Basic information about the data release:
Total sample size: 96,499
Total number of variants analyzed: 16,152,119 variants
Number of disease endpoints (phenotypes) available: 1,122 endpoints
Data released to the partners: Q4 2018 (Nov 27)
Public data release: Jan 14 2020
Thorough documentation is available at: www.finngen.fi/en/r2_documents
How to access the summary statistics:
- Fill this online form to gain access to Finngen GWAS summary statistics.
- Instructions on how to download summary statistics are sent to you by e-mail.
- Download the data
Please remember to acknowledge the FinnGen study when using these results in publications.
You can use the following text:
“We want to acknowledge the participants and investigators of the FinnGen study”
Browsing the results:
The web browser r2.finngen.fi contains all FinnGen GWAS results from release 2 and provides you with three options:
Search for the GWAS result of a variant, phenotype or gene.
Explore the loss-of-function burden (LoF) for gene-phenotypes combinations.
Find a particular phenotype/endpoint.