Variants linked to Colorectal Cancer

Continuously updated · newest added Oct 22, 2026

239 positions on this site are linked to Colorectal Cancer, out of 108,452 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

Metastasis in stage I-III microsatellite instability low/stable colorectal cancer (time to event)

ASTN2 · rs1372330

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Sensitive

Metastasis in stage I-III microsatellite instability low/stable colorectal cancer (time to event)

near KIF16B · rs2327990

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Sensitive

Metastasis in stage I-III microsatellite instability low/stable colorectal cancer (time to event)

near SP9 · rs7582977

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Sensitive

Metastasis in stage I-III microsatellite instability low/stable colorectal cancer (time to event)

near CMPK2 · rs11692570

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Sensitive

Progression free survival in metastatic colorectal cancer (chemotherapy interaction)

GnT-IVa · rs885036

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Sensitive

Colorectal cancer or advanced adenoma

A1CF · rs10821907

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Sensitive

Colorectal cancer

NOTCH4 · rs3830041

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Sensitive

Colorectal cancer

near SLC25A28 · rs2193352

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Sensitive

Distal/Left-sided colorectal cancer

BMP7 · rs6014965

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Sensitive

Colorectal cancer

GATA3 · rs10795668

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Sensitive

Colorectal cancer or advanced adenoma

DUSP10 · rs17011141

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Sensitive

Colorectal cancer

POLD3 · rs57796856

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Sensitive

Colorectal cancer x fine particulate matter exposure levels interaction

HDAC9 · rs6950598

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Sensitive

Colorectal cancer or advanced adenoma

EIF3H · rs6469654

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Sensitive

Colorectal cancer

FHL3 · rs61776719

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Sensitive

Colorectal cancer or advanced adenoma

PITX1 · rs4976270

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Sensitive

Colorectal cancer

PLCB1 · rs2423279

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Sensitive

Colorectal cancer

BMP5 · rs62404966

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Sensitive

Colorectal cancer or advanced adenoma

LRP1 · rs4759277

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Sensitive

Colorectal cancer

RPS21 · rs6061231

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Showing 20 of 239 · page 7 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.