





Key Benefits
- Covers 21,000 Protein-Coding Genes – Extensive analysis for a deeper health understanding.
- High-Depth Sequencing (150X-180X) – Ensures accuracy and reliability.
- Identify Genetic Risk Factors – Understand inherited conditions and predispositions.
- Improve Diagnosis & Treatment – Get personalized insights for better health management.


What You’ll Get in Report
📌 Genetic Variants Analysis – Identify mutations linked to health conditions
📌 Disease Risk Assessment – Evaluate inherited disease risks
📌 Pharmacogenomics Insights – Learn how your genes affect medication response
📌 Carrier Screening – Find out if you're a carrier for inherited disorders
📌 Personalized Recommendations – Insights for better health decisions
Why Choose MapmyGenome?


Who Should Take This Test?
- Individuals with undiagnosed conditions seeking genetic explanations
- Patients with a family history of genetic disorders
- Those exploring personalized medicine for better treatment strategies
- Couples undergoing carrier screening for family planning
How It Works – 4 Simple Steps


How This Test Transforms Your Health
- Discover the Root Cause of Symptoms – Get clarity on unexplained medical conditions.
- Precision Medicine for You – Learn how your genetics influence medication response.
- Proactive Health Management – Take steps to prevent genetic-related health issues.
- Empower Your Family's Health – Identify inherited risks and make informed decisions.
- Long-Term Health Monitoring – Use insights for continuous health optimization.
FAQs
What is Whole Exome Sequencing (WES)?
Whole Exome Sequencing (WES) is a genetic test that analyzes the protein-coding regions of your DNA (exome). These regions contain 21,000 genes and are responsible for most known genetic disorders.
How is WES different from Whole Genome Sequencing (WGS)?
WES focuses only on the exome (protein-coding genes), which is where most disease-causing mutations occur. WGS, on the other hand, sequences the entire genome, including non-coding regions. WES is more cost-effective while still providing valuable insights.
What health conditions can WES help diagnose?
WES can help identify genetic causes of:
- Neurological disorders (e.g., epilepsy, autism, intellectual disabilities)
- Cardiovascular diseases (e.g., inherited heart conditions)
- Metabolic disorders
- Immune system disorders
- Rare genetic conditions
How accurate is WES?
Our WES test provides high-depth sequencing (150X-180X), ensuring high accuracy in detecting genetic variants. However, not all genetic mutations may be identified, and some may require further testing.
Do I need a doctor’s prescription for this test?
Yes, a Test Requisition Form (TRF) is mandatory for WES. We recommend consulting a genetic counselor before and after testing to understand the results better.
What type of sample is required for WES?
We use a saliva or blood sample for sequencing. Your kit will include easy-to-follow instructions for sample collection.
How long does it take to receive my WES report?
It typically takes 4-6 weeks to process your sample and generate a detailed report.