Variants linked to Celiac Disease

Continuously updated · newest added Oct 26, 2026

20,582 positions on this site are linked to Celiac Disease, out of 134,364 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

Strength of the evidence: all 2+ 3+ 4

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TGFBR3 protein levels

ADAMTS5 · rs16979423

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ITGB6 protein levels

near NOTCH1 · rs13295248

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CD101 protein levels

near ATP5MC1P7 · rs10998778

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Impedance of arm left (UKB data field 23110)

RBM6 · rs377609499

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GUSB protein levels

CHPT1 · rs74692062

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GDF2 protein levels

IARS1 · rs559813290

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LILRB5 protein levels

near LILRA5 · rs188240454

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Glucose levels (UKB data field 30740)

SPC25 · rs146779637

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PON2 protein levels

PDK4-AS1 · rs145452862

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SERPINI2 protein levels

near GBGT1 · rs60526253

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F12 protein levels

LMAN2 · rs574659363

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LILRB5 protein levels

LILRB2 · rs140268965

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DYNLT1 protein levels

TRIM58 · rs116559617

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HEPACAM2 protein levels

ST6GAL1 · rs113395872

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PSPN protein levels

PDE3A · rs10841569

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CD46 protein levels

near TSPAN15 · rs972570

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LILRA3 protein levels

LILRA4 · rs56374127

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Haematocrit percentage (UKB data field 30030)

HERPUD1 · rs113286621

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GFRA2 protein levels

near MTCO3P1 · rs9275580

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PLA2G10 protein levels

H1-1 · rs34877685

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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.