a poster presentation for an scientific congress. it is a precision medicine congress. it should be striking.

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This study explores the potential of whole exome sequencing (WES) in routine clinical settings, focusing on 3,889 exomes from Türkiye. It highlights the identification of actionable cancer-related variants, revealing a 5.91% prevalence of pathogenic/likely pathogenic variants and a low rate of actionable findings. The research emphasizes the importance of normalizing genetic variants, understanding inheritance patterns, and validating findings across populations to enhance precision...