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 112,359 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

HGFAC protein levels

FAM193A · rs142467211

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Standard

SPARCL1 protein levels

ARHGAP24 · rs141979424

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Standard

GLO1 protein levels

near ZFAND3-DT · rs141080514

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Standard

SPARCL1 protein levels

HSD17B11 · rs141076398

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Standard

PON1 protein levels

PPP1R9A · rs140326266

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Standard

GLIPR1 protein levels

TRPM3 · rs139726937

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Standard

CPA4 protein levels

CPA4 · rs139700037

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

near RBM38 · rs138749250

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Standard

GLIPR1 protein levels

PCDH15 · rs138672622

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Standard

ARSA protein levels

MAPK8IP2 · rs138520389

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Standard

CD101 protein levels

near Metazoa_SRP · rs138335586

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Standard

TNFRSF11B protein levels

SAMD12-AS1 · rs13274424

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Standard

Mean reticulocyte volume (UKB data field 30260)

near CDCA7 · rs13006456

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Standard

IGF 1 (UKB data field 30770)

XYLT1 · rs12935465

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Standard

FUT8 protein levels

SYNE2 · rs12883524

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Standard

Red blood cell erythrocyte distribution width (UKB data field 30070)

near DAGLB · rs12702503

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Standard

SMOC1 protein levels

near RNU1-70P · rs12496506

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Standard

Leg fat percentage right (UKB data field 23111)

near GADD45G · rs12339822

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Standard

IGFBPL1 protein levels

near U8 · rs12235833

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Standard

ERMAP protein levels

near YRDCP3 · rs12106351

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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.