Variant: rs564398 

    present in Gene: CDKN2B-AS1
    present in Chromosome: 9
    Position on Chromosome: 22029548
    Alleles of this Variant: T/C

rs564398 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.

rs564398 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.

rs564398 in CDKN2B-AS1 gene and Coronary Artery Disease PMID 17634449 2007 Genomewide association analysis of coronary artery disease.

rs564398 in CDKN2B-AS1 gene and Coronary heart disease PMID 29615537 2018 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes.

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

rs564398 in CDKN2B-AS1 gene and Diabetes Mellitus, Non-Insulin-Dependent PMID 17463249 2007 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.

rs564398 in CDKN2B-AS1 gene and Glaucoma PMID 22792221 2012 Common variants on chromosome 9p21 are associated with normal tension glaucoma.

rs564398 in CDKN2B-AS1 gene and Glaucoma, Open-Angle PMID 22428042 2012 Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese.

PMID 22570617 2012 Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.