Variants linked to Celiac Disease

Continuously updated · newest added Oct 26, 2026

3,108 positions on this site are linked to Celiac Disease, out of 131,364 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

Strength of the evidence: all 2+ 3+ 4

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ALCAM protein levels

ABCC6 · rs72653706

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CST3 protein levels

CST3 · rs55837531

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C8B protein levels

C8B · rs146187042

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IRAK4 protein levels

IRAK4 · rs121908002

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Neutrophill percentage (UKB data field 30200)

HLA-DQA1 · rs72848261

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TMPRSS15 protein levels

TMPRSS15 · rs77200626

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NMNAT1 protein levels

NMNAT1 · rs150726175

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SERPINC1 protein levels

SERPINC1 · rs121909551

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RNASEH2A protein levels

RNASEH2B · rs75184679

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DEFA1 or DEFA1B protein levels

MYB · rs210962

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PMM2 protein levels

PMM2 · rs28936415

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IGFBPL1 protein levels

ALDH1B1 · rs7846941

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WASF1 protein levels

SLC22A16 · rs62421680

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PDGFRB protein levels

near U3 · rs554981654

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Gamma glutamyltransferase levels (UKB data field 30730)

GGT1 · rs554233625

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KDR protein levels

near LRRC34P2 · rs548371862

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LTA protein levels

TRIM31 · rs140451451

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CFHR2 protein levels

KCNT2 · rs140074152

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PRR4 protein levels

TAS2R14 · rs117759736

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ENPP7 protein levels

near ENPP7 · rs117593594

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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.