Find answers – fast
Shorten the time it takes to reach an accurate diagnosis of a rare disease.
RareVision
RareVision is a whole genome test for individuals showing clinical signs of a possible genetic condition.
Why RareVision?
Diagnosing a rare disease can take an average of 4 to 5 years1. Almost 40% of rare disease patients2 received a misdiagnosis in their diagnostic odyssey. This delays your ability to start effective treatments for rare disease symptoms that may get worse over time.
RareVision, our whole genome test provides a comprehensive view of your genes to provide new insights into rare or undiagnosed conditions – within two weeks.
How to order a test
We recommend you request your provider or geneticist, who can assess your medical symptoms more accurately, to place an order for you. If you want to initiate the ordering process on your own, you can still do that in the following steps. If you need support in ordering, email us at inquiry@inocras.com.
Sign up
Fill out the order request form and consent form at inocras.com.
Clinical request
An external clinician will review and approve your test request.
Sample collection
Once your test request is approved, we’ll send you a kit with instructions for you to collect your cheek swab sample, along with directions for where to send it.
Genetic counselor appointment
When your report is ready, you will get a notification with a link to make an appointment with a genetic counselor.
Result review
A genetic counselor will review your RareVision report with you.
**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 genomic 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 diagnostic testing for rare disease cases 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 cheek swab sample.
Once your test request is approved, we’ll send you a kit with instructions for you to collect your cheek swab sample, along with directions for where to send it.
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 part of your patient care, 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.