Polygenic Score (PGS) ID: PGS000708

Predicted Trait
Reported Trait Kidney failure
Mapped Trait(s) kidney failure (EFO_1002048)
Additional Trait Information Unadjusted weights
Released in PGS Catalog: Feb. 3, 2021
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Terms and Licenses
Creative Commons Attribution 4.0 International (CC BY 4.0)

Score Details

Score Construction
PGS Name HC294
Development Method
Name snpnet (multi-PRS)
Parameters Weighted combination of multiple biomarker PRS. 1,080,968 variants as input (directly genotyped variants, imputed HLA allelotypes, and CNVs)
Variants
Original Genome Build hg19
Number of Variants 183,272
Effect Weight Type weights.HC294
PGS Source
PGS Catalog Publication (PGP) ID PGP000128
Citation (link to publication) Sinnott-Armstrong N et al. Nat Genet (2021)
Ancestry Distribution
Score Development/Training
European: 100%
223,327 individuals (100%)
PGS Evaluation
European: 100%
5 Sample Sets

Development Samples

Score Development/Training
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
223,327 individuals European
(British)
UKB Training

Performance Metrics

Disclaimer: The performance metrics are displayed as reported by the source studies. It is important to note that metrics are not necessarily comparable with each other. For example, metrics depend on the sample characteristics (described by the PGS Catalog Sample Set [PSS] ID), phenotyping, and statistical modelling. Please refer to the source publication for additional guidance on performance.

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
PPM001608 PSS000829|
European Ancestry|
135,300 individuals
PGP000128 |
Sinnott-Armstrong N et al. Nat Genet (2021)
Reported Trait: Renal failure HR: 1.12 [1.08, 1.16] C-index: 0.667 Age as time scale, sex, batch, PCs(1-10)
PPM001600 PSS000823|
European Ancestry|
87,413 individuals
PGP000128 |
Sinnott-Armstrong N et al. Nat Genet (2021)
Reported Trait: Kidney failure AUROC: 0.56142 Age, sex, PCs(1-10)
PPM001609 PSS000804|
European Ancestry|
135,300 individuals
PGP000128 |
Sinnott-Armstrong N et al. Nat Genet (2021)
Reported Trait: Dialysis HR: 1.13 [1.04, 1.23] C-index: 0.745 Age as time scale, sex, batch, PCs(1-10)
PPM001610 PSS000682|
European Ancestry|
135,300 individuals
PGP000128 |
Sinnott-Armstrong N et al. Nat Genet (2021)
Reported Trait: Diabetic kidney failure in all HR: 1.19 [1.13, 1.26] C-index: 0.779 Age as time scale, sex, batch, PCs(1-10)
PPM001611 PSS000682|
European Ancestry|
135,300 individuals
PGP000128 |
Sinnott-Armstrong N et al. Nat Genet (2021)
Reported Trait: Diabetic kidney failure in diabetics HR: 1.08 [1.02, 1.14] C-index: 0.706 Age as time scale, sex, batch, PCs(1-10)
PPM001612 PSS000683|
European Ancestry|
135,300 individuals
PGP000128 |
Sinnott-Armstrong N et al. Nat Genet (2021)
Reported Trait: Diabetic kidney failure in type 2 diabetics HR: 1.13 [1.04, 1.24] C-index: 0.634 Age as time scale, sex, batch, PCs(1-10)

Evaluated Samples

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
PSS000682 ICD-10 E1[0-4]2
[
  • 1,299 cases
  • , 134,001 controls
]
European
(Finnish)
FinnGen
PSS000683 ICD-10 E1[0-4]2
[
  • 511 cases
  • , 134,789 controls
]
European
(Finnish)
FinnGen
PSS000823 87,413 individuals European UKB
PSS000829 ICD-10 N17
[
  • 3,058 cases
  • , 132,242 controls
]
European
(Finnish)
FinnGen
PSS000804 ICD-10 Z992|Y841
[
  • 595 cases
  • , 134,705 controls
]
European
(Finnish)
FinnGen