SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs147842865 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | STAM | GRCh38.p7 | 10:17703481 | ATTTGCCCTGCGTAC[C/G]TATATATAGTAGCAT | 8027 |
rs147861204 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17668974 | CAGTTGGGTAAATAT[A/G]TGAGAACATGATTGC | 8027 |
rs147932283 | snp | C/G/T | 0.00119737 | 0.0244387 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717311 | GAGGTTGCAGTGAGA[C/G/T]GAGATCACGCCACTG | 8027 |
rs147935092 | snp | C/T | 0.000148264 | 0.00860872 | synonymous-codon | STAM | GRCh38.p7 | 10:17695131 | ATCCAGTCTCTTAAC[C/T]AACCACCAACATGAA | 8027 |
rs147944913 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | STAM | GRCh38.p7 | 10:17681253 | AATTACCTTCTCACC[A/G]TTTTACTACACCCTT | 8027 |
rs147965387 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714668 | AGAATGCAGGACCTA[A/G]TATGCCCCAGGTGCC | 8027 |
rs147968502 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17683988 | GTATGATTGAGCTGC[A/G]TTGCTAGGGTCTAAA | 8027 |
rs147998284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17700950 | TTCATGATTCCTCCT[C/T]GTGTTGAACACTTTC | 8027 |
rs148015924 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688582 | ATTCTCCTGCCGCAG[C/T]CTCCTGAGTAGCTGG | 8027 |
rs148087202 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714448 | TTAAATGAATTGACT[A/G]TATGAATGAATGCTT | 8027 |
rs148090755 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17651866 | CACCTAAATGTGATG[C/T]GAAGTCCTCCTGTCA | 8027 |
rs148141141 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17709220 | AAGTTTTTATTGTTG[A/T]TTTTATTTGCATCTA | 8027 |
rs148155945 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17675335 | GTGGTGAAACCCTGT[C/G]TCCACTAAAAATAAA | 8027 |
rs148208571 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | STAM | GRCh38.p7 | 10:17669732 | AGATGGAGTCTCGCT[C/T]TGTCACCCAGGCTGT | 8027 |
rs148252630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17685648 | TGGGCCACAACCTGA[A/G]CAACTTTATCAGTGC | 8027 |
rs148262001 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | STAM | GRCh38.p7 | 10:17704997 | AGATGGGACCTCTCA[C/T]TGATGAAAAGCTGGA | 8027 |
rs148304265 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17681971 | CATCCCCATGAAATG[C/T]ATGTTTGCTACATTC | 8027 |
rs148313838 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17648523 | GCTCACTCTTTGGGT[A/C]CGTGCTACCTTTAAG | 8027 |
rs148364612 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644228 | TGTCGCGGACCCTGT[A/G]GAGTCGGTCTCTGTT | 8027 |
rs148404200 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17683825 | TCTTCTTCATATCAT[A/G]TCTTCATATCATTTT | 8027 |
rs148427448 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | STAM | GRCh38.p7 | 10:17649715 | ATCTGTCAGAAAACT[A/G]AAGTTATCTTTCTAA | 8027 |
rs148479326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17645960 | TCACCTTTATATTCT[A/G]CTGACTTTGTGAACA | 8027 |
rs148504353 | snp | A/T | 1.66513e-05 | 0.00288537 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688041 | GGGTCATCCTAAAGT[A/T]TGTGAAAAATTAAAG | 8027 |
rs148528938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17702649 | CGAAACAGACTGTGG[A/G]AGACTGTGCTAAGGG | 8027 |
rs148538555 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17706852 | AACTCTCTTAAATAT[C/G]TAATGAACTTCTAGT | 8027 |
rs148551088 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | STAM | GRCh38.p7 | 10:17690795 | TACTGATGCAGTTCT[A/G]TTAGCACTAACTTTT | 8027 |
rs148611961 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17653820 | TACATTTTGGTATCT[A/G]TGGAAGATCCTGGAA | 8027 |
rs148669412 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17711321 | TATAAGGTGATAATA[A/C]GTGACAATTACTGTT | 8027 |
rs148688916 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17676578 | ATATGACCCAGATCT[A/G]TTCATAAAAAGATGA | 8027 |
rs148741484 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17671289 | GTAATGTTTAAATCA[C/T]TCTAAAATAACTTTG | 8027 |
rs148815015 | snp | A/C | 0.00953873 | 0.0683987 | upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17643959 | CGTCCTACGGAGACT[A/C]CTAGCCAAGGGAAAA | 8027 |
rs148920900 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697097 | GCTGTTTTTGTGTGT[C/G]TATGTATTTTTAGTA | 8027 |
rs148982109 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | STAM | GRCh38.p7 | 10:17657044 | GTTGTATGCATGCCC[A/G]TCGGAGGCTTTTTTC | 8027 |
rs149004943 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | STAM | GRCh38.p7 | 10:17709113 | CCTCTGTGGTATTCC[A/G]GTACCAGCCAGCAAG | 8027 |
rs149016660 | in-del | -/AG | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715385 | TAATTGTGAGCTAAA[-/AG]GAGATATATATATAT | 8027 |
rs149031808 | snp | A/G | 3.30557e-05 | 0.00406531 | synonymous-codon | STAM | GRCh38.p7 | 10:17700198 | TCTTACAGTTAAAAC[A/G]GAGAAGAAGACGGTA | 8027 |
rs149058010 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | STAM | GRCh38.p7 | 10:17704306 | TGGGACACTGACAAC[A/G]TAAAAGCAAAATTGG | 8027 |
rs149077180 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17669293 | GTGTCTAAACACATT[C/G]TGCTACCACATGGTT | 8027 |
rs149129166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665809 | ACTTGATTATACCAA[A/G]CCTAAAACTTTAACA | 8027 |
rs149212581 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17678190 | GTGGATTTGCCTGTT[A/G]TAGACATTTCATATA | 8027 |
rs149308964 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688337 | CTAGTTAGTAATACT[A/G]GTTTTCTGGCATTCA | 8027 |
rs149395422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17702377 | CAAGGAAAAAAACAA[G/T]TTGAAATACATGACA | 8027 |
rs149445406 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | STAM | GRCh38.p7 | 10:17698795 | GTTGCAAACTTGCGC[A/G]TCAAGAGCTGTTAGA | 8027 |
rs149468797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17662623 | TGGAGATCATGTACT[C/T]TAGAGGGAGAATGCC | 8027 |
rs149511990 | in-del | -/AT | | | intron-variant | STAM | GRCh38.p7 | 10:17676896 | ATTTAATAATTATAC[-/AT]ATATATATATATATA | 8027 |
rs149532030 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | STAM | GRCh38.p7 | 10:17648859 | ATGCAAGTTTTTTTA[C/T]TGTGGCTCACAATAT | 8027 |
rs149538373 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17710964 | TTTGTGTGTTTCAAC[A/G]GGGAAATGAGGAATT | 8027 |
rs149591310 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17706265 | AGGAAATAGCTTTTA[C/T]ACAGGGTTATGCAGC | 8027 |
rs149602063 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | STAM | GRCh38.p7 | 10:17670853 | CTATATTTTGCTCCT[G/T]TTATATGTTGTGTGG | 8027 |
rs149697183 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17683398 | AACTTCCGGACTCAA[A/G]CCATCTGCCCACCTC | 8027 |
rs149709201 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17673156 | TATTTTTACAAAATA[C/T]TTTGTGTTTATTGCC | 8027 |
rs149832396 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, missense | STAM | GRCh38.p7 | 10:17690203 | GTCCAGTGTTCTTTT[C/T]GCTGCCCGAGTCTGC | 8027 |
rs149857901 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | STAM | GRCh38.p7 | 10:17681169 | TATAGTAGCCATCCT[A/G]ATGGGTGTGAGGTGG | 8027 |
rs149891439 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | STAM | GRCh38.p7 | 10:17686029 | GGTTACAGTAGAAAA[A/T]TAGCAGTATAGAAAT | 8027 |
rs149901146 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | STAM | GRCh38.p7 | 10:17653337 | TTTGTGATGTGTGGA[G/T]TCATCTCACAGAGTT | 8027 |
rs149926713 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17703551 | ATTTTAGTAGTGGTC[A/G]TGGTAAAGTAGATCT | 8027 |
rs149971772 | snp | A/G | 0.000131783 | 0.00811628 | synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714594 | CAGCCAGGCGCCAGT[A/G]TATAGTCCTCCTCCT | 8027 |
rs149980463 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | STAM | GRCh38.p7 | 10:17700351 | TTGCTTTAAGAAAAA[A/C]TTGATTACTTGAGTT | 8027 |
rs149990053 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | STAM | GRCh38.p7 | 10:17665766 | GTTTACTTCATTTAA[A/G]TTGTAGTTTCTTTTT | 8027 |
rs150067561 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713423 | GGCTTGAATAGCTGA[C/T]TGCCTATGCATTCTC | 8027 |
rs150085297 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | STAM | GRCh38.p7 | 10:17677720 | TTGGCACATAATAGA[C/T]ATTCAGTCAATATTA | 8027 |
rs150149460 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17661711 | CACATTTATTACTCA[A/G]TTCTGTCCATCTGCC | 8027 |
rs150219572 | snp | A/T | 0.000707977 | 0.0188013 | intron-variant | STAM | GRCh38.p7 | 10:17684953 | TTATTTCCAGAAATT[A/T]ATTAAGGCAGTCTTC | 8027 |
rs150244595 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | STAM | GRCh38.p7 | 10:17675894 | AAAGGGCCGGTATCC[G/T]TTTGCACTGATACCT | 8027 |
rs150286577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17647355 | GCATTCCTCTTTGAT[A/G]TACAGTATTTTATTC | 8027 |
rs150314424 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698655 | CAAAGAGAAATAGCT[A/G]CCCTATTTAGCTTGC | 8027 |
rs150359831 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | STAM | GRCh38.p7 | 10:17692154 | CACCAAGAGGCTAAT[A/T]TGCCCAGTGTCATCC | 8027 |
rs150382718 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17658496 | AACTATGTCCTTTCT[C/G]ATTTTCTGCCTACCT | 8027 |
rs150455637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706001 | TGAGCCCAGAAGGTC[A/G]AGGCTGCAGTGAGCC | 8027 |
rs150598656 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714849 | ATGAGATTCATTACT[A/G]TCTTAAGATGTGTTT | 8027 |
rs150608643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17679282 | GTGAAGTGGCATCTC[A/G]ATGTGGTTTTGATTT | 8027 |
rs150633430 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | STAM | GRCh38.p7 | 10:17668178 | CAGTGATCCAGTAGC[A/T]AAAATAATTGACAGG | 8027 |
rs150703017 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17690077 | GCCTCTAATCTAATC[C/T]GCTCATTTTTACAGA | 8027 |
rs150748128 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17685965 | GAAAAAGTTTTTGTA[C/T]GTTAAAAGGGAAAAT | 8027 |
rs150823658 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | STAM | GRCh38.p7 | 10:17648558 | GTAACACTCACCACA[A/G]AGGTCCGTGGCTTCA | 8027 |
rs150838031 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17699703 | CCTACGTGGCACGCC[A/G]GATAATACATAGCTG | 8027 |
rs150849046 | snp | C/G | 8.23798e-05 | 0.00641741 | missense | STAM | GRCh38.p7 | 10:17708882 | AGCTGTCTTCTCTCA[C/G]CCAGGCAGTGGTCCC | 8027 |
rs150854827 | in-del | -/TTTTCTC | | | intron-variant | STAM | GRCh38.p7 | 10:17669254 | TGTATTTAAGTCTGT[-/TTTTCTC]TTTTGACCCGTTGGT | 8027 |
rs150876103 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644946 | AAACCGAATTGAGGA[A/C]CTGAGCCTTTGGGAT | 8027 |
rs150907681 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | STAM | GRCh38.p7 | 10:17659631 | ATGCCACCAGGCCCA[A/G]CTAATTATTTTTTTA | 8027 |
rs150944654 | snp | C/T | 6.58903e-05 | 0.00573941 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714736 | GGAGGCAGCCAACAG[C/T]CACCTCAGCCACAGC | 8027 |
rs151003168 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | STAM | GRCh38.p7 | 10:17672575 | GTGCTGAGGGCCATT[C/T]TTGCTCGGAGCATGC | 8027 |
rs151021636 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17661243 | CTTTAGCAGTTTCAT[C/T]TACTGCTTTATGCCA | 8027 |
rs151074076 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | STAM | GRCh38.p7 | 10:17657471 | ATCAGAGTAATGCTG[G/T]CCTCACAGAATGAGT | 8027 |
rs151123839 | snp | A/C | 0.0267878 | 0.112589 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717165 | GTCAGGAGTTCGAGA[A/C]CAGTCTGACCAACAT | 8027 |
rs151139104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17680983 | TCCTTTGGGGTATAT[A/G]CCTGGAAGTGGAATT | 8027 |
rs151190736 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | STAM | GRCh38.p7 | 10:17677089 | CAAGGTGTTCATCAG[C/T]GCTTCATTCTTACTG | 8027 |
rs151234858 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17691906 | GATGTAAAATATAGC[A/T]ACTTTGCATCTGTAG | 8027 |
rs151286260 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17687111 | CTCTTTCTTTAATAC[A/G]GAAGAATAATGCCCT | 8027 |
rs151295999 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | STAM | GRCh38.p7 | 10:17654373 | GACTACATGCGCCCA[C/T]CACCAAGCCTGGCTA | 8027 |
rs180713792 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689689 | ACTCACTGCAGAGAA[A/C]CCACCTAGAATAGGT | 8027 |
rs180727835 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17650624 | ATATGCCCTCAAGGA[C/T]TCCAGGTTTAGATCA | 8027 |
rs180732455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17672183 | TAATCTCACTAACTG[A/G]TGACCGCGCCTAACA | 8027 |
rs180745015 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17657351 | TCTCCTGCCCTGCTC[C/G]TACCTGTCTTACTAC | 8027 |
rs180761236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17698932 | ATGTTTCTTTTCCTT[C/T]ATAGGAAAATGAATC | 8027 |
rs180761838 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | STAM | GRCh38.p7 | 10:17704178 | GCTCACTGCAGCCTT[G/T]ACCTCCTGGGCTCAA | 8027 |
rs180767480 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | STAM | GRCh38.p7 | 10:17666598 | GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 8027 |
rs180778538 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17680598 | TTCTTGTAGAGACAG[G/T]GTCCCACTATATTGC | 8027 |
rs180863997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17653219 | TATAATGACACCCCA[A/G]TTGTAGAATCCATGA | 8027 |
rs180864961 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17661781 | TAATCAAGTTTTTGA[A/G]CATAGCCAAATGGTG | 8027 |
rs180890434 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17683858 | TGAATGCTTAGTACT[A/T]TGAATTTTATATTTT | 8027 |
rs180936482 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17701726 | TTTTCGTTTTTACCC[C/T]CCTCCTCTCCCTTTT | 8027 |
rs180954242 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17669240 | ATTATATTTGCATAT[C/G]TATTTAAGTCTGTTT | 8027 |
rs181157839 | snp | C/T | 0.000247091 | 0.0111123 | synonymous-codon | STAM | GRCh38.p7 | 10:17695134 | CAGTCTCTTAACTAA[C/T]CACCAACATGAAGGC | 8027 |
rs181159428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17707725 | CTGTGTGGGTCTGTC[A/G]TTTAACAGAAGTGCT | 8027 |
rs181174747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17676911 | CATATATATATATAT[A/G]AAAGTTCAGTATTAC | 8027 |
rs181252461 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715322 | TATTTACATGAAGGC[G/T]CATTATGTTGTCGTG | 8027 |
rs181276604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697863 | TCGTTTTTTAATGCT[A/G]GATAGAAGGGATCAA | 8027 |
rs181281410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17711020 | GAAATTGGAAGGAGC[A/G]AGGGCCAGGGTTAGA | 8027 |
rs181291481 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | STAM | GRCh38.p7 | 10:17679810 | CATAGAGTTAGTTTC[A/G]GTAGTTTCCTGTCTT | 8027 |
rs181346710 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665514 | TATATTCTTCTGCAT[G/T]TATTACTTAATTACT | 8027 |
rs181410673 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17676224 | TACTTCCAGGCATGA[G/T]CTGACTTATTTTTAA | 8027 |
rs181418616 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17661353 | AGTGGTAATATGAAG[C/G]CTTTGCCAGTGTCTT | 8027 |
rs181421561 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17646603 | TCTTCAGTGTAGCAA[C/T]ATTGTTTTGCTCCAG | 8027 |
rs181428284 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17668355 | GATAGTACAGAGGTC[A/T]ACTCCGACACAATTT | 8027 |
rs181456069 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | STAM | GRCh38.p7 | 10:17649904 | CGATGTGAGGCACCC[A/G]GGCCCAGCCAATTTG | 8027 |
rs181560596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17664353 | GTATACTCACATGCC[C/T]GCTGTCTGTCTCCAG | 8027 |
rs181563085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17649190 | AGGAGGATTCCTTGA[A/G]GCCAGGAATTGGAGA | 8027 |
rs181567752 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17694430 | CGGAAGAGCAGAAAG[C/G]GTTCTGTGTTGAATT | 8027 |
rs181580503 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17679581 | TTAATTTGCGTGTGT[G/T]TTTTTTTTTTAAATG | 8027 |
rs181673722 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17707385 | ATTGCACTCCAGCCT[A/G]GGCGACAGAGCAAGA | 8027 |
rs181750874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17710714 | GCACTGTCTTTCACC[C/T]CTATAGCCATCCTAT | 8027 |
rs181755885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17658148 | CATCCCACAAATTTT[A/G]CGAAGTTGTATTTTC | 8027 |
rs181768986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17652966 | TGTTTCCTAGGAGAC[A/G]GCCTCTAAATCCTTG | 8027 |
rs181904828 | snp | A/G | 0.000248725 | 0.011149 | intron-variant | STAM | GRCh38.p7 | 10:17704935 | ATTTTTTTTTCTTGT[A/G]CTTTCTTATATTTCT | 8027 |
rs181998173 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17685974 | TTTGTATGTTAAAAG[A/G]GAAAATGCCTCATGT | 8027 |
rs182006310 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | STAM | GRCh38.p7 | 10:17672515 | CTTGTATGTGCTGTC[G/T]CACAATTACAATTCC | 8027 |
rs182013596 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17669707 | CTTTCTTTCTTTTTT[C/T]TTTTTTCTGAGATGG | 8027 |
rs182017499 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | STAM | GRCh38.p7 | 10:17653676 | TGCCCTATACAGTAT[A/G]GTTATTTACATAACA | 8027 |
rs182021178 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697707 | TCAAGCAAAGTTTAA[A/G]TCATAATCTCCCCTC | 8027 |
rs182033710 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | STAM | GRCh38.p7 | 10:17701890 | ATGGCTCTAATGACT[A/G]GTTAACACAGCTGAG | 8027 |
rs182038699 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715774 | ACTACATTTTCGAAG[C/T]CTCTTGTAATTATTT | 8027 |
rs182052677 | snp | A/C | 0.000370277 | 0.0136015 | intron-variant | STAM | GRCh38.p7 | 10:17705771 | GCCCATGTTGTTTTA[A/C]ATTCTCAAATGCACA | 8027 |
rs182057004 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17691720 | AGACATGTAATCAGA[C/T]AATTATAACAGAAGC | 8027 |
rs182059111 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17673119 | CTCTTCTAAGTGCAC[A/G/T]TGCAGATTTTCTCTT | 8027 |
rs182070986 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17691062 | AAAATTTATGTAAAC[C/T]GTAAAACTTATTTCT | 8027 |
rs182234773 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17647526 | TTTTCCCTTAGAGTA[G/T]TAGGAAGCAATTTAG | 8027 |
rs182237443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706941 | TATTATTACAAACCA[A/G]CAAAATATATTTCCA | 8027 |
rs182313923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17675909 | TTTTGCACTGATACC[C/T]ACAAATAGCACTCCA | 8027 |
rs182342904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645050 | AGTTTGAAATGCTAC[A/C]TTTTTGTTGTTTTCT | 8027 |
rs182401119 | snp | A/T | 3.30371e-05 | 0.00406417 | missense | STAM | GRCh38.p7 | 10:17700271 | CCGGAACCAGCCTTT[A/T]TTGATGAAGTAAGTG | 8027 |
rs182497475 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17654501 | TGCTGGGATTACAGG[C/T]GTGGGTCACCGCGCC | 8027 |
rs182506291 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17693565 | TTTTGTGTCTAACAA[A/G]TTTGTTTTTTGTAGA | 8027 |
rs182594429 | snp | C/T | 5.09238e-05 | 0.00504572 | intron-variant | STAM | GRCh38.p7 | 10:17660442 | AAAATAATGTTTCTG[C/T]AATCCCCTTTACAAT | 8027 |
rs182630114 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | STAM | GRCh38.p7 | 10:17658308 | GTAATCACTATGTGA[G/T]TTCTATTGTTTTAGA | 8027 |
rs182635823 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713680 | TCTATCTAGACTCTG[A/T]CCCTTTCTCCCATCT | 8027 |
rs182723794 | snp | C/T | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713460 | TGCCAGTTTTTTGGA[C/T]ATCAAACTTGACAGA | 8027 |
rs182730884 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17699644 | GACCCCTGTCAAGGC[C/T]ACCTGCAAAGTTCTC | 8027 |
rs182791470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17681452 | CATGCTTTCTATGAT[C/T]TTTTATCTTTTTAAA | 8027 |
rs182852287 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716014 | TTCTAATGGAATTAT[C/T]TTGGCTTCTTACTTG | 8027 |
rs182862344 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17678620 | ACTTATTTTATTTTG[G/T]TAAAATATATTTAAC | 8027 |
rs182873399 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17702399 | TACATGACAGAGACT[A/G]TTGTTTGAATGGTAA | 8027 |
rs182929443 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17648350 | TTGTAAAATGGACCA[A/G]TTAGCACTCTGTAAA | 8027 |
rs182985621 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716409 | ACTTAAGGGTAACTT[A/C]AGTGTTTCGCTCAAG | 8027 |
rs182997274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17686997 | ACTTCAAATTATTGC[C/T]GCTATGAAGATACAT | 8027 |
rs183058733 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | STAM | GRCh38.p7 | 10:17650925 | AAAAAATTAGCCGGG[C/T]GTAGTGGCGGGCGCC | 8027 |
rs183111192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17672909 | GGGAAAAGTGAGAGA[G/T]AATTCTCCTTTCCCT | 8027 |
rs183130793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17705215 | TGAGGATTTGATCGA[C/T]CTTTGCAATATAGTC | 8027 |
rs183145872 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17651352 | TAGCATAGCACCTGG[C/G]ATGTAGTAACCAATG | 8027 |
rs183228068 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17670379 | TAAAACGAGTGAGCA[C/G]AGGCAAAATTAGAAG | 8027 |
rs183272048 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | STAM | GRCh38.p7 | 10:17702829 | CCTGGCCAACATGGT[A/G]AAACCCCGTCTCTAC | 8027 |
rs183286059 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17703377 | TTTCACTCTCTGATG[A/G]TTAATTCGTTTCTCA | 8027 |
rs183314960 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | STAM | GRCh38.p7 | 10:17669921 | ATTTTTAGTAGACAC[A/G]TGGTTTCACCATGTT | 8027 |
rs183332886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687537 | AAGGAAAAAAAGTTA[C/T]GTTATTTTGAAGAAA | 8027 |
rs183334656 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17681107 | TGCACAAGTGTTTCA[A/T]TTTCTCCACATCTTT | 8027 |
rs183339004 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17666837 | TGAAAGGACAGCATC[A/G]GTAGAGAAACAGACC | 8027 |
rs183361391 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717059 | AATAGAATAATTTAT[A/G]AAATGAACTAGCTGT | 8027 |
rs183362859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17699108 | CACAGGCCAGATTTC[A/G]GTAGTATGGGCTAGT | 8027 |
rs183397872 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17670938 | AGTATATAAAGATTG[C/T]ATTATTTCTGTTGTG | 8027 |
rs183399036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17655722 | ACTTGGTCAAGACCA[A/G]CCATTACAGATAAGA | 8027 |
rs183401313 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | STAM | GRCh38.p7 | 10:17667402 | GCTGGTATTACAGGC[A/G]TGAGCCACCGCATCC | 8027 |
rs183419138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691375 | TACAAAAAATTAGCC[A/G]GGCGTAGTGGCAGGT | 8027 |
rs183506892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17708312 | GCCCTTTACAAAAAA[A/G]TTTGCTGACCCCTGC | 8027 |
rs183550401 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17686464 | TGACTATAGCCTCTG[C/T]CTCCCGGGTTCAAGT | 8027 |
rs183564651 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | STAM | GRCh38.p7 | 10:17654284 | CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTCACT | 8027 |
rs183634078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17675790 | ACAGAGTTCTTTGGT[A/G]CCTATTGAATTTTTT | 8027 |
rs183818848 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17658981 | TATTTGTTACTGTTT[C/T]CTATTCATTGCCCTT | 8027 |
rs183850076 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692082 | AAATAGGCTGTGAGG[G/T]GCCCATGAGGTGTAG | 8027 |
rs183875685 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17712876 | CGGAGCGGTGGGAGC[G/T]GTAGGGAAGCTCAGT | 8027 |
rs183947861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17693140 | CTAGATTGATGAGAA[A/G]GGTTTTGCAAATTCT | 8027 |
rs183949424 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17708073 | TTTTTTGTATTTTTA[A/G/T]TAGAGACGGGGTTTC | 8027 |
rs183952481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17706817 | TCGTAAAAAACACAA[A/G]ATGCTTTTAGAGCTA | 8027 |
rs183996168 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17715001 | AACTACTTACAACAT[A/T]TAATTCCTTTCATAA | 8027 |
rs184032475 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17706138 | CTGTTTGAAACTTTC[C/T]AAAACTAATGTTTAA | 8027 |
rs184037874 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | STAM | GRCh38.p7 | 10:17674014 | GGCGGGAGAGTCCTT[C/G]GAGGGACTGGAGGTC | 8027 |
rs184042187 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17677936 | TTCCAGGGCTCATTG[G/T]AGTTCAAATTGCCCG | 8027 |
rs184066176 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17701530 | GCTGCAGTGGAAGAA[C/T]TGAGTAGTAGCAACA | 8027 |
rs184083143 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17671818 | CCTGTTATTTTGTTA[C/T]GTCCTGAGAGAGGGA | 8027 |
rs184084771 | snp | A/G | 3.48147e-05 | 0.00417207 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696754 | TTGTTATGGTAAAGC[A/G]TTGTTTTTTGTTTGT | 8027 |
rs184088115 | snp | A/C/T | 0.00455051 | 0.0474827 | intron-variant | STAM | GRCh38.p7 | 10:17708771 | TTTCTCTTTAACCAT[A/C/T]GCAGGTGTATGCAGG | 8027 |
rs184089356 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17656953 | TTTCCTGTGATTCTT[A/C/T]CCTTAGAGTGGGCGG | 8027 |
rs184100312 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643894 | CTTTCTCCTGGCTCT[A/C]CCAGTCACTCCTGGG | 8027 |
rs184120930 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17667559 | AAATACTGAATGCCA[A/G]ATATCATGCTTTGGC | 8027 |
rs184149204 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17679089 | GTACGGATATTGGTT[A/G]GAGTCCCAGCTGGAT | 8027 |
rs184189845 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | STAM | GRCh38.p7 | 10:17664594 | TGAACAGTATTGTAG[C/G]CTGCCATTGAGGTAT | 8027 |
rs184193019 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17662224 | TTCATTTTTTTCCCT[C/T]CTGTATAACATTCAT | 8027 |
rs184201786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17649435 | AAATGCATCTTTACC[C/T]TCTCACTCTGTTTCT | 8027 |
rs184236726 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17674934 | TTGAGACACTCAATC[C/T]TTAAGAATGGAATGA | 8027 |
rs184238383 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | STAM | GRCh38.p7 | 10:17659614 | GCTGGGAATACAGGT[A/G]CATGCCACCAGGCCC | 8027 |
rs184268025 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17651680 | TTAGCAGAGCTTCAG[A/T]TTACATTTCTTTGCA | 8027 |
rs184287957 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642714 | CCTAAGGTTTTAAAA[A/T]TTTTTTTACATGCTT | 8027 |
rs184288156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17681893 | GAGAGCCTAAGCACA[C/T]GATGTTTCGTAGGTT | 8027 |
rs184476853 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17710921 | AATATGTAATATCTG[C/T]TTATCAATATATAAA | 8027 |
rs184477981 | snp | A/G | 0.00874735 | 0.0655527 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717192 | ACATGGTGAAACCCC[A/G]TCTTTACAAAACTAC | 8027 |
rs184483728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697738 | TAGGAAAACAGAAAA[A/G]TATGTTCAAATCTAG | 8027 |
rs184487879 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17679669 | TCTGAGATTTTCTTC[A/G]TGGGAAGTTTTCTTA | 8027 |
rs184615213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17700988 | TGAGGAAAAGCTTAC[A/G]CTAATTTTATATTAA | 8027 |
rs184619432 | snp | C/T | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714123 | ATCTTTGCTTAAGTA[C/T]TGCCTTATTGGAGAG | 8027 |
rs184634426 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17682250 | TATTGTCAGTACTCC[G/T]GTGTCTAGCACTAAA | 8027 |
rs184659172 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689178 | TTTTGGGTAACCTTC[C/T]TTTAGGATGCCCAAC | 8027 |
rs184689672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17668155 | AGGAGTGATGTTGGA[A/G]AGAGAGGCAGTGATC | 8027 |
rs184694123 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17652042 | TGGGCAGATTTCTCA[A/G]TCTCCTCTTTTTGAG | 8027 |
rs184754180 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17663813 | GTATGTATTTTCTTT[A/C]AATAATACTGTTTAA | 8027 |
rs184826790 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17703663 | TCCATTGGTCTGTAC[A/C]ACAAAAGATTCTGAA | 8027 |
rs184834541 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17653062 | TATGCTAATAAGATG[A/T]CTTGGTCTGGGGGCT | 8027 |
rs184867140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17706679 | CCATCGCGCCCGGCC[A/G]AGGCCCATATTTTTA | 8027 |
rs184881635 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | STAM | GRCh38.p7 | 10:17648588 | ATTCTTGACGTCAGC[A/G]AGACCACAAACCCAC | 8027 |
rs184935363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692445 | ATGAGTGTGAGACCT[C/G]TAAAGTACCGGTATA | 8027 |
rs184978096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17668435 | GAACCAATATTGATA[C/G]ATTACTATTAACTAA | 8027 |
rs185023550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17671240 | GAATGGTAAACCACA[A/G]TAAAGCTTTTTTTGT | 8027 |
rs185088818 | snp | C/T | 0.029116 | 0.117091 | intron-variant | STAM | GRCh38.p7 | 10:17656288 | GACAGAGCGAGACTC[C/T]GTCTTAAAAAAAAAA | 8027 |
rs185113544 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688486 | GTTTGTTTTTGAGAC[A/G/T]GAGTCTTTGTTTGTC | 8027 |
rs185139580 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | STAM | GRCh38.p7 | 10:17653324 | TTTGTGAAAATGCTT[A/T]GTGATGTGTGGATTC | 8027 |
rs185248848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695498 | TTTTCGGTTCCACCT[A/G]ATAATATAGATGGTT | 8027 |
rs185250991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17707914 | ACTTTTTTTTGAGAC[A/G]GAGTCTTGCTTTGTC | 8027 |
rs185266471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17677554 | CCCTGGCTCCTAAAA[C/T]AAGTCCAACTGTGAA | 8027 |
rs185333782 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | STAM | GRCh38.p7 | 10:17691385 | TAGCCAGGCGTAGTG[A/G]CAGGTGCCTGTAGTC | 8027 |
rs185335927 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17711495 | TAAAAAAATATAATT[G/T]TATACAACATGATTT | 8027 |
rs185394176 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697970 | TCATCTTTTTATTTC[C/T]AGCAGCTCCTAATAG | 8027 |
rs185396068 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17673046 | TTAAGAAGCTTTTTG[A/G]GAGAGATGAGGATTT | 8027 |
rs185486773 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17694584 | GTTAGGTTGAGTCTT[G/T]AGACTGGTAAGAATT | 8027 |
rs185487992 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17676612 | TGTGGATGAACATAG[A/T]TTTGGCTGTTGTGAC | 8027 |
rs185506276 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17693606 | GAAATGCCATTTGCC[A/G]CTTGCTTTTCTCATG | 8027 |
rs185557163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17661465 | CTTTTGGTCTCACAA[C/T]TTCCAGCTGTCTTTA | 8027 |
rs185563373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17646975 | CTGAATCAGAAATTC[A/G]CTGACTGATTTATAT | 8027 |
rs185589402 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17676008 | TTTACCATTAGATCA[C/G]AGAAGTGACTGCTGA | 8027 |
rs185610978 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17679323 | AATTGCTAGCGATGT[C/T]GAGCATTTGTTATGT | 8027 |
rs185619052 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17707137 | GATACTGGCCGGGTG[C/T]GGTGGCTCATACCTG | 8027 |
rs185620174 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | STAM | GRCh38.p7 | 10:17648670 | TTACCTTACTTCAGT[C/G]ATTGTTATCTCTTAT | 8027 |
rs185629120 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17710205 | CATGCTGCTCTACCT[A/T]CCTTGTTACTAGAGA | 8027 |
rs185729830 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716109 | AATCTTAAATATTTA[C/T]GATTTCCCTGGTTGG | 8027 |
rs185743958 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17663996 | TTTTATGACTACATT[G/T]TTTTAAGGAAAAATA | 8027 |
rs186109023 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17701765 | CTCTCCAACTTTACG[A/G]AAGAAAGGCTTACCG | 8027 |
rs186112910 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17647667 | GTTTCCTTATCTTTA[A/T]TATGGAATATAAGAG | 8027 |
rs186117120 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17669478 | TTTAAATTGGCCTAG[A/T]TTTAAATTAACAAAT | 8027 |
rs186208253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712974 | GGAAATAAAAGAAAT[A/G]AGGTTATGAGGCCTT | 8027 |
rs186240125 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17662130 | TATCCAGTTGCCGTA[C/T]AACAGCTGTGTTCAT | 8027 |
rs186244306 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17684126 | GTCACTTTTTGACCA[A/G]TTTCATGGAGTTTTT | 8027 |
rs186255708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665591 | TGTATTTCTTTTAAG[C/T]CTATTAGTATTGGAC | 8027 |
rs186291786 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715474 | TGTCATCACACCAGC[A/G]TACAGTAGCTAAATT | 8027 |
rs186317937 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715777 | ACATTTTCGAAGTCT[C/T]TTGTAATTATTTGGG | 8027 |
rs186325422 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17702242 | TGAATCTAATACTGA[G/T]AGTATTATCAGTTTA | 8027 |
rs186348307 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17707480 | TTTTTTCCATGTAAA[A/G]TGGGCACGGACTGTG | 8027 |
rs186355221 | snp | G/T | 0.000362184 | 0.0134522 | intron-variant | STAM | GRCh38.p7 | 10:17705547 | GAGCATTATATCATT[G/T]TAGTAACAGCTATGC | 8027 |
rs186365053 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | STAM | GRCh38.p7 | 10:17654285 | TGGAGTGCAGTGGCA[C/T]GATCTCAGCTCACTG | 8027 |
rs186380675 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17686413 | ACAGTGTCTCTCTTT[G/T]TCACCCAGGCTGGAG | 8027 |
rs186387994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17686612 | CTCGAACTCCTGACC[G/T]TGTGATTGCCCACCT | 8027 |
rs186392547 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17669801 | CTCCCAGGTTCACAC[C/T]GTTCTCCTGCCTCAG | 8027 |
rs186399033 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17653783 | ATTCAATGCCATTTT[A/T]TATTAGGGACTTGAG | 8027 |
rs186421147 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17650388 | GACTCTTTACCAGAG[G/T]TGAATAGGCTTCAAA | 8027 |
rs186452247 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17680355 | CAATAACTCCCCATT[C/T]GCTGCTCCCCAGGCC | 8027 |
rs186501117 | snp | A/T | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689748 | AGAGTCTTTGGTTCT[A/T]GTTAACTCAAAACTT | 8027 |
rs186501234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17650741 | GATATTTTTAAAATG[G/T]GAATGTACGCGTGGC | 8027 |
rs186501608 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17672232 | ATAACTGTACAACAG[G/T]ATACCTATAAGTAGA | 8027 |
rs186511269 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17657443 | TCTTGTAATGTTTTT[A/G]TCTGGTTTTGGTATC | 8027 |
rs186566998 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | STAM | GRCh38.p7 | 10:17669951 | TAGCCAGGATGGTCT[C/G]GATCTCCTGACTTCG | 8027 |
rs186606825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17702727 | TATATAAGAAAATGC[C/T]GGCCAGGCGCAGTGG | 8027 |
rs186808888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17670659 | AATATTTTAGTTCAG[C/T]ATGTAGAAGTTTAGT | 8027 |
rs186816985 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17655216 | TGTAAGCTACTTCTG[G/T]TAGGGTATGGCGTGG | 8027 |
rs186918167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17709021 | GCCCCCAGTTATCTA[C/T]AACTATAAAATCTGG | 8027 |
rs186927896 | snp | A/G/T | 0.000138136 | 0.00830978 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696757 | TTATGGTAAAGCATT[A/G/T]TTTTTTGTTTGTCAT | 8027 |
rs186929670 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17672641 | CTTCTTCAGCTGTTG[C/T]TCAAAGTAACAGTTT | 8027 |
rs186972744 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17705179 | GTGGAGAATTAGACT[C/G]ATTTGTCCTTTTTTT | 8027 |
rs187056711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692665 | TTATTTACACAATTT[A/G]ATAGAGGCAGTGATA | 8027 |
rs187058156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713537 | GTCTACTATGGTCCC[A/G]TCATAGTATTCTGAA | 8027 |
rs187104475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17660731 | ACAGCCAATGTACAC[A/G]AGTCAGGGCAACATA | 8027 |
rs187134348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17658239 | GTGTTAGTCTCCATG[C/T]ACTTTGGGATTTTCC | 8027 |
rs187167501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691247 | TGCCTGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 8027 |
rs187176932 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17648508 | ATAAATCTTGGTGCT[A/G]CTCACTCTTTGGGTC | 8027 |
rs187188055 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | STAM | GRCh38.p7 | 10:17680632 | GGCTGGTCTCACACT[C/T]CTTGGCTGGAGCAAT | 8027 |
rs187199933 | snp | A/T | | | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696443 | TAAGAGCCTGTCTTT[A/T]TAGCTCATTACAAAG | 8027 |
rs187202974 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17678683 | TATAATTCAGTGGTA[A/T]TTAGTACATTCACAG | 8027 |
rs187206153 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17663613 | CCTTTAATAGTTATT[A/G]CTCTCTGGTTCTTTT | 8027 |
rs187216452 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712227 | GGTAAACTATTACCC[C/G]CATTTTATAGATGGG | 8027 |
rs187287536 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645444 | GAGTAGAAAAAAGTT[C/G]ACTCCTTACCTCTGC | 8027 |
rs187404607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17699016 | TTGGAAATTAAGCTA[C/T]TTCTGTGTTATACAG | 8027 |
rs187417532 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | STAM | GRCh38.p7 | 10:17666677 | GCTGGGATTACAGGC[A/G]TGAGCCACCCTGCCT | 8027 |
rs187495955 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17708401 | TATCCATTGCAGTCT[A/G]TGGCTACAAAACAAT | 8027 |
rs187551942 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717068 | ATTTATAAAATGAAC[A/T]AGCTGTAACATAGGC | 8027 |
rs187564668 | snp | A/C | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713775 | GTCAGCTATCCTGGT[A/C]CAGAGGGAGCCCGTT | 8027 |
rs187572533 | snp | A/G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17681921 | GTTATATGAATGATT[A/G/T]CTCTGCTTTACTATT | 8027 |
rs187601803 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17655767 | CATTTCCACTGTCCC[C/G]CCAACCCATCTGTGT | 8027 |
rs187613755 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17699256 | TTGGGAGATTCATTG[C/G]AGGAAATGTAATATT | 8027 |
rs187624092 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17703557 | GTAGTGGTCATGGTA[A/G]AGTAGATCTGTTTGG | 8027 |
rs187641151 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687636 | AAAAATGCATAGTCA[C/T]GAACATTAAGAAGTC | 8027 |
rs187645481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17671006 | TCTGTGACATGCCTT[C/T]ATGCTTATGAAAGGC | 8027 |
rs187672241 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17681214 | TTTTTTTTTTTTTTT[G/T]TAATGTAGGTGCTTA | 8027 |
rs187673241 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17667288 | AACGCCACCATGCCC[A/G]GCTATTTTGTATTTT | 8027 |
rs187681031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17650926 | AAAAATTAGCCGGGC[A/G]TAGTGGCGGGCGCCT | 8027 |
rs187681766 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17679133 | GCTTAATTTTTTGAG[G/T]AACTACCACACTTTT | 8027 |
rs187683463 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17702940 | TTGAATCTGGGAGGC[A/G]GAAGGTCGTAGTGAG | 8027 |
rs187701839 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17648664 | CCATTCTTACCTTAC[C/T]TCAGTCATTGTTATC | 8027 |
rs187783214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17667675 | CTAACAGATGATGGT[C/T]AATAGCTAAGAAGCT | 8027 |
rs187791960 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17705805 | AGGTGTGGTAGCTCA[C/T]GCCTGTAATCTCAGC | 8027 |
rs187794353 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17651783 | TTCTTTCAGACTTAC[G/T]TTTCCATTGGCCATT | 8027 |
rs187804963 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17673210 | GTTCCTCCCAGCACT[A/C]CTTATTGTGCGTTTT | 8027 |
rs187837697 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17700665 | TATTGAGTTGAAGGA[A/T]TTGTGTATTTTCCAT | 8027 |
rs187840950 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17667411 | ACAGGCGTGAGCCAC[C/G/T]GCATCCAGCCCATAG | 8027 |
rs187974281 | snp | C/T | 0.00795532 | 0.062565 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716623 | ATTCCTGTTTACCAA[C/T]GTTAAATGTATCATT | 8027 |
rs187982419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17663833 | ATACTGTTTAACATA[C/T]ATCTCCAGTTGTGTT | 8027 |
rs187990042 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17687037 | AATGAACTGGCCAGG[C/T]TTTTTCCCTTAATAA | 8027 |
rs188117604 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17681496 | GTTTTATGGCTTAAC[A/G]TTGTTTATCATGTGT | 8027 |
rs188134107 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17651499 | ACAAGTATGTTAACC[A/G]TCTGATATCCACTGG | 8027 |
rs188273220 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17685815 | ACAACTGCCCACTCA[A/G]CTGTAGAATTCTAGT | 8027 |
rs188275496 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | STAM | GRCh38.p7 | 10:17669555 | TCTTTTTGTTTATAA[A/C]CTTTAGTAGTGTTTT | 8027 |
rs188282572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17693334 | TTTTAAGTCCCTGAT[A/G]GTGGGAATAACATAA | 8027 |
rs188407536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689230 | GTGCTGATTTACTAC[A/G]CTGTCTTTCCCCAGT | 8027 |
rs188423479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17672170 | ATACCTTTTCAGATA[A/G]TCTCACTAACTGGTG | 8027 |
rs188429473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17657239 | GACTGTTAGGAGCTT[C/T]TCTCTCCTTGGTGCA | 8027 |
rs188489692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17674410 | CACATAGTGCCTGGG[A/G]CTAGGGTCATCTGAA | 8027 |
rs188535475 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642784 | TTCATCCAACAGTAT[G/T]TGAGTGTCTGACTCC | 8027 |
rs188562348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17675657 | ACACTAGGCTAGACT[A/G]TGAACTTCATGAAGC | 8027 |
rs188576736 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | STAM | GRCh38.p7 | 10:17659715 | TGATCCTCCCACCTC[A/G]GCCTCCCAAAATGCT | 8027 |
rs188638816 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696023 | CAAATGAGCCCTCTG[G/T]GGTCTCTTTTATAAG | 8027 |
rs188646940 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | STAM | GRCh38.p7 | 10:17662902 | GGCACCAAGCTAGAC[C/G]ACTTCATGTGCATTT | 8027 |
rs188705801 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17669569 | ACCTTTAGTAGTGTT[A/C/T]TTAAGTTTTCCTCTT | 8027 |
rs188771007 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17692250 | ACCACTCATATCGCA[C/G]TACCTTGTTTAAAGG | 8027 |
rs188776704 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17658763 | AAGTGTTGGGATTAC[A/T]GGCAAAAGCCACTGT | 8027 |
rs188835608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17659201 | ACACTGTACCACTTC[A/G]TGTGTAATGCAAGTA | 8027 |
rs188890564 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | STAM | GRCh38.p7 | 10:17664843 | GTAAAGTGCGGCGAT[C/T]TTTTTAAGAGGACAG | 8027 |
rs188899201 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17649563 | TTCATTTTTTTTCCC[C/T]TAATACTTTAGGGAT | 8027 |
rs188918297 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697850 | AAATATCTCATTATC[A/G]TTTTTTAATGCTAGA | 8027 |
rs188920279 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | STAM | GRCh38.p7 | 10:17710972 | TTTCAACGGGGAAAT[G/T]AGGAATTGCTGGTAG | 8027 |
rs188922738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17678023 | ATTTTAGAATATACA[A/G]TTCAGTGGGTTTTAA | 8027 |
rs188935975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17679749 | TGTTTCTTCTTAAGT[C/T]AGTTTCTTTTCTTTT | 8027 |
rs188945839 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | STAM | GRCh38.p7 | 10:17708081 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT | 8027 |
rs188987872 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17648273 | ACGCACCAATCAGTG[C/T]TCTGTAGCTAGCTGG | 8027 |
rs189002381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714235 | AGAACCACTTGACAC[A/G]CGATACATGTGTTTG | 8027 |
rs189038085 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17668311 | AAGGGAAATGAATGC[A/G]CATTGCTTAGCATAA | 8027 |
rs189047967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17652787 | GATATTGTTCAGAAT[A/G]ACTCACTCAATATTC | 8027 |
rs189062402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17701218 | CTGCTGTTACTGCAT[A/G]TAAAGAAAAGATTAA | 8027 |
rs189072562 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17682370 | TTTATCCATTCATCT[C/G]TTGATGGGCATTTGG | 8027 |
rs189079018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17646563 | AGTTGAGAATGTGTC[A/G]GTTGAGCCTGCCAGA | 8027 |
rs189092661 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715573 | GTATTGTGGGACCAT[A/G]AGACAAAATTAAGTA | 8027 |
rs189141012 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17660369 | GATTTGTTGTTAAGA[C/T]TTGATTATACTATAG | 8027 |
rs189222644 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17648876 | GTGGCTCACAATATG[A/G]CTTCTTCCTGTGTGT | 8027 |
rs189236241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17703976 | AAGCTAAAGCTGCTC[C/T]GAAACAAAGCAAAAT | 8027 |
rs189276404 | snp | A/G | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17690121 | ACTCAGAATGGTTAA[A/G]TGACTTGCCCAGGGA | 8027 |
rs189280764 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17672465 | TCCTCAGATTTTTTC[A/C]CAAAAAACTTGTGCC | 8027 |
rs189315058 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17704844 | CTGTAGACTAAGGTT[A/G]AAGAATGTATATTTT | 8027 |
rs189373259 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17701847 | ACCAGGGATGATTTC[A/C]TATACTGGTTTTGGT | 8027 |
rs189381857 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17701621 | GCTTGGCCCTTGGTA[C/T]GGATAATTTAAAGAG | 8027 |
rs189396093 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17668818 | TTCTTATTGCTGAAT[A/C]CTCTTCCATTATATG | 8027 |
rs189418428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17675834 | CTCTAATTTTTATGG[C/T]GGTGATTCACCCTGA | 8027 |
rs189429421 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643916 | ACTCCTGGGGTTGTT[A/C]GTAGGCTTCAGCACG | 8027 |
rs189657943 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17707970 | ATCTCAGCTCGCTGC[A/C]AGCTCCGCCTCCTGG | 8027 |
rs189671719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17683627 | CACTTTTTAATTTTA[C/T]ATATTTTTTTGTCTC | 8027 |
rs189691032 | snp | A/C | 0.00795532 | 0.062565 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715079 | AGAAAGTCAAACTTA[A/C]AAAAACTGTTGTGAC | 8027 |
rs189725192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17653203 | TCATAAATCATACCT[A/G]TATAATGACACCCCA | 8027 |
rs189769586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17658550 | TGGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 8027 |
rs189799582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17653617 | TGTAGAGGAAAAAAT[A/G]TCATGTCTGTACCGA | 8027 |
rs189802791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691496 | GTACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 8027 |
rs189807187 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17673081 | ACCCTTTAAACAGGT[A/G]GGTGATGGAAACCTT | 8027 |
rs189913776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17661663 | ATTAATGACAAGATG[A/C]TTCTTTCATTGCACT | 8027 |
rs189922239 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17647479 | TGCCCTGCGGCTCAG[G/T]TCCGGAGCCTCTTCT | 8027 |
rs189944493 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688806 | AGCTTTATTAATTAG[G/T]TAACACTGTCTTTTT | 8027 |
rs189947798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17707541 | CAGCACCCTGTAGAT[G/T]AACAGCTAGGCCCAA | 8027 |
rs189952210 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17694771 | AGTAGATTTAAGAGT[A/T]TGTATTTTTTATTAC | 8027 |
rs189954413 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17676808 | CCAGAAGTATACTCA[A/C]GTTAAATTCACTTAT | 8027 |
rs189984814 | snp | C/T | 0.0119091 | 0.0762411 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717317 | GCAGTGAGACGAGAT[C/T]ACGCCACTGCATTCC | 8027 |
rs190040790 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | STAM | GRCh38.p7 | 10:17707334 | AGAATGGCATGAACC[C/T]GGGAGGCGGAGGTTG | 8027 |
rs190116499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17676194 | TTAAGGAAGGTTCAC[A/G]ACTTAATTTTCATTT | 8027 |
rs190198021 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17703631 | AGATGTGTGTATGTA[A/T]TAATGGTTTCATTCA | 8027 |
rs190209500 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697175 | CTCAGGTGATCCACC[C/T]GCCTCAGTCTCCCAA | 8027 |
rs190214248 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17671282 | TGAAGATGTAATGTT[G/T]AAATCACTCTAAAAT | 8027 |
rs190273388 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | STAM | GRCh38.p7 | 10:17664009 | TTGTTTTAAGGAAAA[A/G]TATATTAGTATTATA | 8027 |
rs190301297 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17693759 | ATTTTTTTTTACTAA[A/T]ATTAAGCTGCAGTGA | 8027 |
rs190370023 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17661145 | TTTGGCATGTATTAC[A/G]GAGCTTTCCAAACAG | 8027 |
rs190437382 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17710397 | CCTGGCATAGGCCCA[A/C]CCCTACCCATAGAGT | 8027 |
rs190450454 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | STAM | GRCh38.p7 | 10:17657685 | TCTTGTATGTATTTC[A/G]GCAGATTATGTCTTT | 8027 |
rs190454010 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17679334 | ATGTTGAGCATTTGT[C/T]ATGTGCTTATTGGCC | 8027 |
rs190538549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17681441 | TCTTTGGAGAACATG[C/T]TTTCTATGATTTTTT | 8027 |
rs190554741 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17667312 | GTATTTTTAGTAGAC[A/G]TGGGGTTTCAACGTA | 8027 |
rs190562652 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | STAM | GRCh38.p7 | 10:17650982 | AGGCAGGAGAATAGC[A/G]TGAACCTGGGAGGCG | 8027 |
rs190576901 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17699261 | AGATTCATTGGAGGA[A/C]ATGTAATATTCCATC | 8027 |
rs190581355 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, synonymous-codon | STAM | GRCh38.p7 | 10:17713377 | CACAGGACAGCAGGC[G/T]TGAATAGCTGATTGC | 8027 |
rs190684105 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695570 | TGTATATGTACTTAA[A/T]GCAATTTGTAAGAAA | 8027 |
rs190689750 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17686437 | GCTGGAGTACAGTGG[C/T]GTGATCTCAGCTGAC | 8027 |
rs190695180 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | STAM | GRCh38.p7 | 10:17669825 | GCCTCAGCCTCCCCA[A/G]TAGCTGGGACTACAG | 8027 |
rs190716957 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17715919 | AAAGTAATCTACATT[A/C]CTGGCTTTGCTTAAC | 8027 |
rs190722186 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | STAM | GRCh38.p7 | 10:17702303 | GTCATCGGTAGAAAA[A/C]TTTCAAGTATATTAG | 8027 |
rs190734798 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17663105 | ACTATAAATATTCCA[C/T]GTTTTTCCAGTTAAA | 8027 |
rs190761892 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17662196 | AGCTCCTTAGTCTTC[G/T]GAATCATGCATTTTC | 8027 |
rs190835237 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | STAM | GRCh38.p7 | 10:17650808 | CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT | 8027 |
rs190846342 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17680487 | GAGTTCAGTGGCGCA[A/G]TCGTGGCTCACTGCA | 8027 |
rs190871157 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712168 | AGCACTGTGCTGTAT[C/G]CTTTACACAAAGTAA | 8027 |
rs190882187 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17666729 | TTGTCCTGGACTGGA[C/G]TGTGACTATTTCCGG | 8027 |
rs190912489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17650606 | CAGATACCCTGGTAC[C/T]GAATATGCCCTCAAG | 8027 |
rs190946043 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17677622 | TTTCTTCAGTCTAAT[G/T]ATGCTGCTATCCAAA | 8027 |
rs191014686 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17647878 | TCTTGCCTGAGCTCT[C/T]GACCTAGATATCCAT | 8027 |
rs191017321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17670163 | GAAGTCAAGTTGTTG[A/G]CTAGGCAATAGGGAA | 8027 |
rs191044295 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | STAM | GRCh38.p7 | 10:17706052 | TAGCCTGGGCAACAG[C/T]GACACCCTGTCTCTA | 8027 |
rs191091181 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698701 | ACAGTAAAATATTGT[A/G]AAATCCCTTTGTTAT | 8027 |
rs191099443 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | STAM | GRCh38.p7 | 10:17666587 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 8027 |
rs191187319 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17670840 | TGATATTTGTACTCT[A/G]TATTTTGCTCCTTTT | 8027 |
rs191193163 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17655506 | GGTAGTGACTAACTA[A/G]CAGGTGATGCTGTGA | 8027 |
rs191212528 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17703110 | TCTTTGACACTAAAT[A/G]ATTTTAAATATTGTA | 8027 |
rs191220758 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | STAM | GRCh38.p7 | 10:17687373 | CTACTCGGGAGGTTG[A/T]CACAAGAGAATCGCT | 8027 |
rs191263248 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | STAM | GRCh38.p7 | 10:17654359 | TCCCAGGTAGCTGGG[A/T]CTACATGCGCCCACC | 8027 |
rs191354335 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17702767 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCGG | 8027 |
rs191433548 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17692792 | ATCCTGACACTTGAT[C/T]CAAAAGGAAATGATA | 8027 |
rs191449623 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17660166 | AGTATTTCTTATTTT[A/C]GTCTTTCTATTTGCA | 8027 |
rs191477248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706803 | TCAATAAAGTAGTTT[C/T]GTAAAAAACACAAAA | 8027 |
rs191502047 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643803 | CCATTTCCTTCCAGA[G/T]GGAATACAAGGTTAT | 8027 |
rs191504333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691290 | TTGGGAGGCCGAGGC[A/G]GGTGGGTCACGAGGT | 8027 |
rs191570301 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | STAM | GRCh38.p7 | 10:17658302 | TCCATTGTAATCACT[A/G]TGTGATTTCTATTGT | 8027 |
rs191583660 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716282 | TTATTTTCTTTTTGA[G/T]AGAAGATTAAATCTT | 8027 |
rs191592815 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17708300 | TATTTACGTCAGGCC[C/G]TTTACAAAAAAGTTT | 8027 |
rs191594324 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | STAM | GRCh38.p7 | 10:17686746 | TAGTCTCAATAAAGC[A/G]TTTGCAAATCCATTA | 8027 |
rs191635493 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | STAM | GRCh38.p7 | 10:17648582 | GGCTTCATTCTTGAC[A/G]TCAGCGAGACCACAA | 8027 |
rs191655889 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17653839 | AAGATCCTGGAACCA[A/T]TCTCCCATGTATACC | 8027 |
rs191682940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17678477 | CAGGCTGGTCTCGAA[C/T]TCCTGATCTCAGGTG | 8027 |
rs191739694 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | STAM | GRCh38.p7 | 10:17705190 | GACTCATTTGTCCTT[C/T]TTTTTAAAGTGAGGA | 8027 |
rs191812868 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17672880 | GATAAGTAGGTATTT[C/T]TAGGTGGAAAACTGG | 8027 |
rs191818822 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17699060 | GGAGTACCCAAGTGA[G/T]TGGACTTCATGTTCT | 8027 |
rs191914884 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17678974 | GAATTTCCTTAAGGC[C/T]GAATACTATTCCATT | 8027 |
rs191916799 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17663738 | TTAAACAATAATTGA[G/T]ATACCATTCTAATAT | 8027 |
rs191933153 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17701460 | CAAATTTAGCCTGTT[G/T]CCTGTTTATTGGAAC | 8027 |
rs191945899 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696603 | TGAATAGCTTCTTAC[C/G]TTTTCTGAGGCTTCT | 8027 |
rs191946648 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17683202 | AGGGTCTCACTCTGT[C/G]TCTCAGGATGGAGTA | 8027 |
rs191949232 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17708657 | CAGAAATAACTTTGA[A/T]AAAAGGATTCCAGAG | 8027 |
rs191963170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696232 | TTGCCCAAAACCTTA[C/T]GTCTGTTCTTTCAAA | 8027 |
rs191976868 | snp | A/G | 4.95193e-05 | 0.00497566 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714829 | TAAATGCCACTGACA[A/G]TGTTATGAGATTCAT | 8027 |
rs192067064 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642199 | AACATTGTCTAGAAT[A/C]TTGCCACTCAGAGAC | 8027 |
rs192105857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17703571 | AAAGTAGATCTGTTT[A/G]GATTTTTTAAAAAAC | 8027 |
