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 concerns about rare disorders. It is also for patients with symptoms that are impacting their daily health that could be linked to suspected genetic diseases 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 diagnose rare diseases. Our whole genome sequencing test looks at the bigger picture of your genes for a more holistic understanding of how a rare and undiagnosed disease could be affecting your health – all within two weeks.
Identifying your risk can change your future
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 equips you with more information about what might be causing symptoms in you or your children with a suspected genetic disease. Your doctor can potentially use this information to help narrow down a diagnosis, leading to a quicker and more accurate molecular diagnosis than you might receive from other genetic tests.
Whole genome coverage
Standard panel testing looks at less than 0.1% of your genome3, leaving lots of room for unanswered questions. Similarly, whole exome sequencing tests only analyze 1-2% of the human genome. 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
Medical genetics and genetic sequencing 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 providers make informed decisions based on the results of the report. Those results help inform a precision medicine plan tailored to your unique body and health conditions, 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 and disease management.
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, choose your preferred sample collection method, 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 link to make an appointment for a phlebotomist to visit your home and draw your blood. If you choose to provide a buccal (cheek) swab instead of blood, we’ll send you a kit with instructions for you to collect your sample.
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
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 either a blood or buccal (cheek) swab sample.
When you or your provider order your RareVision test, you will have the option of choosing your preferred sample collection type. If you choose a blood sample, 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.
If you choose to provide a buccal (cheek) swab, we’ll send you a kit with instructions for you to collect your sample 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 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.