• Welcome to Phoenix Rising!

    Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of and finding treatments for complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia (FM), long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.

    To become a member, simply click the Register button at the top right.

Fighting Stress with Adenosine Antagonists.

Messages
9
Location
Catalonia, Spain
Hi all!!

I know this post is old, but... I'm interested in AMPD1 and AMPD3...

In AMPD1 I have the heterozygous mutation on rs17602729, and also 3 more mutations, another one heterozygous on rs2010899 with unknown clinical significance, one homozygous on rs761755 also with unknown clinical significance, and have another heterozygous on rs61752479 wich is likely benign allele.

And in AMPD3 I have 30 mutations, 3 in UTR region and 27 Intron, all with unknown clinical significance.

Is it possible that this SNP with unknown clinical significance can be problematic? isn't it?

I want to ask for it to my Dr. when I'll see her next visit...