Variants linked to Celiac Disease

Continuously updated · newest added Oct 24, 2026

20,582 positions on this site are linked to Celiac Disease, out of 113,027 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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SPINK8 protein levels

near SCAP · rs137985341

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CEACAM21 protein levels

near CEACAM21 · rs137932231

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IFNGR1 protein levels

ST3GAL6 · rs13072410

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TCN1 protein levels

HSD17B14 · rs12979373

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Neutrophill percentage (UKB data field 30200)

near FCN1 · rs12554353

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Urate levels (UKB data field 30880)

CFL1 · rs12419727

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INHBB protein levels

near Y_RNA · rs118046313

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Eosinophill percentage (UKB data field 30210)

IKZF2 · rs117954874

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TCN2 protein levels

PES1 · rs117695276

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GLIPR1 protein levels

near OR1J1 · rs117627603

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PON1 protein levels

SLC25A13 · rs116865085

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ADAMTS15 protein levels

near HLA-DQA1 · rs116518618

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CD86 protein levels

CD86 · rs114921667

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CD14 protein levels

CYSTM1 · rs114901832

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Platelet count (UKB data field 30080)

VAMP4 · rs114427647

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ECM1 protein levels

RORC · rs114103746

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ADGRB3 protein levels

near SLC25A6P6 · rs113339974

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SIRPB1 protein levels

SIRPD · rs113200157

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GLIPR1 protein levels

FARS2 · rs112498364

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Neutrophill count (UKB data field 30140)

CASC3 · rs112229539

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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.