Evolve from proactive to predictive care with myGeneticScreen
Empower your population with this innovative testing solution that helps determine genetic risk for three hereditary conditions, enabling individuals and their families to take preventive measures and make informed decisions.
Analyzing risk for three conditions
Hereditary Breast & Ovarian Cancer Syndrome
Caused by genetic variants in the BRCA genes, this increases the lifetime risk of developing breast and ovarian cancer compared with the general population.
Lynch Syndrome
The most common cause of hereditary colorectal cancer³, and can increase the risk of other cancers, including stomach, liver, brain, and pancreatic cancers.
Familial Hypercholesterolemia
An inherited disorder that can increase the risk of cardiovascular diseases at a younger age. Finding and treating this early can reduce coronary heart disease risk by 80%.²
Drive goals forward with myGeneticScreen
A competitive benefit
Drive engagement with your population from home by leveraging this innovative, health-forward screening opportunity.
Improve health outcomes
Aggregate data enables health systems to better understand, and track genetic risk in populations to provide enhanced care.
Reduce long-term costs
Genetic screening facilitates the early detection of health issues to help drive down overall treatment costs per patient.
Which genes do we analyze?
myGeneticScreen analyzes 11 genes associated with three conditions recommended by the Centers for Disease Control and Prevention (CDC) as actionable Tier 1 conditions
Design your solution
Get in touch with us so we can work together to build a solution for your needs
How does this solution work?
Our accessible healthcare solutions are customized to meet your specific goals, and each step of the process can be adapted to best suit your population.
Multi-channel engagement and education
We offer custom-built announcement and engagement strategies to maximize compliance, from fully digital packages to device-free communication. Our Genetics Knowledge Hub was created by experts to guide your people through the basics of genetics and what they'll learn from their results.
Simple saliva sample collection from home
We meet your people where they are with kits delivered directly to their homes. Your people will feel empowered with our easy-to-use sample collection kits, no matter what their experience or digital fluency is. We offer both printed and digital instructions depending on their needs.
Downloadable result report for easy sharing
Our wholly owned solution ensures a streamlined delivery of lab results directly to a secure online account, including detailed breakdowns from the genetics team for further understanding. With these results, the patient and their provider can make informed decisions about their healthcare for life.
Comprehensive patient-friendly result report
Downloadable from their dashboard for providers
Educational factsheets written by experts also available
Genetic counseling with experts through their journey
As part of the myGeneticScreen experience, your people will have access to 1-on-1 counseling sessions with genetic experts.
Pre-test counseling for guidance and to answer any questions.
Post-test counseling to better understand results and make informed decisions on next steps.
Testing for family members on our platform
As these conditions are hereditary, first degree relatives of those affected have a 50% risk to also inherit the mutation. We also offer myGeneticScreen testing to family members to help them understand their risk and take action where needed.
Design your solution
Get in touch with us so we can work together to build a solution for your needs
Developed by genetic and clinical experts
We work with trusted experts to build experiences, so your population can get the answers they need.
Dr. Avni Santani
Chief Genomics Officer
Dr. Robert Mordkin, MD
Chief Medical Officer
Dr. Kate Karfilis
Director of Product - Genomics
Wendi Gill
Genetic Counselor