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SNP information rs2287780

RS2287780

Normal allele: CC

Polymorphism in folic acid pathway genes causing B12 deficiency and increased homocysteine.

Polymorphism rs2287780 is related to topics like this:

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...

DNA methylation genes

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


Mthfr and magnesium DNA

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

Zinc finger protein

Zinc finger proteins constitute the most extensive transcription factor family within the human...

Wilson disease gene

Wilson's disease is an autosomal recessive condition, necessitating that both parents carry at...

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