FinnGen r8 2023 complex disease GWAS: European ancestry

Summary statistics are available for download from FinnGen.

Publications

FinnGen provides genetic insights from a well-phenotyped isolated population.
Kurki MI, et al.
Nature. 2023 Jan;613(7944):508-518. doi: 10.1038/s41586-022-05473-8.
PMID: 36653562

Phenotypes

  • Atopic dermatitis
  • Age-related macular degeneration (AMD)
  • Alzheimer's disease
  • Ankylosing spondylitis
  • Asthma
  • Atrial fibrillation or flutter
  • Myocardial infarction
  • Primary open-angle glaucoma
  • Psoriasis
  • Senile cataract
  • Seropositive rheumatoid arthritis
  • Type 1 diabetes (T1D)
  • Type 2 diabetes (T2D)

Experiment summary

This study analyzed genetic associations for common genetically complex diseases in participants of European ancestry in the FinnGen study.

Dataset ID
Kurki2023_FinnGen_EU