rs574552037
A SNP in the BRIP1 gene on chromosome 17. Its most notable genotype is C;G: Increased cancer risk; ovarian cancer & related
- Gene
- BRIP1
- Location
- Chr 1761,716,043 (GRCh38)
- Highest magnitude
- 6.0Very important
- Tested on
- 23andMe, AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;GMost notableBadIncreased cancer risk; ovarian cancer & related
- G;GGoodcommon in clinvar
On SNPedia: (C;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other BRIP1 SNPs
- rs137852986A;GIncreased cancer risk; ovarian cancer & relatedVery important
- rs149364097C;GOvarian cancer susceptibilityVery important
- rs368796923A;GIncreased cancer risk; ovarian cancer & relatedVery important
- rs575595017A;GIncreased cancer risk; ovarian cancer & relatedVery important
- rs587778134-;TTOvarian cancer susceptibilityVery important
- rs587780226A;GOvarian cancer susceptibilityVery important
- rs587780228A;CIncreased cancer risk; ovarian cancer & relatedVery important
- rs587780236-;AIncreased cancer risk; ovarian cancer & relatedVery important
Notes
From SNPedia
Notes
aka c.2400C>G (p.Tyr800Ter or Y800X), and also c.2400C>T (p.Tyr800=); the former is considered in ClinVar to be pathogenic for ovarian cancer, while the latter is benign
Source and license
Adapted from rs574552037 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.