Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 13
rs1035071612 0.763 0.240 19 11113361 missense variant C/A;T snv 4.0E-06 9
rs79524815 0.851 0.240 7 18658708 intron variant T/G snv 3.8E-02 4
rs34487851 0.882 0.200 2 106026098 regulatory region variant A/G snv 0.28 3