Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,581 positions on this site are linked to Celiac Disease, out of 110,511 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

Platelet crit (UKB data field 30090)

near MYB · rs9321489

See detailed info →
Standard

PVR protein levels

PVR · rs139267469

See detailed info →
Standard

Mean corpuscular haemoglobin (UKB data field 30050)

MIR4435-2HG · rs2334233

See detailed info →
Standard

CTSV protein levels

CHPT1 · rs2559851

See detailed info →
Standard

PYDC1 protein levels

GC · rs705117

See detailed info →
Standard

ICAM2 protein levels

near ST3GAL6-AS1 · rs114321579

See detailed info →
Standard

FGA protein levels

near FGB · rs140473879

See detailed info →
Standard

RNASE1 protein levels

near RNASE1 · rs56216219

See detailed info →
Standard

HPSE protein levels

HPSE · rs61751211

See detailed info →
Standard

DSG4 protein levels

B4GALNT3 · rs2286782

See detailed info →
Standard

PODXL protein levels

near ABO · rs10901257

See detailed info →
Standard

Mean sphered cell volume (UKB data field 30270)

SPTB · rs2038433

See detailed info →
Standard

Monocyte percentage (UKB data field 30190)

NOL4L-DT · rs11699129

See detailed info →
Standard

CTSO protein levels

IGF2R · rs76778371

See detailed info →
Standard

ABO protein levels

ADAMTSL2 · rs28569945

See detailed info →
Standard

ZBTB16 protein levels

ZBTB16 · rs573195

See detailed info →
Standard

NID1 protein levels

near NID1 · rs76183323

See detailed info →
Standard

CXCL6 protein levels

near CXCL6 · rs181216093

See detailed info →
Standard

Haematocrit percentage (UKB data field 30030)

near CETP · rs12720917

See detailed info →
Standard

LGALS4 protein levels

ABO · rs78755596

See detailed info →

Showing 20 of 20581 · page 1016 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.