Predicted Trait | |
Reported Trait | Myocardial infarction |
Mapped Trait(s) | myocardial infarction (EFO_0000612) |
Additional Trait Information | Unadjusted weights |
Score Construction | |
PGS Name | HC326 |
Development Method | |
Name | snpnet (multi-PRS) |
Parameters | Weighted combination of multiple biomarker PRS. 1,080,968 variants as input (directly genotyped variants, imputed HLA allelotypes, and CNVs) |
Variants | |
Original Genome Build | hg19 |
Number of Variants | 183,566 |
Effect Weight Type | weights.HC326 |
PGS Source | |
PGS Catalog Publication (PGP) ID | PGP000128 |
Citation (link to publication) | Sinnott-Armstrong N et al. Nat Genet (2021) |
Ancestry Distribution | |
Score Development/Training | European: 100% 223,327 individuals (100%) |
PGS Evaluation | European: 100% 2 Sample Sets |
Study Identifiers | Sample Numbers | Sample Ancestry | Cohort(s) | Phenotype Definitions & Methods | Age of Study Participants | Participant Follow-up Time | Additional Ancestry Description | Additional Sample/Cohort Information |
---|---|---|---|---|---|---|---|---|
Europe PMC: 10.1038/s41588-020-00757-z |
223,327 individuals | European (British) |
UKB | — | — | — | — | Training |
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 |
---|---|---|---|---|---|---|---|---|
PPM001602 | PSS000826| European Ancestry| 87,413 individuals |
PGP000128 | Sinnott-Armstrong N et al. Nat Genet (2021) |
Reported Trait: Myocardial infarction | — | AUROC: 0.59348 | — | Age, sex, PCs(1-10) | — |
PPM001606 | PSS000827| European Ancestry| 135,300 individuals |
PGP000128 | Sinnott-Armstrong N et al. Nat Genet (2021) |
Reported Trait: Myocardial infarction | HR: 1.19 [1.17, 1.22] | C-index: 0.707 | — | Age as time scale, sex, batch, PCs(1-10) | — |
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 |
---|---|---|---|---|---|---|---|---|
PSS000826 | — | — | 87,413 individuals | — | European | — | UKB | — |
PSS000827 | ICD-10 I21|I22 | — | [
|
— | European (Finnish) |
— | FinnGen | — |