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.

web/package.json

@@ -0,0 +1,23 @@
+{
+  "name": "rarelens-web",
+  "version": "0.1.0",
+  "private": true,
+  "type": "module",
+  "scripts": {
+    "dev": "vite dev",
+    "build": "vite build",
+    "preview": "vite preview",
+    "check": "svelte-kit sync && svelte-check --tsconfig ./tsconfig.json",
+    "test": "vitest run"
+  },
+  "devDependencies": {
+    "@sveltejs/adapter-node": "^5.2.0",
+    "@sveltejs/kit": "^2.5.0",
+    "@sveltejs/vite-plugin-svelte": "^4.0.0",
+    "svelte": "^5.0.0",
+    "svelte-check": "^4.0.0",
+    "typescript": "^5.5.0",
+    "vite": "^5.4.0",
+    "vitest": "^2.0.0"
+  }
+}