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 116,262 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

CTRL protein levels

near SERPINA4 · rs10151340

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Standard

GPIHBP1 protein levels

near RHPN1 · rs10086661

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Standard

PODXL protein levels

PODXL · rs1007340

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Standard

CDH17 protein levels

MYMK · rs9802318

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Standard

STX7 protein levels

near MOXD1 · rs9483433

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Standard

CEACAM6 protein levels

STXBP5 · rs9390458

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Standard

Glycated haemoglobin HbA1c levels (UKB data field 30750)

near LINC03002 · rs9389212

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Standard

TCL1A protein levels

FKBP5 · rs9368885

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Standard

FCRL1 protein levels

FLT3 · rs9319410

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Standard

CD302 protein levels

HLA-DQB1 · rs9273550

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

UBE2O · rs898085

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Standard

ZBTB17 protein levels

ZBTB17 · rs848217

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Standard

EGFR protein levels

EGFR-AS1 · rs845560

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Standard

PNLIPRP2 protein levels

near SNRPGP6 · rs80327955

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Standard

CRISP2 protein levels

near MAX · rs8009396

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Standard

IL7R protein levels

ST3GAL4 · rs80035373

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Standard

IFNL1 protein levels

FAP · rs79854652

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Standard

RGMA protein levels

RECK · rs79792936

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Standard

Alkaline phosphatase (UKB data field 30610)

CMAHP · rs79645378

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Standard

GPC5 protein levels

near MIR17HG · rs79642658

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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.