Genetics Resources & Support

Genetics can be complex, and finding reliable information online is not always easy. This page brings together trusted organisations, patient support groups, educational resources and laboratory information that may help you better understand genetic conditions, genetic testing and inherited health risks. 


Please note that external websites are provided for information only. CKE Genetics is not responsible for the content of third-party websites.

NHS & Genomics Resources

Access trusted information and support from leading NHS and genomics organisations to help you better understand genetic health and testing.

NHS Genomics

Information about how genetics and genomics are used within NHS healthcare.

NHS Health Information

Trusted patient information covering a wide range of health conditions and genetic topics.

Genomics England

Information about genomic medicine, research and national genomic programmes.

Genomics Education Programme

Information about genomic medicine, research and national genomic programmes.

Cancer Genetics Resources

Find trusted information, support services, and educational resources to help you understand inherited cancer risk, genetic testing, and your healthcare options.

Cancer Research UK

Information on inherited cancer risk, cancer genetics, screening and prevention.

Macmillan Cancer Support

Practical and emotional support for people affected by cancer and their families.

Breast Cancer Now

Information about inherited breast cancer, BRCA genes and support services.

Target Ovarian Cancer

Information about ovarian cancer, inherited risk factors and BRCA-related cancers.

Lynch Syndrome UK

Information and support for individuals and families affected by Lynch syndrome.

Rare Disease Resources

Living with a rare disease can be challenging. These trusted organisations offer information, guidance, advocacy, and support for individuals and families affected by rare and genetic conditions.

Genetic Alliance UK

The UK’s national charity supporting people affected by genetic, rare and undiagnosed conditions.

Rare Disease UK

Advocacy, education and support for individuals living with rare diseases.

Unique Rare Chromosome Disorder Support Group

Support and information for families affected by rare chromosome and gene disorders.

Global Genes

International patient support and advocacy organisation for rare diseases.

Inherited Heart Conditions

Learn more about inherited heart conditions and the support available to help individuals and families understand their diagnosis, manage their health, and make informed decisions.

British Heart Foundation

Information on inherited heart conditions and cardiovascular health.

Heart Rhythm Alliance

Resources and support relating to inherited cardiac rhythm disorders.

Carrier Screening & Family Planning

Planning for the future can bring many questions. These resources offer guidance, support, and information on carrier screening, genetic conditions, and reproductive options to help you navigate your family planning journey with confidence.

Sickle Cell Society

Information about sickle cell disease, carrier status and family planning.

Antenatal Results and Choices (ARC)

Support and information for parents facing difficult decisions during pregnancy following screening or diagnostic testing.

Learning About Genetics

Genetics plays an important role in health, inheritance, and disease. Explore trusted educational resources to learn about genes, genetic conditions, inheritance patterns, genetic counselling, and the latest developments in genomic medicine.

MedlinePlus Genetics

Comprehensive information about genetic conditions, genes and inheritance patterns.

National Society of Genetic Counsellors

Information about genetic counselling and the role of genetic counsellors.

Understanding Genetics

Patient-friendly educational resources covering genetics and inherited conditions.

Our Laboratory Partners

CKE Genetics collaborates with carefully selected accredited laboratory partners to provide access to a broad range of high-quality genetic testing services. Together, we support accurate results, informed decision-making, and personalised patient care.

Blueprint Genetics

Specialists in rare disease, hereditary cancer and inherited condition testing.

Fulgent Genetics

Clinical genetic testing across hereditary cancer, reproductive health and rare diseases.

Bioarray

Genetic testing services supporting reproductive and clinical genetics pathways.

MolMart

Exome-based reproductive carrier screening and advanced genomic testing services.

CKE Genetics Services

Our genetic testing services help individuals and families gain greater clarity about inherited conditions, health risks, and reproductive options through expert-led testing and support.

Carrier Screening

Understand your risk of passing on inherited genetic conditions before or during pregnancy.

Cancer Genetics

Assess your inherited risk of cancer and explore appropriate screening and prevention options.

Rare Disease Testing

Explore whether a health condition or symptoms may have an underlying genetic cause.

Proactive Genetic Screening

Gain insight into future genetic health risks and inherited conditions.

General Genetic Consultation

Speak with a genetic counsellor if you are unsure which testing pathway is right for you.

Patient Support Organisations

Living with, or being at risk of, a genetic condition can raise many questions. These trusted patient support organisations provide information, practical guidance, advocacy, and community support for individuals and families affected by inherited conditions.

Alzheimer's Society

Information and support for families affected by dementia and inherited neurological conditions.

Muscular Dystrophy UK

Support, advocacy and information for people affected by muscular dystrophy and related conditions.

Huntington's Disease Association

Explore whether a health condition or symptoms may have an underlying genetic cause.

Fragile X Society

Support and information for individuals and families affected by Fragile X syndrome.

Disclaimer

The information on this page is intended for educational purposes only and should not be considered medical advice. If you have concerns about your health, family history or genetic risk, please book a consultation with one of our genetic counsellors or speak with your healthcare professional.