| Predicted Trait | |
| Reported Trait | Alzheimer's disease |
| Mapped Trait(s) | Alzheimer disease (MONDO_0004975) |
| Score Construction | |
| PGS Name | Alzheimer_s_disease_prscs |
| Development Method | |
| Name | PRS-CS |
| Parameters | PRS-CS-auto in FinnGen, LD reference panel: European ancestry in 1000 Genomes |
| Variants | |
| Original Genome Build | GRCh38 |
| Number of Variants | 1,092,011 |
| Effect Weight Type | beta |
| PGS Source | |
| PGS Catalog Publication (PGP) ID | PGP000364 |
| Citation (link to publication) | Mars N et al. Am J Hum Genet (2022) |
| Ancestry Distribution | |
| Source of Variant Associations (GWAS) | European: 100% 455,258 individuals (100%) |
| PGS Evaluation | European: 100% 1 Sample Sets |
| Study Identifiers | Sample Numbers | Sample Ancestry | Cohort(s) |
|---|---|---|---|
Europe PMC: 30617256 |
[
|
European | NR |
|
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 |
|---|---|---|---|---|---|---|---|---|
| PPM014953 | PSS009939| European Ancestry| 39,444 individuals |
PGP000364 | Mars N et al. Am J Hum Genet (2022) |
Reported Trait: Alzheimer's disease | OR: 1.64 [1.5, 1.79] | — | — | age, sex, 10 PCs, technical covariates | — |
|
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 |
|---|---|---|---|---|---|---|---|---|
| PSS009939 | — | — | 39,444 individuals | — | European (Finnish) |
— | FinnGen | — |