Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10738607
rs10738607
0.810 GeneticVariation BEFREE Four SNPs, rs4977574_A [0.56(0.50-0.63); p < 0.0001], rs10757274_A [0.87(0.77-0.97); p = 0.014], rs10738607_A [0.89(0.80-1.00); p = 0.043] and rs1333045_T [0.54(0.48-0.61); p < 0.0001] residing on the CDKN2B gene were significantly associated with CAD following multivariate adjustments for MI, HTN and DM, while four others were weakly associated with the disease. 29894795

2018

dbSNP: rs10738607
rs10738607
G 0.810 GeneticVariation GWASCAT A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs. 26708285

2016

dbSNP: rs10738607
rs10738607
0.810 GeneticVariation GWASDB A common variant on chromosome 9p21 affects the risk of myocardial infarction. 17478679

2007