Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,582 positions on this site are linked to Celiac Disease, out of 111,519 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

F13B protein levels

CFHR3 · rs188390743

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Standard

GLIPR1 protein levels

near RNU6-63P · rs186967244

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

near PEMT · rs186920574

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Standard

F13B protein levels

KCNT2 · rs185808527

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Standard

GLIPR1 protein levels

near DAPP1 · rs184787145

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Standard

PDGFRB protein levels

HMGXB3 · rs184700209

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Standard

Eosinophill count (UKB data field 30150)

ABCB10 · rs1838463

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Standard

CNTN1 protein levels

HECTD4 · rs182350076

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Standard

IL31RA protein levels

IL6ST-DT · rs182320051

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Standard

GLIPR1 protein levels

near CSF1 · rs182124532

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Standard

MYOC protein levels

PRRC2C · rs181559114

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Standard

MDGA1 protein levels

DNAH8 · rs181490882

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Standard

GLIPR1 protein levels

near RPL31P13 · rs180755973

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Standard

Eosinophill percentage (UKB data field 30210)

TMEM182 · rs180737123

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Standard

Mean corpuscular volume (UKB data field 30040)

near APOOP4 · rs1715086

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Standard

CPXM2 protein levels

CPXM2 · rs1712934

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Standard

VNN1 protein levels

GPLD1 · rs16889389

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Standard

F13B protein levels

near ATP6V1G3 · rs16843226

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Standard

PEAR1 protein levels

ARHGEF11 · rs151236230

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Standard

FCGR3B protein levels

NPEPPS · rs149972127

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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.