rs80359306

A SNP in the BRCA2 gene on chromosome 13. Its most notable genotype is -;A: BRCA2 variant considered pathogenic for breast cancer

Gene
BRCA2
Location
Chr 1332,333,284 (GRCh38)
Highest magnitude
6.0Very important
Tested on
23andMe

Genotypes

As shown in 23andMe and AncestryDNA files.

On SNPedia: (-;-), (-;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Conditions, medicines and genes

Notes

From SNPedia

Notes

rs80359306, also known as c.1813dupA, 2034insA, c.1806_1807insA and p.Gly602_Lys603?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar. dbSNP has merged rs80359307 into this SNP, rs80359306, so it may now also represent c.1813delA, which is also pathogenic in ClinVar for breast cancer.

-;A

See text and links via main rs-page. Note: if the raw data is "DI" for this SNP, due to ambiguity it could either represent c.1813dupA or c.1813delA.

Source and license

Adapted from rs80359306 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.