Test Disclaimer
\nMedical Disclaimer: The Whole Exome Sequencing Test is a specialised genetic investigation intended to support diagnosis and clinical decision-making. Results must always be interpreted by qualified medical and genetic professionals. Information provided is subject to the disclaimer policy and does not replace professional medical advice.
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Whole Exome Sequencing Test
Whole Exome Sequencing Test in Pune, Maharashtra
The Whole Exome Sequencing (WES) Test is an advanced genetic investigation that analyses the protein-coding regions of the genome responsible for most known inherited disorders. In Pune and across Maharashtra, this test is advised when routine tests fail to explain rare diseases, unexplained neurological conditions, developmental delays, or suspected hereditary disorders requiring in-depth genetic evaluation.
At healthcare nt sickcare, the Whole Exome Sequencing Test is supported through a home collection facility and a direct walk-in facility for Pune locals. Due to its complexity, this test is performed with specialist coordination and results are intended to support clinical and genetic counselling decisions.
Genetic Analysis Covered in This Package
- Protein-coding regions (exons) of approximately 20,000 genes
- Genes linked to rare and inherited genetic disorders
- Genes associated with neurological and developmental conditions
- Variants related to undiagnosed and complex syndromes
Test Reporting and Sample Information
- Whole Exome Sequencing Test Reporting: Report available in approximately 45–47 days
- Whole Exome Sequencing Test Sample Type: Whole blood EDTA sample
Frequently Asked Questions
This test is advised for unexplained medical conditions, suspected genetic disorders, developmental delays, rare syndromes, or when standard investigations do not provide a clear diagnosis.
Whole Exome Sequencing helps identify genetic variants responsible for inherited or rare conditions, enabling accurate diagnosis, personalised treatment planning, and genetic counselling.
Fasting is not required for the Whole Exome Sequencing Test. Patients should follow sample collection instructions shared at the time of booking.
Conditions may include developmental delay, unexplained seizures, congenital abnormalities, intellectual disability, or complex multi-system disorders without a confirmed diagnosis.
Test Disclaimer
Medical Disclaimer: The Whole Exome Sequencing Test is a specialised genetic investigation intended to support diagnosis and clinical decision-making. Results must always be interpreted by qualified medical and genetic professionals. Information provided is subject to the disclaimer policy and does not replace professional medical advice.
Original: $31,499.00
-70%$31,499.00
$9,449.70Product Information
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Description
Whole Exome Sequencing Test in Pune, Maharashtra
The Whole Exome Sequencing (WES) Test is an advanced genetic investigation that analyses the protein-coding regions of the genome responsible for most known inherited disorders. In Pune and across Maharashtra, this test is advised when routine tests fail to explain rare diseases, unexplained neurological conditions, developmental delays, or suspected hereditary disorders requiring in-depth genetic evaluation.
At healthcare nt sickcare, the Whole Exome Sequencing Test is supported through a home collection facility and a direct walk-in facility for Pune locals. Due to its complexity, this test is performed with specialist coordination and results are intended to support clinical and genetic counselling decisions.
Genetic Analysis Covered in This Package
- Protein-coding regions (exons) of approximately 20,000 genes
- Genes linked to rare and inherited genetic disorders
- Genes associated with neurological and developmental conditions
- Variants related to undiagnosed and complex syndromes
Test Reporting and Sample Information
- Whole Exome Sequencing Test Reporting: Report available in approximately 45–47 days
- Whole Exome Sequencing Test Sample Type: Whole blood EDTA sample
Frequently Asked Questions
This test is advised for unexplained medical conditions, suspected genetic disorders, developmental delays, rare syndromes, or when standard investigations do not provide a clear diagnosis.
Whole Exome Sequencing helps identify genetic variants responsible for inherited or rare conditions, enabling accurate diagnosis, personalised treatment planning, and genetic counselling.
Fasting is not required for the Whole Exome Sequencing Test. Patients should follow sample collection instructions shared at the time of booking.
Conditions may include developmental delay, unexplained seizures, congenital abnormalities, intellectual disability, or complex multi-system disorders without a confirmed diagnosis.
Test Disclaimer
Medical Disclaimer: The Whole Exome Sequencing Test is a specialised genetic investigation intended to support diagnosis and clinical decision-making. Results must always be interpreted by qualified medical and genetic professionals. Information provided is subject to the disclaimer policy and does not replace professional medical advice.
