DNA health tests
DNA insights can help you transform your healthcare, now and in the future.
A new chapter in health
This isn’t about predicting the future. It’s about shaping it.
With our DNA health tests we can help you understand which medicines work best for you, identify your unique health risks, and turn the page to a healthier future.
This isn't just your life
It's your story
And next chapter?
It's still unwritten because your story isn't set
It's shaped by you
Imagine healthcare that follows your journey
Not the other way around
Imagine that your family history no longer predicts your future
Your lifestyle
Your risk factors
Your health goals
And now, your DNA
A new era in personalised healthcare
Introducing MY Genomic Health
Where we shape tomorrow, together
So pick up the pen
Own your story
For you
And those you love
Bupa My Genomic Health data, 2025
Understanding DNA health tests
Learn about DNA health tests, what the tests look for and the benefits with Dr Rebecca Rohrer.
Transcript
Who are you?
Hey, my name's Dr.
Rebecca r. I'm the Clinical Innovation
and Genomics Director at Bupa.
I am a working GP mom of three
and a young onset breast cancer survivor,
which gives me huge interest in genomics
as an exciting new field of medicine.
What is your background?
I'm the Director of Clinical Innovation
and Genomics at Bupa.
I've got a background working in our
insurance division as well.
As a medical director, I still practise as a gp,
and that gives me a huge vested interest in this shift from
reactive to preventative and personalised medicine.
I love to translate clinical innovation into direct patient
care so that we can benefit the whole customer experience.
What is genomics?
Genomics is the study of all
of the DNA in a living organism.
DNA acts like an alphabet,
and it's used to write the instructions
for everything that your body does.
Specific sections of DNA are called genes,
and each one of those is a unique instruction
for a particular function.
Genomics looks at the bigger picture.
It helps us understand how those genes interact
with each other and with the environment
to shape our traits, influence our health,
and contribute to disease.
What is a human genome?
The human genome is all
of the genetic instructions stored in a person's DNA.
It contains over 3 billion pairs of DNA letters A,
T, C, and G.
And together they code for about 20,000 genes.
These genes are organised into 23 pairs of chromosomes.
We call them pairs
because you inherit one set from your mother
and one set from your father, and this is why certain traits
or risks for diseases can run in families.
How is genomic data used in medicine?
Genomics is a rapidly evolving field that's changing
how we understand and manage medical conditions.
It helps healthcare professionals to personalise treatment,
predict disease risks, find genetic disorders,
and develop targeted therapies based on a person's genes.
What are the benefits of genomic testing?
Genomic testing helps predict disease risks,
identify genetic disorders and personalised treatments.
It enables tailored healthcare solutions by understanding
how genetic variations can affect individual responses
to medications and risk of developing disease.
What is personalised medicine and how does genomics contribute to it?
Personalised medicine is an approach to healthcare
that tailors medical treatment to an individual patient,
including their genetic makeup.
Now, genomics contributes to personalised medicine
by providing insights into
how genetic variations affect individual responses
to medication, the risk of developing disease,
but also to treatment, and that enables us to have effective
and customised healthcare solutions.
How can genomics help predict disease risk?
Genomics helps predict disease risk
by identifying genetic variations associated
with specific diseases.
By analysing an individual's genome,
scientists can assess the likelihood
of developing certain conditions,
and that enables early intervention
and personalised healthcare strategies.
What is pharmacogenomics?
Pharmacogenomics is the study of
how your genetic makeup influences
your response to medicines.
It can predict whether a medicine is likely to work for you,
whether you might experience side effects,
and what dose may be most suitable.
Because this information is based on your unique genetic
profile, pharmacogenomics plays a key role in personalised
medicine.
What is a polygenic risk score?
Polygenic risk score adds up the effects
of changes in lots
of different genes across your whole genome
to estimate your chance of developing a certain condition.
What is a carrier gene?
A carrier gene has a change
or what we call a variant linked to a genetic condition,
but the person doesn't show symptoms
because they can also have healthy copy.
Since we all inherit two copies of each gene,
one from each parent, carriers can pass this change
to their children, and if both parents are carriers
of the same condition, their child could inherit,
both changed copies and could be affected.
Knowing if you are a carrier helps you understand genetic
risks and make informed choices about family planning.
What DNA testing does Bupa offer?
We have three kinds of DNA tests, medication check checks.
Your response to medications,
a health check will reveal your risks
of developing certain conditions.
An advanced, a health check looks at your risk
of developing a wider range of health conditions,
polygenic risk scores, carrier genes,
pharmacogenomics, and traits.
More information about these tests can be found on our
website.
How can your DNA transform your health?
Bupa My Genomic Health combines DNA insights with joined up care. Testing is just the beginning.
With your results, we can give you expert guidance and care that works for you.
Personalised medicine
Understand which medicines work best for your body, with one simple at-home DNA test.
Reveal future health risks
Find which health concerns you’re more likely to develop based on your genes. We can then personalise your care and address risks early.
Small changes, big impact
With a deeper understanding of your health, you can be sure you know the right steps to stay well.
Health services powered by Bupa My Genomic Health
Medication Check
Medication Check analyses your DNA response to over 100 common medicines.
This includes medicines used to treat heart conditions, diabetes, mental health and more.
Get the right medicines and dosages for you, and minimise the chance of side effects.
DNA Health Check
Our DNA Health Check gives you a picture of your current health. It also identifies risks that we can actively help you manage.
From this, we can give you personalised care and advice to help you live healthier for longer.
What is DNA and genomic testing?
What is genomics?
Genomics can be a powerful tool to detect risk of disease. This can help you manage and take action to improve your health.
What is pharmacogenomics?
Pharmacogenomics looks at how your body responds to certain medication types, and can help you get better treatment.
DNA health tests for your employees
With DNA-powered healthcare you can empower your people to feel their best and do their best, so your business can thrive.
My Genomic Health is supplied by Bupa Occupational Health Limited. Registered in England and Wales with registration number 631336. Registered office: 1 Angel Court, London EC2R 7HJ
