Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2910164
rs2910164
0.100 GeneticVariation BEFREE In the subgroups, rs2910164 and rs3746444 were only associated with CVDs, especially CAD. 30642078

2019

dbSNP: rs2910164
rs2910164
0.100 GeneticVariation BEFREE In addition, the presence of a minor allele of the rs2910164 polymorphism was significantly associated with risk of depression in patients with CAD. 29749487

2018

dbSNP: rs2910164
rs2910164
0.100 GeneticVariation BEFREE In the subgroup analysis by race, miR-146a rs2910164 polymorphism was significantly associated with an increased C</span>AD risk in Asians (OR = 1.18; 95% CI 1.04 - 1.33; P = 0.008). 28886326

2017

dbSNP: rs2910164
rs2910164
0.100 GeneticVariation BEFREE Meanwhile, we demonstrated that the G allele of rs2910164 decreased the susce</span>ptibility of CAD. 28489066

2017

dbSNP: rs2910164
rs2910164
0.100 GeneticVariation BEFREE In subgroup analyses, miR‑146a rs2910164 C>G increased the risk of developing CAD in non‑smoking, hypertensive and nondiabetic subgroups. 27430349

2016

dbSNP: rs2910164
rs2910164
0.100 GeneticVariation BEFREE Our data provide the first evidence for the association of miR-146a rs2910164 and TCF21 rs12190287 with CAD in an Iranian population, encouraging further research to elucidate the disease-related effects of miR-146a rs2910164. 26909569

2016

dbSNP: rs2910164
rs2910164
0.100 GeneticVariation BEFREE In conclusion, the current meta-analysis suggests lower risks of CAD for GG, GG + GC genotype and G allele of rs2910164, while rs2910164 is not associated with the risk of IS. 26114385

2015

dbSNP: rs2910164
rs2910164
0.100 GeneticVariation BEFREE The current meta-analysis results showed that rs2910164 CC genotype has a decreased risk with overall cardiovascular diseases and the specific coronary artery disease. 25865299

2015

dbSNP: rs2910164
rs2910164
0.100 GeneticVariation BEFREE This study investigated the influence of the miR-146a GC rs2910164 on miR-146a expression in young South African Indians with CAD. 23794009

2014

dbSNP: rs2910164
rs2910164
0.100 GeneticVariation BEFREE Our data provide the first evidence that the miR-146a rs2910164 polymorphism is associated with increased risk of CAD in Chinese Han population, which may be through influencing the expression levels of the miRNA. 24447667

2014