rs273899700

A SNP in the BRCA1 gene on chromosome 17. Its most notable genotype is -;AGCC: BRCA1 variant considered pathogenic for breast cancer

Gene
BRCA1
Location
Chr 1743,092,414 (GRCh38)
Highest magnitude
6.0Very important
Tested on
Not on consumer chips

Genotypes

As shown in 23andMe and AncestryDNA files.

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

Conditions, medicines and genes

Notes

From SNPedia

Notes

rs273899700, also known as 3233delAGCCinsGA, c.3114_3117delAGCCinsGA and p.Glu1038_Ala1039GluLysfs, is a variant in the BRCA1 gene considered pathogenic for breast cancer in ClinVar.

-;AGCC

Considered pathogenic in ClinVar.

AGCC;GA

see details via ClinVar sidebar/box on associated SNP/rs# page

AGCC;GA

See details at rs273899700

Source and license

Adapted from rs273899700 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.