Health + Talent Geneus DNA (Standard Set)

About This Service

Healthcare innovation and discovering potential from DNA
Simply collect samples from saliva or make an appointment for sampling at Siam Square One, 2nd floor.
Can be tested at any age, young and old, or newborn.
- Let you know yourself and keep you healthy on your own, deep down to the DNA level. And choose the one that suits you best for sustainable health.
- Take a sample from the bulge of the cheek with a simple procedure. It does not hurt and does not require a blood draw. Can be tested at any age, young and old, The U.S. has international lab standards, including CLIA certified, CAP certified, which is the highest recognized in the world.
- Easy-to-understand test reports with personalized advice from experts that will help you take care of your health and longevity.
- See the results on the application 24 hours a day and keep new topics updated. A single examination can bring results for life.
***Once the payment you can make an appointment and show the QR code to pick up the product and collect samples at GeneusDNA's Siam Square One branch, 2nd floor.

Standard Health and talent DNA test by experts in the certified USA laboratory.
Discover 250 reports according to your DNA
- Talent (12 items)
- Genetic and Behavior (11 items)
- Metabolism and weight loss (5 items)
- Food Intolerance from DNA and Food Sensitivity (12 items)
- Health risk assessment (11 items)
- Exercise (9 items)
- Need for vitamins and minerals (12 items)
- Infectious diseases (4 items)
- Genetic disorders carrier and Preconception and Family Planning (101 items)

DNA Vitamin group
- Vitamin A : BCMO1 gene
- Vitamin B6 : NBPF3 gene
- Vitamin B9 – Folate : MTHFR gene
- Vitamin B12 : FUT2 gene
- Vitamin C : SLC23A1 gene
- Vitamin D : GC gene
- Omega-3 : FADS1 gene

Food sensitivities and intolerance
- Lactose Intolerance : MCM6 gene
- Caffeine metabolism : CYP1A2 gene
- Alcohol flush reaction : ALDH2 gene
- Response to dietary saturated fat : APOA2 gene
- Celiac disease : HLA-DQA1, HLA-DQA2

Lifestyle and behavior
- Sweet tooth : SLC2A2 gene
- Satiety – feeling full : FTO gene

Antioxidant
- SOD2 (Manganese Superoxide Dismutase 2)
- GSTP1 (Glutathione Sulfotransferase P1)

Weight loss methods
- Low-carb diet
- Low-fat diet
- Caloric restriction
- Ketogenic Diet
- IF (Intermittent fasting
- Cardio exercise
- Strength training exercise

Sports performance
- VO2 Max efficiency
- Power / Endurance performance
- Injury risk
- Free radicals during exercise
- Post-exercise recovery

Fitness and holistic health
- insu.lin sensitivity response to Cardio exercise
- Glucose response to Cardio exercise
- HDL response to Cardio exercise

Health risk
- Alzheimer’s disease
- Parkinson’s disease
- Age-related macular degeneration
- Hereditary thrombophilia
- Hereditary hemochromatosis
- G6PD
- Type-2 Diabetes
- Hypertension
- Increased LDL
- Increased Triglyceride
- Decreased HDL
- Carrier status and rare disease 101 diseases

Genetic disorders carrier and Preconception and Family Planning (101 items)
Achondrogenesis
Achromatopsia
Acute fatty liver
Alkaptonuria
Alpha-Mannosidosis
ARSACS
Agenesis of the Corpus Callosum with Peripheral Neuropathy
Autosomal Recessive Polycystic Kidney Disease
Andermann syndrome
Beta Thalassemia & related hemoglobinopathies
Bloom syndrome
Biotinidase deficiency
Bardet-Biedl Syndrome
Galactosylceramide beta-galactosidase deficiency
Beta-sacroglycanopathy(Limb-girdle muscular dystrophy)
Caravan Disease
Carnitine Palmitoyltransferase deficiency
Choroideremia
Citrullinemia type I
Citrullinemia type II
Cohen syndrome
Combined Pituitary Hormone Deficiency
Congenital Adrenal Hyperplasia
Congenital Disorder of Glycosylation
Cystic fibrosis
D-Bifunctional Protein Deficiency
Deafness
Diastrophic Dysplasia
Dihydrolipoamide Dehydrogenase deficiency
Dilated Cardiomyopathy
Duchenne Muscular Distrophy
Factor XI Deficiency
Familial Dysautonomia
Familial Mediterranean fever
Fanconi Anemia
Familial Hyperinsu.linism
Gaucher Disease
G6PD
Glutaric acidemia
GRACILE syndrome
Glycogen storage disease type 1a
Glycogen storage disease type 1b
Glycogen storage disease type V
Hemophilia B
Hereditary Fructose Intolerance
Herlitz Junctional Epidermolysis Bullosa
Hexosaminidase A Deficiency(Including Tay-Sachs Disease)
Homocystinuria
Homocysteinemia
Hyperinsu.linism
Inclusion Body Myopathy
Isovaleric Acidemia
Joubert Syndrome
Krabbe Disease
Leigh Syndrome, French Canadian Type
Limb-Girdle Muscular Dystrophy Type 2D
Limb-Girdle Muscular Dystrophy Type 2E
Limb-Girdle Muscular Dystrophy Type 2I