GATA6 and coronary artery disorder: A burden analysis of these rare pathogenic QV highlights GATA6 as the gene with the most significant CHD association (OR = 7.66 [95% CI 3.6–14.47]; p = 1.60E–06), with 9 unique QV present in 10 CHD samples, and the only significant candidate following Bonferroni correction (p = 0.03) (Table 1).