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 113,531 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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Standard

GLIPR1 protein levels

NAALADL2 · rs528826089

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Standard

TRAF3 protein levels

HLA-DQA1 · rs527732063

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Standard

CPVL protein levels

near CYP4V2 · rs4861707

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

near NUP35 · rs4666887

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Standard

TIMD4 protein levels

near TRIM48 · rs4601804

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Standard

COL28A1 protein levels

near EVA1CP3 · rs4476911

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Standard

SMPDL3A protein levels

near RPL23AP48 · rs4464831

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Standard

Platelet crit (UKB data field 30090)

SLC67A1 · rs386111

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Standard

LRP11 protein levels

near RAET1L · rs35037735

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Standard

SPRR3 protein levels

near LCE6A · rs34879209

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Standard

Total bilirubin levels (UKB data field 30840)

near RNU6ATAC · rs34755157

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Standard

Mean reticulocyte volume (UKB data field 30260)

WAC · rs332141

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Standard

TIMD4 protein levels

near IFNGR1 · rs2797670

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Standard

Lymphocyte percentage (UKB data field 30180)

DAP · rs267945

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Standard

MEGF10 protein levels

ROS1 · rs210966

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Standard

TNFRSF9 protein levels

CAMTA1 · rs1986198

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Standard

IL6R protein levels

near ADAR · rs191520357

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Standard

GLIPR1 protein levels

RALYL · rs191234927

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Standard

Direct low density lipoprotein levels (UKB data field 30780)

MARK4 · rs190994764

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Standard

FOLR2 protein levels

near CCDC150 · rs190974050

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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.