Vejthani Hospital Vejthani Hospital

Genetic Health Screening

Type

Blood Testing

Duration

30 min

Results

21 days

Comprehensive genetic screening program through DNA analysis assessing risk factors for various conditions. Valid through December 31, 2025. Includes 6 screening categories: Genetic Cancer Screening (6 items), Cardiovascular Disease risk (5 items), Neurological Disorders risk (3 items), Infectious Disease risk (16 items), Other Genetic Diseases (11 items), and Drug/Medicine Response Assessment (202 medication types). Includes doctor consultations and hospital service fees. Vejthani Q Life Center, 11th Floor.

Genetic health tests analyze your DNA to identify inherited variants that may affect your health risks, medication responses, and nutritional needs. Unlike standard blood tests that measure your current state, genetic tests reveal your underlying predispositions — information that doesn't change over time and only needs to be tested once. Common panels examine variants related to cardiovascular risk (APOE, Factor V Leiden), medication metabolism (pharmacogenomics), methylation (MTHFR), nutrient processing, and disease susceptibility. This information can help personalize your preventive health strategy and medication choices.

Key Details

Type
DNA analysis (one-time test)
Sample
Saliva or cheek swab
Turnaround
2–4 weeks
Results
Lifetime relevance — DNA doesn't change
Common Use
Risk assessment, pharmacogenomics

Who Is This For?

Anyone interested in personalized health insights based on their genetic makeup. People with a family history of genetic conditions who want to know their carrier status. Those wanting to optimize nutrition and supplementation based on genetic variants (e.g., MTHFR for folate metabolism). Patients who have experienced adverse medication reactions and want pharmacogenomic guidance.

What's Included

DNA extraction and analysis
Genetic variant identification
Risk assessment report
Specific genes tested vary by panel

Preparation Required

No fasting required. Sample collection is typically a saliva sample or cheek swab — no blood draw needed for most genetic tests. Results take longer than standard blood tests because DNA analysis requires specialized laboratory processing.

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