Gene: KCND2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3751
Gene Symbol: KCND2
KCND2 		0.020 GeneticVariation disease BEFREE The data suggest that mutations in KCND2 and KCND3 are not a frequent cause of long QT syndrome. 15563876 2005
Entrez Id: 3751
Gene Symbol: KCND2
KCND2 		0.020 GeneticVariation disease BEFREE This information should facilitate the systematic screening of KCND2 and KCND3 exons for mutations in (inherited) arrhythmia syndromes, such as LQTS and Brugada. 10942109 2000