| 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 | — |