Polygenic Score (PGS) ID: PGS000905

Predicted Trait
Reported Trait PR interval
Mapped Trait(s) PR interval (EFO_0004462)
Released in PGS Catalog: Sept. 17, 2021
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PGS obtained from the Catalog should be cited appropriately, and used in accordance with any licensing restrictions set by the authors. See EBI Terms of Use (https://www.ebi.ac.uk/about/terms-of-use/) for additional details.

Score Details

Score Construction
PGS Name PRS743_PR
Development Method
Name Clumping and Thresholding (C+T)
Parameters r^2 = 0.1 in a 250kb region, p = 5e-8, imputation quality > 0.6
Variants
Original Genome Build GRCh37
Number of Variants 743
Effect Weight Type beta
PGS Source
PGS Catalog Publication (PGP) ID PGP000236
Citation (link to publication) Ntalla I et al. Nat Commun (2020)
Ancestry Distribution
Source of Variant
Associations (GWAS)
European: 92.8%
Hispanic or Latin American: 4.4%
African: 2.8%
292,566 individuals (100%)
PGS Evaluation
European: 100%
5 Sample Sets

Development Samples

Source of Variant Associations (GWAS)
Study Identifiers Sample Numbers Sample Ancestry Cohort(s)
GWAS Catalog: GCST010321
Europe PMC: 32439900
271,570 individuals European 35 cohorts
  • AGES
  • ,AMISH
  • ,ARIC
  • ,BRIGHT
  • ,BioMe
  • ,CHRIS
  • ,CHS
  • ,CROATIA-KORCULA
  • ,CROATIA-SPLIT
  • ,ERF
  • ,FHS
  • ,FINCAVAS
  • ,GS:SFHS
  • ,Health2000
  • ,INGI-Carlantino
  • ,INGI-FVG
  • ,JHS
  • ,KORA
  • ,LifeLines
  • ,MESA
  • ,MICROS
  • ,NEO
  • ,ORCADES
  • ,PIVUS
  • ,PREVEND
  • ,PROSPER
  • ,RS
  • ,SHIP
  • ,SardiNIA
  • ,TwinsUK
  • ,UKB
  • ,ULSAM
  • ,WHI
  • ,YFS
  • ,deCODE
GWAS Catalog: GCST010321
Europe PMC: 32439900
8,173 individuals African American or Afro-Caribbean 35 cohorts
  • AGES
  • ,AMISH
  • ,ARIC
  • ,BRIGHT
  • ,BioMe
  • ,CHRIS
  • ,CHS
  • ,CROATIA-KORCULA
  • ,CROATIA-SPLIT
  • ,ERF
  • ,FHS
  • ,FINCAVAS
  • ,GS:SFHS
  • ,Health2000
  • ,INGI-Carlantino
  • ,INGI-FVG
  • ,JHS
  • ,KORA
  • ,LifeLines
  • ,MESA
  • ,MICROS
  • ,NEO
  • ,ORCADES
  • ,PIVUS
  • ,PREVEND
  • ,PROSPER
  • ,RS
  • ,SHIP
  • ,SardiNIA
  • ,TwinsUK
  • ,UKB
  • ,ULSAM
  • ,WHI
  • ,YFS
  • ,deCODE
GWAS Catalog: GCST010321
Europe PMC: 32439900
12,823 individuals Hispanic or Latin American 35 cohorts
  • AGES
  • ,AMISH
  • ,ARIC
  • ,BRIGHT
  • ,BioMe
  • ,CHRIS
  • ,CHS
  • ,CROATIA-KORCULA
  • ,CROATIA-SPLIT
  • ,ERF
  • ,FHS
  • ,FINCAVAS
  • ,GS:SFHS
  • ,Health2000
  • ,INGI-Carlantino
  • ,INGI-FVG
  • ,JHS
  • ,KORA
  • ,LifeLines
  • ,MESA
  • ,MICROS
  • ,NEO
  • ,ORCADES
  • ,PIVUS
  • ,PREVEND
  • ,PROSPER
  • ,RS
  • ,SHIP
  • ,SardiNIA
  • ,TwinsUK
  • ,UKB
  • ,ULSAM
  • ,WHI
  • ,YFS
  • ,deCODE

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
PPM002674 PSS001175|
European Ancestry|
309,269 individuals
PGP000236 |
Ntalla I et al. Nat Commun (2020)
Reported Trait: Atrial fibrillation OR: 0.94
β: -0.058 (0.009)
Baseline age, sex, genotyping array, trait-related principal components
PPM002675 PSS001178|
European Ancestry|
290,252 individuals
PGP000236 |
Ntalla I et al. Nat Commun (2020)
Reported Trait: Distal conduction disease β: 0.105 (0.019)
OR: 1.11
Baseline age, sex, genotyping array, trait-related principal components
PPM002676 PSS001176|
European Ancestry|
309,041 individuals
PGP000236 |
Ntalla I et al. Nat Commun (2020)
Reported Trait: Atrioventricular preexcitation OR: 0.83
β: -0.191 (0.057)
Baseline age, sex, genotyping array, trait-related principal components
PPM002677 PSS001177|
European Ancestry|
309,246 individuals
PGP000236 |
Ntalla I et al. Nat Commun (2020)
Reported Trait: Coronary artery disease OR: 0.99
β: -0.014 (0.007)
Baseline age, sex, genotyping array, trait-related principal components
PPM002678 PSS001182|
European Ancestry|
309,270 individuals
PGP000236 |
Ntalla I et al. Nat Commun (2020)
Reported Trait: Pacemaker OR: 1.06
β: 0.056 (0.016)
Baseline age, sex, genotyping array, trait-related principal components

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
PSS001175 Cases were individuals with atrial fibrillation. Disease status was ascertained based on data from baseline interviews, hospital diagnosis codes (ICD-9 and ICD-10), cause of death codes (ICD-10), and operation codes. Details of individual selections and disease definitions are described in Supplementary Data 23.
[
  • 14,812 cases
  • , 294,457 controls
]
European UKB
PSS001176 Cases were individuals with atrioventricular preexcitation. Disease status was ascertained based on data from baseline interviews, hospital diagnosis codes (ICD-9 and ICD-10), cause of death codes (ICD-10), and operation codes. Details of individual selections and disease definitions are described in Supplementary Data 23.
[
  • 307 cases
  • , 308,734 controls
]
European UKB
PSS001177 Cases were individuals with congential artery disease. Disease status was ascertained based on data from baseline interviews, hospital diagnosis codes (ICD-9 and ICD-10), cause of death codes (ICD-10), and operation codes. Details of individual selections and disease definitions are described in Supplementary Data 23.
[
  • 27,072 cases
  • , 282,174 controls
]
European UKB
PSS001178 Cases were individuals with distal conduction disease. Disease status was ascertained based on data from baseline interviews, hospital diagnosis codes (ICD-9 and ICD-10), cause of death codes (ICD-10), and operation codes. Details of individual selections and disease definitions are described in Supplementary Data 23.
[
  • 2,789 cases
  • , 287,463 controls
]
European UKB
PSS001182 Cases were individuals with a pacemaker. Disease status was ascertained based on data from baseline interviews, hospital diagnosis codes (ICD-9 and ICD-10), cause of death codes (ICD-10), and operation codes. Details of individual selections and disease definitions are described in Supplementary Data 23.
[
  • 3,975 cases
  • , 305,295 controls
]
European UKB