Your genome,finally decoded.
We read your genome and explain what it means for your health, your medicines and your family. It starts at £1,695, with the sample taken at home or at our clinic in Marylebone.
Request a consultationThree billion lettersdecide who you are.
Every cell in your body carries a copy, written in four letters: A, C, G and T.
0.1%
of them make you unique.
Every hero has an origin story. Yours is written in three billion letters, and this is the part only you have. It is why a medicine that works for a friend may not work for you, and why a risk can run in your family.
To read it,we open it.
In the laboratory your DNA is separated into single strands, and the letters along each one are read in turn.
Breast and ovarian cancer
If you carry a change here, screening starts earlier and comes round more often, and preventive surgery becomes a conversation worth having. Your sisters and daughters may want to know too.
Inherited high cholesterol
About one person in 250 has cholesterol that is high from birth, however well they eat. A statin started early takes away most of the risk.
How you respond to clopidogrel
Clopidogrel is the blood thinner usually given after a stent. About a third of people barely activate it. If you are one of them, you are given a different drug from the start.
Where a findingchanges your care.
We check the 84 genes where a result changes what your doctor does. About 6 in every 100 people carry a finding in one of them.
The Sentinel
£1,695
for one person
The 84 genes where a finding changes what a doctor does, with a results consultation with a doctor and the full raw data files.
- A first call with a doctor at no charge
- Report updated if a finding is reclassified
- A registered genetic counsellor where a finding appears
- First specialist consultation, where a finding calls for one
The Vantage
£2,850
for one person
Around 200 heart and cancer genes, Lp(a) and ApoB, a results session with a genetic counsellor, and the full raw data files.
- A first call with a doctor at no charge
- Results consultation with a doctor
- First specialist consultation, where a finding calls for one
- Relatives screened for a family finding at a family rate
The Legacy
Our recommendation
£8,500
for one person
The whole genome, a medicines report, a genetic heart score, carrier status, the Longevity+ blood panel, and a doctor review every year for three years.
- Whole genome, over 500 genes reported
- A registered genetic counsellor before and after
- Full re-reading within two years, and a yearly check against new research
- Relatives screened for a family finding, included for two
The Legacy Family
The Legacy for four people, a named family physician for the year, and a family results meeting with the counsellor.
Who is being read
- You
- Adult
- Child
- Child
£32,500
for four people£32,500 for four, then £7,950 for each person after that
Medicine evolves.Your readingevolves with it.
With The Legacy, your genome is read again in full within two years and checked against new research every year. We tell you if anything changes for you.
One sample.All we will ever need.
Your genome is read once and kept, so every check from here on starts from it.
Request a consultationWhole genome sequencing at The Wellness starts at £1,695 for The Sentinel, which reads the genes where a finding changes what a doctor does and includes a results consultation. Most genomes are reported within twelve weeks of the laboratory receiving the sample.
- What it costs
- The Sentinel £1,695, The Vantage £2,850, The Legacy £8,500.
- How soon
- Most genomes are reported within twelve weeks of the laboratory receiving your sample.
- How to begin
- Request a tier online, then give saliva at home from a couriered kit or blood in Marylebone.
Evidence and questions
Which findings are reported
The American College of Medical Genetics and Genomics keeps a list of genes where a finding is medically actionable, and recommends reporting them from clinical exome and genome sequencing1.
The list is revised as the evidence changes, which is why a stored genome can be read again in later years.
Genetic results and insurance
Under the UK Code on Genetic Testing and Insurance, insurers should not ask for or take into account a predictive genetic test result, except for Huntington’s disease when life cover is over £500,0002.
How genetic data is protected
UK GDPR names genetic data as special category data, which carries extra legal protection3.
Is it right for you
A genome result can reveal a risk you did not expect, and it may also matter to parents, siblings or children.
A genome reads inherited risk and does not diagnose new symptoms, so see a doctor first for those and call 999 in an emergency.
A result with no finding does not rule out every inherited condition, because the report covers known, actionable genes1.
Questions
Will a genetic test affect my life insurance?
For most people, no. The UK code says insurers should not ask for or use a predictive genetic test result, with one exception for Huntington’s disease on life cover over £500,0002.
How does UK law protect my genetic data?
Genetic data is special category data under UK GDPR and carries extra protection3. Your raw data is yours to download, and it is deleted the day you ask.
Which genes does a genome test report?
A clinical report focuses on genes where a finding changes what a doctor does, following the list kept by the American College of Medical Genetics and Genomics1.
Do I speak to a genetic counsellor?
Yes. A genetic counsellor talks with you before the sample is taken and holds your results conversation as soon as the report is ready.
- Lee K, Abul-Husn NS, Amendola LM and others, for the ACMG Secondary Findings Working Group. ACMG SF v3.3 list for reporting of secondary findings in clinical exome and genome sequencing, a policy statement. Genetics in Medicine, 2025. DOI 10.1016/j.gim.2025.101454, PMID 40568962
- Department of Health and Social Care, Code on Genetic Testing and Insurance, GOV.UK, updated March 2026
- Information Commissioner’s Office, What is special category data?
Reviewed 15 October 2026.
How it works
1
A conversation first
One of our doctors calls you to talk through your family history and what you want to know. It is included, and it commits you to nothing.
The era of
personal medicine.
You are part of the first generation who will not be treated as an average.
The genome, and the years ahead.
Our guide to what your genome can tell you now, and what is coming next.
Questions
Medicine made for you.
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