Variant: rs10738607 

    present in Gene: CDKN2B-AS1
    present in Chromosome: 9
    Position on Chromosome: 22088095
    Alleles of this Variant: A/G

rs10738607 in CDKN2B-AS1 gene and Calcification of coronary artery PMID 22144573 2011 Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.

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

rs10738607 in CDKN2B-AS1 gene and Coronary Artery Disease PMID 26708285 2016 Among the four variants reaching GWAS significance in the present study, the rs10738607_G [0.78(0.71-0.85); p = 2.17E-08] in CDNK2A/B gene was associated with CAD.

rs10738607 in CDKN2B-AS1 gene and Myocardial Infarction PMID 17478679 2007 A common variant on chromosome 9p21 affects the risk of myocardial infarction.

PMID 26708285 2016 A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs.

rs10738607 in CDKN2B-AS1 gene and Serum total cholesterol measurement PMID 30275531 2018 Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program.