Variants linked to Prostate Cancer

Continuously updated · newest added Oct 23, 2026

412 positions on this site are linked to Prostate Cancer, out of 108,956 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

Prostate cancer

near WDR11 · rs10886810

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Sensitive

Prostate cancer

NTN1 · rs12449664

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Sensitive

Prostate cancer

FRG1-DT · rs113668862

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Sensitive

Prostate cancer

near B4GALNT2 · rs370406642

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Sensitive

Prostate cancer

near RPL24P7 · rs7618603

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Sensitive

Prostate cancer

near EEF1GP7 · rs11581903

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Sensitive

Prostate cancer

MYO9B · rs10412482

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Sensitive

Prostate cancer

near UNCX · rs75701624

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Sensitive

Prostate cancer

near Y_RNA · rs528765618

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Sensitive

Prostate cancer

LINC01162 · rs2709729

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Sensitive

Prostate cancer

SIDT1 · rs9827928

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Sensitive

Prostate cancer

ARMC2 · rs2038542

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Sensitive

Prostate cancer

near RNU4-10P · rs61390061

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Sensitive

Prostate cancer

LOC340602 · rs5945572

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Sensitive

Prostate cancer

NEDD9 · rs2018336

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Sensitive

Prostate cancer

OSBPL7 · rs142847236

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Sensitive

Prostate cancer

SLC39A1 · rs12027783

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Sensitive

Prostate cancer

AKR1C3 · rs61856137

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Sensitive

Prostate cancer

PCAT1 · rs6983515

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Sensitive

Prostate cancer

AATK · rs11871062

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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.