Variant: rs10811652

present in Gene: CDKN2B-AS1 present in Chromosome: 9 Position on Chromosome: 22077086 Alleles of this Variant: A/C;T

rs10811652 in CDKN2B-AS1 gene and Coronary Artery Disease PMID 30003307 2018 We found genome-wide significant evidence for association with CAD at the previously well-established LPA locus (lead variant: rs74617384; OR 1.38 [95% CI 1.26, 1.51], p = 3.2 × 10<sup>-12</sup>) and at 9p21 (lead variant: rs10811652; OR 1.19 [95% CI 1.13, 1.26], p = 6.0 × 10<sup>-11</sup>).

rs10811652 in CDKN2B-AS1 gene and Diabetes PMID 30003307 2018 Genome-wide association study of coronary artery disease among individuals with diabetes: the UK Biobank.

rs10811652 in CDKN2B-AS1 gene and Diabetes Mellitus PMID 30003307 2018 Genome-wide association study of coronary artery disease among individuals with diabetes: the UK Biobank.

rs10811652 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.