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Clinical Genetics Consultation

A Clinical Genetics Consultation at London Prengnacy 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.

Carrier screening diagram, by London Pregnancy Clinic, explaining how genetic mutations are passed from parents to child, showing that each parent contributes one gene of each pair, with a risk of the child inheriting a genetic condition if both parents carry the same mutation.

The best selection of advanced carrier screenings in London with Genetic Counselling help available

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. This is particularly important 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 (e.g., cancer predisposition)

  • A child has developmental features that may require medical genetics input

  • Same-day, evening, and weekend genetic tests

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.

Carrier Genetic Testing Explained

What are the benefits of genetic testing?

Genetic testing offers several benefits, not just for you, but for your entire family. Here are some key advantages:

  • 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.
  • 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.
  • Personalized Care: With genetic information, doctors can provide more personalized 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.

Overall, genetic testing empowers you with knowledge about your health and your family’s health. It helps you make well-informed decisions and take proactive steps to ensure the best possible outcomes for you and your loved ones.

We STRONGLY recommend having a pre-test counselling session prior to these appointments for an additional £80.

Who is a genetic counsellor?

A genetic counsellor specialising in pregnancy and fertility is a healthcare professional trained in genetics and counselling. They assist individuals and couples during preconception, pregnancy, and the postnatal period. They help assess the risk of inherited conditions, interpret test results like carrier screening or NIPT, and advise on genetic testing options.

These counsellors work with fetal medicine specialists to provide crucial support. They help families navigate the complex landscape of genetic information. This guidance enables families to understand their options for family planning, prenatal screening, and managing potential genetic risks. This support ensures the best possible outcomes for both parents and their future children.

At London Pregnancy we offer Genetic Counselling and Testing/Screening via our partner, Jeen Health.

Who needs a Clinical Genetics consultation?

You may benefit from a Clinical Genetics Consultation if you want clearer answers about inherited risk, unusual results, or unexplained symptoms. This service is particularly helpful for:

  • High-risk or complex family history, including early cancers or repeated patterns

  • Pregnancy and prenatal concerns, including screening results and next-step options

  • Unclear, positive, or unexpected genetic test results, where interpretation affects decisions

  • Rare or undiagnosed symptoms, when other assessments haven’t explained the cause

  • Children with developmental concerns or features suggestive of a genetic condition

  • Planning ahead, when you want prevention advice based on family risk

Early review can reduce uncertainty and guide the most appropriate testing pathway.

Clinical Geneticist vs Genetic Counsellor

Both roles work together, and you may see one or both.

  • Clinical Geneticist: a medical doctor who can assess, diagnose, and oversee medical care
  • Genetic Counsellor: a specialist who explains risk, supports decision-making, and helps you understand testing

Often counselling with a GC (genetic counsellor) is the first step. Complex cases, or results with medical implications, may need a clinical geneticist’s input.

What happens during the appointment?

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.

Carrier screening diagram, by London Pregnancy Clinic, showing the chances of passing on cystic fibrosis if both parents are healthy carriers, with 25% chance of child having CF, 50% chance of child being a carrier, and 25% chance of child not inheriting CF.

Otther 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.

30-Minute Genetic Counselling

Quick, Targeted Support

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

60-Minute Genetic Counselling

Comprehensive, Personalised Support

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

Online Genetic Counselling

In the Comfort of Your Home

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

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 strongly recommend genetic counselling with Jeen’s counsellors before choosing a test. They will guide you and help you select the best test for your needs and requirements.

Carrier Screening Tests

Screening for 787 monogenic conditions

BEACON 787 is one of the most advanced carrier screening tests, detecting a wide variety of severe autosomal recessive and X-linked genetic conditions. We strongly recommend genetic counselling before taking this test. 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.

Karyotype Chromosome Analysis

DIAGNOSTIC CHROMOSOMAL TESTING

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.

NIPD Testing

NON-INVASIVE PRENATAL DIAGNOSIS FOR SINGLE-GENE CONDITIONS

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 strongly recommend counselling and, where needed, clinical genetics input to confirm eligibility, timing, and the most appropriate pathway.

Frequently Asked Questions

Your questions answered

What is a Clinical Genetics Consultation?

A Clinical Genetics Consultation is a doctor-led appointment focused on inherited risk and complex genetic concerns. It helps clarify what results mean in a medical context and sets out a clear plan for next steps, including whether testing is likely to be useful.

How is this different from genetic counselling?

Genetic counselling focuses on education, risk assessment, and decision support around testing. A Clinical Genetics Consultation adds medical assessment by a doctor who can consider diagnoses, interpret complex findings clinically, and advise on management and referrals where appropriate.

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?

Many consultations can be done by secure video when the focus is history and results review. If an examination is needed, we will advise you on the best format.

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?

Only with your consent. We can provide a clear letter summarising the assessment and recommendations that you can share with your care team if you wish.

What if my family history suggests an inherited cancer risk?

A consultation can help assess patterns in your family, estimate risk, and advise on appropriate testing and surveillance pathways. Where relevant, we can also provide a clear summary you can share with your wider medical team.

If you have them, bring previous test results, scan reports, and clinic letters. It also helps to note key family diagnoses and the ages at diagnosis, but you don’t need perfect information to benefit from the consultation.

Do you want to know more about your options of Genetic Tests?

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