| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs1374529 | snp | C/G | 0 | 0 | intron-variant | INTS12 | GRCh38.p7 | 4:105697412 | TCTCTTCCCCCCTCA[C/G]AGGTAACCACTATTC | 57117 |
| rs3213950 | snp | C/T | 0.00546505 | 0.0519871 | utr-variant-5-prime, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105700012 | AGCAGCCATTGCAAA[C/T]GCCTGAAGGAAAAAA | 57117 |
| rs3756260 | snp | C/G | 0.46974 | 0.119223 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105708873 | CGTTTTTCTCCTGGC[C/G]TCTGTGGAGGCGAGT | 57117 |
| rs3796924 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105688603 | ATCTTATCCTTCATT[C/G]CAAAACCATGTTACG | 57117 |
| rs3796925 | snp | A/G | 0.00796804 | 0.0626141 | intron-variant | INTS12 | GRCh38.p7 | 4:105701651 | CTTTTTTTTCTTTAA[A/G]TTCCACTCCTGTGAC | 57117 |
| rs4434257 | snp | A/T | 0.100231 | 0.200173 | intron-variant | INTS12 | GRCh38.p7 | 4:105698220 | CCTTCCTCATTAATG[A/T]AAATGAATATCAACC | 57117 |
| rs4490460 | snp | C/T | 0.245631 | 0.249962 | intron-variant | INTS12 | GRCh38.p7 | 4:105697912 | aaaattagccaagca[C/T]ggtggcatgcacctg | 57117 |
| rs4699196 | snp | C/T | 0.463666 | 0.129795 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709792 | TGTATTTCTATTTTA[C/T]CTAAGCTTATCTGTA | 57117 |
| rs5860807 | in-del | -/T | 0.307176 | 0.243374 | intron-variant | INTS12 | GRCh38.p7 | 4:105698554 | AAAACAATTTTTTTT[-/T]CTTTAGTAATAATAG | 57117 |
| rs6820671 | snp | A/G | 0.345925 | 0.230864 | intron-variant | INTS12 | GRCh38.p7 | 4:105692664 | TATATAGAATGCCTT[A/G]ATTAAATTTGGCTAT | 57117 |
| rs6850604 | snp | G/T | 0.0566069 | 0.158427 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707223 | ACTGACAGCTGCTGT[G/T]CCCCTCTCCATTCCA | 57117 |
| rs7659526 | snp | C/T | 0.347694 | 0.230122 | intron-variant | INTS12 | GRCh38.p7 | 4:105700486 | AATGGTGAAAAGGTA[C/T]ATTAAGTGATTAGCT | 57117 |
| rs10008158 | snp | A/G | 0 | 0 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683066 | AGTGGGCGTAGTGCT[A/G]TTATTGGAACCTATT | 57117 |
| rs10016392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105701606 | AAACCTGCCATTCCC[C/T]CAGCATATACAAGGG | 57117 |
| rs10516523 | snp | G/T | 0.46974 | 0.119223 | intron-variant | INTS12 | GRCh38.p7 | 4:105704106 | CTTTTATAGCAAAAC[G/T]TTCTCAGAAATCATA | 57117 |
| rs10615792 | in-del | -/AT | 0.223225 | 0.248562 | intron-variant | INTS12 | GRCh38.p7 | 4:105690459 | ATAGATTTCAGAGAC[-/AT]ATAAGAGGTAGAATT | 57117 |
| rs10672030 | in-del | -/T | 0 | 0 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710233 | TTTTTTTTTTTTTTT[-/T]GAGCTGGAGTCCTGC | 57117 |
| rs11726569 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | INTS12 | GRCh38.p7 | 4:105685451 | CTATATGACAAATCA[A/G]TAATGGATATGCCTT | 57117 |
| rs11727189 | snp | G/T | 0.0614824 | 0.164198 | intron-variant | INTS12 | GRCh38.p7 | 4:105697983 | tgaacctgggaggga[G/T]agagcgcagtgagcc | 57117 |
| rs11727735 | snp | A/G | 0.0486741 | 0.148216 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710713 | TGTGAAAATTCAGTA[A/G]TTTTATTTCATACTT | 57117 |
| rs11728044 | snp | C/G | 0.0622301 | 0.165053 | intron-variant | INTS12 | GRCh38.p7 | 4:105683629 | TAGTGCTTTAACATA[C/G]TTTTTACCCAACAAA | 57117 |
| rs11940951 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707034 | AAATTTCTTGGCCTA[A/G]CATTTAAGAAGATTC | 57117 |
| rs11941690 | snp | A/C | 0.471768 | 0.115407 | intron-variant | INTS12 | GRCh38.p7 | 4:105690103 | AGCTGAGAAGCAGAA[A/C]ATATGGGAACATGAA | 57117 |
| rs12374256 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | INTS12 | GRCh38.p7 | 4:105696204 | ttgacatatgtatac[A/G]tctgtgacaccatca | 57117 |
| rs12507921 | snp | A/G | 0 | 0 | intron-variant | INTS12 | GRCh38.p7 | 4:105695025 | tgcctcctgggctca[A/G]gcaatcctcccaccc | 57117 |
| rs13111824 | snp | G/T | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710493 | ctcggcttcccaaag[G/T]ggtgggattacaggc | 57117 |
| rs13132641 | snp | A/T | 0.0131051 | 0.0798799 | intron-variant | INTS12 | GRCh38.p7 | 4:105684775 | GTTATGAAAGACCTA[A/T]TTTTTTTTCCTTTTC | 57117 |
| rs13142949 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105702131 | atttatttctatttc[C/T]ttttttttttttttt | 57117 |
| rs17036109 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | INTS12 | GRCh38.p7 | 4:105684085 | ACAGTGACATTTTGG[A/G]TAGGACTGATCTCAT | 57117 |
| rs17036120 | snp | C/G | 0.0614824 | 0.164198 | intron-variant | INTS12 | GRCh38.p7 | 4:105700351 | CAGTACATAGAACTT[C/G]ATGGGTTTACGTCAA | 57117 |
| rs17036123 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | INTS12 | GRCh38.p7 | 4:105701033 | TGCAGCACACTTGCA[C/T]TGCTATAGTTAGGGA | 57117 |
| rs17036125 | snp | A/T | 0.0614824 | 0.164198 | intron-variant | INTS12 | GRCh38.p7 | 4:105702517 | TATAATTGATCTTTA[A/T]CCTCAAGGAGCTTTA | 57117 |
| rs17036129 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | INTS12 | GRCh38.p7 | 4:105703372 | AATTCTTAGGTGATG[C/T]TGGGAATTAGCTGTG | 57117 |
| rs17036133 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | INTS12 | GRCh38.p7 | 4:105703576 | TCCCTACTTTATAGA[A/C]ATCCACCCTGCTAGC | 57117 |
| rs17262443 | snp | C/T | 0.110167 | 0.207236 | intron-variant | INTS12 | GRCh38.p7 | 4:105693649 | AGATCTGTAGAAGAA[C/T]TGCAATGAATTTATT | 57117 |
| rs17262457 | snp | C/T | 0.109461 | 0.206758 | intron-variant | INTS12 | GRCh38.p7 | 4:105697205 | ATAGCTTTGCTGATA[C/T]AGATAACTTGTTATT | 57117 |
| rs17262764 | snp | A/G | 0.46974 | 0.119223 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707852 | TCTGTGATCTCTCCA[A/G]TCTAAATTGGGCATT | 57117 |
| rs28391170 | snp | A/C | 0.342134 | 0.232404 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708089 | CTTCCAATAAACATT[A/C]TTTTAAAGATGCTGC | 57117 |
| rs28403197 | snp | A/G | 0.171704 | 0.237423 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708410 | TGTCCCTAGACCTAG[A/G]AATATGCTCGGTCCG | 57117 |
| rs28414565 | snp | A/C | 0.172351 | 0.237636 | intron-variant | INTS12 | GRCh38.p7 | 4:105683672 | TTAGTTAAACATCTA[A/C]TTCTTTTAGACTTTT | 57117 |
| rs28450989 | snp | C/G | 0.328148 | 0.237472 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105708850 | TATTTTCCACATAAG[C/G]TGGCTGTCGTTTTTC | 57117 |
| rs28628106 | snp | C/T | 0.46974 | 0.119223 | intron-variant | INTS12 | GRCh38.p7 | 4:105686084 | TTTCTTTTTTTGAGT[C/T]GCAGTTTCGCTCTTG | 57117 |
| rs28642176 | snp | A/C | 0.171704 | 0.237423 | intron-variant | INTS12 | GRCh38.p7 | 4:105705027 | ATCACTTCTCACAAT[A/C]CAAAGGTTCAAGAAT | 57117 |
| rs34072732 | snp | A/G | 0.0978298 | 0.198354 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683207 | CAATTTTGCTGTTGA[A/G]GGACCAGCAGAGGAA | 57117 |
| rs34166034 | in-del | -/C | | | intron-variant, utr-variant-5-prime | INTS12 | GRCh38.p7 | 4:105702893 | TATCTTACCTTTACT[-/C]CCCCTTTTCTGTTGC | 57117 |
| rs34234581 | snp | C/T | 0.00192581 | 0.0309709 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682778 | CTTCTTGACCATCTG[C/T]AATCGCTTCATAGCA | 57117 |
| rs34535300 | in-del | -/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105686102 | GTTTCGCTCTTGTCA[-/C]CCCAGGCTGGAGTGC | 57117 |
| rs34567094 | snp | C/T | 0.0499671 | 0.149956 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683155 | GGTTAGCTGACGAAG[C/T]AGCAGGTTTCCCAGT | 57117 |
| rs34938249 | in-del | -/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105685801 | AGGCCAAGATATTAA[-/G]GAAATAATGTAGTAT | 57117 |
| rs34969827 | in-del | -/G | | | frameshift-variant, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682952 | GGAACTAAACTACTT[-/G]GGACTAGGAAGACCT | 57117 |
| rs34994709 | in-del | -/T | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707316 | TTCTCCCTTGAAGCA[-/T]TTTTTTTTTTTTTTT | 57117 |
| rs35236206 | in-del | -/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105697699 | AAAGTCTGTTGATCA[-/C]CTGGTGTAGACTTAG | 57117 |
| rs35370743 | snp | A/G | 0.0904758 | 0.192489 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105683033 | CAAGGTTAGAGGTGG[A/G]GGTGGTTTTAAAGGT | 57117 |
| rs35485586 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698885 | TGTTCTATTTTCTCC[-/T]TTCTCAGTTTGGGAT | 57117 |
| rs35650037 | snp | G/T | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710496 | GGCTTCCCAAAGGGG[G/T]GGGATTACAGGCGTG | 57117 |
| rs35695511 | snp | A/C/G | 0.00382332 | 0.0435557 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105692054 | CTTGTCTGTCACCTG[A/C/G]GGTTTATGACAATCT | 57117 |
| rs35859278 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698892 | TTTTCTCCTTCTCAG[-/T]TTTGGGATCTAAGTC | 57117 |
| rs36020924 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698840 | GATCCTCTCTTGAGC[-/T]TTCAGATTCTGGTTA | 57117 |
| rs36071022 | in-del | -/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105684783 | GACCTAATTTTTTTT[-/C]CCTTTTCTTGCTATT | 57117 |
| rs56843185 | snp | A/G | 0.108755 | 0.206276 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710152 | ATTTCTTTTTATTTT[A/G]TATACTTTGCACTTC | 57117 |
| rs57389075 | in-del | -/TT | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701250 | TTTTTTTTTTTTTTT[-/TT]AAGTTCCCAGGAAGG | 57117 |
| rs57790298 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707331 | TTTTTTTTTTTTTTT[-/TT]GGCACAAGTGTTATG | 57117 |
| rs57956021 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105689362 | CCAATGCACATATGA[A/G]AATCTCACTCAAAGC | 57117 |
| rs59677702 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105685694 | TTCTTCCATATTTAG[G/T]GCTATGCTTAATATT | 57117 |
| rs61732560 | snp | A/G | 0.00072678 | 0.0190489 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693313 | CCTACAAACAACGCA[A/G]GCCAATCCCATCTCC | 57117 |
| rs62320293 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682729 | AAAAACCTACTTGGC[C/T]ACATTACTTCTTGAG | 57117 |
| rs62320294 | snp | C/G/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683158 | TAGCTGACGAAGTAG[C/G/T]AGGTTTCCCAGTATT | 57117 |
| rs62320295 | snp | A/G/T | 6.87924e-05 | 0.00586442 | missense, synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683279 | TACTGACGAGGAAAC[A/G/T]CTGGCACTAGAAGAA | 57117 |
| rs62320296 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | INTS12 | GRCh38.p7 | 4:105696093 | CGGCCTCAAATGATC[C/T]GCCCACCTCGGCCTC | 57117 |
| rs62320297 | snp | C/T | 0.202035 | 0.245356 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105706791 | TCCTGTGGATTCTGA[C/T]GGCAATATTTTTCAC | 57117 |
| rs70941208 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105706971 | AAATAAAAAAAAAAA[-/A]TTCTTGCTGAGAAGT | 57117 |
| rs70941210 | in-del | -/T | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710399 | TTTTTTTTTTTTTTT[-/T]CAGTCGAGGAGGGGT | 57117 |
| rs71586112 | in-del | -/A | 0.5 | 0 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105706960 | CTTTTTCATTAAAAT[-/A]AAAAAAAAAAATTCT | 57117 |
| rs72671808 | snp | A/C | 0.0618563 | 0.164627 | intron-variant | INTS12 | GRCh38.p7 | 4:105684563 | ATAGAGTTCTGAGAT[A/C]TTCGATTTATAAGAG | 57117 |
| rs72671809 | snp | A/C | 0.0622301 | 0.165053 | intron-variant | INTS12 | GRCh38.p7 | 4:105690380 | GAGGCAAGGAGATTT[A/C]TTAAGTGGCTATTGC | 57117 |
| rs72671810 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | INTS12 | GRCh38.p7 | 4:105692596 | AACAAACCCCAACAC[C/T]TGGCATGCACAAAAG | 57117 |
| rs72671811 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | INTS12 | GRCh38.p7 | 4:105694446 | TTCTCACGTCTCAGC[C/T]TCCTGAGGTGCTGGA | 57117 |
| rs72671812 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | INTS12 | GRCh38.p7 | 4:105696133 | TGGGATTAAAGACGT[A/G]TACCACCACACCTGG | 57117 |
| rs72671813 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105696608 | TTTATCAATTTACCT[A/G]TTGATGGATATTTGG | 57117 |
| rs72671815 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | INTS12 | GRCh38.p7 | 4:105697062 | GTTTGTTTTATTACT[A/G]AGTTAAAAGAGTTCT | 57117 |
| rs72671820 | snp | C/T | 0.0934081 | 0.194882 | intron-variant | INTS12 | GRCh38.p7 | 4:105699826 | TTACAAAACTCTCTC[C/T]AAGCTTTTTATTCAT | 57117 |
| rs72671824 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | INTS12 | GRCh38.p7 | 4:105702066 | TAACATGGCCCTTTG[A/G]CCCAGTGGTCCCCAT | 57117 |
| rs72671826 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | INTS12 | GRCh38.p7 | 4:105703345 | GTGGTAGTAGTAGTA[C/T]TGATAGGAGTGAATT | 57117 |
| rs72671828 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | INTS12 | GRCh38.p7 | 4:105703643 | ACTGGGAGGAATATA[C/T]ATACATTCTATCTTC | 57117 |
| rs72671835 | snp | C/T | 0.0614824 | 0.164198 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710199 | AATTTAAACACAGCT[C/T]AAACTTGAGCTTCTG | 57117 |
| rs72969245 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | INTS12 | GRCh38.p7 | 4:105683892 | AAATTTTGAGCAACA[A/G]TTACAGGAGTACAAA | 57117 |
| rs72969249 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | INTS12 | GRCh38.p7 | 4:105691839 | TAATCACATGTACAT[A/G]CTATACATATAAATA | 57117 |
| rs72969253 | snp | A/T | 0.0566069 | 0.158427 | intron-variant | INTS12 | GRCh38.p7 | 4:105704917 | CTAGCATCATCTATT[A/T]TCTGGCCCACTGCAA | 57117 |
| rs72969258 | snp | C/T | 0.0134861 | 0.0810011 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710531 | ACCGCGCCCGGCCTG[C/T]TTTTGTTTTTTTAAA | 57117 |
| rs73837096 | snp | A/C | 0.109461 | 0.206758 | intron-variant | INTS12 | GRCh38.p7 | 4:105685412 | AACTGGTTATTCTTA[A/C]TTCTATTCCAATTCA | 57117 |
| rs73837101 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | INTS12 | GRCh38.p7 | 4:105700361 | AACTTGATGGGTTTA[C/T]GTCAAGTTTACTCTG | 57117 |
| rs73837102 | snp | C/T | 0.5 | 0 | intron-variant | INTS12 | GRCh38.p7 | 4:105700820 | TACATCAAAGGCTTA[C/T]GAAATTCCACAATAC | 57117 |
| rs73839003 | snp | A/C | 0.0494327 | 0.149241 | intron-variant | INTS12 | GRCh38.p7 | 4:105701473 | ATTATTATATACATC[A/C]CCTCTACATAATGAT | 57117 |
| rs73839004 | snp | A/G | 0.109814 | 0.206997 | intron-variant | INTS12 | GRCh38.p7 | 4:105704479 | AACTCTGGGAGTAGG[A/G]TCTAGAAATCTGTGT | 57117 |
| rs73839006 | snp | C/T | 0.108755 | 0.206276 | intron-variant | INTS12 | GRCh38.p7 | 4:105706681 | TCCTGCTCTTACTTT[C/T]AATAAATGACACAAC | 57117 |
| rs74317794 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105683981 | TCATGATTTTAGTTT[A/C]ACAATTTGCCCATGA | 57117 |
| rs74464047 | snp | C/T | 0.108755 | 0.206276 | intron-variant | INTS12 | GRCh38.p7 | 4:105698156 | AGCAAAAAAGTTGTT[C/T]TAGTTGTTGACGGAT | 57117 |
| rs74497593 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | INTS12 | GRCh38.p7 | 4:105695057 | CCACCCGCCCACAAA[C/T]AGCTGGGACTACAGG | 57117 |
| rs74516377 | snp | C/G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691493 | GAGGACAATGAGAAG[C/G/T]AAAGACTAAGCAACA | 57117 |
| rs74673939 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | INTS12 | GRCh38.p7 | 4:105689499 | CTTTTGGTATTTCCC[C/T]ACATTTGCTCTTGGT | 57117 |
| rs74708995 | snp | A/T | 0.0134861 | 0.0810011 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709546 | ATCTCTTGGGTTTTT[A/T]ACTTCTATAGAAAGT | 57117 |
| rs75516903 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | INTS12 | GRCh38.p7 | 4:105684176 | ATCAGAAGCTCACAA[C/T]GGTACCAATGCCACT | 57117 |
| rs75758764 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | INTS12 | GRCh38.p7 | 4:105685154 | CATTTGCTTTTTATA[C/T]GTGAATGGGAACAAT | 57117 |
| rs75818640 | snp | A/T | 0.0524604 | 0.153226 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707065 | AGTAACTGGCACAAA[A/T]ATTATCATTCATCAT | 57117 |
| rs76024642 | snp | A/C/T | 0.0341544 | 0.126217 | intron-variant | INTS12 | GRCh38.p7 | 4:105696394 | CTCCCATCATCATCA[A/C/T]CACTTATCTGTTTTC | 57117 |
| rs76054753 | snp | A/T | 0 | 0 | intron-variant | INTS12 | GRCh38.p7 | 4:105683982 | CATGATTTTAGTTTC[A/T]CAATTTGCCCATGAT | 57117 |
| rs76321687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105704015 | ATTTCCCATATCTTC[C/T]TTTTTTTTTTTTCAG | 57117 |
| rs76419734 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | INTS12 | GRCh38.p7 | 4:105703128 | GGCCAAAACAGACTG[C/T]AAAAGAGCCATATCA | 57117 |
| rs76455970 | snp | C/T | 0.5 | 0 | intron-variant | INTS12 | GRCh38.p7 | 4:105700535 | ACTTTTACCTCAACT[C/T]TTTTTTTTTTTTTTT | 57117 |
| rs76478268 | snp | G/T | 0.5 | 0 | intron-variant | INTS12 | GRCh38.p7 | 4:105687713 | CTTTGGGAGGCTGAG[G/T]CGGGTGGTTCACTTG | 57117 |
| rs76570474 | snp | C/G | 0.000151267 | 0.00869543 | intron-variant | INTS12 | GRCh38.p7 | 4:105686881 | TACAAAATCTTAACT[C/G]AATATACAGAAAGAT | 57117 |
| rs76612485 | snp | C/T | 0.0970103 | 0.197722 | downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682596 | TTTTGTTATATAATA[C/T]TTAGCATTTTAAGGT | 57117 |
| rs77079725 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105700708 | CATATCTACTTAAAA[A/C]ACACACACACACACA | 57117 |
| rs77125802 | snp | A/G | 0.5 | 0 | intron-variant | INTS12 | GRCh38.p7 | 4:105694345 | ATAATTTTTTTTTTA[A/G]GACAGAGTCTTGCAG | 57117 |
| rs77475426 | snp | C/T | 0.0232847 | 0.105357 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710541 | GCCTGTTTTTGTTTT[C/T]TTAAACTTGTTTTAC | 57117 |
| rs77730993 | snp | C/T | 0.109461 | 0.206758 | intron-variant | INTS12 | GRCh38.p7 | 4:105695210 | TATCTATCTTTTCTT[C/T]TTAACAACTGTTCCA | 57117 |
