Genetic / genomic testing
Analysis of genes or genomic panels informing individualized risk assessment and pharmacogenomic considerations, interpreted by qualified clinical staff.
What it is & how it works
Analysis of specific genes or broader genomic panels to inform individualized risk assessment, pharmacogenomic considerations (how a patient may metabolize certain medications), and, in some protocols, nutrigenomic factors relevant to program design.
How it's done
Typically performed via a saliva or blood sample sent for laboratory analysis, with results interpreted by a physician or genetic counsellor and integrated into the broader individualized plan rather than delivered as a standalone report.
Conditions it treats
Why Unfold Longevity
Interpreted by qualified clinical staff and framed as one input among several, not presented as a standalone diagnosis or deterministic prediction — consistent with Unfold Longevity's evidence-bounded language.
Evidence & safety
Interpreted by qualified clinical staff, not presented as a standalone diagnosis.
Related questions
It can inform individualized risk assessment, how you may metabolize certain medications (pharmacogenomics), and in some protocols nutrigenomic factors relevant to program design. It cannot diagnose a condition on its own, and it won't predict your response to every medication.
Results are interpreted by a physician or genetic counsellor as one input among several, not as a standalone diagnosis; genes are only one of many factors affecting disease risk and medication response, and test panels may be less complete for some ancestries or rarer variants. Results are integrated into your broader plan rather than delivered as an isolated report.