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 115,632 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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HDDC2 protein levels

TPD52L1 · rs192152681

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GLIPR1 protein levels

near PHACTR3 · rs191865793

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Glycated haemoglobin HbA1c levels (UKB data field 30750)

UBR1 · rs191443517

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Urate levels (UKB data field 30880)

near SNRPCP13 · rs191114068

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SCARA5 protein levels

SCARA5 · rs191109927

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TREM2 protein levels

SLC15A3 · rs190806225

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PROC protein levels

NDRG3 · rs190616557

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BCHE protein levels

near MTND4P17 · rs190570315

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FCRL3 protein levels

near ETV3 · rs189872396

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SIRPA protein levels

near CKAP2LP1 · rs189684092

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VSIR protein levels

VSIR · rs188863463

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VSIG10 protein levels

SUDS3 · rs188460397

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KAZALD1 protein levels

TLX1NB · rs188436053

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TF protein levels

RAB6B · rs188321313

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AGT protein levels

near LINC01737 · rs188110834

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CRTAP protein levels

CARD11 · rs1878808

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GLIPR1 protein levels

CACNA1I · rs187589115

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WFIKKN2 protein levels

ACSF2 · rs187506037

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GLIPR1 protein levels

SMURF1 · rs187368374

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PNLIPRP1 protein levels

PNLIPRP1 · rs186836921

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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.