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SNP information rs4654748

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:

B6 for mthfr

Vitamin B6, belonging to the group of water-soluble B vitamins, manifests in three primary forms:...

DNA methylation genes

The Genetic Methylation Check examines your DNA to offer insights into your unique methylation...


Folate and mthfr

MTHFR is an enzyme crucial for converting folic acid into an active form known as L-methylfolate,...

Mthfr and B12

Many individuals carry MTHFR mutations without being aware of their MTHFR status, while only a...

Mthfr and magnesium DNA

Magnesium stands out as one of the most vital nutrients for overall health, facilitating over 300...

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