A CLEARER PATH
TO ANSWERS
TO ANSWERS
A CLEARER PATH
TO ANSWERS
TO ANSWERS
Improving The Journey For Patients With Rare Genetic Diseases
Genetic testing has been available for decades, but the standard tests often miss the details that matter most for understanding a patient’s condition. The result can be years of uncertainty, repeated specialist visits and tests that raise more questions than they answer.
Now there’s something better. 3X Genetics has developed a testing platform that delivers the precise data you and your care team need to reach a confident diagnosis, track changes over time, and make well-informed decisions about your care.
What Are The Possible Effects of Delayed Diagnosis?
For rare genetic diseases, delays can have serious consequences: missed opportunities for early intervention, confusion about symptoms and progression, limited access to clinical trials, and extensive specialist visits with costs that can reach $500,000. The uncertainty affects not just patients but family members who may also carry the condition.
Accurate genetic testing helps clinicians understand not only symptoms but personal and family history — essential elements for informed care decisions.
How Do I Test?
Start by speaking with your doctor, whether a primary care physician or a specialist such as a neurologist, cardiologist, or ophthalmologist. They can help determine whether testing is appropriate and provide you with a test kit, or can obtain one by contacting us directly.
The test requires only a saliva sample, which can be collected at a healthcare facility or at home and mailed directly to our CLIA-licensed laboratory for processing by qualified 3X technicians.
Moving Forward With Confidence
A clear diagnosis opens the door to earlier intervention, better-informed care, and the ability to plan for the future. At 3X Genetics, we help patients and families move from uncertainty to understanding through precise testing, clinical expertise and guidance at every step.
