Your health story doesn’t start with symptoms. It starts with your genes.

Many health conditions don’t appear suddenly, they develop quietly over years. Some risks are inherited. Some conditions are silently carried. And some medicines work differently simply because of your DNA.

Genomic Health Insights (GHI) helps you understand these invisible factors early , so you can make smarter, more informed health decisions, before problems arise.

Why people choose this test

• Clarity before symptoms : Understand risks long before disease appears

• One test, lifelong value : Insights relevant across health, family & treatment

• Not just for today : Designed for long-term health planning

• Doctor-backed insights : Actionable, clinically relevant information

• Counselling included : Expert support to help you interpret results

Important to know

• This is not a diagnostic test — it does not confirm disease

• It provides genetic risk insights , not medical diagnoses

• Results should always be interpreted with clinical guidance

Before the Test

• No fasting required

• Continue your regular medications unless your clinician advises otherwise

• Sharing your family medical history during counselling may be helpful

• Eligibility: 18 Years and above

During the Test

• A trained eMedic will visit your home to collect the sample

• Sample type: Blood

• The collection involves a simple needle-based blood draw, similar to any routine blood test, and takes only a few minutes

After the Test

• Turnaround time: 24 days

• Your report will be available once analysis is complete

• After your report is ready, a counselling session will be scheduled to walk you through your findings and answer any questions

Why Should You Take a Genomic Health Insights Test?

Most health checkups tell you how your body is doing today.

Genomic Health Insights helps you understand what you may be predisposed to over your lifetime.

This test is designed for people who want clarity before symptoms appear, abnormalities show up in reports, or uncertainty sets in.

If health conditions run in your family

If you have a family history of cancer, heart disease, diabetes, or other inherited conditions, this test helps clarify whether those risks apply to you personally or are influenced by lifestyle factors.

This understanding can guide earlier, more relevant screening and help reduce unnecessary testing or anxiety.

If your preventive health reports are normal, but you want to be proactive

Even when routine health checkups look normal, some risks remain invisible until much later in life.

Genomic Health Insights can help identify hidden inherited risks early, enabling you to prioritise what truly needs monitoring over time and offering reassurance when genetic risk is low.

If you’re planning a family

Carrier screening helps identify inherited conditions that could be passed on to children.

Having this insight early allows couples to make informed decisions through partner testing, counselling, or planned interventions before pregnancy.

If you’re on, or may need, long-term medications

Your genes can influence how your body responds to certain medicines.

Pharmacogenomic insights help doctors select treatments that are better suited to you, reducing trial-and-error and the risk of adverse reactions over time.

If you’re health-conscious and want personalised insights

If you’re already committed to fitness, nutrition, or lifestyle changes, genetic insights can provide a deeper understanding of how your body responds.

This allows you to personalise your approach rather than rely on one-size-fits-all advice.

How genetic testing fits into preventive healthcare

Think of preventive health as a layered approach:

1. Genetic testing (once in a lifetime)

Understand your lifelong health predispositions and inherited risks, which remain constant over time.

2. Personalised preventive checkups (ongoing)

Use genetic risk insights to decide what to screen, how early, and how frequently, instead of relying only on population averages.

3. Targeted tests & monitoring (as needed)

If preventive checkups show borderline or abnormal results, focused tests help investigate and track specific concerns.

Genomic Health Insights sits at the foundation of this journey. It does not replace routine health checkups, but makes them more relevant and personalised.

Your GHI report may include any one of the below results:

1. Positive / Clinically significant variant identified

A genetic variant was detected that is known to be associated with a higher chance of certain health conditions.

This does not mean you currently have the condition.

During your counselling session, you will be guided on what this result means for you and what conversations to have with your clinician.

2. Negative / No clinically significant variants identified

No variants associated with increased inherited risk were found for the genes screened.

This lowers, but does not completely remove your overall risk, since lifestyle and other non-genetic factors also play a role.