Empowered Myriad Oncology patient

Each step. Every patient. Myriad Oncology.

Delivering comprehensive care at every step of the patient journey with germline and tumor genomic insights to assess hereditary cancer risk, guide treatment selection, and evaluate recurrence risk—all in one streamlined solution.

Empowering confident cancer care at every step

Myriad Oncology offers comprehensive germline and tumor genomic tests that provide clinically actionable insights, helping to tailor treatments for each patient’s unique cancer journey—maximizing their chance for a healthier future.

I’m a provider

I’m a patient

Helping to improve patient outcomes across the cancer care continuum

From risk assessment to therapy selection, Myriad Oncology offers integrated germline and tumor genomic tests that enable a truly personalized approach to cancer prevention and treatment.

Each step. High-Risk Unaffected Diagnosis
- Early stage
Progression
- Late Stage
Survivorship
Every Patient.
Exactly what you need.

Risk Assessment and prevention

Individualized management based on accurate hereditary cancer risk assessment

Surgery guidance

Appropriate surgery decisions based on hereditary cancer syndromes and risk of second primary cancer

Initial treatment guidance

Active surveillance and treatment intensity decisions based on guideline-supported molecular insights

Adjuvant therapy guidance

Adjuvant treatment decisions based on comprehensive guideline-supported germline and tumor genomic testing

Targeted therapy selection

FDA-approved therapies and clinical trial availability based on comprehensive germline and tumor genomic results

Management planning

Management updates and assessment of family members based on hereditary cancer syndromes


Each step.
Every Patient.
Exactly what
you need.
High-Risk Unaffected

Risk Assessment and prevention

Individualized management based on accurate hereditary cancer risk assessment

Diagnosis - Early stage

Surgery guidance

Appropriate surgery decisions based on hereditary cancer syndromes and risk of second primary cancer

Initial treatment guidance

Active surveillance and treatment intensity decisions based on guideline-supported molecular insights

Adjuvant therapy guidance

Adjuvant treatment decisions based on comprehensive guideline-supported germline and tumor genomic testing

Progression - Late Stage

Targeted therapy selection

FDA-approved therapies and clinical trial availability based on comprehensive germline and tumor genomic results

Survivorship

Management planning

Management updates and assessment of family members based on hereditary cancer syndromes

Comprehensive support services for providers and patients

Myriad Oncology provides a comprehensive suite of services and workflow solutions that simplify germline and tumor genomic testing, all at no additional cost to the clinic or patient.

Patient education

Pre- and post-test education as live, point-of-care sessions with a board-certified Genetic Counselor

Affordability

Transparent pricing with personalized cost estimates, financial assistance, and other affordability options, including direct pay

Fast results

Consolidated germline and tumor genomic results are available, on average, 14 days after our lab receives the sample

Easy reporting

The Myriad Management Tool streamlines germline and tumor genomic results into an easy-to-follow report

Provider support

Medical Science Liaisons support providers and their teams in answering clinical, testing, and results-related questions

Lifetime commitment

Myriad’s Variant Classification Program includes a Lifetime Reclassification Commitment to send amended reports if a variant of uncertain significance (VUS) is reclassified and is clinically actionable

Comprehensive support services for providers and patients

Myriad Oncology provides a comprehensive suite of services and workflow solutions that simplify germline and tumor genomic testing, all at no additional cost to the clinic or patient.

Patient education

Pre- and post-test education as live, point-of-care sessions with a board-certified Genetic Counselor

Affordability

Transparent pricing with personalized cost estimates, financial assistance, and other affordability options, including direct pay

Fast results

Consolidated germline and tumor genomic results are available, on average, 14 days after our lab receives the sample

Easy reporting

The Myriad Management Tool streamlines germline and tumor genomic results into an easy-to-follow report

Provider support

Medical Science Liaisons support providers and their teams in answering clinical, testing, and results-related questions

Lifetime commitment

Myriad’s Variant Classification Program includes a Lifetime Reclassification Commitment to send amended reports if a variant of uncertain significance (VUS) is reclassified and is clinically actionable

Myriad Oncology empowers providers and patients with fast, comprehensive answers to help guide management decisions and targeted therapy choices

Comprehensive germline and tumor genomic biomarker testing from a single, trusted source

  • Germline Tests

    Germline hereditary cancer test analyzing 63 clinically-validated genes associated with over 11 cancer types—aligned with national oncology guidelines.

  • Tumor Profiling

    The Precise Tumor® Test is a pan-cancer, comprehensive laboratory test that uses state-of-the-art, next-generation sequencing to discover and target important variants within tumors.

