Anyone ever had a variant of unknown significance with the BRCA2 gene?

I am treating for a recurrence about 1.5 years after RALP. They mentioned an option of doing genetic testing, so I did. I just got a call from one of the staff, letting me know that I had a vus with the BRAC2 gene. She implied it is an important note, and that I should speak to a genetic counselor as well as my doctor at the next appointment. Googling this showed very inconclusive evidence that it could mean anything. Anyone ever experienced this?