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 116,598 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

CPB2 protein levels

near SIAH3 · rs73179218

See detailed info →
Standard

CCL25 protein levels

CYTH2 · rs73050914

See detailed info →
Standard

Lymphocyte percentage (UKB data field 30180)

GLCCI1 · rs73049256

See detailed info →
Standard

GLO1 protein levels

BTBD9 · rs72851404

See detailed info →
Standard

HSBP1 protein levels

CDH13 · rs72793418

See detailed info →
Standard

IL4R protein levels

IL4R · rs72782399

See detailed info →
Standard

Mean corpuscular haemoglobin (UKB data field 30050)

near POT1 · rs727505

See detailed info →
Standard

SLAMF7 protein levels

near MPZ · rs72714960

See detailed info →
Standard

AMY2A protein levels

THAP3P1 · rs72689196

See detailed info →
Standard

ITGBL1 protein levels

ITGBL1 · rs72659186

See detailed info →
Standard

CFHR4 protein levels

near ATP6V1G3 · rs72644145

See detailed info →
Standard

CFP protein levels

ENTPD1-AS1 · rs7077566

See detailed info →
Standard

CSPG4 protein levels

SLC45A4 · rs6983780

See detailed info →
Standard

Peak expiratory flow (UKB data field 3064)

CASC15 · rs6904682

See detailed info →
Standard

TNR protein levels

ZNF366 · rs6888856

See detailed info →
Standard

DCTD protein levels

near CIBAR1P2 · rs6552631

See detailed info →
Standard

PLB1 protein levels

near CDKN2AIPNLP2 · rs6547247

See detailed info →
Standard

LEFTY2 protein levels

UMOD · rs6497475

See detailed info →
Standard

AIF1L protein levels

NUP214 · rs62580390

See detailed info →
Standard

IGF 1 (UKB data field 30770)

near TACR3 · rs62342064

See detailed info →

Showing 20 of 20582 · page 117 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.