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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Apolipoprotein A levels (UKB data field 30630)

LIPC-AS1 · rs192828174

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VNN2 protein levels

near MOXD1 · rs192604223

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TNC protein levels

near NUGGC · rs192503259

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TGFBI protein levels

near LECT2 · rs191708170

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PNLIPRP2 protein levels

near SLC18A2-AS1 · rs191644653

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Lipoprotein A levels (UKB data field 30790)

LINC02901 · rs189685014

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GPR37 protein levels

near SSU72L6 · rs189559591

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ROR1 protein levels

ROR1 · rs189033155

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LHPP protein levels

LHPP · rs188738583

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GLIPR1 protein levels

near NIBAN1 · rs188562472

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MUC2 protein levels

TC2N · rs1884841

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GLIPR1 protein levels

near LINC00867 · rs188013808

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BTD protein levels

near GALNT15 · rs185171146

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LAYN protein levels

ALG9 · rs183706534

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Platelet crit (UKB data field 30090)

near MCAM · rs182494271

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NAPRT protein levels

near ZNF696 · rs182458703

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GALNT3 protein levels

near GALNT3 · rs182293213

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PILRB protein levels

NYAP1 · rs181839139

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CEACAM21 protein levels

CEACAM21 · rs181602484

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SIGLEC10 protein levels

near SIGLEC8 · rs180826286

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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.