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

PINLYP protein levels

near CD177P1 · rs1806750

See detailed info →
Standard

LEG1 protein levels

MGAT5 · rs17764739

See detailed info →
Standard

GHRL protein levels

VPS13C · rs17271193

See detailed info →
Standard

LRPAP1 protein levels

HCG20 · rs17195733

See detailed info →
Standard

TCL1A protein levels

SYNE3 · rs17092581

See detailed info →
Standard

Arm fat percentage left (UKB data field 23123)

near LINC02227 · rs17055814

See detailed info →
Standard

CD300LF protein levels

TMEM104 · rs149794871

See detailed info →
Standard

Triglyceride levels (UKB data field 30870)

near TRIB1AL · rs149719228

See detailed info →
Standard

GLIPR1 protein levels

near Y_RNA · rs149533933

See detailed info →
Standard

RNASET2 protein levels

near CCR6 · rs149498891

See detailed info →
Standard

TIMP3 protein levels

SYN3 · rs148899787

See detailed info →
Standard

HDDC2 protein levels

near HDDC2 · rs148504917

See detailed info →
Standard

CD109 protein levels

ABO · rs148031614

See detailed info →
Standard

TNFRSF1B protein levels

IAH1 · rs147722775

See detailed info →
Standard

CD300LF protein levels

EXOC7 · rs147214267

See detailed info →
Standard

SMPDL3A protein levels

GNPTAB · rs146019182

See detailed info →
Standard

IFNGR2 protein levels

LINC00945 · rs144864589

See detailed info →
Standard

IFNAR1 protein levels

TYK2 · rs143495504

See detailed info →
Standard

TLR1 protein levels

near TMEM156 · rs143324467

See detailed info →
Standard

Red blood cell erythrocyte distribution width (UKB data field 30070)

near POU4F3 · rs1432952

See detailed info →

Showing 20 of 20582 · page 159 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.