SNP information rs371271054
Normal allele: TT
Associated with the occurrence of childhood encephalopathy due to thiaminpyrophosphokinase deficiency. It is a rare treatable neurological disorder caused by mutations in the TPK1 gene.
Polymorphism rs371271054 is related to topics like this:
Cyclin B1 serves as a regulatory protein pivotal in the process of mitosis. It forms complexes with...
Research and publications:
The Genetic Methylation Check examines your DNA to offer insights into your unique methylation...
The biologically active form of vitamin K acts as a co-factor in a reaction crucial for both blood...
Vitamin B2, also known as riboflavin, is a vital nutrient necessary for human health and is part of...