Six homozygous mutations
- Thread starter Jonseeder
- Start date
caledonia
Senior Member
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See the SNPs Interpretation Guide in my signature link.
Note that SNPs are only potentials and may or may not be expressed. It's best to pair genetic testing with functional testing to see what's actually going on in your body.
Note that SNPs are only potentials and may or may not be expressed. It's best to pair genetic testing with functional testing to see what's actually going on in your body.
Some of those SNPs have little or no effect.
The ones that do something are
COMT v158M which slows the enzyme. Supplementation with its cofactor magnesium may be helpful in stimulating the enzyme.
The notion that people with COMT don't tolerate methyl groups is a myth. Some people are sensitive but it has nothing to do with COMT. You may or may not be sensitive - you would have to put it to the test.
MTHFR C677T. This would slow the enzyme. Supplementation with its co-factor vit B2 and with its product methylfolate could be helpful.
MTRR A66G. This would slow the enzyme. Supplementation with methylB12 may be helpful.
Start low and increase slowly with the folate and B12.
The ones that do something are
COMT v158M which slows the enzyme. Supplementation with its cofactor magnesium may be helpful in stimulating the enzyme.
The notion that people with COMT don't tolerate methyl groups is a myth. Some people are sensitive but it has nothing to do with COMT. You may or may not be sensitive - you would have to put it to the test.
MTHFR C677T. This would slow the enzyme. Supplementation with its co-factor vit B2 and with its product methylfolate could be helpful.
MTRR A66G. This would slow the enzyme. Supplementation with methylB12 may be helpful.
Start low and increase slowly with the folate and B12.