Interpreting genetic testing reports from Avise requires understanding several key components. These typically include details about the tested genes, identified variants, and their potential clinical significance. An example might show a specific gene variant linked to an increased risk of a particular condition. The report often categorizes variants as pathogenic, likely pathogenic, benign, likely benign, or of uncertain significance (VUS). Understanding these classifications and their implications is crucial for accurate interpretation.
Accurate interpretation of these reports enables informed decision-making regarding health management. It empowers individuals and healthcare professionals to develop personalized strategies for disease prevention, early detection, and targeted treatment. The development of advanced genetic testing methodologies has revolutionized diagnostic capabilities and personalized medicine, leading to more proactive and effective healthcare approaches.