- genetrackhealthcare@gmail.com
- +91 9311400585
Years of Experience
Rare genetic conditions often require specialized and precise analysis. Our diagnostic genetic testing is designed to detect uncommon variants and mutations, offering clarity, diagnosis, and direction for clinical management and long-term care.
No two individuals respond to medications the same way. Through pharmacogenetic testing, we analyze how your genes influence drug response helping healthcare providers select the safest and most effective medications while minimizing adverse reactions.
For deeper genetic insight, our exome sequencing focuses on protein-coding regions of the genome where most disease-causing mutations occur. This approach is especially valuable for identifying complex or previously undiagnosed genetic conditions.
Genetic results can be complex and emotionally overwhelming. Our experienced genetic counsellors provide compassionate, clear, and personalized guidance helping you understand your results, their implications, and available next steps.
After receiving your results, our counselling services help interpret findings, address uncertain or inconclusive results, and guide decision-making related to follow-up testing, surveillance, or medical care for both you and your family.
If you wish to assess your risk of developing a genetic condition before symptoms appear, presymptomatic testing can provide valuable foresight empowering you to take preventive or proactive health measures.
