rhabdomyolysis Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Breakdown of muscle fibers that leads to the release of muscle fiber contents (myoglobin) into the bloodstream. (Human Phenotype Ontology, HP_0003201)
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