Hepatitis B Gene Set

Dataset GWAS Catalog SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus, which is transmitted_by sexual contact, transmitted_by blood transfusions, and transmitted_by fomites like needles or syringes. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice. (Human Disease Ontology, DOID_2043)
External Link https://www.ebi.ac.uk/gwas/search?query=Hepatitis B
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Genes

5 genes associated with the Hepatitis B phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
HLA-DPA1 major histocompatibility complex, class II, DP alpha 1 1.64948
HLA-DPB1 major histocompatibility complex, class II, DP beta 1 1.58902
HLA-DQB2 major histocompatibility complex, class II, DQ beta 2 1.37564
UBE2L3 ubiquitin-conjugating enzyme E2L 3 0.696558
GRIN2A glutamate receptor, ionotropic, N-methyl D-aspartate 2A 0.405958