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 113,657 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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FCRL5 protein levels

FCRL5 · rs181977070

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GLIPR1 protein levels

LINC00589 · rs181756741

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DDT protein levels

near KLHL5P1 · rs17004186

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Mean corpuscular haemoglobin (UKB data field 30050)

near H2AC2P · rs16890978

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FCRL1 protein levels

FHL1P1 · rs16854644

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CRISP3 protein levels

FEZ2 · rs1544655

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Urate levels (UKB data field 30880)

ABCG2 · rs151297142

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IL12B protein levels

UBLCP1 · rs150942885

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NPTX2 protein levels

ATN1 · rs150902512

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NRP1 protein levels

near PBX4 · rs150824230

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GSTP1 protein levels

near CDK2AP2 · rs150686494

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PEPD protein levels

near PEPD · rs150575334

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AHSG protein levels

CRYGS · rs150441905

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Direct low density lipoprotein levels (UKB data field 30780)

CCDC93 · rs150097723

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CLGN protein levels

near SCOC · rs149966091

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HLA A protein levels

LINC01149 · rs149945939

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SPARCL1 protein levels

AFF1 · rs149580678

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PLXDC1 protein levels

FBXO47 · rs149385639

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Alkaline phosphatase (UKB data field 30610)

ABO · rs148987354

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PON2 protein levels

PPP1R9A-AS1 · rs148089191

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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.