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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COL2A1 protein levels

TUBA1C · rs2878288

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Platelet count (UKB data field 30080)

near SRSF3P6 · rs28438997

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C4BPB protein levels

CD55 · rs28371670

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CD163 protein levels

near MTCO3P1 · rs28371349

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EGFR protein levels

SEC61G-DT · rs2699235

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CXCL12 protein levels

near LINC00841 · rs2624688

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EPPK1 protein levels

FLI1 · rs2509583

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Reticulocyte count (UKB data field 30250)

near RN7SL554P · rs2326843

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Impedance of arm left (UKB data field 23110)

KCNQ1 · rs231341

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CRISP3 protein levels

ATXN1 · rs2301594

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FEV1 FVC ratio Z score (UKB data field 20258)

THRAP3 · rs2242428

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CNTN4 protein levels

B4GALT1 · rs2183124

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PSPN protein levels

EYA4 · rs212775

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HYAL1 protein levels

DOCK3 · rs2125368

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MSTN protein levels

near ADRB2 · rs2116715

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PLXNB2 protein levels

TUBGCP6 · rs200425811

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ADAMTSL2 protein levels

near DBH · rs1989787

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CTSC protein levels

near FOLH1B · rs192642478

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ICAM2 protein levels

ST3GAL6-AS1 · rs191600187

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CLUL1 protein levels

CLUL1 · rs191381354

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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.