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 55
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs35188965 5 1104823 intron variant C/G;T snv 12
rs4760 1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 7