Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4673 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs1883112 0.851 0.200 22 36860804 intron variant G/A snv 0.39 4
rs28937317 0.882 0.120 3 38560418 missense variant T/C snv 3