Genomics is revolutionizing how we understand disease, diagnose conditions, and design individualized care plans. By analyzing your DNA, we can identify risks for conditions that may never present symptoms until it’s too late — such as:
- Cancer (e.g., breast, ovarian, colorectal, prostate, pancreas, etc.)
- Cardiovascular disease (e.g., inherited arrhythmias, early heart attacks)
- Neurological conditions (e.g., epilepsy, Alzheimer’s, Parkinson’s)
- Rare genetic disorders
- Medication sensitivity (Pharmacogenomics)
- Biological-age acceleration (Epigenetic clocks)
Just as a blood pressure reading gives a snapshot of cardiovascular risk, your genetic blueprint reveals lifelong insights that can guide prevention, early intervention, and optimized treatment.
