rs3025039, VEGFA

N. diseases: 62
Disease: Tetralogy of Fallot ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Tetralogy of Fallot
CUI: C0039685
Disease: Tetralogy of Fallot
0.020 GeneticVariation BEFREE Further subgroup analyses according to ethnicity of study participants and type of disease demonstrated that the rs833061 polymorphism was significantly correlated with the risk of CHD in Asians under additive genetic model, and the rs3025039 polymorphism was significantly correlated with the risk of Tetralogy of Fallot (TOF) in dominant, recessive and allele models. 30689460 2018
Tetralogy of Fallot
CUI: C0039685
Disease: Tetralogy of Fallot
0.020 GeneticVariation BEFREE In the single SNP analyses, the mutant homozygous genotypes of -2578C/A (rs699947) and +963C/T (rs3025039) were related with an increased risk of TOF. 25894981 2015