Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs1057519903 0.683 0.080 1 226064434 missense variant A/T snv 28
rs1057519902 0.742 0.160 1 226064451 missense variant G/C snv 16
rs1553260624 0.763 0.080 1 226064454 missense variant G/A snv 14
rs2235544 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 14
rs1052576 0.807 0.200 1 15506048 missense variant T/A;C snv 0.53 9
rs1373481065 0.827 0.040 1 67687668 missense variant A/G snv 4.0E-06 6
rs374052197 0.882 0.040 1 13610421 missense variant G/A;T snv 8.0E-06 5
rs621559 0.827 0.080 1 43179740 intron variant G/A snv 0.18 5
rs745934102 0.882 0.040 1 13607281 missense variant G/A snv 3.2E-05 1.4E-05 5
rs12752552 0.882 0.040 1 64763616 intron variant T/C snv 0.13 4
rs12021720
DBT
0.925 0.160 1 100206504 missense variant T/A;C snv 0.92 3
rs10494090 1.000 0.040 1 108150714 intron variant A/C;G;T snv 2
rs10924303 1.000 0.040 1 245683732 intron variant C/T snv 0.15 2
rs10924690 1.000 0.040 1 246320481 intron variant G/A snv 0.20 2
rs11163687 1.000 0.040 1 83199436 intergenic variant A/G snv 9.6E-02 2
rs11166389 1.000 0.040 1 100000723 non coding transcript exon variant G/A snv 0.15 2
rs11583706 1.000 0.040 1 238358337 intron variant G/T snv 0.17 2