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 114,582 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

FCGR2A protein levels

near RNU6-481P · rs6680657

See detailed info →
Standard

GHRL protein levels

GHRLOS · rs4684677

See detailed info →
Standard

Reticulocyte percentage (UKB data field 30240)

GUSBP5 · rs1912742

See detailed info →
Standard

BPIFA2 protein levels

PRH1 · rs1013311

See detailed info →
Standard

FETUB protein levels

HRG-AS1 · rs146416428

See detailed info →
Standard

COL18A1 protein levels

COL18A1 · rs201662370

See detailed info →
Standard

CREG1 protein levels

near RNU6-1183P · rs182028108

See detailed info →
Standard

Reticulocyte percentage (UKB data field 30240)

KANK2 · rs35312489

See detailed info →
Standard

PODXL protein levels

C1GALT1 · rs767298

See detailed info →
Standard

CA14 protein levels

near CA14 · rs17646887

See detailed info →
Standard

CDCP1 protein levels

CDCP1 · rs79885994

See detailed info →
Standard

SUMF2 protein levels

DENND6A · rs9852409

See detailed info →
Standard

CCL22 protein levels

CCL22 · rs41398344

See detailed info →
Standard

SIRPA protein levels

SIRPA · rs9679973

See detailed info →
Standard

GHR protein levels

GHR · rs4146624

See detailed info →
Standard

CTSZ protein levels

DRAM1 · rs6539021

See detailed info →
Standard

Haematocrit percentage (UKB data field 30030)

near LPL · rs75902744

See detailed info →
Standard

LILRB5 protein levels

near RNU6-1307P · rs180761831

See detailed info →
Standard

CCL17 protein levels

PLCL2 · rs74509702

See detailed info →
Standard

CCL4 protein levels

near MRM1 · rs9330240

See detailed info →

Showing 20 of 20582 · page 988 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.