Predicted Trait | |
Reported Trait | Melanoma |
Mapped Trait(s) | melanoma (EFO_0000756) |
Score Construction | |
PGS Name | Melanoma_PRS68 |
Development Method | |
Name | Genome-wide significant variants |
Parameters | NR |
Variants | |
Original Genome Build | NR |
Number of Variants | 68 |
Effect Weight Type | log(OR) for the effect allele *NOTE* a EAF-normalised weight was used for the PRS (see "variant_description" and dosage_#_weight columns) |
PGS Source | |
PGS Catalog Publication (PGP) ID | PGP000274 |
Citation (link to publication) | Steinberg J et al. Br J Dermatol (2021) |
Ancestry Distribution | |
Source of Variant Associations (GWAS) | European: 100% 411,948 individuals (100%) |
PGS Evaluation | European: 100% 2 Sample Sets |
Study Identifiers | Sample Numbers | Sample Ancestry | Cohort(s) |
---|---|---|---|
Europe PMC: 32341527 |
[
|
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 |
---|---|---|---|---|---|---|---|---|
PPM012812 | PSS009568| European Ancestry| 395,647 individuals |
PGP000274 | Steinberg J et al. Br J Dermatol (2021) |
Reported Trait: Incident invasive melanoma | HR: 1.8 [1.71, 1.88] | — | — | age, sex, self-reported ethnicity, ease of tanning, 20 genetic PCs | subdistribution hazard ratio (and 95% confidence interval) per 1 sd of PRS on log-scale, based on Fine-Grey competing risks regression with death as competing risk |
PPM012815 | PSS009567| European Ancestry| 4,765 individuals |
PGP000274 | Steinberg J et al. Br J Dermatol (2021) |
Reported Trait: Incident invasive melanoma | HR: 1.47 [1.31, 1.67] | — | — | age, sex, self-reported ethnicity, ease of tanning, 20 genetic PCs | subdistribution hazard ratio (and 95% confidence interval) per 1 sd of PRS on log-scale, based on Fine-Grey competing risks regression with death as competing risk |
PPM012818 | PSS009568| European Ancestry| 395,647 individuals |
PGP000274 | Steinberg J et al. Br J Dermatol (2021) |
Reported Trait: Incident invasive melanoma | — | AUROC: 0.685 [0.673, 0.698] | R²: 0.068 [0.059, 0.078] | age, sex | AUC (and 95% confidence interval) for PRS-adjusted age-sex-specific absolute 10-year risk of invasive melanoma; R2 (and 95% confidence interval) based on 1.5% melanoma prevalence for same risk estimates as AUC (95% confidence interval) |
PPM012821 | PSS009567| European Ancestry| 4,765 individuals |
PGP000274 | Steinberg J et al. Br J Dermatol (2021) |
Reported Trait: Incident invasive melanoma | — | AUROC: 0.691 [0.661, 0.722] | R²: 0.072 [0.051, 0.1] | age, sex | AUC (and 95% confidence interval) for PRS-adjusted age-sex-specific absolute 10-year risk of invasive melanoma; R2 (and 95% confidence interval) based on 1.5% melanoma prevalence for same risk estimates as AUC (95% confidence interval) |
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 |
---|---|---|---|---|---|---|---|---|
PSS009567 | invasive melanoma diagnosis record (ICD10 code C43) in Victorian Cancer Registry or the Australian Cancer Database | Mean = 9.7 years | [ ,
39.4 % Male samples |
Mean = 63.52 years Sd = 7.21 years |
European | — | MCCS | — |
PSS009568 | invasive melanoma diagnosis (ICD10 code C43 or ICD9 code 172 for ICD9) in cancer registry records (provided by NHS Digital for England and Wales, and National Records of Scotland, NHS Central Register for Scotland) | Mean = 7.16 years | [ ,
46.4 % Male samples |
Mean = 56.91 years Sd = 7.95 years |
European | — | UKB | — |