Predicted Trait | |
Reported Trait | Epilepsy |
Mapped Trait(s) | epilepsy (EFO_0000474) |
Score Construction | |
PGS Name | INTERVENE_MegaPRS_Epilepsy |
Development Method | |
Name | megaprs.auto |
Parameters | BayesR, p1=0.985, p2=0.005, p3=0.005, p4=0.005 |
Variants | |
Original Genome Build | GRCh37 |
Number of Variants | 605,432 |
Effect Weight Type | beta |
PGS Source | |
PGS Catalog Publication (PGP) ID | PGP000618 |
Citation (link to publication) | Jermy B et al. Nat Commun (2024) |
Study Identifiers | Sample Numbers | Sample Ancestry | Cohort(s) |
---|---|---|---|
GWAS Catalog: GCST007343 Europe PMC: 30531953 |
38,752 individuals | European | NR |
GWAS Catalog: GCST007343 Europe PMC: 30531953 |
3,406 individuals | East Asian | NR |
GWAS Catalog: GCST007343 Europe PMC: 30531953 |
2,731 individuals | African American or Afro-Caribbean | NR |
Study Identifiers | Sample Numbers | Sample Ancestry | Cohort(s) | Phenotype Definitions & Methods | Age of Study Participants | Participant Follow-up Time | Additional Ancestry Description | Additional Sample/Cohort Information |
---|---|---|---|---|---|---|---|---|
— | 404 individuals | European | 1000G | — | — | — | non-Finnish Europeans | — |
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 |
---|---|---|---|---|---|---|---|---|
PPM021223 | PSS011665| European Ancestry| 447,332 individuals |
PGP000618 | Jermy B et al. Nat Commun (2024) |
Reported Trait: Incident Epilepsy | HR: 1.12 [1.09, 1.14] | — | — | PCs 1-10 | — |
PPM021224 | PSS011580| European Ancestry| 20,188 individuals |
PGP000618 | Jermy B et al. Nat Commun (2024) |
Reported Trait: Incident Epilepsy | HR: 1.07 [1.02, 1.11] | C-index: 0.54 [0.53, 0.55] | — | PCs 1-10 | — |
PPM021225 | PSS011579| European Ancestry| 69,715 individuals |
PGP000618 | Jermy B et al. Nat Commun (2024) |
Reported Trait: Incident Epilepsy | HR: 1.1 [1.05, 1.16] | C-index: 0.55 [0.54, 0.57] | — | PCs 1-10 | — |
PPM021226 | PSS011578| European Ancestry| 29,427 individuals |
PGP000618 | Jermy B et al. Nat Commun (2024) |
Reported Trait: Incident Epilepsy | HR: 1.1 [1.02, 1.19] | C-index: 0.54 [0.52, 0.56] | — | PCs 1-10 | — |
PPM021227 | PSS011576| European Ancestry| 44,188 individuals |
PGP000618 | Jermy B et al. Nat Commun (2024) |
Reported Trait: Incident Epilepsy | HR: 1.17 [1.04, 1.32] | — | — | PCs 1-10 | — |
PPM021228 | PSS011577| European Ancestry| 7,018 individuals |
PGP000618 | Jermy B et al. Nat Commun (2024) |
Reported Trait: Incident Epilepsy | HR: 0.98 [0.86, 1.13] | C-index: 0.59 [0.55, 0.63] | — | PCs 1-10 | — |
PPM021230 | PSS011574| European Ancestry| 199,868 individuals |
PGP000618 | Jermy B et al. Nat Commun (2024) |
Reported Trait: Incident Epilepsy | HR: 1.11 [1.08, 1.14] | C-index: 0.55 [0.54, 0.56] | — | PCs 1-10 | — |
PPM021229 | PSS011575| European Ancestry| 412,090 individuals |
PGP000618 | Jermy B et al. Nat Commun (2024) |
Reported Trait: Incident Epilepsy | HR: 1.11 [1.09, 1.13] | C-index: 0.55 [0.55, 0.56] | — | PCs 1-10 | — |
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 |
---|---|---|---|---|---|---|---|---|
PSS011665 | — | — | [
|
— | European | — | UKB | — |
PSS011574 | — | — | [
|
— | European | — | EB | — |
PSS011575 | — | — | [
|
— | European | — | FinnGen | — |
PSS011576 | — | — | [
|
— | European | — | G&H | — |
PSS011577 | — | — | [
|
— | European | — | GS:SFHS | — |
PSS011578 | — | — | [
|
— | European | — | GEL | — |
PSS011579 | — | — | [
|
— | European | — | HUNT | — |
PSS011580 | — | — | [
|
— | European | — | MGBB | — |