Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4664308 0.851 0.160 2 160060986 intron variant A/G snv 0.30 4
rs35771982 0.925 0.120 2 160028907 missense variant G/C snv 0.39 0.35 2
rs17830558 1.000 0.120 2 160021853 intron variant T/G snv 0.39 1