Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,582 positions on this site are linked to Celiac Disease, out of 112,611 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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AMY2B protein levels

CBFA2T3 · rs7405380

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TRAF3 protein levels

HLA-DQA1 · rs6929057

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CBLN4 protein levels

LINC01440 · rs559390

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F12 protein levels

NSD1 · rs114167666

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CD207 protein levels

CREB5 · rs989437

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IL1R2 protein levels

near CYCSP20 · rs7779671

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IL5RA protein levels

BORCS8-MEF2B · rs1005980

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CCL18 protein levels

near EML4-AS1 · rs6715862

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MERTK protein levels

NOX4 · rs564699

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CALCA protein levels

PAX8 · rs3748916

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APOH protein levels

APOH · rs528176736

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BPIFB1 protein levels

near LPL · rs1441754

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Mean sphered cell volume (UKB data field 30270)

CCND3 · rs76624801

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TFPI2 protein levels

near BET1-AS1 · rs116913862

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LILRB1 protein levels

near PPIAP9 · rs2516491

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PLG protein levels

PLG · rs147175166

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Mean corpuscular volume (UKB data field 30040)

LINC01625 · rs139635049

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FLT4 protein levels

near WWP1P1 · rs143565429

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GUSB protein levels

near SEC24D · rs116093021

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Mean corpuscular haemoglobin (UKB data field 30050)

CARMIL1 · rs149124714

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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.