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  • Introduction
  • Data download
  • Data releases
  • How to cite
  • Pheweb Browser
    • Getting started
    • Phenotype list
    • GWAS overview
    • Locus zoom
    • Variant view
    • Gene view / LoF burden
  • Methods
    • Participating biobanks/cohorts
    • Genotypes
      • Genotype data
      • Genotype imputation
      • SISu reference panel
      • Software used
    • Endpoints
    • GWAS
      • Quality control
      • Association tests
      • Workflows
    • Loss of function burden
    • Contact
    • Github
    • FinnGen
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Introduction

NextData download

Last updated 2 years ago

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FinnGen a public-private partnership project combining genotype data from Finnish biobanks and digital health record data from Finnish health registries. FinnGen provides a unique opportunity to study genetic variation in relation to disease trajectories in an isolated population.

FinnGen is a growing project, aiming at 500,000 individuals in 2023.

FinnGen results are subjected to one year embargo and, after that, available to the larger scientific community via the Pheweb browser or through data download.