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 115,170 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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Standard

THBS2 protein levels

DPY19L3 · rs2111504

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Standard

FGFBP2 protein levels

ABCA8 · rs148549682

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Standard

IL12B protein levels

IL12B-AS1 · rs116377621

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Standard

KIR3DL1 protein levels

near LILRP1 · rs138893041

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Standard

ESM1 protein levels

GZMK · rs6875666

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Standard

CD300A protein levels

POC1B · rs75929616

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Standard

ENTPD6 protein levels

NOL4L-DT · rs6058753

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Standard

AFP protein levels

ANKRD17 · rs7692425

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Standard

ANGPTL3 protein levels

ANGPTL3 · rs72649573

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Standard

ANXA2 protein levels

ANXA2 · rs3759911

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Standard

TCN1 protein levels

near TCN1 · rs17154234

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

SEC14L5 · rs9937661

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Standard

EPHA4 protein levels

EPHA4 · rs9758

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Standard

Mean corpuscular haemoglobin (UKB data field 30050)

near ATP6V1G3 · rs78024727

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Standard

CDH5 protein levels

near Y_RNA · rs7863743

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Standard

LPA protein levels

SLC22A2 · rs3912160

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Standard

ABO protein levels

near RALGDS · rs3888561

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Standard

SIGLEC6 protein levels

ST3GAL4 · rs4935967

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Standard

LILRA6 protein levels

LILRB5 · rs190628353

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Standard

PON3 protein levels

PPP1R9A · rs192272865

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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.