Variants linked to Celiac Disease

Continuously updated · newest added Oct 25, 2026

20,582 positions on this site are linked to Celiac Disease, out of 118,864 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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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

SLC45A4 · rs34650936

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Standard

Eosinophill percentage (UKB data field 30210)

ATG5 · rs34599047

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Standard

Whole body water mass (UKB data field 23102)

near ZNF619P1 · rs34013557

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Standard

CA14 protein levels

PRKAG3 · rs33985460

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Standard

CCN5 protein levels

KCNK15-AS1 · rs33932543

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Standard

CRYBB2 protein levels

NOTCH2 · rs327189

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Standard

Platelet count (UKB data field 30080)

near HLA-DQB2 · rs28986344

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Standard

HYAL1 protein levels

near PRSS44P · rs28800005

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Standard

CANT1 protein levels

B4GALT1 · rs2770808

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Standard

ASGR2 protein levels

ASB3 · rs2542572

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Standard

NCAN protein levels

MICA-AS1 · rs2523469

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Standard

PROC protein levels

near HLA-G · rs2517896

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Standard

C1QTNF1 protein levels

C1QTNF1-AS1 · rs2377006

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Standard

CPA4 protein levels

MEFV · rs224222

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Standard

SERPINA11 protein levels

SERPINA9 · rs201966528

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Standard

COMT protein levels

TXNRD2 · rs192748697

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Standard

IL7R protein levels

IL7R · rs192345351

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Standard

LTA protein levels

SLC17A2 · rs191749731

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Standard

PENK protein levels

near RPL37P6 · rs191735561

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Standard

TOR1AIP1 protein levels

TOR1AIP2 · rs191353556

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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.