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 117,186 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

LRRN1 protein levels

SUMF1 · rs187067536

See detailed info →
Standard

PDCD6 protein levels

AHRR · rs187007411

See detailed info →
Standard

GLIPR1 protein levels

ANKFN1 · rs186614287

See detailed info →
Standard

FCGR2A protein levels

ATF6 · rs186297020

See detailed info →
Standard

GLIPR1 protein levels

near MIR552 · rs185737243

See detailed info →
Standard

GLIPR1 protein levels

EYS · rs185214742

See detailed info →
Standard

WFDC12 protein levels

SEMG1 · rs184534879

See detailed info →
Standard

BST1 protein levels

CC2D2A · rs184088904

See detailed info →
Standard

TMPRSS5 protein levels

DRD2 · rs184060585

See detailed info →
Standard

GC protein levels

near GC · rs183901939

See detailed info →
Standard

CLEC4D protein levels

AICDA · rs183539950

See detailed info →
Standard

CELSR2 protein levels

WDR47 · rs183465195

See detailed info →
Standard

Mean corpuscular volume (UKB data field 30040)

near AHI1 · rs182878679

See detailed info →
Standard

CGREF1 protein levels

near DPYSL5 · rs182797402

See detailed info →
Standard

PRTG protein levels

ZNF280D · rs181694090

See detailed info →
Standard

F3 protein levels

SLC44A3-AS1 · rs181425910

See detailed info →
Standard

VWF protein levels

AK8 · rs181224696

See detailed info →
Standard

LRP11 protein levels

TAB2 · rs181134994

See detailed info →
Standard

CRISP2 protein levels

DEFB110 · rs180845231

See detailed info →
Standard

LY75 protein levels

near BAZ2B-AS1 · rs180789648

See detailed info →

Showing 20 of 20582 · page 125 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.