Packages include Whole Exome Sequencing, Genotyping, DNA Methylation, Hereditary Cancer Screening, Carrier Screening, Health Risks Assessment, Ancestry Insights, Customized Wellness Planning, Pharmacogenetics and More.
✅ Secure, Private and Confidential Screening
✅ Personalized Health Insights and Recommendations
✅ Easy to Read Illustrative Reports by Email
✅ Complimentary Consultation with Geneticist
Unveil Your DNA: Discover the Secrets Within
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Embark on a transformative journey of self-discovery with our comprehensive Premium Exclusive DNA Program. Unlock over 500 genetic insights, unraveling the mysteries of your health and innate talents. Tailored for all ages, Premium Exclusive DNA empowers you to make informed decisions for a healthier and more fulfilling life. Embrace the power of your DNA with our cutting-edge analysis and embark on a path to optimized well-being and self-awareness. Your genetic story awaits, discover it with Premium Exclusive DNA today.
Methylation Test
Methylation is a fundamental biochemical process that involves the addition of methyl groups to various molecules, including DNA, proteins, and neurotransmitters. Methylation plays a vital role in gene expression, detoxification, energy production, and neurotransmitter balance. A Methylation Test assesses genetic variations that can impact an individual's methylation capacity. Key components covered by a Methylation Test may include:
Health and Nutrition
Vitamin B6, Vitamin B9 - Folate, Vitamin B12, Vitamin C, Vitamin A, Vitamin D, Omega-3 fatty acids, Copper, Phosphorus, Caffeine sensitivity, Alcohol sensitivity, Calcium, Magnesium, Zinc, Nutrition, Lactose intolerance, Celiac predisposition, Response to saturated fat, Satiety - obesity gene, Liver detoxification, Spice sensitivity, Sweet tooth, Cellular detoxification, Salt sensitivity.
Allergy and Sensitivity
Cockroach allergy, Dust mite allergy, Pet allergy, Atopic dermatitis, Spice sensitivity.
Talent and Abilities
Reading and spelling ability, Language, Musical Ability, Pollen allergy, Intelligence, Mathematical ability, Working memory, Memory ability, Multi-tasking skills, Power sports, Task attention, Creativity, Endurance sports.
DNA Character
Adventurer, Adjuster, Analyst.
Fitness and Sports Performance
VO2 Max - Aerobic potential, Injury risk, Power/Endurance potential, Free radicals during exercise, Post-exercise recovery, Insulin sensitivity response to exercise, HDL response to exercise, Glucose response to exercise.
Healthy Weight
Low-carb diet, Low-calorie diet, Low-fat diet, Cardio exercise, Strength training.
COVID-19 Infection and Severe Symptoms Risk
ABO gene, OAS gene, DDP9 gene.
Behavioral Traits
Addictive Behavior, CCHCR1 gene.
Personality Traits
Intrinsic Motivation to Exercise, Misophonia, Stress management.
Skin and Beauty
Age Spots, Skin Glycation Risk, Morning Person, Freckles, Acne Risk, Stretch Marks, Wrinkles, Keloid Formation, Sun Sensitivity, Cellulite Protection.
Sleep and Environmental Sensitivity
Sleep duration, Deep sleep, Sleep movement, Air pollution, Pollution Sensitivity, Secondhand smoke, Traffic-related pollution.
Neurological and Mental Health
Alzheimer’s disease, Age-related macular degeneration, Health Risk, Parkinson’s disease, Hereditary thrombophilia, Hereditary hemochromatosis, Elevated Triglycerides, Type 2 Diabetes, Androgenetic alopecia, Body odor, Elevated LDL Cholesterol, Decreased HDL Cholesterol, Hypertension.
Physical Traits
Bitter taste sensitivity, Earwax type, Hair thickness, Pain sensitivity, Motion sickness, Age-related hearing loss.
