> 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/variant-view.md).

# Variant view

The variant view has the following URL: `http://r2.finngen.fi/variant/CHR-POS-ALT-REF,` e.g. [`http://r2.finngen.fi/variant/13-80757865-T-TA`](http://results.finngen.fi/variant/13-80757865-T-TA)

* `CHR`: chromosome on hg38 (1-22, X or 23)
* `POS`: position on hg38
* `REF`: reference allele
* `ALT`: alternative allele

![Variant view: displaying on the x-axis all phenotypes and phenotype categories and on the y-axis the p-values.](https://1223477342-files.gitbook.io/~/files/v0/b/gitbook-legacy-files/o/assets%2F-LvPur3Kbj-JuAmvOiI6%2F-LvQB0fYgrFMX4in-8mq%2F-LvQBtsP3gmDzUZFXXR1%2FScreenshot%202019-12-06%20at%2014.33.29.png?alt=media\&token=3656f6f7-b317-40eb-be91-f2cdead55762)