C/T]TCCCCCACGCGGTGG | 55827 |
rs768482368 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040445 | TAAGAAAGGTGAGAG[G/T]TGGTGGTGGCTTAGA | 55827 |
rs768491599 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168014221 | AAAATAGCTCTTGTC[A/G]AGGTCATCAATGACT | 55827 |
rs768494367 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970541 | TAGTCCCAGTTACTC[C/G]GGAGGGAGTGGCAGG | 55827 |
rs768496190 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167981895 | TTGGATATATACCCA[C/G]GATTGGGATTGCTGG | 55827 |
rs768510578 | snp | A/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938739 | GTTTAAGTACTTGTA[A/T]ATAGTTCTATATTTT | 55827 |
rs768521042 | in-del | -/TAGG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000291 | CACAGATCACCATAA[-/TAGG]TAGGATAATAATGAA | 55827 |
rs768616130 | snp | C/T | 1.64944e-05 | 0.00287175 | missense | DCAF6 | GRCh38.p7 | 1:168002552 | GACCCAGAGCAAGGC[C/T]GGAGAGTGAACGAGA | 55827 |
rs768626489 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168069714 | AACTTTTACCAGGAA[A/C]GAGGGAAAACTTCAA | 55827 |
rs768632730 | snp | C/T | 3.30267e-05 | 0.00406353 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974941 | GATGGAGTAATATTT[C/T]ATACCAACGTTGAGC | 55827 |
rs768676017 | snp | C/T | 1.84643e-05 | 0.00303839 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168045222 | TCGAGCAGGACCTGG[C/T]GATAGGTTGGTAAAT | 55827 |
rs768699922 | in-del | -/TTGTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168051789 | TTTTGCTTCTCAAAC[-/TTGTT]TTGTTTTGTGCTGTT | 55827 |
rs768721839 | snp | A/G | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167934967 | AGAACACAGTTTTCC[A/G]GTAGGCAAAGAGAGA | 55827 |
rs768733297 | snp | A/G | 0.000101693 | 0.00712995 | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168022988 | TCATTTTTGTTTCAG[A/G]TTCTCCTTCTTCTGT | 55827 |
rs768753249 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167973379 | ACCCTTTGTAACTAA[C/G]AAGCTGTCTGTGAAG | 55827 |
rs768760979 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024826 | AAAAAAAAAAAAGAT[A/T]ATTCCTTATGGACCT | 55827 |
rs768784509 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064667 | TAAAAGTTAGCATGA[A/C]AATAATTAGAGGAAG | 55827 |
rs768805873 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962329 | TTCATCTGTTTCTCT[G/T]TATAGTTCTGTCAGT | 55827 |
rs768824449 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046596 | TCTTTACCTGTACAC[A/G]GTAATCTTGAGCATT | 55827 |
rs768847242 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054091 | TATATGTTGAAATGA[C/T]AGCAATTCTAACATA | 55827 |
rs768848805 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052947 | CTTCATATTATAGCT[A/G]CTGCCAAAAATTGGT | 55827 |
rs768852034 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019137 | CACTGCAACCTCCAC[A/C]TCCCGGGTTCAAGTG | 55827 |
rs768860737 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941977 | TTCCAATTGCTCCAC[A/G]TTCTCATCAGCATTT | 55827 |
rs768893772 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167960119 | AGCAGCACCATTTGT[C/T]GAAAAGACTATCTGC | 55827 |
rs768895975 | snp | A/G | 7.42198e-05 | 0.00609134 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063610 | GTTTTTTTAATATGT[A/G]ATTCATATAGACGCT | 55827 |
rs768941116 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985390 | GCTTCTAGAGGCTAC[C/T]TGCATTCCTTGGAGC | 55827 |
rs768956496 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168031639 | TTCACTTGGAAGTCA[C/T]ATTTTAACTTGTTAA | 55827 |
rs768963114 | snp | A/G | 1.64836e-05 | 0.0028708 | missense | DCAF6 | GRCh38.p7 | 1:167991303 | GACAGCTCAGTACGA[A/G]TATATGATCGGCGAA | 55827 |
rs768993505 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167996218 | TTGGTTCATTCTTTT[A/G]TCTTAATTTTTTTTG | 55827 |
rs769014287 | snp | C/T | 3.5076e-05 | 0.00418769 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993216 | AAATAACTTCTTGTT[C/T]CTTTTTTAGGGAATT | 55827 |
rs769016719 | snp | A/G | 1.66167e-05 | 0.00288237 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023052 | CGAGCAACAGGGTGC[A/G]TGCAACAGGAGATGC | 55827 |
rs769032640 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168074398 | CCTAGTTCCATCTCA[G/T]TGATGGTAGTGATTT | 55827 |
rs769055857 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005127 | TTCTAGATTTATTTG[A/G]TTTTATGTCTATATT | 55827 |
rs769074638 | snp | A/G | 1.75903e-05 | 0.00296561 | missense | DCAF6 | GRCh38.p7 | 1:168068458 | CACTTAATCATATCC[A/G]AGCTGGTAGGAACTT | 55827 |
rs769086617 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943860 | CATTTTTTTTTTGAG[A/T]TGGAGTCTCACTCTG | 55827 |
rs769091839 | snp | A/G | 1.66863e-05 | 0.0028884 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937032 | GGGCCCCGGGGCGGA[A/G]GCGCTGAGGTCGCCG | 55827 |
rs769114713 | snp | A/T | 1.9071e-05 | 0.00308791 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068316 | AAGGAAAAAATACAG[A/T]TACTTTATGATCTTT | 55827 |
rs769144204 | snp | A/T | 1.66646e-05 | 0.00288652 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991188 | TATGTAATTGGTATT[A/T]TGTTATGTTTTGTAG | 55827 |
rs769153996 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167979282 | AGACCCATTTACCCA[A/G]GATGTTTTTTGCCAA | 55827 |
rs769157653 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022803 | TCAAAGTTACTAAAT[A/G]CTTGCCTGGAATAAC | 55827 |
rs769161919 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945859 | CTTGATTTGGTTTTC[A/G]TTTTGAATCATTATT | 55827 |
rs769178057 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167999787 | AATGTGATGACTGGT[C/T]TGATCTTCCTTCTAG | 55827 |
rs769181701 | snp | C/T | 1.69634e-05 | 0.00291229 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167951841 | AAACTTGAAGCAACC[C/T]TTAATGTGCATGATG | 55827 |
rs769204791 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167934783 | TTACAACACATTTTC[C/T]AGTTTGCCAAGTCTT | 55827 |
rs769282073 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968875 | GGTAAATTTGGAACT[A/G]AGAGGAAATAATTTG | 55827 |
rs769286167 | in-del | -/CTT | 4.04817e-05 | 0.0044988 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993207 | ATTAATTTTAAATAA[-/CTT]CTTGTTTCTTTTTTA | 55827 |
rs769293459 | in-del | -/AACTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035656 | GATGAATTCATTAAC[-/AACTT]AAATGAACAAATTCT | 55827 |
rs769324035 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972974 | CCTCTTAAGTGGAGG[C/T]AAATCATAAATTTTT | 55827 |
rs769339266 | snp | G/T | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935975 | TGGAGTACCCTTCCC[G/T]CGGCTTTCCCTGCCC | 55827 |
rs769370062 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168002231 | ACATATACATGATTT[C/T]AAAGTTGCATTCAGG | 55827 |
rs769381493 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168032879 | CATTTTGAATATTTG[A/G]TTTAGATTTACATAT | 55827 |
rs769400959 | snp | C/T | 3.54453e-05 | 0.00420968 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066341 | CTGAATTGCATGTTT[C/T]TAGGCTTCATATTAA | 55827 |
rs769403115 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167980136 | CAGTGAGCTGAGATC[A/G]TGTCACTGCACTCCA | 55827 |
rs769409094 | in-del | -/CTCT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168014376 | CATTCAGTTCTCCAG[-/CTCT]CTCTCTGGCTTTTCC | 55827 |
rs769414931 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168060845 | AGTGAGCTGAGACCC[C/T]GCCACTGCACTCCAG | 55827 |
rs769419461 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967318 | CTAATAAACTCCCTC[A/T]CTAGAAGGCAAGAGA | 55827 |
rs769432262 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167958836 | TTATCAACATCTTCC[A/G]CCTGAGTGGTACATT | 55827 |
rs769457841 | snp | C/T | | | missense | DCAF6 | GRCh38.p7 | 1:167991232 | ACTGTCGACGTGCTG[C/T]CACGTCTGTTGCTAT | 55827 |
rs769469331 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037667 | ATTTCATACATTGAG[A/G]TAGATGTGTATTATA | 55827 |
rs769488065 | snp | C/G | 8.34202e-05 | 0.0064578 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936883 | CCCCCACGCGGTGGT[C/G]TCCCCTCCCACCCGG | 55827 |
rs769524141 | in-del | -/TGGG | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938881 | ATGGAATTTGTGTAT[-/TGGG]TCTAGGGGAATTGAA | 55827 |
rs769529010 | snp | C/T | 1.65304e-05 | 0.00287488 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002583 | ACGAGATGGTAACTA[C/T]ACTTTGGTCAGCTTT | 55827 |
rs769539041 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986355 | ATCCTCATCAACACT[C/T]GATATTATAAGTCTT | 55827 |
rs769567129 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000919 | TATATAATGATGACG[A/G]TTGTACCTCTTTATG | 55827 |
rs769568432 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168067481 | AGAATTGGACAGAAG[C/T]CTGAGAATAGTTCAC | 55827 |
rs769571652 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030077 | CTGGCTCTGGCATCC[A/G]TGATCATAACCACTT | 55827 |
rs769581421 | snp | A/G | 1.65485e-05 | 0.00287645 | missense | DCAF6 | GRCh38.p7 | 1:168003887 | GAGCAGAGTCCCAAT[A/G]TGTCATTGATGCAGA | 55827 |
rs769616879 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940594 | TTCTCAAATTACTGT[A/T]TACTAGGTGTAGAGT | 55827 |
rs769630775 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970689 | TAAAACACCAATGAT[G/T]CATTATATAGGAAAA | 55827 |
rs769645884 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050666 | GATTAAGTGCAATGT[C/T]TTCCTTCTATTCTAG | 55827 |
rs769673140 | in-del | -/A | 3.38914e-05 | 0.00411638 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966758 | GTAATTTAATGAGAG[-/A]AAAAAAATCAAGAAG | 55827 |
rs769741781 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975619 | GGCATGACCATGGCT[C/G]TCTGCAGCTTCAAAC | 55827 |
rs769822306 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976234 | AGCACTCTGGGAGGC[A/T]GAGGTGGGCGGATCA | 55827 |
rs769831866 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167999692 | TCAGACTTTTATTCT[A/G]CAGCTCCCTTACCTC | 55827 |
rs769860417 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937650 | TTCCCACCCCTGGAA[A/G]ACACACTTGGCATTT | 55827 |
rs769882114 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168073439 | ATTTGAGGAGAGAAC[A/G]ACTATTCTGCTTTCC | 55827 |
rs769886782 | snp | A/T | 6.73514e-05 | 0.00580269 | splice-acceptor-variant | DCAF6 | GRCh38.p7 | 1:167993224 | TCTTGTTTCTTTTTT[A/T]GGGAATTATGCAGGT | 55827 |
rs769896550 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001472 | TTCACTGGTGACTGG[A/T]GAGAATGAAGTTAGT | 55827 |
rs769919967 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168028475 | AGTTTGAAACTTACG[G/T]CTGTAGGCAGTTGTG | 55827 |
rs769939276 | snp | A/G | 2.56927e-05 | 0.00358409 | missense | DCAF6 | GRCh38.p7 | 1:168063638 | GCTCTGCTGTTGCCC[A/G]TATTCAGGAGTTCTT | 55827 |
rs769943643 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071220 | CAGATATGGTTTTTA[C/T]TGTAACCACTCAACT | 55827 |
rs769980031 | in-del | -/TTT | | | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168075850 | TACCCTGAATTTGAC[-/TTT]TTATTTAATGCCTTG | 55827 |
rs769995808 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046648 | GTAAGACTTAGTTCT[A/G]TTTCTTTCCATACCC | 55827 |
rs770068115 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975434 | CCAGTAGACAAAAGA[A/T]TCAGATTCCTAAAGG | 55827 |
rs770068704 | snp | A/G/T | 3.33557e-05 | 0.00408374 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023068 | TGCAACAGGAGATGC[A/G/T]CTATGCCCATCCATC | 55827 |
rs770092272 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943219 | TGGCCGAAATTTGGT[A/C]TTTTTTAAAAAAATT | 55827 |
rs770117727 | snp | A/G | 1.65916e-05 | 0.00288019 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168038480 | AAAACTGAACTTTAC[A/G]GATGAATGGTAAGTT | 55827 |
rs770120942 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974001 | AGCATTCCTACCAAC[A/G]GTGTTTAAGAGTCTG | 55827 |
rs770133529 | snp | A/G | 1.81826e-05 | 0.00301513 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068469 | ATCCGAGCTGGTAGG[A/G]ACTTTAAGTATACTA | 55827 |
rs770135084 | snp | C/T | 3.30464e-05 | 0.00406474 | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167966676 | ATATATTTTATCTGG[C/T]TCAGATGACACCAAA | 55827 |
rs770172280 | snp | C/T | 1.64912e-05 | 0.00287147 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168044929 | TTCACAGCCAAGCCA[C/T]TGGATTCCAACTCAG | 55827 |
rs770177413 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168005297 | AAAATTTGTTTCTCT[A/G]GTATTTACATGAAAA | 55827 |
rs770177497 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062449 | TAAAAACCGCTTTCA[A/G]ACTCCTCTCAGTAAT | 55827 |
rs770181522 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168020127 | AGGCAAGTAATGATA[A/G]ACATTAAATGACCCA | 55827 |
rs770185052 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962832 | TGGTGGCACATGCCT[A/T]TAATCCCAGTTACTT | 55827 |
rs770206178 | snp | C/T | 1.76319e-05 | 0.00296911 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168075376 | GTGTTTCCAGACCGG[C/T]TGGAGGGTGACAGAT | 55827 |
rs770227836 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168045642 | TTGACCCTGGATTAA[A/G]GTAGTGTGTTAGTAG | 55827 |
rs770235328 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168012621 | TAAAATTTCAAGCTG[C/T]TAGCAGAACTGTTAT | 55827 |
rs770252433 | snp | A/G | 3.41869e-05 | 0.00413428 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951868 | GATGGTTGTGTAAGT[A/G]ATAGTTAATTCTCAA | 55827 |
rs770312945 | snp | A/C/T | 0.000196635 | 0.00991372 | synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936965 | CGTGAGGAAAAGGTC[A/C/T]CTCGGGCTGGAGGAC | 55827 |
rs770317401 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968076 | ATCTATTATTTTAAT[A/G]GTAATTCCAAAAATG | 55827 |
rs770320910 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997113 | TATAAAAGGTGCTCA[A/G]AAAATATTTGGTGAA | 55827 |
rs770359052 | in-del | -/TAT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985687 | ATATCTTTGGGCTAC[-/TAT]TATTCTGCTTACCAC | 55827 |
