Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,581 positions on this site are linked to Celiac Disease, out of 110,049 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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Platelet count (UKB data field 30080)

RBMS2 · rs116924969

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CPVL protein levels

ALG1 · rs116891668

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ITGA2 protein levels

NDUFS4 · rs116818570

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ITGA5 protein levels

near FN1-DT · rs11678988

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GM2A protein levels

GM2A · rs116789293

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Lymphocyte count (UKB data field 30120)

PLD3 · rs11666860

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CXCL1 protein levels

near CXCL6 · rs116515151

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GLIPR1 protein levels

OBSCN · rs116347362

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NCAM1 protein levels

near NPM1P5 · rs11630088

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FLRT2 protein levels

near LINC02328 · rs11625375

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IGF 1 (UKB data field 30770)

near RESF1 · rs11611636

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AMPD3 protein levels

SBF2 · rs11604907

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Trunk fat mass (UKB data field 23128)

near JHY · rs11603783

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SCT protein levels

near MIR4686 · rs11603281

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SPINK5 protein levels

near SPINK5 · rs115834550

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CTSE protein levels

GOLT1A · rs11576112

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Alkaline phosphatase (UKB data field 30610)

ECE1 · rs115716053

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LRRC25 protein levels

GOLM1 · rs11559368

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IL17RA protein levels

ADA2 · rs115273803

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ENPP5 protein levels

PTCHD4 · rs115258611

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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.