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 118,864 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

High light scatter reticulocyte percentage (UKB data field 30290)

near IQCF6 · rs73080676

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Standard

Mean corpuscular haemoglobin (UKB data field 30050)

AHI1 · rs72980205

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Standard

CLEC4M protein levels

AK8 · rs72759424

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Standard

CBLIF protein levels

MGAT1 · rs72650619

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Standard

TOR1AIP1 protein levels

LHX4 · rs71630257

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Standard

STXBP1 protein levels

ZNF79 · rs7035039

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Standard

PDGFRA protein levels

FIP1L1 · rs6833442

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

PTPRJ · rs61914723

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Standard

AFAP1 protein levels

SORCS2 · rs60232025

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Standard

PTPRH protein levels

SSC5D · rs59703635

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Standard

PINLYP protein levels

MS4A4A · rs58589035

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Standard

GYS1 protein levels

FAM167A-AS1 · rs58569413

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Standard

GLIPR1 protein levels

CASP8 · rs578158875

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Standard

SERPINA9 protein levels

near SERPINA1 · rs575810488

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Standard

TOR1AIP1 protein levels

RALGPS2 · rs575671452

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Standard

GLIPR1 protein levels

RGS2-AS1 · rs574145602

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Standard

Urate levels (UKB data field 30880)

FLRT1 · rs572740326

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Standard

Alkaline phosphatase (UKB data field 30610)

near NAP1L1P1 · rs571474

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Standard

FCRL3 protein levels

FCRL2 · rs569207310

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Standard

SPAG1 protein levels

SPAG1 · rs567738265

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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.