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 117,438 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

Mean corpuscular haemoglobin (UKB data field 30050)

RAB11FIP3 · rs117622026

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Standard

GLIPR1 protein levels

TRPM3 · rs117593222

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Standard

WFIKKN2 protein levels

SLC38A4-AS1 · rs117492977

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Standard

PTPRB protein levels

PRANCR · rs117462747

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Standard

LEG1 protein levels

THEMIS · rs117412656

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Standard

CCN5 protein levels

KCNK15-AS1 · rs117296501

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Standard

Aspartate aminotransferase levels (UKB data field 30650)

near GPR160P2 · rs117174308

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Standard

MMP1 protein levels

WTAPP1 · rs117129110

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Standard

COL9A1 protein levels

near COL9A1 · rs117122199

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Standard

PON2 protein levels

near COL1A2 · rs117120087

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

SNAP29 · rs117104037

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Standard

Platelet count (UKB data field 30080)

RUNX1 · rs11702406

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Standard

IL1RL2 protein levels

near IL18R1 · rs116643975

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Standard

FASLG protein levels

SLFN12L · rs11654381

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Standard

Neutrophill percentage (UKB data field 30200)

AKAP13 · rs11633087

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Standard

SERPINA3 protein levels

SERPINA12 · rs11625754

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Standard

CPVL protein levels

near LYPLA2P1 · rs116077877

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Standard

IGF 1 (UKB data field 30770)

near KRTAP5-4 · rs11605284

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Standard

MUC2 protein levels

BRSK2 · rs11602061

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Standard

CTSE protein levels

RHEX · rs115992630

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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.