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 116,598 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

MICB or MICA protein levels

LINC00973 · rs62276869

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Standard

COL18A1 protein levels

COL18A1 · rs62216332

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Standard

Neutrophill percentage (UKB data field 30200)

CERKL · rs62189983

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DPP10 protein levels

DPP10 · rs62155342

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SERPINI2 protein levels

TULP2 · rs62128042

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Standard

FABP9 protein levels

THRA · rs62065218

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

near EGR2 · rs61864736

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Standard

Whole body water mass (UKB data field 23102)

LINC01698 · rs60534728

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Standard

IL18RAP protein levels

near IGHV3-7 · rs58291548

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Standard

Red blood cell erythrocyte count (UKB data field 30010)

FAM182A · rs57915816

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Standard

BTC protein levels

near LINC02483 · rs576857546

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IKZF2 protein levels

near IGLC7 · rs5759537

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TNC protein levels

SCARA5 · rs574772914

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IL18 protein levels

IL18 · rs5744254

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CSTB protein levels

PDXK · rs573868774

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SERPINE2 protein levels

SERPINE2 · rs573829890

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Impedance of arm left (UKB data field 23110)

near ZFYVE27 · rs572707716

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Standard

GLIPR1 protein levels

NOC4L · rs571674115

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Standard

MDGA1 protein levels

near MIR4462 · rs571490443

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Standard

Total bilirubin levels (UKB data field 30840)

near LINC01891 · rs571352992

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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.