Publication Information (EuropePMC) | |
Title | Family Clustering of Autoimmune Vitiligo Results Principally from Polygenic Inheritance of Common Risk Alleles. |
PubMed ID | 31327509(Europe PMC) |
doi | 10.1016/j.ajhg.2019.06.013 |
Publication Date | July 18, 2019 |
Journal | Am J Hum Genet |
Author(s) | Roberts GHL, Paul S, Yorgov D, Santorico SA, Spritz RA. |
Polygenic Score ID & Name | PGS Publication ID (PGP) | Reported Trait | Mapped Trait(s) (Ontology) | Number of Variants |
Ancestry distribution GWAS Dev Eval |
Scoring File (FTP Link) |
---|---|---|---|---|---|---|
PGS000738 (CONFIRMED_PGS) |
PGP000145 | Roberts GHL et al. Am J Hum Genet (2019) |
Vitiligo | Vitiligo | 48 | - |
https://ftp.ebi.ac.uk/pub/databases/spot/pgs/scores/PGS000738/ScoringFiles/PGS000738.txt.gz |
PGS Performance Metric ID (PPM) |
Evaluated Score |
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 |
---|---|---|---|---|---|---|---|---|---|
PPM001761 | PGS000738 (CONFIRMED_PGS) |
PSS000907| European Ancestry| 4,008 individuals |
PGP000145 | Roberts GHL et al. Am J Hum Genet (2019) |
Reported Trait: Vitiligo | — | — | Odds Ratio (OR, top 20% vs remaining 80% of score distribution): 4.87 [4.21, 5.64] | — | — |
PPM001762 | PGS000738 (CONFIRMED_PGS) |
PSS000907| European Ancestry| 4,008 individuals |
PGP000145 | Roberts GHL et al. Am J Hum Genet (2019) |
Reported Trait: Vitiligo | — | — | Odds Ratio (OR, top 10% vs remaining 90% of score distribution): 5.26 [4.42, 6.29] | — | — |
PPM001763 | PGS000738 (CONFIRMED_PGS) |
PSS000907| European Ancestry| 4,008 individuals |
PGP000145 | Roberts GHL et al. Am J Hum Genet (2019) |
Reported Trait: Vitiligo | — | — | Odds Ratio (OR, top 10% vs remaining 95% of score distribution): 6.2 [4.96, 7.79] | — | — |
PPM001764 | PGS000738 (CONFIRMED_PGS) |
PSS000907| European Ancestry| 4,008 individuals |
PGP000145 | Roberts GHL et al. Am J Hum Genet (2019) |
Reported Trait: Vitiligo | — | — | Odds Ratio (OR, top 1% vs remaining 99% of score distribution): 8.79 [5.85, 13.78] | — | — |
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 |
---|---|---|---|---|---|---|---|---|
PSS000907 | Cases are individuals with vitiligo. Diagnoses of vitiligo in multiplex-affected subjects and reportedly unaffected family members were verified by manual review of all available phenotype information for each subject. | — | [
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— | European | — | NR | — |