TEST DIRECTORY

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Laboratory：Akiruno

○BRCA1/2 gene single site test

CODE：0R615 1

  • TEST NAME SPECIMEN
    REQUIREMENT
    （ｍL）     CONTAINER CAP COLOR STORE
    TEMPERATURE
    (STABILITY)     TURNAROUND
    TIME (DAY)     METHODOLOGY REFERENCE RANGE
    (UNIT)
  • Ethics recommission
    BRCA1/2 gene single site test
    Blood (EDTA-2K added)
    7.0
    PNM Room temperature
     10-18 Next Generation Sequencing (NGS)

    A method that uses a next-generation sequencer to simultaneously determine the base sequences of a huge number of DNA fragments.

COMMENT


This test is for when a blood relative has undergone a BRCA1/2 gene test and a pathogenic mutation or suspected pathogenic mutation has been found.
Avoid cryopreservation. Please be sure to specify your sex when making your request. Please avoid duplicate requests with other items.
This testing method increases the influence of contamination, so please be careful when handling the specimen. The number of days required may vary depending on the measurement and analysis situation.
●When requesting this inspection
When requesting this inspection, please read the following information and use the special request form.
1. To protect personal information, please anonymize the test subject's name and enter it in the "anonymous code" field.
2. To confirm that the purpose and limitations of the test and the significance of the BRCA1/2 genes have been explained, and that written consent has been obtained from the test subject. , please check.
3. For inquiries about test results, please use an anonymous code.
4. Some of the anonymized personal information will be used by Myriad Genetic Laboratories, Inc. (USA), the measurement and analysis organization for this test, to ensure the quality of the BRCA1/2 genetic test. It may be used to improve.
5. Please check the announcements from related academic societies, etc.
●About submission
・Please be sure to collect the sample into a dedicated blood collection tube and submit it on the same day.
・Samples cannot be returned. Please note.
●Notes regarding entrustment
・Test report for those who have developed breast cancer or ovarian cancer and have found a pathogenic mutation or suspected pathogenic mutation in BRCA1/2 gene testing Please submit a copy along with the special request form, and fill in the mutation information on the special request form.
・Persons with a history of allogeneic bone marrow transplantation cannot request this item.
●How to make a request
1. Access the dedicated request input site (https://db.myriadgenetics-ops.com/secure/login.aspx).
2. After logging in, enter the necessary request information according to the "Myriad Genetics Test Request Input System Operation Guide".
3. After completing the input, please print out the request form and submit it along with the specimen.
*Internet connection environment is required.

Collect blood in a special container, mix well, and store at room temperature. Please avoid duplicate requests with other items.
This testing method increases the influence of contamination, so please be careful when handling the specimen.
Please submit the specimen on the same day after collection.

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