Our advanced research algorithms analyse 700,000 data points to provide you with indepth insights to your health.
As we all know, people with various ethnic backgrounds such as South Asian versus European have varying risk assessments for specific diseases such as diabetes and heart disease.
We are one of the only companies in the UK to perform this examination of your
ancestry before applying our advanced algorithm.
 
Complex Diseases: GWAS In this part of our report, we leverage GWAS publications, a research method comparing DNA markers in individuals with and without certain diseases. While not diagnostic, these studies offer valuable insights for early detection and prevention, highlighting potential genetic factors to monitor. It's important to recognize that complex diseases are influenced by multiple factors beyond genetics, including lifestyle and diet, which often have significant impacts.
 
Complex Diseases: Mutations Here, we delve into mutations within key genes from an oncological perspective. Our focus is on identifying mutations known as pathogenic in major scientific communities, shedding light on potential cancer risks.
 
Biomarkers, Biometrics, and Traits This section employs GWAS statistical analyses to assess your genetic predisposition to specific metabolic parameter abnormalities. By examining biomarkers and biometrics, we provide insights into potential health risks and personalized intervention opportunities.
 
Hereditary Diseases We explore genetic mutations associated with hereditary conditions that can be passed down to future generations. Even if carriers remain symptom-free, there's a risk of transmitting these conditions to offspring. Genetic testing for both prospective parents before conception is essential to mitigate these risks. If hereditary diseases are prevalent in your family, genetic testing offers vital guidance from geneticists on preventive measures and family planning strategies.
 
Here is a list of conditions we test for. Please note the list may vary at time of testing due to various factors not limited to advances in technology or even further scientific data of relevance, etc.
 
Cancers:
Breast cancer
Prostate cancer 
Bladder cancer
Upper aerodigestive tract cancers 
Basal cell carcinoma 
Squamous cell carcinoma
Non-melanoma skin cancer
Glioma 
Hodgkin’s lymphoma 
Diffuse large B cell lymphoma 
Follicular lymphoma 
Testicular germ cell tumor 
Wilms tumor 
Endocrine Disorders:
Hypothyroidism
Type 1 diabetes 
Type 2 diabetes 
Neurological Disorders:
Alzheimer’s disease (late onset)
Parkinson’s disease
Multiple sclerosis
Schizophrenia 
Myasthenia gravis
Neuroblastoma 
Psoriasis 
Respiratory Disorders:
Chronic bronchitis and chronic obstructive pulmonary disease 
Asthma (childhood onset) 
Autoimmune Disorders:
Rheumatoid arthritis
Celiac disease 
Psoriasis 
Cardiovascular Disorders:
Intracranial aneurysm 
Coronary heart disease
Myocardial infarction (early onset)
Musculoskeletal Disorders:
Osteosarcoma
Follicular lymphoma
Gynaecology:
Endometriosis
Genetic Disorders: ( We are not able to distinguish between carrier types within the test limits. )
Microcephaly 3, Primary, Autosomal Recessive
Microcephaly 5, Primary, Autosomal Recessive
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 1
Osteogenesis Imperfecta, Type Ii
Noonan Syndrome 1
Noonan Syndrome-Like Disorder With Or Without Juvenile Myelomonocytic Leukemia
Myopathy, Myofibrillar, 1
Myopathy Centronuclear
Myopathy, Centronuclear, X-Linked
Long Qt Syndrome 1
Leigh Syndrome
Leopard Syndrome 1
Leukoencephalopathy With Vanishing White Matter
Lissencephaly 1
Polymicrogyria, Bilateral Frontoparietal
Niemann-Pick Disease, Type A
Cystinosis, Nephropathic
Nemaline Myopathy 2
Loeys-Dietz Syndrome 2
Maple Syrup Urine Disease
Meckel Syndrome, Type 3
Pontine And Cerebellar Hypoplasia
Metachromatic Leukodystrophy
Methylmalonic Aciduria And Homocystinuria, Cblc Type
Niemann-Pick Disease, Type B
Melanocortin 4 Receptor Deficiency
Albinism, Oculocutaneous, Type Ib
Osteogenesis Imperfecta, Type Iii
Retinitis Pigmentosa
Rubinstein-Taybi Syndrome 
Mucopolysaccharidosis, Type Vii
Mucopolysaccharidosis, Type Iva