I just received the results of a genetic test ordered by my oncologist. It shows that I have a genetic variant in the FANCA gene. I have an appointment with my oncologist in a few weeks and he is going to to set up a meeting with a genetic counselor to go over the results.
From what I can tell, the significance of this variant is a predisposition to PCa, which... as a G9 patient who has already had surgery, radiation, and ADT...may explain why I developed cancer but I'm wondering if it has any significance on future treatment decisions. I suspect this information is important for my son's to know.
I have no doubt that my doctor will explain the test results but I want to go into the appointment with a better understanding so I know what questions to ask. Does anyone have any insights to help me be better informed?
Thanks in advance
Written by
DJBUNK
To view profiles and participate in discussions please or .
Thank you for the reply Nalakrats. One additional factor that I noticed after I posted is that the report states the variant is pathogenic. As a medical neophyte, I had to Google pathogenic. It appears to me that my report is indicating that the FANCA variant was due to exposure or some other external influence. Is that a correct interpretation?
Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.
Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.