Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs368234815 0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs9264942 0.763 0.400 6 31306603 intron variant T/C snv 0.34 15
rs10484554 0.807 0.200 6 31306778 intron variant C/T snv 0.12 11
rs1015164 0.925 3 46410189 intron variant A/C;G;T snv 8
rs183662584 1.000 3 46373218 missense variant G/A snv 5.2E-04 1.5E-04 2