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rs397507222(C;C)

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common in clinvar

Is a	genotype
of	rs397507222
Gene	BRCA1
Chromosome	17
Position	43,091,679
Merged from	Rs886038026
mentioned	by

0

Good

Geno	Mag	Summary
(-;C)	6	BRCA1 variant considered pathogenic for breast cancer (possible; see note)
(C;C)	0	common in clinvar

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Is a genotype