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 131,364 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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Standard

Lymphocyte count (UKB data field 30120)

RASA3 · rs56023786

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Standard

SPINK4 protein levels

SMU1 · rs560214022

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Standard

Urate levels (UKB data field 30880)

CARMIL1 · rs55917698

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Standard

PM20D1 protein levels

LEMD1 · rs55916208

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Standard

GLIPR1 protein levels

TENT5A · rs556344842

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Standard

KLK10 protein levels

KLK10 · rs554122041

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Standard

CLEC6A protein levels

MFAP5 · rs552513581

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Standard

FUT8 protein levels

near FUT8 · rs551609499

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Standard

LPA protein levels

LPAL2 · rs551188427

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Standard

GLIPR1 protein levels

LINC01376 · rs548852870

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Standard

GLIPR1 protein levels

AGBL4 · rs547705894

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Standard

PON1 protein levels

PPP1R9A · rs546577278

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Standard

CXCL6 protein levels

ANKRD17 · rs543982605

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Standard

INHBC protein levels

SHMT2 · rs543672180

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

near TASOR · rs543547362

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Standard

TREH protein levels

IFT46 · rs541229939

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Standard

F12 protein levels

ZNF346 · rs541035816

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Standard

PNLIPRP2 protein levels

PNLIPRP2 · rs540767115

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Standard

Mean corpuscular haemoglobin (UKB data field 30050)

CIMIP4 · rs539673178

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Standard

GLIPR1 protein levels

COPS8-DT · rs535080683

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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.