Variant: rs1412829 

    present in Gene: CDKN2B-AS1
    present in Chromosome: 9
    Position on Chromosome: 22043927
    Alleles of this Variant: A/G

rs1412829 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.

rs1412829 in CDKN2B-AS1 gene and Central Nervous System Neoplasms PMID 19578366 2009 Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.

rs1412829 in CDKN2B-AS1 gene and Glaucoma PMID 21532571 2011 Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1.

rs1412829 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.

rs1412829 in CDKN2B-AS1 gene and Glioma PMID 19578367 2009 Genome-wide association study identifies five susceptibility loci for glioma.

PMID 19578366 2009 Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.

PMID 21531791 2011 Chromosome 7p11.2 (EGFR) variation influences glioma risk.

rs1412829 in 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.

PMID 20512145 2010 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci.

rs1412829 in CDKN2B-AS1 gene and Nasopharyngeal carcinoma PMID 20512145 2010 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci.