Could anyone please help me with these DNA results?
You have the slow versions of MAOA and COMT, hence you're breaking down serotonin, dopamine, epinephrine, and norepinephrine somewhat slowly. But you have the faster version of VDR Taq (VDR Bsm is exactly the same thing usually, just reported backwards), so you are probably producing dopamine (which turns into norepinephrine then epinephrine) at a normal rate. This suggests that you really don't need and wouldn't tolerate extra methyl groups or serotonin and dopamine precursors.
Fortunately you don't have the nasty MTHFR SNP, and the other two have little or no impact by themselves, especially when heterozgyous. Supplementing with methyfolate probably isn't necessary, though you could always try it anyhow or get tested if worried about it.
Your MTR and MTRR could indicate a problem resulting in higher homocysteine and lower B12. Due to your COMT and MAOA issue, hydroxoB12 is a safer bet than methylB12.
BHMT-08 can also result in increased homocysteine. The other BHMT SNPs listed don't have an impact on the gene.
CBS C699T might result in a slight upregulation in disposing of homocysteine via an alternative pathway. The other CBS SNPs don't impact the functioning of their gene.
SHMT1 is typically only relevant when it's homozygous and MTHFR C677T is present. Neither applies to you, so it's unlikely that you need the usual indicated supplements (folate and folinic acid).
ACAT1-02 also isn't shown to have any impact on its gene.
SUMMARY:
HydroxoB12 may be helpful. It also could be a good idea to keep an eye on your homocysteine levels.