rs1333049, CDKN2B-AS1

N. diseases: 60
Disease: Acute myocardial infarction ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
0.030 GeneticVariation BEFREE Homozygous carriers of the rs1333049 C allele on chromosome 9p21 showed a reduced risk of 1 year ReMI in the contemporary percutaneous coronary intervention era, although the C allele had conferred susceptibility to their first AMI. 25232560 2014
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
0.030 GeneticVariation BEFREE For Pakistanis, the odds ratio for MI was 1.13 (95% CI, 1.05 to 1.22; P=2 x 10(-3)) for each copy of the C allele at rs1333049. 20395598 2010
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
0.030 GeneticVariation BEFREE This study examined the association of rs1333049 with myocardial infarction (MI), angiographic severity of CAD and clinical outcome after a first acute MI in Han Chinese. 19548844 2009