Gene: TCN2 ×
Source: BEFREE ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1801198
rs1801198
TCN2
0.010 GeneticVariation BEFREE No significant association was observed between rs1801198 and primary risks of congenital abnormalities, cancer, or Alzheimer disease.<b>Conclusions:</b> Meta-analysis results indicate an influence of rs1801198 on holotranscobalamin and homocysteine concentrations in European-descent subjects. 28814397

2017