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rs397507608(G;G)

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common in clinvar

Is a	genotype
of	rs397507608
Gene	BRCA2
Chromosome	13
Position	32,333,283
mentioned	by

0

Good

Geno	Mag	Summary
(-;G)	6	Likely miscall in Ancestry and possibly 23andMe data; otherwise, BRCA2 variant considered pathogenic for breast cancer
(G;G)	0	common in clinvar

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Is a genotype