Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs63750066
APP
0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 9
rs63750671
APP
0.790 0.240 21 25891858 missense variant G/C snv 8
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 8
rs63749964
APP
0.851 0.080 21 25891783 missense variant A/C snv 4
rs63750734
APP
0.851 0.080 21 25891790 missense variant C/T snv 4
rs63750399
APP
0.882 0.080 21 25891787 missense variant T/A;C snv 3
rs63750643
APP
0.882 0.080 21 25891793 missense variant T/C snv 3
rs63750973
APP
0.882 0.120 21 25891792 missense variant G/A snv 3
rs281865161
APP
0.925 0.080 21 25897626 missense variant TC/GA mnv 2