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 113,783 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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CHI3L1 protein levels

ADORA1 · rs141877540

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GLIPR1 protein levels

MFF-DT · rs141425127

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NAAA protein levels

ART3 · rs141288423

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ENPP2 protein levels

DEPTOR-AS1 · rs140776652

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CEACAM5 protein levels

HNRNPUL1 · rs140148192

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ITGA6 protein levels

RAPGEF4-AS1 · rs140031904

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Platelet distribution width (UKB data field 30110)

SNX9 · rs140002699

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PSAPL1 protein levels

SORCS2 · rs139862842

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FUCA1 protein levels

HIVEP2 · rs139717578

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AMY1A or AMY1B or AMY1C protein levels

near AMY2B · rs139325607

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HSBP1 protein levels

CDH13 · rs139063717

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GSTM4 protein levels

GSTM1 · rs138936893

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NRP1 protein levels

NRP1 · rs138276798

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PSCA protein levels

ZFP41 · rs13279113

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MEGF10 protein levels

near MEGF10 · rs13178512

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COCH protein levels

near FAM124B · rs13001652

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PTPRB protein levels

PTPRB-AS1 · rs12821702

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Pulse rate (UKB data field 102)

CEP85L · rs12197704

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RHOC protein levels

near TAFA3 · rs12129286

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Red blood cell erythrocyte count (UKB data field 30010)

near Y_RNA · rs11892454

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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.