Gene: KCNJ2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3759
Gene Symbol: KCNJ2
KCNJ2 		0.120 GeneticVariation disease BEFREE KCNJ2 variant of unknown significance reclassified as long QT syndrome causing ventricular fibrillation. 21875779 2012
Entrez Id: 3759
Gene Symbol: KCNJ2
KCNJ2 		0.120 GeneticVariation disease BEFREE A 37-year-old Japanese woman experienced aborted sudden cardiac death from ventricular fibrillation and was diagnosed with Andersen-Tawil syndrome by genetic analysis that revealed 2 mutations in the KCNJ2 gene. 22739561 2012
Entrez Id: 3759
Gene Symbol: KCNJ2
KCNJ2 		0.120 Biomarker disease HPO