rs192113928 | snp | A/G | 0.000165843 | 0.00910461 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688140 | TAAGAACCTTAAGGA[A/G]CAAGGAGTTACGTTC | 8027 |
rs192119333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17680821 | CATCCCTGTTATAGC[A/G]TATTCCATGTATGTA | 8027 |
rs192132804 | snp | C/T | | | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717088 | GTAACATAGGCTGGA[C/T]GCAGTGGGTCACACC | 8027 |
rs192208920 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17648310 | GTAAAATGCACCAAT[C/T]AGTGCTCTGTAGCTA | 8027 |
rs192251922 | snp | G/T | 0.0123036 | 0.0774623 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17716934 | AATGACAAGACGAGG[G/T]TAGAAATAGGAGGGG | 8027 |
rs192251945 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | STAM | GRCh38.p7 | 10:17663949 | ACTTTTGTCTTCTTG[G/T]GCTCCTCTTTCTATT | 8027 |
rs192320206 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713668 | TTATCTTCAAAATCT[A/G]TCTAGACTCTGACCC | 8027 |
rs192398639 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17681892 | TGAGAGCCTAAGCAC[A/G]TGATGTTTCGTAGGT | 8027 |
rs192409790 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17651564 | TATTTTACCTCTCCT[C/G]TAAGCTGTTTTTTCT | 8027 |
rs192483091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712555 | GAATTTCCCAACAAT[A/G]GATTTATAAATAACA | 8027 |
rs192580751 | snp | G/T | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17709608 | CTGAAATCTTTTCCT[G/T]GAAGCAAATAAAGGA | 8027 |
rs192651772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17667689 | TCAATAGCTAAGAAG[C/T]TAGTAACCAGAGTGC | 8027 |
rs192659780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17679220 | ACTACATCCCCTCCA[A/G]TATTTGGTATCTTTC | 8027 |
rs192666247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17651974 | TCTCTAATCTTTTGA[A/G]AAGACTATTGAAATT | 8027 |
rs192672644 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17648667 | TTCTTACCTTACTTC[A/C]GTCATTGTTATCTCT | 8027 |
rs192684851 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17700964 | TTGTGTTGAACACTT[C/T]CTAGTATTTGAGGAA | 8027 |
rs192701181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17682107 | AATATATATACCTAT[A/G]TAAGTATCACCCCAA | 8027 |
rs192722490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17700091 | TTTAGCTTGCTGGGA[A/G]TATAAGAAAAATCCC | 8027 |
rs192759078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17667413 | AGGCGTGAGCCACCG[C/T]ATCCAGCCCATAGAA | 8027 |
rs192763681 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17703637 | GTGTATGTAATAATG[A/G]TTTCATTCATTCCAT | 8027 |
rs192799418 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | STAM | GRCh38.p7 | 10:17671724 | AACATATTTGTTAAC[C/G]ATGTTTTTTATTATT | 8027 |
rs192866425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692404 | GCAAAGGAGCCATAG[A/G]GGGAGAACGTTGTAA | 8027 |
rs192876557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17659594 | CCACTTCAGCCTTCT[C/T]GGTAGCTGGGAATAC | 8027 |
rs192941994 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17655927 | ATGATTTTTTTAAAG[A/T]TTTTTTTCCTCCTAC | 8027 |
rs192987822 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17656495 | TGCAATATTACTGTC[G/T]TTAGGTCTTTCCTCT | 8027 |
rs193004745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689012 | TCTCCTTAGTAAGAG[C/G]CGACCAGTACATAAG | 8027 |
rs193044074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706333 | ATATCCATCCCACTC[C/T]AGACCTATTGAATCA | 8027 |
rs193080776 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | STAM | GRCh38.p7 | 10:17674931 | TACTTGAGACACTCA[A/G]TCCTTAAGAATGGAA | 8027 |
rs193144784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17673279 | TTATGAAAGGATGTA[C/T]GTTTTCCACTTAGCG | 8027 |
rs193159426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17671107 | TCATTCAGCAAAGAT[C/T]TGAGTTCCCATGTCT | 8027 |
rs193210430 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17658778 | AGGCAAAAGCCACTG[G/T]GCCTGGCCTCATCCT | 8027 |
rs193292425 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17691967 | ATTACCTCTACATAC[G/T]TTATAAGCCCCGGAG | 8027 |
rs193299456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713807 | AACCCTGTGGAATCT[C/T]ATCACGCTTCTGCTC | 8027 |
rs199630448 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17683119 | CTGTTTTCTCTTTCT[A/G]TCTTTTGTGTATCAA | 8027 |
rs199636279 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17673252 | CTTTATTATAGTTCT[A/G]TTAACTACATTTTAT | 8027 |
rs199678940 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17662063 | CTTGCCTAGGCTAGC[A/G]AATTAACCCACTGGC | 8027 |
rs199745685 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17675517 | CAAAAAAAAAAAAAA[-/A]GATAGTAGCGTTTTC | 8027 |
rs199769248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17646279 | GGGTGTTCAGCCTTA[C/T]CCCTGGCCTTTATCC | 8027 |
rs199779874 | snp | A/G | 0.000291323 | 0.0120655 | intron-variant | STAM | GRCh38.p7 | 10:17705559 | ATTTTAGTAACAGCT[A/G]TGCTTCAAATTATTG | 8027 |
rs199781423 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17672069 | ATTTTCAAAAGTTTT[A/G]TACAGCATAGGATGT | 8027 |
rs199802161 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17692833 | TAATAGATACTACAG[-/T]TTTTTTTTTTAACTA | 8027 |
rs199845803 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17663124 | TTTCCAGTTAAAAAA[C/T]CAATTTGTAATGCAT | 8027 |
rs199850982 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17687499 | GTCTCAAAAAACAAA[A/C]CAAAAAAAAAGAAAA | 8027 |
rs199875490 | snp | C/T | 4.94311e-05 | 0.00497123 | synonymous-codon | STAM | GRCh38.p7 | 10:17705660 | TACCAAGTTAATGAA[C/T]GAAGATCCGATGTAT | 8027 |
rs199887417 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17660586 | GATTTTTATTCTTTC[C/T]TTTTAAAAAACACGA | 8027 |
rs199991053 | in-del | -/T | 0.0240643 | 0.107019 | intron-variant | STAM | GRCh38.p7 | 10:17650255 | GGACACAATGTATAG[-/T]TGGATAGGTATAGGA | 8027 |
rs200122875 | in-del | -/CC | 0.0244538 | 0.107838 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642904 | TAGCTGGGATTACAA[-/CC]GCGCGCACCACCACG | 8027 |
rs200167112 | snp | C/T | 0.000300832 | 0.0122607 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644394 | GGTAAGTGTTTTTGC[C/T]TCTCCCTGCCCATTC | 8027 |
rs200190968 | snp | A/C | 3.29554e-05 | 0.00405914 | missense | STAM | GRCh38.p7 | 10:17705679 | GATCCGATGTATTCC[A/C]TGTATGCAAAGTTAC | 8027 |
rs200238364 | snp | C/T | 0.00199801 | 0.0315438 | intron-variant | STAM | GRCh38.p7 | 10:17695026 | ATAACATTTTGGGTC[C/T]TTAAAAACTCATTGT | 8027 |
rs200264317 | snp | C/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, intron-variant | STAM | GRCh38.p7 | 10:17684691 | CCTAAGGATTGTCTT[C/T]GGTCTATTATGAGAA | 8027 |
rs200330404 | snp | A/G | 1.65611e-05 | 0.00287755 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688053 | AGTATGTGAAAAATT[A/G]AAGGCTCTTATGGTT | 8027 |
rs200423190 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17659125 | AAATCTTTTTTTTTT[-/T]AGTAATTGCCTAAGA | 8027 |
rs200495281 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17668475 | TTTGCATTAAGGTAC[A/T]CTTTGTTTTGTACAG | 8027 |
rs200552264 | snp | C/T | 1.82774e-05 | 0.00302297 | intron-variant | STAM | GRCh38.p7 | 10:17695257 | GTAATGTTAATATTA[C/T]ATTTAAAATTTGTAT | 8027 |
rs200585956 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714530 | GTAATTGAGTGTTTT[C/T]CTTCCTCCACAGTAC | 8027 |
rs200597809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17660447 | AATGTTTCTGCAATC[C/T]CCTTTACAATCTACA | 8027 |
rs200605156 | in-del | -/C | | | intron-variant | STAM | GRCh38.p7 | 10:17706366 | TCCTCAGGGTTGAGG[-/C]CCCTTTTTTTTTTTT | 8027 |
rs200616074 | in-del | -/T | 0.311614 | 0.242289 | intron-variant | STAM | GRCh38.p7 | 10:17680266 | TAAATACCTGCATAA[-/T]GTTGTGAACTCTAGT | 8027 |
rs200627075 | snp | C/T | 0.0176082 | 0.0921631 | synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714606 | AGTATATAGTCCTCC[C/T]CCTGCCGCTACTGCT | 8027 |
rs200632229 | snp | G/T | | | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696515 | TTTTTTCGTATTGGT[G/T]CCTCTTTTTTTGGGA | 8027 |
rs200689272 | in-del | -/AGATAT | | | intron-variant | STAM | GRCh38.p7 | 10:17677160 | TTATTTTGGTGCCAG[-/AGATAT]CTTTGCTTTGGTTTT | 8027 |
rs200739308 | snp | A/G | 0.000149309 | 0.00863901 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644321 | GGAGTCCCCGGGGAC[A/G]CCTCGGCACGCAGCG | 8027 |
rs200766819 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17669012 | ATGGTAAGACTGTTT[-/A]ATCTTTGTTAGAAGC | 8027 |
rs200778551 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17663125 | TTCCAGTTAAAAAAT[C/T]AATTTGTAATGCATC | 8027 |
rs200808235 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17699154 | GGCATTCAAATCCAG[G/T]CTTTGTCATTTATTA | 8027 |
rs200821922 | snp | C/G | 0.000265666 | 0.0115223 | missense | STAM | GRCh38.p7 | 10:17705598 | TTCAGAAAACATTCA[C/G]AACTCTCAGAACTTA | 8027 |
rs200934917 | snp | G/T | 1.67677e-05 | 0.00289544 | intron-variant | STAM | GRCh38.p7 | 10:17684652 | GTATTATTAAGTAAT[G/T]TTTACTTTTCTCATT | 8027 |
rs200965178 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17687501 | CTCAAAAAACAAACC[A/G]AAAAAAAAGAAAAGA | 8027 |
rs201034753 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17681815 | ACTTCAGTAAATGGA[A/G]GACTTGGTTTGCTGT | 8027 |
rs201039968 | snp | C/G/T | 1.64895e-05 | 0.00287132 | missense | STAM | GRCh38.p7 | 10:17700240 | TGATGTTCAGGTAGA[C/G/T]ACAATAGAACCAGAG | 8027 |
rs201053297 | snp | A/G | 1.64827e-05 | 0.00287073 | synonymous-codon | STAM | GRCh38.p7 | 10:17705642 | GGAGGCCCTTTCCTT[A/G]TATACCAAGTTAATG | 8027 |
rs201056538 | snp | A/C | | | synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714630 | TACTGCTGCTGCTGC[A/C]ACTGCCGATGTCACT | 8027 |
rs201065224 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17701276 | GTGTTTATGAAAAAA[A/T]AAAAAGTATGTTTGT | 8027 |
rs201170355 | snp | C/T | 0.000115364 | 0.00759399 | synonymous-codon | STAM | GRCh38.p7 | 10:17708904 | AGTGGTCCCACCATC[C/T]GCAAACCCAGCCCTT | 8027 |
rs201209873 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644150 | GGGGGCTTCCTCGGC[G/T]CCTTGCTGTTGCCGC | 8027 |
rs201231613 | snp | A/G | 1.64779e-05 | 0.00287031 | missense | STAM | GRCh38.p7 | 10:17695167 | AAAAGTTCGTGCTAT[A/G]TATGACTTTGAAGCT | 8027 |
rs201260526 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17680432 | TTTTTTTTTTTTTTT[C/T]TTTTTTTGGAGATAT | 8027 |
rs201295044 | snp | A/G | 0.00199806 | 0.0315443 | intron-variant | STAM | GRCh38.p7 | 10:17705056 | GCATTTATGTTGTGT[A/G]CCTTCTTTCCTGAAG | 8027 |
rs201367097 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17710346 | TGCTGCTGTTCTCTG[G/T]GTGTGACTCTGCTTC | 8027 |
rs201390969 | in-del | -/TAG | | | intron-variant | STAM | GRCh38.p7 | 10:17673292 | ATGTTTTCCACTTAG[-/TAG]CGAACTCAGTGGAAG | 8027 |
rs201399950 | in-del | -/C | | | intron-variant | STAM | GRCh38.p7 | 10:17707900 | TTTTTTTTTAATAAA[-/C]TTTTTTTTGAGACGG | 8027 |
rs201425906 | in-del | -/T | 0.219049 | 0.248077 | intron-variant | STAM | GRCh38.p7 | 10:17681198 | GGTATTGAGATCGTC[-/T]TTTTTTTTTTTTTTT | 8027 |
rs201464850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17658439 | AGTCTATAAATGTCA[A/G]TTGTCAATTATATAC | 8027 |
rs201475289 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17666385 | TTTTTCCTTGGCTTT[G/T]TATTTTTTTTTTTTT | 8027 |
rs201738946 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | STAM | GRCh38.p7 | 10:17705633 | GAAAGTGATGGAGGC[C/T]CTTTCCTTATATACC | 8027 |
rs201773289 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17651215 | TTCTTGCAGGTGTAT[C/T]TCACTCCTTATTGGT | 8027 |
rs201795138 | snp | A/G/T | 0.000116913 | 0.00764492 | intron-variant | STAM | GRCh38.p7 | 10:17660562 | GGGTAAGTATTTAGC[A/G/T]TTTCAAAGGATTTTT | 8027 |
rs201828537 | in-del | -/CAT | | | intron-variant | STAM | GRCh38.p7 | 10:17708593 | ACTAAAAATGAAAAC[-/CAT]CATCAACAGCCTATT | 8027 |
rs201871726 | snp | C/G | 0.00199796 | 0.0315434 | missense | STAM | GRCh38.p7 | 10:17693270 | GTAGCCAAGGATCCT[C/G]GTACTGTGGCTAACA | 8027 |
rs201917144 | in-del | -/AGAAA | | | intron-variant | STAM | GRCh38.p7 | 10:17687523 | AGAAAAGAAAAGAAA[-/AGAAA]GGAAAAAAAGTTATG | 8027 |
rs201928207 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17663123 | TTTTCCAGTTAAAAA[A/T]TCAATTTGTAATGCA | 8027 |
rs201938565 | snp | C/T | 3.29522e-05 | 0.00405894 | synonymous-codon | STAM | GRCh38.p7 | 10:17708850 | CCACCTCCAGAGCTA[C/T]AGTCTTCCCCCGGAG | 8027 |
rs201980854 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17710678 | TTTGTATCCCCACTG[A/T]AGACAGTATCTTGAG | 8027 |
rs202025632 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17660587 | ATTTTTATTCTTTCT[C/T]TTTAAAAAACACGAA | 8027 |
rs202095046 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696817 | CCATCAAGGCATAGG[A/G]TTATTTCCTTCTAAT | 8027 |
rs202140008 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17705906 | GACTCTGTCTCTACC[-/A]AAAAAAAAAAAAAAA | 8027 |
rs202178748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691116 | AGAAGTGTCTGATAA[C/T]TAAAACATTATCTAA | 8027 |
rs202195222 | snp | C/G | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715225 | TTTAATCATAAACAA[C/G]TACCATGTTTCTTAA | 8027 |
rs202226355 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17655531 | CTGTGATATATAGCA[A/G]GTATTATACACCTGT | 8027 |
rs202232803 | in-del | -/TCTC | | | intron-variant | STAM | GRCh38.p7 | 10:17657841 | TAGTAATTGGTGTTT[-/TCTC]TCTCTCTCTTTTTTT | 8027 |
rs367591695 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695617 | TTTTTTTTACACAGA[A/T]CAGTATAGCCATAGG | 8027 |
rs367611486 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17676927 | AAAGTTCAGTATTAC[C/G]TATCTGGTGGAAATA | 8027 |
rs367634267 | snp | C/T | 3.36576e-05 | 0.00410215 | intron-variant | STAM | GRCh38.p7 | 10:17708962 | CCAAAGTAATTTTAC[C/T]GTTGATTCTTGTTTG | 8027 |
rs367655001 | snp | A/C/G | 1.78029e-05 | 0.00298348 | intron-variant | STAM | GRCh38.p7 | 10:17695251 | TGACAGGTAATGTTA[A/C/G]TATTACATTTAAAAT | 8027 |
rs367772416 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17660713 | TGATGATTACACCCA[A/T]GAACAGCCAATGTAC | 8027 |
rs367804747 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17683532 | TTTTTTCATTTTTTT[-/T]CTCTCTGTACTTCAG | 8027 |
rs367879073 | snp | A/G | 3.3036e-05 | 0.0040641 | missense | STAM | GRCh38.p7 | 10:17695207 | AATGAACTTACTTTT[A/G]AAGCTGGAGAAATTA | 8027 |
rs367949559 | snp | C/T | | | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717133 | TTTGGGAGGCCGTGG[C/T]GGGCGGATCATTTGA | 8027 |
rs367999907 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17701535 | AGTGGAAGAATTGAG[C/T]AGTAGCAACAGAGAT | 8027 |
rs368016594 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17657851 | GTGTTTTCTCTCTCT[C/T]TTTTTTTTTTCCTTA | 8027 |
rs368043554 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697072 | TTACAGGCACCCGCC[A/G]CCATGTCCAGCTGTT | 8027 |
rs368109298 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17694204 | GGTTTTTGACCTTAA[A/C]TTTGATAATGGTGTA | 8027 |
rs368123848 | snp | C/T | | | missense, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688115 | AGCTTAGTCTAATAT[C/T]AGCAATGATTAAGAA | 8027 |
rs368140764 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17659363 | TTGTTGCTGTTATTA[C/T]TTAGAATAAACTATT | 8027 |
rs368151211 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17648267 | GTAAAAACGCACCAA[A/T]CAGTGCTCTGTAGCT | 8027 |
rs368157299 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17685135 | TCAAGCCATATTAGA[A/G]TGTTTTTAACCTGTT | 8027 |
rs368172602 | snp | A/G | 1.64819e-05 | 0.00287066 | missense | STAM | GRCh38.p7 | 10:17708905 | GTGGTCCCACCATCC[A/G]CAAACCCAGCCCTTC | 8027 |
rs368289928 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17673542 | TTCATTTTCTCAAAT[G/T]TCAGTTGACAGTTTA | 8027 |
rs368297927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17663025 | TTTTCATTTTGTAGA[C/T]GCTTTCTGTAATAAT | 8027 |
rs368302026 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17665741 | AGAAAGCCTACTAGA[G/T]GTAATCCCTGTTTAC | 8027 |
rs368313917 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17660352 | ATGCTGGCAACTATT[C/T]TGATTTGTTGTTAAG | 8027 |
rs368324610 | snp | C/T | 0.000164756 | 0.00907472 | missense | STAM | GRCh38.p7 | 10:17708861 | GCTACAGTCTTCCCC[C/T]GGAGCAGCTGTCTTC | 8027 |
rs368325190 | snp | A/G | 4.94173e-05 | 0.00497053 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714721 | ACTCTGCCTCAGCCC[A/G]GAGGCAGCCAACAGC | 8027 |
rs368328656 | snp | C/T | 1.70255e-05 | 0.00291761 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644424 | CCTCACCGGACTGCA[C/T]GCTCACTCTGCCAGC | 8027 |
rs368383034 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17679613 | AGTGTTGATGTTAAT[G/T]TTTAAACATTTGGTA | 8027 |
rs368394556 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17671606 | ACTGATGTTACTGAT[A/G]TAGTAACTAGCAGGG | 8027 |
rs368399479 | snp | C/T | 1.64931e-05 | 0.00287163 | intron-variant | STAM | GRCh38.p7 | 10:17684789 | TACCACGAAATTACC[C/T]GCCACAATTGAGCCC | 8027 |
rs368499916 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643710 | AATTCGTTCAGCTCC[A/C]ATGACTTCATCCGAG | 8027 |
rs368590006 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17672080 | TTTTATACAGCATAG[C/G]ATGTCACAAATCTTG | 8027 |
rs368598299 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697077 | GGCACCCGCCGCCAT[A/G]TCCAGCTGTTTTTGT | 8027 |
rs368675082 | snp | A/G | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715791 | TCTTGTAATTATTTG[A/G]GATATCAACAAAATT | 8027 |
rs368710070 | snp | C/G/T | 0.00174984 | 0.029528 | intron-variant | STAM | GRCh38.p7 | 10:17660599 | TCTTTTTAAAAAACA[C/G/T]GAAAGGCCAGGTGCA | 8027 |
rs368719685 | in-del | -/AG | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698508 | TCTGGACGATCTAAA[-/AG]AGAAACTGAAGCATC | 8027 |
rs368752898 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | STAM | GRCh38.p7 | 10:17704709 | ATTTTCTATCCAAAC[A/G]AAGTGTTCTGTTCAA | 8027 |
rs368790325 | snp | A/C | 9.92901e-05 | 0.00704522 | intron-variant | STAM | GRCh38.p7 | 10:17693183 | GAGGAGGAGAATTTG[A/C]TAACAACCCTCAAAT | 8027 |
rs368820883 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642544 | ATGAGGAAACTGAGA[C/T]ACCAAGAGGTGAAGC | 8027 |
rs368860944 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17664835 | GAAATTTTGTAAAGT[A/G]CGGCGATCTTTTTAA | 8027 |
rs368881610 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17676558 | CTTTTACCCTCTTAC[A/G]AACTATATGACCCAG | 8027 |
rs368916030 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17712419 | TATATCTCACACATA[G/T]GGAGTGATGACAAAT | 8027 |
rs368920417 | snp | A/C/G | | | intron-variant, missense | STAM | GRCh38.p7 | 10:17713282 | AGCCGCTCCCCAGGG[A/C/G]ACCTCATGAAGCCCG | 8027 |
rs368942442 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17680011 | GTTTTTCAGTTTTGT[G/T]GATCCTTTAAAAAAA | 8027 |
rs369035726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17701416 | GAAGTGTCACATTGT[A/G]TAGATCAGGAGTTGG | 8027 |
rs369068316 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17709352 | ATATAGTTCTGAGCT[A/G]TCTCTTTAAGACAAA | 8027 |
rs369258609 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17707589 | GGCACCTGCTTTAGA[A/G]TCTTGATCACCAGTT | 8027 |
rs369289055 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17680076 | CTGTTGTCTGTTTTA[C/T]TTATTGCCTCTCTTT | 8027 |
rs369309979 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688939 | TTTATGAATTCCTCT[A/G]TTAACAATGAGAGGA | 8027 |
rs369326666 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17656294 | CGAGACTCCGTCTTA[-/A]AAAAAAAAAAAAAAA | 8027 |
rs369333324 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17679462 | ATTCTGGCTGTTAAT[C/G]TCTTGTCATATATAT | 8027 |
rs369377221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17677947 | ATTGGAGTTCAAATT[A/G]CCCGATAAAAGTTTT | 8027 |
rs369387094 | snp | C/T | 3.31813e-05 | 0.00407302 | intron-variant | STAM | GRCh38.p7 | 10:17704386 | GAAAACATAAAGTTG[C/T]CTAAAGGTTGGTAGC | 8027 |
rs369387534 | snp | A/G | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715853 | TTAAATATGTCTTTA[A/G]CACATTGTATCCTTT | 8027 |
rs369452515 | snp | C/G/T | 0.000116509 | 0.00763166 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644292 | TCGAGCTCTGACTCC[C/G/T]GTGCTGTCGAGAGGG | 8027 |
rs369487262 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17674279 | ATCTCTTACTACACA[A/G]CTCTTAGTAGTAACT | 8027 |
rs369495513 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17700772 | CCCAGCATACTCAAC[A/G]AGGATATTAAGATTG | 8027 |
rs369504779 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17659445 | TATCTTCGGGTATTC[C/T]ATCTTTATTCTCTTC | 8027 |
rs369520806 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17711007 | AATGTAGGATGAGGA[A/C]ATTGGAAGGAGCGAG | 8027 |
rs369538930 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17664837 | AATTTTGTAAAGTGC[A/G]GCGATCTTTTTAAGA | 8027 |
rs369539757 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17681995 | TACATTCTTGGCCTG[C/T]CATTTAAATAGATCT | 8027 |
rs369554893 | snp | A/G | 0.000115452 | 0.00759687 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714522 | GTATTGATGTAATTG[A/G]GTGTTTTTCTTCCTC | 8027 |
rs369610150 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | STAM | GRCh38.p7 | 10:17705043 | AAAGAACATGGGTGC[A/C]TTTATGTTGTGTACC | 8027 |
rs369669679 | snp | C/T | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716619 | ATAAATTCCTGTTTA[C/T]CAATGTTAAATGTAT | 8027 |
rs369702608 | snp | A/G | 1.64893e-05 | 0.0028713 | missense | STAM | GRCh38.p7 | 10:17695073 | TGTCTCTCAAGGAAC[A/G]AAGGCAGCAGTCAAC | 8027 |
rs369762187 | snp | A/T | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643318 | ACGCAACATCTCTAG[A/T]AGATGCTCCTTAAAA | 8027 |
rs369835013 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644038 | GAGGAGTCAGGCAGA[A/G]GGGACTCCCTGTTCA | 8027 |
rs369856491 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698348 | TGAATCAGTTCCTGG[A/G]GAGGATAGAATTGCT | 8027 |
rs369878128 | snp | A/G | | | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696721 | ACAAAAGATAAAGAT[A/G]TACAGAAATAAATAC | 8027 |
rs369913599 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17665546 | ATCGTTACTTATTGA[C/T]TACTTATTGTATCCT | 8027 |
rs369941221 | in-del | -/TCAA | | | intron-variant | STAM | GRCh38.p7 | 10:17708599 | AATGAAAACCATCAA[-/TCAA]CAGCCTATTTCATTG | 8027 |
rs369996357 | in-del | -/AGAAG | | | intron-variant | STAM | GRCh38.p7 | 10:17672870 | TTATCAAATGATAAG[-/AGAAG]TAGGTATTTTTAGGT | 8027 |
rs370051962 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17667593 | ACAGTGGTGAATAAA[A/G]CAGGCATAGCCTTTG | 8027 |
rs370127469 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17674015 | GCGGGAGAGTCCTTG[C/G]AGGGACTGGAGGTCC | 8027 |
rs370155309 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17682992 | ACTGTCTCTCTTTAT[-/A]CCCTGTTAGTATTCC | 8027 |
rs370185389 | snp | C/G | 3.29636e-05 | 0.00405964 | synonymous-codon, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17684711 | TATTATGAGAAGAGT[C/G]AACCACAAAGATCCT | 8027 |
rs370209046 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | STAM | GRCh38.p7 | 10:17705772 | CCCATGTTGTTTTAA[A/G]TTCTCAAATGCACAG | 8027 |
rs370210413 | snp | A/G | 8.3391e-05 | 0.00645667 | intron-variant | STAM | GRCh38.p7 | 10:17708772 | TTCTCTTTAACCATC[A/G]CAGGTGTATGCAGGG | 8027 |
rs370315605 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645029 | GAAGTTGTTGAATCT[A/G]GAAAGAGTTTGAAAT | 8027 |
rs370331643 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17654922 | TTCCAAATTTTCACA[A/C]AGTAGTCTGTATTTC | 8027 |
rs370360652 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17706401 | TTTTTTTTTTTGAGG[C/T]GGAGTCTCACTCCGT | 8027 |
rs370439088 | snp | A/C/G | 3.30606e-05 | 0.00406561 | missense | STAM | GRCh38.p7 | 10:17695214 | TTACTTTTAAAGCTG[A/C/G]AGAAATTATTACAGT | 8027 |
rs370444455 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17662893 | TGAAGACTGGGCACC[A/G]AGCTAGACCACTTCA | 8027 |
rs370446198 | snp | A/C | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698437 | TGCATTGCTATATGA[A/C]TTAAAAAAAAAAAAA | 8027 |
rs370530555 | snp | G/T | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689659 | CAGAAACAATGTTTA[G/T]TTATCAAAGAGTAGA | 8027 |
rs370552404 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697418 | CTAGTGTGTAGTCCC[A/G]GACTTGAAAGCAGTG | 8027 |
rs370593663 | snp | A/T | 0.000313265 | 0.0125114 | intron-variant | STAM | GRCh38.p7 | 10:17684815 | AGCCCCTTTAACTTC[A/T]GATTTTGTGCTTTTA | 8027 |
rs370616007 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17649313 | TGCTGAATCCAGAGG[A/G]TTGGTTGAGCCTGGG | 8027 |
rs370624930 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17674867 | ACAATGAAAAATACC[A/G]TTAGGAAAAAATAAT | 8027 |
rs370731351 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17650934 | GCCGGGCGTAGTGGC[C/G]GGCGCCTGTAGTCCC | 8027 |
rs370852062 | snp | C/T | 6.58935e-05 | 0.00573955 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714760 | CCACAGCAACCATAT[C/T]CTCAGAAGGCTCTGC | 8027 |
rs370853595 | snp | C/T | 1.64803e-05 | 0.00287052 | missense | STAM | GRCh38.p7 | 10:17708903 | CAGTGGTCCCACCAT[C/T]CGCAAACCCAGCCCT | 8027 |
rs370920878 | snp | C/T | | | synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714552 | CCACAGTACAATGGT[C/T]AGTTCCGTTCAAGGA | 8027 |
rs370940096 | snp | C/T | 0.000164736 | 0.0090742 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714587 | CATATCCCAGCCAGG[C/T]GCCAGTATATAGTCC | 8027 |
rs370965756 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17708112 | AGCCAGGATGGTCTC[C/G]ATCTCCTGACCTCGT | 8027 |
rs371026356 | snp | A/G/T | 3.29567e-05 | 0.00405924 | missense | STAM | GRCh38.p7 | 10:17695151 | ACCAACATGAAGGCC[A/G/T]AAAAGTTCGTGCTAT | 8027 |
rs371072460 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17702823 | GACCATCCTGGCCAA[C/T]ATGGTGAAACCCCGT | 8027 |
rs371099441 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17655232 | TAGGGTATGGCGTGG[A/G]CTAGAAGGCTATTCC | 8027 |
rs371145902 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | STAM | GRCh38.p7 | 10:17652336 | AATAAATGATGTGAA[C/T]AATTTTAGATTTCTG | 8027 |
rs371155678 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17667267 | AAGTAGCTGGGATTA[C/T]AGGTGAACGCCACCA | 8027 |
rs371178826 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17662157 | TCATGTTACTCCCCT[A/G]CCTTCCATACTGAGT | 8027 |
rs371252102 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17666551 | AGGCACCCGCCACCA[C/T]GCCCAGCTAATTTTT | 8027 |
rs371255096 | snp | A/C/G | 1.64866e-05 | 0.00287106 | intron-variant | STAM | GRCh38.p7 | 10:17684763 | ACTGTGAGTGGTTTC[A/C/G]TTTTAATCTGTACCA | 8027 |
rs371280959 | snp | A/G | 0.000153988 | 0.00877328 | missense | STAM | GRCh38.p7 | 10:17704432 | CTTAATTCCTGTAGG[A/G]TAAAATGGACCAGTT | 8027 |
rs371331342 | in-del | -/CTAT | | | intron-variant | STAM | GRCh38.p7 | 10:17670761 | ACTGTATATATTTAT[-/CTAT]ATTCACGTTCCATTA | 8027 |
rs371350955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696951 | ACTGAACTTTTTAGA[A/G]CAGTGTTGCCCAGGC | 8027 |
rs371356583 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17707868 | AAGTAGACAAATCCA[G/T]CCTGTTGCCTGTTTT | 8027 |
rs371392755 | snp | C/G | 1.64781e-05 | 0.00287033 | missense | STAM | GRCh38.p7 | 10:17695088 | AAAGGCAGCAGTCAA[C/G]CACCCTTTCCACTTT | 8027 |
rs371399006 | snp | A/T | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689294 | GAAACCATGAACAGA[A/T]ATCTGTGAGTGTGGA | 8027 |
rs371407508 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17695328 | GATTGCAGTTACCAA[A/G]TACAATAATAAATAT | 8027 |
rs371454608 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17679429 | TGTTCGTTGTTGAGA[C/T]GTAGGAGTTCTTTAT | 8027 |
rs371469583 | snp | A/G | | | missense, utr-variant-5-prime, intron-variant | STAM | GRCh38.p7 | 10:17684686 | TTAGACCTAAGGATT[A/G]TCTTCGGTCTATTAT | 8027 |
rs371574843 | snp | C/T | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17681008 | GGAATTGCTGGAGCA[C/T]ATGGTAATTCTATTT | 8027 |
rs371655348 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | STAM | GRCh38.p7 | 10:17674068 | TGATCCAGGGATGAG[A/G]TTCATGGCTGGCTTT | 8027 |
rs371661686 | snp | A/C | 0.000117856 | 0.00767555 | intron-variant | STAM | GRCh38.p7 | 10:17705770 | AGCCCATGTTGTTTT[A/C]AATTCTCAAATGCAC | 8027 |
rs371663939 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17673964 | TGTGTAAGCTCTGAT[C/G]TGTAGGATGAGTAAG | 8027 |
rs371678606 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | STAM | GRCh38.p7 | 10:17665678 | ATCTAACACATATAC[A/C]TAATTACTGAATGAA | 8027 |
rs371678791 | snp | C/T | 4.94474e-05 | 0.00497205 | missense | STAM | GRCh38.p7 | 10:17708906 | TGGTCCCACCATCCG[C/T]AAACCCAGCCCTTCC | 8027 |
rs371763125 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | STAM | GRCh38.p7 | 10:17662079 | ATTAACCCACTGGCA[-/T]TTTTTTTTCTGTTTC | 8027 |
rs371854920 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17694274 | GTTGTTTGCTTTTTT[A/G]TTATGATTTTTACTT | 8027 |
rs371896913 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642180 | AAAATGCACAAAGAA[C/T]AAAAACATTGTCTAG | 8027 |
rs371921230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688912 | ACTTGAGAGATTCTT[C/T]TGTGGAGGAAATTTA | 8027 |
rs371945645 | snp | A/T | 6.6865e-05 | 0.0057817 | intron-variant | STAM | GRCh38.p7 | 10:17660456 | GCAATCCCCTTTACA[A/T]TCTACAGAGAAAGCA | 8027 |
rs371956107 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17655440 | CCTAACCAATACCTA[C/T]TGGTTATTATCCACT | 8027 |
rs371962768 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17687509 | ACAAACCAAAAAAAA[-/A]GAAAAGAAAAGAAAG | 8027 |
rs372010645 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon | STAM | GRCh38.p7 | 10:17704475 | GCAAAGTACAGACCC[C/T]AGTGATGATCAGCCA | 8027 |
rs372014497 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17663697 | CTTGTTATACCTCTT[C/G]TTAATAAAGAGTTGT | 8027 |
rs372077266 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17668027 | GTTATTGGTAATGAC[A/G]AGGTCTGATGACTCC | 8027 |
rs372134009 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17648432 | GGCACCCTAGCCAGC[A/G]GCAGCAACCGGCTCG | 8027 |
rs372136574 | snp | C/G | 3.29641e-05 | 0.00405968 | missense | STAM | GRCh38.p7 | 10:17705703 | AAGTTACAGAATCAG[C/G]CATATTATATGCAGT | 8027 |
rs372221916 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17675168 | CACATGGCCTGATAC[A/T]GCTTTTAGTTTATGA | 8027 |
rs372263762 | snp | A/C/T | 0.000167464 | 0.00914918 | intron-variant | STAM | GRCh38.p7 | 10:17660454 | CTGCAATCCCCTTTA[A/C/T]AATCTACAGAGAAAG | 8027 |
rs372301159 | snp | C/T | 8.24953e-05 | 0.0064219 | missense | STAM | GRCh38.p7 | 10:17700209 | AAACAGAGAAGAAGA[C/T]GGTACAATTTAGTGA | 8027 |
rs372330843 | snp | G/T | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688508 | TTGTTTGTCGCCCTG[G/T]GTAGAGTGCAGTAGC | 8027 |
rs372453892 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17678801 | ATTTCCCCTCCTAGC[C/T]ACTAGTTACTTTTTT | 8027 |
rs372479341 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17693401 | TAAATAGAACTTTAT[A/G]GCAAAAAGCTGAAAT | 8027 |
rs372521273 | in-del | -/CTC/CTCTA/CTCTT | 0.16381 | 0.255787 | intron-variant | STAM | GRCh38.p7 | 10:17657850 | GTGTTTTCTCTCTCT[-/CTC/CTCTA/CTCTT]TTTTTTTTTTTCCTT | 8027 |
rs372564298 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17646739 | AGAGATTCCCAGTAC[A/C]TAAGCCTTGCACAGA | 8027 |
rs372592177 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17712830 | GGGAGCAGTGCACAA[A/G]TGCAGGGACTTGAGA | 8027 |
rs372627119 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon | STAM | GRCh38.p7 | 10:17708835 | GAACGCGCAGATGAG[C/T]CACCTCCAGAGCTAC | 8027 |
rs372752736 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17703380 | CACTCTCTGATGATT[A/G]ATTCGTTTCTCAAGC | 8027 |
rs372753227 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17705137 | TTGTGGAGGAACCAA[C/T]TCTCATTCACATATC | 8027 |
rs372760504 | snp | A/G | 1.65119e-05 | 0.00287327 | synonymous-codon | STAM | GRCh38.p7 | 10:17693242 | AGAACAAGCAAAAGC[A/G]AGCCCAGCTCTTGTA | 8027 |
rs372779527 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17660029 | TGGTTTTCTTTCCTT[C/T]AGTCCCCTCTCCATA | 8027 |
rs372888359 | snp | G/T | 3.32281e-05 | 0.0040759 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644309 | TGCTGTCGAGAGGGA[G/T]TCCCCGGGGACACCT | 8027 |
rs372899044 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17662879 | GTGACAGTTTCTGTT[C/G]AAGACTGGGCACCAA | 8027 |
rs373078460 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17706229 | TTATGCTAATAGTTT[G/T]TTGTTGTTGTTGTTG | 8027 |
rs373106562 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696981 | CTGGAGTGCAGTGGT[A/G]CGAGCTCGGATCATT | 8027 |
rs373121185 | snp | A/G | 0.000198666 | 0.0099646 | intron-variant | STAM | GRCh38.p7 | 10:17693173 | GGGTGGGTGAGAGGA[A/G]GAGAATTTGATAACA | 8027 |
rs373129544 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643885 | ACCTGCTTTCTTTCT[C/G]CTGGCTCTCCCAGTC | 8027 |
rs373182985 | in-del | -/TAA | 0.00478085 | 0.0486577 | intron-variant | STAM | GRCh38.p7 | 10:17670797 | TAAGAAATGCCTACT[-/TAA]TAAGCTTAACATTAA | 8027 |
rs373202489 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17674680 | TTTATTGGTCAAGCA[A/G]GTCACTGAAGTCAGT | 8027 |
rs373209507 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17711692 | GGAGGTGTGAAAGGC[A/G]TGGTATGTATCGGCA | 8027 |
rs373209935 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17654857 | ATGTTTCTTGAAGCA[G/T]TGCAAACACCTGAGA | 8027 |
rs373270069 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17677047 | TTTAAGCTAGTATGT[A/G]AAAAGATACTGCTGT | 8027 |
rs373382713 | snp | A/G | 0.000191716 | 0.00978884 | intron-variant | STAM | GRCh38.p7 | 10:17708725 | CAGAGAAAGTTCAGT[A/G]TGCTTATTAAAATTT | 8027 |
rs373455172 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17671154 | CTGCTAGGTCCTGGT[A/G]TACTAAGACCTATAA | 8027 |
rs373468780 | snp | A/G/T | 3.30815e-05 | 0.00406692 | intron-variant | STAM | GRCh38.p7 | 10:17704943 | TTCTTGTACTTTCTT[A/G/T]TATTTCTTCACATCT | 8027 |
rs373489236 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17656249 | CAGTGAGCCGAGATC[A/G]CACCACTGCACTCCA | 8027 |
rs373595036 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17702963 | GTAGTGAGCCAAGAT[A/C]ATGCCACTGCACTCC | 8027 |
rs373598981 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17660612 | CACGAAAGGCCAGGT[A/G]CAGTGGCTTGCACCT | 8027 |
rs373694726 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17700465 | CAGTCCTTTGTTTGC[C/T]GTGCCAGAGCCTCAT | 8027 |
rs373764775 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant | STAM | GRCh38.p7 | 10:17705052 | GGGTGCATTTATGTT[A/G]TGTACCTTCTTTCCT | 8027 |
rs373780461 | snp | C/G | 1.65323e-05 | 0.00287505 | intron-variant | STAM | GRCh38.p7 | 10:17704570 | GTTAGAGGTTAATAA[C/G]TGGTGTCCTGTTAAA | 8027 |
rs373786637 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689490 | TCTTAAAAAAATTTT[G/T]GTTTAAAATTTTCTT | 8027 |
rs373790412 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17669269 | TTTTCTCTTTTGACC[C/T]GTTGGTATGTGTCTA | 8027 |
rs373793472 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17692839 | GATACTACAGTTTTT[A/T]TTTTAACTATTTATG | 8027 |
rs373798864 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697005 | GATCATTGCAACCTC[C/T]GCCTCCTGGGTTCAG | 8027 |
rs373821070 | snp | C/T | 1.65814e-05 | 0.00287931 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644330 | GGGGACACCTCGGCA[C/T]GCAGCGGAGATGCCT | 8027 |
rs373827392 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17679209 | GTTCTAATTTCACTA[C/T]ATCCCCTCCAATATT | 8027 |
rs373852452 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon | STAM | GRCh38.p7 | 10:17695098 | GTCAACCACCCTTTC[C/T]ACTTTGTATCCAAGC | 8027 |
rs373896095 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17666778 | AAGAATATTTCCTGA[G/T]TTTTGTAAGGGAAAA | 8027 |
rs373897408 | snp | A/C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17646009 | AGGTAAATTTCTTAA[A/C/T]GTCAAACCCGTTCCT | 8027 |
rs373949067 | snp | C/T | 0.000461893 | 0.0151899 | intron-variant | STAM | GRCh38.p7 | 10:17705061 | TATGTTGTGTACCTT[C/T]TTTCCTGAAGCTATC | 8027 |
rs373954360 | snp | C/T | 0.00755907 | 0.0610114 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643462 | GTTTTTTTCTGTTTT[C/T]TTTTTTTTGCTCAGT | 8027 |
rs374018862 | snp | A/G | 1.64779e-05 | 0.00287031 | missense | STAM | GRCh38.p7 | 10:17695165 | CGAAAAGTTCGTGCT[A/G]TATATGACTTTGAAG | 8027 |
rs374258125 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17686454 | TGATCTCAGCTGACT[A/G]TAGCCTCTGCCTCCC | 8027 |
rs374373647 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17670707 | GAAGTCCTTTGGGAC[A/T]TACATGAACATGTTT | 8027 |
rs374383496 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17672803 | GGAAACTGACCTTAA[G/T]AATGTTGTTCTTCTG | 8027 |
rs374402428 | snp | C/T | 0.000313286 | 0.0125118 | intron-variant | STAM | GRCh38.p7 | 10:17684774 | TTTCATTTTAATCTG[C/T]ACCACGAAATTACCT | 8027 |
rs374442557 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17682177 | CTTATGCAAGTACTA[A/G]TATGCATTGTCACTA | 8027 |
rs374460456 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17667917 | AGTCAGTTGCCCTGA[-/A]TGAGCGCAGAGCTGG | 8027 |
rs374464303 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17677250 | TTCATTTCAACACCC[C/G]TTTCCCCACCATCCT | 8027 |
rs374511706 | snp | A/C | 1.6554e-05 | 0.00287693 | synonymous-codon | STAM | GRCh38.p7 | 10:17708784 | ATCGCAGGTGTATGC[A/C]GGGCCTCCTCCAAGT | 8027 |
rs374537930 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17672144 | TGGCTTCCTCCTATA[C/T]AGCAATGGAAATACC | 8027 |
rs374542642 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17667067 | AGTGAGAAATCTAAT[G/T]GATATTTAGGATTCT | 8027 |
rs374571069 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17686611 | TCTCGAACTCCTGAC[C/T]TTGTGATTGCCCACC | 8027 |
rs374614211 | snp | A/G | 0.000119154 | 0.00771769 | intron-variant | STAM | GRCh38.p7 | 10:17705567 | AACAGCTATGCTTCA[A/G]ATTATTGTGTCATGT | 8027 |
rs374650240 | in-del | -/G | | | intron-variant | STAM | GRCh38.p7 | 10:17703306 | TCCATTTCAAAAAAA[-/G]CAGAATTATTTTGAC | 8027 |
rs374663209 | in-del | -/A | 0.302184 | 0.244493 | intron-variant | STAM | GRCh38.p7 | 10:17675503 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAG | 8027 |
rs374711515 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17694110 | ATTGTCTTTTGTTAA[A/G]TAAAATAATGATATG | 8027 |
rs374805372 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17653214 | ACCTATATAATGACA[A/C]CCCAATTGTAGAATC | 8027 |
rs374848479 | snp | A/G | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689736 | CACTAAATATCTAGA[A/G]TCTTTGGTTCTTGTT | 8027 |
rs374977551 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17693891 | TTGTTAAATGGTTGT[-/T]ATGATTTCCTTTTCC | 8027 |
rs374978051 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17699319 | TATTTCCCTTCCTTA[A/C]ATTGCCCCCTCCTGT | 8027 |
rs375019329 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17648402 | GGGCGGGGACAAATA[A/C]GAGAATAAAAGCTGG | 8027 |
rs375049726 | snp | C/T | | | synonymous-codon | STAM | GRCh38.p7 | 10:17704484 | AGACCCCAGTGATGA[C/T]CAGCCAGACCTACCA | 8027 |
rs375051606 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17687336 | AAAAATTAGCTGGGC[A/G]TGGTGGTGCGCGCCT | 8027 |
rs375062849 | snp | C/T | 3.34018e-05 | 0.00408654 | intron-variant | STAM | GRCh38.p7 | 10:17660561 | TGGGTAAGTATTTAG[C/T]GTTTCAAAGGATTTT | 8027 |
rs375088702 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17683907 | TTCCTGTTAAGGAGT[A/G]TTGGACTTTATTTTT | 8027 |
rs375091489 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17682184 | AAGTACTAATATGCA[G/T]TGTCACTATAGATTA | 8027 |
rs375096931 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17654008 | TGTATCCAGTTGGTC[A/G]GAAGTGCCTGGGGAC | 8027 |
rs375126960 | snp | A/G | | | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695574 | TATGTACTTAATGCA[A/G]TTTGTAAGAAATATA | 8027 |
rs375167534 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17657787 | TTCTTTTTAATGTCC[A/T]TGGGGTTTGTAGTGA | 8027 |
rs375313229 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644283 | CATCCTACGTCGAGC[C/T]CTGACTCCCGTGCTG | 8027 |
rs375316303 | snp | C/G | 6.76053e-05 | 0.00581361 | intron-variant | STAM | GRCh38.p7 | 10:17708970 | ATTTTACTGTTGATT[C/G]TTGTTTGGAGTTAGT | 8027 |
rs375321364 | snp | A/G | 1.69063e-05 | 0.00290738 | intron-variant | STAM | GRCh38.p7 | 10:17684639 | GGGGAAGCTAGATGT[A/G]TTATTAAGTAATTTT | 8027 |
rs375329299 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17680789 | CTTATTTCACTTAGC[A/G]TAATGGCTTTAAAGT | 8027 |
rs375357156 | snp | C/T | 8.23608e-05 | 0.00641667 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714682 | AATATGCCCCAGGTG[C/T]CAAACTATAACTTAA | 8027 |
rs375372161 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17702543 | TAACATTTTAAATGT[A/G]TAAGAAATGAGATGT | 8027 |
rs375437972 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17663399 | TCTCAGTATATTCCT[C/T]AATATTTGAATTGTC | 8027 |
rs375508475 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17687408 | CCGCATCCCCCACCC[C/G]CCTCTGGGAGGCGGA | 8027 |
rs375511561 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17665849 | AAATTTTTTTCTAAC[A/G]TCTCAAGATATTCAC | 8027 |
rs375511802 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17656678 | GTTTTTGTAATCGGT[C/G]GAAGGTATCTGAGTT | 8027 |
rs375533840 | snp | C/T | 3.29544e-05 | 0.00405908 | synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714558 | TACAATGGTCAGTTC[C/T]GTTCAAGGAAACACA | 8027 |
rs375584219 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643714 | CGTTCAGCTCCCATG[A/C]CTTCATCCGAGCAAG | 8027 |
rs375596615 | snp | A/G | | | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696660 | ATTGGCTTTTTCAGT[A/G]GGTTATTGTGAGATT | 8027 |
rs375611263 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17671093 | TAAAAATATTTAGTT[A/C]ATTCAGCAAAGATTT | 8027 |
rs375711527 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17703214 | TGTGTGTGGTAGGCA[A/T]ACTTTCTTGACATGT | 8027 |
rs375739061 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17668367 | GTCAACTCCGACACA[A/G/T]TTTCCCCAATTATTC | 8027 |
rs375743228 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | STAM | GRCh38.p7 | 10:17705072 | CCTTCTTTCCTGAAG[C/G]TATCACTGTACTGCA | 8027 |
rs375749603 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17676445 | CTGACATATGTAGGC[A/T]GTTATGTACATTCCT | 8027 |
rs375778964 | snp | A/C | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687606 | ACTAGGCCCCAGATA[A/C]TTAAGCATCATGGAA | 8027 |
rs375811987 | snp | A/G | 4.9458e-05 | 0.00497258 | missense | STAM | GRCh38.p7 | 10:17705631 | GTGAAAGTGATGGAG[A/G]CCCTTTCCTTATATA | 8027 |
rs375834131 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17675892 | CCAAAGGGCCGGTAT[C/G]CTTTTGCACTGATAC | 8027 |
rs375849651 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17668110 | GAAAGCATCACTTAC[A/T]CTGTTATTAAAAGCT | 8027 |
rs375855378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17661144 | TTTTGGCATGTATTA[C/T]AGAGCTTTCCAAACA | 8027 |
rs375938525 | snp | A/G | 9.97589e-05 | 0.00706183 | missense | STAM | GRCh38.p7 | 10:17708941 | CAGCAGACTCAGGCC[A/G]CTTACCCAAAGTAAT | 8027 |
rs376019961 | snp | C/T | 8.23825e-05 | 0.00641751 | missense | STAM | GRCh38.p7 | 10:17708857 | CAGAGCTACAGTCTT[C/T]CCCCGGAGCAGCTGT | 8027 |
rs376024433 | snp | C/T | 0.000134251 | 0.00819191 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644404 | TTTGCCTCTCCCTGC[C/T]CATTCCTCACCGGAC | 8027 |
rs376163229 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17654948 | ATTTCAGCCAGCCTA[C/G]ATTCTTCATTATACT | 8027 |
rs376259120 | snp | C/T | 3.32674e-05 | 0.0040783 | intron-variant | STAM | GRCh38.p7 | 10:17684664 | AATTTTTACTTTTCT[C/T]ATTTTTTTAGACCTA | 8027 |
rs376354086 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17709698 | AGAAGTTTCTAGGTA[A/G]CACAGGCACAACTTC | 8027 |
rs376467317 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17666711 | CTTTGGCTTTGTATT[A/G]TTTTGTCCTGGACTG | 8027 |
rs376487907 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17706906 | GCAGTGAAAAAAAAA[-/A]TGAGGTAAAAACCTG | 8027 |
rs376521317 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17701163 | GAGATTTCTTGAATT[A/T]AGTTAATCACTCCTA | 8027 |
rs376576585 | in-del | -/TTCT | | | intron-variant | STAM | GRCh38.p7 | 10:17703094 | ATGTAGAAACCCTAC[-/TTCT]TTGACACTAAATAAT | 8027 |
rs376599070 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17652072 | GTATTAGTGTAAGGA[A/T]ATTCTCAGGATAAAA | 8027 |
rs376599582 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17692119 | TTATCGTAGTCATTT[-/T]ATTGATGAGGAATTT | 8027 |
rs376656791 | snp | A/G | 1.65798e-05 | 0.00287917 | missense, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696804 | GGAAAGGTGAAACCC[A/G]TCAAGGCATAGGGTT | 8027 |
rs376659810 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | STAM | GRCh38.p7 | 10:17704557 | CAAATAAAGAGTAGT[C/T]AGAGGTTAATAACTG | 8027 |
rs376671889 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17712960 | TTCCGTATTTTCAAG[G/T]AAATAAAAGAAATGA | 8027 |
rs376715165 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17651774 | GAGGATAATTTCTTT[C/T]AGACTTACTTTTCCA | 8027 |
rs376758308 | snp | A/C | 1.67438e-05 | 0.00289338 | intron-variant | STAM | GRCh38.p7 | 10:17705758 | TAAGCTTTTAGAAGC[A/C]CATGTTGTTTTAAAT | 8027 |
rs376793961 | snp | A/G | 3.29489e-05 | 0.00405874 | synonymous-codon | STAM | GRCh38.p7 | 10:17695128 | CACATCCAGTCTCTT[A/G]ACTAACCACCAACAT | 8027 |
rs376812321 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17694929 | ATGTATCAGGATATG[G/T]TCTAGTTTCTAACTA | 8027 |
rs376842869 | snp | C/T | 6.68192e-05 | 0.00577972 | intron-variant | STAM | GRCh38.p7 | 10:17700315 | TAGGAGTTGGTACTT[C/T]GTATTGAAATTTAAA | 8027 |
rs376861625 | in-del | -/C/CC/CCC | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714312 | TATTTCCGCAAACCA[-/C/CC/CCC]CCCCCCCCAACTTTT | 8027 |
rs376914995 | snp | A/G | 7.08328e-05 | 0.00595075 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687980 | TGTCTGTATTAAATC[A/G]TTGGCTAGGAAATTG | 8027 |
rs376937466 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17693072 | ATTCATTTCCCTCTC[C/T]CTTTTAAGGTGGAAG | 8027 |
rs376954775 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17670289 | ATAGAATGAGACTTA[C/T]AGAATTCTGATGACT | 8027 |
rs376993493 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17702827 | ATCCTGGCCAACATG[A/G]TGAAACCCCGTCTCT | 8027 |
rs377038873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17667615 | TAGCCTTTGCCGTCA[A/G]TGGTGCTAATATTCT | 8027 |
rs377123637 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17677864 | ATAATTATTAAAAAG[G/T]ATTTTTTTGTATTTA | 8027 |
rs377163011 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17685713 | CCTATGGTGGAAAAC[A/T]TGCAGCTGGCTAGGT | 8027 |
rs377172455 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17682544 | TTGATTTCCAAATAT[C/T]TGGGTATTTTTATGC | 8027 |
rs377214453 | in-del | -/GTA | | | intron-variant | STAM | GRCh38.p7 | 10:17669904 | TTTTTTTTTTTTTTT[-/GTA]TTTTTAGTAGACACG | 8027 |
rs377247704 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17680702 | GCAAGTCACTGTGCC[C/T]GGCCTTGATTTTGAC | 8027 |
rs377347777 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17692306 | ATGTGTAATTAACAG[A/G]TTGAGGGATGCTTCA | 8027 |
rs377367206 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17679575 | TGATGTTTAATTTGC[A/G]TGTGTTTTTTTTTTT | 8027 |
rs377433144 | snp | C/T | 3.29538e-05 | 0.00405904 | missense | STAM | GRCh38.p7 | 10:17705018 | AAAAGCTGGAAGATA[C/T]TGATAGGTAAAAGAA | 8027 |
rs377442031 | in-del | -/GGTTGAG | 0.00874735 | 0.0655527 | intron-variant | STAM | GRCh38.p7 | 10:17692305 | AATGTGTAATTAACA[-/GGTTGAG]GGATGCTTCATTGAC | 8027 |
rs377551390 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17711217 | TCACTGTTTTTCAGA[C/T]TTCTGTCATCCTAGG | 8027 |
rs377570488 | snp | G/T | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689224 | AAATATGTGCTGATT[G/T]ACTACACTGTCTTTC | 8027 |
rs377690223 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714623 | CTGCCGCTACTGCTG[C/T]TGCTGCAACTGCCGA | 8027 |
rs377692538 | snp | A/G | 6.59283e-05 | 0.00574106 | missense, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17684733 | AAAGATCCTCACGTT[A/G]CTATGCAGGCTTTGA | 8027 |
rs377739589 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17706000 | TTGAGCCCAGAAGGT[C/T]GAGGCTGCAGTGAGC | 8027 |
rs386741501 | multinucleotide-polymorphism | ATG/GTC | | | intron-variant | STAM | GRCh38.p7 | 10:17654793 | ATATTTTTCAAAAAA[ATG/GTC]TAGGTCTTGTTGTTT | 8027 |
rs386741502 | multinucleotide-polymorphism | AGG/TGT | | | intron-variant | STAM | GRCh38.p7 | 10:17655346 | ATTAATTCTTATGCA[AGG/TGT]AATTAATCTGTGTGA | 8027 |
rs386741503 | multinucleotide-polymorphism | AGG/GGA | | | intron-variant | STAM | GRCh38.p7 | 10:17674870 | ATGAAAAATACCATT[AGG/GGA]AAAAAATAATTCTAA | 8027 |
rs527273473 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17706575 | TAGTAGAGACGGGGT[A/T]TCGCCGTGTTAGCCA | 8027 |
rs527304348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712086 | AGGCAACTGGGTGGA[C/T]GGTGGAACTGTAAAT | 8027 |
rs527366498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17661420 | TTCCTGAAACTTTCC[C/G]TGATTCATTTTTTAT | 8027 |
rs527387682 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17660658 | CGGTAGGATGAGGTG[A/G]GAGGATCGCTTGAGC | 8027 |
rs527392911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17666960 | TCACTTATTGACTAC[C/T]TATTGTTTGCTAGAC | 8027 |
rs527448237 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696383 | AAAAAAAACCTTGCT[A/G]CTGTGTACCAGAAAG | 8027 |
rs527450343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689662 | AAACAATGTTTATTT[A/G]TCAAAGAGTAGACTC | 8027 |
rs527467284 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17666090 | CGTGAGGATAAATAC[A/T]GATTATCTTCAATAA | 8027 |
rs527476752 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17655976 | TTAAGTTGCTTTTTT[C/T]TTTTTCTTTTTTTGG | 8027 |
rs527485541 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17695971 | TCTGGTTTGTAGAAG[C/G]CTGTCATTTTGCTGT | 8027 |
rs527539104 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644557 | GGCGCATCCTCTTTG[A/G]AAGAAATGGGACTCA | 8027 |
rs527539211 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17650949 | GGGCGCCTGTAGTCC[A/C]AGCTACTCAGGAGGC | 8027 |
rs527558411 | snp | A/G | 0.00835141 | 0.0640778 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17716830 | TACTTTAAAACTGTT[A/G]CTGTGTTAGTTTATG | 8027 |
rs527579106 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17653392 | TTGTTTTGATAAAAC[A/G]GGATAAAAACTCTGA | 8027 |
rs527612700 | snp | C/T | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17690284 | CAGTGGAGTGAATGC[C/T]GGCAAGAGCATTATG | 8027 |
rs527644768 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | STAM | GRCh38.p7 | 10:17694326 | TTGTTCCCTACCTCA[A/G]GGTCCTAAAAGATAG | 8027 |
rs527650426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687913 | TTCTTGTCTATAGCT[A/G]TGCATAACTTGTGAT | 8027 |
rs527650470 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17655118 | TTTACCTGTCTTTCA[A/G]TTTGCTTTGGGCTTT | 8027 |
rs527678586 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17654709 | AAACTTGAGCAATGA[C/T]AGGTAAATTTGAGCT | 8027 |
rs527687594 | snp | A/G | 0.000100524 | 0.00708887 | intron-variant | STAM | GRCh38.p7 | 10:17700321 | TTGGTACTTTGTATT[A/G]AAATTTAAATGGTTT | 8027 |
rs527713855 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17660066 | AAAAAAAAATCCACA[A/G]AACTAGCTAAATAAT | 8027 |
rs527743145 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17649359 | TGAGCTATGACTGCA[C/T]TCTTGCCTGGGCAAG | 8027 |
rs527769102 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688883 | AATCAGGATATCCTT[A/T]AAAGTTAGGGATGAC | 8027 |
rs527783714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17683022 | CTTGTTATGAAAACT[A/G]CTAACGGTAGTGAAT | 8027 |
rs527815780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688460 | GAAATTTTTTGGTAT[A/G]GTTTTTGTTTGTTTG | 8027 |
rs527848075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17677529 | CTGCAAGTCAGTATG[A/G]GGTCACGGACCCTGG | 8027 |
rs527870004 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716533 | ATCTGTCGGATTATA[A/T]TCTTTTCCACTCCAA | 8027 |
rs527876507 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644054 | GGGACTCCCTGTTCA[G/T]CCTTTACCGATGGGG | 8027 |
rs527906174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17649942 | TTTAGTGTTGTAGTT[A/G]TCTTGACTTGAAACC | 8027 |
rs527906957 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716179 | GTTGAGTCGAACATC[A/G]TATTTAATGAATTGA | 8027 |
rs527977276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17672019 | TACTAAAAAGTACTT[G/T]TCAACTGAGATATAG | 8027 |
rs528082441 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715080 | GAAAGTCAAACTTAC[A/G]AAAACTGTTGTGACA | 8027 |
rs528091973 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | STAM | GRCh38.p7 | 10:17648240 | ATTGTAAAATGCACC[G/T]ATCAGTGCTCTGTAA | 8027 |
rs528132223 | snp | G/T | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644959 | GACCTGAGCCTTTGG[G/T]ATGTCTCTCTTAGGC | 8027 |
rs528143754 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715512 | CAATTATAGCAAATG[A/G]TAATGTTCCCTTTTG | 8027 |
rs528159797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17670056 | TTCTTAAAGGGTAGA[C/T]GGGATTATAGCATCT | 8027 |
rs528168338 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17646786 | TTATTTTTTAATAGT[A/G]TAACATATAGAATAC | 8027 |
rs528293227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704692 | GAATTTGAATTCTTA[C/T]AATTTTCTATCCAAA | 8027 |
rs528313211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17709869 | CGAAGTGACCTTAAG[A/G]GGGATGATGGCAAGG | 8027 |
rs528318037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17670573 | TACATTGTGTTTTGT[C/T]TGACTGAAATATACC | 8027 |
rs528321654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17664703 | AAGACAAATTCAGGT[A/G]GAGTCTTTTGAAGTA | 8027 |
rs528321822 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17706569 | TATTTTTAGTAGAGA[C/T]GGGGTTTCGCCGTGT | 8027 |
rs528359446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17659286 | GCTGTCATTCATTCT[A/G]CTTACATGGAAGCAT | 8027 |
rs528396234 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17665134 | TTTAGTCAGAACTGT[C/G]ACCAGGAAACATGGC | 8027 |
rs528532752 | snp | C/G | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714224 | TCTTACCAGTTAGAA[C/G]CACTTGACACACGAT | 8027 |
rs528535467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17675426 | GGAGAATTGCTTGAA[C/T]CCGGGAAGTGGAGGT | 8027 |
rs528580753 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17663340 | TTTAGACACATGCTC[A/T]TTTTTTTTAGTTTTT | 8027 |
rs528711897 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17657903 | ATCGGTTTTATTGAT[A/C]TTTTAAAATAACCAG | 8027 |
rs528713333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17653616 | TTGTAGAGGAAAAAA[C/T]ATCATGTCTGTACCG | 8027 |
rs528781077 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17687409 | CGCATCCCCCACCCC[C/G]CTCTGGGAGGCGGAG | 8027 |
rs528789565 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | STAM | GRCh38.p7 | 10:17703231 | CTTTCTTGACATGTG[C/G]TTTTGTTTTTTAAGA | 8027 |
rs528823427 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697076 | AGGCACCCGCCGCCA[C/T]GTCCAGCTGTTTTTG | 8027 |
rs528831928 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17647176 | TCAGTAAACATTTAT[A/G]GAATAAATGAATCTC | 8027 |
rs528844595 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17690696 | ACCTCTGAAGATATA[G/T]TTTTCTAAGTATATT | 8027 |
rs528868602 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17649301 | ATTTACTCGGGATGC[C/T]GAATCCAGAGGATTG | 8027 |
rs528887386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17651147 | TCAGCAGGGCATGTA[A/G]GGCCTCTTATATTTG | 8027 |
rs528889343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17656695 | AAGGTATCTGAGTTA[C/T]TGGCAGTGAGTCTGT | 8027 |
rs528914027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17662446 | GATCCTCTGAATCCT[C/T]AAAGCACTCTATCAA | 8027 |
rs528927050 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17656155 | AAAAATTAGCTGGAC[A/G]TTGTGGCATGTGCCT | 8027 |
