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 111,183 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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B3GNT7 protein levels

near ARMC9 · rs140736199

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GLIPR1 protein levels

near CARS1P2 · rs140473166

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TIMP4 protein levels

SYN2 · rs140219161

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GLIPR1 protein levels

near RPL9P21 · rs138531342

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FUCA1 protein levels

CNR2 · rs138396102

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CEACAM21 protein levels

near PSG7 · rs138049621

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LEG1 protein levels

IKZF2 · rs1372133

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COL9A1 protein levels

COL19A1 · rs13208290

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CD200R1 protein levels

ST3GAL3 · rs12024345

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SGSH protein levels

PGBD1 · rs115837789

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Impedance of whole body (UKB data field 23106)

DDC-AS1 · rs11575301

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Platelet crit (UKB data field 30090)

PARP11-AS1 · rs113136983

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DYNLT1 protein levels

SH3BP5L · rs1127427

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APOBR protein levels

HIRIP3 · rs112533759

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SERPINI1 protein levels

HLA-DQA1 · rs112216801

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NAPRT protein levels

TIGD5 · rs111956838

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Gamma glutamyltransferase levels (UKB data field 30730)

SLC17A8 · rs11110365

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Total protein levels (UKB data field 30860)

LINC02458 · rs11105192

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NRP2 protein levels

PARD3B · rs10490277

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CTHRC1 protein levels

BAALC-AS1 · rs10088427

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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.