Your genome,finally decoded.

The Sentinel is £1,695 and reads the 84 genes where a finding changes what a doctor does. The Vantage is £2,850 and reads around 200 heart and cancer genes, with Lp(a) and ApoB. The Legacy is £8,500 and reads the whole genome, with a medicines report, a genetic heart score, carrier status, the Longevity+ blood panel and a doctor review every year for three years. The Legacy Family is £32,500 for four people, with further members at £7,950 each, and for family offices, up to six people across three generations start from £47,500. Every option begins with a free call with one of our doctors.

A geneticist takes you through it before anyone else does, and your doctor turns it into a plan the same week. Where a finding calls for a specialist, we book that appointment for you rather than handing you a letter. Most findings are things that can be watched or acted on early, which is the reason to look.

Saliva at home, from a kit couriered to your door and returned in the prepaid box, or a blood draw in Marylebone with the counsellor’s first conversation on the same visit. The genome is the same either way.

Most genomes are reported within twelve weeks of the laboratory receiving the sample, and the counsellor books your results conversation as soon as the report is signed. The first conversation happens before the sample, so you know what can and cannot be found before you give it.

It reads the eighty one genes on the ACMG list where a finding changes what a doctor does, your carrier status where you ask for it, how your body handles the medicines you are most likely to be prescribed, and your polygenic risk for coronary disease. Most people learn that nothing on the list needs acting on. It does not diagnose every condition, it does not replace your history, your examination or your blood work, and it does not predict a life.

You, the counsellor and your doctor at The Wellness. Your raw data is yours to download at any time and is deleted the day you ask. It is never sold and never shared for research without your written consent. Under the code agreed between the UK government and the insurance industry you do not have to disclose a predictive genomic result to an insurer, with one exception for Huntington’s disease on life cover above £500,000.

Because what is known about a genome changes every year while the sequence itself does not. Each year the laboratory re reads your stored genome against what has been learned since, without a second sample, and the counsellor writes to you only when something has changed.