TCN2, transcobalamin 2, 6948

N. diseases: 104; N. variants: 30
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0598608
Disease: Hyperhomocysteinemia
Hyperhomocysteinemia
0.020 GeneticVariation disease BEFREE Our results, if confirmed in other populations, highlight the necessity for investigation of the transcobalamin II C776G polymorphism in the research for hyperhomocysteinemia risk factors. 16820193 2007
CUI: C0598608
Disease: Hyperhomocysteinemia
Hyperhomocysteinemia
0.020 GeneticVariation disease LHGDN Our results, if confirmed in other populations, highlight the necessity for investigation of the transcobalamin II C776G polymorphism in the research for hyperhomocysteinemia risk factors. 16820193 2007
CUI: C0598608
Disease: Hyperhomocysteinemia
Hyperhomocysteinemia
0.020 GeneticVariation disease BEFREE Because Hcy metabolism is impaired in renal failure, MTHFR 677 C>T, GCP2 1561C>T, RFC1 80G>A, and TCN2 776G>C may further aggravate hyperhomocysteinemia in these patients. 12694331 2003