


Have a family history of heart disease, especially if it involves early-onset heart disease (before age 55 in men, 65 in women), sudden cardiac death, or known inherited heart conditions.
Have been diagnosed with heart conditions that may have a genetic basis, such as hypertrophic cardiomyopathy, arrhythmias, or familial hypercholesterolemia.
Experience unexplained symptoms like fainting, arrhythmias, or heart failure, particularly at a young age, which may suggest an underlying genetic cause.
Have relatives with identified genetic mutations related to heart disease, even if they currently show no symptoms themselves.
Are considering proactive measures to understand their genetic risk and manage their heart health more effectively.
Are planning to undergo major heart surgery or procedures, as understanding genetic risks can influence surgical decisions and post-operative care strategies.
Meet with healthcare provider to discuss why you want the test.This initial consultation helps identify your reasons for testing, such as diagnosing a genetic condition or assessing risks for inherited diseases.
DNA sample is collected, usually from blood, saliva, or a cheek swab. This sample contains your genetic material, which will be analyzed in the lab. The collection process is quick and simple.
DNA extracted & analysed. Techniques like PCR or DNA sequencing are used to examine your genes for any variations or mutations. Helps to identify genetic changes that might be linked to specific health conditions.
The lab sends a report to your healthcare provider, who will explain the results. It might show normal results, or it could indicate genetic variations that could affect your health or require further action.
After receiving results, you’ll have a follow-up discussion with healthcare provider. They’ll explain what the results mean for your health & guide you on next steps such as lifestyle changes, further tests, or treatments.
It analyzes your DNA for genetic risks related to heart conditions.
Those with a family history of heart conditions or early-onset heart disease.
DNA is collected and analyzed to identify heart disease-related genetic variations.
They indicate your genetic risk for heart disease.
Early risk detection and personalized heart health management.
Follow your healthcare provider’s personalized plan for prevention and monitoring.
Lillian Pratt
Chief Marketing Officer
Mrs. Sarita Sonar
Chief Finance Officer
Mrs. Jannie James
Chief Operating Officer
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A Doctor of Philosophy, leading Genomics and Proteomics researcher and a scientist whose work involves using Big Data and AI resources, Dr Roberto specialises in the study of Epigenetics.
John Gladwin is a distinguished figure in the software and IT services industry, with a career spanning over three decades. His expertise covers a broad spectrum including sales, marketing, operations, and corporate strategy.
Priya John has extensive experience in supply chains and developing in emerging markets. Priya’s leadership has been instrumental in scaling her company’s global presence, establishing market leadership in customer relationship management, and business process outsourcing services.