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You're here because your pediatrician suggested Nurture Genomics' genomic screening service for your healthy baby. This page is designed to help you understand — in simple, honest terms — what Nurture does, how it works, and what you should consider before saying "yes."
In the U.S., every baby usually gets state newborn screening, which tests for a fixed number of serious treatable conditions using a blood-spot test. In Utah, babies are tested for 52 conditions.
In the U.S., every baby usually gets state newborn screening, which tests for a fixed number of serious treatable conditions using a blood-spot test. In Utah, babies are tested for 52 conditions.
Nurture uses whole-genome sequencing to screen for 400+ medically actionable, childhood-onset conditions — much more than standard newborn screening.
Nurture combines testing with ongoing support: genetic counseling, help navigating next steps, and care coordination if the test finds something important.
Your doctor will use a gentle cheek swab to collect a DNA sample — no blood draw required.
Nurture analyzes your child's DNA (their "genome") and looks at more than 400 genes linked to treatable childhood conditions.
We know test results aren't always easy to understand. That's why in addition to your lab report, Nurture provides a patient guide that tells you in clear language what the results mean for your child and outlines next steps in their care.
From the very beginning of the process, you will have access to Nurture's team of trained genetic counselors. They'll help you understand what the results mean, answer questions, and support you in next steps.
If a risk is found, Nurture works with you and your pediatrician to connect you with the right specialists and coordinate next steps in your child's care.
Yes. Many serious but treatable genetic conditions don't show symptoms at first. Nurture gives you a chance to catch those risks early.
Yes. Nurture partners with a well-established clinical lab that meets strict privacy and security standards. Your personal data won't be shared without your permission.
This program is offered at no cost to you through a collaboration between Intermountain Health and Nurture Genomics. Your insurance will not be billed for the genetic test or the genetic counseling included in this program. If the results suggest that your child may need additional testing or follow-up medical visits, those services would be billed to you or your insurance in the same way as any other healthcare visit or test.
No — Nurture is meant to add to state-provided newborn screening, not replace it. The two work together to give you more information.
Nurture includes more than 400 genetic conditions in this screening. These conditions were chosen based on two main criteria:
No. This test is intended for healthy children to identify possible future health risks. It is not designed to diagnose conditions that are already suspected or present. If your child has symptoms or you are concerned about a known genetic condition in your family, talk with your provider about diagnostic genetic testing.
Yes. In some cases, genetic findings may have implications for siblings, parents, or other relatives. If this happens, your care team will explain what the results may mean for your family and discuss next steps.
Nurture may be a good fit if you want extra peace of mind for your baby's future — especially if you value:
Before you decide, you might ask your pediatrician or a genetic counselor about how genetic screening fits with your family's values and what you hope to learn.
Nurture's genomic screening is available in select pediatrician offices at Intermountain Healthcare. Ask your pediatrician if it is right for your baby. Have a question for us? Contact Nurture's support team at support@nurturegenomics.com.
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