rhabdomyolysis Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Necrosis or disintegration of skeletal muscle often followed by myoglobinuria. (Experimental Factor Ontology, EFO_0003867)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0003201
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Genes

1 genes associated with the rhabdomyolysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
RYR2 ryanodine receptor 2 (cardiac) 1.12851