For Patients
At Otogenetics, we are dedicated to advancing healthcare through cutting-edge genetic testing.
Patients Introduction
As a next-generation sequencing laboratory, our focus is on providing comprehensive and accurate carrier screening for prenatal and inherited cancer, as well as offering non-invasive prenatal testing for expecting mothers. Our state-of-the-art technology and expert team work tirelessly to deliver reliable results that empower you and your healthcare provider to make informed decisions about your health and your family’s future. Whether you are planning a family, expecting a baby, or seeking insights into your genetic health, Otogenetics is here to support you every step of the way. Trust us to provide the clarity and peace of mind you deserve with our innovative and personalized genetic testing solutions.
GxVISION® Carrier Screening
Carrier screening is genetic testing that determines whether an asymptomatic person has a genetic mutation or abnormalities associated with a particular disorder that may be passed on to children.
EnVISION Non-Invasive Prenatal® Screening
Advancements in genetic testing have enabled the most accurate and sensitive detection of fetal chromosomal abnormalities via the analysis of cell free DNA (cfDNA) derived from fetal placenta in the maternal blood. The American College of Obstetricians and Gynecologists (ACOG) and the Society for Maternal Fetal Medicine (SMFM) jointly and specifically stated in the new clinical management guidelines (ACOG Practice Bulletin #226, 2020) that NIPT is the most sensitive and specific screening test for common fetal aneuploidies, and that all pregnant women, regardless of age or other risk factors, should be offered prenatal screening for fetal chromosomal abnormalities.
GxVISION® Hereditary Cancer Risk Assessment
Hereditary cancers constitute 5-10% of all cancer cases. Genetic testing plays a crucial role in diagnosing these conditions, identifying at-risk patients, and ultimately improving outcomes.
FAQ’s Billing & Insurance FAQs
Every patient should have access to highly accurate and affordable genetic testing. Otogenetics is committed to work with each patient to reach payment solutions. These may include:
- Working with your insurance provider to verify coverage.
- Flexible payment options billed over several months.
- Financial assistance for patients who qualify.
We encourage patients to call us for all billing questions, and to discuss payment solutions.
Please call us toll free at 1-855-686-4363, option 1.
Otogenetics is committed to working with patients to ensure that everyone has access to testing
without financial burden.
* Medicaid patients will NOT have patient out of pocket responsibility.
* We treat all out-of-network claims as if they are in-network.
* We will work with all insurers (primary and secondary policies) to maximize your qualified coverage.
Otogenetics testing service is covered by many insurance plans, the exact amount you owe may vary based on your individual plan and financial situation.
Here is our commitment to you regarding costs:
- We will reach out to you if we estimate your cost could be more than $50 (the average out of pocket Otogenetics patients pay).
- We will discuss the estimate with you, and review your affordability.
You may receive information from your insurer, known as an Explanation of Benefits (EOB), regarding the test you received from Otogenetics.
An EOB from your insurer is NOT A BILL.
A bill for the test(s) provided by Otogenetics comes ONLY from Otogenetics.
If there is any patient out of pocket cost after Otogenetics has exhausted all options for reimbursement coverage and financial assistance, Otogenetics will reach out to you, the patient.