MyRisk with RiskScore

More than 1 in 4 patients you see today will meet criteria for hereditary cancer testing.1

Now featured in Obstetrics & Gynecology Learn more about how Myriad’s recently published study helps providers more than double the completion rate of the hereditary cancer risk assessment test.

Do you know your patient's remaining lifetime risk of developing breast cancer?

Myriad’s comprehensive breast cancer risk assessment program can help your practice identify patients at high-risk for breast cancer, and provide resources for medical management.

8 out of 10 providers agreed that the program’s online screening tool helped them meet ACOG guidelines, recommending hereditary cancer risk assessment for all patients.2

Meet MyRisk® with RiskScore®

Request more information about your hereditary genetic testing options and how MyRisk can benefit your patients.

Screen efficiently

A patient’s personal and family history could be the only sign that they are at an increased risk for breast cancer.

Accurate patient identification that fits any workflow:

  • Paper screening—short form & comprehensive family history questionnaires
  • MyGeneHistory® (digital screening tool)
  • Integrated EMR patient identification

Patient education:

  • Speak with a board-certified genetic counselor
  • Patient education video

Evaluate effectively

The MyRisk hereditary cancer test evaluates genes associated with hereditary cancer, delivering unsurpassed technical accuracy with over 99.99% sensitivity and specificity.3

RiskScore is the first and only comprehensive breast cancer risk assessment that includes a polygenic score validated for all ancestries.

Diagnose accurately

With over 99.99% sensitivity and specificity and the industry’s most definitive variant classification4, the MyRisk hereditary cancer test allows providers to accurately diagnose hereditary cancer syndromes associated with certain genetic mutations, such as BRCA1 and BRCA2, which are linked to an increased risk of breast and ovarian cancers.

For patients who test negative for breast cancer-associated genetic mutations, RiskScore provides eligible patients with a five-year and remaining lifetime risk of breast cancer, allowing providers to stratify breast cancer risk more comprehensively.

Manage appropriately

Patients and providers can make more confident and informed medical management decisions for managing risk.2

Impact of MyRisk® with RiskScore®

  • Screening tools can increase patient identification by 30%.2
  • End-to-end integration can lead to 50% more patients being appropriately offered testing.2
  • Patient education can lead to 40% more patients submitting a test.2

Comprehensive support

Myriad Genetics supports patients and healthcare providers throughout the genetic testing process, with pre-test educations with a board-certified genetic counselor, billing support, clear results reporting, and post-test consultations.

Cost should not be a barrier

95% of private insurers have coverage for hereditary cancer testing.5

Myriad is committed to providing patients with access to accurate and affordable genetic results through extensive coverage with most insurance plans and financial assistance programs. 

MyRisk Patient Story

Forging a path forward

Lisa’s mom’s battle with breast cancer inspired her to get genetic testing and make a life-saving choice. Her story is a testament to courage and resilience.

Meet MyRisk® with RiskScore®

Request more information about your hereditary genetic testing options and how MyRisk can benefit your patients.

References:
  1. American Cancer Society.
  2. Adkins RT, Waldman RN, DeFrancesco MS, Feltz JP, Welling DS, Neiman WA. Use of Virtual Patient Education to Improve Provider Compliance with Hereditary Cancer Assessment Guidelines and Genetic Testing in a Community OB/GYN Setting. Poster presented at: ACOG Annual Clinical and Scientific Meeting; May 17 – 19, 2024; San Francisco, CA.
  3. Myriad MyRisk® Plus Technical Specifications, Myriad Genetic Laboratories, 2024
  4. Mundt, Erin, et al. “Driving Down the Rate of Variants of Uncertain Significance as the Myriad myRisk® Multigene Panel Grows.”
  5. Based on internal Myriad data, 2024