Gene: SCN1A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A 		0.110 GeneticVariation phenotype BEFREE This kind of myoclonus is an intrinsic feature of DS associated with SCN1A mutations, and may be a cause of disability. 28126647 2017
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A 		0.110 Biomarker phenotype HPO