rs786202434
A SNP in the RAD51D gene on chromosome 17. Its most notable genotype is -;A: Ovarian cancer susceptibility
- Gene
- RAD51D
- Location
- Chr 1735,107,380 (GRCh38)
- Highest magnitude
- 6.0Very important
- Tested on
- 23andMe, AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- -;-Goodcommon in clinvar
- -;AMost notableBadOvarian cancer susceptibility
SNPedia records rs786202434 on the minus strand: (-;-), (-;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other RAD51D SNPs
- rs200564819A;GOvarian cancer susceptibilityVery important
- rs374357106G;TOvarian cancer susceptibilityVery important
- rs587780104A;GOvarian cancer susceptibilityVery important
- rs587780105-;GOvarian cancer susceptibilityVery important
- rs587781527GGAGGTC;TGAGGTTOvarian cancer susceptibilityVery important
- rs587782695A;GOvarian cancer susceptibilityVery important
- rs587782736-;AAOvarian cancer susceptibilityVery important
- rs730881943-;TAOvarian cancer susceptibilityVery important
Source and license
Adapted from rs786202434 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.