| Predicted Trait | |
| Reported Trait | Psoriasis |
| Mapped Trait(s) | psoriasis (EFO_0000676) |
| Additional Trait Information | Score was developed using GWAS of psoriasis susceptibility and tested on prediction of severe psoriasis (vs. non-severe disease) |
| Score Construction | |
| PGS Name | GWS-noHLA |
| Development Method | |
| Name | Clumping and thresholding |
| Parameters | GWAS filtered for variants with P<5E-8, top variant taken for each independent LD block of the genome (defined in Berisa et al. 2016, PMID:26395773). |
| Variants | |
| Original Genome Build | hg19 |
| Number of Variants | 64 |
| Effect Weight Type | beta |
| PGS Source | |
| PGS Catalog Publication (PGP) ID | PGP000760 |
| Citation (link to publication) | Saklatvala JR et al. Genome Med (2025) |
| Ancestry Distribution | |
| Source of Variant Associations (GWAS) | European: 100% 52,950 individuals (100%) |
| PGS Evaluation | European: 100% 4 Sample Sets |
| Study Identifiers | Sample Numbers | Sample Ancestry | Cohort(s) |
|---|---|---|---|
| — | [
|
European | CASP, Genizon, KIEL, UCSF, WTCCC |
|
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 |
|---|---|---|---|---|---|---|---|---|
| PPM023016 | PSS012098| European Ancestry| 9,426 individuals |
PGP000760 | Saklatvala JR et al. Genome Med (2025) |
Reported Trait: Severe psoriasis | OR: 1.22 [1.15, 1.3] | — | — | — | — |
| PPM023020 | PSS012094| European Ancestry| 14,167 individuals |
PGP000760 | Saklatvala JR et al. Genome Med (2025) |
Reported Trait: Severe psoriasis | OR: 1.25 [1.18, 1.31] | — | — | — | — |
| PPM023024 | PSS012096| European Ancestry| 8,603 individuals |
PGP000760 | Saklatvala JR et al. Genome Med (2025) |
Reported Trait: Severe psoriasis | OR: 1.23 [1.17, 1.31] | — | — | — | — |
| PPM023028 | PSS012095| European Ancestry| 12,708 individuals |
PGP000760 | Saklatvala JR et al. Genome Med (2025) |
Reported Trait: Severe psoriasis | OR: 1.19 [1.15, 1.24] | — | — | — | — |
|
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 |
|---|---|---|---|---|---|---|---|---|
| PSS012094 | — | — | [
|
— | European (Estonian) |
— | EB | — |
| PSS012095 | — | — | [
|
— | European (Finnish) |
— | FinnGen | — |
| PSS012096 | — | — | [
|
— | European (Norwegian) |
— | HUNT | — |
| PSS012098 | — | — | [
|
— | European (British) |
— | UKB | — |