Predicted Trait | |
Reported Trait | Inflammatory bowel disease (IBD) |
Mapped Trait(s) | inflammatory bowel disease (EFO_0003767) |
Score Construction | |
PGS Name | ldpred2.auto.GCST004131.IBD |
Development Method | |
Name | LDpred2-auto |
Parameters | auto |
Variants | |
Original Genome Build | GRCh38 |
Number of Variants | 1,018,068 |
Effect Weight Type | beta |
PGS Source | |
PGS Catalog Publication (PGP) ID | PGP000517 |
Citation (link to publication) | Monti R et al. Am J Hum Genet (2024) |
Ancestry Distribution | |
Source of Variant Associations (GWAS) | |
Score Development/Training | European: 100% 5,340 individuals (100%) |
PGS Evaluation | European: 66.7% South Asian: 33.3% 6 Sample Sets |
Study Identifiers | Sample Numbers | Sample Ancestry | Cohort(s) |
---|---|---|---|
GWAS Catalog: GCST004131 Europe PMC: 28067908 |
59,957 individuals | NR, European | 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 |
---|---|---|---|---|---|---|---|---|
— | 5,340 individuals | European | UKB | — | — | — | — | — |
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 |
---|---|---|---|---|---|---|---|---|
PPM019252 | PSS011231| European Ancestry| 396,819 individuals |
PGP000517 | Monti R et al. Am J Hum Genet (2024) |
Reported Trait: Inflammatory bowel disease | OR: 1.98269 [1.93792696, 2.02848131] β: 0.68445 [0.66161882, 0.70728739] |
AUROC: 0.68464 [0.67874717, 0.6905373] | R²: 0.072 [0.06730218, 0.0770144] | 0 | beta = log(or)/sd_pgs |
PPM019253 | PSS011244| South Asian Ancestry| 44,057 individuals |
PGP000517 | Monti R et al. Am J Hum Genet (2024) |
Reported Trait: Inflammatory bowel disease | OR: 1.96487 [1.79443565, 2.15148758] β: 0.67543 [0.58469057, 0.7661595] |
AUROC: 0.68609 [0.6621402, 0.71004923] | R²: 0.06963 [0.05194957, 0.09014172] | 0 | beta = log(or)/sd_pgs |
PPM019254 | PSS011260| European Ancestry| 66,865 individuals |
PGP000517 | Monti R et al. Am J Hum Genet (2024) |
Reported Trait: Inflammatory bowel disease | OR: 1.53961 [1.46795237, 1.61475975] β: 0.43153 [0.38386848, 0.47918619] |
AUROC: 0.61629 [0.6026057, 0.62997539] | R²: 0.02895 [0.02234833, 0.03618136] | 0 | beta = log(or)/sd_pgs |
PPM019255 | PSS011288| South Asian Ancestry| 9,326 individuals |
PGP000517 | Monti R et al. Am J Hum Genet (2024) |
Reported Trait: Inflammatory bowel disease | OR: 1.7204 [1.47508928, 2.00651675] β: 0.54256 [0.38871852, 0.69640026] |
AUROC: 0.64259 [0.59747381, 0.68771596] | R²: 0.0437 [0.02067683, 0.073914] | 0 | beta = log(or)/sd_pgs |
PPM019256 | PSS011273| European Ancestry| 90,274 individuals |
PGP000517 | Monti R et al. Am J Hum Genet (2024) |
Reported Trait: Inflammatory bowel disease | OR: 1.95616 [1.85139121, 2.06685554] β: 0.67098 [0.61593736, 0.72602839] |
AUROC: 0.68274 [0.66821232, 0.69727153] | R²: 0.06887 [0.0582775, 0.08158032] | 0 | beta = log(or)/sd_pgs |
PPM019251 | PSS011220| European Ancestry| 199,274 individuals |
PGP000517 | Monti R et al. Am J Hum Genet (2024) |
Reported Trait: Inflammatory bowel disease | OR: 1.37223 [1.31427216, 1.43274448] β: 0.31644 [0.27328302, 0.35959182] |
AUROC: 0.58458 [0.57191218, 0.59724852] | R²: 0.01565 [0.01132517, 0.02036671] | 0 | beta = log(or)/sd_pgs |
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 |
---|---|---|---|---|---|---|---|---|
PSS011273 | — | — | [
|
— | European | — | UKB | — |
PSS011244 | — | — | [
|
— | South Asian | — | G&H | — |
PSS011220 | — | — | [
|
— | European | — | EB | — |
PSS011288 | — | — | [
|
— | South Asian | — | UKB | — |
PSS011260 | — | — | [
|
— | European | — | HUNT | — |
PSS011231 | K11_IBD_STRICT, ICD10: K50|K51, ICD9: 555|556 | — | [
|
— | European | — | FinnGen | — |