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SNP information rs371271054

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:

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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