| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs532688325 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056667 | CCGAGATCTGTCTCC[G/T]CCCCTTCCTCCTCCT | 1840 |
| rs532724448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113091973 | ACAGGTGCTGAAGTC[A/G]GGAGGACTCAGGCAG | 1840 |
| rs532808304 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097843 | TCGTTGGGAGTGGGC[A/G]GTGGGGTGGCTAATT | 1840 |
| rs532843372 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DTX1 | GRCh38.p7 | 12:113082303 | GCTCAAAGTCCCCAA[C/T]GCTCCATCTCCAAGA | 1840 |
| rs532966201 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086920 | AAACACTCCCCCCAC[C/T]CTGCCCCCCACCTGA | 1840 |
| rs533020861 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069561 | TGATGAATCCCAGAG[A/G]AGAGTTTGGAGGGAA | 1840 |
| rs533029572 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113063328 | ATCTTCCCTGGGGGG[A/T]CATTTACATCCCCTG | 1840 |
| rs533077626 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113092766 | TTTCCTGGAACGTTT[G/T]ATGGAAATTAATAAT | 1840 |
| rs533347695 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056124 | CCCTCCCCTGGTCCC[A/G]CCCCTCTCACCTGGA | 1840 |
| rs533350192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113067601 | TGCAGCAGGTGCTCA[A/G]TAAATACTTGAAGGC | 1840 |
| rs533384336 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056023 | CCACCATTTATTGAG[C/T]ACCAGTTGTTTGCAG | 1840 |
| rs533420215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113061490 | AGGGAGCAGACCTGA[A/G]TGCCAACGGTGTGAC | 1840 |
| rs533435754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113074064 | GGTGAAATCCCGTCT[C/T]TACGAAAAATACAAA | 1840 |
| rs533438218 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113066948 | TCCTTGCTCGGCCAC[C/G]CTGGCCAAGCGCCTC | 1840 |
| rs533472853 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113073336 | TCTCTCTAACTCACC[G/T]CCTCCCGGGCCTACT | 1840 |
| rs533532987 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113079162 | AAGAACCAAGCCCTG[A/C]GGGGTGGCAATGAGA | 1840 |
| rs533560375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113093844 | CCTTGCCCTGGCCCC[A/G]TCTTTCACCAGCTCC | 1840 |
| rs533567079 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082565 | AACCACCTCCCAGCC[C/T]TCCCAACCCTGGTCT | 1840 |
| rs533581450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113078592 | CATGTGCATATTACA[A/G]ATGGGGAAGCCAAGG | 1840 |
| rs533597670 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DTX1 | GRCh38.p7 | 12:113093401 | AGGCCCTTCAGGGGC[C/T]TTCAAGGGGCTGAGT | 1840 |
| rs533654618 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113084954 | TCTTCCTCTCTGGTC[G/T]TCAGTTTTTGCATCT | 1840 |
| rs533731234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113060905 | TCCGGGACCTAGCTG[A/G]GTTGGGTATGGGCGG | 1840 |
| rs533798205 | snp | G/T | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055350 | AGTCTCCTGTGAGAA[G/T]AATCTGCTGACAGCC | 1840 |
| rs533892089 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113093451 | AACCCTCCCACCCAC[C/G]CGAGGGCCCCGGGAT | 1840 |
| rs533956332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113059573 | CCCTGAGTCATTGCC[C/T]GGTGGTATCTGTGAC | 1840 |
| rs533957689 | in-del | -/GGG | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113064073 | TGGGGCTTGTTGTCA[-/GGG]GGGTCTAGCCCAAGG | 1840 |
| rs534048950 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113066509 | CTCCAGCCTGAGTAA[C/T]AGAGTGAGACTCCGT | 1840 |
| rs534062921 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066184 | ACCTCGGGGAATGCT[A/G]TTGGTGAGGGCCAGG | 1840 |
| rs534095536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113072629 | ATTAATACCCCCATT[G/T]TATAGATAAGGGCAC | 1840 |
| rs534131914 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097368 | GCAAACTGGAGGATG[C/T]GGGGCAAGCCCTTAG | 1840 |
| rs534199288 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055652 | GCCTGGGGAGGGGAG[C/G]TCCCTCCAGCTGGCC | 1840 |
| rs534266204 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113070924 | CCTGGAAGCAATGGT[A/G]TGAGGATGGAATGAG | 1840 |
| rs534353139 | snp | A/G | | | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096277 | GGGAGGCCGAGGTGG[A/G]AGGATCACTTGAGGC | 1840 |
| rs534369520 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113095527 | CTCTCACATTCCTCC[A/C]AAAAGCAGCACCCGA | 1840 |
| rs534370964 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057146 | CCGCGCATCCCCGTG[C/T]TTCCCGGCGCACCCC | 1840 |
| rs534382315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113081174 | ATGGTGAAACCCCAT[C/G]TCTACTAAAAATACA | 1840 |
| rs534419776 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113075221 | ATGCTGAGTTGCCTA[C/G]GCACAGTCACAGAGC | 1840 |
| rs534421094 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113087983 | GCCCTGATCTACCCT[C/G]CCCAGGCCTGAGCCA | 1840 |
| rs534507900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113076874 | ACTGCATGGGGCCTA[C/T]GTGCATGGCCTTGGT | 1840 |
| rs534509211 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113087455 | TGCAGTGGGGGTGGC[A/G]GCAGGGACTTGGCCC | 1840 |
| rs534673622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113064851 | GGTGCCTTCAGCCAT[A/G]GGATGTGCATGGTGT | 1840 |
| rs534748459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113063289 | GGTTTGAGAATGGCT[A/T]TCTGCTCCCAGAGAA | 1840 |
| rs534799336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113083593 | GGCCTCCCGAAATTC[C/T]GGGATTACAGGCATG | 1840 |
| rs534808728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113070395 | CACGTGCCCCCTTCC[C/T]GTCAGGGTCTGGGTG | 1840 |
| rs534840365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113091287 | CTGGAATATGTGAGT[A/G]TGTGTGTATCTTAAT | 1840 |
| rs534930250 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113090119 | TTTCCACCCAATTTA[A/T]AGGTAGTCCTGGAGA | 1840 |
| rs534937768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113058605 | CAGTCTAACCTTGTC[C/T]AGTTTAAGACTTGGA | 1840 |
| rs534994825 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097144 | ATAGCTCCCTGAGAG[A/G]GCCAAGCAGAGAGTA | 1840 |
| rs535024033 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058093 | GCCAGACGGTCCTTG[A/C]TGTCCCCCTGGGGAG | 1840 |
| rs535086131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113070867 | TCACCTCTCCGGGCC[C/T]CAGTTTCCTCATCTG | 1840 |
| rs535119080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113077326 | GCCTGTGCTGACCCC[C/T]CAACCTCCCGCCCAC | 1840 |
| rs535178995 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096483 | AGAAAAAAAAGAAAA[A/G]GAAAGAAAAGAAAAG | 1840 |
| rs535270619 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097491 | CACCCACTGATTGGG[A/C]AATTGTGGGCCCATG | 1840 |
| rs535290741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113071062 | CCAGCTTCCCTTTCT[C/T]TTCATCTCTCAAGCT | 1840 |
| rs535327988 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113084757 | TCCCCATTTTTCAAA[A/T]GAGGAAACTGAGGCT | 1840 |
| rs535441514 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113058791 | ACAGCAGTAGCATGG[A/G]ATTGTAGAATAAGGG | 1840 |
| rs535465216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113066331 | GTCAGGAGTTCGAGA[C/T]CAGCCTGGCCAACAT | 1840 |
| rs535497212 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057948 | ATAAGAGAGACACTT[C/G]CTTTCCAGGGCAGCA | 1840 |
| rs535634572 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113092837 | ACCACTAGTAGTTGG[G/T]TTTCAGGCACAGCGG | 1840 |
| rs535642072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113078298 | TGTTCCCACACATCT[A/G]TCTCCATGCATAAGG | 1840 |
| rs535815203 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097565 | GCCAGCACGAGCGGG[A/G]ACTAGAGGGTCCTGA | 1840 |
| rs535818376 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113059334 | TGGAGAAAATGAGAG[A/G]ATGATGTTGGTGGCA | 1840 |
| rs535823369 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113061951 | CCTCAAGTGAGCCGC[C/T]CGCCTCGGCCTCCCA | 1840 |
| rs535853563 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083974 | CTCAGCAAGGATCAG[C/T]TTGCAAGGGAGGTGT | 1840 |
| rs535934059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113068766 | GGCGCCATGTGAGAA[G/T]GCACTGAACATTGCA | 1840 |
| rs535935954 | in-del | -/TG | 0.0138799 | 0.0821421 | intron-variant | DTX1 | GRCh38.p7 | 12:113088841 | TCTCCTCAAAAGTTT[-/TG]TTGTTGTTGTTGTTG | 1840 |
| rs535955319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113071794 | TGGGCAGGCGGGCAG[C/T]GGCGGGCGCTGCGGG | 1840 |
| rs535966136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113074958 | AGGTTTGGGGCAGGG[A/G]AGAGCAGAGCTGAGT | 1840 |
| rs535985483 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076472 | GGAAAAAAAAAAAAA[A/G]AAAAAGTGGGGCCGG | 1840 |
| rs536021659 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113088612 | TTAAAGTATAATTTT[A/T]AAAAAAGACTATAAT | 1840 |
| rs536095544 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113056723 | AGCACGGCCGAGGCC[C/T]CCTCCCACCCGCGAG | 1840 |
| rs536189575 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056343 | AGGCCTTGTCAGCAC[A/C]CTCCCACCCCCAGGA | 1840 |
| rs536189590 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113062648 | GTGGTGTGTACCAAG[G/T]TACACGTGCGTGTGC | 1840 |
| rs536205134 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113089110 | GAGTGTGCCATGAGG[A/G]TATCTGGGAAGAGCA | 1840 |
| rs536224317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113069349 | TGGCGTATGAGTGCC[C/T]GCCTCCGCCTGCCAG | 1840 |
| rs536243525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113076031 | GGGAGAAAATGGAGC[A/G]GGGAAGGAGAGAGGG | 1840 |
| rs536283254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113082406 | AGGAAGATAGGGGTG[A/G]CAGACCCTGGCTTCT | 1840 |
| rs536369108 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | DTX1 | GRCh38.p7 | 12:113081892 | TTTTTTACCCCAAAT[C/G]GGGGTACAAGGCCAG | 1840 |
| rs536396846 | snp | A/C | 1.64754e-05 | 0.00287009 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095327 | TCCCTCTCTGCAGGG[A/C]CCTGAGCACCCCAAC | 1840 |
| rs536515780 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113063397 | CTGAATTTCCCACCC[A/T]GTTCACACAGCTGGA | 1840 |
| rs536628526 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113056806 | GTCCACGCGCGGAAA[C/G]CTCGGCGCGGCGGCC | 1840 |
| rs536665231 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091529 | GTGTGTAATGTGTCC[C/T]GGGGAGTATGATAAG | 1840 |
| rs536721572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113062664 | TACACGTGCGTGTGC[A/G]TACACACACACAGCA | 1840 |
| rs536723724 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084531 | GCTGAGACTAAAGGT[A/G]TGCACCACCATGCCC | 1840 |
| rs536776863 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113089532 | AGGCCCGCAGGCAGC[A/G]GTCGCTTGTCCAGGC | 1840 |
| rs536832706 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113064098 | CCAAGGCAGGGACAG[C/T]CTGCACTACCCTGGA | 1840 |
| rs536893673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113089581 | ACTCGGAGGAAACAG[C/T]GTGTCCCACATCAAA | 1840 |
| rs537033229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113063183 | GGGAAGCCCAAGGCC[A/G]AAGGGTATGCTCAGC | 1840 |
| rs537155176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069402 | TCCGAGTGCCACGCA[A/G]CCCTTCAGCCTTCCT | 1840 |
| rs537168008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113076095 | GATGATGGTAAATGA[A/G]GGAATGTCTGAATGC | 1840 |
| rs537180134 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088817 | CCTGGGCAACACAGC[A/G]AGGCCCTGTCTCCTC | 1840 |
| rs537208024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113090002 | TGCTTGGAGAGCTGT[A/G]CTGAGGACTCTGCTA | 1840 |
| rs537318402 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057835 | AGAGGGACCAAGAGA[A/C]AACACGGAAGAGGCT | 1840 |
| rs537324019 | snp | A/G/T | 0.000115348 | 0.00759354 | missense | DTX1 | GRCh38.p7 | 12:113095361 | GGGAAGAAGTTCACC[A/G/T]CAAGAGGATTCCCTC | 1840 |
| rs537396399 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057102 | TCCGCGACGCGACCC[C/T]CGAGGGGCCCTGGGC | 1840 |
| rs537448250 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113073567 | CTTTCATATCAATAG[C/T]CATAGCTCCGTGCCT | 1840 |
| rs537568769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113079258 | TGGTCCCCAAGAGGA[A/G]GAGAGGGCACCCAAA | 1840 |
| rs537578088 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DTX1 | GRCh38.p7 | 12:113079725 | GTGTGTGTGTGTGTG[C/T]GTGTGTGTGTGTTAG | 1840 |
| rs537638891 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057965 | TTTCCAGGGCAGCAC[C/G]CTTTATCGGAGAAGG | 1840 |
| rs537718783 | snp | A/T | 0.0551013 | 0.156571 | intron-variant | DTX1 | GRCh38.p7 | 12:113067890 | AAAACAAAAAAAAAA[A/T]TAGCTAGACATGATG | 1840 |
| rs537810063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113088068 | CTAGGCTGGCTCAAC[C/T]CCAGATGGCTCCACA | 1840 |
| rs537932050 | snp | A/G | 0.000733983 | 0.019143 | intron-variant | DTX1 | GRCh38.p7 | 12:113093496 | GTCGGGGGTTTGGGC[A/G]GGGATGGCGCCCCGC | 1840 |
| rs538131463 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075635 | CGCAGAGCTTTGGCA[A/C]ACATGAAGCTGTGGT | 1840 |
| rs538149095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113067117 | ATGCAGAACAAAGGA[C/T]GAGGCAATCAAAGGA | 1840 |
| rs538175107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113081224 | GGTACACACCTGTAA[C/T]CCCAGCTACTGGGAG | 1840 |
| rs538224530 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113068045 | TCCTGTCTCAAAAAA[A/T]AAATAAATAAATAAA | 1840 |
| rs538282653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113087568 | GTGACAGGCTCACAC[C/G]CCTAGAAAGGAGAAA | 1840 |
| rs538322934 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113074224 | ACAGAGAAAGACTCT[C/G]TCTCATATATATATA | 1840 |
| rs538351202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113073695 | CTTTCAGCCCTGAGT[A/G]GGGACACACCAGTGT | 1840 |
| rs538359743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113080368 | CCTTACAAAAAGAGG[A/G]GCTGGAGGTCCCAGA | 1840 |
| rs538379618 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075684 | GCCCTCCTTTATGAA[A/T]GGGGGCCCACCTGGC | 1840 |
| rs538381889 | in-del | -/A | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RASAL1, DTX1 | GRCh38.p7 | 12:113098491 | CTGTAGTTCTGGTGG[-/A]TGCTGCGGCTTCGGG | 1840 |
| rs538434760 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075264 | AAGTCAGGACTTGAA[G/T]TGAGGGCTGTCTGCC | 1840 |
| rs538440620 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113068874 | CTGACAGTGGAAGTC[A/G]GGGAAGTTCAAATCC | 1840 |
| rs538445547 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058131 | GTTGCCGCCTGCTGC[C/G]AGGCCCAGGAGGAGC | 1840 |
| rs538450032 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113094313 | GTCATTTTCACCCAT[A/G]TTTTCCACTAAATGT | 1840 |
| rs538464331 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113081687 | AACTTCAAGGGGGCT[C/T]GAAGGGCGTGGTGTG | 1840 |
| rs538497891 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113061792 | CTGCAGCCTCTTTCC[A/C]CGGGTTCAAGTGATT | 1840 |
| rs538587269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113061298 | GAGGAAGGCCTGGAA[A/C]CCTATTGCGATTGGC | 1840 |
| rs538589124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113068614 | TTAGAGTGTGAGGCT[C/G]TGCAGACAGCTTGTG | 1840 |
| rs538764480 | snp | A/G | 1.6951e-05 | 0.00291122 | missense | DTX1 | GRCh38.p7 | 12:113094811 | CCATCTGCATGGAGC[A/G]ACTGGTCACAGCATC | 1840 |
| rs538764549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113088120 | CCTGGCCCCTGACTC[A/G]GAAACTCCAGGACCC | 1840 |
| rs538992008 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056183 | TCAGGGCTGGGAACT[A/G]GGTACTGGCAGGAGA | 1840 |
| rs539036291 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113070869 | ACCTCTCCGGGCCTC[A/G]GTTTCCTCATCTGTA | 1840 |
| rs539211123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113062747 | GTGCAGTGCAGCCAG[C/T]GGAAGAAAGCCCCGG | 1840 |
| rs539253695 | in-del | -/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113085055 | TCAGGCCCGTACCCT[-/T]TTTTTTTTTTTTTAG | 1840 |
| rs539302655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069475 | CCACCCTGGCCTGGC[C/T]TCCAGCAGACCCTGG | 1840 |
| rs539436998 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084260 | TCCAGTGCGTTGGAA[C/T]ACAGCTGTGGAGCAG | 1840 |
| rs539620772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113065700 | AGCGGGGCTGTGGAG[A/G]GGATGGTGAAGAAGG | 1840 |
| rs539794241 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113054919 | CTTGTGGGGCAGTTA[G/T]GAAGAGTAGTAAGTA | 1840 |
| rs539836416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113071842 | GAGGACAGCAGCTGC[C/T]CTAATTACTCCTGCT | 1840 |
| rs540016647 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113098273 | TGCTCCCTGGCACAA[C/T]GACAAGAAACAAGGA | 1840 |
| rs540017522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113079870 | GGCCCCCTTCTTGAC[A/C]ACTTCTGAGCTGGGA | 1840 |
| rs540032363 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113087412 | GGCACCTGGTCCCCC[G/T]GGCTTGCAGCGATGT | 1840 |
| rs540067669 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113086877 | CAGTGACTGTCACCC[C/T]GCCTCACCGCTGCTG | 1840 |
| rs540194983 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097875 | TCTTCGGCCAACCAG[A/G]GGCCTGTTGCCCAGG | 1840 |
| rs540250575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113071297 | TTGTGCAGTCCTCCA[A/G]CTGACACTGACCAAA | 1840 |
| rs540358336 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113092591 | TCCAGAAGAGAAAAA[A/C]AATTCATCACCAAAT | 1840 |
| rs540395732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113091641 | CTGTGTGTCTGCACC[C/T]ACTGCAGCAGTACCC | 1840 |
| rs540417920 | snp | A/G | 3.295e-05 | 0.00405881 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095333 | TCTGCAGGGCCCTGA[A/G]CACCCCAACCCCGGG | 1840 |
| rs540423885 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097703 | TACCCCATCCTCTCC[A/G]CCAAATCGCTCCCAA | 1840 |
| rs540537761 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113065806 | AGGACGGGGAGGCCA[C/G/T]GGGGAGGCCAAGGGG | 1840 |
| rs540592968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113079328 | TTGATAATGATGGTC[C/T]GAGATCACCAAAGCT | 1840 |
| rs540771488 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DTX1 | GRCh38.p7 | 12:113090232 | CTAGAGGTGCTTGAA[A/G]AATGGGCAGGAAAGA | 1840 |
| rs540856708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069649 | CACAGGCTGCAGCTC[A/G]AATCCCAGCCCAGCC | 1840 |
| rs540979863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113082055 | CCTCTGACCTGCCAG[A/G]GCTCTGTTGTCTCCA | 1840 |
| rs540982706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075853 | GTGACCTAATGAATT[C/T]ATTCATTCATTCAAC | 1840 |
| rs541007808 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057850 | CAACACGGAAGAGGC[C/T]GGACCTCGAACAGGG | 1840 |
| rs541068483 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113096010 | CAGGAGTTTGAGACC[A/G]GCCTGGACAACATGG | 1840 |
| rs541089190 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083265 | AAGGTTTCAACACAT[A/G]ACTTCTTTGGGGCAC | 1840 |
| rs541093584 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057435 | GGGCCCTCTCCCCTC[A/T]TGTCTCCTGGCAGGT | 1840 |
| rs541096917 | snp | C/T | 1.65329e-05 | 0.0028751 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095158 | GCCCGGCTTCCCTGA[C/T]ACCCAGACCATCCGC | 1840 |
| rs541160344 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113056859 | CGCGGAGGCGGGACC[A/G]CGGCTCCCTCCCACT | 1840 |
| rs541246869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113076256 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 1840 |
| rs541248891 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113089301 | CAGGTGTTAACTGTG[A/T]GCAAAGTGGGAGCTG | 1840 |
| rs541312977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113090383 | AGGGTCAAATGAATA[C/T]TCAGTGCCCCTCTTC | 1840 |
| rs541376402 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113081841 | TGGAGACCACCGGGG[A/G]ATAGAGGCTCCCTTC | 1840 |
| rs541378534 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096654 | GGAGGGAGGCTGAGG[C/T]TGGTGGGCTGGAAGC | 1840 |
| rs541803196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113076298 | ACCCCATCTCTACTA[A/G]AAATACAAAAATTAG | 1840 |
| rs541807105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113083015 | AGAAGTCCGAGATCA[C/G]GGTGTCACAGGGTAG | 1840 |
| rs541892823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113082615 | TTTTTTGTTTTTAGA[A/G]ACAGAGCCTCGCTCT | 1840 |
| rs541926846 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057884 | GCTGCCTCACTCCCT[A/G]CCTGAGCCAGCCGAG | 1840 |
| rs541997279 | snp | A/C | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055946 | ACAGGGGGACTGGCC[A/C]TCCCGTTAACACTTG | 1840 |
| rs541997774 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113081324 | ACAGAGTGAGACTCC[A/G]TCTCCAAAAAAATTA | 1840 |
| rs542063420 | snp | G/T | 0.00199481 | 0.0315187 | missense | DTX1 | GRCh38.p7 | 12:113078008 | CCACGGAGCCCGGGC[G/T]CCCCCGGCGGAGCGC | 1840 |
| rs542168882 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113077023 | CCCTGGAGAGGTGGA[C/G]GGTGGGGGAGCCCTC | 1840 |
| rs542176623 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113090986 | TCCCCACAGGCGGTG[A/C/T]GGAATCGTGTGTCCG | 1840 |
| rs542249934 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097222 | AAACACACATGTCCT[A/G]TTGAACTCATGCACG | 1840 |
| rs542280448 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067288 | TCCCAGGGCCCTCCC[C/G]CTGGCTGGGGTAAGC | 1840 |
| rs542283149 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | DTX1 | GRCh38.p7 | 12:113061393 | TGAGGGTTTTTCCCT[A/C]GCTTTACCCAGGAGC | 1840 |
| rs542283429 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113059683 | AAGGACCAGCTGATG[G/T]GGTTTGGGGAAGTTC | 1840 |
| rs542322333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113060539 | CCCTGGGGTAGGAAG[A/G]GGCAGAGGACATTTA | 1840 |
| rs542375503 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113081339 | GTCTCCAAAAAAATT[A/T]AAAAAAGAGAGAGAT | 1840 |
| rs542463078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113080901 | GATCACTTGAGCCCA[A/G]TAGGTCAAGGCTGCA | 1840 |
| rs542494215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113084333 | GGACAGTGATAGCTG[C/T]GGGCCTATTTCCATT | 1840 |
| rs542499897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113087725 | TTTGGGGTCTGCTGG[A/G]TAAGTGTGAGGTATC | 1840 |
| rs542617461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113093310 | CCCCGCCCCCGAGAT[A/G]GGCTGGTGAGCGTGG | 1840 |
| rs542683088 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092982 | GGTCCTGGCCACCCC[C/G]GCCCCATAATAGGAT | 1840 |
| rs542824757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113089014 | AGCAAGATCTTGTCT[A/G]TAAATAAATAACTAA | 1840 |
| rs542854671 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DTX1 | GRCh38.p7 | 12:113088245 | ATAGAGTTCATCTCA[C/T]GTGCCATCTCTGCTC | 1840 |
| rs542893452 | snp | A/G | 8.47637e-05 | 0.00650958 | intron-variant | DTX1 | GRCh38.p7 | 12:113094110 | ATGAGGTGAGGAGGG[A/G]ATGGGGGGGCTGGGG | 1840 |
| rs542926950 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | DTX1 | GRCh38.p7 | 12:113086092 | GGACAACATAGTGAG[A/G]CTCCACCTTTACAAA | 1840 |
| rs543003923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069495 | GCAGACCCTGGAGAA[C/T]CTGGGCCAGCTTCAA | 1840 |
| rs543172903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075679 | TCAGTGCCCTCCTTT[A/T]TGAAAGGGGGCCCAC | 1840 |
| rs543226574 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057255 | AGGCGGAGAGTCTCG[G/T]AAAACCGCGCCCCCG | 1840 |
| rs543312635 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113056895 | GGGAGCCCAGGAGGC[A/G]GCGGTGCTGGAGCGC | 1840 |
| rs543346589 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087598 | AGGGAGAGGGTGGGG[C/G]GTCCCTAAAGCACTG | 1840 |
| rs543366798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113085983 | GTTAAAAAGCAAGGT[A/G]TGGTCCAGGCACTGT | 1840 |
| rs543444604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113070085 | CTCACAGATGGCATC[C/T]GGTGTGCTCCTAACT | 1840 |
| rs543444743 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113063174 | GCCACATATGGGAAG[-/C]CCAAGGCCGAAGGGT | 1840 |
| rs543451842 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113056949 | GAAGAGAGGCGGTGA[A/G]AACGCGGGTGCTTAG | 1840 |
| rs543477577 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056409 | CTTCAAGATCTTTCT[A/T]TAGACAGTCTCTGGA | 1840 |
| rs543516490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113062146 | CTGTCTAGATTTTCT[A/G]ATTGTAAAATTCTTG | 1840 |
| rs543523980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113093815 | CCTCACCTCCATTGC[C/T]TGATCTCAGCTCCCC | 1840 |
| rs543543587 | snp | A/C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086130 | TAAATTAGCTGGGTG[A/C/T]GGTGGTGCGTGCCTG | 1840 |
| rs543565074 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113090288 | ATGCATTCCTATAAA[A/T]GTATAGAGAGGGAGG | 1840 |
| rs543654393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096571 | ATGCAAAGGAAATGG[C/T]CAAGCCAGCAGTACG | 1840 |
| rs543796466 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113063505 | CACCTATCTGCCTGG[G/T]ATCTCCCATGTCGCT | 1840 |
| rs543836350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113072833 | CTTAGCCTCCTGAGT[A/G]ACTGGGATTACAGGC | 1840 |
| rs543863837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113066543 | AAAAAAAAAAAAAAG[A/G]ATCGTAGTGGGTGGG | 1840 |
| rs543921893 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113071993 | TAGCTGGCCCTGACG[G/T]GCTCCCAGAGTCCTT | 1840 |
| rs544046634 | snp | C/T | 0.00104898 | 0.0228777 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093216 | GCCGGTCCATCCGGC[C/T]CTGGCAGGTGAGGTC | 1840 |
| rs544107944 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057359 | CCCTTCGGTTCCCCA[C/T]TGTTCTCAGCCGAAT | 1840 |
| rs544364372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113086414 | AATCGGTGGGAAAGA[A/G]GTAAGAGAGGAAAAG | 1840 |
| rs544440181 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113065070 | GGTAGAGGAGGCCTC[A/G]TGGGGCCCACTGGGG | 1840 |
| rs544474557 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113095239 | TCTGGCCCCCAGCCC[C/G]CACACCCCTCCAACT | 1840 |
| rs544478286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113061472 | AAAAGAGCCTCAACC[A/G]GCAGGGAGCAGACCT | 1840 |
| rs544501699 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113088031 | AAAGACTTCAGCCCA[C/G]CTGTAGAGCACAGAG | 1840 |
