My Whole Genome Sequencing
A genetic approach to personalize health and prevent disease
[ about My Whole Genome Sequencing ]
The Genome Risk Test offers clinical-grade Whole Genome Sequencing (WGS) to identify genetic predispositions for over 650 hereditary diseases. It integrates genomics into routine health check-ups, enabling personalized medical care and early intervention strategies. The test is designed for healthy individuals seeking proactive health management through comprehensive genetic insights.
Providing:
- A comprehensive, easy-to-understand report
- Interpretation by expert geneticists using public, private, and proprietary databases
- Clinically actionable insights for physicians
- Lifetime updates as scientific knowledge evolves
[who is it for]
for both men and women
adults only
[About My Whole Genome Sequencing]
What Does It Analyze?
Analyzes thousands of genetic variants across the entire genome. Key areas include:
Hereditary diseases (+650 conditions)
Carrier status (+225 conditions)
Multifactorial diseases (15 conditions)
Pharmacogenomics (+150 drug response markers)
Genetic traits (+50 traits related to diet, behavior, longevity, and more)
Ancestry insights
[test results]
What does the report provide?
Drug Efficacy Panel
- Identifies optimal medications and dosages
- Highlights risk of adverse reactions or therapeutic failure
- Includes clinical recommendations based on CPIC and DPWG guidelines
Pharmacogenetic Results
- Categorizes metabolizer status (e.g., poor, intermediate, ultrarapid)
- Suggests alternative agents when necessary
- Provides lifetime value as genetic data can be reused for future prescriptions
[Advantages]
Benefits of the test
heathcare providers
Reduce adverse drug reactions (which account for ~3.5% of hospital admissions)
Improve treatment efficacy and safety
Save time and resources by avoiding trial-and-error prescribing
patients
Receive safer, more effective medications
Avoid unnecessary side effects
Benefit from lifelong pharmacogenomic insights
Your Health Journey Made Simple
Four easy steps to unlock
your genetic insights.
01
Order Kit
Request your DNA kit online
02
Collect Sample
Quick, painless (at home or clinic)
03
Send to Lab
Secured and processed in world-class facilities
04
Get Results
Available in 6 to 8 weeks after the sample is received in the lab.
[our Professionals]
We offer you our team of professionals with
whom you can arrange a genetic counselling
consultation in person or online, to answer your
questions and analyse your specific case.