rs528979715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17685748 | GAGCGGGACAAGGCA[C/T]TCTGTTTTTCTATTG | 8027 |
rs529041678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17679827 | TAGTTTCCTGTCTTT[A/G]TAGGAATTTGTCCAT | 8027 |
rs529042353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713419 | AACAGGCTTGAATAG[A/C]TGACTGCCTATGCAT | 8027 |
rs529044895 | snp | A/G | 0.000164902 | 0.00907876 | intron-variant | STAM | GRCh38.p7 | 10:17684795 | GAAATTACCTGCCAC[A/G]ATTGAGCCCCTTTAA | 8027 |
rs529076417 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17666644 | CCTTGTGATCTGCCC[A/G]CCTTGGCCTCCCAAA | 8027 |
rs529093538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17646145 | CCAACTCAGAATCCA[A/G]CTTGTTACACCTGAG | 8027 |
rs529104663 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17693487 | TCACATGTATCCTTT[C/T]AGTCTATGTTTTTAT | 8027 |
rs529108283 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713975 | ACCCCCTGCGGCCCC[C/T]TCTGCCGCAGCACTC | 8027 |
rs529123218 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17686669 | GGCATGAGCCACCGC[A/G]CCCAGCCAACATCCT | 8027 |
rs529138095 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17665879 | CATGATTTCTACTGC[A/G]CAATTTCCAGTGTGT | 8027 |
rs529180155 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17674909 | AAATTATAAATTCCA[A/C]TTTTGATACTTGAGA | 8027 |
rs529224684 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17684153 | TTTTCACCTGTGCAT[G/T]CGTGGGTTTTTCAGA | 8027 |
rs529236516 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17692508 | TAACTGGCAGAATGG[C/T]TGGAAATGAGGTTGG | 8027 |
rs529248948 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644450 | CCAGCCCCTGCCTGC[A/C]TTCAGGACCCTCGGG | 8027 |
rs529272811 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17670419 | TTTACTTCCCATTTT[A/G]TGTTTTTTTCTACCT | 8027 |
rs529325896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17672674 | CTTTAATAATTGAGG[A/G]AAAGTTGGCTGTATT | 8027 |
rs529335875 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17694801 | CCCAGAATAATTTAC[A/G]TTGTATTTGTTCAGT | 8027 |
rs529373597 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17694415 | ACTCTAAAACAAGAG[C/T]GGAAGAGCAGAAAGG | 8027 |
rs529401207 | snp | A/G | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714122 | CATCTTTGCTTAAGT[A/G]TTGCCTTATTGGAGA | 8027 |
rs529443463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706904 | AATGCAGTGAAAAAA[A/G]AATGAGGTAAAAACC | 8027 |
rs529483830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17673228 | TATTGTGCGTTTTCC[C/T]CCTCATGGCTTTATT | 8027 |
rs529527993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17661873 | TCCTCCCACTATGAC[A/G]TTCCCAAAGAATCTC | 8027 |
rs529529110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712732 | GTGGAAACGCATGTA[A/T]TCCGTTGGAAACAGG | 8027 |
rs529530445 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | STAM | GRCh38.p7 | 10:17667158 | TGAGACAGAGTTTCA[C/G]TTTTGTTGCCCAGGC | 8027 |
rs529562448 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17667464 | CTTGATTTCCATGTT[A/T]CACTCAGTTTCGTAA | 8027 |
rs529600288 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17702373 | AGTTCAAGGAAAAAA[A/C]CAATTTGAAATACAT | 8027 |
rs529708791 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17710648 | TTTCCTGGCTGGTAG[G/T]TGCCTTTTTACTTGT | 8027 |
rs529717898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17666457 | TGGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG | 8027 |
rs529864764 | snp | A/G | | | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717021 | AAGAAATCTTTCATT[A/G]ATAGCTGTCCTTATT | 8027 |
rs529924985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17700743 | GTATTCATATCATGC[A/G]AGAACTCCTGTTTCC | 8027 |
rs529952928 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17650135 | ATAAATCATAAGCTA[A/G]ATGAATCTTAAATGT | 8027 |
rs530008308 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17699492 | TTATGTTAAATTGTT[C/T]TTAAAGATTGCTTTG | 8027 |
rs530016048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692964 | ACTTGTGTACCATAT[A/G]CTTTTAGTTGAACCT | 8027 |
rs530046398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704915 | AATATCTATCAAAGG[C/T]TCACATTTTTTTTTC | 8027 |
rs530096822 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17683069 | GGATTACAATCTTAA[-/T]CTGCCATTTTTCTAG | 8027 |
rs530108068 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17659203 | ACTGTACCACTTCAT[A/G]TGTAATGCAAGTACC | 8027 |
rs530142857 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17658683 | GTAGAGGAGAGGTTT[C/T]GTCATGTTGCCCAGG | 8027 |
rs530186607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688343 | AGTAATACTAGTTTT[C/T]TGGCATTCAGAGGTG | 8027 |
rs530199477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687837 | CTTTAATTTGAAGTG[A/G]GATATATATGATGGG | 8027 |
rs530223350 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715770 | TTACACTACATTTTC[A/G]AAGTCTCTTGTAATT | 8027 |
rs530234476 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17706792 | TCAGACATATCTCAA[A/T]AAAGTAGTTTCGTAA | 8027 |
rs530330069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17648700 | TAGTCAGTGGCAAGA[A/G]CCTTCTGGTAGGTTT | 8027 |
rs530393939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17677325 | TTTATAAACAAAATA[A/C]ATAATCAATTTTATT | 8027 |
rs530429399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17676711 | ACCATCTTTCACTCG[C/T]GAAAGGGTACTGCCA | 8027 |
rs530431291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17682941 | GCACATTTAGAATTA[C/T]GTTTCCTTGGGGGAC | 8027 |
rs530437053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17647038 | TGGTGATAGCTTTTC[A/C]CTTGGAAGAAACACC | 8027 |
rs530501462 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17675668 | GACTATGAACTTCAT[A/G]AAGCAGGGTCAGTCT | 8027 |
rs530542427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17653123 | AAAGGATTTGGGCTT[G/T]GAGTCATAGGACCTC | 8027 |
rs530581064 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642515 | CACAACCCTATTATT[C/T]CTGTTTCTTACACAT | 8027 |
rs530645515 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644176 | GCCGCCGCCGCAGCT[A/G]CTGCCGCGGTTGGTG | 8027 |
rs530659868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17669654 | CTGCTGTTTCAGTGG[C/G]GTTTTTCTTTCACTG | 8027 |
rs530660634 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | STAM | GRCh38.p7 | 10:17676112 | TTTGTTTGGGAAATT[A/G]GAAAGGTCTATTGCA | 8027 |
rs530716555 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17709086 | CCCCATTTGTGCTAA[A/T]GAGTGGTGGAGCCTC | 8027 |
rs530797525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17664648 | AGAAGACTATAACAT[G/T]TAAGTGGGTTGAGAG | 8027 |
rs530798613 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | STAM | GRCh38.p7 | 10:17707488 | ATGTAAAGTGGGCAC[A/G]GACTGTGTTCAGATT | 8027 |
rs530830412 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, stop-lost | STAM | GRCh38.p7 | 10:17713379 | CAGGACAGCAGGCTT[C/G]AATAGCTGATTGCCT | 8027 |
rs530838698 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17663543 | TTTTTCCTTTTCTTC[C/T]TCCTTCCCTCCTTTT | 8027 |
rs530877484 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17662807 | GTGTTTATAACAGTA[A/C]CTGGCACATGGCTGA | 8027 |
rs530912745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17668108 | TTGAAAGCATCACTT[A/G]CACTGTTATTAAAAG | 8027 |
rs530998517 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | STAM | GRCh38.p7 | 10:17657144 | TCACTCACTCAGTGC[C/G]TGAGATTTTATTGGA | 8027 |
rs531001146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17668751 | CATCTTTCACTTACC[A/G]GTATGCATTTAAGGT | 8027 |
rs531011818 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17651351 | TTAGCATAGCACCTG[A/G]CATGTAGTAACCAAT | 8027 |
rs531037770 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | STAM | GRCh38.p7 | 10:17674870 | ATGAAAAATACCATT[A/G]GGAAAAAATAATTCT | 8027 |
rs531063972 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17687321 | GTCTGCTAAAAGTAC[-/A]AAAATTAGCTGGGCA | 8027 |
rs531077059 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17702860 | TAAAAATACAAAGAT[C/T]CGCTGGACGTGGTGG | 8027 |
rs531082772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17707979 | CGCTGCCAGCTCCGC[C/T]TCCTGGGTTCAGGCC | 8027 |
rs531140550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17703385 | TCTGATGATTAATTC[A/G]TTTCTCAAGCTATTT | 8027 |
rs531143239 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691856 | ATGACAATATACATT[A/C]ATAACTTTTCATGAT | 8027 |
rs531155000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17675039 | TCTGTGTTGAAAGAT[A/G]TACCCATTTGTGTGT | 8027 |
rs531177857 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17702244 | AATCTAATACTGAGA[G/T]TATTATCAGTTTACA | 8027 |
rs531339736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696539 | TTTGGGAGAGAGTCC[A/G]TAACTGCAGAGCATG | 8027 |
rs531382208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17661482 | TCCAGCTGTCTTTAT[A/G]TAGATGGCATCTGTA | 8027 |
rs531382881 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17667439 | TAGAATTTTTTTTTT[A/T]AAACGTGATCTTGAT | 8027 |
rs531406966 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17656083 | GTGAGTCACCAGGTC[A/C]GGAGATTGAGACCAT | 8027 |
rs531410694 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697218 | ACAGGCGTGAGCCAT[C/T]GCACCTGGCCTAACT | 8027 |
rs531446948 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17655627 | CTCTCAGTAGTAGGT[C/G]AAAATGAGGAAATAA | 8027 |
rs531488505 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17685007 | AAATCTTCACAGAGG[A/T]CTATTCTGTGCTTTT | 8027 |
rs531527628 | snp | C/T | 0.0123036 | 0.0774623 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714967 | AGGTTCTTCCCCCCC[C/T]GCCCCTGCAGAGGAA | 8027 |
rs531533298 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17651672 | TTTTCTGGTTAGCAG[A/G]GCTTCAGATTACATT | 8027 |
rs531594893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17646069 | GCACCTTCTTGCCTT[C/T]ATGCTTTTGTCCTAC | 8027 |
rs531606618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17650056 | GTCAGACTGCTTTGG[A/G]CCAGTCCACATCCTA | 8027 |
rs531644078 | snp | A/C/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698125 | ATCTTTAAGAAAATG[A/C/G]TGCGCTCTCATAGTT | 8027 |
rs531655136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17685675 | GTGCCTGAGAATGTT[C/G]AAGGCCCCAGTTTGG | 8027 |
rs531708882 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17683551 | TCTGTACTTCAGTTT[G/T]GGTACTTTCAGCATA | 8027 |
rs531804462 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644100 | TTTGAGACAGGCAGC[A/G]CCAAGGTCGCCCAGA | 8027 |
rs531828686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17678402 | TTGGATGGGGTACAT[C/G]CCACTGTGCCTGGCT | 8027 |
rs531901176 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17679902 | GTCTTTTAAAATCCT[A/T]TTTATTTCAGTGAGG | 8027 |
rs531915795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17672613 | ATCTAACATAGTCCT[A/G]TATGCAAGCCAGCTT | 8027 |
rs531930667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706622 | CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC | 8027 |
rs531952030 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17711567 | GGGTTTGAGGAAGTT[A/T]TCCAAGAGGGTTATT | 8027 |
rs531974478 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17672145 | GGCTTCCTCCTATAT[A/G]GCAATGGAAATACCT | 8027 |
rs531999769 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716078 | TCATGCGAAAAATGT[C/T]TTCCACTGACATTGT | 8027 |
rs532091720 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17671130 | CCATGTCTTTTAGCT[A/G]CTGTGTGTCTGCTAG | 8027 |
rs532091744 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17676658 | GCCTTGGACAATTGT[A/T]GTTTATGCCTGCTGT | 8027 |
rs532126856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17710037 | AGCTGTTCTTAGAGT[A/G]GCATGTTGCTTTACA | 8027 |
rs532222796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665661 | TTAGTGGCATGTAGA[A/G]TATCTAACACATATA | 8027 |
rs532223822 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17700811 | TGACTGAGGAAGGGA[C/T]ACTCATTGACTATCT | 8027 |
rs532225732 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17678479 | GGCTGGTCTCGAACT[C/T]CTGATCTCAGGTGAT | 8027 |
rs532265890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688489 | TGTTTTTGAGACGGA[A/G]TCTTTGTTTGTCGCC | 8027 |
rs532284143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17660119 | TTTATAAAGATTTAC[C/T]AGCAAGTAAATAATC | 8027 |
rs532289594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17705150 | AACTCTCATTCACAT[A/G]TCTTGTGCTAGATGT | 8027 |
rs532294360 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17710525 | TCATTCCTGCATATT[C/G]TTTAGTTGTTAGCTT | 8027 |
rs532331709 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17711789 | ACTGCCAAGGTCGAA[A/G]AATGCTTGTTCTAGA | 8027 |
rs532353353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17705511 | TTTGCCATTTTTGAT[A/G]TTTTGATGTATCATT | 8027 |
rs532380471 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704020 | ATAAGAGGTGGAAGA[A/C]CTCACGCATTGTAAG | 8027 |
rs532471111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17694473 | ATCAATGCACTGATA[C/T]TACATTTCAGAGCCT | 8027 |
rs532482480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17700702 | AGATAATGTCAAATT[A/G]TTGAGCAAAACAAGT | 8027 |
rs532511065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17658103 | ATGTATTCAATGCTA[C/T]AAATTTCCCTCTAAC | 8027 |
rs532565027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17648321 | CAATCAGTGCTCTGT[A/G]GCTAGCTAGAGGTTT | 8027 |
rs532631794 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642137 | TTTGAAAGGAATACA[C/T]GCTCATCATTAAAAT | 8027 |
rs532634012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692874 | AAGTAGTCATCTCTT[G/T]CTGTCTCCCAGCCTC | 8027 |
rs532687403 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17660730 | AACAGCCAATGTACA[C/T]GAGTCAGGGCAACAT | 8027 |
rs532708836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17687458 | CGAGCCACTGCAGTC[C/T]GGCTTCTGCCACAGG | 8027 |
rs532744636 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17658809 | TTAACTTTTAATCTC[G/T]ATGTGTTTTTATGTC | 8027 |
rs532776738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17653626 | AAAAATATCATGTCT[A/G]TACCGAACACATAGA | 8027 |
rs532874627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17681506 | TTAACATTGTTTATC[A/G]TGTGTAATATCCATA | 8027 |
rs532880089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17680484 | CTGGAGTTCAGTGGC[A/G]CAATCGTGGCTCACT | 8027 |
rs532887308 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687809 | TCTCCAAAATCTTAT[C/T]ACCTATTTAATGCTT | 8027 |
rs532895916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17686217 | AGAGATTCTAATACC[A/G]TGTTTTTTGTAATGT | 8027 |
rs532942801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17674963 | GACAAAATGTGATAC[A/G]AGGGTTTCTTCATTT | 8027 |
rs532948312 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697731 | TCCCCTCTAGGAAAA[C/G]AGAAAAATATGTTCA | 8027 |
rs532974230 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17657061 | CGGAGGCTTTTTTCC[C/G]TTTTCTGGTGGAGTG | 8027 |
rs533004671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714031 | TTGGTGTTTTCTCTC[C/T]TCAAAGGCTTCTTTC | 8027 |
rs533128568 | snp | C/T | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689568 | GTTTTTACTACTCAG[C/T]ATAGTTTCTAGAATC | 8027 |
rs533151171 | snp | A/G | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688313 | TTGTGTTAGTAACTA[A/G]TTGTATTGCTAGTTA | 8027 |
rs533159332 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17675375 | TGAGTATGGTAGTGC[C/G]TGCCTGTTATCTCAG | 8027 |
rs533173960 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645123 | TTGCTTTTGGTTTTT[A/T]ATTTTATTTTATTTT | 8027 |
rs533262558 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | STAM | GRCh38.p7 | 10:17664889 | AAGGACTTTAGGAGG[A/G]GCATTTCACTTTCAG | 8027 |
rs533342462 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17702803 | TCACGAGGTCAGGAC[A/G]TTGAGACCATCCTGG | 8027 |
rs533416524 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17663214 | AACGTTATTCTCCCA[C/G]AAATGTTTATTATTA | 8027 |
rs533417757 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, missense | STAM | GRCh38.p7 | 10:17713349 | AGATGCGTATTTCTC[C/T]TCCGTACTTCCCCAC | 8027 |
rs533428387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17656734 | GCACCAATCTCAGTT[C/T]TTGCCTCCTCAGAAG | 8027 |
rs533511965 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17707008 | CTTTACATGAGAATG[C/G]ATGCAATGCAGTGTA | 8027 |
rs533581233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17707389 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC | 8027 |
rs533588843 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17691021 | TTCAAATCTGTCTAA[C/T]TGTGAAGTTTGCCAA | 8027 |
rs533597022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17660240 | AATGCCTTTTATTTT[A/T]TACTAAGTAAAGAGG | 8027 |
rs533659272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17654872 | GTGCAAACACCTGAG[A/G]TAGTATTTTAGGTCT | 8027 |
rs533717689 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644198 | CGGTTGGTGGGGTTG[G/T]GTGAGAGGAGGAGCT | 8027 |
rs533720785 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17703246 | CTTTTGTTTTTTAAG[A/C]CTGCTTAAAATGAAA | 8027 |
rs533756061 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17698793 | GGGTTGCAAACTTGC[A/C/G]CGTCAAGAGCTGTTA | 8027 |
rs533771597 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17650179 | TCCTGAAGTGTGATA[A/C/T]GATAGAAAGACCTTG | 8027 |
rs533779224 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643883 | CAACCTGCTTTCTTT[C/T]TCCTGGCTCTCCCAG | 8027 |
rs533819929 | snp | A/G | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715187 | TTAACACTGTGTTAA[A/G]TTAATTTACGTTGCT | 8027 |
rs533912993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17693656 | TATTCGTGTGATATA[G/T]CCATTAACTGTTCTA | 8027 |
rs533917676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688709 | CTCAGGTGTTCTGCC[C/T]GCCTCGGCCTCCCAA | 8027 |
rs533924199 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17676547 | TGCCCCCTTTTCTTT[C/T]ACCCTCTTACGAACT | 8027 |
rs533929968 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715305 | AAACAAAGTTGTTAG[C/T]GTATTTACATGAAGG | 8027 |
rs533959425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17677678 | AAAGTAGAAGAAAAA[A/T]GTTTTAGGATTAAAA | 8027 |
rs533967762 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17690144 | CCAGGGACACAGCTC[-/A]ATAGTTGACAGCTGG | 8027 |
rs533981571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689079 | ACTTTGCTCTCCTGT[C/T]CACCCTTGTGCCAAA | 8027 |
rs533998412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17683294 | TCAGGCCATTCACTG[C/T]GCCCATAGGAGCTGG | 8027 |
rs534005681 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643155 | GACTTCATTTTTAAT[C/G]AATTTTTAAGCACTC | 8027 |
rs534030570 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716417 | GTAACTTAAGTGTTT[C/T]GCTCAAGTGTTGTGT | 8027 |
rs534040087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17711786 | GACACTGCCAAGGTC[A/G]AAGAATGCTTGTTCT | 8027 |
rs534086859 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17671451 | TTAGACATCTCCTCT[C/T]TTACAGATGAGGTCT | 8027 |
rs534151478 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17710186 | CCTCTGTTTGACTAT[C/G]TCACATGCTGCTCTA | 8027 |
rs534166906 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17681829 | AGGACTTGGTTTGCT[G/T]TGAATGTTTTGAACA | 8027 |
rs534171053 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17652534 | TCAACTATGATAGTA[A/G]GCAATTTATATTTGA | 8027 |
rs534171160 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17673499 | TCAGTCACGGGAGAG[C/T]AACAGCAGTTGCTAA | 8027 |
rs534177612 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642547 | AGGAAACTGAGACAC[C/T]AAGAGGTGAAGCAAT | 8027 |
rs534178496 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17648789 | TAAAAATGTTAGATA[A/T]TGTCAGTTACCTGCT | 8027 |
rs534281641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17670256 | ATTTTACTAAGTCTT[A/G]AAAACATCGTATATT | 8027 |
rs534281911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17669136 | ATGGTTCTAACTTTA[C/T]TCTTTTCTATTTGGC | 8027 |
rs534282121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17675739 | CTTGTCACCTAGAAG[C/G]TAATTAATGAACGTT | 8027 |
rs534303144 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642947 | TTTGTACTTTTAGTA[A/G]AGACGGGGTTTCACC | 8027 |
rs534396003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17705231 | CTTTGCAATATAGTC[A/C]AAAGGACCAGCGTAG | 8027 |
rs534435147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17669713 | TTCTTTTTTTTTTTT[C/T]CTGAGATGGAGTCTC | 8027 |
rs534460780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17699812 | TCTTGAAGGATTAGT[A/G]ATTTAAAAAGAGGGT | 8027 |
rs534470502 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17681085 | CGTTTTACATTCCCA[C/T]CAACAGTGCACAAGT | 8027 |
rs534477319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665748 | CTACTAGATGTAATC[C/T]CTGTTTACTTCATTT | 8027 |
rs534497700 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17699114 | CCAGATTTCAGTAGT[A/T]TGGGCTAGTAGAGCA | 8027 |
rs534587690 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17661634 | ACCTACTTTCTTTCA[C/G]TTTTTCCATTTCTAT | 8027 |
rs534630556 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714697 | CCAAACTATAACTTA[A/G]CATCATCAACTCTGC | 8027 |
rs534642759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17693146 | TGATGAGAAAGGTTT[C/T]GCAAATTCTTAGGGT | 8027 |
rs534655800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17687306 | ATGGTAAAACCCCGC[A/G]TCTGCTAAAAGTACA | 8027 |
rs534668236 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704123 | ATTTAAACAGGGTCT[G/T]GCACTGTTGTCCAGA | 8027 |
rs534764883 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17652041 | CTGGGCAGATTTCTC[A/C]ATCTCCTCTTTTTGA | 8027 |
rs534833465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17698784 | TGAGAAAAGGGGTTG[C/G]AAACTTGCGCGTCAA | 8027 |
rs534885613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17647977 | TTAGTTCTTTGCCCA[A/G]ACCTGCTCATTCCTT | 8027 |
rs534923209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17653365 | GTTAAATGTTTGTTT[C/T]GGTAAAACAGGTTGT | 8027 |
rs534937337 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17646490 | TTTAGCATTCAAGAT[A/T]GTTTTATACTCCTTA | 8027 |
rs534973195 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | STAM | GRCh38.p7 | 10:17687495 | CTCTGTCTCAAAAAA[C/T]AAACCAAAAAAAAAG | 8027 |
rs535033369 | snp | A/C | 0.00256709 | 0.0357345 | missense, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696848 | TTTGTGACTGCAGAT[A/C]TCACTGCTGAACCAG | 8027 |
rs535034826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17702958 | AGGTCGTAGTGAGCC[A/C]AGATCATGCCACTGC | 8027 |
rs535076361 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | STAM | GRCh38.p7 | 10:17683631 | TTTTAATTTTACATA[-/T]TTTTTTGTCTCTAGA | 8027 |
rs535097149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644935 | GGCAACGACTGAAAC[C/T]GAATTGAGGACCTGA | 8027 |
rs535142489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712469 | TTAGTTGGAGAAATG[C/T]AGCATTAAATTACCG | 8027 |
rs535150084 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17700450 | TTGAAACTTCCTCTC[C/T]AGTCCTTTGTTTGCC | 8027 |
rs535189581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17707643 | TCATGTTCAATTTTC[A/G]AAGAATGACAAAATA | 8027 |
rs535235409 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17661964 | TCATTAATTTAATTG[A/T]AAATTTTTAACTACT | 8027 |
rs535269997 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643335 | GATGCTCCTTAAAAC[C/T]TCTCCATCACACAGA | 8027 |
rs535284589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17707147 | GGGTGCGGTGGCTCA[C/T]ACCTGTAATCCCAGC | 8027 |
rs535293212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712986 | AATGAGGTTATGAGG[C/T]CTTCCCTTCCACTAG | 8027 |
rs535300639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714240 | CACTTGACACACGAT[A/G]CATGTGTTTGTTACC | 8027 |
rs535346365 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17709633 | AAAGGATAGGCTTTT[A/T]AGAGTTTACCAACGT | 8027 |
rs535349268 | snp | A/T | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645303 | GAATGTAATCATTAC[A/T]GTGAATAAGGACAAC | 8027 |
rs535364696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17680758 | CATCATACAGCATTT[C/G]TCCTGTTGTGACCAG | 8027 |
rs535388303 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17650291 | TTGAATTCACTTTCT[A/T]CTTTGGTAAATAGGG | 8027 |
rs535410315 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17678058 | TTCATAAGTTTGTGC[A/G]ACAGTATCTAATTCC | 8027 |
rs535472985 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17650754 | TGTGAATGTACGCGT[G/T]GCCCCTCCGTTTAAA | 8027 |
rs535567518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17672190 | ACTAACTGGTGACCG[C/T]GCCTAACATTGAGCT | 8027 |
rs535604667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17673410 | TTCGTGTTTTGCTCA[G/T]TGACTTTTTTTTGAG | 8027 |
rs535605610 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17710290 | GAGATAACCTGTTGG[C/T]AGGTGCTTTAACAGT | 8027 |
rs535628164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17701730 | CGTTTTTACCCCCCT[C/T]CTCTCCCTTTTCAAT | 8027 |
rs535630100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695556 | AAAAACACTGAGTAT[A/G]TATATGTACTTAATG | 8027 |
rs535697142 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17707587 | AGGGCACCTGCTTTA[G/T]AGTCTTGATCACCAG | 8027 |
rs535710862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17660829 | AAAGAGAATATTTTT[A/G]TTAAAAAGATTTGAA | 8027 |
rs535749676 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17667466 | TGATTTCCATGTTTC[A/C]CTCAGTTTCGTAACA | 8027 |
rs535806256 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17668920 | AAAGCTGCTATAAAC[A/G]TGAATTTGCAGCCTT | 8027 |
rs535834689 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17678748 | ACTTTTTCATCATCC[C/T]ACGTAGAAACTCTAC | 8027 |
rs535835482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17705983 | TGAGGTGGGAGGATA[A/G]CTTGAGCCCAGAAGG | 8027 |
rs535850960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17649852 | TCCTAGCCTCAAGTG[A/G]TCTGCCTGCCTCAGC | 8027 |
rs535880746 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716804 | AGCCTTATAAAGGTT[G/T]AAATGATGAGTACTT | 8027 |
rs535934000 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | STAM | GRCh38.p7 | 10:17700813 | ACTGAGGAAGGGACA[C/T]TCATTGACTATCTAT | 8027 |
rs535967258 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17665869 | AAGATATTCACATGA[G/T]TTCTACTGCGCAATT | 8027 |
rs536049236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17649549 | TAAGATGAGAACTTT[C/T]CATTTTTTTTCCCCT | 8027 |
rs536123340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17650332 | CCATTATACATCATG[C/T]GGATGCTATGAGGAT | 8027 |
rs536128712 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643851 | GAGGAAAAAAGGCGC[A/G]CAGCTCGACCCGAAC | 8027 |
rs536161881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17655446 | CAATACCTATTGGTT[A/G]TTATCCACTTGGTCT | 8027 |
rs536231576 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17710457 | ACATGTTTATTTCAA[C/T]AGGTGTCTTTTGAAG | 8027 |
rs536300686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17648449 | CAGCAACCGGCTCGG[A/G]TCCCCTTCCATGCTG | 8027 |
rs536349873 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717226 | AATTAGCTGGGCGTG[A/G]TGGCAGGCACCTGGT | 8027 |
rs536373522 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17687483 | CACAGGGTGAGACTC[A/T]GTCTCAAAAAACAAA | 8027 |
rs536390694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17693840 | GTGTGACTAAAAGCA[A/G]TATTGTTGGATCATG | 8027 |
rs536422058 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17677407 | AATCATCTTTAGATT[-/A]TTTTTTACTGATTTT | 8027 |
rs536456575 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642479 | AATAAGCGTTTTGCT[A/T]GTACTAATTCATTTG | 8027 |
rs536497369 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17710120 | CCTGACTTAATAGGA[A/C]CCTGCAGCTATTTTA | 8027 |
rs536514972 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716301 | AGATTAAATCTTTAG[A/C]CAGTAATCTTAAGGG | 8027 |
rs536593074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17674667 | ACTTCCACTATATTT[G/T]ATTGGTCAAGCAAGT | 8027 |
rs536600590 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | STAM | GRCh38.p7 | 10:17702776 | GCACTTCGGGAGGCC[A/G]AGGCGGGCAGATCAC | 8027 |
rs536617746 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17680531 | CCACCTCAGCCTCTC[C/G]AATAGCTGGGACTAC | 8027 |
rs536661493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692406 | AAAGGAGCCATAGGG[A/G]GAGAACGTTGTAAGT | 8027 |
rs536676818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713612 | GGTTCTAAACCTCAG[A/G]CATTCTGGACTCTTC | 8027 |
rs536732755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17681715 | GGCATATCTGTGTCC[A/G]GAACATAGCATGTTT | 8027 |
rs536760505 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17668329 | TTGCTTAGCATAATG[A/C]ATATTGAACAGATAG | 8027 |
rs536768142 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17707487 | CATGTAAAGTGGGCA[C/T]GGACTGTGTTCAGAT | 8027 |
rs536805453 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17699632 | TTGGAAGACTGAGAC[A/C]CCTGTCAAGGCCACC | 8027 |
rs536841377 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17709461 | AGAAGGTAAGCACCC[A/T]TGTTTCTCAGGAGGC | 8027 |
rs536867179 | in-del | -/TTTTTTTT | 0.104938 | 0.20361 | intron-variant | STAM | GRCh38.p7 | 10:17678261 | TTCATGTGGTGTAAT[-/TTTTTTTT]TTTTTTTTTGGAAGA | 8027 |
rs536931505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17664842 | TGTAAAGTGCGGCGA[C/T]CTTTTTAAGAGGACA | 8027 |
rs537041449 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714108 | GCTTACTTTTTCCAC[A/C]TCTTTGCTTAAGTAT | 8027 |
rs537085394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17661704 | TCACCTTCACATTTA[C/T]TACTCAATTCTGTCC | 8027 |
rs537102891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17708210 | AAATAAACTTTTATC[A/G]GAACACAGCCACTCT | 8027 |
rs537110558 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17656349 | CTTGTTTGCCCATGG[C/G]TAATACTGGAGAAAT | 8027 |
rs537149447 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17662023 | CCATTTTTATTTGTC[C/G]TACTTTACTTTGGAC | 8027 |
rs537164550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17675065 | TGTGTATTTATAAAT[A/C]TGAACAGCTGACAGA | 8027 |
rs537258319 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17690926 | CTTTGAATAAAAAGT[G/T]CAGTTCAGAAACATG | 8027 |
rs537275952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17656768 | GAATTCATCTAAGGG[A/G]CGTAAGGCAGAAAAA | 8027 |
rs537285022 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17663549 | CTTTTCTTCTTCCTT[C/G]CCTCCTTTTTCTTCT | 8027 |
rs537345775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697487 | TTTTACTAATCATAT[A/G]AAAGTTTTTTGTTTG | 8027 |
rs537397888 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17707157 | GCTCATACCTGTAAT[C/T]CCAGCACGTTGGGAG | 8027 |
rs537399080 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17683651 | TTGTCTCTAGACTTT[C/T]ATCTGGGCCCTTTTT | 8027 |
rs537453115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695487 | TAATCTATTCATTTT[C/T]GGTTCCACCTAATAA | 8027 |
rs537464364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17701871 | TTTTGGTATTAAGAA[A/G]GTCATGGCTCTAATG | 8027 |
rs537469383 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17655380 | TAACCTGCTTTTGCT[A/G]TCTTCTATGTTAGAA | 8027 |
rs537486913 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17685415 | CCTCAAAAGTGGTGG[C/T]GGGGGAGTTTCCACA | 8027 |
rs537496190 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17662317 | TTTGTTTCTTGAGGA[C/T]GGAATGTTTTCCTCT | 8027 |
rs537624764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691261 | CGGTGGCTCACGCCT[A/G]TAATCCTAGCACTTT | 8027 |
rs537639140 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17651967 | AAAAAGTTCTCTAAT[C/G]TTTTGAAAAGACTAT | 8027 |
rs537640608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712414 | AACTTTATATCTCAC[A/G]CATATGGAGTGATGA | 8027 |
rs537686922 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644699 | TGCTTCTGGAAGAAC[A/C]GCGAAGGGCTTAAGG | 8027 |
rs537700744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17646436 | ACCTTCTTACAAAAT[C/T]CTCTAACTTATTTTA | 8027 |
rs537718750 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17673619 | CTGTGTAACCCTGGG[C/T]CCTGCCTTCAGCAGC | 8027 |
rs537730356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17667360 | AACCCCTCACCTTGT[A/G]ATCTGCCCTCCTCAG | 8027 |
rs537804340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17683110 | ATGTTTCTTCTGTTT[C/T]CTCTTTCTGTCTTTT | 8027 |
rs537812732 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17664178 | TTACATATTCACAGA[A/T]CAACTTAGTAATAGA | 8027 |
rs537831690 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17653266 | CCATCGAAACCTACA[C/G]TGAAAAACCGAATAT | 8027 |
rs537923698 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17674401 | AGTTGTAGTCACATA[A/G]TGCCTGGGACTAGGG | 8027 |
rs537929128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17678312 | CAGGCTAGAATGCAG[C/T]GGCACAATCTCAGTT | 8027 |
rs537931129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17684475 | TCATCTACGATTACT[A/G]ATAAGAGAGCCTGTT | 8027 |
rs537932598 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17671413 | GTCTAGGAGTTTTGT[A/G]TTAACATTCTGATAA | 8027 |
rs537963189 | snp | A/T | 3.29549e-05 | 0.00405911 | missense | STAM | GRCh38.p7 | 10:17705670 | ATGAACGAAGATCCG[A/T]TGTATTCCATGTATG | 8027 |
rs537969147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17677576 | AACTGTGAAAAAGGC[A/G]AAATCTAAATAATAG | 8027 |
rs537980531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689757 | GGTTCTTGTTAACTC[A/C]AAACTTGGTTTGACC | 8027 |
rs538023690 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17659622 | TACAGGTGCATGCCA[-/C]CAGGCCCAGCTAATT | 8027 |
rs538035671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17700563 | TGCCTAGGTTGTTTA[C/T]AGTTTTTACAGTGTA | 8027 |
rs538037301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706202 | TGGCAGTTACAGCAT[A/G]TAATATACTAATTAT | 8027 |
rs538102032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712893 | TAGGGAAGCTCAGTA[C/T]GTGAGGGGTGCAGCT | 8027 |
rs538124500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17673329 | AGAACTTGGTAATAA[A/G]TAGAACTTTATAAGG | 8027 |
rs538151314 | snp | A/C | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715421 | TGTGTATATATATAT[A/C]TCTACATGTCTTTCT | 8027 |
rs538194576 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | STAM | GRCh38.p7 | 10:17677001 | CATAATAGTGGTTAA[C/G]TTCTGTTTTGTAGAC | 8027 |
rs538281178 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643241 | CATTTGGAGATGCCG[A/T]AATTTGCGGGATAAT | 8027 |
rs538354368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17670905 | GTTACAAATCAAATT[C/T]GCATTTTGAATATGT | 8027 |
rs538412581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687541 | AAAAAAAGTTATGTT[A/G]TTTTGAAGAAATTAA | 8027 |
rs538425870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17693740 | GACCTGTGGATTATT[C/T]CTGATTTTTTTTTAC | 8027 |
rs538464531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17699676 | ACTGGCATGGACGGC[A/G]CTCTCTAAACGCCTA | 8027 |
rs538480791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665790 | TCTTTTTAAATCTTG[A/G]AATACTTGATTATAC | 8027 |
rs538493584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17659369 | CTGTTATTATTTAGA[A/G]TAAACTATTTTTTGT | 8027 |
rs538494283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17654947 | TATTTCAGCCAGCCT[A/G]GATTCTTCATTATAC | 8027 |
rs538536695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17682346 | TTACATTGTGTTAAT[A/G]TATTACAATTTATCC | 8027 |
rs538540922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17660306 | GATAATGAGCGTACA[C/T]CTTTTCAAGATGGCC | 8027 |
rs538542693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17666540 | GCTGGGACTACAGGC[A/G]CCCGCCACCATGCCC | 8027 |
rs538568924 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | STAM | GRCh38.p7 | 10:17654324 | ACCTCCCAGGTTCAC[A/G]CCATTCTCCTGCCTC | 8027 |
rs538661513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704153 | ACTGAAGTGCAGTGG[C/T]GAGATCATAGCTCAC | 8027 |
rs538683218 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17676522 | GGAAGCTGCAACGGT[A/G]TAGAAATACTGCCCC | 8027 |
rs538750308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17680770 | TTTGTCCTGTTGTGA[C/T]CAGCTTATTTCACTT | 8027 |
rs538788598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692385 | AAGGGAAAAAGTGAA[C/T]GGAGCAAAGGAGCCA | 8027 |
rs538835351 | snp | A/G | 0.000243153 | 0.0110235 | intron-variant | STAM | GRCh38.p7 | 10:17693340 | GTCCCTGATGGTGGG[A/G]ATAACATAAGCCTTT | 8027 |
rs538924802 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715151 | CCATTTTGAATCACA[A/G]TGGTGATCGTGTGAA | 8027 |
rs538947441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17648579 | CGTGGCTTCATTCTT[C/G]ACGTCAGCGAGACCA | 8027 |
rs538955865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696041 | TCTCTTTTATAAGGT[A/C]GCTAATCTCATTCAT | 8027 |
rs538959340 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17676216 | TTTTCATTTACTTCC[A/T]GGCATGAGCTGACTT | 8027 |
rs539004677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691978 | ATACGTTATAAGCCC[C/T]GGAGGTAATGTTACA | 8027 |
rs539033151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17679340 | AGCATTTGTTATGTG[C/T]TTATTGGCCCTTTGT | 8027 |
rs539046312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17713155 | GTGACCATTCTCTTT[G/T]CCCTTCTGCCTCACC | 8027 |
rs539052533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17685284 | TTTCAGAAACACTGC[A/G]AAAAGTCTATGGCAC | 8027 |
rs539073182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17657350 | CTCTCCTGCCCTGCT[C/T]GTACCTGTCTTACTA | 8027 |
rs539076699 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17707271 | AAAATTTAGCCTGGC[A/G]TGGTGGTGGGTGCCT | 8027 |
rs539080382 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17710699 | GTATCTTGAGAGCTG[C/G]CACTGTCTTTCACCT | 8027 |
rs539096641 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17678169 | ACTAATCTACTTTCT[A/C]TCTGTGTGGATTTGC | 8027 |
rs539107171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713522 | CCCTCCCACCCCCGA[A/G]TCTACTATGGTCCCA | 8027 |
rs539133176 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17652792 | TGTTCAGAATGACTC[A/G]CTCAATATTCTTGGG | 8027 |
rs539166059 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | STAM | GRCh38.p7 | 10:17686496 | ATTCTCCTGCCTCAG[C/T]CTCCTGAGTAGCTGG | 8027 |
rs539216891 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714752 | CACCTCAGCCACAGC[A/G]ACCATATTCTCAGAA | 8027 |
rs539232478 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17708103 | CACTGTGTTAGCCAG[G/T]ATGGTCTCGATCTCC | 8027 |
rs539237546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17703024 | AAAAAAAAAAAAAAA[A/G]AAAGAAAAGAAAAGA | 8027 |
rs539269339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17707671 | ATAAAGTTAGGAGGA[C/G]TGGTATAGCTGTGTT | 8027 |
rs539398561 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697468 | GATATTCAGAAGGAG[A/C]CATTTTTACTAATCA | 8027 |
rs539406003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17666625 | GATGGTCTCGATATC[C/T]TGACCTTGTGATCTG | 8027 |
rs539437101 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17646359 | GGACATTGCTAAATG[C/T]CCCCTGGAAGGACAA | 8027 |
rs539473588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645406 | CCTTAGAGCATGTCA[C/T]TGAAACTTGGAAGTT | 8027 |
rs539516379 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17674594 | CTAAGAGCTAGTGCT[C/G]CAGGAGACCCAAATG | 8027 |
rs539519790 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642693 | GCCGAAATGGAATTG[C/T]TGGGTCCTAAGGTTT | 8027 |
rs539602165 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17668265 | GGAGCTGGGCAGTTT[G/T]AGGAAAGAGGGAGAG | 8027 |
rs539613489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689995 | GAAAAGGAAGAATTA[A/G]TGATTGTGCCATATG | 8027 |
rs539664133 | in-del | -/C | 0.00597247 | 0.0543191 | intron-variant | STAM | GRCh38.p7 | 10:17684421 | CATTTTATTTTCAAA[-/C]CTTTTTTTTTTTCCT | 8027 |
rs539686719 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17669372 | TTTTTTTTTTTTTCC[A/G]GAAATGTTGTTTTAG | 8027 |
rs539768098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17662959 | GCAGCTGCAAAGCCC[C/T]TCCTCTCTCTCTTCA | 8027 |
rs539826656 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706689 | CGGCCGAGGCCCATA[A/T]TTTTAAAGCTTCGTA | 8027 |
rs539862696 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706299 | ATCAGCCATCACACT[G/T]TTGAAAAAAATTACA | 8027 |
rs539864729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712300 | AGATTCTAAACCAGA[C/T]ATTCTGACTCCAGAA | 8027 |
rs539885691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17662584 | CTTCTGTTGCACATG[A/G]GAAAGAAGCAAATAG | 8027 |
rs539901269 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643594 | GCTGTCTGCAGATTC[C/T]AAAGCCGGGCGTTCA | 8027 |
rs539923744 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716065 | CTTTTCTTTTAATTC[A/G]TGCGAAAAATGTTTT | 8027 |
rs539962770 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17669752 | ACCCAGGCTGTAGTG[A/C]AGTGGCGCAATCTCA | 8027 |
rs539993114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696687 | GATTCAAATTTTGTA[A/G]TAGTGTAAGTTGAAT | 8027 |
rs540022420 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17694830 | GTAAAAATAGGAGTT[C/T]TCATGCTGTTCCAAT | 8027 |
rs540062469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17677139 | TTAATGGTTCAGTAG[A/C]CAATTTTATTTTGGT | 8027 |
rs540074363 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17661972 | TTAATTGAAAATTTT[C/T]AACTACTGTGTGTTA | 8027 |
rs540108256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17651361 | ACCTGGCATGTAGTA[A/G]CCAATGGATACGTTT | 8027 |
rs540135397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665983 | AAGAGAACTTTCACA[A/G]TGATAATAGCCGTTT | 8027 |
rs540148252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17650831 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCGGATTA | 8027 |
rs540160790 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17692660 | TTCCCTTATTTACAC[A/T]ATTTAATAGAGGCAG | 8027 |
rs540211385 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17713034 | TGTCAAGAACCCTGG[C/T]GATGCCCATACTGCT | 8027 |
rs540220659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689143 | AAAATCAAGAAATGT[A/C]TTTTTTATTCCTATT | 8027 |
rs540231703 | snp | A/G | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716586 | ATATACTTTTCTGCA[A/G]TTTTTCTTTGTCTTT | 8027 |
rs540239740 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687738 | GACACTTTTCCTTGT[C/G]TTACTGATGTACAAA | 8027 |
rs540254639 | snp | C/G | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714230 | CAGTTAGAACCACTT[C/G]ACACACGATACATGT | 8027 |
rs540263850 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17708419 | GCTACAAAACAATGA[A/G]TTCAAATACACTTTC | 8027 |
rs540266016 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714964 | TAGAGGTTCTTCCCC[C/G]CCCGCCCCTGCAGAG | 8027 |
rs540277457 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | STAM | GRCh38.p7 | 10:17681217 | TTTTTTTTTTTTTTA[A/C]TGTAGGTGCTTATAG | 8027 |
rs540294862 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | STAM | GRCh38.p7 | 10:17655891 | CCCTCTGCTTCTGTA[C/T]AGCTGTTGTTTTGAA | 8027 |
rs540338515 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642829 | CTTTGCAATTTTTTT[C/T]TTTTTTTGAGACGGA | 8027 |
rs540352836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17676582 | GACCCAGATCTATTC[A/G]TAAAAAGATGATTTT | 8027 |
rs540367903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17690668 | GATTTTTGTTAGGGC[A/G]TACTTAACAAAAACC | 8027 |
rs540433294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17664890 | AGGACTTTAGGAGGA[C/G]CATTTCACTTTCAGT | 8027 |
rs540453264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17699270 | GGAGGAAATGTAATA[C/T]TCCATCAAGCATATT | 8027 |
rs540470281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17710490 | CATTTTCTTGAAATA[C/T]TTAGCCCTCTCGTCC | 8027 |
rs540479532 | snp | G/T | 3.36995e-05 | 0.00410471 | intron-variant | STAM | GRCh38.p7 | 10:17700326 | ACTTTGTATTGAAAT[G/T]TAAATGGTTTTGCTT | 8027 |
rs540490688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706017 | AGGCTGCAGTGAGCC[A/G]TGTTCACACCACTGC | 8027 |
rs540520220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17660089 | TAAATAATTAACTTA[A/C]TTACCTGAAACATTT | 8027 |
rs540532442 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17710963 | GTTTGTGTGTTTCAA[C/T]GGGGAAATGAGGAAT | 8027 |
rs540600764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17676007 | ATTTACCATTAGATC[A/G]GAGAAGTGACTGCTG | 8027 |
rs540607269 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17659034 | TTCACTCTTTTTTTG[A/G]CTTTTGTGATTTTAA | 8027 |
rs540616099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697699 | TTTAGTCATCAAGCA[A/T]AGTTTAAGTCATAAT | 8027 |
rs540640819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17675458 | GCAGTGAACTGAGAT[C/T]GCACCACTGCATTCC | 8027 |
rs540649644 | in-del | -/A | 0.00279162 | 0.0372561 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643188 | TGATTACTATGTATT[-/A]ATCCTGTGTTGACAT | 8027 |
rs540682265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691504 | GCCTGGGCGACAGAG[C/T]GAGACTCAAATAAAT | 8027 |
rs540751771 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17657592 | TGAACCCATCTGGGC[C/T]TGTGCTTTCTGTTTT | 8027 |
rs540763012 | snp | C/T | 0.457504 | 0.139435 | intron-variant | STAM | GRCh38.p7 | 10:17669884 | CAATTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 8027 |
rs540783983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17658549 | TTGGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 8027 |
rs540827314 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17657456 | TTGTCTGGTTTTGGT[A/G]TCAGAGTAATGCTGG | 8027 |
rs540841249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17699001 | ATTATATTTCTTAGG[C/T]TGGAAATTAAGCTAT | 8027 |
rs540929781 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17702022 | TCCATCTTTCAGAAG[A/C/G]TACCGAAAGAACTTA | 8027 |
rs541110626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17652473 | TGCTGATAACTGTAT[C/T]ATATGTTCCTGGATG | 8027 |
rs541174797 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645101 | TGATGATGTCAATTC[A/G]ATAGGTTTGCTTTTG | 8027 |
rs541197427 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17673985 | GATGAGTAAGCGTTG[A/C]CTAAGAACAGCAGGG | 8027 |
rs541212510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17679137 | AATTTTTTGAGGAAC[A/T]ACCACACTTTTCACA | 8027 |
rs541274172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17652978 | GACAGCCTCTAAATC[C/G]TTGGAATTTTCTGAG | 8027 |
rs541321472 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17702791 | GAGGCGGGCAGATCA[C/T]GAGGTCAGGACATTG | 8027 |
rs541342432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17647472 | AGTTGAGTGCCCTGC[A/G]GCTCAGTTCCGGAGC | 8027 |
rs541357298 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17667939 | CAGAGCTGGGTTTCA[G/T]AGTGAGTTAGAAAAA | 8027 |
rs541360200 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17680866 | CTTATCCATTTATGC[G/T]TCTGTGGACACTTGG | 8027 |
rs541360394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17662543 | GATATAAACCTAGTA[C/G]ATTTGTAGAATGAAT | 8027 |
rs541361589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17674747 | TGAAGGGAAATGGTA[A/G]GTTCATGTCAAAGGA | 8027 |
rs541462194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17646018 | TCTTAATGTCAAACC[C/T]GTTCCTAGTAGCTGT | 8027 |
rs541465548 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717128 | AGCACTTTGGGAGGC[C/T]GTGGCGGGCGGATCA | 8027 |
rs541487009 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17705986 | GGTGGGAGGATAGCT[C/T]GAGCCCAGAAGGTCG | 8027 |
rs541526895 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17711999 | TAATTACACATTGGG[C/T]GACATGGTTGGGAGA | 8027 |
rs541527938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706469 | CTGCAAGCTCCGCCT[C/T]CCGGGTTCTCGCCAT | 8027 |
rs541558958 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17666766 | GTAGGAAGTTGAAAG[A/T]ATATTTCCTGATTTT | 8027 |
rs541560016 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17685530 | GATTTATTAGGGGAA[C/T]TTACACAGGAGGGCT | 8027 |
rs541581313 | snp | C/T | | | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695490 | TCTATTCATTTTCGG[C/T]TCCACCTAATAATAT | 8027 |
rs541611499 | snp | A/G/T | 0.000329573 | 0.0128328 | synonymous-codon, missense | STAM | GRCh38.p7 | 10:17705702 | AAAGTTACAGAATCA[A/G/T]CCATATTATATGCAG | 8027 |
rs541617956 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17661341 | CTTGATATTTGCAGT[A/G]GTAATATGAAGCCTT | 8027 |
rs541621694 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17679562 | AAACTTTTAATTTTG[A/G]TGTTTAATTTGCGTG | 8027 |
rs541640701 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17682146 | GCATTTAATCACTCC[C/T]AAAAGTTCCTTCCAC | 8027 |
rs541676705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17707866 | AGAAGTAGACAAATC[C/T]AGCCTGTTGCCTGTT | 8027 |
rs541680488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, missense | STAM | GRCh38.p7 | 10:17713324 | TGCCGTGGATCTGCC[C/G]AGGATTCCCAGATGC | 8027 |
rs541680567 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17660840 | TTTTATTAAAAAGAT[A/T]TGAAGAATCATCTCA | 8027 |
rs541686405 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17699791 | TTCTACCAAATGAGA[-/T]TTTTTTCTTGAAGGA | 8027 |
rs541740759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17655545 | AGGTATTATACACCT[A/G]TAAAATATTTGGTCA | 8027 |
rs541768263 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17662489 | TTGTGTTTTTTCCTG[C/T]ATTTTAGTAACTTAT | 8027 |
rs541802436 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17703874 | ACTGAAACAGCTGCT[A/G]TATTCACCATGGGCA | 8027 |
rs541819274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17678323 | GCAGCGGCACAATCT[C/T]AGTTCACTGTAACCT | 8027 |
rs541820708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17683947 | GTTACATTCGTCTGT[A/G]GCTTATGTTGTTAGG | 8027 |
rs541821346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17671989 | CTGTCACTGCTCGGC[A/G]TATGGTTTTTATGAT | 8027 |
rs541862781 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | STAM | GRCh38.p7 | 10:17690985 | CTCTACTGGTAGAGA[-/T]TTCTTCACACACCAT | 8027 |
rs541873338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17700611 | TTTTTTGAACATCTA[C/T]CTTTGTGTTTCTTTA | 8027 |
rs541875355 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17694185 | ATTGTAGGTATCTAC[C/T]CCTGGTTTTTGACCT | 8027 |
rs541887518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17705370 | TTCTGGTACAGTCAG[C/G]TACGATAAGACGGAG | 8027 |
rs541931186 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17667790 | GAGACAGAGTTCAAA[C/G]CACTGCATCCCAGAA | 8027 |
rs541969917 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17667401 | TGCTGGTATTACAGG[A/C]GTGAGCCACCGCATC | 8027 |
rs541983037 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17672423 | ACATGTTTAACCTAC[G/T]GAATTTAACTGTATT | 8027 |
rs542000891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17701945 | AAAAATAGGACCAAA[A/G]TGAATTTTCAGCTAG | 8027 |
rs542037652 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706778 | TAGCCTTTTGCAGGT[C/G]AGACATATCTCAATA | 8027 |
rs542094479 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716522 | TTTTGATAAATATCT[A/G]TCGGATTATAATCTT | 8027 |
rs542099509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696372 | TGTTGGGAGAAAAAA[A/C]AAACCTTGCTGCTGT | 8027 |
rs542114358 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644041 | GAGTCAGGCAGAGGG[G/T]ACTCCCTGTTCAGCC | 8027 |
rs542129315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17661741 | CTTCATAATCTCTCA[A/G]AATGTTGACGTTTTA | 8027 |
rs542200759 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17660301 | CAAGAGATAATGAGC[A/G]TACATCTTTTCAAGA | 8027 |
rs542235487 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17693478 | CAATTACTGTCACAT[A/G]TATCCTTTCAGTCTA | 8027 |
rs542288055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17660337 | ATGAAAATAACTAGA[A/C]TGCTGGCAACTATTC | 8027 |
rs542361026 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | STAM | GRCh38.p7 | 10:17681276 | ACACCCTTAAGTTTT[C/T]TTGGGTTATGTTTTC | 8027 |
rs542390228 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17680260 | TGGTATTAAATACCT[G/T]CATAATGTTGTGAAC | 8027 |
rs542430905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688354 | TTTTCTGGCATTCAG[A/G]GGTGCCAGAAAAGTA | 8027 |
rs542452487 | snp | A/T | | | upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644005 | ACTAATTCCACTCTT[A/T]TGTGTGACTAATTAA | 8027 |
rs542453509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17649258 | ACAATAAAAAAGTTA[A/G]CTGGCATGGTGGTAT | 8027 |
rs542455903 | snp | A/G | | | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696266 | ATGTATTGAGTGCTT[A/G]CTAGCTTTCCATATA | 8027 |
rs542517933 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17646265 | TCCTGTGCAATGTAG[A/G]GTGTTCAGCCTTATC | 8027 |
rs542519692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17710291 | AGATAACCTGTTGGT[A/G]GGTGCTTTAACAGTG | 8027 |
rs542621813 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17692698 | CTGTCAGAATTAACT[A/C/G]CTTGTAATTTGGTTT | 8027 |
rs542712227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714234 | TAGAACCACTTGACA[C/T]ACGATACATGTGTTT | 8027 |
rs542750416 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17675262 | TAATTCCAGCCCTTT[-/G]GGAGGCCAAGGTGGG | 8027 |
rs542806330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17669832 | CCTCCCCAGTAGCTG[C/G]GACTACAGGCACCCG | 8027 |
rs542892773 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17658462 | TTATATACAGTTGAT[G/T]GATGGTGTTGTTGAG | 8027 |
rs542931624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17657883 | TTTAGCTTGGCTAGC[A/G]GCATATCGGTTTTAT | 8027 |
rs542967385 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17700303 | TTTCCATGGTGATAG[A/G]AGTTGGTACTTTGTA | 8027 |
rs542967767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17664375 | TGTCTCCAGAACTTA[C/T]CCATCATCCCAAACT | 8027 |
rs543005201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17702773 | CCAGCACTTCGGGAG[A/G]CCGAGGCGGGCAGAT | 8027 |
rs543071196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17708347 | GAAAGTTAGCTTGCT[C/T]TATTGTTCAATAAAC | 8027 |
rs543088531 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17656977 | TGGGCGGCCCACATG[C/T]GCAGTGCCCTCCTTA | 8027 |
rs543097869 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17669369 | GTTTTTTTTTTTTTT[C/T]CCGGAAATGTTGTTT | 8027 |
rs543230885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17704163 | AGTGGCGAGATCATA[A/G]CTCACTGCAGCCTTG | 8027 |
rs543231694 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17698953 | AAAATGAATCAGCTG[C/T]AGAATTTTGCTTTTG | 8027 |
rs543266099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691095 | CCAGGCATACCTGTA[A/G]TTTTCAGAAGTGTCT | 8027 |
rs543269605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17703866 | TCTGCCTTACTGAAA[C/T]AGCTGCTGTATTCAC | 8027 |
rs543292822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17651747 | AAGATTTTTGAAGAA[C/T]TGATTTGCAAAGAGG | 8027 |
rs543320449 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17678050 | TTAATATGTTCATAA[A/G]TTTGTGCAACAGTAT | 8027 |
rs543330156 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17670640 | CGTACTGAATTTAAT[C/T]CTCAATATTTTAGTT | 8027 |
rs543431224 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | STAM | GRCh38.p7 | 10:17707287 | TGGTGGTGGGTGCCT[A/G]TAGTCCCAGCTACTT | 8027 |
