Genetic Tesults

I'm waiting on results of gene testing which I undertook mostly at the request of my 37 year old daughter . I was diagnosed at 61 , mum same time as me when she was 81 and her mum died at 41 from bc. So my daughter is justifiably concerned. The genetic counsellor advised there was a less than 1 % chance that I have the mutation based on stats. As much  as I was happy about the low % it meant I had to pay 600$ for the test as it was apparently only govt funded if there was a 10% risk or more. What surprised me was the advice that if I have the mutation there is an increased risk of ovarian cancer and surgery would be recommended.