Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1906
Gene Symbol: EDN1
EDN1 		0.410 GeneticVariation disease UNIPROT Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears. 24268655 2013
Entrez Id: 1906
Gene Symbol: EDN1
EDN1 		0.410 GeneticVariation disease BEFREE Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears. 24268655 2013
Entrez Id: 1906
Gene Symbol: EDN1
EDN1 		0.410 CausalMutation disease CLINVAR