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 118,864 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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F12 protein levels

near NHP2 · rs181723718

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Mean corpuscular haemoglobin (UKB data field 30050)

near MEMO1P2 · rs181340624

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PVALB protein levels

near CSF2RB · rs180909678

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HAVCR1 protein levels

SGCD · rs180885052

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CD300A protein levels

ATP2B1 · rs17782847

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CXCL12 protein levels

near RPL9P21 · rs17156619

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GASK1A protein levels

near POMGNT2 · rs17075257

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ENPP6 protein levels

PROM1 · rs16892927

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Eosinophill count (UKB data field 30150)

CSF2RB · rs16845

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KLRF1 protein levels

near IL15 · rs1519548

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MGMT protein levels

MGMT · rs151132897

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SCP2 protein levels

FAM30A · rs150829198

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SEMA4D protein levels

SEMA4D · rs150158729

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CD8A protein levels

NOTCH4 · rs150079294

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LAMB1 protein levels

LAMB4 · rs149493645

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Mean reticulocyte volume (UKB data field 30260)

ANK1 · rs149446140

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MSMB protein levels

ANTXRL · rs149322374

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F11 protein levels

near CRYGS · rs149084848

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CD300LF protein levels

near USH1G · rs148894191

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CPPED1 protein levels

near SHISA9 · rs148578856

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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.