Myriad Genetics, Inc. · NASDAQ:MYGN

Myriad Genetics — Investor Presentation (February 2024)

12 slides from Myriad Genetics's investor presentation, February 2024

  1. Slide 1: Foresight #RareDiseaseDay Information Kit

    Foresight” #RareDiseaseDay Information Kit Let’s honor this #RarestDay by spreading the word Myriad genetics

  2. Slide 2: Table of Contents

    Table of Contents You can help make undiagnosed rare disease #MoreRare Throughout this guide, you will find useful information to build Ashley's inspiring story Learn about rare disease awareness of Rare Disease Day Learn about Foresight® Carrier Screen and the benefits of carrier Social media kit s

  3. Slide 3: Leap Day comes every 4 years—and this year, February 29 is Rare Disease Day

    Leap Day comes every 4 years—and this year, February 29 is Rare Disease Day, too. But did you know? Most kids living with a rare disease must wait even longer to get a correct diagnosis, specialized care, and support. 4.8 years is the typical waiting time for a rare disease diagnosis* The good news?

  4. Slide 4: Ashley's inspiring story

    Ashley Is 26, pregnant, ana experiencing a complication-free pregnancy. Ashley delivers Christopher. At around 18 months, has not yet started walking. 7 Foresight me: "s Ashley and her husband learn about the Ashley's ®@ = “SESS inspiring story. Christopher gets medical Interventions and extensive p

  5. Slide 5: Rare Disease Facts: Rare disease isn't rare at all

    RARE DISEASE FACTS Rare disease isn’t rare at all By definition, individual rare diseases affect 200,000 people or less. But the overall community living with rare disease across the globe is anything but small. = SS 38 8 38 8 af 58 Q SS SS G8 GS SS SL mee ae LO,OOO+ 1in1i3 400 million types of rare

  6. Slide 6: Rare Disease Facts: The journey to diagnosis can be isolating

    RARE DISEASE FACTS The journey to diagnosis can be isolating Families navigating mysterious symptoms and healthcare choices may not know where to turn for help. Until they have a correct diagnosis, it may be hard to identify the right dedicated support groups for them, with a community of families w

  7. Slide 7: How Foresight Helps: Early insights matter

    HOW FORESIGHT HELPS OPTIONS THAT MAY HELP BEFORE PREGNANCY Early insights matter @ If every family received a genetic Foresight In vitro fertilization: embryo _-Family-building options: from Carrier Screen before or during pregnancy, Genetic testing can be done adoption to sperm or ege many could fi

  8. Slide 8: How Foresight Helps: Foresight is for every parent-to-be

    HOW FORESIGHT HELPS Foresight is for every 1 in 300 838% arent-to-be | ot pregnancies are affected by the of people who carry a risk of cystic fibrosis, conditions Foresight screens*® spinal muscular atrophy, and fragile X Anyone can have a baby with an inherited by syndrome have no known family his

  9. Slide 9: Know Your Risk

    “1 in 40 people are “Once we had carriers carrier screening of Spinal R A R E D I S E A S E D AY Muscular done, we were Know Atrophy and don’t know it. able to make a My husband plan.” Your and I are two of them.” Ashley Pantier Risk. Ashley Pantier Mom of two children with Spinal Muscular Atrophy S

  10. Slide 10: Rare Disease Day social media posts

    Having a rare FEBRUARY Rare disease can be Disease hard, getting Day a diagnosis Andrea Pirages MS, Board-Certified Genetic Counselor shouldn’t be. and Carrier Screening Advocate Suggested copy: Considered the #RarestDay on the calendar, February 29th comes only Suggested copy: For some rare disease

  11. Slide 11: Q: Knowledge Is Power

    Knowledge Q: Is Power I would not do anything differently, so why do a reproductive carrier screen? Suggested copy: A: In fact, there are many proactive things you can do when armed with the Suggested copy: Many of us are carriers of inherited conditions and don’t know it. In fact, 88% knowledge a c

  12. Slide 12: Myriad Genetics Foresight Carrier Screen References

    Myriad genetics Foresight’ Carrier Screen Refrences: 1, Rare disease facts. Global Genes. https://globalgenes.org/rare-disease-facts. Published September 5, 2023. Accessed December 21, 2023. 2. Rare diseases. National Institutes of Health. https://www.nih.gov/about-nih/what-we-do/nih- turning-discov

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