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health
  • Health Insight Test

    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
      £380.00Price

      ANYONE  CAN TAKE  THE TEST

      • Pro-active, health-conscious people who wish to prepare for the future.

      • Anybody with a family or personal history of unfavourable medication reactions.

      • whenever the course of treatment is not working.

      • People who are on multiple medications.

      • People taking or starting certain specific medications.

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