Source: ALL
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
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
rs63750921
APP
0.882 0.200 21 25891820 missense variant G/C snv 4
rs63749810
APP
0.882 0.200 21 25891853 missense variant C/T snv 3