Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs7330796 13 75324027 intron variant T/C snv 0.76 1
rs2877716 3 123375604 intron variant T/C snv 0.76 4