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 109,124 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

FGF5 protein levels

near CFAP299 · rs559977552

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Standard

FGFBP1 protein levels

PROM1 · rs55937602

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Standard

KLRD1 protein levels

near KLRF1 · rs55927238

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Standard

PLTP protein levels

near MMP9 · rs559072266

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Standard

Mean corpuscular haemoglobin (UKB data field 30050)

PSORS1C1 · rs558745444

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Standard

GLIPR1 protein levels

near LINC01444 · rs558741222

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

near CCDC66 · rs558367900

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Standard

EPPK1 protein levels

MROH1 · rs558162702

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Standard

PGLYRP2 protein levels

SLC1A6 · rs55786704

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Standard

CLIC5 protein levels

CLIC5 · rs55766431

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Standard

LRRC37A2 protein levels

MAPT · rs556596824

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Standard

PLA2G2A protein levels

PLA2G5 · rs555191407

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Standard

LGALS9 protein levels

KSR1 · rs554902175

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Standard

ITGA6 protein levels

ITGA6 · rs554725581

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Standard

MMP8 protein levels

near MMP7 · rs554141289

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Standard

CCL13 protein levels

GASK1A · rs553601709

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Standard

PILRA protein levels

COL26A1 · rs553286849

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Standard

IL2RA protein levels

IL2RA · rs553112485

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Standard

MMP7 protein levels

WTAPP1 · rs552306

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Standard

GLIPR1 protein levels

PNLIPRP3 · rs551987600

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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.