BRCA 1 and 2 mutations 8 SNP

BRCA 1 and 2 mutations 8 SNP test is an advanced genetic blood analysis used to detect specific mutations in the BRCA1 and BRCA2 genes. These genes play a key role in regulating cell growth and repairing DNA damage. Mutations in these genes can increase the risk of hereditary breast and ovarian cancer in women, as well as prostate cancer in men.

Who conducts the BRCA 1 and 2 mutations 8 SNP test?

Genetic Laboratory Belgrade, IntroLab, is equipped with top-notch staff and technology to perform this analysis. Using Next-Generation Sequencing (NGS), we precisely analyze eight single nucleotide polymorphisms (SNPs) in the BRCA1 and BRCA2 genes. SNPs are variations at the single nucleotide level in DNA that may indicate the presence of certain mutations.

Who is this test for?

This test is specifically designed for individuals with a family history of breast, ovarian, or prostate cancer, as well as those who want to proactively identify their risk of developing these cancers. The sample for analysis is usually taken from peripheral blood, and the procedure is quick, painless, and safe.

What makes the BRCA 1 and 2 mutations 8 SNP test unique?

The key advantage of the BRCA 1 and 2 Mutations 8 SNP test is its high reliability and accuracy. Identifying mutations in the BRCA1 and BRCA2 genes allows for early detection of potential genetic risks and enables a personalized approach to the treatment and prevention of certain diseases. Our laboratory follows strict quality control protocols, ensuring accurate results.

Interpreting the test results

Once we receive the test results, our team of geneticists will carefully analyze and interpret them. We will then provide you with clear and understandable reports, explaining the results in detail and offering recommendations for further action. Our experts are also available to provide you with all the necessary information and advice on the next steps.