Genetic Testing - HealthBanksUS

SmartParenting Genetic Testing

HealthBanks is proud to offer SmartParenting Genetic Testing to protect the health of your newborn. Our parent carrier and newborn genetic testing services can help uncover the genetic conditions that could be passed on to your child and identify potential health risks for your baby before symptoms arises.


Carrier Genetic Testing

Newborn Genetic Testing

Parent Carrier Genetic Testing

A healthy baby begins with healthy genes. Yours!
Even if you don’t have family history of a genetic condition, you may carry a risk of passing one on to your children
Samples Collected from: Dad or Pregnant mom
30 Genes for Mom and 28 genes for Dad, Test coverage: 99% at 20x Del/Dup > 2 Exon
Screens for autosomal recessive and X-linked conditions: Cystic Fibrosis, Muscular Dystrophy, Hemoglobinopathies, Spinal Muscular Atrophy (SMA)Fragile X, Duchenne

Newborn Genetic Testing

Identify DNA changes that could cause severe or life-altering symptoms in an infant
Analyze 255 genes and over 200 conditions
Clear and concise reporting of diagnostic results that are medically actionable
Results are provided directly to your pediatrician or provider with clear follow-up recommendations
Target Conditions include: Metabolic, Blood & Immunodeficiency Disorders, Hearing & Vision Loss, Cardiac Conditions, Pediatric Cancers, Epilepsy, and others
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