Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,581 positions on this site are linked to Celiac Disease, out of 110,175 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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IL1RN protein levels

near IL1A · rs115231944

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HRG protein levels

HRG · rs115043810

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CD38 protein levels

C1QTNF7-AS1 · rs114839377

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Mean corpuscular haemoglobin (UKB data field 30050)

GPX6 · rs114053137

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CCL8 protein levels

ASIC2 · rs113703560

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HPGDS protein levels

near BMPR1B-DT · rs113271995

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LAYN protein levels

HOATZ · rs113215371

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FGFBP1 protein levels

near FGFBP1 · rs113210349

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NELL1 protein levels

ESRRG · rs113112728

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SERPINE2 protein levels

WDFY1 · rs113018545

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ENPP2 protein levels

TAF2 · rs112562547

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DSG3 protein levels

ATP2B1 · rs112389263

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Alkaline phosphatase (UKB data field 30610)

near KIAA0319 · rs112356786

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KLK7 protein levels

near GDF3 · rs112264763

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MMP1 protein levels

PDGFD · rs11226148

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Triglyceride levels (UKB data field 30870)

DSCAML1 · rs11216398

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EXOSC10 protein levels

near IGHV3-7 · rs111932469

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Alkaline phosphatase (UKB data field 30610)

ARMH3 · rs11191199

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GPR37 protein levels

near POT1-AS1 · rs111816406

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CCL17 protein levels

LINC02323 · rs11160693

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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.