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rs397507741(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs397507741
GeneBRCA2
Chromosome13
Position32,339,121
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;C) 6 BRCA2 variant considered pathogenic for breast cancer
(C;C) 0 common in clinvar