Genetic Testing Clinic Prices UK
Genetic testing clinics analyse DNA to identify hereditary disease risk, pharmacogenomic markers, and carrier status for inherited conditions. Tests can guide cancer screening, fertility decisions, medication choices, and lifestyle changes. Because results carry medical and ethical implications, clinics pair laboratory analysis with pre- and post-test counselling.
Specialist centres like London Genetics Centre, Newson Health Genomics, and North West Genomics Laboratory Hub offer targeted panels (BRCA, Lynch syndrome), whole exome sequencing, carrier screening, and pharmacogenomics. Appointments include a detailed family history, discussion of potential outcomes, and informed consent to ensure you’re ready for the information DNA testing reveals.
Genetic Testing Clinic Workflow
📄 Pre-test counselling
Genetic counsellors explain test scope, limitations, and inheritance patterns. You discuss how results may affect insurance, family planning, or relatives.
🧪 Sample collection
Blood samples or cheek swabs are taken in clinic or via home kits. Some tests require fasting or specific timing.
🔬 Laboratory analysis
UKAS-accredited labs analyse DNA using targeted panels or whole exome sequencing. Turnaround varies from 4 to 12 weeks.
🧠 Post-test consultation
Clinicians review results, explain risk levels, and outline screening or preventive options. Letters summarise findings for your GP and specialists.
How Much is Genetic Testing in the UK?
Single-condition panel (e.g. BRCA): £450 to £720.
Comprehensive hereditary cancer panel: £850 to £1 250.
Whole exome sequencing: £1 950 to £2 800 including counselling and medical recommendations.
Link results to ongoing health monitoring with private blood tests and specialist consultations.
Factors Driving Price
🧑⚕️ Counselling requirements
Pre- and post-test sessions with genetic counsellors add to costs but ensure responsible use of results.
🧪 Test complexity
Broad panels and exome sequencing analyse thousands of genes, increasing lab time and data interpretation.
📦 Family cascade testing
Testing relatives adds discounted follow-up costs but provides clarity for the wider family.
🧬 Interpretation updates
Some clinics include re-analysis if gene classifications change, while others charge extra.
How to Approach Genetic Testing Wisely
💡 Define your goals
Choose panels aligned to family history or clinical concern; avoid broad tests without clear action plans.
🤝 Check NHS eligibility
Individuals meeting NICE criteria (e.g. strong family cancer history) may access NHS-funded testing.
📅 Plan emotional support
Inform relatives about potential results and ensure counselling is available to interpret implications.
FAQs
Do I need a GP referral?
Private clinics accept self-referrals, but sharing reports with your GP ensures follow-up screening is coordinated.
Will results affect insurance?
Life insurers in the UK follow the Genetics & Insurance Moratorium, limiting use of predictive tests. Still, discuss implications with counsellors.
Can children be tested?
Usually only when results influence childhood medical care. Clinics advise on timing and ethics for paediatric testing.
Are results confidential?
Clinics follow GDPR and medical confidentiality. You control who receives copies of the report.
Can I use results for precision medicine?
Yes—clinicians use pharmacogenomic panels to tailor medications (e.g. antidepressants, anticoagulants). Share findings with prescribing doctors.
Conclusion
Genetic testing offers powerful insight when paired with expert counselling and clear action plans. Define your goals, involve your healthcare team, and use post-test guidance to turn genetic data into proactive care. 😁
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Alan Frost |
| Grew up in and live in Birmingham. Writer, publisher, editor, EFL teacher, composer. |
