rs80358920

A SNP in the BRCA2 gene on chromosome 13. Its most notable genotype is C;T: Possible miscall in data from Ancestry v2c chip; otherwise, BRCA2 variant considered pathogenic for breast cancer

Gene
BRCA2
Location
Chr 1332,346,841 (GRCh38)
Highest magnitude
6.0Very important
Tested on
AncestryDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

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

Conditions, medicines and genes

Notes

From SNPedia

Notes

rs80358920, also known as R2318X, c.6952C>T and p.Arg2318Ter, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar. On their v4 chip, 23andMe called this i5009344, and it was prone to being a false positive (miscall).

C;T

See details at rs80358920.

Source and license

Adapted from rs80358920 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.