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 115,128 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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ADAM15 protein levels

ASH1L · rs567052197

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GLIPR1 protein levels

near FOXF2 · rs566546724

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VSIG10 protein levels

VSIG10 · rs566273753

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SHMT1 protein levels

TOM1L2 · rs564144962

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FCGR3B protein levels

NECTIN4-AS1 · rs563818196

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PTPRM protein levels

near LRRC30 · rs56252937

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Platelet distribution width (UKB data field 30110)

FLI1 · rs56145199

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CCL13 protein levels

near LINC01989 · rs561396857

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MRI1 protein levels

ADGRL1-AS1 · rs561262294

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PNLIPRP2 protein levels

PNLIPRP3 · rs561218694

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GLIPR1 protein levels

PTPRD · rs560492673

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BST1 protein levels

CC2D2A · rs559795739

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GLIPR1 protein levels

near RPL9P18 · rs558063500

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CEACAM21 protein levels

LIPE-AS1 · rs557769897

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CTBS protein levels

DDAH1 · rs557599360

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Eosinophill percentage (UKB data field 30210)

UHRF2 · rs555891873

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IL1R2 protein levels

near PDCL3 · rs555503283

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CRTAM protein levels

near CRTAM · rs554612995

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NPHS1 protein levels

ZNF461 · rs554467444

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GLIPR1 protein levels

EPIC1 · rs554416011

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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.