BRCA - JScreen
BRCA TESTING

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Knowing if you have a BRCA mutation can save your life.

While anyone can have a BRCA mutation, Ashkenazi (Eastern and Central European – for example Germany, Poland, Russia) Jews are at 10 times greater risk – even if they don’t have a personal or close family history of cancer. Having a BRCA mutation puts a person at risk for certain cancers, including breast, ovarian, pancreatic and prostate. Anyone with a mutation also has a 50% chance of passing it down to each of his/her children, regardless of their gender.

JScreen at Emory University, in partnership with the Winship Cancer Institute, has launched The PEACH BRCA Study in the metro-Atlanta area. The purpose of this study is to evaluate a new BRCA education and screening program for men and women with Ashkenazi Jewish background.

The study benefits include:

  • Learning about your risk for certain cancers, including breast, ovarian, pancreatic and prostate
  • Receiving information that will help inform your medical management and reproductive planning
  • Gaining important health information that can be shared with family members

The study is open to 500 participants.

Who Is Eligible?

To participate in The PEACH BRCA Study, individuals must meet ALL of the following criteria:

  • Have at least one Ashkenazi (Eastern and Central European – for example Germany, Poland, Russia) Jewish grandparent
  • Are at least 25 years old
  • Reside in the metro-Atlanta area (open to both men & women)
  • Have not had BRCA testing in the past
  • No personal or close significant family history of BRCA-related cancers or a BRCA mutation

What Is The Process?

The first step is to complete an online eligibility questionnaire. Participants will collect a saliva sample at home for genetic testing and receive their BRCA results by a certified genetic counselor by phone or secure video. In addition, they will complete two surveys. Testing is FREE! Participants will not be charged and will not be asked to provide health insurance information.

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Not eligible or not ready to get tested yet?

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FAQs

1. INFORMATION ABOUT BRCA

What is BRCA?

The name “BRCA” is an abbreviation for “BReast CAncer gene.” We all have two BRCA genes, BRCA1 and BRCA2. These genes are important because they repair DNA breaks that might lead to cancer. When either BRCA gene is not working properly (in other words, when there is a mutation in one of these genes), it may not be effective at preventing cancer. Because of this, people with a BRCA mutation are more likely to develop certain cancers, such as breast, ovarian, pancreatic, and prostate cancers.

Why should I consider doing BRCA testing?

People who carry BRCA mutations are at increased risk for certain cancers, including breast, ovarian, pancreatic, and prostate cancers. Information about carrier status can help guide medical management. For example, female carriers may elect to have increased cancer surveillance (such as frequent mammograms and breast MRIs), or risk-reducing surgeries (such as preventative mastectomies and removal of ovaries). Male carriers are encouraged to have yearly clinical breast and prostate exams. Carriers who know their status are encouraged to speak with a genetic counselor and appropriate medical specialists, as well as discuss with other family members who are also at-risk to carry mutations. Knowing this information can be life-saving for yourself and others.

Which cancers are associated with BRCA?

Female carriers of BRCA mutations are at increased risk to develop breast and ovarian cancers. Males with mutations are at increased risk for breast and prostate cancers. Both females and males with mutations are at risk for pancreatic cancer and may have an increased risk of melanoma. While the risks are increased, not all BRCA carriers will develop cancer.

Can men have BRCA mutations?

Yes. A parent with a BRCA mutation has a 50% chance of passing it on to each of his/her children (son or daughter). This means that both men and women are at equal risk for inheriting a BRCA mutation. Males with a BRCA mutation are at increased risk for breast, prostate and pancreatic cancers.

If I have a mutation, will my kids have it too?

Each child (son or daughter) has a 50% chance of inheriting a BRCA mutation. Reproductive options, such as in vitro fertilization with genetic testing of the embryo, are available to BRCA carriers who are planning on having a child and want to avoid passing down their mutation.

What does being Ashkenazi Jewish have to do with BRCA?

While anyone could have a mutation in his/her BRCA genes, individuals with Ashkenazi Jewish (Eastern and Central European) background are at 10 times greater risk. One in 40 Ashkenazi Jews will have a mutation—even if there is no family history of BRCA-related cancer.

Is all cancer hereditary?

No. Most cancer happens by chance. However, some cancers are due to hereditary changes in genes, even if cancer hasn’t been seen in the family. For example, about 5-10% of breast cancers and about 20-25% of ovarian cancers are due to inherited genetic changes that increase the risk to develop these types of cancer. Many cases of breast and ovarian cancers are due to BRCA mutations, but there are other genes that increase the risk for these and other forms of cancer. It is important to consult with a genetic counselor if you think that you or a family member might have a hereditary cancer risk.

2. BRCA TESTING THROUGH JSCREEN

How is BRCA testing different than JScreen’s reproductive carrier screening panel?

JScreen’s reproductive carrier screening panel tests for diseases like Tay-Sachs and cystic fibrosis, many of which present in infancy or early childhood. Most carriers of these diseases have no symptoms, but may pass down their genetic mutations to their children. If two carriers of the same disease have a child together, there is a 25% chance for that child to be affected with the disease. So, the JScreen reproductive carrier panel is designed to provide you with information about the health of your children.

