# 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 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` --- # Agent Instructions: Querying This Documentation If you need additional information that is not directly available in this page, you can query the documentation dynamically by asking a question. Perform an HTTP GET request on the current page URL with the `ask` query parameter: ``` GET https://docs.finngen.fi/finngen-data-specifics/green-library-data-aggregate-data/core-analysis-results-files/chip-gwas.md?ask= ``` The question should be specific, self-contained, and written in natural language. The response will contain a direct answer to the question and relevant excerpts and sources from the documentation. Use this mechanism when the answer is not explicitly present in the current page, you need clarification or additional context, or you want to retrieve related documentation sections.