Variants linked to Prostate Cancer

Continuously updated · newest added Oct 23, 2026

416 positions on this site are linked to Prostate Cancer, out of 109,712 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Prostate Cancer

Sensitive

Prostate cancer

near SALL3 · rs9959454

See detailed info →
Sensitive

Prostate cancer

INHBB · rs11900747

See detailed info →
Sensitive

Prostate cancer

ADAM15 · rs146564277

See detailed info →
Sensitive

Prostate cancer

MYO9B · rs10421727

See detailed info →
Sensitive

Prostate cancer

SUGCT · rs12701832

See detailed info →
Sensitive

Prostate cancer

TEX11 · rs13441059

See detailed info →
Sensitive

Prostate cancer

EEFSEC · rs149272765

See detailed info →
Sensitive

Prostate cancer

GMEB2 · rs381331

See detailed info →
Sensitive

Prostate cancer

CTD-2194D22.4 · rs13177600

See detailed info →
Sensitive

Prostate cancer

GATA2-AS1 · rs4857898

See detailed info →
Sensitive

Prostate cancer

near RPL19P16 · rs4558107

See detailed info →
Sensitive

Prostate cancer

LINC00506 · rs77171792

See detailed info →
Sensitive

Prostate cancer

near LINC01509 · rs12156453

See detailed info →
Sensitive

Prostate cancer

PCAT1 · rs201495744

See detailed info →
Sensitive

Prostate cancer

KRT8 · rs4919743

See detailed info →
Sensitive

Prostate cancer

LINC00506 · rs77464751

See detailed info →
Sensitive

Cancer of prostate (PheCode 185)

FOXP4 · rs4714482

See detailed info →
Sensitive

Prostate cancer

FOXP4 · rs4714485

See detailed info →
Sensitive

Prostate cancer

ANO7 · rs76832527

See detailed info →
Sensitive

Prostate cancer

near SMIM38 · rs12275055

See detailed info →

Showing 20 of 416 · page 15 of 21

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.