Coding variant results including CHIP EWAS (Exome-Wide Association Scan)

These files contain the results of GWAS scans (additive & recessive), as well as additive chip-genotype scans for coding variants. The variants included are those coding variants with INFO > 0.6. Additive, recessive and chip genotype additive scans were performed for these variants. Release endpoints were used. Chip analysis was performed for endpoints that have at least 50 cases among the chip genotyped samples.

Data access

Results are published in green library, under gs://finngen-production-library-green/finngen_R12/finngen_R12_analysis_data/coding/.

Results can also be browsed using the https://dev2.finngen.fi table browser.

More information about the files in green library can be found in the documentation at green library: gs://finngen-production-library-green/finngen_R12/finngen_R12_analysis_data/coding/finngen_R12_coding.md