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 118,294 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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Standard

TACSTD2 protein levels

MYSM1 · rs116375857

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Standard

ECM1 protein levels

near RN7SL480P · rs115911336

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Standard

CRLF1 protein levels

EGF · rs11568994

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Standard

HAVCR1 protein levels

ITK · rs113512645

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Standard

SPINK2 protein levels

near HOPX · rs113193015

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Standard

CFHR5 protein levels

near NEK7 · rs112250744

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Standard

Immature reticulocyte fraction (UKB data field 30280)

near OR9H1 · rs111942141

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

KDM2B · rs111556339

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Standard

Calcium levels (UKB data field 30680)

near FERRY3 · rs11063179

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Standard

DNPEP protein levels

near NIFKP3 · rs11054685

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Standard

COL15A1 protein levels

TGFBR1 · rs10988705

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Standard

TPMT protein levels

RNF144B · rs10949517

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Standard

Urate levels (UKB data field 30880)

ZKSCAN5 · rs10230784

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Standard

ENPP2 protein levels

CUX1 · rs9690066

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Standard

Basal metabolic rate (UKB data field 23105)

near ENTPD4-DT · rs9644077

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Standard

Gamma glutamyltransferase levels (UKB data field 30730)

NFKBIB · rs9636109

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Standard

PCDH17 protein levels

near RPP40P2 · rs9538365

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Standard

Eosinophill count (UKB data field 30150)

POLR1HASP · rs9261043

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Standard

CDKN1A protein levels

near GPR166P · rs80296862

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Standard

Lymphocyte count (UKB data field 30120)

EPS15L1 · rs79788231

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Showing 20 of 20582 · page 146 of 1030

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.