Simple, transparent pricing
Choose the option that best fits your needs. Get instant access to structured research insights.
Single Report
Perfect for individuals or families looking for a comprehensive overview of a single genetic finding.
- Single gene report generation
- Personal online report dashboard
- Downloadable PDF format
- Access to your report through your account
Institutional & Volume
For clinics, institutions, and patient advocacy groups needing multiple reports or ongoing access.
- Custom pricing for your needs
- Dedicated support
- Flexible invoicing
- All Single Report features
Notes
All purchases are one-time payments. No subscription required. Prices shown exclude applicable sales tax or VAT, which will be calculated at checkout based on your location. Please review our Refund Policy for more details.
In their words
Immediately after receiving a diagnosis, feeling overwhelmed and alone, we were able to run a report on Geneformation and understand what research was already out there and how we could progress it further. It gave us a foundation from which we were able to take action, and instead of feeling helpless, we were able to identify a path forward.
It turns a variant into a world. Reading the report, I recognized the first 15 to 20 hours of my own effort, already assembled. It compresses the distance between ‘we found a mutation’ and ‘here is what is known,’ which can otherwise take months of a physician’s time.
Geneformation is an exceptional resource for families, researchers, and clinicians alike. I used it to analyze cases studied in my own lab and was amazed that, in less than an hour, it produced a comprehensive summary that saved many hours of literature review and even uncovered an important publication I had missed. It has the potential to become an invaluable tool for advancing rare disease research and patient care.
Shared with permission. Educational research support — not medical advice, and not a description of any medical outcome.
Educational Research Support
Our reports organize publicly available research findings for informational purposes. They are not a diagnosis or medical advice. Always discuss findings and decisions with your clinician or genetic counselor.
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