| rs77908234 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | INTS12 | GRCh38.p7 | 4:105684302 | CTTCTTATTGACACC[C/T]TTTCTACCTTTATAC | 57117 |
| rs78000015 | snp | A/T | 0.5 | 0 | intron-variant | INTS12 | GRCh38.p7 | 4:105689758 | AAATAAAAAAAAAAT[A/T]AGCTAGGCCTGGTGG | 57117 |
| rs78609538 | snp | C/G | 0 | 0 | intron-variant | INTS12 | GRCh38.p7 | 4:105695026 | GCCTCCTGGGCTCAA[C/G]CAATCCTCCCACCCC | 57117 |
| rs78831757 | in-del | -/CTTTT | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710387 | AATCACACTCGGCTC[-/CTTTT]TTTTTTTTTTTTTTT | 57117 |
| rs78889671 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707870 | TAAATTGGGCATTCA[G/T]ATATAAATATAAGTA | 57117 |
| rs78988212 | snp | G/T | 0.0970103 | 0.197722 | intron-variant | INTS12 | GRCh38.p7 | 4:105693598 | AGTCCATTTTACAGA[G/T]ATATTCACATAGTTA | 57117 |
| rs79009646 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | INTS12 | GRCh38.p7 | 4:105689317 | ATCAGGTCCTATTTA[C/T]AATATCTTTGAGATA | 57117 |
| rs79565208 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707331 | ATTTTTTTTTTTTTT[G/T]GGCACAAGTGTTATG | 57117 |
| rs79571438 | snp | A/C | 0.0486741 | 0.148216 | intron-variant | INTS12 | GRCh38.p7 | 4:105695041 | GCAATCCTCCCACCC[A/C]CCACCCGCCCACAAA | 57117 |
| rs79577293 | snp | C/G | 0 | 0 | intron-variant | INTS12 | GRCh38.p7 | 4:105705297 | ATGAGAATCTAATGC[C/G]TGATGATCTGTCACA | 57117 |
| rs79691691 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | INTS12 | GRCh38.p7 | 4:105688247 | GGAAAGATGCTTCCC[A/G]CCAGCCATTCCATAG | 57117 |
| rs79721545 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | INTS12 | GRCh38.p7 | 4:105697382 | TATAAATGGGAATAA[C/T]ACACAACAATTTCAG | 57117 |
| rs79866548 | snp | A/C/G | 0.0050069 | 0.0497871 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682704 | TTTCATCTTTAGGCT[A/C/G]ATATGATACAAAAAC | 57117 |
| rs79889591 | snp | A/T | 0.5 | 0 | intron-variant | INTS12 | GRCh38.p7 | 4:105689756 | AAAAATAAAAAAAAA[A/T]TTAGCTAGGCCTGGT | 57117 |
| rs80067572 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | INTS12 | GRCh38.p7 | 4:105691576 | ACATCTTATCCATGC[A/G]GTGGTTTAAGCTCAC | 57117 |
| rs80245547 | snp | C/T | 0.0622301 | 0.165053 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707798 | TATTTATCGAATGAA[C/T]GAACTAGGTTTTTTG | 57117 |
| rs80340943 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | INTS12 | GRCh38.p7 | 4:105691692 | TAAAATGTTTGTCAA[C/T]ACATTGACAGACTAG | 57117 |
| rs112015248 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710630 | ATTAGCTTTTCTAAC[A/T]AAGAATAAATACTTG | 57117 |
| rs112037309 | snp | A/G | 0.109461 | 0.206758 | intron-variant | INTS12 | GRCh38.p7 | 4:105695979 | CTGCCTCAGCCTCCC[A/G]TGTATCTGGGACTAC | 57117 |
| rs112119830 | snp | A/C | 0.0614824 | 0.164198 | intron-variant | INTS12 | GRCh38.p7 | 4:105695935 | CTTGGCTCACTGCAA[A/C]CTCTGCCTCCTGGGT | 57117 |
| rs112172458 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | INTS12 | GRCh38.p7 | 4:105689774 | AGCTAGGCCTGGTGG[C/T]ACATGCCTGTAGTCC | 57117 |
| rs112481782 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | INTS12 | GRCh38.p7 | 4:105697791 | GTGGTGACACATGCC[C/T]GTAATCCCAGCACTT | 57117 |
| rs112980957 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | INTS12 | GRCh38.p7 | 4:105693570 | GAGTGAGAAGGACAA[C/T]TGGCAATGAACAAGT | 57117 |
| rs113183096 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | INTS12 | GRCh38.p7 | 4:105692479 | ACAGAGTAAGACTCT[A/G]TCTCAAAAAAAAAAA | 57117 |
| rs113227484 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105695885 | ACAGAGTCTCACTCT[G/T]TTGCCCAGGCTGGAG | 57117 |
| rs113398996 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | INTS12 | GRCh38.p7 | 4:105693620 | ACATAGTTAGGGACA[A/G]ATGTGCACATTAAAG | 57117 |
| rs113664959 | snp | A/G | 0.5 | 0 | intron-variant | INTS12 | GRCh38.p7 | 4:105703924 | ATAAAAAAGGAGAAG[A/G]TAGCTCTCTATGTAG | 57117 |
| rs113721485 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | INTS12 | GRCh38.p7 | 4:105686157 | AAACTTCGCCTCTGG[A/G]GTTCAAGCGATTCTC | 57117 |
| rs114171212 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | INTS12 | GRCh38.p7 | 4:105695034 | GGCTCAAGCAATCCT[C/T]CCACCCCCCACCCGC | 57117 |
| rs114327899 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | INTS12 | GRCh38.p7 | 4:105683627 | TTTAGTGCTTTAACA[G/T]AGTTTTTACCCAACA | 57117 |
| rs114695427 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | INTS12 | GRCh38.p7 | 4:105683948 | AGTGTACAATTTTTA[C/T]GATGTGTTAAAAAGT | 57117 |
| rs114727759 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | INTS12 | GRCh38.p7 | 4:105705232 | ATTCTCATAGGAATG[C/T]GAATCCTATGTGAAC | 57117 |
| rs114953181 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | INTS12 | GRCh38.p7 | 4:105704253 | TAAACCTAATACATA[C/T]GATTGTCCCTCCTAC | 57117 |
| rs115033976 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | INTS12 | GRCh38.p7 | 4:105698072 | AACAACAGAAAAACA[A/G]AAACGTGTATTGTGT | 57117 |
| rs115061828 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | INTS12 | GRCh38.p7 | 4:105687743 | GAGGTCAGGAGTTTG[C/T]GAACAGCCAGAACAG | 57117 |
| rs115191172 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | INTS12 | GRCh38.p7 | 4:105706532 | TGGGATTACAAGTGC[A/G]AGCCAAATCTCTTAA | 57117 |
| rs115302648 | snp | A/C | 0.00666572 | 0.0573448 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105683007 | ACTGAGCGACTAAGG[A/C]CAGTTTTACCCAAGG | 57117 |
| rs115307578 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | INTS12 | GRCh38.p7 | 4:105700100 | GTTTTTTAATTTGTA[A/G]TAGATAATACTGTAC | 57117 |
| rs115483565 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704014 | TATTTCCCATATCTT[C/T]TTTTTTTTTTTTTCA | 57117 |
| rs116514173 | snp | A/G | 0.245346 | 0.249957 | intron-variant | INTS12 | GRCh38.p7 | 4:105696014 | GCACCACCACACCCG[A/G]CTGATTTTTGTAGTT | 57117 |
| rs116536772 | snp | C/G | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709655 | TTTGGGATGAGATGA[C/G]TTGTTTTTTTCCCCT | 57117 |
| rs116832590 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | INTS12 | GRCh38.p7 | 4:105704223 | TCTCATGAGTCATTC[A/G]CCGCCTCAGTCAGGT | 57117 |
| rs116879534 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | INTS12 | GRCh38.p7 | 4:105700758 | ACAGAGCCTATGATG[C/T]TTTGTGTCCTAAAGA | 57117 |
| rs116957480 | snp | A/C/G | 0.0170251 | 0.090679 | intron-variant, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105689211 | GACCCTGCCATACAC[A/C/G]ATCACAACATTCTTA | 57117 |
| rs118073909 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | INTS12 | GRCh38.p7 | 4:105683840 | GAAAGAAGACAGCTG[C/T]ATAGATTCTAAACCC | 57117 |
| rs137865784 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | INTS12 | GRCh38.p7 | 4:105690950 | AAACCAAACTGAGCA[G/T]AACAGATTGTAACTT | 57117 |
| rs137906545 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105705016 | AAAATCCTTTTATCA[C/T]TTCTCACAATCCAAA | 57117 |
| rs137972099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105701150 | AAGCACATCTGAAAA[C/T]GGATTTTGTTGTCCC | 57117 |
| rs138257061 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | INTS12 | GRCh38.p7 | 4:105684795 | TTTTCCTTTTCTTGC[A/T]ATTAAACATAAAACT | 57117 |
| rs138296247 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105689884 | GCACTCCAGCCTAGA[A/C]AACAGAGTGAGACCC | 57117 |
| rs138554330 | snp | C/T | 5.01274e-05 | 0.00500612 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683266 | TTAAGCCACTAGTTA[C/T]TGACGAGGAAACGCT | 57117 |
| rs138606174 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710137 | GATTTGAGAATCATC[A/G]TTTCTTTTTATTTTA | 57117 |
| rs138639452 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | INTS12 | GRCh38.p7 | 4:105705115 | TGCAGCAGGAGGTGA[A/G]CAGTAGGCAAGCGAG | 57117 |
| rs138838235 | in-del | -/A | 0.0486741 | 0.148216 | intron-variant | INTS12 | GRCh38.p7 | 4:105697429 | AGGGGGGAAGAGAAG[-/A]AAAAAGGAAGGAGGA | 57117 |
| rs138886381 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | INTS12 | GRCh38.p7 | 4:105689764 | AAAAAAAATTAGCTA[C/G]GCCTGGTGGCACATG | 57117 |
| rs138923976 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | INTS12 | GRCh38.p7 | 4:105685392 | AACTCTAATTACTTT[C/T]AATAAACTGGTTATT | 57117 |
| rs139147352 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | INTS12 | GRCh38.p7 | 4:105692226 | TGCTGGCTCATGCCT[A/G]TAATCCCAGCACTTT | 57117 |
| rs139189162 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105705494 | TGAAACCATGTCTTC[A/C]ATGAAACTGGTCCCT | 57117 |
| rs139324824 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | INTS12 | GRCh38.p7 | 4:105694865 | CTGTTCAGGTGCATA[C/T]CACTCTATAAAGTTT | 57117 |
| rs139355447 | snp | C/T | 9.52753e-05 | 0.00690135 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105692070 | GGTTTATGACAATCT[C/T]GGTGGTAGAGATTAT | 57117 |
| rs139504996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105687262 | GTTGCTGAGGGCAAA[C/T]TAAAACACAGCTCAG | 57117 |
| rs139553859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105687456 | ATTTTATAAGCATCT[C/T]CAGTTTTATTTTGAC | 57117 |
| rs139945314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105701970 | ACACCAACATTCCAG[C/T]TGGAACCTTGGAGTC | 57117 |
| rs139964617 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | INTS12 | GRCh38.p7 | 4:105698187 | GAGTTAAGTTTTAAC[A/T]CCATTATTTCACATT | 57117 |
| rs140052930 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707500 | TCTCTCCTTCTACAC[A/T]ATTGTAGCCATTTCC | 57117 |
| rs140407528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105684462 | CTCTGAAATAGTTGA[C/T]AAAACATTTTTAGCT | 57117 |
| rs140414330 | in-del | -/A | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703116 | CCTAAACCCATGGCC[-/A]AAAACAGACTGCAAA | 57117 |
| rs140447872 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | INTS12 | GRCh38.p7 | 4:105698852 | GAGCTTCAGATTCTG[A/G]TTAGACTTGAGCTAG | 57117 |
| rs140717055 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105706496 | CTCAAACAATCCTCC[A/C/T]GTTGTGGCTTCCCAA | 57117 |
| rs140805616 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | INTS12 | GRCh38.p7 | 4:105703563 | AAGCCCTGTAGTTTC[C/T]CTACTTTATAGACAT | 57117 |
| rs140810789 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105708993 | TCACGCACCCTCCCT[G/T]CCTGGCCGCGCCTCT | 57117 |
| rs141049529 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694550 | AGGGTGGCCAACTCC[C/T]GACCTGCTGACCTCA | 57117 |
| rs141093981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708389 | GAGGCAGGATTCCAA[A/G]TCCCTTGTCCCTAGA | 57117 |
| rs141157660 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | INTS12 | GRCh38.p7 | 4:105700101 | TTTTTTAATTTGTAA[C/T]AGATAATACTGTACA | 57117 |
| rs141192797 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105692725 | CTTTCTCTCAGAAGG[C/T]AGTAGACTCTGATTA | 57117 |
| rs141226582 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | INTS12 | GRCh38.p7 | 4:105689397 | ATAGTTAGAATGACT[A/G]TATTTAGAATCCCCA | 57117 |
| rs141267498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105705379 | CAAGGTTCCCACTGA[C/T]TCTACATTATGGTGA | 57117 |
| rs141555014 | snp | C/T | 0.000285866 | 0.011952 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683270 | GCCACTAGTTACTGA[C/T]GAGGAAACGCTGGCA | 57117 |
| rs141564437 | snp | A/C | 1.64996e-05 | 0.0028722 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105686774 | ACCAATGGATCTTTG[A/C]CAGCTGGAGTTACAG | 57117 |
| rs141758012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105703966 | TCTGGATCCTATCTC[G/T]TCTTGTCCCCTCTTG | 57117 |
| rs141802402 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | INTS12 | GRCh38.p7 | 4:105702180 | TCGCTCTGTCGCCCA[A/G]GCTGGAGTGCAGTGG | 57117 |
| rs141853457 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | INTS12 | GRCh38.p7 | 4:105699669 | CCCCAGCTGATTTTT[C/G]TATGTGGTGTAACAG | 57117 |
| rs142027677 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | INTS12 | GRCh38.p7 | 4:105686389 | TCATGGCACCTCGCC[C/T]GAATTTAAACCAGAT | 57117 |
| rs142134796 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | INTS12 | GRCh38.p7 | 4:105691837 | ATTAATCACATGTAC[A/T]TACTATACATATAAA | 57117 |
| rs142140494 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690213 | TGAGAGAGAGGGCTG[-/T]TAAGGTAGAGTCGGG | 57117 |
| rs142172284 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | INTS12 | GRCh38.p7 | 4:105683428 | ACCAAATTAGGTTCT[C/T]ATGAAGCTGATCTGA | 57117 |
| rs142455399 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | INTS12 | GRCh38.p7 | 4:105705026 | TATCACTTCTCACAA[G/T]CCAAAGGTTCAAGAA | 57117 |
| rs142494240 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105701638 | AACAGCCTAATCTCT[G/T]TTTTTTCTTTAAATT | 57117 |
| rs142497611 | in-del | -/T | 0.0509478 | 0.151255 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709965 | ATTAAGCTATGCGGG[-/T]TTTTTTTTTCTTTTT | 57117 |
| rs142510677 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | INTS12 | GRCh38.p7 | 4:105699040 | CCAGGCAGGTACTAC[A/C]CTAGGTAACTCATTT | 57117 |
| rs142820343 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | INTS12 | GRCh38.p7 | 4:105703411 | ATATAGCACAAAAAT[C/T]GCCATTACTGAACAA | 57117 |
| rs142846724 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | INTS12 | GRCh38.p7 | 4:105684859 | CTTCACAAAAGAAAA[C/T]CCACCTTTAGTAATT | 57117 |
| rs142911266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707772 | CTTGAAACTTAATAA[A/G]GGCTCAAAAATATTT | 57117 |
| rs143163648 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | INTS12 | GRCh38.p7 | 4:105683835 | TGAGAGAAAGAAGAC[A/G]GCTGTATAGATTCTA | 57117 |
| rs143350013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105695383 | ATAGCTATCAATATA[C/T]ATTCACTGAGTGTTG | 57117 |
| rs143436191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105691279 | AGGTGGAGAATAAGA[C/T]ATTATGGCAATTTCT | 57117 |
| rs143438675 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105704861 | CATACCTCAAATCTA[C/T]CCACCCTTTTCAATC | 57117 |
| rs143528639 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105698508 | CACAACAAATTTTTC[A/T]TGTTCTTTAAGAGAT | 57117 |
| rs143545291 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710480 | ATGATCCGCCCGCCT[C/T]GGCTTCCCAAAGTGG | 57117 |
| rs143567053 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105692870 | CTAATTATCCACAGT[C/T]CTTAGCACATTACTG | 57117 |
| rs143820409 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699895 | GCCCCGAGCCAAAGA[C/T]TCATCAAGCAGTGCT | 57117 |
| rs143834873 | in-del | -/AAG | 0.00716266 | 0.059414 | intron-variant | INTS12 | GRCh38.p7 | 4:105684737 | GAGAAAAAGTTAGTC[-/AAG]AAGTAAACCTTTAAT | 57117 |
| rs144126812 | snp | A/G | 0 | 0 | intron-variant | INTS12 | GRCh38.p7 | 4:105692539 | CTGGTAAAGTTTGGT[A/G]TATTAAAAAGAAAAA | 57117 |
| rs144231959 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | INTS12 | GRCh38.p7 | 4:105706469 | GGTCTTGCTATGTTG[C/T]TCTTATCTGGTCTCA | 57117 |
| rs144499591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105696049 | TACAGATGGCGTTTC[A/T]CCATGTTGGCCACAC | 57117 |
| rs144619017 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | INTS12 | GRCh38.p7 | 4:105702464 | TTCTATTTATTTTTT[A/T]AAAATCTATTCATAT | 57117 |
| rs144640222 | snp | C/T | 0.0134861 | 0.0810011 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709970 | AGCTATGCGGGTTTT[C/T]TTTTCTTTTTTTTTA | 57117 |
| rs144650579 | snp | C/T | 0.00196426 | 0.0312773 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699931 | CTTTTCAGCAGAATC[C/T]TTACTCTTTGAATGC | 57117 |
| rs144678574 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | INTS12 | GRCh38.p7 | 4:105706618 | GGCATCTCAAATTCA[A/G]TTACAACTAAAATTG | 57117 |
| rs144680414 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | INTS12 | GRCh38.p7 | 4:105705041 | TCCAAAGGTTCAAGA[A/G]TAAGATTCTTAACAA | 57117 |
| rs144768612 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | INTS12 | GRCh38.p7 | 4:105703614 | TCTCTGCCTGCACCC[A/G]AACTCTAAGTGCAAC | 57117 |
| rs144825445 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105686385 | TGAGTCATGGCACCT[C/T]GCCTGAATTTAAACC | 57117 |
| rs145035273 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | INTS12 | GRCh38.p7 | 4:105689642 | GCATGGTGGCTCATG[A/C]CTATAATCCCAGCAC | 57117 |
| rs145055502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105685221 | GTGAATTTTTTATTA[A/C]AGAAACACAAAACCT | 57117 |
| rs145084546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105687322 | GGGAGAAAAAAACTA[C/T]TGATAAATGATTAAA | 57117 |
| rs145106449 | in-del | -/T | 0.0271762 | 0.113356 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708484 | TGAAAGGGGAGAGCA[-/T]GTCAGTCTAGGGCAC | 57117 |
| rs145174807 | snp | C/T | 0.00619209 | 0.0552965 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682913 | TCCACTATTTCCATT[C/T]CCACTTAGTTGGCTG | 57117 |
| rs145257296 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | INTS12 | GRCh38.p7 | 4:105699018 | TTCAGTGACAGCCTA[C/T]TATGTACCAGGCAGG | 57117 |