rs770392371 | snp | A/G | 2.75281e-05 | 0.00370989 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993186 | AATGTTTTTCTTTAA[A/G]ACATTATTAATTTTA | 55827 |
rs770413389 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168068011 | GTCACTAAAGTTATC[A/C]GTTCTCCTATAGGGA | 55827 |
rs770424625 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167953205 | CCAAGGACACCTCTG[C/T]CTTGTATATTTTATG | 55827 |
rs770448813 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168010500 | TTTTTTGCTTTACCC[C/T]TTGTATTCTTGAATT | 55827 |
rs770504552 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167991701 | TCTGTTCGATGCCTT[C/T]TCCCCTAGCTCATGG | 55827 |
rs770506213 | snp | A/G | 0.000249124 | 0.0111579 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066496 | TACTTACTATAGACC[A/G]TATTTCAATTTGTTC | 55827 |
rs770513325 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167980369 | GATCATATGGTAATT[A/C]CATTTTTAAGTTTTT | 55827 |
rs770517007 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971703 | ATCATTGCAATTATC[A/G]ATATGTTATTTTCAT | 55827 |
rs770528435 | snp | A/G | 2.91907e-05 | 0.00382027 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937025 | TGAGCGGGGGCCCCG[A/G]GGCGGAGGCGCTGAG | 55827 |
rs770540473 | snp | A/G | 1.65045e-05 | 0.00287263 | missense | DCAF6 | GRCh38.p7 | 1:168044611 | GAATCATCAGAGGAT[A/G]TGACAAAATATCAGG | 55827 |
rs770540548 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036389 | TTACACTTCTCTCAC[A/G]TCTGCTTTTGTTTTC | 55827 |
rs770550847 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167979609 | TCATTTATCTAGGCT[G/T]TGTGCTGTGGCTCAT | 55827 |
rs770555176 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168012821 | AAATATTGAATAAAT[G/T]GTTCATAAGATTATC | 55827 |
rs770555742 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046788 | TTCCAAAACCCAGGG[C/T]TGAGAGCTAGATTCT | 55827 |
rs770589194 | snp | A/T | 1.72534e-05 | 0.00293708 | splice-acceptor-variant | DCAF6 | GRCh38.p7 | 1:168004531 | TAACATGTGTTTTGA[A/T]GGTGGAACAAGTCAA | 55827 |
rs770626191 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982564 | TCTGGATATTAAACC[-/T]TCGTCAGGTGCATAG | 55827 |
rs770632797 | snp | A/G | 1.72299e-05 | 0.00293508 | missense | DCAF6 | GRCh38.p7 | 1:168068449 | TGTTGGCTTCACTTA[A/G]TCATATCCGAGCTGG | 55827 |
rs770633784 | in-del | -/G | 1.7693e-05 | 0.00297425 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993491 | CGGTGGCTCACGCCT[-/G]GTAATCCCAGCGCTT | 55827 |
rs770668813 | in-del | -/TT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961755 | TACAGGTTGAGTGTC[-/TT]TAATTTGAAAATCTG | 55827 |
rs770670114 | snp | G/T | 3.30972e-05 | 0.00406786 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974955 | TTATACCAACGTTGA[G/T]CAAGATGCAGAAACC | 55827 |
rs770684058 | snp | G/T | 1.67147e-05 | 0.00289086 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044701 | TTAGATAATTGCTTT[G/T]TATGGGAAAATAAAA | 55827 |
rs770685290 | snp | A/G | 5.743e-05 | 0.00535833 | missense | DCAF6 | GRCh38.p7 | 1:168063659 | AGGAGTTCTTCAGAC[A/G]GAGAAAAGAAAGGAA | 55827 |
rs770687349 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019460 | GAGCTATATGTACAT[A/G]TATCAGATGAATGTC | 55827 |
rs770690890 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167990168 | AAAATATTATGAATA[A/T]GCCTAGGCAACATAG | 55827 |
rs770697986 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052819 | CTCATCACCTCTTAC[C/G]TGGTGTACTGAGGGA | 55827 |
rs770698749 | snp | C/T | | | missense | DCAF6 | GRCh38.p7 | 1:168004713 | CAGAAAGCCCTCATT[C/T]TACTCCTTTGCTATC | 55827 |
rs770720328 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961310 | TGCAGTGGCGCGATC[G/T]CGGCTCAATGCAAGC | 55827 |
rs770743039 | in-del | -/AATAT | 1.69798e-05 | 0.00291369 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966771 | GAAAAAAAATCAAGA[-/AATAT]AGGCAGAAATGAAGA | 55827 |
rs770751654 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168026305 | TAATATTCGTTAAAC[A/G]AGTGAGTAAATGAAT | 55827 |
rs770810300 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948416 | GCTCTGAGAAAATAA[A/G]TTTTGCCCAACCTAA | 55827 |
rs770851450 | in-del | -/TTGT | 3.60669e-05 | 0.00424643 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068468 | ATCCGAGCTGGTAGG[-/TTGT]AACTTTAAGTATACT | 55827 |
rs770867605 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168074838 | GAGCATACTGTACTC[A/C]CCAGTTTGTAAGTTT | 55827 |
rs770869600 | snp | C/T | 0.000115355 | 0.00759368 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063784 | GTTCATGGCATTTTT[C/T]GGTGAAATTGCAGTT | 55827 |
rs770878378 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017226 | TAATAAAACATTTTT[-/G]TTTTTTTTTTTGCTG | 55827 |
rs770882889 | snp | C/T | 1.69576e-05 | 0.00291179 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935737 | GGGTCCATTACCTGC[C/T]GGATGGTTGTACAAC | 55827 |
rs770903802 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167953387 | ACATTATTATTATTA[C/T]TGATAGTGCTTACTA | 55827 |
rs770904428 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017487 | TTGTAACTAGTTCAC[A/G]GATTTGAATTGAAGC | 55827 |
rs770969340 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167951655 | CGGAGGTTAAATTGC[C/T]CAGTATCACTCAGTT | 55827 |
rs770995998 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167978018 | TTTGTTGTTGTTTTT[A/G]TATCTGGCTTTTTTT | 55827 |
rs771003822 | snp | A/G | 1.73613e-05 | 0.00294624 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951901 | CTGAAGGGATTTGAT[A/G]CTAAGTGTTTAAGTG | 55827 |
rs771053002 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168044320 | ATACTCCCTCCCAAA[A/G]TAACAATATGACAAT | 55827 |
rs771072017 | in-del | -/TT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009439 | TTCTGTCTCTCTCTC[-/TT]TCTTTCTTTCTGTCT | 55827 |
rs771076510 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058893 | GTTTTCTACTGGGTT[C/G]TTTTAATTGAGTTGT | 55827 |
rs771079467 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167956440 | CTGATATTGGTAATA[-/T]TTTTCTCCATGTTTT | 55827 |
rs771080892 | snp | A/G | 1.66479e-05 | 0.00288508 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038499 | GAATGGTAAGTTAAT[A/G]TTTTTGTAAAGATGT | 55827 |
rs771082066 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954434 | AGATTTGTGCTTAAA[-/T]TTTTTATTTTTTATT | 55827 |
rs771115202 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995055 | AGAAGGGTATGATGG[C/T]TAATAAAATGATTTT | 55827 |
rs771169160 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168032104 | TGACATAGAGTTGAG[C/T]TGTGATTGCCAGAAG | 55827 |
rs771169297 | snp | C/T | 1.75289e-05 | 0.00296043 | missense | DCAF6 | GRCh38.p7 | 1:168075401 | ACAGATCAGAAGGCT[C/T]TGGTCAAGAGAATGA | 55827 |
rs771217130 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007591 | ACTAGATTTTTCGAC[A/C]CGGTTGCATTTAACA | 55827 |
rs771219225 | snp | A/G | 1.65392e-05 | 0.00287564 | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167966697 | TGACACCAAATTAGT[A/G]ATTAGTAATCCTTAC | 55827 |
rs771253053 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975613 | TGCAGTGGCATGACC[A/G]TGGCTCTCTGCAGCT | 55827 |
rs771262652 | snp | G/T | 1.71029e-05 | 0.00292424 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993468 | AAAACCATGTCCTTT[G/T]GCCGGGCGCGGTGGC | 55827 |
rs771290421 | in-del | -/AAGTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167987257 | ATAACTTTTTATCTG[-/AAGTT]AAGTTAATGCTAATC | 55827 |
rs771320629 | snp | A/G | 1.67663e-05 | 0.00289532 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004808 | GGTGAGGATAAGTAT[A/G]CTGTGGTTCATCTAA | 55827 |
rs771353743 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054757 | TTTTCTTTTCTAAGA[A/G]CTACTAAGCTAATAT | 55827 |
rs771371769 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167999477 | AAAGTCCTAAATGGC[A/G]TCTGCTTCTGATAGA | 55827 |
rs771373802 | in-del | -/AAAG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168045356 | CATTCATATAAACTT[-/AAAG]AAAGAAACTTTACAG | 55827 |
rs771376104 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167988229 | GCAGTGGTGCAATCC[G/T]AGCTCACTGCAGCCT | 55827 |
rs771398657 | in-del | -/TGT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034071 | TTAACCAGTTATTAA[-/TGT]TGTTGATATGAATTA | 55827 |
rs771443662 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167957236 | TAATTTTATCATCTG[A/T]AAAAGAGTACCAATT | 55827 |
rs771491194 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986330 | TCAGCAATGTGTTCC[A/G]TAACTCCACATCCTC | 55827 |
rs771509803 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964769 | TTCTCAGTTTTGTAC[A/G]TTTTTATTGATATAT | 55827 |
rs771510767 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064526 | TAGGTTAAAAAATAA[C/T]ATTTGGGTTGGGGAA | 55827 |
rs771528551 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970299 | ATGTATATTTGAAAA[A/T]ATGATACTCTTTCTC | 55827 |
rs771531376 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944133 | AGGGGTGAGCCACCA[C/T]GCCCAGCCTGATTTC | 55827 |
rs771571439 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943257 | ATCCTGGCTATTCTG[A/C]ACCCTTTCTATTTCC | 55827 |
rs771578101 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035143 | ACCTTGGAATATATA[C/T]TGTCACTAATACTGC | 55827 |
rs771652729 | snp | A/G | 0.000370651 | 0.0136084 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044713 | TTTGTATGGGAAAAT[A/G]AAAAGCCTTAATCTA | 55827 |
rs771658102 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168014058 | TTCCCTTGATTCTTT[A/G]TAACCCTGACAATGA | 55827 |
rs771660414 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167958204 | GCCGTATTTAAGAAA[A/C]TTGCTTAATCACTGG | 55827 |
rs771683046 | in-del | -/TTAAG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168010809 | TCTTTCAGTTATTTC[-/TTAAG]TTAAGCCTAGAAATG | 55827 |
rs771689994 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986114 | AATTTAATCCCAGTT[G/T]ATTGTTGGATATTTG | 55827 |
rs771693904 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167999694 | AGACTTTTATTCTAC[A/G]GCTCCCTTACCTCTA | 55827 |
rs771727508 | snp | C/T | 1.64953e-05 | 0.00287182 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167987545 | CTCTTGTGGTGAAGA[C/T]GGAACTGTTAGGTGG | 55827 |
rs771736321 | snp | C/T | 5.13773e-05 | 0.00506814 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987458 | CCGTCTGTTTAAATG[C/T]TCGTATGATTATCTG | 55827 |
rs771739803 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972062 | GGTTTCGCCATGTTG[A/G]GCAGGCTGGTCTCGA | 55827 |
rs771746333 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050334 | TTTATTCAGTCATCA[C/T]TGTAACCATGATTTC | 55827 |
rs771775545 | snp | A/G | 0.000198265 | 0.00995456 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168044913 | AGCACAATCAGATAA[A/G]TTCACAGCCAAGCCA | 55827 |
rs771798143 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013177 | TGAAAAGAAAGCAGT[A/G]TGCCACTGAGCATCA | 55827 |
rs771817573 | snp | C/T | 1.68935e-05 | 0.00290628 | upstream-variant-2KB, missense, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935765 | AACGGCCTCAATTTC[C/T]CGGGCAGCATCAGCT | 55827 |
rs771825936 | snp | A/G | 1.66843e-05 | 0.00288823 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038510 | TAATATTTTTGTAAA[A/G]ATGTTCTTAGCCATT | 55827 |
rs771832631 | snp | A/G | 6.63911e-05 | 0.00576118 | missense | DCAF6 | GRCh38.p7 | 1:168004664 | TCTACATCCTCTACA[A/G]TGTCAGCTCAGGCTC | 55827 |
rs771842259 | snp | A/G | 4.9458e-05 | 0.00497258 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168004747 | TCCAGACAGTGAACA[A/G]AGGCAGTCTGTTGAG | 55827 |
rs771846582 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041254 | TCAGATACTTTGCCC[A/G]GTTTTCTATGGTGTT | 55827 |
rs771888438 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168053805 | ATCATGTTATTTTTG[A/C]AGTTTACGCAAGCTG | 55827 |
rs771913118 | snp | A/G | 1.66217e-05 | 0.0028828 | missense | DCAF6 | GRCh38.p7 | 1:168065677 | GATCGGCACACTGCT[A/G]AGCATTTGATGCTTC | 55827 |
rs771925290 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167981605 | ATCCAGTGTGTAGCT[C/T]CTACTTATAAGTGAG | 55827 |
rs771977419 | snp | A/G | 4.35825e-05 | 0.00466791 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935863 | CGAGGGATCGTTGGC[A/G]GCCGGGTGGGAGCGT | 55827 |
rs771987968 | in-del | -/T | 4.3928e-05 | 0.00468637 | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075472 | TTAAATGTTCTGAAA[-/T]TTGTATAAGACATTT | 55827 |
rs772044474 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168031235 | ATCTCAAGAAAAATC[A/G]GAAAAATTCTAAAAT | 55827 |
rs772095137 | in-del | -/TAAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967566 | TTTTAGAAATATGAC[-/TAAA]TAGTTATTTTAAAAT | 55827 |
rs772100173 | in-del | -/AAC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167993759 | CGTCTCAGAAAAAAC[-/AAC]AACAACAACAACAAC | 55827 |
rs772126340 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995146 | TTTCCCCTTGAAATA[C/T]ATGGGTAAGTAAAGT | 55827 |
rs772137347 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962765 | TTCAAGACCAGCCTG[A/G]CCAACGTGGCAAAAC | 55827 |
rs772143033 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940664 | TTTATTATCCCATAT[A/G]TATACGGTTTTGTAA | 55827 |
rs772152608 | snp | A/T | 1.65209e-05 | 0.00287405 | missense | DCAF6 | GRCh38.p7 | 1:168045091 | AATCCTGAGCCTCAG[A/T]TCCAAACAGAAGCCA | 55827 |
rs772191895 | snp | C/T | | | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168015819 | GCTTTGCTTCGTAAG[C/T]GCCTGCAACAACTGA | 55827 |
rs772202603 | snp | A/G | | | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168076200 | TTCTATACTCTTACA[A/G]TAAAGTAAGCTACAG | 55827 |
rs772211621 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167983338 | CTGTTTGTTGTTGTC[A/G]TTGCTGTTTGTTTAG | 55827 |
rs772213681 | in-del | -/ATC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167955486 | CAGGCATCTAGTAGT[-/ATC]ATGTTGTGGTTACAT | 55827 |
