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Caffeine is the most widely consumed psychoactive substance globally, found in coffee, tea, energy drinks, and some medications. The way your body processes caffeine depends largely on genetic factors, specifically how fast or slow caffeine is metabolized.

This test analyses specific genetic variations that affect how efficiently your body breaks down caffeine. People with certain genetic variations metabolize caffeine more slowly, leading to prolonged effects and potentially stronger stimulation. Slow metabolizers may also be at a higher risk for side effects like headaches, insomnia, and an increased risk of heart issues. Understanding your caffeine metabolism rate can help manage caffeine consumption for better health outcomes.

Cholesterol plays a vital role in heart health, but imbalances can lead to serious conditions like atherosclerosis, heart attacks, and strokes. High cholesterol is a major risk factor for cardiovascular diseases, which are the leading cause of death globally.

This test analyses genetic variations that affect how your body processes cholesterol. Identifying these variations can help understand your risk for high cholesterol and related health issues, providing insights into better managing your cardiovascular health.

Folic acid is essential for the proper functioning of the nervous, circulatory, and cardiovascular systems. This vitamin plays a key role in the metabolism of amino and nucleic acids, and deficiencies can lead to serious conditions like nervous system disorders and anaemia. It is also particularly important for women planning pregnancy, as folic acid is vital for foetal development.

This test analyses genetic variations that affect how efficiently your body converts folic acid. Changes in this gene can reduce folic acid absorption, increasing the risk of deficiency. Understanding your genetic predisposition can help manage folic acid levels for better health.

Lactose intolerance occurs when the body cannot properly digest lactose, a sugar found in dairy products, due to a lack of the lactase enzyme.

Our Lactose Intolerance Genetic Test analyses genetic variations that determine how well your body produces the enzyme needed to break down lactose. Identifying these variations helps determine your level of lactose tolerance, allowing you to manage symptoms and adjust your diet accordingly.

Peanut allergy is a serious condition that can trigger life-threatening reactions, such as anaphylaxis, after consuming peanuts.

This test analyses specific genetic variations that are associated with an increased susceptibility to the development of peanut allergies and play a key role in hereditary peanut allergy. Understanding your genetic predisposition can help manage the risk of severe allergic reactions, enabling better lifestyle choices and preventive measures.

Vitamin C is essential for immune function and overall health, acting as a powerful antioxidant. However, not everyone metabolizes vitamin C efficiently due to genetic factors.

This test analyses specific genetic variations that affect how your body processes vitamin C. Certain genetic deletions can reduce your ability to metabolize this vitamin, leading to lower levels despite similar dietary intake. Understanding your genetic predisposition can help ensure you meet your body's vitamin C needs through diet and supplementation.

Vitamin D is essential for maintaining healthy bones, muscles, and immune function. It is primarily produced in the skin through sun exposure, but genetic factors can affect how well your body metabolizes and transports this crucial nutrient.

This test analyses specific genetic variations that influence the efficiency of vitamin D metabolism. People with certain genetic changes may have a reduced ability to process vitamin D, leading to deficiency even with normal sun exposure or dietary intake. In the UAE, despite ample sunlight, vitamin D deficiency is widespread due to limited sun exposure and lifestyle factors. Understanding your genetic predisposition can help manage vitamin D levels to prevent associated health issues.

Vitamin E is a powerful antioxidant, essential for immune function, skin health, and proper nerve and muscle function. Vitamin E also contributes to the maintenance of the proper functions of the reproductive organs of men and women, while during pregnancy, an optimal amount aids in the development of the foetus. 

This test analyses specific genetic variations that affect how your body metabolizes fats, which are necessary for absorbing vitamin E. People with certain genetic changes may struggle to efficiently absorb vitamin E, leading to potential deficiencies. Understanding your genetic predisposition can help manage vitamin E levels, promoting overall health and vitality.

Fructose intolerance is a condition where the body cannot properly digest fructose, a sugar found in fruits, honey, and certain vegetables. This can lead to digestive issues such as bloating, abdominal pain, and diarrhoea, as well as more severe complications like liver problems and hypoglycaemia.

This test analyses specific genetic variations that affect how the body metabolizes fructose. People with certain changes in their genes may have reduced ability to process fructose, leading to intolerance. Understanding your genetic predisposition can help manage symptoms and prevent long-term health complications.

Iron is essential for oxygen transport, immune system function, and many other vital processes. Low iron levels can result in anaemia, causing symptoms like fatigue, weakness, and dizziness. While environmental factors can influence iron levels, genetic factors also play a significant role.

Our Iron Metabolism Genetic Test analyses variations in a key gene that helps regulate iron levels in the body. Certain genetic changes can predispose individuals to iron deficiency anaemia, making it harder to maintain healthy iron levels. Understanding your genetic predisposition can help identify the cause of chronic low iron and guide appropriate management.

