Variants linked to Celiac Disease

Continuously updated · newest added Oct 25, 2026

20,582 positions on this site are linked to Celiac Disease, out of 117,874 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

HMCN2 protein levels

NCS1 · rs183365707

See detailed info →
Standard

GALNT10 protein levels

near FAM114A2 · rs150111861

See detailed info →
Standard

CD55 protein levels

CR2 · rs149295608

See detailed info →
Standard

TIMP4 protein levels

SYN2 · rs149250423

See detailed info →
Standard

CDSN protein levels

near MUC22 · rs147851553

See detailed info →
Standard

SMAD5 protein levels

near SFRP2 · rs147316129

See detailed info →
Standard

MATN2 protein levels

SCARA5 · rs147205924

See detailed info →
Standard

SPINK1 protein levels

near PPP2R2B · rs146844692

See detailed info →
Standard

CDA protein levels

VWA5B1 · rs146161197

See detailed info →
Standard

HYAL1 protein levels

STIMATE · rs145387116

See detailed info →
Standard

LEG1 protein levels

KIAA0408 · rs145321441

See detailed info →
Standard

COMP protein levels

near COMP · rs145122962

See detailed info →
Standard

HDGF protein levels

near KRT8P45 · rs144403686

See detailed info →
Standard

C4BPB protein levels

PFKFB2 · rs143736099

See detailed info →
Standard

ECM1 protein levels

RPRD2 · rs142691903

See detailed info →
Standard

GLIPR1 protein levels

GRIN2A · rs142327197

See detailed info →
Standard

DKK3 protein levels

LINC02547 · rs141508763

See detailed info →
Standard

GLIPR1 protein levels

near TMF1P1 · rs141129736

See detailed info →
Standard

RNASE10 protein levels

near SETP1 · rs140702176

See detailed info →
Standard

CD38 protein levels

C1QTNF7 · rs139878157

See detailed info →

Showing 20 of 20582 · page 139 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.