Scope
Stop guessing
Know before
One cheek swab screens for 1,000+ conditions
Empowered Parenting in
Three Steps
No appointments, doctor visits, or tears required
Order online and register through secure parent portal
Collect sample and send to be sequenced in our accredited lab
Reports for conditions and medication response provided by licensed genetic counselors
Real Families. Real Results. Real Peace of Mind.
Explore how early genetic screening can save lives
Method
Timing
Follow-up
State Newborn Screening
~30-60 treatable conditions
Heel-prick blood test + hearing + pulse
Within 48 hours of birth
None
Fore Genomics Screening
~1,000+ treatable conditions
Simple at-home cheek swab
Any age from newborn through childhood
Annually
Why Genetic Screening is
Essential
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Fore’s genetic health screening goes beyond the basic conditions your state screens for—covering 1,000+ conditions and providing insights on over 100 medications.
Identify Risks Early
Before health conditions become problems
Personalize Medication
Based on your child’s genetics
Partner with Your Pediatrician
Easily share results with your child’s doctor
Stay One Step Ahead
On-going support provided by Fore’s genetic counselor
Team Up
with Your Pediatrician
Fore is built to collaborate with your child’s doctor. Your child’s results can be integrated into regular check-ups.
Easily share digital results with your pediatrician
Use our secure platform to keep track of updates and follow-ups
Get real-time support from our network of licensed physicians and genetic counselors
Frequently Asked Questions
What is included in Fore’s Genetic Health Screen?
There exists a multitude of genetic conditions that may manifest in childhood or adulthood, varying in their treatability. Fore’s genetic screening specifically targets detectable genetic alterations associated with childhood-onset conditions. We screen for hundreds of pediatric-onset conditions, where identifying an elevated risk could significantly alter the child's medical care. This encompasses a range of disorders, including blood disorders, neurological conditions, metabolic disorders, immune system impairments, endocrine disorders, and more. Fore is designed as a screening tool for seemingly healthy infants and children. If you have concerns about your child's health and seek a genetic diagnosis, kindly reach out to us for further guidance.
How is Fore’s Genetic Health Screening different from other DNA testing services?
Fore utilizes cutting-edge technology to sequence your child’s whole genome (100% of their DNA) and examine it for hundreds of medically significant conditions. But it's not just a test; Fore offers a comprehensive care service. This service includes access to genetic counselors, medical specialists, and care navigators who are there to assist you in comprehending the results, leveraging the insights effectively, and determining the best course of action moving forward.
Is Fore only useful for children with a family history of genetic conditions?
No, family history is indeed a crucial factor in assessing risk, but it doesn't provide the complete picture. Many genetic conditions are inherited unknowingly within families. Some are transmitted silently through carriers who show no symptoms (unaffected carriers) and pass on a single genetic alteration for the condition. For a child to be affected, both parents must be carriers, yet since most families are unaware of carrying such conditions, they remain "hidden," lacking any apparent family history. Moreover, certain conditions, known as X-linked disorders, predominantly manifest in males rather than females. In such cases, the mother may be an unaffected carrier, and several generations of unaffected carrier females may precede the birth of an affected male, masking any evident family history. Lastly, genetic conditions can emerge in a family due to new genetic variations occurring spontaneously in the egg or sperm that form the child. These alterations are spontaneous and not linked to any familial history of the condition.
Will insurance or my health saving account cover the cost of Fore’s service?
No. Insurance doesn’t typically cover genetic screening for healthy newborns. Fore has partnered with payment solutions providers to allow use of HSA and FSA funds at checkout.
Why would I need Fore for my child if I’ve already had carrier testing?
Carrier screening detects genetic diseases that require both parents to be carriers to have an affected child (autosomal recessive), or where the mother may be a carrier and has an increased risk of having an affected son (X-linked recessive). The range of conditions screened for varies between testing labs, from a few to hundreds. Usually, these conditions are chosen based on their frequency and severity rather than their treatability. Testing can occur before conception or during pregnancy. Fore's service focuses on the baby and occurs after birth and is designed to grow as your child ages.
Data Privacy: How will Fore share my child’s data?
As a parent or legal guardian you are in control of your child’s data. Fore will not share your child’s data without your written consent. We partner with DNAnexus, a trusted and widely adopted platform used by leading hospitals and research institutions, to store and manage data securely. DNAnexus maintains rigorous compliance with key privacy and security standards.
Can my child’s genetic information be used against them?
Genetic Information Non-Discrimination Act (GINA 2008) safe guards individuals against genetic discrimination in both the workplace and health insurance realm. For instance, health insurance providers are prohibited from setting premiums based on genetic health data, and employers are barred from making hiring or firing decisions based on genetic health information. Additionally, various state laws extend protection against genetic discrimination to other insurance benefits.
