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.

api/tests/test_health.py

@@ -0,0 +1,12 @@
+import pytest
+from httpx import ASGITransport, AsyncClient
+
+from app.main import app
+
+
+@pytest.mark.asyncio
+async def test_health():
+    async with AsyncClient(transport=ASGITransport(app=app), base_url="http://test") as c:
+        r = await c.get("/health")
+    assert r.status_code == 200
+    assert r.json() == {"status": "ok"}