Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs10224210 1.000 0.040 7 151716108 intron variant T/C snv 0.21 8
rs963837 0.925 0.120 11 30727543 intergenic variant T/C snv 0.35 8
rs8096658 0.925 0.120 18 79396537 intron variant C/G snv 0.39 5