| rs544515022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113068143 | CAGTCTCCAGCCTAG[G/T]CATGAGCAGCATTCA | 1840 |
| rs544575323 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113074031 | AGGTCAGGAGTTCGA[C/G]ACCAGCCTGGCCAAC | 1840 |
| rs544663310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113079977 | GTGAAAACGCTGTGT[A/G]CCTGAACACAGCATC | 1840 |
| rs544667939 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113067281 | ACCACCTTCCCAGGG[A/C/T]CCTCCCCCTGGCTGG | 1840 |
| rs544756094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113087599 | GGGAGAGGGTGGGGG[A/G]TCCCTAAAGCACTGT | 1840 |
| rs544843524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113093524 | CGCCCTGTGACTGCG[C/T]CCCCTAACCCCCAGG | 1840 |
| rs544843662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113087126 | AGGACCGGGAGGGTT[C/G]AAGAGTGACCCCCGC | 1840 |
| rs544880265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113093253 | AGGGCGGGAAAGAAG[A/G]GCGGGGCCCACTAGG | 1840 |
| rs544912079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113067490 | CACAAAGGCTGCAAA[C/T]TCAGATGCTTACAGG | 1840 |
| rs544991593 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082518 | TTGAGGAGCCAGGCA[A/G]ACAGGTCTACCCACT | 1840 |
| rs545000066 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RASAL1, DTX1 | GRCh38.p7 | 12:113098510 | TGCGGCTTCGGGCAA[A/C]CCCTGCTGGCCACCC | 1840 |
| rs545013711 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061667 | TGCTCACCACTGTGG[A/G]TACAAGAGAGACAAG | 1840 |
| rs545052247 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113059747 | TAACCCCAGGCTGGT[A/G]GGATGCTCGCTTTCC | 1840 |
| rs545098230 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113074594 | TTTACTCCAAGTGAG[A/C/T]GGAAGCCAGGAAGGA | 1840 |
| rs545139727 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113080046 | TTTTGCTCTCCAGGA[C/G]GAGGGTTGGCATGGA | 1840 |
| rs545249574 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056523 | GATTCAAGCCGGTGA[C/T]TCCTAAACATCCCAC | 1840 |
| rs545414582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113068191 | GTATTTGGTTATTCA[C/T]TCATTTATTCATTCA | 1840 |
| rs545665311 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | DTX1 | GRCh38.p7 | 12:113062762 | GGAAGAAAGCCCCGG[-/T]TGTCAGGCTGGGGCC | 1840 |
| rs545680906 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113062294 | CTTTGTGGGACCTGC[A/C]GTCTCTGTTGTAACT | 1840 |
| rs545715923 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069042 | TTATCATTATTATCA[G/T]AACAACCTGCCCCAG | 1840 |
| rs545721758 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113061506 | TGCCAACGGTGTGAC[C/G]TCAGGCCTCTCCAGG | 1840 |
| rs545807632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113070560 | CTCAGAACCCTCCCC[C/T]TTCTCCATGGAGTCA | 1840 |
| rs545955103 | snp | C/T | 1.86468e-05 | 0.00305337 | missense | DTX1 | GRCh38.p7 | 12:113058223 | CACGGTGGGCTGATG[C/T]CTGTGAATGGTCTGG | 1840 |
| rs546101575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113068165 | CAGCATTCAGTTAGG[C/T]TCATTCAGATGTATT | 1840 |
| rs546195627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113086213 | GCAGTGAGCCAAGAT[C/T]GAGCCACTGCACTCC | 1840 |
| rs546260195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113091449 | TCTGTGTGTCTGTGT[A/G]TGCATGTATCTGTGA | 1840 |
| rs546300603 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097419 | GGCAAAGAGGGACTC[C/G]GGAAACTCAGTGTAC | 1840 |
| rs546303112 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097607 | TGCCTCTTCATCTCT[C/T]TGGACTCTGATCTCC | 1840 |
| rs546399631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113070754 | CTGTGCTACCACTTG[A/G]TGAGGTTGAACCCCA | 1840 |
| rs546547621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113065454 | GCGCCTTCCGGGCTG[C/G]GGGTGGGGATGCCCG | 1840 |
| rs546568951 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097303 | AGACCCCATGACCCC[C/T]CCATGTGGATCCCCA | 1840 |
| rs546638615 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113072172 | TTCCCACTCCTCCAA[A/G]TGCCAAGTAGGTTGC | 1840 |
| rs546650804 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091915 | ACGTATCCAGCCTGG[C/G]TTCCATGCCCATCAA | 1840 |
| rs546652296 | snp | A/C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057760 | AGGGCTGGCTGAGAG[A/C/T]CGCAGGAGCAGCAGG | 1840 |
| rs546739811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113063973 | GGCCCCCCAGACAGG[C/T]CTTAGGGATAGAAAA | 1840 |
| rs546786298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113059867 | CCAGTTCTTCAGTCT[C/T]ACTAGCCACACTTCA | 1840 |
| rs546789067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113084632 | TCAAGTGATCCTCTC[A/G]CCTTGGCCTCCCAAA | 1840 |
| rs546825028 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113059256 | ATGGGATTCAGTGGT[C/G]TTGGTGACATTGATA | 1840 |
| rs546827664 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DTX1 | GRCh38.p7 | 12:113083603 | AATTCTGGGATTACA[A/G]GCATGAGCCACTGCG | 1840 |
| rs546913681 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113090617 | CATCCTGCCTCCCTC[A/G]GGAGCTGTGTTCATT | 1840 |
| rs546998545 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113066241 | CTAAGAATCATGGGG[G/T]GTGTAGGCCGGGTGT | 1840 |
| rs547021753 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113071759 | GTCCATGGCCAGCCT[G/T]GGCCGGAGAGGCGGA | 1840 |
| rs547056298 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113093795 | CTTATTCTTAGCATT[G/T]ACTACCTCACCTCCA | 1840 |
| rs547095268 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113065405 | CTCGCCCGGGCCACC[A/G]AGTACCTTGGACAGC | 1840 |
| rs547121299 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113070855 | CCTCCCAAGAGTTCA[C/T]CTCTCCGGGCCTCAG | 1840 |
| rs547153629 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113081134 | GATCACTTGAGGCCA[C/G]GAGTTCGAGACCAGC | 1840 |
| rs547188794 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097954 | GCCAAGATTTAAAGG[A/G]ATGCCAGCGATTGCT | 1840 |
| rs547268099 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056670 | AGATCTGTCTCCTCC[C/T]CTTCCTCCTCCTCCG | 1840 |
| rs547360922 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113082327 | TCCAAGAAACCCCCC[A/G]GGGAAAATCCCTCTG | 1840 |
| rs547399348 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113089513 | GGCTGGCTCCCCTTC[C/T]GGGAGGCCCGCAGGC | 1840 |
| rs547409985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113081406 | TCAGCTTTCATGGCC[C/T]AGTGTTAATTCTCCA | 1840 |
| rs547555874 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RASAL1, DTX1 | GRCh38.p7 | 12:113098325 | CCTCGAGGGAAATAC[A/G]GAGGAGCTGGGAGAC | 1840 |
| rs547670931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113082657 | CTGGAGTACAGTGGC[A/G]CAATCACAGCTCCTG | 1840 |
| rs547876206 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057018 | GCTCGGGGACGTCTG[G/T]GCTGGGGAAGCGGGG | 1840 |
| rs547926649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069358 | AGTGCCCGCCTCCGC[C/T]TGCCAGCAGCCTCCA | 1840 |
| rs547976862 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057585 | CCTCCCCCGTGCGTT[C/T]TGCGGCCACCCAGGC | 1840 |
| rs548017622 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057070 | GCAGAGACGATCCAG[C/T]TCCTGGCTTCGCCCC | 1840 |
| rs548028888 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113082226 | TCCCTCCCCACCCAC[G/T]CAGATGCTGCCCAGC | 1840 |
| rs548051683 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113077162 | CGCCCCAGTGCTATG[C/G]GCTGAACCTTTAGCC | 1840 |
| rs548184595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113082742 | GTGGGACTACAGGCA[C/T]GCACCACCACACCCA | 1840 |
| rs548258472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113083379 | TACCCAGGCTGGAGT[A/G]CAGTGGTGCAATCTT | 1840 |
| rs548289497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075223 | GCTGAGTTGCCTACG[C/T]ACAGTCACAGAGCTG | 1840 |
| rs548300673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113090412 | TCCTGGGGCCCCCCC[A/G]CAGGGTGCCCGACAA | 1840 |
| rs548466190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096252 | TGCACACCTGTAATC[C/G]CTGCACTTGGGGAGG | 1840 |
| rs548542357 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113087177 | AATCTGAGCCTCCAA[G/T]ACCACTCACACCTCA | 1840 |
| rs548675616 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113054840 | CTTGGGTAAGCTACT[C/T]AGCCTTTCTGAGCTT | 1840 |
| rs548723633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113064663 | CTGAGTTTATTTCCT[C/T]CTCTGTAAAATGGGG | 1840 |
| rs548851841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113080082 | GGGAAGCTGTAATTT[C/T]CCAGGGATGCATCAC | 1840 |
| rs548852674 | snp | C/G | | | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096230 | ACAGGCAGGCCAAGC[C/G]CAGTGGTGCACACCT | 1840 |
| rs548861471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113067823 | GATCACTTGAGCACA[A/G]GAGTTTAAGACCAGC | 1840 |
| rs548924113 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113065635 | GAGATGGAAGCTGTG[A/G]TGGGAAGCGTGGGGG | 1840 |
| rs549123892 | snp | A/G | | | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058184 | CTGGCCCCTGAGGCA[A/G]TGGCGGCCATGTCAC | 1840 |
| rs549241537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113073482 | TGGCTGGAACATGGT[A/G]GGTGCCCAGGGACCT | 1840 |
| rs549308983 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088526 | TGATGAGTTAATGGG[C/T]GCAGCACACCAGCAT | 1840 |
| rs549476560 | snp | A/G | 0 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113068333 | ACACCTCCGCACCTA[A/G]TGAGCTATGTGCTTT | 1840 |
| rs549518971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113061040 | ATCCCCTTATGTTCC[C/T]GAGTCCCCAGACTTG | 1840 |
| rs549519512 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083861 | CAGAGCCCTTTACAG[A/G]TTGGGTGACCTTGGA | 1840 |
| rs549562664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113088487 | TTAAAGAGGGATAAC[A/G]TTAGGAGATATATCT | 1840 |
| rs549568173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113081538 | CAAAGAGTAAATGAA[A/G]ACGATCTCTGGAGTG | 1840 |
| rs549646573 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113094642 | TAAAACAATGTATGG[G/T]GCAGAGGGTGTGTCC | 1840 |
| rs549681566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113074843 | GAGGTGGGATATGAG[A/G]TAGAAGTCAAGGATG | 1840 |
| rs549700595 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113061685 | CAAGAGAGACAAGCA[A/G]AAGATCTTAAATCTT | 1840 |
| rs549705175 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056534 | GTGACTCCTAAACAT[C/T]CCACTCCCTGCCTCA | 1840 |
| rs549766566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113094742 | GTGCTGACCCAGTAG[G/T]TGCCCTGCCCTCCCC | 1840 |
| rs549771320 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087018 | GGCCGTGGGAACAGC[C/T]GGTCCTGCCCTCCCC | 1840 |
| rs549872569 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DTX1 | GRCh38.p7 | 12:113088533 | TTAATGGGCGCAGCA[C/T]ACCAGCATGGCACAT | 1840 |
| rs549882108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113063374 | CCTCCGAGGGCCTCA[C/T]CCAGACCCTGAATTT | 1840 |
| rs550101573 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084380 | TGTCCCAGGCTCTCA[A/G]TTTCATGGCTTTTTT | 1840 |
| rs550131061 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097761 | GACTTCAGGAGCGAA[A/C]GGAGGAGGCCTAGTT | 1840 |
| rs550183929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113081728 | GGCTAGAGGTGTGGG[A/G]AGGGCTGGAGTGAGG | 1840 |
| rs550211784 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056576 | GGGTCAGAAGGCCCC[C/T]TGGGGTCTCGGGAGG | 1840 |
| rs550342783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113058550 | CTGCTGATGCCAAAT[C/T]CCTTCCCCATCTCCC | 1840 |
| rs550354447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075942 | AAAATCCCTGACCTT[A/G]TGGCTATTACATTCT | 1840 |
| rs550427389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113089359 | GGGATCTGATTTGGG[A/G]CTGGGAAAGGCAGAG | 1840 |
| rs550517741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113091128 | AGAGGGGCGGCAGTA[A/G]CAGGTGCGGTACTGG | 1840 |
| rs550717483 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057953 | AGAGACACTTGCTTT[C/G]CAGGGCAGCACCCTT | 1840 |
| rs550749914 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113079061 | TTTGCAAATTCTTGG[G/T]TTAAGGTGTCCCAGG | 1840 |
| rs550761378 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055458 | CATGGACCCCAGAAG[G/T]CCATCCAGGGACCCT | 1840 |
| rs550798225 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113054868 | CTTCAGGAGGTTTTT[C/T]GTTTCCTTGTGTAAA | 1840 |
| rs550832061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113084796 | CTAAGACATTTGCAC[A/G]AGGTAACACAATTAG | 1840 |
| rs550926690 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113085755 | TTTGGGGCCCTGGGG[A/T]CACAGCAGTGAACTA | 1840 |
| rs550980928 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | DTX1 | GRCh38.p7 | 12:113066395 | TTAGTGGGCATGGTG[A/G]TGGGCGCCTGTAATC | 1840 |
| rs551041673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113073185 | TTCACCTCACCAGGA[A/G]CTGAATGGTGGTACT | 1840 |
| rs551111220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113072242 | TGCCTGGTGCTCCAA[A/C]CATAGTTGCATATCT | 1840 |
| rs551131349 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088603 | CCCTAGAACTTAAAG[C/T]ATAATTTTAAAAAAA | 1840 |
| rs551188234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113059180 | GGGTCTTGGTGACAA[C/T]GGAGGGATGGATGAT | 1840 |
| rs551190527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113060648 | AGGCCTGGACAGCCA[C/T]GCAAAGAACTTTGAA | 1840 |
| rs551239303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113073394 | AAATCAATCTGCACA[C/T]ACTCAATTAAAATGA | 1840 |
| rs551327097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113079613 | ACTGACTGCAACTTC[C/T]GCCTCCAGGGTTCAA | 1840 |
| rs551441371 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076142 | GCTGAAGATGGAGAA[C/T]ACATAAAGGTATCAA | 1840 |
| rs551491159 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097455 | ATGCCTCACCCATTC[C/T]GTGTCATCACCCATG | 1840 |
| rs551791368 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055558 | CTCTCTCTTTAGTCT[A/T]CAGCAGGTGAAAGCA | 1840 |
| rs551793870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113060906 | CCGGGACCTAGCTGG[G/T]TTGGGTATGGGCGGC | 1840 |
| rs551911844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113063231 | CCAGGAGCCATCAGG[C/G]TCTTGGGGTGAGGGG | 1840 |
| rs551923196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113066959 | CCACCCTGGCCAAGC[A/G]CCTCTCCCTCTCTGG | 1840 |
| rs551978542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113087918 | GATCCTGGACCCCTC[C/T]AGGGGACAGAGAGAG | 1840 |
| rs552005460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113076367 | AGGAGGCTGAGGCAG[A/G]AGAATCGCTTGAACC | 1840 |
| rs552015582 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113093883 | CTAACCTCCAGCAAC[C/T]CCTGACCTCTGACCC | 1840 |
| rs552103053 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113093410 | AGGGGCCTTCAAGGG[G/T]CTGAGTGGGTGGGGC | 1840 |
| rs552238851 | snp | C/T | 0.0172898 | 0.0913561 | intron-variant | DTX1 | GRCh38.p7 | 12:113078138 | GGGAGGGGGCCTCTG[C/T]GTCGTCCGCAGGCAA | 1840 |
| rs552249058 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069766 | CTGGGGCTGCTGTGA[C/G]GACTGGGAGATGATG | 1840 |
| rs552328601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113084485 | CGACCTCCTGGGCTC[A/G]AGCAATCCTCCTGCC | 1840 |
| rs552446427 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057665 | GGCAGGAGCCGTCGG[A/G]GAAGGGGGCCCAGAC | 1840 |
| rs552498356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096257 | ACCTGTAATCCCTGC[A/G]CTTGGGGAGGCCGAG | 1840 |
| rs552565558 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113093933 | TGACCCCGGCCAACC[C/G]TTGCCAGCCTGACCC | 1840 |
| rs552638882 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113081711 | TGGTGTGTTCAGGGA[A/G]GGGCTAGAGGTGTGG | 1840 |
| rs552682903 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074235 | CTCTCTCTCATATAT[A/G]TATATAGTCAGTCAG | 1840 |
| rs552730255 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113058602 | GGGCAGTCTAACCTT[G/T]TCCAGTTTAAGACTT | 1840 |
| rs552750123 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076754 | GAACTAATGCAAGAA[C/T]TGTTGAATGACTAAA | 1840 |
| rs552906637 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058116 | CTGGGGAGAGAGGAA[C/G]TTGCCGCCTGCTGCC | 1840 |
| rs553024281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113089655 | GCTACCCTGGGTTCT[C/T]GCAGGAGGCCTGCAG | 1840 |
| rs553037269 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113064244 | CAGGGAGCGGCCCAT[C/G]TCTGGTAGCAGCAGG | 1840 |
| rs553041186 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113072332 | AACAAATAATGACAG[C/T]GTGAGGACAGACATG | 1840 |
| rs553117604 | snp | A/C/T | 0.00755907 | 0.0610114 | intron-variant | DTX1 | GRCh38.p7 | 12:113066452 | AGAATCACTTGAACC[A/C/T]GGGAGGTGGAGGTAG | 1840 |
| rs553177614 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088064 | CTCTCTAGGCTGGCT[C/T]AACTCCAGATGGCTC | 1840 |
| rs553178736 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069115 | ACAGCGCCTGGCACA[C/T]AGTAGGCCCTCTGGG | 1840 |
| rs553270562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113058662 | TAGGGCCTTGAGCAA[C/G]TTGCATCATCTCTCT | 1840 |
| rs553299922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113082901 | CAGCGACTGGCCTGT[C/T]TCTATGACTTTAAGT | 1840 |
| rs553309920 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113091329 | TGTGGGGGGCGTGCC[C/G]TGAAGTGTGCCTGTG | 1840 |
| rs553311117 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113061368 | GCAAGAGGCCTCCTC[A/T]CCAGATATGTGAGGG | 1840 |
| rs553338625 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DTX1 | GRCh38.p7 | 12:113090133 | ATAGGTAGTCCTGGA[A/G]AAAAAAAGAGATACT | 1840 |
| rs553344711 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097508 | ATTGTGGGCCCATGG[A/G]GTGGAAGCCCCCAGA | 1840 |
| rs553387669 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087698 | GACTGAGTCCTGAGG[C/G]TCCTGGGGCTCTTTG | 1840 |
| rs553397289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113068065 | AAATAAATAAATACA[A/G]GTCACTATTTTTTAA | 1840 |
| rs553434093 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113067324 | CCTCCCCAGCTTCCT[C/G]TGTTCTAGGGGGCGA | 1840 |
| rs553461359 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055667 | GTCCCTCCAGCTGGC[C/T]GGAGAGCCAGAGCTG | 1840 |
| rs553667283 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113061931 | AGCTGGTCTTGAACT[C/G]CTGGCCTCAAGTGAG | 1840 |
| rs553742598 | snp | C/T | 6.34457e-05 | 0.00563195 | intron-variant | DTX1 | GRCh38.p7 | 12:113093525 | GCCCTGTGACTGCGC[C/T]CCCTAACCCCCAGGG | 1840 |
| rs553761618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113081835 | AGGTTCTGGAGACCA[C/G]CGGGGGATAGAGGCT | 1840 |
| rs553815205 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113074239 | CTCTCATATATATAT[A/G]TAGTCAGTCAGGTAA | 1840 |
| rs553847470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113081278 | AGGTTGCAGTGAGCC[A/G]AGATCACGCCACTGC | 1840 |
| rs553884176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113088126 | CCCTGACTCGGAAAC[C/T]CCAGGACCCAGTGCC | 1840 |
| rs554025463 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097740 | GAGCCAAAGGCTGGC[A/G]CTTCTGACTTCAGGA | 1840 |
| rs554106378 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056360 | TCCCACCCCCAGGAA[C/T]AGTTAGAGGAGGAAA | 1840 |
| rs554110807 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075548 | AAGGCTCTGAGAAGT[A/C]CTGCGGCCTGGACCT | 1840 |
| rs554116206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069918 | TCCAGAAGGTCACAT[A/G]GCAATCCAGGGTTGG | 1840 |
| rs554240540 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113078288 | CACCTTTACATGTTC[C/G]CACACATCTATCTCC | 1840 |
| rs554366883 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113056865 | GGCGGGACCGCGGCT[C/G]CCTCCCACTCCGGGG | 1840 |
| rs554429665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069483 | GCCTGGCTTCCAGCA[A/G]ACCCTGGAGAACCTG | 1840 |
| rs554450796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113062791 | CCACAGGGGAGAAGC[C/T]AGGCTCTGGCCCCAC | 1840 |
| rs554561480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113088265 | CATCTCTGCTCCAGG[G/T]CAGTGACTTCCTGGA | 1840 |
| rs554584793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113076055 | GAGAGGGGAAAGTAC[A/G]TGGGGGGTGCACATT | 1840 |
| rs554586714 | in-del | -/GTT | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088863 | GTTGTTGTTGTTGTT[-/GTT]TAAGCTGGGTGTGGT | 1840 |
| rs554597286 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113061981 | AAAGTGCTGGGATTA[A/C]AAGCGTGAGCCACTG | 1840 |
| rs554621570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075627 | GGGGAGCACGCAGAG[C/T]TTTGGCAAACATGAA | 1840 |
| rs554623529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113082425 | ACCCTGGCTTCTTCC[A/G]CCTAAAGCTTTCCAT | 1840 |
| rs554634388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113068797 | AAGGGTGGACACTGG[C/G]ACATGGGGAGGAGGC | 1840 |
| rs554697354 | snp | A/G | | | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058189 | CCCTGAGGCAGTGGC[A/G]GCCATGTCACGGCCA | 1840 |
| rs554754977 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | DTX1 | GRCh38.p7 | 12:113088618 | TATAATTTTAAAAAA[A/T]GACTATAATGTCAGG | 1840 |
| rs554760447 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | DTX1 | GRCh38.p7 | 12:113075963 | ATTACATTCTAGCGA[C/G]GGGGGGACAGACAGA | 1840 |
| rs554839071 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113094607 | AAATAAATAAAATAA[C/T]GAAGAAGAAGAAAAG | 1840 |
| rs554844980 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096999 | GCAAATGCCTCCTTC[A/G]CCAGGTGTGTCCTGG | 1840 |
| rs554903414 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113070069 | GGCTCCAGCTGGACC[A/T]CTCACAGATGGCATC | 1840 |
| rs555032927 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DTX1 | GRCh38.p7 | 12:113072729 | TTTTTTTTGAGACAG[A/G]GTCTTGCTTTGTCGC | 1840 |
| rs555041777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113078616 | GCCAAGGCTGGGAAA[A/G]CTATGGTGCCTTCTC | 1840 |
| rs555161152 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057763 | GCTGGCTGAGAGCCG[A/C]AGGAGCAGCAGGCTG | 1840 |
| rs555173523 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069842 | AAGGTGTTGGGTGCC[A/G]CTGTTGTCCTTGTTG | 1840 |
| rs555250893 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057260 | GAGAGTCTCGGAAAA[A/C]CGCGCCCCCGGCCCC | 1840 |
| rs555350605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113071929 | CCAGTAAACAGGCAG[A/G]AAAATCGATACCTGG | 1840 |
| rs555359921 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113066522 | AACAGAGTGAGACTC[C/T]GTCTCAAAAAAAAAA | 1840 |
| rs555572608 | snp | C/G/T | 0.000271691 | 0.0116525 | intron-variant | DTX1 | GRCh38.p7 | 12:113093149 | GCTGCGGCCTCTTCT[C/G/T]TTCTCCCCGCAGGGT | 1840 |
| rs555587079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113067019 | CCAGGCTGCTACTGC[C/T]GCCTGCACAGACAGC | 1840 |
| rs555654096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113068108 | TGTGAACCAGAACAA[A/G]ACCATATCCGCCCAG | 1840 |
| rs555687416 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061677 | TGTGGGTACAAGAGA[A/G]ACAAGCAAAAGATCT | 1840 |
| rs555691035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113067173 | GCTGCAGCACAGCCA[C/T]CTCTTGTCCCGATGA | 1840 |
| rs555751338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113093453 | CCCTCCCACCCACCC[A/G]AGGGCCCCGGGATTC | 1840 |
| rs555782931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113073595 | CCTCGATTTCTCCAG[C/G]TATTGGGGCCTGTCC | 1840 |
| rs555803771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113087006 | GTGGCTGCCCCGGGC[C/T]GTGGGAACAGCCGGT | 1840 |
| rs555967552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113074967 | GCAGGGGAGAGCAGA[A/G]CTGAGTTCAAGGTGC | 1840 |
| rs556058766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113087499 | CCAGGACTGTGGGGG[A/G]AGGAGGGGGAGAAGG | 1840 |
| rs556204060 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113079802 | GACCTCTTGTGATCT[A/G]CCAGCCTTGGCCTCC | 1840 |
| rs556282937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113080619 | GGAATGGAATGGAAC[A/G]GAATGGAAAACAGAA | 1840 |
| rs556311041 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055734 | ACCCTGCCTAGTGTA[C/T]CCCCATCTGCCCCGG | 1840 |
| rs556326959 | in-del | -/A | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086262 | AACCCTGTATCAAGA[-/A]AAAAAAAAAAAAAGC | 1840 |
| rs556349459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113061217 | GGAAAAGGGAAAAAA[A/G]ACACTCATTCCTAAA | 1840 |
| rs556420306 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055168 | AGGTGACATTTAATC[A/T]GACCTTAAATAGCAT | 1840 |
| rs556436858 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113062179 | ATGTTCATTGAAGCT[A/G]AACTTGAACTTTGAG | 1840 |
| rs556484587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113081228 | CACACCTGTAATCCC[A/G]GCTACTGGGAGGATT | 1840 |
| rs556497776 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113058509 | TCACTACCTTGCAGC[C/G]TAGGATGCTGAAAAT | 1840 |
| rs556523306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113088118 | GCCCTGGCCCCTGAC[C/T]CGGAAACTCCAGGAC | 1840 |
| rs556633289 | snp | A/G | 1.90954e-05 | 0.00308988 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096931 | TCCGAGGCTGCAGCC[A/G]AGGCTTGAGGCCCAA | 1840 |
| rs556687784 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113090711 | ACAGCCCTCAGAGGG[G/T]TCTGGGATGGGAGTC | 1840 |
| rs556744731 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069439 | GCACTGCAGACCCCC[A/T]CTCCTCCCCTTGTCT | 1840 |
| rs556871270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075012 | CAGGGAAGGGTCATG[A/G]ACCTGGCTCCCAGGG | 1840 |
| rs556962351 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087527 | AGGCAGCTATGAGGC[A/G]GAGACAGCCCTGAAA | 1840 |
| rs557025752 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113064236 | TGTAGGGGCAGGGAG[C/T]GGCCCATCTCTGGTA | 1840 |
| rs557070352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113064962 | GAGGAACACTTACAG[A/G]TGGAGGAAACAGCAG | 1840 |
| rs557076654 | in-del | -/ACA | 0.00199481 | 0.0315187 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113054890 | TTGTGTAAAATGAGG[-/ACA]ACATTACCTTCCTTG | 1840 |
