Variants linked to Prostate Cancer

Continuously updated · newest added Oct 22, 2026

408 positions on this site are linked to Prostate Cancer, out of 108,620 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

DLEU1 · rs1327653

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Sensitive

Prostate cancer

SEPTIN2 · rs116154780

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Sensitive

Prostate cancer

NUF2 · rs6660538

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Sensitive

Prostate cancer

POU2F2 · rs61088131

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Sensitive

Prostate cancer

MRPS6 · rs10154043

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Sensitive

Prostate cancer

MYO9B · rs11666569

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Sensitive

Prostate cancer

near INHBB · rs10204633

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Sensitive

Prostate cancer

LINC01798 · rs62145819

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Sensitive

Prostate cancer

AC011747.3 · rs62106670

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Sensitive

Prostate cancer

FGD1 · rs4826594

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Sensitive

Prostate cancer

ACADSB · rs12263012

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Sensitive

Prostate cancer

near CHORDC1P1 · rs6738169

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Sensitive

Prostate cancer

ASB1 · rs473651

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Sensitive

Prostate cancer

PCAT1 · rs114705582

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Sensitive

Prostate cancer

near SMIM38 · rs4620729

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Sensitive

Prostate cancer

STK39 · rs16854905

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Sensitive

Prostate cancer

MECOM · rs142436749

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Sensitive

Prostate cancer

INTS4 · rs12796422

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Sensitive

Prostate cancer

near RPS3A · rs77063077

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Sensitive

Prostate cancer

SH3D19 · rs147762399

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Showing 20 of 408 · page 1 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.