rs397509299(C;C)

common in clinvar

Is a	genotype
of	rs397509299
Gene	BRCA1, NBR2
Chromosome	17
Position	43,124,042
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6	BRCA1 variant considered pathogenic for breast cancer