Gene: APP ×
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: rs63750579
rs63750579
APP
13 0.742 0.280 21 25891856 missense variant C/G;T snv 0.010 1.000 1 2002 2002
dbSNP: rs63750671
rs63750671
APP
8 0.790 0.240 21 25891858 missense variant G/C snv 0.010 1.000 1 2002 2002