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    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

    Genomic Health Insights Test Parameters in Bangalore

    Adult-Onset Risk

    Inherited cancer risk

    (12+ cancer tissue types)

    Inherited cardiovascular risk

    (12 conditions including cardiomyopathy, arrhythmia, lipid disorders, etc.)

    Inborn errors of metabolism

    (58 conditions across 12 metabolic pathways)

    Carrier Screening

    • Over 175 inherited conditions

      • Hemoglobinopathies

      • Metabolic conditions

      • Severe childhood-onset genetic disorders

      • Neuromuscular disorders

      • Cystic fibrosis-related variants

    Pharmacogenomics

    110 medicines

    Guidance for approximately

    Genomic Health Insights Test Preparation

    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.

    Interpretations

    Results & Interpretation

    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.

    Frequently Asked Questions About Genomic Health Insights Test in Bangalore

    GHI is a DNA-based screening that helps you understand your inherited health risks, whether you carry certain genetic conditions, and how your body may respond to some medicines. It is not a diagnostic test , but a screening test to learn more about your genetic health.

    GHI looks at three things:

    • Adult-onset health risks : Inherited tendencies for certain conditions

    • Carrier status : Whether you carry variants that may matter for future children

    • Pharmacogenomics : How your genes may affect your response to certain medicines

    No, you do not need to fast or stop taking your regular medications before the test.

    If your clinician has given you any specific instructions about a particular medicine, please follow those.

    A trained Medic will collect a blood sample from your home using a standard needle-based blood draw.

    This test may be helpful for:

    • Adults who want to take a proactive approach to their long-term health

    • Couples planning a pregnancy

    • Individuals with a family history of inherited conditions

    • Anyone who wants to understand how their genes may influence their response to certain medicines

    • People who are simply curious about their genetic risks

    A positive result simply means that a genetic variant was found that may be linked to a higher chance of certain health conditions. It does not mean you currently have the condition.

    Your counselling session will help you understand what this finding means for you and what you may want to discuss with your clinician.

    A negative result means that no clinically significant variants were identified in the genes screened.

    This is generally reassuring, but it does not remove all health risks. Lifestyle, environment, and other non-genetic factors still play an important role.

    No,it will not diagnose any existing medical conditions.. It only helps assess inherited genetic risk.

    You will receive your report within 24 days from the date of testing.

    Within 2 days of your report being released, you will receive a call for a counselling session with a genetic counsellor. They will walk you through your report, explain each finding in simple terms, and answer any questions you may have. They will also guide you on what to discuss with your clinician, if needed.

    If your sample cannot be processed, a re-collection will be arranged so it can be processed again.

    Genomic Health Insights is meant for individuals who can legally provide consent. Only people 18 years and above can take this test.

    Your data is encrypted and anonymised and stored securely on India-based servers.

    Your results can be accessed only by you and by anyone you explicitly authorise , with two-factor authentication ensuring an additional layer of protection.

    Your genetic data is never sold or shared with pharmaceutical companies or third parties. Your demographic and contact information is used only to reach you regarding your test.

    Yes. You can request deletion of your genetic data after your report has been delivered.

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    Payment & Refund Policy

    • We do not accept cash payments
    • All modes of online payment are accepted
    • Refunds will be credited back to the source of payment within 5-7 working days of order cancellation.