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rs397507891(G;G)

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common in clinvar

Is a	genotype
of	rs397507891
Gene	BRCA2
Chromosome	13
Position	32,346,897
mentioned	by

0

Good

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

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Is a genotype