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

GLIPR1 protein levels

PRKCA · rs572498461

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Standard

MSMB protein levels

MARCHF8 · rs571711119

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Standard

DBH protein levels

SARDH · rs571389818

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Standard

LECT2 protein levels

near SMAD5-AS1 · rs570982670

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Standard

IL1RL1 protein levels

TBC1D8 · rs569369028

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CSTB protein levels

GATD3 · rs569184758

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Whole body water mass (UKB data field 23102)

ZBTB38 · rs568652489

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BPIFB1 protein levels

BPIFB4 · rs567934675

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TYRO3 protein levels

near ISCA1P4 · rs567821651

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Standard

GLIPR1 protein levels

LAMC3 · rs566887843

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Standard

ICAM2 protein levels

near OR5K4 · rs566182728

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

TASOR · rs566010972

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Standard

GLIPR1 protein levels

KALRN · rs565397907

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Standard

GLIPR1 protein levels

near LINC02772 · rs564421226

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FUCA1 protein levels

ADAT2 · rs563517232

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FEV1 FVC ratio Z score (UKB data field 20258)

CROCC2 · rs56331064

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Standard

GLIPR1 protein levels

near NKX1-1 · rs563231753

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Standard

PNLIPRP2 protein levels

PNLIPRP2 · rs563177170

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

near RNU6-543P · rs56089551

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Standard

NAAA protein levels

NAAA · rs560825914

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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.