The GNT. Polygenic Risk is a genetic test that estimates the relative likelihood of developing common diseases based on the combination of many genetic variants (polygenic risk scores or PRS). Based on this data, the report presents a risk percentile (compared to the rest of the population), classifies it into a risk category, and includes prevention and screening recommendations adapted to the clinical context.

Its objective is to provide a risk stratification useful in clinical practice, which complements information from the clinical history, lifestyle habits, and other biomarkers. In this way, it helps to personalize prevention, better plan screenings, and adjust therapeutic goals according to each person’s individual risk.