Vitamin B12 is crucial for producing red blood cells, supporting the nervous system, and aiding various metabolic functions. Deficiencies can lead to symptoms like anaemia, dizziness, weakness, and neurological issues.

This test analyses specific genetic variations that affect the production of an enzyme involved in the absorption of vitamin B12 in the small intestine and its transport between the cells in the human body. People with an unfavourable genetic variant have a higher risk of vitamin B12 deficiency, related to the malabsorption of this vitamin. Understanding your genetic predisposition can help manage vitamin B12 levels to support overall health.

Breast and ovarian cancers can develop due to genetic mutations that impair DNA repair mechanisms, leading to uncontrolled cell growth. 

This test analyses specific variations in genes responsible for tumour suppression and DNA repair. Mutations in these genes can lead to a lifetime likelihood of breast cancer to over 80%. Identifying mutations that significantly increase cancer risk helps you and your healthcare provider make informed health decisions. Early detection is crucial in breast and ovarian cancers, as it can greatly improve treatment outcomes. By knowing your risk, you and your healthcare provider can make informed decisions about monitoring and preventive strategies.

Colorectal cancer is the second leading cause of cancer deaths globally, with cases expected to rise by 71.5% by 2035. Risk factors include unhealthy lifestyle choices like poor diet, obesity, excessive alcohol consumption, smoking, and genetic predisposition.

This test detects mutations in genes that regulate cell division and inhibit tumour growth. These mutations significantly increase the risk of conditions like familial adenomatous polyposis coli (FAP) and hereditary mixed polyposis syndrome (HMPS), which can lead to cancer. Early detection and awareness empower you to adopt healthier habits and engage in monitoring strategies, which is crucial given the rising prevalence of this serious disease.

Lung cancer is the second most common cancer and the leading cause of cancer deaths worldwide. While smoking is the main cause, genetic factors also significantly impact risk by affecting how your body handles harmful substances like nicotine. 

This test analyses specific genes that are responsible for the production of proteins that inhibit the growth and reproduction of damaged cells, as well as regulate the aging process of cells and the binding of harmful substances entering the lungs, including nicotine. Abnormalities in the indicated genes result in the formation of a protein that does not respond to DNA damage, increases the negative effects of smoking and the risk of addiction to nicotine, thus leading to a much greater risk of respiratory cancer.

Pancreatic cancer is seventh among cause of death from cancer. This type of cancer is highly lethal and is still characterised by low 5-year survival rate. Pancreatic cancer is more frequent in developed countries.

This test analyses specific variations that impair enzyme production in the pancreas, leading to chronic inflammation and increasing cancer risk. These genetic mutations affect enzymes essential for protein digestion and protecting the pancreas from self-damage. By identifying these variations, you and your healthcare provider can take proactive steps for monitoring and prevention, empowering you to make informed health decisions.

Prostate cancer is the third most common cancer in men. While it primarily affects men over 60, cases in younger men are on the rise. Risk factors include age, obesity, smoking, lack of activity, and notably, genetic predisposition.

This test analyses specific genetic variations that impair proteins responsible for preventing tumour development. Mutations in these genes may account for 30-40% of early-onset prostate cancer cases. Understanding your genetic predisposition empowers you to take proactive steps - such as regular screenings and lifestyle adjustments - for early detection and effective treatment.

Skin cancer, including melanoma, arises from abnormal skin cell growth, often due to UV exposure. Genetic factors significantly increase melanoma risk.

This test detects mutations in genes that are responsible for the production of proteins that inhibit the development of skin cancer, as well as for proper pigmentation, which is crucial for the protection of the skin. These variations can impair proteins that prevent cancer, raising your risk. By identifying these variations, you and your healthcare provider can take proactive steps for monitoring and prevention, empowering you to make informed health decisions.

Our Basic STD Package tests for four common sexually transmitted infections: Chlamydia trachomatis, HPV types 16 and 18, Syphilis (Treponema pallidum), and Gonorrhoea (Neisseria gonorrhoeae). These STIs often show no symptoms but can lead to serious health issues if left untreated.

Our Advanced STD Package tests for ten common infections: Chlamydia trachomatis, HPV types 16 and 18, Syphilis (Treponema pallidum), Gonorrhoea (Neisseria gonorrhoeae), Gardnerella vaginalis, Mycoplasma hominis and genitalium, Ureaplasma parvum and urealyticum, and Trichomonas vaginalis.

Quickly screen for Opiates, Cannabinoids, Barbiturates, Benzodiazepines, Amphetamines, Cocaine, Methadone/EDDP, Pregabalin, Tramadol, Fentanyl, and Synthetic Cannabinoids with our easy-to-use rapid test. The plastic strip changes colour upon contact with specific drugs, providing results in minutes.

