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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RTN4IP1 protein levels

QRSL1 · rs2054365

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Haematocrit percentage (UKB data field 30030)

CETP · rs181381869

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MICB or MICA protein levels

near HLA-DQB2 · rs149109754

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FLT4 protein levels

near WWP1P1 · rs79243979

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C2 protein levels

near MTCO3P1 · rs41288885

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CLEC11A protein levels

near GPR32P1 · rs1975032

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CDH5 protein levels

ADAMTSL2 · rs187182154

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IL12B protein levels

IL12B-AS1 · rs151160735

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FAM3D protein levels

near GBGT1 · rs140167248

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IL18 protein levels

NAIP · rs115486998

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MLN protein levels

ITPR3 · rs77770551

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MICB or MICA protein levels

TAP2 · rs10484565

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FGFBP2 protein levels

near LINC01482 · rs569449632

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SLAMF1 protein levels

near SLAMF6 · rs9726326

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MILR1 protein levels

DDX42 · rs7220095

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Trunk fat mass (UKB data field 23128)

near MC4R · rs79566431

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LILRB4 protein levels

SKIC2 · rs492899

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CLPS protein levels

near SLC26A8 · rs150916167

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Haemoglobin concentration (UKB data field 30020)

PRKCE · rs7598174

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CFHR4 protein levels

CFHR5 · rs12097550

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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.