The BRCA test is different in that it could tell you if you carry a genetic mutation that would predispose you to certain cancers. If you do carry a mutation, each of your children has a 50% chance of inheriting that mutation and its associated cancer risks. As you can see, the BRCA test may give you information about your own health, as well as risks to your family members.

How do I participate in The PEACH BRCA Study?

To participate, you will need to meet the following initial eligibility criteria: live in the greater metropolitan Atlanta area, be at least 25 years old, have at least one Ashkenazi Jewish grandparent, never have had BRCA testing, and have little or no personal or close family history of BRCA-related cancer. You will be asked to complete a questionnaire about your family’s health history and a genetic counselor will review it and let you know if you are eligible. If you think you may be eligible to participate, click here to get started.

Is JScreen’s BRCA test the same as 23andMe’s BRCA test?

No. 23andMe looks for the presence of three specific BRCA mutations that are commonly found in Ashkenazi (Eastern and Central European) Jews. JScreen’s BRCA test is more comprehensive, because it also screens for hundreds of other mutations in the BRCA genes.

Can I participate in the study if I have a personal or family history of breast, ovarian, pancreatic, or prostate cancer?

It depends. We will ask all interested participants for a detailed cancer family history. A genetic counselor will review your responses and will let you know if your history puts you at higher risk to have a genetic mutation that predisposes you to any of these types of cancer. If there is a higher risk, you are not eligible to participate in the study. Individuals with significant personal or family histories of cancer should meet one-on-one with a genetic counselor, who can recommend more comprehensive testing (which will likely be covered by insurance) than BRCA1/2.

3. INSURANCE

Does insurance cover BRCA testing?

Most insurance carriers will cover BRCA testing and genetic counseling if the individual has a personal or significant family history of BRCA-related cancers.

If you meet eligibility criteria for The PEACH BRCA Study, which includes having no personal or significant family history of BRCA-related cancers, you will not be asked to provide your insurance information and there will be no cost to you. The study will use grant funding to pay for your testing and genetic counseling.

If my insurance company learns I am BRCA-positive, will my insurance coverage change?

It depends on what type of insurance you have and where you live. According to the GINA law, health insurance companies that provide plans for businesses with 15 or more employees cannot change your coverage based on the results of your genetic testing. However, other types of insurance, such as life, disability, and long-term care, do not have restrictions about using your genetic information to set their plans, and each state has its own mandates regarding the use of genetic information. You can learn more about this topic here.

If my employer learns I am BRCA-positive, are there grounds for firing me?

The GINA law makes it illegal for employers with 15 or more employees to use your genetic information to make decisions about hiring, firing, promotion, pay, privileges or terms. In other words, your employer may not use family health history and genetic test results in making decisions about your employment. Please be aware that GINA’s protections in employment do not extend to the US military or employees of the federal government.

I am worried about my results getting in the wrong hands. How will you ensure that all of my information is kept private?

The privacy of your health information is very important to us. To protect your personal health information, we will follow federal and state privacy laws, including the Health Insurance Portability and Accountability Act and regulations (HIPAA). The only people who will have access to your medical and genetic information will be the study team, its overseers, and the laboratory. Each study participant will also be given a copy of his/her results after they are reviewed with a genetic counselor and will have the option to share them with their personal health-care provider.

Invitae (the testing lab) and Emory University notice of privacy practices.

Resources

Sharsheret

Sharsheret is the national non-profit organization supporting Jewish women and families facing breast and ovarian cancer.

Komen Atlanta

Komen Atlanta saves lives by meeting the most critical needs in our communities and investing in breakthrough research to prevent and cure breast cancer.

FORCE

FORCE provides information, support, research and advocacy programs for the hereditary cancer community.

Winship Cancer Center

The Winship Genetic Counseling Program provides personalized risk assessment, information about testing options and consultations to discuss test results.

NSGC

The National Society of Genetic Counselors (NSGC) Find a Genetic Counselor directory offers access to over 3,300 genetic counselors (US and Canada).

Bright Pink

Bright Pink helps to save lives from breast and ovarian cancer by empowering women to know their risk and manage their health proactively.

Yodeah

Yodeah’s mission is to educate and facilitate cost-effective testing for hereditary cancer genetic mutations such as BRCA in the Jewish community.

TEAL

TEAL promotes public awareness and education of ovarian cancer, provides support to survivors, and raises funds for research.

HIS Breast Cancer Awareness

HIS Breast Cancer is a non-profit organization providing awareness, education and support of male breast cancer and BRCA genetic mutations.

We Get it Too

The mission of Wegetittoo.org is to bring awareness and education of male breast cancer while stressing the importance of early detection and screening

The PEACH BRCA Study is made possible thanks to the generosity of the Marcus Foundation, the Florence and Laurence Spungen Family Foundation, the Kay Family Foundation Fund of the Community Foundation of Greater Atlanta, and The Jewish Women’s Fund of Atlanta.

About JScreen

JScreen is a not-for-profit program that is part of Emory University School of Medicine’s Department of Human Genetics. With a mission to prevent Jewish genetic diseases, JScreen makes genetic screening and counseling convenient and affordable.

Contact JScreen

Contact our staff with any questions about our program.

JScreen at Emory University
Department of Human Genetics
5115 New Peachtree Road, Suite 301
Atlanta, GA 30341
Office: 404-778-8640
[email protected]

Genetic counselors can be reached at [email protected]