Hero_Image_Fore_Genomics_Nov_15_2024 - Fore Genomics, Inc.

Genetic Screening For 500+ Conditions & 100+ Medications.

Take control of your child's health with proactive health screening

Order Now

Finally... A Health Solution Designed For Children

Set your child up for a healthy life with genetic health screening. Health screening vital for early detection of manageable conditions in childhood. Recommended for ages 0-5, it remains available for children up to 18 years old.

Fore Genomics Health Screen with 5-Year Membership - Fore Genomics, Inc.

Why Screen?

Newborns receive basic state-sponsored screening for a handful of conditions, but Fore goes further—providing insights into hundreds of conditions. With Fore’s advanced genetic screening, you gain the knowledge to protect and support your baby’s health from day one. It’s the peace of mind every parent deserves.

Pediatric_Genetic_Health_Screening_Report - Fore Genomics, Inc.

What We Screen For

Risks of neurological and cardiovascular conditions, metabolic disorders, and even pediatric cancers. With this knowledge, you and your child’s doctor can stay ahead—monitoring, preventing, and creating personalized care plans to ensure your little one thrives to their fullest potential

Lifelong Insights

Personalized Medicine is driven by individual health insights based on your genetic profile, resulting in tailored care planning. Engage with our interactive content to learn more about the benefits of the Fore Genomics' Genetic Health Screening. Using genetic health screening builds the foundation for a healthy life.

Order For Your Child Today

Save $500.00
Fore Genomics Health Screen
Fore Genomics Health Screen
Sale price$499.00 Regular price$999.00
5.0
Fore Genomics Gift Card - Fore Genomics, Inc.
Fore Genomics Gift Card
Sale priceFrom $250.00

Customer Reviews

Based on 5 reviews
100%
(5)
0%
(0)
0%
(0)
0%
(0)
0%
(0)
M
Morgan
Prepared

During my pregnancy journey I learned my family had a history of genetic disease. Once my child was born I knew I needed Fore's genetic health screen to ensure I was prepared for any potential disease my child may have to face.

M
Mandy
Reports were clear and easy to understand

The service was very easy to use. Everything went as expected without delays. Reports were clear and the information was easy to understand. The peace of mind that comes with the knowledge of my child's potential to develop disease is invaluable.

S
Suzanne
Great preventative care

From a family with physicians and lots of experience around healthcare solutions, this has been a great preventative care experience.

A
Ashley

My family is focused on healthy living and being able to be proactive about healthcare for our kids is important to us. I have seen a number of family health solutions and this peaked my interest as something to increase the knowledge of my child’s health. The post-test genetic counseling session was very insightful and the most valuable part of the experience for my family.

N
Nick
Great to see a solution introduced to families directly

I work in healthcare and am always looking for the newest technologies that can help families live healthier lives. A lot is focused on helping adults and very little focused on helping kids. Understanding DNA and genetic health risk early in life really helps build a lifetime of precisions healthcare. It’s great to see a solution introduced to families directly. I had my questions about how easily the results translate to our pediatrician. It’s been a very smoothprocess and our pediatrician is receptive to this extra insight.

These tests were developed and performance characteristics were determined by Fore Genomics, Inc. in collaboration with Fore’s service providers. The US Food and Drug Administration (FDA) has not approved or cleared these tests; however, FDA clearance approval is not currently required for clinical use. These tests are used for clinical purposes, and therefore validation was done as required under the requirements of the Clinical Laboratory Improvement Act (CLIA) of 1988. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions. The chance of a false negative or a false-positive result due to laboratory error cannot be completely excluded. These results should not be regarded as investigational or for research.