| rs557101219 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113079264 | CCAAGAGGAAGAGAG[G/T]GCACCCAAAACCAAC | 1840 |
| rs557104289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113058860 | CACAGGCAGTAAGTC[A/T]GTGTATTGTTGTATT | 1840 |
| rs557176914 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113064031 | GAGAACCCCTTCCCC[C/T]TTCCCCCTTCTCCCT | 1840 |
| rs557188451 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113065612 | AGTCTGACCTGGAGA[C/G]GAAGGAGGAGATGGA | 1840 |
| rs557234833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113071131 | CAGTTTCCCATGTTG[G/T]CCTTGGCCTGTCTCT | 1840 |
| rs557273652 | snp | A/C | 1.67393e-05 | 0.00289299 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077476 | GTCGTCGGCGCCGGG[A/C]AAGGGCATCGTGTGG | 1840 |
| rs557276283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113086049 | AAGGTGGGAGGATCA[C/T]TTGAGCCCAGGAATT | 1840 |
| rs557296246 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113091060 | GCTTGTAGGGCTGAG[C/T]GCATGCTCCTCTGGG | 1840 |
| rs557418904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113091228 | GTATGTGTGTGTCCC[C/T]GTGTGTGCACAAGTC | 1840 |
| rs557444025 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058139 | CTGCTGCCAGGCCCA[C/G]GAGGAGCTGGGCCTG | 1840 |
| rs557467742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113090778 | CACCAAGTGGGTGTG[C/T]GTGCGCTGCACCTGT | 1840 |
| rs557470121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113084827 | GACTCAGATTCAAAA[A/G]CCCAAGTTGACCAGC | 1840 |
| rs557677331 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113092204 | AAGAGGTGAAATTAC[G/T]CGGCCAGGATTGCAC | 1840 |
| rs557745547 | snp | A/C/T | 3.31286e-05 | 0.00406982 | missense | DTX1 | GRCh38.p7 | 12:113077561 | ACCATCCAGAACGCC[A/C/T]ACGAGAAGCAGCACC | 1840 |
| rs557833624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113084167 | TGTAACAGACAGGGC[A/G]GGGAGCCAGCTGGCA | 1840 |
| rs557901482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113064081 | TGTTGTCAGGGTCTA[A/G]CCCAAGGCAGGGACA | 1840 |
| rs557939054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113066453 | GAATCACTTGAACCC[A/G]GGAGGTGGAGGTAGC | 1840 |
| rs557974054 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061889 | TTTTGTATTTTTAGT[A/G]GAGATGGGGTTTTAC | 1840 |
| rs557986499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113059480 | TGTGATGGCTGATGA[C/T]GGAGATAAAATCGAT | 1840 |
| rs557995227 | in-del | -/G | 0.0138799 | 0.0821421 | intron-variant | DTX1 | GRCh38.p7 | 12:113088845 | CTCAAAAGTTTTGTT[-/G]TTGTTGTTGTTGTTG | 1840 |
| rs558025298 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113065704 | GGGCTGTGGAGGGGA[A/T]GGTGAAGAAGGTGGT | 1840 |
| rs558062079 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | DTX1 | GRCh38.p7 | 12:113071818 | CTGCGGGGTGCAGGG[C/G]CCAGCGGGGAGGACA | 1840 |
| rs558077541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113079872 | CCCCCTTCTTGACCA[C/T]TTCTGAGCTGGGAGA | 1840 |
| rs558158367 | snp | A/C/G | 8.34796e-05 | 0.00646019 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096849 | TGGATCCAACCTCAC[A/C/G]GGCCACGGCTACCCG | 1840 |
| rs558219785 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075783 | AAATGAAGGAATGGA[C/T]GAATGCAGGGATGAG | 1840 |
| rs558222065 | snp | A/C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RASAL1, DTX1 | GRCh38.p7 | 12:113098527 | CCTGCTGGCCACCCT[A/C/T]GGGATAGCGCCGTGT | 1840 |
| rs558238664 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113085635 | ACCCTTTGTCTCCCA[C/T]CTTTTCTGTAGTTTG | 1840 |
| rs558257388 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057121 | GGGGCCCTGGGCCGC[G/T]CCTGCAGCGCCGCGC | 1840 |
| rs558304563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113080480 | TGCAGTAAGAATTTG[A/G]GAACCTTCTCTCTGG | 1840 |
| rs558478952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113064155 | CAGGACCCTTTGGGA[C/T]CCTCTCTCCAGCCTC | 1840 |
| rs558488446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113086919 | CAAACACTCCCCCCA[C/T]CCTGCCCCCCACCTG | 1840 |
| rs558550845 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113056807 | TCCACGCGCGGAAAG[C/G]TCGGCGCGGCGGCCG | 1840 |
| rs558566508 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113070373 | AGGATGTCCCATGAC[C/T]GCCTCCCACGTGCCC | 1840 |
| rs558633188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113062670 | TGCGTGTGCGTACAC[A/G]CACACAGCACCAGTC | 1840 |
| rs558718426 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113082495 | AAAGGGATGGAGGTG[C/G]GGGGTCTTTGAGGAG | 1840 |
| rs558740041 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097124 | TGTCAGGCTGGCCCC[A/G]AATCATAGCTCCCTG | 1840 |
| rs558749234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113084546 | ATGCACCACCATGCC[C/T]GGCCAATTTTTTATT | 1840 |
| rs558758054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113076837 | TCATTGAATGAGTGA[A/G]CAAACTATAATGAAG | 1840 |
| rs558918221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113088708 | AAAATAAAGTGGTTG[C/T]GGCCAGGCACAGTGG | 1840 |
| rs558948842 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060833 | GGGTAGGTGTCACTC[C/T]TTGCTAGGAGGTCTG | 1840 |
| rs558958229 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113071265 | GCCGCCCCCACACCC[A/G]GTCTCAGGGGCCCAG | 1840 |
| rs559179527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113070086 | TCACAGATGGCATCC[A/G]GTGTGCTCCTAACTG | 1840 |
| rs559201170 | snp | A/C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056206 | GCAGGAGATTCAGAT[A/C/T]GGGGTTGGTGTCTGG | 1840 |
| rs559406529 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057457 | CTGGCAGGTCGCGAG[C/T]ACGAGTGGGGTGGGG | 1840 |
| rs559409610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113082088 | CACATGCCGCTCCCC[C/G]ACAGCCGACATCATT | 1840 |
| rs559448257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113088895 | TGGTGTGTGCCAGTA[A/G]TCCCAGCTACTCAAG | 1840 |
| rs559450283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113081470 | AACAAGACAAACAAG[A/G]CCTGTGTCCTCCCGG | 1840 |
| rs559534199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113088445 | GAAGAGGCGGCGTGG[A/G]CCAGATCATACAGGG | 1840 |
| rs559576219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113083351 | TTTTTTTTTTGAGAC[C/T]GTCTTGCTCTGTTAC | 1840 |
| rs559597573 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113069650 | ACAGGCTGCAGCTCG[A/C]ATCCCAGCCCAGCCG | 1840 |
| rs559616648 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113090878 | TGTCAGGAGGTGTGG[C/G]TCAGAGCATGTGCGC | 1840 |
| rs559630999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075879 | TCAACAAATATCGCT[C/T]GAGCACCTGCTGTGT | 1840 |
| rs559634597 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113086402 | GAGGCTCAGGGCAAT[C/T]GGTGGGAAAGAAGTA | 1840 |
| rs559701594 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DTX1 | GRCh38.p7 | 12:113092792 | ATAATGCTACATCTA[A/G]CAAGCTTTGAGAGAT | 1840 |
| rs559716416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113089912 | ACACTCAGCAAGAGC[A/G]GGGTTACCCACTGGG | 1840 |
| rs559801933 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113064742 | TACATAAATGAGATA[C/T]GTAGATAAAAGCTTG | 1840 |
| rs559928604 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113086573 | TGCTGAGCATAGACC[A/G]CAGTGGGGCTGAAGC | 1840 |
| rs559937152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113087620 | AAAGCACTGTTCAAC[C/T]TCCTTCTCCCCATAA | 1840 |
| rs559974138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113087156 | CAGCCCCCATACCTC[C/T]AGATAAATCTGAGCC | 1840 |
| rs559991232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113063072 | GCTTGCTCGCTTCGC[A/G]GTACTGAGCCAAGTG | 1840 |
| rs560108740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113080060 | AGGAGGGTTGGCATG[A/G]AGGGCGGGGAAGCTG | 1840 |
| rs560118595 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | DTX1 | GRCh38.p7 | 12:113076535 | TTGGGAGGCCAAGGC[A/G]GTTGGATTGCTTGAG | 1840 |
| rs560126984 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113072191 | CAAGTAGGTTGCCCG[C/T]CTCGCTTGCAGATGT | 1840 |
| rs560605495 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056080 | CCTGCCCTTCTCTTC[C/T]TCCAGGATCTCACCT | 1840 |
| rs560636306 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055362 | GAAGAATCTGCTGAC[A/T]GCCAGAGCCCTTCTT | 1840 |
| rs560646966 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113090513 | TTTCACAGGACTCTA[G/T]CCCCATTACAGGTGG | 1840 |
| rs560667795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113080868 | TAGTCCCAGTTACTC[A/G]GAAGGCTGAGGCAAG | 1840 |
| rs560749938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113062320 | TAACTATTCAACTCT[A/G]TCGGAGCAGAAAAGC | 1840 |
| rs560752269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113081364 | AGAGATTTGAAAGCT[A/G]CTGTTCTAGAGGAGG | 1840 |
| rs560754333 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113074685 | ATGGGAAATGGATTA[C/G]AGAGGCCAGTCATGA | 1840 |
| rs560783845 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056525 | TTCAAGCCGGTGACT[C/T]CTAAACATCCCACTC | 1840 |
| rs560841605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113080922 | CAAGGCTGCAGTGAC[C/T]TGTGATCACACCACT | 1840 |
| rs560869801 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113072850 | CTGGGATTACAGGCA[C/T]GTACCACCACGCCTG | 1840 |
| rs560884556 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113068535 | AGATGGAACAGCATA[C/T]GCAAATACAGAGGCA | 1840 |
| rs561030029 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113065229 | TCAGGCACTTCCTAC[A/C]GTCTGTCTGGGTTCC | 1840 |
| rs561094859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113088588 | CGTTGTGCACATGTA[C/T]CCTAGAACTTAAAGT | 1840 |
| rs561206612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113095258 | ACCCCTCCAACTCCT[C/T]CAGATGCTTCTCCAC | 1840 |
| rs561217837 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056544 | AACATCCCACTCCCT[C/G]CCTCACGCTCTGCTT | 1840 |
| rs561246496 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086070 | CCCAGGAATTTGAGA[A/C]CAGCCTGGACAACAT | 1840 |
| rs561410202 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113069123 | TGGCACATAGTAGGC[A/C]CTCTGGGAGTGTTTA | 1840 |
| rs561539099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113065232 | GGCACTTCCTACAGT[C/G]TGTCTGGGTTCCCTT | 1840 |
| rs561581365 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113056905 | GAGGCGGCGGTGCTG[C/G]AGCGCGAGCCGGAGC | 1840 |
| rs561624651 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113071302 | CAGTCCTCCAGCTGA[A/C]ACTGACCAAAGCCCC | 1840 |
| rs561699625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113065953 | TGCTCCCAGGCCTCC[A/G]CCCGCCACCTCTGTC | 1840 |
| rs561713319 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069268 | ACTTCCTGCTTTGCT[A/G]GGGATCTGAATCCCC | 1840 |
| rs561750669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113091764 | TGACCTGAACAGGCA[C/T]GGCCAGAGCCAAGGG | 1840 |
| rs561782632 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113098036 | TCCTCCTCGCCTGGT[C/G]TTTTCCTGCCAAGAG | 1840 |
| rs561791531 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097720 | CAAATCGCTCCCAAT[G/T]TTGAGAGCCAAAGGC | 1840 |
| rs561900661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113073090 | CCGAGCTCAGGATTT[A/G]GCACACAGGGGAAGT | 1840 |
| rs562154805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113078970 | TTTAACCAGAGCAGC[C/T]CTTTTTGGAAACACT | 1840 |
| rs562170987 | snp | C/G | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056020 | CACCCACCATTTATT[C/G]AGCACCAGTTGTTTG | 1840 |
| rs562222662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113066784 | CCTCAAGGTGCTTCT[A/G]TTCTGGGGGTGAGGG | 1840 |
| rs562240554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113092621 | TGCTTTTGAAAACCT[A/G]GACTTATCATTGTTA | 1840 |
| rs562317572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113067429 | GTCTCTAATTTGCCA[A/G]GTGATCTTGCCCAAG | 1840 |
| rs562386205 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113059067 | ATTGGGGATGGGGGG[C/T]GTTGGTGGTGTTGAT | 1840 |
| rs562401652 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | DTX1 | GRCh38.p7 | 12:113073933 | AGAATGCATGCAGAT[G/T]AATACATCATGTCAC | 1840 |
| rs562492844 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RASAL1, DTX1 | GRCh38.p7 | 12:113098498 | TCTGGTGGATGCTGC[A/G]GCTTCGGGCAACCCC | 1840 |
| rs562542119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113066547 | AAAAAAAAAAGAATC[A/G]TAGTGGGTGGGGAGA | 1840 |
| rs562555340 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113086507 | AAGGGAACCAGCAGG[C/G]CTGTGTGTTGGGAGA | 1840 |
| rs562575351 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069485 | CTGGCTTCCAGCAGA[A/C]CCTGGAGAACCTGGG | 1840 |
| rs562869340 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DTX1 | GRCh38.p7 | 12:113079492 | CTGACTTCCTGGGTT[C/T]GAATCCCCTCTTGGC | 1840 |
| rs562872277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113074047 | ACCAGCCTGGCCAAC[A/G]TGGTGAAATCCCGTC | 1840 |
| rs562961401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113073248 | CAACCCCTCATTTTG[C/T]AGGTGGGGAAACTGA | 1840 |
| rs562985999 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079021 | GCATGATTTTATTAA[C/G]GATGGGCACCCAGCT | 1840 |
| rs563018473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113060804 | GTAGAGGGCAGGGCT[A/G]TGAGAGCAGAAGTGG | 1840 |
| rs563140939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113061474 | AAGAGCCTCAACCGG[A/C]AGGGAGCAGACCTGA | 1840 |
| rs563180952 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057605 | GCCACCCAGGCCTTC[C/T]AGGACACCGTGGAGA | 1840 |
| rs563278251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113076342 | TGCATGCCTGTAGTC[C/T]CAGCTACTCAGGAGG | 1840 |
| rs563289166 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057912 | GAGGGGGCCAAGGAC[C/T]TTAGAGCTGTTTCCT | 1840 |
| rs563368834 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062436 | TTCACGGGTCATGAA[A/G]TATTCTTTTTTTTCC | 1840 |
| rs563375597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113064363 | GGCTAACTCCAGAAG[C/G]CTGTTTTGAAACTAA | 1840 |
| rs563398881 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DTX1 | GRCh38.p7 | 12:113082164 | CCAGACATTGGCCTG[A/G]AAAACAGAAGATGTG | 1840 |
| rs563502822 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113072031 | GAGCTGGCCAACGCT[G/T]ATGTTGAGAATCCTC | 1840 |
| rs563547565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113091003 | GAATCGTGTGTCCGC[A/G]TGTGGACGGCAGGCC | 1840 |
| rs563573806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113063632 | ATGCCATACCCGAGG[C/T]TGCAAGCCTGGCCTT | 1840 |
| rs563638558 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113083411 | GCTCACTGCAACCTC[C/T]ACCTCCCAGGTTCAA | 1840 |
| rs563650130 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060072 | ACATTGCTAGGTACC[C/T]ACAGAGTGCTTACCA | 1840 |
| rs563714140 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113083387 | CTGGAGTGCAGTGGT[A/G]CAATCTTGGCTCACT | 1840 |
| rs563733565 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097234 | CCTGTTGAACTCATG[C/T]ACGCACACCCACGTG | 1840 |
| rs563753133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113090418 | GGCCCCCCCGCAGGG[C/T]GCCCGACAAGAAAAT | 1840 |
| rs563809804 | in-del | -/AAAA | | | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096440 | GCAAGACTCTGCCTC[-/AAAA]AAAAAAAAAAAAAAA | 1840 |
| rs563997895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113085195 | TCTGGGACTACAGGC[A/G]CACGCCACCAACCCG | 1840 |
| rs564023683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113077106 | GGTGGCTCTCCCGCC[C/T]CTACGCCCAATCTAC | 1840 |
| rs564043641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113071214 | CACCCTGTCTCTGCC[C/T]CAGGCATGAAGCAGT | 1840 |
| rs564062927 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113083147 | CTTAGAAGGACATCA[C/G]TCCTATTGGATTAGG | 1840 |
| rs564186916 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087912 | TTTCGGGATCCTGGA[C/T]CCCTCTAGGGGACAG | 1840 |
| rs564304710 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113091861 | CCCCCAAGGCCTTCA[-/G]GCTGACCCCTGGATT | 1840 |
| rs564309685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113066669 | TGTGTGATTGTGGTC[A/G]CTATTCATTCATTCA | 1840 |
| rs564357837 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113065133 | TAGCAGCCAGGCCCC[C/G]GGGGACTCACAGCCA | 1840 |
| rs564389711 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057928 | TTAGAGCTGTTTCCT[C/G]CGGCATAAGAGAGAC | 1840 |
| rs564531374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113091548 | GAGTATGATAAGTCT[A/G]TGTGGTCTTCTCCAT | 1840 |
| rs564595390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113059755 | GGCTGGTAGGATGCT[C/T]GCTTTCCCTCTAGAG | 1840 |
| rs564616295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113091040 | CAGGCTGCAGCGCGC[C/T]GGGGGCTTGTAGGGC | 1840 |
| rs564663503 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113078777 | ATGGTGGCTCGAGCA[A/T]GCATCAGCTGCTTGT | 1840 |
| rs564704857 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069588 | GGAAACAGAACACTG[A/C]GGGATTATTGATCAT | 1840 |
| rs564713273 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113079045 | CCCAGCTTGTATCAA[-/G]TTTGCAAATTCTTGG | 1840 |
| rs564714553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113073005 | AGCCACTGCACCTGG[C/T]TCGACCCGAGAGACT | 1840 |
| rs564747356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069253 | GTCCCCTCCCCCTCC[A/G]CTTCCTGCTTTGCTA | 1840 |
| rs564800293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113079313 | GCATGGCCGGGGGAA[C/T]TGATAATGATGGTCC | 1840 |
| rs564845946 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056517 | GACAAAGATTCAAGC[C/T]GGTGACTCCTAAACA | 1840 |
| rs564919199 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113088380 | TGCTAGGAGGACAGT[A/T]GTGGTATGCACTCAT | 1840 |
| rs564935992 | snp | C/G | 0.000420492 | 0.0144938 | intron-variant | DTX1 | GRCh38.p7 | 12:113094144 | GGCCCTGGCATGGAG[C/G]GGGCAGGAACCCTCA | 1840 |
| rs565022680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113093825 | ATTGCCTGATCTCAG[C/T]TCCCCTTGCCCTGGC | 1840 |
| rs565089654 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057380 | TCAGCCGAATGCTCT[A/C]CTGGGAAGGGGGGAG | 1840 |
| rs565192109 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062241 | ATGCAGGAGCTGGCT[A/G]ATTTTTTTCTAATAG | 1840 |
| rs565199085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113089856 | GCTGAGATCTAAATC[C/T]TTCCCTTCCTGGAGT | 1840 |
| rs565220510 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113081379 | ACTGTTCTAGAGGAG[G/T]CTGAAAATTACTCAG | 1840 |
| rs565323743 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113056973 | TGCTTAGGGACCCCA[C/T]CCCCGGCTCCCGCTG | 1840 |
| rs565327585 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113081198 | AAATACAAAAATTAG[C/T]TGAGCATGGTGGTAC | 1840 |
| rs565504786 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113064845 | ATGCACGGTGCCTTC[A/G]GCCATGGGATGTGCA | 1840 |
| rs565510471 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057040 | GAAGCGGGGCTGTTA[C/T]CCCCAGGGCGGGAGG | 1840 |
| rs565520764 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086131 | AAATTAGCTGGGTGC[A/G]GTGGTGCGTGCCTGT | 1840 |
| rs565551539 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056672 | ATCTGTCTCCTCCCC[C/T]TCCTCCTCCTCCGCC | 1840 |
| rs565560747 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DTX1 | GRCh38.p7 | 12:113075214 | CCCAGAGATGCTGAG[C/T]TGCCTACGCACAGTC | 1840 |
| rs565753827 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113082346 | AAAATCCCTCTGGCT[C/G]TCAAGACCCGTGGAG | 1840 |
| rs565790978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113089514 | GCTGGCTCCCCTTCC[A/G]GGAGGCCCGCAGGCA | 1840 |
| rs565826209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113081160 | CCAGCATGGCCAACA[C/T]GGTGAAACCCCATCT | 1840 |
| rs565870215 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069325 | CCAGAAAGCCCCCCA[A/T]ACAGCCCATGGCGTA | 1840 |
| rs565910048 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087147 | TGACCCCCGCAGCCC[C/T]CATACCTCTAGATAA | 1840 |
| rs565967238 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060324 | GTGCTGGAGGACCTA[C/T]ACTGAAGGTCCTGGT | 1840 |
| rs565985741 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083537 | TGGCATGTTGGTCAG[G/T]CTGGTCTCGAACTCC | 1840 |
| rs566085858 | snp | G/T | 0.000988028 | 0.0222045 | intron-variant | DTX1 | GRCh38.p7 | 12:113095320 | TGTACTGTCCCTCTC[G/T]GCAGGGCCCTGAGCA | 1840 |
| rs566113002 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113085867 | GTAGAAAGTAGTAAC[C/T]GCTACAGAGGAAAAA | 1840 |
| rs566145520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113070261 | ATTATGACTTCTGGG[C/T]TGGTGAAGGATTCAG | 1840 |
| rs566196145 | snp | A/G | 0.000412642 | 0.0143579 | intron-variant, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096688 | CTGTGACCTCCTCCC[A/G]GCCCCACTGTGTCCC | 1840 |
| rs566236776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113091235 | TGTGTCCCCGTGTGT[A/G]CACAAGTCTCTGTAT | 1840 |
| rs566352985 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069989 | CCTCAGTTTCCTCCC[A/C]CAGAACATGGGCTCA | 1840 |
| rs566608303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113072495 | ATGTGGGTAACATAT[A/G]TAATATCAGCCATTG | 1840 |
| rs566715447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113079621 | CAACTTCTGCCTCCA[A/G]GGTTCAAGTGATTCT | 1840 |
| rs566761434 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055025 | CCAAGATGAATATGA[C/T]GGCTATCTCACTCTA | 1840 |
| rs566800415 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113065441 | CAACGACCCGCCCGC[C/G]CCTTCCGGGCTGGGG | 1840 |
| rs566812835 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113074091 | CAAAAAAAATCAGCT[A/G]GGTGACACATACCTG | 1840 |
| rs566830836 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055597 | CATTGACCCAATCTG[A/G]AAAAGCCCATCCAAC | 1840 |
| rs566856856 | snp | C/T | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113054891 | TGTGTAAAATGAGGA[C/T]AACATTACCTTCCTT | 1840 |
| rs566900800 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069232 | TGGAGGACTGTCCAG[C/T]CCTCTGTCCCCTCCC | 1840 |
| rs566937495 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113079749 | GTGTTAGTGGAGATG[A/G]GATTTCACCATGTTT | 1840 |
| rs566970752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113067767 | CCATTTGAGGTGGCT[C/G]ATGCCTGGAATCCCA | 1840 |
| rs567007635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113066966 | GGCCAAGCGCCTCTC[C/T]CTCTCTGGGCTCCTT | 1840 |
| rs567022847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113093899 | CCTGACCTCTGACCC[C/T]GGCCAACCCTTGCCA | 1840 |
| rs567052634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113087923 | TGGACCCCTCTAGGG[G/T]ACAGAGAGAGGTGGC | 1840 |
| rs567125603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113087429 | GCTTGCAGCGATGTC[C/T]TTCAAGTCTCTGCAG | 1840 |
| rs567196791 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113093440 | CCCAAGAGCGCAACC[C/G]TCCCACCCACCCGAG | 1840 |
| rs567216274 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113074104 | CTGGGTGACACATAC[C/G]TGTAATGCCAGCTAC | 1840 |
| rs567248698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113073557 | AACCCCGCCCCTTTC[A/G]TATCAATAGCCATAG | 1840 |
| rs567253014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113080132 | CCTGGTCATTCCTCT[C/T]GGAGGAGAGGGTCAT | 1840 |
| rs567289141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113086041 | GGGAGGCTAAGGTGG[A/G]AGGATCACTTGAGCC | 1840 |
| rs567435996 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113067109 | ACCCTGAGATGCAGA[A/C]CAAAGGACGAGGCAA | 1840 |
| rs567441347 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113068608 | GTGTGGTTAGAGTGT[A/G]AGGCTGTGCAGACAG | 1840 |
| rs567454860 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113067869 | AAACCCCATCTCCAC[C/G]AAATAAAAACAAAAA | 1840 |
| rs567628299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113093948 | CTTGCCAGCCTGACC[C/T]CTGCCCTCTGACCCC | 1840 |
| rs567704006 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056158 | GGTGGGTGCTTTGGG[C/G]GAAGTGGGCTCAGGG | 1840 |
| rs567740366 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055668 | TCCCTCCAGCTGGCC[A/G]GAGAGCCAGAGCTGG | 1840 |
| rs567816410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113088527 | GATGAGTTAATGGGC[A/G]CAGCACACCAGCATG | 1840 |
| rs567871855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113081679 | GCATGAACAACTTCA[A/G]GGGGGCTCGAAGGGC | 1840 |
| rs568072698 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057937 | TTTCCTCCGGCATAA[C/G]AGAGACACTTGCTTT | 1840 |
| rs568136345 | in-del | -/C | 0.0174175 | 0.0916809 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056120 | GTCCCCTCCCCTGGT[-/C]CCCACCCCTCTCACC | 1840 |
| rs568139241 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057761 | GGGCTGGCTGAGAGC[C/G]GCAGGAGCAGCAGGC | 1840 |
| rs568144981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113064519 | TCAGAGTCTAGTGAA[C/G]GTGAAGGCAAATGCA | 1840 |
| rs568195887 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | DTX1 | GRCh38.p7 | 12:113083336 | ATAATTTACCAATAC[-/T]TTTTTTTTTGAGACC | 1840 |
| rs568266097 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113054849 | GCTACTTAGCCTTTC[G/T]GAGCTTCAGGAGGTT | 1840 |
| rs568277860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113084634 | AAGTGATCCTCTCGC[C/T]TTGGCCTCCCAAAGC | 1840 |
| rs568279806 | snp | C/T | 1.93287e-05 | 0.00310869 | intron-variant | DTX1 | GRCh38.p7 | 12:113077399 | CGCCCGCTGTGCTGA[C/T]GCCTCCTCCCCATTT | 1840 |
| rs568290573 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076376 | AGGCAGGAGAATCGC[G/T]TGAACCTGGAGGCGG | 1840 |
| rs568304226 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113090648 | GACTTCCATCACACC[A/G]GCGCCTCCTCAAGGG | 1840 |
| rs568353243 | snp | A/G | 6.70893e-05 | 0.00579139 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096792 | CACCACGGGCGAGTC[A/G]GACACCGTGGTGTGG | 1840 |
| rs568393183 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113059283 | GATAGTTGTGTTGGT[A/G]GTGGTGCTGGAAGTG | 1840 |
| rs568455064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113071776 | GCCGGAGAGGCGGAC[A/G]GATGGGCAGGCGGGC | 1840 |
| rs568573948 | snp | A/G | 0.0130372 | 0.0796784 | intron-variant | DTX1 | GRCh38.p7 | 12:113078124 | AGACGGGGCCCAGGG[A/G]GAGGGGGCCTCTGCG | 1840 |
