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.

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VIT protein levels

VIT · rs139300543

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LY6D protein levels

near GML · rs138823042

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IL32 protein levels

ZNF816-ZNF321P · rs138017999

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Platelet count (UKB data field 30080)

DYNC1H1 · rs13749

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Lymphocyte count (UKB data field 30120)

PEBP4 · rs13275018

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GLIPR1 protein levels

EYS · rs13213455

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MELTF protein levels

BDH1 · rs13088613

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DYNLT1 protein levels

OR2L5 · rs12753585

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APOBR protein levels

GSG1L · rs12444488

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FCGR2A protein levels

near RNU6-481P · rs12141690

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GP1BB protein levels

near PNRC2P1 · rs12081886

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CLEC4C protein levels

near NIFKP3 · rs118176172

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TNFRSF11B protein levels

SAMD12-AS1 · rs118076946

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PRSS53 protein levels

ARMC5 · rs117947985

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Apolipoprotein A levels (UKB data field 30630)

SIK3 · rs117892218

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Neutrophill count (UKB data field 30140)

near ATP5F1EP2 · rs117808697

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AFP protein levels

ARL10 · rs11744825

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Impedance of whole body (UKB data field 23106)

EBF1 · rs11741461

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CNTN5 protein levels

CNTN5 · rs117365839

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LGALS1 protein levels

TRIOBP · rs117262262

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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.