rs543439818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689420 | CTGAGCACTCTTGAG[A/G]TGTGAAGACTCAAAA | 8027 |
rs543476063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695834 | TCTTCCTGTAGTGTC[C/T]CTCTTACTTACTGCC | 8027 |
rs543523992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17663008 | TATCTTTACTTCGGT[A/G]TTTTTCATTTTGTAG | 8027 |
rs543548590 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17684082 | TGACGACTGTGTGAG[C/T]GTTGGATCTCTTTAG | 8027 |
rs543553950 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17650472 | CTTTTTGTCTGTTTT[C/G]ATAGTTGGTACCTAA | 8027 |
rs543560358 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17662335 | AATGTTTTCCTCTTT[A/T]ATTTCCCATCTCTGT | 8027 |
rs543579537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691467 | AGCTTGCAGTGAGCC[A/G]AGATCTCGCCACTGT | 8027 |
rs543667398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17646744 | TTCCCAGTACATAAG[A/C]CTTGCACAGAGTCCA | 8027 |
rs543684716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17656983 | GCCCACATGCGCAGT[A/G]CCCTCCTTATACTTG | 8027 |
rs543721357 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17706834 | TGCTTTTAGAGCTAA[C/G]AAAACTCTCTTAAAT | 8027 |
rs543732848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17679491 | ATGATTTGGAAATAT[G/T]TTCTCCCATTCTGTG | 8027 |
rs543749877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17686127 | GCTTTATGCAGTTAA[C/T]ATTTATTTTCTACTA | 8027 |
rs543788167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17673157 | ATTTTTACAAAATAT[C/T]TTGTGTTTATTGCCA | 8027 |
rs543791996 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17643927 | TGTTAGTAGGCTTCA[G/T]CACGCCTGAAGGACC | 8027 |
rs543845831 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17650898 | GTGAAACCCCATCTC[C/T]ACTAAAAATACAAAA | 8027 |
rs543852364 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643708 | CCAATTCGTTCAGCT[C/T]CCATGACTTCATCCG | 8027 |
rs543862841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17650867 | TCAGCAGATCGAGAC[C/G]ATCCTGGCTAACATG | 8027 |
rs543880500 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17652968 | TTTCCTAGGAGACAG[C/G]CTCTAAATCCTTGGA | 8027 |
rs543939348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17711187 | TCTTGTTACATAAAA[G/T]TTTGGTGTTAAAGCT | 8027 |
rs543958496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17666436 | GTCTTGCTTTGTTGC[C/T]CAGGCTGGAGTGCAG | 8027 |
rs543961865 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17671941 | TTACTGTCTTTTCAA[A/T]GACAATAATTTCCTT | 8027 |
rs544062050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17713234 | CTTCAAGGTCCAGTG[C/T]ACAGTAGATGGACTG | 8027 |
rs544082118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17661203 | TATGGGTGATTTCTT[C/T]AGCTCCTGGGCTAAC | 8027 |
rs544084563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17673832 | TAACTATTAGTGTTA[C/T]AACTATTATCTGACA | 8027 |
rs544117337 | snp | C/G | 1.65669e-05 | 0.00287805 | synonymous-codon, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17660474 | TACAGAGAAAGCAAC[C/G]AGCGAGATGAATACT | 8027 |
rs544156937 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17677261 | ACCCCTTTCCCCACC[A/G]TCCTTTCCAAAAGTC | 8027 |
rs544199032 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704877 | TTACTCCAAATTAAA[A/T]CTTTTATTCCTTAAA | 8027 |
rs544205772 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688792 | AATATACACAAAATA[C/G]CTTTATTAATTAGGT | 8027 |
rs544206277 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17665259 | CATATGCATATGCAT[A/G]TATATTTATGTTTGT | 8027 |
rs544228946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17682909 | TATATATTTTGAAGT[C/T]CTATTTTTGTGTTCA | 8027 |
rs544260228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17705259 | TAGATAGGTCGTTTT[A/G]AAAACAAGGGCTAGC | 8027 |
rs544344815 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17672328 | AAATTTCACTTTTCT[G/T]GGAAAAGAGAATTGC | 8027 |
rs544349853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17677755 | TTTTGTGTGTTGTTT[C/T]TCCCTTCACCATGCT | 8027 |
rs544367242 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697284 | AAAAATGCAAATTCA[-/T]TTAAGAAGTCTTACA | 8027 |
rs544410559 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | STAM | GRCh38.p7 | 10:17706402 | TTTTTTTTTTGAGGC[A/G]GAGTCTCACTCCGTG | 8027 |
rs544463416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17684596 | CCCTTTTTATCGTAG[C/T]CTTTTGTCTATAACA | 8027 |
rs544465901 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17694015 | TGTCCTGTTATTTTA[A/G]TTTTTATTTTTTTGA | 8027 |
rs544513131 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17691468 | GCTTGCAGTGAGCCA[A/G]GATCTCGCCACTGTA | 8027 |
rs544549404 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17707630 | AAGCAAAAAACCTTC[A/G]TGTTCAATTTTCGAA | 8027 |
rs544654665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17699467 | TTTGGAGGTTGTTAT[A/G]TAGCTACTGTTATGT | 8027 |
rs544711533 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17674962 | TGACAAAATGTGATA[C/T]AAGGGTTTCTTCATT | 8027 |
rs544743382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17686761 | GTTTGCAAATCCATT[A/G]TATGCTCCTTGACCA | 8027 |
rs544769041 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17681235 | TAGGTGCTTATAGGT[A/G]TAAATTACCTTCTCA | 8027 |
rs544806668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17687348 | GGCATGGTGGTGCGC[A/G]CCTGTAATCCTACTC | 8027 |
rs544946273 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715411 | TATATATGTGTGTGT[A/G]TATATATATATCTAC | 8027 |
rs544960063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688314 | TGTGTTAGTAACTAG[C/T]TGTATTGCTAGTTAG | 8027 |
rs544968431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17676396 | GTAATACTGGTAAAT[A/G]ATGAAATTGAATTTG | 8027 |
rs545028109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17657623 | AGAAGATTATTAATT[A/G]TTGATTCAGTTTTTT | 8027 |
rs545049072 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17645975 | ACTGACTTTGTGAAC[A/T]CATATTTGCATTGGA | 8027 |
rs545087808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17647510 | CTCCTTCCACTTTTT[G/T]TTTTCCCTTAGAGTA | 8027 |
rs545119746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17679180 | TTTTACATTCCCACC[A/G]GCAATGTACAAGGGT | 8027 |
rs545121139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17652171 | ACAAACCCTGTTTTT[A/G]TCTTAGAAAATAAAT | 8027 |
rs545180335 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, missense | STAM | GRCh38.p7 | 10:17713359 | TTCTCCTCCGTACTT[A/C]CCCACAGGACAGCAG | 8027 |
rs545249250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17648015 | GCCCTTCTCAGTAGA[C/T]GACAACATGATTACT | 8027 |
rs545273873 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642653 | CTTTGTTCATGTTTT[A/T]AAAGAATGTCTTTAG | 8027 |
rs545305057 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714319 | CGCAAACCACCCCCC[C/G]CAACTTTTTTTACAC | 8027 |
rs545309955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17663218 | TTATTCTCCCAGAAA[C/T]GTTTATTATTATTTT | 8027 |
rs545341661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17672109 | TGACTCCTTTTTCCA[A/G]CAATAGCTTTAAATA | 8027 |
rs545388049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17686046 | AGCAGTATAGAAATA[C/T]AGTAAGAATGTAAAA | 8027 |
rs545391062 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17708292 | ACTTAAAATATTTAC[A/G]TCAGGCCCTTTACAA | 8027 |
rs545395120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706793 | CAGACATATCTCAAT[A/G]AAGTAGTTTCGTAAA | 8027 |
rs545428203 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17686399 | TTTTTTTTTTTGAGA[C/T]AGTGTCTCTCTTTGT | 8027 |
rs545428993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691378 | AAAAAATTAGCCAGG[C/T]GTAGTGGCAGGTGCC | 8027 |
rs545429837 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17706578 | TAGAGACGGGGTTTC[C/G]CCGTGTTAGCCAGGT | 8027 |
rs545450350 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17707203 | TCACGAGGTCAGGAG[A/T]TGGAGACCATCCTGG | 8027 |
rs545455186 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713811 | CTGTGGAATCTTATC[A/C/G]CGCTTCTGCTCAGAA | 8027 |
rs545477655 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | STAM | GRCh38.p7 | 10:17674791 | TTATCTTTGGAATAC[A/G]TAATTTGCCTGAGGC | 8027 |
rs545505673 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17656032 | AAGGTAGTTTCCTCA[C/T]GCCTGCAATCCCAGC | 8027 |
rs545541253 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17702212 | TAATAATAATCATTA[C/T]CTTATACATATGAAT | 8027 |
rs545581717 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17673246 | TCATGGCTTTATTAT[A/G]GTTCTATTAACTACA | 8027 |
rs545615471 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17703285 | TAATTTACATTGAAA[A/C]TTGGTATCCATTTCA | 8027 |
rs545652574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17707953 | TGGAGTGCAGTGGCG[C/T]GATCTCAGCTCGCTG | 8027 |
rs545665620 | in-del | -/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643906 | CTCCCAGTCACTCCT[-/G]GGGGTTGTTAGTAGG | 8027 |
rs545702485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696414 | AGCAATGATTTAGGA[A/G]TGGAGACTGAAAATA | 8027 |
rs545718811 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17655999 | TTTTTTGGTCTTTTT[C/G]TTTATCTTCCACATT | 8027 |
rs545861882 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon | STAM | GRCh38.p7 | 10:17695143 | AACTAACCACCAACA[C/T]GAAGGCCGAAAAGTT | 8027 |
rs545892858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17661765 | CGTTTTAAAGTCTCC[C/T]TAATCAAGTTTTTGA | 8027 |
rs546005211 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17655069 | ATACATCGGGAAGCC[A/C]TTCCTGATTCTCCTC | 8027 |
rs546005444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17690423 | AAAGTATGTAACAGC[C/T]AATCTTGTCATAGTG | 8027 |
rs546101967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17656529 | GCTGACATAGAGCCC[C/T]CAGAAAAGAGTCTTC | 8027 |
rs546119073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17684601 | TTTATCGTAGTCTTT[C/T]GTCTATAACAGTTAA | 8027 |
rs546182909 | in-del | -/AAA | | | intron-variant | STAM | GRCh38.p7 | 10:17651089 | AAAAAAAAAAAAAAA[-/AAA]GTTCTGAAGAATCTA | 8027 |
rs546186947 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17665795 | TTAAATCTTGAAATA[C/T]TTGATTATACCAAAC | 8027 |
rs546210053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17678358 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 8027 |
rs546245951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17676193 | ATTAAGGAAGGTTCA[C/T]GACTTAATTTTCATT | 8027 |
rs546265266 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17655491 | TTTTAGTTGTCCGGT[G/T]GTAGTGACTAACTAG | 8027 |
rs546279841 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17664708 | AAATTCAGGTAGAGT[A/C]TTTTGAAGTAGAGGA | 8027 |
rs546280115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17670576 | ATTGTGTTTTGTTTG[A/G]CTGAAATATACCTTA | 8027 |
rs546285724 | snp | C/T | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713962 | CTCTCCCCTCGGCAC[C/T]CCCTGCGGCCCCCTC | 8027 |
rs546302042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17660992 | AGTGATTTCTCAGTT[A/G]CCAAGTTTCATGGTT | 8027 |
rs546318505 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17670155 | TAACAACAGAAGTCA[A/C]GTTGTTGACTAGGCA | 8027 |
rs546336382 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17667681 | GATGATGGTCAATAG[A/C]TAAGAAGCTAGTAAC | 8027 |
rs546381781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17683469 | ACCCAAGCTATTTTA[C/T]TTTCATTTTTCTCTT | 8027 |
rs546391527 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17657992 | CTAATTTTTGTTGTT[G/T]GTTTTCTTCTGCTTG | 8027 |
rs546406623 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643416 | CATTTTGGGTTGCTA[A/G]GAATCACTCACTGAT | 8027 |
rs546446041 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644076 | CCGATGGGGCAGGCT[C/T]GGGGCAGCTTTGAGA | 8027 |
rs546447718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17693680 | TGTTCTATAATATCC[A/G]GTGTACTAATGAGTG | 8027 |
rs546469360 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17678989 | TGAATACTATTCCAT[G/T]GTATATCACATTTTG | 8027 |
rs546473133 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17699584 | TAATGTCAAATGATA[A/G]TATTATATAACTAGA | 8027 |
rs546492796 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644949 | CCGAATTGAGGACCT[C/G]AGCCTTTGGGATGTC | 8027 |
rs546533993 | snp | C/T | 0.00101657 | 0.0225223 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644389 | ATGTTGGTAAGTGTT[C/T]TTGCCTCTCCCTGCC | 8027 |
rs546578067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17675752 | AGGTAATTAATGAAC[A/G]TTAGTTATGGAAAGT | 8027 |
rs546612347 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17646801 | ATAACATATAGAATA[C/T]AGTGTATAGAATACA | 8027 |
rs546613973 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17659332 | AATATATATAAAATC[A/G]TAGGTAATGAATACA | 8027 |
rs546641665 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | STAM | GRCh38.p7 | 10:17665150 | ACCAGGAAACATGGC[C/T]CTCAGTGGTGTTGTG | 8027 |
rs546662543 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715108 | ACAAATGTTATGTAC[A/G]TATATTGATATGTAA | 8027 |
rs546670892 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17711623 | AAGATGTTCTGTCAC[A/G]TCAGAGATGTGGTAG | 8027 |
rs546726828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17658802 | TCATCCTTTAACTTT[C/T]AATCTCTATGTGTTT | 8027 |
rs546730093 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | STAM | GRCh38.p7 | 10:17709163 | TCGCTCAACTCATGT[A/C]ATCTGGTTTCAGCCT | 8027 |
rs546749769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17653231 | CCAATTGTAGAATCC[A/G]TGAAGGTACATTTCC | 8027 |
rs546775668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17657918 | CTTTTAAAATAACCA[A/G]CTTTTGGTTGTGCTG | 8027 |
rs546809618 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17699150 | GATTGGCATTCAAAT[C/T]CAGGCTTTGTCATTT | 8027 |
rs546978258 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17700454 | AACTTCCTCTCCAGT[C/G]CTTTGTTTGCCGTGC | 8027 |
rs547026317 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17668885 | CATCTTGTTGGCTCC[C/G]AGTTTTGGTGATTTT | 8027 |
rs547128334 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17670265 | AGTCTTAAAAACATC[A/G]TATATTTTATAGAAT | 8027 |
rs547170545 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17679644 | GAATTCACCAGTGAA[A/G]CTTTCTGTTTCTGAG | 8027 |
rs547195711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17687056 | TTCCCTTAATAAGCA[A/G]TGAGTAAAATAATTT | 8027 |
rs547198478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645371 | AAAGGTGGATGTTGA[A/G]TTTTTCTTTTTAAAC | 8027 |
rs547257681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17708080 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT | 8027 |
rs547258264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17680479 | CCAGGCTGGAGTTCA[A/G]TGGCGCAATCGTGGC | 8027 |
rs547301077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713983 | CGGCCCCCTCTGCCG[C/T]AGCACTCGTGGCCTG | 8027 |
rs547362695 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645449 | GAAAAAAGTTCACTC[C/T]TTACCTCTGCCACTT | 8027 |
rs547378402 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17651288 | CATACCTATTTGTTC[A/C]TTAATCCTCAGTAGG | 8027 |
rs547381954 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17707624 | ACAAGGAAGCAAAAA[A/T]CCTTCATGTTCAATT | 8027 |
rs547385644 | snp | A/G | | | downstream-variant-500B | STAM | GRCh38.p7 | 10:17716879 | TGAAAATACCAGGGG[A/G]AAAAAATCCAATGAA | 8027 |
rs547407466 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17678073 | AACAGTATCTAATTC[A/C]TGAACAATCATCATC | 8027 |
rs547526440 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17680447 | CTTTTTTTGGAGATA[C/T]GGTCTTACTCTGTCA | 8027 |
rs547526451 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17656730 | GTCTGCACCAATCTC[A/C]GTTCTTGCCTCCTCA | 8027 |
rs547531410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17672706 | GACACATTTGAGAGA[C/T]GGTTCATGAGTTCTC | 8027 |
rs547538831 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17651829 | CATCTTCGGGCTGAC[G/T]GAATGACAGTCCTTT | 8027 |
rs547544810 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706668 | CCAGGTGTGAGCCAT[C/G]GCGCCCGGCCGAGGC | 8027 |
rs547578735 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17704634 | CATTTCTCACTTCTC[C/T]TTGACCCAGGCTCAC | 8027 |
rs547590370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17679852 | GTCCATTTTAACTAG[A/G]TTATCCAATTTGTTG | 8027 |
rs547592045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17673247 | CATGGCTTTATTATA[A/G]TTCTATTAACTACAT | 8027 |
rs547641301 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696635 | CTTCTTTTGTAATAA[A/G]GGAAGATTCATTGGC | 8027 |
rs547708782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17701749 | TCCCTTTTCAATTCT[C/T]CTCTCCAACTTTACG | 8027 |
rs547760372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17668224 | GATTTTTAAATAAAC[G/T]GCAACATGAGGGGAC | 8027 |
rs547815507 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644520 | GCTCCCTCCTTCAGA[C/G]CTGGGAGGAGGTTGA | 8027 |
rs547851345 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665705 | TGAAAATTAGTAATT[G/T]TTAGTAATTATCTCA | 8027 |
rs547860624 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717268 | CTCAGGAGGCTGAGG[C/T]GAGAGAATTGCTTGA | 8027 |
rs547923627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712266 | GACCTGGAGACAAAA[C/T]GGAAGTCCCACTTAG | 8027 |
rs547940582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17655327 | GAATTGTTTGGATCT[C/T]TGTATTAATTCTTAT | 8027 |
rs547940930 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17667507 | TCTTTAATTCGTTTC[A/T]TTCTCTTTGCGTTCG | 8027 |
rs548009957 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17658810 | TAACTTTTAATCTCT[A/T]TGTGTTTTTATGTCT | 8027 |
rs548076108 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689013 | CTCCTTAGTAAGAGC[C/G/T]GACCAGTACATAAGT | 8027 |
rs548082050 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17691577 | AATCCAGTTAAGTGA[A/G]GAATGTAGAACTGTA | 8027 |
rs548105617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17661918 | ATCCATCCCTTTGTT[A/G]TATTTACATTTTAGT | 8027 |
rs548178903 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644178 | CGCCGCCGCAGCTGC[G/T]GCCGCGGTTGGTGGG | 8027 |
rs548198098 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17682547 | ATTTCCAAATATTTG[A/G]GTATTTTTATGCTAT | 8027 |
rs548203400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17700419 | TTCAAGCAATATAGA[C/T]GATGCAGACTGTTTT | 8027 |
rs548206698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17699533 | GAAATCTGTGCTTCT[A/G]GCCAATGAATTGTTG | 8027 |
rs548207143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17693081 | CCTCTCCCTTTTAAG[A/G]TGGAAGCTGCTGCAG | 8027 |
rs548215412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17671246 | TAAACCACAGTAAAG[C/T]TTTTTTTGTAGCATT | 8027 |
rs548271130 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706092 | AATAAATAAATAAAT[G/T]CTCAAATGCATTTGA | 8027 |
rs548298179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17666463 | GCAGTGGCACGATCT[C/T]GGCTCACTGCAAGCT | 8027 |
rs548320446 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17661471 | GTCTCACAACTTCCA[C/G]CTGTCTTTATGTAGA | 8027 |
rs548351174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687885 | CATTAGTTTTATTTC[A/G]AATAACTATATTTTC | 8027 |
rs548376072 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17648726 | GGTTTCTTTGTTACC[A/T]CTCTTGCCTCTACAA | 8027 |
rs548482512 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716164 | TTAAACAACGGAAAA[G/T]TTGAGTCGAACATCA | 8027 |
rs548529395 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642998 | CTCCTGACCTCAGGT[C/G]ATCTGCCGGCCTCGG | 8027 |
rs548556244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17681045 | ATTCGAGGAACCAGT[A/G]TACTGTTTTACACAG | 8027 |
rs548557684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17687484 | ACAGGGTGAGACTCT[C/G]TCTCAAAAAACAAAC | 8027 |
rs548566112 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17656390 | TTGGAAGTTCTGATC[A/G]TGTGGTTAGGTCTCA | 8027 |
rs548719107 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17654267 | TTGCTCTGTCACCCA[G/T]GCTGGAGTGCAGTGG | 8027 |
rs548725890 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17686950 | CTGGTATCTGTGAAG[G/T]TTTCTTTATATCTAT | 8027 |
rs548746165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17683000 | CTCTTTATCCCTGTT[A/C]GTATTCCTTGTTATG | 8027 |
rs548746884 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | STAM | GRCh38.p7 | 10:17647562 | TGTTAAGAATTCAGA[C/G]TGGGGCCACACTGCT | 8027 |
rs548782167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17676765 | CATGCTTGTAATCAA[C/T]TTTCATTTGTCATTG | 8027 |
rs548833560 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17699103 | ACTGGCACAGGCCAG[A/T]TTTCAGTAGTATGGG | 8027 |
rs548879709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17670009 | TGCTGGGATCACAGG[C/T]GTGAGCCACTGCGCC | 8027 |
rs548881552 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643721 | CTCCCATGACTTCAT[C/T]CGAGCAAGTTTGTCA | 8027 |
rs548908014 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645655 | AAATGAGTGTCCTGA[-/T]ATCTTAGCAGTGGAC | 8027 |
rs548945552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17670768 | TATATTTATATTCAC[A/G]TTCCATTATCTCATA | 8027 |
rs548947559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17709097 | CTAATGAGTGGTGGA[A/G]CCTCTGTGGTATTCC | 8027 |
rs549010690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704615 | GATAATATTAAAAAT[A/G]GAACATTTCTCACTT | 8027 |
rs549037100 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | STAM | GRCh38.p7 | 10:17662267 | TCTGAGTTCCAGTGC[-/T]TTTTTTTCTACCTTA | 8027 |
rs549040979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17708659 | GAAATAACTTTGAAA[A/C]AAGGATTCCAGAGTG | 8027 |
rs549041209 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17664655 | TATAACATGTAAGTG[G/T]GTTGAGAGGGAAAAG | 8027 |
rs549041541 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17666965 | TATTGACTACTTATT[C/G]TTTGCTAGACTCTGT | 8027 |
rs549062308 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717134 | TTGGGAGGCCGTGGC[A/G]GGCGGATCATTTGAG | 8027 |
rs549062667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17656795 | AAAAGAGATGAAGCA[A/G]GTTTCAGAGCAGGAG | 8027 |
rs549076553 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715073 | GTCTGCAGAAAGTCA[A/G]ACTTACAAAAACTGT | 8027 |
rs549099383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17662815 | AACAGTACCTGGCAC[A/G]TGGCTGAATGAGTGC | 8027 |
rs549115319 | snp | C/G | 0.000399281 | 0.0141238 | synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714675 | AGGACCTAATATGCC[C/G]CAGGTGCCAAACTAT | 8027 |
rs549173968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17669684 | GATTGGGAATTTCCC[C/T]TCTTTTTCTTTCTTT | 8027 |
rs549180185 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696016 | GCAGGGGCAAATGAG[A/C]CCTCTGGGGTCTCTT | 8027 |
rs549202667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704101 | TGGTTGGTTGGTTTA[C/T]TTATTTATTTAAACA | 8027 |
rs549206283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17663316 | TTGTTTTTATCCAGT[A/G]TCAATAGGTTTAGAC | 8027 |
rs549214789 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17708016 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTGC | 8027 |
rs549245326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17668754 | CTTTCACTTACCAGT[A/G]TGCATTTAAGGTTCC | 8027 |
rs549285683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17652654 | TTCTTTTAAAAAATG[C/T]ACTTAAAAAAAAAAC | 8027 |
rs549293200 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17658712 | GGCTGGTCTTGAACT[C/G]CTGGGCTCAAATGAT | 8027 |
rs549339325 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17676209 | GACTTAATTTTCATT[G/T]ACTTCCAGGCATGAG | 8027 |
rs549363924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692273 | TTTAAAGGTGTTATC[A/G]TAATAACAAACAAGA | 8027 |
rs549408174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17674308 | CTGTCCTAACACTTA[G/T]CTTAAAAGAGCAGTT | 8027 |
rs549464180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697230 | CATCGCACCTGGCCT[A/G]ACTTTTCTTTTTCAT | 8027 |
rs549466055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17703448 | AAATAATTACTTTGC[G/T]TAGGATTAGTAGTCT | 8027 |
rs549504757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17702923 | TGAGGCAGGAGAATC[A/G]CTTGAATCTGGGAGG | 8027 |
rs549594808 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17675386 | GTGCCTGCCTGTTAT[A/C]TCAGCTACTTGGAAG | 8027 |
rs549634055 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17647054 | CTTGGAAGAAACACC[C/G]AAAGATGTTACTAGA | 8027 |
rs549669625 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644858 | TAACGGTAACTGAAG[A/G]AGGGAGCTCTGGTTA | 8027 |
rs549751681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17655629 | CTCAGTAGTAGGTCA[A/G]AATGAGGAAATAAGT | 8027 |
rs549751734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17661832 | GGCTGTATACCCTCC[A/G]CTCTAGCTTTTTTTG | 8027 |
rs549799705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17690613 | GTAGATTTTAAAGCC[A/G]CTTAGTTACTTAAGT | 8027 |
rs549811529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17646101 | CTTATGCTTTCTTTT[A/G]TCTTTCAACATATCC | 8027 |
rs549828397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17651059 | GACAGAGCGAGAGTC[C/T]GTCTCAAAAAAAAAA | 8027 |
rs549873657 | snp | C/G | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697228 | GCCATCGCACCTGGC[C/G]TAACTTTTCTTTTTC | 8027 |
rs549982943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17711591 | GGTTATTCTTAGCCA[C/G]TAGAAAAAAAGTGAG | 8027 |
rs549990481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645188 | ATTTGAGTTTCCGGG[G/T]AGAGAATTTTGGTTT | 8027 |
rs550004651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706208 | TTACAGCATATAATA[C/T]ACTAATTATGCTAAT | 8027 |
rs550024271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17685032 | GCTTTTTAAGAAATC[C/T]TTTCTAGGCTGTGTC | 8027 |
rs550025026 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17701647 | AAGAGAATCTTTTCC[A/G]ATCCTCAGTTACCAT | 8027 |
rs550025668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713395 | AATAGCTGATTGCCT[A/G]TGCAGGACAACAGGC | 8027 |
rs550061934 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706625 | ACCTCGTGATCCACC[C/G]GCCTCGGCCTCCCAA | 8027 |
rs550148797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17679809 | TCATAGAGTTAGTTT[C/T]GGTAGTTTCCTGTCT | 8027 |
rs550189177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17650067 | TTGGGCCAGTCCACA[C/T]CCTACATACTTGGAC | 8027 |
rs550290697 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17665236 | TCTGTTCTTTAAACT[C/G]ACATATACATATGCA | 8027 |
rs550314556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17672628 | GTATGCAAGCCAGCT[G/T]CTTCAGCTGTTGCTC | 8027 |
rs550317173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17660120 | TTATAAAGATTTACT[A/G]GCAAGTAAATAATCT | 8027 |
rs550319800 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644156 | TTCCTCGGCTCCTTG[C/G]TGTTGCCGCCGCCGC | 8027 |
rs550343103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17710086 | AGAAGGTAGGAATTG[G/T]TGAGAAGACACTAGG | 8027 |
rs550378779 | in-del | -/GA | | | intron-variant | STAM | GRCh38.p7 | 10:17703028 | AAAAAAAAAAAAAAA[-/GA]AAAGAAAAGAAAAGA | 8027 |
rs550479074 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17647232 | TGAATTTAGAAGAAA[C/T]GTAAAGATAACTTAT | 8027 |
rs550490194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17694541 | TGGTGGAGATAGAGA[C/T]ACGTTTGAGATCTAT | 8027 |
rs550563436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688562 | CTGCCTCCTGGGTTC[A/G]GGTGATTCTCCTGCC | 8027 |
rs550583691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17663766 | TATTATTGAGGTTTT[A/T]AAAAAATGTCAGGCC | 8027 |
rs550595994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17704336 | GAGTCTCCATAACTA[C/T]GAATTTCAAAAGTTT | 8027 |
rs550655885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17710526 | CATTCCTGCATATTC[G/T]TTAGTTGTTAGCTTA | 8027 |
rs550676684 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17671212 | CCTCCAATATAGACG[A/T]ACATATGTCCTTGAA | 8027 |
rs550695622 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17705169 | TGTGCTAGATGTGGA[G/T]AATTAGACTCATTTG | 8027 |
rs550698041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17699036 | GTGTTATACAGAAGC[A/G]CACAACACGGAGTAC | 8027 |
rs550759027 | snp | C/T | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17692910 | TGGTTTTGGAGTTTT[C/T]TTAAACACGTTGAAA | 8027 |
rs550773367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17653631 | TATCATGTCTGTACC[A/G]AACACATAGAGACAT | 8027 |
rs550816378 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17680219 | ATTGTAGCAAAATAA[A/C]CATAGCATAAAATTT | 8027 |
rs550822672 | snp | A/G | 0.0244538 | 0.107838 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642905 | TAGCTGGGATTACAA[A/G]CGCGCACCACCACGC | 8027 |
rs550939105 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17686245 | TGTAGGTGAAAAATG[G/T]GGTATACTTACCTAT | 8027 |
rs550943988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17664600 | GTATTGTAGGCTGCC[A/G]TTGAGGTATTCTAAA | 8027 |
rs550971568 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715716 | CACCAAAGATAGAGG[C/T]AATGGATAGAAATTT | 8027 |
rs550979041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698537 | ATCAGAGCCTATGTA[A/G]TGGGGTTGTAGTTCT | 8027 |
rs551025652 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17652014 | CTCTGTGTATGTTTT[C/T]TCTGGGTACTGCTGG | 8027 |
rs551071090 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | STAM | GRCh38.p7 | 10:17653284 | AAAAACCGAATATTC[C/T]GCGATAAAAACTGGA | 8027 |
rs551109170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17658618 | CGGGTTTGAGTGATC[C/T]TCCTATCTCAGCCTC | 8027 |
rs551128618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17652585 | TTAATAAGTTTTAAT[A/G]TGCTTAGCTATTATG | 8027 |
rs551170884 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687832 | TAATGCTTTAATTTG[A/T]AGTGAGATATATATG | 8027 |
rs551170918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17681641 | GATTTAATATTTTGA[A/G]GCTATCCTTTTGACT | 8027 |
rs551208213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17687459 | GAGCCACTGCAGTCC[A/G]GCTTCTGCCACAGGG | 8027 |
rs551225959 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704058 | GTGGCTTGATTTCTT[C/G]TCGCTTAAGAGAATC | 8027 |
rs551258165 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17648679 | TTCAGTCATTGTTAT[C/G]TCTTATAGTCAGTGG | 8027 |
rs551260358 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17692689 | AGTGATATACTGTCA[C/G]AATTAACTACTTGTA | 8027 |
rs551264750 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17708605 | AAACCATCAACAGCC[A/T]ATTTCATTGAAAAGC | 8027 |
rs551274618 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715156 | TTGAATCACAGTGGT[A/G]ATCGTGTGAATATAT | 8027 |
rs551327247 | snp | A/G | 0.000798403 | 0.0199641 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714549 | CCTCCACAGTACAAT[A/G]GTCAGTTCCGTTCAA | 8027 |
rs551454637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17668071 | GTTAATAAGATGTGA[C/T]AGAAGTTGAAAAGCC | 8027 |
rs551490284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17667580 | ATGCTTTGGCTATAC[A/C]GTGGTGAATAAAGCA | 8027 |
rs551501456 | snp | A/G | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715034 | TGAAAGAATTGATAC[A/G]AGGCTATTTGTCTCG | 8027 |
rs551502021 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17646909 | TATCACTTAACACTC[A/C/G]TATACATTTGCACAT | 8027 |
rs551519300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17655001 | ACTTTTTACTTTATT[C/T]ACTTAATTAGAAACA | 8027 |
rs551554374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17675000 | CTAACATTTAATTAT[A/G]ACTTTTGACATGGAA | 8027 |
rs551633032 | snp | A/C/G | 1.64784e-05 | 0.00287035 | missense | STAM | GRCh38.p7 | 10:17695087 | CAAAGGCAGCAGTCA[A/C/G]CCACCCTTTCCACTT | 8027 |
rs551653175 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698302 | GGGCTGGTAATGATG[C/T]TTTGTTTGTTTTTGG | 8027 |
rs551667356 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17673382 | AGTTGTACAATAGTG[A/T]AAAGCAGTATTTTTC | 8027 |
rs551668535 | snp | A/G | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716764 | TTACAACCCATATAC[A/G]TTTTTCTTTACCTTT | 8027 |
rs551723976 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696707 | GTAAGTTGAATACTA[C/G]AAAAGATAAAGATGT | 8027 |
rs551736714 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716223 | ATACTATAAATGAAA[A/T]TTTCATTTTTATTTT | 8027 |
rs551831527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17650189 | TGATATGATAGAAAG[A/G]CCTTGGGCTTTGGGC | 8027 |
rs551883038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695392 | GATTTGCTTGTGTTA[C/T]ACTGGGTGGATTCTT | 8027 |
rs551923784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17700823 | GGACACTCATTGACT[A/G]TCTATTGAAACAAAT | 8027 |
rs551935290 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17701915 | GCTGAGATGGTTCCA[C/T]ATTTTTTGTTTTTAA | 8027 |
rs551995145 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697253 | TTTTTCATATGTATC[C/T]ATGTAGAGGTCATTG | 8027 |
rs552024842 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17680927 | ATGCTGCTATGAACA[C/T]GGGTATACCACTATC | 8027 |
rs552053734 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644569 | TTGAAAGAAATGGGA[C/G]TCATCCTGTGAAATG | 8027 |
rs552061985 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17683218 | TCTCAGGATGGAGTA[C/T]GGTGGTGCCATCACA | 8027 |
rs552142895 | snp | C/T | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689887 | GAGGATTTATATGCA[C/T]GTTGAGGTCTGAGAA | 8027 |
rs552182523 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17663842 | AACATACATCTCCAG[G/T]TGTGTTTTTTCTTTC | 8027 |
rs552211000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17695986 | GCTGTCATTTTGCTG[C/T]GTCCTCCCATGGCAG | 8027 |
rs552227332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17655602 | ATTAAACTCACTTGA[C/T]GTACTTCTGCTCTCA | 8027 |
rs552228422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17678557 | CCACGCCCAACCTCA[C/T]GTAGTGTAATTCTTC | 8027 |
rs552262743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689126 | TTTATGTCATGTAGA[A/G]AAAAATCAAGAAATG | 8027 |
rs552279919 | snp | A/C | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715754 | GGAAAGAAAACCTGA[A/C]TTACACTACATTTTC | 8027 |
rs552325216 | in-del | -/T | 0.00993419 | 0.0697739 | intron-variant | STAM | GRCh38.p7 | 10:17683525 | TGTTAAATTTTTTCA[-/T]TTTTTTTCTCTCTGT | 8027 |
rs552373790 | snp | A/C | 0.00279162 | 0.0372561 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716220 | TTCATACTATAAATG[A/C]AAATTTCATTTTTAT | 8027 |
rs552378640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17684335 | TTTTTCCAGTTTTCT[A/C]ATTGTTTACAACGGG | 8027 |
rs552400412 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17710855 | TAAAAATTCCTTGCA[A/G]AGGCTTCACAAAGGC | 8027 |
rs552424146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689684 | AGTAGACTCACTGCA[G/T]AGAACCCACCTAGAA | 8027 |
rs552430952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17683037 | GCTAACGGTAGTGAA[C/T]AGATAAAAGTGTAGT | 8027 |
rs552479666 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712307 | AAACCAGACATTCTG[A/C]CTCCAGAACCCAGCG | 8027 |
rs552524085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17682263 | CCTGTGTCTAGCACT[A/G]AATGTGTTTCTAAGA | 8027 |
rs552546708 | snp | A/G | 3.46909e-05 | 0.00416464 | intron-variant | STAM | GRCh38.p7 | 10:17684937 | AATAAGGTAAGGAGC[A/G]TTATTTCCAGAAATT | 8027 |
rs552647657 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17681332 | TAATTTCCCCTGTGA[-/T]TTTTTTTCATTGACC | 8027 |
rs552705038 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643220 | TCAATATTAGTTTCC[A/C]CGCTACATTTGGAGA | 8027 |
rs552727873 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17649363 | CTATGACTGCACTCT[A/T]GCCTGGGCAAGAGAG | 8027 |
rs552738311 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17660234 | AAAATCAATGCCTTT[C/T]ATTTTATACTAAGTA | 8027 |
rs552772454 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17671381 | CATTGTTGAGAGTCT[C/G]TAAATCCCTGGCATG | 8027 |
rs552784244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17658322 | ATTTCTATTGTTTTA[G/T]ATTTGTCTTGGTTTG | 8027 |
rs552785285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692458 | CTGTAAAGTACCGGT[A/G]TAGAGACTGCTCAGG | 8027 |
rs552804908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704135 | TCTTGCACTGTTGTC[C/T]AGACTGAAGTGCAGT | 8027 |
rs552932334 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17672061 | ATAGGAGAATTTTCA[A/T]AAGTTTTATACAGCA | 8027 |
rs553045002 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698238 | AATTCAAAAACATGT[C/T]AACCTTGTTTAAATG | 8027 |
rs553112910 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17647118 | GATTTTTTCACTGCC[A/G]TATCCCTAGCTGTAG | 8027 |
rs553131331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17674771 | CAAAGGAATTATTAT[C/T]ATAGTTATCTTTGGA | 8027 |
rs553269030 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17680763 | TACAGCATTTGTCCT[G/T]TTGTGACCAGCTTAT | 8027 |
rs553295169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17675187 | TTTAGTTTATGAACA[C/T]TCATAAAAGCCTAAT | 8027 |
rs553307620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17686375 | TACTTAATAACATCC[C/T]GCCTTTTTTTTTTTT | 8027 |
rs553318249 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17648009 | ATCCTTGCCCTTCTC[A/T]GTAGACGACAACATG | 8027 |
rs553386134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17686015 | AATGAATAGTTCCAG[G/T]TTACAGTAGAAAAAT | 8027 |
rs553393513 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17646047 | GTACCACCCAGTTCA[A/G]ACACAGGCACCTTCT | 8027 |
rs553470616 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712476 | GAGAAATGTAGCATT[A/T]AATTACCGTCTCTTA | 8027 |
rs553561489 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17655368 | AATCTGTGTGAATAA[A/C]CTGCTTTTGCTATCT | 8027 |
rs553563347 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713794 | AGGGAGCCCGTTAAA[A/C]CCTGTGGAATCTTAT | 8027 |
rs553572019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706782 | CTTTTGCAGGTCAGA[C/T]ATATCTCAATAAAGT | 8027 |
rs553688633 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644939 | ACGACTGAAACCGAA[C/T]TGAGGACCTGAGCCT | 8027 |
rs553705196 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17665005 | CATATTATTTTAACC[G/T]TTTTTTCTCTTTTGG | 8027 |
rs553709064 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17678862 | CTAGATACCTCATGG[A/G]AGTGGAAACATAGAA | 8027 |
rs553717032 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17654457 | TCTATCTCCTGACCT[C/T]GTGATCCGCCCACCT | 8027 |
rs553752906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17702980 | TGCCACTGCACTCCA[A/G]CCTGGGAGACAGAGT | 8027 |
rs553789094 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17676542 | AATACTGCCCCCTTT[G/T]CTTTTACCCTCTTAC | 8027 |
rs553851367 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17657495 | AATGAGTTAGGAAGT[A/G]TCTCCTCTGCTTCTA | 8027 |
rs553897035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17677620 | AATTTCTTCAGTCTA[A/T]TGATGCTGCTATCCA | 8027 |
rs553940159 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17699686 | ACGGCGCTCTCTAAA[C/G]GCCTACGTGGCACGC | 8027 |
rs553975210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17667697 | TAAGAAGCTAGTAAC[C/G]AGAGTGCTATAATGG | 8027 |
rs553982523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17700628 | TTTGTGTTTCTTTAG[A/G]GTAGATATTCAGGAG | 8027 |
rs553983609 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17707166 | TGTAATCCCAGCACG[C/T]TGGGAGGCCGAGGCG | 8027 |
rs554021581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17660349 | AGAATGCTGGCAACT[A/G]TTCTGATTTGTTGTT | 8027 |
rs554045671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17702659 | TGTGGAAGACTGTGC[C/T]AAGGGCAAGGAATCC | 8027 |
rs554203184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17702747 | AGGCGCAGTGGCTCT[C/T]GCCTGTAATCCCAGC | 8027 |
rs554241199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17648980 | TCCTGCCTCTGTAGC[C/T]ATATGGTACTCTTTG | 8027 |
rs554247979 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706278 | TATACAGGGTTATGC[A/T]GCAGAATCAGCCATC | 8027 |
rs554280072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17654372 | GGACTACATGCGCCC[A/G]CCACCAAGCCTGGCT | 8027 |
rs554287008 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17666604 | GGGTTTCACCGTGTT[A/G]GCCAGGATGGTCTCG | 8027 |
rs554302506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17649559 | ACTTTTCATTTTTTT[C/T]CCCCTAATACTTTAG | 8027 |
rs554381383 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17655453 | TATTGGTTATTATCC[A/G]CTTGGTCTTTACTAG | 8027 |
rs554474878 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17690739 | GTACAGAAGAAAATA[A/G]TGTAAAAATATTAAG | 8027 |
rs554485870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17682502 | GTTCTGTGATTTCAT[C/T]TGTTGTAAGCCTTAG | 8027 |
rs554523720 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17659595 | CACTTCAGCCTTCTC[A/G]GTAGCTGGGAATACA | 8027 |
rs554542578 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17650384 | TTCTGACTCTTTACC[A/T]GAGTTGAATAGGCTT | 8027 |
rs554560861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665379 | AAGTCTAATTCCTAT[A/C]CCTGTTTCGCTGCTC | 8027 |
rs554599766 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17693894 | TTAAATGGTTGTTAT[C/G]ATTTCCTTTTCCATT | 8027 |
rs554613224 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17660314 | GCGTACATCTTTTCA[A/G]GATGGCCATGAAAAT | 8027 |
rs554629436 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715229 | ATCATAAACAACTAC[A/C]ATGTTTCTTAATGTT | 8027 |
rs554637433 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17699754 | GGAGTAGTGTGGATT[A/T]TCTGTCAAACCAGAT | 8027 |
rs554698127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17687222 | GCTCATGCCTGTAAT[C/T]GCAGCACTTTGGGAG | 8027 |
rs554781670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688590 | GCCGCAGCCTCCTGA[A/G]TAGCTGGGACTACAT | 8027 |
rs554851128 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17678861 | TCTAGATACCTCATG[A/G]AAGTGGAAACATAGA | 8027 |
rs554908208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17655585 | GCTTTTTATTTTCTG[C/T]GATTAAACTCACTTG | 8027 |
rs554925890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17675073 | TATAAATATGAACAG[C/T]TGACAGATAGGGAAT | 8027 |
rs554926664 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716350 | CAGATTTAAAGCACC[A/G]TAGTTTTAAATCTGA | 8027 |
rs555029284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17709011 | CTGTTTAAGTGCCCC[C/T]AGTTATCTATAACTA | 8027 |
rs555039503 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642494 | TGTACTAATTCATTT[A/G]ATCCTCACAACCCTA | 8027 |
rs555045009 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715217 | TATTTTATTTTAATC[A/G]TAAACAACTACCATG | 8027 |
rs555051253 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17703150 | GTAAGCAAACAAAAC[A/G]GAAACCATCTGTGTG | 8027 |
rs555093152 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17710631 | CTGTGTGTGTACTTC[C/T]GTTTCCTGGCTGGTA | 8027 |
rs555153274 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17676656 | TTGCCTTGGACAATT[G/T]TAGTTTATGCCTGCT | 8027 |
rs555164764 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17669846 | GGGACTACAGGCACC[A/C]GCCCCTATGCCCTAT | 8027 |
rs555210446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692423 | AGAACGTTGTAAGTA[C/G]AAGTAAATGAGTGTG | 8027 |
rs555220446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17676243 | ACTTATTTTTAATAG[G/T]TATGACTTCACCTAG | 8027 |
rs555311413 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17662025 | ATTTTTATTTGTCCT[A/G]CTTTACTTTGGACGT | 8027 |
rs555387481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17707811 | TTTGGGTAGTTAAGA[C/T]TTCAATCTCTTTAGA | 8027 |
rs555605458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17686528 | AATACAGGCATGCGC[C/T]ACCACGCCTGGCTGG | 8027 |
rs555630389 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17652726 | ATTAAAATGCACTAC[C/T]AGACCAAAGTAATAA | 8027 |
rs555640430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692096 | GTGCCCATGAGGTGT[A/G]GGTGCTATTATCGTA | 8027 |
rs555653971 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17681194 | AGGTGGTATTGAGAT[C/T]GTCTTTTTTTTTTTT | 8027 |
rs555675341 | snp | A/G | | | intron-variant, missense | STAM | GRCh38.p7 | 10:17713336 | GCCGAGGATTCCCAG[A/G]TGCGTATTTCTCCTC | 8027 |
rs555678769 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17685969 | AAGTTTTTGTATGTT[A/G]AAAGGGAAAATGCCT | 8027 |
rs555712870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691283 | TAGCACTTTGGGAGG[C/T]CGAGGCGGGTGGGTC | 8027 |
rs555730486 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | STAM | GRCh38.p7 | 10:17658246 | TCTCCATGTACTTTG[G/T]GATTTTCCAGCTATC | 8027 |
rs555798165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17690945 | TTCAGAAACATGCGG[C/T]TTCACATAGCTTATT | 8027 |
rs555824892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17651511 | ACCATCTGATATCCA[C/G]TGGATTAAGAACTTG | 8027 |
rs555838717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17702634 | ACAAAATTTGAAGAG[C/T]GAAACAGACTGTGGA | 8027 |
rs555840932 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696311 | TAGGAGTGTACTCTT[A/T]GCGAATGTTTTGCAC | 8027 |
rs555886731 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645634 | GCTACCTTTTTTGTT[C/T]CACCTTAAATGAGTG | 8027 |
rs555937845 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17701704 | CCGAGAACATTCTCT[C/T]CTACCATTTTCGTTT | 8027 |
rs555943367 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17679580 | TTTAATTTGCGTGTG[-/T]TTTTTTTTTTTAAAT | 8027 |
rs555966032 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644728 | GGCGTATGTTGGCTA[C/G]ATTAGGATTGTAAAC | 8027 |
rs555976207 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17711873 | GTAGATGGATTCATA[C/G]GGGCAAGATTAGAAG | 8027 |
rs555994352 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17654345 | CTCCTGCCTCAGCCT[C/G]CCAGGTAGCTGGGAC | 8027 |
rs556081497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17650319 | GGGATAGCAATATCC[A/G]TTATACATCATGCGG | 8027 |
rs556108098 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17671917 | ATATACAGGAATTAG[A/T]ATTTAAATTTACTGT | 8027 |
rs556122787 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | STAM | GRCh38.p7 | 10:17692811 | AGGAAATGATAACTC[-/T]TAACTATTAATAGAT | 8027 |
rs556152773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689192 | CCTTTAGGATGCCCA[A/G]CTAATCAAGAGGCTT | 8027 |
rs556164441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17677017 | TTCTGTTTTGTAGAC[A/C]GTTCTGAAGGGATTT | 8027 |
rs556209873 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17661982 | ATTTTTAACTACTGT[A/G]TGTTACATATCGCGT | 8027 |
rs556239694 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17710261 | CGGGGCCTTGGGAAA[G/T]TATCCTTGTGAATGA | 8027 |
rs556253274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17684491 | ATAAGAGAGCCTGTT[A/G]ATTTTGTTTGAAAAA | 8027 |
rs556255130 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17678313 | AGGCTAGAATGCAGC[A/G]GCACAATCTCAGTTC | 8027 |
rs556268644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17670919 | TTGCATTTTGAATAT[C/G]TTCAGTATATAAAGA | 8027 |
rs556437732 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17706756 | GGTTGTGTACACTCA[A/G]TATGTATAGCCTTTT | 8027 |
rs556470300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17667370 | CTTGTGATCTGCCCT[A/C]CTCAGCCTCCCAAAG | 8027 |
rs556505374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17664836 | AAATTTTGTAAAGTG[C/T]GGCGATCTTTTTAAG | 8027 |
rs556542406 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17664354 | TATACTCACATGCCC[A/G]CTGTCTGTCTCCAGA | 8027 |
rs556573807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17649811 | ATAGATGGGGTTTTG[C/G]CATATTGGCCAGGCT | 8027 |
rs556584136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17694876 | TTAAACTTTCAGTTG[C/T]GAATGAATGAATAAA | 8027 |
rs556595613 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17707913 | AACTTTTTTTTGAGA[C/T]GGAGTCTTGCTTTGT | 8027 |
rs556666484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17671442 | AAGGAGGTATTAGAC[A/G]TCTCCTCTTTTACAG | 8027 |
rs556667870 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17658853 | TTATAGACAACATAC[A/T]GTTGTGTGTTGTTTT | 8027 |
rs556684216 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17710369 | TCTGCTTCTGCATTC[A/G]GGATGTGAAATCCCT | 8027 |
rs556740507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665533 | TACTTAATTACTTAT[C/T]GTTACTTATTGACTA | 8027 |
rs556747138 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17693392 | AAGGTAAAATAAATA[G/T]AACTTTATAGCAAAA | 8027 |
rs556783001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695488 | AATCTATTCATTTTC[A/G]GTTCCACCTAATAAT | 8027 |
rs556890926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17646619 | ATTGTTTTGCTCCAG[A/G]AAAGCTTACTTTTTA | 8027 |
rs556891670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17655439 | ACCTAACCAATACCT[A/G]TTGGTTATTATCCAC | 8027 |
rs556912647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687552 | TGTTATTTTGAAGAA[A/G]TTAAATTTTCAAAAT | 8027 |
rs556919825 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17670187 | TAGGGAATGGGATCC[A/G]ATGCGAGCTGATTTT | 8027 |
rs556930442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17660737 | AATGTACACGAGTCA[A/G]GGCAACATAGTGAGA | 8027 |
rs556965884 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17715935 | CTGGCTTTGCTTAAC[A/G]TTTATATAGGTATTG | 8027 |
rs557022453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692650 | TTGTTGTGTATTCCC[G/T]TATTTACACAATTTA | 8027 |
rs557027231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17652807 | ACTCAATATTCTTGG[A/G]CTTTAGAGGGGTTGA | 8027 |
rs557034487 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704742 | TTTTAGAACCTGGTA[A/C]AATGAAAAATGGCAC | 8027 |
rs557049320 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17653492 | GGGTGATGAAGCTTC[C/G]TAGCACAGAAGCTTT | 8027 |
rs557095627 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17699213 | TTTCCAAACTACCTT[A/G]TTTATAAAAAGGGCA | 8027 |
rs557102526 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17691986 | TAAGCCCCGGAGGTA[A/G]TGTTACATACTTTTT | 8027 |
rs557147669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17693743 | CTGTGGATTATTTCT[G/T]ATTTTTTTTTACTAA | 8027 |
rs557249874 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715453 | TAGCCTCTGCATACT[A/G]CTGGCTGTCATCACA | 8027 |
rs557300171 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642686 | TTAATTTGCCGAAAT[A/G]GAATTGCTGGGTCCT | 8027 |
rs557376960 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17668943 | GCAGCCTTTTGTGTT[G/T]ACATCGTTTTAAGTT | 8027 |
rs557386113 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17649934 | GGTAATATTTTAGTG[C/T]TGTAGTTATCTTGAC | 8027 |
rs557391919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17686499 | CTCCTGCCTCAGCCT[C/T]CTGAGTAGCTGGGAA | 8027 |
rs557408380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17707680 | GGAGGACTGGTATAG[C/G]TGTGTTTATAATGAA | 8027 |
rs557415516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714322 | AAACCACCCCCCCCA[A/G]CTTTTTTTACACAAT | 8027 |
rs557453012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17680813 | TTAAAGTTCATCCCT[G/T]TTATAGCGTATTCCA | 8027 |
rs557477935 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17690895 | GTTACATTTAGAACC[G/T]GATGATAGAAAGGAA | 8027 |
rs557479877 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17667720 | TATAATGGAAAATAA[A/C]AAGGTAGACTGGTAT | 8027 |
rs557554201 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | STAM | GRCh38.p7 | 10:17675282 | GCCAAGGTGGGTGGA[A/T]CACCTGAGGTCAGGA | 8027 |
rs557569451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17703036 | AAAAAAAGAAAAGAA[A/G]AGAAAAGAAAAGAAA | 8027 |
rs557586194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713526 | CCCACCCCCGAGTCT[A/G]CTATGGTCCCATCAT | 8027 |
rs557608598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17674605 | TGCTCCAGGAGACCC[A/G]AATGTACTCCACATG | 8027 |
rs557667197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704154 | CTGAAGTGCAGTGGC[A/G]AGATCATAGCTCACT | 8027 |
rs557693815 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17648509 | TAAATCTTGGTGCTG[C/T]TCACTCTTTGGGTCC | 8027 |
rs557693938 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17667295 | CCATGCCCGGCTATT[C/G/T]TGTATTTTTAGTAGA | 8027 |
rs557731003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17666640 | CTGACCTTGTGATCT[A/G]CCCGCCTTGGCCTCC | 8027 |
rs557731800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697971 | CATCTTTTTATTTCC[A/T]GCAGCTCCTAATAGT | 8027 |
rs557800057 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17673907 | CCAGGCACAGCTTGA[C/T]GTGGGGAGCTGTCAA | 8027 |
rs557861584 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17661674 | GATGATTCTTTCATT[G/T]CACTAAAACTTGAGT | 8027 |
rs557905360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17701261 | TTTTCATCTTTAAGC[A/G]TGTTTATGAAAAAAT | 8027 |
rs557912261 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17653526 | TTTGGAACCCTCCCA[C/G]ATCTAGCTCCATACA | 8027 |
rs557925740 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17667742 | GACTGGTATGAGGGG[G/T]TTACGTTTATGCTAT | 8027 |
rs557929536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17690827 | ATGTAAAGATAGAAG[C/T]AGGCTAGCAGCACCG | 8027 |
rs557941570 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17646203 | TTTCTCAGTAGCAAC[A/G]TTATTGACGGTTTGG | 8027 |
rs557951216 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17662966 | CAAAGCCCCTCCTCT[C/G]TCTCTTCACTTTGTT | 8027 |
rs557954334 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17690014 | TTGTGCCATATGTAC[C/T]CTTGTTTGGTTAATC | 8027 |
rs558000771 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17655498 | TGTCCGGTGGTAGTG[A/C]CTAACTAGCAGGTGA | 8027 |
rs558019505 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17708036 | GCTGGGACTGCAGGC[A/G]CCCGCCACCACGCCT | 8027 |
rs558024549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17652237 | TGTAGGTAGTTTATA[G/T]CCTTCTGATTAAAAA | 8027 |
rs558061029 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17669120 | TTAGGCAGTATGAAG[C/T]ATGGTTCTAACTTTA | 8027 |
rs558061373 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | STAM | GRCh38.p7 | 10:17656966 | TTCCCTTAGAGTGGG[C/T]GGCCCACATGCGCAG | 8027 |
rs558074207 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17652669 | CACTTAAAAAAAAAA[-/C]AACCTGCTTGGCTAC | 8027 |
rs558083056 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | STAM | GRCh38.p7 | 10:17677865 | AATTATTAAAAAGGA[-/T]TTTTTTTGTATTTAT | 8027 |
rs558083106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17649048 | ATATTCATCACACCC[A/G]TTCAGGACTCTGTTC | 8027 |
rs558113281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17663488 | CAACTTCAGTGAATT[C/T]GATAATGAAGGTGGA | 8027 |
rs558120090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17679028 | TTCTTTCGTTGATGG[A/G]CATTTGGCTGTTGTG | 8027 |
rs558181636 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17651365 | GGCATGTAGTAACCA[A/G]TGGATACGTTTTAGC | 8027 |
rs558194613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696274 | AGTGCTTGCTAGCTT[C/T]CCATATACTAGAGTT | 8027 |
rs558286153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17650832 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATTAT | 8027 |
rs558361703 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716431 | TCGCTCAAGTGTTGT[G/T]TTCTGATTTCCTGTG | 8027 |
rs558366995 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644202 | TGGTGGGGTTGGGTG[A/G]GAGGAGGAGCTGTCG | 8027 |
