Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs13387042 0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 16