| rs145418027 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105704043 | CAGCCTTTCTACTGG[C/T]ATCTTTTCATTGACA | 57117 |
| rs145606118 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105689241 | AACTAGGTCTTCCTA[A/C]AATGATGTGTACCGC | 57117 |
| rs145728309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105692989 | AAAAGCAATCACCAT[A/G]GCCTTAGATTATCAA | 57117 |
| rs146009095 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | INTS12 | GRCh38.p7 | 4:105697793 | GGTGACACATGCCTG[C/T]AATCCCAGCACTTTG | 57117 |
| rs146172950 | snp | A/C/T | 0.00146907 | 0.0270645 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683278 | TTACTGACGAGGAAA[A/C/T]GCTGGCACTAGAAGA | 57117 |
| rs146409698 | snp | A/G | 0.0138799 | 0.0821421 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105708836 | ACGGCCGGCGCGAGT[A/G]TTTTCCACATAAGGT | 57117 |
| rs146434206 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105687969 | AAAAAAACAACAACA[A/G]AAAAAAAAACAGCAA | 57117 |
| rs146521085 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105692717 | ATTTTTGCCTTTCTC[C/G/T]CAGAAGGTAGTAGAC | 57117 |
| rs146532670 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105689280 | CCCCAGTTTGAGGAA[A/T]CTGTTTGAGGAGAAA | 57117 |
| rs146581425 | in-del | -/A | 0.0614824 | 0.164198 | intron-variant | INTS12 | GRCh38.p7 | 4:105693870 | GATATAAATATTATC[-/A]ATATACCCATTAGAT | 57117 |
| rs146732187 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | INTS12 | GRCh38.p7 | 4:105699348 | CAAAACATATATTCT[C/T]TTCACATAAAGCTGC | 57117 |
| rs146895177 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | INTS12 | GRCh38.p7 | 4:105694581 | AGTGATCCTCCTGCC[C/T]TGACCTCCCAAAGTG | 57117 |
| rs147147175 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | INTS12 | GRCh38.p7 | 4:105691461 | AGTACATAGGAAGAA[C/T]GAGGTAATGGTCACT | 57117 |
| rs147273938 | snp | A/T | 9.92047e-05 | 0.0070422 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695520 | TAAAATCTTACTTTA[A/T]CAGCAGGTCTCTTTT | 57117 |
| rs147326838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105690747 | TTAGATATTAAAGGA[A/G]CTAAAGTGATAATAA | 57117 |
| rs147350041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105686551 | TCCCTTTCTACCTAA[C/T]ATAATAGTAGTAAAG | 57117 |
| rs147591408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105687344 | ATGATTAAACTTTTT[C/G]AGGTTTTTCCACATT | 57117 |
| rs147614165 | snp | A/G | 3.29511e-05 | 0.00405887 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683151 | TTCTGGTTAGCTGAC[A/G]AAGTAGCAGGTTTCC | 57117 |
| rs147779765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682382 | CGTCCCTGCCGCCAC[A/G]TAAGGCACCTCATTC | 57117 |
| rs147870230 | snp | A/C/T | 0.00028162 | 0.0118631 | synonymous-codon, missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699961 | CAAGAAACCTAGTGC[A/C/T]TTCAAAAAAATGGGA | 57117 |
| rs147906829 | snp | A/C | 0.0252325 | 0.109451 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105706807 | GGCAATATTTTTCAC[A/C]CTTGTCCTACTTTTC | 57117 |
| rs147917525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105703761 | AGATCAGTTATACTT[C/T]CTCCATTTTCTTTTA | 57117 |
| rs147940674 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | INTS12 | GRCh38.p7 | 4:105699468 | ATTCAATTTATTTTG[C/T]TGAAAGATCTGTCCT | 57117 |
| rs148127910 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | INTS12 | GRCh38.p7 | 4:105694480 | ACAGGTGTGCGCCAC[C/T]ACACCTGGCTAATTT | 57117 |
| rs148182120 | snp | A/G | 0.00173559 | 0.0294072 | utr-variant-5-prime, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105700013 | GCAGCCATTGCAAAC[A/G]CCTGAAGGAAAAAAA | 57117 |
| rs148385844 | snp | C/T | 4.94956e-05 | 0.00497447 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105686764 | TGGTTTCTTAACCAA[C/T]GGATCTTTGACAGCT | 57117 |
| rs148445846 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105697683 | ACTATTTGGCTCTTT[A/T]TAAAGTCTGTTGATC | 57117 |
| rs148493396 | snp | A/G | 4.98186e-05 | 0.00499067 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699971 | AGTGCTTTCAAAAAA[A/G]TGGGATCAAGTTCCA | 57117 |
| rs148499272 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | INTS12 | GRCh38.p7 | 4:105702725 | TCTACTTGTTCTTTG[C/T]TACAGAAGCCTCCAA | 57117 |
| rs148580917 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | INTS12 | GRCh38.p7 | 4:105686386 | GAGTCATGGCACCTC[A/G]CCTGAATTTAAACCA | 57117 |
| rs148633669 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | INTS12 | GRCh38.p7 | 4:105691696 | ATGTTTGTCAATACA[C/T]TGACAGACTAGTAAG | 57117 |
| rs148858103 | snp | C/T | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710319 | TCCGCCTCCCGGGCT[C/T]AAGCAATTCTCCTGC | 57117 |
| rs148900366 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | INTS12 | GRCh38.p7 | 4:105688643 | CCCTCACAGTAAAAC[A/T]GAAACATATGGCTCC | 57117 |
| rs148953427 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105693180 | CCACCCCAGTTCCAA[A/C]TAGTAAAAACAAAAT | 57117 |
| rs149069973 | snp | C/T | 8.23798e-05 | 0.00641741 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683172 | GCAGGTTTCCCAGTA[C/T]TGTTTTGTGTTGTTG | 57117 |
| rs149225450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105704515 | CTTCCAGGCAATTCT[A/G]TCTACTCTAAAGTTT | 57117 |
| rs149258182 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105696005 | ACTACAGGTGCACCA[A/C/T]CACACCCGGCTGATT | 57117 |
| rs149408719 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | INTS12 | GRCh38.p7 | 4:105686336 | TCAGGTAATCCACCC[A/G]CCTTGGCCTCCCAAA | 57117 |
| rs149639641 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | INTS12 | GRCh38.p7 | 4:105690486 | GAATTAGCAAATCTG[A/G]TAAACAATGGGATAT | 57117 |
| rs149713078 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | INTS12 | GRCh38.p7 | 4:105687771 | CAGCCTGGCCCACAT[A/G]GTGAAACCCCGTCTC | 57117 |
| rs149864959 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105708746 | TTCCCACAGTAGGGG[C/T]GGGGGAAACGTTTGG | 57117 |
| rs149999091 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | INTS12 | GRCh38.p7 | 4:105698914 | ATCTAAGTCCACAGA[C/G]CTGAGTGATTTGGAG | 57117 |
| rs150315577 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | INTS12 | GRCh38.p7 | 4:105700157 | AAAAGTTATTACAAA[C/T]AAAAGTAAATTTCCT | 57117 |
| rs150356619 | snp | G/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105683023 | CAGTTTTACCCAAGG[G/T]TAGAGGTGGAGGTGG | 57117 |
| rs150398564 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | INTS12 | GRCh38.p7 | 4:105684566 | GAGTTCTGAGATATT[C/T]GATTTATAAGAGAAG | 57117 |
| rs150452511 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | INTS12 | GRCh38.p7 | 4:105689857 | GCTGCAGTGAGCCAT[A/G]GTCATGCTACTGCAC | 57117 |
| rs150472974 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | INTS12 | GRCh38.p7 | 4:105703969 | GGATCCTATCTCTTC[C/T]TGTCCCCTCTTGAAC | 57117 |
| rs150790953 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | INTS12 | GRCh38.p7 | 4:105705406 | GTGAGTTGTCCAATT[A/T]TTTTATTATATATTA | 57117 |
| rs151045255 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | INTS12 | GRCh38.p7 | 4:105703415 | AGCACAAAAATCGCC[A/T]TTACTGAACAATGAT | 57117 |
| rs151098627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708050 | AAACTTTGTTCTTCA[C/T]GACTTCGCAAGCTCT | 57117 |
| rs151227498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105684024 | TATCATGTAAGAGTC[C/T]CCTGCTCCTTTAATA | 57117 |
| rs151247998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105698571 | TTTTTTTCTTTAGTA[A/G]TAATAGGTTTCCCTA | 57117 |
| rs180752799 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105705376 | GCTCAAGGTTCCCAC[C/T]GATTCTACATTATGG | 57117 |
| rs180817722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105697544 | TAAATAGTTTTTTAT[A/C]AACAGTTATATTAGA | 57117 |
| rs180835641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105686599 | TAGCCATTTAGTATA[C/T]AAAGTTTCTCATTAA | 57117 |
| rs181162096 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105702027 | ATAAAACTTAACAGG[A/C]TTTGTACCCCTCCCC | 57117 |
| rs181294091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105685901 | AAGAGGTAGATAACA[C/T]TGAAAGTTTATTATA | 57117 |
| rs181312144 | snp | A/G/T | 0.00993419 | 0.0697739 | intron-variant | INTS12 | GRCh38.p7 | 4:105697036 | TTTGCCCATTTAAAA[A/G/T]AAATGAATCTGTTTG | 57117 |
| rs181391210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105703566 | CCCTGTAGTTTCCCT[A/G]CTTTATAGACATCCA | 57117 |
| rs181592762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105701540 | GCTGGTCACCATGTA[C/T]GTTCTGAGGAAAAAA | 57117 |
| rs181653554 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709966 | ATTAAGCTATGCGGG[G/T]TTTTTTTTCTTTTTT | 57117 |
| rs181737920 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105691559 | AAATATCGCCTCTGT[A/C]CACATCTTATCCATG | 57117 |
| rs181810632 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105696493 | GCTTCTTCTACTCAG[C/T]ATATTTATTTTGAGA | 57117 |
| rs181909258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105683869 | CCATTAAAAAAAAAT[A/G]TCCTCCTAAATTTTG | 57117 |
| rs181986012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105706125 | TGCTTTTGGTATTGT[C/T]CAAGTATTTGTCCTT | 57117 |
| rs182005409 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | INTS12 | GRCh38.p7 | 4:105702425 | ACAGGCGTGAGCCAC[C/T]GCGCCCAGCCAATTT | 57117 |
| rs182158639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105690839 | GACAATTTCCAATTC[C/T]TAGTGGTTTCTTATC | 57117 |
| rs182204553 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105689192 | GAACTGAAGAATAAC[C/T]TTGGACCCTGCCATA | 57117 |
| rs182240174 | snp | A/T | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707360 | TGTCCCCTACAAAAC[A/T]CTGAGTACTTTAAGG | 57117 |
| rs182257616 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105687780 | CCACATGGTGAAACC[A/C]CGTCTCTACTAAAAA | 57117 |
| rs182425733 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105708961 | GAAGGCGCAGGCGGC[C/T]CAGGTCGCCGACACG | 57117 |
| rs182565987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105693722 | GAACAGTTTAACAAA[C/T]ATTTGTATTTCTCTT | 57117 |
| rs182697252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105699784 | TTTTGAGATGGTCTA[C/T]ATGTTATCAATGTAG | 57117 |
| rs182783757 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant, utr-variant-5-prime | INTS12 | GRCh38.p7 | 4:105703001 | TCATAAAGAGGTCAG[A/C]AACTTGGTGTAACTG | 57117 |
| rs182834767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105694613 | TGGGATTACAGGCAT[A/G]AGCCACCACACCCAG | 57117 |
| rs183148807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105698168 | GTTCTAGTTGTTGAC[A/G]GATGAGTTAAGTTTT | 57117 |
| rs183172467 | snp | A/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105688414 | GCCATACTATATAGT[A/T]TGGGTCCTTAAATCT | 57117 |
| rs183340723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105684448 | AATTTAGAACTTTAC[G/T]CTGAAATAGTTGATA | 57117 |
| rs183425440 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105706639 | ACTAAAATTGAGATT[C/T]TGATTATCTTCCCGA | 57117 |
| rs183589297 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105702853 | ACTTATGGTTATGTG[C/G]TTTATATTTTATATT | 57117 |
| rs183657785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708053 | CTTTGTTCTTCATGA[C/T]TTCGCAAGCTCTTGC | 57117 |
| rs183673532 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690641 | AGCTATAGAAGCTCA[C/T]CCAGGAAGAGGGTTA | 57117 |
| rs183694290 | snp | A/C | 0.00478085 | 0.0486577 | upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105708737 | AAACAAAGGTTCCCA[A/C]AGTAGGGGCGGGGGA | 57117 |
| rs183829643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105695331 | ACTTAACTTTAAAAT[C/T]TGTAAATTTTACTCA | 57117 |
| rs183842325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105686155 | GCAAACTTCGCCTCT[A/G]GGGTTCAAGCGATTC | 57117 |
| rs183872874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105689669 | GCACTTTGGGAGGCC[A/G]AGGCAGGAGGATCAC | 57117 |
| rs184073107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105694475 | GAACTACAGGTGTGC[A/G]CCACCACACCTGGCT | 57117 |
| rs184167010 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | INTS12 | GRCh38.p7 | 4:105690426 | GATTTGTGGAACAGG[G/T]TAATAAAAGAGAAAT | 57117 |
| rs184526294 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105700172 | TAAAAGTAAATTTCC[G/T]TCTTATTCCTGACAG | 57117 |
| rs184591428 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | INTS12 | GRCh38.p7 | 4:105704872 | TCTATCCACCCTTTT[C/T]AATCCTTACTACTAC | 57117 |
| rs184748566 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | INTS12 | GRCh38.p7 | 4:105701353 | ACCCATGGAAAGGAA[A/T]CCAAAGGCCAGTACT | 57117 |
| rs184889390 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | INTS12 | GRCh38.p7 | 4:105701866 | AAGTATTTATTGCTA[C/T]GTATTTCTACAATCA | 57117 |
| rs184986813 | snp | C/T | 6.59033e-05 | 0.00573997 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683070 | GGCGTAGTGCTGTTA[C/T]TGGAACCTATTTTGG | 57117 |
| rs184988699 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708296 | AGAATGGGGGATGGT[C/T]CTTGACAGGGGAGCC | 57117 |
| rs185099846 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105685152 | GACATTTGCTTTTTA[A/T]ATGTGAATGGGAACA | 57117 |
| rs185105779 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105703255 | GTTTCATTTAAAAAG[A/T]AGATGTTGCTTTCAA | 57117 |
| rs185225709 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105685780 | TATTTTTTTCCATGA[C/T]ATAAAAAGGCCAAGA | 57117 |
| rs185317518 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | INTS12 | GRCh38.p7 | 4:105693998 | TTTGGCAATGCCTAG[C/T]AATGTTGAAGATGTC | 57117 |
| rs185357983 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105703518 | GTGGTCCACCCTTTC[A/T]ATACCTCTTTCAGTA | 57117 |
| rs185663841 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | INTS12 | GRCh38.p7 | 4:105696044 | TTCAGTACAGATGGC[A/G]TTTCACCATGTTGGC | 57117 |
| rs185689590 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105688458 | TTTTTATACTACATA[A/C]CTTCCACATCAAAGT | 57117 |
| rs185695621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105706792 | CCTGTGGATTCTGAC[A/G]GCAATATTTTTCACA | 57117 |
| rs185824135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105692145 | ATTTGCCTAAGAAAA[C/T]ATACCATTAAACATT | 57117 |
| rs186049940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105683525 | TGATACCATATTCTT[A/G]TTCTAATGATTCCAA | 57117 |
| rs186171855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105696644 | CTGCAGTTTGGGACT[A/G]TTACAAATAAAGCTG | 57117 |
| rs186182758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105702030 | AAACTTAACAGGCTT[G/T]GTACCCCTCCCCTAA | 57117 |
| rs186232328 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105684258 | ATATTAGGCACAAAT[C/G]TACGTATTCAAATTA | 57117 |
| rs186236674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105702433 | GAGCCACCGCGCCCA[A/G]CCAATTTATTTCTAT | 57117 |
| rs186384591 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | INTS12 | GRCh38.p7 | 4:105687011 | TATCATATTAATGGT[C/T]TTACAGATTGTATTA | 57117 |
| rs186396683 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105705728 | GCCACCCCCACCTCC[A/G]TCTTAAGTCACCTCT | 57117 |
| rs186506809 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | INTS12 | GRCh38.p7 | 4:105697344 | AGTCTATTTTACTGT[A/G]ATAATATGTAAAAGT | 57117 |
| rs186653632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105689250 | TTCCTACAATGATGT[A/G]TACCGCAGAACTTGC | 57117 |
| rs186659839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707458 | ATAGAATTACTGGAA[C/T]TAAGTGATCAAAGTA | 57117 |
| rs186763152 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | INTS12 | GRCh38.p7 | 4:105687821 | AGCTGGGCATGGTGG[C/T]GGGTGCCTGTAATTC | 57117 |
| rs186822512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105684940 | TGGCATTTCATTTTA[A/G]TGGCTTGCTGTTGCT | 57117 |
| rs186977804 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105706141 | CAAGTATTTGTCCTT[C/G]GCTATCTTCTTAGTT | 57117 |
| rs187150100 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709352 | TTGATATTTGCTGTT[A/C]AGTGTTACTTCAAGA | 57117 |
| rs187260188 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | INTS12 | GRCh38.p7 | 4:105694950 | TTTTTTTTGAGACAG[A/C]GCCTCACTCTGTCAC | 57117 |
| rs187344723 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | INTS12 | GRCh38.p7 | 4:105691057 | TTCATAGGAATAAAT[A/G]AAAACACTTCCTATT | 57117 |
| rs187356153 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105697639 | TAGTTGCAATGGAGA[A/C]CATCTGGCACACAAA | 57117 |
| rs187394178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105698481 | AAACCTAAGGGCAGC[A/G]TGCTTTTTAATCACA | 57117 |
| rs187500974 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105700287 | GTAGGCCTCTCCCTG[C/G]CACAGAACTCCTTCC | 57117 |
| rs187797062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105685461 | AATCAATAATGGATA[C/T]GCCTTGGATAGCAAA | 57117 |
