Understanding Health Risks
Genetic testing can identify if you or your partner are carriers of genes for certain genetic conditions. This helps you understand the risk of passing these conditions to your children.
Clinical Genetics Consultation
A Clinical Genetics Consultation at London Pregnancy Clinic, delivered in partnership with Jeen Health, provides a doctor-led review of complex family history, pregnancy concerns, or unclear genetic results.
In a 30–90 minute appointment (£400), you’ll receive clear interpretation, personalised testing recommendations, and a practical plan for next steps.
Doctor-led review for complex genetic concerns
Genetic questions can feel overwhelming, especially in pregnancy, when decisions can be time-sensitive. At London Pregnancy Clinic, we offer Clinical Genetics Consultations, delivered in partnership with Jeen Health, to provide clear medical guidance when family history, symptoms, or genetic results are complex or uncertain.
This service is ideal if you need a medical genetics specialist (a clinical geneticist) to review your case, interpret results, and recommend the most appropriate next steps, including whether further testing is worthwhile.
Importance of a Clinical Geneticist
Some situations need more than counselling alone. A Clinical Genetics Consultation brings in a doctor specialising in genetic conditions who can medically assess risk, consider diagnoses, and advise on clinical management.
A clinical geneticist can also advise on the most appropriate type of testing (and whether testing is likely to be informative), which is especially helpful when patients feel they’re being offered “more tests” without clarity.
You may benefit from a clinical geneticist’s input when:
- A result could change medical decisions (pregnancy, surgery, surveillance)
- Symptoms suggest a genetic condition but the cause is unclear
- Results are positive, unexpected, or complex to interpret
- Family history suggests a hereditary syndrome
- A child has developmental features that may require medical genetics input
- You want prevention advice or a clear testing pathway based on your family risk
A genetic counsellor and a clinical geneticist work together, and you may need one or both — often counselling with a genetic counsellor is the first step, while complex cases or results with medical implications may need a clinical geneticist’s input. If you’re not sure whether you need a genetic counsellor or a clinical geneticist, contact us directly and we’ll help advise on the right appointment for you.
What your consultation involves
Your consultation is structured, calm, and designed to be easy to follow. The clinical geneticist reviews your personal medical history and your family history in detail, then integrates any relevant test results, scan findings, and clinic letters. You’ll receive a clear explanation of what the evidence suggests, what remains uncertain (if anything), and which options are most appropriate next.
If testing is recommended, you’ll be guided through what the test can realistically answer, its limitations, and what different outcomes would mean for you. You’ll leave with a practical plan, which may include further testing, reassurance and watchful waiting, pregnancy-related pathways, or referrals and surveillance recommendations where appropriate.
Appointments last 30–90 minutes, depending on complexity.
Informed Decisions
Knowing your genetic risks lets you make informed decisions about your pregnancy and family planning. You can consider options like IVF with preimplantation genetic testing (PGT-M) testing, early interventions, or other preventive measures.
Personalised Care
With genetic information, doctors can provide more personalised care. They can recommend specific tests, treatments, or lifestyle changes to help manage or reduce health risks.
Family Health Insights
Genetic testing can reveal important health information that may affect other family members. If a genetic condition is identified, other relatives can also get tested and take steps to manage their health.
Early Intervention
Detecting genetic conditions early can lead to earlier interventions and better management of the condition. This can improve the quality of life for affected individuals.
Peace of Mind
For some, genetic testing provides peace of mind. Knowing your genetic information can alleviate uncertainties about potential health risks.
Preventive Measures
Genetic testing allows for preventive measures to be taken, potentially reducing the risk of having a child with a genetic syndrome.
Other Genetic Counselling Services
At London Pregnancy Clinic, we commit to providing personalised and compassionate genetic counselling tailored to your unique needs. We offer various types of genetic counselling to suit different requirements through Jeen Health. Contact us today to learn more about our genetic counselling services and discover how we can support you throughout your pregnancy journey.
Quick, Targeted Support
30-Minute Genetic Counselling
Our 30-minute genetic counselling session is ideal for those seeking quick yet expert advice on specific genetic concerns. Whether you’re looking for clarity on genetic tests or help interpreting your results, our experienced counsellors provide clear and actionable guidance. Book this session if you need: Pre-test counselling for NIPT or carrier screening; Help interpreting genetic test results; Support with understanding Down syndrome test outcomes; Guidance on further testing or treatment options. 30 min appointment.
Comprehensive, Personalised Support
60-Minute Genetic Counselling
Our 60-minute genetic counselling session offers an in-depth, face-to-face review of your genetic concerns. This session provides detailed, tailored advice on your family’s medical history and hereditary risks, empowering you to make informed decisions about your health and pregnancy. Book this session if you need: A comprehensive review of your family’s medical history and hereditary risks; Personalised advice on genetic tests like NIPT and carrier screening; Preconception counselling to assess genetic risks before trying to conceive. 60 min appointment.
In the Comfort of Your Home
Online Genetic Counselling
Our online genetic counselling sessions provide personalised, expert guidance without the need to leave your home. Whether you need quick answers or a comprehensive review, we offer flexible options to suit your needs. Choose between our 30-minute and 60-minute sessions for tailored support on genetic tests, family history, and hereditary risks. Book the session that suits your needs to receive expert genetic counselling, all from the comfort of your home. 30-60 min appointment. book 30 Min now – £80; book 60 Min now – £140.
