|
rs1063192
|
CDKN2B;CDKN2B-AS1
|
Glaucoma, Open-Angle
|
|
0.810 |
GeneticVariation |
GWASDB |
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.
|
22570617 |
2012 |
|
rs1063192
|
CDKN2B;CDKN2B-AS1
|
Glaucoma, Open-Angle
|
|
0.810 |
GeneticVariation |
BEFREE |
The CDKN2B variant rs1063192 also was found to be associated more strongly with advanced OAG.
|
22840486 |
2012 |
|
rs1063192
|
CDKN2B;CDKN2B-AS1
|
Glaucoma, Open-Angle
|
T |
0.810 |
GeneticVariation |
GWASDB |
A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma.
|
22419738 |
2012 |
|
rs1063192
|
CDKN2B;CDKN2B-AS1
|
Glaucoma, Open-Angle
|
T |
0.810 |
GeneticVariation |
GWASCAT |
A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma.
|
22419738 |
2012 |
|
rs1063192
|
CDKN2B;CDKN2B-AS1
|
Glioma
|
|
0.710 |
GeneticVariation |
BEFREE |
We hypothesized that CCDKN2A/B rs1063192 and rs4977756 and also the long noncoding RNA (lncRNA) CDKN2BAS rs2157719 glioma susceptibility polymorphisms identified by genome-wide association studies may contribute to medulloblastoma predisposition.
|
29314442 |
2018 |
|
rs1063192
|
CDKN2B;CDKN2B-AS1
|
Glaucoma
|
|
0.710 |
GeneticVariation |
BEFREE |
Stratification analysis by type of glaucoma revealed that rs1063192</span> polymorphism conferred a protective factor of primary open-angle glaucoma (POAG) and non-POAG.
|
28416752 |
2017 |
|
rs1063192
|
CDKN2B;CDKN2B-AS1
|
Glioma
|
|
0.710 |
GeneticVariation |
GWASDB |
Chromosome 7p11.2 (EGFR) variation influences glioma risk.
|
21531791 |
2011 |
|
rs1063192
|
CDKN2B;CDKN2B-AS1
|
Glaucoma
|
|
0.710 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1.
|
21532571 |
2011 |
|
rs1063192
|
CDKN2B;CDKN2B-AS1
|
Glioma
|
|
0.710 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies five susceptibility loci for glioma.
|
19578367 |
2009 |
|
rs1063192
|
CDKN2B;CDKN2B-AS1
|
Diabetes Mellitus, Non-Insulin-Dependent
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes.
|
30054458 |
2018 |
|
rs2069426
|
CDKN2B;CDKN2B-AS1
|
Precursor Cell Lymphoblastic Leukemia Lymphoma
|
A |
0.700 |
GeneticVariation |
GWASCAT |
GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21.
|
29348612 |
2018 |
|
rs3217978
|
CDKN2B;CDKN2B-AS1
|
Coronary Artery Disease
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.
|
29212778 |
2018 |
|
rs1063192
|
CDKN2B;CDKN2B-AS1
|
Nasopharyngeal Neoplasms
|
|
0.700 |
GeneticVariation |
GWASCAT |
A GWAS Meta-analysis and Replication Study Identifies a Novel Locus within CLPTM1L/TERT Associated with Nasopharyngeal Carcinoma in Individuals of Chinese Ancestry.
|
26545403 |
2016 |
|
rs3217992
|
CDKN2B;CDKN2B-AS1
|
Coronary Artery Disease
|
T |
0.700 |
GeneticVariation |
GWASDB |
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
|
24262325 |
2014 |
|
rs2069416
|
CDKN2B;CDKN2B-AS1
|
Calcification of coronary artery
|
|
0.700 |
GeneticVariation |
GWASDB |
Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study.
|
23394302 |
2013 |
|
rs3217992
|
CDKN2B;CDKN2B-AS1
|
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
|
|
0.700 |
GeneticVariation |
GWASDB |
Large-scale association analysis identifies new risk loci for coronary artery disease.
|
23202125 |
2013 |
|
rs3217992
|
CDKN2B;CDKN2B-AS1
|
Calcification of coronary artery
|
|
0.700 |
GeneticVariation |
GWASDB |
Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study.
|
23394302 |
2013 |
|
rs2069416
|
CDKN2B;CDKN2B-AS1
|
Glaucoma, Open-Angle
|
|
0.700 |
GeneticVariation |
GWASDB |
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.
|
22570617 |
2012 |
|
rs2069418
|
CDKN2B;CDKN2B-AS1
|
Glaucoma, Open-Angle
|
|
0.700 |
GeneticVariation |
GWASDB |
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.
|
22570617 |
2012 |
|
rs3217992
|
CDKN2B;CDKN2B-AS1
|
Glaucoma
|
|
0.700 |
GeneticVariation |
GWASDB |
Common variants on chromosome 9p21 are associated with normal tension glaucoma.
|
22792221 |
2012 |
|
rs3217992
|
CDKN2B;CDKN2B-AS1
|
Glaucoma, Open-Angle
|
|
0.700 |
GeneticVariation |
GWASDB |
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.
|
22570617 |
2012 |
|
rs1063192
|
CDKN2B;CDKN2B-AS1
|
Calcification of coronary artery
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.
|
22144573 |
2011 |
|
rs2069416
|
CDKN2B;CDKN2B-AS1
|
Calcification of coronary artery
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.
|
22144573 |
2011 |
|
rs2069418
|
CDKN2B;CDKN2B-AS1
|
Calcification of coronary artery
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.
|
22144573 |
2011 |
|
rs3217992
|
CDKN2B;CDKN2B-AS1
|
Glioma
|
|
0.700 |
GeneticVariation |
GWASDB |
Chromosome 7p11.2 (EGFR) variation influences glioma risk.
|
21531791 |
2011 |