Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,580 positions on this site are linked to Celiac Disease, out of 109,292 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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Standard

Monocyte percentage (UKB data field 30190)

IRF8 · rs537343928

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Standard

MATN2 protein levels

MATN2 · rs536274639

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Standard

AHSG protein levels

DNAJB11 · rs535800631

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Standard

CPA2 protein levels

ZC3HC1 · rs535754752

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Standard

Platelet crit (UKB data field 30090)

WIPF2 · rs534576060

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Standard

HGFAC protein levels

ADD1 · rs533007714

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Standard

GLIPR1 protein levels

FHIT · rs531245799

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Standard

CLEC4C protein levels

near CD163 · rs530859990

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Standard

PM20D1 protein levels

CDK18 · rs529164454

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Standard

GLIPR1 protein levels

near CYCSP30 · rs528984303

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Standard

FRZB protein levels

near DNAJC10 · rs528385365

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Standard

Gamma glutamyltransferase levels (UKB data field 30730)

ADORA2A-AS1 · rs528130589

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Standard

GLIPR1 protein levels

ZFPM2 · rs527508621

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Standard

Whole body water mass (UKB data field 23102)

OPRM1 · rs514980

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Standard

CELSR2 protein levels

FNDC7 · rs4970744

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Standard

IDI2 protein levels

ADARB2 · rs4880785

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

PACS1 · rs484983

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Standard

CPXM1 protein levels

TMC2 · rs4815323

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Standard

Lymphocyte count (UKB data field 30120)

RBBP8-AS1 · rs4800137

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Standard

VCPKMT protein levels

DMAC2L · rs4548791

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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.