| rs187811856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105703412 | TATAGCACAAAAATC[A/G]CCATTACTGAACAAT | 57117 |
| rs187897904 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | INTS12 | GRCh38.p7 | 4:105703122 | ACCCATGGCCAAAAC[A/G]GACTGCAAAAGAGCC | 57117 |
| rs187963756 | snp | A/G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105708738 | AACAAAGGTTCCCAC[A/G/T]GTAGGGGCGGGGGAA | 57117 |
| rs188175654 | snp | C/T | 5.2932e-05 | 0.00514424 | intron-variant | INTS12 | GRCh38.p7 | 4:105700039 | AAAAAGAGAAAGTAA[C/T]CTAGAAGACAATGCA | 57117 |
| rs188237763 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | INTS12 | GRCh38.p7 | 4:105702908 | CCCCCTTTTCTGTTG[A/C]CTTCTCTAATCTCTG | 57117 |
| rs188322281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105686424 | GATTGAAGACAAATA[C/T]CTAACCAGATGAGAA | 57117 |
| rs188330323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105705057 | TAAGATTCTTAACAA[A/G]GTCTCCAATTCTCTA | 57117 |
| rs188404736 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105684526 | ATGCATACATTTTTA[A/T]TCAATGTGAAAAGTA | 57117 |
| rs188422232 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | INTS12 | GRCh38.p7 | 4:105690052 | TTATTTGCAAAGCAG[A/T]TAAAAGAATAAACAG | 57117 |
| rs188460501 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690512 | GATATGGAATTAAAA[G/T]AGGCATCAAAGATGT | 57117 |
| rs188473924 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708427 | ATATGCTCGGTCCGC[A/G]TGTCCCGGCCCGCAA | 57117 |
| rs188705335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708175 | CACCTGGAATCGCAG[A/G]AGAAAAGGCTCCGAT | 57117 |
| rs188879869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105697012 | TTGGTAAACTATTTG[A/G]TAAAATATTTTGCCC | 57117 |
| rs189053841 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105694498 | ACCTGGCTAATTTTT[A/G]TATTTTTAGTAGAGA | 57117 |
| rs189239359 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | INTS12 | GRCh38.p7 | 4:105701416 | GTATTTCTAAGAATT[C/T]AACAAAATTGAAAAG | 57117 |
| rs189260758 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105706740 | TCTTTCCTTCACTGA[C/G]TCTTTCCCTACTCCT | 57117 |
| rs189330446 | snp | C/T | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695608 | GAAGACTGGATGATA[C/T]TTTGGGCTCTTGCTT | 57117 |
| rs189350574 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690670 | TAGAACCATAAACAT[A/G]GATTTGACATAAATC | 57117 |
| rs189372318 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105705855 | ACACTGTTAATTATG[C/T]AAATAATCTTTCTTT | 57117 |
| rs189499866 | snp | C/T | 1.64953e-05 | 0.00287182 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683212 | TTGCTGTTGAAGGAC[C/T]AGCAGAGGAAGTTTT | 57117 |
| rs189541631 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | INTS12 | GRCh38.p7 | 4:105702285 | GGACTACAGGCGCCC[A/G]CCACCACACCCGGCT | 57117 |
| rs189541903 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105683733 | TTAATTCACTCTTAA[C/T]AGCAAAAATGCCCAT | 57117 |
| rs189783626 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105701991 | CCTTGGAGTCAGTTC[G/T]TTTTATGCAATCTTG | 57117 |
| rs189888302 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | INTS12 | GRCh38.p7 | 4:105703545 | AGTACTCTAGGCACC[C/G/T]GAAAGCCCTGTAGTT | 57117 |
| rs189949186 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | INTS12 | GRCh38.p7 | 4:105688702 | CCTTCCACCCACATC[C/T]AGCACTCCTGAGGTT | 57117 |
| rs189964757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105706886 | TATGGCAATAACCTC[A/G]TTATTTTCCTTGACT | 57117 |
| rs190123360 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | INTS12 | GRCh38.p7 | 4:105685816 | AGAAATAATGTAGTA[C/T]GATTTCAAGGATGCA | 57117 |
| rs190172953 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | INTS12 | GRCh38.p7 | 4:105691318 | TTAAAAGAAAAATTA[C/T]GAAATTCATTTATCA | 57117 |
| rs190296573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105693073 | AGAAAATGTTACAAC[A/G]TAACAGATTTAAAAG | 57117 |
| rs190427459 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709474 | ACTACTTAACATTTA[C/T]TCCAAAGGACTTGCT | 57117 |
| rs190457315 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | INTS12 | GRCh38.p7 | 4:105699061 | TAACTCATTTACTGG[A/C]TCTCCTTCAATTTTT | 57117 |
| rs190561206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105696379 | TATAGAAAAATATGT[C/T]TCCCATCATCATCAT | 57117 |
| rs190600116 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | INTS12 | GRCh38.p7 | 4:105702797 | CCCTGACTTTTGTTT[A/C]CTCACCAAACAGAAA | 57117 |
| rs190684557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105684261 | TTAGGCACAAATGTA[C/T]GTATTCAAATTAATT | 57117 |
| rs190835456 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | INTS12 | GRCh38.p7 | 4:105687420 | AATTTCTATGTTATG[A/G]AAGAATTTTCACCCA | 57117 |
| rs190880705 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | INTS12 | GRCh38.p7 | 4:105694467 | AGGTGCTGGAACTAC[A/G]GGTGTGCGCCACCAC | 57117 |
| rs190977632 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105697507 | TGATTGTTTAGACAA[C/T]GGGTTAGCAAACTGA | 57117 |
| rs191252254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105684666 | CTTATGAAGTTATCC[A/G]GAGAAGAAAAACTAC | 57117 |
| rs191388127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105685009 | TACTATCAGGACACA[C/T]AGAAGTAATATAACA | 57117 |
| rs191396258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105703136 | CAGACTGCAAAAGAG[C/T]CATATCATTCTTACT | 57117 |
| rs191414047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105706531 | CTGGGATTACAAGTG[C/T]GAGCCAAATCTCTTA | 57117 |
| rs191420872 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | INTS12 | GRCh38.p7 | 4:105690582 | ATAGAACAACTTTCA[C/G]TTTTAAATATATTGA | 57117 |
| rs191508399 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, utr-variant-5-prime | INTS12 | GRCh38.p7 | 4:105703000 | GTCATAAAGAGGTCA[A/G]CAACTTGGTGTAACT | 57117 |
| rs191528455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708583 | CACCTCGCTCCTGGC[A/G]CGGGGGTCTCGAGCC | 57117 |
| rs191664518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105687964 | ATCTCAAAAAAACAA[C/T]AACAGAAAAAAAAAC | 57117 |
| rs191778243 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | INTS12 | GRCh38.p7 | 4:105694987 | TGGAGTGCAGTGGCA[C/T]GATCACCGCTCACTG | 57117 |
| rs192295280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105703413 | ATAGCACAAAAATCG[C/T]CATTACTGAACAATG | 57117 |
| rs192361388 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105697927 | TGGTGGCATGCACCT[G/T]TAGTCTTAGCTACTC | 57117 |
| rs192455633 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105700165 | TTACAAATAAAAGTA[A/T]ATTTCCTTCTTATTC | 57117 |
| rs192521919 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105700861 | TGTTTTTAGTTAATA[A/C]CAATGCTATCATGTG | 57117 |
| rs192594769 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707644 | GTAGTACAATGTTCC[C/T]ATCTGTAAAATTCTC | 57117 |
| rs192707274 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | INTS12 | GRCh38.p7 | 4:105695757 | CAATTTTCAGTTAAA[A/C]ATTAAGACATTTCAT | 57117 |
| rs192893349 | snp | A/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708219 | AGTGGCTGAAAGCTG[A/T]CAGCAAACACTTAGA | 57117 |
| rs192964704 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | INTS12 | GRCh38.p7 | 4:105694531 | GGGTTTTGCCATGTT[C/G]GCCAGGGTGGCCAAC | 57117 |
| rs193108687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105690225 | GCTGTAAGGTAGAGT[C/T]GGGTCAAAAAGAGAA | 57117 |
| rs193119627 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | INTS12 | GRCh38.p7 | 4:105689370 | CATATGAGAATCTCA[C/T]TCAAAGCAATTATAG | 57117 |
| rs199536680 | snp | A/G | 0.00109808 | 0.0234058 | intron-variant | INTS12 | GRCh38.p7 | 4:105686844 | TTTTTTGAGCCTGCA[A/G]AAATCAGTGGATTAA | 57117 |
| rs199563408 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105700551 | TTTTTTTTTTTTTTT[A/G]TAAACTCACCTCTTC | 57117 |
| rs199575533 | snp | G/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693399 | AATCCTTGCTACTTT[G/T]GACAGTAATGGGAGA | 57117 |
| rs199615374 | snp | A/G | 0.000536788 | 0.0163739 | intron-variant | INTS12 | GRCh38.p7 | 4:105699808 | AATGTAGTACTACAG[A/G]CCTTACAAAACTCTC | 57117 |
| rs199935244 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105705149 | AGCTTCATTTGTATT[C/T]ACAGCCACTCCCATC | 57117 |
| rs200072162 | in-del | -/A | | | intron-variant | INTS12 | GRCh38.p7 | 4:105689746 | ATCTCTACAAAAAAT[-/A]AAAAAAAAAATTAGC | 57117 |
| rs200134002 | snp | C/T | 0.00079065 | 0.019867 | intron-variant | INTS12 | GRCh38.p7 | 4:105695472 | TTTCTGCTTATGGAA[C/T]AACTAATTTACTTTC | 57117 |
| rs200200573 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703236 | TTAATATATTAAATG[-/T]TAGGTTTCATTTAAA | 57117 |
| rs200401019 | in-del | -/A | 0.0225045 | 0.103662 | intron-variant | INTS12 | GRCh38.p7 | 4:105685972 | CCAATAAGAAGGGAG[-/A]AAAAAAAAATTACAA | 57117 |
| rs200480077 | snp | C/T | 6.62669e-05 | 0.00575578 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105686713 | TTCTGTTCTCTTAAA[C/T]GCTAGAAAAGTTGTC | 57117 |
| rs200608396 | in-del | -/A | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710235 | TGGGCCCATCAATTT[-/A]TTTTTTTTTTTTTTT | 57117 |
| rs200817001 | snp | C/T | 0.00030102 | 0.0122646 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105692128 | TGCCAGATGCCACCA[C/T]CATTTGCCTAAGAAA | 57117 |
| rs200982175 | in-del | -/A | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707563 | CACCCCTGCCCCCAC[-/A]AAAAAAAACTCCAAA | 57117 |
| rs201024656 | snp | C/G | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683145 | ACAGGTTTCTGGTTA[C/G]CTGACGAAGTAGCAG | 57117 |
| rs201181296 | in-del | -/T | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707317 | TTCTCCCTTGAAGCA[-/T]TTTTTTTTTTTTTTG | 57117 |
| rs201252780 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105705150 | GCTTCATTTGTATTT[A/C]CAGCCACTCCCATCA | 57117 |
| rs201400294 | snp | C/T | 0.000593648 | 0.0172183 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695534 | ATCAGCAGGTCTCTT[C/T]TCAGCTTCCTTCTTT | 57117 |
| rs201470493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105689193 | AACTGAAGAATAACC[C/T]TGGACCCTGCCATAC | 57117 |
| rs201529721 | in-del | -/TA | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710234 | GTGGGCCCATCAATT[-/TA]TTTTTTTTTTTTTTT | 57117 |
| rs201573430 | snp | A/C/G | 0.000510826 | 0.0159737 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683193 | TGTGTTGTTGAACTC[A/C/G]ATTTTGCTGTTGAAG | 57117 |
| rs201639517 | snp | A/G | 0.000232292 | 0.0107746 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699885 | TGGAATCAATGCCCC[A/G]AGCCAAAGATTCATC | 57117 |
| rs201746596 | snp | C/T | | | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683175 | GGTTTCCCAGTATTG[C/T]TTTGTGTTGTTGAAC | 57117 |
| rs201819140 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693389 | GCCATAGGTAAATCC[C/T]TGCTACTTTGGACAG | 57117 |
| rs201904886 | in-del | -/AAC | 0.00835141 | 0.0640778 | intron-variant | INTS12 | GRCh38.p7 | 4:105687959 | ACTCCATCTCAAAAA[-/AAC]AACAACAGAAAAAAA | 57117 |
| rs202054559 | snp | A/G | 0.00038088 | 0.0137947 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105686714 | TCTGTTCTCTTAAAC[A/G]CTAGAAAAGTTGTCT | 57117 |
| rs202081372 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105688180 | TATTCATCATTATTA[G/T]TTACAAAGGATAATC | 57117 |
| rs202144950 | in-del | -/A | | | intron-variant | INTS12 | GRCh38.p7 | 4:105683859 | GATTCTAAACCCATT[-/A]AAAAAAAATGTCCTC | 57117 |
| rs202166150 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701234 | TACACATCCCTAGGC[-/T]TTTTTTTTTTTTTTT | 57117 |
| rs367662887 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105686615 | AAGTTTCTCATTAAA[-/T]TTTTTTATCAAGCAA | 57117 |
| rs367719662 | in-del | -/TA | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690462 | GATTTCAGAGACATA[-/TA]AGAGGTAGAATTAGC | 57117 |
| rs367825208 | snp | A/C/G | 0.000139743 | 0.00835796 | intron-variant | INTS12 | GRCh38.p7 | 4:105700029 | CCTGAAGGAAAAAAA[A/C/G]AGAAAGTAATCTAGA | 57117 |
| rs367854913 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105693126 | AGTTGACAATTTTCA[A/G]TATGCTAAATTGTTA | 57117 |
| rs368243689 | snp | A/G | 9.94794e-05 | 0.00705194 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105686816 | GGGGCTGGTTTCTGC[A/G]GTGGTTTCTGAGTTT | 57117 |
| rs368347244 | snp | A/C | 2.85238e-05 | 0.00377638 | intron-variant | INTS12 | GRCh38.p7 | 4:105691963 | TTAAAATAAAGAAAA[A/C]TATGATTCCTACCAT | 57117 |
| rs368418043 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105699305 | ATTATAAGATTTAAG[C/T]GGGATTTAAAACAGG | 57117 |
| rs368453978 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105689149 | AAGCTGGGGAAAAAC[G/T]CCACTACTGCGTAGA | 57117 |
| rs368522548 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701995 | GGAGTCAGTTCTTTT[C/T]ATGCAATCTTGCCAT | 57117 |
| rs368542851 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704668 | GTGCCTCCTATGCAA[C/T]GTGTCTCCAACAGAG | 57117 |
| rs368658206 | snp | A/G | | | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693403 | CTTGCTACTTTGGAC[A/G]GTAATGGGAGATGAC | 57117 |
| rs368760359 | snp | A/G | 3.29457e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682976 | AAGACCTACTTTGCT[A/G]ACATTGTCACAACTA | 57117 |
| rs368763704 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694775 | TTCAAATGTATTTTT[C/T]TCTAACTACTAAAAT | 57117 |
| rs368812389 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105687728 | GCGGGTGGTTCACTT[G/T]AGGTCAGGAGTTTGC | 57117 |
| rs368817731 | snp | C/T | 2.24924e-05 | 0.00335346 | intron-variant | INTS12 | GRCh38.p7 | 4:105692162 | TACCATTAAACATTA[C/T]ACTACTTTTTTAAAT | 57117 |
| rs368870007 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694928 | ATCTTTTCTTTCTTG[C/T]TTTCCTTTTTTTTTG | 57117 |
| rs368875197 | snp | A/C | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105706860 | TTCAGGTTTTATTAG[A/C]TTACTTGAACTATGG | 57117 |
| rs369141401 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105697645 | CAATGGAGACCATCT[G/T]GCACACAAAATCTAG | 57117 |
| rs369271958 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105706257 | CAACTTCAATCTCTT[C/T]TTTTTTTTTTTTTTT | 57117 |
| rs369296850 | snp | A/G | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709880 | TTTAAACATGTAAAC[A/G]TAGTCATTTAAATCC | 57117 |
| rs369456312 | snp | C/G/T | 3.29936e-05 | 0.00406152 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693471 | TATCAACTCCTTCAG[C/G/T]GATGTCTGATTTCAT | 57117 |
| rs369479502 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | INTS12 | GRCh38.p7 | 4:105703997 | AACCTTGGCCTATGG[A/G]TTATTTCCCATATCT | 57117 |
| rs369523774 | in-del | -/A | | | intron-variant | INTS12 | GRCh38.p7 | 4:105685549 | TTAAAAGTATTTCGT[-/A]TTCATATTCTTTTTC | 57117 |
| rs369802109 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691531 | GCAGCTGGAAAGACA[A/G]ATATGCACATATAAA | 57117 |
| rs370095926 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105696222 | TGTGACACCATCACT[A/G]CAATCAACATAATGA | 57117 |
| rs370124072 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708269 | GATCAAAGCATCACA[C/G]ATCGAAGTCCTAGAA | 57117 |
| rs370142546 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105696606 | TATTTATCAATTTAC[C/T]TATTGATGGATATTT | 57117 |
| rs370294113 | snp | C/G | 0.000115311 | 0.00759224 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682798 | GCTTCATAGCATTGA[C/G]CTGTGATTCTTGTGA | 57117 |
| rs370403762 | snp | A/C | 3.29565e-05 | 0.00405921 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695568 | TTTTCAGTTGTGAGG[A/C]CCTTGCCATTATTAT | 57117 |
| rs370699451 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105700535 | CTTTTACCTCAACTC[-/T]TTTTTTTTTTTTTTT | 57117 |
| rs370808431 | snp | A/T | 1.70606e-05 | 0.00292062 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682694 | ATAATAAGCCTTTCA[A/T]CTTTAGGCTAATATG | 57117 |
| rs370919655 | snp | C/T | 6.60807e-05 | 0.0057477 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699913 | ATCAAGCAGTGCTTT[C/T]AGCTTTTCAGCAGAA | 57117 |
| rs370960804 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | INTS12 | GRCh38.p7 | 4:105706410 | CAGGCATGCACCACC[A/G]TAACCATGCCCAGGT | 57117 |
| rs371055305 | snp | A/G | 1.65726e-05 | 0.00287855 | intron-variant | INTS12 | GRCh38.p7 | 4:105695672 | TGGCTCCACATCCTA[A/G]AAGATGAAAAAAGGT | 57117 |
| rs371369571 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701085 | ATCTCCCATTTTCAG[A/G]GGTTTATAACACCAT | 57117 |
| rs371555245 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698453 | CTGATCAAGAGAAAT[A/G]AACTCTAGCTAGAAA | 57117 |
| rs371654175 | snp | G/T | 2.17205e-05 | 0.00329542 | intron-variant | INTS12 | GRCh38.p7 | 4:105692153 | AAGAAAACATACCAT[G/T]AAACATTACACTACT | 57117 |
| rs371683806 | snp | G/T | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709600 | GGTTTCAAAAACGTT[G/T]GCTAATACACGTACT | 57117 |
| rs371735272 | snp | G/T | | | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693453 | ATCTAGGTTTCTTTG[G/T]AATATCAACTCCTTC | 57117 |
