Background Long-QT syndrome (LQTS) is a cardiac repolarization abnormality that can lead to sudden cardiac death. The most common causes are rare coding variants in the genes , , and . The data on LQTS epidemiology are limited, and information on expressivity and penetrance of pathogenic variants is sparse. Methods and Results We screened for rare coding variants associated with the corrected QT (QTc) interval in Iceland. We explored the frequency of the identified variants, their penetrance, and their association with severe events. Twelve variants were associated with the QTc interval. Five in 1, 3 in , 2 in cardiomyopathy genes and , and 2 in genes where coding variants have not been associated with the QTc interval, and The combined carrier frequency of the 8 variants in the previously known LQTS genes was 530 per 100 000 individuals (1:190). p.Tyr315Cys and p.Leu273Phe in were associated with having a mean QTc interval longer than 500 ms ( =4.2×10 ; odds ratio OR, 38.6; =8.4×10 , OR, 26.5; respectively), and p.Leu273Phe was associated with sudden cardiac death ( =0.0034; OR, 2.99). p.Val215Met in was carried by 1 in 280 Icelanders, had a smaller effect on the QTc interval ( =1.8×10 ; effect, 22.8 ms), and did not associate with severe clinical events. Conclusions The carrier frequency of associating variants in LQTS genes was higher than previous estimates of the prevalence of LQTS. The variants have variable effects on the QTc interval, and carriers of p.Tyr315Cys and p.Leu273Phe have a more severe disease than carriers of p.Val215Met. These data could lead to improved identification, risk stratification, and a more precise clinical approach to those with QTc prolongation.