rs80356847(A;C)
Likely to be a BRCA1 pathogenic mutation, but uncertainty remains
- Magnitude
- 6.0Very important
- Repute
- Bad
- On SNPedia
- rs80356847(G;T)Minus strand
- Gene
- BRCA1
Other genotypes of rs80356847
Notes
From SNPedia
See text; most sources indicate this is likely to be pathogenic BRCA1 mutation, but as the main rs-page discusses, in ClinVar it is currently annotated as either a variant of uncertain significance or as likely benign.
Source and license
Adapted from rs80356847(G;T) on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.