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 118,864 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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IL12B protein levels

LPP · rs66702144

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CRISP2 protein levels

near UTF1 · rs74973131

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CPB2 protein levels

CPB2-AS1 · rs74859256

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Mean corpuscular volume (UKB data field 30040)

LINC01475 · rs10883368

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TFPI protein levels

near TFPI · rs75921449

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LILRB1 protein levels

near TSPAN15 · rs2082206

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CXCL16 protein levels

HLA-DQA1 · rs114005998

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RNASEH2A protein levels

RNASEH2B-AS1 · rs61962192

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PDGFB protein levels

PCSK6 · rs11639051

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SIGLEC10 protein levels

LIM2-AS1 · rs180985088

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VNN1 protein levels

LINC00326 · rs1947640

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MICB or MICA protein levels

near RN7SKP186 · rs112865839

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Apolipoprotein A levels (UKB data field 30630)

LIPG · rs8094774

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ITIH3 protein levels

NEK4 · rs181819742

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SIGLEC9 protein levels

LINC00973 · rs73147949

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KIR2DS4 protein levels

near LILRP2 · rs138850542

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PSCA protein levels

PSCA · rs142914096

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OBP2B protein levels

LINC01502 · rs697449

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GOLGA3 protein levels

CHFR · rs11147139

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Total protein levels (UKB data field 30860)

RCN3 · rs186451245

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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.