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 118,420 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

BTN3A2 protein levels

near ZNF184 · rs79225736

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Standard

ADGRE2 protein levels

DNAJB1 · rs772111893

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Standard

IL5RA protein levels

CRBN · rs76714935

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Standard

Total bilirubin levels (UKB data field 30840)

near TRPM8 · rs765651860

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Standard

Reticulocyte count (UKB data field 30250)

near RN7SL416P · rs76238526

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Standard

CD48 protein levels

near GLRX5P2 · rs761875896

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Standard

CRTAC1 protein levels

TBCCD1 · rs75769344

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Standard

NAP1L4 protein levels

KCNQ1-AS1 · rs74395370

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Standard

CCL25 protein levels

near FCER2 · rs73491778

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Standard

F11 protein levels

ADIPOQ · rs73187705

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Standard

CNDP1 protein levels

CNDP1 · rs72981715

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Standard

Monocyte percentage (UKB data field 30190)

LITAF · rs72781032

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Standard

COMMD1 protein levels

PTPN9 · rs72732847

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Standard

PTPRM protein levels

near PTPRM · rs7241477

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

PAFAH1B1 · rs7213463

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Standard

CTRL protein levels

near RNASE1 · rs7142320

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Standard

TREH protein levels

near FXYD6 · rs7121851

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Standard

LILRB2 protein levels

near LILRA4 · rs6417165

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Standard

Urate levels (UKB data field 30880)

MEPE · rs60944451

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Standard

FAM3D protein levels

ADAMTS13 · rs587620599

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Showing 20 of 20582 · page 147 of 1030

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.