Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs699947
rs699947
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.050 GeneticVariation BEFREE Our overall and subgroup analyses suggested that rs699947 polymorphism was significantly associated with CHD susceptibility in both Caucasians and Asians, rs1570360 polymorphism was significantly associated with CHD susceptibility in Caucasians, and rs3025039 polymorphism was significantly associated with CHD susceptibility in Asians. 30317903

2018

dbSNP: rs699947
rs699947
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.050 GeneticVariation BEFREE In conclusion, our findings suggest that VEGFA rs699947 C>A, rs3025039 C>T and rs2010963 G>C polymorphisms are risk factors for CHD. 28430629

2017

dbSNP: rs699947
rs699947
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.050 GeneticVariation BEFREE Genetic polymorphisms on VEGF (rs699947) and KDR (rs2305948and rs1870377), as well as relevant haplotypes, may serve as genetic markers that might be useful in future investigations on the pathogenesis of CHD. 26726843

2016

dbSNP: rs699947
rs699947
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.050 GeneticVariation BEFREE All of the combined effects of rs699947 (CC/CA) and rs2305948 (TT), rs3025039 (TT) and rs2305948 (TT), rs3025039 (CT) and rs1870377 (AA) had positive effects on the risk of CHD, respectively (all P < 0.05). 27175642

2016

dbSNP: rs699947
rs699947
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.050 GeneticVariation BEFREE We were unable to find strong association between analyzed polymorphisms in growth factors and the severity of coronary artery disease, although there was a trend toward association between rs699947 and the severity of CAD in patients without previous MI. 27835972

2016