Variants linked to Celiac Disease

Continuously updated · newest added Oct 24, 2026

20,582 positions on this site are linked to Celiac Disease, out of 115,422 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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BPIFB1 protein levels

LINC02240 · rs331759

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Red blood cell erythrocyte count (UKB data field 30010)

HLA-DPB2 · rs3130223

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RGMB protein levels

LINC01846 · rs28850011

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CPXM2 protein levels

CHST15 · rs28419428

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PNLIPRP2 protein levels

near ATRNL1 · rs2782884

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SERPINI2 protein levels

PRDM16 · rs2742677

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TNXB protein levels

SCARA5 · rs2685419

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KLK4 protein levels

KLK15 · rs2560935

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DPP7 protein levels

FGL1 · rs2517331

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Mean corpuscular haemoglobin (UKB data field 30050)

MDFI · rs2268412

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CPVL protein levels

FUT8 · rs2149839

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RNASET2 protein levels

TRPS1 · rs2142333

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CFC1 protein levels

GALNT3 · rs2113841

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SHMT1 protein levels

near RPL13P12 · rs2089461

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KLK1 protein levels

near PRB1 · rs2059763

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LRG1 protein levels

PLIN5 · rs200877814

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SCARA5 protein levels

near CLU · rs1982229

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Platelet distribution width (UKB data field 30110)

C11orf65 · rs1961319

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GLIPR1 protein levels

near LINC02540 · rs192368824

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GLIPR1 protein levels

LINC01250 · rs192200807

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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.