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rs80359716(AG;AG)

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common in clinvar

Is a	genotype
of	rs80359716
Gene	BRCA2
Chromosome	13
Position	32,371,005
Merged into	Rs80359714
mentioned	by

0

Good

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

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Is a genotype