| 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 | — |