| Predicted Trait | |
| Reported Trait | Multiple sclerosis | 
| Mapped Trait(s) | multiple sclerosis (MONDO_0005301) | 
| Score Construction | |
| PGS Name | PGS_MS_Brain | 
| Development Method | |
| Name | Genome-wide significant variants | 
| Parameters | NR | 
| Variants | |
| Original Genome Build | GRCh37 | 
| Number of Variants | 476,399 | 
| Effect Weight Type | NR | 
| PGS Source | |
| PGS Catalog Publication (PGP) ID | PGP000334 | 
| Citation (link to publication) | Shams H et al. Brain (2022) | 
| Ancestry Distribution | |
| Source of Variant Associations (GWAS) | European: 100% 41,505 individuals (100%) | 
| PGS Evaluation | European: 100% 2 Sample Sets | 
| Study Identifiers | Sample Numbers | Sample Ancestry | Cohort(s) | 
|---|---|---|---|
| — | [ 
 | European | IMSGC | 
| 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 | 
|---|---|---|---|---|---|---|---|---|
| PPM014749 | PSS009883| European Ancestry| 253,419 individuals | PGP000334 | Shams H et al. Brain (2022) | Reported Trait: Multiple sclerosis | — | AUROC: 0.73 [0.72, 0.74] | Odds ratio (OR, top 10% vs median): 5.3 [4.7, 6.0] | — | — | 
| PPM014750 | PSS009882| European Ancestry| 938 individuals | PGP000334 | Shams H et al. Brain (2022) | Reported Trait: Multiple sclerosis | — | AUROC: 0.8 [0.76, 0.82] | Odds ratio (OR, top 10% vs median): 15.0 [10.4, 24.0] | — | — | 
| 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 | 
|---|---|---|---|---|---|---|---|---|
| PSS009882 | — | — | [ 
 | — | European | — | KP | — | 
| PSS009883 | — | — | [ 
 | — | European | — | UKB | — |