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 113,699 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

SIGLEC6 protein levels

TRIM40 · rs757260

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FCAMR protein levels

SLC2A2 · rs61791106

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Mean sphered cell volume (UKB data field 30270)

TFEB · rs561111743

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SMPDL3A protein levels

near CHPT1 · rs150043343

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Haemoglobin concentration (UKB data field 30020)

near ATP2A2 · rs10774599

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CDH5 protein levels

near FAM163B · rs11791358

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Mean corpuscular volume (UKB data field 30040)

near PDGFRA · rs542853222

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GSTA3 protein levels

HEPHL1 · rs4408267

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SCARB2 protein levels

SMPDL3A · rs13192569

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SMPDL3A protein levels

CHPT1 · rs147240250

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Impedance of whole body (UKB data field 23106)

ADAMTSL3 · rs9989259

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High light scatter reticulocyte count (UKB data field 30300)

LINC01524 · rs4431004

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Basal metabolic rate (UKB data field 23105)

HSPA5-DT · rs35843221

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CDH2 protein levels

CDH1 · rs2011779

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BTN3A2 protein levels

NLRC5 · rs154045

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MUC2 protein levels

BCAT2 · rs150454672

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Haematocrit percentage (UKB data field 30030)

SLC12A3 · rs141724276

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ABO protein levels

ABO · rs8176766

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Mean reticulocyte volume (UKB data field 30260)

CCND3 · rs577951214

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Reticulocyte count (UKB data field 30250)

ERLEC1 · rs2542589

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Showing 20 of 20582 · page 996 of 1030

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.