First Genetic Genie is reporting the CYP2D6 S486T the wrong way round. GG is the normal ancestral allele. BUT this is one of those tricky changes of G to C and the way it is reported depends on the orientation. It needs to be checked very carefully to really determine whether you are wild type or variant.
Having said that the frequency of minor allele is 0.4012. In other words the variant is very common.
Even if you have the variant, this in itself doesn't mean much, nor do the other CYP SNPs for which you are +/-.
Combinations of SNPs can have very marked effects of the activity of the CYP enzymes (all of them, not just 2D6) and working these out can be a nightmare.
Here for example is the SNPedia entry for CYP 2D6, listing the SNPs that constitute the various phenotypically defined alleles.
You need more info than genetic genie provides to work out if you really have any of these alleles (and maybe not even then!).
I can't remember what LiveWello reports. Promethease makes an attempt to work out the CYP alleles but it is all very confusing.
The same sort of comment applies to NAT. It is combinations that matter, not individual SNPs. Again I know that Promethease tries to classify you as low, high or intermediate metaboliser based on all your NAT SNPs, don't know about LiveWello.
The two GSTP1 SNPs definitely slow the enzyme, but the effect with +/- is small. Supplements which stimulate glutathione production might be a good idea.
The SOD2 A16V definitely does something. +/+ has a 30-40% reduction in activity. This is the manganese dependant version of the enzyme operating in mitochondria. Supplementation with Mn may help to stimulate a sluggish enzyme.