Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,581 positions on this site are linked to Celiac Disease, out of 110,679 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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SEMA3G protein levels

POLR1HASP · rs9260181

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Monocyte percentage (UKB data field 30190)

HSD11B1-AS1 · rs909710

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APP protein levels

MED12L · rs8180086

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GAS6 protein levels

TMCO3 · rs78321687

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PLA2G2A protein levels

PLA2G5 · rs77631878

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CTRB1 protein levels

ZNRF1 · rs77214773

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SELPLG protein levels

SSH1 · rs76304752

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GLIPR1 protein levels

near LINC00670 · rs760491887

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Red blood cell erythrocyte count (UKB data field 30010)

DNM3 · rs7534393

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MST1 protein levels

near CCR3 · rs745575679

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SERPINA4 protein levels

near SERPINA1 · rs74393562

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CLGN protein levels

near SCOC · rs73855403

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CGREF1 protein levels

near SLC2A6 · rs736418

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CCL4 protein levels

near TBC1D3JP · rs72818318

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LILRB2 protein levels

KCNT2 · rs72732226

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CTSH protein levels

CHRNA5 · rs72648879

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CRH protein levels

ZNF316 · rs6979882

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KIR2DL3 protein levels

near SUMO2P1 · rs6928280

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SELL protein levels

FIRRM · rs6660060

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IL18BP protein levels

MYH9-DT · rs62228881

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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.