Variants linked to Celiac Disease

Continuously updated · newest added Oct 24, 2026

20,582 positions on this site are linked to Celiac Disease, out of 114,834 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

CPA2 protein levels

near CPA4 · rs77283237

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Standard

ERMAP protein levels

BACE2 · rs76880931

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Standard

ATRN protein levels

PTPRA · rs765688128

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Standard

SIRPB1 protein levels

near SIRPB3P · rs764738917

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Standard

PTPRH protein levels

near TMEM86B · rs76396579

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Standard

RGMA protein levels

RGMA · rs76069502

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Standard

ASRGL1 protein levels

FTH1 · rs76059597

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Standard

CASP8 protein levels

STRADB · rs75850762

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Standard

MFGE8 protein levels

near LPL · rs75835816

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Standard

PNLIPRP2 protein levels

HSPA12A · rs75572469

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Standard

CPVL protein levels

CHN2 · rs755624627

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Standard

LRRC25 protein levels

KANSL1 · rs75449579

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Standard

ANXA2 protein levels

near FOXB1 · rs75225982

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

near COX6CP2 · rs75133182

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

SELENON · rs7513196

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Standard

Creatinine levels (UKB data field 30700)

PPP6R2 · rs7511047

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Standard

GALNT3 protein levels

TTC21B · rs74447004

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Standard

MUC2 protein levels

FER1L6 · rs74403458

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Standard

Neutrophill count (UKB data field 30140)

near ATP6V0D2 · rs74323915

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Standard

Lymphocyte count (UKB data field 30120)

LINC03002 · rs73775366

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Showing 20 of 20582 · page 94 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.