Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,582 positions on this site are linked to Celiac Disease, out of 111,939 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

GLIPR1 protein levels

CNGB1 · rs754969083

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Standard

CEACAM16 protein levels

CEACAM16-AS1 · rs74853593

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Standard

PON1 protein levels

PEG10 · rs748059231

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Standard

PLAUR protein levels

ADK · rs74656412

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Standard

IL27 protein levels

ERLIN1 · rs746231265

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Standard

GLIPR1 protein levels

near PPARGC1A · rs745479389

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Standard

ICAM4 protein levels

near PAFAH2 · rs74467743

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Standard

Weight (UKB data field 21002)

near RBMS3 · rs7426945

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Standard

Red blood cell erythrocyte count (UKB data field 30010)

TAF4B · rs72880146

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Standard

Alkaline phosphatase (UKB data field 30610)

MRS2 · rs72833061

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Standard

UMOD protein levels

GP2 · rs72776650

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

DSTYK · rs72741195

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Standard

CCL4 protein levels

near RPL17P16 · rs67536946

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Standard

PSAPL1 protein levels

near SCNN1G · rs62031940

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Standard

AAMDC protein levels

near TENM4 · rs60245057

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Standard

KIR3DL1 protein levels

near NCR1 · rs587712555

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Standard

ECM1 protein levels

RPRD2 · rs587594426

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Standard

GLIPR1 protein levels

RPS6KA2 · rs575009066

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Standard

GLIPR1 protein levels

near LINC02483 · rs573651169

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Standard

GLIPR1 protein levels

DENND1B · rs573448885

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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.