SNP information rs228587
Normal allele: CC
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 rs228587 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:
29426041 Genetic Polymorphisms in Cytokine Genes in Colombian Patients with Ocular Toxoplasmosis.
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...