The patients are required to answer a Health and lifestyle questionnaire followed by blood sample collection. We use NGS whole-exome sequencing, to look at over 20000 plus genes and their mutations from the collected sample. The molecular data generated is then compared to peer-reviewed databases with over 3 million patients’ genomic data. We achieve this using smart cloud solutions proprietary to GenepoweRx. Based on the insights generated, we provide a clinically actionable report and further patient counselling.