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rs41293497(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs41293497
GeneBRCA2
Chromosome13
Position32,340,037
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;C) 6 considered a causal BRCA2 breast cancer mutation
(C;C) 0 common in clinvar
(C;G) 6 BRCA2 variant considered pathogenic for breast cancer