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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Standard

LRRC37A2 protein levels

GPATCH8 · rs9635715

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FUT3 or FUT5 protein levels

NRTN · rs544548654

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CSTB protein levels

PDXK · rs117050103

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SCGB3A1 protein levels

near SCGB3A1 · rs307802

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DYNLT1 protein levels

near OR2W3 · rs548712666

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PYDC1 protein levels

near ADAMTS3 · rs114204813

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Lymphocyte count (UKB data field 30120)

near RPL3P2 · rs62400295

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IL6R protein levels

CHRNB2 · rs12125018

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KIR2DL2 protein levels

near LILRP2 · rs117351201

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SIGLEC7 protein levels

SIGLEC9 · rs67621164

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MILR1 protein levels

near SMURF2 · rs181638288

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TDGF1 protein levels

CELSR3 · rs11706153

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Mean corpuscular haemoglobin (UKB data field 30050)

HBS1L · rs139369617

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FAP protein levels

near HLA-B · rs9266043

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FOXO1 protein levels

FOXO1 · rs17061453

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SIGLEC9 protein levels

HLA-DQA1 · rs9260

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IL17C protein levels

ZC3H18 · rs17700884

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TNFSF10 protein levels

near CFHR1 · rs7519758

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PILRB protein levels

MEPCE · rs150881124

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DNPH1 protein levels

near SLC22A7 · rs6901866

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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.