Variants linked to Colorectal Cancer

Continuously updated · newest added Oct 22, 2026

240 positions on this site are linked to Colorectal 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 Colorectal Cancer

Sensitive

Colorectal cancer

RPS21 · rs6061231

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Sensitive

Colorectal cancer

SLC25A26 · rs812481

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Sensitive

Colorectal cancer

SLC25A28 · rs1035209

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Sensitive

Colorectal cancer

near DUSP10 · rs6691195

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Sensitive

Colorectal cancer or advanced adenoma

SMAD9 · rs7333607

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Sensitive

Cancer (pleiotropy)

FRY · rs56084662

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Sensitive

Colorectal cancer

near ATF1 · rs11169572

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Sensitive

Colorectal cancer

POU2AF3 · rs3802842

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Sensitive

Distal/Left-sided colorectal cancer

STK11 · rs62131228

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Sensitive

Colorectal cancer

ENTPD7 · rs11190164

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Sensitive

Colorectal cancer

LAMA5 · rs2427308

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Sensitive

Colorectal cancer

FKBP5 · rs16878812

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Sensitive

Colorectal cancer

DENND5B · rs77969132

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Sensitive

Colorectal cancer

LAMC1 · rs10911251

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Sensitive

Colorectal cancer

near PLEKHG6 · rs10849438

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Sensitive

Colorectal cancer or advanced adenoma

LINC00603 · rs12514517

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Sensitive

Colorectal cancer or advanced adenoma

BMP4 · rs4901473

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Sensitive

Colorectal cancer

NXN · rs73975588

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Sensitive

Colorectal cancer

GPATCH1 · rs7252505

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Sensitive

Colorectal cancer or advanced adenoma

MZF1 · rs73068325

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Showing 20 of 240 · page 8 of 12

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.