Variant: rs9632884 

    present in Gene: CDKN2B-AS1
    present in Chromosome: 9
    Position on Chromosome: 22072302
    Alleles of this Variant: G/A;C

rs9632884 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.

rs9632884 in CDKN2B-AS1 gene and Calcification of coronary artery 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.

rs9632884 in CDKN2B-AS1 gene and Carotid Atherosclerosis PMID 30510157 2018 GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes.

rs9632884 in CDKN2B-AS1 gene and Coronary Artery Disease PMID 17634449 2007 Genomewide association analysis of coronary artery disease.

rs9632884 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.