rs1412829, CDKN2B-AS1

N. diseases: 14
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Glioma
CUI: C0017638
Disease: Glioma
0.810 GeneticVariation BEFREE In conclusion, we found an association between rs1412829 and rs4977756 (9p21.3, CDKN2B-AS1) and global DNA methylation pattern in glioma, for which a trend was seen also in the TCGA glioblastoma dataset. 27780202 2016
Glioma
CUI: C0017638
Disease: Glioma
0.810 GeneticVariation GWASDB Chromosome 7p11.2 (EGFR) variation influences glioma risk. 21531791 2011
Glioma
CUI: C0017638
Disease: Glioma
0.810 GeneticVariation GWASDB Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. 19578366 2009
Glioma
CUI: C0017638
Disease: Glioma
0.810 GeneticVariation GWASCAT Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. 19578366 2009
Glioma
CUI: C0017638
Disease: Glioma
0.810 GeneticVariation GWASDB Genome-wide association study identifies five susceptibility loci for glioma. 19578367 2009