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 114,498 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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TNN protein levels

TNR · rs148934644

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CNPY4 protein levels

near LINC00533 · rs148390159

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Calcium levels (UKB data field 30680)

CASR · rs148148022

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TREH protein levels

BCL9L · rs148145020

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GLIPR1 protein levels

CTB-1I21.1 · rs147845487

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OGN protein levels

ROR2 · rs147837729

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TNC protein levels

SCARA5 · rs147766672

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BPIFB1 protein levels

BPIFB3 · rs146748300

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RECK protein levels

CLTA · rs146610298

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PROCR protein levels

TLDC2 · rs146529747

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CLEC4D protein levels

near AICDA · rs146476683

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ICAM4 protein levels

CR1 · rs146066196

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FCGR2A protein levels

FCRLB · rs145739258

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Mean sphered cell volume (UKB data field 30270)

near LRRC36 · rs145600544

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Reticulocyte count (UKB data field 30250)

ABCB6 · rs145526996

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IL15 protein levels

near LINC02276 · rs145484302

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SPAG1 protein levels

RGS22 · rs145416166

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F12 protein levels

UNC5A · rs144524143

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CDHR1 protein levels

near LINC01519 · rs144152883

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SIGLEC1 protein levels

HSPA12B · rs143974404

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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.