GeneBaby

Comprehensive Newborn Genetic Screening

What's Tested

Comprehensive analysis of 229+ genetic markers across 6 critical pediatric health categories

Metabolic Disorders

45+ Genes

PKU, MCAD deficiency, galactosemia, and other metabolic conditions

Immune Deficiencies

38+ Genes

SCID, chronic granulomatous disease, and immune system disorders

Developmental Markers

42+ Genes

Growth patterns, cognitive development, and milestone indicators

Genetic Syndromes

51+ Genes

Down syndrome, cystic fibrosis, sickle cell, and chromosomal conditions

Cardiac Conditions

29+ Genes

Congenital heart defects and cardiovascular genetic markers

Sensory Disorders

24+ Genes

Hearing loss, vision impairments, and sensory processing conditions

Why Choose GeneBaby

Give your child the advantage of early genetic insights

Early Intervention

Detect potential health issues before symptoms appear, enabling proactive treatment and better outcomes

Family Planning

Understand carrier status and hereditary conditions for informed future family decisions

Personalized Care

Tailor medical care, nutrition, and developmental support based on genetic profile

Peace of Mind

Comprehensive screening provides reassurance and clarity about your baby's genetic health

Sample Report

Clear, comprehensive genetic insights designed for parents and pediatricians

Choose Your Package

Flexible plans for comprehensive newborn genetic screening

Essential

Core newborn screening

$99/month

Basic metabolic screening
Common genetic conditions
Digital report access
Email support
Results in 7-10 days

Premium

Comprehensive pediatric genetics

$179/month

Complete 229+ gene analysis
All 6 health categories
Developmental markers
Carrier status screening
Priority processing (5-7 days)
Genetic counselor consultation
Lifetime report access

Family

Multiple children coverage

$299/month

All Premium features
Up to 3 children
Family genetic pattern analysis
Sibling comparison reports
Quarterly health updates
Dedicated support team
Unlimited consultations

How It Works

Simple, safe, and stress-free genetic screening for your baby

Order Your Kit

Choose your package and receive a pediatric-safe collection kit within 2-3 business days

Collect Sample

Gentle cheek swab collection - safe, painless, and takes less than 60 seconds

Lab Analysis

CLIA-certified lab analyzes 229+ genetic markers with pediatric expertise

Get Results

Receive comprehensive report with actionable insights and genetic counseling

Frequently Asked Questions

Absolutely! GeneBaby uses a simple, non-invasive cheek swab that is completely safe and painless for infants. Our collection method is specifically designed for newborns and young children.

Testing can be done anytime after birth. Many parents choose to test within the first few weeks to get early insights, but testing is beneficial at any age during infancy and early childhood.

GeneBaby screens for 229+ genetic markers across metabolic disorders, immune deficiencies, developmental conditions, genetic syndromes, cardiac conditions, and sensory disorders - far more comprehensive than standard newborn screening.

Our testing uses clinical-grade sequencing with 99.5% accuracy. All analysis is performed in CLIA-certified, CAP-accredited laboratories specializing in pediatric genetics.

Many insurance plans cover expanded newborn genetic screening. We provide detailed documentation for reimbursement. Contact your insurance provider for specific coverage details.

If any genetic markers are identified, you'll receive a consultation with a pediatric genetic counselor who will explain the findings, discuss next steps, and coordinate with your pediatrician for appropriate care.

Give Your Baby the Best Start

Join thousands of parents who trust GeneBaby for comprehensive newborn genetic screening

Start Screening Talk to a Counselor