| GWAS snp
|
| PMID
|
[PMID 21531791 ]
|
| Trait
|
|
| Title
|
Chromosome 7p11.2 (EGFR) variation influences glioma risk.
|
| Risk Allele
|
|
| P-val
|
5E-16
|
| Odds Ratio
|
1.2600 [NR]
|
| GWAS snp
|
| PMID
|
[PMID 22570617]
|
| Trait
|
|
| Title
|
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.
|
| Risk Allele
|
|
| P-val
|
2E-18
|
| Odds Ratio
|
1.4500 None
|
[PMID 19578366] Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.
[PMID 23111177] CDKN2B-AS1 Genotype-Glaucoma Feature Correlations in Primary Open-Angle Glaucoma Patients From the United States
[PMID 25239644] Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers
[PMID 25861811] A common variant near TGFBR3 is associated with primary open angle glaucoma
[PMID 25711633] Genetic Variants Associated With Different Risks for High Tension Glaucoma and Normal Tension Glaucoma in a Chinese Population
[PMID 26014354] CCDC26, CDKN2BAS, RTEL1 and TERT Polymorphisms in pediatric brain tumor susceptibility
[PMID 29261660] Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7.
[PMID 32933932] Genetic analysis of primary open-angle glaucoma-related risk alleles in a Korean population: the GLAU-GENDISK study.
]
