Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6329
Gene Symbol: SCN4A
SCN4A 		0.600 GeneticVariation disease UNIPROT A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis. 26659129 2016
Entrez Id: 6329
Gene Symbol: SCN4A
SCN4A 		0.600 GeneticVariation disease UNIPROT Defective fast inactivation recovery of Nav 1.4 in congenital myasthenic syndrome. 25707578 2015
Entrez Id: 6329
Gene Symbol: SCN4A
SCN4A 		0.600 Biomarker disease GENOMICS_ENGLAND Correlating phenotype and genotype in the periodic paralyses. 15534250 2004
Entrez Id: 6329
Gene Symbol: SCN4A
SCN4A 		0.600 GeneticVariation disease UNIPROT Myasthenic syndrome caused by mutation of the SCN4A sodium channel. 12766226 2003
Entrez Id: 6329
Gene Symbol: SCN4A
SCN4A 		0.600 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 6329
Gene Symbol: SCN4A
SCN4A 		0.600 GeneticVariation disease CLINVAR
Entrez Id: 6329
Gene Symbol: SCN4A
SCN4A 		0.600 CausalMutation disease CLINVAR