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 118,042 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

PSAPL1 protein levels

RHBDF2 · rs62085058

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Standard

IGF 1 (UKB data field 30770)

EIF4G3 · rs61781099

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LCP1 protein levels

near LINC01198 · rs578151302

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SNCG protein levels

WAPL · rs576511427

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TFRC protein levels

UBXN7 · rs573927306

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HLA A protein levels

near H2BC14 · rs573545584

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Platelet crit (UKB data field 30090)

RPH3A · rs568027852

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CHRDL2 protein levels

POLD3 · rs567180256

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

SDF2 · rs565038522

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GLIPR1 protein levels

CXADR · rs564747473

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PRR4 protein levels

PRR4 · rs563262154

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GLIPR1 protein levels

ATOSA · rs562881779

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GLIPR1 protein levels

near TSPAN19 · rs562763018

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GLIPR1 protein levels

LINC00922 · rs560493697

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NCR3LG1 protein levels

NUCB2 · rs559087735

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SHMT1 protein levels

near LGALS9C · rs551297983

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ADAM15 protein levels

DAP3 · rs549525988

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MFAP4 protein levels

SLC47A1 · rs546115820

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CST7 protein levels

near LINC02967 · rs545157740

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Standard

GLIPR1 protein levels

RGS2-AS1 · rs541904313

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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.