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

ICAM1 protein levels

ICAM1 · rs115766769

See detailed info →
Standard

Creatinine levels (UKB data field 30700)

SNUPN · rs113023713

See detailed info →
Standard

Eosinophill percentage (UKB data field 30210)

TSBP1 · rs112891419

See detailed info →
Standard

KLRD1 protein levels

PRR4 · rs111644153

See detailed info →
Standard

Lymphocyte count (UKB data field 30120)

POC1B · rs10777162

See detailed info →
Standard

CELSR2 protein levels

LINC02227 · rs10069648

See detailed info →
Standard

Mean corpuscular volume (UKB data field 30040)

LRRC78P · rs9755193

See detailed info →
Standard

Mean reticulocyte volume (UKB data field 30260)

GGT5 · rs9608253

See detailed info →
Standard

LCP1 protein levels

LRRC63 · rs9595454

See detailed info →
Standard

Lymphocyte percentage (UKB data field 30180)

LNCARSR · rs946806

See detailed info →
Standard

NFATC3 protein levels

TSBP1-AS1 · rs9268430

See detailed info →
Standard

CD6 protein levels

near RNU6-283P · rs9266522

See detailed info →
Standard

PTPRF protein levels

near LINC02571 · rs9264898

See detailed info →
Standard

PIK3AP1 protein levels

POLR1HASP · rs9260595

See detailed info →
Standard

CD300LF protein levels

IFITM2 · rs909097

See detailed info →
Standard

TIMP3 protein levels

LARGE1 · rs8139322

See detailed info →
Standard

NELL2 protein levels

near CD209 · rs8109492

See detailed info →
Standard

MYH9 protein levels

GP6-AS1 · rs8099942

See detailed info →
Standard

F3 protein levels

SLC44A3-AS1 · rs80237439

See detailed info →
Standard

DPT protein levels

LINC00970 · rs80080096

See detailed info →

Showing 20 of 20582 · page 161 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.