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SNP information rs10933203

RS10933203

Normal allele: CC

The breakage results in impairment of the protein's ability to transport thiamine into cells, resulting in decreased absorption of vitamin B1 from food. Thiamine-reactive encephalopathy characterised by seizures responding to high doses of thiamine may develop.

Polymorphism rs10933203 is related to topics like this:

CCNB1 cyclin B1

Cyclin B1 serves as a regulatory protein pivotal in the process of mitosis. It forms complexes with...

DNA methylation genes

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

Vitamin k

The biologically active form of vitamin K acts as a co-factor in a reaction crucial for both blood...

Vitamin b2 mthfr

Vitamin B2, also known as riboflavin, is a vital nutrient necessary for human health and is part of...

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