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 117,438 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

SPINK4 protein levels

SPINK4 · rs138047894

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Standard

WFDC12 protein levels

SEMG2 · rs138018319

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Standard

Alkaline phosphatase (UKB data field 30610)

near CLDN23 · rs13274856

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Standard

FEV1 FVC ratio Z score (UKB data field 20258)

ROS1 · rs1321815

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Standard

CD83 protein levels

near LINC01108 · rs13216588

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Standard

ROBO1 protein levels

ADAM17 · rs13019008

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Standard

Red blood cell erythrocyte count (UKB data field 30010)

BCL11B · rs12895055

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Standard

CD99L2 protein levels

near MIR4299 · rs12798718

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Standard

PRCP protein levels

SCARB2 · rs12640185

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Standard

LAMP1 protein levels

near ADPRHL1 · rs12583834

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

near DAZAP2 · rs12579227

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Standard

KLRK1 protein levels

near KLRC1 · rs12370050

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IL15 protein levels

JAK1 · rs12031995

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Standard

APRT protein levels

GALNS · rs118019723

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Standard

FOLR3 protein levels

near RN7SKP297 · rs117970241

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Standard

MMP10 protein levels

PDGFD · rs117884485

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Standard

GYS1 protein levels

PINX1 · rs117786147

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Standard

CPA2 protein levels

NACC2 · rs117711787

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Standard

Platelet distribution width (UKB data field 30110)

LFNG · rs11770785

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Standard

Total bilirubin levels (UKB data field 30840)

LINC02889 · rs11768350

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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.