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: rs200396597
rs200396597
APP
2 1.000 0.080 21 25881743 missense variant C/T snv 7.0E-06 0.010 1.000 1 2018 2018