Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6640
Gene Symbol: SNTA1
SNTA1 		0.700 GeneticVariation disease UNIPROT Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex. 18591664 2008
Entrez Id: 6640
Gene Symbol: SNTA1
SNTA1 		0.700 Biomarker disease GENOMICS_ENGLAND alpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruption. 19684871 2008
Entrez Id: 6640
Gene Symbol: SNTA1
SNTA1 		0.700 GeneticVariation disease UNIPROT alpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruption. 19684871 2008
Entrez Id: 6640
Gene Symbol: SNTA1
SNTA1 		0.700 Biomarker disease GENOMICS_ENGLAND Short QT syndrome. 16301704 2005
Entrez Id: 6640
Gene Symbol: SNTA1
SNTA1 		0.700 Biomarker disease CTD_human
Entrez Id: 6640
Gene Symbol: SNTA1
SNTA1 		0.700 CausalMutation disease CLINVAR