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 113,783 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 (Tractor method with African ancestry)

near SEC61GP1 · rs571678895

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Sensitive

Bipolar disorder or inflammatory bowel disease (MTAG)

INAVA · rs12132298

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Sensitive

Inflammatory bowel disease

near DLD · rs6961243

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Sensitive

Inflammatory bowel disease

LINC00598 · rs17061048

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Sensitive

Inflammatory bowel disease

GATD3 · rs59998884

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Sensitive

Inflammatory bowel disease

near C6orf15 · rs1265061

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Sensitive

Extraintestinal manifestations in inflammatory bowel disease (primary sclerosing cholangitis)

near HLA-DQA2 · rs9276456

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Sensitive

Inflammatory bowel disease (Tractor method with European ancestry)

HLA-DMB · rs188746689

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Sensitive

Inflammatory bowel disease

IFNG-AS1 · rs35788599

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Sensitive

Bipolar disorder or inflammatory bowel disease (MTAG)

STIMATE-MUSTN1 · rs7612624

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Sensitive

Bipolar disorder or inflammatory bowel disease (MTAG)

LINC00243 · rs1264372

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Sensitive

Inflammatory bowel disease

near MIR4679-2 · rs73370726

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Sensitive

Colorectal cancer vs inflammatory bowel disease

near ATP8B4 · rs541295

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Sensitive

Bipolar disorder or inflammatory bowel disease (MTAG)

NDUFAF7 · rs11679617

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Sensitive

Bipolar disorder or inflammatory bowel disease (MTAG)

ALOX5AP · rs9671125

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Sensitive

Inflammatory bowel disease

near C6orf15 · rs11754821

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Sensitive

Inflammatory bowel disease

BTNL2 · rs2395158

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Sensitive

Inflammatory bowel disease (Tractor method with European ancestry)

near HLA-DRA · rs115406035

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Sensitive

Inflammatory bowel disease

near CYCSP42 · rs2823286

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Sensitive

Inflammatory bowel disease

IL18RAP · rs6708413

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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.