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. 2020 Jan 27;141(6):418–428. doi: 10.1161/CIRCULATIONAHA.119.043132

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© 2020 The Authors.

Circulation is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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Figure 1. — Disease causality classification and level of evidence scores for genes reported in LQTS. A, Validity scores according to the ClinGen curation framework and final classifications of the Working Group. Genetic and experimental evidence scores of each one of the 3 blinded curating teams are detailed. Complete list of references used for scoring of these genes is available in the supplements. B, Distribution of genes according to classification. *Genes with strong or definitive evidence for causality in LQTS with atypical features. †Genes with definitive evidence for causality in inherited multiorgan syndrome including QT prolongation but only moderate or limited evidence for isolated LQTS. ‡Genes with strong level of evidence for causality in acquired LQTS but only limited or disputed evidence for congenital LQTS.