rs41293497(C;C)

common in clinvar

Is a	genotype
of	rs41293497
Gene	BRCA2
Chromosome	13
Position	32,340,037
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(A;C)	6	considered a causal BRCA2 breast cancer mutation
(C;C)	0	common in clinvar
(C;G)	6	BRCA2 variant considered pathogenic for breast cancer