Does anyone have nonclassic CAH?

I'm currently 12 twelve weeks pregnant and I found out my husband and I are both carriers for ncah, right around the time I got pregnant. We have the option to test our baby for the condition, either through an amniocentesis in utero, or I can wait until after she's born. There is a risk of 1/400 chance that the amino could result in a miscarriage. I'm not sure if I should take that risk when I could test the baby right after it's born. A diagnosis would only provide me with the information, it wouldn't change my mind about the pregnancy.

For those who have this condition, what have been your symptoms? Is there any advice you would give to me as someone who could pass this down to my daughter. There is a 1 in 4 chance that would happen.