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 114,330 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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Pulse rate (UKB data field 102)

near RPL19P11 · rs1921102

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SHBG protein levels

ATP1B2 · rs191963994

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Reticulocyte percentage (UKB data field 30240)

near SYT11 · rs191668849

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IL17RB protein levels

CHDH · rs191380308

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IL7R protein levels

near RANBP3L · rs191161905

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MSMB protein levels

MARCHF8 · rs191058732

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Mean reticulocyte volume (UKB data field 30260)

near HNRNPA1P41 · rs190935558

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NPTX1 protein levels

TRIM39-RPP21 · rs190763129

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GLIPR1 protein levels

PDSS2 · rs190569705

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MATN2 protein levels

LAPTM4B · rs190105774

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HDGF protein levels

MEF2D · rs189841063

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GDF2 protein levels

BICD2 · rs189444416

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ICAM2 protein levels

near CLDND1-AS1 · rs189364736

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ARHGEF5 protein levels

near RN7SKP174 · rs189343723

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CDH15 protein levels

near CDT1 · rs189143366

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FASLG protein levels

near CH25H · rs188493056

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SIRPA protein levels

SIRPG-AS1 · rs188141382

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CDA protein levels

EIF4G3 · rs187675206

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PROK1 protein levels

LAMTOR5-AS1 · rs187542070

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CYTL1 protein levels

STX18-AS1 · rs187350495

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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.