Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,580 positions on this site are linked to Celiac Disease, out of 109,292 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

NR4A3 · rs551948134

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Standard

GLIPR1 protein levels

near TFDP1P1 · rs551282675

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Standard

Alkaline phosphatase (UKB data field 30610)

DCDC2 · rs551242721

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Standard

GLIPR1 protein levels

BTBD9 · rs551188543

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Standard

GLIPR1 protein levels

near MIR4472-1 · rs551103340

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Standard

PDGFRB protein levels

CDX1 · rs550378547

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Standard

Haematocrit percentage (UKB data field 30030)

ALDH1A2 · rs550028412

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Standard

FCRL5 protein levels

CD5L · rs548321309

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Standard

F13B protein levels

CFHR5 · rs546653826

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Standard

Mean corpuscular haemoglobin (UKB data field 30050)

near SOCAR · rs545147184

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Standard

CD177 protein levels

ZNF180 · rs544300143

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Standard

GLIPR1 protein levels

near DTL · rs544053754

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IL17RB protein levels

SFMBT1 · rs544027378

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Standard

GLIPR1 protein levels

near Y_RNA · rs542495534

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Standard

HSBP1 protein levels

CDH13 · rs541852631

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Standard

GLIPR1 protein levels

near PON2 · rs540323102

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Standard

PSG1 protein levels

LIPE-AS1 · rs539721608

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Standard

Glycated haemoglobin HbA1c levels (UKB data field 30750)

TET1 · rs539453406

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

FAR2 · rs538778348

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Standard

GLIPR1 protein levels

LINC02096 · rs537810812

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Showing 20 of 20580 · page 14 of 1029

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.