Your blueprint for earlier answers, clearer decisions, and a longer, healthier life.

VitalRisk™ analyzes the unique combination of your genetics, key biomarkers, and evidence-based clinical risk factors to build a personalized risk profile for major conditions, including heart disease, diabetes, stroke, certain cancers, and neurodegenerative diseases.

What You Get

• Whole-Genome Sequencing (WGS): An evaluation of your DNA—the body’s instruction manual.

• Personalized Polygenic Risk Scores (PRS): Advanced calculations that measure how your genes influence your risk for common diseases.

• AI-Enhanced Clinical Modeling: We combine genetic risk with biomarker trends, family history, and other clinical thresholds to create an individualized risk gradient.

• Action-Ready Insights: Your report highlights what’s relevant for you, including recommended lifestyle modifications, optional follow-up testing, and targeted prevention strategies discussed with your physician.

Why It Matters

Most chronic diseases develop silently for years. VitalRisk™ helps identify hidden susceptibility early—before symptoms appear—so you and your care team can take meaningful steps to prevent disease, slow progression, or personalize your long-term health strategy.

Who It’s For

Anyone who wants to move beyond reactive medicine and take a proactive, personalized approach to their health—especially those with family histories of heart disease, diabetes, cancer, or Alzheimer’s, or anyone wanting a deeper understanding of their body’s long-term roadmap.

A precision-medicine tool that elevates care, improves early detection, and strengthens the provider–patient relationship.

The VitalRisk™ assessment tool is a comprehensive, whole-genome–based disease-risk evaluation designed to integrate seamlessly into your existing clinical workflow. Using whole-genome sequencing, polygenic risk scoring, and evidence-based clinical modeling, VitalRisk™ helps identify high-risk patients long before traditional markers or symptoms emerge—supporting proactive, data-driven care.

Why Providers Use VitalRisk™

• Earlier Detection & Better Stratification
  VitalRisk™ identifies elevated genetic susceptibility to conditions like heart disease, diabetes, stroke, select cancers, and neurodegenerative disorders—allowing you to risk-stratify patients with greater precision.

• Actionable, Clinically Interpretable Reports
  Each patient report synthesizes genomic findings, PRS values, biomarker inputs, and clinical thresholds to present clear, prioritized risk categories. Reports are built to support clinical decision-making, not overwhelm it.

• Enhanced Patient Engagement
  Genomic insights motivate patients to participate more actively in prevention, lifestyle change, and long-term care planning. Providers often see improved compliance and deeper trust.

Contact us for more information on becoming a clinical partner.