Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3025039
rs3025039
VEGFA
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.040 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
dbSNP: rs3025039
rs3025039
VEGFA
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.040 GeneticVariation BEFREE Overall, our findings indicate that VEGF rs699947, rs1570360, and rs3025039 polymorphisms may affect CHD susceptibility. 30317903

2018
dbSNP: rs3025039
rs3025039
VEGFA
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.040 GeneticVariation BEFREE A significant association between VEGFA rs3025039 C>T polymorphism and risk of CHD was also found. 28430629

2017
dbSNP: rs3025039
rs3025039
VEGFA
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.040 GeneticVariation BEFREE Genotype CT of rs3025039, TT of rs2305948, and AA of rs1873077 were associated with a reduced risk of CHD when smoking, alcohol intake and diabetes were considered, while homozygote GG of rs1570360 might elevate the susceptibility to CHD (all P < 0.05) for patients who were addicted to smoking or those with hypertension. 27175642

2016