TCF7L2, transcription factor 7 like 2, 6934

N. diseases: 257; N. variants: 70
Disease: Neural Tube Defects ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3814573
rs3814573
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C0027794
Disease:
Neural Tube Defects 		0.010 GeneticVariation BEFREE Furthermore, the maternal genotype for TCF7L2 rs3814573 suggested an increased NTD risk among obese women. 23132673 2012