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
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs4665987 0.925 0.120 2 27532958 upstream gene variant G/A;T snv 6