| rs371771059 | snp | C/T | 0.00052309 | 0.0161639 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105691983 | ATTCCTACCATTCTT[C/T]TCATTTGTCTGGTAC | 57117 |
| rs371844878 | snp | A/T | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709612 | GTTTGCTAATACACG[A/T]ACTTCCCATCCCAAC | 57117 |
| rs371972946 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691913 | TCAAATCTTTGTTTT[A/G]AAAGCACATACCAAC | 57117 |
| rs372025672 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | INTS12 | GRCh38.p7 | 4:105697031 | AATATTTTGCCCATT[A/T]AAAAGAAATGAATCT | 57117 |
| rs372111433 | snp | C/T | 1.66183e-05 | 0.00288251 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105686833 | TGGTTTCTGAGTTTT[C/T]TGAGCCTGCAAAAAT | 57117 |
| rs372183863 | snp | A/C | 0.000307953 | 0.0124049 | intron-variant | INTS12 | GRCh38.p7 | 4:105700040 | AAAAGAGAAAGTAAT[A/C]TAGAAGACAATGCAC | 57117 |
| rs372202558 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105683854 | GTATAGATTCTAAAC[C/T]CATTAAAAAAAAATG | 57117 |
| rs372298044 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105704850 | AACCTCTTAAACATA[A/C/T]CTCAAATCTATCCAC | 57117 |
| rs372378109 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | INTS12 | GRCh38.p7 | 4:105692181 | ACTTTTTTAAATGCC[A/G]TAATTTAAAGTTATT | 57117 |
| rs372473026 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704710 | CTATTCCCTTTTCTC[C/T]TAACCAGTTCTTCCT | 57117 |
| rs372483512 | in-del | -/CCAAAAAGGTTGTGGA | 0.0134861 | 0.0810011 | intron-variant | INTS12 | GRCh38.p7 | 4:105705514 | AACTGGTCCCTGGTG[-/CCAAAAAGGTTGTGGA]CCATTGCTCTACATG | 57117 |
| rs372484470 | in-del | -/TCT | | | intron-variant | INTS12 | GRCh38.p7 | 4:105689507 | TTTCCCCACATTTGC[-/TCT]TCTTGGTGTATTCTA | 57117 |
| rs372504520 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703154 | TATCATTCTTACTAT[A/G]GATTAGAGTTCTAGA | 57117 |
| rs372606580 | snp | A/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695622 | ATTTTGGGCTCTTGC[A/T]TAATGGAAATGTTTT | 57117 |
| rs372755279 | snp | A/C | 1.70694e-05 | 0.00292137 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682695 | TAATAAGCCTTTCAT[A/C]TTTAGGCTAATATGA | 57117 |
| rs372874344 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694913 | TCTATACTCTTTCCC[A/G]TCTTTTCTTTCTTGC | 57117 |
| rs372893258 | snp | A/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105700637 | TGATCACATTTAGAT[A/T]GTGGTATCTCATGCA | 57117 |
| rs373018303 | snp | C/T | 1.84425e-05 | 0.0030366 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683295 | CTGGCACTAGAAGAA[C/T]TTCCTGAAATAACTG | 57117 |
| rs373337496 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693415 | GACAGTAATGGGAGA[C/T]GACTGTGTTTCTGGT | 57117 |
| rs373478327 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | INTS12 | GRCh38.p7 | 4:105688507 | ACTTATAAAGCAACA[A/G]TTAGATCAAGAATAT | 57117 |
| rs373526628 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710267 | TTTTGAGCTGGAGTC[C/G]TGCTCTGTCGCCTGG | 57117 |
| rs373654955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105692822 | TGTTGTTGTTCTTCA[C/T]TAATATGAGTCACCT | 57117 |
| rs374190362 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105686954 | GAACATTTTAAAAAA[C/T]AGTGTGATGATAATG | 57117 |
| rs374640619 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703200 | TGTGTGTATGAAAGA[A/G]AAATGTATATATGAA | 57117 |
| rs374662805 | snp | A/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710709 | TTGCTGTGAAAATTC[A/G/T]GTAATTTTATTTCAT | 57117 |
| rs374938337 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105705844 | TAATATTAATCACAC[C/T]GTTAATTATGTAAAT | 57117 |
| rs374976724 | snp | A/T | 2.23102e-05 | 0.00333985 | intron-variant | INTS12 | GRCh38.p7 | 4:105692159 | ACATACCATTAAACA[A/T]TACACTACTTTTTTA | 57117 |
| rs375086284 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105703762 | GATCAGTTATACTTC[C/T]TCCATTTTCTTTTAA | 57117 |
| rs375108724 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699994 | AAGTTCCAAGTTCAC[A/G]GTAGCAGCCATTGCA | 57117 |
| rs375144856 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690639 | TTAGCTATAGAAGCT[C/T]ACCCAGGAAGAGGGT | 57117 |
| rs375236716 | snp | C/T | 0.000215451 | 0.0103769 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105686815 | AGGGGCTGGTTTCTG[C/T]GGTGGTTTCTGAGTT | 57117 |
| rs375256586 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105684486 | TTTAGCTCTTGAAAT[A/C]AAGGTAGCCTTCAAT | 57117 |
| rs375258685 | snp | C/G/T | 0.000184669 | 0.0096073 | intron-variant | INTS12 | GRCh38.p7 | 4:105686646 | CTATTTTTTAGTCAA[C/G/T]TAAACTTTAAGATAT | 57117 |
| rs375350671 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105707992 | ACAGAAACTGTTCAC[A/G]TAGAGTGCAGTATTA | 57117 |
| rs375509645 | in-del | -/AC | 0.00597247 | 0.0543191 | intron-variant | INTS12 | GRCh38.p7 | 4:105687267 | TGAGGGCAAATTAAA[-/AC]ACAGCTCAGATCATT | 57117 |
| rs375619490 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695654 | TGTGCTTGAAATTTT[A/G]GGTGGCTCCACATCC | 57117 |
| rs375643308 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | INTS12 | GRCh38.p7 | 4:105691936 | ATACCAACAAAAACA[C/T]TGACAGACTGTTTAA | 57117 |
| rs375774999 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105696508 | CATATTTATTTTGAG[A/G]TTCATCCATGTTGTT | 57117 |
| rs375844746 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682221 | ATCAATTAGGAAAAT[A/C]CATTGATATGAGAAA | 57117 |
| rs376088212 | snp | A/G | 0.000235754 | 0.0108546 | intron-variant | INTS12 | GRCh38.p7 | 4:105695495 | TTACTTTCTTTTAAC[A/G]AGATTAAAATAAAAT | 57117 |
| rs376474171 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105689683 | CGAGGCAGGAGGATC[A/G]CTTGAGGTCAGGAGT | 57117 |
| rs376474601 | snp | C/T | 1.66974e-05 | 0.00288936 | intron-variant | INTS12 | GRCh38.p7 | 4:105693294 | TGTGGCAAGGTACAA[C/T]TTACCTACAAACAAC | 57117 |
| rs376517193 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693445 | TTTCTCCAATCTAGG[C/T]TTCTTTGGAATATCA | 57117 |
| rs376750449 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105701880 | ATGTATTTCTACAAT[C/G]ACAGGTAAGAGGTTT | 57117 |
| rs376873641 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | INTS12 | GRCh38.p7 | 4:105697566 | TATATTAGAACACAG[A/C]CACACCCATTCATTT | 57117 |
| rs376952478 | in-del | -/AAAAGGTTGTGGACCA | | | intron-variant | INTS12 | GRCh38.p7 | 4:105705517 | TGGTCCCTGGTGCCA[-/AAAAGGTTGTGGACCA]TTGCTCTACATGATT | 57117 |
| rs376992002 | snp | C/T | 6.59011e-05 | 0.00573988 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682785 | ACCATCTGTAATCGC[C/T]TCATAGCATTGAGCT | 57117 |
| rs377070986 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703069 | ACACCAAATCATGTT[A/G]CTTCTATACAATTCC | 57117 |
| rs377108302 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704901 | ACCACCCTAGACCAA[C/T]CTAGCATCATCTATT | 57117 |
| rs377244087 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105686112 | TTGTCACCCAGGCTG[G/T]AGTGCAATGGTGCTA | 57117 |
| rs377327307 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105692622 | AAAAGCATAAGCTTT[G/T]AAAGCTTATGGTCAA | 57117 |
| rs377532933 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704851 | ACCTCTTAAACATAC[C/T]TCAAATCTATCCACC | 57117 |
| rs377718836 | snp | G/T | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710720 | ATTCAGTAATTTTAT[G/T]TCATACTTGGTAACA | 57117 |
| rs386678096 | multinucleotide-polymorphism | CGC/TGT | | | intron-variant | INTS12 | GRCh38.p7 | 4:105697791 | GTGGTGACACATGCC[CGC/TGT]AATCCCAGCACTTTG | 57117 |
| rs397976617 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698562 | AAAACAATTTTTTTT[-/T]CTTTAGTAATAATAG | 57117 |
| rs527276270 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105705712 | CTTCAGTAGAAAGTG[C/T]GCCACCCCCACCTCC | 57117 |
| rs527746417 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105689159 | AAAACTCCACTACTG[C/T]GTAGAGAGAAAACTA | 57117 |
| rs527780462 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701251 | TTTTTTTTTTTTTTT[-/T]AAGTTCCCAGGAAGG | 57117 |
| rs527810646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105689636 | AGCCTGGCATGGTGG[C/T]TCATGCCTATAATCC | 57117 |
| rs528152654 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105693874 | TAAATATTATCAATA[C/T]ACCCATTAGATTTGG | 57117 |
| rs528251580 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105697788 | GGTGTGGTGACACAT[A/G]CCTGTAATCCCAGCA | 57117 |
| rs528271800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708468 | GGAAGCACAGTCCTC[A/G]CTGAAAGGGGAGAGC | 57117 |
| rs528471198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105705721 | AAAGTGTGCCACCCC[C/T]ACCTCCATCTTAAGT | 57117 |
| rs528492767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105706680 | GTCCTGCTCTTACTT[C/T]CAATAAATGACACAA | 57117 |
| rs528497297 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694933 | TCTTTCTTGCTTTCC[-/T]TTTTTTTTTGAGACA | 57117 |
| rs528747517 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707443 | AACAAAATAATGGCT[A/C]TAGAATTACTGGAAT | 57117 |
| rs528761145 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703424 | ATCGCCATTACTGAA[A/C]AATGATCTTTTTTCT | 57117 |
| rs528908929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105685235 | AAAGAAACACAAAAC[C/T]TCTTAATCAAAACAA | 57117 |
| rs528944586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105692291 | GAGTTCAAGACCAGC[C/T]TGGCTGACACGGTGA | 57117 |
| rs529088690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707695 | CTTAATTCATTAATC[C/T]CACTGGTCTGTAAAC | 57117 |
| rs529357180 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105683690 | CTTTTAGACTTTTCT[A/C/T]CAAATAACTAGGGAT | 57117 |
| rs529486664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105706622 | TCTCAAATTCAGTTA[C/T]AACTAAAATTGAGAT | 57117 |
| rs529497635 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105698657 | CCATATTGATTTGGT[A/C]GATCTGAACTCACTG | 57117 |
| rs529561931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105699740 | TAATTTCTTCATGCT[A/C]CAAGGAAAGATTATT | 57117 |
| rs529900158 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105703420 | AAAAATCGCCATTAC[A/T]GAACAATGATCTTTT | 57117 |
| rs529965651 | snp | A/G | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710481 | TGATCCGCCCGCCTC[A/G]GCTTCCCAAAGTGGT | 57117 |
| rs529988239 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | INTS12 | GRCh38.p7 | 4:105702918 | TGTTGCCTTCTCTAA[A/T]CTCTGTTACTTTTCC | 57117 |
| rs530082188 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | INTS12, GSTCD | GRCh38.p7 | 4:105708812 | TTCCGGTCCGCCGGA[A/T]TATGAATGACGGCCG | 57117 |
| rs530083100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105694410 | TGCTCACTGTAACCT[C/T]CGCCTGCTGGGTTAG | 57117 |
| rs530140875 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698041 | GGTAACACAGTGAGA[A/C]CCTGTCTCAACAAAA | 57117 |
| rs530157981 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703306 | TAATATTTACCACTT[C/T]AAAGCTTTCGCTGAC | 57117 |
| rs530350249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105687231 | TCTTGGGGTCTAGGC[A/G]TAAGTCGACTCCTCA | 57117 |
| rs530380337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105686632 | TTTTTATCAAGCAAC[C/T]ATTTTTTAGTCAACT | 57117 |
| rs530614287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105687195 | TCTCATTGGGGTTTG[C/T]CAAATACACAAGAGT | 57117 |
| rs530675087 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105697218 | TATAGATAACTTGTT[A/G]TTTGTTGTCATTAAT | 57117 |
| rs530709445 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709772 | ATTATTGATAAAGAA[C/G]GTGGTGTATTTCTAT | 57117 |
| rs530777216 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105695488 | AACTAATTTACTTTC[G/T]TTTAACAAGATTAAA | 57117 |
| rs530799181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707478 | TGATCAAAGTATAGT[A/G]GTCTTATCTCTCCTT | 57117 |
| rs530800072 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105708892 | GTGGAGGCGAGTGGT[C/T]TGCGGGCAGCAGCTC | 57117 |
| rs530975234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105700271 | AACGTTTTAAATCCA[C/G]GTAGGCCTCTCCCTG | 57117 |
| rs531065163 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | INTS12 | GRCh38.p7 | 4:105701031 | AATGCAGCACACTTG[C/T]ATTGCTATAGTTAGG | 57117 |
| rs531127606 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105694239 | AAATCTAGATCTACA[A/T]GCATTAACAAAGATA | 57117 |
| rs531187456 | snp | A/T | 6.61452e-05 | 0.0057505 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693486 | TGATGTCTGATTTCA[A/T]CTATAAAAAGCAGGC | 57117 |
| rs531422159 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701776 | GTGCTGACCAAAGGG[C/T]TGACACCTAAAAGAA | 57117 |
| rs531562841 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683124 | GTTGCCAGACCAGTC[A/G]AACCCACAGGTTTCT | 57117 |
| rs531584529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105697722 | AGACTTAGTAAAGTG[C/T]TGAAGAAAATGTTAA | 57117 |
| rs531662012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105695702 | TACCAGTAATTAAAT[A/G]TTTAGACTGATCATC | 57117 |
| rs531724258 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105688127 | AGAGTTTAGCATAGT[G/T]TCTGGAAAATGTTGA | 57117 |
| rs531758588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105689133 | ATGAGTCTCTCACCT[A/G]AAGCTGGGGAAAAAC | 57117 |
| rs531848213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105696286 | CCCTTTGTAATTACT[C/T]TCTTACAGGTATACA | 57117 |
| rs532173418 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105693136 | TTTCAATATGCTAAA[C/T]TGTTATATGGGCAGT | 57117 |
| rs532263000 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105696485 | TTGGTCTGGCTTCTT[C/T]TACTCAGCATATTTA | 57117 |
| rs532313203 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698799 | GACAAAATGCCAGTG[-/T]TTACTTGGGCTCTGA | 57117 |
| rs532350454 | snp | A/G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105692894 | ATTACTGTGCACACA[A/G/T]AGGGTGCTCAATAAA | 57117 |
| rs532377077 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105689739 | AAGACTCCATCTCTA[C/T]AAAAAATAAAAAAAA | 57117 |
| rs532487917 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105695014 | ACTGCAATCTCTGCC[A/T]CCTGGGCTCAAGCAA | 57117 |
| rs532817603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105692241 | GTAATCCCAGCACTT[C/T]GGGAGGCCAAGGCAG | 57117 |
| rs532902365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105699601 | AAATTAAAGTAAGTC[A/G]TAAACAAGTGAATTC | 57117 |
| rs532998599 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105698541 | ACTTCCATTTTAGAA[A/C]CCCATTAAAACAATT | 57117 |
| rs533544396 | snp | A/C | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710163 | TTTTATATACTTTGC[A/C]CTTCTACGTGTTTTT | 57117 |
| rs533608120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105705805 | TCACTGTTACATAGC[A/C]CAAAAACATTCTGTA | 57117 |
| rs533612581 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105697276 | GAATTCCCCCTCCCC[C/T]AAAAGGAGGGCACTT | 57117 |
| rs533614597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105689279 | GCCCCAGTTTGAGGA[A/C]TCTGTTTGAGGAGAA | 57117 |
| rs533829755 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682548 | CATTAGAATAAAAAT[A/G]TTGAAGATTGATTTA | 57117 |
| rs534137177 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105704335 | CCTCAGTGCTAGGTT[C/G]TGGGTCTCTTCTTGA | 57117 |
| rs534256100 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105703216 | AAATGTATATATGAA[A/C]GATATTTAATATATT | 57117 |
| rs534620281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105706952 | AGTTTTCTTCTTTTT[C/T]ATTAAAATAAAAAAA | 57117 |
| rs534690946 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | INTS12 | GRCh38.p7 | 4:105706244 | ATATGTTTTACCCCA[A/G]CTTCAATCTCTTTTT | 57117 |
| rs535163934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105684081 | CTGCACAGTGACATT[C/T]TGGGTAGGACTGATC | 57117 |
| rs535203215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105684136 | GGTATAACACTTCAA[C/T]TTCTCTGATTAACTT | 57117 |
| rs535213103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105692329 | TCTCTACTAAAAATA[C/T]AAAAATCAGCTGGGC | 57117 |
| rs535231578 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105702041 | GCTTTGTACCCCTCC[C/T]CTAAATTACTAACAT | 57117 |
| rs535307019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105691788 | AAAAAGAGAAAAATG[C/T]ACATAACATGGTCTG | 57117 |
| rs535389405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105706503 | AATCCTCCTGTTGTG[G/T]CTTCCCAAAGTGCTG | 57117 |
| rs535513248 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105702416 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 57117 |
| rs535829080 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682675 | TATTACAGATTATAT[A/C]ATAATAATAAGCCTT | 57117 |
| rs535993760 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | INTS12, GSTCD | GRCh38.p7 | 4:105708644 | ATAACTCACCGTTCC[G/T]CCCCGCCCTGCCGAT | 57117 |
| rs536029425 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704060 | TCTTTTCATTGACAT[C/T]AAATATATTCAAACA | 57117 |
