rs201765376, MTR

N. diseases: 12
Disease: Hyperhomocysteinemia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
0.010 GeneticVariation BEFREE To conclude, PD cases exhibited hyperhomocysteinemia and MTRR 66 A>G and cSHMT 1420 C>T gene variants were shown to modulate PD risk by altering the homocysteine levels. 24686188 2014