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 118,864 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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LILRB2 protein levels

near TSEN34 · rs79970109

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GLIPR1 protein levels

FEM1B · rs79638346

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CDSN protein levels

ERRFI1-DT · rs78924983

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FCRL6 protein levels

near TOX-DT · rs7826351

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C1S protein levels

near ACSM4 · rs781418882

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GLIPR1 protein levels

PROZ · rs776682230

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TNR protein levels

TNR · rs77466222

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Mean sphered cell volume (UKB data field 30270)

near LINC01478 · rs77351486

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GAL protein levels

near RN7SL147P · rs77116725

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Impedance of arm left (UKB data field 23110)

EBF1 · rs7705707

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GLIPR1 protein levels

near RPL7P20 · rs764598190

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DSG4 protein levels

CDKAL1 · rs76235859

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CD302 protein levels

near RNU2-21P · rs75912194

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LAYN protein levels

LINC02762 · rs75770864

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OGN protein levels

SPTLC1 · rs75641053

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HLA A protein levels

SLC17A1 · rs75479767

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BMP4 protein levels

NBL1 · rs7546665

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GLIPR1 protein levels

near EYA1 · rs754355259

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SERPINA5 protein levels

near RPSAP4 · rs75248972

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VNN1 protein levels

near RPS12 · rs749031709

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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.