rs397507872(GT;GT)

common in clinvar

Is a	genotype
of	rs397507872
Gene	BRCA2
Chromosome	13
Position	32,340,990
mentioned	by

Magnitude

0

Repute

Good

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