rs772253664 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019730 | AAAGTAATTTTTATA[C/T]CCCAAAAGGGTGTAA | 55827 |
rs772256413 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168067854 | CACGAGTATTCAAGT[A/G]ATCCTATTCTTGGTA | 55827 |
rs772257997 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167983729 | TAATGTCTAATTCTT[A/T]CTTTTACTTTTAACT | 55827 |
rs772286593 | snp | C/T | 1.65567e-05 | 0.00287716 | missense, intron-variant, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167966708 | TAGTAATTAGTAATC[C/T]TTACAGCAGAAAGGT | 55827 |
rs772306588 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168010421 | GTTGGCTTTGGAGTT[-/G]TTGTAGCTAAATTAG | 55827 |
rs772370904 | snp | A/C | 1.73489e-05 | 0.00294519 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004839 | TGATTTTTGATAGTG[A/C]AAATTTCTTTACTGG | 55827 |
rs772390194 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030190 | GGTTCAGTGTGGAAC[A/G]TAGGAGAGTGGGCCT | 55827 |
rs772427764 | snp | A/G | 5.52207e-05 | 0.00525426 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022956 | AGTTTTCTGCTGCTT[A/G]CTTTTAAGTTGAAAT | 55827 |
rs772431302 | snp | G/T | 1.76163e-05 | 0.0029678 | missense | DCAF6 | GRCh38.p7 | 1:168045215 | CAAGGTATCGAGCAG[G/T]ACCTGGTGATAGGTT | 55827 |
rs772458678 | in-del | -/CTATGAAAAACA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168029812 | AGTGAAACCCCGTCT[-/CTATGAAAAACA]CAAAAAATTAGCCAG | 55827 |
rs772469711 | in-del | -/C | 3.3888e-05 | 0.00411617 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004820 | TATGCTGTGGTTCAT[-/C]TAATGATTTTTGATA | 55827 |
rs772480046 | in-del | -/ATTGT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167987843 | AGAACTTATATTTTA[-/ATTGT]ACATTTAAAATATAT | 55827 |
rs772521242 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168042953 | TACCTTTCTAGTTGT[-/A]AAATATAAAAATCCT | 55827 |
rs772523350 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036019 | GTGGGCCGAGATCGC[A/G]CCATTGCACTCCAGT | 55827 |
rs772536160 | in-del | -/AG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944118 | AAGTGCTGGGATCAC[-/AG]GGGTGAGCCACCACG | 55827 |
rs772549706 | snp | C/T | 4.94417e-05 | 0.00497176 | missense | DCAF6 | GRCh38.p7 | 1:167991298 | GTTCTGACAGCTCAG[C/T]ACGAATATATGATCG | 55827 |
rs772558754 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943629 | ATCACCTGAATAACG[C/T]TCTTTGTCCTCATTA | 55827 |
rs772561667 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167987405 | TTTGTAACCTTTACC[G/T]TAATCATTTTATGAA | 55827 |
rs772570780 | snp | G/T | 3.35261e-05 | 0.00409413 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066353 | TTTCTAGGCTTCATA[G/T]TAATATATAAATTTT | 55827 |
rs772576222 | in-del | -/TCTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019114 | AGTGCAGTGGTGCTA[-/TCTT]GGCTCACTGCAACCT | 55827 |
rs772615529 | snp | A/T | 1.65151e-05 | 0.00287355 | missense, utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936952 | ACCTGTTGTGGGACG[A/T]GAGGAAAAGGTCCCT | 55827 |
rs772650242 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941647 | GCTTGAGGTTTGGAA[A/T]ATTGTTCTAGATGGT | 55827 |
rs772674652 | snp | A/G | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167936093 | CCCCGGCAGGAGAGA[A/G]GGAGGAGCCATGGCA | 55827 |
rs772689660 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168059035 | TTTAGGCTGTTTTTT[C/G]ATGAACCATTTTTAA | 55827 |
rs772699391 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977921 | TATTCTGAATTCTAA[C/T]ACTGGAGTTTTCTGT | 55827 |
rs772714836 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009677 | TGTCCTGGCTTATCA[C/T]TTGGCCAACTTCCTT | 55827 |
rs772724789 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167988506 | AAGGCCTGAGAAATC[A/C]TTCAGTCTTTTGACC | 55827 |
rs772760115 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968882 | TTGGAACTGAGAGGA[A/G]ATAATTTGATAAGTG | 55827 |
rs772782332 | in-del | -/G | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998404 | TGGTTGCTGAAGGTT[-/G]GGGCTGTGACAGTTT | 55827 |
rs772790181 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035738 | TTGACATGTTTTGTA[A/C]TATGTAGATTATATT | 55827 |
rs772847109 | snp | C/G/T | 0.000243701 | 0.0110363 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936885 | CCCACGCGGTGGTCT[C/G/T]CCCTCCCACCCGGCT | 55827 |
rs772848453 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967525 | TTCTTTACACTTGAC[A/G]TAACAGTTAAATGAG | 55827 |
rs772862612 | snp | C/T | 1.65641e-05 | 0.00287781 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002588 | ATGGTAACTATACTT[C/T]GGTCAGCTTTTCTTT | 55827 |
rs772881350 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959833 | TTTTCTTGACATTGT[A/C]TTTTGCAGGGTGGAA | 55827 |
rs772881878 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168033161 | ACTTTGTGATTCTTA[C/T]GCAAAAGACTTGAAA | 55827 |
rs772882433 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167990130 | TAATTTTTTGTTATA[G/T]TTTAATAGCAGTGAT | 55827 |
rs772893173 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168060857 | CCCCGCCACTGCACT[C/T]CAGCCTAGGTGATAA | 55827 |
rs772926521 | snp | A/C/T | 3.30089e-05 | 0.00406246 | missense, synonymous-codon | DCAF6 | GRCh38.p7 | 1:168044610 | AGAATCATCAGAGGA[A/C/T]GTGACAAAATATCAG | 55827 |
rs772934981 | snp | A/T | | | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167991260 | TATTTGCCCACCAAT[A/T]CCATATTACCTTGCT | 55827 |
rs772965470 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167979522 | TGATCATATTGTAGC[A/C]TATGTCAGAATTTAT | 55827 |
rs772974103 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945514 | TTTTCTTTTTTGAGA[C/T]GGAGTCTCACTCTGT | 55827 |
rs772986076 | snp | A/C | 1.7345e-05 | 0.00294486 | synonymous-codon, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974841 | TTAGGTTTTGACAAC[A/C]ATTCGTTCAGGGCAC | 55827 |
rs772986253 | snp | A/G | 1.65493e-05 | 0.00287652 | missense | DCAF6 | GRCh38.p7 | 1:168003900 | ATGTGTCATTGATGC[A/G]GAGAATGTCTGATAT | 55827 |
rs772987885 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168060089 | TAATTGTCCCCTGCT[C/G]ATATTTAGAAATGCA | 55827 |
rs773022731 | in-del | -/AAACA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167989079 | GCGAGACTCCATCTC[-/AAACA]AAACAAAACAAAACA | 55827 |
rs773037457 | snp | A/G | 0.000115703 | 0.00760515 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974950 | ATATTTTATACCAAC[A/G]TTGAGCAAGATGCAG | 55827 |
rs773055401 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050687 | TCTATTCTAGCTTCA[A/G]TGAGTGTTTCTGTTT | 55827 |
rs773070897 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168051487 | ACATATTTTTGAGTA[C/G]ATCTTTAAAGTGAAC | 55827 |
rs773074846 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971948 | GCAACCTCCACCTCC[C/T]GGGTTCAAGTGATTC | 55827 |
rs773083314 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168043963 | TTAAGTTTAGATTTC[A/G]GGAAGGTTAGTAAAA | 55827 |
rs773086668 | snp | A/G | | | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168015919 | CTGATCAGTCTTCTC[A/G]TGAGGGCTCTTCACA | 55827 |
rs773092879 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168036312 | ATCATTTAAATTCCA[C/G]AAGGCTTCTCATAAC | 55827 |
rs773115054 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168015662 | TAATTTGTTTATAGT[A/G]TTCCTCTATGAGACA | 55827 |
rs773137150 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940619 | TAGAGTAGTGCTTTT[A/G]GAAATCAGTGATTTA | 55827 |
rs773148530 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167949625 | CCAATGTAAACCTGA[A/G]GCTCATACTGCTTGC | 55827 |
rs773151204 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970700 | TGATTCATTATATAG[C/G]AAAAAAAGCTTTTTG | 55827 |
rs773200897 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001122 | CCTGGGCAACATAGC[C/T]AGACTCCATCTCTAA | 55827 |
rs773205997 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001493 | TGAAGTTAGTGGAAA[A/G]ATAGGAAATCAATGG | 55827 |
rs773239040 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959089 | CTTTTTATAGTCTCC[A/T]TAGTTAAGCCTTTTC | 55827 |
rs773283748 | snp | A/C/G | 3.89706e-05 | 0.00441408 | synonymous-codon, missense | DCAF6 | GRCh38.p7 | 1:168063658 | CAGGAGTTCTTCAGA[A/C/G]GGAGAAAAGAAAGGA | 55827 |
rs773289536 | snp | G/T | 1.66502e-05 | 0.00288527 | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168023006 | CTCCTTCTTCTGTGG[G/T]TAACAAACAGCTCGG | 55827 |
rs773291697 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167952795 | AACTTTCTACTTAAC[A/G]TGTCCAGTTGCATGT | 55827 |
rs773317953 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168027003 | ACGCAGGGCAGAAAG[A/T]ATGCCATATCCAAAA | 55827 |
rs773326971 | snp | C/T | 1.64977e-05 | 0.00287203 | missense | DCAF6 | GRCh38.p7 | 1:167993358 | TCGTTAGTTACTCTT[C/T]AGATTACATATATCT | 55827 |
rs773345515 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962929 | CCACTGCACGCCAGC[C/G]TGGCGATGAAGCGAG | 55827 |
rs773372841 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975460 | AAAGGATATTAATGA[C/G]CTTAAGACCTGAGCT | 55827 |
rs773380695 | snp | G/T | 1.67702e-05 | 0.00289566 | missense | DCAF6 | GRCh38.p7 | 1:167993226 | TTGTTTCTTTTTTAG[G/T]GAATTATGCAGGTCG | 55827 |
rs773431515 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961697 | AGTATGGTGTTGAAA[C/T]GAAGTGGTGAGAGAG | 55827 |
rs773444009 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168042851 | GAGTAAAGTGTGTTA[C/T]GATAGTCATCTTGAT | 55827 |
rs773445731 | snp | C/T | 1.72015e-05 | 0.00293265 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951884 | ATAGTTAATTCTCAA[C/T]TCTGAAGGGATTTGA | 55827 |
rs773473315 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041397 | TTTCAGTTTACTTAC[A/C]GTGGTTTTGCCTTAT | 55827 |
rs773493459 | snp | C/T | 1.83041e-05 | 0.00302518 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068471 | CCGAGCTGGTAGGAA[C/T]TTTAAGTATACTACT | 55827 |
rs773507871 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168025852 | AGCCTTTCAAAAGAA[C/T]CCAAATCCATACCTT | 55827 |
rs773517418 | in-del | -/AAC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167993756 | CTCCGTCTCAGAAAA[-/AAC]AACAACAACAACAAC | 55827 |
rs773522806 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070129 | TTGGTTTTAGAATTA[A/G]ATAAGGTGTTTTATA | 55827 |
rs773532508 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168025575 | GAGTTTTTACATACC[-/T]TTTTGTTCATCAGCA | 55827 |
rs773533764 | snp | C/T | 7.4308e-05 | 0.00609496 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937045 | GAGGCGCTGAGGTCG[C/T]CGCCTAGAGTGGGGG | 55827 |
rs773537616 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071229 | TTTTTATTGTAACCA[C/T]TCAACTCTGCCATTG | 55827 |
rs773553931 | snp | C/T | 1.7653e-05 | 0.00297089 | missense | DCAF6 | GRCh38.p7 | 1:168004575 | CTCTTCCTACGGTCC[C/T]ATCAAGTCCTGATTT | 55827 |
rs773565927 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997169 | CCTAGGTTATTTCAC[A/G]TACTCAGAAAGTCAA | 55827 |
rs773567318 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974040 | TAAGCTTGTTTGTAG[A/G]GTCTGTTGTCAAGCT | 55827 |
rs773568586 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168033996 | AGTGCCCTAAAAGAA[A/G]ATACAACATAGTTTT | 55827 |
rs773571370 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046684 | GAGTTCCTTAGAATG[C/T]CATTACCACTTAATT | 55827 |
rs773573179 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986313 | ACCATTTTATACTCC[C/T]ATCAGCAATGTGTTC | 55827 |
rs773595864 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054459 | CATGATCCAATCACC[-/T]TTTTAAAGACCCCAC | 55827 |
rs773598028 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022716 | TATCTACCTTGCACC[C/T]TGTGCCTCTGGTATA | 55827 |
rs773617534 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943226 | AATTTGGTCTTTTTT[A/T]AAAAAATTTATAGTT | 55827 |
rs773619409 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167942109 | TCGCTCTTGTCGCCC[A/G]GGCTGGAGTGCAATG | 55827 |
rs773639274 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167992140 | ACTGAATTTGAATCT[A/C]ATATAAACTAATGCT | 55827 |
rs773748203 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998348 | TTTTGCTGGTGGAGG[A/G]GCTTACCTTAATGTT | 55827 |
rs773783534 | snp | G/T | 1.65438e-05 | 0.00287605 | missense | DCAF6 | GRCh38.p7 | 1:168004676 | ACAATGTCAGCTCAG[G/T]CTCATTCGACATCAT | 55827 |
rs773785664 | in-del | -/ATAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939763 | GGGAAACTCTGCGTC[-/ATAA]ATAAATAAATAAATA | 55827 |
rs773796445 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968016 | GATTACAGGCATGAG[C/T]CACCACGCCCAGCCC | 55827 |
rs773819539 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168044805 | TAGAGGAATTAGACA[-/T]CATATTAGAATGTGT | 55827 |
rs773851962 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985879 | CCCATAAGTCCTTTG[C/T]ACCCCCTCAAAGGGT | 55827 |
rs773883007 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971980 | CGTGCCTTAGCCTCC[C/T]GAGTAGCTGGGACTA | 55827 |
rs773893367 | snp | G/T | 3.31186e-05 | 0.00406918 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974959 | ACCAACGTTGAGCAA[G/T]ATGCAGAAACCAACA | 55827 |
rs773894025 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034082 | TTAATGTTGTTGATA[C/T]GAATTATTTATTTCT | 55827 |
rs773898800 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954761 | CCGGCAAATTTTTGT[A/G]TTTTTAAGAGCTTTA | 55827 |
rs773907759 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168063194 | AATAGAAGTCTATCC[A/G]CTGCTATTATATATT | 55827 |
rs773949589 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168048455 | AAGTCATTTCTGACA[A/C]ATTTACTGAAAATAT | 55827 |
rs773997741 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944288 | AACATACTGGTGCAC[A/G]TATCTTTTAGATATA | 55827 |
rs774005674 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948468 | TATTTAAACCTAATC[C/T]AACATTTCTTGCCCC | 55827 |
rs774017641 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052843 | TGAGGGAGTTCTCCA[A/G]CTCCTTCTACTCCTG | 55827 |
