Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs201085152
rs201085152
APP
3 0.925 0.080 21 25975072 missense variant G/A;T snv 1.6E-05; 3.6E-05 0.010 1.000 1 2008 2008
dbSNP: rs63750424
rs63750424
MAPT
30 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.010 1.000 1 2008 2008