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Congenital heart disease (CHD) has genetic causes in less than 40% of cases, and interpreting the significance of uncertain genetic variants is difficult. Researchers aimed to enhance the diagnostic classification of CHD variants by studying the impact of noncanonical splice region variants on RNA splicing. They analyzed data from thousands of CHD patients and their parents and used computational and in vitro methods. They identified 127 variants that affect splicing, leading to loss of function, including some in known CHD genes. They confirmed the impact of one variant on RNA splicing in a patient's cardiac tissue. The study highlights the importance of identifying splice-altering variants for improving genetic diagnoses of CHD.
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