| rs568611818 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097070 | CCGCAGCCATTCAGG[A/G]GACCTGCCTGGTGGC | 1840 |
| rs568743850 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097970 | ATGCCAGCGATTGCT[C/G]TTTTCAAAACCTACC | 1840 |
| rs568909291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113090737 | GAGTCCTGGCCACGT[A/G]ATACTATCCTGTATA | 1840 |
| rs569048026 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113079105 | ACCCAGTGAGCTGCT[G/T]TTGGGTGCCTACCCT | 1840 |
| rs569105858 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113084797 | TAAGACATTTGCACA[A/G]GGTAACACAATTAGG | 1840 |
| rs569126104 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096026 | GCCTGGACAACATGG[C/T]GAAACCCCGTCTCTA | 1840 |
| rs569162939 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113059439 | GGTTGTAATGATGGT[G/T]ATGTTGATGGTTGCG | 1840 |
| rs569264775 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113098151 | GCCTCGGGCTGGAAG[C/G]GGTGGGGGCGGTGAA | 1840 |
| rs569276928 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113056801 | AGTCTGTCCACGCGC[C/G/T]GAAAGCTCGGCGCGG | 1840 |
| rs569278337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113066941 | AGTTGTGTCCTTGCT[C/T]GGCCACCCTGGCCAA | 1840 |
| rs569336753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113086857 | CCCCGCTAGCCACTG[A/G]TGTGCAGTGACTGTC | 1840 |
| rs569364920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113066421 | TAATCCCAGCTACTC[A/G]GGAGGCCAAGGCAGG | 1840 |
| rs569393999 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055482 | GGACCCTAGGCTAAA[A/G]TCCCAGAACTCAGTG | 1840 |
| rs569402617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113072278 | AGTAGTCTTTGTCCT[C/T]CCAAAAGTGATCTAC | 1840 |
| rs569459920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113093387 | CGTGGCCCGCAGAAA[G/T]GCCCTTCAGGGGCCT | 1840 |
| rs569501583 | in-del | -/AAATA | 0.00597247 | 0.0543191 | intron-variant | DTX1 | GRCh38.p7 | 12:113076609 | TGTCTCTAAATAAAT[-/AAATA]AAATAAAATAACATA | 1840 |
| rs569515024 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113054907 | AACATTACCTTCCTT[A/G]TGGGGCAGTTATGAA | 1840 |
| rs569539384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113071495 | GACGCAGACCCTGTG[A/G]CCAGCACAGCAGGGT | 1840 |
| rs569544687 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DTX1 | GRCh38.p7 | 12:113093046 | TGCAGTTGGCAGAGA[A/G]GTACAAAGAGGCCAG | 1840 |
| rs569556489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069795 | TGTGTGTGAGCCCCT[A/G]GCACAGTTGCTGGCA | 1840 |
| rs569593744 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113071559 | TGGGCCACCAGCCTG[A/T]GGCCCAGCCTCTTTC | 1840 |
| rs569594267 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057080 | TCCAGCTCCTGGCTT[C/T]GCCCCCTCCGCGACG | 1840 |
| rs569726413 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113069390 | GGTGGTAGCCTCTCC[A/G]AGTGCCACGCAGCCC | 1840 |
| rs569794374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075225 | TGAGTTGCCTACGCA[C/T]AGTCACAGAGCTGGA | 1840 |
| rs569852401 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096243 | GCGCAGTGGTGCACA[C/T]CTGTAATCCCTGCAC | 1840 |
| rs569927302 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084837 | CAAAAACCCAAGTTG[A/C]CCAGCATATTGGGGA | 1840 |
| rs569941599 | snp | A/G | 1.6476e-05 | 0.00287014 | missense | DTX1 | GRCh38.p7 | 12:113095349 | CACCCCAACCCCGGG[A/G]AGAAGTTCACCGCAA | 1840 |
| rs570001705 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113082774 | CTAATTTTTTAAAAT[G/T]TTTTGTAGGGACAGG | 1840 |
| rs570012035 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056231 | GTCTGGGCATCGCTC[C/T]AAGCTTTTGTGATCC | 1840 |
| rs570040990 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113077180 | TGAACCTTTAGCCCC[C/G]GCCCCCCTCACCCTG | 1840 |
| rs570088880 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113089977 | ACTGGCTATACTGAT[G/T]GATAGAGGCTGCTTG | 1840 |
| rs570119134 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057954 | GAGACACTTGCTTTC[C/T]AGGGCAGCACCCTTT | 1840 |
| rs570170815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113082477 | AGTGCAGCCTATGAG[A/G]GGAAAGGGATGGAGG | 1840 |
| rs570324430 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057703 | AGGCGAGAAGCCCCA[A/C]TGAAGCCGGGCGCAG | 1840 |
| rs570392928 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057925 | ACTTTAGAGCTGTTT[C/T]CTCCGGCATAAGAGA | 1840 |
| rs570436051 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057145 | GCCGCGCATCCCCGT[A/G]CTTCCCGGCGCACCC | 1840 |
| rs570501898 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084215 | CTGCGGGGGTGGGGA[A/C]GATCCGCCCTGTCCC | 1840 |
| rs570530942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113070862 | AGAGTTCACCTCTCC[C/G]GGCCTCAGTTTCCTC | 1840 |
| rs570556845 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113063269 | GCCACTGGCAGTCGG[C/G]GAAAGGTTTGAGAAT | 1840 |
| rs570645674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113090461 | ACTCTCATCCCTGCG[A/C]CAAATGATGAGCTTT | 1840 |
| rs570681172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113059195 | TGGAGGGATGGATGA[C/T]GGTGACGTGGCAGTG | 1840 |
| rs570691978 | snp | C/T | 3.34001e-05 | 0.00408643 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096810 | CACCGTGGTGTGGAA[C/T]GAGATCCACCACAAG | 1840 |
| rs570848843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113078215 | ACAATAATAATAATG[A/G]CGATAAGTAATATCC | 1840 |
| rs570902796 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113083487 | CCTGCCACCATGACC[A/G]GCTATTTTTTGTATT | 1840 |
| rs570933211 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113074192 | CGAGATCACGCCACT[G/T]CACTCCAGGCTGGGT | 1840 |
| rs570964304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113058604 | GCAGTCTAACCTTGT[C/T]CAGTTTAAGACTTGG | 1840 |
| rs571320683 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113062521 | AGATGGTGGGTGGAT[G/T]TGGCCTGTGTGCTGC | 1840 |
| rs571378266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113088119 | CCCTGGCCCCTGACT[C/T]GGAAACTCCAGGACC | 1840 |
| rs571416552 | snp | C/G | 7.0599e-05 | 0.00594092 | intron-variant | DTX1 | GRCh38.p7 | 12:113093989 | CTGAGCCAAGCCTTC[C/G]GGGACAGACTCTGGG | 1840 |
| rs571427331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113061771 | CAGTGGTGTGATGTC[A/G]GCTCACTGCAGCCTC | 1840 |
| rs571629764 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056588 | CCCTTGGGGTCTCGG[A/G]AGGGCCTGGCCGAGG | 1840 |
| rs571655373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113089469 | CCTGTGCCAGCCTGG[A/G]CCCCCAAGAAGGCAG | 1840 |
| rs571771248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075959 | GGCTATTACATTCTA[A/G]CGAGGGGGGGACAGA | 1840 |
| rs571835588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113067337 | CTCTGTTCTAGGGGG[C/T]GAAGGTTCACTTGTT | 1840 |
| rs571872276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075434 | TTAAGGGACTTTCCC[A/G]CAGTTGAGGGGAAGT | 1840 |
| rs572036445 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113068082 | TCACTATTTTTTAAA[G/T]GTAAATAGCATGTGA | 1840 |
| rs572125875 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113085206 | AGGCGCACGCCACCA[A/G]CCCGGCTAATTTTTT | 1840 |
| rs572163301 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113081836 | GGTTCTGGAGACCAC[C/T]GGGGGATAGAGGCTC | 1840 |
| rs572184722 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059545 | TGGAGATTTGTCATC[A/G]TTGGGGAGATCTCCC | 1840 |
| rs572338465 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113095006 | AGTGGGGTTTGGGGG[G/T]GTGCTGGGAACTCAC | 1840 |
| rs572340936 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055861 | CCCCAATCTAAACAC[A/C]CCCAGGCCCCAGGTG | 1840 |
| rs572418095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069091 | GTTGACTTACACGAA[A/G]CATTTAGAACAGCGC | 1840 |
| rs572459206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075081 | CAGAGTAGACACGGT[A/G]TTTATCTCAATTGAT | 1840 |
| rs572572635 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113084833 | GATTCAAAAACCCAA[G/T]TTGACCAGCATATTG | 1840 |
| rs572589702 | snp | A/C/T | 3.33975e-05 | 0.0040863 | intron-variant | DTX1 | GRCh38.p7 | 12:113095244 | CCCCCAGCCCCCACA[A/C/T]CCCTCCAACTCCTCC | 1840 |
| rs572640791 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057222 | GGAAGGCTCCGGGAG[A/C]CAAGGAGGGCGCCCC | 1840 |
| rs572676367 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069490 | TTCCAGCAGACCCTG[C/G]AGAACCTGGGCCAGC | 1840 |
| rs572678517 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113056873 | CGCGGCTCCCTCCCA[C/T]TCCGGGGGGAGCCCA | 1840 |
| rs572734827 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113071256 | GTGGCTGTGGCCGCC[C/T]CCACACCCGGTCTCA | 1840 |
| rs572766583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113062816 | CCCCACAGGGGCTGC[A/G]GTTTGTTCAGCCGTG | 1840 |
| rs572780412 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113078491 | TTATTCTGCCAAACA[C/G]TTCTACCATGTGCAT | 1840 |
| rs572790774 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061532 | CCAGGTCTCAGTTTC[C/T]ACATCCGTGAAATGG | 1840 |
| rs572808804 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | DTX1 | GRCh38.p7 | 12:113081949 | CTTGGTGCTGCCATC[A/G]GTGGGGAGCTATAGA | 1840 |
| rs572947627 | in-del | -/TTTC | 0.0325976 | 0.123435 | intron-variant | DTX1 | GRCh38.p7 | 12:113072706 | TTTTCTTTTTTTTTT[-/TTTC]TTTTTTTTTTTTTTT | 1840 |
| rs572948421 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097687 | GTTCTCCCATCCTCC[C/T]TACCCCATCCTCTCC | 1840 |
| rs573131056 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066671 | TGTGATTGTGGTCAC[C/T]ATTCATTCATTCATC | 1840 |
| rs573135167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113093093 | GCCAGAGACAGAAGG[A/C]AAGCCAGGTCCCCTG | 1840 |
| rs573383099 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113070890 | CTCATCTGTAAAATG[G/T]AAATAGTCCTGGTCC | 1840 |
| rs573422692 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113089267 | GTTCAGAGGGTAGAT[A/G]GGGGCCAGATCAGGA | 1840 |
| rs573427201 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059570 | TCTCCCTGAGTCATT[A/G]CCCGGTGGTATCTGT | 1840 |
| rs573446877 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113064754 | ATATGTAGATAAAAG[C/G]TTGGAGGATACTACT | 1840 |
| rs573499799 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113079323 | GGGAATTGATAATGA[G/T]GGTCCGAGATCACCA | 1840 |
| rs573594992 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DTX1 | GRCh38.p7 | 12:113072779 | TGTGATCTCAGCTCA[C/T]TGCAACCTCTGCCTC | 1840 |
| rs573623397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113086924 | ACTCCCCCCACCCTG[C/T]CCCCCACCTGAAGCA | 1840 |
| rs573755099 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113060246 | ATCTCTGCTGTGTGT[C/T]AATTTCTGTGCTAAG | 1840 |
| rs573755109 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066443 | CAAGGCAGGAGAATC[A/C]CTTGAACCCGGGAGG | 1840 |
| rs573909763 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113066536 | CCGTCTCAAAAAAAA[A/T]AAAAAGAATCGTAGT | 1840 |
| rs573926725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113087518 | AGGGGGAGAAGGCAG[C/T]TATGAGGCAGAGACA | 1840 |
| rs573932317 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087535 | ATGAGGCAGAGACAG[A/C]CCTGAAAGTGGGGAA | 1840 |
| rs573976886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113059664 | TTGGCATGTTTGACC[C/T]CCCAAGGACCAGCTG | 1840 |
| rs573999161 | in-del | -/GTGT | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079734 | TGTGTGTGTGTGTGT[-/GTGT]TAGTGGAGATGGGAT | 1840 |
| rs574060783 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113079969 | CCCACCATGTGAAAA[C/T]GCTGTGTACCTGAAC | 1840 |
| rs574194139 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113068118 | AACAAAACCATATCC[A/C/G]CCCAGCTTGCAGTCT | 1840 |
| rs574335890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113074404 | TATTCCAGGCAGAGG[A/G]AACAGCCAGTGAGAA | 1840 |
| rs574338140 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113071483 | AACTGCCTGGGGGAC[G/T]CAGACCCTGTGGCCA | 1840 |
| rs574352751 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113078299 | GTTCCCACACATCTA[C/T]CTCCATGCATAAGGA | 1840 |
| rs574415050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113089682 | GCAGTTAGAGAGAAG[C/T]TGGAGACTACCTCGG | 1840 |
| rs574426299 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DTX1 | GRCh38.p7 | 12:113073939 | CATGCAGATTAATAC[A/G]TCATGTCACAGCCTG | 1840 |
| rs574463003 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113082593 | TCTCTTTGTTTCTGT[G/T]TCTTTGTTTTTTGTT | 1840 |
| rs574492841 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058125 | GAGGAAGTTGCCGCC[C/T]GCTGCCAGGCCCAGG | 1840 |
| rs574659264 | in-del | -/GGAATGGAATGGAATGGAAA | 0.0154538 | 0.0865337 | intron-variant | DTX1 | GRCh38.p7 | 12:113080613 | GGAATGGAATGGAAT[-/GGAATGGAATGGAATGGAAA]GGAACGGAATGGAAA | 1840 |
| rs574670467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113085080 | TTTTAGATGGAGTCT[C/T]ACTTTGTTGTCCAGG | 1840 |
| rs574861634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113064259 | CTCTGGTAGCAGCAG[A/G]TCCAGCTAATCCATA | 1840 |
| rs574876547 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113073343 | AACTCACCTCCTCCC[A/G]GGCCTACTGTGGAGG | 1840 |
| rs574907502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113071023 | TTTCCCTGATTCTCC[A/G]TGATGGTCTCAGCCT | 1840 |
| rs575041623 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DTX1 | GRCh38.p7 | 12:113091389 | TTCCCTAGTGTGTGC[A/G]GTATGTTCCCCAAGT | 1840 |
| rs575066409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069870 | TTGTAGGAGACAGGT[A/G]AGCAGCCATGCAGAT | 1840 |
| rs575165041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113083988 | GCTTGCAAGGGAGGT[A/G]TGAACTCTGCAGAGA | 1840 |
| rs575299488 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | DTX1 | GRCh38.p7 | 12:113077082 | TATCTTGGCACCCCC[A/C]CCCTGTTTGGTGGCT | 1840 |
| rs575370438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113064999 | TTCAGCAGGGTCCTG[A/G]AGGAGGGTCTCAGGC | 1840 |
| rs575509825 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | DTX1 | GRCh38.p7 | 12:113086701 | TATGCTTTTATTTTT[A/T]AAAAATCCACATTTT | 1840 |
| rs575571236 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113071140 | ATGTTGGCCTTGGCC[C/T]GTCTCTGACAGTCTC | 1840 |
| rs575624700 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060441 | CAGGGAAGGCTAGCC[C/T]GAGAAAGTGATGTTT | 1840 |
| rs575635816 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056398 | AGCTCTGAATGCTTC[A/G]AGATCTTTCTTTAGA | 1840 |
| rs575657239 | snp | C/G | 5.00138e-05 | 0.00500044 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077488 | GGGCAAGGGCATCGT[C/G]TGGGAGTGGGAGAAC | 1840 |
| rs575688945 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113058876 | GTGTATTGTTGTATT[A/T]TTATGAGTCCCATTT | 1840 |
| rs575706153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113091441 | CCCTGGTATCTGTGT[A/G]TCTGTGTGTGCATGT | 1840 |
| rs575726694 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055914 | GTGTGTCTCAGCCGC[A/T]TCCAGCTTGCTGGAG | 1840 |
| rs575727727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113065696 | AGGTAGCGGGGCTGT[A/G]GAGGGGATGGTGAAG | 1840 |
| rs575736669 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097596 | TTTTGTGTCTGTGCC[G/T]CTTCATCTCTCTGGA | 1840 |
| rs575779660 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113079284 | CCAAAACCAACTGTG[A/C]TTCAATCACTATGGC | 1840 |
| rs575789552 | snp | C/T | 0.0103295 | 0.0711199 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057867 | GACCTCGAACAGGGG[C/T]GGCTGCCTCACTCCC | 1840 |
| rs575818284 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113078742 | CCATCTGTCCTTGTC[C/G]CAGTCCATGCCCACC | 1840 |
| rs575950489 | in-del | -/C | 3.58815e-05 | 0.0042355 | intron-variant | DTX1 | GRCh38.p7 | 12:113093505 | TGGGCGGGGATGGCG[-/C]CCCCGCCCTGTGACT | 1840 |
| rs575959220 | in-del | -/AG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092700 | TATGTTGTGAATTTC[-/AG]AGAGGGAGACAGTGA | 1840 |
| rs575959358 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066919 | GAGTCTCCTCTAGGT[C/T]CCGCATAGTTGTGTC | 1840 |
| rs576017993 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113092224 | CAGGATTGCACAGCT[C/G]ACAGTGATGATACCG | 1840 |
| rs576079620 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | DTX1 | GRCh38.p7 | 12:113076094 | GGATGATGGTAAATG[A/C]AGGAATGTCTGAATG | 1840 |
| rs576176488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113075672 | TAAAGCCTCAGTGCC[C/T]TCCTTTATGAAAGGG | 1840 |
| rs576231926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113088633 | AGACTATAATGTCAG[C/G]TCGTGATTAGTGCTA | 1840 |
| rs576256375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113095692 | GAGAAACTAAGTGGC[A/G]GAGCTGGGATTTGAG | 1840 |
| rs576288287 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113081085 | AATATTTGAGGCGGG[C/T]GTAGTGGCTCACTTT | 1840 |
| rs576348709 | snp | C/T | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055894 | CCACCCCCCTCCCAG[C/T]CAATGTGTGTCTCAG | 1840 |
| rs576350745 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082994 | CTCTTTCACATTCTT[A/G]AGACTAGAAGTCCGA | 1840 |
| rs576362871 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113058752 | GATTAAATAAAATTG[C/T]GCTCACTGAGCACAG | 1840 |
| rs576657142 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057337 | CCGTACGCCCCCCTT[A/G]CTGTCCCCCTTCGGT | 1840 |
| rs576694003 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113063488 | CTGGAGCTGGGGAGG[C/G]GCACCTATCTGCCTG | 1840 |
| rs576750119 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055719 | AGCAGCCTGCCCCTG[A/T]CCCTGCCTAGTGTAT | 1840 |
| rs576849655 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113064233 | ATGTGTAGGGGCAGG[A/G]AGCGGCCCATCTCTG | 1840 |
| rs576861221 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113056858 | GCGCGGAGGCGGGAC[C/T]GCGGCTCCCTCCCAC | 1840 |
| rs576884048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113070383 | ATGACCGCCTCCCAC[A/G]TGCCCCCTTCCCGTC | 1840 |
| rs576888777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113063544 | GCTGCTGGAGGGGTG[C/T]ATGGCAGCCTCCTGC | 1840 |
| rs576899783 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113095510 | ATCATTCCCAATCCC[G/T]GCTCTCACATTCCTC | 1840 |
| rs576903488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113088709 | AAATAAAGTGGTTGC[A/G]GCCAGGCACAGTGGC | 1840 |
| rs576969903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113070099 | CCGGTGTGCTCCTAA[C/T]TGCTCCGTGCCTCTG | 1840 |
| rs577044775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113062732 | GTGTATGTGCCTCCC[A/G]TGCAGTGCAGCCAGC | 1840 |
| rs577075908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113082021 | TCTCTTTGGGGGTGC[A/G]GATCATTAAACATGT | 1840 |
| rs577091151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113090309 | GAGAGGGAGGAAGTT[A/G]GAGTGGTGACAGCTG | 1840 |
| rs577095087 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082323 | CATCTCCAAGAAACC[A/C]CCCGGGGAAAATCCC | 1840 |
| rs577166535 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060573 | CCGTTCTGTTTGGGA[C/T]GCATCTCCCACCAAG | 1840 |
| rs577217731 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113089594 | AGCGTGTCCCACATC[A/T]AAAGGGGGCCGGGTG | 1840 |
| rs577301434 | snp | C/T | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055451 | GGGACTTCATGGACC[C/T]CAGAAGGCCATCCAG | 1840 |
| rs577311493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DTX1 | GRCh38.p7 | 12:113076838 | CATTGAATGAGTGAG[C/T]AAACTATAATGAAGA | 1840 |
| rs577344088 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075607 | CCCGTGGAGCCTTGC[C/T]GTCAGGGGAGCACGC | 1840 |
| rs577366323 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113072894 | TTTTTTAGTAGAGAT[C/T]GGGGGTTTCACCATG | 1840 |
| rs577436061 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097141 | ATCATAGCTCCCTGA[A/G]AGGGCCAAGCAGAGA | 1840 |
| rs577447500 | snp | A/C | 6.02283e-05 | 0.0054873 | intron-variant | DTX1 | GRCh38.p7 | 12:113093242 | AGGTCTGGCCCAGGG[A/C]GGGAAAGAAGGGCGG | 1840 |
| rs577464359 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058027 | TGGCCATCCCACATT[C/T]CTTTAACGGAGGTCT | 1840 |
| rs577475256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096643 | TGGCAGGGGAGGGAG[A/G]GAGGCTGAGGCTGGT | 1840 |
| rs577503588 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057848 | GACAACACGGAAGAG[G/T]CTGGACCTCGAACAG | 1840 |
| rs577553745 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074898 | AAGAGCATCCGGAAG[C/T]GCAGGAGCTGCCAGG | 1840 |
| rs577601819 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083330 | CCTTTTATAATTTAC[C/T]AATACTTTTTTTTTT | 1840 |
| rs577725191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113087597 | AAGGGAGAGGGTGGG[A/G]GGTCCCTAAAGCACT | 1840 |
| rs577756502 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DTX1 | GRCh38.p7 | 12:113087124 | GGAGGACCGGGAGGG[C/T]TGAAGAGTGACCCCC | 1840 |
| rs577865415 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055169 | GGTGACATTTAATCA[A/G]ACCTTAAATAGCATT | 1840 |
| rs577899807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113060301 | ACAAAGTCATCAGTC[A/G]AGGTCTTGTGCTGGA | 1840 |
| rs577941755 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DTX1 | GRCh38.p7 | 12:113081253 | AGGATTGCGTGAACC[C/T]GGGAGGTGGAGGTTG | 1840 |
| rs578218928 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113075029 | CCTGGCTCCCAGGGG[A/T]GAAGACGGGGCCAAA | 1840 |
| rs578229165 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113069466 | GTCTCCCCACCACCC[G/T]GGCCTGGCTTCCAGC | 1840 |
| rs578240558 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DTX1 | GRCh38.p7 | 12:113068988 | ACTCAGTGTTTGTAC[A/G]AGACAGTGATCGTAA | 1840 |
| rs578262317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113068184 | TTCAGATGTATTTGG[C/T]TATTCATTCATTTAT | 1840 |
| rs745350108 | snp | A/G | 1.73048e-05 | 0.00294144 | intron-variant | DTX1 | GRCh38.p7 | 12:113093497 | TCGGGGGTTTGGGCG[A/G]GGATGGCGCCCCGCC | 1840 |
| rs745359772 | snp | C/T | 1.64838e-05 | 0.00287083 | missense | DTX1 | GRCh38.p7 | 12:113095376 | GCAAGAGGATTCCCT[C/T]GCCACTGCTATCTAC | 1840 |
| rs745403217 | snp | A/G | 2.36947e-05 | 0.00344192 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093558 | GACCGGGATACTGCT[A/G]TGCGCGGCCGGGCTG | 1840 |
| rs745443569 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076999 | CCCCCACTTCAGTGT[C/T]TGTCTTGGCCCTGGA | 1840 |
| rs745446738 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062700 | CTGCTCGCACAATGC[C/T]GACACACACATGCCC | 1840 |
| rs745473622 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113094587 | TTAATAAAAATAAAT[A/C]AATAAAATAAATAAA | 1840 |
| rs745495467 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113064145 | CTCCTGGTTACAGGA[C/T]CCTTTGGGACCCTCT | 1840 |
| rs745608665 | snp | A/C | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113054763 | AGGCAGCATGGTGCT[A/C]TGGGAGGTGCAAAAG | 1840 |
| rs745763546 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113089161 | GTGCAAAGGCCCTGG[A/G]GTGGGAGTGTGCCTG | 1840 |
| rs745779873 | snp | C/T | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055868 | CTAAACACCCCCAGG[C/T]CCCAGGTGGTCCACC | 1840 |
| rs745922880 | snp | C/G | 0.00218579 | 0.0329866 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077836 | GGCCTCGCAGCGCCG[C/G]AAGGCGCCCCCCGCG | 1840 |
| rs745952528 | snp | C/T | 2.56151e-05 | 0.00357867 | intron-variant, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096708 | CACTGTGTCCCTGTC[C/T]CCCCAGGTGCTGCGG | 1840 |
| rs746017780 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113080320 | TGAAGTATCAGTTAT[A/G]GCCCCTTATAGACAG | 1840 |
| rs746025585 | snp | A/G | 1.6836e-05 | 0.00290133 | intron-variant | DTX1 | GRCh38.p7 | 12:113095020 | GGGTGCTGGGAACTC[A/G]CTGCCAGCCTCCCCT | 1840 |
| rs746035722 | snp | C/T | 1.74998e-05 | 0.00295797 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077608 | ATCGCTAGGCTTCTG[C/T]TACCTCATCTACTTC | 1840 |
| rs746068757 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113081746 | GGCTGGAGTGAGGCG[C/T]CAGCAAGAAGGAGAA | 1840 |
| rs746134201 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113068690 | GGCACTAGGGAGCTA[C/T]TGATAGCTGTGGAGC | 1840 |
| rs746199861 | snp | C/T | 1.70816e-05 | 0.00292242 | missense | DTX1 | GRCh38.p7 | 12:113058439 | TCCATGCACCAGTTT[C/T]GCCAGGACACAGGTG | 1840 |
| rs746216207 | in-del | -/CACACC/CACT | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062069 | ACACACACACACACA[-/CACACC/CACT]CTCCAACATAATGCT | 1840 |
| rs746218020 | in-del | -/G | 3.65477e-05 | 0.00427464 | intron-variant | DTX1 | GRCh38.p7 | 12:113094107 | CTGATGAGGTGAGGA[-/G]GGGATGGGGGGGCTG | 1840 |
| rs746249802 | snp | A/G | 1.99698e-05 | 0.00315983 | intron-variant | DTX1 | GRCh38.p7 | 12:113094740 | CAGTGCTGACCCAGT[A/G]GGTGCCCTGCCCTCC | 1840 |
| rs746293156 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113073576 | CAATAGCCATAGCTC[C/T]GTGCCTCGATTTCTC | 1840 |
| rs746346440 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074501 | GAGTGAGTGATAAGG[A/G]GGAGGTAGACAATGC | 1840 |
| rs746354499 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059756 | GCTGGTAGGATGCTC[A/G]CTTTCCCTCTAGAGC | 1840 |
| rs746407667 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061246 | AATGGACTCCTGGGA[C/G]CCTGCCAGGAACCCC | 1840 |
| rs746424025 | in-del | -/TG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091511 | CTGTGTACTTAAACA[-/TG]TGTGTGTAATGTGTC | 1840 |
| rs746474876 | in-del | -/AC | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062033 | AATATTATATTTCAT[-/AC]ACACACACACACACA | 1840 |
| rs746512358 | snp | C/G | 1.73141e-05 | 0.00294223 | missense | DTX1 | GRCh38.p7 | 12:113093668 | GCGTGCCCGGGGTGT[C/G]CCGCAAGACCAAGAA | 1840 |
| rs746517355 | snp | A/T | 1.7968e-05 | 0.00299728 | missense | DTX1 | GRCh38.p7 | 12:113058230 | GGCTGATGCCTGTGA[A/T]TGGTCTGGGCTTCCC | 1840 |
| rs746573544 | snp | C/T | | | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095381 | AGGATTCCCTCGCCA[C/T]TGCTATCTACCCAAC | 1840 |
| rs746597229 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096954 | AGGCCCAAGGCTGCC[C/T]ACCTTCCCTCCTGCT | 1840 |
| rs746646289 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113085337 | TTACAGGCGTGAGCC[A/G]CAGTGCCCAGCCAGG | 1840 |
