Transform patient care with polygenic risk assessment - the future of personalized medicine
Polygenic Risk Scores synthesize information from thousands of genetic markers to evaluate an individual's inherited susceptibility to common health conditions. By analyzing numerous genetic variants simultaneously, PRS delivers a comprehensive genetic risk profile that enables healthcare providers to customize prevention approaches and treatment strategies according to each patient's unique genetic makeup.
Beyond Single-Gene Analysis: Unlike traditional genetic tests that focus on individual mutations, PRS evaluates the cumulative impact of many genetic variants, providing a more complete picture of disease predisposition.
PRS provides nuanced insights into patient risk profiles, enabling more precise categorization beyond conventional risk factors and family history alone.
Incorporate PRS into clinical decision-making to guide tailored screening schedules, lifestyle modifications, and early intervention strategies based on genetic predisposition.
Early identification of at-risk individuals through PRS enables proactive management and monitoring, leading to better long-term health results and reduced disease burden.
Incorporating PRS testing into your practice is straightforward with our streamlined process and clinician-friendly reporting system.
Simple DNA collection via saliva sample or buccal swab
Advanced genomic sequencing and analysis
Comprehensive PRS calculation with clinical interpretation
Clear, actionable reports for clinical decisions
Our comprehensive portfolio includes PRS evaluations for numerous common conditions with significant genetic components.
Join the growing community of forward-thinking healthcare providers who are leveraging polygenic risk assessment to deliver more personalized, predictive, and preventive care.
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