Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs1045485 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs3745274 0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30
rs5010528 0.827 0.240 6 31273255 intron variant A/G snv 0.15 9
rs4917014 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 8
rs3815087 0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25 8
rs2779249 0.851 0.200 17 27801555 intron variant C/A snv 0.33 7
rs28399499 0.827 0.280 19 41012316 missense variant T/C snv 5.1E-03 2.2E-02 6
rs9469003 0.882 0.160 6 31440051 intron variant T/C snv 0.22 6
rs3130501 0.851 0.280 6 31168676 intron variant A/G snv 0.78 4
rs2844665 0.882 0.200 6 31039078 downstream gene variant T/C snv 0.65 3
rs6500265 0.882 0.240 16 49912759 intergenic variant C/G;T snv 0.27 3
rs9933632 0.882 0.240 16 49906847 intergenic variant G/T snv 0.31 3
rs79908535 0.882 0.280 5 132679856 missense variant G/A snv 6.8E-05 2.8E-05 3
rs41544623 0.882 0.280 6 31411083 missense variant C/T snv 3
rs3094188 0.882 0.200 6 31174468 intron variant C/A;T snv 0.68 3
rs2734583 0.882 0.240 6 31537703 intron variant A/G snv 0.10 3
rs6016348 0.925 0.160 20 40410188 regulatory region variant C/T snv 0.28 2
rs9888871 0.925 0.160 16 49916730 downstream gene variant G/C snv 0.19 2
rs384129 0.925 0.160 11 22670928 intron variant T/A snv 2
rs16957893 0.925 0.160 15 73437142 intergenic variant G/C snv 4.9E-02 2