rs774031099 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168008123 | TACAGGTTCCTGCCA[C/T]CACACCCAGCAAATT | 55827 |
rs774039125 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046855 | ATAAATGAGCTAATG[G/T]CTTATTTTTCTACAT | 55827 |
rs774068704 | snp | C/T | 1.72868e-05 | 0.00293992 | missense | DCAF6 | GRCh38.p7 | 1:168004539 | GTTTTGAAGGTGGAA[C/T]AAGTCAATCAGATAT | 55827 |
rs774101424 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968130 | GGTAGTAGCAACCGT[A/G]TATTGGTGATTGTAT | 55827 |
rs774115894 | snp | A/G | 1.648e-05 | 0.0028705 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063789 | TGGCATTTTTTGGTG[A/G]AATTGCAGTTTCATG | 55827 |
rs774121713 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997562 | TTTTCTATTCATGTT[A/G]CTAGGTATGGTTTCC | 55827 |
rs774129176 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168026517 | CAACCTAAGGCAATA[C/G]TGGTGAGAAGTGGGA | 55827 |
rs774144475 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167991408 | CTATGACATTTTCAG[-/T]TTTTAAAATTTCTTG | 55827 |
rs774154568 | in-del | -/A | 1.71879e-05 | 0.00293149 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004029 | CATCAGAAAGCTGGC[-/A]AAAACTACTTATTGA | 55827 |
rs774165192 | snp | C/T | 1.66513e-05 | 0.00288537 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038501 | ATGGTAAGTTAATAT[C/T]TTTGTAAAGATGTTC | 55827 |
rs774170552 | snp | A/G | 1.82294e-05 | 0.003019 | missense | DCAF6 | GRCh38.p7 | 1:168063665 | TCTTCAGACGGAGAA[A/G]AGAAAGGAAAGAAAT | 55827 |
rs774183666 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168074994 | CTTTTTACAAACAGA[A/G]TTACACAAATCCTCA | 55827 |
rs774210001 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040107 | GGGAAACCTAGGCAT[C/T]ATTGAGAAGGTGACA | 55827 |
rs774216953 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168012900 | CTGAGATCTTGCTGT[C/T]TGCCACTTCACCAAG | 55827 |
rs774236386 | in-del | -/ATA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168017691 | AACTTTATCTTATAC[-/ATA]ATAATTAAATGCAGT | 55827 |
rs774245662 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167993877 | CAAGGCACTTACAGT[G/T]CAGAAAACAAAAAAC | 55827 |
rs774285503 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939566 | CAGGAGTTTGAGACC[A/G]GCCTGGCCAACATGG | 55827 |
rs774304956 | snp | C/G | 1.68701e-05 | 0.00290427 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023097 | TCCATAGCTTTATTG[C/G]AATGCATATACTAAG | 55827 |
rs774355460 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935664 | CAGTTGTCAGAGGGC[C/T]TCTAAAAGGTCCATT | 55827 |
rs774380123 | snp | A/C | 1.64982e-05 | 0.00287208 | intron-variant | DCAF6 | GRCh38.p7 | 1:168075328 | TAATAATTGTAATTA[A/C]TAAAAGTATTTCTCT | 55827 |
rs774401588 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168002844 | AGTATAAGAATGCCC[-/A]TTACCCCATAGTACG | 55827 |
rs774406443 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007624 | GGCTGTCACTCCTTC[C/T]TGAAACACTTTCCTT | 55827 |
rs774424061 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019579 | TGCTGGCTCCTGCTC[A/G]GAGTGACAGCACCCT | 55827 |
rs774445190 | in-del | -/GGCAG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167966773 | AAAAAAAATCAAGAA[-/GGCAG]AAATGAAGAAACTGT | 55827 |
rs774471144 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961312 | CAGTGGCGCGATCTC[A/G]GCTCAATGCAAGCTC | 55827 |
rs774504428 | snp | A/G | 1.76434e-05 | 0.00297008 | missense | DCAF6 | GRCh38.p7 | 1:168075407 | CAGAAGGCTCTGGTC[A/G]AGAGAATGAAAATGA | 55827 |
rs774523099 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030159 | TGAGTGTTATATAAG[A/G]AAGGGGAAATAGCAG | 55827 |
rs774541413 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167953612 | TTAATTATTATTATT[-/A]TTCTTTGATATGGGG | 55827 |
rs774555211 | in-del | -/TTA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167978574 | TCTTATTTTATTTTG[-/TTA]TTATTAATTTATAGG | 55827 |
rs774557257 | snp | C/T | 4.94425e-05 | 0.0049718 | missense | DCAF6 | GRCh38.p7 | 1:168044971 | GACCTCAATCTTGAT[C/T]GCTCTTGTGGGGTTC | 55827 |
rs774565385 | snp | C/T | 3.30077e-05 | 0.00406236 | missense | DCAF6 | GRCh38.p7 | 1:167993369 | TCTTCAGATTACATA[C/T]ATCTTTTTGACCCGA | 55827 |
rs774566538 | snp | A/G | 3.30349e-05 | 0.00406403 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168004684 | AGCTCAGGCTCATTC[A/G]ACATCATCTCCCACA | 55827 |
rs774599147 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168029524 | TAATAATAACAGCAA[C/T]AACAACATAAGACAC | 55827 |
rs774615994 | snp | A/G | 1.66994e-05 | 0.00288953 | missense | DCAF6 | GRCh38.p7 | 1:167987592 | AAACTAGCTGCACAA[A/G]AGAAGATTGTAAAGA | 55827 |
rs774620118 | snp | A/C/T | 8.58515e-05 | 0.00655128 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993471 | ACCATGTCCTTTGGC[A/C/T]GGGCGCGGTGGCTCA | 55827 |
rs774643412 | in-del | -/TG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001616 | CTGTAGCTGTAAAAC[-/TG]AGATTTTATGAAGTT | 55827 |
rs774672203 | in-del | -/TG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168066804 | TAATTTTATTATAAC[-/TG]TTTCTCCAAAAGCCT | 55827 |
rs774685491 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058316 | CAGTTTTTCTTGCGT[A/G]TATACCAAGGAATGG | 55827 |
rs774689355 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986406 | ATGGTATAGCTGTAT[A/G]TCTTTGTGGTGGTAA | 55827 |
rs774690784 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168044328 | TCCCAAAATAACAAT[A/T]TGACAATAAAAAGGA | 55827 |
rs774704706 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167963024 | TAGCACTTTGGGAGG[A/C]CAAGGCGGGTGGATC | 55827 |
rs774707894 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019444 | ATTCAGGGTTTTGAA[G/T]GAGCTATATGTACAT | 55827 |
rs774731371 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000132 | AGAAATTGGAAGGCT[C/G]GAGAGGGAGAGAGAT | 55827 |
rs774759088 | snp | A/G | 1.65408e-05 | 0.00287578 | missense, intron-variant, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167966698 | GACACCAAATTAGTA[A/G]TTAGTAATCCTTACA | 55827 |
rs774769794 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982069 | ATAATAGCCATTCTC[A/G]CTCATATGAGATGGT | 55827 |
rs774777867 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168074473 | CCTTCATAAAACTTA[C/T]ATTCATTTATTCAGT | 55827 |
rs774840991 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071346 | CAGTGGCTCACGCCT[A/G]TAATCTCAGCACTTT | 55827 |
rs774848637 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167958218 | ACTTGCTTAATCACT[A/G]GTCGTGAAGATTTAT | 55827 |
rs774905854 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167987460 | GTCTGTTTAAATGTT[C/T]GTATGATTATCTGCA | 55827 |
rs774906003 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986244 | GCTGGGTTATAGGAG[-/A]AGCATATGATCAGCT | 55827 |
rs774947619 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057544 | TTTCATTATTGCTTT[C/G]AAATTGCTGGATAAT | 55827 |
rs774958943 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167955683 | GGATTCCTTTTATTT[C/T]GTTTTCTTGACTTAT | 55827 |
rs774960627 | in-del | -/GT/GTGTGG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985208 | TGTGTGTGTGTGTGT[-/GT/GTGTGG]GTGGTGTGTGTGTGT | 55827 |
rs774980861 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168054786 | ATAAGAAAAATGTAT[A/G]CATAGTATAAATTAA | 55827 |
rs774992258 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964781 | TACGTTTTTATTGAT[A/G]TATCCTCAAGGTCAG | 55827 |
rs774993264 | snp | C/T | 9.9036e-05 | 0.00703621 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168065721 | TCATGTGGTAAACTG[C/T]CTGCAGCCACATCCG | 55827 |
rs775003616 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167988293 | AGCCTCCCGAGTAGC[C/T]GGGACTACGGGTGTG | 55827 |
rs775011701 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035145 | CTTGGAATATATACT[A/G]TCACTAATACTGCAG | 55827 |
rs775017582 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168020485 | ATGAGACATGCTGAG[C/G]TTAGTACTGAGTGAG | 55827 |
rs775030164 | in-del | -/TTC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168010805 | ATCTCTTTCAGTTAT[-/TTC]TTCTTAAGTTAAGCC | 55827 |
rs775057489 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050344 | CATCATTGTAACCAT[A/G]ATTTCCTTATTTCTC | 55827 |
rs775066952 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168048636 | AACATAGATATTTTT[A/G]AATGGAATGCTCTTC | 55827 |
rs775078479 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167969066 | TTTTTTTTTACCATT[C/G]TGACCAAGTTATTTA | 55827 |
rs775087680 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168026807 | TGCTGGAAGTCACCA[A/C]AGTGATCTGAGGTAG | 55827 |
rs775092667 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167963235 | TGCTGCTTCACTTCA[A/G]CCTGGGCAAAAGCGT | 55827 |
rs775124602 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938050 | AAAAGTTAGCATGCA[A/G]TTTTTTAATTCTTTT | 55827 |
rs775175827 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013183 | GAAAGCAGTATGCCA[C/G]TGAGCATCACCATTT | 55827 |
rs775180638 | snp | A/C/T | 3.31836e-05 | 0.00407319 | missense | DCAF6 | GRCh38.p7 | 1:168004665 | CTACATCCTCTACAA[A/C/T]GTCAGCTCAGGCTCA | 55827 |
rs775191284 | snp | C/T | 1.6483e-05 | 0.00287076 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063806 | ATTGCAGTTTCATGC[C/T]CTGAGTGTTTTTCCA | 55827 |
rs775218749 | in-del | -/AG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167963494 | CACCCAGGCTGGAGT[-/AG]AGTGGTTCAATCTCA | 55827 |
rs775237339 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168047114 | TTGAAACACAGTACT[A/G]TAACATTAATGAGAA | 55827 |
rs775244110 | snp | A/G | 1.66087e-05 | 0.00288168 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168065679 | TCGGCACACTGCTGA[A/G]CATTTGATGCTTCTG | 55827 |
rs775293799 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168069350 | ACTATTCTAGCTGAT[C/T]TACAGCATTCTTTTC | 55827 |
rs775305846 | snp | A/G | 1.64961e-05 | 0.00287189 | missense | DCAF6 | GRCh38.p7 | 1:167987546 | TCTTGTGGTGAAGAT[A/G]GAACTGTTAGGTGGT | 55827 |
rs775307232 | snp | A/G | 1.72746e-05 | 0.00293888 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993476 | GTCCTTTGGCCGGGC[A/G]CGGTGGCTCACGCCT | 55827 |
rs775335391 | snp | A/G | 1.66938e-05 | 0.00288905 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038513 | TATTTTTGTAAAGAT[A/G]TTCTTAGCCATTTTG | 55827 |
rs775339918 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972263 | TGGCTGTATAGATTT[-/G]GTTTCAACAATTAAA | 55827 |
rs775355967 | snp | C/T | 1.82334e-05 | 0.00301933 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168075426 | GAATGAAAATGAGGA[C/T]GAGGAATAATAAACT | 55827 |
rs775368331 | snp | A/G | | | intron-variant, missense | DCAF6 | GRCh38.p7 | 1:168015826 | TTCGTAAGCGCCTGC[A/G]ACAACTGAGGCTTAA | 55827 |
rs775509987 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948563 | ACTTACAAAGTTGTA[A/G]TTTATTTAATGGTTT | 55827 |
rs775517869 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168051880 | CTAGTTATCACTTTC[-/T]TTTTTTTTTTTTTTC | 55827 |
rs775517935 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064538 | TAACATTTGGGTTGG[G/T]GAAGTAATTAGCTCT | 55827 |
rs775521083 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936319 | TTTCACTTTGATTAA[A/G]CAGGCCCGTAGTTAA | 55827 |
rs775524899 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941866 | TTGTGGGATTGCTGA[C/T]TTGTATGGTAAGTAT | 55827 |
rs775536645 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168063078 | GCCAAACCTGGCTGA[-/T]TTTTTTGTATTTTTA | 55827 |
rs775543392 | in-del | -/AATTA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167988151 | CTTATGCTTTAATAC[-/AATTA]AATTAATTAATTAAT | 55827 |
rs775543772 | in-del | -/AC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167951096 | TAACTTATAGCACTT[-/AC]ACCGATTATTGTTTT | 55827 |
rs775550943 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995981 | TATGTAAAACTTAAT[A/G]TAGAATTATGTATAA | 55827 |
rs775570015 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001283 | GAGAAGAGTGTGAGA[A/C]CCTGCCTGGAAAAAA | 55827 |
rs775580997 | snp | C/T | 1.79364e-05 | 0.00299464 | missense | DCAF6 | GRCh38.p7 | 1:168045218 | GGTATCGAGCAGGAC[C/T]TGGTGATAGGTTGGT | 55827 |
rs775589525 | in-del | -/ATTG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034658 | TGGCACACATTTATA[-/ATTG]ATGTATATTCATAGT | 55827 |
rs775599904 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167949393 | AATATATATTTGCAC[C/G]CAACACTGGAGTACT | 55827 |
rs775639517 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168069358 | AGCTGATTTACAGCA[C/T]TCTTTTCTTCTGTGA | 55827 |
rs775657151 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022300 | ACGAAGCTGTTCTAT[C/T]TGAAGCCAAGGTAGA | 55827 |
rs775684260 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167955613 | TTTATAGGATATTCT[A/G]TGTAAATAATCAAGT | 55827 |
rs775684282 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167983460 | GGTTAGATAGAGATT[A/T]CTTTAAATGCCTTGA | 55827 |
rs775700593 | snp | C/T | 0.000223839 | 0.0105768 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015762 | TGTCTTTTCACCTTT[C/T]TTTTCCTATTTGTGT | 55827 |
rs775710407 | snp | A/T | 3.31203e-05 | 0.00406928 | synonymous-codon, intron-variant, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167966709 | AGTAATTAGTAATCC[A/T]TACAGCAGAAAGGTA | 55827 |
rs775718274 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972222 | GCCTTATTGCTGTTT[A/T]TCTGCAGTATCATAC | 55827 |
rs775725220 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168067876 | TTCTTGGTACTTAAG[C/G]CTCAGTTTCTTGTTA | 55827 |
rs775729606 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168051629 | ACATGAAACATATAG[C/G]AACAATCAGAAATGT | 55827 |
rs775739978 | snp | C/T | 1.65291e-05 | 0.00287476 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168045105 | GTTCCAAACAGAAGC[C/T]ACTGGGCCTTCAGCT | 55827 |
rs775746423 | snp | A/G | | | missense | DCAF6 | GRCh38.p7 | 1:168004661 | CCTTCTACATCCTCT[A/G]CAATGTCAGCTCAGG | 55827 |