| rs746737507 | snp | C/T | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056387 | GAAAGGAGGCTAGCT[C/T]TGAATGCTTCAAGAT | 1840 |
| rs746758458 | snp | A/T | 1.67536e-05 | 0.00289423 | splice-acceptor-variant | DTX1 | GRCh38.p7 | 12:113095040 | CAGCCTCCCCTGCCC[A/T]GGATGGCAGCCTGCA | 1840 |
| rs746852687 | in-del | -/TTT | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062027 | CTTGAAAATATTATA[-/TTT]CATACACACACACAC | 1840 |
| rs746942397 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113064317 | GCTGTCTGTATTTCT[A/G]CTATTGCAGACCCAT | 1840 |
| rs747022650 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113072028 | GCAGAGCTGGCCAAC[A/G]CTGATGTTGAGAATC | 1840 |
| rs747079734 | snp | A/G | 0.000126992 | 0.00796743 | missense | DTX1 | GRCh38.p7 | 12:113094049 | GCAGGTAAGAATCCC[A/G]AGGATGTGGTTCGAA | 1840 |
| rs747114323 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082890 | GGCGTGAGCCACAGC[A/G]ACTGGCCTGTCTCTA | 1840 |
| rs747136391 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092067 | AATATGCCTGTTTTA[C/T]AGATAAGGTAACTGA | 1840 |
| rs747149969 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113068787 | GAACATTGCAAAGGG[A/T]GGACACTGGGACATG | 1840 |
| rs747174484 | snp | C/G | 0.000109141 | 0.00738636 | missense | DTX1 | GRCh38.p7 | 12:113093166 | TCTCCCCGCAGGGTC[C/G]CCGCACTCCCGGTGA | 1840 |
| rs747200879 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113070122 | TGCCTCTGTTTTCTC[A/G]CCTCTAAAATGGGGC | 1840 |
| rs747262659 | snp | A/G | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055966 | GTTAACACTTGAGCC[A/G]CTGCCATTTCCAGCC | 1840 |
| rs747371751 | snp | A/C | 0.000142111 | 0.00842825 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077432 | AGTACAGGCACCATG[A/C]GGCCCGTGCGGCGCA | 1840 |
| rs747414364 | snp | A/C | 1.83092e-05 | 0.0030256 | intron-variant | DTX1 | GRCh38.p7 | 12:113058495 | GCCCCGCCGAGCCAT[A/C]ACTACCTTGCAGCGT | 1840 |
| rs747451954 | snp | C/T | 1.99459e-05 | 0.00315794 | intron-variant | DTX1 | GRCh38.p7 | 12:113094745 | CTGACCCAGTAGGTG[C/T]CCTGCCCTCCCCAGT | 1840 |
| rs747494057 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084970 | TCAGTTTTTGCATCT[A/G]TGAAATGGGACTGGC | 1840 |
| rs747503669 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092858 | GGCACAGCGGCCAAC[G/T]AAAGGAGCCCTCAGA | 1840 |
| rs747579956 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083095 | GTGTCCTCATATGGT[C/G]TTCCCTCTGTACCTG | 1840 |
| rs747703600 | snp | A/G | 1.66888e-05 | 0.00288862 | missense | DTX1 | GRCh38.p7 | 12:113058409 | CAGCTTGTGCCCTAC[A/G]TCATCGACCTGCAGT | 1840 |
| rs747734580 | snp | C/G | 6.76567e-05 | 0.00581582 | intron-variant | DTX1 | GRCh38.p7 | 12:113094019 | GTACCCTCAAACCCA[C/G]CCCGCTGTGTCCCTG | 1840 |
| rs747735678 | in-del | -/AGGGCGTGCTTCGGCACA | 1.67915e-05 | 0.00289749 | cds-indel | DTX1 | GRCh38.p7 | 12:113094834 | CAGCATCAGGCTACG[-/AGGGCGTGCTTCGGCACA]AGGGCGTGCTTCGGC | 1840 |
| rs747784366 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074713 | TGAGTCTACTGCAAT[A/G]GTCCAGGCAGGAGAG | 1840 |
| rs747813644 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113073945 | GATTAATACATCATG[C/T]CACAGCCTGGCGCAG | 1840 |
| rs747818661 | snp | A/G | 1.66338e-05 | 0.00288386 | missense | DTX1 | GRCh38.p7 | 12:113058319 | CGGCCCTACACGGCC[A/G]CCGTGTGCCACCACA | 1840 |
| rs747878200 | snp | A/G | 9.71345e-05 | 0.00696835 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093177 | GGTCCCCGCACTCCC[A/G]GTGAAGAACTTGAAT | 1840 |
| rs747945791 | snp | C/T | | | stop-gained | DTX1 | GRCh38.p7 | 12:113094061 | CCCGAGGATGTGGTT[C/T]GAAGATACATGCAGA | 1840 |
| rs748010454 | snp | A/T | 0.000105833 | 0.00727361 | intron-variant | DTX1 | GRCh38.p7 | 12:113093489 | GCCAGTGGTCGGGGG[A/T]TTGGGCGGGGATGGC | 1840 |
| rs748115584 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113071615 | TCTTAGACCCATTGT[C/T]CTGGCTGAAAATCTA | 1840 |
| rs748116120 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066999 | ATCATCCCTCTGGAG[C/T]TGCTCCAGGCTGCTA | 1840 |
| rs748147823 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074736 | CAGGAGAGATAACAT[C/G]GCGGGGACTGGGTGG | 1840 |
| rs748162200 | snp | A/G | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056086 | CTTCTCTTCCTCCAG[A/G]ATCTCACCTCCTGGC | 1840 |
| rs748214328 | snp | A/T | 3.7435e-05 | 0.00432621 | intron-variant | DTX1 | GRCh38.p7 | 12:113094767 | CTCCCCAGTCCTCAG[A/T]CTCCCCTGCTGCCAC | 1840 |
| rs748267457 | snp | G/T | 1.68216e-05 | 0.00290009 | missense | DTX1 | GRCh38.p7 | 12:113094856 | TGCTTCGGCACAAGG[G/T]CGTGCGGCCTGAGCT | 1840 |
| rs748268956 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088842 | CTCCTCAAAAGTTTT[G/T]TTGTTGTTGTTGTTG | 1840 |
| rs748293481 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069539 | ACTAATGGGCCACAG[C/G]TTAGCCTGATGAATC | 1840 |
| rs748397231 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059266 | GTGGTGTTGGTGACA[C/T]TGATAGTTGTGTTGG | 1840 |
| rs748406959 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113090331 | TGACAGCTGCCCCCC[G/T]GAGGAAGGCCCTGGA | 1840 |
| rs748466176 | snp | C/T | 1.75379e-05 | 0.00296119 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096912 | GCTCACAGCCCAGGG[C/T]GTATCCGAGGCTGCA | 1840 |
| rs748474594 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113063865 | CGGGGAAAACACCTC[C/T]AGAATTAGACACCAA | 1840 |
| rs748534327 | snp | A/G | 3.3018e-05 | 0.00406299 | missense | DTX1 | GRCh38.p7 | 12:113095400 | TATCTACCCAACAAC[A/G]AGAAAGGCCGGAAGG | 1840 |
| rs748551666 | in-del | -/GTGT | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091285 | CCCTGGAATATGTGA[-/GTGT]GTGTGTATCTTAATC | 1840 |
| rs748590423 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113094350 | GTTTTGCTTTTGATA[C/G]TTAAGCCCTTAATTC | 1840 |
| rs748604667 | snp | A/G | 1.69046e-05 | 0.00290723 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077461 | CAACTTCTACGACCC[A/G]TCGTCGGCGCCGGGC | 1840 |
| rs748631080 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083516 | TTTTTAGTAGAGACG[A/G]AGTTTTGGCATGTTG | 1840 |
| rs748654335 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113081156 | GAGACCAGCATGGCC[A/G]ACATGGTGAAACCCC | 1840 |
| rs748662716 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083008 | TGAGACTAGAAGTCC[A/G]AGATCACGGTGTCAC | 1840 |
| rs748717925 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113070206 | CTAAACACAGCCTGG[A/G]GCAGAAAAGTGTGCT | 1840 |
| rs748743756 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113080217 | CAACAGAGAGCAGAC[C/T]TGAGGGGGTCAAAGA | 1840 |
| rs748780572 | snp | C/T | 1.65296e-05 | 0.00287481 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095149 | CCACTCGCTGCCCGG[C/T]TTCCCTGATACCCAG | 1840 |
| rs748833568 | snp | A/G | 0.000234472 | 0.010825 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093183 | CGCACTCCCGGTGAA[A/G]AACTTGAATGGTACT | 1840 |
| rs748904459 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075891 | GCTCGAGCACCTGCT[A/G]TGTGCAGGTGCTGGG | 1840 |
| rs748937745 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060591 | ATCTCCCACCAAGGG[A/G]AAGATGGTGCAAGAT | 1840 |
| rs748998143 | snp | C/G | 5.48501e-05 | 0.00523661 | intron-variant | DTX1 | GRCh38.p7 | 12:113058487 | TGCCACCCGCCCCGC[C/G]GAGCCATCACTACCT | 1840 |
| rs749069556 | snp | A/C | 2.13404e-05 | 0.00326646 | missense | DTX1 | GRCh38.p7 | 12:113058209 | TGTCACGGCCAGGCC[A/C]CGGTGGGCTGATGCC | 1840 |
| rs749130810 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097882 | CCAACCAGGGGCCTG[C/T]TGCCCAGGCAACTCA | 1840 |
| rs749153071 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113068395 | GAGTCCCCAAGGAGC[A/G]AGTGGTTTGCCCTAA | 1840 |
| rs749157720 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067030 | CTGCTGCCTGCACAG[A/G]CAGCAGTGGCAGGCC | 1840 |
| rs749159344 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113072235 | GGCTTTGTGCCTGGT[A/G]CTCCAAACATAGTTG | 1840 |
| rs749173378 | snp | A/C/T | 1.74128e-05 | 0.00295062 | intron-variant | DTX1 | GRCh38.p7 | 12:113093495 | GGTCGGGGGTTTGGG[A/C/T]GGGGATGGCGCCCCG | 1840 |
| rs749254480 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092345 | AAAAAAAAAAGGTAC[C/T]ATATTGTCCCCATTT | 1840 |
| rs749256440 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059588 | CGGTGGTATCTGTGA[C/G]AAGCTCCATGGGCAG | 1840 |
| rs749309569 | snp | C/T | 6.74445e-05 | 0.0058067 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113094926 | GCTGTGCCTCGTGGC[C/T]ATGTACTCCAATGGC | 1840 |
| rs749361573 | snp | A/C | 1.67083e-05 | 0.00289031 | missense | DTX1 | GRCh38.p7 | 12:113077588 | CACCCGTGGCTCGAC[A/C]TCTCATCGCTAGGCT | 1840 |
| rs749392214 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113090434 | GCCCGACAAGAAAAT[A/C]AAGACACCTCCACTC | 1840 |
| rs749445285 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079113 | AGCTGCTGTTGGGTG[A/C]CTACCCTGGACTCCA | 1840 |
| rs749532883 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113080142 | CCTCTCGGAGGAGAG[G/T]GTCATGGGGACAAAC | 1840 |
| rs749679407 | snp | C/T | 1.72961e-05 | 0.00294071 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093690 | GACCAAGAAGAAGCA[C/T]CTTAAAAAGAGTACG | 1840 |
| rs749699353 | in-del | -/TTTTTTTT | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079518 | TTGGCCACTTCTCTT[-/TTTTTTTT]TTTTTTTTTTTTTTT | 1840 |
| rs749739327 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083905 | TGGCCTCTCTAGCCT[C/T]AGTCTCCCCATCTGT | 1840 |
| rs749821377 | in-del | -/C | 9.25712e-05 | 0.00680272 | intron-variant | DTX1 | GRCh38.p7 | 12:113093264 | GAAGGGCGGGGCCCA[-/C]TAGGAGGCAGCTCCG | 1840 |
| rs749977372 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069000 | TACAAGACAGTGATC[A/G]TAATAGTTATCATTA | 1840 |
| rs750014713 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113078446 | TTCCATGTTTATTAT[C/T]TGCTAAACCCGTTAT | 1840 |
| rs750062510 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113090892 | GGTCAGAGCATGTGC[A/G]CATGTGTCCTCGTGT | 1840 |
| rs750159675 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083275 | CACATGACTTCTTTG[A/G]GGCACAGTTCAGCCC | 1840 |
| rs750224436 | snp | A/T | 5.30209e-05 | 0.00514856 | intron-variant | DTX1 | GRCh38.p7 | 12:113093742 | CGAGATGAACCCCAC[A/T]AAGCCTTGACCACAA | 1840 |
| rs750267730 | snp | G/T | 1.7663e-05 | 0.00297173 | missense | DTX1 | GRCh38.p7 | 12:113093637 | GTGAGCAAGAGCGAC[G/T]TGAAGCCCGTGCCTG | 1840 |
| rs750351562 | in-del | -/AA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076460 | AATACTCTGCCTGGA[-/AA]AAAAAAAAAAAAAAA | 1840 |
| rs750371572 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062214 | GACTGCCCTAGCTTT[C/G]CTAGTTTCCCAATGC | 1840 |
| rs750416103 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113056921 | AGCGCGAGCCGGAGC[A/C]GGAGCCGGAGACGAA | 1840 |
| rs750448975 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076268 | GTTCGAGACCAGCCT[C/G]GCCAACATGGCAAAA | 1840 |
| rs750482454 | in-del | -/TGTGTG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079695 | ACCATTCCCGGCTAC[-/TGTGTG]TGTGTGTGTGTGTGT | 1840 |
| rs750486432 | snp | C/T | 4.95798e-05 | 0.0049787 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095134 | GTTCCACCTCATCCC[C/T]CACTCGCTGCCCGGC | 1840 |
| rs750556161 | snp | C/G | 6.30815e-05 | 0.00561576 | intron-variant | DTX1 | GRCh38.p7 | 12:113093156 | CCTCTTCTCTTCTCC[C/G]CGCAGGGTCCCCGCA | 1840 |
| rs750641705 | snp | A/C | | | missense | DTX1 | GRCh38.p7 | 12:113077535 | CGGCCTACGATATGG[A/C]CATCTGCATCACCAT | 1840 |
| rs750676112 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082798 | GGACAGGATCTCACT[A/G]TGTTGCCCAGGCTGG | 1840 |
| rs750677868 | snp | C/T | 6.75664e-05 | 0.00581194 | intron-variant | DTX1 | GRCh38.p7 | 12:113094958 | ACAAGGTGGGTTGGG[C/T]GGGACAATGGCTGAG | 1840 |
| rs750703600 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059783 | GAGCTGTGCCAACCA[A/C]TATGTTAGCCACCAA | 1840 |
| rs750760596 | snp | A/G | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055494 | AAAATCCCAGAACTC[A/G]GTGATCCTGTGGGAG | 1840 |
| rs750827888 | snp | C/G | 2.98503e-05 | 0.00386319 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096978 | TCCTGCTTTGCCCCT[C/G]GTCCGGCAAATGCCT | 1840 |
| rs750860198 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086377 | GCCTGAGAAGGCCAG[C/T]GTGGTTGGAGAGGCT | 1840 |
| rs750862912 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087590 | AAGGAGAAAGGGAGA[A/G]GGTGGGGGGTCCCTA | 1840 |
| rs750919269 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088326 | ATCTTGGCTTAGCGG[C/T]AAGGCATGCCGAAAT | 1840 |
| rs750952551 | in-del | -/CT | | | intron-variant | DTX1 | GRCh38.p7 | 12:113073873 | AAGCAGACAAGATCC[-/CT]CTGACTTTGCAGCTG | 1840 |
| rs750989261 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075525 | GCCCCAAGACACAGA[G/T]CAGGCTAAAGGCTCT | 1840 |
| rs751016661 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088149 | CCAGTGCCAGCTGCA[C/T]CACCAACCAGCTGGG | 1840 |
| rs751052771 | snp | C/T | 1.71534e-05 | 0.00292855 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096762 | AAGACTCATCTTCAC[C/T]ATCGGCACGTCCAAC | 1840 |
| rs751067725 | snp | G/T | 7.07389e-05 | 0.0059468 | intron-variant | DTX1 | GRCh38.p7 | 12:113093992 | AGCCAAGCCTTCGGG[G/T]ACAGACTCTGGGTAC | 1840 |
| rs751101381 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086752 | AGTATTACATTTCAG[A/G]GGTTTGAAAATGTTA | 1840 |
| rs751103596 | snp | C/T | 1.66955e-05 | 0.0028892 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096846 | GTTTGGATCCAACCT[C/T]ACGGGCCACGGCTAC | 1840 |
| rs751159811 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066757 | CACAATCAACAGGAC[A/G]GACACAGAAGCCCTC | 1840 |
| rs751167862 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113068366 | TGGGAGCATTGCAGG[C/T]GCAAGGTGCTATGGA | 1840 |
| rs751209635 | snp | A/G | 1.66774e-05 | 0.00288763 | intron-variant | DTX1 | GRCh38.p7 | 12:113093127 | TCGCTTCGGGGGCTG[A/G]AGTCCAGCTGCGGCC | 1840 |
| rs751252170 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113081242 | CAGCTACTGGGAGGA[C/T]TGCGTGAACCCGGGA | 1840 |
| rs751271904 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067836 | CAGGAGTTTAAGACC[A/T]GCCTGAGCAATGTAG | 1840 |
| rs751339024 | in-del | -/AA | 1.66575e-05 | 0.00288591 | frameshift-variant | DTX1 | GRCh38.p7 | 12:113077517 | CGACGGCGGCGCATG[-/AA]GACGGCCTACGATAT | 1840 |
| rs751369923 | snp | C/G | 0.00107403 | 0.0231487 | intron-variant | DTX1 | GRCh38.p7 | 12:113058473 | AGACACCCACCCCAT[C/G]CCACCCGCCCCGCCG | 1840 |
| rs751496108 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059074 | ATGGGGGGCGTTGGT[A/G]GTGTTGATGGTGGGG | 1840 |
| rs751631269 | snp | G/T | 8.5848e-05 | 0.00655108 | intron-variant | DTX1 | GRCh38.p7 | 12:113093259 | GGAAAGAAGGGCGGG[G/T]CCCACTAGGAGGCAG | 1840 |
| rs751749017 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084577 | TTTGTAGAGATGGGC[A/G]TCTCACTATGTTGCC | 1840 |
| rs751773154 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083381 | CCCAGGCTGGAGTGC[A/G]GTGGTGCAATCTTGG | 1840 |
| rs752050039 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113063506 | ACCTATCTGCCTGGT[A/G]TCTCCCATGTCGCTC | 1840 |
| rs752104332 | snp | A/G | 1.65359e-05 | 0.00287536 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058166 | CCTGCAATAGTGGGG[A/G]ACCTGGCCCCTGAGG | 1840 |
| rs752161227 | snp | A/G | 3.70982e-05 | 0.00430671 | intron-variant | DTX1 | GRCh38.p7 | 12:113058480 | CACCCCATGCCACCC[A/G]CCCCGCCGAGCCATC | 1840 |
| rs752185172 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084722 | ATTCTCACAGATACT[C/T]AATGTGGCAGGTTCT | 1840 |
| rs752245433 | snp | A/G | 5.03728e-05 | 0.00501835 | missense | DTX1 | GRCh38.p7 | 12:113094834 | ACAGCATCAGGCTAC[A/G]AGGGCGTGCTTCGGC | 1840 |
| rs752305774 | snp | A/G | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055469 | GAAGGCCATCCAGGG[A/G]CCCTAGGCTAAAATC | 1840 |
| rs752320841 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RASAL1, DTX1 | GRCh38.p7 | 12:113098422 | TCTAACTAGGGAAAA[A/G]CAGGGATGGACCCCA | 1840 |
| rs752427309 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060448 | GGCTAGCCTGAGAAA[A/G]TGATGTTTGAACAGA | 1840 |
| rs752430683 | snp | A/G | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055540 | CCCTGCCCTATGCAA[A/G]GCCTCTCTCTTTAGT | 1840 |
| rs752504741 | in-del | -/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087566 | GGTGACAGGCTCACA[-/C]CCCCTAGAAAGGAGA | 1840 |
| rs752647431 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092221 | GGCCAGGATTGCACA[G/T]CTGACAGTGATGATA | 1840 |
| rs752673841 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061744 | TCTCACTCTGTCTCC[C/T]AGGCTAGAGTACAGT | 1840 |
| rs752727829 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061947 | CTGGCCTCAAGTGAG[C/G]CGCCCGCCTCGGCCT | 1840 |
| rs752771858 | snp | A/G | 1.69484e-05 | 0.002911 | missense | DTX1 | GRCh38.p7 | 12:113058256 | TTCCCACCGCAGAAC[A/G]TGGCCCGGGTGGTGG | 1840 |
| rs752776561 | snp | A/G | 2.90584e-05 | 0.00381161 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058178 | GGGGACCTGGCCCCT[A/G]AGGCAGTGGCGGCCA | 1840 |
| rs752817368 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060314 | TCGAGGTCTTGTGCT[A/G]GAGGACCTACACTGA | 1840 |
| rs752819127 | snp | A/G | 3.79708e-05 | 0.00435706 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093609 | CCCCAAGCCCATCCT[A/G]CACCCGCCGCCCGTG | 1840 |
| rs752889840 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074386 | CTGGGAATGGTGAGG[C/T]CATATTCCAGGCAGA | 1840 |
| rs752933948 | in-del | -/C | 4.26958e-05 | 0.00462018 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096941 | AGCCAAGGCTTGAGG[-/C]CCCAAGGCTGCCCAC | 1840 |
| rs753155493 | snp | A/C | 8.51028e-05 | 0.00652259 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077689 | CCGCCGCCTGGACCT[A/C]GCCTACCCGCTCACC | 1840 |
| rs753187291 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113065242 | ACAGTCTGTCTGGGT[A/T]CCCTTCACCCAGCCA | 1840 |
| rs753191974 | snp | A/C | 1.68607e-05 | 0.00290346 | missense | DTX1 | GRCh38.p7 | 12:113094908 | TGGCCACATGTACCA[A/C]CTGCTGTGCCTCGTG | 1840 |
| rs753200557 | in-del | -/CTC | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056279 | CTCTCTGGCTTCAGT[-/CTC]CTCATCTGTACTCTT | 1840 |
| rs753221340 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113070730 | CTCCATCGCTGGAAG[C/T]ATCCTAGGCTGTGCT | 1840 |
| rs753240718 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066460 | TTGAACCCGGGAGGT[A/G]GAGGTAGCAGTGAGC | 1840 |
| rs753253220 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075514 | TCACTTCATCAGCCC[C/G]AAGACACAGAGCAGG | 1840 |
| rs753280687 | snp | A/G | 5.06308e-05 | 0.00503119 | missense | DTX1 | GRCh38.p7 | 12:113094880 | CTGAGCTCGTGGGCC[A/G]CCTGGGCCGCTGTGG | 1840 |
| rs753338520 | snp | C/T | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055730 | CCTGACCCTGCCTAG[C/T]GTATCCCCATCTGCC | 1840 |
| rs753351408 | snp | C/T | 7.39508e-05 | 0.00608029 | intron-variant | DTX1 | GRCh38.p7 | 12:113077415 | GCCTCCTCCCCATTT[C/T]GAGTACAGGCACCAT | 1840 |
| rs753471133 | snp | C/T | 6.71377e-05 | 0.00579348 | missense | DTX1 | GRCh38.p7 | 12:113094846 | TACGAGGGCGTGCTT[C/T]GGCACAAGGGCGTGC | 1840 |
| rs753523425 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076819 | AACAGATTGATGAAT[C/G]AATCATTGAATGAGT | 1840 |
| rs753534816 | snp | A/C | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056659 | GCTCAGGGCCGAGAT[A/C]TGTCTCCTCCCCTTC | 1840 |
| rs753628900 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086443 | AGGCGCCAGGTCACA[C/G]AGGGTCTGGAAGGTT | 1840 |
| rs753713602 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084490 | TCCTGGGCTCAAGCA[A/G]TCCTCCTGCCTCAGC | 1840 |
| rs753727899 | snp | A/C | 1.81992e-05 | 0.0030165 | missense | DTX1 | GRCh38.p7 | 12:113093620 | TCCTGCACCCGCCGC[A/C]CGTGAGCAAGAGCGA | 1840 |
| rs753742097 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083250 | GAGGTCCTGAGGCTT[A/G]AGGTTTCAACACATG | 1840 |
| rs753786871 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082670 | GCGCAATCACAGCTC[C/T]TGGCAGCCTGAAACT | 1840 |
| rs753818468 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066394 | ATTAGTGGGCATGGT[C/G]GTGGGCGCCTGTAAT | 1840 |
| rs753838114 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069411 | CACGCAGCCCTTCAG[C/T]CTTCCTTAGGCAGCA | 1840 |
| rs753912514 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087333 | TTTGTCTAGGCAGAC[A/G]GAGGTGCTGGGGTAA | 1840 |
| rs753945996 | in-del | -/GGAATGGAAT | | | intron-variant | DTX1 | GRCh38.p7 | 12:113080618 | GGAATGGAATGGAAC[-/GGAATGGAAT]GGAATGGAAAACAGA | 1840 |
| rs753984479 | in-del | -/C | | | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057572 | CCACGCCGCACCCCT[-/C]CCCCCGTGCGTTCTG | 1840 |
| rs754046207 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062269 | TAGCATCAGATAATA[A/T]ATCTTTTAACTTTGT | 1840 |
| rs754056155 | snp | C/G | 1.67691e-05 | 0.00289556 | missense | DTX1 | GRCh38.p7 | 12:113058275 | CCCGGGTGGTGGTGT[C/G]GGAGTGGCTGAATGA | 1840 |
| rs754064729 | snp | C/T | 1.7581e-05 | 0.00296483 | intron-variant | DTX1 | GRCh38.p7 | 12:113093727 | ACGCCCTGCCTCACA[C/T]GAGATGAACCCCACT | 1840 |
| rs754076005 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060845 | CTCCTTGCTAGGAGG[C/T]CTGGTGTTCTGCAGG | 1840 |
| rs754109603 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075235 | ACGCACAGTCACAGA[A/G]CTGGAAAGTCAGAAA | 1840 |
| rs754150128 | snp | C/T | 6.94806e-05 | 0.00589368 | intron-variant | DTX1 | GRCh38.p7 | 12:113093146 | CCAGCTGCGGCCTCT[C/T]CTCTTCTCCCCGCAG | 1840 |
| rs754242357 | snp | A/G | 3.30945e-05 | 0.0040677 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095104 | GACGGGTACGCAGCC[A/G]CCTGGGAAGATGGAG | 1840 |
| rs754281265 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097504 | GGCAATTGTGGGCCC[A/G]TGGGGTGGAAGCCCC | 1840 |
| rs754315228 | snp | A/G | 0.000576701 | 0.0169711 | missense | DTX1 | GRCh38.p7 | 12:113077801 | GTCAACAGCACGCGC[A/G]CCGCCTCCAACGCCA | 1840 |
| rs754522488 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079970 | CCACCATGTGAAAAC[A/G]CTGTGTACCTGAACA | 1840 |
| rs754564591 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097593 | TGATTTTGTGTCTGT[A/G]CCTCTTCATCTCTCT | 1840 |
| rs754568004 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066868 | ATATAGGACTGTCCC[C/T]TACCTTGGAGCCCAG | 1840 |
| rs754571803 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113081246 | TACTGGGAGGATTGC[C/G]TGAACCCGGGAGGTG | 1840 |
| rs754668631 | snp | C/T | 5.12772e-05 | 0.0050632 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096765 | ACTCATCTTCACTAT[C/T]GGCACGTCCAACACC | 1840 |
| rs754810506 | snp | A/C | 0.0410057 | 0.137191 | intron-variant | DTX1 | GRCh38.p7 | 12:113058476 | CACCCACCCCATGCC[A/C]CCCGCCCCGCCGAGC | 1840 |
| rs754830929 | in-del | -/A | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069637 | GCAGCCTGGATCCAC[-/A]GGCTGCAGCTCGAAT | 1840 |
| rs754841449 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113090193 | AGGGGTGAGGCAGAC[C/G]TAGACTTAACCAGGT | 1840 |
| rs754892597 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113090982 | TACTTCCCCACAGGC[A/G]GTGCGGAATCGTGTG | 1840 |
| rs754896614 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113078772 | CTCACATGGTGGCTC[A/G]AGCAAGCATCAGCTG | 1840 |
| rs754955356 | in-del | -/CATACACA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062030 | GAAAATATTATATTT[-/CATACACA]CACACACACACACAC | 1840 |
| rs755003776 | snp | C/G/T | 6.61041e-05 | 0.00574876 | missense | DTX1 | GRCh38.p7 | 12:113095135 | TTCCACCTCATCCCC[C/G/T]ACTCGCTGCCCGGCT | 1840 |
| rs755020287 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066400 | GGGCATGGTGGTGGG[C/T]GCCTGTAATCCCAGC | 1840 |
| rs755033562 | snp | A/C | 3.18811e-05 | 0.00399244 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058168 | TGCAATAGTGGGGGA[A/C]CTGGCCCCTGAGGCA | 1840 |
| rs755182659 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084878 | CCAGCCAGCCTGTAC[G/T]GTTTTGGATCATGGT | 1840 |
| rs755201215 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057733 | GGGTCTGGGACGCAG[C/T]TGGGAGTGCAAAGGG | 1840 |
| rs755203395 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113072595 | CATTTTGTTTCCCCA[A/G]TAATTCTTTGGGGTA | 1840 |
| rs755206055 | in-del | -/GCGCCGCCGCCT | 0.000119787 | 0.00773815 | cds-indel | DTX1 | GRCh38.p7 | 12:113077659 | CCGCCAGACGCGCCG[-/GCGCCGCCGCCT]GCGCCGCCGCCTGGA | 1840 |
| rs755246547 | snp | A/C | 8.66514e-05 | 0.00658165 | intron-variant | DTX1 | GRCh38.p7 | 12:113093260 | GAAAGAAGGGCGGGG[A/C]CCACTAGGAGGCAGC | 1840 |
| rs755248429 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060104 | GTCTGGAAACACAGG[C/T]GAATTCATAACAAAT | 1840 |
| rs755281779 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075688 | TCCTTTATGAAAGGG[C/G]GCCCACCTGGCAGTC | 1840 |
| rs755319781 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088525 | ATGATGAGTTAATGG[G/T]CGCAGCACACCAGCA | 1840 |
| rs755327446 | snp | C/G | 1.74958e-05 | 0.00295764 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077437 | AGGCACCATGCGGCC[C/G]GTGCGGCGCAACTTC | 1840 |
| rs755350817 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062590 | GCATGGGGTAAGACC[A/G]TGCTGGTGCCACAGG | 1840 |
| rs755390154 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091301 | TGTGTGTGTATCTTA[A/G]TCCATGTATGTTTGT | 1840 |
| rs755553596 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113071365 | TTTTCTGCCAAACAT[A/T]TTTAAGCAACTAGGG | 1840 |
| rs755587017 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097848 | GGGAGTGGGCAGTGG[A/G]GTGGCTAATTGTCTT | 1840 |
| rs755587609 | snp | C/T | 5.04274e-05 | 0.00502107 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113094851 | GGGCGTGCTTCGGCA[C/T]AAGGGCGTGCGGCCT | 1840 |
| rs755607511 | snp | C/T | 5.72426e-05 | 0.00534958 | intron-variant | DTX1 | GRCh38.p7 | 12:113077402 | CCGCTGTGCTGACGC[C/T]TCCTCCCCATTTCGA | 1840 |
| rs755623456 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113090675 | AGGGGCTCAATCCAG[A/G]TGTCTGCTCCAGACC | 1840 |
| rs755642443 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RASAL1, DTX1 | GRCh38.p7 | 12:113098479 | GCCAGGACGCCCCTG[C/T]AGTTCTGGTGGATGC | 1840 |
| rs755660510 | snp | C/T | 0.000218942 | 0.0104606 | intron-variant | DTX1 | GRCh38.p7 | 12:113058484 | CCATGCCACCCGCCC[C/T]GCCGAGCCATCACTA | 1840 |
| rs755693434 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087732 | TCTGCTGGGTAAGTG[C/T]GAGGTATCCTGAAGG | 1840 |
| rs755931687 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091016 | GCGTGTGGACGGCAG[A/G]CCGTTCTGCAGGCTG | 1840 |
