The script [vepAllInOne.py](bh19-rare-diseases/associations/vepmining) retrives information about (allele frequencies)[https://en.wikipedia.org/wiki/Allele\_frequency] in several populations available in the (Ensembl)[http://www.ensembl.org/index.html] databse. This is done throug (this endpoint)[https://rest.ensembl.org/documentation/info/vep\_id\_post] of the Ensembl API.
The script [vepAllInOne.py](bh19-rare-diseases/associations/vepmining) retrives information about [allele frequencies](https://en.wikipedia.org/wiki/Allele\_frequency) in several populations available in the [Ensembl](http://www.ensembl.org/index.html) databse. This is done throug [this endpoint](https://rest.ensembl.org/documentation/info/vep\_id\_post) of the Ensembl API.
```commandline
python3 vepAllInOne.py -f <single column of rsid input file > -t < float, allele frequency threshold below with variant is retained >
