COMT V158M rs4680 AG +/-
COMT H62H rs4633 CT +/-
COMT P199P rs769224 GG -/-
VDR Bsm rs1544410 CC -/-
VDR Taq rs731236 AA +/+
MAO-A R297R rs6323 TT +/+
ACAT1-02 rs3741049 GG -/-
MTHFR C677T rs1801133 GG -/-
MTHFR 03 P39P rs2066470 GG -/-
MTHFR A1298C rs1801131 GG +/+
MTR A2756G rs1805087 AG +/-
MTRR A66G rs1801394 AG +/-
MTRR H595Y rs10380 __ no call
MTRR K350A rs162036 AG +/-
MTRR R415T rs2287780 __ no call
MTRR A664A rs1802059 GG -/-
BHMT-02 rs567754 CT +/-
BHMT-04 rs617219 __ no call
BHMT-08 rs651852 CT +/-
AHCY-01 rs819147 TT -/-
AHCY-02 rs819134 __ no call
AHCY-19 rs819171 TT -/-
CBS C699T rs234706 GG -/-
CBS A360A rs1801181 AG +/-
CBS N212N rs2298758 __ no call
Here are the homozygous MTHFR mutations labeled as risk in @Valentijn 's thread http://forums.phoenixrising.me/index.php?threads/interesting-mthfr-variations.24543/
rs1476413....G35A....TT +/+
rs4846049....A372C...TT +/+
I've done a bit of reading, but really haven't learned anything practical. Any input apreciated.
COMT H62H rs4633 CT +/-
COMT P199P rs769224 GG -/-
VDR Bsm rs1544410 CC -/-
VDR Taq rs731236 AA +/+
MAO-A R297R rs6323 TT +/+
ACAT1-02 rs3741049 GG -/-
MTHFR C677T rs1801133 GG -/-
MTHFR 03 P39P rs2066470 GG -/-
MTHFR A1298C rs1801131 GG +/+
MTR A2756G rs1805087 AG +/-
MTRR A66G rs1801394 AG +/-
MTRR H595Y rs10380 __ no call
MTRR K350A rs162036 AG +/-
MTRR R415T rs2287780 __ no call
MTRR A664A rs1802059 GG -/-
BHMT-02 rs567754 CT +/-
BHMT-04 rs617219 __ no call
BHMT-08 rs651852 CT +/-
AHCY-01 rs819147 TT -/-
AHCY-02 rs819134 __ no call
AHCY-19 rs819171 TT -/-
CBS C699T rs234706 GG -/-
CBS A360A rs1801181 AG +/-
CBS N212N rs2298758 __ no call
Here are the homozygous MTHFR mutations labeled as risk in @Valentijn 's thread http://forums.phoenixrising.me/index.php?threads/interesting-mthfr-variations.24543/
rs1476413....G35A....TT +/+
rs4846049....A372C...TT +/+
I've done a bit of reading, but really haven't learned anything practical. Any input apreciated.