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rs397507900(C;C)

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common in clinvar

Is a	genotype
of	rs397507900
Gene	BRCA2
Chromosome	13
Position	32,355,036
mentioned	by

0

Good

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

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Is a genotype