Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750066
APP
0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 3
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 3
rs63749964
APP
0.851 0.080 21 25891783 missense variant A/C snv 2
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 2
rs193922916
APP
0.827 0.080 21 25897619 missense variant G/A;C snv 1
rs63750064
APP
0.925 0.080 21 25897605 missense variant C/G;T snv 1