| rs536041934 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105687666 | ACCCAGCAACTGGCT[C/G]GGTGCAGTGGCTCAC | 57117 |
| rs536129228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105698005 | CAGTGAGCCAAGATT[A/G]TGCCACTGCACTCCA | 57117 |
| rs536236604 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709010 | CTGGCCGCGCCTCTG[C/T]GACCAGGTAAAGAGG | 57117 |
| rs536298443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105685607 | CTTACAGTCACTTAG[A/C]TAAGGCAATAACTTT | 57117 |
| rs536437592 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105686589 | TTCTAAAATATAGCC[A/C]TTTAGTATATAAAGT | 57117 |
| rs536491748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105688401 | TGGGCTACTGTTTGC[C/T]ATACTATATAGTTTG | 57117 |
| rs536498740 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690557 | AATTGCAGAAAAAAA[A/G]AACTGGATAATAGAA | 57117 |
| rs536704706 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694978 | CACCCAGGCTGGAGT[A/G]CAGTGGCACGATCAC | 57117 |
| rs536724312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105692686 | TTTGGCTATTTTCTC[A/G]TCATTTCTCGTCATA | 57117 |
| rs536828229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105693746 | TTCTCTTTGTACTCT[C/T]CTATCTACTAAAGAA | 57117 |
| rs536885200 | snp | A/G | 0.001718 | 0.0292583 | intron-variant | INTS12 | GRCh38.p7 | 4:105686854 | CTGCAAAAATCAGTG[A/G]ATTAAATCAGATACA | 57117 |
| rs537031052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105707952 | GTCCAAAGTTGATCA[C/T]ATGCACGTGCCCCAG | 57117 |
| rs537062080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105700583 | GTTCTCTGCCCCAAC[C/T]CTAAATGTCTCAGAA | 57117 |
| rs537120817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105706778 | AAATAATCAGAATTC[C/T]TGTGGATTCTGACGG | 57117 |
| rs537289525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105695043 | AATCCTCCCACCCCC[C/T]ACCCGCCCACAAACA | 57117 |
| rs537314298 | snp | A/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698358 | TTCTTACACAAATCT[A/T]GTGATGAAAATATTC | 57117 |
| rs537433144 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105701165 | TGGATTTTGTTGTCC[C/T]CTCCCCTCCAGCTTC | 57117 |
| rs537650793 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105707999 | CTGTTCACATAGAGT[A/G]CAGTATTATCGTTGC | 57117 |
| rs537657380 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105696572 | GAATAATATTCCATT[A/G]AATGAATAGACTACA | 57117 |
| rs537691997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105684830 | GCCATATGGTTAAAT[G/T]ATCTTTCAAAAAACT | 57117 |
| rs537754477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105685553 | AAGTATTTCGTATTC[A/G]TATTCTTTTTCATCA | 57117 |
| rs537835408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105696570 | CTGAATAATATTCCA[C/T]TGAATGAATAGACTA | 57117 |
| rs537894977 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105689254 | TACAATGATGTGTAC[C/T]GCAGAACTTGCCCCA | 57117 |
| rs538173646 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709363 | TGTTAAGTGTTACTT[A/C]AAGACCTCTTGGGTC | 57117 |
| rs538237120 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690263 | ATATGCATCCTAATG[A/C]GTATAATCTCATTAT | 57117 |
| rs538307416 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105691094 | TTAACTGATTAAAAA[G/T]TAAAATGGGTATCCC | 57117 |
| rs538316738 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709951 | TCATATTTAATAAAC[A/G]TTAAGCTATGCGGGT | 57117 |
| rs538608594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105703037 | ATCTACACATACAAA[A/G]ATATTTTCCTGGAGT | 57117 |
| rs538616688 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105695343 | AATTTGTAAATTTTA[A/C]TCATTTTTTGAAAAG | 57117 |
| rs538668281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105695996 | GTATCTGGGACTACA[C/G]GTGCACCACCACACC | 57117 |
| rs538856604 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | GSTCD, INTS12 | GRCh38.p7 | 4:105709132 | GTGGGAAGGACAAGG[A/G]CGTGGTATCATCGTC | 57117 |
| rs539026233 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694268 | TACATTTCAAAAGCA[C/T]ATAGTTGAGTGGAGA | 57117 |
| rs539096809 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682639 | AAATTTGATTATGAA[G/T]ACTTTTATTAAATTA | 57117 |
| rs539101023 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105690651 | GCTCACCCAGGAAGA[G/T]GGTTAGAACCATAAA | 57117 |
| rs539261126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105706440 | TAATTTTGTTGTTTT[C/T]TAAGTAGAGCCAGGG | 57117 |
| rs539451984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105703776 | CCTCCATTTTCTTTT[A/G]AAATTGCTTCTGTGT | 57117 |
| rs539488241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707226 | GACAGCTGCTGTGCC[C/T]CTCTCCATTCCAAAC | 57117 |
| rs539683476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105689978 | TAGAATGTGTCCAGT[C/T]TTGAGCTCTGCTTAA | 57117 |
| rs539869382 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710520 | AGGCGTGAGCCACCG[C/T]GCCCGGCCTGTTTTT | 57117 |
| rs540058605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105704650 | GACATGGATATATCA[C/T]TGGTGCCTCCTATGC | 57117 |
| rs540090775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105704432 | TAGAAATACAAACTC[C/T]TGGTCTCCATTCCTA | 57117 |
| rs540238848 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105702702 | TTTATTCATTTCTCT[A/T]TTCCCATTCTACTTG | 57117 |
| rs540404385 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105708827 | TTATGAATGACGGCC[G/T]GCGCGAGTATTTTCC | 57117 |
| rs540449373 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105687888 | AACCCATTAGGTGGA[C/G]GTTGCAGTGAGCCGA | 57117 |
| rs540493127 | snp | C/T | 1.70694e-05 | 0.00292137 | intron-variant | INTS12 | GRCh38.p7 | 4:105695484 | GAACAACTAATTTAC[C/T]TTCTTTTAACAAGAT | 57117 |
| rs540539153 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | INTS12 | GRCh38.p7 | 4:105698313 | TTCTTATCCATGCTA[A/C]AGTTTGAGAAACACT | 57117 |
| rs540805706 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105692835 | CATTAATATGAGTCA[A/C]CTAAAGGTGAGTACT | 57117 |
| rs540870884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105685099 | TTTTTAACTATAAAT[A/G]TTTTCTTGCCTATTT | 57117 |
| rs541011071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105698528 | CTTTAAGAGATAAAC[C/T]TCCATTTTAGAACCC | 57117 |
| rs541287312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105700064 | AATGCACAATTATCT[A/G]TGTTAAAGTTTTACT | 57117 |
| rs541338751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105705341 | TCCCCAGATGAAACC[A/G]TCTAGCTGCAGGAAA | 57117 |
| rs541416103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105690188 | GTGTATGAATGTGTA[C/T]GCTGAAGCAGTGAGA | 57117 |
| rs541445330 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105705566 | AATACATATAAAGCA[G/T]TTACAACAGTACCTG | 57117 |
| rs541506143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105697597 | TATAATGTATGGCTG[C/T]GTTCACATTACCATG | 57117 |
| rs541621180 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | INTS12 | GRCh38.p7 | 4:105699366 | CACATAAAGCTGCCA[C/T]TGGCTGCTTTGTTAT | 57117 |
| rs541667203 | snp | C/T | 3.1094e-05 | 0.00394285 | intron-variant | INTS12 | GRCh38.p7 | 4:105691954 | ACAGACTGTTTAAAA[C/T]AAAGAAAAATATGAT | 57117 |
| rs541756799 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105698419 | CTTTAAAAACCTATA[A/G]CAAAGTAGTTTCTGA | 57117 |
| rs541987681 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703330 | CGCTGACCTAGGGAA[A/G]TGGTAGTAGTAGTAT | 57117 |
| rs541991502 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105696302 | TCTTACAGGTATACA[C/T]CCTATAGAAAAATAT | 57117 |
| rs542015122 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105683795 | TGAAGAGATTCAGTC[A/C]ATATTTATTTACTGA | 57117 |
| rs542132578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105690009 | GTGCTATGCCAATGA[A/G]TACATGCTCTTACTG | 57117 |
| rs542217712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105689502 | TTGGTATTTCCCCAC[A/G]TTTGCTCTTGGTGTA | 57117 |
| rs542242104 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105696910 | AGGTATGTAGTGATA[A/T]CTCATTTAGATTTAA | 57117 |
| rs542639110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105693808 | GTATCTACCATACAG[A/G]CTTAACACATATTTG | 57117 |
| rs542724573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105684383 | AATTTTACAAAATAA[A/C]ATCCTACTTAAAAAA | 57117 |
| rs542776102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105693114 | GAAAGACAAAATAGT[C/T]GACAATTTTCAATAT | 57117 |
| rs542776178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105700720 | AAACACACACACACA[C/T]ACACACACACACACA | 57117 |
| rs542877134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105686902 | ACAGAAAGATAATAA[C/T]CCCTCACAGGACTCA | 57117 |
| rs543061784 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | INTS12 | GRCh38.p7 | 4:105693010 | AGATTATCAAAGGCA[C/T]ATATATCATAATATA | 57117 |
| rs543199367 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105686012 | GCTCAAGTAGTGTGG[G/T]GAGCAAAATTGTTGC | 57117 |
| rs543263224 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105700151 | TCACCAAAAAGTTAT[A/T]ACAAATAAAAGTAAA | 57117 |
| rs543508700 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105683730 | AATTTAATTCACTCT[C/T]AATAGCAAAAATGCC | 57117 |
| rs543516891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105691109 | GTAAAATGGGTATCC[C/T]GAGTTTTTACTTTTA | 57117 |
| rs543645238 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694959 | AGACAGCGCCTCACT[A/C]TGTCACCCAGGCTGG | 57117 |
| rs543815444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105683651 | CCCAACAAAGTATTA[C/T]CGACCTTAGTTAAAC | 57117 |
| rs543877593 | snp | A/C | 0 | 0 | intron-variant | INTS12 | GRCh38.p7 | 4:105684242 | ATATTTTTTCACTTT[A/C]ATATTAGGCACAAAT | 57117 |
| rs544044305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105706602 | TATGTGATTCCTTAA[C/T]GGCATCTCAAATTCA | 57117 |
| rs544285240 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105687075 | GAAATAATACAGAAG[A/C]GGGTTAGTTAAATAC | 57117 |
| rs544399121 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105702479 | AAAAATCTATTCATA[A/T]ACAGAGTGATAATAG | 57117 |
| rs544476277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105694863 | CACTGTTCAGGTGCA[C/T]ACCACTCTATAAAGT | 57117 |
| rs544492213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105687204 | GGTTTGTCAAATACA[C/T]AAGAGTTTTCTTCTT | 57117 |
| rs544540721 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105701936 | CAGCACCTAGATTAC[A/G]AGACTGCGGAAGTCA | 57117 |
| rs544608111 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105684105 | ACTGATCTCATTCTC[C/T]GATATATTTCATAAG | 57117 |
| rs544803010 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105695428 | ATACCCATTATTATA[C/T]AAAAGAAATAGGCAT | 57117 |
| rs544835642 | snp | A/C | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707059 | AGATTCAGTAACTGG[A/C]ACAAAAATTATCATT | 57117 |
| rs544877732 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105683431 | AAATTAGGTTCTTAT[A/G]AAGCTGATCTGAAAA | 57117 |
| rs544996850 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | INTS12 | GRCh38.p7 | 4:105687012 | ATCATATTAATGGTC[C/T]TACAGATTGTATTAG | 57117 |
| rs545249036 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709574 | AGTTTAATTTGCATG[A/G]AAGTTGCTTTGGTTT | 57117 |
| rs545581169 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | INTS12, GSTCD | GRCh38.p7 | 4:105708717 | GGCCGGCTCCGAAAG[A/C]AGGAAAACAAAGGTT | 57117 |
| rs545582256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105705391 | TGATTCTACATTATG[A/G]TGAGTTGTCCAATTA | 57117 |
| rs545687775 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105684924 | GCATGTTCTATGTGT[C/G]TGGCATTTCATTTTA | 57117 |
| rs545711982 | in-del | -/A | | | intron-variant | INTS12 | GRCh38.p7 | 4:105687969 | AAAAAACAACAACAG[-/A]AAAAAAAAACAGCAA | 57117 |
| rs545717339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105704855 | CTTAAACATACCTCA[A/G]ATCTATCCACCCTTT | 57117 |
| rs545775516 | snp | C/T | | | intron-variant, utr-variant-5-prime | INTS12 | GRCh38.p7 | 4:105702886 | AGTTTTCTATCTTAC[C/T]TTTACTCCCCCTTTT | 57117 |
| rs545806515 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105700089 | TTTACTTTTCTGTTT[C/T]TTAATTTGTAATAGA | 57117 |
| rs546007048 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105702806 | TTGTTTCCTCACCAA[A/T]CAGAAAACAGTAGTT | 57117 |
| rs546021993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105690416 | ACAAGTAATGGATTT[A/G]TGGAACAGGGTAATA | 57117 |
| rs546051396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105689005 | AATGTATAAAATTCT[C/G]CACTAAGGCACTAAC | 57117 |
| rs546146396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105696770 | GCTTAATTACTTGAG[A/G]AACTGCCAAACTGTG | 57117 |
| rs546179675 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105696255 | ATATCCATCATCTCT[C/T]CAAATTTCCTTGTGG | 57117 |
| rs546387998 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105700204 | CATTATCTAGTTCCT[C/T]CCCCCTGAAACAACT | 57117 |
| rs546425917 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | GSTCD, INTS12 | GRCh38.p7 | 4:105709103 | GTCTGCAGGGCTGAG[A/G]ATGCGGGGGAAGGGT | 57117 |
| rs546534851 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709813 | CTTATCTGTAAAAAC[A/C]ATGTTTACAGGAGAA | 57117 |
| rs546582561 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105694425 | CCGCCTGCTGGGTTA[C/G]AGTGATTCTCACGTC | 57117 |
| rs546606147 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105703466 | TATCCTTGATTTATT[A/G]CAGTATGCCGTTTAC | 57117 |
| rs546681485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105686640 | AAGCAACTATTTTTT[A/C]GTCAACTAAACTTTA | 57117 |
| rs546719150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105701280 | GGTATTAGTTATCTA[C/T]CTGATAACTACAAAA | 57117 |
| rs546809341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105688448 | TTCGTATCACTTTTT[A/G]TACTACATACCTTCC | 57117 |
| rs546978289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105690638 | GTTAGCTATAGAAGC[C/T]CACCCAGGAAGAGGG | 57117 |
| rs546994637 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105691523 | AGAGAAATGCAGCTG[A/G/T]AAAGACAGATATGCA | 57117 |
| rs547116529 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105697802 | TGCCTGTAATCCCAG[A/C]ACTTTGGGAAGCCAA | 57117 |
| rs547236557 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703605 | GCCATTCTCTCTCTG[C/T]CTGCACCCAAACTCT | 57117 |
| rs547342815 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105683868 | CCCATTAAAAAAAAA[G/T]GTCCTCCTAAATTTT | 57117 |
| rs547600280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105697329 | AAGGCAGCTGAGTGC[A/G]GTCTATTTTACTGTG | 57117 |
| rs547688682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105705032 | TTCTCACAATCCAAA[A/G]GTTCAAGAATAAGAT | 57117 |
| rs547802477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105697758 | CAGATTAAACTTAAA[A/G]ATGTGTGGTGGGCAG | 57117 |
| rs547923033 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105704346 | GGTTCTGGGTCTCTT[C/G]TTGACTTGTTCTACA | 57117 |
| rs547926336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105704291 | TCAGTCATCTTTGTA[C/G]GTTCCTCCTATCCAA | 57117 |
| rs548189889 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | INTS12 | GRCh38.p7 | 4:105689782 | CTGGTGGCACATGCC[C/T]GTAGTCCCAGCTACT | 57117 |
| rs548222100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105690515 | ATGGAATTAAAAGAG[A/G]CATCAAAGATGTTTT | 57117 |
| rs548285321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105689140 | TCTCACCTGAAGCTG[A/G]GGAAAAACTCCACTA | 57117 |
| rs548536287 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105695364 | TTTTGAAAAGTCAAA[A/C]TCTATAGCTATCAAT | 57117 |
| rs548582410 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105700934 | AAGAAATTATCAAAA[C/T]AAAAATGTATTCTTT | 57117 |
| rs548782984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105700388 | TCTGTATCAAAATTT[C/T]TTCTCTCAAACCTTA | 57117 |
| rs548838927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105684589 | AAGAGAAGGAATCCA[A/G]ATATTTGTCCACATA | 57117 |
| rs548863540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707734 | AGCAGGAACTTGTTT[C/T]GTTCACTGTTATTTC | 57117 |
| rs549375194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105684529 | CATACATTTTTAATC[A/T]ATGTGAAAAGTAACA | 57117 |
| rs549418354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105706137 | TGTCCAAGTATTTGT[C/T]CTTGGCTATCTTCTT | 57117 |
| rs549528793 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690007 | AAGTGCTATGCCAAT[A/G]AATACATGCTCTTAC | 57117 |
| rs549546202 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105691717 | GACTAGTAAGGAATA[G/T]TCATAATTTGTGTGT | 57117 |
| rs549592560 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105699757 | AAGGAAAGATTATTT[C/T]GGCAGAGATTGTTTT | 57117 |
| rs549601306 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105690100 | GAAGCTGAGAAGCAG[-/AA]AAAATATGGGAACAT | 57117 |
