Find answers – faster

Shorten the time it takes to reach an accurate diagnosis of a rare disease.

RareVision

RareVision is a whole genome test that looks at the bigger picture of your genes for a more holistic understanding of how rare disease could affect your health.

Who is RareVision for?

RareVision is for patients who are looking for more answers about their symptoms and want a clear diagnosis of a rare disease, or those who have hereditary disease concerns. It is also for patients with symptoms that are impacting their daily health that could be linked to genetic disease and those who want insights into genetic disease to plan for the future of their families.

It can take an average of 4-5 years¹ to get a diagnosis of a rare disease. Our whole genome test looks at the bigger picture of your genes for a more holistic understanding of how rare disease could affect your health, all within two weeks.

RareVision patients receive:

Whole genome genetic testing that looks at your genes to assess your risk of rare disease
Personalized support from a genetic counselor to help you understand the test findings and answer your questions
Actionable suggestions to help you take control of your health
2-week turnaround time*

Price: $2,400**

*2 weeks from receipt of your blood samples at our lab.
**The listed price is a general estimate. The price may vary depending on your country and the specific scope of services we provide tailored to your needs.

Order now

Identifying your risk can change your future

Almost 40% of rare disease patients² received a misdiagnosis in their journey. This delays your ability to start effective treatments for rare disease symptoms that may get worse over time.

RareVision equips you with more information about what might be causing your or your child’s symptoms. Your doctor can potentially use this information to help narrow down a diagnosis, leading to a quicker and more accurate diagnosis than you might receive from other standard panel tests.

Whole genome coverage

Standard panel testing looks at less than 0.1% of your genome³, leaving lots of room for unanswered questions. Because RareVision looks at your whole genomic makeup, you and your provider will have access to the most comprehensive type of genomic testing.

Easy-to-understand reports

Genetic data can be confusing. With RareVision, you’ll receive a comprehensive report that is easy to understand. It will provide insights to help you and your healthcare provider make informed decisions tailored to your unique body, empowering you on your healthcare journey.

Genetic counseling support

In addition to your test report, you’ll receive automatic access to genetic counseling to guide you through your results line by line. We’ll make sure you and your provider understand the findings and potential treatment options to help you make more informed decisions about your health.

How to order a test

If you need support, email us at inquiry@inocras.com. We can help facilitate the process by working with you.

Sign up

Fill out the order request form and consent form at our patient portal.

Clinical request

An external clinician will review and approve your test request.

Blood sample collection

Once your test request is approved, we’ll send you a link to make an appointment for a phlebotomist to visit your home and draw your blood.

Genetic counselor appointment

You will get a notification when your report is ready. Go to the link we send to you and make an appointment with a genetic counselor to review your result.

Result review

Genetic counselor will review your RareVision report with you.

Order now

Teen receives definitive diagnosis & possible cure

Chloe, 17, had severe symptoms that affected her intestines. Doctors suspected inflammatory bowel disease (IBD), but finding the exact cause remained a challenge. Her results from RareVision revealed two disease-causing changes to her DNA that confirmed her diagnosis of early-onset IBD. She learned that IBD caused by her mutations can be treated, and even cured, through hematopoietic stem cell transplantation. She is now actively preparing for transplantation, a potential treatment for her condition.

Family finds answers for perplexing symptoms

Andrew, a 1-year-old boy, was experiencing a myriad of perplexing symptoms, including decreased muscle tone, facial abnormalities, and developmental delays. With the hope of finding answers, Andrew’s provider ordered the RareVision test. The results revealed a change to his DNA that supported a definitive diagnosis of a rare genetic disorder called Noonan syndrome. This finding provided a roadmap for his future care that allowed his family to take proactive steps in managing his health and to make empowered family planning decisions.

**While all patient names provided are fictionalized to ensure privacy and confidentiality, the age, disease information, and diagnostic process in the testimonials are based on real cases. Please note that clinical outcomes may vary for each individual

Your questions – answered

If you don’t see your question answered here, please contact us at inquiry@inocras.com.

How can I order a test?

RareVision tests can be ordered online using our secure portal. Once you fill out the order form, a telehealth provider will review your test order request and the test will be ordered after they review your order and information. Click here to be directed to the order form.

Is the test covered by insurance?

Currently, our whole genome sequencing tests are not yet covered by insurance in the US. We are working on insurance coverage to provide easy access to all patients.

Outside of the US, our products may be covered by insurance, but it varies significantly by the country and types of insurance. We suggest reaching out to your insurer to confirm. If you need any support exploring it, please contact us at inquiry@inocras.com.

Is testing expensive?

We understand that cost is an important consideration for patients, and we believe that access to whole genome testing should not be solely limited by cost. We strive to offer this valuable testing at an average comparable price so that it’s accessible to as many people as possible.

It’s important to note that the cost of genomic testing can vary depending on several factors, such as the specific test and additional services included. We recommend reaching out to our team at inquiry@inocras.com to discuss specific pricing details and any available financial assistance programs.

What kind of samples are collected, and who collects them?

For RareVision, we will need a blood sample. To collect your blood sample, we provide an at-home blood-draw service, where a phlebotomist will come to your home and collect your blood at your convenience.

How will my test results be shared with me?

Once your test is done, your results will be shared with a genetic counselor, who will then share the results with you directly. We will send you an email for you to make an appointment with a genetic counselor and discuss your results.

What if I have questions about my results?

Our team of in-house experts will explain the results to your provider and offer recommendations for how to use them. As a patient, you’ll also receive genetic counseling to walk through the results and make sure you understand your test findings and your options – at no additional cost.