> For the complete documentation index, see [llms.txt](https://finngen.gitbook.io/documentation/llms.txt). Markdown versions of documentation pages are available by appending `.md` to page URLs; this page is available as [Markdown](https://finngen.gitbook.io/documentation/r2/pheweb/phenotype-list.md).

# Phenotype list

![Genome-wide significant loci = ??](https://1223477342-files.gitbook.io/~/files/v0/b/gitbook-legacy-files/o/assets%2F-LvPur3Kbj-JuAmvOiI6%2F-LxLy0KXeywAEYF4WU6O%2F-LxM5IL6aDbZG8ehvx2_%2Fscreenshot_phenotypelist_anno.png?alt=media\&token=921d061c-fd54-497e-adfb-6edd10c9818e)

Contains all endpoints/phenotypes for which a GWAS was run (if more than 100 cases). 

| Column                           | Description                                                           |
| -------------------------------- | --------------------------------------------------------------------- |
| **phenotype**                    | [Endpoint](/documentation/r2/methods/endpoints.md) description        |
| **category**                     | 13 phenotype **categories**                                           |
| **genome-wide significant loci** | Variant(s) with $$P \leq 5 \cdot 10^{-8}$$ within a +/- 500kb window. |