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i5009188

From SNPedia

23andMe dataI5009188
23andMe searchI5009188
opensnpI5009188
GeneBRCA2
Chromosome13
Position32911328
iGeno Mag Summary
(D;I) 5 likely to be a BRCA2 pathogenic variant but see discussion
(I;I) 0 normal

Due to 23andMe's secrecy policy about what exactly is being assayed at the location they call i5009188, it is not possible to be sure whether this is a pathogenic (or benign) BRCA2 gene mutation.

The best guess is that this SNP is equivalent to rs80359358, but it could also be rs80359356 or rs80359357, all three of which are considered pathogenic for breast cancer in ClinVar. It could also be something else entirely; only 23andMe knows.

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.