Find the test that answers your question.

Genetic testing can be clinically valuable across many areas of health, including earlier screening and personalised medical care. At iGenetx, we see genetics as a lifelong resource that supports informed, proactive health decisions. The first step is a conversation with our team, who will help you decide whether genetic testing is right for you and which test fits.

iGenetx offers genetic services for individuals seeking a proactive, personalised approach to their health, as well as for those with symptoms, medical histories, or family backgrounds that warrant genetic investigation. Before you buy, our team will talk it through with you and help you choose the test that fits your question.

Being a carrier of a genetic variant is common and not inherently harmful. Identifying carrier status is beneficial, as it enables preventive strategies, informed monitoring, and personalised healthcare planning. Early awareness often leads to better outcomes and more effective medical management.

Not necessarily. Humans have two copies of most genes. In recessive conditions, disease develops only when both gene copies are affected. Carriers usually have one normal and one altered copy and do not develop the disease themselves. However, this information is important for family planning, as two carriers of the same condition may have children at risk.

No. Your genetic sequence remains unchanged throughout your life. What evolves is scientific knowledge. As research progresses, new discoveries may emerge, making your genome a lifelong resource that can be revisited to inform future healthcare decisions.

The cost of genetic testing depends on the technology used, the amount of DNA analysed, and the level of clinical expertise required for interpretation. Whole genome sequencing provides the most comprehensive and clinically impactful data. At iGenetx, every report is reviewed by a geneticist. The conversation with our team before you buy is free, and a genetic counselling session after your results is available and charged separately.