Research Details

  • About the Study

    “Understanding Genetic Risks of Cardiovascular diseases in India”

    Cardiovascular diseases are a leading health concern in India. Our research aims to uncover genetic factors contributing to these conditions, paving the way for personalized prevention and treatment strategies tailored to the Indian population.

    To learn about factors that influence cardiac conditions, scientific experts and researchers at Mapmygenome analyze the GENES of those who have diagnosed cardiac conditions using our most advanced genomic testing.

  • Who is Eligible to Participate

    Inclusion Criteria

    You are eligible to participate if you have doctor confirmed diagnosis of any of the following conditions

    • Coronary Artery Disease (CAD)
    • Myocardial Infarction (MI)
    • Atrial Fibrillation (AF)
    • Hypertrophic Cardiomyopathy (HCM)

    You are 18 years or older

  • Benefits to Participants

    Free Genomepatri with Counseling worth 7999

    Genomepatri is Mapmygenome’s DNA-based health and wellness solution that gives a comprehensive genetic assessment based on 100+ easy-to-read reports. The report contains insights into your genetic makeup, susceptibility to health conditions and how you respond to medications. Genomepatri helps you to learn about your parents/grandparents’ genes, that impact their lifestyle, diet, behavior, and fitness, and eventually find clues to their healthy longevity.

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Limited Spots Available. Seeking 500 Participants

Frequently Asked Questions

HOW WILL I RECEIVE THE GENOMEPATRI KIT?

Genomepatri test kit can either be mailed to your postal address or
our technician will deliver the kit and collect the sample from your
home.

HOW IS THE SAMPLE COLLECTED?

Genomepatri’s sample collection kit has a buccal/saliva swab which
is used for collecting a saliva sample. It is very easy to use and the kit comes with printed instructions on how to do the sampling. After you complete the sampling, all you have to do is inform us and we will pick
it up for processing.

WHAT TECHNOLOGY IS USED FOR GENOMEPATRI?

Genomepatri uses a DNA sequencing technology called genotyping which is performed on microarrays.

HOW DO YOU DO THE ANALYSIS?

We screen your genetic data for the presence of “markers” in your DNA
- which are single letter variations - to calculate your lifestyle
disease risk, predisposition to traits, drug response, etc. We have
developed a robust algorithm which is used for analysis, based on
genetic markers present in your DNA sample. These single letter
variations are known as Single Nucleotide Polymorphisms or SNPs.

WHEN WILL I GET THE RESULTS?

The results will be ready after 3 weeks and a genetic counselor will
schedule a session to explain the results to you in the language of your choice.

Publications and Findings