$990
Detect genetic health risks before symptoms arise. Comprehensive clinical genetic testing with complete pharmacogenomics profiling included.
Inherited genetic predispositions do not always manifest in childhood. Many severe conditions arise in adulthood: hereditary cancers, cardiac arrhythmias, vascular aneurysms, metabolic complications, and adverse drug reactions.
Our clinical Whole Exome Sequencing is designed for every proactive adult — yourself, your partner, and your family. Full pharmacogenomic profiling is included to guide safe, personalized medications and dosages.
When genetic insight is urgently needed by a physician, there is often no time to wait. Being informed empowers prevention.
Do you know what genetic variants you carry?
Carrier status for cystic fibrosis, spinal muscular atrophy, metabolic storage disorders, and other inherited conditions that may impact family planning.
Hereditary breast, ovarian, colorectal (Lynch syndrome), gastric, pancreatic, and prostate cancer risks with actionable screening protocols.
Familial hypercholesterolemia, hypertrophic cardiomyopathy, long QT syndrome, Brugada syndrome, thoracic aortic aneurysms.
Individual metabolic response and adverse reaction risks for statins, anticoagulants, antidepressants, cardiovascular drugs, and chemotherapy.
Отчет основан на анализе более 3600 генов. Полный список генов и заболеваний
Genetic testing provides risk assessment and evidence-based guidance. It does not replace a clinical diagnosis. Consult with your healthcare provider.
Individuals who want to identify hidden hereditary health risks early and adopt personalized screening protocols.
Those with relatives diagnosed with early-onset cancer, sudden cardiac events, stroke, or unexplained hereditary illness.
Patients preparing for surgery or taking long-term medications who need precise pharmacogenomic dosing guidance.
Partners planning pregnancy who want to screen for recessive carrier risks for their future children.
Exome sequencing analyzes the protein-coding regions of your DNA where 85% of disease-causing mutations reside.
Identifies pathogenic variants before clinical symptoms develop, when interventions are most effective.
Lifelong utility: your DNA sequence does not change. Your data can be re-analyzed as new scientific discoveries emerge.
All your clinical test results are synthesized in one secure portal, while our AI assistant clarifies complex terminology and variant annotations — empowering you to collaborate effectively with your healthcare providers.
All reports and genomic findings in a single dashboard: actionable health priorities and full variant details.
Context-aware answers tailored to your genomic data: clear clinical explanations and key questions for your physician.
Engage dynamically with your findings: filter by clinical relevance, navigate risk profiles, and prepare for doctor visits.
Comprehensive test — sequencing and interpretation
$350
Explore an example of our comprehensive clinical exome report.
Order your test online or consult with our genetic team today.
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