rs587780875

A SNP in the BRIP1 gene on chromosome 17. Its most notable genotype is A;C: Increased cancer risk; ovarian cancer & related

Gene
BRIP1
Location
Chr 1761,793,687 (GRCh38)
Highest magnitude
6.0Very important
Tested on
Not on consumer chips

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. A;CMost notableBadIncreased cancer risk; ovarian cancer & relatedVery important · 6.0
  2. A;AGoodcommon in clinvarTypical · 0.0

SNPedia records rs587780875 on the minus strand: (G;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Other BRIP1 SNPs

All BRIP1 SNPs

Notes

From SNPedia

Notes

A;C

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Source and license

Adapted from rs587780875 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.