rs558457277 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17679020 | TTTATCCATTCTTTC[A/G]TTGATGGACATTTGG | 8027 |
rs558467677 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645425 | AACTTGGAAGTTTAT[A/G]TAAGAGTAGAAAAAA | 8027 |
rs558482364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17654906 | TGTTGTTCTCTTATT[A/G]TTCCAAATTTTCACA | 8027 |
rs558487898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17677711 | ATTGAATGCTTGGCA[C/T]ATAATAGACATTCAG | 8027 |
rs558502766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644978 | TCTCTCTTAGGCTAG[A/G]TCTCTGCACTTTAAA | 8027 |
rs558559962 | in-del | -/TA | | | intron-variant | STAM | GRCh38.p7 | 10:17664083 | TTGTTTTAAAAGAAA[-/TA]AAACATTTACGTGTA | 8027 |
rs558585712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688727 | CTCGGCCTCCCAAAG[C/T]GCTAGGATTACAGGT | 8027 |
rs558593956 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17712725 | TCTTACAGTGGAAAC[A/G]CATGTATTCCGTTGG | 8027 |
rs558612165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17710199 | ATGTCACATGCTGCT[C/G]TACCTTCCTTGTTAC | 8027 |
rs558656361 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17676333 | GAGAGGAGCTCCATC[G/T]TAAATCTCCTTTCTT | 8027 |
rs558672173 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17716930 | TTCAAATGACAAGAC[A/G]AGGGTAGAAATAGGA | 8027 |
rs558695981 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17678279 | TTTTTTTGGAAGACA[G/T]AGTCTCGCTGTGTTG | 8027 |
rs558740480 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17711140 | GCAGGTTTTTTAGCA[A/C]TCCTCAGTTTATATA | 8027 |
rs558774715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17705253 | CCAGCGTAGATAGGT[C/T]GTTTTAAAAACAAGG | 8027 |
rs558800349 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17683849 | TCATTTTATTGAATG[A/C]TTAGTACTTTGAATT | 8027 |
rs558849638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17672289 | ATTGTTGAAAACTTA[C/T]TGTGGGCCATTCAAA | 8027 |
rs558867595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706314 | TTTGAAAAAAATTAC[A/G]GATATATCCATCCCA | 8027 |
rs558908251 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17711797 | GGTCGAAGAATGCTT[A/G]TTCTAGATACCATCT | 8027 |
rs558975954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17654474 | TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 8027 |
rs558986977 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17704849 | GACTAAGGTTAAAGA[A/G]TGTATATTTTTATTA | 8027 |
rs558987942 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17686202 | TACAACTGTTTATGA[A/C]GAGATTCTAATACCA | 8027 |
rs558997886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17699858 | GAATTCACTTAGGCC[A/G]TTGTAAAACTTTGCT | 8027 |
rs559013934 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17659633 | GCCACCAGGCCCAGC[G/T]AATTATTTTTTTAAA | 8027 |
rs559020584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645879 | TTCTTAATACTTGCT[G/T]CTTCTGTTTACAGCA | 8027 |
rs559033883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691509 | GGCGACAGAGCGAGA[C/T]TCAAATAAATAAATA | 8027 |
rs559051255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17676809 | CAGAAGTATACTCAC[A/G]TTAAATTCACTTATA | 8027 |
rs559087412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17663202 | TTTCTTAATGTTAAC[A/G]TTATTCTCCCAGAAA | 8027 |
rs559132381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17670264 | AAGTCTTAAAAACAT[C/T]GTATATTTTATAGAA | 8027 |
rs559148008 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17686629 | GTGATTGCCCACCTC[A/G]GCCTTCCAAAGTGCT | 8027 |
rs559211738 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17708445 | CTTTCTAAATATCCT[C/T]TGGGATTCCTTAAAA | 8027 |
rs559214469 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714965 | AGAGGTTCTTCCCCC[C/G]CCGCCCCTGCAGAGG | 8027 |
rs559216973 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17703379 | TCACTCTCTGATGAT[G/T]AATTCGTTTCTCAAG | 8027 |
rs559251297 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714452 | ATGAATTGACTATAT[A/C/G]AATGAATGCTTAGTA | 8027 |
rs559273117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17680920 | GTGAATAATGCTGCT[A/G]TGAACACGGGTATAC | 8027 |
rs559303101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17656731 | TCTGCACCAATCTCA[G/T]TTCTTGCCTCCTCAG | 8027 |
rs559334113 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17675519 | AAAAAAAAAAAAAAG[A/G]TAGTAGCGTTTTCTG | 8027 |
rs559339140 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17683688 | TTTCTTCATCATTAT[A/G]TGGATGATTTCCAGC | 8027 |
rs559478446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17685570 | AGGAGGGTTTAAGGA[A/G]TTTGGCTCAGGGTTG | 8027 |
rs559480852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17646842 | TTTTCTTTCACCATA[C/T]CTACCAATGAATATG | 8027 |
rs559481016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17652981 | AGCCTCTAAATCCTT[C/G]GAATTTTCTGAGTGA | 8027 |
rs559490903 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17673802 | TCTAACACAAAGCAG[G/T]CACTCCCTAAGCGTT | 8027 |
rs559626921 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17653275 | CCTACACTGAAAAAC[C/T]GAATATTCCGCGATA | 8027 |
rs559676937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712084 | CCAGGCAACTGGGTG[C/G]ACGGTGGAACTGTAA | 8027 |
rs559689370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17679149 | AACTACCACACTTTT[C/T]ACAGTAGCTACACCA | 8027 |
rs559870735 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17666475 | TCTTGGCTCACTGCA[A/T]GCTCCGCCTGCCGGG | 8027 |
rs559877169 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, missense | STAM | GRCh38.p7 | 10:17713342 | GATTCCCAGATGCGT[A/T]TTTCTCCTCCGTACT | 8027 |
rs559881965 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17655559 | TGTAAAATATTTGGT[C/G]AGAGTTGACTGCTTT | 8027 |
rs559915707 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17712747 | TTCCGTTGGAAACAG[A/G]AAGACAGGAAGTAGA | 8027 |
rs559918038 | in-del | -/TTATTG | 0.0017594 | 0.0296075 | intron-variant | STAM | GRCh38.p7 | 10:17654226 | TTGTTATTATTATTA[-/TTATTG]TTATTATTATTTTTG | 8027 |
rs559964953 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17661187 | GATTAATTGGTGTGG[A/T]TATGGGTGATTTCTT | 8027 |
rs559995755 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17655938 | AAAGTTTTTTTTCCT[C/T]CTACGTGTGTATTCT | 8027 |
rs560017312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17702802 | ATCACGAGGTCAGGA[C/T]ATTGAGACCATCCTG | 8027 |
rs560033275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17662544 | ATATAAACCTAGTAG[A/G]TTTGTAGAATGAATG | 8027 |
rs560041578 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643858 | AAAGGCGCACAGCTC[C/G]ACCCGAACTCAACCT | 8027 |
rs560041966 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17650560 | AATTTTCTACATTCT[A/C]AACAACAAATGTATC | 8027 |
rs560171080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17672436 | ACTGAATTTAACTGT[A/G]TTCTTTTCCAGCCTC | 8027 |
rs560184609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17694914 | AATGATTTTTGTTCA[A/G]TGTATCAGGATATGT | 8027 |
rs560216264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706479 | CGCCTTCCGGGTTCT[C/T]GCCATTCTCCTGCCT | 8027 |
rs560256678 | snp | C/G | | | intron-variant, missense | STAM | GRCh38.p7 | 10:17713293 | AGGGGACCTCATGAA[C/G]CCCGGTGATTCTGAA | 8027 |
rs560296080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17661403 | ACCCCTAAATATAGA[C/T]GTTCCTGAAACTTTC | 8027 |
rs560366293 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17670085 | CTGTGTATCTGGAAG[A/G]GAATGATGCACTTTG | 8027 |
rs560410355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17711295 | AAAGCTACCTGTAGC[A/G]ATGGTAGTATTATAA | 8027 |
rs560435783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17695933 | TCTCACAGACAGATT[A/G]ACTGTGTGTTGAAGG | 8027 |
rs560436661 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17691761 | GCCTGTTACAATGTT[C/G]CAGTCAGTGTTCTAA | 8027 |
rs560455393 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17675683 | GAAGCAGGGTCAGTC[C/T]CTTCTTGTTCACTAC | 8027 |
rs560458961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17690269 | TCTAGACCAGGCTTC[C/T]AGTGGAGTGAATGCT | 8027 |
rs560503494 | snp | A/C | 0.0149756 | 0.0852264 | intron-variant | STAM | GRCh38.p7 | 10:17660049 | CCCTCTCCATATTAT[A/C]AAAAAAAAAATCCAC | 8027 |
rs560552412 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17683014 | TAGTATTCCTTGTTA[A/T]GAAAACTGCTAACGG | 8027 |
rs560594613 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17654703 | TTACCAAAACTTGAG[C/T]AATGATAGGTAAATT | 8027 |
rs560618617 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17691847 | GCCCTGGGAATGACA[A/G]TATACATTCATAACT | 8027 |
rs560644085 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17649930 | ATTTGGTAATATTTT[A/G]GTGTTGTAGTTATCT | 8027 |
rs560728587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17670527 | CTTACATTAAAGTTT[C/T]TGGTGATTCCTCTCT | 8027 |
rs560751534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17687394 | GAGAATCGCTTGAAC[C/T]GCATCCCCCACCCCC | 8027 |
rs560796562 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17709197 | ATTTTTAATACTACT[A/C]TAACCATAAGTTTTT | 8027 |
rs560880867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17709800 | CTCAAAGAGTTACGT[A/G]TTAGAGATGCTTGGG | 8027 |
rs560890235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17671014 | ATGCCTTCATGCTTA[C/T]GAAAGGCATCTAAAT | 8027 |
rs560908913 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714368 | ATATTTTTAATGCAA[G/T]GCCTGATATCACAAA | 8027 |
rs560929120 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17657833 | TTCTGATATTAGTAA[C/T]TGGTGTTTTCTCTCT | 8027 |
rs560994267 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17682057 | AAGAGCATCCCTTGT[A/T]TGTGTATGGTTTGAT | 8027 |
rs561016442 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642715 | CTAAGGTTTTAAAAA[A/T]TTTTTTACATGCTTC | 8027 |
rs561051046 | snp | A/G | 0.000131835 | 0.00811788 | missense | STAM | GRCh38.p7 | 10:17704972 | CTTGTCATTTTAGCA[A/G]TGTGTCACCAGATGG | 8027 |
rs561073963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17648662 | CACCATTCTTACCTT[A/G]CTTCAGTCATTGTTA | 8027 |
rs561117271 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17674899 | CTAATAAACAAAATT[A/G]TAAATTCCACTTTTG | 8027 |
rs561208248 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17703941 | ATCTTGAGATGGATA[A/C/G]TACACTTGTTGGCAT | 8027 |
rs561245111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17708349 | AAGTTAGCTTGCTCT[A/G]TTGTTCAATAAACTG | 8027 |
rs561262947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17675391 | TGCCTGTTATCTCAG[C/T]TACTTGGAAGGCTGA | 8027 |
rs561298546 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17708035 | AGCTGGGACTGCAGG[C/T]GCCCGCCACCACGCC | 8027 |
rs561329165 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17668065 | ATCGGAGTTAATAAG[A/G]TGTGATAGAAGTTGA | 8027 |
rs561345663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17663903 | AATGGTAAACATAAG[C/G]GTCATATTAGGACAT | 8027 |
rs561397684 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17679342 | CATTTGTTATGTGCT[C/T]ATTGGCCCTTTGTGT | 8027 |
rs561412863 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17649293 | GTAGTCCCATTTACT[C/T]GGGATGCTGAATCCA | 8027 |
rs561416572 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697677 | AATGAATCTTCATAA[G/T]GATGAGTTTAGTCAT | 8027 |
rs561454412 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697066 | CTGGGATTACAGGCA[C/G]CCGCCGCCATGTCCA | 8027 |
rs561464486 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17703161 | AAACGGAAACCATCT[C/G]TGTGTTAATGGACTC | 8027 |
rs561519214 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17664377 | TCTCCAGAACTTATC[C/T]ATCATCCCAAACTGA | 8027 |
rs561536388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692742 | TTTGAGCATTTATAT[C/T]GTTTTATATATATAT | 8027 |
rs561549649 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17667855 | ACAAGGTAGAGAAAA[C/G]TTGATGCCTTCTAAG | 8027 |
rs561573486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704166 | GGCGAGATCATAGCT[C/T]ACTGCAGCCTTGACC | 8027 |
rs561635997 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17670692 | ATCTGCTTTTCTAAT[G/T]AAGTCCTTTGGGACT | 8027 |
rs561689203 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17661872 | GTCCTCCCACTATGA[C/T]GTTCCCAAAGAATCT | 8027 |
rs561726004 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17686147 | ATTTTCTACTAATTA[A/T]TAAACATTGTCTTTT | 8027 |
rs561764850 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691473 | CAGTGAGCCAAGATC[G/T]CGCCACTGTACTCCA | 8027 |
rs561767909 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716330 | GGTGACTAATTTCAC[A/C]GACTCAGATTTAAAG | 8027 |
rs561791957 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17691104 | CCTGTAGTTTTCAGA[A/C]GTGTCTGATAATTAA | 8027 |
rs561815583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17678462 | TTTCACCATGTTGGC[C/T]AGGCTGGTCTCGAAC | 8027 |
rs561852331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17684103 | ATCTCTTTAGCATAT[C/T]GCCCTCGGTCACTTT | 8027 |
rs561868558 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17646759 | CCTTGCACAGAGTCC[A/T]GTAGACTCATATTAT | 8027 |
rs561893240 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17646110 | TCTTTTATCTTTCAA[C/T]ATATCCTTGTGTGTT | 8027 |
rs561918694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17680378 | CCCAGGCCCCCTGGC[A/G]ACCACCATTCTACTT | 8027 |
rs561949232 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17685724 | AAACATGCAGCTGGC[C/T]AGGTCACAGAGCGGG | 8027 |
rs561964941 | snp | G/T | | | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696422 | TTTAGGAATGGAGAC[G/T]GAAAATAAGAGCCTG | 8027 |
rs561971310 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17686533 | AGGCATGCGCCACCA[C/T]GCCTGGCTGGTTTTT | 8027 |
rs561975927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17679068 | AATACTACTCTGAAC[A/G]TGGGTGTACGGATAT | 8027 |
rs562002201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17673938 | GGGCCTAAGTTCCTC[A/G]GTTTAAGAGATGTGT | 8027 |
rs562011901 | snp | A/G | 1.64866e-05 | 0.00287106 | missense, utr-variant-5-prime, intron-variant | STAM | GRCh38.p7 | 10:17684697 | GATTGTCTTCGGTCT[A/G]TTATGAGAAGAGTGA | 8027 |
rs562038477 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645065 | ATTTTTGTTGTTTTC[A/T]GAATCACTGGTATTA | 8027 |
rs562042478 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17712211 | AATAACCTGTGAAGT[C/T]GGTAAACTATTACCC | 8027 |
rs562083647 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17672467 | CTCAGATTTTTTCCC[A/G]AAAAACTTGTGCCTG | 8027 |
rs562228483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17707293 | TGGGTGCCTATAGTC[C/T]CAGCTACTTGGGAGG | 8027 |
rs562250787 | snp | C/G | 3.43401e-05 | 0.00414353 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644430 | CGGACTGCACGCTCA[C/G]TCTGCCAGCCCCTGC | 8027 |
rs562393360 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17662837 | AATGAGTGCAACTCT[A/G]CCTGCTTTTGATTGA | 8027 |
rs562405950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665676 | ATATCTAACACATAT[A/G]CATAATTACTGAATG | 8027 |
rs562489071 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17649519 | ATTATCTTTTGTGTG[C/G]AATATAAACTCCATT | 8027 |
rs562490917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17655223 | TACTTCTGGTAGGGT[A/G]TGGCGTGGACTAGAA | 8027 |
rs562496820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704892 | TCTTTTATTCCTTAA[A/C]TTATACAAATATCTA | 8027 |
rs562498320 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | STAM | GRCh38.p7 | 10:17706404 | TTTTTTTTGAGGCGG[A/G]GTCTCACTCCGTGGC | 8027 |
rs562530280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17666719 | TTGTATTGTTTTGTC[A/C]TGGACTGGACTGTGA | 8027 |
rs562588288 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17706053 | AGCCTGGGCAACAGC[A/G]ACACCCTGTCTCTAA | 8027 |
rs562621113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17700051 | TGCCAAAATCTGCAA[C/G]TCAGTTATTTCTTAA | 8027 |
rs562624867 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17711249 | CAGTCTTATTGTTAG[C/T]TGGGGAAGGTGTCAC | 8027 |
rs562648107 | snp | C/T | 3.32281e-05 | 0.0040759 | missense | STAM | GRCh38.p7 | 10:17695226 | CTGGAGAAATTATTA[C/T]AGTTCTTGATGACAG | 8027 |
rs562663431 | snp | C/T | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714304 | GTATAGACTTATTTC[C/T]GCAAACCACCCCCCC | 8027 |
rs562704474 | snp | C/T | 0.000444704 | 0.0149048 | synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714775 | TCTCAGAAGGCTCTG[C/T]TATAGGACCCGGTGT | 8027 |
rs562752260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695859 | ACTGCCTTAGTCCAT[C/T]TGGGCTGCCGTAACA | 8027 |
rs562763218 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17668123 | ACACTGTTATTAAAA[A/G]CTCCAAGAATTAGGA | 8027 |
rs562788603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17701321 | ACTCAAACTTATTAC[C/T]ATGTTTTAAAAATAA | 8027 |
rs562822337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17693621 | ACTTGCTTTTCTCAT[A/G]CAACATTATGTTTGA | 8027 |
rs562885829 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642923 | CGCACCACCACGCCC[A/G]GCTAATTTTTTGTAC | 8027 |
rs562889870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17664623 | ATTCTAAATACCTGA[G/T]GTGCTTTAGAGAAGA | 8027 |
rs562892276 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17657285 | ACTTTTAGAGAGGCA[A/G]TGTGATAATTGCTGA | 8027 |
rs562924286 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17670411 | CAGATTTCTTTACTT[C/G]CCATTTTATGTTTTT | 8027 |
rs562950116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17654229 | GTTATTATTATTATT[A/G]TTATTATTTTTGAGA | 8027 |
rs563015376 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17680982 | GTCCTTTGGGGTATA[A/T]ACCTGGAAGTGGAAT | 8027 |
rs563036868 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716117 | ATATTTACGATTTCC[C/T]TGGTTGGGCTATACT | 8027 |
rs563052992 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17686807 | GTGCACTTAGAAAGA[A/T]TTTTTTTTCTTCTAA | 8027 |
rs563083057 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17659890 | AGTCCCTCAATTTTT[A/G]TTGAGAAAGTGTTTA | 8027 |
rs563157798 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17682735 | CCATGGGTGGGTGGA[G/T]TGTTGTGTAATGCCA | 8027 |
rs563181478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17682212 | TTAAATTTCCTTTTC[C/T]AGAATTTCATAAAAT | 8027 |
rs563233547 | snp | C/T | 1.64931e-05 | 0.00287163 | intron-variant | STAM | GRCh38.p7 | 10:17704540 | CTTTTCTATTTACCT[C/T]GCAAATAAAGAGTAG | 8027 |
rs563270168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17647514 | TTCCACTTTTTTTTT[C/T]CCCTTAGAGTATTAG | 8027 |
rs563390143 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17648052 | TGTCACTGAGCTCCA[A/G]TGTCTAGGAGTATCA | 8027 |
rs563399297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17669966 | CGATCTCCTGACTTC[A/G]TGATCCGCCCATCTC | 8027 |
rs563443311 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17663314 | TTTTGTTTTTATCCA[G/T]TATCAATAGGTTTAG | 8027 |
rs563464121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17709066 | TGGTCAGCGTCATGC[A/G]GCCGCCCCATTTGTG | 8027 |
rs563495584 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17654540 | CCAGGTATTATTTAA[-/G]GTCAATGTGTTACTA | 8027 |
rs563523723 | snp | A/T | 0.00308573 | 0.0391579 | intron-variant | STAM | GRCh38.p7 | 10:17663288 | TATAGCTTTAAAAAT[A/T]TTTTTTGTCTTTTTG | 8027 |
rs563592483 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17674818 | AGGCCTGTTAGTTCC[A/G]TAAGTGTTGAATCAG | 8027 |
rs563672457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17680330 | ACTGTATACCCATTA[A/G]ACAATTAAACAATAA | 8027 |
rs563680264 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17679174 | ACACCATTTTACATT[C/T]CCACCGGCAATGTAC | 8027 |
rs563685022 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17657089 | GTGCCCCAGGAAGGT[C/T]GTATACTGCCATTTT | 8027 |
rs563699990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17674282 | TCTTACTACACAACT[C/G]TTAGTAGTAACTGTC | 8027 |
rs563715714 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17686402 | TTTTTTTTGAGACAG[C/T]GTCTCTCTTTGTCAC | 8027 |
rs563753545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17668696 | CTTTTCCAAATGTTG[C/T]GTAATTGGGATCGTA | 8027 |
rs563764358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17707964 | GGCGCGATCTCAGCT[C/T]GCTGCCAGCTCCGCC | 8027 |
rs563801578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17707485 | TCCATGTAAAGTGGG[C/T]ACGGACTGTGTTCAG | 8027 |
rs563818158 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17677721 | TGGCACATAATAGAC[A/G]TTCAGTCAATATTAG | 8027 |
rs563828533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17703356 | TTTTTAGCATACTTA[C/T]GTCACTTTCACTCTC | 8027 |
rs563838933 | snp | A/C | | | upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644071 | CTTTACCGATGGGGC[A/C]GGCTCGGGGCAGCTT | 8027 |
rs563881370 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17701543 | AATTGAGTAGTAGCA[A/G]CAGAGATCATATGGC | 8027 |
rs563940140 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17673138 | AGATTTTCTCTTACC[A/T]TGTATTTTTACAAAA | 8027 |
rs563941756 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17646310 | ACTAGATGCCGGTGA[C/T]ACCCAGCCCCCACTC | 8027 |
rs563981106 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17647605 | CAGGTTTGCTGCTTA[C/T]CGGTAGTGTGATTTT | 8027 |
rs563988705 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17703733 | TCCCAAATAGGAAAA[C/T]AGAGAAACCACTAGT | 8027 |
rs564022413 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17650688 | TGTTCTTCCCTGCTT[-/C]CAGTTTTTCCCTAGT | 8027 |
rs564049733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17667438 | ATAGAATTTTTTTTT[A/T]AAAACGTGATCTTGA | 8027 |
rs564092962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17667041 | GGTACTGTAGATTCT[C/T]TCAACTTTCAAGTGA | 8027 |
rs564106674 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | STAM | GRCh38.p7 | 10:17664094 | GAAATAAAACATTTA[C/T]GTGTACTTCCAAAAT | 8027 |
rs564143606 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17686814 | TAGAAAGAATTTTTT[C/T]TCTTCTAATAGAGTA | 8027 |
rs564172346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665594 | ATTTCTTTTAAGTCT[A/G]TTAGTATTGGACAAA | 8027 |
rs564209220 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17646702 | TGAAATATTACAAAA[A/G]GTTTATCTAAGAAGA | 8027 |
rs564225255 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17649754 | CTTCATTCATTATTT[-/G]GTAACATTTTTGTTT | 8027 |
rs564242058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688889 | GATATCCTTAAAAGT[C/T]AGGGATGACTTGAGA | 8027 |
rs564328991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17654734 | TGAGCTAGTTCTCCT[C/G]TTTTCCCTCTTCCAA | 8027 |
rs564375093 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714017 | TTCCTTGAACATGCT[C/T]GGTGTTTTCTCTCCT | 8027 |
rs564421289 | in-del | -/TGTCTCAT | 0.149586 | 0.231715 | intron-variant | STAM | GRCh38.p7 | 10:17691511 | GACAGAGCGAGACTC[-/TGTCTCAT]AAATAAATAAATAAA | 8027 |
rs564433711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17706614 | TTGATCTCCTGACCT[C/T]GTGATCCACCCGCCT | 8027 |
rs564471474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17655101 | TCTCTCTCTCCAGGA[C/T]CTTTACCTGTCTTTC | 8027 |
rs564511568 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642831 | TTGCAATTTTTTTCT[C/T]TTTTTGAGACGGAGT | 8027 |
rs564523085 | snp | G/T | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689767 | AACTCAAAACTTGGT[G/T]TGACCAGCATCACTG | 8027 |
rs564555690 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644081 | GGGGCAGGCTCGGGG[C/G]AGCTTTGAGACAGGC | 8027 |
rs564561158 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17677980 | CTTTTATAAATACAT[A/T]TATATTTCACATACC | 8027 |
rs564600674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17649996 | CCCTGCCTCTGCTAA[A/C]TCATCATATGTCTTT | 8027 |
rs564607874 | snp | A/G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17692156 | CCAAGAGGCTAATTT[A/G/T]CCCAGTGTCATCCAG | 8027 |
rs564618982 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17712533 | TTGTGCCAAGTACAA[C/G]AGCACTGAATTTCCC | 8027 |
rs564665380 | snp | A/T | 0.000798403 | 0.0199641 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717173 | TTCGAGACCAGTCTG[A/T]CCAACATGGTGAAAC | 8027 |
rs564693941 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715589 | AGACAAAATTAAGTA[C/T]GATCACATTCTTTAT | 8027 |
rs564717283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665602 | TAAGTCTATTAGTAT[C/T]GGACAAATTTGGAAA | 8027 |
rs564769699 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714612 | TAGTCCTCCTCCTGC[C/T]GCTACTGCTGCTGCT | 8027 |
rs564886853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17682587 | ATCAATTTGTAGTTT[A/G]ATTTTGTTATGGTCA | 8027 |
rs564888454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17709027 | AGTTATCTATAACTA[C/T]AAAATCTGGCTAATA | 8027 |
rs564952508 | snp | C/G | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713696 | CCCTTTCTCCCATCT[C/G]CACCATTACTGCCGT | 8027 |
rs564965629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17710501 | AATATTTAGCCCTCT[C/T]GTCCTGGCTCATTCC | 8027 |
rs564998292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17710011 | AATGAATACCCTTCT[A/G]GAAAATAAACAGCTG | 8027 |
rs565009334 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17694462 | AAAGCAGGATAATCA[A/G]TGCACTGATATTACA | 8027 |
rs565023649 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716068 | TTCTTTTAATTCATG[C/T]GAAAAATGTTTTCCA | 8027 |
rs565024746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17705502 | GTACTACTTTTTGCC[A/G]TTTTTGATATTTTGA | 8027 |
rs565047635 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17700337 | AAATTTAAATGGTTT[G/T]GCTTTAAGAAAAAAT | 8027 |
rs565075132 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17655971 | TTCTCTTAAGTTGCT[G/T]TTTTCTTTTTCTTTT | 8027 |
rs565157875 | snp | A/T | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716513 | TAAGTTAGTTTTTGA[A/T]AAATATCTGTCGGAT | 8027 |
rs565193463 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17706033 | TGTTCACACCACTGC[A/C]GTCTAGCCTGGGCAA | 8027 |
rs565236340 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17704001 | CAAAATCCTCTGGCA[C/T]GACATAAGAGGTGGA | 8027 |
rs565254481 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | STAM | GRCh38.p7 | 10:17669888 | TCTTTTCTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 8027 |
rs565302587 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17653618 | GTAGAGGAAAAAATA[G/T]CATGTCTGTACCGAA | 8027 |
rs565346576 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17657123 | TCTTAATGCCCCTGC[C/T]TGGGCTCACTCACTC | 8027 |
rs565422335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17664465 | TTTGTAGTTTGCCTT[C/T]AATATTTTAAATTAT | 8027 |
rs565438246 | snp | C/T | 0 | 0 | intron-variant | STAM | GRCh38.p7 | 10:17685761 | CACTCTGTTTTTCTA[C/T]TGGGACACAGAAAGA | 8027 |
rs565444183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17659020 | TTCCCATTTTCTATT[C/T]CACTCTTTTTTTGGC | 8027 |
rs565513051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17699272 | AGGAAATGTAATATT[C/T]CATCAAGCATATTCA | 8027 |
rs565516067 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692804 | GATCCAAAAGGAAAT[G/T]ATAACTCTAACTATT | 8027 |
rs565541804 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687742 | CTTTTCCTTGTCTTA[C/T]TGATGTACAAACCTT | 8027 |
rs565545377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713452 | TCTTTGCTTGCCAGT[G/T]TTTTGGACATCAAAC | 8027 |
rs565589118 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17687439 | GGTTGCAGTGTGCTG[A/G]GATCGAGCCACTGCA | 8027 |
rs565598412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17654172 | GTAGAGGGTTTCTGC[A/G]TTTGAAAGTTAAGTT | 8027 |
rs565645014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645399 | AACTCTTCCTTAGAG[C/T]ATGTCACTGAAACTT | 8027 |
rs565697830 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17678592 | GTTCGTTTATGTTGT[A/G]GCTTGTATTAGTACT | 8027 |
rs565725337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17672725 | TCATGAGTTCTCCAA[C/T]AGTTAAATCCCTAAT | 8027 |
rs565778235 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17679326 | TGCTAGCGATGTTGA[C/G]CATTTGTTATGTGCT | 8027 |
rs565822025 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17658822 | TCTATGTGTTTTTAT[A/G]TCTAAAATGAGTTTC | 8027 |
rs565870703 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17668245 | ATGAGGGGACTGACG[A/T]GATTGGAGCTGGGCA | 8027 |
rs565908603 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17674494 | CTGGGACCTCACCTG[A/C/G]CTATCAGGTGAAACT | 8027 |
rs565920101 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17662957 | TTGCAGCTGCAAAGC[C/G]CCTCCTCTCTCTCTT | 8027 |
rs565933895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17668898 | CCCAGTTTTGGTGAT[G/T]TTTAATAAAGCTGCT | 8027 |
rs565990758 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | STAM | GRCh38.p7 | 10:17703023 | CAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 8027 |
rs565992841 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17699389 | ATTGACCACATTGAT[A/G]CAAGGATTAAAAATA | 8027 |
rs566008061 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17690801 | TGCAGTTCTGTTAGC[A/C]CTAACTTTTGATGTA | 8027 |
rs566046418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712277 | AAAACGGAAGTCCCA[C/T]TTAGCTAAGATTCTA | 8027 |
rs566047188 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696661 | TTGGCTTTTTCAGTG[G/T]GTTATTGTGAGATTC | 8027 |
rs566160408 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17704701 | TTCTTATAATTTTCT[A/G]TCCAAACGAAGTGTT | 8027 |
rs566169103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17706950 | AAACCAACAAAATAT[A/G]TTTCCATAATTTAAA | 8027 |
rs566219694 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692492 | TGCTAGCAGTTTCTG[A/G/T]TAACTGGCAGAATGG | 8027 |
rs566245462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17655734 | CCAACCATTACAGAT[A/G]AGAATCTTGGTATGA | 8027 |
rs566270202 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17654842 | ACTCTTGGCATTCTG[A/T]TGTTTCTTGAAGCAG | 8027 |
rs566279665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17661648 | AGTTTTTCCATTTCT[A/G]TTAATGACAAGATGA | 8027 |
rs566286312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17656266 | ACCACTGCACTCCAG[C/G]CTGGGTGACAGAGCG | 8027 |
rs566290795 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17649071 | CTCTGTTCAAACGTC[A/G]TTTTCTGAGACGCTT | 8027 |
rs566375966 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17665371 | ACATTGACAAGTCTA[A/T]TTCCTATCCCTGTTT | 8027 |
rs566437718 | snp | C/G | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715046 | TACAAGGCTATTTGT[C/G]TCGTAAACCTGGTCT | 8027 |
rs566466557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17700805 | TGCACATGACTGAGG[A/G]AGGGACACTCATTGA | 8027 |
rs566475254 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17665740 | CAGAAAGCCTACTAG[A/G/T]TGTAATCCCTGTTTA | 8027 |
rs566527540 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17649622 | AATTATTTATCAAAT[A/G]ATGAATTATTGGTGT | 8027 |
rs566548691 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688682 | TGGCCAGGCTGGTTT[C/T]GAACTCCTGACCTCA | 8027 |
rs566573316 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17693660 | CGTGTGATATATCCA[G/T]TAACTGTTCTATAAT | 8027 |
rs566595376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17694746 | AAAATATCTGCAGCT[A/G]AAAAAGAAAAGTAGA | 8027 |
rs566614597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17684177 | TTTCAGAAGGTCTTC[A/G]CTGATACTTGGAAAG | 8027 |
rs566643179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644530 | TCAGAGCTGGGAGGA[A/G]GTTGAGGGCTTGGCG | 8027 |
rs566727010 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715775 | CTACATTTTCGAAGT[C/T]TCTTGTAATTATTTG | 8027 |
rs566739404 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17670870 | TATATGTTGTGTGGA[G/T]TATGTTTTATGTAAT | 8027 |
rs566756504 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17692176 | GTGTCATCCAGCTAG[-/A]AAGTGGTAGATCTGG | 8027 |
rs566806268 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644183 | CCGCAGCTGCTGCCG[C/T]GGTTGGTGGGGTTGG | 8027 |
rs566815941 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17716842 | GTTACTGTGTTAGTT[G/T]ATGCCTTCCCATTAT | 8027 |
rs566855167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17681780 | CTGCCTGGTAACTGG[A/C]ATCATGGGCAAGGAA | 8027 |
rs566858322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17710725 | CACCTCTATAGCCAT[C/T]CTATGTAGCACACAG | 8027 |
rs566871381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17653758 | GAGGATGTGCAAAGG[C/T]TTTATGCAAATTCAA | 8027 |
rs566874224 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17687346 | TGGGCATGGTGGTGC[A/G]CGCCTGTAATCCTAC | 8027 |
rs566916930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17675708 | CACTACTTTATTCCT[A/G]AAGCCTTGCATAATG | 8027 |
rs566920961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17682245 | AATAGTATTGTCAGT[A/G]CTCCTGTGTCTAGCA | 8027 |
rs566942833 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643009 | AGGTGATCTGCCGGC[C/T]TCGGCCTCCCAGAGT | 8027 |
rs566953935 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17675099 | GGAATCTTAACTGAT[G/T]AGGTAGTCATGAAGA | 8027 |
rs566959007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687911 | TTTTCTTGTCTATAG[C/G]TATGCATAACTTGTG | 8027 |
rs566997157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17648730 | TCTTTGTTACCACTC[C/T]TGCCTCTACAATCAG | 8027 |
rs567008809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665394 | CCCTGTTTCGCTGCT[C/T]TCATCTTCTATAAGT | 8027 |
rs567079481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17705228 | GACCTTTGCAATATA[A/G]TCAAAAGGACCAGCG | 8027 |
rs567085442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698733 | TATTGTATATAAATA[A/G]TATATTTTTTTACAC | 8027 |
rs567111870 | snp | A/G | | | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717215 | AAAACTACAAAAATT[A/G]GCTGGGCGTGGTGGC | 8027 |
rs567244306 | snp | A/G | | | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695528 | TACATTATTTAAAAG[A/G]TTACAGTTTTAGAAA | 8027 |
rs567246387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704117 | TTATTTATTTAAACA[A/G]GGTCTTGCACTGTTG | 8027 |
rs567265994 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17693852 | GCAATATTGTTGGAT[C/G]ATGGCATTGGTACAT | 8027 |
rs567266008 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17647565 | TAAGAATTCAGACTG[G/T]GGCCACACTGCTTGG | 8027 |
rs567277842 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717187 | GACCAACATGGTGAA[A/T]CCCCGTCTTTACAAA | 8027 |
rs567282945 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17673897 | ACCTAACATTCCAGG[C/G]ACAGCTTGATGTGGG | 8027 |
rs567285022 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17708678 | GATTCCAGAGTGGTG[A/G]TTTTTCTTGTTTTTG | 8027 |
rs567289408 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17683612 | CTGATTAATTCCATC[C/T]ACTTTTTAATTTTAC | 8027 |
rs567377015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17700734 | TTTACACTCGTATTC[A/G]TATCATGCGAGAACT | 8027 |
rs567416020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704633 | ACATTTCTCACTTCT[C/T]CTTGACCCAGGCTCA | 8027 |
rs567460089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17656851 | GCAGGAAAGAAAGGA[A/G]AGTGCCCTTGGAAGA | 8027 |
rs567520858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17652005 | CAAATGAGGCTCTGT[A/G]TATGTTTTTTCTGGG | 8027 |
rs567530096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17662858 | TTTTGATTGAAGTCA[C/T]ATTTTGTGACAGTTT | 8027 |
rs567543101 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17657203 | TGCATTCATTTAACA[C/G]TTTAATGTTTAACAC | 8027 |
rs567712141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17663334 | AATAGGTTTAGACAC[A/G]TGCTCATTTTTTTTA | 8027 |
rs567746333 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697844 | TTGGCAAAATATCTC[A/G]TTATCGTTTTTTAAT | 8027 |
rs567767045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17703477 | CTTTATTTGCCCTGC[A/G]TACCTATATATAGTA | 8027 |
rs567840986 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17672622 | AGTCCTGTATGCAAG[C/G]CAGCTTCTTCAGCTG | 8027 |
rs567868408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17686355 | CAGTGAACATATTGG[C/T]TTTGTACTTAATAAC | 8027 |
rs567923810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17700447 | TTTTTGAAACTTCCT[C/T]TCCAGTCCTTTGTTT | 8027 |
rs567970153 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17663932 | ATTCCTGGGCCCTAG[A/G]CACTTTTGTCTTCTT | 8027 |
rs567987326 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17675406 | CTACTTGGAAGGCTG[A/C]GGTGGGAGAATTGCT | 8027 |
rs568007310 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643099 | TGACAAAACATTATC[C/T]AACTGCTACTTTAAT | 8027 |
rs568021318 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645163 | TGACTTGAAGATAAT[A/G]ATTATGGGAATTTGA | 8027 |
rs568030789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17685088 | GTTTTGTTGAAGAGA[C/T]TGCGGATTCATGTAA | 8027 |
rs568035686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17650751 | AAATGTGAATGTACG[C/T]GTGGCCCCTCCGTTT | 8027 |
rs568045006 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713405 | TGCCTATGCAGGACA[A/G]CAGGCTTGAATAGCT | 8027 |
rs568047857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17656121 | AACACAGTGAAACCC[A/G]TCTCTACTAAAAATA | 8027 |
rs568084953 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17655644 | AAATGAGGAAATAAG[G/T]GTACTCTGTTGATCT | 8027 |
rs568092700 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689904 | TTGAGGTCTGAGAAG[C/G]ACTGCTGCTCTAGAG | 8027 |
rs568109960 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17651060 | ACAGAGCGAGAGTCC[C/G]TCTCAAAAAAAAAAA | 8027 |
rs568144683 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17677590 | CAAAATCTAAATAAT[A/G]GTGTTAAAGTACATA | 8027 |
rs568146567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17683668 | TCTGGGCCCTTTTTA[A/G]TATATTTCTTCATCA | 8027 |
rs568196313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644901 | CAAACATGTTAGGAG[C/T]GATGAAGATGAAATA | 8027 |
rs568263370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17707585 | AGAGGGCACCTGCTT[C/T]AGAGTCTTGATCACC | 8027 |
rs568316642 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17674336 | GTTTATTATATCTCA[A/C]AGTTATGTGGGTTAA | 8027 |
rs568317553 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644167 | CTTGCTGTTGCCGCC[C/G]CCGCAGCTGCTGCCG | 8027 |
rs568354494 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17671458 | TCTCCTCTTTTACAG[A/T]TGAGGTCTGTCAAAG | 8027 |
rs568363295 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17702647 | AGCGAAACAGACTGT[G/T]GAAGACTGTGCTAAG | 8027 |
rs568372506 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17650126 | GTCAGCCTCATAAAT[C/G]ATAAGCTAGATGAAT | 8027 |
rs568434214 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17701661 | CGATCCTCAGTTACC[A/G]TAGCATTCTTTCCTA | 8027 |
rs568573933 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17659567 | TCAACCTCTTGGGCT[A/C]AAGTGATCCTCCCAC | 8027 |
rs568578308 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17711593 | TTATTCTTAGCCAGT[A/C]GAAAAAAAGTGAGGA | 8027 |
rs568645576 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17709874 | TGACCTTAAGGGGGA[C/T]GATGGCAAGGCCCAC | 8027 |
rs568656053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712735 | GAAACGCATGTATTC[C/T]GTTGGAAACAGGAAG | 8027 |
rs568668755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17660757 | ACATAGTGAGACCCC[A/G]TCTCTTAAAAAAGAA | 8027 |
rs568694710 | snp | A/C | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689984 | TACTCTTGTAAGAAA[A/C]GGAAGAATTAATGAT | 8027 |
rs568735227 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645748 | AGTTAGCACACACTA[C/T]AGGACACAGCAGCTC | 8027 |
rs568834246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665365 | AGATGGACATTGACA[A/G]GTCTAATTCCTATCC | 8027 |
rs568841181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17693775 | ATTAAGCTGCAGTGA[A/G]TATTCTTGTACATAT | 8027 |
rs568909904 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17692116 | CTATTATCGTAGTCA[-/T]TTTATTGATGAGGAA | 8027 |
rs568922235 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697828 | GATATGCTACAGTTA[G/T]TTGGCAAAATATCTC | 8027 |
rs568944585 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17648890 | GGCTTCTTCCTGTGT[G/T]TCTGATATGATTATG | 8027 |
rs568957106 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17700396 | ATTTTTGTATTTTTT[A/T]ATAAAAATTCAAGCA | 8027 |
rs568977909 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17699768 | TTCTGTCAAACCAGA[-/C]TTTTTTTTTTCTACC | 8027 |
rs568999505 | snp | C/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688078 | ATGGTTGAATGGACA[C/G]ATGAATTTAAGAATG | 8027 |
rs569109219 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17667020 | TTGATTATCACAGCA[A/G]TTCTAGGTACTGTAG | 8027 |
rs569118691 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17690618 | TTTTAAAGCCACTTA[C/G]TTACTTAAGTTATTA | 8027 |
rs569174775 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687734 | AGCAGACACTTTTCC[-/T]TGTCTTACTGATGTA | 8027 |
rs569180241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17649529 | GTGTGGAATATAAAC[C/T]CCATTAAGATGAGAA | 8027 |
rs569183242 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17652246 | TTTATATCCTTCTGA[A/T]TAAAAAAAAAATACT | 8027 |
rs569296146 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17653667 | TTGTCATTATGCCCT[A/G]TACAGTATAGTTATT | 8027 |
rs569316697 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17687472 | CCGGCTTCTGCCACA[G/T]GGTGAGACTCTGTCT | 8027 |
rs569352928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692944 | TCTCTAGTCTGTCTT[C/T]TCTGACTTGTGTACC | 8027 |
rs569357836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17680002 | TAACCAAAGGTTTTT[C/T]AGTTTTGTTGATCCT | 8027 |
rs569379630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17653638 | TCTGTACCGAACACA[C/T]AGAGACATTTTTCTT | 8027 |
rs569421876 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17680530 | TCCACCTCAGCCTCT[C/G/T]GAATAGCTGGGACTA | 8027 |
rs569443165 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17648442 | CCAGCAGCAGCAACC[A/G]GCTCGGGTCCCCTTC | 8027 |
rs569482268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17709342 | ATTTTAAAATATATA[C/G]TTCTGAGCTGTCTCT | 8027 |
rs569486351 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17670512 | TCAAGACATACCAAT[C/G]TTACATTAAAGTTTT | 8027 |
rs569516062 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17681701 | TGAATTTATTGGGAG[A/G]CATATCTGTGTCCAG | 8027 |
rs569526884 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17699557 | ATTGTTGATCCCTCA[A/G]TGACCACTTTTTAAT | 8027 |
rs569529314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17710099 | TGTTGAGAAGACACT[A/T]GGGTTCCTGACTTAA | 8027 |
rs569570371 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715765 | CTGAATTACACTACA[C/T]TTTCGAAGTCTCTTG | 8027 |
rs569596517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698624 | AGGAAATAGAAGTCT[A/G]TTTCACTTAGCCTGT | 8027 |
rs569613366 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17701662 | GATCCTCAGTTACCA[C/T]AGCATTCTTTCCTAA | 8027 |
rs569647104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17708189 | GCCACCATGCCTGGC[A/G]GCTTTAAATAAACTT | 8027 |
rs569655742 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17659263 | TCCTTCCCATCCCTT[A/G]CGTCATTGCTGTCAT | 8027 |
rs569685921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714079 | CTTTCCTAGGGAATC[C/T]ATCTGGCTCACTCGC | 8027 |
rs569782651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17668996 | CATGATTGCTAGATC[A/G]TATGGTAAGACTGTT | 8027 |
rs569826927 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17669643 | TGTCCTTTTTGCTGC[A/T]GTTTCAGTGGGGTTT | 8027 |
rs569866400 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17663508 | ATGAAGGTGGATCTG[C/T]TTGTTCTTTTAGTCA | 8027 |
rs569927476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17657399 | GGATTTTTGCATTTA[C/T]GTTCATGAGAGATAT | 8027 |
rs569953418 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17712892 | GTAGGGAAGCTCAGT[A/C]CGTGAGGGGTGCAGC | 8027 |
rs569969310 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17680771 | TTGTCCTGTTGTGAC[C/T]AGCTTATTTCACTTA | 8027 |
rs570032258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17707076 | CAAGGACCCCCTTTT[C/T]ACAAACTCATCACGG | 8027 |
rs570106660 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697176 | TCAGGTGATCCACCC[A/G]CCTCAGTCTCCCAAA | 8027 |
rs570128813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696709 | AAGTTGAATACTACA[A/G]AAGATAAAGATGTAC | 8027 |
rs570132221 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17685323 | TTTTATCTTTATCAA[C/T]AAGGCTGCTTCCTGG | 8027 |
rs570192627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17702516 | TTAATGTCCTGGGAA[C/T]CTTATCCTTTGTAAC | 8027 |
rs570215705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17651403 | ATAATCAAGTTAGAA[A/G]TAGATGTGGGGACTA | 8027 |
rs570250395 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17656323 | AAAAAAAGATAGTTT[C/T]AGATAGCTTGCTTGT | 8027 |
rs570255746 | in-del | -/TC | | | intron-variant | STAM | GRCh38.p7 | 10:17669893 | CTTTTCTTTTTTTTT[-/TC]TTTTTTTTTTGTATT | 8027 |
rs570281875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644574 | AGAAATGGGACTCAT[C/T]CTGTGAAATGGGCCT | 8027 |
rs570298683 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17651950 | AAGTTGCTGCTTATC[A/C]GAAAAAGTTCTCTAA | 8027 |
rs570325611 | snp | C/T | 9.89103e-05 | 0.00703174 | intron-variant | STAM | GRCh38.p7 | 10:17704531 | AAGGTAAAACTTTTC[C/T]ATTTACCTTGCAAAT | 8027 |
rs570327550 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17680952 | ACTATCTCCTCCAGA[C/G]CCTGCCTGCTTTCAG | 8027 |
rs570329854 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644224 | GAGCTGTCGCGGACC[C/T]TGTAGAGTCGGTCTC | 8027 |
rs570381105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695426 | TTGTTGTTTAATTTT[G/T]TTCTTATTTATTACT | 8027 |
rs570483596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17660723 | ACCCATGAACAGCCA[A/G]TGTACACGAGTCAGG | 8027 |
rs570498471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17655603 | TTAAACTCACTTGAC[A/G]TACTTCTGCTCTCAG | 8027 |
rs570559660 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17682335 | GGGAAGAGGTATTAC[A/C]TTGTGTTAATATATT | 8027 |
rs570606662 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17660146 | AATCTTTTGCTAATG[A/T]AAATAGTATTTCTTA | 8027 |
rs570621563 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17683103 | ATTGGTTATGTTTCT[A/T]CTGTTTTCTCTTTCT | 8027 |
rs570678976 | snp | A/G | 1.67604e-05 | 0.00289481 | intron-variant | STAM | GRCh38.p7 | 10:17705760 | AGCTTTTAGAAGCCC[A/G]TGTTGTTTTAAATTC | 8027 |
rs570695914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17672857 | TGTGTTATGGTCATT[C/T]ATCAAATGATAAGTA | 8027 |
rs570706035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17684386 | TTCCACCCTGGCTGG[A/T]AGTGGAAGTCATGGC | 8027 |
rs570731921 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17678558 | CACGCCCAACCTCAT[A/G]TAGTGTAATTCTTCT | 8027 |
rs570735315 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715912 | ATGTTTCAAAGTAAT[A/C]TACATTCCTGGCTTT | 8027 |
rs570757991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712325 | CCAGAACCCAGCGCA[C/T]AGACTCTATATTACG | 8027 |
rs570899365 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17677564 | TAAAATAAGTCCAAC[A/T]GTGAAAAAGGCAAAA | 8027 |
rs570964835 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716246 | TTTATTTTCTAAGAC[G/T]GTTGTAATCAGGTAG | 8027 |
rs570964912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17647481 | CCCTGCGGCTCAGTT[C/G]CGGAGCCTCTTCTCT | 8027 |
rs570969779 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17664772 | TTGTGTTTCAGGCAA[A/C]AATCTAGATTTAGAA | 8027 |
rs571002253 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643755 | CACGCAGCTAATTAA[A/G]CTGTTTACCTAGAAG | 8027 |
rs571061511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17671402 | CCCTGGCATGAGTCT[A/G]GGAGTTTTGTATTAA | 8027 |
rs571085616 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17700479 | CCGTGCCAGAGCCTC[A/T]TTATTTTAAATTCCT | 8027 |
rs571117672 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17707181 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACGAGGT | 8027 |
rs571125289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665193 | TAATTCCTTCTCTTA[A/G]AAAGGAAAAAACCAG | 8027 |
rs571191828 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17685772 | TCTATTGGGACACAG[A/C]AAGAAAGCAGGGAGA | 8027 |
rs571194014 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687974 | TTAAAATGTCTGTAT[G/T]AAATCATTGGCTAGG | 8027 |
rs571221159 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | STAM | GRCh38.p7 | 10:17675241 | TGGGCACGTGGCTTA[C/T]GCCTGTAATTCCAGC | 8027 |
rs571221978 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715136 | TAACTGCATTAGTGG[A/C]CATTTTGAATCACAG | 8027 |
rs571298141 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17660756 | AACATAGTGAGACCC[C/G]GTCTCTTAAAAAAGA | 8027 |
rs571305776 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698520 | AAAAGAGAAACTGAA[A/G]CATCAGAGCCTATGT | 8027 |
rs571336374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17653789 | TGCCATTTTATATTA[A/G]GGACTTGAGCATCCA | 8027 |
rs571404789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17678474 | GGCCAGGCTGGTCTC[A/G]AACTCCTGATCTCAG | 8027 |
rs571450667 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17652788 | ATATTGTTCAGAATG[A/C]CTCACTCAATATTCT | 8027 |
rs571503556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697907 | CCACAAGATGCTTAG[A/G]TGTTTTTTAGTTTAT | 8027 |
rs571529815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17657343 | GAGAACCCTCTCCTG[C/T]CCTGCTCGTACCTGT | 8027 |
rs571559796 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17654323 | CACCTCCCAGGTTCA[C/T]GCCATTCTCCTGCCT | 8027 |
rs571684359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17663429 | CAGTTGGGGATTTTA[A/G]TTGACATTATACTAA | 8027 |
rs571756181 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17658088 | ATTCTTTTTAAAAAT[A/G]TGTATTCAATGCTAT | 8027 |
rs571783957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691976 | ACATACGTTATAAGC[A/C]CCGGAGGTAATGTTA | 8027 |
rs571802862 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698401 | TCAAGGATCTCATGT[A/G]GATCCTGGAGCCATT | 8027 |
rs571815428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17653256 | ATTTCCCAGTCCATC[A/G]AAACCTACACTGAAA | 8027 |
rs571820318 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17675772 | TTATGGAAAGTATTA[G/T]TAACAGAGTTCTTTG | 8027 |
rs571852815 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | STAM | GRCh38.p7 | 10:17706786 | TGCAGGTCAGACATA[C/T]CTCAATAAAGTAGTT | 8027 |
rs571860317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17681097 | CCACCAACAGTGCAC[A/G]AGTGTTTCAATTTCT | 8027 |
rs571884345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17681505 | CTTAACATTGTTTAT[C/T]ATGTGTAATATCCAT | 8027 |
rs571885291 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714712 | ACATCATCAACTCTG[C/T]CTCAGCCCGGAGGCA | 8027 |
rs571907528 | snp | A/G | | | intron-variant, synonymous-codon, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17684849 | TCTAGGAGCATGTGT[A/G]TCAAACTGTGGCAAA | 8027 |
rs571913840 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17647483 | CTGCGGCTCAGTTCC[A/G]GAGCCTCTTCTCTCC | 8027 |
rs571918404 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17687110 | TCTCTTTCTTTAATA[C/T]GGAAGAATAATGCCC | 8027 |
rs571941343 | snp | A/G | | | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695810 | AATCAGTTCAAATTG[A/G]TTTAAAGTTCTTCCT | 8027 |
rs571950245 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17653805 | GGACTTGAGCATCCA[C/T]ACATTTTGGTATCTG | 8027 |
rs572090352 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17655415 | TTAGGGTAGCTAGGT[A/G]GGTACCCTACCTAAC | 8027 |
rs572097983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17666619 | AGCCAGGATGGTCTC[C/G]ATATCCTGACCTTGT | 8027 |
rs572136547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17665950 | ATGGGCTGAACAGCC[C/T]TCATTTGTTTAGAAA | 8027 |
rs572144985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17673635 | CCTGCCTTCAGCAGC[C/G]CTCATGATGGGGAGA | 8027 |
rs572197738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695596 | AGAAATATATAATCT[A/G]TTGAGTTTTTTTTAC | 8027 |
rs572201493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17656517 | CTTTCCTCTTGGGCT[A/G]ACATAGAGCCCCCAG | 8027 |
rs572202053 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17657550 | TTAGTATAATTTCTT[C/T]CTTAAATATTTGGTA | 8027 |
rs572211163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17702026 | TCTTTCAGAAGATAC[C/T]GAAAGAACTTAATGA | 8027 |
rs572213388 | snp | A/T | | | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696150 | AAGACACAAACATTC[A/T]GACATATTTTAACAT | 8027 |
rs572239224 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | STAM | GRCh38.p7 | 10:17661750 | CTCTCAAAATGTTGA[C/T]GTTTTAAAGTCTCCT | 8027 |
rs572239564 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17660242 | TGCCTTTTATTTTAT[A/G]CTAAGTAAAGAGGCA | 8027 |
rs572257521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689276 | GACTGTAATGAGTGA[C/T]GTGAAACCATGAACA | 8027 |
rs572277104 | snp | C/T | 0.000464728 | 0.0152364 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696897 | CAGCCTGCCAATAAA[C/T]GATGTTTTCTAATCC | 8027 |
rs572293917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697452 | TCCAAGCAACATGTC[A/G]GATATTCAGAAGGAG | 8027 |
rs572360888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17691061 | AAAAATTTATGTAAA[C/T]CGTAAAACTTATTTC | 8027 |
rs572373866 | snp | C/T | | | missense | STAM | GRCh38.p7 | 10:17700218 | AGAAGACGGTACAAT[C/T]TAGTGATGATGTTCA | 8027 |
rs572400871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17654464 | CCTGACCTCGTGATC[C/T]GCCCACCTCGGCCTC | 8027 |
rs572403278 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17660989 | ATTAGTGATTTCTCA[G/T]TTACCAAGTTTCATG | 8027 |
rs572418648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689973 | ACAAAGGGACTTACT[A/C]TTGTAAGAAAAGGAA | 8027 |
rs572618988 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17667190 | GGAGTGCGATGGTGC[A/G]ATCTCAGCTCACTGC | 8027 |
rs572635935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17684599 | TTTTTATCGTAGTCT[C/T]TTGTCTATAACAGTT | 8027 |
rs572642528 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17649008 | TTGCCTGGGATACTC[C/G]TCACCCAGGTATTTG | 8027 |
rs572649977 | snp | C/G | 0.00318978 | 0.0398085 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717160 | TTGAGGTCAGGAGTT[C/G]GAGACCAGTCTGACC | 8027 |
rs572686386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17678342 | TCACTGTAACCTGCA[C/T]CTCCCAGGTTCAAGC | 8027 |
rs572723068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17683994 | TTGAGCTGCATTGCT[A/G]GGGTCTAAACTCCCC | 8027 |
rs572767078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17671679 | TGTACGTTTTTAGTC[C/T]GACATAGGTTATTAG | 8027 |
rs572803834 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17671052 | TACTCAGTATTCAAG[A/G]AGCATTCATATTATC | 8027 |
rs572809506 | snp | G/T | 1.65622e-05 | 0.00287764 | missense, utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644342 | GCACGCAGCGGAGAT[G/T]CCTCTTTTTGCCACC | 8027 |
rs572827727 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | STAM | GRCh38.p7 | 10:17693907 | ATGATTTCCTTTTCC[A/T]TTGGCAGTGTATGAA | 8027 |
rs572910833 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643878 | GAACTCAACCTGCTT[G/T]CTTTCTCCTGGCTCT | 8027 |
rs572992103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17683250 | CTCACTGCATCCTCG[A/G]CCTCTGGGGCTCAAG | 8027 |
rs573057131 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17677669 | AAAATCAGTAAAGTA[G/T]AAGAAAAAAGTTTTA | 8027 |
