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: rs429358
rs429358
APOE
66 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.800 0
dbSNP: rs63750771
rs63750771
PSEN1
1 1.000 0.080 14 73186896 missense variant T/C snv 0.010 1.000 1 2002 2002