Genetic Insights Service
Empowering patients to understand genetic results and advocate for their health with confidence and clarity.
Easy-to-read summaries of your results, plus templates for contacting labs, researchers, and doctors so you’re prepared for every appointment.
Clear Reports & Advocacy Tools
Connect with labs, researchers, and rare disease groups to share your data, contribute to research, or find others with similar results.
Patient Research Connections
Get help requesting, organizing, and reviewing your raw genetic files so you can go beyond standard lab summaries.
Raw Data Support
Secure Genetic File Transfer & Cleanup
Retrieve, verify, format, and securely send your genetic data to doctors, geneticists, or research programs.
A Closer Look at Our Services
Our services give you clarity and direction after receiving genetic test results. We don’t just summarize your variants, we help you take the next step, whether that’s preparing for a specialist visit, contacting labs studying your gene, or submitting your story to research registries.
Variant Interpretation
We analyze your genome or exome in full, using trusted databases, literature searches, and advanced tools to identify the variants that matter most. You’ll receive a clear explanation of what’s known, what’s being studied, and what to bring to your provider so you can move forward with confidence.
Research Support
We investigate your variants using peer-reviewed studies, historical classifications, and emerging insights. Every finding is curated and explained to help you make informed decisions and stay up to date with the science behind your DNA.
Patient Advocacy
We give you actionable tools to advocate for yourself or your family from templates for contacting labs to curated lists of rare disease platforms where you can share your data and connect with others. You’ll feel supported and prepared, not just waiting for answers.
Easy Reports
Each report is tailored to your unique results and goals, whether it’s a simple variant summary or a fully annotated, literature-backed document. Our reports are formatted for clarity so both you and your doctor can quickly understand the information and decide on next steps.