Our clinical genetics service serves over five million people. Our team works together to offer accurate information and support.
Regional genetics clinics offer services to diagnose and assess the risk of you or your family inheriting a genetic condition. It is not always possible to make a specific diagnosis for a family or child, however, a genetic assessment will help you to understand the possible diagnoses and treatment options.
Because diagnosis and testing will often have an impact on the wider family, the genetic counselling process includes an explanation and risk assessment with any available options for family members.
It may take time to adjust to new diagnoses and to decide on the best possible course of action. Our team will provide up-to-date and unbiased information. We suggest asking for an update when the affected person and family members reach reproductive age, and before a new pregnancy. Testing, risk-reducing treatment and research options change over time.
Commitment to research
The genetics clinic is part of the Division of Medical and Molecular Genetics at King’s College London. Our team are committed to genetic research and academic excellence.
100,000 Genomes project
The South London Genomic Medicine Centre (GMC), hosted by Guy’s and St Thomas’, is one of the centres taking part in the 100,000 Genomes Project.
The national programme will focus on cancer and rare diseases and will enable pioneering research to decode 100,000 human genomes, a scale not seen anywhere else in the world.
Find out how Guy's and St Thomas' are involved in the 100,000 Genomes Project.
A collaboration between King’s Health Partners and PHG Foundation has been undertaking a health economic analysis into the cost effectiveness of using exome sequencing as a routine clinical test. The results from the pilot project, which was funded by Guy’s and St Thomas’ NHS Foundation Trust, are now published in the free report Whole-exome sequencing in clinical genetics: A health economic evaluation.
This is an evidence-based economic evaluation to assess the costs of routine clinical use of exome sequencing in clinical genetics. The results show that if used as a near first line and sequencing costs could be reduced further, the test would represent cost-effective use of NHS resources given the much higher detection rate.
- From the 4th of September 2017 we will be offering an updated prenatal array CGH service with higher resolution analysis. Please go to our Prenatal Referrals Page for further information. We have a Prenatal Genomics Education Day planned for the 8th September 2017 at Guys Clinical Genetics Service which will outline this update please contact firstname.lastname@example.org if you are interested in attending