Genetic Screening Tests
London Pregnancy Clinic offers a wide range of advanced and effective genetic screening tests. The best time for carrier screening is before pregnancy; for NIPT, it is at 10 gestational weeks. Our tests cover various types of genetic conditions. We only support testing with a pre-test appointment with a genetics clinician. They will guide you and help you select the best test for your needs and requirements.
What we look at
Screening for 1,008 genes
Carrier Screening Tests
Beacon One+ is one of the most advanced carrier screening tests, detecting a wide variety of severe autosomal recessive and X-linked genetic conditions. We only support testing with a pre-test appointment with a genetics clinician. If a genetic condition is found, post-test counselling is included in the price. We also recommend that both parents undergo simultaneous carrier screening testing. This ensures a comprehensive understanding of potential genetic risks.
Diagnostic chromosomal testing
Karyotype Chromosome Analysis
Karyotype chromosome analysis examines the complete set of chromosomes to identify changes in chromosome number or structure. It is commonly used in fertility and recurrent miscarriage workups, and can be helpful when there is a personal or family history suggesting chromosomal rearrangements. At London Pregnancy Clinic, results are interpreted with clinical context and clear guidance, so you understand what the finding means and how it may affect your reproductive options.
Non-invasive prenatal diagnosis for single-gene conditions
NIPD Testing
When there is a known familial condition or a specific inherited risk, NIPD can provide more targeted answers than screening alone. This test is used for certain single-gene disorders and can be a valuable option when you need clarity without invasive procedures. We only support testing with a pre-test appointment with a genetics clinician to confirm eligibility, timing, and the most appropriate pathway.
Your questions answered
Why do you recommend counselling or a clinical genetics review before genetic tests?
Because the value of a genetic test depends on choosing the right test for the right question and understanding its limitations. Counselling and clinical review help avoid unnecessary testing, reduce anxiety caused by misunderstood results, and ensure there is a practical plan for every possible outcome.
Do I have to have genetic counselling before booking a Clinical Genetics Consultation?
Not always. Some patients come directly for a medical genetics opinion, especially if they already have results to interpret or a complex history. If counselling would be helpful first, we can advise on the best order for your situation.
What happens if I already have a genetic test result from another clinic?
You can bring external results, including uncertain or unexpected findings, and we will review what they mean, how reliable they are in context, and what follow-up (if any) is recommended.
Will I definitely need genetic testing after the consultation?
No. In many cases, the most helpful outcome is reassurance, a clarified risk assessment, or a monitoring plan. If testing is recommended, it’s because it is likely to add meaningful information for decisions or medical care.
Can you help with pregnancy-related genetic questions and screening results?
Yes. We regularly support patients who have concerns arising from screening results, family history, previous pregnancy outcomes, or questions about the most appropriate next steps and timing.
Can the clinical geneticist consultation be online?
Yes, the clinical geneticist consultation can be online in many cases. When the focus is reviewing your personal and family history and interpreting existing results, a secure video appointment usually works just as well as coming in person. If a physical examination turns out to be helpful, our team will let you know and advise on the best format for your situation.
At London Pregnancy Clinic we offer both in-clinic and remote appointments, and our online genetic counselling sessions follow the same approach. When you book, tell us whether you would prefer video or a clinic visit, and share any test results, scan reports, and clinic letters beforehand so the specialist can review them in advance and make the most of your time together.
What does a “variant of uncertain significance” mean?
It means a genetic change has been found but current evidence does not confirm whether it is harmful. We explain what this means in practical terms, whether it should change care, and what (if anything) can clarify it over time.
Will you share my results with my GP or specialist?
We will only share your results with your GP or specialist with your consent. Your genetic information is confidential, and nothing is sent to anyone else without your agreement. After your consultation, we can provide a clear letter summarising the assessment, what your results mean, and any recommendations, so your wider care team has the full picture if you choose to involve them.
Many patients find it reassuring to keep their own GP informed, particularly where surveillance or follow-up may be arranged locally. You are welcome to share the letter yourself, or ask us to send it directly to a named clinician. If you have questions about referrals or how your results fit with NHS care, our genetic testing and counselling team is happy to talk this through with you.
Contact
Do you want to know more about your options of Genetic Tests?
Sources & clinical references
The figures and clinical statements on this page are drawn from the sources below. Guidance evolves — always discuss your individual circumstances with a clinician.
- NHSGenetic and genomic testing2024
- Royal College of Obstetricians and GynaecologistsNon-invasive Prenatal Testing for Chromosomal Abnormality using Maternal Plasma DNA (Scientific Impact Paper No. 15)2014
- Human Fertilisation and Embryology AuthorityPre-implantation genetic testing for monogenic disorders (PGT-M) and chromosomal structural rearrangements (PGT-SR)
- NHS England Genomics Education Programme (GeNotes)Variant of uncertain significance (VUS) — Knowledge Hub2024
- MedlinePlus Genetics, US National Library of MedicineWhat are the uses of genetic testing?