This study characterizes a large early onset atrial fibrillation family and identifies a rare causative mutation (R231H) in the KCNQ1 gene. The age of this mutation is ~5000 years, as estimated using IBD-coalescent methods. The geographic distribution and demographic history of the mutation is described. Induced pluripotent stem cell derived cardiomyocytes carrying the mutation have abbreviated action potential duration, indicating a gain-of-function. This data resource provides exome or whole genome sequencing data for six patients and RNA-seq data from the cardiomyocyte experiments.

Leveraging Extended Families for Cardiovascular Disease Genomic Discovery

Atrial Fibrillation study with RNA-Seq, SNP/CNV Genotypes (NGS) + 3 more data on dbGaP (10 participants)