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 110,847 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

GPA33 protein levels

BIVM-ERCC5 · rs61966043

See detailed info →
Standard

ADAMTS8 protein levels

ZBTB44 · rs61915097

See detailed info →
Standard

IGF 1 (UKB data field 30770)

near EED · rs61904289

See detailed info →
Standard

PAPPA protein levels

near PRG2 · rs61888916

See detailed info →
Standard

GLIPR1 protein levels

near AKR1C5P · rs587680093

See detailed info →
Standard

SCGB1A1 protein levels

near P3H2 · rs58312266

See detailed info →
Standard

GIMAP7 protein levels

near ALDH7A1P3 · rs577958186

See detailed info →
Standard

PCSK7 protein levels

near BUD13 · rs577035642

See detailed info →
Standard

GLIPR1 protein levels

near DDI2 · rs576035541

See detailed info →
Standard

MILR1 protein levels

near RPL31P57 · rs574735450

See detailed info →
Standard

GLIPR1 protein levels

near CFAP100-DT · rs570504160

See detailed info →
Standard

GLIPR1 protein levels

MACROD2 · rs566462617

See detailed info →
Standard

AGT protein levels

near SNRPD2P2 · rs563236016

See detailed info →
Standard

PON1 protein levels

PPP1R9A · rs561167305

See detailed info →
Standard

GLIPR1 protein levels

PLBD1 · rs560760440

See detailed info →
Standard

LILRA2 protein levels

NPAS2 · rs56044389

See detailed info →
Standard

GLIPR1 protein levels

near MLLT3 · rs559736252

See detailed info →
Standard

ADGRB3 protein levels

near ADGRB3 · rs559339345

See detailed info →
Standard

IL34 protein levels

HYDIN · rs557618123

See detailed info →
Standard

SERPINB8 protein levels

near SERPINB8 · rs556872466

See detailed info →

Showing 20 of 20581 · page 36 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.