Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1455858 0.925 0.080 7 136946956 intron variant T/C snv 0.69 3