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 118,294 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

ZP3 protein levels

HIP1 · rs147359763

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Standard

LEG1 protein levels

near DUS3L · rs146393151

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Standard

CD8A protein levels

HCP5 · rs146121051

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Standard

GLIPR1 protein levels

CSRNP2 · rs145731739

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Standard

TCTN3 protein levels

ENTPD1-AS1 · rs144972697

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Standard

FLT4 protein levels

near OR5K3 · rs143692707

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Standard

Haematocrit percentage (UKB data field 30030)

RFLNA · rs142073102

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Standard

GLIPR1 protein levels

PHLPP1 · rs141154802

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Standard

MGMT protein levels

MGMT · rs139219283

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Standard

GPC5 protein levels

GPC5 · rs138846693

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

near EHD3 · rs13420414

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Standard

Haemoglobin concentration (UKB data field 30020)

UBE2E2 · rs12489408

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Standard

CSPG4 protein levels

REPS1 · rs12175880

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Standard

GC protein levels

near HNRNPA1P67 · rs11942445

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Standard

CD163 protein levels

B3GAT1 · rs11822913

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Standard

GLIPR1 protein levels

PSD3 · rs118027861

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Standard

CCN4 protein levels

NDRG1 · rs117934693

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Standard

SMPD1 protein levels

HPX · rs117801081

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Standard

Impedance of arm left (UKB data field 23110)

near CABCOCO1 · rs117508839

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Standard

CPOX protein levels

SLC31A1 · rs116786854

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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.