Gene: MYCN ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4613
Gene Symbol: MYCN
MYCN 		0.110 GeneticVariation disease BEFREE Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia. 21224895 2011
Entrez Id: 4613
Gene Symbol: MYCN
MYCN 		0.110 Biomarker disease HPO
Entrez Id: 4613
Gene Symbol: MYCN
MYCN 		0.110 GeneticVariation disease CLINVAR