  • Genomic prognostic test for patients newly diagnosed with early-stage, estrogen-receptor-positive, HER2-negative breast cancer.

  • The Prolaris® Test is a molecular diagnostic test that helps determine the aggressiveness of a prostate cancer tumor to guide the best treatment decisions for prostate cancer patients.

  • HRD Status

    The most comprehensive FDA-approved tumor test that determines HRD status in women with ovarian cancer.

  • FDA-approved germline companion diagnostic test for patients with breast, ovarian, pancreatic and prostate cancer.

  • IHC Stains

    FDA-approved assay to identify patients with ovarian cancer who may qualify for treatment with mirvetuximab*

  • Offered together with Precise Tumor to measure protein expression and identify patients who may benefit from immunotherapy

Previous Test
    Next Test

    Are you missing critical insights that could impact cancer care?

    The MyRisk® Hereditary Cancer Test focuses exclusively on genes backed by clinical evidence and cited in national oncology guidelines—so every result has the potential to inform care.1-3

    100%

    of genes strongly recommended by ASCO guidelines are tested to help ensure no relevant findings are missed1-3

    100%

    of genes tested are cited in national oncology guidelines, helping to avoid the uncertainty associated with non-actionable results1-3

    Affordable genetic testing

    Excellent insurance coverage

    The majority of patients face no out-of-pocket costs for MyRisk testing8

    Clear cost estimates

    Patients will know what their costs are—if any—before the test is run.

    Financial assistance

    Myriad offers assistance to manage out-of-pocket costs as well as a direct pay option.

    See the latest research and insights

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    Groundbreaking research to support patient health

    Myriad conducts industry-leading, innovative genetic research and testing to further the science of care. Our scientific studies have been published in prominent journals and at global conferences and feature breakthrough insights for improved patient treatments and outcomes

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    Stay in the know

    Stay up to date on the latest industry information on our blog featuring healthcare professionals, patients, and Myriad leadership.

    Get started with Myriad Oncology

    Request more information from our team.

    Request more information about how Myriad Oncology can benefit you/your patients.

    Get started with Myriad Oncology

    Request more information about how Myriad’s Oncology solutions can benefit you/your patients.


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    References:
    1. Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines.) Genetic/Familial High-Risk Assessment: Breast, Ovarian, Pancreatic, and Prostate. V1.2026. ©National Comprehensive Cancer Network, Inc. 2025. All rights reserved. Accessed September 4, 2025. To view the most recent and complete version of the guideline, go online to NCCN.org. NCCN makes no warranties of any kind whatsoever regarding their content, use or application and disclaims any responsibility for their application or use in any way.
    2. Tung N, Ricker C, Messersmith H, et al. Selection of Germline Genetic Testing Panels in Patients With Cancer: ASCO Guideline. J Clin Oncol. 2024;42(21):2599-2615.
    3. Internal product development data on file at Myriad Genetics, Inc. Last updated 2025.
    4. Mundt E, McGreevy K, Nix P, Cummings S. Myriad’s Multidisciplinary Approach and Consistent Investment in Variant Classification for Clinical Decision Making [White paper]. Myriad Genetics. 2025.
    5. Gradishar W, Johnson K, Brown K, et al. Clinical Variant Classification: A Comparison of Public Databases and a Commercial Testing Laboratory. Oncologist. 2017;22(7):797-803.
    6. Nix P, Mundt E, Manley S, Coffee B, Roa B. Functional RNA Studies Are a Useful Tool in Variant Classification but Must Be Used With Caution: A Case Study of One BRCA2 Variant. JCO Precis Oncol. 2020;4:730-735.
    7. Nix P, Mundt E, Cummings SA, Roa B, Enhancing variant interpretation in hereditary cancer testing with RNA analysis from residual blood samples. J Clin Oncol. 2025;43(16_suppl):e22595.
    8. Data on File at Myriad Genetics, Inc. Based on a review of 12 months of past claim data for major insurance carriers across the US, the majority of patients face no out-of-pocket costs for their MyRisk test. Last updated 2024.

    ©2025 Myriad Genetics, Myriad Oncology, MyRisk, Precise Tumor, MyChoice, Prolaris, BRACAnalysis CDx, RiskScore, and their respective logos, are either trademarks or registered trademarks of Myriad Genetics, Inc. and its subsidiaries in the United States and other jurisdictions. EndoPredict and the EndoPredict logo are either trademarks or registered trademarks of Eurobio Scientific. Eurobio Scientific has licensed the EndoPredict test to Myriad Genetics in select territories.