Genetic Insights Service
Empowering patients to understand genetic results and advocate for their health with confidence and clarity.
Variant Interpretation
Specializing in identifying and explaining gene variants from whole genome or exome sequencing to make informed decisions with their healthcare team.
Research Support
Finding and summarizing variant-specific medical research to help individuals and families navigate complex genetic findings and take next steps with confidence.
Creating easy-to-understand reports based on your test results, along with templates for contacting labs, researchers, and doctors — so you’re prepared to advocate for yourself.
Clear Reports & Advocacy Tools
Helping you connect with labs, researchers, and rare disease organizations to share your genetic data, contribute to research, or find others with similar results.
Patient Research Connections
Most labs only provide a filtered summary of your results but that doesn’t mean there’s nothing more to find. We guide you through requesting your raw sequencing files or supplemental reports and help you look beyond the standard findings. This service is especially valuable if you’ve been told your results were “negative” but still don’t have answers.
Raw Data Support
Secure Genetic File Transfer & Cleanup
Need help getting your DNA data to your doctor or geneticist? We’ll guide you on how to securely log into platforms like Sequencing.com or 23andMe, retrieve your genetic data files, verify they're complete and correctly formatted, and upload them to a provider-approved location.
A Closer Look at Our Services
Our services are built to give you clarity and direction after receiving genetic test results. We don’t just research and summarize your variants, we help you take the next step, whether that means preparing for a doctor’s appointment, connecting with labs studying your gene, or submitting your genetic story to research platforms and patient registries.
Variant Interpretation
We use a combination of trusted genetic databases, literature searches, and AI-assisted tools to analyze your variants. You’ll receive a clear explanation of what’s known, what’s being studied, and what to bring to your provider for further conversation helping you navigate your health journey with confidence and purpose.
Research Support
We research your variant(s) using trusted scientific resources and advanced tools, including AI-assisted methods, to find the most relevant studies, historical classifications, and emerging insights. Every detail is curated and explained to help you make informed decisions, advocate for yourself, and stay current with evolving knowledge.
Patient Advocacy
We provide actionable resources to help you advocate for yourself or your family, including templates for contacting labs, suggestions for what to share with specialists, and curated lists of rare disease platforms and research initiatives where you can contribute your data or connect with others. Whether you're undiagnosed or exploring a variant of uncertain significance, we help you feel like you're part of the process not just waiting for answers.
Easy Reports
Each report is tailored to your unique results and goals, from basic variant summaries to fully annotated reference documents. We combine professional formatting, AI-generated structure, and human review to make complex genetic data clear and usable.