Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,582 positions on this site are linked to Celiac Disease, out of 112,149 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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LY75 protein levels

LY75-CD302 · rs113023766

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FRZB protein levels

near HLA-DQB1 · rs2856694

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MUC16 protein levels

GAL3ST2 · rs150107870

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Platelet count (UKB data field 30080)

RHCE · rs909832

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LTBP2 protein levels

near AREL1 · rs888414

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CD244 protein levels

near RN7SL51P · rs35808670

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PTPRM protein levels

near ABO · rs141638449

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KIR2DL3 protein levels

HCG22 · rs13209912

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ITGAV protein levels

ITGAV · rs13006483

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MEP1B protein levels

near LINC02132 · rs16940186

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SMPDL3A protein levels

DRAM1 · rs7302651

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CCL25 protein levels

B4GALNT3 · rs7306988

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C1QTNF1 protein levels

C1QTNF1-AS1 · rs181647086

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ICAM2 protein levels

ST3GAL6 · rs540295212

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SCGB3A2 protein levels

TP63 · rs1515498

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IL7R protein levels

CAPSL · rs75159651

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Direct low density lipoprotein levels (UKB data field 30780)

near APOC1 · rs182067414

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GABARAP protein levels

near MTCO3P1 · rs11967437

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CD207 protein levels

near HLA-DQA1 · rs539981616

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C1RL protein levels

CLSTN3 · rs113899462

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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.