rs573193062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17647975 | TCTTAGTTCTTTGCC[C/G]AAACCTGCTCATTCC | 8027 |
rs573218156 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17711105 | TCAAGGTCAGTGAGG[A/T]TTGTTGTTGTTTTTG | 8027 |
rs573227860 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | STAM | GRCh38.p7 | 10:17681188 | GGTGTGAGGTGGTAT[A/T]GAGATCGTCTTTTTT | 8027 |
rs573294682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17709012 | TGTTTAAGTGCCCCC[A/G]GTTATCTATAACTAT | 8027 |
rs573350884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704785 | AGATTAATATTTTAG[A/G]TTAAGTTGTCACCAT | 8027 |
rs573375484 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17650659 | TCTCTCAGATTAGTA[C/T]AGTAGCTTCCAGCTG | 8027 |
rs573378550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17675960 | TGAGTACTTCCAACA[C/T]GATGAATGGGCAAAA | 8027 |
rs573383406 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | STAM | GRCh38.p7 | 10:17660279 | TTGTGAATAGGGAAA[A/G]TAATTGCAAGAGATA | 8027 |
rs573394204 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | STAM | GRCh38.p7 | 10:17680146 | TTGCTCTTTTTCCTC[A/G]TTTCTTAAGGTATAA | 8027 |
rs573398868 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17650840 | GGAGGCCGAGGTGGG[C/T]GGATTATGAGGTCAG | 8027 |
rs573427531 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697693 | GATGAGTTTAGTCAT[C/G]AAGCAAAGTTTAAGT | 8027 |
rs573447235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17699778 | ACCAGATTTTTTTTT[C/T]CTACCAAATGAGATT | 8027 |
rs573464053 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692129 | CATTTTATTGATGAG[G/T]AATTTGAGGCACCAA | 8027 |
rs573503142 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17670250 | TTTTTTATTTTACTA[A/T]GTCTTAAAAACATCG | 8027 |
rs573549936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17663103 | CAACTATAAATATTC[C/T]ATGTTTTTCCAGTTA | 8027 |
rs573559472 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17707828 | TCAATCTCTTTAGAT[G/T]AAAAAAATGCATTTT | 8027 |
rs573574600 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17669095 | TTTGATCTATTTGGA[A/G]TTTATCCTGTTAGGC | 8027 |
rs573605120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17699267 | ATTGGAGGAAATGTA[A/G]TATTCCATCAAGCAT | 8027 |
rs573622100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17692443 | AAATGAGTGTGAGAC[C/G]TGTAAAGTACCGGTA | 8027 |
rs573631281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17663640 | TTTTAAATCCCCATT[A/G]AGTTAATCTTCAAGC | 8027 |
rs573675682 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | STAM | GRCh38.p7 | 10:17650924 | CAAAAAATTAGCCGG[A/G]CGTAGTGGCGGGCGC | 8027 |
rs573675751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17656434 | TCACTGTAGGTTGGT[C/G]TGGTGGGCCATTGAC | 8027 |
rs573710371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17655919 | GAAATATAATGATTT[C/T]TTTAAAGTTTTTTTT | 8027 |
rs573716832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17703630 | TAGATGTGTGTATGT[A/C]ATAATGGTTTCATTC | 8027 |
rs573733885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17657046 | TGTATGCATGCCCAT[C/T]GGAGGCTTTTTTCCC | 8027 |
rs573834472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17651523 | CCACTGGATTAAGAA[C/G]TTGTATTCTTTGATT | 8027 |
rs573866161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17686532 | CAGGCATGCGCCACC[A/G]CGCCTGGCTGGTTTT | 8027 |
rs573892360 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17647471 | AAGTTGAGTGCCCTG[A/C/T]GGCTCAGTTCCGGAG | 8027 |
rs573894765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17657540 | TTACACAGAATTAGT[A/G]TAATTTCTTCCTTAA | 8027 |
rs573970855 | snp | A/G | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713710 | TCCACCATTACTGCC[A/G]TGGCTCTTCTGCTGG | 8027 |
rs573995373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17673981 | GTAGGATGAGTAAGC[A/G]TTGACTAAGAACAGC | 8027 |
rs573995723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17680117 | TCCTTCTCCTTTGCT[G/T]GCTTTGGGTTTCCTT | 8027 |
rs574035304 | snp | A/C | | | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696410 | AAAGAGCAATGATTT[A/C]GGAATGGAGACTGAA | 8027 |
rs574073995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17690965 | CATAGCTTATTTCTG[C/T]GCTTCTCTACTGGTA | 8027 |
rs574077821 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717105 | CAGTGGGTCACACCT[C/G]TAATCCCAGCACTTT | 8027 |
rs574264229 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, synonymous-codon | STAM | GRCh38.p7 | 10:17713296 | GGACCTCATGAAGCC[C/G]GGTGATTCTGAATGC | 8027 |
rs574373713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17650330 | ATCCATTATACATCA[G/T]GCGGATGCTATGAGG | 8027 |
rs574519010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706769 | CAATATGTATAGCCT[C/T]TTGCAGGTCAGACAT | 8027 |
rs574539226 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17667383 | CTCCTCAGCCTCCCA[A/T]AGTGCTGGTATTACA | 8027 |
rs574553766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17712427 | ACACATATGGAGTGA[A/T]GACAAATAATGCCTT | 8027 |
rs574563128 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17661293 | TTTGTGCACTTTCAT[G/T]TGAAAAAGATTAGGA | 8027 |
rs574585505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706443 | GAGTGCAGTGCTGCA[A/G]TCTCAGCTCACTGCA | 8027 |
rs574589749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17678321 | ATGCAGCGGCACAAT[C/T]TCAGTTCACTGTAAC | 8027 |
rs574590982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17700572 | TGTTTACAGTTTTTA[C/T]AGTGTAGTAGTGAGA | 8027 |
rs574596461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17661719 | TTACTCAATTCTGTC[C/G]ATCTGCCTTCATAAT | 8027 |
rs574618795 | in-del | -/T | 0.196206 | 0.244144 | intron-variant | STAM | GRCh38.p7 | 10:17679581 | TTAATTTGCGTGTGT[-/T]TTTTTTTTTTAAATG | 8027 |
rs574627566 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17700074 | TTTCTTAAATTGCGC[C/G/T]TTTTAGCTTGCTGGG | 8027 |
rs574658649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17701405 | TAAGGATTTTTGAAG[C/T]GTCACATTGTATAGA | 8027 |
rs574716309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17672939 | TGTTCTTTGTCCCTG[C/T]CCCTGACCCCTATCT | 8027 |
rs574751212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17705323 | GAGCTCACAAATGAC[C/T]CATATGTTAGTAACT | 8027 |
rs574787944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17710282 | TTGTGAATGAGATAA[C/G]CTGTTGGTAGGTGCT | 8027 |
rs574820205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17701904 | TAGTTAACACAGCTG[A/G]GATGGTTCCATATTT | 8027 |
rs574835141 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17694183 | TTATTGTAGGTATCT[A/T]CTCCTGGTTTTTGAC | 8027 |
rs574895070 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17707930 | GAGTCTTGCTTTGTC[A/G]CCCAGGCTGGAGTGC | 8027 |
rs574930128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17658446 | AAATGTCAATTGTCA[A/G]TTATATACAGTTGAT | 8027 |
rs574941374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17686168 | ATTGTCTTTTAATGT[C/T]CTGAATGTCCATCGA | 8027 |
rs574946195 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17683911 | TGTTAAGGAGTATTG[G/T]ACTTTATTTTTTCAG | 8027 |
rs575023456 | snp | A/C | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688600 | CCTGAGTAGCTGGGA[A/C]TACATGCACGTGCAG | 8027 |
rs575062559 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17654988 | TTTTGATGACTTTAC[A/T]TTTTACTTTATTCAC | 8027 |
rs575099573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688807 | GCTTTATTAATTAGG[C/T]AACACTGTCTTTTTA | 8027 |
rs575100807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17660329 | AGATGGCCATGAAAA[C/T]AACTAGAATGCTGGC | 8027 |
rs575172665 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17652846 | GGAGCAGGCTCTGGG[A/T]CTCCTCAATCAGAGC | 8027 |
rs575211811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17648064 | CCAATGTCTAGGAGT[A/G]TCACTGATTCTTCTT | 8027 |
rs575222209 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17711257 | TTGTTAGTTGGGGAA[C/G]GTGTCACTGATGACG | 8027 |
rs575244068 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17646112 | TTTTATCTTTCAACA[G/T]ATCCTTGTGTGTTAA | 8027 |
rs575259286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17687355 | TGGTGCGCGCCTGTA[A/G]TCCTACTCGGGAGGT | 8027 |
rs575260775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17653867 | ACCAAGAGACAACTG[C/T]GTATCTCTATTGGCT | 8027 |
rs575270419 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17699239 | GGGCATATCTCATAA[G/T]ATTGGGAGATTCATT | 8027 |
rs575278528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687634 | GAAAAAATGCATAGT[C/T]ATGAACATTAAGAAG | 8027 |
rs575318831 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17693473 | AGAGGCAATTACTGT[A/C]ACATGTATCCTTTCA | 8027 |
rs575323132 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | STAM | GRCh38.p7 | 10:17665424 | TTACCACTTACGTAA[A/G]TTTTGTATCTTTCCA | 8027 |
rs575328932 | snp | G/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715461 | GCATACTACTGGCTG[G/T]CATCACACCAGCGTA | 8027 |
rs575415828 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17670444 | CTACCTTCACTGTGC[A/T]GTGTGCTTAGGTGCT | 8027 |
rs575422896 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17663834 | TACTGTTTAACATAC[A/T]TCTCCAGTTGTGTTT | 8027 |
rs575505588 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17664366 | CCCGCTGTCTGTCTC[C/G]AGAACTTATCCATCA | 8027 |
rs575572055 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17646649 | AAAGTTGCTCAGGTT[C/T]TGGTATTGGACCAAT | 8027 |
rs575603033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17707253 | TCTCTGCTCAAAATA[C/T]AAAAAATTTAGCCTG | 8027 |
rs575653454 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17715949 | CGTTTATATAGGTAT[G/T]GTTTTCTTTCACACT | 8027 |
rs575694395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714333 | CCCAACTTTTTTTAC[A/C]CAATGGTTAAATAAC | 8027 |
rs575703014 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17702293 | ATCCCATATGGTCAT[C/T]GGTAGAAAACTTTCA | 8027 |
rs575728860 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17703092 | CTATGTAGAAACCCT[A/G]CTTCTTTGACACTAA | 8027 |
rs575731025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17676435 | AGTTCATCAGCTGAC[A/G]TATGTAGGCAGTTAT | 8027 |
rs575752146 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17680332 | TGTATACCCATTAAA[A/C]AATTAAACAATAACT | 8027 |
rs575761992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17708337 | CCCTGCTTTAGAAAG[G/T]TAGCTTGCTCTATTG | 8027 |
rs575765503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17707724 | CCTGTGTGGGTCTGT[C/T]GTTTAACAGAAGTGC | 8027 |
rs575797993 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17648642 | ATCATCACCTTTTTC[G/T]GTCTCACCATTCTTA | 8027 |
rs575841010 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17675862 | TGAAAGTCTTGCTTA[C/T]CTAATTAGATTAATC | 8027 |
rs575870647 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | STAM | GRCh38.p7 | 10:17673294 | TGTTTTCCACTTAGC[A/G]AACTCAGTGGAAGAT | 8027 |
rs575880780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17703752 | GAAACCACTAGTCTT[C/T]CTCCTTCCTTTTATG | 8027 |
rs575910216 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | STAM | GRCh38.p7 | 10:17683351 | ATTTTTTGTAGAGAT[A/G]GGGTTTCACAGTGTT | 8027 |
rs576001240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17673756 | AGACTCTGGAGTCAG[A/G]TTGTCTGCTTGTGAG | 8027 |
rs576040060 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704157 | AAGTGCAGTGGCGAG[A/T]TCATAGCTCACTGCA | 8027 |
rs576130709 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17674933 | CTTGAGACACTCAAT[C/G]CTTAAGAATGGAATG | 8027 |
rs576303431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17656973 | AGAGTGGGCGGCCCA[C/T]ATGCGCAGTGCCCTC | 8027 |
rs576310795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17679475 | ATCTCTTGTCATATA[C/T]ATGATTTGGAAATAT | 8027 |
rs576315339 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17654772 | TTACATATTGGTGAT[A/C]GATTAATATTTTTCA | 8027 |
rs576340290 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | STAM | GRCh38.p7 | 10:17656564 | TTCTTGGAGGGTAAC[A/G]GTACAAATGTTGAAT | 8027 |
rs576342334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17663004 | TTTTTATCTTTACTT[C/T]GGTGTTTTTCATTTT | 8027 |
rs576347837 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17685454 | CCCCAAACTGTTCCA[G/T]ATAGGGCCAGATGAG | 8027 |
rs576395753 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17660376 | TGTTAAGACTTGATT[A/G]TACTATAGTTTTGTG | 8027 |
rs576401554 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17655712 | TTTCATTATCACTTG[G/T]TCAAGACCAACCATT | 8027 |
rs576417059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17655872 | TTCCAGTCAAGACTG[A/G]TTACCCTCTGCTTCT | 8027 |
rs576439331 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17657083 | GGTGGAGTGCCCCAG[A/G]AAGGTCGTATACTGC | 8027 |
rs576453732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17690036 | TGGTTAATCTAGAAT[C/T]TTAGCCACGGAAACA | 8027 |
rs576458064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17662252 | CATTTCAGCTCAACT[A/G]TCTGAGTTCCAGTGC | 8027 |
rs576490777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696277 | GCTTGCTAGCTTTCC[A/G]TATACTAGAGTTTAC | 8027 |
rs576712823 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17700599 | GAGATTTTTTTTTTT[A/T]TTGAACATCTATCTT | 8027 |
rs576738420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17666380 | AAATGTTTTTCCTTG[A/G]CTTTGTATTTTTTTT | 8027 |
rs576782121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17654939 | GTAGTCTGTATTTCA[C/G]CCAGCCTAGATTCTT | 8027 |
rs576794328 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17703102 | ACCCTACTTCTTTGA[C/T]ACTAAATAATTTTAA | 8027 |
rs576804221 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17709664 | GTATTCTAGAAGTTA[C/T]GACATTCTAGCTGGC | 8027 |
rs576862734 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688730 | GGCCTCCCAAAGTGC[C/T]AGGATTACAGGTGTG | 8027 |
rs576918870 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716461 | GTTTAAAATATGTTG[C/T]CCTGCCCTGAAGTCA | 8027 |
rs576922319 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687762 | GTACAAACCTTGCTT[C/T]GTTGCAAAATATTCT | 8027 |
rs576965973 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17704865 | TGTATATTTTTATTA[C/T]TCCAAATTAAATCTT | 8027 |
rs576983282 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17657241 | CTGTTAGGAGCTTCT[C/G]TCTCCTTGGTGCAAG | 8027 |
rs577009950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17678285 | TGGAAGACAGAGTCT[C/T]GCTGTGTTGCCCAGG | 8027 |
rs577025437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17705257 | CGTAGATAGGTCGTT[C/T]TAAAAACAAGGGCTA | 8027 |
rs577070340 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17672291 | TGTTGAAAACTTACT[A/G]TGGGCCATTCAAAGA | 8027 |
rs577083359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17706038 | ACACCACTGCAGTCT[A/G]GCCTGGGCAACAGCG | 8027 |
rs577182799 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715383 | TACTAATTGTGAGCT[A/G]AAGAGATATATATAT | 8027 |
rs577326773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17664928 | TATTTTTTAAATCAA[A/G]ATGATTTGTAACTAG | 8027 |
rs577335992 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | STAM | GRCh38.p7 | 10:17699867 | TAGGCCATTGTAAAA[C/T]TTTGCTTTTGTCCTC | 8027 |
rs577346916 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | STAM | GRCh38.p7 | 10:17692184 | CAGCTAGAAAGTGGT[A/G]GATCTGGGATTTGAA | 8027 |
rs577380587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17664943 | AATGATTTGTAACTA[A/G]TAATATATAGTAGAA | 8027 |
rs577396879 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17659124 | TAAAATCTTTTTTTT[A/T]TAGTAATTGCCTAAG | 8027 |
rs577496648 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17662453 | TGAATCCTCAAAGCA[C/G]TCTATCAAAACTATT | 8027 |
rs577496761 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17693994 | AATCTGGTAGGTTTA[A/C]AATGATGTCCTGTTA | 8027 |
rs577531712 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698260 | GTTTAAATGGCATTG[C/T]GTAGTGTGCTGACTT | 8027 |
rs577572363 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | STAM | GRCh38.p7 | 10:17703662 | TTCCATTGGTCTGTA[C/T]AACAAAAGATTCTGA | 8027 |
rs577618930 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | STAM | GRCh38.p7 | 10:17654367 | AGCTGGGACTACATG[C/T]GCCCACCACCAAGCC | 8027 |
rs577620039 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698499 | GTTTTTCACTCTGGA[C/T]GATCTAAAAGAGAAA | 8027 |
rs577622637 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17652995 | TGGAATTTTCTGAGT[G/T]ATAAGAGCATCTTTG | 8027 |
rs577625241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17658390 | TGCATGAGAGCTTGG[A/G]AAGAATGTGTATTCT | 8027 |
rs577649229 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17708126 | CGATCTCCTGACCTC[A/G]TGATCTGCCTGCCTC | 8027 |
rs577680851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17704143 | TGTTGTCCAGACTGA[A/C]GTGCAGTGGCGAGAT | 8027 |
rs577787728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17653412 | AAAAACTCTGAACAC[C/T]GAAGCTCAGTTAAGC | 8027 |
rs577831311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17654987 | GTTTTGATGACTTTA[C/T]TTTTTACTTTATTCA | 8027 |
rs577841940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17676034 | GCTGATAGAATTCAT[A/T]AAAAAAAAAATCTGT | 8027 |
rs577913072 | snp | A/G | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715505 | TTTGGTGCAATTATA[A/G]CAAATGATAATGTTC | 8027 |
rs577928623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17668514 | GTTTTGACAGTGTAT[A/G]TAATGACATGTGTCT | 8027 |
rs577990331 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17694062 | GTTCTTTTTTTGTAT[A/G]TTCACTGGTCATTAT | 8027 |
rs578041876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17685609 | TTCTGTGTGTTTAGC[A/G]ACATACTTGATCTTT | 8027 |
rs578054811 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17655975 | CTTAAGTTGCTTTTT[A/T]CTTTTTCTTTTTTTG | 8027 |
rs578146582 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | STAM | GRCh38.p7 | 10:17674790 | GTTATCTTTGGAATA[A/C]ATAATTTGCCTGAGG | 8027 |
rs578199485 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714313 | TATTTCCGCAAACCA[A/C]CCCCCCCAACTTTTT | 8027 |
rs578202293 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | STAM | GRCh38.p7 | 10:17707915 | CTTTTTTTTGAGACG[A/G]AGTCTTGCTTTGTCG | 8027 |
rs578204277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | STAM | GRCh38.p7 | 10:17675204 | CATAAAAGCCTAATT[A/G]AAGATAATAGCATTT | 8027 |
rs745496250 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17692022 | AAACCCTGAATGAGC[C/G]CATCTCATCTGATTT | 8027 |
rs745716563 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645490 | GGTGAAATCATAGGC[A/G]AGTTAAATTCTTTGA | 8027 |
rs745976199 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696920 | TCTAATCCTTTTCTT[A/G]ATGGAAGTTGAGTAA | 8027 |
rs746019172 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17651344 | AAAGCACTTAGCATA[A/G]CACCTGGCATGTAGT | 8027 |
rs746028984 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17666678 | CTGGGATTACAGGCA[G/T]GAGCCACCCTGCCTG | 8027 |
rs746042481 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17686704 | TTTTAAAAAATTTCC[C/T]TTTATTAAACAAATT | 8027 |
rs746243941 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17685345 | GCTTCCTGGCCATCA[A/C]AGGATTTTAATACTA | 8027 |
rs746564226 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17658372 | GTCTGTCTTGGTGAA[C/T]GCTGCATGAGAGCTT | 8027 |
rs746618213 | snp | C/T | | | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696257 | TTCAAAAACATGTAT[C/T]GAGTGCTTGCTAGCT | 8027 |
rs747178048 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17651559 | GTCCCTATTTTACCT[C/G]TCCTCTAAGCTGTTT | 8027 |
rs747587605 | in-del | -/TGGCGCGA | | | intron-variant | STAM | GRCh38.p7 | 10:17707948 | CAGGCTGGAGTGCAG[-/TGGCGCGA]TCTCAGCTCGCTGCC | 8027 |
rs747669835 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17709601 | CTCTGAGCTGAAATC[-/T]TTTCCTTGAAGCAAA | 8027 |
rs747672498 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643490 | AGTCTAGGGAGGCTA[C/T]CTTGGGCTGTGAAAG | 8027 |
rs747755995 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17678689 | TCAGTGGTATTTAGT[A/G]CATTCACAGTATTAT | 8027 |
rs747959064 | in-del | -/TAAT | | | intron-variant | STAM | GRCh38.p7 | 10:17677586 | AAGGCAAAATCTAAA[-/TAAT]AGTGTTAAAGTACAT | 8027 |
rs747979930 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698157 | TTGCCAGGGTGTCTG[A/G]TGTCATTTTTATAGA | 8027 |
rs748066951 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716360 | GCACCGTAGTTTTAA[A/C]TCTGAGCCTGTGAAA | 8027 |
rs748117187 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17651015 | GCTTGCGGTGAGCCA[A/G]GATCACACCACTGCA | 8027 |
rs748243707 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17703144 | TATTCTGTAAGCAAA[A/C]AAAACGGAAACCATC | 8027 |
rs748326842 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17654358 | CTCCCAGGTAGCTGG[A/G]ACTACATGCGCCCAC | 8027 |
rs748623864 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644853 | TTTTGTAACGGTAAC[C/T]GAAGGAGGGAGCTCT | 8027 |
rs749010279 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17709892 | TGGCAAGGCCCACAT[A/G]TCAGAAAACAGGGCA | 8027 |
rs749163696 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17660366 | TCTGATTTGTTGTTA[A/T]GACTTGATTATACTA | 8027 |
rs749433169 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17683028 | ATGAAAACTGCTAAC[A/G]GTAGTGAATAGATAA | 8027 |
rs749622200 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17675314 | TTTGAGACCAGCCTG[C/G]CCAATGTGGTGAAAC | 8027 |
rs749674480 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17655942 | TTTTTTTTCCTCCTA[C/T]GTGTGTATTCTTTTT | 8027 |
rs749981904 | in-del | -/G | | | intron-variant | STAM | GRCh38.p7 | 10:17665455 | TTCTTTTACACAAAT[-/G]TGAATACATTTTCCC | 8027 |
rs750020085 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17686180 | TGTCCTGAATGTCCA[C/T]CGAGATTACAACTGT | 8027 |
rs750071377 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17649230 | GCAACATAATGAGAC[C/T]CTGTCTCTACAAACA | 8027 |
rs750117968 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17667522 | ATTCTCTTTGCGTTC[A/G]TCATTTTTTCTTTTA | 8027 |
rs750192688 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17682254 | GTCAGTACTCCTGTG[C/T]CTAGCACTAAATGTG | 8027 |
rs750317388 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17702862 | AAAATACAAAGATTC[G/T]CTGGACGTGGTGGTG | 8027 |
rs750505822 | snp | G/T | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688996 | AGCACCTGAAGCATT[G/T]TCTCCTTAGTAAGAG | 8027 |
rs750574138 | in-del | -/CTTAAA | | | intron-variant | STAM | GRCh38.p7 | 10:17661121 | TTAGGGGAATAGAAT[-/CTTAAA]CTTTTTGGCATGTAT | 8027 |
rs750613759 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17709277 | ATTTATGTTTAGTGA[A/C]TATAATTTGTCATTT | 8027 |
rs750717977 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17678249 | GTGATCAACTTTCTT[C/T]ATGTGGTGTAATTTT | 8027 |
rs750843711 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17659669 | GGCCTTGCTCTGCTG[A/C]CCAGACTGGTCTCCA | 8027 |
rs751092644 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698073 | TACTTCACTTCTCTT[C/T]CAAGAGAAGGCTTGA | 8027 |
rs751180874 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17699485 | GCTACTGTTATGTTA[A/G]ATTGTTTTTAAAGAT | 8027 |
rs751236672 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17652087 | TATTCTCAGGATAAA[A/G]TGAGATCATTATGAA | 8027 |
rs751448882 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17684209 | GCCTCTAGGCAGAAA[A/G]TTGAGGCAAACTTCT | 8027 |
rs751460681 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716080 | ATGCGAAAAATGTTT[C/T]CCACTGACATTGTAA | 8027 |
rs751745318 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17654279 | CCAGGCTGGAGTGCA[A/G]TGGCATGATCTCAGC | 8027 |
rs752041561 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17661490 | TCTTTATGTAGATGG[C/G]ATCTGTATTTGCAGC | 8027 |
rs752044314 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17660035 | TCTTTCCTTCAGTCC[C/T]CTCTCCATATTATCA | 8027 |
rs752317327 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17681546 | GAATAATATATTGTA[G/T]TATTTCTAGTTCAAA | 8027 |
rs752712609 | in-del | -/TTTC | | | intron-variant | STAM | GRCh38.p7 | 10:17669688 | GGAATTTCCCTTCTT[-/TTTC]TTTCTTTCTTTCTTT | 8027 |
rs752724387 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17705212 | AAGTGAGGATTTGAT[C/T]GACCTTTGCAATATA | 8027 |
rs752894130 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17676416 | AATTGAATTTGATGC[G/T]TTCAGTTCATCAGCT | 8027 |
rs753146195 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17649139 | CTGAATGCAGTGGCT[C/G]ACGCCAGTAACCCCT | 8027 |
rs753645884 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17702758 | CTCTCGCCTGTAATC[C/G]CAGCACTTCGGGAGG | 8027 |
rs753647073 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17699837 | GAGGGTTTATTTTAA[A/G]TTGCAGAATTCACTT | 8027 |
rs753842298 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17654093 | CTTCAACCTGTGAAG[C/T]CTTTGCTGACTGGGT | 8027 |
rs754274790 | snp | A/C | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715616 | TTATTTCTCATTTTA[A/C]AGAAATGATGTTGGT | 8027 |
rs754296535 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17693725 | GTCTTCCTACTGATG[A/G]ACCTGTGGATTATTT | 8027 |
rs754767074 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17667746 | GGTATGAGGGGGTTA[C/G]GTTTATGCTATAATT | 8027 |
rs755276907 | snp | A/C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17711704 | GGCGTGGTATGTATC[A/C/G]GCATTCCAGCAGCAC | 8027 |
rs755573794 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17709580 | GTTTTTTCTGCTTTA[A/G]TGGGACTCTGAGCTG | 8027 |
rs755699102 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17663720 | AGAGTTGTTTGAAAA[G/T]GATTAAACAATAATT | 8027 |
rs756179859 | in-del | -/CT | | | intron-variant | STAM | GRCh38.p7 | 10:17706839 | TTAGAGCTAAGAAAA[-/CT]CTCTTAAATATCTAA | 8027 |
rs756206022 | in-del | -/CTG | | | intron-variant | STAM | GRCh38.p7 | 10:17657095 | CAGGAAGGTCGTATA[-/CTG]CCATTTTGTCTCTTA | 8027 |
rs756437014 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17673245 | CTCATGGCTTTATTA[G/T]AGTTCTATTAACTAC | 8027 |
rs756606401 | in-del | -/TT | | | intron-variant | STAM | GRCh38.p7 | 10:17646818 | GTGTATAGAATACAC[-/TT]AACAATTTTTTCTTT | 8027 |
rs756716913 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17665198 | CTTCTCTTAAAAAGG[-/A]AAAAAACCAGACAAA | 8027 |
rs756822813 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17647262 | TTTCATCAAGTTTGT[A/G]TTTCAAAGTCTCTAG | 8027 |
rs756839222 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17649196 | ATTCCTTGAGGCCAG[A/G]AATTGGAGACCAGTC | 8027 |
rs756937776 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17680670 | CCTTCATCTCCCAAA[A/G]TGCTGGAATTATAGG | 8027 |
rs756985086 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17702768 | TAATCCCAGCACTTC[A/G]GGAGGCCGAGGCGGG | 8027 |
rs757003983 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17712321 | GACTCCAGAACCCAG[C/T]GCATAGACTCTATAT | 8027 |
rs757247069 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17700071 | TTATTTCTTAAATTG[C/T]GCCTTTTAGCTTGCT | 8027 |
rs757380840 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17667923 | TTGCCCTGAATGAGC[A/G]CAGAGCTGGGTTTCA | 8027 |
rs757616690 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17676670 | TGTAGTTTATGCCTG[C/G]TGTTCCTCTGTTATG | 8027 |
rs757636838 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17656053 | CAATCCCAGCACTTT[C/G]GGAGGCCAAGGTGGG | 8027 |
rs757835164 | in-del | -/T | | | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695785 | TAAAATTTGCAGGTG[-/T]TTTTTTAAAAATCAG | 8027 |
rs757873516 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17676963 | AACTGAATTAAAAAT[G/T]CATAGGACAGAATGA | 8027 |
rs758106926 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17649495 | TAGTGACCTGACATT[A/G]ATTGATTGATTATCT | 8027 |
rs758297587 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17703061 | AAGAAAATACTTGCA[A/G]AAGCAGACTAATCAT | 8027 |
rs758484467 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17669865 | CCTATGCCCTATGCC[C/T]GGCCAATTCTTTTCT | 8027 |
rs758575065 | snp | C/T | | | upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644110 | GCAGCGCCAAGGTCG[C/T]CCAGATTCCCGACAA | 8027 |
rs758754692 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17659756 | GCATGAGCCATCCTG[C/G]CTAGCCTCTAATGCT | 8027 |
rs758952996 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17658070 | TATTGATTTTAGATC[G/T]TGATTCTTTTTAAAA | 8027 |
rs758992603 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17678276 | TTTTTTTTTTGGAAG[A/G]CAGAGTCTCGCTGTG | 8027 |
rs759026670 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17653716 | AATTAGGCATGATAA[A/G]TGATCTAGAGAAATT | 8027 |
rs759374574 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643856 | AAAAAGGCGCACAGC[C/T]CGACCCGAACTCAAC | 8027 |
rs759810598 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17663048 | GTAATAATTGGGTCA[A/G]TTGCTTGAAGTTGTT | 8027 |
rs760512955 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17671904 | TTAATTTAGTAATAT[A/G]TACAGGAATTAGAAT | 8027 |
rs760531560 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17653978 | AATCCTGAAGGGTAG[C/T]GGGAACTTCCAGTTT | 8027 |
rs760929675 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696993 | GGTGCGAGCTCGGAT[C/T]ATTGCAACCTCCGCC | 8027 |
rs761122932 | in-del | -/C | | | intron-variant | STAM | GRCh38.p7 | 10:17685637 | TTTTAGTGTTTTGGG[-/C]CACAACCTGAACAAC | 8027 |
rs761377917 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17686068 | AATGTAAAATTCTGT[A/G]CTTTTCGAACATCAT | 8027 |
rs761400021 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17667275 | GGGATTACAGGTGAA[C/T]GCCACCATGCCCGGC | 8027 |
rs761422670 | in-del | -/TT | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715778 | CATTTTCGAAGTCTC[-/TT]GTAATTATTTGGGAT | 8027 |
rs761685570 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17676145 | AGAAAGCACAGTAGC[A/T]CAGTTTGGATATTTG | 8027 |
rs761920580 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17709161 | ACTCGCTCAACTCAT[A/G]TAATCTGGTTTCAGC | 8027 |
rs762010473 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17711084 | CTCGAGCTTTCTAGC[A/G]GCAAATCAAGGTCAG | 8027 |
rs762013835 | in-del | -/A | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697404 | TGGGACCGTTTCTCT[-/A]AGTGTGTAGTCCCAG | 8027 |
rs762366306 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17650666 | GATTAGTACAGTAGC[C/T]TCCAGCTGTTCTTCC | 8027 |
rs762679650 | snp | A/G | | | synonymous-codon | STAM | GRCh38.p7 | 10:17708796 | TGCAGGGCCTCCTCC[A/G]AGTGGTGCCTACCTG | 8027 |
rs762742417 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17706716 | CGTATGTAATTATTT[A/G]CTTAAGAACCTTAGT | 8027 |
rs762908727 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17677633 | TAATGATGCTGCTAT[C/T]CAAAAATTTTAATCT | 8027 |
rs762994184 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17646364 | TTGCTAAATGCCCCC[-/T]GGAAGGACAAAATAC | 8027 |
rs763119188 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17662736 | TACCACCTAAGAATA[A/T]TAATAGTATCATCTT | 8027 |
rs763404119 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17700819 | GAAGGGACACTCATT[A/G]ACTATCTATTGAAAC | 8027 |
rs763470116 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17683436 | CAAAATGCTGGAATT[A/G]TAGGTGTGAGCTGCT | 8027 |
rs763900068 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17674232 | TCAAACCTACCAGCC[A/G]TCAGCTTCCTTTGTT | 8027 |
rs764289939 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17657098 | GAAGGTCGTATACTG[A/C]CATTTTGTCTCTTAA | 8027 |
rs764404926 | snp | C/G | | | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695565 | GAGTATGTATATGTA[C/G]TTAATGCAATTTGTA | 8027 |
rs764717539 | snp | A/G | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715567 | TTCAGAGTATTGTGG[A/G]ACCATGAGACAAAAT | 8027 |
rs764764962 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17649142 | AATGCAGTGGCTCAC[A/G]CCAGTAACCCCTACA | 8027 |
rs765063641 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17656782 | GGCGTAAGGCAGAAA[A/T]AGAGATGAAGCAAGT | 8027 |
rs765241278 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17674647 | GTTATGTGTCTCAGA[A/C]TGTCACTTCCACTAT | 8027 |
rs765300342 | snp | A/G | | | upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644015 | CTCTTATGTGTGACT[A/G]ATTAAAAGAGGAGTC | 8027 |
rs765419648 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17679935 | GAGAGTAATGTTCCC[C/T]CTTTGTTTTTTGATT | 8027 |
rs765443385 | in-del | -/TA | | | intron-variant | STAM | GRCh38.p7 | 10:17711149 | TAGCACTCCTCAGTT[-/TA]TATATATATCTGAGA | 8027 |
rs765510077 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17660950 | TTCTTCTGGAATCTC[A/G]TTTTTTCCACTGATT | 8027 |
rs765573300 | in-del | -/TTG | | | intron-variant | STAM | GRCh38.p7 | 10:17709214 | AACCATAAGTTTTTA[-/TTG]TTGTTTTTATTTGCA | 8027 |
rs765711772 | snp | C/T | | | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717294 | CTTGAACCTGGGAGA[C/T]GGAGGTTGCAGTGAG | 8027 |
rs765752990 | in-del | -/TG | | | intron-variant | STAM | GRCh38.p7 | 10:17652002 | ATTCAAATGAGGCTC[-/TG]TGTATGTTTTTTCTG | 8027 |
rs765995368 | snp | G/T | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687850 | TGAGATATATATGAT[G/T]GGTTTTTTCATAGTG | 8027 |
rs766241252 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17706745 | GTTCTTCATCAGGTT[A/G]TGTACACTCAATATG | 8027 |
rs766391436 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17657003 | CCTTATACTTGGGAG[A/G]TGAGCATGCACAGTG | 8027 |
rs766442690 | in-del | -/GAG | | | intron-variant | STAM | GRCh38.p7 | 10:17693168 | TCTTAGGGTGGGTGA[-/GAG]GAGGAGAATTTGATA | 8027 |
rs766483019 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17662835 | TGAATGAGTGCAACT[C/G]TGCCTGCTTTTGATT | 8027 |
rs766483958 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17658784 | AAGCCACTGTGCCTG[A/G]CCTCATCCTTTAACT | 8027 |
rs766912879 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17680189 | GATTTGAGATCTTTT[C/T]CCCCAATTCTTTAGA | 8027 |
rs767126649 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17652427 | GTGTAGGAAAGTAAT[A/T]AAGTAGTTCATGAGT | 8027 |
rs767299047 | snp | A/G | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689998 | AAGGAAGAATTAATG[A/G]TTGTGCCATATGTAC | 8027 |
rs767365009 | in-del | -/T | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688370 | GGTGCCAGAAAAGTA[-/T]TATAATGGAATATTA | 8027 |
rs767412086 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643857 | AAAAGGCGCACAGCT[C/G]GACCCGAACTCAACC | 8027 |
rs767477020 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17686422 | CTCTTTGTCACCCAG[A/G]CTGGAGTACAGTGGC | 8027 |
rs767640990 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17674762 | AGTTCATGTCAAAGG[-/A]ATTATTATCATAGTT | 8027 |
rs767787522 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17694996 | TTTTTCTACTTCTTC[A/G]GACTGTTGGATATAA | 8027 |
rs767867954 | in-del | -/TAA | | | intron-variant | STAM | GRCh38.p7 | 10:17646533 | TACATAGGAGGTGTT[-/TAA]TAATGTTTGTTGAGT | 8027 |
rs768140021 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17663357 | TTTTTTTAGTTTTTC[A/G]TATTTATTTTTAAAC | 8027 |
rs768625612 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17647637 | GGCCTAGTTGCTTAG[A/G]TAATCTGTGTCTCAG | 8027 |
rs768670534 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17700430 | TAGACGATGCAGACT[C/G]TTTTTTGAAACTTCC | 8027 |
rs768698800 | in-del | -/AG | | | intron-variant | STAM | GRCh38.p7 | 10:17712911 | GAGGGGTGCAGCTGC[-/AG]AGAGTTGATCAGTGT | 8027 |
rs768867861 | snp | A/C | | | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717208 | TCTTTACAAAACTAC[A/C]AAAATTAGCTGGGCG | 8027 |
rs769107058 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17687352 | TGGTGGTGCGCGCCT[A/G]TAATCCTACTCGGGA | 8027 |
rs769182137 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17685714 | CTATGGTGGAAAACA[C/T]GCAGCTGGCTAGGTC | 8027 |
rs769245052 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17709641 | GGCTTTTAAGAGTTT[-/A]CCAACGTGTATTCTA | 8027 |
rs769345769 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643601 | GCAGATTCCAAAGCC[A/G]GGCGTTCAGGGACTC | 8027 |
rs769352732 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17667170 | TCACTTTTGTTGCCC[A/G]GGCTGGAGTGCGATG | 8027 |
rs769439510 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17708548 | CTTTAATGCTTCAGT[A/G]TGGAGATAACATGAG | 8027 |
rs769656182 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17677596 | CTAAATAATAGTGTT[A/G]AAGTACATAATTTCT | 8027 |
rs769704343 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17682811 | GTACTTTTTTTTCTT[G/T]TGTTATCAAGTCATT | 8027 |
rs769792902 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645874 | ACAGCTTCTTAATAC[C/T]TGCTTCTTCTGTTTA | 8027 |
rs770011956 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17699167 | AGGCTTTGTCATTTA[C/T]TAGCTTTCTCTTTTA | 8027 |
rs770033572 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17700787 | AAGGATATTAAGATT[C/G]TTTGCACATGACTGA | 8027 |
rs770373996 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17670869 | TTATATGTTGTGTGG[-/A]TTATGTTTTATGTAA | 8027 |
rs770459751 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17673377 | ATATTAGTTGTACAA[C/T]AGTGAAAAGCAGTAT | 8027 |
rs770470301 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17709894 | GCAAGGCCCACATGT[C/T]AGAAAACAGGGCATT | 8027 |
rs770654713 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17661821 | TTTTCTTCAGGGGCT[A/G]TATACCCTCCACTCT | 8027 |
rs770693658 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17660411 | AAATGTGATTATGTA[G/T]CTTTTAAAGATTTGA | 8027 |
rs770963388 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17679025 | CCATTCTTTCGTTGA[C/T]GGACATTTGGCTGTT | 8027 |
rs771872475 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17660643 | GTAGGCCCAGCCCCT[C/G]GGTAGGATGAGGTGG | 8027 |
rs772104313 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17662035 | GTCCTACTTTACTTT[G/T]GACGTTCCTTACCTT | 8027 |
rs772525634 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17706054 | GCCTGGGCAACAGCG[A/G]CACCCTGTCTCTAAA | 8027 |
rs772597757 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17666838 | GAAAGGACAGCATCA[G/T]TAGAGAAACAGACCT | 8027 |
rs772760134 | snp | C/T | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689754 | TTTGGTTCTTGTTAA[C/T]TCAAAACTTGGTTTG | 8027 |
rs772881047 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687776 | TCGTTGCAAAATATT[C/T]TGAAAAGTCCTTTCA | 8027 |
rs773317641 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17645941 | TTAGCTAGCAACTAC[C/G]CAATCACCTTTATAT | 8027 |
rs773584415 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17651889 | TCCTGTCAGCATTTC[G/T]TACCTCCCCAGATCT | 8027 |
rs773787203 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17653470 | GATACACACTGATGT[A/G]TTTGGAGGGTGATGA | 8027 |
rs773892172 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17673386 | GTACAATAGTGAAAA[A/G]CAGTATTTTTCGTGT | 8027 |
rs773987821 | snp | A/G | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689948 | GCAAGTGAAAACTGC[A/G]TTTCAGTCCACAAAG | 8027 |
rs774072938 | snp | C/G/T | 1.6492e-05 | 0.00287154 | missense, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688096 | GAATTTAAGAATGAT[C/G/T]CACAGCTTAGTCTAA | 8027 |
rs774154709 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17679078 | TGAACATGGGTGTAC[A/G]GATATTGGTTAGAGT | 8027 |
rs774434952 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17664397 | TCCCAAACTGAAACC[A/C]TGTGCCCATTAAACA | 8027 |
rs774549663 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17694887 | GTTGTGAATGAATGA[A/G]TAAACTGACAAAATG | 8027 |
rs774954667 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17681306 | CCTTTTCATTAATCT[C/T]AAAGTATTTTCTAAT | 8027 |
rs775031281 | snp | A/G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17703612 | ATATACTTATATATC[A/G/T]TATAGATGTGTGTAT | 8027 |
rs775140348 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17673967 | GTAAGCTCTGATCTG[C/T]AGGATGAGTAAGCGT | 8027 |
rs775301105 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645562 | TCCATTCTGCAGTTA[A/G]ATAATATGTCTAGAG | 8027 |
rs775323470 | snp | C/T | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17690030 | CTTGTTTGGTTAATC[C/T]AGAATCTTAGCCACG | 8027 |
rs775389536 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17712894 | AGGGAAGCTCAGTAC[A/G]TGAGGGGTGCAGCTG | 8027 |
rs775400344 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17662073 | CTAGCGAATTAACCC[A/G]CTGGCATTTTTTTTC | 8027 |
rs776003458 | in-del | -/AAAT | | | intron-variant | STAM | GRCh38.p7 | 10:17706067 | GACACCCTGTCTCTA[-/AAAT]AAATAAATAAATAAA | 8027 |
rs776166144 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17685615 | GTGTTTAGCAACATA[C/T]TTGATCTTTTAGTGT | 8027 |
rs776540257 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17647661 | GTCTCAGTTTCCTTA[A/T]CTTTAATATGGAATA | 8027 |
rs776648226 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17692629 | AGTGTGAATTGAATT[A/G]TATGTTTGTTGTGTA | 8027 |
rs776736487 | snp | G/T | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17681010 | AATTGCTGGAGCATA[G/T]GGTAATTCTATTTTT | 8027 |
rs776819568 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17660719 | TTACACCCATGAACA[A/G]CCAATGTACACGAGT | 8027 |
rs777041570 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697284 | TAAAAATGCAAATTC[A/G]TTAAGAAGTCTTACA | 8027 |
rs777212885 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17668495 | GTTTTGTACAGGTCA[A/G]TGGGTTTTGACAGTG | 8027 |
rs777281170 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17680603 | GTAGAGACAGGGTCC[C/T]ACTATATTGCCCAGG | 8027 |
rs777472677 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17699707 | CGTGGCACGCCAGAT[A/G]ATACATAGCTGATTT | 8027 |
rs777550306 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17651057 | GTGACAGAGCGAGAG[C/T]CCGTCTCAAAAAAAA | 8027 |
rs777572078 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17661763 | GACGTTTTAAAGTCT[C/G]CTTAATCAAGTTTTT | 8027 |
rs777834877 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17652522 | GTAAGATAGCACTCA[A/G]CTATGATAGTAGGCA | 8027 |
rs777983471 | in-del | -/C | | | intron-variant | STAM | GRCh38.p7 | 10:17703586 | GGATTTTTTAAAAAA[-/C]ATAAATACATATATA | 8027 |
rs778456861 | in-del | -/C | | | intron-variant | STAM | GRCh38.p7 | 10:17692021 | TAAACCCTGAATGAG[-/C]CCATCTCATCTGATT | 8027 |
rs778515327 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17649225 | TCTGGGCAACATAAT[A/G]AGACCCTGTCTCTAC | 8027 |
rs778822078 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17700072 | TATTTCTTAAATTGC[A/G]CCTTTTAGCTTGCTG | 8027 |
rs779207108 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17657309 | TTGCTGAATCACCCA[A/G]CATTCCTAGTGGGTG | 8027 |
rs779275774 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17707225 | CCATCCTGGCTAACA[C/T]GGTGAAACCCTGTCT | 8027 |
rs779277482 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17685213 | CTAATTAAATAATAT[C/T]AGTCTATTTTACATA | 8027 |
rs779851369 | in-del | -/C | | | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17715981 | GATTTTTGGGTTGCT[-/C]TTTCTGGCCTTTTAA | 8027 |
rs779977873 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17684154 | TTTCACCTGTGCATG[C/T]GTGGGTTTTTCAGAA | 8027 |
rs780012699 | in-del | -/G | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714403 | AAAATAACAATGTTT[-/G]GCACATTATAGCTGT | 8027 |
rs780426611 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17659844 | AGAAGTTCTGCTAAC[A/G]TTGCTTTCAAGGCAG | 8027 |
rs780596889 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17658134 | CACTGCTTTTGTTGC[A/G]TCCCACAAATTTTGC | 8027 |
rs780920229 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17651002 | CCTGGGAGGCGGAGC[C/T]TGCGGTGAGCCAAGA | 8027 |
rs781006991 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17678502 | CAGGTGATCCGCCTG[C/T]CTCGGCCTCCCAAAG | 8027 |
rs781098054 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17665906 | GTGTGAGTAACTAGT[G/T]AAGAATGCCCAGCCA | 8027 |
rs781116547 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17649566 | ATTTTTTTTCCCCTA[A/T]TACTTTAGGGATAGT | 8027 |
rs781376686 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17655501 | CCGGTGGTAGTGACT[A/C]ACTAGCAGGTGATGC | 8027 |
rs781649115 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17691143 | CTAAAGAAAATTGCA[A/G]CTAGAGATAGGTCAG | 8027 |
rs781655655 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644794 | TTGAGCGTCTGGAAC[C/T]GGCAGAATGTTTTAG | 8027 |
rs781785813 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688964 | AGAGGACTTTAGAAG[A/G]GGTAAATGGGAAGAG | 8027 |
rs781788116 | snp | A/G | 3.29565e-05 | 0.00405921 | missense | STAM | GRCh38.p7 | 10:17695090 | AGGCAGCAGTCAACC[A/G]CCCTTTCCACTTTGT | 8027 |
rs781789859 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17692498 | CAGTTTCTGGTAACT[A/G]GCAGAATGGTTGGAA | 8027 |
rs781789901 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642835 | AATTTTTTTCTTTTT[C/T]TGAGACGGAGTTTCG | 8027 |
rs781790602 | snp | G/T | 1.72567e-05 | 0.00293735 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696900 | CCTGCCAATAAATGA[G/T]GTTTTCTAATCCTTT | 8027 |
rs781790994 | snp | A/G | 1.65302e-05 | 0.00287486 | intron-variant | STAM | GRCh38.p7 | 10:17704416 | CTTTTTATATTAACT[A/G]CTTAATTCCTGTAGG | 8027 |
rs781794267 | snp | C/G | 3.30803e-05 | 0.00406682 | missense | STAM | GRCh38.p7 | 10:17693259 | GCCCAGCTCTTGTAG[C/G]CAAGGATCCTGGTAC | 8027 |
rs781797154 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17656033 | AGGTAGTTTCCTCAC[A/G]CCTGCAATCCCAGCA | 8027 |
rs781797614 | snp | A/C/G | 3.45855e-05 | 0.00415834 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644429 | CCGGACTGCACGCTC[A/C/G]CTCTGCCAGCCCCTG | 8027 |
rs781798498 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17660433 | AAGATTTGAAAAATA[A/G]TGTTTCTGCAATCCC | 8027 |
rs781799049 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17686484 | CGGGTTCAAGTGATT[C/G]TCCTGCCTCAGCCTC | 8027 |
rs781802519 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17646156 | TCCAACTTGTTACAC[C/T]TGAGTCATTTCCTGA | 8027 |
rs781805217 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17678201 | TGTTGTAGACATTTC[A/G]TATAAATGGAGCTCT | 8027 |
rs781805537 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17675917 | TGATACCTACAAATA[C/G]CACTCCATGTGGTGG | 8027 |
rs781806065 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17659264 | CCTTCCCATCCCTTG[C/T]GTCATTGCTGTCATT | 8027 |
rs781806131 | snp | A/G | 3.29527e-05 | 0.00405898 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714559 | ACAATGGTCAGTTCC[A/G]TTCAAGGAAACACAT | 8027 |
rs781808328 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17674369 | GCTGGGCAGTTCTTG[C/T]GTGGGGTCTGTCATG | 8027 |
rs781809428 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17680589 | TTTAAAAATTTCTTG[C/T]AGAGACAGGGTCCCA | 8027 |
rs781810287 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17655154 | ATTTGAAACCCTTTC[A/G]ATCTTAAATCTAAGT | 8027 |
rs781810428 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17683217 | CTCTCAGGATGGAGT[A/G]CGGTGGTGCCATCAC | 8027 |
rs781811113 | in-del | -/AT | | | intron-variant | STAM | GRCh38.p7 | 10:17676898 | TTAATAATTATACAT[-/AT]ATATATATATATAAA | 8027 |
rs781813389 | snp | G/T | 1.64917e-05 | 0.00287151 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714814 | GTGGCAGATACCTGC[G/T]AAATGCCACTGACAA | 8027 |
rs781814136 | snp | A/G | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713633 | TGGACTCTTCTGTTC[A/G]TTATCATATTTTGAA | 8027 |
rs781814621 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17691245 | AATGCCTGGCCGGGC[A/G]CGGTGGCTCACGCCT | 8027 |
rs781816370 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17711272 | GGTGTCACTGATGAC[A/G]GTTTTCTAAAGCTAC | 8027 |
rs781816952 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17686525 | GGGAATACAGGCATG[C/T]GCCACCACGCCTGGC | 8027 |
rs781817414 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17682753 | TTGTGTAATGCCAGT[C/T]AGGTCAAGTTTCATG | 8027 |
rs781817529 | snp | A/T | 1.64757e-05 | 0.00287012 | missense | STAM | GRCh38.p7 | 10:17704483 | CAGACCCCAGTGATG[A/T]TCAGCCAGACCTACC | 8027 |
rs781817992 | snp | A/G | 3.2962e-05 | 0.00405954 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714544 | TTCTTCCTCCACAGT[A/G]CAATGGTCAGTTCCG | 8027 |
rs781818802 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17655295 | TGCCTGCAAGTAAAT[C/T]GCTTTATTGAGATCA | 8027 |
rs781819077 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644264 | TTTTGCCTGAGGAGT[C/T]TTCCATCCTACGTCG | 8027 |
rs781821125 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17652922 | AAATTCTCTTATAGT[A/G]TTGAATGATAAATAA | 8027 |
rs781822302 | snp | C/G | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687586 | TAACATGCAGTGTAC[C/G]TCAAACTAGGCCCCA | 8027 |
rs781822595 | snp | A/T | 1.64893e-05 | 0.0028713 | missense | STAM | GRCh38.p7 | 10:17700241 | GATGTTCAGGTAGAG[A/T]CAATAGAACCAGAGC | 8027 |
rs781824632 | snp | C/G | 3.30049e-05 | 0.00406219 | missense | STAM | GRCh38.p7 | 10:17708924 | ACCCAGCCCTTCCTA[C/G]TCAGCAGACTCAGGC | 8027 |
rs781824698 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17681249 | TATAAATTACCTTCT[C/T]ACCGTTTTACTACAC | 8027 |
rs781824956 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17691289 | TTTGGGAGGCCGAGG[C/T]GGGTGGGTCACGAGG | 8027 |
rs781825104 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17648569 | CACAAAGGTCCGTGG[C/G]TTCATTCTTGACGTC | 8027 |
rs781830348 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17680259 | ATGGTATTAAATACC[C/T]GCATAATGTTGTGAA | 8027 |
rs781830434 | in-del | -/A | 1.65395e-05 | 0.00287567 | intron-variant | STAM | GRCh38.p7 | 10:17693198 | TAACAACCCTCAAAT[-/A]ACTGTGTTCCTCTTT | 8027 |
rs781831522 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17694961 | ACTATTGAAGGAAGA[A/G]TACCTTTTATCTTGA | 8027 |
rs781834494 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17650152 | TGAATCTTAAATGTT[A/C]ATGTCACATTCTCCT | 8027 |
rs781835507 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17704377 | TAATAAAGTGAAAAC[A/T]TAAAGTTGCCTAAAG | 8027 |
rs781836085 | snp | A/G | 1.70953e-05 | 0.00292359 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688199 | AATGAAGTTGTGTGT[A/G]TGCTACAGTTTGTTT | 8027 |
rs781837138 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17708552 | AATGCTTCAGTATGG[A/T]GATAACATGAGTTTA | 8027 |
rs781837733 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17667961 | TTAGAAAAATAGAAG[A/G]TGATGGTTGGAAGGT | 8027 |
rs781839550 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17672936 | CCCTGTTCTTTGTCC[C/T]TGCCCCTGACCCCTA | 8027 |
rs781842487 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17666922 | TCATCAAAGTCTTTT[A/G]AATGCTCTTTTAAGA | 8027 |
rs781843420 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17671581 | GGTGTCCCATGACAG[G/T]CGGGTTACTACTGAT | 8027 |
rs781844548 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17675623 | CTTATACAGGGATTC[A/T]CTTAAGTTTTAGAAA | 8027 |
rs781845005 | snp | A/C/T | 3.29469e-05 | 0.00405864 | synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714720 | AACTCTGCCTCAGCC[A/C/T]GGAGGCAGCCAACAG | 8027 |
rs781846010 | snp | C/G | 3.29457e-05 | 0.00405854 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714654 | TGTCACTCTGTACCA[C/G]AATGCAGGACCTAAT | 8027 |
rs781847810 | snp | A/G | 1.65143e-05 | 0.00287348 | missense, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17660517 | GGCCTCATTTTGGAT[A/G]TCTGTGATAAAGTTG | 8027 |
rs781848088 | snp | A/C/T | 3.29647e-05 | 0.00405971 | missense, synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714543 | TTTCTTCCTCCACAG[A/C/T]ACAATGGTCAGTTCC | 8027 |
rs781848218 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17712233 | CTATTACCCCCATTT[C/T]ATAGATGGGGAAGCT | 8027 |
rs781849078 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17698805 | TGCGCGTCAAGAGCT[G/T]TTAGAATATGAAGTC | 8027 |
rs781849453 | snp | A/G | 1.64942e-05 | 0.00287173 | intron-variant | STAM | GRCh38.p7 | 10:17684758 | CTTTGACTGTGAGTG[A/G]TTTCATTTTAATCTG | 8027 |
rs781849539 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17653551 | CATACAGGTGGTTGT[C/T]TGTATCTGGGGGTCT | 8027 |
rs781849965 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17663061 | CAATTGCTTGAAGTT[C/G]TTTGTCAAAAGGCAA | 8027 |
rs781851628 | snp | C/G | 4.98824e-05 | 0.00499387 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644300 | TGACTCCCGTGCTGT[C/G]GAGAGGGAGTCCCCG | 8027 |
rs781852810 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17677448 | TTCAAATAATTCTTT[A/G]TATCTGGCCTTTACC | 8027 |
rs781859426 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17670365 | TAATGTGACTTGTCT[A/G]AAACGAGTGAGCAGA | 8027 |
rs781862099 | snp | C/T | 1.64773e-05 | 0.00287026 | intron-variant | STAM | GRCh38.p7 | 10:17660597 | TTTCTTTTTAAAAAA[C/T]ACGAAAGGCCAGGTG | 8027 |
rs781862985 | snp | A/G | 4.94466e-05 | 0.00497201 | synonymous-codon | STAM | GRCh38.p7 | 10:17695080 | CAAGGAACAAAGGCA[A/G]CAGTCAACCACCCTT | 8027 |
rs781863042 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17648396 | GGACATGGGCGGGGA[C/G]AAATAAGAGAATAAA | 8027 |
rs781863160 | snp | A/G | 1.64909e-05 | 0.00287144 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688101 | TAAGAATGATCCACA[A/G]CTTAGTCTAATATCA | 8027 |
rs781863253 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689057 | GTGGATATGGCTAAA[C/T]AGCTTAACTTTGCTC | 8027 |
rs781864025 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17679235 | ATATTTGGTATCTTT[A/C]CTTTCTTAAAAAAAT | 8027 |
rs781865904 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17701374 | AATACATTAAATTAT[A/G]CAACTAGCAAACCAT | 8027 |
rs781866374 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17710076 | CAAAGGGGCTAGAAG[A/G]TAGGAATTGTTGAGA | 8027 |
rs781867625 | snp | A/C | 1.70749e-05 | 0.00292184 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696889 | GTATTTTCCAGCCTG[A/C]CAATAAATGATGTTT | 8027 |
rs781867826 | snp | C/T | | | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696313 | GGAGTGTACTCTTTG[C/T]GAATGTTTTGCACTG | 8027 |
rs781869476 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17703008 | GTAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 8027 |
rs781869999 | snp | C/T | 4.94507e-05 | 0.00497221 | intron-variant | STAM | GRCh38.p7 | 10:17705058 | ATTTATGTTGTGTAC[C/T]TTCTTTCCTGAAGCT | 8027 |
rs781870396 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17668845 | TATGGATGTTCTACA[A/G]TTTGTTTATTAACCT | 8027 |
rs781871371 | snp | A/G | 1.66399e-05 | 0.00288438 | intron-variant, missense, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17684914 | CTAGTGAAGTAAGCA[A/G]CGTATTAAATAAGGT | 8027 |
rs781871708 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17665752 | TAGATGTAATCCCTG[A/T]TTACTTCATTTAAGT | 8027 |
rs781872656 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17657191 | CTCCCTGGTGCCTGC[A/G]TTCATTTAACACTTT | 8027 |
rs781875033 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17703487 | CCTGCGTACCTATAT[A/G]TAGTAGCATAACCAT | 8027 |
rs781876250 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17656120 | TAACACAGTGAAACC[C/T]GTCTCTACTAAAAAT | 8027 |
rs781877501 | snp | G/T | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697330 | ATATTTTTCTTACCA[G/T]TTGATTACAGTGTGA | 8027 |
rs781877747 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17672745 | AAATCCCTAATCAAA[A/G]AAAATGGAGTAACTG | 8027 |
rs781880033 | snp | G/T | 1.68715e-05 | 0.00290439 | intron-variant | STAM | GRCh38.p7 | 10:17684644 | AGCTAGATGTATTAT[G/T]AAGTAATTTTTACTT | 8027 |
rs781881416 | snp | A/G | 1.64893e-05 | 0.0028713 | synonymous-codon | STAM | GRCh38.p7 | 10:17695071 | GTTGTCTCTCAAGGA[A/G]CAAAGGCAGCAGTCA | 8027 |
rs781882391 | snp | A/G | | | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696349 | AGTGTCATCTTTGAC[A/G]TTCGTTCTGTTGGGA | 8027 |
