Variants linked to Crohn's Disease

Continuously updated · newest added Oct 21, 2026

107 positions on this site are linked to Crohn's Disease, out of 102,854 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 Crohn's Disease

Sensitive

Crohn's disease

LINC00824 · rs6651252

See detailed info →
Sensitive

Crohn's disease

near TNFSF15 · rs10817678

See detailed info →
Sensitive

Fever in mesalamine-treated irritable bowel disease

OTUD7A · rs77344822

See detailed info →
Sensitive

Poor prognosis in Crohn's disease

IGFBP1 · rs75764599

See detailed info →
Sensitive

Crohn's disease

UBE2L3 · rs2256609

See detailed info →
Sensitive

Crohn's disease

THADA · rs10495903

See detailed info →
Sensitive

Crohn's disease

TNFSF11 · rs2062305

See detailed info →
Sensitive

Crohn's disease

FUT2 · rs281379

See detailed info →
Sensitive

Crohn's disease

IL12RL2 · rs2058660

See detailed info →
Sensitive

Crohn's disease

near TRIB1 · rs1551398

See detailed info →
Sensitive

Crohn's disease

MUC19 · rs11175593

See detailed info →
Sensitive

Crohn's disease

IRGM · rs7714584

See detailed info →
Sensitive

Crohn's disease

IRGM · rs11747270

See detailed info →
Sensitive

Crohn's disease

SLCO6A1 · rs7705924

See detailed info →
Sensitive

Crohn's disease

SBNO2 · rs2024092

See detailed info →
Sensitive

Crohn's disease

near THEMIS · rs13204742

See detailed info →
Sensitive

Crohn's disease

CD27 · rs7954567

See detailed info →
Sensitive

Crohn's disease

STARD10 · rs11235667

See detailed info →
Sensitive

Crohn's disease

TBC1D1 · rs1487630

See detailed info →
Sensitive

Crohn's disease

near IRF1 · rs2188962

See detailed info →

Showing 20 of 107 · page 2 of 6

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.