Variant: rs10757278 

    present in Gene: CDKN2B-AS1
    present in Chromosome: 9
    Position on Chromosome: 22124478
    Alleles of this Variant: A/G

rs10757278 in CDKN2B-AS1 gene and Calcification of coronary artery PMID 23727086 2013 Candidate gene association study of coronary artery calcification in chronic kidney disease: findings from the CRIC study (Chronic Renal Insufficiency Cohort).

PMID 23394302 2013 Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study.

PMID 22144573 2011 Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.

rs10757278 in CDKN2B-AS1 gene and Coronary heart disease PMID 22751097 2012 Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.

PMID 23364394 2013 A genome-wide association study of a coronary artery disease risk variant.

PMID 21347282 2011 Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.

rs10757278 in CDKN2B-AS1 gene and Major Depressive Disorder PMID 23377640 2013 Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.

rs10757278 in CDKN2B-AS1 gene and Myocardial Infarction PMID 17478679 2007 A common variant on chromosome 9p21 affects the risk of myocardial infarction.