Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,581 positions on this site are linked to Celiac Disease, out of 110,679 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

PDCD1LG2 protein levels

DCBLD2 · rs138571278

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Standard

MEGF10 protein levels

VPS25P1 · rs12758626

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Standard

Mean sphered cell volume (UKB data field 30270)

near CD5L · rs12728978

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Standard

FCGR2A protein levels

near OLFML2B · rs12563944

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Standard

NUDT10 protein levels

near C1S · rs12366520

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Standard

Alkaline phosphatase (UKB data field 30610)

near SPTLC1P2 · rs12192336

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Standard

CRISP2 protein levels

near ADGRF1 · rs11967940

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

ZNF217-AS1 · rs11907600

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Standard

FAM171B protein levels

CALCRL-AS1 · rs11904848

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

SDCBP2 · rs117816499

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Standard

TMEM132A protein levels

near SLC15A3 · rs117695129

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Standard

KIR3DL1 protein levels

near LILRP1 · rs117173177

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Standard

Platelet count (UKB data field 30080)

SH2B3 · rs116869429

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Standard

CRHBP protein levels

WDR41 · rs114864585

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Standard

FGFR4 protein levels

near SUDS3P1 · rs113234961

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Standard

CD58 protein levels

PTPRF · rs1065771

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Standard

Mean reticulocyte volume (UKB data field 30260)

DOCK7 · rs10493326

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Standard

THBD protein levels

GOLIM4 · rs9813779

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Standard

SERPINB1 protein levels

near SERPINB9 · rs9501897

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Standard

CFP protein levels

near NOTCH4 · rs9267918

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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.