Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3825942 0.716 0.320 15 73927241 missense variant G/A;C;T snv 0.18; 4.5E-06 15
rs1900004 0.827 0.040 10 68241124 intron variant C/T snv 0.39 5
rs3793342 0.851 0.040 7 150998107 intron variant G/A snv 0.13 4