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Table 4 Comparison of different selection criteria for BRCA1/2 testing in our cohort

From: High frequency of pathogenic non-founder germline mutations in BRCA1 and BRCA2 in families with breast and ovarian cancer in a founder population

Criteria

Sensitivity

Specificity

Accuracy

NCCN

100%

50%

64%

Manchester scoring system

85.7%

88.9%

87.5%

Swedish Breast cancer group

57.1%

88.9%

75%