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abstract
Highlights
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- The impact of mutation position and family history on ovarian cancer (OC) risks was assessed.
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- In BRCA1 families women with a mutation within the OCCR region have higher OC risks.
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- In BRCA2 families, mutation position did not significantly affect the OC risk.
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- In BRCA2 families, a family history including only OC presented a strong impact on OC risk.
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