Data download

To download FinnGen summary statistics you will need to fill the online form at this link. You will then receive an email containing the detailed instructions for downloading the data.

Using FinnGen data for publications

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 FinnGen study.

Manifest

The Manifest file with the link to all the downloadable summary statistics is available at: https://storage.googleapis.com/finngen-public-data-r2/summary_stats/r2_manifest.tsv

Description

GWAS summary stats (tab-delimited, bgzipped, genome build 38, filtered to INFO > 0.6, tabix index files included) are named as {endpoint}.gz. For example, endpoint I9_CHD has I9_CHD.gz and I9_CHD.gz.tbi.

To learn more about the methods used, see section GWAS.

The {endpoint}.gz have the following structure:

Column name

Description

chrom

chromosome on build GRCh38 (1-22, X)

pos

position in base pairs on build GRCh38

ref

reference allele

alt

alternative allele (effect allele)

rsids

variant identifier

nearest_genes

nearest gene name from variant

pval

p-value from SAIGE

beta

effect size estimated with SAIGE for the alternative allele

sebeta

standard deviation of effect size estimated with SAIGE

maf

minor allele frequency

maf_cases

minor allele frequency among cases

maf_controls

minor allele frequency among controls

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