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Normal allele: CC
Transcobalamin deficiency.
Polymorphism rs34324219 is related to topics like this:
Mthfr and B12 Many individuals carry MTHFR mutations without being aware of their MTHFR status, while only a...
Many individuals carry MTHFR mutations without being aware of their MTHFR status, while only a...
Research and publications:
28334792 GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians.
Magnesium stands out as one of the most vital nutrients for overall health, facilitating over 300...
Zinc finger proteins constitute the most extensive transcription factor family within the human...
Wilson's disease is an autosomal recessive condition, necessitating that both parents carry at...