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 112,859 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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GLIPR1 protein levels

ABR · rs191202493

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TREH protein levels

BCL9L · rs191036003

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CLEC4C protein levels

near GDF3 · rs190700056

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EPHB6 protein levels

TRBVB · rs190588589

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OXT protein levels

PTPRA · rs190393862

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CST5 protein levels

near CST5 · rs190025292

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KLB protein levels

near PDS5A · rs189032404

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CA5A protein levels

SLC7A5-AS1 · rs188359514

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Mean reticulocyte volume (UKB data field 30260)

ANK1 · rs188146372

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GFRAL protein levels

HCRTR2 · rs188055163

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RTN4R protein levels

near LINC02891 · rs188007688

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IFNAR1 protein levels

near LINC01548 · rs186965033

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MMP1 protein levels

PDGFD · rs186748123

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Alkaline phosphatase (UKB data field 30610)

STKLD1 · rs186469807

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Neutrophill count (UKB data field 30140)

near TBC1D14 · rs185679641

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GLIPR1 protein levels

near Y_RNA · rs184003341

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TNFSF11 protein levels

MAL2-AS1 · rs183744316

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HBZ protein levels

LUC7L · rs183229266

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MMP1 protein levels

near RNU7-159P · rs182844815

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TNFRSF8 protein levels

near FAM20B · rs182537901

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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.