| rs755944021 | snp | C/T | 0.00014281 | 0.00844895 | intron-variant | DTX1 | GRCh38.p7 | 12:113093534 | CTGCGCCCCCTAACC[C/T]CCAGGGATGACCGGG | 1840 |
| rs755979668 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082656 | GCTGGAGTACAGTGG[C/T]GCAATCACAGCTCCT | 1840 |
| rs756036012 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113063851 | GCTTTTCCCATCACC[A/G]GGGAAAACACCTCCA | 1840 |
| rs756164577 | snp | C/T | 1.65059e-05 | 0.00287275 | intron-variant | DTX1 | GRCh38.p7 | 12:113095275 | AGATGCTTCTCCACC[C/T]TGCCACCACCTGTTC | 1840 |
| rs756177831 | snp | G/T | 1.68493e-05 | 0.00290248 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058264 | GCAGAACGTGGCCCG[G/T]GTGGTGGTGTGGGAG | 1840 |
| rs756192889 | in-del | -/C | 8.20513e-05 | 0.0064046 | intron-variant | DTX1 | GRCh38.p7 | 12:113093124 | ACGTCGCTTCGGGGG[-/C]TGGAGTCCAGCTGCG | 1840 |
| rs756211964 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076373 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGAGG | 1840 |
| rs756249445 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057582 | ACCCCTCCCCCGTGC[G/T]TTCTGCGGCCACCCA | 1840 |
| rs756260866 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113085209 | CGCACGCCACCAACC[C/T]GGCTAATTTTTTATA | 1840 |
| rs756271941 | in-del | -/TTTTTTTTT | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079516 | TCTTGGCCACTTCTC[-/TTTTTTTTT]TTTTTTTTTTTTTTT | 1840 |
| rs756300071 | snp | C/T | 2.44717e-05 | 0.00349789 | missense | DTX1 | GRCh38.p7 | 12:113058197 | CAGTGGCGGCCATGT[C/T]ACGGCCAGGCCACGG | 1840 |
| rs756462869 | in-del | -/TTTTTTTTT | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079517 | CTTGGCCACTTCTCT[-/TTTTTTTTT]TTTTTTTTTTTTTTT | 1840 |
| rs756510084 | snp | A/G | 0.000142949 | 0.00845305 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077722 | GGGCTCCATCCCTAA[A/G]TCGCAGTCGTGGCCC | 1840 |
| rs756576630 | snp | C/T | 1.68613e-05 | 0.00290351 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113094920 | CCACCTGCTGTGCCT[C/T]GTGGCCATGTACTCC | 1840 |
| rs756620146 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083756 | TCTCTCTTTCTCTGT[C/T]TTCTGCCTTTTCCTC | 1840 |
| rs756680926 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088398 | GGTATGCACTCATAT[A/G]TTTGACATTCCTGCT | 1840 |
| rs756697150 | snp | C/G | 1.69269e-05 | 0.00290915 | intron-variant | DTX1 | GRCh38.p7 | 12:113095002 | ACGGAGTGGGGTTTG[C/G]GGGGGTGCTGGGAAC | 1840 |
| rs756727557 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066729 | CCAGGCACTGTCCGG[G/T]CACTAGGAATGTCAC | 1840 |
| rs756758797 | snp | C/G/T | 1.64735e-05 | 0.00286993 | synonymous-codon, missense | DTX1 | GRCh38.p7 | 12:113077530 | ATGGACGGCCTACGA[C/G/T]ATGGACATCTGCATC | 1840 |
| rs756768589 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088285 | GACTTCCTGGAGCAC[C/T]GTGTTGAGGAGGATT | 1840 |
| rs756796860 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113089937 | ACTGGGCCAGACTGG[A/G]CATTATATAGACCTG | 1840 |
| rs756802835 | snp | A/G | 1.82988e-05 | 0.00302474 | intron-variant | DTX1 | GRCh38.p7 | 12:113077418 | TCCTCCCCATTTCGA[A/G]TACAGGCACCATGCG | 1840 |
| rs757042093 | snp | C/T | 2.04966e-05 | 0.00320123 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058213 | ACGGCCAGGCCACGG[C/T]GGGCTGATGCCTGTG | 1840 |
| rs757046432 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113093759 | AGCCTTGACCACAAC[C/T]CTGTGACCCCTGGTC | 1840 |
| rs757074315 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113081688 | ACTTCAAGGGGGCTC[A/G]AAGGGCGTGGTGTGT | 1840 |
| rs757104501 | snp | C/T | 1.6741e-05 | 0.00289314 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058283 | GTGGTGTGGGAGTGG[C/T]TGAATGAGCACAGCC | 1840 |
| rs757105080 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069814 | CAGTTGCTGGCACTG[C/T]GGAGCATTCGGTAAG | 1840 |
| rs757111605 | in-del | -/ACAC | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062040 | ATTTCATACACACAC[-/ACAC]ACACACACACACACA | 1840 |
| rs757182551 | in-del | -/GC | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082416 | GGGTGGCAGACCCTG[-/GC]TTCTTCCGCCTAAAG | 1840 |
| rs757189148 | snp | C/G | 1.66371e-05 | 0.00288414 | intron-variant | DTX1 | GRCh38.p7 | 12:113095443 | CGTGAGGGCATGGGA[C/G]ATAGGCACAGGCAGG | 1840 |
| rs757191295 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079996 | GAACACAGCATCTAC[A/G]CTGGCAGTAGTTCAG | 1840 |
| rs757235984 | snp | C/T | 1.68397e-05 | 0.00290165 | intron-variant | DTX1 | GRCh38.p7 | 12:113095017 | GGGGGGTGCTGGGAA[C/T]TCACTGCCAGCCTCC | 1840 |
| rs757263716 | snp | C/T | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055747 | TATCCCCATCTGCCC[C/T]GGGGAGGCAGGCGTG | 1840 |
| rs757289343 | snp | C/G | 0.000515597 | 0.0160478 | missense | DTX1 | GRCh38.p7 | 12:113077831 | ATCCTGGCCTCGCAG[C/G]GCCGCAAGGCGCCCC | 1840 |
| rs757308877 | snp | C/T | 2.43176e-05 | 0.00348686 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093553 | GGGATGACCGGGATA[C/T]TGCTGTGCGCGGCCG | 1840 |
| rs757328959 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061202 | TGCCCCCTGTTTGCC[G/T]GAAAAGGGAAAAAAA | 1840 |
| rs757364308 | snp | C/T | 4.95855e-05 | 0.00497899 | missense | DTX1 | GRCh38.p7 | 12:113095123 | GGGAAGATGGAGTTC[C/T]ACCTCATCCCCCACT | 1840 |
| rs757384373 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076136 | GAGTGGGCTGAAGAT[A/G]GAGAATACATAAAGG | 1840 |
| rs757413834 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092651 | AATGATATGTTCTTA[C/T]GCAGGGCTTGTCAGA | 1840 |
| rs757460584 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062361 | ATATGTAAGTGAATG[C/T]GTGTGGCTGTGTTCT | 1840 |
| rs757474243 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113095548 | CAGCACCCGAACAGT[A/G]ACGACCACAGCCACC | 1840 |
| rs757510373 | in-del | -/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113058696 | CCTCAGTTTCCTCAT[-/C]TGCAAAATGGGTAGA | 1840 |
| rs757587824 | snp | A/G | 5.08522e-05 | 0.00504217 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096771 | CTTCACTATCGGCAC[A/G]TCCAACACCACGGGC | 1840 |
| rs757667381 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097516 | CCCATGGGGTGGAAG[C/T]CCCCAGATGACTGAG | 1840 |
| rs757723412 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113085222 | CCCGGCTAATTTTTT[A/G]TATTTTTTGTAGAGG | 1840 |
| rs757772756 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086099 | ATAGTGAGACTCCAC[C/T]TTTACAAAATTTTTT | 1840 |
| rs757777910 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097933 | TGGCTGCCACGGTGG[A/G]AGTCAGCCAAGATTT | 1840 |
| rs757840523 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084807 | GCACAAGGTAACACA[A/G]TTAGGACTCAGATTC | 1840 |
| rs757846818 | snp | A/G | 1.85506e-05 | 0.00304548 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096735 | GCGGCTGCTCATCAC[A/G]GCCTGGGAGAGAAGA | 1840 |
| rs757876060 | snp | C/T | 0.000151163 | 0.00869244 | intron-variant | DTX1 | GRCh38.p7 | 12:113095461 | AGGCACAGGCAGGGG[C/T]TCCAGCAACCACTGG | 1840 |
| rs757929003 | snp | C/T | 1.74824e-05 | 0.0029565 | missense | DTX1 | GRCh38.p7 | 12:113093649 | GACGTGAAGCCCGTG[C/T]CTGGCGTGCCCGGGG | 1840 |
| rs757976064 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113078546 | AGGAGAGCTATGGTG[A/C]CTTCTCATTTATTCC | 1840 |
| rs757991840 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066608 | CCTGAGCCTCTGAGC[C/T]TCTGTTTCCTCACCT | 1840 |
| rs758081381 | in-del | -/CAAAAAAA | | | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096439 | AGCAAGACTCTGCCT[-/CAAAAAAA]AAAAAAAAAAAAAAA | 1840 |
| rs758141950 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113085327 | AGTGCTGGGATTACA[A/G]GCGTGAGCCACAGTG | 1840 |
| rs758174679 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083294 | ACAGTTCAGCCCATA[A/G]CAATGTGTCTGTGTG | 1840 |
| rs758178005 | in-del | -/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061913 | GTTTTACCCTGTTGG[-/C]CAAGCTGGTCTTGAA | 1840 |
| rs758228152 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113070951 | TGAGTGAGTGCAAGG[A/C]GAGTGCTGAGTGCAG | 1840 |
| rs758228929 | snp | C/T | | | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057103 | CCGCGACGCGACCCC[C/T]GAGGGGCCCTGGGCC | 1840 |
| rs758279955 | in-del | -/AAAAA | | | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096443 | AGACTCTGCCTCAAA[-/AAAAA]AAAAAAAAAAAAAAA | 1840 |
| rs758282914 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113078216 | CAATAATAATAATGA[C/T]GATAAGTAATATCCA | 1840 |
| rs758302185 | snp | C/T | 1.66032e-05 | 0.0028812 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058369 | GGACGCTCGCGGTTC[C/T]GTGGTCCTGGGGCAG | 1840 |
| rs758355234 | snp | C/T | 0.000167157 | 0.0091406 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058294 | GTGGCTGAATGAGCA[C/T]AGCCGCTGGCGGCCC | 1840 |
| rs758431069 | snp | A/G | 5.63618e-05 | 0.00530827 | missense | DTX1 | GRCh38.p7 | 12:113093163 | TCTTCTCCCCGCAGG[A/G]TCCCCGCACTCCCGG | 1840 |
| rs758432034 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113093804 | AGCATTTACTACCTC[A/G]CCTCCATTGCCTGAT | 1840 |
| rs758483921 | snp | A/G | 0.00019378 | 0.00984136 | intron-variant | DTX1 | GRCh38.p7 | 12:113093244 | GTCTGGCCCAGGGCG[A/G]GAAAGAAGGGCGGGG | 1840 |
| rs758549641 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082833 | AAACTCCTGGCCTCA[A/G]GCATCCGCCTGCCTC | 1840 |
| rs758613768 | snp | A/C | 1.67871e-05 | 0.00289711 | intron-variant | DTX1 | GRCh38.p7 | 12:113095033 | TCACTGCCAGCCTCC[A/C]CTGCCCAGGATGGCA | 1840 |
| rs758683003 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086431 | TAAGAGAGGAAAAGG[C/T]GCCAGGTCACACAGG | 1840 |
| rs758732852 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091437 | GGCTCCCTGGTATCT[C/G]TGTGTCTGTGTGTGC | 1840 |
| rs758737904 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074525 | ACAATGCCAGAGGAG[A/G]ACAGGGCCCCACAAT | 1840 |
| rs758754897 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RASAL1, DTX1 | GRCh38.p7 | 12:113098335 | AATACGGAGGAGCTG[A/G]GAGACACTGTGATCA | 1840 |
| rs758783949 | snp | C/T | 3.24217e-05 | 0.00402614 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096981 | TGCTTTGCCCCTGGT[C/T]CGGCAAATGCCTCCT | 1840 |
| rs758845785 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087596 | AAAGGGAGAGGGTGG[A/G]GGGTCCCTAAAGCAC | 1840 |
| rs758897148 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075553 | TCTGAGAAGTCCTGC[A/G]GCCTGGACCTTGGGT | 1840 |
| rs758980988 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062496 | CTTACTTCCTGAGCT[G/T]CACGATAGCAGATGG | 1840 |
| rs759000343 | snp | C/T | 5.00923e-05 | 0.00500436 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096848 | TTGGATCCAACCTCA[C/T]GGGCCACGGCTACCC | 1840 |
| rs759015998 | snp | A/G | 6.70297e-05 | 0.00578882 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096868 | CACGGCTACCCGGAC[A/G]CTAGCTACCTAGACA | 1840 |
| rs759055372 | snp | C/G | 5.66043e-05 | 0.00531968 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096929 | TATCCGAGGCTGCAG[C/G]CAAGGCTTGAGGCCC | 1840 |
| rs759091080 | snp | C/G | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056617 | GGATTTGGGGCGCCC[C/G]GAGACTCGCGTGTCA | 1840 |
| rs759103743 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092122 | TCAAGGTTGTCACTG[C/T]AGCAGTTTTGTGGTT | 1840 |
| rs759156734 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113093400 | AAGGCCCTTCAGGGG[C/T]CTTCAAGGGGCTGAG | 1840 |
| rs759264141 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083108 | GTCTTCCCTCTGTAC[C/T]TGTCTGTGTCTTAAT | 1840 |
| rs759273535 | snp | G/T | 3.32817e-05 | 0.00407919 | missense | DTX1 | GRCh38.p7 | 12:113077507 | GAGTGGGAGAACGAC[G/T]GCGGCGCATGGACGG | 1840 |
| rs759296454 | snp | C/T | 1.68417e-05 | 0.00290182 | missense | DTX1 | GRCh38.p7 | 12:113094871 | GCGTGCGGCCTGAGC[C/T]CGTGGGCCGCCTGGG | 1840 |
| rs759329934 | snp | C/G | 4.96709e-05 | 0.00498327 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093207 | TGGTACTGGGCCGGT[C/G]CATCCGGCCCTGGCA | 1840 |
| rs759373277 | in-del | -/CC | 1.65897e-05 | 0.00288003 | intron-variant | DTX1 | GRCh38.p7 | 12:113095433 | GTGCCCAGCCGTGAG[-/CC]GGCATGGGAGATAGG | 1840 |
| rs759390309 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074185 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 1840 |
| rs759409473 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086456 | CACAGGGTCTGGAAG[A/G]TTGCGGTTAGGACTT | 1840 |
| rs759420239 | in-del | -/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079244 | GGGGGTTTGGACTGT[-/G]GTCCCCAAGAGGAAG | 1840 |
| rs759473108 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074998 | CTGTTAAACCTCTCC[A/G]GGGAAGGGTCATGAA | 1840 |
| rs759513469 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067761 | GTGAGGCCATTTGAG[G/T]TGGCTCATGCCTGGA | 1840 |
| rs759531292 | snp | C/T | 3.36293e-05 | 0.00410043 | missense | DTX1 | GRCh38.p7 | 12:113094823 | AGCGACTGGTCACAG[C/T]ATCAGGCTACGAGGG | 1840 |
| rs759624535 | snp | G/T | 4.9675e-05 | 0.00498348 | intron-variant | DTX1 | GRCh38.p7 | 12:113095421 | GGCCGGAAGGTGGGT[G/T]CCCAGCCGTGAGGGC | 1840 |
| rs759677695 | snp | C/T | 1.9147e-05 | 0.00309405 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093606 | GGCCCCCAAGCCCAT[C/T]CTGCACCCGCCGCCC | 1840 |
| rs759688462 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113085801 | CTCTCTTGGAGCTCA[C/T]ATTCTAGTGGGAGAC | 1840 |
| rs759694939 | in-del | -/A | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092539 | TCATTTGAAGAGAGG[-/A]TAGTACCTTGTCACA | 1840 |
| rs759716509 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066420 | GTAATCCCAGCTACT[C/T]GGGAGGCCAAGGCAG | 1840 |
| rs759723717 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083282 | CTTCTTTGGGGCACA[A/G]TTCAGCCCATAACAA | 1840 |
| rs759790756 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097288 | AGAGAAGAGACAGAA[A/G]GACCCCATGACCCCC | 1840 |
| rs759930221 | in-del | -/C | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056192 | GGAACTGGGTACTGG[-/C]AGGAGATTCAGATCG | 1840 |
| rs759999653 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113090616 | CCATCCTGCCTCCCT[C/T]GGGAGCTGTGTTCAT | 1840 |
| rs759999709 | snp | A/G | 9.05387e-05 | 0.00672764 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113078034 | AGCGCGCACCCCGGG[A/G]CAGAACAACCTCAAC | 1840 |
| rs760031672 | snp | C/T | 1.74857e-05 | 0.00295678 | intron-variant | DTX1 | GRCh38.p7 | 12:113093713 | AGAGTACGCCCTCCA[C/T]GCCCTGCCTCACACG | 1840 |
| rs760043485 | snp | C/T | | | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058060 | AGGCCTCAGAGAGAA[C/T]CCAGAGTTAGAAAGG | 1840 |
| rs760138547 | snp | A/G/T | 5.03489e-05 | 0.00501721 | missense | DTX1 | GRCh38.p7 | 12:113094840 | TCAGGCTACGAGGGC[A/G/T]TGCTTCGGCACAAGG | 1840 |
| rs760148107 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083212 | CTCTTTAAAGACCCC[A/G]TCTCTAAATACAGTC | 1840 |
| rs760221120 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082599 | TGTTTCTGTGTCTTT[C/G]TTTTTTGTTTTTAGA | 1840 |
| rs760320274 | in-del | -/A | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092327 | CCTCACAGCAGATTA[-/A]AAAAAAAAAAAAGGT | 1840 |
| rs760358106 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113070624 | GCACCCACATACCCA[C/T]CTCTAGGCAGTGGGT | 1840 |
| rs760427480 | snp | C/T | 2.57192e-05 | 0.00358593 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096968 | CCACCTTCCCTCCTG[C/T]TTTGCCCCTGGTCCG | 1840 |
| rs760439219 | snp | C/T | 2.76591e-05 | 0.00371871 | missense | DTX1 | GRCh38.p7 | 12:113077645 | ATGTCGCAGATGAAC[C/T]GCCAGACGCGCCGGC | 1840 |
| rs760442881 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061802 | TTTCCCCGGGTTCAA[C/G]TGATTCTCGTGCCTC | 1840 |
| rs760552377 | snp | A/G | 4.97393e-05 | 0.0049867 | intron-variant | DTX1 | GRCh38.p7 | 12:113095429 | GGTGGGTGCCCAGCC[A/G]TGAGGGCATGGGAGA | 1840 |
| rs760559432 | in-del | -/GGAGAAAG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087577 | TCACACCCCTAGAAA[-/GGAGAAAG]GGAGAGGGTGGGGGG | 1840 |
| rs760586880 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076043 | AGCGGGGAAGGAGAG[A/T]GGGGAAAGTACGTGG | 1840 |
| rs760672136 | snp | A/G | 1.66575e-05 | 0.00288591 | stop-gained | DTX1 | GRCh38.p7 | 12:113077517 | ACGACGGCGGCGCAT[A/G]GACGGCCTACGATAT | 1840 |
| rs760730807 | snp | G/T | 6.75311e-05 | 0.00581042 | intron-variant | DTX1 | GRCh38.p7 | 12:113094966 | GGTTGGGCGGGACAA[G/T]GGCTGAGGAGTGGGC | 1840 |
| rs760777788 | snp | C/T | 1.75203e-05 | 0.00295971 | intron-variant | DTX1 | GRCh38.p7 | 12:113093721 | CCCTCCACGCCCTGC[C/T]TCACACGAGATGAAC | 1840 |
| rs760786131 | snp | C/T | 1.66001e-05 | 0.00288094 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058336 | CGTGTGCCACCACAT[C/T]GAGAACGTGCTGAAG | 1840 |
| rs760832800 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097369 | CAAACTGGAGGATGC[C/G]GGGCAAGCCCTTAGG | 1840 |
| rs760866691 | snp | A/G | 3.72065e-05 | 0.00431299 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093615 | GCCCATCCTGCACCC[A/G]CCGCCCGTGAGCAAG | 1840 |
| rs760889931 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086022 | CCTGTAATCCCAGCA[C/G]TTTGGGAGGCTAAGG | 1840 |
| rs760910804 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079308 | CTATGGCATGGCCGG[A/G]GGAATTGATAATGAT | 1840 |
| rs761037508 | snp | A/G | 1.97011e-05 | 0.0031385 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096726 | CCAGGTGCTGCGGCT[A/G]CTCATCACGGCCTGG | 1840 |
| rs761047158 | in-del | -/A | | | intron-variant | DTX1 | GRCh38.p7 | 12:113078119 | GGTAAGACGGGGCCC[-/A]AGGGGGAGGGGGCCT | 1840 |
| rs761115928 | snp | C/T | 4.96726e-05 | 0.00498335 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095170 | TGATACCCAGACCAT[C/T]CGCATCGTCTATGAC | 1840 |
| rs761153392 | snp | G/T | 1.73246e-05 | 0.00294312 | splice-donor-variant | DTX1 | GRCh38.p7 | 12:113058453 | TCGCCAGGACACAGG[G/T]GAGCAGACACCCACC | 1840 |
| rs761194219 | snp | C/T | 1.6886e-05 | 0.00290564 | intron-variant | DTX1 | GRCh38.p7 | 12:113094977 | ACAATGGCTGAGGAG[C/T]GGGCAGGGAACGGAG | 1840 |
| rs761249409 | snp | C/T | 5.19683e-05 | 0.0050972 | missense | DTX1 | GRCh38.p7 | 12:113077663 | CAGACGCGCCGGCGC[C/T]GCCGCCTGCGCCGCC | 1840 |
| rs761411555 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092762 | CTTCTTTCCTGGAAC[A/G]TTTTATGGAAATTAA | 1840 |
| rs761425758 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113070271 | CTGGGTTGGTGAAGG[A/T]TTCAGTGAAGTCTCT | 1840 |
| rs761430189 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061016 | GGGACCCCCATTTCT[A/G]TTCCCAGCATCCCCT | 1840 |
| rs761584184 | snp | C/T | 1.68658e-05 | 0.0029039 | missense | DTX1 | GRCh38.p7 | 12:113094888 | GTGGGCCGCCTGGGC[C/T]GCTGTGGCCACATGT | 1840 |
| rs761608190 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113072441 | GCTTTGCTGGATGAA[C/T]AGGAGTTTGCCAAGT | 1840 |
| rs761627309 | snp | A/C | 1.91031e-05 | 0.0030905 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096730 | GTGCTGCGGCTGCTC[A/C]TCACGGCCTGGGAGA | 1840 |
| rs761649108 | snp | C/T | | | synonymous-codon | DTX1 | GRCh38.p7 | 12:113094932 | CCTCGTGGCCATGTA[C/T]TCCAATGGCAACAAG | 1840 |
| rs761712030 | snp | A/G | 1.75968e-05 | 0.00296616 | intron-variant | DTX1 | GRCh38.p7 | 12:113093733 | TGCCTCACACGAGAT[A/G]AACCCCACTAAGCCT | 1840 |
| rs761739604 | snp | C/T | 0.000100052 | 0.00707219 | missense | DTX1 | GRCh38.p7 | 12:113078086 | ACCAGCGTGAGCGCG[C/T]GCGCCTCCATCCCGC | 1840 |
| rs761753550 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084310 | TCCACCCCACGTGGT[A/G]GGTGGGAGGACAGTG | 1840 |
| rs761787100 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087340 | AGGCAGACGGAGGTG[C/T]TGGGGTAAGGAAAGG | 1840 |
| rs761825166 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113070825 | GTGGCATCATTCCCA[A/G]CCCTCTGCTCTCACC | 1840 |
| rs761990937 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088306 | GAGGAGGATTCTGAA[A/G]TTGCATCTTGGCTTA | 1840 |
| rs762008401 | snp | A/C | 1.74827e-05 | 0.00295652 | intron-variant | DTX1 | GRCh38.p7 | 12:113058460 | GACACAGGTGAGCAG[A/C]CACCCACCCCATGCC | 1840 |
| rs762139351 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113063353 | CCCCTGCCACTGGGA[C/G]AGCCGCCTCCGAGGG | 1840 |
| rs762158056 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067409 | GGAGCCTGGGTCCAA[A/G]GCCTGTCTCTAATTT | 1840 |
| rs762163064 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113098194 | CCTCCTAGTCCTAGT[C/T]TCCAAGAATGCAGAG | 1840 |
| rs762192180 | snp | A/G | 5.56726e-05 | 0.00527572 | intron-variant | DTX1 | GRCh38.p7 | 12:113094109 | GATGAGGTGAGGAGG[A/G]GATGGGGGGGCTGGG | 1840 |
| rs762202158 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069088 | AGAGTTGACTTACAC[A/G]AAGCATTTAGAACAG | 1840 |
| rs762231749 | in-del | -/ACACACAC | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062033 | AATATTATATTTCAT[-/ACACACAC]ACACACACACACACA | 1840 |
| rs762258338 | snp | C/T | 5.11653e-05 | 0.00505767 | intron-variant | DTX1 | GRCh38.p7 | 12:113093508 | GGCGGGGATGGCGCC[C/T]CGCCCTGTGACTGCG | 1840 |
| rs762303453 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067635 | AATGGGGCCAGCATA[A/T]CTCAGCTCCTGCTCA | 1840 |
| rs762364786 | snp | A/G | 1.65718e-05 | 0.00287848 | missense | DTX1 | GRCh38.p7 | 12:113095177 | CAGACCATCCGCATC[A/G]TCTATGACATCCCCA | 1840 |
| rs762376479 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059594 | TATCTGTGACAAGCT[A/C]CATGGGCAGTGGGGA | 1840 |
| rs762548356 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113056884 | CCCACTCCGGGGGGA[A/G]CCCAGGAGGCGGCGG | 1840 |
| rs762577986 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113078810 | AAAGTATTTCCCCAT[A/G]GGCTGCACCTGAAAT | 1840 |
| rs762602833 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113090903 | GTGCGCATGTGTCCT[C/T]GTGTGCAGTGAGTCA | 1840 |
| rs762618389 | snp | A/G | 3.59363e-05 | 0.00423873 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096919 | GCCCAGGGCGTATCC[A/G]AGGCTGCAGCCAAGG | 1840 |
| rs762638971 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113095929 | AAAAACAGGCAGGGC[C/T]GGGTGTGGTGGCTCA | 1840 |
| rs762648652 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061497 | AGACCTGAGTGCCAA[C/T]GGTGTGACCTCAGGC | 1840 |
| rs762651695 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091945 | ACAGCAAGACACCAG[C/T]TCCCCTGCATAAACA | 1840 |
| rs762776864 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084421 | GACAGGGTCTCACTC[C/T]GTCACCCAGGCTGGA | 1840 |
| rs762822623 | snp | A/C | 0.0307044 | 0.120039 | intron-variant | DTX1 | GRCh38.p7 | 12:113058466 | GGTGAGCAGACACCC[A/C]CCCCATGCCACCCGC | 1840 |
| rs762843247 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097200 | AGAGACCCGCCCCCT[C/T]ACACACAAACACACA | 1840 |
| rs762879544 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074141 | GTCTGAGGCAGGAGA[A/G]TCGTTTGAACCTGGG | 1840 |
| rs762925937 | in-del | -/CGACGGCGGC | 1.66435e-05 | 0.0028847 | frameshift-variant | DTX1 | GRCh38.p7 | 12:113077503 | GTGGGAGTGGGAGAA[-/CGACGGCGGC]GCATGGACGGCCTAC | 1840 |
| rs762960270 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083606 | TCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC | 1840 |
| rs762979797 | snp | C/T | 3.34024e-05 | 0.00408657 | intron-variant | DTX1 | GRCh38.p7 | 12:113095220 | TGGGCTCCCCTTCCG[C/T]CTCTCTGGCCCCCAG | 1840 |
| rs763025523 | in-del | -/C | 6.74491e-05 | 0.00580689 | intron-variant | DTX1 | GRCh38.p7 | 12:113095010 | GGGTTTGGGGGGGTG[-/C]TGGGAACTCACTGCC | 1840 |
| rs763030792 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095336 | GCAGGGCCCTGAGCA[C/T]CCCAACCCCGGGAAG | 1840 |
| rs763129140 | in-del | -/GA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086163 | GTCCCAGCTACACAG[-/GA]GGCTGAGGTGGGAGG | 1840 |
| rs763197363 | snp | C/T | 3.95531e-05 | 0.0044469 | intron-variant | DTX1 | GRCh38.p7 | 12:113077390 | GCAGACCAACGCCCG[C/T]TGTGCTGACGCCTCC | 1840 |
| rs763277883 | snp | A/G | 3.90755e-05 | 0.00441998 | missense | DTX1 | GRCh38.p7 | 12:113093599 | TGACGCGGGCCCCCA[A/G]GCCCATCCTGCACCC | 1840 |
| rs763349356 | snp | C/G | 1.72427e-05 | 0.00293616 | missense | DTX1 | GRCh38.p7 | 12:113058244 | AATGGTCTGGGCTTC[C/G]CACCGCAGAACGTGG | 1840 |
| rs763354643 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097987 | TTTCAAAACCTACCA[-/G]TCCCACTGTGGGTGG | 1840 |
| rs763382342 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076374 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGAGGC | 1840 |
| rs763445414 | snp | A/G | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055503 | GAACTCAGTGATCCT[A/G]TGGGAGTATCGTCAG | 1840 |
| rs763515842 | snp | C/T | 3.42483e-05 | 0.00413799 | intron-variant | DTX1 | GRCh38.p7 | 12:113093514 | GATGGCGCCCCGCCC[C/T]GTGACTGCGCCCCCT | 1840 |
| rs763525237 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113089099 | GCTAAGTGAGGGAGT[A/G]TGCCATGAGGATATC | 1840 |
| rs763624901 | snp | A/G | 0.000215889 | 0.0103874 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096972 | CTTCCCTCCTGCTTT[A/G]CCCCTGGTCCGGCAA | 1840 |
| rs763641509 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083222 | ACCCCGTCTCTAAAT[A/G]CAGTCACATTCTGAG | 1840 |
| rs763653742 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061701 | AAGATCTTAAATCTT[C/T]TTTTTTTCTTCTTTT | 1840 |
| rs763660432 | snp | C/G | 1.87166e-05 | 0.00305908 | intron-variant | DTX1 | GRCh38.p7 | 12:113077409 | GCTGACGCCTCCTCC[C/G]CATTTCGAGTACAGG | 1840 |
| rs763672904 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113089739 | TAAATAAATAACAGT[C/T]CCACAGTGACACCCC | 1840 |
| rs763730414 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113070645 | GGCAGTGGGTTCAGA[G/T]CGGGACCATGCTCTA | 1840 |
| rs763758735 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088073 | CTGGCTCAACTCCAG[A/G]TGGCTCCACAGACCA | 1840 |
| rs763784086 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113070180 | TAAACACACTCTTTC[A/G]CTTGAATGAGCTAAA | 1840 |
| rs763867005 | in-del | -/TACA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062032 | AAATATTATATTTCA[-/TACA]CACACACACACACAC | 1840 |
| rs763926472 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062143 | CTTCTGTCTAGATTT[C/T]CTAATTGTAAAATTC | 1840 |
| rs764005756 | snp | C/T | 1.66056e-05 | 0.00288141 | missense | DTX1 | GRCh38.p7 | 12:113077520 | ACGGCGGCGCATGGA[C/T]GGCCTACGATATGGA | 1840 |
| rs764009375 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082617 | TTTTGTTTTTAGAGA[C/G]AGAGCCTCGCTCTTA | 1840 |
