Unlock the power of genetics

At Myriad Genetics, we believe in the power of human understanding. That’s why we offer a personal and thoughtful genetic insights experience for providers and the women who rely on them.

Myriad Women's Health Portals

Prenatal Login Hereditary Cancer Login

Your partner in patient care

We provide transformative genetic insights that let you focus on what you do best, offering definitive results and support whenever you need it.

MyRisk® Hereditary Cancer Test

Help patients get ahead of cancer with our hereditary cancer test

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Prequel® Prenatal Screen

Get reliable results the first time with noninvasive prenatal screening

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Foresight® Carrier Screen

Identify couples at risk to pass down serious, prevalent, clinically-actionable inherited conditions

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We’re reimagining the future of genetics

50%

of hereditary cancers are non BRCA1/2

Learn how to identify more patients at high risk for hereditary cancer

100X

lower false positive rates from cfDNA screening compared to standard screening3

Learn why NIPS leads to fewer unnecessary invasive procedures

86%

of affected pregnancies no longer missed1

Learn how ECS detects more at-risk couples for serious conditions

Patient resources

 
Carrier screening resources

Prenatal screening resources

Register your kit or view results

Why genetic screening and testing?

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Supporting services with Myriad Complete™

Myriad offers the following through Myriad Complete to help your patient navigate through the testing/screening process.

Education

We provide resources to help educate your patients about Myriad products.

Access

We offer a comprehensive program to make genetic products accessible for more of your patients.

Results

We deliver screening and testing results effectively and thoroughly so you can focus on care plans.

Consults

We provide consults from patient educators, who are genetic counselors, tailored to help your patient understand their results.

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All patients deserve genetic insights

At Myriad Genetics, you can count on us to do the heavy lifting in the moments that matter.

References

  1. Hogan et al. Validation of an Expanded Carrier Screen that Optimizes Sensitivity via Full-Exon Sequencing and Panel-wide Copy Number Variant Identification. Clinical Chemistry 2018; doi:10.1373/clinchem.2018.286823
  2. Ghiossi, C.E., Goldberg, J.D., Haque, I.S. et al. J Genet Counsel (2017). https://doi.org/10.1007/s10897-017-0160-1.
  3. Norton, M. et al Cell free DNA analysis for noninvasive examination of trisomy. The New England Journal of Medicine April 2015; 372: 1589-1597.
  4. BRCA1/BRCA2 Frequency: Gabai-Kapara E, Lahad A, Kaufman B, et al. Population-based screening for breast and ovarian cancer risk due to BRCA1 and BRCA2. Proc Natl Acad Sci U S A. 2014.