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 117,648 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

PRELP protein levels

near MIR3622B · rs500458

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Standard

CFHR2 protein levels

ZBTB41 · rs41314027

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

GPR15 · rs3749260

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Standard

SIGLEC8 protein levels

ETFB · rs370777932

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Standard

Eosinophill percentage (UKB data field 30210)

CDK6 · rs34257565

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Standard

MAN2B2 protein levels

LINC02481 · rs28656105

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Standard

IL15RA protein levels

near LASTR · rs28653026

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Standard

OSMR protein levels

near HLA-DRB9 · rs2187822

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Standard

GLIPR1 protein levels

BAZ2B · rs193052873

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Standard

GASK1A protein levels

near RNU6-367P · rs192299009

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Standard

LRG1 protein levels

SEMA6B · rs190218798

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Standard

REG3G protein levels

near REG3G · rs187827476

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Standard

PGLYRP2 protein levels

WIZ · rs186729461

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Standard

MEP1B protein levels

near RPS27P28 · rs186668345

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Standard

GLIPR1 protein levels

RHPN2 · rs182621702

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Standard

Whole body water mass (UKB data field 23102)

SPRY4-AS1 · rs181895

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Standard

ULBP2 protein levels

RAET1L · rs181620867

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Standard

CNTN5 protein levels

CNTN5 · rs181105372

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Standard

EFCAB2 protein levels

EFCAB2 · rs181058360

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Standard

FCAMR protein levels

PIGR · rs17018064

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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.