Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs371271054
rs371271054
0.800 GeneticVariation UNIPROT Thiamine pyrophosphokinase deficiency in encephalopathic children with defects in the pyruvate oxidation pathway. 22152682

2011

dbSNP: rs387906935
rs387906935
0.800 GeneticVariation UNIPROT Thiamine pyrophosphokinase deficiency in encephalopathic children with defects in the pyruvate oxidation pathway. 22152682

2011

dbSNP: rs387906936
rs387906936
0.700 GeneticVariation UNIPROT Thiamine pyrophosphokinase deficiency in encephalopathic children with defects in the pyruvate oxidation pathway. 22152682

2011