SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs731570 | snp | A/T | 0.424037 | 0.179474 | intron-variant | DTX1 | GRCh38.p7 | 12:113059814 | CCACATGTGGCTACT[A/T]AAATTTACATTAATT | 1840 |
rs733174 | snp | C/T | 0.264906 | 0.249555 | intron-variant | DTX1 | GRCh38.p7 | 12:113060540 | TTAAATGTCCTCTGC[C/T]CCTTCCTACCCCAGG | 1840 |
rs737633 | snp | A/G | 0.163564 | 0.234582 | intron-variant | DTX1 | GRCh38.p7 | 12:113066920 | GGACACAACTATGCG[A/G]GACCTAGAGGAGACT | 1840 |
rs936386 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | DTX1 | GRCh38.p7 | 12:113065366 | GGGCCGTGCGCACCC[A/G]GCTGCAGACCTGGAT | 1840 |
rs1074161 | snp | C/T | 0.149999 | 0.229128 | intron-variant | DTX1 | GRCh38.p7 | 12:113081938 | CCACTGATGGCAGCA[C/T]CAAGCCCAGGCTTCC | 1840 |
rs1284866 | snp | A/G | 0.373598 | 0.21731 | intron-variant | DTX1 | GRCh38.p7 | 12:113076389 | ctcaatgcaatctcc[A/G]cctccaggttcaagc | 1840 |
rs1284867 | snp | C/T | 0.490398 | 0.0686206 | intron-variant | DTX1 | GRCh38.p7 | 12:113076153 | CTTTTTTTAAATTGA[C/T]ACCTTTATGTATTCT | 1840 |
rs1284868 | snp | C/T | 0.495708 | 0.0461266 | intron-variant | DTX1 | GRCh38.p7 | 12:113069297 | TGGTCACCTGGCTTC[C/T]CACACACCCAGCAGG | 1840 |
rs1284869 | snp | A/G | 0.372189 | 0.218105 | intron-variant | DTX1 | GRCh38.p7 | 12:113068239 | CCTCTGTGGTCAGGA[A/G]TGCAGGGAGGTAGGT | 1840 |
rs1284870 | snp | A/G | 0.319616 | 0.240112 | intron-variant | DTX1 | GRCh38.p7 | 12:113067369 | ATTTCCACAGGGCCA[A/G]GTGAGTAACACCTTG | 1840 |
rs1299753 | snp | A/G | 0.498945 | 0.022939 | intron-variant | DTX1 | GRCh38.p7 | 12:113072908 | accagcctggcccac[A/G]tggtgaaacccccga | 1840 |
rs1300122 | snp | A/G | 0.365439 | 0.221752 | intron-variant | DTX1 | GRCh38.p7 | 12:113076682 | ttcattcaatgattc[A/G]ttcattcattgattc | 1840 |
rs1379862 | snp | A/G | 0 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113060624 | CAGGCCTGTACATCC[A/G]GTCCTTGCTCAGCTG | 1840 |
rs1379863 | snp | C/T | 0.116488 | 0.211364 | intron-variant | DTX1 | GRCh38.p7 | 12:113090062 | GATGTCTGCCACAGG[C/T]AGGAGACCAACCAGT | 1840 |
rs1466325 | snp | C/G | 0.474903 | 0.109173 | intron-variant | DTX1 | GRCh38.p7 | 12:113087872 | GGGGACTTGGCTGCC[C/G]TAAAGGGAGGGTCAG | 1840 |
rs1545661 | snp | C/T | 0.099723 | 0.199792 | intron-variant | DTX1 | GRCh38.p7 | 12:113086838 | ACCCTCCCCCACTTT[C/T]CTGCCCCGCTAGCCA | 1840 |
rs1551618 | snp | A/C | 0 | 0 | intron-variant | DTX1 | GRCh38.p7 | 12:113073421 | GGCAGCCTCACTCTG[A/C]TGCCTGATTTATCAT | 1840 |
rs1585243 | snp | C/G | 0.438806 | 0.163867 | intron-variant | DTX1 | GRCh38.p7 | 12:113079601 | GGCACAATCTCCACT[C/G]ACTGCAACTTCTGCC | 1840 |
rs1619738 | snp | C/G | 0.467642 | 0.123012 | intron-variant | DTX1 | GRCh38.p7 | 12:113088479 | ggtcatgcttaaaga[C/G]ggataacattaggag | 1840 |
rs1625170 | snp | A/G | 0.2897 | 0.246828 | intron-variant | DTX1 | GRCh38.p7 | 12:113093490 | CGCCATCCCCGCCCA[A/G]ACCCCCGACCACTGG | 1840 |
