rs169547(A;G)

Benign variant

Is a	genotype
of	rs169547
Gene	BRCA2
Chromosome	13
Position	32,355,250
mentioned	by

Magnitude

1

Repute

Good

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;G)	1	Benign variant
(G;G)	0	common in complete genomics