Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6606
Gene Symbol: SMN1
SMN1
0.030 GeneticVariation disease BEFREE Survival of motor neuron 1 (SMN1) is well-known as a causative gene for spinal muscular atrophy (SMA) and mutations of glycyl- and tyrosyl-tRNA synthetases are identified as a cause of distal SMA and Charcot-Marie-Tooth disease. 22083460 2012
Entrez Id: 6606
Gene Symbol: SMN1
SMN1
0.030 Biomarker disease BEFREE A patient with both Charcot-Marie-Tooth disease (CMT 1A) and mild spinal muscular atrophy (SMA 3). 18337101 2008
Entrez Id: 6606
Gene Symbol: SMN1
SMN1
0.030 GeneticVariation disease BEFREE SMN gene analysis of the spinal form of Charcot-Marie-Tooth disease. 9192274 1997