TKT and Schnyder corneal dystrophy: While the general trend is significant, the observation that 2/4 of the individual SNPs nominally associated with SCD actually show the opposite direction of effect, including TKT/CACNA1D/PRKCD, suggests the need to further elucidate how each of these variants modifies both the underlying QRS/QT interval trait as well as the potential role in SCD.