Automatically query genomic variants.
Just have docker and docker compose installed, run as a service using the following command:
docker compose up -d
Afterwards the service will be exposed on Port 5001. This can be configured by changing the Port in the Dockerfile and the docker-compose.yml.
Just query a genomic position in hg19 or grch37 syntax including ref and alt allele. Currently only single nucleotide exchanges (both coding and non-coding) are supported.