Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs63750306
PSEN1
0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs1223904774
APP
0.790 0.120 21 25891772 missense variant C/T snv 4.0E-06 7.0E-06 8
rs74315411
PRNP
0.882 0.160 20 4699767 missense variant A/G snv 4
rs201085152
APP
0.925 0.080 21 25975072 missense variant G/A;T snv 1.6E-05; 3.6E-05 3