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 117,186 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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SERPINA11 protein levels

SERPINA5 · rs17753261

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Leg fat percentage right (UKB data field 23111)

ZBTB20 · rs17685222

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C1QTNF9 protein levels

near HLA-DQB1 · rs17205886

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PTPRM protein levels

CFAP77 · rs17149282

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VCAN protein levels

PXYLP1 · rs16851191

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ENDOU protein levels

near LMTK3 · rs1643494

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Aspartate aminotransferase levels (UKB data field 30650)

HLA-H · rs1611464

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SULT2A1 protein levels

near VSTM5 · rs1573567

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GM2A protein levels

GM2A · rs151286974

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PON1 protein levels

PPP1R9A · rs151225924

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SMPDL3A protein levels

SMPDL3A · rs150818386

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SNCG protein levels

GRID1 · rs150809249

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GLIPR1 protein levels

IL7 · rs149759353

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CDHR5 protein levels

DEAF1 · rs149498490

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GLIPR1 protein levels

GBX2-AS1 · rs149261166

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SMOC2 protein levels

SMOC2 · rs149250393

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Eosinophill percentage (UKB data field 30210)

TMEM182 · rs149243557

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CBLN4 protein levels

near CBLN4 · rs149181323

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CD109 protein levels

CD109 · rs149134447

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MICB or MICA protein levels

near OR5V1 · rs148250332

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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.