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 118,864 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

SNX15 protein levels

CARNS1 · rs56389755

See detailed info →
Standard

GLIPR1 protein levels

LINC01818 · rs56356459

See detailed info →
Standard

CD300LF protein levels

HID1 · rs561282132

See detailed info →
Standard

GLIPR1 protein levels

near RPL35AP11 · rs560457449

See detailed info →
Standard

GLIPR1 protein levels

near RPL35AP22 · rs560009324

See detailed info →
Standard

GLIPR1 protein levels

DGCR5 · rs557597283

See detailed info →
Standard

ITGB7 protein levels

ITGAE · rs551820103

See detailed info →
Standard

LGALS8 protein levels

LGALS8-AS1 · rs550734969

See detailed info →
Standard

TNXB protein levels

TNXB · rs545295609

See detailed info →
Standard

GLIPR1 protein levels

near OR52M1 · rs545217172

See detailed info →
Standard

GLIPR1 protein levels

TIAM2 · rs544766632

See detailed info →
Standard

GLIPR1 protein levels

PGRMC2 · rs543163029

See detailed info →
Standard

GLIPR1 protein levels

LINC02177 · rs541619090

See detailed info →
Standard

PINLYP protein levels

CD177P1 · rs541117269

See detailed info →
Standard

GLIPR1 protein levels

LINC00276 · rs538970708

See detailed info →
Standard

GLIPR1 protein levels

near LINC01179 · rs535985675

See detailed info →
Standard

CTSH protein levels

near CRABP1 · rs535307686

See detailed info →
Standard

CSF2RB protein levels

NCF4 · rs532588816

See detailed info →
Standard

GLIPR1 protein levels

SLC35F3 · rs532298969

See detailed info →
Standard

CLSTN2 protein levels

near TRMT112P5 · rs530949872

See detailed info →

Showing 20 of 20582 · page 156 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.