Evidence grading
Every genomic marker in our library is mapped to a 5-tier evidence system. We use established clinical consensus (STRONG/VALIDATED) to separate proven risk from emerging research.
Heritable Health Science
The methodology of clinical telegenomics
Heritable Health combines advanced bioinformatics with direct clinician oversight to ensure that genetic data is understood accurately and applied responsibly in a medical context.
Three commitments
How a report becomes clinical guidance
Clinician-in-the-loop
Bioinformatics can only go so far. We pair every report with a human clinician who reviews the data against your personal and family medical history.
Direct-to-Provider
We coordinate findings with your primary care team. Our summaries are formatted for inclusion in medical records, supporting ongoing management and follow-up.
The 5-tier evidence scale
Proven risk on the left, emerging research on the right.
- 01StarkClinical consensus
- 02ValidatedGuideline and FDA backed
- 03MäßigReplicated findings
- 04EmergingActive research
- 05ExploratoryEarly signal
Genetic insight has clinical limits
Our methodology is designed to prioritize findings that have clear clinical next steps. We do not provide speculative risk scores, and we distinguish clearly between proven medical risk and emerging genomic research.
- Strict adherence to clinical-genomics literature.
- Clear labelling of uncertainty and evidence tiers.
- HIPAA-grade data isolation and encryption.
- Focus on actionable clinical next steps.