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Mapmygenome’s BRCAMap test covers both BRCA1 and BRCA2 genes (Full sequence analysis for coding regions). Blood specimen is collected from the individual for DNA extraction and analysis (Next Generation Sequencing). Validation by Sanger sequencing for pathogenic variants found (if any). This includes: - Primary Genotype Report - Personalised Genetic Counseling session (~45 mins) - Recommendations and guidelines from our counselor. This may include other screening tests if any. A physician's summary or a genetic counseling session is necessary before purchase.

What is BRCAMap ?

BRCAMap is a targeted next generation sequencing(NGS) Panel for BRCA 1 & BRCA 2 full gene sequencing to assess the BRCA mutations that are responsible for the majority of hereditary breast and ovarian cancers.

BRCAMap can be performed on somatic samples(tissue samples) if the patient is currently diagnosed with cancer or Germline samples(Blood) for the patients who are at risk of developing cancer.

BRCA testing for breast cancer

Almost 12% of women in the general population develop breast cancer during their lifetime. In India, almost 1 in 28 women are diagnosed with breast cancer

70 to 85% of Hereditary Breast and Ovarian Cancer cases are caused by mutations in either the BRCA1 or BRCA2 gene

BRCA genes are popularly known as breast cancer, early onset genes. They are “tumor suppressors'' in nature. BRCA genes repair damages or double stranded breaks in DNA and restore genomic integrity of human cells. Hence they play a vital role in maintaining normal cell growth in the body .

Harmful mutations or changes in the two genes have been associated with increased risk of cancers. Most common types of cancers with BRCA in women include breast and ovarian. Defective BRCA genes account for nearly 5-10% of breast cancer cases, while the rest are sporadic in nature.

Who should be tested ?

  • Strong family history of breast, ovarian, fallopian tube, peritoneal, prostate, or pancreatic cancer (BRCA1&2 mutations are inherited, family members with either BRCA1 or BRCA2 mutations usually share the same mutation.)
  • Personal history of Breast/ovarian cancers and meets the criteria related to : age of diagnosis, type of cancer/Bilateral Cancers ancestry.
  • Personal/family history of ovarian, fallopian tube, or primary peritoneal cancer.
  • History of breast cancer in Males.
  • A relative with a known deleterious mutation in BRCA1 or BRCA2 genes.
  • Ashkenazi Jewish or Eastern European ancestry.

Test sample requirements

FFPE (Formalin-Fixed Paraffin-Embedded) Sample - Somatic cases

Blood Sample - Germline cases

How it Works?


Sample Collection

Your Doctor places a request for the test. The sample is tested for the susceptibility.


Lab Processing

The sample processed using NGS Technique


Data Analysis

Your genetic sequence is subjected to extensive analysis and a report is generated based on the genetic findings


Genetic Counseling

Our genetic counselor will discuss your results at a time and day convenient for you.

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