New.myriadpro.com is a subdomain of myriadpro.com, which was created on 2010-04-29,making it 14 years ago.
Description:Find out how MyRisk comprehensive risk assessments provide actionable genetic testing insights to help patients and providers make informed medical...
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Patients I need help with… Understanding hereditary cancer risk What is my risk of developing hereditary cancer? Treating cancer What are my treatment options? Guiding prenatal care Am I having a boy or girl? Is my baby at risk for a genetic condition? Managing mental health How might my genes affect my medication outcomes? (sidebar parent) About genetic testing Affordability Financial assistance Patient Resources How does genetic testing work? Patient record request Blood draw locator Prostate Cancer What are my treatment options? Providers My patient needs a test for… Assessing hereditary cancer risk What is my patient’s risk of developing hereditary cancer? Cancer treatment What is the best treatment for my patient? Prenatal care What is the predicted fetal sex of my patient’s baby? What is a pregnancy’s risk of a genetic disease? Mental health treatment How will my patient metabolize or respond to certain medications? (sidebar parent) About our tests Myriad test catalog Scientific Publications MyRisk ® gene table Affordability Financial assistance EMR Integrations Provider resources Order a test kit Order patient materials Documents & forms Scope of service & lab certificates Provider portal Blood draw locator Prostate Cancer Treatment What are my patient’s treatment options? Biopharma Our Tests Tests for… (column wrapper) Prenatal care Fetal sex Chromosome conditions Genetic diseases Cancer risk assessment Hereditary cancer Mental health Depression Anxiety ADHD (column wrapper) Cancer management Breast cancer Ovarian cancer Pancreatic cancer Prostate cancer Endometrial cancer Other cancers All tests (sidebar parent) TESTS BY SPECIALTY Oncology Urology Imaging OB/GYN Mental Health Internal/Primary care All tests TESTS BY NAME BRACAnalysis CDx ® EndoPredict ® Foresight ® GeneSight ® MyChoice ® CDx MyRisk ® (cancer treatment) MyRisk ® (cancer risk) Prequel ® Precise ™ Tumor Prolaris ® SneakPeek ® About About (column wrapper) About Myriad Leadership Investor relations (column wrapper) Press releases Careers Contact (sidebar parent) Myriad Genetics Laboratory and Support Center 322 North 2200 West Salt Lake City, UT 84116 Corporate Phone: (801) 584-3600 Corporate Fax: (801) 584-3640 PORTALS ORDER Search: Portals Order Search: Patients I need help with… Understanding hereditary cancer risk What is my risk of developing hereditary cancer? Treating cancer What are my treatment options? Guiding prenatal care Am I having a boy or girl? Is my baby at risk for a genetic condition? Managing mental health How might my genes affect my medication outcomes? (sidebar parent) About genetic testing Affordability Financial assistance Patient Resources How does genetic testing work? Patient record request Blood draw locator Prostate Cancer What are my treatment options? Providers My patient needs a test for… Assessing hereditary cancer risk What is my patient’s risk of developing hereditary cancer? Cancer treatment What is the best treatment for my patient? Prenatal care What is the predicted fetal sex of my patient’s baby? What is a pregnancy’s risk of a genetic disease? Mental health treatment How will my patient metabolize or respond to certain medications? (sidebar parent) About our tests Myriad test catalog Scientific Publications MyRisk ® gene table Affordability Financial assistance EMR Integrations Provider resources Order a test kit Order patient materials Documents & forms Scope of service & lab certificates Provider portal Blood draw locator Prostate Cancer Treatment What are my patient’s treatment options? Biopharma Our Tests Tests for… (column wrapper) Prenatal care Fetal sex Chromosome conditions Genetic diseases Cancer risk assessment Hereditary cancer Mental health Depression Anxiety ADHD (column wrapper) Cancer management Breast cancer Ovarian cancer Pancreatic cancer Prostate cancer Endometrial cancer Other cancers All tests (sidebar parent) TESTS BY SPECIALTY Oncology Urology Imaging OB/GYN Mental Health Internal/Primary care All tests TESTS BY NAME BRACAnalysis CDx ® EndoPredict ® Foresight ® GeneSight ® MyChoice ® CDx MyRisk ® (cancer treatment) MyRisk ® (cancer risk) Prequel ® Precise ™ Tumor Prolaris ® SneakPeek ® About About (column wrapper) About Myriad Leadership Investor relations (column wrapper) Press releases Careers Contact (sidebar parent) Myriad Genetics Laboratory and Support Center 322 North 2200 West Salt Lake City, UT 84116 Corporate Phone: (801) 584-3600 Corporate Fax: (801) 584-3640 Take the next step with MyRisk ® Interested in learning more about the MyRisk test and your ordering options? Fill out the form below to get started. Request information Back Order MyRisk Providers Patients Resources Documents & forms I am a: Please select... Health Care Provider Patient Specialty Please select... Gynecology IVF Internal Medicine MFM Obstetrics/Gynecology Other - Women’s Health Primary Care I don’t have my healthcare provider’s information You agree to be contacted with newsletters, marketing or promotional materials and other information that may be of interest to you. You may opt-out of receiving communications from us by following the unsubscribe link or the instructions provided in any email we send. For further information on our privacy practices and commitment to protecting your privacy, please visit our Privacy Policy. Hidden Fields Google Account ID Web_Form_URL__c Google_Client_Id__c GCLID UTM Medium UTM Source UTM Campaign UTM Content UTM Term AE_First_Name AE_Last_Name Hidden test fields Contact Information MyRisk ® Hereditary Cancer Test The all-in-one hereditary cancer test, risk assessment, and care plan MyRisk with RiskScore ® is a powerful tool that evaluates 48 genes to help healthcare providers identify their patients’ risk of developing 11 different types of hereditary cancer. More than a test, MyRisk’s clear, actionable results are the foundation for personalized care plans that can be used to help patients make confident, informed decisions about their medical management. Know Your Risk. Plan for your Future. MyRisk ® Hereditary Cancer Test The all-in-one hereditary cancer test, risk assessment, and care plan MyRisk with RiskScore ® is a powerful tool that evaluates 48 genes to help healthcare providers identify their patients’ risk of developing 11 different types of hereditary cancer. More than a test, MyRisk’s clear, actionable results are the foundation for personalized care plans that can be used to help patients make confident, informed decisions about their medical management. Know Your Risk. Plan for your Future. Why MyRisk? For patients with family history of certain cancers , hereditary cancer testing is the primary way to determine if they are at an increased risk of developing specific types of cancer. MyRisk with RiskScore evaluates 48 genes associated with hereditary cancer risk to identify genetic changes associated with an increased cancer risk. When combined with family history and other clinical factors, MyRisk with RiskScore provides each patient with a cancer risk assessment individualized to them. Nearly 1 in 4 patients 1 meet criteria for hereditary cancer testing MyRisk is more than a test Delivers personalized care plans The MyRisk Management Tool offers personalized guidance for patients and providers to work together to reduce risk of developing cancer or detect it at an earlier, more treatable stage. Guides medical management decisions Because of the precision science behind MyRisk, 53% of patients 2 qualify for a medical management change that may help lower cancer risk, as opposed to only 10% with other hereditary cancer tests. Gives a precise answer about breast cancer risk As the only hereditary cancer test designed for patients of all ancestries, the RiskScore component of MyRisk gives patients both a five-year and lifetime risk estimate of developing breast cancer. This is calculated using a combination of clinical risk factors, family history, and unique genetic,...
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