rs188483654

This is a intron variant variant in the URGCP gene.

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GWAS Catalog Trait Associations (1)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

eosinophilic esophagitis

Chang X et al. “A genome-wide association meta-analysis identifies new eosinophilic esophagitis loci.” The Journal of Allergy and Clinical Immunology 149(3):988-998 (2022)

Allele C

OR 5.68

p 9.0e-9

N 7,836

Meta-analysis

European

About URGCP

URG4 is upregulated in the presence of hepatitis B virus (HBV)-encoded X antigen (HBxAg) and may contribute to the development of hepatocellular carcinoma by promoting hepatocellular growth and survival (Tufan et al., 2002 [PubMed 12082552]).[supplied by OMIM, Mar 2008]

View all URGCP variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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