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Private Genetic Testing UK: Future-proof your Health.
Can’t link you to Genghis Khan*… but can map your cancer risk.
Can’t link you to Genghis Khan*… but can map your cancer risk.
*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.
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.
Testing 50 Genes Linked With Various Cancers
Testing ~800 Conditions That Could Affect Your Baby
Over 5,000 diseases are linked to genetic mutations
Up to 10% of those are due to genetic mutations we test for, such as BRCA1, BRCA2 and more.
From the ~800 genes we screen for in our carrier screening test. Making this test actionable and clinically significant.
However, some mutations such as BRCA1 can indicate a risk of >70% for breast cancer in your lifetime.
However, this varies by ethnicity and can be increased due to genetic variation.
Trusted specialists
Speak to our expert genetic specialist,
design your personalised test
Get your test through the mail,
easy oral self-swab
Get your detailed report and
recommendations
Smooth appointment process, short wait time, and a professional doctor. No complaints. Had the genetic cancer test and checked for vitamin deficiency- was fast and easy, great location and great space.
I am still in the process but so far my experience has been so positive. Everyone I have spoken to on the phone has been really helpful and kind. The people I have spoke to have really gone out of their way to explain things so I understand the process.
Great service from Ailidh and the team. Fair prices and very supportive. Recommended
I had a great experience with Jeen [the London Pregnancy Clinic] for my carrier screening. The staff was kind, professional, and attentive, and I received my results much faster than expected. I highly recommend them!
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.
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.
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.
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.
A registered genetic counsellor with a special interest in cancer genetics, including supporting families affected with Lynch syndrome or Hereditary Breast and Ovarian Cancer syndrome. Lily also has an interest in visual communication and scientific content development.
An HCPC-registered genetic counsellor with expertise in prenatal, reproductive, and cancer genetics, as well as rare diseases. Clair has a particular interest in immunology and haematology genetics and is passionate about integrating genetics into holistic patient care.
Catrina has extensive experience across both the NHS and private sector, and has specialist interests in prenatal genetics. She also has clinical experience in cardiac genetics and is passionate about supporting individuals and families through informed reproductive decision-making.
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.
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.
A dedicated midwife with over five years of experience across home births and tertiary hospitals, Saskia is passionate about empowering women through informed, holistic, and family-centred care. She is committed to supporting confident, positive birth experiences for every family.
An experienced midwife with a Master’s in Advanced Midwifery Practice and a background in fetal medicine and early pregnancy care. Siobhan provides NIPT counselling and is passionate about delivering safe, personalised maternity care.
A GP with extensive international experience in women’s and sexual health, Dr Uddin trained at Guy’s, King’s and St Thomas’ in London and has worked in Australia, the US, and the NHS. She provides holistic, patient-centred care at Spital Clinic.
A GP with a special interest in women’s health, lifestyle changes and menopause care, Dr Whittle trained in London and holds a BMS Menopause Certificate. She is passionate about holistic, accessible gynaecology and women’s health services.
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.
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.
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.
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.
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.
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.
Our team of Expert Specialists is here to help. Whether you're curious about testing, your results, or what’s right for you. We're just a message away.
