Variants linked to Celiac Disease

Continuously updated · newest added Oct 26, 2026

20,582 positions on this site are linked to Celiac Disease, out of 119,364 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

Haemoglobin concentration (UKB data field 30020)

near LINC02537 · rs12660375

See detailed info →
Standard

CD6 protein levels

MVB12A · rs10406088

See detailed info →
Standard

ADAMTS13 protein levels

LNPEP · rs27291

See detailed info →
Standard

Haematocrit percentage (UKB data field 30030)

NUP93 · rs540077191

See detailed info →
Standard

IL12B protein levels

LPP · rs116392971

See detailed info →
Standard

RGMA protein levels

TPM2 · rs2789750

See detailed info →
Standard

DSG4 protein levels

WNT3 · rs199528

See detailed info →
Standard

CST5 protein levels

near CSTP1 · rs145856484

See detailed info →
Standard

CCN5 protein levels

KCNK15-AS1 · rs61011644

See detailed info →
Standard

TGFA protein levels

PSMD3 · rs4795412

See detailed info →
Standard

SEMA3G protein levels

CDH23 · rs4747199

See detailed info →
Standard

SEPTIN3 protein levels

ELL2 · rs6890954

See detailed info →
Standard

PLXNA4 protein levels

PLXNA4 · rs6467443

See detailed info →
Standard

FLT4 protein levels

near WWP1P1 · rs4378915

See detailed info →
Standard

SERPINA11 protein levels

MYPOP · rs12976652

See detailed info →
Standard

GPC5 protein levels

near MIR17HG · rs16945768

See detailed info →
Standard

LTA protein levels

near LINC02571 · rs117298325

See detailed info →
Standard

ICAM5 protein levels

S1PR2 · rs7246367

See detailed info →
Standard

Total protein levels (UKB data field 30860)

RPL13A · rs12985239

See detailed info →
Standard

CD160 protein levels

near LINC02725 · rs482246

See detailed info →

Showing 20 of 20582 · page 972 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.