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 103,022 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Sensitive

Crohn's disease

LGALS9 · rs2945412

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Sensitive

Crohn's disease

FADS1 · rs102275

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Sensitive

Crohn's disease

ATG16L1 · rs2241880

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Sensitive

Crohn's disease

ZFP36L1 · rs4902642

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Sensitive

Crohn's disease

ICOSLG · rs762421

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Sensitive

Crohn's disease

C11orf30 · rs7927997

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Sensitive

Crohn's disease

near TNFSF18 · rs9286879

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Sensitive

Crohn's disease

STARD10 · rs11235667

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Sensitive

Crohn's disease

ADAM30 · rs3897478

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Sensitive

Crohn's disease

CD27 · rs7954567

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Sensitive

Crohn's disease

MST1 · rs9858542

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Sensitive

Crohn's disease

NDFIP1 · rs6863411

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Sensitive

Crohn's disease

HLA-B · rs114985235

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Sensitive

Crohn's disease

near THEMIS · rs13204742

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Sensitive

Crohn's disease

IRGM · rs11747270

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Sensitive

Crohn's disease

MUC19 · rs11175593

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Sensitive

Crohn's disease

THADA · rs10495903

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Sensitive

Crohn's disease

PTGER4 · rs4613763

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Sensitive

Crohn's disease

MAP3K7IP1 · rs2413583

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Sensitive

Crohn's disease

MUC19 · rs11564258

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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.