Testing for >1000 conditions using your DNA

Genetic Testing for
hereditary cancer

Private Genetic Testing UK: Future-proof your Health.

Genetic Testing
And Counselling
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Genetic Conditions
we test for

Can’t link you to Genghis Khan*… but can map your cancer risk.

High Blood Pressure
Leukaemia Cancer
Cystic Fibrosis
Colon Cancer
Melanoma cancer
High Blood Pressure
Leukaemia cancer
Cystic Fibrosis
Colon cancer
Melanoma cancer
Nervous System
Brain Tumours
Hromosomal Instability
Ovarian cancer
Pancreas cancer
Nervous System
Brain Cancer
Chromosomal Instability
Ovarian Cancer
Pancreatic Cancer
Sarcomas Cancer
Heart Health
Lymphoma Cancer
Kidney Cancer
Thyroid cancer
Sarcomas cancer
Heart Attack
Lymphoma cancer
Kidneys cancer
Thyroid cancer


*Genghis Khan conquered half the world and fathered enough children that 1 in 200 men today might carry his DNA. Fun fact, but we’re less interested in ancient empires and more in mapping something truly powerful: your genetic risk for cancer.

What do we test for?

Know your genes, protect your future. Over 5,000 diseases are linked to genetic mutations. Early insights through genetic testing can help with prevention, early detection and personalised healthcare decisions.

Other Genetic Conditions

Over 5,000 diseases are linked to genetic mutations

Coming Soon
Hereditary Cancer Risk

Testing 50 Genes Linked With Various Cancers

Learn More
Other Genetic Conditions

Over 5,000 diseases are linked to genetic mutations

Coming Soon
1 in 2

Are estimated to have cancer in their lifetime in the UK

Up to 10% of those are due to genetic mutations we test for, such as BRCA1, BRCA2 and more.

>90%

Of the population will carry one or more mutation

From the ~800 genes we screen for in our carrier screening test. Making this test actionable and clinically significant.

13%

General risk for breast cancer in a women's lifetime in the UK

However, some mutations such as BRCA1 can indicate a risk of >70% for breast cancer in your lifetime.

1 in 8

Men will have develop prostate cancer in their lifetime

However, this varies by ethnicity and can be increased due to genetic variation.

How it works

Chat with our Genetic Counsellor, receive your at-home DNA kit with a quick cheek swab, send it back, and get your results in under 4 weeks.

How it works

Chat with our Genetic Counsellor, receive your at-home DNA kit with a quick cheek swab, send it back, and get your results in under 4 weeks.

1

Genetic Counselling

Speak to our expert genetic specialist,
design your personalised test

2

Get your test

in 1-2 working days,
easy oral self-swab

3

Get your report

Get your detailed report
and recommendations

Cancer Risk Assessment Tool

Disclaimer! This tool provides approximate cancer risk estimates based on genetic and ethnic factors. It is for educational purposes only and should not replace professional medical advice. Risk estimates are based on population-level data and may not reflect your individual circumstances. Always consult a healthcare provider or genetic counsellor for personalised risk assessment and screening recommendations.

Cancer Risk Assessment Tool

Meet our Team

Fetal Medicine Specialist at University College London and Founder of the London Pregnancy Clinic, a pioneer in early prenatal diagnostics and Non-Invasive Prenatal Testing (NIPT), leading the integration of innovative genetic testing and carrier screening into early pregnancy care.

Dr Anju Kulkarni

Consultant Clinical Geneticist and Medical Oncologist at Guy’s and St Thomas’ Hospital specialises in cancer genetics, genomic testing, and digital innovation, advising on genomic boards and helping develop tools like QGenome and Nucleus to improve patient care.

Dr Vishakha Tripathi

Experienced genetic counsellor and clinical scientist with expertise in cancer genetic testing, genetic counselling and decision making support. She works across the NHS, Cancer Alliances and private providers including her company DNA Connect.

Brings extensive NHS experience, specialising in prenatal genomics, cleft genetics, and patient education, and actively contributes to developing genomic education programmes for healthcare professionals through the North Thames Genomic Medicine Alliance.

Genomics Education Development Lead, specialising in cancer genetics, digital education tools, and visual communication, with a background spanning clinical practice at St George’s Hospital and content development for NHS England’s Genomics Education Programme.

University Hospital Lewisham, with expertise in gynaecological oncology, colposcopy, and advanced laparoscopic surgery, offering comprehensive care for early pregnancy complications, fertility, and pelvic floor disorders.

Dr Spyros Bakalis

Fetal Medicine Specialist at Guy’s and St Thomas’ hospital, with a subspecialty in maternal and fetal medicine, focusing on high-risk pregnancies including those complicated by maternal cardiac disease and cancer, and has contributed significant research on fetal growth / placental abnormalities.

Dr Diane Nzelu

Consultant in Maternal–Fetal Medicine at UCLH and Obstetric Lead for the North Central London Maternal Medicine Network. She has a special interest in hypertensive disorders of pregnancy and the management of medically complex cases, and has published widely on this topic. She also contributes to global maternal health initiatives.

Frequently
Asked Questions

What is genetic testing?

Genetic testing looks at your DNA to find changes or variants in your genes. These changes can tell us if you’re at risk for certain inherited conditions, like hereditary cancers or if you’re a carrier for a genetic condition.

What can genetic testing tell me?

It can reveal if you have a higher genetic risk for certain cancers (like breast, ovarian or bowel), if you’re a carrier for inherited conditions, or if you have a genetic condition that could impact your health or your family’s.

Will the results tell me if I’ll definitely get a disease?

The meaning of your results depends on the type of test you've had — some genetic tests are screening tools that assess the likelihood or risk of a condition, while others are more diagnostic in nature.

Genetic tests can look for variations in your DNA that may be associated with certain conditions. In some cases, a result may indicate an increased risk, but not a certainty, of developing a condition. In others, it may suggest you carry a genetic change without it ever affecting your health.

Not all people with a disease-causing variant will go on to develop the condition, and some without a detectable variant may still be affected due to non-genetic factors such as environment, lifestyle, or chance.

Always discuss your results with a qualified healthcare provider or genetic counsellor to fully understand what they may (or may not) mean for you and your family.

How does it work?

It’s simple. You’ll first speak with one of our expert Genetic Counsellors. Depending on your location and the type of test, you’ll either receive a saliva kit in the post for an at-home cheek swab, or we’ll arrange a at-home blood sample collection.

Blood draws can be done at our partner clinic in Shoreditch, Spital Clinic, or by a mobile phlebotomist visiting your home. Your sample is then sent to a certified lab in the UK or US, and results are typically ready in under 4 weeks.

Is my data safe and private?

Yes. At Jeen Health, your data is encrypted and stored securely on our GDPR compliant servers, as well as with our vetted laboratories. Your results are only shared with you and your dedicated Genetic Counsellor, never with insurers or third parties.

Is genetic testing only for people with a family history of disease?

Not at all. While a strong family history increases your risk, many people with genetic conditions have no known family history. Testing helps you uncover hidden risks you wouldn’t otherwise know about.

Get in touch

Our team of expert Genetic Counsellors is here to help. Whether you're curious about testing, your results, or what’s right for you — we're just a message away.

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