Variants linked to Colorectal Cancer

Continuously updated · newest added Oct 22, 2026

239 positions on this site are linked to Colorectal Cancer, out of 108,284 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

near LINC01228 · rs61336918

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Sensitive

Colorectal cancer

near FMN1 · rs57284764

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Sensitive

Colorectal cancer

near RNU6-996P · rs10978941

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Sensitive

Colorectal cancer

ANO1 · rs10751097

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Sensitive

Colorectal cancer

RHPN2 · rs6510329

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Sensitive

Colorectal cancer

TMPRSS12 · rs1961622

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Sensitive

Colorectal cancer

near EPS15P1 · rs4236382

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Sensitive

Colorectal cancer

near PLCL1 · rs6434979

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Sensitive

Colorectal cancer (age of onset)

near ZKSCAN8P1 · rs13197175

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Sensitive

Colorectal cancer

ARHGAP11A-SCG5 · rs7494781

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Sensitive

TGF-beta 2 levels in metastatic colorectal cancer

LINC02869 · rs11118119

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Sensitive

Colorectal cancer

near UBA52P7 · rs12822984

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Sensitive

Colorectal cancer

DIP2B · rs11169484

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Sensitive

CD73 levels in metastatic colorectal cancer

NT5E · rs2229523

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Sensitive

Colorectal cancer

POU5F1B · rs1562871

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Sensitive

Colorectal cancer

PNKD · rs7557709

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Sensitive

Colorectal cancer

LAMC1 · rs34099011

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Sensitive

Colorectal cancer

near CTIF · rs4939824

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Sensitive

Colorectal cancer

near SLC6A18 · rs4583925

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Sensitive

Colorectal cancer

near RNU7-147P · rs4675253

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Showing 20 of 239 · page 4 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.