| rs549603059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105692301 | CCAGCCTGGCTGACA[C/T]GGTGAAACCCTGTCT | 57117 |
| rs549647432 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105691666 | CCACTTCTCAGTGCT[G/T]CATGGTATTTTAAAA | 57117 |
| rs549701581 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105685455 | ATGACAAATCAATAA[C/T]GGATATGCCTTGGAT | 57117 |
| rs549727249 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105698696 | GCAATGAGAATGGAT[A/G]GAAGAAATGAAGTCA | 57117 |
| rs549750465 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105692268 | GCAGGCGGATCATTT[G/T]AAGTCAGGAGTTCAA | 57117 |
| rs550358586 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105705904 | CCATGAAGGCAGGCA[A/G]TGGATTGGTCTTGCC | 57117 |
| rs550688015 | in-del | -/TTCT | 0.00676609 | 0.0577691 | intron-variant | INTS12 | GRCh38.p7 | 4:105693847 | CAAATTCGGATTCCC[-/TTCT]TTAAGATATAAATAT | 57117 |
| rs550719801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105693539 | TGGTAGAATAAACTT[C/T]AAGTCACTGAAAGAC | 57117 |
| rs550754120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105702879 | ATATTTTAGTTTTCT[A/G]TCTTACCTTTACTCC | 57117 |
| rs550874233 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105708902 | GTGGTCTGCGGGCAG[C/T]AGCTCCCAGAGGCAG | 57117 |
| rs550910070 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709381 | GACCTCTTGGGTCAC[A/C]CTAACTTCTCTTCTC | 57117 |
| rs550935754 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709786 | AGGTGGTGTATTTCT[A/G]TTTTACCTAAGCTTA | 57117 |
| rs550939506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105702196 | GCTGGAGTGCAGTGG[A/C]ATGATCTCGGCTCAT | 57117 |
| rs550986472 | snp | A/C | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707316 | TTTCTCCCTTGAAGC[A/C]TTTTTTTTTTTTTTT | 57117 |
| rs551107804 | snp | C/T | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105706820 | ACACTTGTCCTACTT[C/T]TCACTTCCACTGCTA | 57117 |
| rs551249394 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105701456 | TCACTTCTTAAAATT[A/T]TATTATTATATACAT | 57117 |
| rs551292703 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105694320 | ACACACACAGTATGA[A/T]AACATTTACATAATT | 57117 |
| rs551328498 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105685557 | ATTTCGTATTCATAT[G/T]CTTTTTCATCACATC | 57117 |
| rs551564710 | snp | A/T | 0.00835141 | 0.0640778 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105708862 | AAGGTGGCTGTCGTT[A/T]TTCTCCTGGCGTCTG | 57117 |
| rs551697009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105684386 | TTTACAAAATAACAT[C/T]CTACTTAAAAAATGG | 57117 |
| rs551738700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708481 | TCACTGAAAGGGGAG[A/G]GCAGTCAGTCTAGGG | 57117 |
| rs551776565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707452 | ATGGCTATAGAATTA[C/T]TGGAATTAAGTGATC | 57117 |
| rs551833352 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709965 | CATTAAGCTATGCGG[G/T]TTTTTTTTTCTTTTT | 57117 |
| rs551892052 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710570 | ACTTGTAGCTTTTGT[A/T]TCATCATCTGTGATT | 57117 |
| rs551901689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105706357 | ACTCCTGGGCTCAAG[C/T]GATCCTCCTGCCTCA | 57117 |
| rs551948969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682349 | ATACGGGGAGGAAAA[C/T]AGAAAACTATGTTGG | 57117 |
| rs551994863 | snp | C/T | 4.9675e-05 | 0.00498348 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693309 | CTTACCTACAAACAA[C/T]GCAGGCCAATCCCAT | 57117 |
| rs552038564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105695902 | TGCCCAGGCTGGAGT[A/G]GAGTGCTGTGGCACA | 57117 |
| rs552112823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105703529 | TTTCAATACCTCTTT[C/T]AGTACTCTAGGCACC | 57117 |
| rs552127986 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105692342 | TACAAAAATCAGCTG[C/G/T]GCATGGTGGTACACA | 57117 |
| rs552143069 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105687346 | GATTAAACTTTTTGA[C/G]GTTTTTCCACATTGC | 57117 |
| rs552155632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105688090 | TCAAAGGTGGGTTAT[A/G]AGGATGAATTATGAT | 57117 |
| rs552224483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105697081 | TAAAAGAGTTCTTCA[C/T]AGATTTTGGGCACAA | 57117 |
| rs552275705 | snp | C/T | 4.94458e-05 | 0.00497197 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695552 | AGCTTCCTTCTTTAC[C/T]TTTTCAGTTGTGAGG | 57117 |
| rs552398961 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105689754 | CAAAAAATAAAAAAA[A/T]AATTAGCTAGGCCTG | 57117 |
| rs552411224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682186 | TAAAAAAGGTAAAGA[C/T]ATAATATGAAGTATG | 57117 |
| rs552647570 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105702329 | TTTTAGTACAGACGG[G/T]GTTTCATCATGTTAG | 57117 |
| rs552706889 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | INTS12 | GRCh38.p7 | 4:105686958 | ATTTTAAAAAATAGT[A/G]TGATGATAATGAATA | 57117 |
| rs552956719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105694562 | TCCCGACCTGCTGAC[C/T]TCAAGTGATCCTCCT | 57117 |
| rs552957894 | in-del | -/T | 0.00200803 | 0.0316225 | intron-variant | INTS12 | GRCh38.p7 | 4:105684775 | TTATGAAAGACCTAA[-/T]TTTTTTTTCCTTTTC | 57117 |
| rs553018383 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | INTS12, GSTCD | GRCh38.p7 | 4:105708675 | CCGTCTGTTCCCGGT[G/T]GTCCCTTCGGAAACG | 57117 |
| rs553148606 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105699171 | GTTTCCTTATGTAAA[A/G]TGAAGAAAACAGTTA | 57117 |
| rs553221690 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105684975 | ATTGCTTTTCAACAG[G/T]ATGACAGATGGTTTA | 57117 |
| rs553325114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105685676 | TTTTTTTTTTAATAT[C/T]TTTTCTTCCATATTT | 57117 |
| rs553476734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105689897 | GAAAACAGAGTGAGA[A/C]CCTGTCTCAGAAAAA | 57117 |
| rs553899707 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105696674 | GTTATGAATATTCAT[A/G]TACAAGTATTTATAT | 57117 |
| rs553906501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105704748 | TCCCTTTTTCAAATG[A/G]TATTTACCCTATTGC | 57117 |
| rs554175627 | snp | A/G/T | 1.84364e-05 | 0.00303609 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683293 | CGCTGGCACTAGAAG[A/G/T]ATTTCCTGAAATAAC | 57117 |
| rs554226375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105689255 | ACAATGATGTGTACC[A/G]CAGAACTTGCCCCAG | 57117 |
| rs554288483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105696609 | TTATCAATTTACCTA[C/T]TGATGGATATTTGGG | 57117 |
| rs554461661 | in-del | -/TAT | 0.00358779 | 0.0422022 | intron-variant | INTS12 | GRCh38.p7 | 4:105687048 | AAACAGTAAAGATAA[-/TAT]TAAGCTTTAGAAATA | 57117 |
| rs554679000 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105688684 | CTTTCAATCTTAACA[A/C]TGCCTTCCACCCACA | 57117 |
| rs554699040 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105703187 | ACAAAGTCCTGTGTG[A/T]GTGTATGAAAGAAAA | 57117 |
| rs554821777 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694713 | AAGTATGAAAACATA[C/T]GGGATAATATACTCC | 57117 |
| rs555006490 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710076 | ACACCTGAAAGTATC[A/G]TTTTGTGAGGTCTCA | 57117 |
| rs555282184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105699370 | TAAAGCTGCCATTGG[C/T]TGCTTTGTTATTATC | 57117 |
| rs555358022 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | INTS12 | GRCh38.p7 | 4:105706510 | CTGTTGTGGCTTCCC[A/C]AAGTGCTGGGATTAC | 57117 |
| rs555679386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105706873 | AGCTTACTTGAACTA[C/T]GGCAATAACCTCGTT | 57117 |
| rs555752998 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105705257 | GTGAACTGTGCATGT[G/T]TGTGATCTACGTTGT | 57117 |
| rs555815010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105690781 | TGAAACAGTTGAGTA[C/T]ATACTAAAGAAAGAT | 57117 |
| rs555877119 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105683357 | CATTAGAGCCAAGTT[G/T]AATCAGTACCTGTAT | 57117 |
| rs555938831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105704544 | TTGGGAATTATTGCC[C/T]TAGACAATTTGATCT | 57117 |
| rs556360229 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691422 | TATTAAAGGCAGGTA[C/T]GTTAGTCAACAGTAA | 57117 |
| rs556441365 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105689990 | AGTCTTGAGCTCTGC[A/T]TAAGTGCTATGCCAA | 57117 |
| rs556569246 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105703808 | TCAGTAGATGGCCTC[A/T]CCTACTTCACAAAGA | 57117 |
| rs556741872 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105690707 | AATGGAGGAGAAAAA[A/C]CTTGGGGGAAGAACA | 57117 |
| rs556799425 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105696813 | TATATTTCCACCAAG[C/T]ATATATGAGAGAGTT | 57117 |
| rs556965303 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708601 | GGGGTCTCGAGCCTC[C/T]AGGAGGCCAGGAGCA | 57117 |
| rs556965643 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105700589 | TGCCCCAACCCTAAA[C/T]GTCTCAGAAAACATA | 57117 |
| rs557078315 | snp | C/T | 1.67295e-05 | 0.00289214 | intron-variant | INTS12 | GRCh38.p7 | 4:105686866 | GTGGATTAAATCAGA[C/T]ACAAAATCTTAACTG | 57117 |
| rs557097990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708011 | AGTGCAGTATTATCG[C/T]TGCCATTTCATAATG | 57117 |
| rs557159394 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105699294 | ATCATCACACAATTA[A/C/T]AAGATTTAAGTGGGA | 57117 |
| rs557220868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105691922 | TGTTTTGAAAGCACA[C/T]ACCAACAAAAACATT | 57117 |
| rs557266506 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | INTS12 | GRCh38.p7 | 4:105694488 | GCGCCACCACACCTG[A/G]CTAATTTTTGTATTT | 57117 |
| rs557275646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105701533 | TCATGGGGCTGGTCA[C/T]CATGTACGTTCTGAG | 57117 |
| rs557433424 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105706974 | ATAAAAAAAAAAATT[C/T]TTGCTGAGAAGTTAG | 57117 |
| rs557690739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105694474 | GGAACTACAGGTGTG[C/T]GCCACCACACCTGGC | 57117 |
| rs557754433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105700076 | TCTATGTTAAAGTTT[C/T]ACTTTTCTGTTTTTT | 57117 |
| rs557813916 | snp | A/C | | | intron-variant, utr-variant-5-prime | INTS12 | GRCh38.p7 | 4:105702984 | TTTACTTTCTACAGC[A/C]GTCATAAAGAGGTCA | 57117 |
| rs558081742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105700533 | CCACTTTTACCTCAA[C/T]TCTTTTTTTTTTTTT | 57117 |
| rs558198754 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105691813 | GGTCTGGTCTTTAGC[A/G]ATAGAAATATTAATC | 57117 |
| rs558550110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105687759 | GAACAGCCAGAACAG[C/T]CTGGCCCACATGGTG | 57117 |
| rs558610048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105688597 | AGAGCCATCTTATCC[C/T]TCATTGCAAAACCAT | 57117 |
| rs558661431 | snp | C/T | 0.000132426 | 0.00813607 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105686716 | TGTTCTCTTAAACGC[C/T]AGAAAAGTTGTCTCT | 57117 |
| rs558692878 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709270 | TCCCCCTAGCCAGTC[C/T]CTCATGTCTTCCTCT | 57117 |
| rs558846782 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105696579 | ATTCCATTGAATGAA[C/T]AGACTACAATTTATT | 57117 |
| rs558856680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105701918 | AGATTAGGTGACAAG[A/G]GTCAGCACCTAGATT | 57117 |
| rs558921692 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105695345 | TTTGTAAATTTTACT[C/T]ATTTTTTGAAAAGTC | 57117 |
| rs559213510 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | INTS12 | GRCh38.p7 | 4:105698575 | TTTCTTTAGTAATAA[C/T]AGGTTTCCCTATCTG | 57117 |
| rs559252257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105686259 | ACCCCTGGCTAATTT[C/T]TGTATTTTTAGTAGA | 57117 |
| rs559359016 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | INTS12 | GRCh38.p7 | 4:105695180 | GCAGTCTACCTGCCT[C/T]GGCCTCCCAAAGTGT | 57117 |
| rs559466709 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105693127 | GTTGACAATTTTCAA[G/T]ATGCTAAATTGTTAT | 57117 |
| rs559466818 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105700783 | TAAAGAGCTTAAAAA[A/T]TAGCCAAGATGGATA | 57117 |
| rs559528079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105693870 | GATATAAATATTATC[A/G]ATATACCCATTAGAT | 57117 |
| rs559795745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105706652 | TTCTGATTATCTTCC[C/T]GAAAAGTTCCTTGTC | 57117 |
| rs560007245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707341 | TTTTTTGGCACAAGT[A/G]TTATGTCCCCTACAA | 57117 |
| rs560088751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105694988 | GGAGTGCAGTGGCAC[A/G]ATCACCGCTCACTGC | 57117 |
| rs560266262 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105688771 | ATAAAGACTAATTAT[C/G]ATGAAGCCCCAGGAA | 57117 |
| rs560383133 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709493 | AAAGGACTTGCTTCA[C/T]TTGGGGCCATTTGCT | 57117 |
| rs560393743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105703476 | TTATTGCAGTATGCC[A/G]TTTACTTCCTATCCA | 57117 |
| rs560398107 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105688218 | ATCCAGAAAAATCCA[C/T]GCATACTGAACGGGG | 57117 |
| rs560453315 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105687908 | CAGTGAGCCGAGATC[A/G]CACCACTGCCCTCCA | 57117 |
| rs560593491 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691796 | AAAAATGCACATAAC[A/G]TGGTCTGGTCTTTAG | 57117 |
| rs560630480 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105685783 | TTTTTTCCATGATAT[A/G]AAAAGGCCAAGATAT | 57117 |
| rs560650766 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105689702 | GAGGTCAGGAGTTCG[A/G]GACCAGCCCTGGCAA | 57117 |
| rs560917065 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | INTS12, GSTCD | GRCh38.p7 | 4:105708808 | CTTTTTCCGGTCCGC[C/G]GGATTATGAATGACG | 57117 |
| rs561110528 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105692217 | GGCCAGGTGTGCTGG[C/T]TCATGCCTGTAATCC | 57117 |
| rs561167754 | in-del | -/A/T | 0.0146672 | 0.084371 | intron-variant | INTS12 | GRCh38.p7 | 4:105704014 | ATTTCCCATATCTTC[-/A/T]TTTTTTTTTTTTTCA | 57117 |
| rs561169259 | in-del | -/TAAA | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691891 | ATTTTTTCAATATCT[-/TAAA]TATTCAAATCTTTGT | 57117 |
| rs561225582 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105701947 | TTACAAGACTGCGGA[A/T]GTCATCAACACCAAC | 57117 |
| rs561233327 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709790 | GGTGTATTTCTATTT[C/T]ACCTAAGCTTATCTG | 57117 |
| rs561279987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105695450 | AATAGGCATAAAACA[C/T]TGTTTCTTTCTGCTT | 57117 |
| rs561488735 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105687206 | TTTGTCAAATACACA[A/G]GAGTTTTCTTCTTGG | 57117 |
| rs561686002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105691389 | CAATATAACAAATGA[A/G]AAGATATTTCACTAT | 57117 |
| rs561689778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105705660 | TAGCTATCTGACTTA[C/T]TTCAAGTCCTCCAAT | 57117 |
| rs561888615 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105689514 | CACATTTGCTCTTGG[G/T]GTATTCTAGTCATGT | 57117 |
| rs561906394 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105705154 | CATTTGTATTTACAG[C/T]CACTCCCATCACTTG | 57117 |
| rs562112800 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | INTS12 | GRCh38.p7 | 4:105704250 | AGGTAAACCTAATAC[A/G]TACGATTGTCCCTCC | 57117 |
| rs562144531 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105683731 | ATTTAATTCACTCTT[A/G]ATAGCAAAAATGCCC | 57117 |
| rs562205709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105696989 | CATATGGCATACATA[C/T]ATCTTCTTTGGTAAA | 57117 |
| rs562435976 | snp | C/T | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682849 | CTGAGGGAGAGCTGC[C/T]GGATTCTGAAGTAGT | 57117 |
| rs562514087 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | INTS12 | GRCh38.p7 | 4:105688109 | ATGAATTATGATTAT[G/T]TAAGAGTTTAGCATA | 57117 |
| rs562638964 | in-del | -/ATA | 0.00716266 | 0.059414 | intron-variant | INTS12 | GRCh38.p7 | 4:105689531 | TATTCTAGTCATGTT[-/ATA]ATATTAGCCATGACT | 57117 |
| rs562648203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105697705 | CTGTTGATCACTGGT[A/G]TAGACTTAGTAAAGT | 57117 |
| rs562711526 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105696268 | CTCCAAATTTCCTTG[G/T]GGCCCTTTGTAATTA | 57117 |
| rs562781327 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105697114 | CCTTTATCAGATATA[C/T]GATTTGCAAATATTT | 57117 |
| rs562818354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707007 | CTTTCTACCACCTTC[A/G]AAATAAAGACCAAAT | 57117 |
| rs562824862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105689014 | AATTCTCCACTAAGG[C/T]ACTAACTGCCAGAAT | 57117 |
| rs562959337 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708612 | CCTCCAGGAGGCCAG[A/G]AGCAGAGTCGCTCAG | 57117 |
| rs562961659 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710211 | GCTCAAACTTGAGCT[A/T]CTGTAGTAGTGGGCC | 57117 |
