Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs79184941 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 18
rs121913478 0.708 0.640 10 121515280 missense variant T/C snv 13
rs4430796 0.790 0.280 17 37738049 intron variant A/G snv 0.52 7