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rs397507785(T;T)

From SNPedia
common in clinvar
Is agenotype
ofrs397507785
GeneBRCA2
Chromosome13
Position32,339,794
Merged fromRs863224466
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;T) 6 BRCA2 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar