Empower your family’s health with the most comprehensive Genetic Health Exam for newborns and children.
Most parents don’t realize just how limited standard newborn testing can be. Fore’s genetic health screening goes beyond the basic conditions your state screens for—covering over 800+ conditions and providing insights on 100+ medications.
Catch hidden health conditions sooner.
Avoid adverse drug reactions and tailor treatments.
Share results seamlessly with your child’s healthcare team.
Ongoing guidance and support from genetic counselors.
Your child’s results are physician-approved and ready to be shared with pediatricians and other care providers.
Fore and its network of partners are committed to advancing personalized healthcare by delivering the highest quality service. Together, they provide expertise in sequencing, analysis, genetic counseling, clinical planning, security, and privacy.
Fore screens for 800+ conditions compared to roughly ~50 in state tests, plus medication response insights.
No. Our test only requires a painless cheek swab—easy for both parent and child.
You’ll receive final results in about 4 weeks. Once available, you can consult with our genetic counselors.
Yes. Fore’s process is physician-approved and conducted in CLIA/CAP-accredited labs.
We provide a detailed clinical action plan and connect you with board-certified genetic counselors to help you take the next step.
Fore believes in collaboration. Your child’s results can seamlessly integrate into regular checkups and healthcare plans. Together with your pediatrician, you can stay ahead of potential issues and ensure that proper management and treatments are precisely tailored to your child's needs.
Once you have your child’s genetic report, you don’t have to navigate it alone. Our board-certified genetic counselors provide personalized guidance, answer your questions, and help you create a clear action plan. Plus, you’ll have continuous access to easy-to-understand resources in our online portal—so you’re always informed.