DSP VUS *not asking for medical advice just opinions/support*
I have quite a bit of health anxiety. Always have related to heart stuff because my dad (he’s okay!) had a rare congenital heart defect when i was young. Totally unrelated to this. Long story short— I’ve had about all the cardiac testing you can have. Most recently an MRI after i had a 2 week monitor show a single 10 beat run of NSVT. My mri was normal. But my doctor decided to do genetic testing on my about this condition i specifically found in a google spiral. And what are the odds i find out i have a DSP vus variant. On the clinvar database it has 4 labs calling it VUS and one lab calling it likely benign. My doctor thinks I’m fine especially with my structure being normal and believes the NSVT was related to my POTS and he just signed up for updates on the gene. But basically told me to live my life with no restrictions. I’m having a hard time with that.