Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,581 positions on this site are linked to Celiac Disease, out of 110,511 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

GRN protein levels

SLC25A24 · rs149486864

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Standard

SNCG protein levels

BMPR1A · rs149360987

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Standard

FCRL3 protein levels

near FCRL4 · rs149128095

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Standard

AMY2B protein levels

near AMY1C · rs148480463

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Standard

MST1 protein levels

PRSS50 · rs148134755

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Standard

GLIPR1 protein levels

near MTND4LP25 · rs146606540

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Standard

PTH1R protein levels

near ELP6 · rs145628067

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Standard

GLIPR1 protein levels

near RPL21P44 · rs145333293

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Standard

TYRO3 protein levels

STARD9 · rs145036897

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

CD226 · rs144408230

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Standard

FLT4 protein levels

BTNL8 · rs142848432

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Standard

VNN2 protein levels

VNN2 · rs142626186

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Standard

SCG3 protein levels

TMOD3 · rs142502020

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Standard

Alkaline phosphatase (UKB data field 30610)

near CLEC10A · rs142467156

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Standard

SGSH protein levels

CARD14 · rs142078801

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Standard

LEFTY2 protein levels

DNAH14 · rs141859902

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Standard

IL17D protein levels

IFT88 · rs140911986

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Standard

DPP6 protein levels

DPP6 · rs140187322

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Standard

SCN4B protein levels

SCN4B · rs140122876

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Standard

CD34 protein levels

near CELP · rs139744322

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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.