Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,580 positions on this site are linked to Celiac Disease, out of 110,006 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

GLIPR1 protein levels

near SMARCE1 · rs142225540

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ENPP5 protein levels

CYP39A1 · rs141566557

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Mean corpuscular volume (UKB data field 30040)

DDC · rs141421210

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NMI protein levels

near FABP5P10 · rs141096755

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PRTG protein levels

PRTG · rs140985611

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SEMA3G protein levels

SLC26A8 · rs140674756

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CPB2 protein levels

LCP1 · rs140642876

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PALM2 protein levels

PALM2AKAP2 · rs140463474

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IL1RL1 protein levels

RFX8 · rs140330695

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GLIPR1 protein levels

near RN7SKP120 · rs140154972

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CTRB1 protein levels

near RPL18P13 · rs140073569

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PCDHB15 protein levels

NRG2 · rs139934873

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QDPR protein levels

near RPS7P6 · rs139922615

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F12 protein levels

NSD1 · rs139601377

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KLRB1 protein levels

near KLRB1 · rs139487897

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KLRF1 protein levels

KLRF1 · rs139455560

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RELT protein levels

FCHSD2 · rs139395844

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Platelet distribution width (UKB data field 30110)

near NINJ2-AS1 · rs139313514

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FRZB protein levels

near NCKAP1 · rs139240008

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SEMA7A protein levels

near LINC02255 · rs138171763

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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.