Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507866(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs397507866
GeneBRCA2
Chromosome13
Position32,340,902
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 6 Likely miscall in Ancestry v2c data; otherwise, BRCA2 variant considered pathogenic for breast cancer