Predicted Trait | |
Reported Trait | Heart failure |
Mapped Trait(s) | heart failure (EFO_0003144) |
Score Construction | |
PGS Name | PRS39_HF |
Development Method | |
Name | Genome-wide significant SNPs |
Parameters | NR |
Variants | |
Original Genome Build | NR |
Number of Variants | 39 |
Effect Weight Type | beta |
PGS Source | |
PGS Catalog Publication (PGP) ID | PGP000511 |
Citation (link to publication) | Rasooly D et al. Nat Commun (2023) |
Ancestry Distribution | |
Source of Variant Associations (GWAS) | European: 100% 1,266,315 individuals (100%) |
PGS Evaluation | European: 100% 1 Sample Sets |
Study Identifiers | Sample Numbers | Sample Ancestry | Cohort(s) |
---|---|---|---|
GWAS Catalog: GCST90274223 Europe PMC: 37429843 |
1,266,315 individuals | European | HERMES, MVP |
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 |
---|---|---|---|---|---|---|---|---|
PPM019123 | PSS011190| European Ancestry| 75,119 individuals |
PGP000511 | Rasooly D et al. Nat Commun (2023) |
Reported Trait: Heart failure | OR: 1.28 [1.24, 1.31] | — | — | — | — |
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 |
---|---|---|---|---|---|---|---|---|
PSS011190 | — | — | [ ,
43.9 % Male samples |
— | European | — | BioVU | — |