Gene: SCN4A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6329
Gene Symbol: SCN4A
SCN4A 		0.110 GeneticVariation disease BEFREE De novo variant in SCN4A causes neonatal sodium channel myotonia with general muscle stiffness and respiratory failure. 31732390 2019
Entrez Id: 6329
Gene Symbol: SCN4A
SCN4A 		0.110 Biomarker disease HPO