Hi,
I've done an at-home genetic test (23andme/Promethease) which shows that I have genes rs1801131 (A;C) and rs1801133 (C:T).
From what I've read so far these two genes together can cause miscarriage and birth defects, as they significantly reduce absorption of folate.
We're going to start TTC at the end of this year, and I want to be as prepared as possible. I think my best bet would to start taking a strong methylfolate now (I'm already taking a regular strength l-methylfolate) and continue during (hopefully) pregnancy, so I want to see my GP about getting a prescription strength supplement.
However, I really hate wasting doctor's time, and I also hate the thought of them just not knowing what I'm talking about. So, does anyone have experience with discussing these genes with their doctor, were they happy to discuss it and test folate & B12 levels, or not?
Thanks!