rs775763544 | snp | C/T | 1.79451e-05 | 0.00299537 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974809 | TAAGTTACCATTAAC[C/T]GCTTTCTTTGTGTGT | 55827 |
rs775769947 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167981294 | TTTTTGCATATGTAG[A/G]GTAAGGGTCTAAGTT | 55827 |
rs775821269 | snp | A/G | 3.56996e-05 | 0.00422475 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022968 | CTTACTTTTAAGTTG[A/G]AATCTCATTTTTGTT | 55827 |
rs775822639 | in-del | -/TGT | 0.000309741 | 0.0124409 | intron-variant | DCAF6 | GRCh38.p7 | 1:168015967 | GTTATTAATGTCAAG[-/TGT]CCTTAAGCAGCTGAT | 55827 |
rs775825049 | snp | A/G | 1.65449e-05 | 0.00287614 | missense | DCAF6 | GRCh38.p7 | 1:167991204 | TGTTATGTTTTGTAG[A/G]ATATTTTAATTAACT | 55827 |
rs775829144 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167951088 | CACTATACTAACTTA[C/T]AGCACTTACACCGAT | 55827 |
rs775847017 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030328 | GGAAGCATGAATAGC[A/G]TATTGCAGAGCCTCT | 55827 |
rs775854115 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168008691 | CCTCACTGTGGACGT[A/G]TAAGAATTTATATGG | 55827 |
rs775876588 | snp | A/G | 0.000807229 | 0.0200739 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167991299 | TTCTGACAGCTCAGT[A/G]CGAATATATGATCGG | 55827 |
rs775917698 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168073046 | CCGGGTGTGGTGGCA[C/T]GCTCCTGTAGTCCCA | 55827 |
rs775960345 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168021708 | TGGTGATACTAGAAG[A/G]TGGAAGATTTAAAGT | 55827 |
rs775960391 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168006857 | AACGGACAATGGGAA[C/T]ATGAAAATTTGCTAC | 55827 |
rs775988345 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057664 | CTACCCTCCTTGAGC[G/T]CTCAGTTCAGTGGGA | 55827 |
rs776019371 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167983240 | TAGCATTGAATCTGT[-/A]GGTTGTGTTGGGCTG | 55827 |
rs776038481 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001784 | TGAAATAAAAAGCAC[A/G]GATGGAGAAATTAGG | 55827 |
rs776040887 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964994 | TAATCATAGTTGTTT[C/T]GGATTCCTGGTCTTA | 55827 |
rs776056211 | in-del | -/G | 3.3618e-05 | 0.00409974 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966756 | TGTAATTTAATGAGA[-/G]GAAAAAAAATCAAGA | 55827 |
rs776065626 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935041 | TATCTGTCATTCTCA[C/T]AGACCGCGTATTACA | 55827 |
rs776092154 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168059240 | CCCTGCCCCATTTAG[A/T]TAGCCAGTTTTTCCC | 55827 |
rs776093679 | in-del | -/AGG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962861 | TTGGGAGGCTGAGGC[-/AGG]AGAATTGCTTGAACC | 55827 |
rs776102053 | snp | A/T | 1.65269e-05 | 0.00287457 | missense | DCAF6 | GRCh38.p7 | 1:168065696 | ATTTGATGCTTCTGG[A/T]AGCTGATAATCATGT | 55827 |
rs776103460 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072454 | TCACTCTTAAGCTTT[A/G]ATTTCTTTATTTATT | 55827 |
rs776105800 | in-del | -/TCT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009323 | CTTTCTCTTCTCTTC[-/TCT]TCTTCTTTCCTTCCT | 55827 |
rs776126236 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030068 | CCAAGAGGTCTGGCT[C/T]TGGCATCCGTGATCA | 55827 |
rs776141431 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941282 | CTTAAGGCAGGACAC[A/C]AAAGGCATATAAGTA | 55827 |
rs776145502 | snp | C/T | 2.28794e-05 | 0.00338218 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043182 | TATAAAATTGCAGCA[C/T]TGGATGTTTATCTAC | 55827 |
rs776145516 | snp | A/G | 1.88795e-05 | 0.00307236 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066517 | CAATTTGTTCCTAAA[A/G]TGCTTCCCTAAGAAA | 55827 |
rs776146136 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007844 | TTTAATATCTCCTGT[A/G]AATTCATGACTCACA | 55827 |
rs776148658 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168021857 | GGGCAATCTTAAAAT[A/G]CCTACTTTTTGGGAA | 55827 |
rs776156549 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167991140 | CTAATGAGAAAATAT[C/T]TTAAATATAATTTCA | 55827 |
rs776157066 | snp | A/C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967226 | AGACAAAAACAGCCA[A/C/G]ATGACTGCGGTGTGA | 55827 |
rs776177195 | snp | A/C | 9.63623e-05 | 0.0069406 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065571 | TTTGAATTTTTAAAT[A/C]ATTTTTTTTAACCCT | 55827 |
rs776201210 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062801 | CAGTTCTGTCACCAA[A/G]TCATTTCTTAAGAGA | 55827 |
rs776204372 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167958655 | CTTAATGGCTCAGAC[A/T]TTTCATTGTAAAATA | 55827 |
rs776219499 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168014286 | ATCTCTTTTAGTATA[C/G]TAGCAGCATTTCACA | 55827 |
rs776277105 | snp | C/T | 3.30387e-05 | 0.00406427 | missense | DCAF6 | GRCh38.p7 | 1:167987568 | TTAGGTGGTTTGATA[C/T]ACGCATCAAAACTAG | 55827 |
rs776281166 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977858 | TCACAAAGCAAATCT[A/G]TTCATGTAACTACCA | 55827 |
rs776284776 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167970604 | CACTCCAAGTCTGGA[G/T]GACAGCAAGAGCTGA | 55827 |
rs776287395 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058970 | TACTAATCCACTATC[A/G]TGTATTAGTGTACAA | 55827 |
rs776294135 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945415 | GTGTTTTGTAGTTCT[C/T]CTTGTAGGGATTTTA | 55827 |
rs776298525 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168073202 | AAGAAAAAGAAAAAC[A/C]GTATACATAGAAGTG | 55827 |
rs776330085 | snp | A/T | 1.66983e-05 | 0.00288944 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991184 | ACTATATGTAATTGG[A/T]ATTATGTTATGTTTT | 55827 |
rs776354760 | snp | A/C | 1.6691e-05 | 0.00288881 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065795 | TTATTTGTATGACTC[A/C]TCAGTCATACAAAAT | 55827 |
rs776388282 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167987752 | ATTTTTAAATTTTTG[G/T]TTTGCTAAAATATTT | 55827 |
rs776399810 | snp | A/G | 1.90431e-05 | 0.00308564 | intron-variant | DCAF6 | GRCh38.p7 | 1:168043145 | CAGTGAAACAAGTAA[A/G]GTGTTATTTTGCTTT | 55827 |
rs776407093 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167988603 | GATCATTTTGAAGTA[A/G]TAAATGAAATAAGAA | 55827 |
rs776427619 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168069634 | AGCACATCTGAAAAA[-/T]TTGAAAGAAGACCCA | 55827 |
rs776455592 | snp | A/T | 7.05144e-05 | 0.00593736 | splice-acceptor-variant | DCAF6 | GRCh38.p7 | 1:167974828 | TTCTTTGTGTGTTTT[A/T]GGTTTTGACAACAAT | 55827 |
rs776464027 | snp | A/C | 3.43418e-05 | 0.00414364 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936872 | CCTCCTCCCCTCCCC[A/C]ACGCGGTGGTCTCCC | 55827 |
rs776477159 | in-del | -/ACACACAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167992276 | CACACACACACACAC[-/ACACACAA]ACACACAAACACCGA | 55827 |
rs776479393 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982481 | CTCCTGACCTCATGA[C/T]CTGCCTGCCTCAGCC | 55827 |
rs776488031 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976484 | CTCAAAAATAAAAAA[C/T]AAAAATAAAGTCTAC | 55827 |
rs776499401 | snp | C/T | 1.65386e-05 | 0.00287559 | missense | DCAF6 | GRCh38.p7 | 1:168045119 | CCACTGGGCCTTCAG[C/T]TCATGAAGAAACATC | 55827 |
rs776501149 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168069875 | AATATATTTTGTTCA[A/G]TAACAGCAAGTAACC | 55827 |
rs776507523 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168003016 | CTTTAAGATAGCACA[C/G]TTGAAAATAGAATTA | 55827 |
rs776531024 | snp | A/C | 1.66991e-05 | 0.00288951 | intron-variant | DCAF6 | GRCh38.p7 | 1:167966739 | AAAGTAGTTTAAAAA[A/C]TCTGTAATTTAATGA | 55827 |
rs776558110 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064807 | AAATTTTTTAAAATC[C/G]TTGTTTGAAATACAA | 55827 |
rs776561770 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167950654 | CCTTTGTGACAGTAT[A/G]CAGAAAGTATAGGCA | 55827 |
rs776562932 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168069579 | CCACAGAAAGTAGAC[A/G]GCGTATAGCGTTTTT | 55827 |
rs776597902 | in-del | -/TAAT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168025022 | ATTAACAATGAAGAA[-/TAAT]TAAGGCAAAATACAA | 55827 |
rs776674283 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167969296 | CTCATAGAATGTAAT[C/G]TTCAGCCAAGTAGTT | 55827 |
rs776702506 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167947398 | GATCTTTATTTCTTT[C/T]CTTCTGCTAGTTTTG | 55827 |
rs776704522 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975239 | GCAAGTAATAGTACT[C/T]TAAGATGGGTTTGTA | 55827 |
rs776707096 | snp | C/T | 1.65201e-05 | 0.00287398 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974945 | GAGTAATATTTTATA[C/T]CAACGTTGAGCAAGA | 55827 |
rs776732862 | snp | A/G | 1.66299e-05 | 0.00288352 | intron-variant | DCAF6 | GRCh38.p7 | 1:168023057 | AACAGGGTGCGTGCA[A/G]CAGGAGATGCGCTAT | 55827 |
rs776754561 | snp | C/T | | | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935073 | AAACAGAGATCTAGG[C/T]TTTTGCTCAAGGTCA | 55827 |
rs776763492 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167973430 | TTCTTTCCTAACAGT[C/G]TTTCCCCCAGTGGTT | 55827 |
rs776770181 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168008677 | AAAAAAATCAAACTC[C/T]TCACTGTGGACGTAT | 55827 |
rs776789468 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040241 | AGCAGAAGCATCAGA[C/T]CTAGTATGTTCAAGG | 55827 |
rs776789509 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168053807 | CATGTTATTTTTGCA[G/T]TTTACGCAAGCTGGC | 55827 |
rs776791066 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168004905 | GTTGGAATAAATGAT[C/T]AAAATGACATGTAAT | 55827 |
rs776830788 | snp | A/G | 1.83623e-05 | 0.00302998 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068333 | ACTTTATGATCTTTG[A/G]TACGATTTTTAACTT | 55827 |
rs776853637 | in-del | -/CTCTCTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009409 | TCTTTCTTTCTCTCT[-/CTCTCTT]TTGTTTCTTTCTGTC | 55827 |
rs776857844 | snp | C/T | 1.72913e-05 | 0.0029403 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993218 | ATAACTTCTTGTTTC[C/T]TTTTTAGGGAATTAT | 55827 |
rs776859560 | in-del | -/G | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937073 | GGGAGGGGGCACGCT[-/G]CCGGGTCTGTTGGAG | 55827 |
rs776875406 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972445 | TTTAGTGTGATTTTT[A/G]TGGACAGTCACTGTA | 55827 |
rs776881929 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052948 | TTCATATTATAGCTG[A/C]TGCCAAAAATTGGTC | 55827 |
rs776883528 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022667 | AGAAGGGCAAGGAGT[A/C]TTGTGTAGTGAACTA | 55827 |
rs776896546 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168051001 | CTTCTTTTGCCACAG[C/G]TAACCACCTTTCCTA | 55827 |
rs776898825 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167984089 | CTCACTATTCTTTCT[A/G]AGATCCAGTTATTTG | 55827 |
rs776912687 | snp | C/T | 2.11553e-05 | 0.00325226 | synonymous-codon, utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936986 | GCTGGAGGACCCGTC[C/T]CGGCTGCGGAGTCGA | 55827 |
rs776920107 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962348 | GTTCTGTCAGTTTTT[-/A]ATCTCACATATTTCG | 55827 |
rs776925705 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030512 | ATGGAGTATGGAGAA[-/T]TGATTAGAGACTGAA | 55827 |
rs776926593 | snp | C/T | 1.64944e-05 | 0.00287175 | missense | DCAF6 | GRCh38.p7 | 1:167991312 | GTACGAATATATGAT[C/T]GGCGAATGCTGGGCA | 55827 |
rs776965744 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941229 | AGTATTGAAAAATGA[C/T]GGTCAATTGTGACAA | 55827 |
rs776988478 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168048672 | AACTACAGCAAGTCT[A/G]TGTAAATGTAACTGG | 55827 |
rs777076741 | snp | A/T | 1.6476e-05 | 0.00287014 | missense | DCAF6 | GRCh38.p7 | 1:167991271 | CAATACCATATTACC[A/T]TGCTGTTGGTTGTTC | 55827 |
rs777085169 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030400 | AGGACAAAGTGACTT[C/T]TTGGACATTTTTAGG | 55827 |
rs777149256 | snp | C/G | 1.75881e-05 | 0.00296543 | missense | DCAF6 | GRCh38.p7 | 1:168068460 | CTTAATCATATCCGA[C/G]CTGGTAGGAACTTTA | 55827 |
rs777184622 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167996225 | ATTCTTTTGTCTTAA[C/T]TTTTTTTGTACTTTC | 55827 |
rs777194786 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041519 | TTTAGTATCAAAAAC[-/T]GTATATTCCTTCTAG | 55827 |
rs777225430 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971414 | ATAGTTGGAGCCCAC[C/T]AAGTCTTAGTAAAAC | 55827 |
rs777266047 | in-del | -/AC | 1.91444e-05 | 0.00309384 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068312 | CTTCAAGGAAAAAAT[-/AC]AGTTACTTTATGATC | 55827 |
rs777283556 | snp | C/G/T | 0.000406088 | 0.0142437 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044720 | GGGAAAATAAAAAGC[C/G/T]TTAATCTATGTTAAT | 55827 |
rs777326131 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962647 | TTGTTTTTTGATCCA[C/T]TCTGACAGTCTCTGT | 55827 |
rs777333676 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937608 | CGTTTTGACCGCTTA[A/G]AGGTGGTGTAGGGTT | 55827 |
rs777340480 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167991586 | CATAACAAATGACCA[C/T]AAACTGGGTATCTTA | 55827 |
rs777364772 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019414 | TCATATAAAGGCCCC[C/T]ATAAGGTTGATAGCA | 55827 |
rs777414255 | snp | C/T | 1.74686e-05 | 0.00295534 | intron-variant | DCAF6 | GRCh38.p7 | 1:167951792 | ATTTGTTCTTTCTTT[C/T]TAAACAGGAAGAAGA | 55827 |
rs777429828 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961305 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCAATG | 55827 |
rs777436170 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948289 | GCTGAGCCTCTCATA[C/T]CTGGATCTCTAAATC | 55827 |
rs777438694 | snp | A/G | 1.77792e-05 | 0.00298149 | intron-variant | DCAF6 | GRCh38.p7 | 1:168066493 | TTGTACTTACTATAG[A/G]CCATATTTCAATTTG | 55827 |
