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 117,790 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

Pulse rate (UKB data field 102)

RFT1 · rs7645611

See detailed info →
Standard

PGLYRP4 protein levels

GATAD2B · rs75864455

See detailed info →
Standard

Reticulocyte count (UKB data field 30250)

CARMIL1 · rs73734011

See detailed info →
Standard

SMPD1 protein levels

near BNIP1 · rs72816168

See detailed info →
Standard

CA3 protein levels

near REXO1L8P · rs7002221

See detailed info →
Standard

Mean sphered cell volume (UKB data field 30270)

BRD2 · rs620202

See detailed info →
Standard

CD6 protein levels

near PGA3 · rs61899463

See detailed info →
Standard

FOLR3 protein levels

GCNT2 · rs597697

See detailed info →
Standard

FLT4 protein levels

near RPL19P7 · rs577988435

See detailed info →
Standard

GLIPR1 protein levels

LIMASI · rs571132541

See detailed info →
Standard

SIRPA protein levels

SIRPA · rs562732426

See detailed info →
Standard

GLIPR1 protein levels

HLCS · rs558350758

See detailed info →
Standard

GLIPR1 protein levels

near EDN1 · rs555352209

See detailed info →
Standard

GFRAL protein levels

COL21A1 · rs551489368

See detailed info →
Standard

Haematocrit percentage (UKB data field 30030)

SLC12A3 · rs551114142

See detailed info →
Standard

MPI protein levels

THSD4 · rs549767941

See detailed info →
Standard

CDNF protein levels

FAM171A1 · rs549652490

See detailed info →
Standard

IGFBP3 protein levels

near TTC4P1 · rs549297536

See detailed info →
Standard

GLIPR1 protein levels

near MTCYBP36 · rs547557575

See detailed info →
Standard

GLIPR1 protein levels

CRACDL · rs538995720

See detailed info →

Showing 20 of 20582 · page 137 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.