Variants linked to Celiac Disease

Continuously updated · newest added Oct 24, 2026

20,582 positions on this site are linked to Celiac Disease, out of 115,254 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

GLIPR1 protein levels

near LINC01925 · rs538335991

See detailed info →
Standard

KLK1 protein levels

near RNU6-317P · rs537198000

See detailed info →
Standard

PNLIPRP2 protein levels

near PNLIPRP2 · rs535709001

See detailed info →
Standard

GLIPR1 protein levels

near ARL2BPP3 · rs535234392

See detailed info →
Standard

GLIPR1 protein levels

CYP2AB1P · rs531327448

See detailed info →
Standard

IL17RB protein levels

CACNA1D · rs531100596

See detailed info →
Standard

NELL2 protein levels

ANO6 · rs530927231

See detailed info →
Sensitive

Takes medication for celiac disease/sprue?

near DDX59-AS1 · rs530510527

See detailed info →
Standard

GLIPR1 protein levels

TBC1D19 · rs530336726

See detailed info →
Standard

SERPINA9 protein levels

near SERPINA11 · rs530141464

See detailed info →
Standard

SDCCAG8 protein levels

near SEPTIN14P21 · rs529258134

See detailed info →
Standard

IGFBP3 protein levels

ADCY1 · rs529162863

See detailed info →
Standard

CSF3 protein levels

near CSF3R · rs529033484

See detailed info →
Standard

GLIPR1 protein levels

near ATP6V0E1P4 · rs528492691

See detailed info →
Standard

SEMA3G protein levels

SLC26A8 · rs528129103

See detailed info →
Standard

PSAPL1 protein levels

SORCS2 · rs527891677

See detailed info →
Standard

COL5A1 protein levels

FLI1 · rs519913

See detailed info →
Standard

REG3A protein levels

TBXAS1 · rs4725857

See detailed info →
Standard

Urate levels (UKB data field 30880)

HS3ST1 · rs4697886

See detailed info →
Standard

FCGR3B protein levels

near RHBDF2 · rs4647859

See detailed info →

Showing 20 of 20582 · page 100 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.