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 115,758 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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PTPRH protein levels

RDH13 · rs1654446

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LPO protein levels

near RNA5SP94 · rs155568

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VWC2 protein levels

near DDX43P2 · rs151323932

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GLIPR1 protein levels

RFWD3 · rs151148478

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CCN3 protein levels

COLEC10 · rs151034823

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UBE2L6 protein levels

ZDHHC5 · rs150928534

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CCL3 protein levels

SLFN12L · rs150907804

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AXIN1 protein levels

AXIN1 · rs150847929

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Mean sphered cell volume (UKB data field 30270)

near SLC20A2 · rs150747022

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PBLD protein levels

CTNNA3 · rs150628384

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PALM protein levels

near CAPN8 · rs150394890

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Monocyte percentage (UKB data field 30190)

near ECPAS · rs150360581

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MPO protein levels

USP32 · rs150205652

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CEACAM21 protein levels

near CEACAM6 · rs150127461

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MATN3 protein levels

WDR35 · rs150080038

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PRG3 protein levels

SLC43A3 · rs149820828

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SUSD4 protein levels

near SUSD4 · rs149727351

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IL17RB protein levels

CACNA1D · rs149607505

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TMEM106A protein levels

DMXL2 · rs149605042

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AIF1 protein levels

near HLA-DQB2 · rs149548865

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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.