| rs764034190 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113098103 | GCCCCGTTGGGGAGT[A/G]ATGGCTTGCAAGAGA | 1840 |
| rs764049667 | snp | C/G | 1.6593e-05 | 0.00288031 | intron-variant | DTX1 | GRCh38.p7 | 12:113095435 | TGCCCAGCCGTGAGG[C/G]CATGGGAGATAGGCA | 1840 |
| rs764071516 | in-del | -/G | 0.00197844 | 0.0313896 | intron-variant | DTX1 | GRCh38.p7 | 12:113094113 | AGGTGAGGAGGGGAT[-/G]GGGGGGCTGGGGGAG | 1840 |
| rs764089026 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074441 | GAGGCTGGACAGTGC[C/T]TGGTGTATTTGAGGA | 1840 |
| rs764253013 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113065779 | GTGATGAGAGGGTGA[C/T]GAGGAGGGGCCAGGA | 1840 |
| rs764344755 | snp | G/T | 1.67719e-05 | 0.0028958 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058273 | GGCCCGGGTGGTGGT[G/T]TGGGAGTGGCTGAAT | 1840 |
| rs764389287 | snp | C/T | 1.84578e-05 | 0.00303786 | missense | DTX1 | GRCh38.p7 | 12:113093617 | CCATCCTGCACCCGC[C/T]GCCCGTGAGCAAGAG | 1840 |
| rs764391245 | snp | C/T | 5.87078e-05 | 0.00541761 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096727 | CAGGTGCTGCGGCTG[C/T]TCATCACGGCCTGGG | 1840 |
| rs764480308 | snp | A/G/T | 3.37366e-05 | 0.00410699 | intron-variant | DTX1 | GRCh38.p7 | 12:113095007 | GTGGGGTTTGGGGGG[A/G/T]TGCTGGGAACTCACT | 1840 |
| rs764487338 | snp | G/T | 7.34511e-05 | 0.00605972 | intron-variant | DTX1 | GRCh38.p7 | 12:113093140 | TGGAGTCCAGCTGCG[G/T]CCTCTTCTCTTCTCC | 1840 |
| rs764536095 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075663 | GGTTTGGAGTAAAGC[C/T]TCAGTGCCCTCCTTT | 1840 |
| rs764629407 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113056824 | CGGCGCGGCGGCCGA[C/G]GGGCCTGGGAGGGAA | 1840 |
| rs764684782 | snp | A/G | 4.96496e-05 | 0.0049822 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095101 | GAAGACGGGTACGCA[A/G]CCGCCTGGGAAGATG | 1840 |
| rs764744078 | snp | C/T | 1.71452e-05 | 0.00292785 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077668 | GCGCCGGCGCCGCCG[C/T]CTGCGCCGCCGCCTG | 1840 |
| rs764772924 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113072204 | CGTCTCGCTTGCAGA[C/T]GTCTTCTTTGCACCA | 1840 |
| rs764817306 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113089976 | AACTGGCTATACTGA[C/T]TGATAGAGGCTGCTT | 1840 |
| rs764835647 | snp | A/G | 1.66236e-05 | 0.00288297 | missense | DTX1 | GRCh38.p7 | 12:113058391 | CTGGGGCAGGTGGAC[A/G]CCCAGCTTGTGCCCT | 1840 |
| rs764973286 | in-del | -/AAAA | | | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096444 | GACTCTGCCTCAAAA[-/AAAA]AAAAAAAAAAAAAAA | 1840 |
| rs765057305 | snp | A/T | 3.5312e-05 | 0.00420175 | intron-variant | DTX1 | GRCh38.p7 | 12:113093740 | CACGAGATGAACCCC[A/T]CTAAGCCTTGACCAC | 1840 |
| rs765098566 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066418 | CTGTAATCCCAGCTA[C/T]TCGGGAGGCCAAGGC | 1840 |
| rs765144907 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086475 | CGGTTAGGACTTTGG[C/G]TTTTGCTCTGCATGA | 1840 |
| rs765207829 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088324 | GCATCTTGGCTTAGC[A/G]GTAAGGCATGCCGAA | 1840 |
| rs765215495 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084413 | GTGTGTGAGACAGGG[C/T]CTCACTCCGTCACCC | 1840 |
| rs765366584 | snp | C/T | 1.65272e-05 | 0.0028746 | missense | DTX1 | GRCh38.p7 | 12:113095130 | TGGAGTTCCACCTCA[C/T]CCCCCACTCGCTGCC | 1840 |
| rs765384668 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075506 | CAAAAGACTCACTTC[A/G]TCAGCCCCAAGACAC | 1840 |
| rs765486555 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067833 | GCACAGGAGTTTAAG[A/C]CCAGCCTGAGCAATG | 1840 |
| rs765518114 | snp | A/C/T | 0.008839 | 0.06589 | intron-variant | DTX1 | GRCh38.p7 | 12:113058462 | CACAGGTGAGCAGAC[A/C/T]CCCACCCCATGCCAC | 1840 |
| rs765650396 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113098276 | TCCCTGGCACAATGA[C/T]AAGAAACAAGGAACT | 1840 |
| rs765677870 | snp | C/T | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055462 | GACCCCAGAAGGCCA[C/T]CCAGGGACCCTAGGC | 1840 |
| rs765708684 | snp | C/T | 0.00031732 | 0.012592 | intron-variant | DTX1 | GRCh38.p7 | 12:113095218 | GGTGGGCTCCCCTTC[C/T]GCCTCTCTGGCCCCC | 1840 |
| rs765803475 | snp | A/G/T | 0.000129999 | 0.00806137 | intron-variant | DTX1 | GRCh38.p7 | 12:113093243 | GGTCTGGCCCAGGGC[A/G/T]GGAAAGAAGGGCGGG | 1840 |
| rs765871367 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092964 | CATTGGAACCTGGGC[A/G]GAGGTCCTGGCCACC | 1840 |
| rs765901849 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059963 | GTTGCAGAAAGTTCT[A/G]TTACACCATGCTAGT | 1840 |
| rs765935539 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113090921 | GTGCAGTGAGTCAGC[A/G]TGTCCTCCTGCGCCC | 1840 |
| rs765937702 | snp | C/T | 1.73243e-05 | 0.0029431 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096755 | GGGAGAGAAGACTCA[C/T]CTTCACTATCGGCAC | 1840 |
| rs765988518 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092055 | AAGTGAGGTGTTAAT[A/C]TGCCTGTTTTACAGA | 1840 |
| rs766028821 | in-del | -/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067891 | AAACAAAAAAAAAAA[-/T]AGCTAGACATGATGG | 1840 |
| rs766078692 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075330 | CTGTTCTCACTCACT[C/T]CTCCCCCAAATACTG | 1840 |
| rs766112060 | snp | C/T | 1.65603e-05 | 0.00287747 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095095 | CGGGGAGAAGACGGG[C/T]ACGCAGCCGCCTGGG | 1840 |
| rs766114921 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113085677 | TCCTTTATAGCATAT[G/T]TTCATCTGTTTTTTA | 1840 |
| rs766119003 | in-del | -/T | 1.66414e-05 | 0.00288452 | frameshift-variant | DTX1 | GRCh38.p7 | 12:113077516 | AACGACGGCGGCGCA[-/T]GGACGGCCTACGATA | 1840 |
| rs766149525 | snp | A/G | 1.78969e-05 | 0.00299135 | intron-variant | DTX1 | GRCh38.p7 | 12:113058471 | GCAGACACCCACCCC[A/G]TGCCACCCGCCCCGC | 1840 |
| rs766165800 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113058616 | TGTCCAGTTTAAGAC[C/T]TGGATTCCAATGCAG | 1840 |
| rs766172287 | in-del | -/AAAAAAAA | | | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096440 | GCAAGACTCTGCCTC[-/AAAAAAAA]AAAAAAAAAAAAAAA | 1840 |
| rs766300565 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095342 | CCCTGAGCACCCCAA[C/T]CCCGGGAAGAAGTTC | 1840 |
| rs766333628 | snp | A/G | | | synonymous-codon | DTX1 | GRCh38.p7 | 12:113078022 | CGCCCCCGGCGGAGC[A/G]CGCACCCCGGGGCAG | 1840 |
| rs766404906 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113064835 | CACTAGGCAGATGCA[C/T]GGTGCCTTCAGCCAT | 1840 |
| rs766441593 | in-del | -/AATA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059846 | AACTAAGTAAAATGT[-/AATA]AAAATCCAGTTCTTC | 1840 |
| rs766463161 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113063453 | CAGAAGCTCCCAGCT[C/T]GCTCCCTGGCCTCAT | 1840 |
| rs766633116 | snp | G/T | 3.91443e-05 | 0.00442387 | intron-variant | DTX1 | GRCh38.p7 | 12:113077394 | ACCAACGCCCGCTGT[G/T]CTGACGCCTCCTCCC | 1840 |
| rs766642742 | snp | C/T | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055528 | CGTCAGACTTGGCCC[C/T]GCCCTATGCAAAGCC | 1840 |
| rs766655143 | in-del | -/AG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113078120 | GGTAAGACGGGGCCC[-/AG]GGGGAGGGGGCCTCT | 1840 |
| rs766686137 | snp | A/G | | | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096063 | ATACAAAAATTATCC[A/G]GAGTGGTGGAGTGCG | 1840 |
| rs766730153 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088460 | ACCAGATCATACAGG[A/G]CCTGGTCATGCTTAA | 1840 |
| rs766783302 | snp | C/T | 1.71478e-05 | 0.00292807 | missense | DTX1 | GRCh38.p7 | 12:113058247 | GGTCTGGGCTTCCCA[C/T]CGCAGAACGTGGCCC | 1840 |
| rs766834427 | snp | C/T | 3.33428e-05 | 0.00408293 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058158 | GAGCTGGGCCTGCAA[C/T]AGTGGGGGACCTGGC | 1840 |
| rs766854481 | snp | C/T | 3.32099e-05 | 0.00407478 | intron-variant | DTX1 | GRCh38.p7 | 12:113093520 | GCCCCGCCCTGTGAC[C/T]GCGCCCCCTAACCCC | 1840 |
| rs766919057 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091048 | AGCGCGCCGGGGGCT[G/T]GTAGGGCTGAGCGCA | 1840 |
| rs767108880 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113081254 | GGATTGCGTGAACCC[A/G]GGAGGTGGAGGTTGC | 1840 |
| rs767154437 | in-del | -/CCT | 4.20106e-05 | 0.00458296 | intron-variant, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096678 | GGAAGCTGCCTGTGA[-/CCT]CCTCCTCCCGGCCCC | 1840 |
| rs767163815 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113068130 | TCCGCCCAGCTTGCA[A/G]TCTCCAGCCTAGTCA | 1840 |
| rs767163919 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082494 | GAAAGGGATGGAGGT[C/G]GGGGGTCTTTGAGGA | 1840 |
| rs767250827 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075078 | CATCAGAGTAGACAC[A/G]GTATTTATCTCAATT | 1840 |
| rs767286756 | snp | A/G | 1.66396e-05 | 0.00288436 | missense | DTX1 | GRCh38.p7 | 12:113077513 | GAGAACGACGGCGGC[A/G]CATGGACGGCCTACG | 1840 |
| rs767325743 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074336 | ATGTTTGAACACACA[A/C]CTGTAAGAAAGAAGG | 1840 |
| rs767421067 | snp | C/T | 1.67992e-05 | 0.00289816 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113094830 | GGTCACAGCATCAGG[C/T]TACGAGGGCGTGCTT | 1840 |
| rs767425097 | in-del | -/TTTTTTTTTT | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079516 | TCTTGGCCACTTCTC[-/TTTTTTTTTT]TTTTTTTTTTTTTTT | 1840 |
| rs767432693 | snp | A/T | 1.90264e-05 | 0.00308429 | missense | DTX1 | GRCh38.p7 | 12:113093608 | CCCCCAAGCCCATCC[A/T]GCACCCGCCGCCCGT | 1840 |
| rs767647816 | snp | C/T | 0.000122861 | 0.00783681 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058173 | TAGTGGGGGACCTGG[C/T]CCCTGAGGCAGTGGC | 1840 |
| rs767659565 | snp | C/T | 4.96644e-05 | 0.00498294 | intron-variant | DTX1 | GRCh38.p7 | 12:113095422 | GCCGGAAGGTGGGTG[C/T]CCAGCCGTGAGGGCA | 1840 |
| rs767719944 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097307 | CCCATGACCCCCCCA[C/T]GTGGATCCCCATCTG | 1840 |
| rs767767534 | in-del | -/GCC | 0.00514135 | 0.0504405 | cds-indel | DTX1 | GRCh38.p7 | 12:113077860 | CCCCGCGCCCCCGCT[-/GCC]GCCGCCGCCGCCACC | 1840 |
| rs767806383 | snp | C/T | 0.000154204 | 0.00877943 | intron-variant | DTX1 | GRCh38.p7 | 12:113093528 | CTGTGACTGCGCCCC[C/T]TAACCCCCAGGGATG | 1840 |
| rs767833903 | snp | C/G | | | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077470 | CGACCCGTCGTCGGC[C/G]CCGGGCAAGGGCATC | 1840 |
| rs767969703 | snp | A/G | | | upstream-variant-2KB, intron-variant | DTX1 | GRCh38.p7 | 12:113057171 | CACCCCAGCGCACCC[A/G]GCATCCCCCCGGCAG | 1840 |
| rs767971099 | snp | A/C | 1.66112e-05 | 0.00288189 | stop-gained | DTX1 | GRCh38.p7 | 12:113058327 | CACGGCCACCGTGTG[A/C]CACCACATTGAGAAC | 1840 |
| rs767978079 | snp | C/T | | | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058174 | AGTGGGGGACCTGGC[C/T]CCTGAGGCAGTGGCG | 1840 |
| rs768022485 | snp | C/G | 1.69619e-05 | 0.00291216 | missense | DTX1 | GRCh38.p7 | 12:113058255 | CTTCCCACCGCAGAA[C/G]GTGGCCCGGGTGGTG | 1840 |
| rs768048317 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113065475 | GGGATGCCCGGGACA[C/G]ACCCCCTCGCAGCCC | 1840 |
| rs768063861 | snp | A/C/G | 0.000119229 | 0.00772029 | intron-variant | DTX1 | GRCh38.p7 | 12:113095001 | AACGGAGTGGGGTTT[A/C/G]GGGGGGTGCTGGGAA | 1840 |
| rs768073379 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079182 | TGGCAATGAGAGGAA[A/G]GATCAAAGACCTTGA | 1840 |
| rs768133605 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113064993 | GGGTCCTTCAGCAGG[A/G]TCCTGGAGGAGGGTC | 1840 |
| rs768136495 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113071898 | AGGACTCCAGGGACA[C/T]AGCCTTTAATAACTA | 1840 |
| rs768187961 | snp | A/G | 3.27102e-05 | 0.00404401 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096983 | CTTTGCCCCTGGTCC[A/G]GCAAATGCCTCCTTC | 1840 |
| rs768238335 | snp | C/T | 3.4617e-05 | 0.00416021 | missense | DTX1 | GRCh38.p7 | 12:113093670 | GTGCCCGGGGTGTGC[C/T]GCAAGACCAAGAAGA | 1840 |
| rs768248899 | in-del | -/G | 0.00197844 | 0.0313896 | intron-variant | DTX1 | GRCh38.p7 | 12:113094112 | AGGTGAGGAGGGGAT[-/G]GGGGGGGCTGGGGGA | 1840 |
| rs768309364 | snp | A/G | 1.78519e-05 | 0.00298758 | missense | DTX1 | GRCh38.p7 | 12:113058232 | CTGATGCCTGTGAAT[A/G]GTCTGGGCTTCCCAC | 1840 |
| rs768348251 | snp | C/T | 2.07153e-05 | 0.00321826 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093583 | GGGCTGCCCGTGTGC[C/T]TGACGCGGGCCCCCA | 1840 |
| rs768462274 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060595 | CCCACCAAGGGGAAG[A/G]TGGTGCAAGATGGCA | 1840 |
| rs768465173 | snp | G/T | 3.37633e-05 | 0.00410859 | intron-variant | DTX1 | GRCh38.p7 | 12:113094971 | GGCGGGACAATGGCT[G/T]AGGAGTGGGCAGGGA | 1840 |
| rs768539647 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076054 | AGAGAGGGGAAAGTA[C/T]GTGGGGGGTGCACAT | 1840 |
| rs768541695 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088816 | GCCTGGGCAACACAG[C/T]GAGGCCCTGTCTCCT | 1840 |
| rs768593919 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113085676 | TTCCTTTATAGCATA[C/T]GTTCATCTGTTTTTT | 1840 |
| rs768619446 | snp | A/G | 5.53986e-05 | 0.00526272 | missense | DTX1 | GRCh38.p7 | 12:113077646 | TGTCGCAGATGAACC[A/G]CCAGACGCGCCGGCG | 1840 |
| rs768675367 | snp | C/T | 3.33795e-05 | 0.00408517 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095059 | TGGCAGCCTGCAGTG[C/T]CCCACCTGCAAGGCC | 1840 |
| rs768679677 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113072344 | CAGTGTGAGGACAGA[C/T]ATGCAATAAAAGACT | 1840 |
| rs768717751 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113068849 | CACTCTGGTGGCATG[A/G]GCCAGAGGGCTGACA | 1840 |
| rs768771037 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113070134 | CTCGCCTCTAAAATG[A/G]GGCAATAACACCCCC | 1840 |
| rs768797162 | snp | A/G | 1.68746e-05 | 0.00290466 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096886 | AGCTACCTAGACAAC[A/G]TGCTGGCTGAGCTCA | 1840 |
| rs768839188 | snp | C/T | 6.62274e-05 | 0.00575407 | missense | DTX1 | GRCh38.p7 | 12:113095171 | GATACCCAGACCATC[C/T]GCATCGTCTATGACA | 1840 |
| rs768931233 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092941 | CACTAAAGTCTAAGG[A/G]TGCATCCCATTGGAA | 1840 |
| rs768996902 | snp | A/G | 1.83417e-05 | 0.00302829 | intron-variant | DTX1 | GRCh38.p7 | 12:113058499 | CGCCGAGCCATCACT[A/G]CCTTGCAGCGTAGGA | 1840 |
| rs769045372 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091655 | CCACTGCAGCAGTAC[C/T]CAAGCCTGCCAAGGG | 1840 |
| rs769058803 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088195 | CATTTCCCTTCTCTG[G/T]GCTTCAGTCCCATCA | 1840 |
| rs769061882 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061430 | ATGTCAAGAAAGGAC[A/G]TCTTGTCCTCATTGG | 1840 |
| rs769201819 | in-del | -/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113082859 | CCTCAGCCTCCAAAA[-/G]GTGCTGGGAATTATA | 1840 |
| rs769211091 | snp | C/G | 1.73366e-05 | 0.00294415 | intron-variant | DTX1 | GRCh38.p7 | 12:113058454 | CGCCAGGACACAGGT[C/G]AGCAGACACCCACCC | 1840 |
| rs769230290 | in-del | -/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113078899 | GGTGACCTGGAATCG[-/T]GGGGGGTGGGGTAAT | 1840 |
| rs769254978 | in-del | -/AAA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076459 | CAATACTCTGCCTGG[-/AAA]AAAAAAAAAAAAAAA | 1840 |
| rs769261718 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113085524 | TGGTTCCTTCTTTTG[C/T]CAATTACTTGTGTAT | 1840 |
| rs769274808 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059886 | AGCCACACTTCAAGT[A/G]CTCATAGCCACATGT | 1840 |
| rs769316492 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086686 | TTCTTGCAGTGATTT[A/T]ATGCTTTTATTTTTA | 1840 |
| rs769367510 | snp | A/G | 4.97269e-05 | 0.00498608 | missense | DTX1 | GRCh38.p7 | 12:113095084 | AAGGCCATCTACGGG[A/G]AGAAGACGGGTACGC | 1840 |
| rs769386039 | snp | A/G | 1.67172e-05 | 0.00289108 | missense | DTX1 | GRCh38.p7 | 12:113058412 | CTTGTGCCCTACATC[A/G]TCGACCTGCAGTCCA | 1840 |
| rs769419508 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074729 | GTCCAGGCAGGAGAG[A/G]TAACATGGCGGGGAC | 1840 |
| rs769437286 | snp | A/C | 1.66225e-05 | 0.00288287 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058321 | GCCCTACACGGCCAC[A/C]GTGTGCCACCACATT | 1840 |
| rs769440988 | in-del | -/G | 6.81013e-05 | 0.0058349 | intron-variant | DTX1 | GRCh38.p7 | 12:113095000 | AACGGAGTGGGGTTT[-/G]GGGGGGGTGCTGGGA | 1840 |
| rs769560618 | snp | A/G | 1.67511e-05 | 0.00289401 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096796 | ACGGGCGAGTCGGAC[A/G]CCGTGGTGTGGAACG | 1840 |
| rs769610375 | snp | C/G | 0.00121433 | 0.0246108 | missense | DTX1 | GRCh38.p7 | 12:113078089 | AGCGTGAGCGCGCGC[C/G]CCTCCATCCCGCCGG | 1840 |
| rs769705063 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079050 | CTTGTATCAAGTTTG[C/T]AAATTCTTGGGTTAA | 1840 |
| rs769754903 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113065814 | GAGGCCACGGGGAGG[A/C]CAAGGGGTTGGGGCA | 1840 |
| rs769802838 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113089214 | AGACCAGGGTGGCTG[A/G]AGTGGAGTGGGAGAG | 1840 |
| rs769810465 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067001 | CATCCCTCTGGAGCT[A/G]CTCCAGGCTGCTACT | 1840 |
| rs769814839 | snp | C/G | 4.7848e-05 | 0.00489098 | missense | DTX1 | GRCh38.p7 | 12:113093178 | GTCCCCGCACTCCCG[C/G]TGAAGAACTTGAATG | 1840 |
| rs769844860 | snp | C/T | 8.26371e-05 | 0.00642742 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095146 | CCCCCACTCGCTGCC[C/T]GGCTTCCCTGATACC | 1840 |
| rs769994337 | snp | C/G | 1.68556e-05 | 0.00290302 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077464 | CTTCTACGACCCGTC[C/G]TCGGCGCCGGGCAAG | 1840 |
| rs770052305 | snp | C/G | 2.0253e-05 | 0.00318215 | intron-variant | DTX1 | GRCh38.p7 | 12:113077376 | GCCCTTCCAGCCGCG[C/G]AGACCAACGCCCGCT | 1840 |
| rs770081786 | snp | A/C | 1.65135e-05 | 0.00287341 | missense | DTX1 | GRCh38.p7 | 12:113095403 | CTACCCAACAACGAG[A/C]AAGGCCGGAAGGTGG | 1840 |
| rs770176972 | snp | C/T | 1.76235e-05 | 0.0029684 | intron-variant | DTX1 | GRCh38.p7 | 12:113094783 | CTCCCCTGCTGCCAC[C/T]TGCAGGACTGCACCA | 1840 |
| rs770418984 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074809 | GAAGGTGGAGATGAC[G/T]GGATTTACTGACAGA | 1840 |
| rs770443174 | in-del | -/A | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086104 | AGACTCCACCTTTAC[-/A]AAAATTTTTTTAAAT | 1840 |
| rs770449960 | in-del | -/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088842 | CTCCTCAAAAGTTTT[-/G]TTGTTGTTGTTGTTG | 1840 |
| rs770453820 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075961 | CTATTACATTCTAGC[A/G]AGGGGGGGACAGACA | 1840 |
| rs770521391 | snp | A/C | | | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096935 | AGGCTGCAGCCAAGG[A/C]TTGAGGCCCAAGGCT | 1840 |
| rs770631802 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067074 | ATGAGGGAGTCTGGC[A/G]CTGGGCCCTGGAGCT | 1840 |
| rs770789647 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097944 | GTGGGAGTCAGCCAA[C/G]ATTTAAAGGGATGCC | 1840 |
| rs770821504 | in-del | -/AAATAAATA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113094583 | TCTCTTAATAAAAAT[-/AAATAAATA]AAATAAATAAAATAA | 1840 |
| rs770840978 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086761 | TTTCAGGGGTTTGAA[A/G]ATGTTAAAGTACTGA | 1840 |
| rs770880667 | snp | C/G | 3.61441e-05 | 0.00425097 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096921 | CCAGGGCGTATCCGA[C/G]GCTGCAGCCAAGGCT | 1840 |
| rs770881701 | in-del | -/C | 1.65551e-05 | 0.00287702 | frameshift-variant | DTX1 | GRCh38.p7 | 12:113095170 | TGATACCCAGACCAT[-/C]CGCATCGTCTATGAC | 1840 |
| rs770925152 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087179 | TCTGAGCCTCCAATA[A/C]CACTCACACCTCAAA | 1840 |
| rs770929713 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083367 | GTCTTGCTCTGTTAC[C/T]CAGGCTGGAGTGCAG | 1840 |
| rs770996258 | snp | A/G | 1.67947e-05 | 0.00289777 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077593 | GTGGCTCGACCTCTC[A/G]TCGCTAGGCTTCTGC | 1840 |
| rs771003813 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113080156 | GGGTCATGGGGACAA[A/G]CAGAGGTGTGTCCCA | 1840 |
| rs771049060 | snp | C/T | 5.04944e-05 | 0.00502441 | missense | DTX1 | GRCh38.p7 | 12:113094861 | CGGCACAAGGGCGTG[C/T]GGCCTGAGCTCGTGG | 1840 |
| rs771282138 | snp | C/G | | | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057957 | ACACTTGCTTTCCAG[C/G]GCAGCACCCTTTATC | 1840 |
| rs771384225 | in-del | -/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113063383 | GCCTCACCCAGACCC[-/T]GAATTTCCCACCCAG | 1840 |
| rs771433085 | snp | C/T | 2.25157e-05 | 0.00335519 | missense | DTX1 | GRCh38.p7 | 12:113093566 | TACTGCTGTGCGCGG[C/T]CGGGCTGCCCGTGTG | 1840 |
| rs771449972 | snp | A/G | 1.65282e-05 | 0.00287469 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095411 | CAACGAGAAAGGCCG[A/G]AAGGTGGGTGCCCAG | 1840 |
| rs771463239 | snp | A/G | 1.95185e-05 | 0.00312392 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093600 | GACGCGGGCCCCCAA[A/G]CCCATCCTGCACCCG | 1840 |
| rs771488666 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113094622 | CGAAGAAGAAGAAAA[A/G]AAAATAAAACAATGT | 1840 |
| rs771516456 | in-del | -/TTG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088842 | TCCTCAAAAGTTTTG[-/TTG]TTGTTGTTGTTGTTG | 1840 |
| rs771660342 | snp | A/G | 1.64849e-05 | 0.00287092 | missense | DTX1 | GRCh38.p7 | 12:113095377 | CAAGAGGATTCCCTC[A/G]CCACTGCTATCTACC | 1840 |
| rs771706036 | snp | C/T | 1.8504e-05 | 0.00304165 | missense | DTX1 | GRCh38.p7 | 12:113058224 | ACGGTGGGCTGATGC[C/T]TGTGAATGGTCTGGG | 1840 |
| rs771760072 | snp | C/T | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113054951 | TATTTAAGTGCCTGG[C/T]ACATAATAGGCACTC | 1840 |
| rs771798553 | snp | A/T | 3.37462e-05 | 0.00410755 | intron-variant | DTX1 | GRCh38.p7 | 12:113094964 | TGGGTTGGGCGGGAC[A/T]ATGGCTGAGGAGTGG | 1840 |
| rs771815949 | snp | A/C/G | 1.64768e-05 | 0.00287021 | synonymous-codon, missense | DTX1 | GRCh38.p7 | 12:113095354 | CAACCCCGGGAAGAA[A/C/G]TTCACCGCAAGAGGA | 1840 |
| rs771912351 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083121 | ACCTGTCTGTGTCTT[A/T]ATCTTCTCTTCTTAG | 1840 |
| rs772029371 | snp | C/T | 5.05412e-05 | 0.00502673 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113094872 | CGTGCGGCCTGAGCT[C/T]GTGGGCCGCCTGGGC | 1840 |
| rs772119988 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113068692 | CACTAGGGAGCTATT[A/G]ATAGCTGTGGAGCAG | 1840 |
| rs772262066 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067507 | CAGATGCTTACAGGG[C/T]CTGGGCAACTAATAG | 1840 |
| rs772277056 | snp | C/G | 1.78742e-05 | 0.00298945 | missense | DTX1 | GRCh38.p7 | 12:113077617 | CTTCTGCTACCTCAT[C/G]TACTTCAACAGCATG | 1840 |
| rs772328217 | snp | A/C | 0.000827472 | 0.0203237 | missense | DTX1 | GRCh38.p7 | 12:113077841 | CGCAGCGCCGCAAGG[A/C]GCCCCCCGCGCCCCC | 1840 |
| rs772474000 | snp | A/G | 1.70892e-05 | 0.00292306 | missense | DTX1 | GRCh38.p7 | 12:113058440 | CCATGCACCAGTTTC[A/G]CCAGGACACAGGTGA | 1840 |
| rs772480005 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113073667 | TAACAGAGGAGAGGG[C/T]AGAGGACAAGCTCTT | 1840 |
| rs772483016 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113081286 | GTGAGCCGAGATCAC[C/G]CCACTGCACTCCAGC | 1840 |
| rs772491457 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097969 | GATGCCAGCGATTGC[G/T]CTTTTCAAAACCTAC | 1840 |
| rs772495341 | snp | C/G | 1.67363e-05 | 0.00289272 | intron-variant | DTX1 | GRCh38.p7 | 12:113094030 | CCCACCCCGCTGTGT[C/G]CCTGCAGGTAAGAAT | 1840 |
| rs772603999 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059785 | GCTGTGCCAACCAAT[A/T]TGTTAGCCACCAACC | 1840 |
| rs772620740 | snp | G/T | 5.24379e-05 | 0.00512018 | intron-variant | DTX1 | GRCh38.p7 | 12:113093714 | GAGTACGCCCTCCAC[G/T]CCCTGCCTCACACGA | 1840 |
| rs772666461 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074123 | AATGCCAGCTACTTG[A/G]GAGTCTGAGGCAGGA | 1840 |
| rs772719370 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074730 | TCCAGGCAGGAGAGA[C/T]AACATGGCGGGGACT | 1840 |
| rs772758951 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091765 | GACCTGAACAGGCAC[A/G]GCCAGAGCCAAGGGG | 1840 |
| rs772784416 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059907 | AGCCACATGTGTCTT[A/G]TGGTACCTTGTGGGC | 1840 |
| rs772810139 | in-del | -/G | 6.81013e-05 | 0.0058349 | intron-variant | DTX1 | GRCh38.p7 | 12:113095001 | AACGGAGTGGGGTTT[-/G]GGGGGGTGCTGGGAA | 1840 |
| rs772831452 | snp | C/G | 7.2889e-05 | 0.00603649 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113078103 | CGCCTCCATCCCGCC[C/G]GGGTAAGACGGGGCC | 1840 |
| rs772847249 | snp | C/T | 1.65666e-05 | 0.00287802 | missense | DTX1 | GRCh38.p7 | 12:113095091 | TCTACGGGGAGAAGA[C/T]GGGTACGCAGCCGCC | 1840 |
| rs772900345 | snp | A/G | 6.61168e-05 | 0.00574926 | missense | DTX1 | GRCh38.p7 | 12:113095147 | CCCCACTCGCTGCCC[A/G]GCTTCCCTGATACCC | 1840 |
| rs772910068 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113094219 | TTCCTTTCTTCACTT[C/T]ATGAGGTTTTTTGAT | 1840 |
| rs772927773 | snp | A/C | 8.70133e-05 | 0.00659538 | intron-variant | DTX1 | GRCh38.p7 | 12:113094111 | TGAGGTGAGGAGGGG[A/C]TGGGGGGGCTGGGGG | 1840 |
| rs772987117 | snp | A/G | 9.52381e-05 | 0.0069 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093180 | CCCCGCACTCCCGGT[A/G]AAGAACTTGAATGGT | 1840 |
| rs773095370 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113089096 | TGTGCTAAGTGAGGG[A/C]GTGTGCCATGAGGAT | 1840 |
| rs773105205 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066014 | TCTGGAATCACAACC[A/G]GTGGTAGCCAGTCCC | 1840 |
| rs773106047 | snp | C/T | 1.79149e-05 | 0.00299285 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096918 | AGCCCAGGGCGTATC[C/T]GAGGCTGCAGCCAAG | 1840 |
| rs773127297 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084416 | TGTGAGACAGGGTCT[C/T]ACTCCGTCACCCAGG | 1840 |
| rs773143354 | snp | A/G | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056308 | TCTTCAGATTCCACG[A/G]TTCCAACTGAGTCTG | 1840 |
| rs773182515 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113085549 | GTGTATTTCTTTGGC[G/T]TATCCTTCCCTGGAG | 1840 |
| rs773287455 | in-del | -/G | 3.13858e-05 | 0.0039613 | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058171 | AATAGTGGGGGACCT[-/G]GCCCCTGAGGCAGTG | 1840 |
| rs773406571 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069104 | AAGCATTTAGAACAG[C/T]GCCTGGCACATAGTA | 1840 |
| rs773439961 | snp | C/T | 1.69746e-05 | 0.00291325 | stop-gained | DTX1 | GRCh38.p7 | 12:113094810 | ACCATCTGCATGGAG[C/T]GACTGGTCACAGCAT | 1840 |
