Variants linked to Celiac Disease

Continuously updated · newest added Oct 22, 2026

20,580 positions on this site are linked to Celiac Disease, out of 108,452 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

CFP protein levels

C3 · rs147859257

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Standard

RNASE6 protein levels

METTL17 · rs147069902

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

near ART2BP · rs145864192

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Standard

AFP protein levels

NSMCE3 · rs145058546

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Standard

PDCD5 protein levels

DPY19L3 · rs143976902

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Standard

TSPAN8 protein levels

TSPAN8 · rs143621199

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Standard

KLK1 protein levels

C19orf48P · rs143534987

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Standard

NAAA protein levels

UTP20 · rs143470856

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Standard

PENK protein levels

near CHCHD7 · rs142865918

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Standard

CXCL12 protein levels

LINC00840 · rs142691515

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Standard

CCL23 protein levels

CCL14 · rs142032662

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Standard

TXNDC15 protein levels

CDKN2AIPNL · rs141449831

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Standard

SLITRK6 protein levels

near SLITRK6 · rs139714614

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Standard

CD300E protein levels

CD300LD-AS1 · rs138343633

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Standard

Platelet distribution width (UKB data field 30110)

near RRP7A · rs138160110

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Standard

PILRB protein levels

near RNU6-393P · rs137925042

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Standard

Creatinine levels (UKB data field 30700)

near LINC01991 · rs13069721

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Standard

GALNT3 protein levels

SCN3A · rs13011459

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Standard

PHACTR2 protein levels

PHACTR2 · rs12527367

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Standard

CPA4 protein levels

near AREG · rs1246411

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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.