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.

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.

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:

• MTHFR Gene: The methylenetetrahydrofolate reductase (MTHFR) gene is a key player in folate metabolism and methylation. Variations in this gene can affect how the body processes and utilizes folate.
• MTR and MTRR Genes: These genes are involved in the conversion of homocysteine to methionine, a process crucial for methylation. Variations may impact this conversion and influence overall methylation status.
• COMT Gene: The catechol-O-methyltransferase (COMT) gene regulates the breakdown of catecholamines, including dopamine, norepinephrine, and epinephrine. Genetic variations in COMT can influence neurotransmitter balance.
• BHMT Gene: The betaine-homocysteine methyltransferase (BHMT) gene is involved in an alternative pathway for homocysteine metabolism. Genetic variations may