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 117,690 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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KEL protein levels

near KEL · rs118063764

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Immature reticulocyte fraction (UKB data field 30280)

TTLL9 · rs11700068

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CYTL1 protein levels

near MSX1 · rs116521001

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PODXL protein levels

near RPUSD4 · rs11605334

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BCHE protein levels

near LINC01322 · rs115620280

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TFRC protein levels

UBXN7 · rs115160695

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ARSB protein levels

DMGDH · rs114447964

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Lymphocyte count (UKB data field 30120)

near TBC1D12 · rs112497462

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BCAM protein levels

DDX31 · rs112481484

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TACSTD2 protein levels

JUN-DT · rs112388692

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FCN2 protein levels

B3GNT6 · rs11237062

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DYNLT1 protein levels

ARHGEF3 · rs11130550

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PAMR1 protein levels

CD44 · rs11033008

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Monocyte percentage (UKB data field 30190)

near NCOA1 · rs10190597

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TNFSF13B protein levels

ATP6V1G2-DDX39B · rs9267487

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PLXDC1 protein levels

LRRC37A11P · rs78188373

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IL17RB protein levels

near CYCSP20 · rs7799991

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FUT8 protein levels

FGFR3P1 · rs7775117

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TGFBI protein levels

TGFBI · rs7723865

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VSTM1 protein levels

VSTM1 · rs76638738

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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.