rs1625761 | snp | C/T | 0.482008 | 0.0931261 | intron-variant | DTX1 | GRCh38.p7 | 12:113079125 | GTGCCTACCCTGGAC[C/T]CCAGATTCAGTCATC | 1840 |
rs1625812 | snp | A/C | 0.375598 | 0.21616 | intron-variant | DTX1 | GRCh38.p7 | 12:113079147 | TCAGTCATCTGAGCA[A/C]AGAACCAAGCCCTGA | 1840 |
rs1625847 | snp | C/T | 0.370568 | 0.219005 | intron-variant | DTX1 | GRCh38.p7 | 12:113079157 | GAGCAAAGAACCAAG[C/T]CCTGAGGGGTGGCAA | 1840 |
rs1626561 | snp | A/T | 0.466412 | 0.125164 | intron-variant | DTX1 | GRCh38.p7 | 12:113079200 | TCAAAGACCTTGAAC[A/T]TGGGACAGACCAGAA | 1840 |
rs1628251 | snp | A/C | 0.470715 | 0.117409 | intron-variant | DTX1 | GRCh38.p7 | 12:113082891 | GCGTGAGCCACAGCG[A/C]CTGGCCTGTCTCTAT | 1840 |
rs1628639 | snp | C/T | 0.22263 | 0.248497 | intron-variant | DTX1 | GRCh38.p7 | 12:113093094 | TCAGGGGACCTGGCT[C/T]GCCTTCTGTCTCTGG | 1840 |
rs1674089 | snp | A/C | 0.478603 | 0.101197 | intron-variant | DTX1 | GRCh38.p7 | 12:113059024 | GCACGACTCCACCCC[A/C]CAAACCAACACTTGG | 1840 |
rs1674091 | snp | A/G | 0.316485 | 0.240998 | intron-variant | DTX1 | GRCh38.p7 | 12:113090783 | AGTGGGTGTGTGTGC[A/G]CTGCACCTGTGTGCA | 1840 |
rs1674092 | snp | C/T | 0.222333 | 0.248464 | intron-variant | DTX1 | GRCh38.p7 | 12:113091088 | GGGTTTGCTGCCCAC[C/T]TTACCCAGCTCTGTG | 1840 |
rs1674093 | snp | A/G | 0.220843 | 0.248294 | intron-variant | DTX1 | GRCh38.p7 | 12:113091392 | CCTAGTGTGTGCGGT[A/G]TGTTCCCCAAGTAGA | 1840 |
rs1674094 | snp | C/T | 0.268724 | 0.249298 | intron-variant | DTX1 | GRCh38.p7 | 12:113092102 | CAAGAAGTTAAGTGA[C/T]TTGTTCAAGGTTGTC | 1840 |
rs1674095 | snp | A/T | 0.318036 | 0.240564 | intron-variant | DTX1 | GRCh38.p7 | 12:113093500 | GGGGTTTGGGCGGGG[A/T]TGGCGCCCCGCCCTG | 1840 |
rs1674096 | snp | A/G | 0.347914 | 0.230028 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | RASAL1, DTX1 | GRCh38.p7 | 12:113098391 | AGGACCCTGTCCTTG[A/G]GGAGGAGGGTCAGGT | 1840 |
rs1674117 | snp | A/G | 0.495634 | 0.0465208 | intron-variant | DTX1 | GRCh38.p7 | 12:113086010 | CTGTGGCTCACACCT[A/G]TAATCCCAGCACTTT | 1840 |
rs1674119 | snp | C/T | 0.225005 | 0.248747 | intron-variant | DTX1 | GRCh38.p7 | 12:113088299 | ctgtgttgaggagga[C/T]tctgaagttgcatct | 1840 |
rs1674120 | snp | C/T | 0.313814 | 0.241719 | intron-variant | DTX1 | GRCh38.p7 | 12:113088440 | TGGCAGAAGAGGCgg[C/T]gtggaccagatcata | 1840 |
rs1674122 | snp | A/G | 0.465052 | 0.127485 | intron-variant | DTX1 | GRCh38.p7 | 12:113079689 | CATGCCACCATTCCC[A/G]GCTACTGTGTGTGTG | 1840 |
rs1674123 | snp | C/T | 0.498652 | 0.0259235 | intron-variant | DTX1 | GRCh38.p7 | 12:113073425 | CTGGGGCAGCCTCAC[C/T]CTGATGCCTGATTTA | 1840 |
rs1732784 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | DTX1 | GRCh38.p7 | 12:113059122 | accaccaacacaacc[A/G]ctaacactgtctcct | 1840 |
