Any help is greatly appreciated. Trying to keep all this straight is no easy task!
Me:
Here are your homozygous mutations as indicated in your SNP gene table above (not including MTHFR):
DETOX
Homozygous
CYP1A2 164A>C rs762551 CC +/+
CYP2D6 S486T rs1135840 GG +/+
Heterozygous
CYP1B1 L432V rs1056836 CG +/-
CYP1B1 N453S rs1800440 CT +/-
CYP1B1 R48G rs10012 CG +/-
CYP2D6 2850C>T rs16947 AG +/-
GSTP1 I105V rs1695 AG +/-
SOD2 A16V rs4880 AG +/-
NAT2 I114T rs1801280 CT +/-
NAT2 K268R rs1208 GG +/+
Me:
Here are your homozygous mutations as indicated in your SNP gene table above (not including MTHFR):
- COMT V158M
- COMT H62H
- MAO-A R297R
- BHMT-08
- VDR Bsm
- VDR Taq
- MTRR A66G
- BHMT-02
- AHCY-01
- AHCY-19
- CBS A360A
DETOX
Homozygous
CYP1A2 164A>C rs762551 CC +/+
CYP2D6 S486T rs1135840 GG +/+
Heterozygous
CYP1B1 L432V rs1056836 CG +/-
CYP1B1 N453S rs1800440 CT +/-
CYP1B1 R48G rs10012 CG +/-
CYP2D6 2850C>T rs16947 AG +/-
GSTP1 I105V rs1695 AG +/-
SOD2 A16V rs4880 AG +/-
NAT2 I114T rs1801280 CT +/-
NAT2 K268R rs1208 GG +/+