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 | — |