Variant: rs1063192 

    present in Gene: CDKN2B;CDKN2B-AS1
    present in Chromosome: 9
    Position on Chromosome: 22003368
    Alleles of this Variant: G/A;T

rs1063192 in CDKN2B;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.

rs1063192 in CDKN2B;CDKN2B-AS1 gene and Diabetes Mellitus, Non-Insulin-Dependent PMID 30054458 2018 Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes.

rs1063192 in CDKN2B;CDKN2B-AS1 gene and Glaucoma PMID 21532571 2011 Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1.

rs1063192 in CDKN2B;CDKN2B-AS1 gene and Glaucoma, Open-Angle PMID 22419738 2012 A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma.

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

rs1063192 in CDKN2B;CDKN2B-AS1 gene and Glioma PMID 21531791 2011 Chromosome 7p11.2 (EGFR) variation influences glioma risk.

PMID 19578367 2009 Genome-wide association study identifies five susceptibility loci for glioma.

rs1063192 in CDKN2B;CDKN2B-AS1 gene and Nasopharyngeal Neoplasms PMID 26545403 2016 A GWAS Meta-analysis and Replication Study Identifies a Novel Locus within CLPTM1L/TERT Associated with Nasopharyngeal Carcinoma in Individuals of Chinese Ancestry.