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 113,826 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

IL4R protein levels

near KATNIP · rs75157252

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Standard

CELSR2 protein levels

WDR47 · rs74969346

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Standard

ENPP5 protein levels

RCAN2 · rs748654645

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Standard

CTRL protein levels

LINC02057 · rs74568270

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Standard

Red blood cell erythrocyte distribution width (UKB data field 30070)

HBB · rs74234654

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Standard

GPNMB protein levels

near DNAJC13 · rs73860747

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Standard

Eosinophill percentage (UKB data field 30210)

near HMGA1P3 · rs73206888

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Standard

TMPRSS5 protein levels

near MBNL1 · rs73154145

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Standard

Haematocrit percentage (UKB data field 30030)

PDE3A · rs73067286

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

near ITPR2 · rs7305031

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Standard

Neutrophill percentage (UKB data field 30200)

GLCCI1 · rs73049270

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Standard

GLIPR1 protein levels

PALLD · rs72975216

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Standard

ICAM2 protein levels

near RN7SL18P · rs72899532

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Standard

GALNT3 protein levels

near SLC38A11 · rs72870713

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Standard

CD2AP protein levels

PTCHD4 · rs72867944

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Standard

INHBB protein levels

near LINC01101 · rs72833847

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ASGR2 protein levels

LINC01118 · rs72804495

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Standard

CD101 protein levels

CD101 · rs72699134

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Standard

CA3 protein levels

CA1 · rs72682933

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Standard

ICAM4 protein levels

near ZBTB7A · rs7259699

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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.