present in Gene: HCN4
present in Chromosome: 15
Position on Chromosome: 73329719
Alleles of this Variant: C/G;T
rs794727637 in
HCN4 gene and
Brugada Syndrome 8
PMID 25145518 2014 The symptom complex of familial sinus node dysfunction and myocardial noncompaction is associated with mutations in the HCN4 channel.
PMID 26206080 2015 HCN4 mutation as a molecular explanation on patients with bradycardia and non-compaction cardiomyopathy.
PMID 25145517 2014 HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy.