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

i5009351

From SNPedia
23andMe dataI5009351
23andMe searchI5009351
opensnpI5009351
Gene (via rs)BRCA2

aliasrs397507866
Rs_StabilizedOrientationplus
RsGeno 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