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

Cancer (pleiotropy)

near MXRA8 · rs186507655

See detailed info →
Sensitive

Colorectal cancer

near DUSP10 · rs6658977

See detailed info →
Sensitive

Colorectal cancer or advanced adenoma

DACT1 · rs8020436

See detailed info →
Sensitive

Colorectal cancer or advanced adenoma

SF3A3 · rs4360494

See detailed info →
Sensitive

Colorectal cancer

RHPN2 · rs73039434

See detailed info →
Sensitive

Colorectal cancer

SMAD6 · rs4776316

See detailed info →
Sensitive

Proximal colorectal cancer

RIN3 · rs61975764

See detailed info →
Sensitive

Colorectal cancer

DIP2B · rs34245511

See detailed info →
Sensitive

Colorectal cancer

NABP1 · rs11903757

See detailed info →
Sensitive

Colorectal cancer

near CCND2 · rs4572213

See detailed info →
Sensitive

Colorectal cancer

MAMSTR · rs12979278

See detailed info →
Sensitive

Distal/Left-sided colorectal cancer

KLF14 · rs73161913

See detailed info →
Sensitive

Colorectal cancer

AS1 · rs704017

See detailed info →
Sensitive

Colorectal cancer

NOS1 · rs73208120

See detailed info →
Sensitive

Colorectal cancer

near BMP2 · rs6085661

See detailed info →
Sensitive

Colorectal cancer

RTEL1-TNFRSF6B · rs3787089

See detailed info →
Sensitive

Proximal colorectal cancer

BCL11B · rs80158569

See detailed info →
Sensitive

Colorectal cancer

SLCO2A1 · rs113569514

See detailed info →
Sensitive

Colorectal cancer or advanced adenoma

EIF3H · rs117079142

See detailed info →
Sensitive

Colorectal cancer or advanced adenoma

HAO1 · rs11087784

See detailed info →

Showing 20 of 239 · page 11 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.