Hi all, I have a daughter with a rare genetic disorder and I am pregnant with my third child. My second baby did not have the genetic disorder. I was told I would have a 1% chance of having a another child with disorder, since it did not come from her dad or myself. With my third child all preliminary genetic tests were normal, but they are going to want me to do an amniocentesis. I’m not sure if I want to do this because it is risky. What do you think?