For Providers
Clinical-grade genetic screening. Actionable results.
GeneSprout is a trusted partner for comprehensive genetic screening, with results you can act on.
Why it matters
Genetic screening as a clinical tool, not a consumer product.
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Most genetic conditions in children go undetected until symptoms appear
More than 4% of children have a GeneSprout screenable genetic condition, yet the average time from first symptoms to diagnosis is over four years. Many of the conditions GeneSprout screens for are actionable from day one — but only if identified before harm accumulates. Extensive pediatric genetic screening gives clinicians the information they need to act early, not reactively.
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Your patients' families are asking questions you may not yet have answers to
Parents today are proactive about their children's health. Many are already researching genetic testing independently, often without clinical guidance. GeneSprout gives you a trusted option to offer them — so the conversation happens in your office, with your oversight, rather than outside the care relationship.
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Results in weeks — not months
Traditional genetic diagnostic workups can take months to complete, often requiring multiple specialist visits before a sample is even collected. GeneSprout returns whole exome and whole genome sequencing results in four weeks or less — so your patients spend less time waiting and more time on the right care path.
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A partner for providers — not just families
GeneSprout is designed to support providers and parents. Our team of expert pediatricians monitors ongoing research and guidelines so that you have access to the most up-to-date information.
What we offer
A screening program built for clinical practice.
GeneSprout gives providers a rigorous, supported pathway to add pediatric genetic screening to their practice — whether through direct patient referrals or a formal practice partnership.
Comprehensive screening for 2,200+ actionable conditions
Whole exome and whole genome sequencing across cardiovascular, metabolic, neurological, and oncologic conditions — curated for clinical relevance and focused exclusively on findings where early knowledge changes care.
Simple referral pathway for any practice
Referring a patient to GeneSprout requires no EHR integration or practice-level agreement. Any provider can refer a patient directly to GeneSprout’s website.
Actionable findings only — no anxiety without action
GeneSprout focuses on conditions that are actionable during childhood, where early insight can meaningfully guide care or intervention. GeneSprout does not report on findings that lack clear clinical action and may only increase parental anxiety.
Result summaries for clinicians
GeneSprout can provide a copy of the report that includes recommended next steps to clinicians, when appropriate consent is in place. Because most practicing pediatricians were not trained to interpret genetic sequencing results, GeneSprout helps fill this gap.
Health navigation that supports your team
When a finding is identified, our health navigators can engage the family directly — answering questions, and ensuring their follow-up with your team. We extend your capacity without adding to your workload.
Practice and health system partnerships
For practices and health systems seeking deeper integration, GeneSprout offers formal partnership arrangements — including volume pricing, co-branded patient materials, and dedicated clinical support.
How it works
Two ways to bring GeneSprout to your patients.
Refer a patient directly
The simplest path — refer a patient directly to GeneSprout, or generate a referral via Provider Referral page. No formal agreement required. The family orders, collects, and ships the sample. When the results are ready, we'll make it easy for the family to share back to you.
Or connect for a practice partnership
For practices and health systems that want deeper integration — direct referrals, patient outreach support, or EMR-adjacent workflows — reach out to our provider partnerships team to explore what's possible.
Learn more
Resources for clinicians.
Our Screening Science
What we test for and why.
Whole exome and whole genome sequencing covering 2,200+ actionable conditions — with ACMG-classified variants and a curated condition list built for clinical use.
Health Navigation
How we support your patients after a finding.
Our health navigation team is available to provide guidance to your care team – supporting your team with recommendations and answering family questions.
For Families
See what your patients experience.
Understand the end-to-end GeneSprout journey from the family perspective — so you can speak to it with confidence when recommending it to patients.