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 118,714 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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HDL cholesterol levels (UKB data field 30760)

ZBTB4 · rs8075009

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HDDC2 protein levels

near HEY2-AS1 · rs79920868

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CNTN1 protein levels

REDIC1 · rs7960814

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Eosinophill percentage (UKB data field 30210)

near SETP16 · rs79504890

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FGF2 protein levels

IL21-AS1 · rs78722717

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DPT protein levels

LINC00970 · rs78491951

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PLXDC1 protein levels

LAMTOR4 · rs7785392

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LEG1 protein levels

near KIAA0408 · rs77632450

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IL7R protein levels

UGT3A2 · rs775207584

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IL1RAP protein levels

OSTN · rs77487185

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LRIG1 protein levels

near RPL21P41 · rs77208322

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SIGLEC6 protein levels

LINC01412 · rs77066002

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PDGFRB protein levels

NDST1-AS1 · rs76802053

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HPGDS protein levels

near PDLIM5 · rs76798504

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NRCAM protein levels

NRCAM · rs75616307

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GLIPR1 protein levels

near LINC01163 · rs753728280

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GLIPR1 protein levels

SYT1 · rs749592679

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DLL1 protein levels

near LINC00574 · rs74769859

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LTA protein levels

DDR1 · rs74689782

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RTN4R protein levels

TANGO2 · rs73150851

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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.