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 114,834 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

SERPINA9 protein levels

near LINC02571 · rs9264954

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CD72 protein levels

POLR1HASP · rs9260535

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TCN1 protein levels

PLA2G4C · rs8109684

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TPSAB1 protein levels

ARSG · rs8075388

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IGF 1 (UKB data field 30770)

near RNU7-134P · rs8065258

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VSIR protein levels

CHST3 · rs80210009

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Neutrophill count (UKB data field 30140)

EXOC3L2 · rs79744739

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ORM1 protein levels

near LINC01252 · rs7959807

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Platelet distribution width (UKB data field 30110)

DGAT2 · rs7947512

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UMOD protein levels

ACSM5P1 · rs79386529

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PSAPL1 protein levels

near EEF1GP2 · rs79286622

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LYPD3 protein levels

near HSD17B14 · rs79179496

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TNN protein levels

near KIAA0040 · rs78301951

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LECT2 protein levels

SLC25A48 · rs781235830

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NECTIN4 protein levels

NECTIN4 · rs78105657

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GLIPR1 protein levels

near SGO1P2 · rs778857109

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CDH17 protein levels

near CDH17 · rs77829097

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CD83 protein levels

near RNF182 · rs77757414

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MARCO protein levels

near TRAPPC3L · rs7751233

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CDHR5 protein levels

near IFITM3-AS1 · rs77358882

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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.