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 25
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7