The science behind PRS

Discover how genetics is revolutionizing personalized medicine and improving patients' lives

What are PRS?

Polygenic Risk Scores (PRS) are like a personalized score that summarizes how your genes influence the risk of developing certain diseases.

This is how the PRS work

Make data-driven decisions and anticipate potential risks

We identify genetic variants that may influence health

Based on large-scale genetic studies (GWAS), the variants associated with specific diseases are selected.

We assign a weight to each variant based on its importance in the risk.

We add the weighted values to generate a unique score.

The weighted variants are combined into a score that represents the polygenic risk.

How are the results interpreted?

PRS analyzes small differences in DNA (genetic variants) and adds their impact to generate a personalized score. This score compares the predisposition to certain diseases with that of the general population, helping to identify relative risks and make preventive decisions.

This allows to identify those who could benefit from specific interventions and to compare their score with the general population to better understand their relative risk.

Take advantage of all the benefits

Customization

Customization

Adjust health recommendations based on each patient's unique genetics

Customization

Adjust health recommendations based on each patient's unique genetics

Prevention

Prevention

Identify risks before symptoms appear

Prevention

Identify risks before symptoms appear

Scientific Backup

Scientific Backup

Based on genome-wide association studies (GWAS) with millions of data points.

Scientific Backup

Based on genome-wide association studies (GWAS) with millions of data points.

We value privacy

Genetic information is extremely sensitive. At N-GENE, we guarantee total protection of patient data through advanced encryption measures and strict data handling policies. We do not share or use genetic information for any purpose without the user's explicit consent.

Explore more about genetics

Access educational articles to learn about genetics and the scientific evidence that supports its integration in consultation

Glossary of genetic terms

In this article you will learn the most commonly used genetic terms explained in a simple manner.

Glossary of genetic terms

In this article you will learn the most commonly used genetic terms explained in a simple manner.

Genome-Wide Association Studies (GWAS)

This article explains the importance of these studies in modern genetics and their usefulness in the field of precision health.

What is the difference between mutation and polymorphism?

This article provides the key insights to understand the difference between these genetic changes and what types there are.

Reasons to integrate genetics into the consultation

This article discusses the advantages of knowing the patient's genetic information in the nutrition consultation.

Discover how N-GENE can transform your medical consultation

Fundamental today, essential tomorrow

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N-GENE Application

Frequently Asked Questions

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N-GENE Application

Frequently Asked Questions