rs1732785 | snp | A/G | 0.421684 | 0.181726 | intron-variant | DTX1 | GRCh38.p7 | 12:113058508 | TTTTCAGCATCCTAC[A/G]CTGCAAGGTAGTGAT | 1840 |
rs1732786 | snp | C/T | 0.481009 | 0.0955756 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057841 | AGGTCCAGCCTCTTC[C/T]GTGTTGTCTCTTGGT | 1840 |
rs1732790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DTX1 | GRCh38.p7 | 12:113093924 | TGGCAAGGGTTGGCC[A/G]GGGTCAGGCTGGCAA | 1840 |
rs1732791 | snp | A/G | 0.221439 | 0.248363 | intron-variant | DTX1 | GRCh38.p7 | 12:113092809 | GGTGTAGCTATTTTA[A/G]CATCTCTCAAAGCTT | 1840 |
rs1732792 | snp | C/T | 0.269267 | 0.249256 | intron-variant | DTX1 | GRCh38.p7 | 12:113092787 | TCAAAGCTTGTTAGA[C/T]GTAGCATTATTAATT | 1840 |
rs1732793 | snp | C/T | 0.22263 | 0.248497 | intron-variant | DTX1 | GRCh38.p7 | 12:113091127 | CAGTACCGCACCTGC[C/T]ACTGCCGCCCCTCTC | 1840 |
rs1732794 | snp | C/T | 0.314787 | 0.241459 | intron-variant | DTX1 | GRCh38.p7 | 12:113091019 | CTGCAGCCTGCAGAA[C/T]GGCCTGCCGTCCACA | 1840 |
rs1732795 | snp | A/G | 0.304438 | 0.244001 | intron-variant | DTX1 | GRCh38.p7 | 12:113091010 | GCAGAACGGCCTGCC[A/G]TCCACACGCGGACAC | 1840 |
rs1732796 | snp | C/T | 0.251296 | 0.249997 | intron-variant | DTX1 | GRCh38.p7 | 12:113088540 | tgtatacatgtgcca[C/T]gctggtgtgctgcgc | 1840 |
rs1732797 | snp | C/G | 0.347694 | 0.230122 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113098162 | GAAGGGGTGGGGGCG[C/G]TGAAGCAGTGGCAGA | 1840 |
rs1732800 | snp | G/T | 0.492823 | 0.0594727 | intron-variant | DTX1 | GRCh38.p7 | 12:113074068 | aaatcccgtctctac[G/T]aaaaatacaaaaaaa | 1840 |
rs1732801 | snp | A/G | 0.383439 | 0.21141 | intron-variant | DTX1 | GRCh38.p7 | 12:113074069 | aatcccgtctctacg[A/G]aaaatacaaaaaaaa | 1840 |
rs1732802 | snp | C/T | 0.482384 | 0.0921818 | intron-variant | DTX1 | GRCh38.p7 | 12:113079926 | CTTGAGCCTCAGTTT[C/T]GTCATCTGTCAAATG | 1840 |
rs1732803 | snp | G/T | 0.492287 | 0.0616198 | intron-variant | DTX1 | GRCh38.p7 | 12:113082011 | AAGGAAGTTTTCTCT[G/T]TGGGGGTGCGGATCA | 1840 |
rs1732805 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113060959 | GACTCCCCACAAGGC[C/T]GCCAAGCTGGCAACT | 1840 |
rs1882195 | snp | C/G | | | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056096 | GGGGACCCTGGCCAG[C/G]AGGTGAGATCCTGGA | 1840 |
rs1902953 | snp | C/T | 0.289683 | 0.24683 | | | GRCh38.p7 | 12:113062323 | GCTGCTTTTCTGCTC[C/T]GATAGAGTTGAATAG | 1840 |
rs1902954 | snp | C/T | 0.21695 | 0.247806 | | | GRCh38.p7 | 12:113060504 | TGCACTGGCTGTGCC[C/T]TCTGCCTGGGACACT | 1840 |
rs1902956 | snp | C/T | | | | | GRCh38.p7 | 12:113054848 | agctacttagccttt[C/T]tgagcttcaggaggt | 1840 |
rs2243396 | snp | C/T | 0.331674 | 0.236282 | intron-variant | DTX1 | GRCh38.p7 | 12:113095319 | CTGTACTGTCCCTCT[C/T]TGCAGGGCCCTGAGC | 1840 |
rs2243397 | snp | C/T | 0.328556 | 0.237346 | intron-variant | DTX1 | GRCh38.p7 | 12:113095245 | CCCCAGCCCCCACAC[C/T]CCTCCAACTCCTCCA | 1840 |
