Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs368234815 0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15