Predicted Trait | |
Reported Trait | Lung cancer |
Mapped Trait(s) | lung carcinoma (EFO_0001071) |
Score Construction | |
PGS Name | PGS20_LC |
Development Method | |
Name | Genome-wide significant SNPs |
Parameters | p<1.9E-03 |
Variants | |
Original Genome Build | GRCh37 |
Number of Variants | 20 |
Effect Weight Type | log(OR) |
PGS Source | |
PGS Catalog Publication (PGP) ID | PGP000387 |
Citation (link to publication) | Qin N et al. Lancet Oncol (2022) |
Ancestry Distribution | |
Source of Variant Associations (GWAS) | European: 100% 85,716 individuals (100%) |
PGS Evaluation | European: 100% 1 Sample Sets |
Study Identifiers | Sample Numbers | Sample Ancestry | Cohort(s) |
---|---|---|---|
GWAS Catalog: GCST004748 Europe PMC: 2860473 |
85,716 individuals | European | NR |
PGS Performance Metric ID (PPM) |
PGS Sample Set ID (PSS) |
Performance Source | Trait |
PGS Effect Sizes (per SD change) |
Classification Metrics | Other Metrics | Covariates Included in the Model |
PGS Performance: Other Relevant Information |
---|---|---|---|---|---|---|---|---|
PPM015574 | PSS009988| European Ancestry| 450,821 individuals |
PGP000387 | Qin N et al. Lancet Oncol (2022) |
Reported Trait: Lung cancer | — | — | Hazard ratio (HR, high vs low risk): 1.48 [1.31, 1.68] | — | — |
PPM015576 | PSS009988| European Ancestry| 450,821 individuals |
PGP000387 | Qin N et al. Lancet Oncol (2022) |
Reported Trait: Lung cancer x autosomal mosaic loss abnormalities interaction | HR: 1.95 [1.02, 3.7] | — | — | — | — |
PGS Sample Set ID (PSS) |
Phenotype Definitions and Methods | Participant Follow-up Time | Sample Numbers | Age of Study Participants | Sample Ancestry | Additional Ancestry Description | Cohort(s) | Additional Sample/Cohort Information |
---|---|---|---|---|---|---|---|---|
PSS009988 | — | — | [ ,
46.0 % Male samples |
— | European | — | UKB | — |