Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1805017
rs1805017
PLA2G7
0.040 GeneticVariation BEFREE Polymorphisms in rs1805017 and rs1805018, additional interaction between rs1805017 and smoking, and haplotype containing the rs1805017-H and rs1805018-T alleles were associated with increased CHD risk. 29728838

2018
dbSNP: rs1805017
rs1805017
PLA2G7
0.040 GeneticVariation BEFREE These findings indicated that R92H variant in PLA2G7 gene might contribute to CHD susceptibility in a southern Chinese population. 25690150

2015
dbSNP: rs1805017
rs1805017
PLA2G7
0.040 GeneticVariation BEFREE The R92H polymorphism was highly related to the plasma PAF-AH levels and the risk of CHD, especially among patients with BSS, even with the adjustment for the effects of traditional factors. 25034894

2014
dbSNP: rs1805017
rs1805017
PLA2G7
0.040 GeneticVariation BEFREE 14 association studies focusing on three polymorphisms (A379V, V279F and R92H) in PLA2G7 gene and risk of CHD were included in meta-analysis, covering a total of 8,280 cases and 5,656 controls. 20926117

2010