Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11614913
rs11614913
HOXC6 ; MIR196A2
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.050 GeneticVariation BEFREE Our data suggests that the T allele of the miRNA-196a2 C/T (rs11614913) polymorphism is associated with the risk of developing CAD, but no association with restenosis was observed. 30560371

2019
dbSNP: rs11614913
rs11614913
HOXC6 ; MIR196A2
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.050 GeneticVariation BEFREE Our study suggests that miR-196a2 rs11614913 T > C may contribute to CAD susceptibility but further well-designed studies with larger sample size and comprehensive data are needed to confirm our findings and provide a profound conclusion. 30072171

2018
dbSNP: rs11614913
rs11614913
HOXC6 ; MIR196A2
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.050 GeneticVariation BEFREE Furthermore, miR‑149 rs2292832 C>T and miR‑196a2 rs11614913 T>C was shown to increase CAD risk in females and patients aged >63 years old. 27430349

2016
dbSNP: rs11614913
rs11614913
HOXC6 ; MIR196A2
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.050 GeneticVariation BEFREE We observed no association of the other two SNPs in miR-196a2 (rs11614913) and miR-499 (rs3746444) with the CAD incidence. 24447667

2014
dbSNP: rs11614913
rs11614913
HOXC6 ; MIR196A2
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.050 GeneticVariation BEFREE Cox regression analysis showed that age, smoking status, numbers of pathological changes in coronary arteries, rs11614913 T → C, and diabetes mellitus were associated with serious prognosis of CAD. 22159951

2012