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 114,960 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

TFF3 protein levels

near RANP1 · rs6909620

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PPCDC protein levels

TMEM266 · rs67306087

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CD177 protein levels

LYPD5 · rs6509117

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HAVCR1 protein levels

SGCD · rs62380676

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PDGFRA protein levels

near LNX1 · rs62297751

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CYTL1 protein levels

near CYTL1 · rs62290428

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SCARF2 protein levels

CYBRD1 · rs62181672

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UMOD protein levels

near GPATCH2L · rs61979234

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OMD protein levels

STAB2 · rs61937794

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CCS protein levels

PC · rs61890458

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PNLIPRP2 protein levels

MIR3663HG · rs61873576

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APOM protein levels

near BTN2A3P · rs60632935

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SCGN protein levels

KIF2C · rs60452778

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PRG2 protein levels

LINC02391 · rs59601864

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Red blood cell erythrocyte distribution width (UKB data field 30070)

U2SURP · rs59236208

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VSTM1 protein levels

CNOT3 · rs587752317

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SLC39A5 protein levels

SPINT2 · rs58749430

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Apolipoprotein A levels (UKB data field 30630)

near KANK3 · rs58181566

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CTSF protein levels

near C11orf86 · rs58090285

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TACSTD2 protein levels

DAB1 · rs577819993

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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.