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 homozygous double mutation in SMN1: a complicated genetic diagnosis of SMA. 24498607 2013
Entrez Id: 6607
Gene Symbol: SMN2
SMN2 		0.100 GeneticVariation phenotype CLINVAR Spinal muscular atrophy diagnostics. 17761649 2007