My ActX Genomic Profile vs Hypercholesterolemia

ActX makes it easy to personalize your health care based on your DNA. Use My ActX Genomic Profile to view the results of your ActX analysis anytime, or share access with your health care provider. Help your physician use genetics to pick the best medication for you. Learn about your hereditary medical risks and work with your physician to reduce them. Focus on risks that you can do something about. Our simple saliva test makes it easy to have your DNA analyzed. As new research becomes available, ActX reanalyzes your genetic data and notifies you and your physician about changes to your profile. The My ActX Genomic Profile is intended for existing ActX customers. ActX analysis must be authorized by a licensed healthcare provider. FEATURES: DRUG-GENOME INTERACTIONS: Our Med Check functionality lets you enter the name of a medication to find out if there could be side effect, efficacy or dosage issues due to your genetics. You can also check the Medications section in your Profile to view the complete list of medications affected by your genetics. HEREDITARY RISKS: Your personalized profile offers insights into your actionable genetic risks, including cancer, cardiovascular, and metabolic risks. Our detailed summaries and additional resources can help you understand how your genes can impact your health. CARRIER STATUS: Your profile also shows genetic conditions that you carry and could pass on to your children. Carriers do not normally develop a disease, but if the other parent is also a carrier, then there is a chance that children could develop a genetic condition. SHARE WITH YOUR DOCTOR: The My ActX Genomic Profile app allows you to share your genetic information with the other healthcare providers involved in your care. Simply press “Share” and enter your doctor’s information. In less than 60 seconds, your doctor can get the information they need to personalize your medical care. Not an ActX customer? Visit our website to learn more about how ActX is personalizing medical care with genetics: https://www.actx.com/patient_home. What is your DNA telling you? Website: https://www.actx.com/ Facebook: https://www.facebook.com/actxinc/ Twitter: https://twitter.com/ActX IMPORTANT NOTE: ActX is a screening service and not intended for the diagnosis of high risk patients. The Service looks only at selected variants (DNA variations) for the targeted genes and not for all possible genetic variants. The features described outline the ActX Full Service option. Other ActX packages do not necessarily include all of the above information.

@Point of Care™ with Cognitive AI is a clinical decision-making mobile platform. Hypercholesterolemia @Point of Care™ provides a streamlined clinical decision support tool for clinicians to obtain content when it is needed—enabling better decisions, better outcomes, and better care. With Cognitive AI, clinicians use @Point of Care™ to easily access curated, evidence-based, and disease-specific medical content. Clinicians navigate content by asking voice-enabled natural language questions. With Cognitive AI, confidence-rated answers to efficiently incorporate best treatment options happen more quickly and decisions are made faster to improve patient outcomes at the point of care. Hypercholesterolemia @Point of Care™ is designed to: • Support discovery and practice change • Provide relevant, evidence-based disease-specific medical content • Improve patient outcomes at the point of care Features: • Continually updated Hypercholesterolemia content • Topics in diagnosis, treatment, and care management developed with expert physician authors • Case studies, videos, and interviews • Access to actionable patient-recorded data • Detailed reference list with access to original sources • Continuing medical education credit (CME/CE) • Surveys and peer polling • Patient education resources to share with patients