Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,582 positions on this site are linked to Celiac Disease, out of 111,519 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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MEP1A protein levels

ABO · rs13291798

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PYY protein levels

BCL2 · rs72943036

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TGFBR3 protein levels

UMOD · rs13333226

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Forced expiratory volume in 1 second FEV1 Z score (UKB data field 20256)

near U3 · rs7517716

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Whole body water mass (UKB data field 23102)

ARID5B · rs68156080

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Reticulocyte percentage (UKB data field 30240)

PANK2-AS1 · rs6052139

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SNAP25 protein levels

CLASRP · rs553008235

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HBEGF protein levels

RUNX1 · rs11700551

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RILP protein levels

near NLRP6 · rs58512066

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Mean corpuscular haemoglobin (UKB data field 30050)

JAK2 · rs73393498

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PLA2G7 protein levels

near LPA · rs374071816

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ALPP protein levels

near ABO · rs7030248

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CHIT1 protein levels

LINC02929 · rs2893907

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OLFM4 protein levels

KCNJ15 · rs9305635

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NT5C3A protein levels

CARINH · rs11951091

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CCL18 protein levels

near MAFB · rs56206139

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CCL8 protein levels

CADM3 · rs2746041

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SERPINI2 protein levels

GFI1B · rs78218908

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FLT1 protein levels

near OBP2B · rs7023066

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PNLIPRP1 protein levels

SORBS2 · rs11724862

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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.