Variants linked to Celiac Disease

Continuously updated · newest added Oct 22, 2026

20,580 positions on this site are linked to Celiac Disease, out of 108,620 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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SEMA3G protein levels

near SLC26A8 · rs12191244

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PGLYRP2 protein levels

BRD4 · rs117955143

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TACSTD2 protein levels

near TSPYL5 · rs117788373

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Impedance of arm right (UKB data field 23109)

SLIT3 · rs11740226

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CKAP4 protein levels

CKAP4 · rs117044974

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GALNT3 protein levels

SCN2A · rs116803598

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GSTM4 protein levels

near SARS1 · rs116645638

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TYRO3 protein levels

near ARHGEF28P1 · rs115524806

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CD27 protein levels

ZNF384 · rs113756914

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Neutrophill count (UKB data field 30140)

CLEC4M · rs113080783

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MANSC1 protein levels

DSTYK · rs11240373

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FCRL1 protein levels

near FCRL5 · rs111824950

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SLAMF1 protein levels

near SETP9 · rs111817279

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Platelet count (UKB data field 30080)

RNF115 · rs10797658

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ADAM8 protein levels

ALS2 · rs10211223

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Urate levels (UKB data field 30880)

near MIRLET7A1HG · rs10118003

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MEPE protein levels

near LINC03020 · rs10095629

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BTD protein levels

near GALNT15 · rs987858

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FOLR1 protein levels

GMNC · rs9838279

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PCDHB15 protein levels

SP110 · rs957682

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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.