Variants linked to Inflammatory Bowel Disease

Continuously updated · newest added Oct 24, 2026

57 positions on this site are linked to Inflammatory Bowel Disease, out of 113,657 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 Inflammatory Bowel Disease

Sensitive

Inflammatory bowel disease

CPEB4 · rs72810983

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Sensitive

Inflammatory bowel disease

near TTC33 · rs1505992

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Sensitive

Inflammatory bowel disease

GSDMB · rs12946510

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Sensitive

Inflammatory bowel disease

FLJ20306 · rs11768365

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Sensitive

Inflammatory bowel disease

METTL10 · rs111456533

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Sensitive

Inflammatory bowel disease

CUL1 · rs243505

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Sensitive

Inflammatory bowel disease

IMPG2 · rs503734

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Sensitive

Inflammatory bowel disease

ITGB8 · rs149169037

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Sensitive

Inflammatory bowel disease

ITGA4 · rs6740847

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Sensitive

Inflammatory bowel disease

FOXP1 · rs2593855

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Sensitive

Inflammatory bowel disease

PLCG2 · rs11548656

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Sensitive

Thiopurine-induced leukopenia in inflammatory bowel disease

FTO · rs79206939

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Sensitive

Inflammatory bowel disease

PMVK · rs3766920

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Sensitive

Inflammatory bowel disease

BTBD8 · rs34856868

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Sensitive

Inflammatory bowel disease

YDJC · rs2266959

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Sensitive

Inflammatory bowel disease

MAP3K8 · rs1042058

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Sensitive

Inflammatory bowel disease

PHACTR2 · rs12199775

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Sensitive

Inflammatory bowel disease

BACH2 · rs1847472

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Sensitive

Response to thiopurine immunosuppressants in inflammatory bowel disease (pancreatitis) (azathioprine and mercaptopurine)

HLA region · rs6935723

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Sensitive

Inflammatory bowel disease

near ZBTB40 · rs12568930

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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.