Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,582 positions on this site are linked to Celiac Disease, out of 111,393 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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SPARCL1 protein levels

KLHL8 · rs565455465

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Whole body water mass (UKB data field 23102)

NEK6 · rs56141370

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CD5L protein levels

near LINC01929 · rs55966171

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PYDC1 protein levels

near GC · rs555939398

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GLIPR1 protein levels

RN7SL752P · rs555069857

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PDCD6 protein levels

PLEKHG4B · rs553215629

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GLIPR1 protein levels

DAAM2 · rs551879834

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LAMB1 protein levels

near NRCAM · rs550160485

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TPSAB1 protein levels

near C1QTNF8 · rs545706912

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MAN2B2 protein levels

KIAA0232 · rs538581873

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ITGB6 protein levels

near RBMS1 · rs537357220

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GLIPR1 protein levels

TOP2B · rs532685040

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TGFBI protein levels

near WHRN · rs4998152

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Eosinophill percentage (UKB data field 30210)

BAZ1A · rs4982216

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DSG4 protein levels

GNB1L · rs4819523

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VNN1 protein levels

VNN3P · rs45513492

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NOMO1 protein levels

SMG1 · rs4286096

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F3 protein levels

ABCD3 · rs4148038

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CD101 protein levels

IGSF3 · rs41275572

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Eosinophill percentage (UKB data field 30210)

EFCC1 · rs395020

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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.