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rs397507908(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs397507908
GeneBRCA2
Chromosome13
Position32,355,114
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6 BRCA2 variant considered pathogenic for breast cancer