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 113,489 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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RAB44 protein levels

near RNU1-88P · rs190919633

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CEACAM21 protein levels

PCAT19 · rs189905360

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CFHR4 protein levels

near ASPM · rs189750892

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GPR37 protein levels

near POT1-AS1 · rs189155821

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Lipoprotein A levels (UKB data field 30790)

near MAS1 · rs188853201

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CXCL6 protein levels

near AFP · rs188410248

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DKK4 protein levels

near SFRP1 · rs187208870

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GLIPR1 protein levels

PAXIP1 · rs186565388

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KIR2DL2 protein levels

near OR2B6 · rs186367440

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ALPP protein levels

DIS3L2 · rs186079931

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ADGRE1 protein levels

INSR · rs185963644

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PROK1 protein levels

KCNC4 · rs185491604

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Apolipoprotein A levels (UKB data field 30630)

near CETP · rs184617400

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GLIPR1 protein levels

near HAUS4P1 · rs184610420

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AGT protein levels

GALNT2 · rs184569164

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GIMAP7 protein levels

near ALDH7A1P3 · rs184088138

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VSIG10 protein levels

VSIG10 · rs183562350

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Platelet distribution width (UKB data field 30110)

DNM3 · rs183458045

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PENK protein levels

PENK-AS1 · rs182347467

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MATN2 protein levels

MATN2 · rs182070549

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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.