| rs562995126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105702843 | AAAATAAAACACTTA[C/T]GGTTATGTGGTTTAT | 57117 |
| rs563102678 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105699547 | TAAGTTGTGGTTACA[C/T]TCAGCAGCTTAAAAA | 57117 |
| rs563250363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105693019 | AAGGCATATATATCA[G/T]AATATAATAATCACT | 57117 |
| rs563282765 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105692269 | CAGGCGGATCATTTG[A/T]AGTCAGGAGTTCAAG | 57117 |
| rs563352025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105699738 | TATAATTTCTTCATG[A/C]TACAAGGAAAGATTA | 57117 |
| rs563354031 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707221 | TGACTGACAGCTGCT[C/G]TGCCCCTCTCCATTC | 57117 |
| rs563602362 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105697216 | GATATAGATAACTTG[C/T]TATTTGTTGTCATTA | 57117 |
| rs563787636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105691110 | TAAAATGGGTATCCC[A/G]AGTTTTTACTTTTAA | 57117 |
| rs563899053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105685148 | AAAAGACATTTGCTT[C/T]TTATATGTGAATGGG | 57117 |
| rs564024779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105692236 | TGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCAA | 57117 |
| rs564036364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105698529 | TTTAAGAGATAAACT[C/T]CCATTTTAGAACCCC | 57117 |
| rs564083455 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105699596 | ATCGGAAATTAAAGT[A/T]AGTCGTAAACAAGTG | 57117 |
| rs564090052 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105684519 | TGTCTGCATGCATAC[A/C]TTTTTAATCAATGTG | 57117 |
| rs564211246 | snp | A/C | 0 | 0 | intron-variant | INTS12 | GRCh38.p7 | 4:105706538 | TACAAGTGCGAGCCA[A/C]ATCTCTTAAATTTGA | 57117 |
| rs564283832 | snp | C/T | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682998 | TCACAACTAACTGAG[C/T]GACTAAGGCCAGTTT | 57117 |
| rs564391816 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105700112 | GTAATAGATAATACT[A/G]TACACATGATATAAA | 57117 |
| rs564444909 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105705673 | TATTTCAAGTCCTCC[A/G]ATATACTCTTTCTTA | 57117 |
| rs564591064 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105697604 | TATGGCTGCGTTCAC[A/T]TTACCATGGCAGAAT | 57117 |
| rs564815305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105694651 | TATGTAGATCTAAAA[A/G]CAGAGAAATAATCTA | 57117 |
| rs565022675 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | INTS12 | GRCh38.p7 | 4:105687054 | TAAAGATAATATTAA[A/G]CTTTAGAAATAATAC | 57117 |
| rs565229752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708177 | CCTGGAATCGCAGGA[A/G]AAAAGGCTCCGATTC | 57117 |
| rs565401935 | in-del | -/TTCT | 0.00557542 | 0.0525036 | intron-variant | INTS12 | GRCh38.p7 | 4:105698511 | AACAAATTTTTCATG[-/TTCT]TTAAGAGATAAACTT | 57117 |
| rs565434882 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105700202 | GGCATTATCTAGTTC[A/C]TTCCCCCTGAAACAA | 57117 |
| rs565447916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105694167 | AAACTGGTTAATCAT[C/T]CCCCTATGATAAATC | 57117 |
| rs565574269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105700448 | GCAGGTGTTTGTGTG[C/T]GTAAGGGCTATCGTA | 57117 |
| rs565581849 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105700908 | TCACTTTTTCAAAGA[A/C]CTCTCCAGGCAAGAA | 57117 |
| rs565745727 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105684623 | TGAAAATTGATAGGA[A/T]GTTTTCTTACAGTAA | 57117 |
| rs565763316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708457 | ACTCCCTCGGAGGAA[A/G]CACAGTCCTCACTGA | 57117 |
| rs565980238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707768 | AGTGCTTGAAACTTA[A/C]TAAGGGCTCAAAAAT | 57117 |
| rs566065239 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105705288 | GTGCTCCTCATGAGA[A/C]TCTAATGCCTGATGA | 57117 |
| rs566114188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105684123 | TATATTTCATAAGGG[C/T]ATAACACTTCAACTT | 57117 |
| rs566240264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105692302 | CAGCCTGGCTGACAC[A/G]GTGAAACCCTGTCTC | 57117 |
| rs566374037 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105687090 | AGGGTTAGTTAAATA[A/C]CATTTTAACAAGATA | 57117 |
| rs566387159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105691767 | ATATTAGAATTAGAT[A/G]AAACTAAAAAGAGAA | 57117 |
| rs566460273 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709914 | ATAATAAACTGTTAT[A/G]ACACAACTAAGTGAT | 57117 |
| rs566501519 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105686650 | TTTTTAGTCAACTAA[A/T]CTTTAAGATATAATC | 57117 |
| rs566515097 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | GSTCD, INTS12 | GRCh38.p7 | 4:105709108 | CAGGGCTGAGGATGC[A/G]GGGGAAGGGTGGGAA | 57117 |
| rs566582647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105702344 | GGTTTCATCATGTTA[A/G]CCAGGATGGTCTCGA | 57117 |
| rs566622720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105693610 | AGATATATTCACATA[G/T]TTAGGGACAGATGTG | 57117 |
| rs566783134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105696422 | TTCTGTAACAATACA[C/T]TAGTTTGCATTTCCT | 57117 |
| rs567378918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708629 | GCAGAGTCGCTCAGC[A/G]TAACTCACCGTTCCG | 57117 |
| rs567417784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105687465 | GCATCTTCAGTTTTA[C/T]TTTGACCAATAACTG | 57117 |
| rs567432794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105695835 | GAGAAATAATTGATA[C/T]ACAAACTGTACCTTT | 57117 |
| rs567460595 | snp | A/G | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710383 | CCACAATCACACTCG[A/G]CTCCTTTTTTTTTTT | 57117 |
| rs567557715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105702273 | CCCGAGTAGCTGGGA[A/C]TACAGGCGCCCGCCA | 57117 |
| rs567618228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105693555 | AAGTCACTGAAAGAC[A/G]AGTGAGAAGGACAAT | 57117 |
| rs567805099 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105696614 | AATTTACCTATTGAT[G/T]GATATTTGGGTTGTC | 57117 |
| rs567815576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105697253 | TGCATAAACTTTGGC[A/G]GCTCTTGGAATTCCC | 57117 |
| rs567842950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105694396 | AGTGGCACAATCTCT[C/G]CTCACTGTAACCTCC | 57117 |
| rs567928146 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105685597 | AAGCTTACTACTTAC[A/T]GTCACTTAGATAAGG | 57117 |
| rs568242491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682431 | GGCTTTGCTAGAAGA[C/T]GAACTATTTCTTTTT | 57117 |
| rs568438699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105688257 | TTCCCGCCAGCCATT[C/T]CATAGTCTTTGATAA | 57117 |
| rs568606226 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710691 | AACAAGCACAGGTAT[C/T]GTTTGCTGTGAAAAT | 57117 |
| rs568727535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105696494 | CTTCTTCTACTCAGC[A/G]TATTTATTTTGAGAT | 57117 |
| rs568931643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105704305 | AGGTTCCTCCTATCC[A/C]ATTAAAAATGAGTTC | 57117 |
| rs568939524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105696013 | TGCACCACCACACCC[A/G]GCTGATTTTTGTAGT | 57117 |
| rs569006485 | snp | A/C/T | 0.00174752 | 0.0295081 | intron-variant | INTS12 | GRCh38.p7 | 4:105686848 | TTGAGCCTGCAAAAA[A/C/T]CAGTGGATTAAATCA | 57117 |
| rs569018904 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105687355 | TTTTGAGGTTTTTCC[A/C]CATTGCAAAACTAGG | 57117 |
| rs569151717 | in-del | -/T | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707317 | TCTCCCTTGAAGCAT[-/T]TTTTTTTTTTTTTTG | 57117 |
| rs569392712 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105683408 | TGGGAAATTTAAATC[A/T]CACCACCAAATTAGG | 57117 |
| rs569838270 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | INTS12 | GRCh38.p7 | 4:105695393 | ATATATATTCACTGA[A/G]TGTTGATTATTATAT | 57117 |
| rs569891423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105693696 | CCAGCAAGATAGAAA[C/T]AAATAAATCAGAACA | 57117 |
| rs570083843 | snp | C/G/T | 5.01688e-05 | 0.00500822 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683267 | TAAGCCACTAGTTAC[C/G/T]GACGAGGAAACGCTG | 57117 |
| rs570093881 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105704500 | AAATCTGTGTTAAGC[C/G]TTCCAGGCAATTCTA | 57117 |
| rs570119028 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105690713 | GGAGAAAAAACTTGG[C/G]GGAAGAACAGTGCTT | 57117 |
| rs570206690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105689898 | AAAACAGAGTGAGAC[C/T]CTGTCTCAGAAAAAG | 57117 |
| rs570220679 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | INTS12 | GRCh38.p7 | 4:105690648 | GAAGCTCACCCAGGA[A/G]GAGGGTTAGAACCAT | 57117 |
| rs570355957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105705218 | ACTGGTGGAATTAGA[C/T]TCTCATAGGAATGCG | 57117 |
| rs570368487 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105705998 | AAGTAAATACTTGTT[A/G]TCTACTTCCAATTTC | 57117 |
| rs570523163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105697858 | AGTTTGAGACCAACC[C/T]GGGCAACATGGCAAA | 57117 |
| rs570990946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105697334 | AGCTGAGTGCAGTCT[A/G]TTTTACTGTGATAAT | 57117 |
| rs571079275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105704399 | CTGAGTCAGCAGCAT[A/G]GGTATCACGTCAGAA | 57117 |
| rs571383895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105702068 | ACATGGCCCTTTGAC[C/T]CAGTGGTCCCCATGG | 57117 |
| rs571537544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105701471 | ATATTATTATATACA[C/T]CACCTCTACATAATG | 57117 |
| rs571560869 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708495 | GAGCAGTCAGTCTAG[C/G]GCACGCAACCGCCCG | 57117 |
| rs571586438 | in-del | -/A | 0.108048 | 0.20579 | intron-variant | INTS12 | GRCh38.p7 | 4:105692484 | GTAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 57117 |
| rs571646625 | snp | C/G | 4.98923e-05 | 0.00499436 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699883 | ACTGGAATCAATGCC[C/G]CGAGCCAAAGATTCA | 57117 |
| rs571731552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105706696 | CAATAAATGACACAA[C/T]TTTCTTTTAGTCAGG | 57117 |
| rs571838944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105685499 | TGGCAAATTAAAATG[A/G]AAAATAATCTCCAAA | 57117 |
| rs571969868 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105699453 | AATTATCCTACCCAT[A/C]TTCAATTTATTTTGT | 57117 |
| rs572301036 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105686183 | TTCTCCTGCCTCAGC[C/T]TCCCAAGTAGCTGAT | 57117 |
| rs572420421 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694576 | CCTCAAGTGATCCTC[C/T]TGCCTTGACCTCCCA | 57117 |
| rs572463721 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105704593 | GATTACTAATACATC[G/T]CTGCAGTCCATGTGT | 57117 |
| rs572510448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105698110 | AAAAATTGAAGACAA[A/G]GTCATGCAGTATTAA | 57117 |
| rs572529651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105687747 | TCAGGAGTTTGCGAA[C/T]AGCCAGAACAGCCTG | 57117 |
| rs572647515 | snp | G/T | 0.00169577 | 0.029069 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682895 | TCCACTAGGTCCTGA[G/T]GTTCCACTATTTCCA | 57117 |
| rs572708975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105683530 | CCATATTCTTGTTCT[A/G]ATGATTCCAAAAGAA | 57117 |
| rs572754773 | snp | G/T | | | intron-variant, utr-variant-5-prime | INTS12 | GRCh38.p7 | 4:105703010 | GGTCAGCAACTTGGT[G/T]TAACTGTGTTGATCT | 57117 |
| rs572911671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105695333 | TTAACTTTAAAATTT[A/G]TAAATTTTACTCATT | 57117 |
| rs573043396 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | INTS12 | GRCh38.p7 | 4:105694461 | CTCCTGAGGTGCTGG[-/A]ACTACAGGTGTGCGC | 57117 |
| rs573365059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708140 | GTTCTTGGTTCTGGA[C/T]AACACTGATACCTTA | 57117 |
| rs573398339 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | INTS12, GSTCD | GRCh38.p7 | 4:105708710 | CCGCACTGGCCGGCT[C/T]CGAAAGCAGGAAAAC | 57117 |
| rs573430260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105700794 | AAAAATAGCCAAGAT[C/G]GATAAAGATATACAT | 57117 |
| rs573729764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105700122 | ATACTGTACACATGA[C/T]ATAAAATTTAAAATC | 57117 |
| rs573792380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105700690 | GTCTCTGAGGGATAA[C/T]ATCATATCTACTTAA | 57117 |
| rs573831429 | snp | C/T | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707914 | AGATCCATTTTTCAC[C/T]CTACCTGGCAATCTC | 57117 |
| rs573914501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105684888 | TTAAAAGACCAACAC[C/T]TAGGAAGTACAAGCA | 57117 |
| rs574070390 | snp | A/C/G | 0.000134891 | 0.00821156 | intron-variant | INTS12 | GRCh38.p7 | 4:105691929 | AAAGCACATACCAAC[A/C/G]AAAACATTGACAGAC | 57117 |
| rs574193058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105690619 | AGTATCTATAGACTA[C/T]CTAGTTAGCTATAGA | 57117 |
| rs574447113 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105688701 | GCCTTCCACCCACAT[A/C]TAGCACTCCTGAGGT | 57117 |
| rs574477425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105689274 | AACTTGCCCCAGTTT[A/G]AGGAATCTGTTTGAG | 57117 |
| rs574535930 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105699337 | GTGTTTGGTATCAAA[A/C]CATATATTCTTTTCA | 57117 |
| rs574754334 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105702594 | TTATTACAATCAATT[A/C]TCCTTTCTGACTACA | 57117 |
| rs574779269 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709452 | CAGAAAGCAGTTCTA[G/T]GTGAATACTACTTAA | 57117 |
| rs574816772 | snp | G/T | 3.42519e-05 | 0.00413821 | intron-variant | INTS12 | GRCh38.p7 | 4:105695479 | TTATGGAACAACTAA[G/T]TTACTTTCTTTTAAC | 57117 |
| rs574818528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105703190 | AAGTCCTGTGTGTGT[A/G]TATGAAAGAAAAATG | 57117 |
| rs575027325 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710118 | AGACTGAAAAGGTCA[A/G]TGAGATTTGAGAATC | 57117 |
| rs575417066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105687769 | AACAGCCTGGCCCAC[A/G]TGGTGAAACCCCGTC | 57117 |
| rs575557396 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710260 | TTTTTTTTTTTGAGC[C/T]GGAGTCCTGCTCTGT | 57117 |
| rs575670181 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708188 | AGGAGAAAAGGCTCC[G/T]ATTCCAAACCAATCA | 57117 |
| rs575824686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105694793 | TAACTACTAAAATCT[C/T]AATTACTATATGTAG | 57117 |
| rs575873516 | in-del | -/T | 0.0588605 | 0.161139 | intron-variant | INTS12 | GRCh38.p7 | 4:105685661 | GAGAATTTGAGGCTA[-/T]TTTTTTTTTAATATT | 57117 |
| rs575879468 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691098 | CTGATTAAAAAGTAA[A/G]ATGGGTATCCCGAGT | 57117 |
| rs575910125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105701935 | TCAGCACCTAGATTA[C/T]AAGACTGCGGAAGTC | 57117 |
| rs575945812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105698416 | GGGCTTTAAAAACCT[A/G]TAACAAAGTAGTTTC | 57117 |
| rs576386396 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105696863 | ACCAATGCTTTGTAT[G/T]GCTACTCTTTTTAAA | 57117 |
| rs576536666 | snp | G/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682630 | AAACAATAGAAATTT[G/T]ATTATGAAGACTTTT | 57117 |
| rs576625726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105703925 | TAAAAAAGGAGAAGG[C/T]AGCTCTCTATGTAGT | 57117 |
| rs576666363 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105697459 | AATGGGTCCTCAGAT[A/C]TAGTGGTGGCAGGGC | 57117 |
| rs576678966 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105690008 | AGTGCTATGCCAATG[A/T]ATACATGCTCTTACT | 57117 |
| rs577140584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105688799 | GAAGTACTTCTGCCT[A/G]TGAGATCATGTTTCA | 57117 |
| rs577289965 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710195 | CTTTAATTTAAACAC[A/G]GCTCAAACTTGAGCT | 57117 |
| rs577318822 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105706659 | TATCTTCCCGAAAAG[C/T]TCCTTGTCCTGCTCT | 57117 |
| rs577488518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105696719 | TTATTTCTCTAGAAA[A/T]AATAGGAGTGGGTTA | 57117 |
| rs577771564 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105706553 | AATCTCTTAAATTTG[A/C]ATCCCATGTTTCCAA | 57117 |
| rs577853919 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | INTS12 | GRCh38.p7 | 4:105700553 | TTTTTTTTTTTTTCT[A/C]AACTCACCTCTTCAG | 57117 |
| rs577864448 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105693692 | GAAACCAGCAAGATA[A/G]AAATAAATAAATCAG | 57117 |
| rs577995844 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691484 | TGGTCACTTGAGGAC[A/C]ATGAGAAGGAAAGAC | 57117 |
| rs578095544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | INTS12 | GRCh38.p7 | 4:105683637 | TAACATAGTTTTTAC[C/T]CAACAAAGTATTATC | 57117 |
| rs578203103 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105687756 | TGCGAACAGCCAGAA[C/G]AGCCTGGCCCACATG | 57117 |