Genetic Counselling 101: Decode Your Gs and Cs!!
Genetic counselling is a communication process that helps individuals and families understand and adapt to the medical, psychological, and familial implications of genetic contributions to disease. But what does that actually mean in practice? Let’s break it down.
What Is Genetic Counselling?
A genetic counsellor is a healthcare professional with specialised training in medical genetics and counselling. They work with individuals and families to:
Interpret family and medical histories to assess the chance of disease occurrence or recurrence
Educate about inheritance, testing, management, prevention, resources, and research
Counsel to promote informed choices and adaptation to the risk or condition
Support individuals in understanding their genetic test results and what they mean for their health and their family’s health
When Should You See a Genetic Counsellor?
You have a personal or family history of a genetic condition or birth defect
You are planning a pregnancy and want to understand your carrier status
You have had recurrent pregnancy losses
You have received a genetic test result and need help understanding it
You have a family history of hereditary cancer (breast, ovarian, colorectal, etc.)
You have a child with a developmental delay, intellectual disability, or birth defect
You are of advanced maternal age (35+) and planning a pregnancy
What Happens in a Genetic Counselling Session?
A typical genetic counselling session at MapmyGenome includes:
A detailed review of your personal and family medical history (three-generation pedigree)
Assessment of your genetic risk based on your history and any available test results
Discussion of available genetic testing options and what they can and cannot tell you
Interpretation of genetic test results in the context of your personal and family history
Guidance on next steps — including surveillance, preventive measures, and reproductive options
Emotional support and referrals to relevant specialists or support groups
Decoding Your Gs and Cs
Your DNA is made up of four bases: Adenine (A), Thymine (T), Guanine (G), and Cytosine (C). The sequence of these bases encodes all the information needed to build and run your body. Variations in this sequence — called SNPs (single nucleotide polymorphisms) or mutations — can influence your risk for certain diseases, your response to medications, and many other traits. A genetic counsellor helps you understand what these variations mean for you specifically.
Book a Genetic Counselling Session
MapmyGenome’s certified genetic counsellors provide expert, personalised guidance for individuals and families — whether you’re interpreting a Genomepatri result, planning a pregnancy, or navigating a hereditary condition. CAP & NABL-accredited laboratory.



