Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,580 positions on this site are linked to Celiac Disease, out of 109,838 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

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

near CACNA2D3 · rs1458978

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Standard

VIT protein levels

STRN · rs145720518

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Standard

GLIPR1 protein levels

HPCAL1 · rs145647824

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Standard

GLIPR1 protein levels

XKR4 · rs145394085

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Standard

GRN protein levels

near PSAP · rs145123284

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Standard

CLEC1A protein levels

near OLR1 · rs144911919

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Standard

Apolipoprotein A levels (UKB data field 30630)

near INTS10 · rs144907154

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Standard

PIK3IP1 protein levels

SFI1 · rs144440001

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Standard

Impedance of arm left (UKB data field 23110)

near RNPC3-DT · rs144268600

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Standard

IFNGR2 protein levels

near LINC01548 · rs144076161

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Standard

TDRKH protein levels

near SELENBP1 · rs143764512

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Standard

CRISP3 protein levels

near RNU7-65P · rs143746475

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Standard

Platelet crit (UKB data field 30090)

ATXN2 · rs143423998

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Standard

ABO protein levels

near MYMK · rs143235471

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Standard

FGFBP2 protein levels

PROM1 · rs143196221

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Standard

High light scatter reticulocyte percentage (UKB data field 30290)

near SMOX · rs143125043

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Standard

ITGBL1 protein levels

FGF14 · rs143072050

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Standard

GALNT10 protein levels

MFAP3 · rs142677471

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Standard

IFI30 protein levels

KCNN1 · rs142319812

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

ARHGEF3 · rs142293866

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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.