Variant: rs10120688 

    present in Gene: CDKN2B-AS1
    present in Chromosome: 9
    Position on Chromosome: 22056500
    Alleles of this Variant: G/A

rs10120688 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.

rs10120688 in CDKN2B-AS1 gene and Glaucoma PMID 22792221 2012 Common variants on chromosome 9p21 are associated with normal tension glaucoma.

rs10120688 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.

rs10120688 in CDKN2B-AS1 gene and Glioma PMID 21531791 2011 Chromosome 7p11.2 (EGFR) variation influences glioma risk.