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 118,864 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

KIRREL2 protein levels

near PGAP6 · rs148233424

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Standard

FUCA1 protein levels

EEF1A1P48 · rs148102454

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Standard

FGL1 protein levels

MTUS1-DT · rs147569921

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Standard

FAM171B protein levels

LINC01473 · rs147312753

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Standard

PCDHB15 protein levels

PCDHB14 · rs145769211

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Standard

GPC5 protein levels

LINC00379 · rs145194592

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Standard

Alkaline phosphatase (UKB data field 30610)

PRSS55 · rs144943733

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Standard

IL34 protein levels

PHLPP2 · rs144818546

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Standard

IL17D protein levels

IFT88 · rs144621025

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Standard

LILRB1 protein levels

near H4C5 · rs144462190

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Standard

GALNT3 protein levels

SCN1A · rs144134844

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Standard

LY6D protein levels

near LY6D · rs143839725

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Standard

Gamma glutamyltransferase levels (UKB data field 30730)

MARK3 · rs143574994

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

NOL4L · rs143458646

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Standard

Mean reticulocyte volume (UKB data field 30260)

FBXW4 · rs143263487

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Standard

CRYGD protein levels

ZNF813 · rs143093299

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Standard

PCDHB15 protein levels

TAF7 · rs142607585

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Standard

Platelet crit (UKB data field 30090)

ATXN2 · rs140820516

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Standard

CSTB protein levels

GATD3 · rs140713369

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Standard

KITLG protein levels

CD40 · rs139401012

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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.