rs777446554 | snp | A/C/T | 5.50964e-05 | 0.00524835 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937020 | CTGGGTGAGCGGGGG[A/C/T]CCCGGGGCGGAGGCG | 55827 |
rs777451190 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168026282 | AAAATCATACATCAT[C/G]TGGTAAATAATATTC | 55827 |
rs777458038 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168006233 | TGCTAAATTCCTTTC[A/G]ATATTTAATGTAAGT | 55827 |
rs777466961 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168021062 | TTAATATTTTAAATA[C/G]TTCAAGAGTTTGAAA | 55827 |
rs777474770 | snp | A/G | 1.73315e-05 | 0.00294371 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004512 | TTAAAATTTGAATTT[A/G]CCTTAACATGTGTTT | 55827 |
rs777510660 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974578 | TAAACTAAATAAATG[G/T]AAATATGCATGTTTT | 55827 |
rs777518422 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001698 | GCAAAGAGCCAAGAG[-/A]GAGAAAATGGATGTA | 55827 |
rs777527882 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070788 | GGTAATGGTTTGCAT[A/G]GATCATTCTAGACTC | 55827 |
rs777529905 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167996640 | CCTGTCGGACCTAAA[A/G]CAAAACTGAAGTCCT | 55827 |
rs777552501 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168031193 | GATGAAAGTAGAAAG[A/G]AGAGGACAGAGTAAG | 55827 |
rs777561945 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168018906 | TTGACTGCTTTATGC[C/G]TCAGTTTCCCAATTA | 55827 |
rs777580185 | snp | C/T | 1.67063e-05 | 0.00289014 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168068402 | AGAAACTAGAAACAC[C/T]ATTACAGTTCCAGCC | 55827 |
rs777595309 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941816 | TACATCTTGGACAAA[A/G]TAACTAGGGTCGAAC | 55827 |
rs777620393 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167973126 | ACAGCGTTAAAGAAC[A/G]TGATATTTATCTTGT | 55827 |
rs777627850 | in-del | -/T | 1.74142e-05 | 0.00295073 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993218 | ATAACTTCTTGTTTC[-/T]TTTTTAGGGAATTAT | 55827 |
rs777633179 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168041087 | TCCCTTGAAAACGGG[C/T]ATGTTTAATAGAACC | 55827 |
rs777650714 | in-del | -/AGTC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167999236 | TAGTGGGCTTCAAAT[-/AGTC]AGTAAAACATGCTGT | 55827 |
rs777671449 | snp | A/G | 1.66699e-05 | 0.00288698 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044895 | ACAACTTTATTTTCT[A/G]ACAGCACAATCAGAT | 55827 |
rs777711628 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167953825 | GCTGGTCTTGAACTC[C/T]TGGCCTCAGGTGATC | 55827 |
rs777715641 | snp | G/T | 2.24434e-05 | 0.00334981 | intron-variant | DCAF6 | GRCh38.p7 | 1:167975056 | TATATATGTAAGTAT[G/T]TATATTTTTGATTAA | 55827 |
rs777726521 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052666 | TGCCCGTTATGACTA[G/T]TCTTCATTAGGGACT | 55827 |
rs777772025 | in-del | -/GTAAT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062460 | TTCAAACTCCTCTCA[-/GTAAT]GCCTGTTTTCCTGAA | 55827 |
rs777783495 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939670 | TGGGAGGCTGAGGCA[A/G]GAGAATAGCTTGAAC | 55827 |
rs777795633 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943978 | CAAGTAGTTGGGACT[A/G]CAGGTGCCCGCCACC | 55827 |
rs777812418 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168069044 | CATAAATGTCCCCAT[A/T]CGTTTGGTATTAGCT | 55827 |
rs777816305 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058547 | TCATGTTTTTCAGCC[C/T]GATCTCCTGATCTGG | 55827 |
rs777827127 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064082 | AGTTTCTGGTGGATT[-/T]TTTTTTTTTTTTTTT | 55827 |
rs777839942 | snp | C/T | 1.75968e-05 | 0.00296616 | upstream-variant-2KB, intron-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935715 | GGTCTCGATAAGGAG[C/T]CATTCAGGGTCCATT | 55827 |
rs777853037 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062338 | TATGGGCCTGTTTTG[C/T]TTGCAAAAATTCATT | 55827 |
rs777876929 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168031801 | GCCACATGGCGTGGG[C/T]GTATTTACTTATTTT | 55827 |
rs777928479 | snp | A/G | 0.000111651 | 0.0074708 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935846 | GCGGCCGACATCGCC[A/G]CCGAGGGATCGTTGG | 55827 |
rs777965290 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168028514 | GGCACTAATTTTCTG[C/T]TATAGATTTAAAGAA | 55827 |
rs778009946 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976251 | AGGTGGGCGGATCAC[C/T]TGAGGCCAGGAATTT | 55827 |
rs778031663 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034686 | CATAGTAATGCTCAA[C/T]AAATTATAGTTATTA | 55827 |
rs778036796 | snp | A/G | 7.0425e-05 | 0.00593359 | missense | DCAF6 | GRCh38.p7 | 1:168065603 | AGATAAAAGAAGCCA[A/G]TTTCTGGGGTGCTAA | 55827 |
rs778038840 | snp | A/G | 1.66241e-05 | 0.00288302 | intron-variant | DCAF6 | GRCh38.p7 | 1:168038491 | TTACAGATGAATGGT[A/G]AGTTAATATTTTTGT | 55827 |
rs778053664 | in-del | -/ACATA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057613 | TTATGTGCTAGATAC[-/ACATA]TCTGGTGGGTGCTGG | 55827 |
rs778081523 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944526 | ATAAGGTGATATCTC[A/G]TTGTGAATTTGATTT | 55827 |
rs778095844 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972005 | GGACTACAGGGATGC[A/G]CCACCATACCCGGCT | 55827 |
rs778107633 | snp | A/G | 1.85541e-05 | 0.00304577 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974786 | AAATGAATATTTCTA[A/G]GAAATAATAAGTTAC | 55827 |
rs778107959 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057176 | TGTGCCATTCTACCT[A/G]TGTGTAATGGTGTTT | 55827 |
rs778113242 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168063914 | ATGGTTCTTTTAGCC[C/T]TATAATATATTGTGA | 55827 |
rs778125926 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013421 | TATCTGGAGAGGCTG[A/T]AAGTTTATTTGGTAG | 55827 |
rs778154272 | snp | C/G | 8.24967e-05 | 0.00642196 | missense | DCAF6 | GRCh38.p7 | 1:168045055 | ACTAGCACTGAGAGT[C/G]CTACCAATGAAAATA | 55827 |
rs778187932 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072858 | TGTCTCTTCATATCA[G/T]TATCTTCCCCAGTTT | 55827 |
rs778215695 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168042927 | ACATTTTACTTGTGA[A/G]TTTTTTGGTCTACCT | 55827 |
rs778216095 | snp | C/T | 8.26521e-05 | 0.006428 | missense, intron-variant, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167966687 | CTGGCTCAGATGACA[C/T]CAAATTAGTAATTAG | 55827 |
rs778236670 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168016096 | TTGCATATGGGTGGT[A/G]TTCAACATCACGTGT | 55827 |
rs778247234 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964727 | TTATGTTTTGTTTTG[C/G]TTTTTTTCAGTCTTT | 55827 |
rs778247370 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167990204 | CCCTATTTGTACAAA[A/T]TTTTTTTTAAAAAAT | 55827 |
rs778254661 | snp | A/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938543 | TAGAGTGGTGATTAA[A/T]CATTTTAAAATTGAA | 55827 |
rs778266584 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938457 | TCTTCTTTAAGTAGA[C/T]GTTCGCCCTTACAGC | 55827 |
rs778329582 | snp | A/G/T | 3.3028e-05 | 0.00406363 | missense | DCAF6 | GRCh38.p7 | 1:167993280 | GTTTTATTCCTTCCC[A/G/T]TCTTAATAATAAGTC | 55827 |
rs778335278 | in-del | -/TTTTA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030424 | TTTTAGGTTTCGCAT[-/TTTTA]TTTTAAGAACAGAGG | 55827 |
rs778335500 | snp | A/T | 1.65149e-05 | 0.00287353 | intron-variant | DCAF6 | GRCh38.p7 | 1:168002452 | ATGAGTTTTAGACTT[A/T]CATAGAATTTACCCG | 55827 |
rs778352392 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167949290 | ATTTCTGAACATCTT[C/T]GGAGCAGAGGCACTA | 55827 |
rs778393229 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167982310 | GCAGTGGTGCGATCT[C/T]GGCTCACAGCAACCT | 55827 |
rs778396497 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168027655 | TTCCATAGCATTTTC[A/G]TAGATTTCTTTACTT | 55827 |
rs778466242 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968575 | CGTGGGGAAATGAGG[C/T]AGGAGAAGCTGTCGG | 55827 |
rs778475222 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168064281 | TCTCTAAGATCTTTT[A/G]TAGTTTTTACGATCT | 55827 |
rs778495040 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167993011 | TCTAGACAATCATGA[A/G]TTTTTTTGGTAGAGG | 55827 |
rs778496443 | snp | A/G | 1.69798e-05 | 0.00291369 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167951827 | TTATCCAAAGATTAA[A/G]ACTTGAAGCAACCCT | 55827 |
rs778504701 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168029373 | AGTGGTGGAGCCATA[G/T]TTGTATGTCTGTACT | 55827 |
rs778505600 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168068656 | TGAACTACATTTGTC[A/G]TAAAATGGTCAAAAT | 55827 |
rs778506478 | in-del | -/TAAT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168040023 | AGTTTATTATAAACA[-/TAAT]TAATAAGTGTACCAT | 55827 |
rs778523288 | in-del | -/AC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167992259 | GCCAGGATTACACAC[-/AC]ACACACACACACACA | 55827 |
rs778528302 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995954 | GTGGAAGTAGAGGTA[C/T]AAGTAAATAAATATG | 55827 |
rs778531223 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974329 | TATCAATTTTAAACT[G/T]TATTACTGTCACAGT | 55827 |
rs778541401 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167939910 | ATTGTCTATCTACAG[A/G]GTTGTAGATTTAAGT | 55827 |
rs778552117 | snp | C/G/T | 0.000105015 | 0.00724553 | missense, stop-gained | DCAF6 | GRCh38.p7 | 1:168068457 | TCACTTAATCATATC[C/G/T]GAGCTGGTAGGAACT | 55827 |
rs778563506 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167949308 | AGCAGAGGCACTAGT[C/T]GTTTTGTTCTGGACT | 55827 |
rs778571242 | snp | A/G | 1.67337e-05 | 0.00289251 | missense | DCAF6 | GRCh38.p7 | 1:168004652 | TTTCTTCAGCCTTCT[A/G]CATCCTCTACAATGT | 55827 |
rs778583233 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167994175 | ACTATTTCTAAAACC[G/T]TATCCCTAACAGTGA | 55827 |
rs778584321 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168065402 | GTCCTCCTGCCTTGG[A/C]CTCCCAAAGTGCTGG | 55827 |
rs778584916 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013865 | ATCCTCCTACCTCAG[C/T]CTCCCGAGGGGCCAC | 55827 |
rs778589122 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167981470 | GGGGTACAAATGATC[C/G]TGTTACCCAGGAACT | 55827 |
rs778626476 | snp | A/C | 1.64982e-05 | 0.00287208 | missense | DCAF6 | GRCh38.p7 | 1:167987532 | CTTACACTTTTCTCT[A/C]TTGTGGTGAAGATGG | 55827 |
rs778630694 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961346 | CTCCCGGGTTCATGC[C/T]ATTCTTCTGCCTCAG | 55827 |
rs778635475 | snp | A/T | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997557 | GATTTTTTTCTATTC[A/T]TGTTACTAGGTATGG | 55827 |
rs778642156 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167989860 | GCAAAATTCTATCTC[-/A]AAAAAAAAAAAAAAA | 55827 |
rs778668564 | snp | C/T | 1.85159e-05 | 0.00304264 | intron-variant | DCAF6 | GRCh38.p7 | 1:168075358 | TTTGCGATTCTCTTA[C/T]CTGTGTTTCCAGACC | 55827 |
rs778683169 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070981 | ATCATTTCTCTGTCA[C/T]GGGTTTGCAAAGCCT | 55827 |
rs778689903 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019087 | GGAGTCTCGCTTTGT[C/T]GCCCAAGCTGGAGTG | 55827 |
rs778693904 | in-del | -/CAT | 3.63646e-05 | 0.00426392 | intron-variant | DCAF6 | GRCh38.p7 | 1:168068469 | TCCGAGCTGGTAGGA[-/CAT]ACTTTAAGTATACTA | 55827 |
rs778785543 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168055025 | GTTTTTAACTTGATA[G/T]ACTGAAGAACAGTGG | 55827 |
rs778822344 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985385 | TTCCAGCTTCTAGAG[G/T]CTACTTGCATTCCTT | 55827 |
rs778834196 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976082 | TTACATTTATTGTGA[A/G]TTCTGATATATTTGG | 55827 |
rs778834422 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943818 | CTCTAGTTCCATCCA[C/T]GTTGCTGTATATGTC | 55827 |
rs778840349 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962684 | TTTTAGGCTGGGTGC[A/G]GTGGCTCACCCCTGT | 55827 |
rs778847087 | snp | A/G | 1.65477e-05 | 0.00287638 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065768 | TATCTTTTCTAGGAC[A/G]AGGGCTAGAAATTAT | 55827 |
rs778857293 | snp | A/G | 1.69292e-05 | 0.00290935 | upstream-variant-2KB, missense, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935739 | GTCCATTACCTGCTG[A/G]ATGGTTGTACAACGG | 55827 |
rs778869676 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168010268 | ATTGTCTCATTATAT[A/G]TATATATATTTGTTT | 55827 |
rs778877335 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168053589 | GCTCAGTGTTCCAAA[A/G]TTCTCCCTTTCAGAA | 55827 |
rs778902348 | snp | C/T | 3.4132e-05 | 0.00413096 | missense | DCAF6 | GRCh38.p7 | 1:168043107 | TTCGTCCCACAGAGC[C/T]CAGTGCAACCACCAG | 55827 |
rs778923372 | snp | A/G | 1.71997e-05 | 0.0029325 | missense | DCAF6 | GRCh38.p7 | 1:168065650 | TCTGACTGTGGCCAC[A/G]TTTTCATCTGGGATC | 55827 |
rs778943974 | snp | A/C/G | 3.36356e-05 | 0.00410084 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991168 | TCACCTCTGCTGTAT[A/C/G]ACTATATGTAATTGG | 55827 |
rs778948843 | snp | C/T | 0.000117447 | 0.00766222 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935858 | GCCGCCGAGGGATCG[C/T]TGGCAGCCGGGTGGG | 55827 |
rs778954939 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167966448 | TTATGTGTGGCCGGA[C/G]ACAATTCTTCTTCTT | 55827 |
rs778967217 | snp | A/G | 4.51355e-05 | 0.00475034 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936906 | CCACCCGGCTCAGGC[A/G]GAGCCATGTCTCGGG | 55827 |
rs778969859 | snp | A/C | 8.77655e-05 | 0.00662382 | intron-variant | DCAF6 | GRCh38.p7 | 1:168045242 | GGTTGGTAAATTTTT[A/C]ATTAACATGAACTGT | 55827 |
rs778972485 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168019836 | CTGTGCAAGCAGGCT[C/G]TAAACAACACCAGAT | 55827 |
rs778987268 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168050128 | CATAGTCTTGAATAG[G/T]TTTTAATTATAGCCT | 55827 |
rs779002675 | in-del | -/A | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168034771 | TTAAGGGTTTTAAAT[-/A]AAAATCTACCTTTTA | 55827 |
