Variants linked to Celiac Disease

Continuously updated · newest added Oct 24, 2026

20,582 positions on this site are linked to Celiac Disease, out of 115,842 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

AGRN protein levels

near C1orf159 · rs149229450

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Standard

FCRL3 protein levels

near KIRREL1 · rs149011295

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Standard

GLIPR1 protein levels

near SRSF3P6 · rs148795359

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

TAOK1 · rs148379086

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Standard

STX7 protein levels

TAAR1 · rs148062999

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Standard

PROC protein levels

near CBFA2T2 · rs147460174

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Standard

HLA DRA protein levels

BRD2 · rs147269908

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Standard

PSAP protein levels

CDH23 · rs146781648

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Standard

GLIPR1 protein levels

near LINC02183 · rs146762438

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Standard

CA5A protein levels

near KLHDC4 · rs146741548

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Standard

Pulse rate (UKB data field 102)

PREP · rs146643077

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Standard

IL1R1 protein levels

COPG2 · rs145003280

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Standard

MSMB protein levels

MARCHF8 · rs144972605

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Standard

CD209 protein levels

near CD209 · rs144968292

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Standard

TGFBI protein levels

TGFBI · rs144900214

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Standard

GLIPR1 protein levels

LBX1-AS1 · rs144874650

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Standard

FASLG protein levels

FAS · rs144792567

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Standard

GLIPR1 protein levels

near LZTS1 · rs144715749

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Standard

IL7R protein levels

PRLR · rs144514645

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Standard

PTPRB protein levels

PTPRB-AS1 · rs144514589

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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.