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 111,645 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

GLIPR1 protein levels

near U3 · rs149562983

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Standard

GLIPR1 protein levels

near HERPUD2 · rs149428613

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Standard

Platelet distribution width (UKB data field 30110)

PKN2-AS1 · rs1490738

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Standard

CD33 protein levels

near SIGLEC8 · rs148660547

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Standard

ADGRE1 protein levels

MGAT5 · rs147513032

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Standard

LAMB1 protein levels

near BUB3P1 · rs147452799

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Standard

TPK1 protein levels

TPK1 · rs147310986

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Standard

LTBP3 protein levels

PACS1 · rs146513911

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Standard

CRELD1 protein levels

CIDECP1 · rs145794253

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

TAOK1 · rs145772295

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Standard

PGLYRP1 protein levels

near IGFL1 · rs145319099

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Standard

HRG protein levels

HRG-AS1 · rs145254686

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Standard

CHIT1 protein levels

LINC02929 · rs145247798

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Standard

TP53I3 protein levels

FAM228B · rs144231256

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Standard

PLTP protein levels

near RPS2P7 · rs143759668

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Standard

IL17RB protein levels

near CABYRP1 · rs143729350

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Standard

KLKB1 protein levels

TLR3 · rs143546139

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Standard

VWF protein levels

near CELP · rs142810361

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Standard

CPA2 protein levels

near CPA2 · rs142650013

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Standard

HBZ protein levels

CAPN15 · rs141885650

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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.