Variant: rs10116277 

    present in Gene: CDKN2B-AS1
    present in Chromosome: 9
    Position on Chromosome: 22081398
    Alleles of this Variant: G/T

rs10116277 in CDKN2B-AS1 gene and Ankle brachial pressure index (observable entity) PMID 22199011 2012 Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies.

rs10116277 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.

rs10116277 in CDKN2B-AS1 gene and Glaucoma, Open-Angle PMID 22570617 2012 Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.

rs10116277 in CDKN2B-AS1 gene and Glioma PMID 21531791 2011 Chromosome 7p11.2 (EGFR) variation influences glioma risk.

rs10116277 in CDKN2B-AS1 gene and Myocardial Infarction PMID 17478679 2007 A common variant on chromosome 9p21 affects the risk of myocardial infarction.