rs397507776(C;C)

common in clinvar

Is a	genotype
of	rs397507776
Gene	BRCA2
Chromosome	13
Position	32,339,605
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(-;C)	6	BRCA2 variant considered pathogenic for breast cancer
(C;C)	0	common in clinvar