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 114,792 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

LILRA6 protein levels

near MIR4752 · rs149354341

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Standard

Immature reticulocyte fraction (UKB data field 30280)

near LINC01625 · rs60562771

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Standard

CCDC50 protein levels

near IGHV1-67 · rs2583285

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Standard

PILRB protein levels

STAG3L5P-PVRIG2P-PILRB · rs141587987

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Standard

CSF2RB protein levels

CSF2RB · rs7292430

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Standard

LILRB2 protein levels

RPS9 · rs118125339

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Sensitive

Coeliac disease

HLA-DPB1 · rs72500564

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Standard

DTD1 protein levels

DTD1 · rs6081238

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Standard

KYNU protein levels

KYNU · rs17808482

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Standard

ERBB2 protein levels

IKZF3 · rs3764354

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Standard

ANGPT2 protein levels

MCPH1 · rs1968586

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Standard

PXN protein levels

GCN1 · rs555994863

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Standard

Reticulocyte percentage (UKB data field 30240)

ANK1 · rs80008824

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Standard

BLMH protein levels

STAB1 · rs138055453

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Standard

CHIT1 protein levels

near ADORA1 · rs72739545

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Standard

SPINK2 protein levels

near ORM2 · rs10982164

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Standard

S100A14 protein levels

S100A14 · rs11548102

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Standard

INSL4 protein levels

near INSL4 · rs41313766

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Standard

MST1 protein levels

ARIH2 · rs34221642

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Standard

ADAM15 protein levels

MEX3A · rs3814314

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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.