Brugada Syndrome data for rare variant association analysis

The directory contains data described by Le Scouarnec et al. (2015) for the rare variant association analysis of Brugada syndrome (BrS). The quality control of this processed data is further detailed in the publication.<br>The directory contains:<br>-files named .txt. These files are genotype files with each row corresponding to a SNV and each column corresponding to an individual. SNV identifiers are indicated in the first column CHROM_POS_REF_ALT. Positions are according to the GRCh37/hg19 assembly. Other column names are the individual identifiers. Genotypes are coded 0, 1 or 2 according to the number of alternative alleles.<br>- a file named "phenotypes_BrS.txt". This file contains two columns: the individual identifier and the phenotype (affected: 1, unaffected: 0).<br>