rs779040587 | in-del | -/CTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167980589 | GCTTCTTTTCATATG[-/CTT]CTTCTTGGCCATCTG | 55827 |
rs779108235 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168003437 | GACTTTAAGGAAACT[G/T]CATGCAAAAGCATAA | 55827 |
rs779136808 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168074118 | CATTGGTTTGACATT[C/G]GATTAGAGTTGGCAT | 55827 |
rs779138385 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058899 | TACTGGGTTGTTTTA[A/C]TTGAGTTGTTTTTCT | 55827 |
rs779170001 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168022607 | ATGCTTCGAATCCTC[C/G]AAGGCAGGATGAAAA | 55827 |
rs779186411 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035959 | CCCAGCTACTCTGGA[A/G]GCTGAGGCAGGAGAA | 55827 |
rs779197718 | in-del | -/TG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945455 | AATATATTCCTAGTT[-/TG]TGTGTGTGTGTGTAT | 55827 |
rs779239220 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167978714 | GATGGGGTCTCACTT[C/T]TTCACCCAGGCTGGA | 55827 |
rs779258249 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049994 | AATGCCAAATCTGTT[A/G]TAAGTGATTTGACGG | 55827 |
rs779259755 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168008462 | TCCTGTATCTAAACT[A/G]TAACCTGGGTCTTTT | 55827 |
rs779267742 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168032315 | TAGGGTAGATAGATC[A/T]TCTCTGTTAGCAGTC | 55827 |
rs779280007 | in-del | -/A | 8.05429e-05 | 0.00634547 | intron-variant | DCAF6 | GRCh38.p7 | 1:167987630 | ATTAAATTTTTATAC[-/A]AATGATGCAGAAAAA | 55827 |
rs779281211 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167990481 | GACCAATAATAGCAG[C/G]CATTTCTAATGGTAC | 55827 |
rs779289037 | snp | A/C | 1.7465e-05 | 0.00295503 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:168045213 | TGCAAGGTATCGAGC[A/C]GGACCTGGTGATAGG | 55827 |
rs779294264 | in-del | -/GA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167944689 | TTTGAGTTCCTTGTG[-/GA]TAGTCTGGATATTAG | 55827 |
rs779352599 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168051090 | AGGTCGCTTTCCACA[A/G]ACTATATTTAGCTGC | 55827 |
rs779355647 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062656 | ATTATGGACGTCTGG[A/T]CTGTTATATGTCAAA | 55827 |
rs779357428 | snp | A/G | 1.84025e-05 | 0.0030333 | intron-variant | DCAF6 | GRCh38.p7 | 1:167974792 | ATATTTCTAGGAAAT[A/G]ATAAGTTACCATTAA | 55827 |
rs779357492 | snp | A/C | 1.66029e-05 | 0.00288117 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003855 | AACTCACTGATAAGA[A/C]CTATATTGTAATAGG | 55827 |
rs779368846 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168016443 | ATTATTTCCTTCTGT[C/G]ATTATTTGAAAATTT | 55827 |
rs779375873 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968501 | CTCTAGAGCACTGAG[A/G]AATACTTTTTAAGGA | 55827 |
rs779380388 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167992847 | ACGTTGCATACTAAT[A/G]TATGTAGTATGCTAA | 55827 |
rs779397634 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954174 | CCATGCCTGGCTAAT[G/T]TTTGAATTTCTAGTA | 55827 |
rs779411467 | snp | G/T | 1.64746e-05 | 0.00287002 | intron-variant | DCAF6 | GRCh38.p7 | 1:168022946 | ATTGCTGTGCAGTTT[G/T]CTGCTGCTTACTTTT | 55827 |
rs779419870 | in-del | -/CTC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009411 | TTTCTTTCTCTCTCT[-/CTC]TTTTGTTTCTTTCTG | 55827 |
rs779420731 | snp | C/T | 3.30442e-05 | 0.0040646 | missense | DCAF6 | GRCh38.p7 | 1:168044914 | GCACAATCAGATAAG[C/T]TCACAGCCAAGCCAT | 55827 |
rs779481095 | snp | A/G | 1.65026e-05 | 0.00287246 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974911 | AATGATAAACAGATT[A/G]TATCCTGCTCTGGAG | 55827 |
rs779507873 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167958088 | TTTCCCTTCATTCTA[C/T]GGGTTGTCTTTTTGC | 55827 |
rs779526805 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167995569 | CCTGTAATCCCAGCT[A/T]CTTGGGAGGTTGAGG | 55827 |
rs779527979 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168014974 | AGCAGTTATCCCCAC[A/G]TGACACAAACACATA | 55827 |
rs779529804 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167999496 | GCTTCTGATAGAAGG[C/G]TGTTTCATTTGCATT | 55827 |
rs779583450 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168067541 | AGACAGAAGGATCAG[-/C]ATGTGCCAAAGCATG | 55827 |
rs779660437 | snp | A/G | 1.67223e-05 | 0.00289151 | synonymous-codon, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974979 | AGAAACCAACAGACA[A/G]TGCCAATTTACGTGT | 55827 |
rs779725806 | snp | G/T | 2.42198e-05 | 0.00347985 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | DCAF6, MPC2 | GRCh38.p7 | 1:167935891 | CGTGGCTGTGTTCTC[G/T]TCCCTGGCTGACAAC | 55827 |
rs779731642 | in-del | -/AC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168029821 | CCGTCTCTATGAAAA[-/AC]ACAAAAAATTAGCCA | 55827 |
rs779795095 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976145 | AAAAAAAGTTTCCAA[C/T]CTCCATTAACCCTCC | 55827 |
rs779849250 | in-del | -/TG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977889 | CTAGCACATTAAGTA[-/TG]TCCCAAAAGCTCCCT | 55827 |
rs779863487 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940172 | TTCAGAAAACTTCCT[A/G]TTATGTTGTGGGAAT | 55827 |
rs779869746 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167966789 | GCAGAAATGAAGAAA[C/T]TGTGAACAGTCATAG | 55827 |
rs779883136 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167964021 | TGTGCTAGATATAAG[C/T]ATAGATGATCAAATA | 55827 |
rs779928551 | snp | A/G | 1.65828e-05 | 0.00287943 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065786 | GGCTAGAAATTATTT[A/G]TATGACTCATCAGTC | 55827 |
rs779929482 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168028118 | CATCTTGTTTAGTTT[A/C]AACAGTATGTTTTAA | 55827 |
rs779936864 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168043889 | TCAGCTTAACTACTT[G/T]TTCATGATAGTTTAG | 55827 |
rs779943551 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168000917 | ATTATATAATGATGA[C/T]GGTTGTACCTCTTTA | 55827 |
rs779999715 | snp | A/G | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167997931 | TCCTCAGGGAAATGC[A/G]GATCACAACCACAGT | 55827 |
rs780002986 | snp | C/T | 0.000320598 | 0.0126569 | missense, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936918 | GGCAGAGCCATGTCT[C/T]GGGGTGGCTCCTACC | 55827 |
rs780031439 | in-del | -/CTC | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167998070 | ATATGAGCCATACTT[-/CTC]CTCCCAGATATACAG | 55827 |
rs780046777 | snp | C/T | 1.65899e-05 | 0.00288005 | intron-variant | DCAF6 | GRCh38.p7 | 1:168003861 | CTGATAAGACCTATA[C/T]TGTAATAGGAGAGCA | 55827 |
rs780053774 | snp | A/T | 3.29533e-05 | 0.00405901 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167991254 | TGTTGCTATTTGCCC[A/T]CCAATACCATATTAC | 55827 |
rs780083529 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954223 | GTTGGCTAGGCTGGC[A/C]TCGAACTCCTGACCT | 55827 |
rs780100258 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007270 | CCCTTCTCTTGCATT[A/G]TCATTGCCTTTTTTT | 55827 |
rs780107753 | snp | A/G | 1.6582e-05 | 0.00287936 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044557 | CTCATGGATACCAAG[A/G]GATGACTGTAATTTG | 55827 |
rs780127062 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168053550 | TGGCAAGGAAAAAAG[A/G]TCAGACACAGTGGAA | 55827 |
rs780133597 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009864 | TTTACTATGATAAGC[C/T]CTCTTGAAGACAGGA | 55827 |
rs780138103 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024719 | TGAGGGAGGAGAATC[A/G]CTTGAACCTGGGAGG | 55827 |
rs780173301 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167942819 | AATCAATTGACCATA[A/T]ATGTTTAAGTCAATT | 55827 |
rs780181955 | snp | A/G | 1.64895e-05 | 0.00287132 | missense | DCAF6 | GRCh38.p7 | 1:168002516 | AGCGTTTGAGACTTC[A/G]TGGTGATTGGTCAGA | 55827 |
rs780184114 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985152 | GTGGCAATTCAAGAT[A/G]AGATTTAGGTGAGAT | 55827 |
rs780190155 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062302 | TCTGGTTATACTGTT[C/T]CTAAATTCTGGTGCT | 55827 |
rs780217874 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168010398 | TGGTAAATCTAGAGG[A/G]GTCACAGTGTTGGCT | 55827 |
rs780247118 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167947604 | TTTTTTTAAATTTCT[G/T]TCTTAATTTCTTCAT | 55827 |
rs780261715 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167979978 | ACGAGGTCAAGAGAT[G/T]GAGACCATCCTGGCC | 55827 |
rs780281651 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167978894 | ACTCCTGGGCTCAAG[C/T]GATCCTCCTGCCTCT | 55827 |
rs780284763 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167952931 | ATTATCAAGATTTTG[C/T]CATATTTTCTTTTCT | 55827 |
rs780296172 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052357 | GTTTTAGAAAAGCTG[A/C]AACACTAAAGTAGAG | 55827 |
rs780309629 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167983489 | GAACCAATAAGCCTT[-/C]CAGTCTTTGTCAAAG | 55827 |
rs780311345 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168012168 | ATTTATAGCAGGCAG[A/G]TAAAGTGCCACCAAA | 55827 |
rs780313833 | in-del | -/TG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959391 | TCGTGTGCAGGTGTA[-/TG]TGTGGACATACGTTT | 55827 |
rs780351813 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167967844 | CAAGCGATTCTCCTG[C/T]CTCAGCCTCCCAAGG | 55827 |
rs780378139 | snp | C/G | | | intron-variant, upstream-variant-2KB | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167996770 | AGGCCAAGCATGACT[C/G]TATTTTAGGATTTTG | 55827 |
rs780379649 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168060532 | TTTGATACAGTTCTC[A/G]TTTATTCATAATTAT | 55827 |
rs780398016 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167953865 | GGCCTCCAAAAGTGC[-/T]TGGGATTGCAGGTGT | 55827 |
rs780417626 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024011 | CTTGAACCCAGAAAT[C/T]TGAGACCAGCCTGGT | 55827 |
rs780440274 | snp | C/T | 4.97913e-05 | 0.00498931 | intron-variant, stop-gained | DCAF6 | GRCh38.p7 | 1:168023044 | TCACTTGACGAGCAA[C/T]AGGGTGCGTGCAACA | 55827 |
rs780453773 | snp | C/T | 1.75554e-05 | 0.00296267 | intron-variant | DCAF6 | GRCh38.p7 | 1:168063600 | ATTTATTTTTGTTTT[C/T]TTAATATGTAATTCA | 55827 |
rs780456850 | snp | A/G | 3.30104e-05 | 0.00406252 | missense, utr-variant-5-prime | DCAF6 | GRCh38.p7 | 1:167974932 | TGCTCTGGAGATGGA[A/G]TAATATTTTATACCA | 55827 |
rs780473740 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168074322 | ACTGAACTGTTTTCC[A/T]TATGCTTAACCTTAA | 55827 |
rs780485628 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046405 | GAAAGAAGACAGGCA[A/G]AAATCCTGAAGAGGA | 55827 |
rs780494438 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168038511 | AATATTTTTGTAAAG[A/T]TGTTCTTAGCCATTT | 55827 |
rs780501817 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168038592 | TTGTTTTGCTATAAG[G/T]TATTGGTTTTCAAAC | 55827 |
rs780527480 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971265 | CTGTGTTCCTGTCTT[G/T]TGGATAACTCTATTA | 55827 |
rs780543654 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959652 | GATTATCTTTTCATA[C/T]GCTCGTTTGCAATCT | 55827 |
rs780556752 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167960966 | ATACTGAATCTTTCT[A/G]TTTATTAATATGGAA | 55827 |
rs780560869 | snp | A/G | 1.65329e-05 | 0.0028751 | missense | DCAF6 | GRCh38.p7 | 1:168038434 | TTTTAAGTTTGCACT[A/G]CAGCACAGAAGGAAC | 55827 |
rs780561750 | snp | A/G | 6.59707e-05 | 0.00574291 | missense | DCAF6 | GRCh38.p7 | 1:168004763 | AGGCAGTCTGTTGAG[A/G]CATCTGGACACCACA | 55827 |
rs780562598 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167945799 | CCACCACACCCGGCC[-/T]TTTTTTTTTTTGTTA | 55827 |
rs780564151 | snp | A/G | | | utr-variant-3-prime | DCAF6 | GRCh38.p7 | 1:168075725 | TGGGAGCTTGGATCA[A/G]TGTTGAAGAATAATT | 55827 |
rs780564591 | snp | C/T | 2.73295e-05 | 0.00369649 | intron-variant | DCAF6 | GRCh38.p7 | 1:167993188 | TGTTTTTCTTTAAAA[C/T]ATTATTAATTTTAAA | 55827 |
rs780574252 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168068761 | CGTGCATATTCTTTA[A/G]TGGTAGGTTTGTTGA | 55827 |
rs780632189 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167993558 | AGTTTGCAACCAGCC[C/T]GACCAACATGGAGAA | 55827 |
rs780656618 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961151 | ACTTGTTCATTTCTG[G/T]TATTTAGGAAAATAA | 55827 |
rs780705724 | in-del | -/TAT | 3.35824e-05 | 0.00409757 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991352 | CAGGTAAGAAGATAA[-/TAT]TAGAGAAAATATAGG | 55827 |
rs780737563 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167973064 | AAGTAACTAATGGCT[G/T]TATGTAGTGTGTAGT | 55827 |
rs780744489 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948051 | TCTTAGTACTCCAGT[G/T]TCGGGTGCAAATATG | 55827 |
rs780758535 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168004276 | TCTGAGAATGGAAAT[A/G]TATAAAATTCTGTGT | 55827 |
rs780765244 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168074498 | TTCAGTAAACCTTCA[C/T]TGAACATCCTATACT | 55827 |
rs780770200 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168002145 | CATCACAATAGAAAA[C/T]TAAGGCTCAAGATGG | 55827 |
rs780803282 | snp | A/C | 0.000160527 | 0.00895754 | intron-variant | DCAF6 | GRCh38.p7 | 1:168019591 | CTCAGAGTGACAGCA[A/C]CCTGTGGAGTCTGCT | 55827 |
rs780839739 | snp | C/T | 1.70638e-05 | 0.00292089 | missense | DCAF6 | GRCh38.p7 | 1:168066454 | ATTTTTAACCGAAAA[C/T]TTGCTGATGAAGTAA | 55827 |
rs780840068 | snp | A/G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971895 | GAGTCTTGCTCTGTC[A/G/T]CCCAGGCTGCAGTGC | 55827 |
rs780850929 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959733 | GTTTCTTATTGTAGT[A/G]TTTTAAGAGTTCTTT | 55827 |
rs780853672 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168051429 | TAGAAATAGTGTCAC[A/G]TATCAAGATGATATA | 55827 |
rs780862263 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168044154 | TACTGAGGGGAGGTT[A/T]TAGCTGAATGTCAAA | 55827 |
