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 110,679 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

IGF2R protein levels

MAS1 · rs12207188

See detailed info →
Standard

CD302 protein levels

POLR1HASP · rs9260603

See detailed info →
Standard

ICAM2 protein levels

near RPL19P7 · rs74459479

See detailed info →
Standard

TFF1 protein levels

near GKN2 · rs12990985

See detailed info →
Standard

DNAJC6 protein levels

RFX2 · rs10418205

See detailed info →
Standard

ALCAM protein levels

near ABCC1 · rs12448760

See detailed info →
Standard

ACE protein levels

near PPIAP55 · rs185105129

See detailed info →
Standard

FOLR2 protein levels

MS4A14 · rs950803

See detailed info →
Standard

SLAMF7 protein levels

CD244 · rs115868021

See detailed info →
Standard

PLAUR protein levels

LY75-CD302 · rs72955755

See detailed info →
Standard

PGLYRP1 protein levels

PSMD3-AS1 · rs12450688

See detailed info →
Standard

COLEC12 protein levels

COLEC12 · rs55639531

See detailed info →
Standard

GGT5 protein levels

GGT5 · rs140980900

See detailed info →
Standard

NELL1 protein levels

LRP1 · rs141826184

See detailed info →
Standard

Mean corpuscular volume (UKB data field 30040)

USP49 · rs34718512

See detailed info →
Standard

DEFA1 or DEFA1B protein levels

HLA-DPA1 · rs3128959

See detailed info →
Standard

TSPAN8 protein levels

GPR39 · rs2241764

See detailed info →
Standard

TNFRSF19 protein levels

LINC00323 · rs62217923

See detailed info →
Standard

PRR4 protein levels

B3GNT3 · rs34262244

See detailed info →
Standard

NCAM1 protein levels

LINC00393 · rs1887646

See detailed info →

Showing 20 of 20581 · page 1015 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.