Gene: SMN2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6607
Gene Symbol: SMN2
SMN2 		0.100 CausalMutation phenotype CLINVAR A leaky splicing mutation affecting SMN1 exon 7 inclusion explains an unexpected mild case of spinal muscular atrophy. 21542063 2011
Entrez Id: 6607
Gene Symbol: SMN2
SMN2 		0.100 GeneticVariation phenotype CLINVAR