Gene: SCN2A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6326
Gene Symbol: SCN2A
SCN2A 		0.110 GeneticVariation phenotype BEFREE Here, we described a Chinese family with 2 members having juvenile-onset myoclonus and identified a novel SCN2A point mutation within this family. 30813219 2019
Entrez Id: 6326
Gene Symbol: SCN2A
SCN2A 		0.110 Biomarker phenotype HPO