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 116,094 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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SUSD4 protein levels

TLR5 · rs115937574

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ACAN protein levels

near PSAP · rs11593281

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Haemoglobin concentration (UKB data field 30020)

PADI2 · rs11585299

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MEGF10 protein levels

near SELENOTP2 · rs115579804

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KIT protein levels

KIT · rs115028437

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MEGF10 protein levels

LMNB1 · rs114725221

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ADAM23 protein levels

MYOSLID · rs114617574

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GLIPR1 protein levels

NDEL1 · rs114610120

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SPINK6 protein levels

FBXO38-DT · rs114544021

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ADAM23 protein levels

near HNRNPA1P51 · rs114477007

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APOC1 protein levels

RELB · rs114248186

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Eosinophill count (UKB data field 30150)

BTLA · rs114092838

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GLIPR1 protein levels

SYNPR-AS1 · rs114083793

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TALDO1 protein levels

near EPS8L2 · rs113451909

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Impedance of whole body (UKB data field 23106)

HCP5 · rs113340460

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SNCG protein levels

near RNU6-529P · rs113130693

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CCL17 protein levels

near PLCL2 · rs113080155

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IL1RL1 protein levels

near CFAP144P2 · rs112853373

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PXN protein levels

RNF10 · rs112788889

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CLEC1A protein levels

near KRT17P8 · rs112712075

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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.