rs63750399(A;A)

common in clinvar

Is a	genotype
of	rs63750399
Gene	APP
Chromosome	21
Position	25,891,787
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;G)	7	Mutation considered pathogenic for Alzheimer disease
(A;T)	7	Mutation considered pathogenic for Alzheimer disease