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 113,321 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 THSD7A · rs6977013

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Standard

GDNF protein levels

GDNF-AS1 · rs67437118

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Standard

Mean corpuscular haemoglobin (UKB data field 30050)

MUC4 · rs67175307

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Standard

SPINK2 protein levels

IGFBP7-AS1 · rs62308338

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Standard

Impedance of arm left (UKB data field 23110)

EFL1P1 · rs62026522

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Standard

PBLD protein levels

CTNNA3 · rs61866885

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Standard

CGREF1 protein levels

PRR30 · rs61741796

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Standard

FABP9 protein levels

near S100A10 · rs58680739

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Standard

CD70 protein levels

near TUBB4A · rs57961423

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Standard

IGF2R protein levels

NCOA7-AS1 · rs579477

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Standard

SPINK8 protein levels

SHISA5 · rs576345181

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Standard

GLIPR1 protein levels

VSTM2B-DT · rs575159876

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Standard

GLIPR1 protein levels

SMARCA4 · rs574326907

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

ANKMY1 · rs573972313

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Standard

PON1 protein levels

PPP1R9A · rs570174677

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Standard

VCAN protein levels

near RNU4-11P · rs569968574

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Standard

GLIPR1 protein levels

near Y_RNA · rs569725477

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Standard

GLIPR1 protein levels

near SLAIN2 · rs569500423

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Standard

GLIPR1 protein levels

near MTDH · rs567431003

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Standard

LRRN1 protein levels

SUMF1 · rs567424316

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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.