Gene: RYR1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6261
Gene Symbol: RYR1
RYR1 		0.500 GermlineCausalMutation disease ORPHANET RYR1 mutations are a common cause of congenital myopathies with central nuclei. 20839240 2010
Entrez Id: 6261
Gene Symbol: RYR1
RYR1 		0.500 Biomarker disease CTD_human Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene. 17376685 2007