Carrier Status
Achondrogenesis, Acute fatty liver, Alpha-Mannosidosis, Agenesis of the Corpus Callosum with Peripheral Neuropathy, Achromatopsia, Alkaptonuria, ARSACS, Autosomal Recessive Polycystic Kidney Disease, Andermann syndrome, Bloom syndrome, Bardet-Biedl Syndrome, Beta-sacroglycanopathy (Limb-girdle muscular dystrophy), Carnitine Palmitoyltransferase deficiency, Citrullinemia type I, Cohen syndrome, Congenital Adrenal Hyperplasia, Cystic fibrosis, Deafness, Dihydrolipoamide Dehydrogenase deficiency, Duchenne Muscular Dystrophy, Familial Dysautonomia, Beta Thalassemia & related hemoglobinopathies, Biotinidase deficiency, Galactosylceramide beta-galactosidase deficiency, Caravan Disease, Choroideremia, Citrullinemia type II, Combined Pituitary Hormone Deficiency, Congenital Disorder of Glycosylation, D-Bifunctional Protein Deficiency, Diastrophic Dysplasia, Dilated Cardiomyopathy, Factor XI Deficiency, Familial Mediterranean fever, Fanconi Anemia, Gaucher Disease, Glutaric acidemia, Glycogen storage disease type 1a, Glycogen storage disease type V, Hereditary Fructose Intolerance, Hexosaminidase A Deficiency (Including Tay Sachs Disease), Homocysteinemia, Inclusion Body Myopathy, Joubert Syndrome, Leigh Syndrome, French Canadian Type, Limb-Girdle Muscular Dystrophy Type 2E, Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD), Maple Syrup Urine Disease Type 1A, Mucolipidosis, Methylmalonic Acidemia, Muscular dystrophy-dystroglycanopathy, Neuronal Ceroid Lipofuscinosis, Northern Epilepsy, Pendred Syndrome, Pompe Disease, Pseudocholinesterase Deficiency, Primary Hyperoxaluria type III, Rhizomelic Chondrodysplasia Punctata Type 1, Sickle Cell Anemia, Familial Hyperinsulinism, G6PD, GRACILE syndrome, Glycogen storage disease type 1b, Hemophilia B, Herlitz Junctional Epidermolysis Bullosa, Homocystinuria, Hyperinsulinism, Isovaleric Acidemia, Krabbe Disease, Limb-Girdle Muscular Dystrophy Type 2D, Limb-Girdle Muscular Dystrophy Type 2I, Maple Syrup Urine Disease Type 1B, Maple Syrup Urine Disease Type III, Metachromatic Leukodystrophy, Mucopolysaccharidosis, Nemaline Myopathy, Niemann-Pick Disease, Oculocutaneous Albinism, Polyglandular Autoimmune Syndrome, Primary Carnitine Deficiency, Primary Hyperoxaluria type II, Pycnodysostosis, Salla Disease, Sjogren-Larsson Syndrome, Tyrosinemia Type I, Usher Syndrome type 1F, Usher Syndrome type 3A, Zellweger Syndrome Spectrum.
Ancestry
For this report, Geneus DNA will analyze genes to identify DNA similarities based on populations of each race collected from around the world.
DNA Fun Facts
Asparagus Odor Detection, Romantic relationship status.
Cancer Risk
Breast Cancer, Colorectal Cancer, Pancreatic Cancer, Prostate Cancer, Gastric Cancer, Ovarian Cancer, Lung Cancer, Skin Cancer, Urinary Bladder Cancer, Cervical Cancer, Melanoma Cancer.
Premium Health Risk
Osteoarthritis, Osteoporosis, Periodontitis, Telomere length, Lipoprotein a or Lp(a), Glaucoma, Gallstones, Varicose veins, Migraine, Systemic Lupus Erythematosus (SLE), Anxiety, Asthma.
Drug Response
Cardiovascular drugs, Anti-inflammatory drugs, Antibacterial drugs, Antifungal drugs, Antiviral drugs, Skeletal Muscle Relaxants, Antidepressant drugs, Sedative drugs, Gastrointestinal drugs, Antipsychotic drugs, Immunological drugs, Anticonvulsant drugs, Antineoplastic drugs, Antiemetics drugs, and Antigout drugs.
Heart Diseases
This test analyzes genes related to various types of genetically inherited heart diseases within the family, such as severe heart muscle disease, severe heart arrhythmias, and severe hyperlipidemia.
Brain Disorders
This test analyzes genes related to brain and nervous system diseases that are inherited genetically.
Cardiovascular Disease Risk
This test analyzes genes involved in various inherited cardiovascular diseases: Stroke, Coronary artery disease, Atherosclerosis.
Genetic Height
This report will analyze genes related to growth and hormone production, which constitute factors influencing an individual's height. The results of your genetic analysis will be utilized to estimate your height based on the average height for your race.
Detoxification DNA Test
Detoxification DNA Test analyzes specific genetic markers associated with the body's detoxification processes. The human body has sophisticated mechanisms to eliminate toxins and harmful substances, and these processes are influenced by various genes. The Detoxification DNA Test provides insights into how efficiently an individual's body processes and removes toxins, pollutants, and other environmental stressors.
Examining the genetic code to analyze individual characteristics lifestyle, design balancing food and nutrition including the exercise that is most appropriate for you. It can also predict the risk of diseases that will be caused by genetic factors to be used as information to reduce the risk of disease in the future.
Do you experience symptoms of gut microbiome imbalance?
Signs may include:
Did you know that the gut houses over 5,000 types of microorganisms? Our Gut Microbiome Screening examines more than 100 different microorganisms in your body.
This screening uses stool samples to evaluate gut bacteria, providing key insights into:
Importance of Gut Microbiome Screening
A balanced gut microbiome supports a protective mucus layer that guards against harmful bacteria and inflammation. An imbalance may elevate the risk of diseases such as inflammatory bowel disease (IBD) and irritable bowel syndrome (IBS), and increase susceptibility to conditions triggered by pathogenic bacteria.
How the Test is Conducted
The test involves Next Generation Sequencing (NGS) and uses a swab similar to an ATK test. It can be completed at home or in the hospital. If done at home, a hospital staff member will collect the swab and send it to Korea for analysis. The process is quick and straightforward.
Benefits of the Screening
Next Steps After Results
A doctor will interpret your results, assess your risk for conditions related to gut microbiota, such as IBS, obesity, diabetes, migraines, anxiety, and depression. They will offer advice on:
Recommendations for a Healthy Gut
Who Should Consider This Screening?
This screening is suitable for individuals with symptoms such as:
