Get started with Myriad’s Prenatal Screening

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Get started with Myriad's Prenatal Screening

Request more information about how Myriad’s prenatal screening options can benefit your patients.

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Prenatal Genetic Screening

Plan and prepare for your pregnancy and your family

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.

Prenatal Genetic Screening

Plan and prepare for your pregnancy and your family

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 insights for informed plans

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.

Foresight Test Kit

Foresight® Carrier Screen

Genetic screening for inherited conditions

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.

ForeSight Test Kit
Prequel Text Kit

Prequel® Prenatal Screen

Early insights into your baby’s development

As early as week eight, 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.

Prequel Text Kit

SneakPeek® Early Gender Test

Determines fetal sex as early as six weeks into pregnancy

SneakPeek is a gender test that identifies the fetal sex of the baby

SneakPeek Test Kit

Foresight patient story

Early insights helped Ashley prepare

Foresight empowered Ashley with answers about spinal muscular atrophy, enabling her to make time-sensitive decisions about her family’s health.

Focused on serious conditions

Focused on serious conditions

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.

Foresight

Prequel

Dedicated to making prenatal screening available to all patients

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.

Affordable

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.*

*Applies to Prequel and Foresight only
66% of patients pay zero dollars out-of-pocket
  • Broad in-network status with health plans
  • 66% of patients qualify for financial assistance and payment plans5
  • Personalized cost estimates
    ($150 is the average out-of-pocket cost)5
*Applies to Prequel and Foresight only

Reliable and actionable

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.

Reliable and actionable

Secure

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.

Secure

Myriad prenatal care resources

References:
  1. Foresight® Residual Risk Table. https://myriad-library.s3.amazonaws.com/mwh/disease-detection-fact-sheet.pdf.
  2. Hogan, et al. Clin Chem 2018; doi:10.1373/clinchem.2018.286823.
  3. Hancock S, Ben-Shachar R, Adusei C, et al. Clinical experience across the fetal-fraction spectrum of a non-invasive prenatal screening approach with low test-failure rate. Ultrasound Obstet Gynecol. 2020;56(3):422-430. doi:10.1002/uog.21904.
  4. Muzzey D, Goldberg JD, Haverty C. Noninvasive prenatal screening for patients with high body mass index: Evaluating the impact of a customized whole genome sequencing workflow on sensitivity and residual risk. Prenat Diagn. 2020;40(3):333-341. doi:10.1002/pd.5603.
  5. Internal Data, 2021