What’s Analyzed
[ 229+ Genes · 6 Categories ]Comprehensive screening across 6 critical health categories — the most complete newborn panel available.
Metabolic Disorders
PKU, Galactosemia, MCAD deficiency, Maple syrup urine disease, and 30+ more conditions affecting how your baby processes nutrients and produces energy.
Immune Deficiencies
SCID, Common variable immunodeficiency, Wiskott-Aldrich syndrome. Early detection protects your baby from infections that could be life-threatening.
Developmental Markers
Fragile X, Rett syndrome, Angelman syndrome, Prader-Willi syndrome. Understanding developmental genetics helps create personalized growth milestones.
Genetic Syndromes
Down syndrome markers, Turner syndrome, Klinefelter syndrome. Comprehensive syndromic screening provides clarity and helps families plan appropriate care.
Cardiac Conditions
Long QT syndrome, Hypertrophic cardiomyopathy, Brugada syndrome. Genetic cardiac screening identifies hidden heart risks before they become emergencies.
Sensory Disorders
Congenital hearing loss, Retinitis pigmentosa, Usher syndrome. Early genetic identification allows intervention before critical developmental windows close.
What parents ask us
[ Key Genes + Answers ]Is genetic testing safe for my newborn?
[ Non-invasive cheek swab collection ]GeneBaby uses a simple, painless cheek swab that collects DNA from cells inside your baby’s mouth. The process takes less than 60 seconds, causes zero discomfort, and has been safely used on over 50,000 newborns.
Our CLIA-certified lab follows the highest safety and security standards for sample handling.
My baby seems healthy. Why would I need genetic screening?
[ 229+ genes analyzed for hidden conditions ]Most genetic conditions don’t show symptoms at birth but can be detected through DNA analysis. Research shows that 95% of conditions we detect are highly treatable when caught early, dramatically improving outcomes.
Early identification allows for preventive care, dietary modifications, and medical interventions before symptoms appear.
What if you find something concerning in my baby’s results?
[ Board-certified genetic counselors available ]If we detect a significant variant, you’ll receive a detailed report with clear explanations and actionable recommendations.
Our team of board-certified genetic counselors and pediatric specialists is available to walk you through the findings, answer all questions, and connect you with appropriate healthcare providers for follow-up care.
How It Works
[ From Swab To Answers ]Order your kit
Choose your plan and receive your DNA collection kit with free shipping directly to your door — sterile cheek swabs, collection tubes, prepaid return envelope, and detailed instructions. Gentle pediatric swabs included.
Collect sample at home
Use the painless cheek swab to gently collect DNA from inside your baby’s mouth. The entire process takes less than 60 seconds and causes zero discomfort.
Lab analysis
Your sample arrives at our CLIA-certified laboratory where our team of geneticists analyzes 229+ genes using next-generation sequencing technology. Our AI-powered analysis cross-references findings against 2M+ clinical data points.
Review results
Receive your comprehensive genetic report within 5-7 days — detailed findings, personalized care recommendations, and actionable insights. Board-certified genetic counselors are available to answer questions and guide next steps.
What’s in your report
- Findings across all 6 pediatric health categories
- Carrier status — PKU, cystic fibrosis & more
- Pediatric care plan & developmental milestones
- Pharmacogenomics — pain management & antibiotics
- Pediatrician-ready findings and next steps
- Genetic counselor support for your family
Included With Your Membership
[ GeneBaby + 10 More Tests ]GeneBaby is included with your Gene Matrix Membership — along with all 10 other genetic tests. No per-test fees. No surprises.
A standalone panel at typical lab pricing — a separate order, a separate kit, and a report that never updates.
This test individually: $799. With your membership: included at $89/mo (or $59/mo billed annually) along with all 10 other tests.
No per-test fees. No surprises. 30-day guarantee. HSA/FSA eligible.
GeneBaby changed their lives
[ Verified Results ]“GeneBaby detected a rare metabolic disorder in our daughter at 3 weeks old — before any symptoms appeared. Our pediatrician was able to start dietary intervention immediately. She is now 2 years old and thriving. This test changed everything.”
Rachel & James T. — Seattle, WA · MCAD deficiency detected at 3 weeks
“Lucas tested positive for G6PD deficiency at birth through GeneBaby. Thanks to early detection, we’ve been able to avoid trigger medications and foods that could have caused a severe hemolytic crisis. Our doctor said this information is life-saving.”
Jennifer Rodriguez — Austin, TX · Lucas, 7 months old
Frequently asked
GeneBaby is designed for newborns and infants up to 24 months old. The test can be performed as early as birth, providing crucial genetic insights during the most critical developmental period.
We use a simple, painless cheek swab method that can be performed at home. The kit includes detailed instructions and all necessary materials. The process takes less than 2 minutes and causes no discomfort to your baby.
GeneBaby analyzes 229+ genes associated with pediatric health conditions including metabolic disorders, immune deficiencies, developmental markers, genetic syndromes, cardiac conditions, and sensory disorders.
Results are typically available within 5-7 business days after our lab receives your sample. You will receive an email notification when your report is ready to view.
Coverage varies by insurance provider. We provide detailed receipts that you can submit to your insurance company for potential reimbursement. Our team can also help verify your coverage before ordering.
If we detect any significant variants, your report will include detailed information and personalized recommendations. We also offer genetic counseling services to help you understand the results and next steps.