DNA health testing uses genomic analysis to identify variations in your genetic code — known as single nucleotide polymorphisms (SNPs) — that may influence your predisposition to certain health conditions, your response to nutrients and medications, and your metabolic characteristics.

It is important to understand what DNA testing does and does not tell you: genetic variants indicate predispositions and risk modifiers — they are probabilistic rather than deterministic. A variant associated with increased cancer risk does not mean you will develop cancer; it means your baseline risk may be different from the general population. This information is most valuable when interpreted by a clinician who can contextualise it within your overall health picture and use it to guide personalised prevention strategies.

Our DNA health testing uses validated laboratory analysis and is interpreted by trained clinical practitioners — not an automated algorithm alone.