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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

Group of drugs: Cardiovascular drugs, Anti-inflammatory drugs, Antibacterial drugs

Name of each drug: Simvastatin, Atorvastatin, Clopidogrel, Warfarin, Acenocoumarol, Phenprocoumon, Celecoxib, Flurbiprofen, Ibuprofen, Lornoxicam Meloxicam, Piroxicam, Tenoxicam, Flucloxacilin, Amikacin, Gentamicin, Kanamycin, Paromomycin, Plazomicin, Streptomycin, Tobramycin, Antifungal drugs, Antiviral drugs, Skeletal Muscle Relaxants, Antidepressant drugs, Sedative drugs, Voriconazole, Flucytosine, Efavirenz, Abacavir, Nevirapine, Atazanavir, Succinylcholine, Amitriptyline, Clomipramine, Doxepin, Imipramine, Trimipramine, Citalopram, Escitalopram, Sertraline, Desflurane, Enflurane, Halothane, Isoflurane, Methoxyflurane, Sevoflurane, Gastrointestinal drugs, Antipsychotic drugs, Immunological drugs, Anticonvulsant drugs, Antineoplastic drugs, Antiemetics drugs, Omeprazole, Dexlansoprazole, Lansoprazole, Pantoprazole, Clozapine, Olanzapine, Siponimod, Azathioprine, Tacrolimus, Phenytoin, Fosphenytoin, Carbamazepine, Oxcarbazepine, Lamotrigine, Mercaptopurine, Thioguanine, Cisplatin, Capecitabine, Fluorouracil, Tegafur, Irinotecan, Granisetron, Docetaxel, Antigout drugs, Allopurinol

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.

Arrhythmogenic right ventricular dysplasia, familial 1, Arrhythmogenic right ventricular dysplasia, familial 2, Arrhythmogenic right ventricular dysplasia 8, Arrhythmogenic right ventricular cardiomyopathy, type 10, Arrhythmogenic right ventricular cardiomyopathy, type 12, Familial hypertrophic cardiomyopathy 1, Familial hypertrophic cardiomyopathy 3, Familial hypertrophic cardiomyopathy 5, Arrhythmogenic right ventricular dysplasia 9, Arrhythmogenic right ventricular cardiomyopathy, type 11, Cardiomyopathy, Familial hypertrophic cardiomyopathy 2, Familial hypertrophic cardiomyopathy 4, Familial hypertrophic cardiomyopathy 6, Familial hypertrophic cardiomyopathy 7, Familial hypertrophic cardiomyopathy 9, Familial hypertrophic cardiomyopathy 11, Familial hypertrophic cardiomyopathy 13, Familial hypertrophic cardiomyopathy 15, Familial hypertrophic cardiomyopathy 17, Familial hypertrophic cardiomyopathy 19, Fabry disease, Marfan syndrome, Cerebral arteriovenous malformation, Cerebral cavernous malformations 3, Cerebral cavernous malformations 1, Familial hypertrophic cardiomyopathy 8, Familial hypertrophic cardiomyopathy 10, Familial hypertrophic cardiomyopathy 12, Familial hypertrophic cardiomyopathy 14, Familial hypertrophic cardiomyopathy 16, Familial hypertrophic cardiomyopathy 18, Familial hypertrophic cardiomyopathy 20, Ehlers-Danlos syndrome, type 4, Cardiofaciocutaneous syndrome 1, Cerebral cavernous malformation, Cerebral cavernous malformations 2, Primary pulmonary hypertension 1, Essential hypertension, Primary dilated cardiomyopathy, Long QT syndrome, Familial hypercholesterolemia 2, Catecholaminergic polymorphic ventricular tachycardia, Brugada syndrome, Familial hypercholesterolemia 1, Familial hypercholesterolemia 3, Congenital heart disease, Familial hypercholesterolemia 4

Brain Disorders

This test analyzes genes related to brain and nervous system diseases that are inherited genetically.

Charcot-Marie-Tooth Disease (Covers more than 55 diseases), Hereditary Motor Neuropathies (Covers more than 23 diseases), Hereditary Sensory and Autonomic Neuropathy (Covers 11 diseases), Hereditary Sensory Neuropathy (Covers 4 diseases), Neuropathic Amyloidosis (Covers 3 diseases), Other Neuropathies and related disorders (Covers 16 diseases), Riboflavin Transporter Deficiency (Covers 2 diseases), A group of genetic diseases can cause abnormalities of the autonomic nervous system, which controls bodily functions outside of the mind's control, such as heart rate, blood pressure, and sweating, A group of genetic diseases associated with abnormalities in the sensory nervous system, A group of neurological diseases caused by a protein called amyloid, which accumulates in various tissues and organs, Other disease groups related to genetic disorders of the nervous system, A group of diseases that affect the nerves, causing hearing loss due to damage to the sound-sensing nerves in the inner ear

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.