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
rs201085152
APP
0.925 0.080 21 25975072 missense variant G/A;T snv 1.6E-05; 3.6E-05 3