Didn’t do NIPT test and I’m freaking out.

FTM here. 32F. Husband is 35M. I’m 14 weeks today. At my 9 week appt - when the OB presented the option to do the NIPT test, she made it sound like it wasn’t something people normally do and can be costly. She recommended just doing the initial genetic screen where it tests only 3 genetic disorders including cystic fibrosis and 2 others. My husband and I weren’t very familiar with any of this so we just agreed with the initial test. They lost my vial and didn’t have the results at my most recent appt on Monday so I had to redraw. Still don’t have the results.

I started researching NIPT and it sounds like this is something most people do opt into and when talking to friends about it, almost everyone did it. I’m freaking out now that I didn’t. It seems like it’s something that’s done between 9 - 13 weeks. Is this something you did / would recommend others do? Does it even make sense for me to do it at this point? Would an anatomy scan be able to tell me of any genetic disorders anyway? I hope I haven’t made a mistake by not doing it and am still considering messaging my OB saying I want to do it. Aside from Marfans syndrome, which isn’t tested for in the NIPT, we don’t have any history of genetic disorders. Just looking for opinions here.