Predicted Trait | |
Reported Trait | Hearing difficulty |
Mapped Trait(s) | age-related hearing impairment (EFO_0005782) |
Score Construction | |
PGS Name | PRS_HD |
Development Method | |
Name | PRSice |
Parameters | INFO: 0.9, MAF: 0.01, clump-r2: 0.1, p≤ 0.48; software version = 2.1.3.beta |
Variants | |
Original Genome Build | hg19 |
Number of Variants | 100,325 |
Effect Weight Type | beta |
PGS Source | |
PGS Catalog Publication (PGP) ID | PGP000165 |
Citation (link to publication) | Cherny SS et al. Eur J Hum Genet (2020) |
Ancestry Distribution | |
Source of Variant Associations (GWAS) | European: 100% 250,389 individuals (100%) |
PGS Evaluation | European: 100% 1 Sample Sets |
Study Identifiers | Sample Numbers | Sample Ancestry | Cohort(s) |
---|---|---|---|
GWAS Catalog: GCST008899 Europe PMC: 31564434 |
250,389 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 |
---|---|---|---|---|---|---|---|---|
PPM001938 | PSS000972| European Ancestry| 3,636 individuals |
PGP000165 | Cherny SS et al. Eur J Hum Genet (2020) |
Reported Trait: Hearing difficulties | — | — | R²: 0.0911 | Age, sex | — |
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 |
---|---|---|---|---|---|---|---|---|
PSS000972 | Hearing difficulty cases were defined as responding either ‘Yes, diagnosed by doctor or health professional’ or ‘Yes, not diagnosed by health professional’ to ‘Do you suffer from hearing loss?’ while participants that responded ‘No’ were assigned as controls. | — | [ ,
8.5 % Male samples |
Mean = 60.34 years Sd = 10.18 years |
European (British) |
— | TwinsUK | — |