I had the maternal genetic testing done and the fetal too. My baby girl got the green light 💗

But they told me I am in the grey zone for fragile X. So normal is below 45. Grey zone is 45-54. Pre mutation is 55-200 and mutation is over 200.

So I was told I am not a carrier but my children could be carriers and their children could possibly have fragile x.

I believe there is power in knowledge but I am a worrier and now my doctor has me concerned about potential grandchildren😣

Just curious if there is anyone else out there with experience or knowledge on this.