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 110,511 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

GLIPR1 protein levels

near SLC16A14 · rs190742417

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NOMO1 protein levels

ABCC6 · rs190354733

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SCG3 protein levels

MAPK6 · rs189698618

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GLIPR1 protein levels

CREB3L1 · rs187528053

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CD200R1 protein levels

NECTIN3-AS1 · rs186378597

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MDGA1 protein levels

ZFAND3 · rs186186238

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GLIPR1 protein levels

EXT2 · rs185400560

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F13B protein levels

KCNT2 · rs185028083

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CFHR2 protein levels

CFH · rs184482827

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Platelet crit (UKB data field 30090)

RCL1 · rs182851782

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Monocyte percentage (UKB data field 30190)

near IRF8 · rs182321587

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SCARB2 protein levels

FAM47E · rs182113748

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CEACAM21 protein levels

near RN7SL718P · rs181473436

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QSOX1 protein levels

CEP350 · rs181098546

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SPON1 protein levels

SPON1 · rs181056763

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MMP10 protein levels

MMP1 · rs17879960

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B4GAT1 protein levels

CACNB2 · rs1757210

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IL34 protein levels

PDPR · rs150239000

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HMCN2 protein levels

HMCN2 · rs150120510

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CD300A protein levels

POC1B · rs149492467

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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.