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 112,691 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

IL6R protein levels

KCNN3 · rs573939130

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Standard

GLIPR1 protein levels

CCSER2 · rs573869341

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

VAMP4 · rs570382952

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Standard

GLIPR1 protein levels

LINC01609 · rs569069269

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Standard

ATXN3 protein levels

TRIP11 · rs568801221

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Standard

LPA protein levels

LPA · rs568254317

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Standard

IL1RL1 protein levels

near SLC9A4 · rs564450062

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Standard

GLIPR1 protein levels

near CBLN2 · rs563191290

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Standard

Platelet count (UKB data field 30080)

ARHGEF3 · rs56187327

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Standard

WFIKKN1 protein levels

PIGQ · rs560390178

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Standard

TCN1 protein levels

near LINC02571 · rs56006638

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Standard

GRHPR protein levels

POLR1E · rs55983514

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Standard

GLIPR1 protein levels

PARD3B · rs559681044

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Standard

GLIPR1 protein levels

near LINC01821 · rs558578246

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Standard

CSTB protein levels

AGPAT3 · rs555746939

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Standard

Alkaline phosphatase (UKB data field 30610)

near NBPF3 · rs555280546

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Standard

MBL2 protein levels

near RPL31P44 · rs555259909

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Standard

GLIPR1 protein levels

ATP11A · rs554162695

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Standard

ITPA protein levels

ATRN · rs554125541

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Standard

GLIPR1 protein levels

CLASP2 · rs553022786

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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.