Variants linked to Celiac Disease

Continuously updated · newest added Oct 25, 2026

20,582 positions on this site are linked to Celiac Disease, out of 117,102 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

ADGRB3 protein levels

COL9A1 · rs190824522

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Standard

GLIPR1 protein levels

MYO5B · rs190594941

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HAVCR1 protein levels

SGCD · rs190555844

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Standard

CEACAM21 protein levels

near TPM3P5 · rs190444279

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Standard

NCAM2 protein levels

NCAM2 · rs190441810

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Standard

BCHE protein levels

near LINC01322 · rs189677132

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GLIPR1 protein levels

near LINC02500 · rs189525155

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Standard

Haematocrit percentage (UKB data field 30030)

ALDH1A2 · rs189452693

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Standard

Apolipoprotein A levels (UKB data field 30630)

near LNC-RHL1 · rs189391949

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GRN protein levels

near AMIGO1 · rs189318337

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CD109 protein levels

CD109 · rs188913865

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CD101 protein levels

LINC01525 · rs188895907

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GLIPR1 protein levels

PGCKA1 · rs188652567

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Standard

GLIPR1 protein levels

near LINC02211 · rs188550874

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

near DSTYK · rs188249176

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Standard

SMPDL3A protein levels

TRDN · rs188242249

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SCG3 protein levels

DMXL2 · rs188230429

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GLIPR1 protein levels

ANKS1B · rs187864864

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SPAG1 protein levels

near ANKRD46 · rs187668085

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Standard

ECM1 protein levels

near CA14 · rs187487814

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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.