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
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs560887 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 14