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 111,813 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Celiac Disease

Standard

MST1 protein levels

QRICH1 · rs62262510

See detailed info →
Standard

IL10 protein levels

IL10RA · rs3135932

See detailed info →
Standard

ALPI protein levels

near Y_RNA · rs609202

See detailed info →
Standard

PTP4A3 protein levels

RIDA · rs2242197

See detailed info →
Standard

MSR1 protein levels

MSR1 · rs138749399

See detailed info →
Standard

LRRC37A2 protein levels

WNT3 · rs118058613

See detailed info →
Standard

FUT3 or FUT5 protein levels

FUT3 · rs28742587

See detailed info →
Standard

BPIFB1 protein levels

BPIFB1 · rs117258330

See detailed info →
Standard

REG3A protein levels

near RPL36AP45 · rs17338413

See detailed info →
Standard

NIT1 protein levels

NIT1 · rs76502631

See detailed info →
Standard

PRSS22 protein levels

near PRSS22 · rs8046218

See detailed info →
Standard

CCL13 protein levels

near CCL13 · rs3136674

See detailed info →
Standard

AMY1A or AMY1B or AMY1C protein levels

near AMY2B · rs113630435

See detailed info →
Standard

CREG1 protein levels

GNPTAB · rs183530599

See detailed info →
Standard

PRSS27 protein levels

PRSS27 · rs71386687

See detailed info →
Standard

APOBR protein levels

SGF29 · rs138534121

See detailed info →
Standard

FUT3 or FUT5 protein levels

FUT5 · rs8101625

See detailed info →
Standard

PTGR1 protein levels

LRRC37A5P · rs59773154

See detailed info →
Standard

PDGFC protein levels

ORM1 · rs113354603

See detailed info →
Standard

CLPS protein levels

CLPS · rs116063149

See detailed info →

Showing 20 of 20582 · page 1008 of 1030

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.