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i5009344

From SNPedia
23andMe dataI5009344
23andMe searchI5009344
opensnpI5009344
Gene (via rs)BRCA2

aliasrs80358920
Rs_StabilizedOrientationplus
RsGeno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6 Possible miscall in data from Ancestry v2c chip; otherwise, BRCA2 variant considered pathogenic for breast cancer

Removed from 23andMe due to unreliability https://www.reddit.com/r/23andme/comments/53ay25/23andme_raw_data_accuracy_promethease_analysis/d8coyol

For information about causal/pathogenic BRCA2 mutations and what they imply about the odds of developing breast cancer, please see the BRCA2 page and links from that page.