We’re not a testing company, we’re a clinical genetics practice. Our focus is interpretation, integration, and prevention. We use medical-grade hereditary testing alongside nutrigenomic analysis to create actionable, evidence-based care plans your patients can actually use.

By identifying individual risk factors, genetic counselors can help develop a tailored plan that may include lifestyle accommodations, nutrition strategies, and appropriate screening recommendations, all aimed at optimizing long-term health and well-being.

Never. We complement existing care by focusing on prevention and proactive wellness. Our recommendations are meant to support, not replace, ongoing care with their medical team.

We work with CLIA-certified labs for hereditary cancer, preconception, connective tissue disorder, cardiovascular, and Alzheimer’s testing, as well as validated nutrigenomics panels. Each test is chosen based on clinical appropriateness, family history, and patient goals.

Absolutely. We review the patient’s history, assess indications, and determine which testing is appropriate. You don’t have to select a specific panel, we handle that part.

You’ll receive a concise clinical summary with results interpretation, key findings, and recommendations for follow-up or screening. We can also collaborate directly if you’d like to discuss the results or management options.

We use nutrigenomic data to guide practical lifestyle and nutrition choices that support each patient’s unique metabolic and disease risk profile, always in the context of clinical genetics, not as a stand-alone wellness add-on.

No. Our supplement protocols are evidence-based recommendations, not product-driven. We help patients identify what’s truly supportive, not what’s marketable.

Many genetic tests can be billed through insurance when criteria are met. Our interpretation and consultative services are private-pay, allowing for a more comprehensive, patient-centered approach.