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BRCA1 & BRCA2: Genetic testing for hereditary breast and ovarian cancer patient guide What is Hereditary Cancer? Breast cancer is the most common cancer in women in the U.S. (it affects about 1 in
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How to fill out brca1 brca2 genetic testing:

01
Find a reputable genetic testing provider or clinic that offers brca1 brca2 genetic testing. This can typically be done through a referral from a healthcare professional or through online research.
02
Schedule an appointment with the chosen provider or clinic. This may involve filling out forms or providing some basic personal and medical information.
03
Attend the appointment and meet with a genetic counselor or healthcare professional who specializes in genetic testing. They will explain the process, potential outcomes, and answer any questions or concerns.
04
Provide a DNA sample, usually through a simple blood draw or saliva sample. The provider will collect the necessary sample and send it to a laboratory for testing.
05
Wait for the test results. The timeframe for receiving results can vary, so it is important to inquire about the estimated turnaround time during the appointment.
06
Once the results are ready, schedule a follow-up appointment with the genetic counselor or healthcare professional to discuss the findings and implications. They will provide guidance on understanding the test results and the potential risks and advantages associated with them.

Who needs brca1 brca2 genetic testing:

01
Individuals with a family history of breast or ovarian cancer. This includes individuals who have a first-degree relative (parent, sibling, or child) who has been diagnosed with breast or ovarian cancer, especially at a young age.
02
Individuals with a personal history of breast or ovarian cancer, particularly if they were diagnosed before the age of 50.
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Individuals with a family history of male breast cancer.
04
Individuals of Ashkenazi Jewish descent, as there is a higher prevalence of brca1 brca2 gene mutations in this population.
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Individuals who have had multiple primary breast or ovarian cancers.
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Individuals who have had breast cancer in both breasts (bilateral breast cancer).
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Individuals with a family history of certain rare cancer types, such as pancreatic cancer, prostate cancer, or aggressive forms of melanoma.
It is important to note that the decision to undergo brca1 brca2 genetic testing should be made in consultation with a healthcare professional or genetic counselor, as they will be able to provide personalized advice based on an individual's specific situation and medical history.
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BRCA1 and BRCA2 genetic testing is a type of genetic test that looks for mutations in the BRCA1 and BRCA2 genes which are associated with an increased risk of breast and ovarian cancer.
Individuals with a family history of breast or ovarian cancer, or those who are at high risk for developing these cancers, may be required to undergo BRCA1 and BRCA2 genetic testing.
To fill out BRCA1 and BRCA2 genetic testing, individuals need to consult with a healthcare provider or genetic counselor who can order the test and help interpret the results.
The purpose of BRCA1 and BRCA2 genetic testing is to identify individuals who may have an increased risk of developing breast or ovarian cancer so that appropriate preventive measures can be taken.
BRCA1 and BRCA2 genetic testing typically reports any mutations or variants found in these genes and provides information on the associated cancer risks.
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