Predicted Trait | |
Reported Trait | Congenital deficiency of other clotting factors (including factor VII) |
Mapped Trait(s) | congenital vitamin K-dependent coagulation factors deficiency (MONDO_0015722) |
Additional Trait Information | hematopoietic |
Score Construction | |
PGS Name | portability-PLR_286.12 |
Development Method | |
Name | Penalized regression (bigstatsr) |
Parameters | HapMap3 variants |
Variants | |
Original Genome Build | GRCh37 |
Number of Variants | 45 |
Effect Weight Type | beta |
PGS Source | |
PGS Catalog Publication (PGP) ID | PGP000263 |
Citation (link to publication) | Privé F et al. Am J Hum Genet (2022) |
Ancestry Distribution | |
Score Development/Training | European: 100% 391,124 individuals (100%) |
PGS Evaluation | European: 75% South Asian: 25% 4 Sample Sets |
Study Identifiers | Sample Numbers | Sample Ancestry | Cohort(s) | Phenotype Definitions & Methods | Age of Study Participants | Participant Follow-up Time | Additional Ancestry Description | Additional Sample/Cohort Information |
---|---|---|---|---|---|---|---|---|
— | 391,124 individuals | European | UKB | — | — | — | UK (+ Ireland) | — |
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 |
---|---|---|---|---|---|---|---|---|
PPM009505 | PSS009296| European Ancestry| 19,864 individuals |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Reported Trait: Congenital deficiency of other clotting factors (including factor VII) | — | — | Partial Correlation (partial-r): 0.0562 [0.0424, 0.0701] | sex, age, birth date, deprivation index, 16 PCs | — |
PPM009506 | PSS009070| European Ancestry| 4,108 individuals |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Reported Trait: Congenital deficiency of other clotting factors (including factor VII) | — | — | Partial Correlation (partial-r): 0.0487 [0.018, 0.0792] | sex, age, birth date, deprivation index, 16 PCs | — |
PPM009507 | PSS008624| European Ancestry| 6,613 individuals |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Reported Trait: Congenital deficiency of other clotting factors (including factor VII) | — | — | Partial Correlation (partial-r): 0.0377 [0.0136, 0.0618] | sex, age, birth date, deprivation index, 16 PCs | — |
PPM009508 | PSS008178| South Asian Ancestry| 6,272 individuals |
PGP000263 | Privé F et al. Am J Hum Genet (2022) |
Reported Trait: Congenital deficiency of other clotting factors (including factor VII) | — | — | Partial Correlation (partial-r): 0.0354 [0.0106, 0.0601] | sex, age, birth date, deprivation index, 16 PCs | — |
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 |
---|---|---|---|---|---|---|---|---|
PSS009070 | — | — | 4,108 individuals | — | European | Poland (NE Europe) | UKB | — |
PSS008624 | — | — | 6,613 individuals | — | European | Italy (South Europe) | UKB | — |
PSS009296 | — | — | 19,864 individuals | — | European | UK (+ Ireland) | UKB | — |
PSS008178 | — | — | 6,272 individuals | — | South Asian | India (South Asia) | UKB | — |