Understand your starting point
Build a private picture of family history and genetic-origin context. This helps add relevant testing; it never removes the universal screening core.
For individuals and couples planning a pregnancy
ClaviGenix™
Understand inherited risk before pregnancy.
A clear, private way to organize verified carrier-screening results and understand whether two partners share a clinically meaningful inherited-disease risk.
Research prototype with synthetic data only. No clinical service is currently offered.
A three-stage path
From your history to a clear, explainable report
Each stage adds context while keeping the underlying laboratory evidence, rules, and limitations visible.
Use verified laboratory results
The future service accepts structured results from approved, attended testing—not uploaded screenshots, emailed reports, or mailed samples.
See what the findings mean together
Versioned clinical rules compare two partners’ verified findings and explain the evidence, limits, and appropriate next step without judging the relationship.
Privacy and trust
Your information should serve you—not define you.
Future ClaviGenix records use a service-specific code instead of ordinary identifying details. Health plans and public programs may fund access, but funding does not grant them access to individual genetic findings.
Read the privacy commitmentsAbout us
Co-authoring future generations calls for thoughtful, informed choices.
ClaviGenix brings clinical perspective and technology research together around a participant-first, explainable approach to preconception information.