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. Author manuscript; available in PMC: 2009 Apr 17.
Published in final edited form as: Curr Treat Options Oncol. 2007 Feb;8(1):61–73. doi: 10.1007/s11864-007-0021-5

Table 3.

Results of genetic screening for BRCA1/2 mutations

Result Interpretation
Positive for deleterious mutation Individual has high risk of breast and ovarian cancer
Negative for a mutation Result interpreted with caution especially in the setting of a strong family history
Mutation of unknown significance Mutation has not been definitively shown to be deleterious either because it is rare or because it may not completely track with the family history of the individual
Mutation favoring benign polymorphism Although not certain these mutations seem to not be associated with a high risk for breast and ovarian cancer