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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FLT4 protein levels

near WWP1P1 · rs148387678

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FUCA1 protein levels

IFNLR1 · rs10903035

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KIR2DL3 protein levels

LILRB4 · rs11574578

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GP1BB protein levels

POLR1HASP · rs9260043

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AMY1A or AMY1B or AMY1C protein levels

THAP3P1 · rs144738643

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FAM3B protein levels

near HLA-DQB1 · rs3129777

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AMY2A protein levels

near RNPC3-DT · rs28702555

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CD1C protein levels

BACH2 · rs62408222

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CLEC4C protein levels

CD163L1 · rs180879827

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PM20D1 protein levels

MFSD4A-AS1 · rs139936227

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CD300A protein levels

ATP2B1 · rs61926781

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GC protein levels

near GC · rs143862434

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PRTG protein levels

BANP · rs4843292

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Reticulocyte percentage (UKB data field 30240)

USP4 · rs35220094

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CRH protein levels

EYA1 · rs13263939

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Mean corpuscular haemoglobin (UKB data field 30050)

AXIN1 · rs182809760

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IFNGR2 protein levels

HERPUD2 · rs896173

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LRPAP1 protein levels

FAM193A · rs150209965

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MCEMP1 protein levels

MEF2D · rs1342442

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SIRPA protein levels

near SIRPA · rs76991189

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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.