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MyRisk Clinical Handbook Version 3.0: 08/01/2014 Myriad myRisk Clinical Handbook For the most uptodate clinical information please visit www.MyriadPro.com/myRisk. The format and contents of this guide.

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One or more of your genes that were passed down through your family is altered, or carries a genetic mutation, which increases your risk for one or more hereditary cancers. This mutation(s) is considered CLINICALLY SIGNIFICANT and changes to your medical management may be appropriate.

To access an online or PDF copy of your results, please create an online account in our patient portal. Doing so ensures a secure method of accessing your sensitive and private health information.

If you have a BRCA mutation, you have a 50 percent chance of passing the mutation to each of your children. These mutations do not skip generations but sometimes appear to, because not all people with BRCA mutations develop cancer. Both men and women can have BRCA mutations and can pass them onto their children.

There are three possible results you can receive from genetic testing: positive, negative or uncertain. The meaning of these results depends on multiple factors, such as the type of genetic testing that was performed and your personal and family history, among others.

Up to 10% of all cancers may be caused by inherited genetic changes. Inheriting a cancer-related genetic change doesn't mean you will definitely get cancer. It means that your risk of getting cancer is increased.

What will the MyRiskâ„¢ test results tell me? The MyRiskâ„¢ test report typically provides results in three main categories: Positive, Negative, or VUS (Variants of Uncertain Significance). A positive result means our test found a variant in a specific gene that is associated with a higher risk of hereditary cancer.

Each gene tested with MyRisk links to one or more of 11 cancer sites: Breast, Ovarian, Colorectal, Uterine, Skin, Pancreatic, Gastric, Prostate, Renal, Lung, and Endocrine.

By analyzing small pieces of DNA from your baby's placenta, called cell-free DNA, we can determine the chance that your baby has a chromosome abnormality associated with a certain genetic condition. Results are available in approximately 7-10 days.

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© Copyright 1997-2025
airSlate Legal Forms, Inc.
3720 Flowood Dr, Flowood, Mississippi 39232
Form Packages
Adoption
Bankruptcy
Contractors
Divorce
Home Sales
Employment
Identity Theft
Incorporation
Landlord Tenant
Living Trust
Name Change
Personal Planning
Small Business
Wills & Estates
Packages A-Z
Form Categories
Affidavits
Bankruptcy
Bill of Sale
Corporate - LLC
Divorce
Employment
Identity Theft
Internet Technology
Landlord Tenant
Living Wills
Name Change
Power of Attorney
Real Estate
Small Estates
Wills
All Forms
Forms A-Z
Form Library
Customer Service
Terms of Service
DMCA Policy
About Us
Blog
Affiliates
Contact Us
Privacy Notice
Delete My Account
Site Map
All Forms
Search all Forms
Industries
Forms in Spanish
Localized Forms
Legal Guides
Real Estate Handbook
All Guides
Prepared for You
Notarize
Incorporation services
Our Customers
For Consumers
For Small Business
For Attorneys
Our Sites
US Legal Forms
USLegal
FormsPass
pdfFiller
signNow
airSlate workflows
DocHub
Instapage
Social Media
Call us now toll free:
1-877-389-0141
As seen in:
  • USA Today logo picture
  • CBC News logo picture
  • LA Times logo picture
  • The Washington Post logo picture
  • AP logo picture
  • Forbes logo picture
© Copyright 1997-2025
airSlate Legal Forms, Inc.
3720 Flowood Dr, Flowood, Mississippi 39232