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With carrier and prenatal screening, you can gain the knowledge and insight you and your healthcare provider need to make critical and time-sensitive decisions before and during pregnancy.
Genetic screenings both before and during pregnancy help you understand your baby’s risk of inheriting a serious health condition or a chromosomal condition. Knowing this information helps you and your healthcare provider create informed plans for care and support before, during, and after your pregnancy.
Before or during pregnancy, Foresight can help determine whether you and your partner or donor carry inherited health conditions, such as cystic fibrosis, that you might pass on to a child.
Designed for all ancestries
Foresight’s detection rate is >99% across ancestries for most of the conditions on our panel1 – giving you reliable results to manage your family planning journey.
Industry-leading detection rates
Most couples are not carriers of the same condition. Knowing whether you and your partner are among those at higher risk is important to plan for your pregnancy and delivery. One in 22 couples screened using the Foresight Universal Panel is found to be at higher risk of passing one of the serious and actionable conditions to a child – leading the industry in detection.2
Pre- and post-screen support
We partner with your healthcare provider to ensure that you have answers to all your questions. Every Foresight Carrier Screen includes scheduled or on-demand consultations with our board-certified genetic counselors.
As early as week 10, Prequel can identify whether your baby may have an increased risk for a chromosomal condition like Down, Edwards, or Patau syndrome. This early insight into your baby’s development can help you plan and prepare with confidence.
Prequel can also screen for the expected sex of your baby or babies in a singleton or twin pregnancy.
Answers for everyone
Prequel provides results to >99.9% of patients.3 Our advanced science and technology work for any expectant parent regardless of ancestry or BMI, including those with twin and IVF pregnancies.4,5
Screens for the most serious conditions
Prequel analyzes all chromosomes to detect common conditions such as Down, Edwards, Patau, and DiGeorge (22q microdeletion) syndromes.
Support when you need it
We want you to have all the support you need. Every Prequel Prenatal Screen includes scheduled or on-demand consultations with our board-certified genetic counselors, and our payment specialists can help with any questions you may have about the cost of your screen.
SneakPeek is a gender test that identifies the fetal sex of the baby
Foresight empowered Ashley with answers about spinal muscular atrophy, enabling her to make time-sensitive decisions about her family’s health.
Together, Prequel and Foresight screen for hundreds of diseases and serious conditions. Most patients receive a low-risk result on these screens. If your result indicates you are at an elevated risk, you and your healthcare providers will be armed with more information to prepare for pregnancy, a supported delivery and giving your baby the best possible start.
We are committed to providing access to accurate and affordable screening to help patients make informed choices about their health, their families, and their futures.
We understand that every situation is unique, and we don’t want cost to be a barrier. Our financial assistance program takes into account each patient’s ability to pay, working with them directly to find the best option.*
Myriad’s prenatal screens offer industry leading accuracy2,3 and are designed to give patients and their providers the most reliable answers possible.
Each of our prenatal genetic screens delivers clear, actionable results and easy-to-understand reports to ensure that both patients and their healthcare providers can use the information to guide important healthcare decisions.
Myriad believes that results and genetic information belong to the patient. We take multiple steps to ensure that the security and privacy of patient data is not compromised, and we believe that patients should be in control of their information.