SNP information rs4654748
Normal allele: CC
Breakage causes a deficiency of the active form of vitamin B6, pyridoxal-5'-phosphate (p-5-p). Supplemental intake of p-5-p is recommended.
Polymorphism rs4654748 is related to topics like this:
Vitamin B6, belonging to the group of water-soluble B vitamins, manifests in three primary forms:... The Genetic Methylation Check examines your DNA to offer insights into your unique methylation...
Research and publications:
19744961 Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway.
21115529 Genetics and genomics of human ageing.
31666285 Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood.
33170161 Genetic test for the prescription of diets in support of physical activity.
MTHFR is an enzyme crucial for converting folic acid into an active form known as L-methylfolate,...
Many individuals carry MTHFR mutations without being aware of their MTHFR status, while only a...
Magnesium stands out as one of the most vital nutrients for overall health, facilitating over 300...