Variants linked to Prostate Cancer

Continuously updated · newest added Oct 22, 2026

408 positions on this site are linked to Prostate Cancer, out of 108,788 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

VPS53 · rs461251

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Sensitive

Prostate cancer

near COX16 · rs17565772

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Sensitive

Toxicity response to radiotherapy in prostate cancer (rectal bleeding) (time to event)

near RNU2-48P · rs17055178

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Sensitive

Prostate cancer

RFX6 · rs434499

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Sensitive

Conversion from active surveillance to active treatment in prostate cancer

near LINC01101 · rs1404610

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Sensitive

Prostate cancer

HSD17B2-AS1 · rs8052913

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Sensitive

Prostate cancer

NEDD9 · rs4713343

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Sensitive

Prostate cancer

near CDKAL1 · rs9358412

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Sensitive

Prostate cancer

RPL22 · rs4908865

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Sensitive

Prostate cancer

ACOXL-AS1 · rs2165108

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Sensitive

Prostate cancer

FERMT2 · rs12889169

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Sensitive

Toxicity response to radiotherapy in prostate cancer (decreased urine stream) (time to event)

near RPS26P2 · rs10969913

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Sensitive

Prostate cancer

CASC8 · rs9656816

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Sensitive

Prostate cancer

BNIP2 · rs6151589

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Sensitive

Prostate cancer

near MAST2 · rs544780844

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Sensitive

Prostate cancer

CASC19 · rs16902043

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Sensitive

Prostate cancer

STK39 · rs11892008

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Sensitive

Prostate cancer

ZMIZ1-AS1 · rs11002805

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Sensitive

Prostate cancer

near C6orf15 · rs9263523

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Sensitive

Prostate cancer

MEX3D · rs202204141

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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.