rs2246275 | snp | A/G | 0.268452 | 0.249318 | intron-variant | DTX1 | GRCh38.p7 | 12:113092830 | GCCTGAAACCCAACT[A/G]CTAGTGGTGTAGCTA | 1840 |
rs2246844 | snp | C/T | 0.253824 | 0.249971 | intron-variant | DTX1 | GRCh38.p7 | 12:113088534 | catgtgccatgctgg[C/T]gtgctgcgcccatta | 1840 |
rs2254306 | snp | C/G | 0.499437 | 0.0167637 | intron-variant | DTX1 | GRCh38.p7 | 12:113072232 | CCAGGCTTTGTGCCT[C/G]GTGCTCCAAACATAG | 1840 |
rs2254770 | snp | C/G | 0.338523 | 0.233803 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056518 | ATGTTTAGGAGTCAC[C/G]GGCTTGAATCTTTGT | 1840 |
rs2264886 | snp | C/T | 0.113685 | 0.209567 | intron-variant | DTX1 | GRCh38.p7 | 12:113088657 | ttaccttactgaatt[C/T]ttttttcatagcact | 1840 |
rs2264887 | snp | C/T | 0.412249 | 0.190198 | intron-variant | DTX1 | GRCh38.p7 | 12:113080618 | TGGAATGGAATGGAA[C/T]GGAATGGAAAACAGA | 1840 |
rs2279044 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113098092 | GGCTGCAGTCAGCCC[C/T]GTTGGGGAGTGATGG | 1840 |
rs2305905 | snp | A/G | 0.000101329 | 0.00711718 | intron-variant | DTX1 | GRCh38.p7 | 12:113094989 | GAGTGGGCAGGGAAC[A/G]GAGTGGGGTTTGGGG | 1840 |
rs2384077 | snp | A/G | 0.413748 | 0.188909 | intron-variant | DTX1 | GRCh38.p7 | 12:113066691 | ATTCATTCATCAGGA[A/G]TTTCATGAGCACCTA | 1840 |
rs2464289 | snp | A/G | 0.27008 | 0.249192 | intron-variant | DTX1 | GRCh38.p7 | 12:113090407 | GGGCACCCTGCGGGG[A/G]GGCCCCAGGAAGAGG | 1840 |
rs2464290 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113081845 | TCCAGAAGGGAGCCT[C/T]TATCCCCCGGTGGTC | 1840 |
rs2468356 | snp | G/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113091400 | CCCCATCCGTCTACT[G/T]GGGAACATACCGCAC | 1840 |
rs2701622 | snp | C/T | 0.35574 | 0.226537 | intron-variant | DTX1 | GRCh38.p7 | 12:113095541 | GTGGTCGTTACTGTT[C/T]GGGTGCTGCTTTTGG | 1840 |
rs2701623 | snp | A/G | 0.457388 | 0.139608 | intron-variant | DTX1 | GRCh38.p7 | 12:113084969 | CCAGTcccatttcac[A/G]gatgcaaaaactgaa | 1840 |
rs2701624 | snp | A/C | 0.499396 | 0.0173617 | intron-variant | DTX1 | GRCh38.p7 | 12:113072847 | GCGTGGTGGTACGTG[A/C]CTGTAATCCCAGTTA | 1840 |
rs2731303 | snp | G/T | 0.491525 | 0.0645418 | intron-variant | DTX1 | GRCh38.p7 | 12:113085700 | TCAATAAATATGAAT[G/T]AATTAATTAAAAAAC | 1840 |
rs3038192 | in-del | -/GGTAG | | | intron-variant | DTX1 | GRCh38.p7 | 12:113074509 | agggggaagggtagg[-/GGTAG]acaatgccagaggag | 1840 |
rs3038193 | in-del | -/TTTTTTT | | | intron-variant | DTX1 | GRCh38.p7 | 12:113079537 | ttttttttttttttt[-/TTTTTTT]gagatacagtttcac | 1840 |
rs3178412 | snp | A/C | 0 | 0 | missense, utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096917 | CAGCCCAGGGCGTAT[A/C]CGAGGCTGCAGCCAA | 1840 |
rs3180323 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113096944 | CCAAGGCTTGAGGCC[C/T]AAGGCTGCCCACCTT | 1840 |
