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 112,775 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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Total protein levels (UKB data field 30860)

BCL2 · rs4940573

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CCL21 protein levels

NPHP3-ACAD11 · rs200046908

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DSG3 protein levels

B4GALNT3 · rs36078145

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LILRA6 protein levels

RPS9 · rs118183313

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KLK1 protein levels

CYTH2 · rs117877056

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CD209 protein levels

CLEC4M · rs67057658

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Haematocrit percentage (UKB data field 30030)

MPP2 · rs552316287

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IL17RB protein levels

SLCO1B1 · rs17329885

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CGREF1 protein levels

near SLC5A6 · rs77585907

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SIGLEC9 protein levels

CPOX · rs75010511

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PDGFA protein levels

SLC24A3 · rs6112304

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B4GALT1 protein levels

ZNF649 · rs3859454

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DRAXIN protein levels

MIR4432HG · rs76529516

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MCTS1 protein levels

RPL32P1 · rs3097671

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FAM3D protein levels

MED22 · rs141908130

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Standing height (UKB data field 50)

near WNT4 · rs72865212

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FGFBP1 protein levels

near HPRT1P1 · rs4364259

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Mean corpuscular volume (UKB data field 30040)

PLS1 · rs73230507

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TFRC protein levels

RNF168 · rs9837291

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Standing height (UKB data field 50)

near EXOSC9 · rs3828485

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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.