Predicted Trait | |
Reported Trait | Childhood steroid-sensitive nephrotic syndrome |
Mapped Trait(s) | nephrotic syndrome (EFO_0004255) |
Score Construction | |
PGS Name | SSNS-GRS |
Development Method | |
Name | Genome-wide significant SNPs |
Parameters | r2>0.8 |
Variants | |
Original Genome Build | NR |
Number of Variants | 5 |
Effect Weight Type | ln(OR) |
PGS Source | |
PGS Catalog Publication (PGP) ID | PGP000407 |
Citation (link to publication) | Downie ML et al. Pediatr Nephrol (2022) |
Ancestry Distribution | |
Source of Variant Associations (GWAS) | European: 100% 6,064 individuals (100%) |
PGS Evaluation | European: 100% 1 Sample Sets |
Study Identifiers | Sample Numbers | Sample Ancestry | Cohort(s) |
---|---|---|---|
GWAS Catalog: GCST008456 Europe PMC: 31263063 |
6,064 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 |
---|---|---|---|---|---|---|---|---|
PPM016206 | PSS010057| European Ancestry| 597 individuals |
PGP000407 | Downie ML et al. Pediatr Nephrol (2022) |
Reported Trait: Non-monogenic idiopathic nephrotic syndrome | — | AUROC: 0.638 [0.543, 0.733] | — | — | — |
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 |
---|---|---|---|---|---|---|---|---|
PSS010057 | — | — | 597 individuals | — | European | — | NR | BRIDGE |