rs3214864 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | DTX1, RASAL1 | GRCh38.p7 | 12:113097547 | CAGTTCTACAAAAAA[-/A]TGGCCAGCACGAGCG | 1840 |
rs3217697 | in-del | -/AG | 0.22263 | 0.248497 | intron-variant | DTX1 | GRCh38.p7 | 12:113093040 | GTAACTGCAGTTGGC[-/AG]AGAGAGGTACAAAGA | 1840 |
rs3741985 | snp | C/G | 0.480853 | 0.0959518 | upstream-variant-2KB, utr-variant-5-prime | DTX1 | GRCh38.p7 | 12:113057821 | TGTCTCTTGGTCCCT[C/G]TTCCCCGCCAGACAG | 1840 |
rs3741986 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | DTX1 | GRCh38.p7 | 12:113093976 | CCCGAAGGCTTGGCT[C/T]AGAACTGGGTCAGGG | 1840 |
rs3809163 | snp | A/G | 0.169435 | 0.236663 | intron-variant | DTX1 | GRCh38.p7 | 12:113066062 | CTGGGTGGGCTCATG[A/G]GGGTGACTATCTAAG | 1840 |
rs3825200 | snp | A/G | 0.469346 | 0.119947 | intron-variant | DTX1 | GRCh38.p7 | 12:113066092 | CTGCTGGGGGTGTCT[A/G]TGTCAACCCAGAGGC | 1840 |
rs3839970 | in-del | -/CTGC | | | intron-variant | DTX1 | GRCh38.p7 | 12:113089522 | GCGACCGCTGCCTGC[-/CTGC]GGGCCTCCCGGAAGG | 1840 |
rs3847955 | snp | C/T | 0.412416 | 0.190055 | intron-variant | DTX1 | GRCh38.p7 | 12:113087422 | CCCCCGGGCTTGCAG[C/T]GATGTCCTTCAAGTC | 1840 |
rs4561264 | snp | A/G | 0.147321 | 0.227941 | intron-variant | DTX1 | GRCh38.p7 | 12:113081950 | TTGGTGCTGCCATCA[A/G]TGGGGAGCTATAGAG | 1840 |
rs4767061 | snp | C/T | 0.0368353 | 0.130617 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055242 | TGCTAAATCACCATG[C/T]GACCTTGAGCCAATC | 1840 |
rs4767062 | snp | A/C | 0.120326 | 0.21374 | intron-variant | DTX1 | GRCh38.p7 | 12:113076984 | CAGGGCCTGTGATAA[A/C]CCCCACTTCAGTGTC | 1840 |
rs7294709 | snp | C/T | 0.150333 | 0.229274 | intron-variant | DTX1 | GRCh38.p7 | 12:113082877 | gctgggaattatagg[C/T]gtgagccacagcgac | 1840 |
rs7296817 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | DTX1 | GRCh38.p7 | 12:113079330 | GATAATGATGGTCCG[A/C]GATCACCAAAGCTCA | 1840 |
rs7298895 | snp | C/T | 0.345925 | 0.230864 | intron-variant | DTX1 | GRCh38.p7 | 12:113064105 | AGGGACAGCCTGCAC[C/T]ACCCTGGAGGCCTCC | 1840 |
rs7305270 | snp | A/G | 0.0948562 | 0.196037 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113055803 | AGGCCACTGACCCCC[A/G]TCAGCCACCCAGGCT | 1840 |
rs7306576 | snp | C/T | 0.0948562 | 0.196037 | upstream-variant-2KB | DTX1 | GRCh38.p7 | 12:113056111 | CCTGGCCAGGGTCCC[C/T]TCCCCTGGTCCCACC | 1840 |
rs7308220 | snp | G/T | 0.00259286 | 0.0359125 | intron-variant | DTX1 | GRCh38.p7 | 12:113094121 | AGGGGATGGGGGGGC[G/T]GGGGGAGGGCCCTGG | 1840 |
rs7954586 | snp | C/G | 0.0436148 | 0.141086 | intron-variant | DTX1 | GRCh38.p7 | 12:113093533 | ACTGCGCCCCCTAAC[C/G]CCCAGGGATGACCGG | 1840 |
rs7958787 | snp | C/T | | | intron-variant | DTX1 | GRCh38.p7 | 12:113059792 | caaccaatatgttag[C/T]caccaaccacatgtg | 1840 |
rs7960088 | snp | A/G | 0.161924 | 0.233971 | intron-variant | DTX1 | GRCh38.p7 | 12:113075968 | attctagcgaggggg[A/G]gacagacagaaacca | 1840 |