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 118,630 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

DKKL1 protein levels

PRR12 · rs143640150

See detailed info →
Standard

ALCAM protein levels

near SPRING1P3 · rs143482922

See detailed info →
Standard

GLIPR1 protein levels

IQCJ-SCHIP1 · rs143448154

See detailed info →
Standard

GLIPR1 protein levels

PRKAA1 · rs143038748

See detailed info →
Standard

DPP7 protein levels

near FGL1 · rs142527102

See detailed info →
Standard

SPINK6 protein levels

HTR4 · rs141958305

See detailed info →
Standard

VCAN protein levels

near XRCC4 · rs140330682

See detailed info →
Standard

MUC2 protein levels

near LINC02688 · rs140254559

See detailed info →
Standard

AGT protein levels

CAPN9 · rs140053974

See detailed info →
Standard

CD300A protein levels

ATP2B1-AS1 · rs139879110

See detailed info →
Standard

RLN2 protein levels

near RLN2 · rs139835687

See detailed info →
Standard

BTN3A2 protein levels

RIPOR2 · rs139001028

See detailed info →
Standard

CEACAM21 protein levels

near CEACAM3 · rs138380200

See detailed info →
Standard

RNASE6 protein levels

near EDDM3B · rs138059342

See detailed info →
Standard

Mean corpuscular volume (UKB data field 30040)

BEST2 · rs137957583

See detailed info →
Standard

LEG1 protein levels

LINC00970 · rs1322496

See detailed info →
Standard

PLAUR protein levels

HLA-DQA1 · rs1281944

See detailed info →
Standard

PLA2G2A protein levels

near LINC01757 · rs12725354

See detailed info →
Standard

FABP2 protein levels

GSDME · rs12530499

See detailed info →
Standard

REG1B protein levels

HTRA1-AS1 · rs12413994

See detailed info →

Showing 20 of 20582 · page 152 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.