rs1805087, MTR

N. diseases: 135
Disease: 5,10-Methylenetetrahydrofolate reductase deficiency ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
5,10-Methylenetetrahydrofolate reductase deficiency
CUI: C0268615
Disease: 5,10-Methylenetetrahydrofolate reductase deficiency
0.010 GeneticVariation BEFREE The purpose of the study was to determine the frequency of occurrence of polymorphisms of genes MTHFR (C677T), MTR (A2756G), and MTHFD1 (G1958A), as well as to analyze the concentration of homocysteine (Hcy), methionine (Met), asymmetric dimethylarginine (ADMA), and arginine (Arg) in epileptics treatment with antiepileptic drugs (AEDs), and controls. 21543238 2011