| rs773528525 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097844 | CGTTGGGAGTGGGCA[-/G]TGGGGTGGCTAATTG | 1840 |
| rs773620428 | snp | A/G | 4.11963e-05 | 0.00453833 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093585 | GCTGCCCGTGTGCCT[A/G]ACGCGGGCCCCCAAG | 1840 |
| rs773710321 | snp | C/T | 1.65233e-05 | 0.00287426 | missense | DTX1 | GRCh38.p7 | 12:113095409 | AACAACGAGAAAGGC[C/T]GGAAGGTGGGTGCCC | 1840 |
| rs773769178 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061277 | CTCCCACCCCAACCA[C/G]AGAGGGAGGAAGGCC | 1840 |
| rs773780570 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113081021 | TTGCATCATTTCTGC[A/T]TATGTTTAATAGGTT | 1840 |
| rs773791295 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088336 | AGCGGTAAGGCATGC[C/T]GAAATTGATTAGTAA | 1840 |
| rs773798074 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061638 | AACTAATTATCTACT[A/G]TGCATCTAGCACGTG | 1840 |
| rs773827724 | snp | A/C | 8.26918e-05 | 0.00642955 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095161 | CGGCTTCCCTGATAC[A/C]CAGACCATCCGCATC | 1840 |
| rs773979093 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113072399 | AGAACAGAGAAGCCC[A/G]TGTTGGAGGAGATGA | 1840 |
| rs774015603 | snp | G/T | 0.000236008 | 0.0108604 | missense | DTX1 | GRCh38.p7 | 12:113094817 | GCATGGAGCGACTGG[G/T]CACAGCATCAGGCTA | 1840 |
| rs774073151 | in-del | -/GGCCACGTGATACTATCCTGTAT | 1.65921e-05 | 0.00288024 | intron-variant | DTX1 | GRCh38.p7 | 12:113095431 | GGGTGCCCAGCCGTG[-/GGCCACGTGATACTATCCTGTAT]AGGGCATGGGAGATA | 1840 |
| rs774141564 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113093389 | TGGCCCGCAGAAAGG[C/T]CCTTCAGGGGCCTTC | 1840 |
| rs774153722 | snp | C/T | 4.92211e-05 | 0.00496066 | missense | DTX1 | GRCh38.p7 | 12:113093206 | ATGGTACTGGGCCGG[C/T]CCATCCGGCCCTGGC | 1840 |
| rs774183903 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092618 | AAATGCTTTTGAAAA[C/T]CTGGACTTATCATTG | 1840 |
| rs774194774 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113094571 | CAACAGAGCCTGTCT[C/T]TTAATAAAAATAAAT | 1840 |
| rs774220510 | snp | C/G | 1.81421e-05 | 0.00301176 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096922 | CAGGGCGTATCCGAG[C/G]CTGCAGCCAAGGCTT | 1840 |
| rs774338569 | snp | A/G | 4.95913e-05 | 0.00497928 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095414 | CGAGAAAGGCCGGAA[A/G]GTGGGTGCCCAGCCG | 1840 |
| rs774451194 | snp | A/T | 1.71437e-05 | 0.00292772 | missense | DTX1 | GRCh38.p7 | 12:113077603 | CTCTCATCGCTAGGC[A/T]TCTGCTACCTCATCT | 1840 |
| rs774594866 | snp | C/G | 1.66466e-05 | 0.00288496 | missense | DTX1 | GRCh38.p7 | 12:113077503 | GTGGGAGTGGGAGAA[C/G]GACGGCGGCGCATGG | 1840 |
| rs774623498 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113080210 | CCAGTGCCAACAGAG[A/G]GCAGACTTGAGGGGG | 1840 |
| rs774637405 | snp | A/G | 3.3243e-05 | 0.00407681 | missense | DTX1 | GRCh38.p7 | 12:113058322 | CCCTACACGGCCACC[A/G]TGTGCCACCACATTG | 1840 |
| rs774654077 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097237 | GTTGAACTCATGCAC[A/G]CACACCCACGTGCCT | 1840 |
| rs774676784 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067180 | CACAGCCACCTCTTG[G/T]CCCGATGACCGACTG | 1840 |
| rs774692655 | in-del | -/CCGGG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086999 | CTGCACGTGGCTGCC[-/CCGGG]CCGGGCCGTGGGAAC | 1840 |
| rs774794767 | snp | A/T | 1.92188e-05 | 0.00309984 | missense | DTX1 | GRCh38.p7 | 12:113093604 | CGGGCCCCCAAGCCC[A/T]TCCTGCACCCGCCGC | 1840 |
| rs774831457 | snp | A/C/G | 6.83041e-05 | 0.00584363 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058249 | TCTGGGCTTCCCACC[A/C/G]CAGAACGTGGCCCGG | 1840 |
| rs774833229 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113089495 | GGCAGAGCTAGGGGT[A/G]AAGGCTGGCTCCCCT | 1840 |
| rs774857509 | snp | C/T | | | utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113058019 | AGCCTGGATGGCCAT[C/T]CCACATTCCTTTAAC | 1840 |
| rs774864002 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113090614 | TCCCATCCTGCCTCC[C/T]TCGGGAGCTGTGTTC | 1840 |
| rs774870643 | in-del | -/TG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079700 | CCCGGCTACTGTGTG[-/TG]TGTGTGTGTGTGTGT | 1840 |
| rs774947398 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087217 | CCGAGGGGACTTTTA[C/T]ATCCTTTAATCTCTA | 1840 |
| rs774965138 | snp | C/T | 3.63828e-05 | 0.00426498 | intron-variant | DTX1 | GRCh38.p7 | 12:113093504 | TTTGGGCGGGGATGG[C/T]GCCCCGCCCTGTGAC | 1840 |
| rs775024092 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113064302 | CCAACCACCAGTCAC[A/G]CTGTCTGTATTTCTA | 1840 |
| rs775057383 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084083 | CAGAGAGGGGGATTG[A/G]CTCATCTAGGGTCAC | 1840 |
| rs775076085 | snp | C/T | 1.84072e-05 | 0.00303369 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058225 | CGGTGGGCTGATGCC[C/T]GTGAATGGTCTGGGC | 1840 |
| rs775222170 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113058583 | CCTCACCTCCAGAAA[A/C]ACAGGGCAGTCTAAC | 1840 |
| rs775279252 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083172 | ATTAGGGCCCATCCT[A/G]GTGACCTCATTTTAT | 1840 |
| rs775292199 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075182 | TTATGCCCATTTTCA[A/G]CATGAGAAAACTGGG | 1840 |
| rs775322257 | snp | A/G | 1.91944e-05 | 0.00309788 | missense | DTX1 | GRCh38.p7 | 12:113077628 | TCATCTACTTCAACA[A/G]CATGTCGCAGATGAA | 1840 |
| rs775335959 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113063090 | ACTGAGCCAAGTGCC[C/T]GGTTTCCCTCAAAGC | 1840 |
| rs775359324 | snp | A/G | 1.68465e-05 | 0.00290223 | missense | DTX1 | GRCh38.p7 | 12:113094873 | GTGCGGCCTGAGCTC[A/G]TGGGCCGCCTGGGCC | 1840 |
| rs775410118 | snp | A/G | 1.68801e-05 | 0.00290512 | intron-variant | DTX1 | GRCh38.p7 | 12:113094965 | GGGTTGGGCGGGACA[A/G]TGGCTGAGGAGTGGG | 1840 |
| rs775410588 | snp | A/G | | | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077515 | GAACGACGGCGGCGC[A/G]TGGACGGCCTACGAT | 1840 |
| rs775483051 | snp | A/T | 1.74989e-05 | 0.00295789 | intron-variant | DTX1 | GRCh38.p7 | 12:113093718 | ACGCCCTCCACGCCC[A/T]GCCTCACACGAGATG | 1840 |
| rs775561467 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113068784 | ACTGAACATTGCAAA[G/T]GGTGGACACTGGGAC | 1840 |
| rs775671176 | in-del | -/AG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075827 | TGAATTAAAAAAAAA[-/AG]AATCCATTTGTGACC | 1840 |
| rs775708250 | snp | C/T | 2.01157e-05 | 0.00317134 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096724 | CCCCAGGTGCTGCGG[C/T]TGCTCATCACGGCCT | 1840 |
| rs775753236 | in-del | -/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113080090 | TAATTTTCCAGGGAT[-/G]GCATCACAGCCACTA | 1840 |
| rs775824567 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113098064 | GAGAGGGGTGGGTGG[C/T]TCTGTTCCTGGGGGC | 1840 |
| rs775838265 | snp | A/C | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113054978 | ACTCAGTAAATGACA[A/C]CCTTATGTAATGGGG | 1840 |
| rs775900132 | snp | C/G | 1.66056e-05 | 0.00288141 | missense | DTX1 | GRCh38.p7 | 12:113058330 | GGCCACCGTGTGCCA[C/G]CACATTGAGAACGTG | 1840 |
| rs775966876 | snp | C/T | 3.31153e-05 | 0.00406898 | missense | DTX1 | GRCh38.p7 | 12:113095097 | GGGAGAAGACGGGTA[C/T]GCAGCCGCCTGGGAA | 1840 |
| rs776025734 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113080640 | GAAAACAGAATAGAA[C/G]TAGAATAGATTGGCA | 1840 |
| rs776026102 | snp | C/T | 6.37816e-05 | 0.00564683 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113094045 | CCCTGCAGGTAAGAA[C/T]CCCGAGGATGTGGTT | 1840 |
| rs776064738 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091535 | AATGTGTCCCGGGGA[G/T]TATGATAAGTCTGTG | 1840 |
| rs776132940 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113085423 | ACATTGCCAAGCTGA[G/T]AATTCCTAAAGAGAC | 1840 |
| rs776182768 | snp | C/G | 1.74698e-05 | 0.00295544 | missense | DTX1 | GRCh38.p7 | 12:113058239 | CTGTGAATGGTCTGG[C/G]CTTCCCACCGCAGAA | 1840 |
| rs776186506 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113073709 | TAGGGACACACCAGT[A/G]TGGAACAGTCTGAGT | 1840 |
| rs776252968 | snp | A/G | 3.37604e-05 | 0.00410841 | intron-variant | DTX1 | GRCh38.p7 | 12:113094976 | GACAATGGCTGAGGA[A/G]TGGGCAGGGAACGGA | 1840 |
| rs776268282 | in-del | -/CAAA | | | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096439 | AGCAAGACTCTGCCT[-/CAAA]AAAAAAAAAAAAAAA | 1840 |
| rs776295045 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113064385 | TGAAACTAAATTCAT[C/T]GCTCGTATTTGGTAG | 1840 |
| rs776328674 | snp | A/G | 1.66363e-05 | 0.00288407 | missense | DTX1 | GRCh38.p7 | 12:113058316 | TGGCGGCCCTACACG[A/G]CCACCGTGTGCCACC | 1840 |
| rs776369082 | in-del | -/TG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088844 | CCTCAAAAGTTTTGT[-/TG]TTGTTGTTGTTGTTG | 1840 |
| rs776388027 | snp | C/G | 1.66827e-05 | 0.00288809 | missense | DTX1 | GRCh38.p7 | 12:113095061 | GCAGCCTGCAGTGCC[C/G]CACCTGCAAGGCCAT | 1840 |
| rs776437956 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113063267 | CTGCCACTGGCAGTC[A/G]GGGAAAGGTTTGAGA | 1840 |
| rs776443157 | snp | C/G | 3.78136e-05 | 0.00434803 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113078055 | CAACCTCAACCGGCC[C/G]GGGCCCCAGCGCACC | 1840 |
| rs776517949 | snp | C/G | 1.74564e-05 | 0.0029543 | intron-variant | DTX1 | GRCh38.p7 | 12:113058459 | GGACACAGGTGAGCA[C/G]ACACCCACCCCATGC | 1840 |
| rs776575021 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113095464 | CACAGGCAGGGGCTC[C/T]AGCAACCACTGGCCT | 1840 |
| rs776692952 | in-del | -/A | | | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096202 | GAGCAAGACTCCATC[-/A]ACAAAAAAAAAAACA | 1840 |
| rs776792329 | in-del | -/GC | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066717 | CCTACTGTGTGCCAG[-/GC]GCACTGTCCGGGCAC | 1840 |
| rs776905560 | snp | A/G | 1.8789e-05 | 0.00306499 | intron-variant | DTX1 | GRCh38.p7 | 12:113094766 | CCTCCCCAGTCCTCA[A/G]TCTCCCCTGCTGCCA | 1840 |
| rs776943418 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113063463 | CAGCTCGCTCCCTGG[C/T]CTCATATGACTGGAG | 1840 |
| rs776995654 | snp | A/G | 1.85623e-05 | 0.00304645 | intron-variant | DTX1 | GRCh38.p7 | 12:113094108 | TGATGAGGTGAGGAG[A/G]GGATGGGGGGGCTGG | 1840 |
| rs777042656 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076067 | TACGTGGGGGGTGCA[A/C]ATTTTTAAATAGGAT | 1840 |
| rs777051186 | snp | C/T | 1.65704e-05 | 0.00287836 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095176 | CCAGACCATCCGCAT[C/T]GTCTATGACATCCCC | 1840 |
| rs777108960 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067633 | TGAATGGGGCCAGCA[G/T]AACTCAGCTCCTGCT | 1840 |
| rs777139751 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113065260 | CTTCACCCAGCCAGC[A/G]GGTGTCACCCCATTT | 1840 |
| rs777161946 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069075 | ATTTTGTGGCTGAAG[A/G]GTTGACTTACACGAA | 1840 |
| rs777228921 | snp | C/T | 1.834e-05 | 0.00302815 | intron-variant | DTX1 | GRCh38.p7 | 12:113058501 | CCGAGCCATCACTAC[C/T]TTGCAGCGTAGGATG | 1840 |
| rs777276313 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087804 | AAGTAACAAGTCTAG[A/G]CCTGCTGGGGGTGGG | 1840 |
| rs777328428 | in-del | -/A | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076644 | TGGATGACTGCAGGC[-/A]ACGAATGAATGACCT | 1840 |
| rs777379038 | in-del | -/TG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091245 | GTGTGCACAAGTCTC[-/TG]TGTATGTAGGTGTGG | 1840 |
| rs777379341 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113080063 | AGGGTTGGCATGGAG[A/G]GCGGGGAAGCTGTAA | 1840 |
| rs777380882 | snp | A/G | 1.82593e-05 | 0.00302148 | intron-variant | DTX1 | GRCh38.p7 | 12:113058485 | CATGCCACCCGCCCC[A/G]CCGAGCCATCACTAC | 1840 |
| rs777396163 | in-del | -/GAG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074519 | AGGTAGACAATGCCA[-/GAG]GAGGACAGGGCCCCA | 1840 |
| rs777432523 | snp | A/G | 3.34739e-05 | 0.00409095 | missense | DTX1 | GRCh38.p7 | 12:113058415 | GTGCCCTACATCATC[A/G]ACCTGCAGTCCATGC | 1840 |
| rs777497264 | snp | A/C/G | 5.0536e-05 | 0.00502652 | missense | DTX1 | GRCh38.p7 | 12:113093547 | CCCCCAGGGATGACC[A/C/G]GGATACTGCTGTGCG | 1840 |
| rs777503098 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076795 | CTTAAATTAATGAAC[A/T]AAGGCATGAACAGAT | 1840 |
| rs777585807 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092493 | GGGCCAGAGGAAGAG[A/G]AGAGTCAGGATACCT | 1840 |
| rs777640703 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113081412 | TTCATGGCCTAGTGT[G/T]AATTCTCCAAATATG | 1840 |
| rs777710897 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067024 | CTGCTACTGCTGCCT[C/G]CACAGACAGCAGTGG | 1840 |
| rs777776829 | in-del | -/CTCTT | 1.65649e-05 | 0.00287788 | intron-variant | DTX1 | GRCh38.p7 | 12:113093142 | GAGTCCAGCTGCGGC[-/CTCTT]CTCTTCTCCCCGCAG | 1840 |
| rs777781996 | snp | C/T | 5.26413e-05 | 0.00513009 | intron-variant | DTX1 | GRCh38.p7 | 12:113093491 | CAGTGGTCGGGGGTT[C/T]GGGCGGGGATGGCGC | 1840 |
| rs777814639 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097865 | TGGCTAATTGTCTTC[C/G]GCCAACCAGGGGCCT | 1840 |
| rs777817071 | snp | G/T | 1.64996e-05 | 0.0028722 | intron-variant | DTX1 | GRCh38.p7 | 12:113095277 | ATGCTTCTCCACCCT[G/T]CCACCACCTGTTCAT | 1840 |
| rs777863594 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113072960 | GATCCACCCGCCTCA[A/G]CTTCCCAAAGTGTTG | 1840 |
| rs777866361 | snp | A/C/T | 3.29567e-05 | 0.00405924 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095360 | CGGGAAGAAGTTCAC[A/C/T]GCAAGAGGATTCCCT | 1840 |
| rs777879482 | snp | C/T | 4.8129e-05 | 0.00490532 | missense | DTX1 | GRCh38.p7 | 12:113058199 | GTGGCGGCCATGTCA[C/T]GGCCAGGCCACGGTG | 1840 |
| rs777921102 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060805 | TAGAGGGCAGGGCTG[C/T]GAGAGCAGAAGTGGG | 1840 |
| rs777927732 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113068394 | GGAGTCCCCAAGGAG[C/T]GAGTGGTTTGCCCTA | 1840 |
| rs777971051 | snp | A/G | 6.74286e-05 | 0.00580601 | missense | DTX1 | GRCh38.p7 | 12:113094921 | CACCTGCTGTGCCTC[A/G]TGGCCATGTACTCCA | 1840 |
| rs778040871 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069394 | GTAGCCTCTCCGAGT[A/G]CCACGCAGCCCTTCA | 1840 |
| rs778137992 | in-del | -/ACCCCATCCTCTCC | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097689 | TCTCCCATCCTCCCT[-/ACCCCATCCTCTCC]ACCAAATCGCTCCCA | 1840 |
| rs778166167 | snp | A/G | 3.02741e-05 | 0.00389052 | intron-variant, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096699 | TCCCGGCCCCACTGT[A/G]TCCCTGTCCCCCCAG | 1840 |
| rs778187252 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113071670 | GGAGCATTTCCACCA[C/T]TGCTCCCTTAGAAAT | 1840 |
| rs778250420 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088590 | TTGTGCACATGTACC[C/G]TAGAACTTAAAGTAT | 1840 |
| rs778389858 | in-del | -/AT | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091510 | TCTGTGTACTTAAAC[-/AT]GTGTGTGTAATGTGT | 1840 |
| rs778414779 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083824 | CACCCTCCTTCTCTC[C/G]CCTCCTGGACCCAAA | 1840 |
| rs778442674 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084618 | TCAAATTCCTGGGCT[A/C]AAGTGATCCTCTCGC | 1840 |
| rs778449629 | snp | A/G | 0.000517063 | 0.0160706 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113077785 | CCAGCAGTGCCTGCT[A/G]GTCAACAGCACGCGC | 1840 |
| rs778633439 | snp | C/T | 4.94727e-05 | 0.00497332 | intron-variant | DTX1 | GRCh38.p7 | 12:113095290 | CTGCCACCACCTGTT[C/T]ATGGTCTAAATCCCT | 1840 |
| rs778651621 | snp | A/G | 1.81066e-05 | 0.00300882 | splice-acceptor-variant | DTX1 | GRCh38.p7 | 12:113077422 | CCCCATTTCGAGTAC[A/G]GGCACCATGCGGCCC | 1840 |
| rs778898103 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091324 | ATGTTTGTGGGGGGC[A/G]TGCCCTGAAGTGTGC | 1840 |
| rs778919730 | snp | A/G | 1.67321e-05 | 0.00289236 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058291 | GGAGTGGCTGAATGA[A/G]CACAGCCGCTGGCGG | 1840 |
| rs778962161 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087900 | CAGTTGTCAGTGTTT[C/T]GGGATCCTGGACCCC | 1840 |
| rs778962753 | snp | C/T | 9.65135e-05 | 0.00694604 | missense | DTX1 | GRCh38.p7 | 12:113093554 | GGATGACCGGGATAC[C/T]GCTGTGCGCGGCCGG | 1840 |
| rs779019282 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113063377 | CCGAGGGCCTCACCC[A/G]GACCCTGAATTTCCC | 1840 |
| rs779094194 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113092668 | CAGGGCTTGTCAGAG[C/G]CTTTAATATGCTCAG | 1840 |
| rs779103936 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061223 | GGGAAAAAAAACACT[C/G]ATTCCTAAATGGACT | 1840 |
| rs779113022 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113071659 | GCGGAGGAGAAGGAG[C/T]ATTTCCACCACTGCT | 1840 |
| rs779115803 | snp | A/G | 0.000261301 | 0.0114273 | missense | DTX1 | GRCh38.p7 | 12:113077832 | TCCTGGCCTCGCAGC[A/G]CCGCAAGGCGCCCCC | 1840 |
| rs779122834 | snp | C/T | 1.68388e-05 | 0.00290158 | intron-variant | DTX1 | GRCh38.p7 | 12:113095019 | GGGGTGCTGGGAACT[C/T]ACTGCCAGCCTCCCC | 1840 |
| rs779156990 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062426 | TCATATCTTTTTCAC[A/G]GGTCATGAAATATTC | 1840 |
| rs779181161 | in-del | -/GAG | 1.79703e-05 | 0.00299747 | intron-variant | DTX1 | GRCh38.p7 | 12:113094102 | CCCACCTGATGAGGT[-/GAG]GAGGGGATGGGGGGG | 1840 |
| rs779293277 | snp | C/T | 1.69103e-05 | 0.00290773 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096773 | TCACTATCGGCACGT[C/T]CAACACCACGGGCGA | 1840 |
| rs779298324 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113085289 | TCCTGACCTCAAGCA[A/G]TCCACCCACCTTAGC | 1840 |
| rs779383413 | snp | A/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113078573 | TTCCACCAAACAGTT[A/C]TACCATGTGCATATT | 1840 |
| rs779478688 | in-del | -/TGTG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091341 | GCCCTGAAGTGTGCC[-/TGTG]TGTATCCATGTATAT | 1840 |
| rs779619837 | snp | A/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059649 | GCAGCCTAGAAATCC[A/T]TGGCATGTTTGACCC | 1840 |
| rs779630326 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074492 | GCTGGAATGGAGTGA[C/G]TGATAAGGGGGAGGT | 1840 |
| rs779682979 | snp | C/G | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055949 | GGGGGACTGGCCATC[C/G]CGTTAACACTTGAGC | 1840 |
| rs779691369 | snp | G/T | 1.67894e-05 | 0.00289731 | intron-variant | DTX1 | GRCh38.p7 | 12:113095462 | GGCACAGGCAGGGGC[G/T]CCAGCAACCACTGGC | 1840 |
| rs779715260 | snp | C/T | 0.000115564 | 0.00760057 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113095399 | CTATCTACCCAACAA[C/T]GAGAAAGGCCGGAAG | 1840 |
| rs779768333 | snp | C/G/T | 6.70733e-05 | 0.00579076 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113093567 | ACTGCTGTGCGCGGC[C/G/T]GGGCTGCCCGTGTGC | 1840 |
| rs779782765 | in-del | -/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060588 | TGCATCTCCCACCAA[-/G]GGGAAGATGGTGCAA | 1840 |
| rs779809231 | snp | C/G | 0.000315778 | 0.0125614 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096953 | GAGGCCCAAGGCTGC[C/G]CACCTTCCCTCCTGC | 1840 |
| rs779811842 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076177 | AAAAAAGCATAAGGG[G/T]CCCAGGGGCGGTGGC | 1840 |
| rs779879751 | snp | C/G | 1.67719e-05 | 0.0028958 | intron-variant | DTX1 | GRCh38.p7 | 12:113095038 | GCCAGCCTCCCCTGC[C/G]CAGGATGGCAGCCTG | 1840 |
| rs779966752 | snp | A/G | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056184 | CAGGGCTGGGAACTG[A/G]GTACTGGCAGGAGAT | 1840 |
| rs780013460 | snp | C/T | 1.66029e-05 | 0.00288117 | missense | DTX1 | GRCh38.p7 | 12:113058371 | ACGCTCGCGGTTCCG[C/T]GGTCCTGGGGCAGGT | 1840 |
| rs780078089 | in-del | -/A | | | intron-variant, downstream-variant-500B | DTX1, RASAL1 | GRCh38.p7 | 12:113096204 | GCAAGACTCCATCAC[-/A]AAAAAAAAAAACAGG | 1840 |
| rs780127794 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113088680 | TAAGGTAAGGACAAA[G/T]ATGGGCTTTTTAAAA | 1840 |
| rs780164893 | snp | C/T | 1.66474e-05 | 0.00288503 | synonymous-codon | DTX1 | GRCh38.p7 | 12:113058312 | CCGCTGGCGGCCCTA[C/T]ACGGCCACCGTGTGC | 1840 |
| rs780182986 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113090083 | ACCAACCAGTGGTGG[C/T]ATGCATGCTCAATAT | 1840 |
| rs780216540 | snp | A/T | 1.82727e-05 | 0.00302258 | intron-variant | DTX1 | GRCh38.p7 | 12:113058493 | CCGCCCCGCCGAGCC[A/T]TCACTACCTTGCAGC | 1840 |
| rs780285696 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113075638 | AGAGCTTTGGCAAAC[A/G]TGAAGCTGTGGTTTG | 1840 |
| rs780332224 | snp | A/G | 1.68097e-05 | 0.00289906 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096785 | CGTCCAACACCACGG[A/G]CGAGTCGGACACCGT | 1840 |
| rs780341652 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057633 | AGAGGGAACAAGGGG[A/G]CAGGGACGCCCCCTT | 1840 |
| rs780368376 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113067008 | CTGGAGCTGCTCCAG[G/T]CTGCTACTGCTGCCT | 1840 |
| rs780438914 | snp | C/T | 1.99432e-05 | 0.00315772 | intron-variant | DTX1 | GRCh38.p7 | 12:113094743 | TGCTGACCCAGTAGG[C/T]GCCCTGCCCTCCCCA | 1840 |
| rs780498275 | snp | C/T | 1.66299e-05 | 0.00288352 | stop-gained | DTX1 | GRCh38.p7 | 12:113058394 | GGGCAGGTGGACGCC[C/T]AGCTTGTGCCCTACA | 1840 |
| rs780529307 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113087069 | CCCTGCCCCCAACCA[G/T]CTCCTCCCGTTCCTT | 1840 |
| rs780617702 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097057 | CCTGCGGAAGGGGCC[A/G]CAGCCATTCAGGGGA | 1840 |
| rs780665529 | snp | C/T | 1.67775e-05 | 0.00289629 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096874 | TACCCGGACGCTAGC[C/T]ACCTAGACAACGTGC | 1840 |
| rs780716565 | snp | C/T | 3.25759e-05 | 0.0040357 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096982 | GCTTTGCCCCTGGTC[C/T]GGCAAATGCCTCCTT | 1840 |
| rs780726494 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097544 | AGCAGTTCTACAAAA[-/G]GAATGGCCAGCACGA | 1840 |
| rs780775776 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062499 | ACTTCCTGAGCTGCA[C/T]GATAGCAGATGGTGG | 1840 |
| rs780785694 | snp | A/G | 3.41227e-05 | 0.0041304 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096766 | CTCATCTTCACTATC[A/G]GCACGTCCAACACCA | 1840 |
| rs780787756 | snp | A/C | 8.64685e-05 | 0.00657471 | missense | DTX1 | GRCh38.p7 | 12:113093685 | CGCAAGACCAAGAAG[A/C]AGCACCTTAAAAAGA | 1840 |
| rs780806237 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097710 | TCCTCTCCACCAAAT[C/T]GCTCCCAATTTTGAG | 1840 |
| rs780925437 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062128 | TGAAATCAACACAAG[C/T]TTCTGTCTAGATTTT | 1840 |
| rs780936368 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086467 | GAAGGTTGCGGTTAG[A/G]ACTTTGGCTTTTGCT | 1840 |
| rs781092928 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113090302 | AAGTATAGAGAGGGA[A/G]GAAGTTAGAGTGGTG | 1840 |
| rs781104104 | snp | C/T | 4.93157e-05 | 0.00496542 | missense | DTX1 | GRCh38.p7 | 12:113093176 | GGGTCCCCGCACTCC[C/T]GGTGAAGAACTTGAA | 1840 |
| rs781143343 | in-del | -/C | | | intron-variant | DTX1 | GRCh38.p7 | 12:113069942 | GGGTTGGAACCTCAG[-/C]CATGTCACTTACTTA | 1840 |
| rs781145939 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113078933 | AAGCCAGGCAAACGA[A/G]AGTCTGTCTCTCTGC | 1840 |
| rs781208725 | snp | C/T | 5.48642e-05 | 0.00523728 | intron-variant | DTX1 | GRCh38.p7 | 12:113058479 | CCACCCCATGCCACC[C/T]GCCCCGCCGAGCCAT | 1840 |
| rs781215012 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060332 | GGACCTACACTGAAG[G/T]TCCTGGTGTGGTCAG | 1840 |
| rs781244758 | snp | G/T | 0.000123293 | 0.00785055 | intron-variant | DTX1 | GRCh38.p7 | 12:113093488 | GGCCAGTGGTCGGGG[G/T]TTTGGGCGGGGATGG | 1840 |
| rs781249707 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113065481 | CCCGGGACAGACCCC[C/T]TCGCAGCCCTCTCCC | 1840 |
| rs781275547 | snp | C/T | 3.41927e-05 | 0.00413463 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096900 | CGTGCTGGCTGAGCT[C/T]ACAGCCCAGGGCGTA | 1840 |
| rs781334173 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113071561 | GGCCACCAGCCTGAG[A/G]CCCAGCCTCTTTCCC | 1840 |
| rs781341992 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113080014 | GGCAGTAGTTCAGCC[A/G]TGGCCGTTAGGACTA | 1840 |
| rs781419270 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113063625 | TCCAAAGATGCCATA[C/G]CCGAGGCTGCAAGCC | 1840 |
| rs781463465 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057745 | CAGTTGGGAGTGCAA[A/C]GGGCTGGCTGAGAGC | 1840 |
| rs781498169 | in-del | -/CA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084997 | TGGCAACACAGGCCC[-/CA]ATAGTCCATCATGAA | 1840 |
| rs781510694 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113076728 | GTGAACTAGGGCATG[A/G]ATAAGTGAATGAACT | 1840 |
| rs781592142 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113062653 | GTGTACCAAGGTACA[C/T]GTGCGTGTGCGTACA | 1840 |
| rs781647069 | in-del | -/GTGA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091281 | CATTCCCTGGAATAT[-/GTGA]GTGTGTGTGTATCTT | 1840 |
| rs781675893 | snp | A/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086846 | CCACTTTTCTGCCCC[A/G]CTAGCCACTGGTGTG | 1840 |
| rs781753209 | snp | A/G | 1.68117e-05 | 0.00289923 | missense | DTX1 | GRCh38.p7 | 12:113094853 | GCGTGCTTCGGCACA[A/G]GGGCGTGCGGCCTGA | 1840 |
| rs781769396 | snp | C/G | 1.69559e-05 | 0.00291164 | missense | DTX1 | GRCh38.p7 | 12:113077459 | CGCAACTTCTACGAC[C/G]CGTCGTCGGCGCCGG | 1840 |
| rs781769482 | snp | A/G | 1.6857e-05 | 0.00290314 | missense | DTX1 | GRCh38.p7 | 12:113094900 | GGCCGCTGTGGCCAC[A/G]TGTACCACCTGCTGT | 1840 |
| rs796247016 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113090641 | GTTCATTGACTTCCA[G/T]CACACCGGCGCCTCC | 1840 |
| rs796284982 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113066787 | CAAGGTGCTTCTGTT[C/T]TGGGGGTGAGGGGTG | 1840 |
| rs796591346 | in-del | -/CA | | | intron-variant | DTX1 | GRCh38.p7 | 12:113084998 | GGCAACACAGGCCCA[-/CA]TAGTCCATCATGAAG | 1840 |
| rs796631079 | in-del | -/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113061708 | TAAATCTTTTTTTTT[-/T]CTTCTTTTTTTGAGA | 1840 |
| rs796725611 | snp | C/G | | | intron-variant | DTX1 | GRCh38.p7 | 12:113083466 | AAGTAGTGGAGATTA[C/G]AGACACCTGCCACCA | 1840 |
| rs796743490 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113095978 | TTTGGGAGGCTAAGG[C/T]GGGCAGATCACGAGA | 1840 |
| rs796836369 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113065137 | AGCCAGGCCCCGGGG[G/T]ACTCACAGCCACGCT | 1840 |
| rs796870788 | in-del | -/A | | | intron-variant | DTX1 | GRCh38.p7 | 12:113086261 | AAACCCTGTATCAAG[-/A]AAAAAAAAAAAAAAG | 1840 |