Access results

According to the FinnGen consortium agreement, FinnGen results are subjected to one year embargo and, after that, can be made available to the larger scientific community. Data releases are done twice a year. The results can be browsed with the web browser and summary statistics data can be downloaded from Google cloud storage free of charge. The latest release is from June 2022. Please follow the instructions below to access it.

Latest data release:

Total sample size: 309,154 (173,746 females and 135,408 males)

Total number of variants analyzed: 16,962,023 variants

Number of disease endpoints (phenotypes) available: ​3,095 endpoints

Data released to the partners: Q2 2021

Public data release: June 1, 2022

Thorough documentation is available here.

 

Please note that the allele frequency column provides the human reference genome alternative allele (not minor allele) frequency. All effect sizes and allele frequencies are reported in terms of alternate allele.

 

How to access the summary statistics:

  1. Fill this online form to gain access to Finngen GWAS summary statistics. 
  2. Instructions on how to download summary statistics are sent to you by e-mail.
  3. Download the data 

 

Acknowledgements:

When using these results in publications, please remember to:

  1. Acknowledge the FinnGen study. You can use the following text:

“We want to acknowledge the participants and investigators of the FinnGen study”

  1. Cite our latest publication:

Kurki M.I., et al. FinnGen: Unique genetic insights from combining isolated population and national  health register data, medRxiv 2022.03.03.22271360; doi: https://doi.org/10.1101/2022.03.03.22271360

Furthermore, if possible, include "FinnGen" as a keyword for your publication.

 

Browsing the results: 

The web browser r7.finngen.fi contains all FinnGen GWAS results from the latest public release and provides you with three options:

  1. Search for the GWAS result of a variant, phenotype or gene.

  2. Explore the loss-of-function burden (LoF) for gene-phenotypes combinations.

  3. Find a particular phenotype/endpoint.

 

Risteys

Risteys tool (Risteys = intersection in Finnish) allows browsing of the FinnGen data at the phenotype level, including endpoint definitions, statistics about number of individuals, gender distribution, and longitudinal relationships. For this data release, please visit: r7.risteys.finngen.fi.

 

Individual level data

In case you are interested in accessing individual level biobank samples and data or recontacting Finnish biobank participants, please visit the Fingenious portal hosted by the Finnish Biobank Cooperative FINBB for more information.

 

Earlier data releases:

DF6 - January 24 2022

Total sample size: ​260,405 (147,061 females and 113,344 males)

Total number of variants analyzed: 16,962,023 variants

Number of disease endpoints (phenotypes) available: ​2,861 endpoints

Data released to the partners: Q3 2020

Public data release: January 24 2022

Browser: r6.finngen.fi

Thorough documentation is available here.

 

DF5 - May 11 2021

Total sample size: ​218,792

Total number of variants analyzed: 16,962,023 variants

Number of disease endpoints (phenotypes) available: ​2,803 endpoints

Data released to the partners: Q2 2020

Public data release: May 11 2021

Browser: r5.finngen.fi

Thorough documentation is available here

 

DF4 - November 30 2020:

Total sample size: ​176,899

Total number of variants analyzed: 16,962,023 variants

Number of disease endpoints (phenotypes) available: ​2,444 endpoints

Data released to the partners: Q4 2019

Public data release: Nov 30, 2020

Thorough documentation is available here

 

DF3 - June 16 2020:

Total sample size: ​135,638

Total number of variants analyzed: 16,962,023 variants

Number of disease endpoints (phenotypes) available: ​1,801 endpoints

Data released to the partners: Q2 2019 (May)

Public data release: June 16 2020

Thorough documentation is available here

New feature: LD estimation from SISu v3 reference panel

 

DF2 - January 14 2020:

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 here