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rs28897743(G;G)

From SNPedia

common in clinvar
Is agenotype
ofrs28897743
GeneBRCA2
Chromosome13
Position32,346,896
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 6 considered a causal BRCA2 breast cancer mutation
(G;G) 0 common in clinvar
(G;T) 6 BRCA2 variant considered pathogenic for breast cancer