User-friendly and accurate, this test is ideal for workplaces, clinics, and on-site settings. Ensure timely interventions and promote a safer environment with our reliable 12-parameter screening solution.

Coeliac disease (Gluten Intolerance) is an autoimmune condition where the body reacts negatively to gluten, causing inflammation and damage to the intestinal lining. This leads to malabsorption of nutrients, resulting in symptoms like abdominal pain, diarrhoea, and weight loss.

This test analyses specific genetic variations that affect the body’s immune response and tolerance to gluten. People with certain genetic variants are more likely to develop coeliac disease. Understanding your genetic predisposition can help identify gluten intolerance early, allowing for dietary adjustments to avoid long-term health complications.

Alzheimer's disease is a condition that slowly damages memory, thinking skills, and behaviour. This genetic test looks for variations in your DNA that may increase your risk of developing Alzheimer's.

This test identifies genetic variations that may increase the risk of developing Alzheimer’s. The variations analysed in this test affect how the brain works, particularly how well it clears out waste products and keeps nerve cells healthy. People with certain variations are more likely to experience problems in these areas, which can lead to the brain changes seen in Alzheimer’s.

Cardiovascular diseases, including conditions like atherosclerosis, coronary artery disease, heart attacks, and strokes, affect the heart and blood vessels. These diseases are the leading cause of death worldwide, often resulting from the buildup of plaque in arteries, high blood pressure, and poor blood circulation.

This Test analyses specific genetic variations that play a key role in how the body manages blood pressure and processes lipids (fats). These genetic mutations can contribute to the development of heart disease by affecting cholesterol levels and blood vessel health. Understanding your genetic risk helps in managing cardiovascular health and potentially preventing severe outcomes.

COVID-19 is a respiratory disease that can vary greatly in severity, from mild symptoms to severe respiratory failure. 

The test looks for changes in specific genes that affect how well your body manages respiratory infections. Certain genetic variations can lead to an increased risk of complications, such as difficulty breathing or even the need for hospitalization. Understanding these genetic factors can provide insights into your susceptibility to more severe outcomes from COVID-19.

Obesity is a significant health challenge linked to various serious conditions like type II diabetes, hypertension, cardiovascular disease, and certain cancers. It is influenced by both lifestyle and genetic factors that affect fat storage and appetite regulation.

This test analyses specific genetic variations that impact how your body balances carbohydrates and fats. These variations can increase fat storage and affect hunger signals, leading to a higher risk of weight gain. Understanding your genetic predisposition can provide valuable insights into weight management and overall health.

Parkinson’s disease is a progressive neurological condition that affects movement, leading to symptoms like tremors, stiffness, and slow movement. It is caused by the gradual loss of nerve cells in the brain that produce dopamine, a neurotransmitter essential for movement control.

This test analyses specific genetic variations associated with an increased risk of developing the disease. The test focuses on changes in a gene that provides instructions for building a protein involved in the function of nerve cells in the brain. These genetic variations can disrupt the communication between nerve cells, contributing to the development of Parkinson’s. Early identification of genetic risk factors can offer insights into potential disease progression.

Psoriasis is a chronic autoimmune condition that affects the skin, causing red, scaly patches and discomfort. It can also affect joints, leading to psoriatic arthritis.

This test analyses specific genetic variations linked to an increased risk of developing psoriasis. The test focuses on changes in a gene that provides instructions for regulating immune responses. These genetic variations can trigger abnormal immune reactions, which contribute to the skin and joint symptoms of psoriasis. Understanding your genetic risk can provide insights into managing and preventing psoriasis outbreaks.

Hypertension, or high blood pressure, is a common condition that increases the risk of heart disease, stroke, and other health problems. It is influenced by both environmental and genetic factors.

This test focuses on changes in genes that regulate the production of enzymes responsible for controlling blood pressure. These genetic variations can lead to fluctuations in blood pressure, the development of cardiovascular diseases, and changes in blood vessel structure, potentially contributing to atherosclerosis. Understanding these genetic factors can provide important insights into cardiovascular health.

Type II diabetes is a chronic condition in which the body does not regulate blood sugar (glucose) effectively, leading to high blood sugar levels over time. This can result in serious complications, such as cardiovascular disease, kidney failure, and nerve damage.

This test focuses on changes in a gene responsible for how well the body responds to blood sugar levels. These genetic variations can impair insulin production or reduce the effectiveness of insulin, leading to poor blood sugar control. Identifying genetic risk factors can offer insights into managing and potentially preventing the disease.

Androgenetic alopecia, commonly known as male or female pattern baldness, is a hereditary condition that causes hair loss, typically at the temples and top of the head in men and thinning across the scalp in women.

