Initial release: rarelens platform skeleton (AGPL-3.0)

End-to-end variant interpretation platform for rare genetic disease research:
SvelteKit UI, FastAPI + PostgreSQL API, Nextflow/Ensembl VEP pipeline,
LightGBM pathogenicity scoring with MLflow, K8s/ArgoCD/GCP infrastructure.
Public test data only; no clinical claims.

infra/terraform/variables.tf

@@ -0,0 +1,9 @@
+variable "project" { type = string }
+variable "region" {
+  type    = string
+  default = "europe-west2" # London: keeps public genomic test data and the Cambridge team in one jurisdiction
+}
+variable "github_repo" {
+  type    = string
+  default = "lynchaos/rarelens"
+}