rs781882862 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17691813 | GAATGTGTTTTAGAA[C/T]TTCATTTTTAAATTG | 8027 |
rs781883583 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17704187 | AGCCTTGACCTCCTG[G/T]GCTCAAGTGATTCTC | 8027 |
rs781885438 | in-del | -/ATA | 1.75462e-05 | 0.00296189 | intron-variant | STAM | GRCh38.p7 | 10:17693345 | GATGGTGGGAATAAC[-/ATA]ATAAGCCTTTATTTT | 8027 |
rs781886445 | snp | A/G | 1.64885e-05 | 0.00287123 | missense | STAM | GRCh38.p7 | 10:17700235 | AGTGATGATGTTCAG[A/G]TAGAGACAATAGAAC | 8027 |
rs781888849 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17647270 | AGTTTGTATTTCAAA[A/G]TCTCTAGTGACTTCC | 8027 |
rs781889910 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17705521 | TTGATATTTTGATGT[A/G]TCATTATTTAGAGCA | 8027 |
rs781890078 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17671435 | TTCTGATAAGGAGGT[A/G]TTAGACATCTCCTCT | 8027 |
rs781890640 | snp | A/T | 1.65184e-05 | 0.00287384 | missense, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688063 | AAATTAAAGGCTCTT[A/T]TGGTTGAATGGACAG | 8027 |
rs781891079 | snp | C/T | 1.65247e-05 | 0.00287438 | missense, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17660530 | ATATCTGTGATAAAG[C/T]TGGTCAGTCTCGCAC | 8027 |
rs781893540 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17711060 | ACTAGAGGTGTCCTG[C/T]GTATTTGACTCGAGC | 8027 |
rs781893567 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17667767 | TGCTATAATTTTAAT[A/G]TTGAAAAGAGACAGA | 8027 |
rs781894511 | in-del | -/G | | | intron-variant | STAM | GRCh38.p7 | 10:17663715 | AATAAAGAGTTGTTT[-/G]AAAAGGATTAAACAA | 8027 |
rs781897894 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17662774 | GAGTTGTTGTGACTT[G/T]GAGATTAGCTTTATC | 8027 |
rs781900253 | snp | C/T | 3.3066e-05 | 0.00406595 | intron-variant | STAM | GRCh38.p7 | 10:17704944 | TCTTGTACTTTCTTA[C/T]ATTTCTTCACATCTT | 8027 |
rs781900482 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17661612 | CTCCTGTCTCTTTTT[C/G]TTTTAAACCTACTTT | 8027 |
rs781901289 | snp | G/T | 1.74236e-05 | 0.00295152 | intron-variant | STAM | GRCh38.p7 | 10:17708726 | AGAGAAAGTTCAGTA[G/T]GCTTATTAAAATTTT | 8027 |
rs781901627 | snp | C/T | 4.3631e-05 | 0.0046705 | intron-variant | STAM | GRCh38.p7 | 10:17700140 | TAAAGTGCTTTAAAG[C/T]AGAATTTTAAATGTA | 8027 |
rs781904114 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17685448 | GGACTGCCCCAAACT[C/G]TTCCAGATAGGGCCA | 8027 |
rs781906579 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17657997 | TTTTGTTGTTTGTTT[A/T]CTTCTGCTTGCTTAG | 8027 |
rs781907224 | snp | C/G | 4.94319e-05 | 0.00497127 | missense | STAM | GRCh38.p7 | 10:17705668 | TAATGAACGAAGATC[C/G]GATGTATTCCATGTA | 8027 |
rs781908565 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17686666 | ACAGGCATGAGCCAC[C/T]GCGCCCAGCCAACAT | 8027 |
rs781909923 | snp | C/T | 1.8432e-05 | 0.00303573 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696740 | AGAAATAAATACATT[C/T]GTTATGGTAAAGCAT | 8027 |
rs781913829 | snp | C/T | 1.648e-05 | 0.0028705 | missense | STAM | GRCh38.p7 | 10:17704456 | ACCAGTTGCTACAGA[C/T]GCTGCAAAGTACAGA | 8027 |
rs781915088 | snp | C/T | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713949 | GTGATCTTAGCTGCT[C/T]TCCCCTCGGCACCCC | 8027 |
rs781915498 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17709259 | GATAATGTCTTTAAT[C/G]AAATTTATGTTTAGT | 8027 |
rs781915639 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17680846 | TATGTATGTACCACA[G/T]TTTGCTTATCCATTT | 8027 |
rs781916689 | snp | C/G | 1.64925e-05 | 0.00287158 | intron-variant | STAM | GRCh38.p7 | 10:17684788 | GTACCACGAAATTAC[C/G]TGCCACAATTGAGCC | 8027 |
rs781916958 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17705225 | ATCGACCTTTGCAAT[A/G]TAGTCAAAAGGACCA | 8027 |
rs781916991 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17673874 | ATATTTGAGTTTGCA[A/G]GAGGAATACCTAACA | 8027 |
rs781917169 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17677978 | TACTTTTATAAATAC[A/G]TATATATTTCACATA | 8027 |
rs781917344 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17650870 | GCAGATCGAGACCAT[C/G]CTGGCTAACATGGTG | 8027 |
rs781917780 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17648284 | AGTGCTCTGTAGCTA[A/G]CTGGAGGTTTGTAAA | 8027 |
rs781918809 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17682140 | AAGATAGCATTTAAT[C/T]ACTCCCAAAAGTTCC | 8027 |
rs781923333 | snp | A/G | 3.29598e-05 | 0.00405941 | missense | STAM | GRCh38.p7 | 10:17705649 | CTTTCCTTATATACC[A/G]AGTTAATGAACGAAG | 8027 |
rs781924218 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17686176 | TTAATGTCCTGAATG[G/T]CCATCGAGATTACAA | 8027 |
rs781924591 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17706633 | ATCCACCCGCCTCGG[C/T]CTCCCAAAGTGCTGG | 8027 |
rs781924994 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17712087 | GGCAACTGGGTGGAC[A/G]GTGGAACTGTAAATT | 8027 |
rs781925227 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17649823 | TTGCCATATTGGCCA[C/G]GCTGGTCTTGAACTC | 8027 |
rs781926453 | snp | C/G | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715228 | AATCATAAACAACTA[C/G]CATGTTTCTTAATGT | 8027 |
rs781927022 | snp | C/T | 1.65625e-05 | 0.00287766 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644357 | GCCTCTTTTTGCCAC[C/T]AATCCCTTCGATCAG | 8027 |
rs781932197 | snp | A/T | 1.68533e-05 | 0.00290282 | missense, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688168 | TTCCCAGCTATTGGC[A/T]CTCAGGTATTTTGGG | 8027 |
rs781933691 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17667549 | TTTATTTGTCAAATA[A/C]TGAATGCCAAATATC | 8027 |
rs781933999 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17662405 | TCCACAAAGCCTTTC[C/T]TTATCCCCTTTACTG | 8027 |
rs781934455 | snp | A/G | | | upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644025 | TGACTAATTAAAAGA[A/G]GAGTCAGGCAGAGGG | 8027 |
rs781935030 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645085 | CACTGGTATTAGGTA[C/T]TGATGATGTCAATTC | 8027 |
rs781936659 | snp | A/G | 3.38112e-05 | 0.0041115 | intron-variant | STAM | GRCh38.p7 | 10:17700330 | TGTATTGAAATTTAA[A/G]TGGTTTTGCTTTAAG | 8027 |
rs781938220 | snp | A/G | 3.82146e-05 | 0.00437102 | intron-variant | STAM | GRCh38.p7 | 10:17695269 | TTACATTTAAAATTT[A/G]TATGAAAGTGTGTAT | 8027 |
rs781939521 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17661347 | ATTTGCAGTGGTAAT[A/G]TGAAGCCTTTGCCAG | 8027 |
rs781943212 | snp | A/C | 6.58957e-05 | 0.00573964 | missense | STAM | GRCh38.p7 | 10:17695140 | CTTAACTAACCACCA[A/C]CATGAAGGCCGAAAA | 8027 |
rs781943558 | in-del | -/G | | | intron-variant | STAM | GRCh38.p7 | 10:17652925 | TTCTCTTATAGTGTT[-/G]AATGATAAATAATTT | 8027 |
rs781944462 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17666593 | TAGTAGAGACGGGGT[G/T]TCACCGTGTTAGCCA | 8027 |
rs781944684 | in-del | -/AAT | | | intron-variant | STAM | GRCh38.p7 | 10:17701273 | GCGTGTTTATGAAAA[-/AAT]AATAAAAAGTATGTT | 8027 |
rs781946633 | snp | C/T | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715552 | ATTTTGGCATGACAT[C/T]TCAGAGTATTGTGGG | 8027 |
rs781947301 | snp | G/T | 1.65146e-05 | 0.0028735 | missense | STAM | GRCh38.p7 | 10:17693222 | CCTCTTTTTTGTTAG[G/T]CTGCAGAACAAGCAA | 8027 |
rs781948611 | snp | G/T | 3.65999e-05 | 0.00427769 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696918 | TTTCTAATCCTTTTC[G/T]TAATGGAAGTTGAGT | 8027 |
rs781950033 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17678982 | TTAAGGCTGAATACT[A/G]TTCCATTGTATATCA | 8027 |
rs781950104 | in-del | -/T | 0.000119573 | 0.00773126 | intron-variant | STAM | GRCh38.p7 | 10:17705792 | AAATGCACAGTGAGG[-/T]TGTGGTAGCTCATGC | 8027 |
rs781950336 | snp | G/T | 1.6489e-05 | 0.00287128 | intron-variant, missense, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17684844 | TAGCTTCTAGGAGCA[G/T]GTGTATCAAACTGTG | 8027 |
rs781951186 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17693541 | ATCCAAAAACAATAT[C/G]AAGTGCTTTTTTGTG | 8027 |
rs781951684 | snp | C/G | 6.58903e-05 | 0.00573941 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714683 | ATATGCCCCAGGTGC[C/G]AAACTATAACTTAAC | 8027 |
rs781956904 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17711754 | CGTGTAGGGGAGCAG[C/T]GAGAGACATACTTGA | 8027 |
rs781959350 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17711170 | ATATCTGAGAGGCTA[-/T]CTCTTGTTACATAAA | 8027 |
rs781960564 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17656882 | AATCCAAGTGGGTGA[C/G]TTGAAGAGTAAGTGC | 8027 |
rs781960910 | snp | G/T | 1.67798e-05 | 0.00289648 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688161 | AGTTACGTTCCCAGC[G/T]ATTGGCTCTCAGGTA | 8027 |
rs781963601 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643511 | GCTGTGAAAGACATG[G/T]CACCAACCATCACAG | 8027 |
rs781965771 | snp | A/T | 3.30038e-05 | 0.00406212 | missense | STAM | GRCh38.p7 | 10:17700208 | AAAACAGAGAAGAAG[A/T]CGGTACAATTTAGTG | 8027 |
rs781967629 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17655701 | GGAAACAAGAATTTC[A/G]TTATCACTTGGTCAA | 8027 |
rs781968739 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688572 | GGTTCAGGTGATTCT[C/T]CTGCCGCAGCCTCCT | 8027 |
rs781968895 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17667469 | TTCCATGTTTCACTC[-/A]AGTTTCGTAACATGG | 8027 |
rs781969452 | in-del | -/TTTTTTTTTTT | | | intron-variant | STAM | GRCh38.p7 | 10:17669884 | AATTCTTTTCTTTTC[-/TTTTTTTTTTT]TTTTTTTTTTTTTTT | 8027 |
rs781970264 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17652327 | GACAGCCTCAATAAA[C/T]GATGTGAACAATTTT | 8027 |
rs781971654 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17663675 | ATTGTGTGCATAAAT[A/G]GGATATCTTGTTATA | 8027 |
rs781974232 | snp | C/T | 8.51332e-05 | 0.00652375 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688191 | ATTTTGGGAATGAAG[C/T]TGTGTGTGTGCTACA | 8027 |
rs781975701 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17649155 | ACGCCAGTAACCCCT[A/G]CACTTTGGGAGGCTG | 8027 |
rs781976343 | snp | C/T | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715569 | CAGAGTATTGTGGGA[C/T]CATGAGACAAAATTA | 8027 |
rs781976537 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17692331 | GCTTCATTGACAGTG[A/T]TATTTTAGCTGATTA | 8027 |
rs781977378 | snp | C/G | 3.29576e-05 | 0.00405928 | missense | STAM | GRCh38.p7 | 10:17708896 | AGCCAGGCAGTGGTC[C/G]CACCATCCGCAAACC | 8027 |
rs781977405 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17694736 | AAGGTCAAGGAAAAT[A/C]TCTGCAGCTAAAAAA | 8027 |
rs781978133 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643483 | TTTGCTCAGTCTAGG[A/G]AGGCTATCTTGGGCT | 8027 |
rs781979636 | snp | A/G | 1.7002e-05 | 0.0029156 | intron-variant | STAM | GRCh38.p7 | 10:17695013 | ACTGTTGGATATAAT[A/G]ACATTTTGGGTCTTT | 8027 |
rs781979995 | snp | C/T | 3.30295e-05 | 0.0040637 | missense | STAM | GRCh38.p7 | 10:17708791 | GTGTATGCAGGGCCT[C/T]CTCCAAGTGGTGCCT | 8027 |
rs781981248 | snp | G/T | 1.65718e-05 | 0.00287848 | intron-variant | STAM | GRCh38.p7 | 10:17704397 | GTTGCCTAAAGGTTG[G/T]TAGCTTTTTATATTA | 8027 |
rs781982423 | snp | C/T | 1.64852e-05 | 0.00287094 | missense | STAM | GRCh38.p7 | 10:17705635 | AAGTGATGGAGGCCC[C/T]TTCCTTATATACCAA | 8027 |
rs781983251 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17686294 | CCATTTCCAAAAACG[A/T]CTTCCTATAGGCAAG | 8027 |
rs781983299 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17655764 | AGTCATTTCCACTGT[A/C]CCCCCAACCCATCTG | 8027 |
rs781983555 | snp | A/G | 6.888e-05 | 0.00586816 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688018 | TTTATTTCTTTTTCT[A/G]TTTTACAGGGTCATC | 8027 |
rs781984556 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17667444 | TTTTTTTTTTAAAAC[G/T]TGATCTTGATTTCCA | 8027 |
rs781986944 | snp | A/G | | | upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644063 | TGTTCAGCCTTTACC[A/G]ATGGGGCAGGCTCGG | 8027 |
rs781988189 | snp | C/G | 1.77354e-05 | 0.00297781 | intron-variant | STAM | GRCh38.p7 | 10:17693350 | GTGGGAATAACATAA[C/G]CCTTTATTTTTTCTC | 8027 |
rs781988953 | snp | A/G | 1.70414e-05 | 0.00291898 | intron-variant | STAM | GRCh38.p7 | 10:17700180 | AAAGATAACTTTTAC[A/G]TATCTTACAGTTAAA | 8027 |
rs781990449 | snp | C/G | 3.29511e-05 | 0.00405887 | missense | STAM | GRCh38.p7 | 10:17705007 | TCTCATTGATGAAAA[C/G]CTGGAAGATATTGAT | 8027 |
rs781990488 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17699133 | GCTAGTAGAGCAAGA[A/T]AGATTGGCATTCAAA | 8027 |
rs781991721 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17682440 | ACATTCTTATAAAGA[A/G]TACTGGGTAGTATGC | 8027 |
rs781991983 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17666226 | AGGTGGAAAACATCA[G/T]GTAACTTTTTCTTTA | 8027 |
rs781992343 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17657514 | CCTCTGCTTCTATAT[A/G]CTGCAAGAGATTACA | 8027 |
rs781994121 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17661289 | CTTATTTGTGCACTT[C/T]CATGTGAAAAAGATT | 8027 |
rs781997120 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17713011 | CACTAGTCCTTTGGG[A/T]CCGTTCTTGTCAAGA | 8027 |
rs781998051 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17709503 | TATGTGATGACAGAG[G/T]CCCATTTACTTTGCC | 8027 |
rs781998338 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17656293 | GCGAGACTCCGTCTT[-/A]AAAAAAAAAAAAAAA | 8027 |
rs782000018 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17646937 | CATCTTCAAAATTAA[C/T]TGTCTTCAGTCTTAA | 8027 |
rs782001487 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17678168 | CACTAATCTACTTTC[G/T]ATCTGTGTGGATTTG | 8027 |
rs782001833 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17654154 | GGTAGTTAGCAGTGC[A/G]TTGTAGAGGGTTTCT | 8027 |
rs782002006 | snp | A/T | 1.65061e-05 | 0.00287277 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714508 | TGCTCTATAAATCAG[A/T]ATTGATGTAATTGAG | 8027 |
rs782002028 | snp | A/C/G | 3.32745e-05 | 0.00407875 | missense | STAM | GRCh38.p7 | 10:17693284 | TGGTACTGTGGCTAA[A/C/G]AAAAAAGAAGAAGAA | 8027 |
rs782002522 | in-del | -/CTG | 4.94271e-05 | 0.00497102 | cds-indel, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714616 | CTCCTCCTGCCGCTA[-/CTG]CTGCTGCTGCTGCAA | 8027 |
rs782004720 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17671218 | ATATAGACGTACATA[A/T]GTCCTTGAATGGTAA | 8027 |
rs782005322 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17683308 | GCGCCCATAGGAGCT[G/T]GGACCATTTCTGGCT | 8027 |
rs782005670 | snp | A/C | 1.94755e-05 | 0.00312048 | intron-variant | STAM | GRCh38.p7 | 10:17695276 | TAAAATTTGTATGAA[A/C]GTGTGTATGGCTTCT | 8027 |
rs782006068 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17704929 | GTTCACATTTTTTTT[C/T]CTTGTACTTTCTTAT | 8027 |
rs782007404 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17649889 | AAGTGCTGGGATTAC[C/T]GATGTGAGGCACCCG | 8027 |
rs782007775 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17653285 | AAAACCGAATATTCC[A/G]CGATAAAAACTGGAA | 8027 |
rs782009879 | snp | A/C/T | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716574 | ATGGTTTAACTGATA[A/C/T]ACTTTTCTGCAATTT | 8027 |
rs782010823 | snp | A/G | 1.64781e-05 | 0.00287033 | missense | STAM | GRCh38.p7 | 10:17708824 | CTGGTTGCAGGGAAC[A/G]CGCAGATGAGCCACC | 8027 |
rs782010951 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17656854 | GGAAAGAAAGGAAAG[C/T]GCCCTTGGAAGAAAT | 8027 |
rs782014078 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17685002 | TGTTTAAATCTTCAC[A/G]GAGGACTATTCTGTG | 8027 |
rs782014571 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714674 | CAGGACCTAATATGC[C/T]CCAGGTGCCAAACTA | 8027 |
rs782015194 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17687062 | TAATAAGCAATGAGT[A/G]AAATAATTTATTTTG | 8027 |
rs782016467 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17653345 | GTGTGGATTCATCTC[A/G]CAGAGTTAAATGTTT | 8027 |
rs782018290 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17675306 | GTCAGGAGTTTGAGA[A/C]CAGCCTGGCCAATGT | 8027 |
rs782018536 | snp | A/G | 1.65113e-05 | 0.00287322 | synonymous-codon | STAM | GRCh38.p7 | 10:17693239 | TGCAGAACAAGCAAA[A/G]GCAAGCCCAGCTCTT | 8027 |
rs782019129 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17655518 | CTAGCAGGTGATGCT[A/G]TGATATATAGCAGGT | 8027 |
rs782019430 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17650022 | TCTTTGTTTCTATAA[C/T]AGAATATTTGTGTTC | 8027 |
rs782020566 | snp | A/C | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645311 | TCATTACTGTGAATA[A/C]GGACAACCTTATGAA | 8027 |
rs782020889 | snp | C/T | 1.66665e-05 | 0.00288669 | intron-variant | STAM | GRCh38.p7 | 10:17704919 | TCTATCAAAGGTTCA[C/T]ATTTTTTTTTCTTGT | 8027 |
rs782021046 | snp | C/G | 3.31175e-05 | 0.00406911 | missense | STAM | GRCh38.p7 | 10:17705733 | TCATCTGGTGTTTCT[C/G]GTTCTCAGGTAAGCT | 8027 |
rs782023175 | snp | A/T | 1.68462e-05 | 0.00290221 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696876 | CAGAAATGAGTAAGT[A/T]TTTTCCAGCCTGCCA | 8027 |
rs782026278 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17673465 | TCTAGGCCCCATTCG[C/T]AATGACAGTGTTTTA | 8027 |
rs782028019 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714601 | GCGCCAGTATATAGT[C/T]CTCCTCCTGCCGCTA | 8027 |
rs782028886 | snp | C/T | 1.65586e-05 | 0.00287733 | synonymous-codon, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17660477 | AGAGAAAGCAACCAG[C/T]GAGATGAATACTGCT | 8027 |
rs782029189 | snp | C/T | 1.65241e-05 | 0.00287433 | intron-variant | STAM | GRCh38.p7 | 10:17693211 | AATACTGTGTTCCTC[C/T]TTTTTGTTAGGCTGC | 8027 |
rs782029477 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17706529 | GACTACAGGCGCCCG[C/T]CACCACGCCAGGCTA | 8027 |
rs782031422 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17701027 | ATATGTCATTGTCAC[A/G]CCTGAAACAATGTAT | 8027 |
rs782032698 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17702079 | TATGAACAAAATTTC[-/T]CCTCACTTTCAACTA | 8027 |
rs782034842 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17668562 | CGTATCTGTCATTAC[A/C]GTACCATGCTGAATA | 8027 |
rs782035457 | snp | C/G | 1.64895e-05 | 0.00287132 | synonymous-codon, utr-variant-5-prime, intron-variant | STAM | GRCh38.p7 | 10:17684693 | TAAGGATTGTCTTCG[C/G]TCTATTATGAGAAGA | 8027 |
rs782035779 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17710502 | ATATTTAGCCCTCTC[A/G]TCCTGGCTCATTCCT | 8027 |
rs782036090 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17679035 | GTTGATGGACATTTG[A/G]CTGTTGTGAATACTA | 8027 |
rs782037157 | snp | C/G | 1.65792e-05 | 0.00287912 | missense, utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644366 | TGCCACCAATCCCTT[C/G]GATCAGGATGTTGGT | 8027 |
rs782037326 | snp | A/G | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715110 | AAATGTTATGTACAT[A/G]TATTGATATGTAACT | 8027 |
rs782037547 | in-del | -/C | | | intron-variant | STAM | GRCh38.p7 | 10:17658527 | ACCTGTCCATTTCTT[-/C]CTTTTTTTGGTCTTG | 8027 |
rs782037904 | snp | C/T | 1.64768e-05 | 0.00287021 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714785 | CTCTGCTATAGGACC[C/T]GGTGTTCCTCTTGGT | 8027 |
rs782040658 | in-del | -/A | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714424 | TTATAGCTGTTTAGT[-/A]AAAGGTTATTAAATG | 8027 |
rs782041020 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17677908 | TAATTATACTTAAGC[A/G]TATTGCTTTGCTTTC | 8027 |
rs782042236 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17702868 | CAAAGATTCGCTGGA[C/T]GTGGTGGTGTGCGCT | 8027 |
rs782044601 | snp | A/G | 3.29538e-05 | 0.00405904 | missense | STAM | GRCh38.p7 | 10:17705023 | CTGGAAGATATTGAT[A/G]GGTAAAAGAACATGG | 8027 |
rs782047840 | snp | G/T | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698298 | ACCTGGGCTGGTAAT[G/T]ATGTTTTGTTTGTTT | 8027 |
rs782048712 | snp | A/G | 3.30819e-05 | 0.00406692 | missense, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688057 | TGTGAAAAATTAAAG[A/G]CTCTTATGGTTGAAT | 8027 |
rs782048822 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17671143 | CTGCTGTGTGTCTGC[C/T]AGGTCCTGGTATACT | 8027 |
rs782050646 | snp | C/G | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689619 | TTAAACAGAATAATC[C/G]AAGACATTATACATT | 8027 |
rs782050925 | snp | A/G | 6.5912e-05 | 0.00574035 | missense | STAM | GRCh38.p7 | 10:17695160 | AAGGCCGAAAAGTTC[A/G]TGCTATATATGACTT | 8027 |
rs782051640 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17662432 | ACTGACAATGGTATG[A/G]TCCTCTGAATCCTCA | 8027 |
rs782052004 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17657646 | AGTTTTTTAAATAGA[C/T]GTGGGCCATTTAGAT | 8027 |
rs782052642 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643677 | CGCCCTGAACACTCC[C/G]CTCTTGGGATTCAGG | 8027 |
rs782054161 | in-del | -/T | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698421 | TGGAGCCATTTCATC[-/T]TTTTTTTTTTTTTAA | 8027 |
rs782056822 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17712576 | ATAAATAACAATTGG[-/A]GGAAAGTTTAGAAGT | 8027 |
rs782057326 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17661464 | TCTTTTGGTCTCACA[A/G]CTTCCAGCTGTCTTT | 8027 |
rs782057734 | snp | A/G/T | 3.29784e-05 | 0.00406058 | intron-variant, missense, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17684847 | CTTCTAGGAGCATGT[A/G/T]TATCAAACTGTGGCA | 8027 |
rs782057862 | snp | C/G | 1.66081e-05 | 0.00288163 | intron-variant | STAM | GRCh38.p7 | 10:17695045 | AAAACTCATTGTTTT[C/G]TAGCCATTGAGTTGT | 8027 |
rs782059044 | snp | C/T | 1.66109e-05 | 0.00288187 | synonymous-codon, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696856 | TGCAGATCTCACTGC[C/T]GAACCAGAAATGAGT | 8027 |
rs782059335 | snp | C/T | 1.70104e-05 | 0.00291632 | intron-variant | STAM | GRCh38.p7 | 10:17705785 | AAATTCTCAAATGCA[C/T]AGTGAGGTGTGGTAG | 8027 |
rs782060774 | snp | C/T | 1.65181e-05 | 0.00287381 | synonymous-codon, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17660525 | TTTGGATATCTGTGA[C/T]AAAGTTGGTCAGTCT | 8027 |
rs782062008 | snp | A/G | 3.336e-05 | 0.00408398 | intron-variant | STAM | GRCh38.p7 | 10:17660460 | TCCCCTTTACAATCT[A/G]CAGAGAAAGCAACCA | 8027 |
rs782062323 | snp | C/G | 4.94197e-05 | 0.00497066 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714625 | GCCGCTACTGCTGCT[C/G]CTGCAACTGCCGATG | 8027 |
rs782062420 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17650049 | GTTCCCAGTCAGACT[A/G]CTTTGGGCCAGTCCA | 8027 |
rs782063237 | in-del | -/GTGTGATTT | | | intron-variant | STAM | GRCh38.p7 | 10:17672833 | TGACATCTTACAGCA[-/GTGTGATTT]GTGTGATTTGTGTTA | 8027 |
rs782063893 | in-del | -/C | 1.65759e-05 | 0.00287883 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644334 | CACCTCGGCACGCAG[-/C]CGGAGATGCCTCTTT | 8027 |
rs782064013 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17694543 | GTGGAGATAGAGACA[C/T]GTTTGAGATCTATTT | 8027 |
rs782064131 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17708357 | TTGCTCTATTGTTCA[A/G]TAAACTGCAGTTTAG | 8027 |
rs782064534 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17679050 | GCTGTTGTGAATACT[A/G]TTAATACTACTCTGA | 8027 |
rs782064672 | snp | A/G | 1.65108e-05 | 0.00287317 | intron-variant | STAM | GRCh38.p7 | 10:17704427 | AACTACTTAATTCCT[A/G]TAGGATAAAATGGAC | 8027 |
rs782064979 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17647281 | CAAAGTCTCTAGTGA[C/T]TTCCACCTTGCCAAA | 8027 |
rs782065007 | in-del | -/C | | | intron-variant | STAM | GRCh38.p7 | 10:17691045 | TTGCCAAATTGTGAA[-/C]AAAAATTTATGTAAA | 8027 |
rs782069359 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645474 | CCACTTCTCAGCTCA[C/T]GGTGAAATCATAGGC | 8027 |
rs782070280 | in-del | -/C | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645522 | TTCCAGTGTTCTTGT[-/C]TTTAAAGAGGGGAAA | 8027 |
rs782072347 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688494 | TTGAGACGGAGTCTT[C/T]GTTTGTCGCCCTGGG | 8027 |
rs782072891 | snp | C/G | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714422 | CATTATAGCTGTTTA[C/G]TAAAAGGTTATTAAA | 8027 |
rs782073248 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714777 | TCAGAAGGCTCTGCT[A/G]TAGGACCCGGTGTTC | 8027 |
rs782073581 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17699369 | CTTAATATTTTTATG[A/G]ATTGATTGACCACAT | 8027 |
rs782073648 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17683602 | TCATTCTTACCTGAT[C/T]AATTCCATCCACTTT | 8027 |
rs782074362 | snp | A/G | 1.64933e-05 | 0.00287165 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714525 | TTGATGTAATTGAGT[A/G]TTTTTCTTCCTCCAC | 8027 |
rs782077022 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17680324 | ACTGAAACTGTATAC[C/T]CATTAAACAATTAAA | 8027 |
rs782077722 | snp | C/T | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716693 | ATGACATAGTCTCTA[C/T]TATGATTTTTGCCCT | 8027 |
rs782078162 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17687304 | ACATGGTAAAACCCC[A/G]CGTCTGCTAAAAGTA | 8027 |
rs782079208 | snp | C/T | 1.66109e-05 | 0.00288187 | intron-variant | STAM | GRCh38.p7 | 10:17704930 | TTCACATTTTTTTTT[C/T]TTGTACTTTCTTATA | 8027 |
rs782081358 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon | STAM | GRCh38.p7 | 10:17708838 | CGCGCAGATGAGCCA[C/T]CTCCAGAGCTACAGT | 8027 |
rs782082507 | snp | A/C | 1.64988e-05 | 0.00287213 | intron-variant | STAM | GRCh38.p7 | 10:17705065 | TTGTGTACCTTCTTT[A/C]CTGAAGCTATCACTG | 8027 |
rs782084307 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17708570 | TAACATGAGTTTAGC[A/G]TATGTTTAACTAAAA | 8027 |
rs782084768 | snp | A/G | 3.31049e-05 | 0.00406834 | intron-variant | STAM | GRCh38.p7 | 10:17704407 | GGTTGGTAGCTTTTT[A/G]TATTAACTACTTAAT | 8027 |
rs782084982 | snp | G/T | 1.65018e-05 | 0.00287239 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714514 | ATAAATCAGTATTGA[G/T]GTAATTGAGTGTTTT | 8027 |
rs782085409 | snp | A/G | 4.06298e-05 | 0.00450702 | intron-variant | STAM | GRCh38.p7 | 10:17695283 | TGTATGAAAGTGTGT[A/G]TGGCTTCTGTGTTTC | 8027 |
rs782086707 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17658679 | TTTTGTAGAGGAGAG[A/G]TTTCGTCATGTTGCC | 8027 |
rs782088528 | snp | C/G | | | intron-variant, missense | STAM | GRCh38.p7 | 10:17713339 | GAGGATTCCCAGATG[C/G]GTATTTCTCCTCCGT | 8027 |
rs782089274 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17667130 | CAGAGTTAAATAATT[-/T]TTTTTTTTTTTTTGA | 8027 |
rs782091582 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17701240 | AAAGATTAAAACTGG[C/T]TACCTTTTTCATCTT | 8027 |
rs782093182 | snp | C/T | | | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696263 | AACATGTATTGAGTG[C/T]TTGCTAGCTTTCCAT | 8027 |
rs782093950 | snp | C/T | 3.29641e-05 | 0.00405968 | synonymous-codon, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17684729 | CCACAAAGATCCTCA[C/T]GTTGCTATGCAGGCT | 8027 |
rs782094377 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17680849 | GTATGTACCACATTT[C/T]GCTTATCCATTTATG | 8027 |
rs782094693 | in-del | -/T | 1.64993e-05 | 0.00287218 | frameshift-variant | STAM | GRCh38.p7 | 10:17708921 | AAACCCAGCCCTTCC[-/T]TAGTCAGCAGACTCA | 8027 |
rs782094943 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17678007 | TACCATCAAATTTAC[C/T]ATTTTAGAATATACA | 8027 |
rs782096050 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17648390 | TCAGCAGGACATGGG[C/T]GGGGACAAATAAGAG | 8027 |
rs782097321 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17646914 | CTTAACACTCGTATA[C/T]ATTTGCACATCTTCA | 8027 |
rs782098791 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17692633 | GAATTGAATTATATG[-/T]TTTGTTGTGTATTCC | 8027 |
rs782101670 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17710928 | AATATCTGTTTATCA[A/C]TATATAAAAACAGAT | 8027 |
rs782104481 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714688 | CCCCAGGTGCCAAAC[C/T]ATAACTTAACATCAT | 8027 |
rs782105062 | snp | A/G | 1.65452e-05 | 0.00287616 | synonymous-codon, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17660480 | GAAAGCAACCAGCGA[A/G]ATGAATACTGCTGAG | 8027 |
rs782107900 | snp | G/T | 4.95741e-05 | 0.00497841 | missense | STAM | GRCh38.p7 | 10:17708928 | AGCCCTTCCTAGTCA[G/T]CAGACTCAGGCCGCT | 8027 |
rs782111650 | snp | A/G | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689562 | TAGCTGGTTTTTACT[A/G]CTCAGTATAGTTTCT | 8027 |
rs782112022 | snp | C/G | 1.64904e-05 | 0.00287139 | intron-variant, missense, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17684832 | ATTTTGTGCTTTTAG[C/G]TTCTAGGAGCATGTG | 8027 |
rs782112227 | snp | C/T | 1.64863e-05 | 0.00287104 | intron-variant, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714535 | TGAGTGTTTTTCTTC[C/T]TCCACAGTACAATGG | 8027 |
rs782112530 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17705498 | ACTAGTACTACTTTT[A/T]GCCATTTTTGATATT | 8027 |
rs782112937 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17678170 | CTAATCTACTTTCTA[C/T]CTGTGTGGATTTGCC | 8027 |
rs782113066 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17709507 | TGATGACAGAGGCCC[A/G]TTTACTTTGCCATTT | 8027 |
rs782113698 | snp | A/C/G | 0.000164855 | 0.00907755 | missense | STAM | GRCh38.p7 | 10:17708911 | CCACCATCCGCAAAC[A/C/G]CAGCCCTTCCTAGTC | 8027 |
rs782115452 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17671266 | TTTGTAGCATTTTAG[A/G]TGAAGATGTAATGTT | 8027 |
rs782118211 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17649968 | AAACCCAAGAGGCAT[C/G]TTTGAATCATTTCCC | 8027 |
rs782120332 | snp | A/G | 3.33045e-05 | 0.00408058 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644384 | TCAGGATGTTGGTAA[A/G]TGTTTTTGCCTCTCC | 8027 |
rs782121383 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17666611 | ACCGTGTTAGCCAGG[A/G]TGGTCTCGATATCCT | 8027 |
rs782121607 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17662671 | TCTAGCCATTTAGCT[A/G]TGTCATACTGGGTAA | 8027 |
rs782121793 | snp | A/C | | | missense | STAM | GRCh38.p7 | 10:17704480 | GTACAGACCCCAGTG[A/C]TGATCAGCCAGACCT | 8027 |
rs782123183 | snp | C/T | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689778 | TGGTTTGACCAGCAT[C/T]ACTGGCATTACCTGG | 8027 |
rs782124076 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17693570 | TGTCTAACAAATTTG[C/T]TTTTTGTAGATAGTA | 8027 |
rs782125060 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17711019 | GGAAATTGGAAGGAG[C/T]GAGGGCCAGGGTTAG | 8027 |
rs782127115 | in-del | -/C | | | intron-variant | STAM | GRCh38.p7 | 10:17712986 | AATGAGGTTATGAGG[-/C]CTTCCCTTCCACTAG | 8027 |
rs782127899 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant | STAM | GRCh38.p7 | 10:17695005 | TTCTTCAGACTGTTG[A/G]ATATAATAACATTTT | 8027 |
rs782133035 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17675208 | AAAGCCTAATTAAAG[A/G]TAATAGCATTTTTTG | 8027 |
rs782133666 | snp | C/G | | | upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644092 | GGGGCAGCTTTGAGA[C/G]AGGCAGCGCCAAGGT | 8027 |
rs782134607 | in-del | -/A | | | downstream-variant-500B | STAM | GRCh38.p7 | 10:17716879 | GAAAATACCAGGGGG[-/A]AAAAAATCCAATGAA | 8027 |
rs782139022 | in-del | -/TCTCTTC | | | intron-variant | STAM | GRCh38.p7 | 10:17683190 | TGTTTTGAGACAGGG[-/TCTCTTC]TCTCACTCTGTCTCT | 8027 |
rs782139918 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17695008 | TTCAGACTGTTGGAT[A/G]TAATAACATTTTGGG | 8027 |
rs782142397 | in-del | -/T | 1.6473e-05 | 0.00286988 | frameshift-variant, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714689 | CCAGGTGCCAAACTA[-/T]TAACTTAACATCATC | 8027 |
rs782142839 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696989 | CAGTGGTGCGAGCTC[A/G]GATCATTGCAACCTC | 8027 |
rs782143698 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17693659 | TCGTGTGATATATCC[A/G]TTAACTGTTCTATAA | 8027 |
rs782143946 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17652116 | AAGCTTTGAATTCTT[C/T]AGAAGCAAGTCTGTT | 8027 |
rs782145676 | snp | A/G | 1.69129e-05 | 0.00290795 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688176 | TATTGGCTCTCAGGT[A/G]TTTTGGGAATGAAGT | 8027 |
rs782146958 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17666774 | TTGAAAGAATATTTC[C/T]TGATTTTTGTAAGGG | 8027 |
rs782147738 | snp | A/G | 1.90903e-05 | 0.00308947 | intron-variant | STAM | GRCh38.p7 | 10:17695271 | ACATTTAAAATTTGT[A/G]TGAAAGTGTGTATGG | 8027 |
rs782147886 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17648145 | TTTAAAAATATATCC[A/G]GAATTTCATTGACAG | 8027 |
rs782148674 | in-del | -/TTA | | | intron-variant | STAM | GRCh38.p7 | 10:17654217 | CAGGTATTATTGTTA[-/TTA]TTATTATTATTATTA | 8027 |
rs782149741 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17670225 | TTACTTGCCTAGACA[A/G]TGATTTTACTTTTTT | 8027 |
rs782150038 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17701029 | ATGTCATTGTCACAC[C/G]TGAAACAATGTATAT | 8027 |
rs782151838 | snp | C/T | 1.69066e-05 | 0.00290741 | intron-variant | STAM | GRCh38.p7 | 10:17660584 | AGGATTTTTATTCTT[C/T]CTTTTTAAAAAACAC | 8027 |
rs782152352 | snp | A/C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17668608 | AATGACCTGTGCTCC[A/C/G]TCTGTTCATTCCTTT | 8027 |
rs782155089 | snp | A/C | 1.64746e-05 | 0.00287002 | missense | STAM | GRCh38.p7 | 10:17695141 | TTAACTAACCACCAA[A/C]ATGAAGGCCGAAAAG | 8027 |
rs782155818 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17706627 | CTCGTGATCCACCCG[C/T]CTCGGCCTCCCAAAG | 8027 |
rs782156340 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | STAM | GRCh38.p7 | 10:17708825 | TGGTTGCAGGGAACG[C/T]GCAGATGAGCCACCT | 8027 |
rs782156905 | snp | G/T | 1.76083e-05 | 0.00296712 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687996 | TTGGCTAGGAAATTG[G/T]TGCTCTTTTATTTCT | 8027 |
rs782157014 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17702881 | GACGTGGTGGTGTGC[A/G]CTTGTAATCCTAGCT | 8027 |
rs782157800 | snp | G/T | 4.94393e-05 | 0.00497164 | intron-variant | STAM | GRCh38.p7 | 10:17705053 | GGTGCATTTATGTTG[G/T]GTACCTTCTTTCCTG | 8027 |
rs782158313 | in-del | -/T | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715181 | ATATATTTAACACTG[-/T]GTTAAATTAATTTAC | 8027 |
rs782159588 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17686348 | TGTTTTACAGTGAAC[A/G]TATTGGTTTTGTACT | 8027 |
rs782159650 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17655851 | TCTGCTCTTTGAATT[G/T]CAGTGTTCCAGTCAA | 8027 |
rs782160099 | in-del | -/C | | | intron-variant | STAM | GRCh38.p7 | 10:17660312 | GAGCGTACATCTTTT[-/C]AAGATGGCCATGAAA | 8027 |
rs782160633 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17652589 | TAAGTTTTAATATGC[C/T]TAGCTATTATGTTTT | 8027 |
rs782162394 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642458 | TTACTCTATGCCAGG[C/T]ACTGTAATAAGCGTT | 8027 |
rs782163093 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17655058 | TTATTTTCTAAATAC[A/G]TCGGGAAGCCCTTCC | 8027 |
rs782163179 | snp | C/G | 3.30246e-05 | 0.0040634 | missense | STAM | GRCh38.p7 | 10:17693240 | GCAGAACAAGCAAAA[C/G]CAAGCCCAGCTCTTG | 8027 |
rs782163447 | snp | C/T | | | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696177 | ACATTTTTTTTTTTT[C/T]GAGTGGAAGAAAATA | 8027 |
rs782166624 | snp | C/T | 1.69309e-05 | 0.0029095 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696880 | AATGAGTAAGTATTT[C/T]CCAGCCTGCCAATAA | 8027 |
rs782168474 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17692470 | GGTATAGAGACTGCT[C/G]AGGAACTGCTAGCAG | 8027 |
rs782168633 | snp | A/C | 1.64923e-05 | 0.00287156 | intron-variant, synonymous-codon, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17684861 | TGTATCAAACTGTGG[A/C]AAAATTTTTCATTTA | 8027 |
rs782169428 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17678944 | GTCCATCCATGTTGT[A/G]TATAGCATGTGTCAG | 8027 |
rs782170532 | snp | G/T | 1.65594e-05 | 0.0028774 | missense | STAM | GRCh38.p7 | 10:17705734 | CATCTGGTGTTTCTG[G/T]TTCTCAGGTAAGCTT | 8027 |
rs782170663 | snp | A/T | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645098 | TACTGATGATGTCAA[A/T]TCAATAGGTTTGCTT | 8027 |
rs782172361 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17657551 | TAGTATAATTTCTTC[C/T]TTAAATATTTGGTAA | 8027 |
rs782173104 | snp | A/G | 8.23621e-05 | 0.00641672 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714672 | TGCAGGACCTAATAT[A/G]CCCCAGGTGCCAAAC | 8027 |
rs782173237 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17710146 | TTTTAGTATTAGCCG[A/G]AACTGCCACTTTTCC | 8027 |
rs782173546 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17711739 | ACCAAGGGTTGAAAG[C/T]GTGTAGGGGAGCAGC | 8027 |
rs782173869 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17704920 | CTATCAAAGGTTCAC[A/G]TTTTTTTTTCTTGTA | 8027 |
rs782174609 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714879 | TATCCTCAGCTTATA[C/G]GAATCTCTCCAGGTC | 8027 |
rs782175933 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17702453 | GTTTAAATTCCTTTG[A/G]CTATATTTAAAGGAA | 8027 |
rs782179824 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17648852 | AAGGGAAATGCAAGT[G/T]TTTTTATTGTGGCTC | 8027 |
rs782180348 | snp | A/C | 3.29897e-05 | 0.00406125 | intron-variant | STAM | GRCh38.p7 | 10:17704543 | TTCTATTTACCTTGC[A/C]AATAAAGAGTAGTTA | 8027 |
rs782182453 | snp | A/C/T | 0.000164991 | 0.00908129 | missense, synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714600 | GGCGCCAGTATATAG[A/C/T]CCTCCTCCTGCCGCT | 8027 |
rs782186330 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17712949 | GGAGCGTGTGCTTCC[A/G]TATTTTCAAGGAAAT | 8027 |
rs782187336 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17647584 | CACACTGCTTGGATT[C/T]AGTCCCAGGTTTGCT | 8027 |
rs782187629 | snp | A/G | 1.64762e-05 | 0.00287016 | missense | STAM | GRCh38.p7 | 10:17704501 | AGCCAGACCTACCAG[A/G]GCTGCTTCATCTTGA | 8027 |
rs782188254 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17707342 | ATGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 8027 |
rs782190080 | snp | A/G | 1.65408e-05 | 0.00287578 | intron-variant | STAM | GRCh38.p7 | 10:17693195 | TTGATAACAACCCTC[A/G]AATACTGTGTTCCTC | 8027 |
rs782193967 | in-del | -/AAT | | | intron-variant | STAM | GRCh38.p7 | 10:17707413 | GACTCCACCTCAAAA[-/AAT]AATAATAATAATAAT | 8027 |
rs782194989 | snp | A/G | | | stop-gained, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696790 | TGATCCTAACTGGTG[A/G]AAAGGTGAAACCCAT | 8027 |
rs782196229 | snp | A/C | 9.93921e-05 | 0.00704884 | missense, utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644362 | TTTTTGCCACCAATC[A/C]CTTCGATCAGGATGT | 8027 |
rs782197403 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17663614 | CTTTAATAGTTATTG[C/T]TCTCTGGTTCTTTTA | 8027 |
rs782198773 | snp | A/G | 1.64993e-05 | 0.00287218 | missense, utr-variant-5-prime, intron-variant | STAM | GRCh38.p7 | 10:17684683 | TTTTTAGACCTAAGG[A/G]TTGTCTTCGGTCTAT | 8027 |
rs782201817 | in-del | -/T | 1.65034e-05 | 0.00287253 | frameshift-variant | STAM | GRCh38.p7 | 10:17704433 | TTAATTCCTGTAGGA[-/T]AAAATGGACCAGTTG | 8027 |
rs782203428 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17679407 | GCCCATTTTTGAATT[C/G]GGTTGTTGTTCGTTG | 8027 |
rs782204969 | snp | A/G | 3.32535e-05 | 0.00407746 | missense, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688147 | CTTAAGGAACAAGGA[A/G]TTACGTTCCCAGCTA | 8027 |
rs782205134 | snp | C/T | 1.65611e-05 | 0.00287755 | missense | STAM | GRCh38.p7 | 10:17695220 | TTAAAGCTGGAGAAA[C/T]TATTACAGTTCTTGA | 8027 |
rs782205313 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17670473 | CTTGTATGAGCAGTT[A/G]TATTTGAAGGTTAAA | 8027 |
rs782207860 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17662111 | ATCTCTTTTCTAATT[C/G]TTATATCCAGTTGCC | 8027 |
rs782209813 | snp | C/G | 1.64741e-05 | 0.00286998 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714768 | ACCATATTCTCAGAA[C/G]GCTCTGCTATAGGAC | 8027 |
rs782212700 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17665984 | AGAGAACTTTCACAA[C/T]GATAATAGCCGTTTT | 8027 |
rs782214355 | snp | C/G/T | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644679 | AGCATCTGGTGCAGG[C/G/T]ACTGTGCTTCTGGAA | 8027 |
rs782216547 | snp | A/C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17661267 | TATGCCACACAAATG[A/C/G]TATTGTCTTATTTGT | 8027 |
rs782216906 | in-del | -/TTTCTTTTCTTT | | | intron-variant | STAM | GRCh38.p7 | 10:17679751 | TTCTTCTTAAGTCAG[-/TTTCTTTTCTTT]TTTCTTTTCTTTTTT | 8027 |
rs782217338 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17647775 | CTTTTTATTAAGTAA[A/G]ATTTTAAAAAGAACC | 8027 |
rs782221072 | snp | C/G | 0.000187548 | 0.00968189 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688193 | TTTGGGAATGAAGTT[C/G]TGTGTGTGCTACAGT | 8027 |
rs782222963 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17657374 | CTTACTACCTGTAAC[A/G]TTTTGTTGAGGATTT | 8027 |
rs782223116 | snp | G/T | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715725 | TAGAGGCAATGGATA[G/T]AAATTTTTAAACTGG | 8027 |
rs782223467 | snp | A/T | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643311 | AAGTGGGACGCAACA[A/T]CTCTAGTAGATGCTC | 8027 |
rs782223861 | snp | C/G | 4.9561e-05 | 0.00497775 | missense | STAM | GRCh38.p7 | 10:17705610 | TCAGAACTCTCAGAA[C/G]TTAATGTGAAAGTGA | 8027 |
rs782225193 | snp | A/G/T | 3.30122e-05 | 0.00406266 | synonymous-codon | STAM | GRCh38.p7 | 10:17705720 | ATATTATATGCAGTC[A/G/T]TCTGGTGTTTCTGGT | 8027 |
rs782225622 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17664805 | AAAATTATTATTGCT[A/G]TTTGGTGTTAGCCTG | 8027 |
rs782226890 | snp | C/T | 1.81223e-05 | 0.00301012 | intron-variant | STAM | GRCh38.p7 | 10:17695255 | AGGTAATGTTAATAT[C/T]ACATTTAAAATTTGT | 8027 |
rs782227217 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17679637 | TTTGGTAGAATTCAC[C/G]AGTGAAGCTTTCTGT | 8027 |
rs782228400 | snp | C/T | 8.6166e-05 | 0.0065632 | intron-variant | STAM | GRCh38.p7 | 10:17708996 | TTAGTGCTGTTACAG[C/T]TGTTTAAGTGCCCCC | 8027 |
rs782228705 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643896 | TTCTCCTGGCTCTCC[C/G]AGTCACTCCTGGGGT | 8027 |
rs782230648 | snp | A/G | 2.02235e-05 | 0.00317983 | intron-variant | STAM | GRCh38.p7 | 10:17700161 | TTTAAATGTATTATT[A/G]AAAAAAGATAACTTT | 8027 |
rs782231302 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17649849 | AACTCCTAGCCTCAA[A/G]TGATCTGCCTGCCTC | 8027 |
rs782233535 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17659825 | TAATTTTTCTTCTTT[C/G]TTAAGAAGTTCTGCT | 8027 |
rs782233889 | snp | A/G | 1.64798e-05 | 0.00287047 | missense | STAM | GRCh38.p7 | 10:17704974 | TGTCATTTTAGCAAT[A/G]TGTCACCAGATGGGA | 8027 |
rs782234053 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17668053 | ACTCCAAGGTCCATC[A/G]GAGTTAATAAGATGT | 8027 |
rs782237766 | snp | C/G | 6.59022e-05 | 0.00573993 | missense | STAM | GRCh38.p7 | 10:17708873 | CCCCGGAGCAGCTGT[C/G]TTCTCTCAGCCAGGC | 8027 |
rs782239227 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17653255 | CATTTCCCAGTCCAT[C/T]GAAACCTACACTGAA | 8027 |
rs782239485 | snp | A/G | 1.65184e-05 | 0.00287384 | intron-variant | STAM | GRCh38.p7 | 10:17693217 | GTGTTCCTCTTTTTT[A/G]TTAGGCTGCAGAACA | 8027 |
rs782241617 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17692107 | GTGTAGGTGCTATTA[C/T]CGTAGTCATTTTATT | 8027 |
rs782242148 | snp | A/C | 1.67077e-05 | 0.00289026 | missense | STAM | GRCh38.p7 | 10:17695231 | GAAATTATTACAGTT[A/C]TTGATGACAGGTAAT | 8027 |
rs782242673 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17661325 | GCACTGCTGCATTAC[A/C]CTTGATATTTGCAGT | 8027 |
rs782243151 | snp | A/G | 3.29843e-05 | 0.00406092 | missense | STAM | GRCh38.p7 | 10:17705710 | AGAATCAGCCATATT[A/G]TATGCAGTCATCTGG | 8027 |
rs782244307 | snp | C/G | 6.59e-05 | 0.00573983 | missense | STAM | GRCh38.p7 | 10:17695108 | CTTTCCACTTTGTAT[C/G]CAAGCACATCCAGTC | 8027 |
rs782245474 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17663206 | TTAATGTTAACGTTA[C/T]TCTCCCAGAAATGTT | 8027 |
rs782246225 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17664942 | AAATGATTTGTAACT[A/G]GTAATATATAGTAGA | 8027 |
rs782246813 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17687011 | CCGCTATGAAGATAC[A/G]TCAGTATTTTAATGA | 8027 |
rs782248265 | snp | C/T | 5.01509e-05 | 0.00500729 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688155 | ACAAGGAGTTACGTT[C/T]CCAGCTATTGGCTCT | 8027 |
rs782248585 | in-del | -/C | 1.65983e-05 | 0.00288078 | intron-variant | STAM | GRCh38.p7 | 10:17704930 | TTCACATTTTTTTTT[-/C]TTGTACTTTCTTATA | 8027 |
rs782248925 | snp | A/C | 1.65855e-05 | 0.00287967 | intron-variant | STAM | GRCh38.p7 | 10:17700292 | GAAGTAAGTGGTTTC[A/C]ATGGTGATAGGAGTT | 8027 |
rs782250582 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17655421 | TAGCTAGGTAGGTAC[A/C]CTACCTAACCAATAC | 8027 |
rs782250812 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17685981 | GTTAAAAGGGAAAAT[C/G]CCTCATGTTTTTGGG | 8027 |
rs782252000 | snp | A/G | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689840 | CACTCCAGACCTATG[A/G]GTTCATTATCTCCAT | 8027 |
rs782252312 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17700399 | TTTGTATTTTTTTAT[A/G]AAAATTCAAGCAATA | 8027 |
rs782252915 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17652047 | AGATTTCTCAATCTC[C/G]TCTTTTTGAGTATTA | 8027 |
rs782254522 | snp | C/T | 0.000150302 | 0.00866766 | intron-variant | STAM | GRCh38.p7 | 10:17684658 | TTAAGTAATTTTTAC[C/T]TTTCTCATTTTTTTA | 8027 |
rs782256234 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688363 | ATTCAGAGGTGCCAG[A/G]AAAGTATTATAATGG | 8027 |
rs782257515 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17710233 | AGATTACTTGAGACT[C/T]ATTCTTCAAGGTCGG | 8027 |
rs782257932 | snp | A/C/T | 0.000230596 | 0.0107355 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714665 | ACCAGAATGCAGGAC[A/C/T]TAATATGCCCCAGGT | 8027 |
rs782258191 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17681672 | TATATAAAGAGCTCC[C/T]TGTTTATGTTATCTG | 8027 |
rs782258641 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17654553 | AAGGTCAATGTGTTA[C/T]TATGACTTTTTGTGG | 8027 |
rs782259263 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17690360 | CAGGACATAGAAGAG[C/T]AATAGTAAAGATAGG | 8027 |
rs782259364 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17711779 | ACTTGAAGACACTGC[A/C]AAGGTCGAAGAATGC | 8027 |
rs782261486 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17680640 | TCACACTCCTTGGCT[G/T]GAGCAATCCTTCCAC | 8027 |
rs782261673 | in-del | -/A | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643834 | ATAACCGAGAGAGCG[-/A]AGAGGAAAAAAGGCG | 8027 |
rs782265600 | snp | A/C | 0.000115339 | 0.00759318 | missense | STAM | GRCh38.p7 | 10:17708888 | CTTCTCTCAGCCAGG[A/C]AGTGGTCCCACCATC | 8027 |
rs782265840 | snp | A/T | 1.65562e-05 | 0.00287712 | missense, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696827 | ATAGGGTTATTTCCT[A/T]CTAATTTTGTGACTG | 8027 |
rs782267135 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714968 | GGTTCTTCCCCCCCC[G/T]CCCCTGCAGAGGAAT | 8027 |
rs782267551 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643396 | AAGTAAAATAAATAA[A/G]CCAACATTTTGGGTT | 8027 |
rs782268010 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17677848 | ATCCTAATTTTTCTA[C/T]ATAATTATTAAAAAG | 8027 |
rs782268138 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17653782 | AATTCAATGCCATTT[C/T]ATATTAGGGACTTGA | 8027 |
rs782269561 | snp | C/G | 1.65919e-05 | 0.00288022 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644323 | AGTCCCCGGGGACAC[C/G]TCGGCACGCAGCGGA | 8027 |
rs782270760 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon | STAM | GRCh38.p7 | 10:17705010 | CATTGATGAAAAGCT[A/G]GAAGATATTGATAGG | 8027 |
rs782270914 | snp | C/T | 1.65655e-05 | 0.00287793 | missense | STAM | GRCh38.p7 | 10:17708783 | CATCGCAGGTGTATG[C/T]AGGGCCTCCTCCAAG | 8027 |
rs782273741 | snp | A/G/T | 3.32387e-05 | 0.00407658 | missense | STAM | GRCh38.p7 | 10:17708776 | CTTTAACCATCGCAG[A/G/T]TGTATGCAGGGCCTC | 8027 |
rs782274582 | snp | A/G | 1.64912e-05 | 0.00287147 | missense | STAM | GRCh38.p7 | 10:17705627 | TAATGTGAAAGTGAT[A/G]GAGGCCCTTTCCTTA | 8027 |
rs782276274 | snp | C/T | 3.29511e-05 | 0.00405887 | synonymous-codon | STAM | GRCh38.p7 | 10:17704995 | CCAGATGGGACCTCT[C/T]ATTGATGAAAAGCTG | 8027 |
rs782278047 | snp | A/G | 1.7649e-05 | 0.00297055 | intron-variant | STAM | GRCh38.p7 | 10:17693346 | GATGGTGGGAATAAC[A/G]TAAGCCTTTATTTTT | 8027 |
rs782278692 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687763 | TACAAACCTTGCTTC[A/G]TTGCAAAATATTCTG | 8027 |
rs782278702 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17657228 | TAACACTTGTGGACT[C/G]TTAGGAGCTTCTCTC | 8027 |
rs782280363 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714660 | TCTGTACCAGAATGC[A/G]GGACCTAATATGCCC | 8027 |
rs782280415 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17680788 | GCTTATTTCACTTAG[C/T]GTAATGGCTTTAAAG | 8027 |
rs782280606 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17653984 | GAAGGGTAGTGGGAA[C/G]TTCCAGTTTGTATCC | 8027 |
rs782283216 | snp | A/G | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715164 | CAGTGGTGATCGTGT[A/G]AATATATTTAACACT | 8027 |
rs782285408 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17684124 | CGGTCACTTTTTGAC[A/C]AGTTTCATGGAGTTT | 8027 |
rs782286567 | snp | G/T | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644902 | AAACATGTTAGGAGC[G/T]ATGAAGATGAAATAC | 8027 |
rs782287632 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689327 | GGCTTATGTTTTGAC[C/T]ACTTCAGGGAGTCAT | 8027 |
rs782288832 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17671039 | CTAAATAAGGCTCTA[C/T]TCAGTATTCAAGGAG | 8027 |
rs782289453 | snp | C/T | 0.000546082 | 0.0165149 | synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714603 | GCCAGTATATAGTCC[C/T]CCTCCTGCCGCTACT | 8027 |
rs782289795 | in-del | -/AAT | | | intron-variant | STAM | GRCh38.p7 | 10:17707416 | TCCACCTCAAAAAAT[-/AAT]AATAATAATAATAAT | 8027 |
rs782289861 | snp | G/T | 1.86506e-05 | 0.00305368 | intron-variant | STAM | GRCh38.p7 | 10:17684960 | CAGAAATTAATTAAG[G/T]CAGTCTTCTTTCTTC | 8027 |
rs782289982 | snp | C/T | 1.64947e-05 | 0.00287177 | intron-variant | STAM | GRCh38.p7 | 10:17684777 | CATTTTAATCTGTAC[C/T]ACGAAATTACCTGCC | 8027 |
rs782290174 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17707880 | CCAGCCTGTTGCCTG[-/T]TTTTTTTTTTTTTAA | 8027 |
rs782290452 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17648677 | ACTTCAGTCATTGTT[A/T]TCTCTTATAGTCAGT | 8027 |
rs782291025 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17707164 | CCTGTAATCCCAGCA[C/T]GTTGGGAGGCCGAGG | 8027 |
rs782293270 | snp | C/T | 3.33356e-05 | 0.00408248 | intron-variant | STAM | GRCh38.p7 | 10:17660558 | CACTGGGTAAGTATT[C/T]AGCGTTTCAAAGGAT | 8027 |
rs782293800 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17678877 | AGTGGAAACATAGAA[-/T]TTTTTTGTGCTTTTG | 8027 |
rs782293817 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17673195 | CTTCTCACATCCTCT[G/T]TTCCTCCCAGCACTA | 8027 |
rs782294008 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17703838 | TAGAAGAGCAGCTGT[G/T]ATACAGCTGAGCTCT | 8027 |
rs782294189 | in-del | -/T | 1.64997e-05 | 0.00287221 | intron-variant | STAM | GRCh38.p7 | 10:17705062 | ATGTTGTGTACCTTC[-/T]TTCCTGAAGCTATCA | 8027 |
rs782294501 | snp | A/T | 1.70842e-05 | 0.00292264 | intron-variant | STAM | GRCh38.p7 | 10:17660431 | TAAAGATTTGAAAAA[A/T]AATGTTTCTGCAATC | 8027 |
rs782295917 | snp | C/G | 6.60404e-05 | 0.00574594 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714497 | TTATCTGTAGTTGCT[C/G]TATAAATCAGTATTG | 8027 |
rs782301385 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17687290 | GACCAGCCTGGCCAA[C/T]ATGGTAAAACCCCGC | 8027 |
rs782302287 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17666245 | ACTTTTTCTTTACCC[A/G]ACTAATGGATATGTT | 8027 |
rs782304037 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17678546 | GGCGTGAGTCACCAC[A/G]CCCAACCTCATGTAG | 8027 |
rs782304224 | snp | A/T | 1.65023e-05 | 0.00287244 | missense | STAM | GRCh38.p7 | 10:17705617 | TCTCAGAACTTAATG[A/T]GAAAGTGATGGAGGC | 8027 |
rs782304716 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17690897 | TACATTTAGAACCTG[A/T]TGATAGAAAGGAACT | 8027 |
rs782309796 | snp | A/G | 1.726e-05 | 0.00293763 | intron-variant | STAM | GRCh38.p7 | 10:17708998 | AGTGCTGTTACAGCT[A/G]TTTAAGTGCCCCCAG | 8027 |
rs782310878 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17663669 | GCATTTATTGTGTGC[A/C]TAAATGGGATATCTT | 8027 |
rs782311487 | snp | A/G | 1.96872e-05 | 0.00313739 | intron-variant | STAM | GRCh38.p7 | 10:17700163 | TAAATGTATTATTAA[A/G]AAAAGATAACTTTTA | 8027 |
rs782311685 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17692293 | AACAAACAAGAGAAT[A/G]TGTAATTAACAGGTT | 8027 |
rs782312554 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17658641 | TCAGCCTCCTGAGTA[C/T]GTTCAGCTAATTTTT | 8027 |
rs782313732 | snp | C/T | 1.67382e-05 | 0.00289289 | intron-variant | STAM | GRCh38.p7 | 10:17660566 | AAGTATTTAGCGTTT[C/T]AAAGGATTTTTATTC | 8027 |
rs782314871 | snp | A/G | 1.68202e-05 | 0.00289996 | missense, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688165 | ACGTTCCCAGCTATT[A/G]GCTCTCAGGTATTTT | 8027 |
rs782315202 | in-del | -/C | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715054 | TATTTGTCTCGTAAA[-/C]CTGGTCTGCAGAAAG | 8027 |
rs782315946 | snp | A/G | 3.29723e-05 | 0.00406018 | missense | STAM | GRCh38.p7 | 10:17708807 | CTCCAAGTGGTGCCT[A/G]CCTGGTTGCAGGGAA | 8027 |
rs782316816 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17662010 | CGTTCCCTTTTCTCC[A/G]TTTTTATTTGTCCTA | 8027 |
rs782317584 | snp | A/C/G | 8.82895e-05 | 0.00664367 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687989 | TAAATCATTGGCTAG[A/C/G]AAATTGGTGCTCTTT | 8027 |
rs782320922 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17657337 | GTGTGGGAGAACCCT[C/T]TCCTGCCCTGCTCGT | 8027 |
rs782322373 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17654021 | TCAGAAGTGCCTGGG[G/T]ACCCCAGAGCTTGTG | 8027 |
rs782322580 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17710765 | GGCTAGGAACTCAGT[A/C]AATATTTTATGAATA | 8027 |
rs782325176 | in-del | -/T | 0.00013342 | 0.00816653 | intron-variant | STAM | GRCh38.p7 | 10:17705748 | GGTTCTCAGGTAAGC[-/T]TTTAGAAGCCCATGT | 8027 |
rs782327708 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17676295 | TATAATGGGGCAGGA[C/G]TGGGTATAGGGAGGA | 8027 |
rs782332540 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17657434 | CTATAGTTTTCTTGT[A/T]ATGTTTTTGTCTGGT | 8027 |
rs782332717 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17649821 | TTTTGCCATATTGGC[A/C]AGGCTGGTCTTGAAC | 8027 |
rs782333815 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17646803 | AACATATAGAATACA[C/G]TGTATAGAATACACT | 8027 |
rs782334099 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17684387 | TCCACCCTGGCTGGA[A/G]GTGGAAGTCATGGCC | 8027 |
rs782334138 | snp | A/C | 3.30077e-05 | 0.00406236 | missense | STAM | GRCh38.p7 | 10:17700206 | TTAAAACAGAGAAGA[A/C]GACGGTACAATTTAG | 8027 |
rs782335322 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17701779 | GGAAGAAAGGCTTAC[C/T]GCTTGCCCGTAGTGA | 8027 |
rs782335838 | snp | A/C | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689370 | CATTCATCCAGACCT[A/C]CATGTGCTTTCTTCC | 8027 |
rs782338876 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17654123 | TAGTTAGCATCAGAA[A/G]TATGCTAGCCCTCTG | 8027 |
rs782339336 | snp | A/G | 0.000115351 | 0.00759355 | synonymous-codon | STAM | GRCh38.p7 | 10:17708901 | GGCAGTGGTCCCACC[A/G]TCCGCAAACCCAGCC | 8027 |
rs782339607 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17656571 | AGGGTAACGGTACAA[A/G]TGTTGAATCAGCCTT | 8027 |
rs782340621 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689458 | TGGGAGAGGAAGGAA[A/G]CAAAGGACATTCTTC | 8027 |
rs782342409 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17679695 | TCTTAATCAGTAATT[G/T]AGTCTTTTTACTTGT | 8027 |
rs782343204 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17646921 | CTCGTATACATTTGC[A/G]CATCTTCAAAATTAA | 8027 |
rs782345032 | snp | A/C | 1.65564e-05 | 0.00287714 | missense, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696831 | GGTTATTTCCTTCTA[A/C]TTTTGTGACTGCAGA | 8027 |
rs782346668 | snp | A/G | 0.000132092 | 0.00812579 | missense | STAM | GRCh38.p7 | 10:17693225 | CTTTTTTGTTAGGCT[A/G]CAGAACAAGCAAAAG | 8027 |
rs782346776 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17676518 | CATTGGAAGCTGCAA[C/T]GGTATAGAAATACTG | 8027 |
