Sequenced once, useful for the rest of your life. We report only what is clinically actionable, and we agree in advance what you want to know.
What it covers
- Clinically actionable disease variants
- Pharmacogenomics — how you metabolise common medication
- Carrier status, where relevant to family planning
- Raw data provided to you for future reinterpretation
How it is performed
A single blood sample. Sequencing and interpretation take four to six weeks.
How to prepare
No preparation is required. Before testing you will have a consultation about which categories of finding you wish to receive.
How we read it
With a clinician, in person, never by email. Pharmacogenomic findings often change prescribing immediately; risk variants change what we monitor and how often.