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
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33