Variants linked to Ovarian Cancer

Continuously updated · newest added Oct 22, 2026

28 positions on this site are linked to Ovarian Cancer, out of 108,020 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Sensitive

Invasive epithelial ovarian cancer

PLEKHM1 · rs1879586

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Sensitive

Invasive epithelial ovarian cancer

SKAP1 · rs7207826

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Sensitive

Ovarian cancer

BRIP1 · rs34289250

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Sensitive

Basal cell carcinoma

TP53 · rs78378222

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Sensitive

Epithelial ovarian cancer

BABAM1 · rs8170

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Sensitive

Epithelial ovarian cancer

SKAP1 · rs9303542

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Sensitive

Epithelial ovarian cancer

CMYC · rs10088218

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Sensitive

Ovarian cancer

BNC2 · rs3814113

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Questions about variants on this site

What is a "variant" page on this site?

One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.