The uploaded file contains the complete list of genetic variants identified in a pediatric patient following whole exome sequencing (WES). The analysis was refined by applying a targeted filtering approach, focusing exclusively on a curated kidney disease panel. This panel encompasses genes associated with renal pathologies, and only variants with a sequencing depth greater than 20 were retained to ensure reliability and accuracy in the data. These steps aim to provide a robust dataset for investigating potential genetic contributors to the patient's clinical presentation.