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Descriptions :

All areas of the BRCA ½ gene which is the representative cause of hereditary breast cancer are analyzed to diagnose a person’s risk of breast cancer. Mutations in the BRCA ½ gene greatly increase the risk of breast cancer. It is available for both germline and somatic variants detecting SNP and InDel for 53 genes and CNV for BRCA1/2 genes.

Who to test for BRCA

  • Early onset breast cancer (under 50 years of age)
  • Bilateral or multiple breast cancer
  • Diagnosed with both breast and ovarian cancer
  • Family history of breast and/or ovarian cancer
  • Two or more BRCA 1 or 2 related cancers on a single family member


Sample types Concentrations
AxenTM BRCA 1/2

Blood or


5ml of blood


AxenTM BRCA Premium with 53 HBOC related genes

Somatic variants

Germline variants

500ng from FFPE

300ng of dna

MLPA for BRCA1/2 genes gDNA 100ng of dna


Additional information