Variants linked to Celiac Disease

Continuously updated · newest added Oct 24, 2026

20,582 positions on this site are linked to Celiac Disease, out of 113,826 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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SERPINI2 protein levels

near GFI1B · rs7030544

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Calcium levels (UKB data field 30680)

near RPL30P3 · rs6717614

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BDNF protein levels

PEAR1 · rs6671171

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Haematocrit percentage (UKB data field 30030)

GALNT2 · rs6541284

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OSMR protein levels

EGFLAM · rs62353647

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HBZ protein levels

MIR4432HG · rs62144672

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VSIG10 protein levels

VSIG10 · rs61943489

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PROCR protein levels

MMP24OS · rs6058206

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SUSD2 protein levels

SGSM1 · rs6004301

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TMPRSS5 protein levels

near CARD10 · rs6000766

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GLIPR1 protein levels

RPRD2 · rs587662030

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MDGA1 protein levels

ZFAND3 · rs576880607

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GLIPR1 protein levels

NDUFAF6 · rs576154258

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TNFRSF10C protein levels

near TTLL12 · rs5751444

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LRRN1 protein levels

SUMF1 · rs574173016

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GLIPR1 protein levels

GABPA · rs574008456

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SIRPA protein levels

near CKAP2LP1 · rs573843022

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Immature reticulocyte fraction (UKB data field 30280)

OR14A2 · rs573723364

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GLIPR1 protein levels

ASCC3 · rs573658295

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Lipoprotein A levels (UKB data field 30790)

WTAP · rs573550973

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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.