Predicted Trait | |
Reported Trait | Melanoma |
Mapped Trait(s) | melanoma (EFO_0000756) |
Score Construction | |
PGS Name | PRS_Melanoma |
Development Method | |
Name | RiskPipe (clumping and thresholding) |
Parameters | p<1e-6 |
Variants | |
Original Genome Build | hg19 |
Number of Variants | 18 |
Effect Weight Type | beta |
PGS Source | |
PGS Catalog Publication (PGP) ID | PGP000138 |
Citation (link to publication) | Fontanillas P et al. Nat Commun (2021) |
Ancestry Distribution | |
Source of Variant Associations (GWAS) | European: 100% 103,008 individuals (100%) |
PGS Evaluation | European: 100% 1 Sample Sets |
Study Identifiers | Sample Numbers | Sample Ancestry | Cohort(s) |
---|---|---|---|
Europe PMC: 33420020 |
[ ,
42.6 % Male samples |
European | 23andMe |
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 |
---|---|---|---|---|---|---|---|---|
PPM001672 | PSS000872| European Ancestry| 88,924 individuals |
PGP000138 | Fontanillas P et al. Nat Commun (2021) |
Reported Trait: Melanoma | OR: 1.33 [1.29, 1.37] | AUROC: 0.579 | — | — | — |
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 |
---|---|---|---|---|---|---|---|---|
PSS000872 | Melanoma cases were determined by a baseline survey containing 34 questions regarding personal history of skin cancer(including skin cancer type, age at diagnosis, body location, prescribed treatments and information regarding cancer recurrence) | — | [ ,
38.9 % Male samples |
European | — | 23andMe | — |