Variant: rs3217992 

    present in Gene: CDKN2B-AS1;CDKN2B
    present in Chromosome: 9
    Position on Chromosome: 22003224
    Alleles of this Variant: C/T

rs3217992 in CDKN2B-AS1;CDKN2B gene and CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 PMID 23202125 2013 Large-scale association analysis identifies new risk loci for coronary artery disease.

rs3217992 in CDKN2B-AS1;CDKN2B 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.

rs3217992 in CDKN2B-AS1;CDKN2B gene and Coronary Artery Disease PMID 24262325 2014 Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.

rs3217992 in CDKN2B-AS1;CDKN2B gene and Glaucoma PMID 22792221 2012 Common variants on chromosome 9p21 are associated with normal tension glaucoma.

rs3217992 in CDKN2B-AS1;CDKN2B 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.

rs3217992 in CDKN2B-AS1;CDKN2B gene and Glioma PMID 21531791 2011 Chromosome 7p11.2 (EGFR) variation influences glioma risk.