Variants linked to Celiac Disease

Continuously updated · newest added Oct 22, 2026

20,580 positions on this site are linked to Celiac Disease, out of 108,788 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

STAT6 · rs76522381

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Standard

Calcium levels (UKB data field 30680)

HNRNPA1P23 · rs76249487

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Standard

SIGLEC8 protein levels

near ZNF175 · rs761640763

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Standard

KLRD1 protein levels

near SLC25A39P2 · rs75884508

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Standard

MEGF9 protein levels

TRAF1 · rs75538425

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Standard

Mean reticulocyte volume (UKB data field 30260)

NOS1AP · rs7536043

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Standard

CDHR5 protein levels

near DUSP8 · rs75011109

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Standard

GLIPR1 protein levels

near PTCD2P2 · rs74985911

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Standard

FABP9 protein levels

CASC3 · rs74964489

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Standard

CTSH protein levels

LINGO1 · rs749567236

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Standard

OLR1 protein levels

near OR5BE1P · rs74799799

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Standard

AGXT protein levels

GPR35 · rs74270181

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Standard

Lymphocyte count (UKB data field 30120)

OARD1 · rs742495

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Standard

ECM1 protein levels

PLEKHO1 · rs74124334

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Standard

Neutrophill percentage (UKB data field 30200)

B3GNTL1 · rs7406268

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Standard

LILRB1 protein levels

near HLA-DOB · rs73739311

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Standard

Mean corpuscular volume (UKB data field 30040)

C2CD2L · rs72999357

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Standard

PSAP protein levels

near PSAP · rs72804049

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Standard

GDNF protein levels

WDR70 · rs72743175

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Standard

NBL1 protein levels

MICOS10-NBL1 · rs72656086

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Showing 20 of 20580 · page 9 of 1029

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.