Health + Talent Geneus DNA (Standard Set) [Flash Sale eVoucher]

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"