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 112,985 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

CKMT1A or CKMT1B protein levels

TMPRSS11E · rs34638591

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Standard

LRPAP1 protein levels

TRIM38 · rs182712233

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Standard

VCAM1 protein levels

near VCAM1 · rs12732056

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Standard

SIGLEC8 protein levels

LINC01564 · rs12662589

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Sensitive

Coeliac disease

near HLA-DOA · rs9276964

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Standard

SEPTIN3 protein levels

DERL3 · rs3177243

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Standard

DPP4 protein levels

near GNS · rs2682725

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Standard

AMY1A or AMY1B or AMY1C protein levels

near AMY1C · rs189709501

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Standard

SCG3 protein levels

FOXP1 · rs6798507

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Standard

CCL25 protein levels

near RNU6-317P · rs144762712

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Standard

Forced vital capacity FVC Z score (UKB data field 20257)

HTRA1 · rs80232578

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Standard

CD300E protein levels

near HLA-DRB1 · rs3998182

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Standard

ASAH2 protein levels

LINC00536 · rs12056768

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Standard

IL15RA protein levels

LINC01149 · rs9267092

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Standard

CXCL6 protein levels

near CXCL1 · rs1398015

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Standard

FCGR3B protein levels

GSEC · rs77235311

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Standard

CD164 protein levels

CCDC162P · rs9386774

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Standard

F11 protein levels

F11 · rs186377697

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Standard

CD300C protein levels

ATP2B1-AS1 · rs17192565

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Standard

Immature reticulocyte fraction (UKB data field 30280)

NCOA4 · rs75901817

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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.