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
Up to 8% of children are affected by a 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. Broad 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 to the family
GeneSprout is designed to support providers and patients. When a patient's results identify a finding, we provide clinician-facing context. We can support direct communication with your office, and support the care team as needed
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 2,800+ actionable conditions
Whole exome and whole genome sequencing across cardiovascular, metabolic, neurological, and pharmacogenomic conditions — curated for clinical relevance and focused exclusively on findings where early knowledge changes care.
CAP/CLIA-certified laboratory
All testing is processed in a CAP and CLIA-certified lab meeting the same clinical standard as hospital labs. Results are classified using ACMG variant interpretation guidelines.
Clinician-facing result summaries
Alongside the family-facing plain-language report, GeneSprout can provides a clinician summary when requested, including variant classification, relevant literature, and recommended next steps — formatted for direct use in the care setting.
Health navigation that supports your team
When a finding is identified, our health navigation team engages the family directly — answering questions, and ensuring their follow-up with your team. We extend your capacity without adding to your workload.
Simple referral pathway for any practice
Referring a patient to GeneSprout requires no EMR integration or practice-level agreement. Any provider can refer a patient directly through our portal — the family handles the rest.
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 — generate a referral link or provide a patient with your provider code. No formal agreement required. The family orders, collects, and ships the sample. You're notified when results are ready.
Or connect for a practice partnership
For practices and health systems that want deeper integration — volume arrangements, patient outreach support, or EMR-adjacent workflows — reach out to our provider partnerships team to explore what's possible.
Patient collects sample at home
A GeneSprout kit ships directly to the family. A simple cheek swab — no needles, no clinic visit — and the sample is returned by prepaid mail.
Lab analysis and result generation
The sample is processed in our CAP/CLIA-certified lab. Whole exome or whole genome sequencing is performed, and findings are interpreted against our curated condition list by our clinical team.
Results delivered to family and provider
Plain-language results go to the family through a secure portal. When directed by a patient, we'll send your office a clinician summary.
Learn more
Resources for clinicians.
Our Screening Science
What we test for and why.
Whole exome and whole genome sequencing covering 2,800+ 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 works alongside your care team — answering family questions, coordinating referrals, and keeping providers in the loop at every step.
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.