Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs2235544 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 14
rs374524467 0.827 0.040 4 110632961 missense variant A/C snv 8.0E-06 7.0E-06 5
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs865880036 0.827 0.040 15 37098156 missense variant A/C snv 1.3E-04 5
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs118101777 0.614 0.280 15 90087472 missense variant C/T snv 2.0E-03 1.6E-03 42
rs11554137 0.742 0.040 2 208248468 synonymous variant G/A snv 5.1E-02 6.8E-02 13
rs16906252 0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 19
rs1805015 0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205