Lab Testing Made Easy.
Results You Can Understand.

At 41 Genes, we’re dedicated to providing our customers with clear, comprehensive reporting, covering toxicology, cancer genomics, and pharmacogenomics. We offer fast turnarounds to give you the results you need, exactly when you need them. Our reports are in-depth, but always easy to understand, and our experts are on hand with outstanding customer service at all times. We’re here to help you every step of the way!

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Advanced Testing,
Advanced Treatment

Full Spectrum Testing

Full Spectrum Testing

The Power of Precision Medicine

With an estimated 80% of Americans currently on at least one type of medication, pharmacogenetic testing is more essential than ever. Doctors and patients alike understand just how important it is to make a fully informed decision before taking new medications, since the more different prescriptions you take, the higher the risk of an adverse reaction. In fact, around 100,000 people die every single year due to these adverse drug reactions, and it costs the healthcare industry an additional $4 billion dealing with the side effects. That’s why 41 Genes provide such a comprehensive testing process- to help keep patients safe and healthy..

Clinical Testing


    Cancer genomics testing involves carefully checking the patient’s DNA for any mutations known to be linked to a hereditary risk of various types of cancer. Our comprehensive report then indicates just how at risk the patient is of developing these hereditary cancers. That information is vital to physicians, who can use it to create a personalized course of therapy around the individual patient’s needs.

    This innovative genetic testing creates a profile of the patient, which doctors can then use to determine how their body will respond to various medications and treatments.

    Based on early studies, every person is estimated to carry approximately three to five genetic mutations.1 Carrying a mutation does not typically cause any related disorders for that person, but it can mean that their children are at risk for having a disorder.Carrier screening can help detect if a couple is at increased risk of having a baby with a specific inherited disorder, such as Tay-Sachs disease or cystic fibrosis. Integrated Genetics offers choice in carrier screening: from a comprehensive screen for more than 110 disorders to a targeted screening for specific disorders.

Insightful Results

Our powerful platform gives you access to all the results you need, whenever you need them. As well as unpacking what your results mean, we also provide advice on how you can live a healthier lifestyle for a healthier body.

How it Works