rs780867077 | in-del | -/TTTGA | 1.98367e-05 | 0.00314928 | intron-variant | DCAF6 | GRCh38.p7 | 1:168065551 | CTTTGTTTTAATAAC[-/TTTGA]TTTGAATTTTTAAAT | 55827 |
rs780881523 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168018389 | TATTTATTTTTGGTT[A/G]TTCACTCTTTGTCAT | 55827 |
rs780895282 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168047498 | ATATTCTGTACACTC[A/G]TTTGAGTATTTAGCC | 55827 |
rs780899129 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168002858 | CATTACCCCATAGTA[C/T]GTTGGGTATTGTCAG | 55827 |
rs780899855 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030070 | AAGAGGTCTGGCTCT[G/T]GCATCCGTGATCATA | 55827 |
rs780935671 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167965057 | ATGCTGGCTTTATCC[C/G]TTCAAATTGTATTTT | 55827 |
rs780978572 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030872 | GGTGACTTTTTCAGC[C/T]ACTGCAAGAGTAGCT | 55827 |
rs780988164 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168030834 | TTATAGTGCTTTGTG[C/G]GAGGTACTGTTGGAG | 55827 |
rs780989871 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168015401 | AATTAACAAAGCAGC[G/T]TAAATTTTTGTGTAT | 55827 |
rs781021091 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167991263 | TTGCCCACCAATACC[A/G]TATTACCTTGCTGTT | 55827 |
rs781022328 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167952601 | ATTTCAATCCATTGA[C/T]TTGCTACATCTTCTC | 55827 |
rs781034639 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167983507 | GTCTTTGTCAAAGGG[A/G]CCTGTGTGTTTGGGT | 55827 |
rs781072446 | snp | A/G | 3.33918e-05 | 0.00408592 | intron-variant | DCAF6 | GRCh38.p7 | 1:167991344 | AAGAGCTACAGGTAA[A/G]AAGATAATATTAGAG | 55827 |
rs781077170 | snp | G/T | 1.66866e-05 | 0.00288842 | stop-gained | DCAF6 | GRCh38.p7 | 1:168068385 | AACGAACTCATGCTG[G/T]AAGAAACTAGAAACA | 55827 |
rs781117054 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167940375 | GATTCTTTTTTTTGG[C/T]GGGAGGCGGGGGGCA | 55827 |
rs781121310 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024462 | GAAATATTCAGAAAC[-/T]TAATTTTAAAGTGAA | 55827 |
rs781123320 | snp | A/G | 3.0966e-05 | 0.00393472 | missense, intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167936924 | GCCATGTCTCGGGGT[A/G]GCTCCTACCCACACC | 55827 |
rs781126980 | snp | A/G | 1.65647e-05 | 0.00287786 | intron-variant | DCAF6 | GRCh38.p7 | 1:168044676 | TATCAATATAAGTGA[A/G]TTGCTCCCTTTAGAT | 55827 |
rs781130988 | snp | A/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938794 | TTCAGCTATATCTAC[A/T]AACGAGTTAATTAAA | 55827 |
rs781180487 | snp | C/T | 5.22972e-05 | 0.0051133 | intron-variant | DCAF6 | GRCh38.p7 | 1:168004496 | TGGTTTTAGAAAATA[C/T]TTAAAATTTGAATTT | 55827 |
rs781184308 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001243 | CTTACAGTGAGCTAG[G/T]ATGGGACCACTGCAA | 55827 |
rs781203383 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941569 | ATGGGATGCATTCTG[G/T]TTTTTTTCATATTGT | 55827 |
rs781222901 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167966282 | CATCAACTATTAAAT[C/T]AAGCTTGTCTAACAC | 55827 |
rs781230220 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168067341 | ACAATGTAAACAGCT[A/G]GAACATACTGTAGTG | 55827 |
rs781237577 | in-del | -/ATTC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168012481 | CAAGGTATTTATTGT[-/ATTC]AATTTTCAGTTTGGG | 55827 |
rs781365056 | in-del | -/CT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167975976 | CAGTTCTTTTATGTC[-/CT]CATGTTTTTGTATGT | 55827 |
rs781384253 | snp | G/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167937446 | GGTTTAGGTGTCGGC[G/T]GCGACGCGTTGACCA | 55827 |
rs781411805 | snp | C/T | | | intron-variant, upstream-variant-2KB | DCAF6, MPC2 | GRCh38.p7 | 1:167938465 | AAGTAGACGTTCGCC[C/T]TTACAGCATTTTAAT | 55827 |
rs781425283 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168012468 | TTAAAATTCAACCCA[A/C]GGTATTTATTGTATT | 55827 |
rs781442830 | snp | C/G | 1.65304e-05 | 0.00287488 | missense | DCAF6 | GRCh38.p7 | 1:167987504 | CTTCAGATTATGACT[C/G]TACCCAATGACCCTT | 55827 |
rs781445000 | in-del | -/TTAT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167960291 | GTAAAATTTTTATTA[-/TTAT]TTATTTATTTATTTA | 55827 |
rs781445305 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986266 | TGATCAGCTTTAATA[G/T]ATATTGATACATAGT | 55827 |
rs781445391 | snp | A/G | | | intron-variant, downstream-variant-500B | DCAF6, MIR1255B2 | GRCh38.p7 | 1:167999162 | TGGATGACCAGGTGC[A/G]TTGTCAATGCCCAGT | 55827 |
rs781495531 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167968377 | GTGCTGAGATTTAGA[C/T]CTTATTGAAGAGGGT | 55827 |
rs781518233 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168071183 | CTTTCAAAACAGGTC[A/C]GTTAATTTTTTTGTT | 55827 |
rs781535407 | snp | A/G | | | downstream-variant-500B | DCAF6 | GRCh38.p7 | 1:168075891 | ACCCACAGTTTTCCA[A/G]TCTCTCCTGTAGCAT | 55827 |
rs781558113 | snp | C/T | 1.77448e-05 | 0.00297861 | missense | DCAF6 | GRCh38.p7 | 1:168075373 | TCTGTGTTTCCAGAC[C/T]GGTTGGAGGGTGACA | 55827 |
rs781580588 | snp | A/G | 0.000232246 | 0.0107735 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167993422 | TAAAACTCCTTCTGC[A/G]GAAGAGAGAAGAGAA | 55827 |
rs781581187 | snp | A/G | 1.64811e-05 | 0.00287059 | missense | DCAF6 | GRCh38.p7 | 1:168063757 | CGCAACTCCAGGACA[A/G]TGGTACCAAATGTTC | 55827 |
rs781598970 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168062418 | AGTAAAAAGTTTACA[A/G]TATCTTTTTTATGTG | 55827 |
rs781615036 | in-del | -/TTTTTTTTTTTTTTTTTTTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167976887 | TACATCCTTTAGCAG[-/TTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTG | 55827 |
rs781615672 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168025997 | CTTGTACAGGCTGTA[C/T]ATCTCTTGTACATGC | 55827 |
rs781658607 | snp | C/G | 1.6492e-05 | 0.00287154 | synonymous-codon | DCAF6 | GRCh38.p7 | 1:167993314 | CAGAGTGACATCTCT[C/G]TGTTACAGTGAAGAT | 55827 |
rs781669041 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948833 | ATTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTT | 55827 |
rs781675892 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167974052 | TAGAGTCTGTTGTCA[A/G]GCTCTTGAATTTTTG | 55827 |
rs781682020 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167948880 | TGGTCCTGAACTCCT[C/G]ACTTCAGGTGATCCA | 55827 |
rs781707592 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168024541 | CCAGGCGTGGTGGCC[C/T]ACACCTGTATTCCCA | 55827 |
rs781719236 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168010113 | CTAGAAGAGAGATGC[A/T]GTGATTAGCTGTCTA | 55827 |
rs781722393 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168042090 | TCTCTTTTTTTTAAA[A/G]AGTCAATTTGACTTC | 55827 |
rs781755247 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167946265 | TGGCAAATCTAAGAG[-/T]TTTTTGTGGGGAGTC | 55827 |
rs796068023 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167959209 | TCTTTTCATAGCTTC[C/T]AGCTCATTTCTTTTT | 55827 |
rs796073524 | multinucleotide-polymorphism | AGACAGGGTC/TTTTATTTTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049262 | GTTTTATTTTTTTGA[AGACAGGGTC/TTTTATTTTT]TGCCCTGTTGCCCAG | 55827 |
rs796115942 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167977950 | GTTTTTTCTAATACC[A/C]CTGTTTTTCTGTTTT | 55827 |
rs796163238 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167971196 | TTCAAATCTCAGCTC[-/T]TTTTTTGTGATATTT | 55827 |
rs796163639 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168070860 | TTCTCCTTTGCCCAC[A/G]CATGTTCTTAGGGTA | 55827 |
rs796188175 | snp | A/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954245 | TCCTGACCTCAGGTG[A/T]TCCTCCCAAAGTGCT | 55827 |
rs796218213 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972083 | CTGGTCTCGAACTCC[G/T]GACTTCAGGTGATCC | 55827 |
rs796250299 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167962069 | TAGACACTGTTTGAT[C/T]TTTATTCTTTTAAAT | 55827 |
rs796252337 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072800 | GGCTTCCATTGGGAA[A/C]TTTTTTTCTTATCTA | 55827 |
rs796260538 | in-del | CCTTCCTTCCTTCCTTCCTTCCTTCCTTTCTTTCTTTCTTTC/TCTTTCTTTCTT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009362 | TTCCTTCCTTCCTTC[lengthTooLong]CTCTCTCTCTTTTGT | 55827 |
rs796265764 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168057643 | GTGATAATGATAACA[C/G]AACGCCTACCCTCCT | 55827 |
rs796266858 | snp | C/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167943493 | TTCATATTTGTAATG[C/G]TATTTTAGATGATAT | 55827 |
rs796267171 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167954748 | TGAGCCACCGCACCC[A/G]GCAAATTTTTGTATT | 55827 |
rs796281588 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168035935 | AGTGTGGTGGTGGGT[A/G]CCTATAACCCCAGCT | 55827 |
rs796285417 | snp | A/G | | | intron-variant, synonymous-codon | DCAF6 | GRCh38.p7 | 1:168015830 | TAAGCGCCTGCAACA[A/G]CTGAGGCTTAAGAAG | 55827 |
rs796290433 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167961055 | ATAGAAATCTTATAC[A/G]TATTTCATTCAATTT | 55827 |
rs796296341 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167972885 | AGTTTATTTAATAAG[A/G]GAATGCTTTTCAATT | 55827 |
rs796326549 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168007477 | TTATTTATTAACCAA[-/C]CCCCCATCTGCTTTT | 55827 |
rs796339014 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167984452 | ATTATCAAATTCAGT[A/G]TTCTAGTTTTTAAAA | 55827 |
rs796363207 | in-del | -/AA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167992283 | CACACACACACACAC[-/AA]ACACCGAATGCACAT | 55827 |
rs796471165 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168046702 | TTACCACTTAATTTA[G/T]GCAGATGAGGTTAGC | 55827 |
rs796485965 | in-del | -/AAAAAAAAAAAAAAAA | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168072295 | AGGGAGAATCAGTCT[-/AAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 55827 |
rs796492460 | snp | G/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168075110 | CCAAAGAACACTGTT[G/T]GACAACCACTGCAGT | 55827 |
rs796531996 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167957062 | GCATGATGATAAACC[C/T]GGTCCATGTGCTGAC | 55827 |
rs796548935 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009378 | CTTCCTTCCTTCCTT[C/T]CTTCCTTCCTTTCTT | 55827 |
rs796571852 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052886 | CTCCATTGTTTATGA[C/T]ATAAAGAAGAAACAA | 55827 |
rs796573100 | in-del | CC/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037102 | TGAGATTCTCCCCCC[CC/T]TTTTTTTTTTTTTTT | 55827 |
rs796585053 | in-del | -/TT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009414 | CTTTCTCTCTCTCTC[-/TT]TTGTTTCTTTCTGTC | 55827 |
rs796613392 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049862 | GGGTTTCACCGTGTT[A/G]GCCAGGATGATCTCG | 55827 |
rs796639885 | in-del | -/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037096 | GTTCTATGAGATTCT[-/C]CCCCCCCCTTTTTTT | 55827 |
rs796645664 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168011652 | GTCTAGTCTAGTCTA[A/G]TCAGATAGATATAGG | 55827 |
rs796646196 | in-del | -/ATAAAC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168058026 | ACAAAACATAAACAT[-/ATAAAC]ATAAAGTTTTACCCA | 55827 |
rs796657274 | in-del | -/TC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168027477 | TCCTATTTGAATATA[-/TC]TCTGACTAATGATTA | 55827 |
rs796660285 | in-del | -/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167963770 | ATATAGTTTTTTTTT[-/T]CTCCTTCCTTAGTAT | 55827 |
rs796703528 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168052273 | TACTTTTTATCACAA[A/G]TACGCAAAGCTGGTT | 55827 |
rs796733503 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168045461 | TCCATATCTCTAGCA[C/T]TGAGGCTTGCTTCTG | 55827 |
rs796758521 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168037878 | CTAAATTATAGATCT[A/G]TGAGTTTGAAAGAAC | 55827 |
rs796766174 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009366 | CTTCCTTCCTTCCTT[C/T]CTTCCTTCCTTCCTT | 55827 |
rs796769231 | in-del | -/GTTG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168049428 | GTTGTTGTTGTTGTT[-/GTTG]TTTTTTTTTTTTTTT | 55827 |
rs796777218 | in-del | -/TGT | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167942235 | ATGCCCAGCTAATGT[-/TGT]ATTTTTAGTAGACAT | 55827 |
rs796779697 | multinucleotide-polymorphism | GT/TG | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167985210 | TGTGTGTGTGTGTGT[GT/TG]TGTGTGTGTGTGTGG | 55827 |
rs796874289 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168013811 | AGTGCAATGGTGCAG[C/T]CGTGGCTTACTGCAG | 55827 |
rs796897028 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167942088 | TTTTGTTTTTGAGAC[A/G]GAGTTTCGCTCTTGT | 55827 |
rs796898597 | snp | A/C | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168027497 | GACTAATGATTATTT[A/C]AGCATATTTTAAATT | 55827 |
rs796909913 | in-del | -/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168056340 | AGCTGCCAGGGCCTC[-/G]GCGGGCAGGGCGCGG | 55827 |
rs796912105 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167986185 | TGAACATTCTAGTGC[A/G]TGTTTTTACATGCCC | 55827 |
rs796925812 | in-del | -/TCTC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168023912 | ACACGATATTCACTT[-/TCTC]TATTTAAAAAGGCAG | 55827 |
rs796936659 | in-del | -/TTTAAC | | | intron-variant | DCAF6 | GRCh38.p7 | 1:167941883 | TGTATGGTAAGTATG[-/TTTAAC]TTTATAAAAAACTTC | 55827 |
rs796990852 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168001306 | GGAAAAAAAAAAGTT[A/G]AAAATGTAAACATTA | 55827 |
rs796996440 | snp | A/G | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168063502 | CTTTTGGTTGGGGGT[A/G]CCTTATTGAGATAGT | 55827 |
rs797006848 | snp | C/T | | | intron-variant | DCAF6 | GRCh38.p7 | 1:168009389 | CCTTCCTTCCTTCCT[C/T]TCTTTCTTTCTTTCT | 55827 |
rs797015336 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF6, MPC2 | GRCh38.p7 | 1:167936490 | ATCTGGTTAGAGTGG[C/T]CCGAATGCATTCTTC | 55827 |