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

Colorectal cancer

PCNT · rs9983528

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Sensitive

Colorectal cancer (age of onset)

ZSCAN16-AS1 · rs138234416

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Sensitive

Colorectal cancer

near RNY1P8 · rs78341008

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Sensitive

Colorectal cancer

LINC02474 · rs12025420

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Sensitive

Colorectal cancer

near RNA5SP299 · rs9733843

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Sensitive

Colorectal cancer

PGAM1P5 · rs11108175

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Sensitive

Colorectal cancer

EIF3H · rs75128197

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Sensitive

Colorectal cancer

RHPN2 · rs73039433

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Sensitive

Colorectal cancer

GREM1-AS1 · rs1919364

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Sensitive

Colorectal cancer

near SLC25A28 · rs35564340

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Sensitive

Colorectal cancer

XRRA1 · rs117042741

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Sensitive

Colorectal cancer

CCND2-AS1 · rs12822620

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Sensitive

Colorectal cancer

near CASC20 · rs6117251

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Sensitive

Colorectal cancer

near CASC20 · rs961253

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Sensitive

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

ATOH8 · rs13402783

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Sensitive

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

SCFD2 · rs17082301

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Sensitive

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

near CECR2 · rs5749032

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Sensitive

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

BBS9 · rs3815652

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Sensitive

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

PIK3AP1 · rs1023741

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Sensitive

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

BRINP3 · rs10920654

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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.