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 114,960 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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MANSC4 protein levels

near HLA-DRB5 · rs73403122

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SPINK2 protein levels

near SPINK2 · rs73240600

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NCR1 protein levels

ARMC9 · rs73098114

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IGF 1 (UKB data field 30770)

AP1M2 · rs73018660

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Haematocrit percentage (UKB data field 30030)

near MIR4496 · rs7300422

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CFD protein levels

CFD · rs72984026

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ARSA protein levels

PPP6R2 · rs7286685

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LRRC25 protein levels

LINC02522 · rs72819760

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PAM protein levels

near RNA5SP188 · rs72776186

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RLN2 protein levels

near RLN2 · rs72703633

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IL1RL2 protein levels

TET2 · rs72665924

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SPP1 protein levels

near IBSP · rs72655764

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DSG3 protein levels

DSC1 · rs7239227

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Glycated haemoglobin HbA1c levels (UKB data field 30750)

MIDEAS · rs7159714

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TCN1 protein levels

GLYATL2 · rs71486427

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IGF 1 (UKB data field 30770)

GPR83 · rs71477696

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ADAMTS8 protein levels

LINC02873 · rs7117998

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TP53BP1 protein levels

CDSN · rs707913

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ST3GAL1 protein levels

near ST3GAL1 · rs7005676

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Eosinophill count (UKB data field 30150)

EFCC1 · rs693476

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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.