TCN2, transcobalamin 2, 6948

N. diseases: 104; N. variants: 30
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1801198
rs1801198
Entrez Id: 6948
Gene Symbol: TCN2
TCN2
CUI: C0027794
Disease:
Neural Tube Defects
0.010 GeneticVariation BEFREE Maternal 776C>G polymorphism in TCN2 was strongly predictive of NTD in the offspring (p = 0.006). 21770021 2011