This test focuses on changes in a gene that regulates the interaction between hormones and hair follicles. These genetic variations can make hair follicles more sensitive to hormones, leading to hair thinning and loss. Understanding your genetic predisposition can provide insights into hair loss prevention and management.

Dyslexia is a learning disorder that affects reading, writing, and spelling abilities. It is often hereditary and results from differences in how the brain processes language.

This test focuses on changes in genes involved in brain development and communication between brain cells. These genetic variations can impact brain function, particularly in areas related to language processing. Understanding genetic factors associated with dyslexia can provide insights into learning difficulties and educational strategies.

Injury risk refers to an individual’s susceptibility to physical injuries during sports or other physical activities. Certain genetic factors can affect muscle structure and recovery, increasing the risk of strains, sprains, or other injuries.

This test examines specific genetic variations that influence how the body responds to physical stress and recovers from injuries. Variations in these genes can affect muscle structure, tissue recovery, and susceptibility to strains or sprains, providing insights into injury prevention and recovery strategies.

Skin moisture plays a crucial role in maintaining healthy, hydrated skin. Genetic factors can influence how well the skin retains moisture, affecting skin texture and sensitivity.

This test identifies genetic variations that affect the skin’s ability to retain moisture, and efficiently transport water and glycerol between skin cells. Unfavourable changes in the analysed gene results in decreased hydration of the epidermis. People with certain variations may be more prone to dry skin, which can lead to discomfort and increased sensitivity to environmental factors. Understanding your genetic predisposition can help guide skincare practices to maintain optimal skin hydration.

Sport predisposition refers to an individual’s natural inclination or genetic potential for success in certain types of physical activities or sports. Knowledge about sports aptitude is important to help children and young people develop their best qualities.

This test analyses genes that influence encoding of the protein that is the building block of muscles, as well as the proteins responsible for muscle regeneration after damage, the amount of enzyme affecting the blood supply to the tissues, as well as blood pressure. These variations can help determine which sports or physical activities you may naturally be more suited for, providing insights into optimizing athletic performance.

Stress tendencies refer to how an individual’s body responds to stress and the likelihood of experiencing stress-related symptoms. Stress can be caused by any type of physical or emotional stimuli and is an individual matter for each person, however, genes that control the amount of stress hormones produced have a great influence on this differentiation.

This test looks at genetic variations that affect the regulation of stress hormones. Analysed genes are responsible for enzymes involved in switching off the activity and degradation of neurotransmitters, e.g. dopamine, epinephrine and norepinephrine, as well as production of a protein that acts as a receptor for oxytocin. These variations can influence how a person’s body reacts to stressful situations, potentially increasing the risk of anxiety or other stress-related conditions. Understanding your genetic predisposition can provide insights into managing stress and maintaining mental well-being.

Thrombophilia is a condition where blood clots more easily, increasing the risk of serious issues like deep vein thrombosis (DVT) or pulmonary embolisms. It can be genetic or acquired, leading to clots in the legs, arms, abdomen, or brain.

Factor V Leiden (FVL) polymorphism is the most common inherited risk factor for thrombophilia. Our test detects this specific genetic variation. Knowing your FVL status helps you manage health risks - crucial for pregnant women, as pregnancy naturally increases blood clotting and can heighten the risk further.

Thrombophilia is a condition marked by increased blood clotting, leading to clots in deep veins and potentially causing a heart attack, stroke, or pulmonary embolism. It's particularly dangerous during pregnancy due to naturally heightened blood clotting.

Our FVR2 Polymorphism Test detects a specific mutation in the Factor V gene that significantly elevates thrombophilia risk, especially when combined with the Factor V Leiden mutation. Using precise PCR methods, this test determines your genotype to help assess and manage your risk.

Thrombophilia predisposes individuals to form blood clots that can block vessels, leading to conditions like a heart attack, stroke, or deep vein thrombosis. Symptoms may include calf pain, swelling, shortness of breath, or headaches.

The PAI-1 Polymorphism Test analyses a mutation in the PAI-1 gene, which produces a protein crucial for dissolving blood clots. Abnormalities can result in an increased level of the PAI-1 protein in the blood, reducing clot breakdown and raising thrombosis risk. This PCR-based test precisely identifies your genotype to evaluate your thrombophilia risk.

Thrombophilia causes blood to clot more easily, increasing the risk of deep vein thrombosis, pulmonary embolism, and even stroke. Symptoms may include leg pain, swelling, shortness of breath, chest pain, or neurological issues like headaches and visual disturbances.

Our Prothrombin Polymorphism Test detects genetic variations that affect the production of prothrombin—a crucial protein in blood clot formation. Certain changes can elevate prothrombin levels, raising clotting risk. Identifying these variations helps assess your genetic predisposition to thrombophilia, enabling proactive health management.