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rs397507815(CT;CT)

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common in clinvar

Is a	genotype
of	rs397507815
Gene	BRCA2
Chromosome	13
Position	32,340,309
Merged into	Rs80359551
mentioned	by

0

Good

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

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Is a genotype