Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
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
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
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs1050501 0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs3811463 0.752 0.400 1 26427451 3 prime UTR variant T/A;C snv 14
rs396991 0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs4612666 0.763 0.440 1 247435768 intron variant T/C snv 0.65 10
rs1342913 0.851 0.040 1 190151895 intron variant G/A snv 0.61 4
rs1041163 0.882 0.160 1 100718269 upstream gene variant T/C snv 0.18 3
rs3795391 0.882 0.040 1 153390629 non coding transcript exon variant T/C snv 8.3E-02 3
rs3806232 0.882 0.040 1 153391654 upstream gene variant T/C snv 0.15 3
rs1058885 0.925 0.080 1 109923844 missense variant T/C snv 0.38 0.39 2
rs1171989978 1.000 0.040 1 202159420 missense variant G/A snv 4.0E-06 1
rs2297706 1.000 0.040 1 109914244 intron variant C/A;T snv 0.22 0.25 1
rs333967 1.000 0.040 1 109917151 intron variant C/T snv 0.28 1
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1027009063 0.925 0.040 2 8802974 stop gained G/A snv 2
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48