[PMID 19654303
] Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study
| GWAS snp
|
| PMID
|
[PMID 21946350]
|
| Trait
|
|
| Title
|
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.
|
| Risk Allele
|
T
|
| P-val
|
5E-7
|
| Odds Ratio
|
0.0250 [0.015-0.035] unit decrease
|
[PMID 18759969] In search of causal variants: refining disease association signals using cross-population contrasts.
[PMID 19247474] Genome-wide and candidate gene association study of cigarette smoking behaviors.
[PMID 19836008] A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.
[PMID 19955392] Role of 5p15.33 (TERT-CLPTM1L), 6p21.33 and 15q25.1 (CHRNA5-CHRNA3) variation and lung cancer risk in never-smokers.
[PMID 20808433] Associations of variants in CHRNA5/A3/B4 gene cluster with smoking behaviors in a Korean population.
[PMID 21436384] Genetic variability of smoking persistence in African Americans.
[PMID 22430809] Association between a Genome-Wide Association Study-Identified Locus and the Risk of Lung Cancer in Japanese Population.
| GWAS snp
|
| PMID
|
[PMID 23022100]
|
| Trait
|
Serum albumin level
|
| Title
|
Discovery and fine mapping of serum protein loci through transethnic meta-analysis.
|
| Risk Allele
|
C
|
| P-val
|
6E-7
|
| Odds Ratio
|
.01 [0.0048-0.0106] unit increase
|
[PMID 29631575] The genetics of smoking in individuals with chronic obstructive pulmonary disease.
] Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study
