Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,580 positions on this site are linked to Celiac Disease, out of 109,544 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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PEPD protein levels

PRODH · rs759404

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INSR protein levels

INSR · rs1799815

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WASF1 protein levels

SLC22A16 · rs76676412

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CCN2 protein levels

near PIF1 · rs7176023

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SIGLEC9 protein levels

near SLC2A4 · rs5412

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PRSS27 protein levels

SYNGR4 · rs919804

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ABO protein levels

CELP · rs532542696

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ESM1 protein levels

NT5DC2 · rs11709284

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SELE protein levels

STKLD1 · rs188110518

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PNLIPRP1 protein levels

ABO · rs77693339

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SLITRK1 protein levels

GALNT6 · rs3782473

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HCG22 protein levels

TCF19 · rs3130934

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FCRL2 protein levels

near RPL13P12 · rs138019528

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IL12B protein levels

near H3C9P · rs10484439

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PTPRM protein levels

AK8 · rs144590872

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CD209 protein levels

near Y_RNA · rs116851371

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BPIFA2 protein levels

MAMSTR · rs183262653

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PRG2 protein levels

NBEAL2 · rs2305637

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ANGPT1 protein levels

SLC24A3 · rs6081562

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ADGRE1 protein levels

ST3GAL4 · rs4601794

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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.