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
rs63750311 0.790 0.240 14 73192647 missense variant A/C snv 8
rs63750671
APP
0.790 0.240 21 25891858 missense variant G/C snv 8
rs79524815 0.851 0.240 7 18658708 intron variant T/G snv 3.8E-02 4
rs1412095491
APP
0.882 0.200 21 26051053 missense variant C/G snv 4.0E-06 3
rs34487851 0.882 0.200 2 106026098 regulatory region variant A/G snv 0.28 3