rs782348312 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17710163 | ACTGCCACTTTTCCC[C/G]TGCTAGTCCTCTGTT | 8027 |
rs782351109 | snp | C/T | 1.6477e-05 | 0.00287024 | synonymous-codon | STAM | GRCh38.p7 | 10:17705016 | TGAAAAGCTGGAAGA[C/T]ATTGATAGGTAAAAG | 8027 |
rs782351901 | snp | A/G | 3.3983e-05 | 0.00412193 | intron-variant | STAM | GRCh38.p7 | 10:17695011 | AGACTGTTGGATATA[A/G]TAACATTTTGGGTCT | 8027 |
rs782352117 | in-del | -/AT | | | intron-variant | STAM | GRCh38.p7 | 10:17664081 | CTTGTTTTAAAAGAA[-/AT]ATAAAACATTTACGT | 8027 |
rs782352154 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17671145 | GCTGTGTGTCTGCTA[A/G]GTCCTGGTATACTAA | 8027 |
rs782353061 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17681470 | TTATCTTTTTAAATC[C/T]GTAGAGACTTGTTTT | 8027 |
rs782354637 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714923 | ATTCAAGAAGGTAGA[A/C]CTCTCCTCAATTTAC | 8027 |
rs782357156 | snp | A/C | 0.0317867 | 0.121996 | intron-variant | STAM | GRCh38.p7 | 10:17684786 | CTGTACCACGAAATT[A/C]CCTGCCACAATTGAG | 8027 |
rs782357809 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17651948 | AAAAGTTGCTGCTTA[G/T]CAGAAAAAGTTCTCT | 8027 |
rs782358365 | snp | C/T | 6.59859e-05 | 0.00574357 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714519 | TCAGTATTGATGTAA[C/T]TGAGTGTTTTTCTTC | 8027 |
rs782358766 | snp | C/G | 1.73543e-05 | 0.00294565 | intron-variant | STAM | GRCh38.p7 | 10:17693339 | AGTCCCTGATGGTGG[C/G]AATAACATAAGCCTT | 8027 |
rs782359623 | snp | A/C | 1.67276e-05 | 0.00289197 | intron-variant | STAM | GRCh38.p7 | 10:17660455 | TGCAATCCCCTTTAC[A/C]ATCTACAGAGAAAGC | 8027 |
rs782362097 | snp | G/T | 1.93194e-05 | 0.00310794 | intron-variant | STAM | GRCh38.p7 | 10:17684967 | TAATTAAGGCAGTCT[G/T]CTTTCTTCACATATT | 8027 |
rs782363025 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714771 | ATATTCTCAGAAGGC[C/T]CTGCTATAGGACCCG | 8027 |
rs782363303 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17703983 | AGCTGCTCCGAAACA[A/G]AGCAAAATCCTCTGG | 8027 |
rs782364634 | in-del | -/T | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688629 | AGCCAGACCTGGAAA[-/T]TTTTTTTTTTTTTAA | 8027 |
rs782365409 | in-del | -/G | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643853 | GAAAAAAGGCGCACA[-/G]GCTCGACCCGAACTC | 8027 |
rs782366785 | snp | G/T | 3.3112e-05 | 0.00406877 | missense, utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644349 | GCGGAGATGCCTCTT[G/T]TTGCCACCAATCCCT | 8027 |
rs782367018 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17654672 | ACCTTATTATTTTCA[A/G]GGGATTTACAATATA | 8027 |
rs782368173 | snp | A/G | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713893 | TGGCCATCAGGTGCT[A/G]TGTGTTCTCCAGCCC | 8027 |
rs782368626 | in-del | -/TTA | 1.67635e-05 | 0.00289507 | intron-variant | STAM | GRCh38.p7 | 10:17708957 | TTACCCAAAGTAATT[-/TTA]TTACTGTTGATTCTT | 8027 |
rs782368686 | snp | C/T | 1.64743e-05 | 0.00287 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714604 | CCAGTATATAGTCCT[C/T]CTCCTGCCGCTACTG | 8027 |
rs782369485 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17706464 | GCTCACTGCAAGCTC[C/T]GCCTTCCGGGTTCTC | 8027 |
rs782370574 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17673464 | TTCTAGGCCCCATTC[A/G]CAATGACAGTGTTTT | 8027 |
rs782374889 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17710417 | ACCCATAGAGTGTAG[C/G]TATTAATGTCACCTC | 8027 |
rs782375826 | snp | C/T | 1.65094e-05 | 0.00287305 | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714498 | TATCTGTAGTTGCTC[C/T]ATAAATCAGTATTGA | 8027 |
rs782377013 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17668492 | TTTGTTTTGTACAGG[A/T]CAATGGGTTTTGACA | 8027 |
rs782378580 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17690411 | TCTAGATGTTATAAA[A/G]TATGTAACAGCTAAT | 8027 |
rs782378713 | snp | G/T | 1.67287e-05 | 0.00289207 | intron-variant | STAM | GRCh38.p7 | 10:17705756 | GGTAAGCTTTTAGAA[G/T]CCCATGTTGTTTTAA | 8027 |
rs782379290 | snp | C/G | 1.66435e-05 | 0.0028847 | intron-variant | STAM | GRCh38.p7 | 10:17700302 | GTTTCCATGGTGATA[C/G]GAGTTGGTACTTTGT | 8027 |
rs782381190 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17670776 | TATTCACGTTCCATT[A/G]TCTCATAAGAAATGC | 8027 |
rs782384310 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17680694 | TTATAGGTGCAAGTC[A/G]CTGTGCCCGGCCTTG | 8027 |
rs782385895 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17691090 | TCTGACCAGGCATAC[C/T]TGTAGTTTTCAGAAG | 8027 |
rs782386950 | snp | A/G | 1.64895e-05 | 0.00287132 | intron-variant, synonymous-codon, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17684837 | GTGCTTTTAGCTTCT[A/G]GGAGCATGTGTATCA | 8027 |
rs782389207 | snp | C/T | 3.29728e-05 | 0.00406021 | intron-variant | STAM | GRCh38.p7 | 10:17704533 | GGTAAAACTTTTCTA[C/T]TTACCTTGCAAATAA | 8027 |
rs782389768 | snp | C/T | 1.65181e-05 | 0.00287381 | intron-variant | STAM | GRCh38.p7 | 10:17693219 | GTTCCTCTTTTTTGT[C/T]AGGCTGCAGAACAAG | 8027 |
rs782390264 | snp | A/G | 1.64963e-05 | 0.00287192 | missense | STAM | GRCh38.p7 | 10:17705716 | AGCCATATTATATGC[A/G]GTCATCTGGTGTTTC | 8027 |
rs782391537 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17694664 | TGATTTATTAAGTCT[G/T]CAGTGAAGCTTGATA | 8027 |
rs782393000 | snp | A/G | 3.29652e-05 | 0.00405974 | missense, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17684709 | TCTATTATGAGAAGA[A/G]TGAACCACAAAGATC | 8027 |
rs782394449 | snp | A/G | 1.67562e-05 | 0.00289444 | missense, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688159 | GGAGTTACGTTCCCA[A/G]CTATTGGCTCTCAGG | 8027 |
rs782395383 | in-del | -/AT | | | intron-variant | STAM | GRCh38.p7 | 10:17710443 | CCTCTCAAGGAACAC[-/AT]ATGTTTATTTCAACA | 8027 |
rs782395703 | snp | C/G | 1.64746e-05 | 0.00287002 | synonymous-codon | STAM | GRCh38.p7 | 10:17695119 | GTATCCAAGCACATC[C/G]AGTCTCTTAACTAAC | 8027 |
rs782396788 | snp | C/T | 1.65323e-05 | 0.00287505 | intron-variant | STAM | GRCh38.p7 | 10:17693207 | CTCAAATACTGTGTT[C/T]CTCTTTTTTGTTAGG | 8027 |
rs782399972 | in-del | -/TT | 4.94539e-05 | 0.00497238 | intron-variant | STAM | GRCh38.p7 | 10:17704963 | CTTCACATCTTGTCA[-/TT]TTTTAGCAATGTGTC | 8027 |
rs782402555 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698176 | CATTTTTATAGAGAC[A/G]GATTGGTGAGACCCA | 8027 |
rs782402892 | snp | C/T | 1.65688e-05 | 0.00287821 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644363 | TTTTGCCACCAATCC[C/T]TTCGATCAGGATGTT | 8027 |
rs782404576 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17674844 | ATCAGAACTTTGAAC[A/T]TAACAAAACAATGAA | 8027 |
rs782405314 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17671043 | ATAAGGCTCTACTCA[A/G]TATTCAAGGAGCATT | 8027 |
rs782406563 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17703910 | GAATGACAAGTTGTT[A/G]GTCATAAGCAATGCC | 8027 |
rs782409775 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17661326 | CACTGCTGCATTACA[C/T]TTGATATTTGCAGTG | 8027 |
rs782410176 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17666249 | TTTCTTTACCCGACT[A/C]ATGGATATGTTTTGG | 8027 |
rs782410177 | snp | C/T | 1.6476e-05 | 0.00287014 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714783 | GGCTCTGCTATAGGA[C/T]CCGGTGTTCCTCTTG | 8027 |
rs782411103 | snp | A/C | | | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695855 | ACTTACTGCCTTAGT[A/C]CATTTGGGCTGCCGT | 8027 |
rs782411500 | snp | A/G | 1.64909e-05 | 0.00287144 | missense, utr-variant-5-prime, intron-variant | STAM | GRCh38.p7 | 10:17684692 | CTAAGGATTGTCTTC[A/G]GTCTATTATGAGAAG | 8027 |
rs782413686 | snp | A/G | 1.66374e-05 | 0.00288417 | stop-gained, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696787 | TAGTGATCCTAACTG[A/G]TGGAAAGGTGAAACC | 8027 |
rs782414046 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17669774 | GCAATCTCAGCTCAC[C/T]GCAAATGCCGCCTCC | 8027 |
rs782414348 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17657590 | AGTGAACCCATCTGG[A/G]CCTGTGCTTTCTGTT | 8027 |
rs782415155 | snp | G/T | 3.42906e-05 | 0.00414055 | intron-variant | STAM | GRCh38.p7 | 10:17684933 | ATTAAATAAGGTAAG[G/T]AGCATTATTTCCAGA | 8027 |
rs782416461 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714757 | CAGCCACAGCAACCA[C/T]ATTCTCAGAAGGCTC | 8027 |
rs782417395 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17656839 | AAAAGCTTTACAGCA[C/G]GAAAGAAAGGAAAGT | 8027 |
rs782418723 | snp | A/C | 1.7644e-05 | 0.00297013 | intron-variant | STAM | GRCh38.p7 | 10:17693348 | TGGTGGGAATAACAT[A/C]AGCCTTTATTTTTTC | 8027 |
rs782419016 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17687036 | TAATGAACTGGCCAG[G/T]TTTTTTCCCTTAATA | 8027 |
rs782420004 | snp | A/G | 1.658e-05 | 0.00287919 | intron-variant | STAM | GRCh38.p7 | 10:17704393 | TAAAGTTGCCTAAAG[A/G]TTGGTAGCTTTTTAT | 8027 |
rs782421926 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17709059 | ATATCTGTGGTCAGC[A/G]TCATGCGGCCGCCCC | 8027 |
rs782424104 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17693376 | TTCTCTGAGATATTT[A/G]AAGGTAAAATAAATA | 8027 |
rs782424712 | in-del | -/T/TTT | | | intron-variant | STAM | GRCh38.p7 | 10:17686378 | TAATAACATCCCGCC[-/T/TTT]TTTTTTTTTTTTTTT | 8027 |
rs782424831 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17679332 | CGATGTTGAGCATTT[A/G]TTATGTGCTTATTGG | 8027 |
rs782425228 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17679969 | ATAAATTGAGTCACC[C/T]TTCTTTCTTGGCCAG | 8027 |
rs782426079 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17713056 | CATACTGCTAGACTC[C/T]CGGTCAGTTCACCAT | 8027 |
rs782426752 | snp | A/G | 1.65982e-05 | 0.00288077 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644318 | GAGGGAGTCCCCGGG[A/G]ACACCTCGGCACGCA | 8027 |
rs782428139 | snp | A/T | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643440 | CACTGATCAACTTTT[A/T]GCTCCAGTTTTTTTC | 8027 |
rs782429739 | snp | C/G | 1.64776e-05 | 0.00287028 | missense | STAM | GRCh38.p7 | 10:17708893 | CTCAGCCAGGCAGTG[C/G]TCCCACCATCCGCAA | 8027 |
rs782430310 | in-del | -/TCTCT | | | intron-variant | STAM | GRCh38.p7 | 10:17657849 | GGTGTTTTCTCTCTC[-/TCTCT]TTTTTTTTTTTTCCT | 8027 |
rs782436416 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17712428 | CACATATGGAGTGAT[A/G]ACAAATAATGCCTTA | 8027 |
rs782436475 | snp | C/T | 0.00020232 | 0.0100558 | synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714741 | CAGCCAACAGCCACC[C/T]CAGCCACAGCAACCA | 8027 |
rs782438256 | snp | A/G | 1.81632e-05 | 0.00301351 | intron-variant | STAM | GRCh38.p7 | 10:17700171 | TTATTAAAAAAAGAT[A/G]ACTTTTACATATCTT | 8027 |
rs782440234 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17699901 | CTTACTAAACTCTGA[C/T]GTGTAGTAGGTGATT | 8027 |
rs782441042 | snp | A/G | 6.59022e-05 | 0.00573993 | missense | STAM | GRCh38.p7 | 10:17704988 | TGTGTCACCAGATGG[A/G]ACCTCTCATTGATGA | 8027 |
rs782441495 | snp | C/T | 3.47657e-05 | 0.00416913 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688011 | GTGCTCTTTTATTTC[C/T]TTTTCTATTTTACAG | 8027 |
rs782441926 | in-del | -/G | | | intron-variant | STAM | GRCh38.p7 | 10:17647866 | TACTCTCAGCCTCTT[-/G]GCCTGAGCTCTCGAC | 8027 |
rs782443894 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17646160 | ACTTGTTACACCTGA[A/G]TCATTTCCTGATTAC | 8027 |
rs782444341 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17669248 | TGCATATGTATTTAA[A/G]TCTGTTTTTCTCTTT | 8027 |
rs782446155 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17661020 | GTTATTTATGAGTTC[C/T]TTTCTCCTTTGTCAG | 8027 |
rs782449879 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17715934 | CCTGGCTTTGCTTAA[C/T]GTTTATATAGGTATT | 8027 |
rs782450389 | snp | C/T | 1.76487e-05 | 0.00297053 | intron-variant | STAM | GRCh38.p7 | 10:17684943 | GTAAGGAGCATTATT[C/T]CCAGAAATTAATTAA | 8027 |
rs782451102 | snp | C/T | 3.42554e-05 | 0.00413842 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688200 | ATGAAGTTGTGTGTG[C/T]GCTACAGTTTGTTTC | 8027 |
rs782452782 | snp | A/G | 1.65496e-05 | 0.00287655 | synonymous-codon | STAM | GRCh38.p7 | 10:17693263 | AGCTCTTGTAGCCAA[A/G]GATCCTGGTACTGTG | 8027 |
rs782452941 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17711078 | ATTTGACTCGAGCTT[C/T]CTAGCGGCAAATCAA | 8027 |
rs782453901 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17665878 | ACATGATTTCTACTG[C/T]GCAATTTCCAGTGTG | 8027 |
rs782454144 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714656 | TCACTCTGTACCAGA[A/G]TGCAGGACCTAATAT | 8027 |
rs782454833 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17659714 | GTGATCCTCCCACCT[C/T]GGCCTCCCAAAATGC | 8027 |
rs782456550 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697861 | TATCGTTTTTTAATG[C/T]TAGATAGAAGGGATC | 8027 |
rs782456754 | in-del | -/C | | | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696138 | TGAATTTTGGGAAGA[-/C]CACAAACATTCAGAC | 8027 |
rs782458012 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17682709 | GCACATGAAAAAAAA[A/T]GTGTATAATGCCATG | 8027 |
rs782458394 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17667822 | GAAGCAATAGTCTGT[A/C]GGTGAATGCTGAATG | 8027 |
rs782458670 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17692919 | AGTTTTTTTAAACAC[A/G]TTGAAATCTTCTCTA | 8027 |
rs782460919 | snp | C/T | 9.93114e-05 | 0.00704598 | missense, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17660541 | AAAGTTGGTCAGTCT[C/T]GCACTGGGTAAGTAT | 8027 |
rs782462031 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17664732 | TAGAGGAATGTTGTA[C/G]ATTGGAATGCAGTTC | 8027 |
rs782462653 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17704599 | AAGAATGGGTTTTGA[A/G]GATAATATTAAAAAT | 8027 |
rs782465693 | snp | C/T | 0.00020911 | 0.0102231 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696904 | CCAATAAATGATGTT[C/T]TCTAATCCTTTTCTT | 8027 |
rs782465831 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17656549 | AAAGAGTCTTCTGAT[G/T]TCTTGGAGGGTAACG | 8027 |
rs782466728 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17667022 | GATTATCACAGCAGT[C/T]CTAGGTACTGTAGAT | 8027 |
rs782467299 | in-del | -/T | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17716587 | TATACTTTTCTGCAA[-/T]TTTTCTTTGTCTTTT | 8027 |
rs782467535 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17691946 | TACACTGTAGTTGTC[A/G]TGTGTATTACCTCTA | 8027 |
rs782468669 | snp | A/G | | | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696499 | CATCTGAAGCTGACA[A/G]TTTTTTCGTATTGGT | 8027 |
rs782468775 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17675653 | AAAAACACTAGGCTA[A/G]ACTATGAACTTCATG | 8027 |
rs782471599 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17709872 | AGTGACCTTAAGGGG[G/T]ATGATGGCAAGGCCC | 8027 |
rs782471783 | in-del | -/T | 0.000954181 | 0.0218215 | intron-variant | STAM | GRCh38.p7 | 10:17704921 | TATCAAAGGTTCACA[-/T]TTTTTTTTCTTGTAC | 8027 |
rs782473176 | snp | A/G | 1.86611e-05 | 0.00305454 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696729 | TAAAGATGTACAGAA[A/G]TAAATACATTTGTTA | 8027 |
rs782473882 | snp | A/G | 1.70816e-05 | 0.00292242 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644425 | CTCACCGGACTGCAC[A/G]CTCACTCTGCCAGCC | 8027 |
rs782474731 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697127 | AGAGACAGGGTTTCA[C/T]CATGTTGGCCAGGCT | 8027 |
rs782475026 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17658150 | TCCCACAAATTTTGC[A/G]AAGTTGTATTTTCAC | 8027 |
rs782475532 | snp | A/G | 0.000164946 | 0.00907996 | missense, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688117 | CTTAGTCTAATATCA[A/G]CAATGATTAAGAACC | 8027 |
rs782475654 | in-del | -/CC/CCC | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714309 | ACTTATTTCCGCAAA[-/CC/CCC]CCACCCCCCCCAACT | 8027 |
rs782475914 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17659898 | AATTTTTGTTGAGAA[A/C]GTGTTTATTTCCTCT | 8027 |
rs782480058 | snp | A/T | 1.65277e-05 | 0.00287464 | missense | STAM | GRCh38.p7 | 10:17693253 | AAGCAAGCCCAGCTC[A/T]TGTAGCCAAGGATCC | 8027 |
rs782483268 | in-del | -/C | | | intron-variant | STAM | GRCh38.p7 | 10:17687010 | GCCGCTATGAAGATA[-/C]ATCAGTATTTTAATG | 8027 |
rs782486456 | snp | C/T | 3.29554e-05 | 0.00405914 | missense | STAM | GRCh38.p7 | 10:17705680 | ATCCGATGTATTCCA[C/T]GTATGCAAAGTTACA | 8027 |
rs782489092 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17686791 | AAAATACAGATTACA[C/T]GTGCACTTAGAAAGA | 8027 |
rs782489767 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17661716 | TTATTACTCAATTCT[C/G]TCCATCTGCCTTCAT | 8027 |
rs782490486 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17680625 | TTGCCCAGGCTGGTC[C/T]CACACTCCTTGGCTG | 8027 |
rs782490692 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644237 | CCCTGTAGAGTCGGT[A/C]TCTGTTGCTCTTTTT | 8027 |
rs782492006 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17675502 | AGTGAGACTCTGTCT[-/A]CAAAAAAAAAAAAAA | 8027 |
rs782493156 | snp | C/G | 4.94271e-05 | 0.00497102 | missense | STAM | GRCh38.p7 | 10:17704493 | TGATGATCAGCCAGA[C/G]CTACCAGAGCTGCTT | 8027 |
rs782495133 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17654514 | GGCGTGGGTCACCGC[A/G]CCCGGCTAAACCAGG | 8027 |
rs782495202 | snp | A/G | 1.648e-05 | 0.0028705 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714547 | TTCCTCCACAGTACA[A/G]TGGTCAGTTCCGTTC | 8027 |
rs782499709 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17661829 | AGGGGCTGTATACCC[A/T]CCACTCTAGCTTTTT | 8027 |
rs782500226 | snp | C/G | 1.80234e-05 | 0.00300189 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696747 | AATACATTTGTTATG[C/G]TAAAGCATTGTTTTT | 8027 |
rs782500771 | snp | C/T | 1.64939e-05 | 0.0028717 | missense | STAM | GRCh38.p7 | 10:17700250 | GTAGAGACAATAGAA[C/T]CAGAGCCGGAACCAG | 8027 |
rs782501849 | snp | A/G | 1.74385e-05 | 0.00295278 | intron-variant | STAM | GRCh38.p7 | 10:17708727 | GAGAAAGTTCAGTAT[A/G]CTTATTAAAATTTTA | 8027 |
rs782502288 | snp | C/T | 1.64806e-05 | 0.00287054 | missense | STAM | GRCh38.p7 | 10:17704970 | ATCTTGTCATTTTAG[C/T]AATGTGTCACCAGAT | 8027 |
rs782505074 | in-del | -/G | 1.65179e-05 | 0.00287379 | intron-variant | STAM | GRCh38.p7 | 10:17693217 | GTGTTCCTCTTTTTT[-/G]TTAGGCTGCAGAACA | 8027 |
rs782505227 | snp | A/C | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17689173 | TTCTATTTTGGGTAA[A/C]CTTCCTTTAGGATGC | 8027 |
rs782505495 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17707090 | TCACAAACTCATCAC[A/G]GTGAGGTGAGGTTAT | 8027 |
rs782505895 | snp | A/G | 8.24545e-05 | 0.00642032 | intron-variant | STAM | GRCh38.p7 | 10:17684778 | ATTTTAATCTGTACC[A/G]CGAAATTACCTGCCA | 8027 |
rs782506519 | snp | A/G | 5.27412e-05 | 0.00513496 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688225 | TGTTTCTCTTAAATA[A/G]CTATATTTATTTGAA | 8027 |
rs782506890 | snp | A/T | 6.67791e-05 | 0.00577798 | missense | STAM | GRCh38.p7 | 10:17693299 | CAAAAAAGAAGAAGA[A/T]GATTTAGCAAAAGGT | 8027 |
rs782507726 | snp | C/T | 1.69243e-05 | 0.00290893 | intron-variant | STAM | GRCh38.p7 | 10:17708972 | TTTACTGTTGATTCT[C/T]GTTTGGAGTTAGTGC | 8027 |
rs782508590 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17660742 | ACACGAGTCAGGGCA[A/G]CATAGTGAGACCCCG | 8027 |
rs782509845 | in-del | -/C | | | intron-variant | STAM | GRCh38.p7 | 10:17650037 | TAGAATATTTGTGTT[-/C]CCAGTCAGACTGCTT | 8027 |
rs782510597 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643254 | CGTAATTTGCGGGAT[A/G]ATTTCCATTTACGTA | 8027 |
rs782513894 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714564 | GGTCAGTTCCGTTCA[A/G]GGAAACACATATCCC | 8027 |
rs782514963 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17653001 | TTTCTGAGTGATAAG[A/C]GCATCTTTGTTATTT | 8027 |
rs782515164 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17676698 | ATGTCCAGTTAACAC[A/C]ATCTTTCACTCGCGA | 8027 |
rs782515665 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716123 | ACGATTTCCCTGGTT[A/G]GGCTATACTATTATT | 8027 |
rs782515699 | snp | A/G | 0.000129249 | 0.0080379 | intron-variant | STAM | GRCh38.p7 | 10:17700151 | AAAGTAGAATTTTAA[A/G]TGTATTATTAAAAAA | 8027 |
rs782516943 | snp | G/T | 1.66189e-05 | 0.00288256 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644307 | CGTGCTGTCGAGAGG[G/T]AGTCCCCGGGGACAC | 8027 |
rs782518808 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17679422 | GGGTTGTTGTTCGTT[A/G]TTGAGATGTAGGAGT | 8027 |
rs782519517 | in-del | -/G | | | intron-variant | STAM | GRCh38.p7 | 10:17690308 | CATTATGTCTTGATT[-/G]GTAGAGAAACTAGCT | 8027 |
rs782520375 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687679 | TAAAGGAACTGTATC[A/G]TTTATTCTCTCCTTC | 8027 |
rs782522322 | snp | C/G | 1.64732e-05 | 0.0028699 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714637 | GCTGCTGCAACTGCC[C/G]ATGTCACTCTGTACC | 8027 |
rs782523099 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17681296 | GTTATGTTTTCCTTT[C/T]CATTAATCTCAAAGT | 8027 |
rs782524823 | snp | G/T | 0.000313012 | 0.0125063 | synonymous-codon | STAM | GRCh38.p7 | 10:17708862 | CTACAGTCTTCCCCC[G/T]GAGCAGCTGTCTTCT | 8027 |
rs782524900 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17691314 | ACGAGGTCAGGAGAT[A/C]GAGACCATCCTGGCT | 8027 |
rs782525335 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17681197 | GGTATTGAGATCGTC[-/T]TTTTTTTTTTTTTTT | 8027 |
rs782529155 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17686534 | GGCATGCGCCACCAC[A/G]CCTGGCTGGTTTTTG | 8027 |
rs782530289 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17712557 | ATTTCCCAACAATAG[A/T]TTTATAAATAACAAT | 8027 |
rs782532102 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17651729 | ATCAGGGATATTAGA[C/T]GAAAGATTTTTGAAG | 8027 |
rs782533373 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17706071 | ACCCTGTCTCTAAAA[C/T]AAATAAATAAATAAA | 8027 |
rs782533589 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17681414 | TTCTTTGTTCTTTCA[A/G]ATTTTATTCTGTCTT | 8027 |
rs782534017 | snp | C/G | 1.64955e-05 | 0.00287184 | missense | STAM | GRCh38.p7 | 10:17708800 | GGGCCTCCTCCAAGT[C/G]GTGCCTACCTGGTTG | 8027 |
rs782534673 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17658003 | TGTTTGTTTTCTTCT[A/G]CTTGCTTAGTTTGGA | 8027 |
rs782537087 | snp | A/C | 4.94287e-05 | 0.00497111 | missense | STAM | GRCh38.p7 | 10:17704506 | GACCTACCAGAGCTG[A/C]TTCATCTTGAAGGTA | 8027 |
rs782537641 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17671824 | ATTTTGTTATGTCCT[A/G]AGAGAGGGATAATGA | 8027 |
rs782538440 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643864 | GCACAGCTCGACCCG[A/C]ACTCAACCTGCTTTC | 8027 |
rs782539324 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17716272 | GGTAGCTTGTTTATT[C/T]TCTTTTTGAGAGAAG | 8027 |
rs782540034 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17703500 | ATATAGTAGCATAAC[C/T]ATGTAAAAACCATGC | 8027 |
rs782540506 | snp | A/C | 1.67897e-05 | 0.00289733 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644405 | TTGCCTCTCCCTGCC[A/C]ATTCCTCACCGGACT | 8027 |
rs782541241 | snp | C/T | 1.72427e-05 | 0.00293616 | intron-variant | STAM | GRCh38.p7 | 10:17705548 | AGCATTATATCATTT[C/T]AGTAACAGCTATGCT | 8027 |
rs782543067 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17650368 | GTGAAAACACATGAC[A/G]TTCTGACTCTTTACC | 8027 |
rs782543368 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17647547 | AGCAATTTAGCTTAG[C/T]GTTAAGAATTCAGAC | 8027 |
rs782547420 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17675794 | AGTTCTTTGGTACCT[A/G]TTGAATTTTTTTTTA | 8027 |
rs782548323 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17677469 | GGCCTTTACCATGCA[C/T]TGAAATGATTGTTTT | 8027 |
rs782549529 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17653553 | TACAGGTGGTTGTTT[G/T]TATCTGGGGGTCTGC | 8027 |
rs782550685 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17686667 | CAGGCATGAGCCACC[A/G]CGCCCAGCCAACATC | 8027 |
rs782550914 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17646115 | TATCTTTCAACATAT[C/T]CTTGTGTGTTAAGGC | 8027 |
rs782552412 | snp | G/T | 1.64928e-05 | 0.00287161 | missense, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688084 | GAATGGACAGATGAA[G/T]TTAAGAATGATCCAC | 8027 |
rs782553191 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17678706 | ATTCACAGTATTATG[C/T]AACCAACACCACTAT | 8027 |
rs782553455 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17712361 | ATTATAGCCCATACC[A/G]TTGTCAATAATAGTA | 8027 |
rs782553749 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17670437 | TTTTTTTCTACCTTC[A/G]CTGTGCTGTGTGCTT | 8027 |
rs782553909 | snp | C/T | 6.59011e-05 | 0.00573988 | missense | STAM | GRCh38.p7 | 10:17704495 | ATGATCAGCCAGACC[C/T]ACCAGAGCTGCTTCA | 8027 |
rs782554172 | snp | A/G | | | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696456 | TTATAGCTCATTACA[A/G]AGACTTCTTACTCTG | 8027 |
rs782554798 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17674000 | ACTAAGAACAGCAGG[A/G]CGGGAGAGTCCTTGG | 8027 |
rs782554877 | in-del | -/A | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688531 | CAGTAGCGTGATCTC[-/A]GGCTCACTGCCACCT | 8027 |
rs782557443 | snp | C/T | 3.33411e-05 | 0.00408282 | missense, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688151 | AGGAACAAGGAGTTA[C/T]GTTCCCAGCTATTGG | 8027 |
rs782558957 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17679270 | AGCCTAGTGAGTGTG[A/C]AGTGGCATCTCAATG | 8027 |
rs782564050 | snp | C/T | 1.65488e-05 | 0.00287647 | intron-variant | STAM | GRCh38.p7 | 10:17693191 | GAATTTGATAACAAC[C/T]CTCAAATACTGTGTT | 8027 |
rs782564535 | snp | A/G | 1.65272e-05 | 0.0028746 | missense, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17660532 | ATCTGTGATAAAGTT[A/G]GTCAGTCTCGCACTG | 8027 |
rs782567044 | snp | C/G | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644518 | AGGCTCCCTCCTTCA[C/G]AGCTGGGAGGAGGTT | 8027 |
rs782568722 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17672925 | AATTCTCCTTTCCCT[C/G]TTCTTTGTCCCTGCC | 8027 |
rs782570790 | snp | A/G/T | 3.30073e-05 | 0.00406236 | synonymous-codon | STAM | GRCh38.p7 | 10:17700258 | AATAGAACCAGAGCC[A/G/T]GAACCAGCCTTTATT | 8027 |
rs782571168 | snp | C/G | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697876 | CTAGATAGAAGGGAT[C/G]AAAGAAAATTACAAA | 8027 |
rs782572896 | in-del | -/G | 1.88382e-05 | 0.003069 | intron-variant | STAM | GRCh38.p7 | 10:17700168 | GTATTATTAAAAAAA[-/G]ATAACTTTTACATAT | 8027 |
rs782574476 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17648849 | TTAAAGGGAAATGCA[A/G]GTTTTTTTATTGTGG | 8027 |
rs782575957 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17669410 | TTCCCCTTCCTACTC[C/T]CATTAAATAAACTTT | 8027 |
rs782577349 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17658096 | TAAAAATATGTATTC[A/G]ATGCTATAAATTTCC | 8027 |
rs782577972 | snp | C/T | 1.70708e-05 | 0.00292149 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696762 | GTAAAGCATTGTTTT[C/T]TGTTTGTCATAGTGA | 8027 |
rs782579954 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17701550 | TAGTAGCAACAGAGA[G/T]CATATGGCCTGCAAA | 8027 |
rs782580550 | snp | C/T | 1.64757e-05 | 0.00287012 | missense | STAM | GRCh38.p7 | 10:17704994 | ACCAGATGGGACCTC[C/T]CATTGATGAAAAGCT | 8027 |
rs782581052 | snp | A/G | 3.29843e-05 | 0.00406092 | synonymous-codon | STAM | GRCh38.p7 | 10:17705624 | ACTTAATGTGAAAGT[A/G]ATGGAGGCCCTTTCC | 8027 |
rs782582591 | snp | G/T | 1.6473e-05 | 0.00286988 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714657 | CACTCTGTACCAGAA[G/T]GCAGGACCTAATATG | 8027 |
rs782583229 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714749 | AGCCACCTCAGCCAC[A/G]GCAACCATATTCTCA | 8027 |
rs782583282 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17711710 | GTATGTATCGGCATT[C/T]CAGCAGCACACTTAC | 8027 |
rs782583780 | snp | C/T | 1.65296e-05 | 0.00287481 | missense, utr-variant-5-prime, intron-variant | STAM | GRCh38.p7 | 10:17684676 | TCTCATTTTTTTAGA[C/T]CTAAGGATTGTCTTC | 8027 |
rs782585860 | in-del | -/T | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697303 | AGAAGTCTTACAGAA[-/T]TTATACATTATATAT | 8027 |
rs782587115 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17661722 | CTCAATTCTGTCCAT[C/G]TGCCTTCATAATCTC | 8027 |
rs782587789 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643367 | AATAATTTTTATTGG[G/T]TAACTAAACTTATAA | 8027 |
rs782587883 | snp | A/G | 4.94279e-05 | 0.00497107 | missense | STAM | GRCh38.p7 | 10:17708885 | TGTCTTCTCTCAGCC[A/G]GGCAGTGGTCCCACC | 8027 |
rs782590339 | snp | C/T | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17690009 | AATGATTGTGCCATA[C/T]GTACCCTTGTTTGGT | 8027 |
rs782590691 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17654491 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTGGG | 8027 |
rs782591508 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17706164 | TTTAAAATTAAAATA[A/C]AGTTTAACGGAATTT | 8027 |
rs782591639 | snp | A/C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17683268 | TCTGGGGCTCAAGTG[A/C/G]ACCTCCCACCTCAGG | 8027 |
rs782591677 | snp | A/C/T | 1.64727e-05 | 0.00286986 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714673 | GCAGGACCTAATATG[A/C/T]CCCAGGTGCCAAACT | 8027 |
rs782592955 | snp | A/G/T | 3.73806e-05 | 0.00432309 | intron-variant | STAM | GRCh38.p7 | 10:17700168 | GTATTATTAAAAAAA[A/G/T]ATAACTTTTACATAT | 8027 |
rs782593753 | snp | A/G | 1.65023e-05 | 0.00287244 | synonymous-codon | STAM | GRCh38.p7 | 10:17705717 | GCCATATTATATGCA[A/G]TCATCTGGTGTTTCT | 8027 |
rs782594577 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17710191 | GTTTGACTATGTCAC[A/G]TGCTGCTCTACCTTC | 8027 |
rs782596835 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17681486 | GTAGAGACTTGTTTT[A/G]TGGCTTAACATTGTT | 8027 |
rs782598564 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714957 | GACTTTTTAGAGGTT[C/T]TTCCCCCCCCGCCCC | 8027 |
rs782599282 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17681427 | CAGATTTTATTCTGT[C/G]TTTGGAGAACATGCT | 8027 |
rs782599861 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17694031 | TTTTTATTTTTTTGA[G/T]TGCTAGTGAGACTGA | 8027 |
rs782602805 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17690291 | GTGAATGCTGGCAAG[A/G]GCATTATGTCTTGAT | 8027 |
rs782605449 | snp | A/G | 1.70252e-05 | 0.00291759 | intron-variant | STAM | GRCh38.p7 | 10:17708984 | TCTTGTTTGGAGTTA[A/G]TGCTGTTACAGCTGT | 8027 |
rs782606823 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | STAM | GRCh38.p7 | 10:17708872 | CCCCCGGAGCAGCTG[C/T]CTTCTCTCAGCCAGG | 8027 |
rs782607180 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17651997 | TTGAAATTCAAATGA[G/T]GCTCTGTGTATGTTT | 8027 |
rs782607586 | snp | G/T | 2.14927e-05 | 0.00327809 | intron-variant | STAM | GRCh38.p7 | 10:17700152 | AAGTAGAATTTTAAA[G/T]GTATTATTAAAAAAA | 8027 |
rs782612476 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17665945 | ATATGATGGGCTGAA[C/G]AGCCTTCATTTGTTT | 8027 |
rs782613197 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17657172 | GGAGCCCCCTTTTTT[C/G]CTTCTCCCTGGTGCC | 8027 |
rs782613239 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17650571 | TTCTAAACAACAAAT[A/G]TATCCTGTCTACCCT | 8027 |
rs782613399 | in-del | -/CCA/CCCCG | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17714318 | CGCAAACCACCCCCC[-/CCA/CCCCG]CCAACTTTTTTTACA | 8027 |
rs782614079 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17649613 | GCACTCAAGAATTAT[G/T]TATCAAATAATGAAT | 8027 |
rs782614712 | snp | G/T | 3.31082e-05 | 0.00406854 | missense, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17660542 | AAGTTGGTCAGTCTC[G/T]CACTGGGTAAGTATT | 8027 |
rs782616531 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17674432 | TCATCTGAAGGCTTC[A/G]CTGGGATGGATGCTT | 8027 |
rs782617291 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17657726 | GTCCATTTCATCTAG[A/G]TTATCAATTTTGTGG | 8027 |
rs782620190 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17653104 | AAGGACTAACCATGT[G/T]ATTAAAGGATTTGGG | 8027 |
rs782620191 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17703784 | CCAACTGAAACACTG[A/G]TAGAAAGAAAATGTG | 8027 |
rs782620574 | in-del | -/T | 0.000954181 | 0.0218215 | intron-variant | STAM | GRCh38.p7 | 10:17704920 | TATCAAAGGTTCACA[-/T]TTTTTTTTTCTTGTA | 8027 |
rs782621356 | in-del | -/ATCA | | | intron-variant | STAM | GRCh38.p7 | 10:17708594 | CTAAAAATGAAAACC[-/ATCA]ATCAACAGCCTATTT | 8027 |
rs782621517 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17679385 | GAAATGTCTATTCAA[A/G]TCCTTTGCCCATTTT | 8027 |
rs782624944 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643848 | CGAGAGGAAAAAAGG[A/C]GCACAGCTCGACCCG | 8027 |
rs782625039 | snp | C/G | | | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717286 | GAGAATTGCTTGAAC[C/G]TGGGAGACGGAGGTT | 8027 |
rs782625536 | in-del | -/A | | | intron-variant | STAM | GRCh38.p7 | 10:17700792 | ATTAAGATTGTTTGC[-/A]ACATGACTGAGGAAG | 8027 |
rs782626094 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17712582 | AACAATTGGAGGAAA[C/G]TTTAGAAGTAGGCAG | 8027 |
rs782626781 | snp | C/T | 1.70729e-05 | 0.00292167 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644426 | TCACCGGACTGCACG[C/T]TCACTCTGCCAGCCC | 8027 |
rs782628434 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17651834 | TCGGGCTGACTGAAT[G/T]ACAGTCCTTTCCTCA | 8027 |
rs782629866 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17679496 | TTGGAAATATTTTCT[C/T]CCATTCTGTGGGTTG | 8027 |
rs782629968 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17650197 | AGAAAGACCTTGGGC[-/T]TTTGGGCTTAAATTG | 8027 |
rs782630045 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17681356 | ATTGACCCATTGGCT[A/G]TTTAGGAGGATGTTG | 8027 |
rs782630913 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17670972 | TCTTTTGTACTTTTA[C/T]ATTAGAATTCTCTTA | 8027 |
rs782632582 | snp | A/C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17683047 | GTGAATAGATAAAAG[A/C/T]GTAGTTGGATTACAA | 8027 |
rs782633173 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17662069 | TAGGCTAGCGAATTA[A/G]CCCACTGGCATTTTT | 8027 |
rs782634695 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644714 | AGCGAAGGGCTTAAG[A/G]CGTATGTTGGCTAGA | 8027 |
rs782636427 | snp | A/G | 1.65811e-05 | 0.00287929 | missense | STAM | GRCh38.p7 | 10:17708780 | AACCATCGCAGGTGT[A/G]TGCAGGGCCTCCTCC | 8027 |
rs782638753 | snp | A/G | 3.295e-05 | 0.00405881 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714586 | ACATATCCCAGCCAG[A/G]CGCCAGTATATAGTC | 8027 |
rs782639677 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17655325 | ATGAATTGTTTGGAT[A/C]TTTGTATTAATTCTT | 8027 |
rs782641729 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17648666 | ATTCTTACCTTACTT[C/T]AGTCATTGTTATCTC | 8027 |
rs782642113 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17663168 | TGTTGTAGCACAAAG[C/G]TGTAGAGATCAATTT | 8027 |
rs782642202 | snp | C/T | 6.60502e-05 | 0.00574637 | synonymous-codon | STAM | GRCh38.p7 | 10:17695206 | CAATGAACTTACTTT[C/T]AAAGCTGGAGAAATT | 8027 |
rs782645025 | snp | C/T | 6.72506e-05 | 0.00579834 | intron-variant | STAM | GRCh38.p7 | 10:17693316 | ATTTAGCAAAAGGTG[C/T]GTTTTTAAGTCCCTG | 8027 |
rs782646477 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17691979 | TACGTTATAAGCCCC[A/G]GAGGTAATGTTACAT | 8027 |
rs782647447 | snp | C/T | | | intron-variant, downstream-variant-500B | STAM, LOC105376438 | GRCh38.p7 | 10:17695629 | AGAACAGTATAGCCA[C/T]AGGGAACAAATTTAT | 8027 |
rs782651940 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17705815 | GCTCATGCCTGTAAT[C/G]TCAGCAATTTGGGAG | 8027 |
rs782653203 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17668015 | AGAGGGTTTTCAGTT[A/G]TTGGTAATGACAAGG | 8027 |
rs782653338 | snp | C/T | 1.65078e-05 | 0.00287291 | intron-variant | STAM | GRCh38.p7 | 10:17684970 | TTAAGGCAGTCTTCT[C/T]TCTTCACATATTTTA | 8027 |
rs782653805 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17660031 | GTTTTCTTTCCTTCA[G/T]TCCCCTCTCCATATT | 8027 |
rs782654321 | snp | A/G | | | synonymous-codon | STAM | GRCh38.p7 | 10:17708898 | CCAGGCAGTGGTCCC[A/G]CCATCCGCAAACCCA | 8027 |
rs782654616 | snp | C/T | 6.59805e-05 | 0.00574333 | intron-variant | STAM | GRCh38.p7 | 10:17684779 | TTTTAATCTGTACCA[C/T]GAAATTACCTGCCAC | 8027 |
rs782655586 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17655411 | GATTTTAGGGTAGCT[A/G]GGTAGGTACCCTACC | 8027 |
rs782655705 | snp | A/C | 1.64898e-05 | 0.00287135 | synonymous-codon | STAM | GRCh38.p7 | 10:17700237 | TGATGATGTTCAGGT[A/C]GAGACAATAGAACCA | 8027 |
rs782655880 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643262 | GCGGGATAATTTCCA[C/T]TTACGTACAAGATGT | 8027 |
rs782657899 | snp | A/G | 6.62175e-05 | 0.00575364 | intron-variant | STAM | GRCh38.p7 | 10:17693172 | AGGGTGGGTGAGAGG[A/G]GGAGAATTTGATAAC | 8027 |
rs782658456 | snp | C/T | | | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696618 | CTTTTCTGAGGCTTC[C/T]TCTTCTTTTGTAATA | 8027 |
rs782659916 | snp | C/T | 1.66485e-05 | 0.00288513 | intron-variant | STAM | GRCh38.p7 | 10:17660556 | CGCACTGGGTAAGTA[C/T]TTAGCGTTTCAAAGG | 8027 |
rs782660653 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17671957 | GACAATAATTTCCTT[G/T]AGAGTATACAATCTT | 8027 |
rs782661386 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17667062 | TTTCAAGTGAGAAAT[C/G]TAATTGATATTTAGG | 8027 |
rs782662657 | in-del | -/TGATAGATATTTGTATA | 1.64727e-05 | 0.00286986 | intron-variant | STAM | GRCh38.p7 | 10:17705060 | TATGTTGTGTACCTT[-/TGATAGATATTTGTATA]CTTTCCTGAAGCTAT | 8027 |
rs782664718 | snp | A/C | 4.94833e-05 | 0.00497385 | intron-variant | STAM | GRCh38.p7 | 10:17684775 | TTCATTTTAATCTGT[A/C]CCACGAAATTACCTG | 8027 |
rs782665460 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17646155 | ATCCAACTTGTTACA[C/G]CTGAGTCATTTCCTG | 8027 |
rs782665591 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17703511 | TAACCATGTAAAAAC[C/T]ATGCATGGAGAAAGG | 8027 |
rs782668350 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643867 | CAGCTCGACCCGAAC[C/T]CAACCTGCTTTCTTT | 8027 |
rs782670929 | snp | A/T | 3.32364e-05 | 0.00407641 | synonymous-codon | STAM | GRCh38.p7 | 10:17693281 | TCCTGGTACTGTGGC[A/T]AACAAAAAAGAAGAA | 8027 |
rs782675017 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17667220 | CAACTTCTGCCTCCC[A/C]AGTTCAAGCGATTCT | 8027 |
rs782677115 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17692750 | TTTATATCGTTTTAT[A/G]TATATATCTGAGTTC | 8027 |
rs782677485 | snp | A/G | 1.64852e-05 | 0.00287094 | missense | STAM | GRCh38.p7 | 10:17705707 | TACAGAATCAGCCAT[A/G]TTATATGCAGTCATC | 8027 |
rs782678180 | snp | A/G | 1.66266e-05 | 0.00288323 | synonymous-codon | STAM | GRCh38.p7 | 10:17695227 | TGGAGAAATTATTAC[A/G]GTTCTTGATGACAGG | 8027 |
rs782682445 | snp | C/T | 1.64846e-05 | 0.0028709 | intron-variant | STAM | GRCh38.p7 | 10:17704529 | TGAAGGTAAAACTTT[C/T]CTATTTACCTTGCAA | 8027 |
rs782682847 | snp | A/G | | | intron-variant, utr-variant-3-prime | STAM | GRCh38.p7 | 10:17713589 | CCAGTTATTTCTACC[A/G]GTTTTTAGGTTCTAA | 8027 |
rs782683477 | snp | C/G | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687688 | TGTATCATTTATTCT[C/G]TCCTTCCCACTTTTT | 8027 |
rs782685108 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17686083 | ACTTTTCGAACATCA[C/T]GGTTAAATGATAATT | 8027 |
rs782686337 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17684105 | CTCTTTAGCATATCG[A/C]CCTCGGTCACTTTTT | 8027 |
rs782687683 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | STAM | GRCh38.p7 | 10:17695105 | ACCCTTTCCACTTTG[C/T]ATCCAAGCACATCCA | 8027 |
rs782688723 | snp | A/G | 1.66838e-05 | 0.00288818 | synonymous-codon, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688152 | GGAACAAGGAGTTAC[A/G]TTCCCAGCTATTGGC | 8027 |
rs782689369 | snp | G/T | 8.28397e-05 | 0.00643529 | intron-variant | STAM | GRCh38.p7 | 10:17700287 | TTGATGAAGTAAGTG[G/T]TTTCCATGGTGATAG | 8027 |
rs782690774 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17673761 | CTGGAGTCAGATTGT[C/T]TGCTTGTGAGGTTCT | 8027 |
rs782692573 | snp | A/G | 1.72502e-05 | 0.0029368 | intron-variant | STAM | GRCh38.p7 | 10:17705550 | CATTATATCATTTTA[A/G]TAACAGCTATGCTTC | 8027 |
rs782699553 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17685092 | TGTTGAAGAGACTGC[A/G]GATTCATGTAACTTT | 8027 |
rs782700563 | snp | G/T | 1.67579e-05 | 0.00289459 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644401 | GTTTTTGCCTCTCCC[G/T]GCCCATTCCTCACCG | 8027 |
rs782701137 | snp | C/T | 1.72826e-05 | 0.00293956 | intron-variant | STAM | GRCh38.p7 | 10:17705538 | CATTATTTAGAGCAT[C/T]ATATCATTTTAGTAA | 8027 |
rs782702785 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17650094 | GGACATTTTTTTAGT[C/G]TGCTTTGCTTAGTCC | 8027 |
rs782702794 | snp | C/T | 1.65108e-05 | 0.00287317 | missense | STAM | GRCh38.p7 | 10:17693226 | TTTTTTGTTAGGCTG[C/T]AGAACAAGCAAAAGC | 8027 |
rs782704568 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714692 | AGGTGCCAAACTATA[A/G]CTTAACATCATCAAC | 8027 |
rs782705530 | snp | C/T | 4.98451e-05 | 0.004992 | synonymous-codon | STAM | GRCh38.p7 | 10:17708940 | TCAGCAGACTCAGGC[C/T]GCTTACCCAAAGTAA | 8027 |
rs782707456 | snp | A/T | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697100 | GTTTTTGTGTGTGTA[A/T]GTATTTTTAGTAGAG | 8027 |
rs782709165 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17709687 | TAGCTGGCAACAGAA[A/G]TTTCTAGGTAGCACA | 8027 |
rs782710758 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688521 | TGGGTAGAGTGCAGT[A/G]GCGTGATCTCGGCTC | 8027 |
rs782711483 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17666821 | CTGGATATTCTAGAG[G/T]TGAAAGGACAGCATC | 8027 |
rs782713068 | snp | A/G | 1.64944e-05 | 0.00287175 | synonymous-codon | STAM | GRCh38.p7 | 10:17700213 | AGAGAAGAAGACGGT[A/G]CAATTTAGTGATGAT | 8027 |
rs782713114 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17692483 | CTCAGGAACTGCTAG[C/T]AGTTTCTGGTAACTG | 8027 |
rs782713744 | snp | A/C | 1.66571e-05 | 0.00288587 | missense, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696864 | TCACTGCTGAACCAG[A/C]AATGAGTAAGTATTT | 8027 |
rs782713954 | snp | C/G | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688898 | AAAAGTTAGGGATGA[C/G]TTGAGAGATTCTTTT | 8027 |
rs782714187 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17705086 | GCTATCACTGTACTG[C/T]AAAGTGGGCTATAAC | 8027 |
rs782715694 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17698630 | TAGAAGTCTATTTCA[C/T]TTAGCCTGTCAAAGA | 8027 |
rs782717624 | snp | G/T | 1.65707e-05 | 0.00287838 | splice-acceptor-variant | STAM | GRCh38.p7 | 10:17695048 | ACTCATTGTTTTCTA[G/T]CCATTGAGTTGTCTC | 8027 |
rs782718363 | snp | G/T | 3.41058e-05 | 0.00412938 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688194 | TTGGGAATGAAGTTG[G/T]GTGTGTGCTACAGTT | 8027 |
rs782720576 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17706632 | GATCCACCCGCCTCG[A/G]CCTCCCAAAGTGCTG | 8027 |
rs782720706 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17711997 | AATAATTACACATTG[C/G]GTGACATGGTTGGGA | 8027 |
rs782721292 | in-del | -/T | | | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696164 | AGACATATTTTAACA[-/T]TTTTTTTTTTTTTGA | 8027 |
rs782721393 | snp | A/C | 1.66186e-05 | 0.00288254 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644308 | GTGCTGTCGAGAGGG[A/C]GTCCCCGGGGACACC | 8027 |
rs782721519 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17702882 | ACGTGGTGGTGTGCG[C/T]TTGTAATCCTAGCTA | 8027 |
rs782721640 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17671958 | ACAATAATTTCCTTT[A/G]GAGTATACAATCTTC | 8027 |
rs782722569 | snp | A/G | 1.65225e-05 | 0.00287419 | missense, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17660529 | GATATCTGTGATAAA[A/G]TTGGTCAGTCTCGCA | 8027 |
rs782722920 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17705325 | GCTCACAAATGACCC[A/G]TATGTTAGTAACTAG | 8027 |
rs782723655 | in-del | -/T | 1.70717e-05 | 0.00292157 | intron-variant | STAM | GRCh38.p7 | 10:17660434 | AGATTTGAAAAATAA[-/T]GTTTCTGCAATCCCC | 8027 |
rs782724040 | snp | A/G | 1.6477e-05 | 0.00287024 | missense | STAM | GRCh38.p7 | 10:17705024 | TGGAAGATATTGATA[A/G]GTAAAAGAACATGGG | 8027 |
rs782725078 | snp | A/G | 1.66255e-05 | 0.00288314 | missense, utr-variant-5-prime, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688043 | GTCATCCTAAAGTAT[A/G]TGAAAAATTAAAGGC | 8027 |
rs782726524 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17701090 | CAACTTGGTGACACA[C/G]CATACTTTTTGGAGC | 8027 |
rs782726894 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17668842 | TTATATGGATGTTCT[A/C]CAGTTTGTTTATTAA | 8027 |
rs782727769 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17678147 | CCTCTCCTCATTCCT[C/G]GAAACCACTAATCTA | 8027 |
rs782728128 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17670226 | TACTTGCCTAGACAA[C/T]GATTTTACTTTTTTA | 8027 |
rs782728630 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17673915 | AGCTTGATGTGGGGA[A/G]CTGTCAAGGGCCTAA | 8027 |
rs782731329 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17682749 | ATTGTTGTGTAATGC[C/T]AGTCAGGTCAAGTTT | 8027 |
rs782731820 | snp | C/T | 0.000218695 | 0.0104547 | intron-variant | STAM | GRCh38.p7 | 10:17660576 | CGTTTCAAAGGATTT[C/T]TATTCTTTCTTTTTA | 8027 |
rs782733181 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714644 | CAACTGCCGATGTCA[C/T]TCTGTACCAGAATGC | 8027 |
rs782733683 | snp | G/T | 1.64781e-05 | 0.00287033 | synonymous-codon, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714618 | TCCTCCTGCCGCTAC[G/T]GCTGCTGCTGCAACT | 8027 |
rs782734043 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17672377 | TTAGTTTTCCTTGAT[A/C]CTCTGACTGTAGAAT | 8027 |
rs782735787 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644166 | CCTTGCTGTTGCCGC[A/C]GCCGCAGCTGCTGCC | 8027 |
rs782736735 | snp | G/T | 1.64773e-05 | 0.00287026 | missense | STAM | GRCh38.p7 | 10:17695156 | CATGAAGGCCGAAAA[G/T]TTCGTGCTATATATG | 8027 |
rs782738528 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17648391 | CAGCAGGACATGGGC[A/G]GGGACAAATAAGAGA | 8027 |
rs782740972 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17659307 | ATGGAAGCATACATA[A/T]GAATATCAGAATATA | 8027 |
rs782741588 | snp | A/T | 1.6549e-05 | 0.0028765 | intron-variant | STAM | GRCh38.p7 | 10:17704408 | GTTGGTAGCTTTTTA[A/T]ATTAACTACTTAATT | 8027 |
rs782743052 | snp | G/T | 1.65938e-05 | 0.00288039 | intron-variant | STAM | GRCh38.p7 | 10:17704933 | ACATTTTTTTTTCTT[G/T]TACTTTCTTATATTT | 8027 |
rs782743102 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17652258 | TGATTAAAAAAAAAA[-/T]ACTTGTTCTTTTATA | 8027 |
rs782744402 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17693537 | GTGTATCCAAAAACA[A/T]TATCAAGTGCTTTTT | 8027 |
rs782744516 | snp | C/G | | | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696301 | AGTTTACACCTAGGA[C/G]TGTACTCTTTGCGAA | 8027 |
rs782745930 | snp | A/G | | | intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17689953 | TGAAAACTGCGTTTC[A/G]GTCCACAAAGGGACT | 8027 |
rs782747269 | snp | C/G | 4.94287e-05 | 0.00497111 | synonymous-codon | STAM | GRCh38.p7 | 10:17708841 | GCAGATGAGCCACCT[C/G]CAGAGCTACAGTCTT | 8027 |
rs782747726 | snp | C/T | 1.64844e-05 | 0.00287087 | stop-gained | STAM | GRCh38.p7 | 10:17695078 | CTCAAGGAACAAAGG[C/T]AGCAGTCAACCACCC | 8027 |
rs782749996 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17657925 | AATAACCAGCTTTTG[G/T]TTGTGCTGATTTTCT | 8027 |
rs782750157 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17648525 | TCACTCTTTGGGTCC[A/G]TGCTACCTTTAAGAG | 8027 |
rs782750329 | snp | A/C/G | 4.94754e-05 | 0.0049735 | intron-variant | STAM | GRCh38.p7 | 10:17684771 | TGGTTTCATTTTAAT[A/C/G]TGTACCACGAAATTA | 8027 |
rs782750474 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17667679 | CAGATGATGGTCAAT[A/T]GCTAAGAAGCTAGTA | 8027 |
rs782750536 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17691284 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGGTCA | 8027 |
rs782752295 | snp | G/T | 1.65329e-05 | 0.0028751 | missense | STAM | GRCh38.p7 | 10:17693255 | GCAAGCCCAGCTCTT[G/T]TAGCCAAGGATCCTG | 8027 |
rs782755618 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17670149 | TTGGGATAACAACAG[A/G]AGTCAAGTTGTTGAC | 8027 |
rs782756813 | snp | A/G | | | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17687566 | AATTAAATTTTCAAA[A/G]TGATTAACATGCAGT | 8027 |
rs782759771 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642468 | CCAGGCACTGTAATA[A/C]GCGTTTTGCTTGTAC | 8027 |
rs782760745 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17666647 | TGTGATCTGCCCGCC[A/T]TGGCCTCCCAAAGCG | 8027 |
rs782760981 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17642750 | TATTTCCCTTAGGAA[G/T]ATTATACAGTATTTA | 8027 |
rs782762817 | snp | C/T | 1.65105e-05 | 0.00287315 | missense | STAM | GRCh38.p7 | 10:17693241 | CAGAACAAGCAAAAG[C/T]AAGCCCAGCTCTTGT | 8027 |
rs782762930 | snp | A/C/G | 0.000112339 | 0.00749389 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696725 | AAGATAAAGATGTAC[A/C/G]GAAATAAATACATTT | 8027 |
rs782763918 | snp | A/T | 1.64879e-05 | 0.00287118 | utr-variant-3-prime, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714807 | CCTCTTGGTGGCAGA[A/T]ACCTGCTAAATGCCA | 8027 |
rs782764899 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17661564 | TGGATATCGTTCTAT[A/G]TAAGCCTTCATCTCA | 8027 |
rs782764919 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17657677 | TGTCTGTTTCTTGTA[C/T]GTATTTCAGCAGATT | 8027 |
rs782767745 | snp | A/C | 1.93616e-05 | 0.00311134 | intron-variant | STAM | GRCh38.p7 | 10:17695275 | TTAAAATTTGTATGA[A/C]AGTGTGTATGGCTTC | 8027 |
rs782767888 | snp | C/T | 1.66023e-05 | 0.00288113 | intron-variant | STAM | GRCh38.p7 | 10:17704927 | AGGTTCACATTTTTT[C/T]TTCTTGTACTTTCTT | 8027 |
rs782771353 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17662710 | TCTTTCTGGGCCTTA[C/T]TTTTCCAGTTTACCA | 8027 |
rs782771469 | snp | C/T | 1.70548e-05 | 0.00292012 | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17696887 | AAGTATTTTCCAGCC[C/T]GCCAATAAATGATGT | 8027 |
rs782771756 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17665322 | TAAGTATGTATTCAC[A/G]TGGCTCAAATGTTAA | 8027 |
rs782772445 | snp | A/C | | | intron-variant | STAM | GRCh38.p7 | 10:17670330 | TTTTGCAGATGAGAA[A/C]ACTAAAGCCCTGAGA | 8027 |
rs782772560 | snp | A/C | | | intron-variant, stop-gained | STAM | GRCh38.p7 | 10:17713356 | TATTTCTCCTCCGTA[A/C]TTCCCCACAGGACAG | 8027 |
rs782776127 | snp | G/T | 1.73763e-05 | 0.00294752 | intron-variant | STAM | GRCh38.p7 | 10:17708740 | ATGCTTATTAAAATT[G/T]TAGAATTGAATATGA | 8027 |
rs782777553 | snp | A/G | 1.65064e-05 | 0.00287279 | intron-variant, missense, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17684880 | ATTTTTCATTTAGAA[A/G]TATGTTCAAGAGATT | 8027 |
rs782777666 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17685411 | GTTGCCTCAAAAGTG[A/G]TGGCGGGGGAGTTTC | 8027 |
rs782779571 | snp | A/G | | | synonymous-codon | STAM | GRCh38.p7 | 10:17695146 | TAACCACCAACATGA[A/G]GGCCGAAAAGTTCGT | 8027 |
rs782781448 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | STAM, STAM-AS1 | GRCh38.p7 | 10:17643784 | AGATGATCCAAAGGA[A/G]TTTCCATTTCCTTCC | 8027 |
rs782786062 | snp | A/T | | | intron-variant | STAM | GRCh38.p7 | 10:17679234 | AATATTTGGTATCTT[A/T]CCTTTCTTAAAAAAA | 8027 |
rs782786691 | snp | A/G | | | intron-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696183 | TTTTTTTTTTGAGTG[A/G]AAGAAAATAAAGTTT | 8027 |
rs782787234 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644179 | GCCGCCGCAGCTGCT[G/T]CCGCGGTTGGTGGGG | 8027 |
rs782788567 | in-del | -/G | | | intron-variant | STAM | GRCh38.p7 | 10:17693666 | ATATATCCATTAACT[-/G]TTCTATAATATCCAG | 8027 |
rs782789447 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644239 | CTGTAGAGTCGGTCT[C/G]TGTTGCTCTTTTTGC | 8027 |
rs782790171 | snp | A/G | | | utr-variant-3-prime | STAM | GRCh38.p7 | 10:17715663 | GAAGATAGTAATTAG[A/G]TTTCTAAGCTGTATA | 8027 |
rs782790827 | snp | G/T | 1.86719e-05 | 0.00305542 | intron-variant, nc-transcript-variant | STAM, LOC105376438 | GRCh38.p7 | 10:17696730 | AAAGATGTACAGAAA[G/T]AAATACATTTGTTAT | 8027 |
rs782792530 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17687443 | GCAGTGTGCTGAGAT[C/T]GAGCCACTGCAGTCC | 8027 |
rs782792998 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17648446 | CAGCAGCAACCGGCT[C/T]GGGTCCCCTTCCATG | 8027 |
rs782793266 | snp | A/C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17712422 | ATCTCACACATATGG[A/C/G]GTGATGACAAATAAT | 8027 |
rs782795383 | snp | C/T | | | downstream-variant-500B | STAM | GRCh38.p7 | 10:17717218 | ACTACAAAAATTAGC[C/T]GGGCGTGGTGGCAGG | 8027 |
rs782796569 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17655128 | TTTCAATTTGCTTTG[A/G]GCTTTGCATTATTTG | 8027 |
rs782796868 | snp | G/T | 1.67944e-05 | 0.00289775 | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644408 | CCTCTCCCTGCCCAT[G/T]CCTCACCGGACTGCA | 8027 |
rs782799215 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon | STAM | GRCh38.p7 | 10:17705666 | GTTAATGAACGAAGA[C/T]CCGATGTATTCCATG | 8027 |
rs782800117 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17675673 | TGAACTTCATGAAGC[A/G]GGGTCAGTCTCTTCT | 8027 |
rs782800339 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17674245 | CCGTCAGCTTCCTTT[A/G]TTAGAGGCTGTTCTA | 8027 |
rs782802702 | snp | C/T | 1.64901e-05 | 0.00287137 | synonymous-codon | STAM | GRCh38.p7 | 10:17704442 | GTAGGATAAAATGGA[C/T]CAGTTGCTACAGATG | 8027 |
rs782803251 | in-del | -/T | | | intron-variant, upstream-variant-2KB | STAM, LOC105376438 | GRCh38.p7 | 10:17697850 | AATATCTCATTATCG[-/T]TTTTTTAATGCTAGA | 8027 |
rs782805317 | snp | C/G | 1.69573e-05 | 0.00291177 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688182 | CTCTCAGGTATTTTG[C/G]GAATGAAGTTGTGTG | 8027 |
rs782807282 | snp | A/C | 0.000369196 | 0.0135817 | missense, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714631 | ACTGCTGCTGCTGCA[A/C]CTGCCGATGTCACTC | 8027 |
rs782807833 | snp | A/C | 1.64822e-05 | 0.00287068 | missense, intron-variant, utr-variant-5-prime | STAM | GRCh38.p7 | 10:17684734 | AAGATCCTCACGTTG[A/C]TATGCAGGCTTTGAC | 8027 |
rs782808693 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17676790 | TCATTGGAAGGATAA[C/T]AGCCAGAAGTATACT | 8027 |
rs782809738 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17647253 | GATAACTTATTTCAT[C/G]AAGTTTGTATTTCAA | 8027 |
rs782810599 | snp | A/G | 5.2516e-05 | 0.00512398 | intron-variant, upstream-variant-2KB | STAM | GRCh38.p7 | 10:17688222 | GTTTGTTTCTCTTAA[A/G]TAGCTATATTTATTT | 8027 |
rs782812014 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17682524 | AAGCCTTAGATATTT[G/T]TTATTTGATTTCCAA | 8027 |
rs782812829 | snp | A/G | 1.72311e-05 | 0.00293518 | intron-variant | STAM | GRCh38.p7 | 10:17660592 | TATTCTTTCTTTTTA[A/G]AAAACACGAAAGGCC | 8027 |
rs782813583 | snp | G/T | | | intron-variant | STAM | GRCh38.p7 | 10:17691203 | GAACACCAAAAAGTT[G/T]TTTTCTTCTCAGCTC | 8027 |
rs782814044 | snp | C/G | | | intron-variant | STAM | GRCh38.p7 | 10:17649989 | ATCATTTCCCTGCCT[C/G]TGCTAAATCATCATA | 8027 |
rs782815288 | snp | A/G | 1.66291e-05 | 0.00288345 | utr-variant-5-prime, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17644295 | AGCTCTGACTCCCGT[A/G]CTGTCGAGAGGGAGT | 8027 |
rs782815724 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17706757 | GTTGTGTACACTCAA[C/T]ATGTATAGCCTTTTG | 8027 |
rs782817033 | snp | C/T | | | intron-variant | STAM | GRCh38.p7 | 10:17701444 | TGGCAAACTCTTAGG[C/T]CAAATTTAGCCTGTT | 8027 |
rs782817755 | in-del | -/AGA | 1.64735e-05 | 0.00286993 | cds-indel, downstream-variant-500B | STAM | GRCh38.p7 | 10:17714763 | AGCAACCATATTCTC[-/AGA]AGAAGGCTCTGCTAT | 8027 |
rs782818072 | snp | C/T | | | intron-variant, upstream-variant-2KB | STAM, STAM-AS1 | GRCh38.p7 | 10:17645168 | TGAAGATAATAATTA[C/T]GGGAATTTGAGTTTC | 8027 |
rs782819206 | snp | A/G | | | intron-variant | STAM | GRCh38.p7 | 10:17671394 | CTCTAAATCCCTGGC[A/G]TGAGTCTAGGAGTTT | 8027 |
rs796143846 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17700601 | GATTTTTTTTTTTTT[-/T]GAACATCTATCTTTG | 8027 |
rs796853720 | in-del | -/T | | | intron-variant | STAM | GRCh38.p7 | 10:17667129 | GCAGAGTTAAATAAT[-/T]TTTTTTTTTTTTTTG | 8027 |
rs117774687 | snp | G/T | 0.0327778 | 0.123752 | | | | : | GAAAAGGGAGAGGAG[G/T]GGGGTAAAAACGAAA | 8027 |