Given a model that is already trained, which features does it rely on causally versus spuriously? Existing methods require access to the training procedure and cannot answer this post-hoc. We introduce the \textbf{Normalised Sensitivity Ratio~(NSR)}, a post-hoc, model-agnostic diagnostic for this question under a structured-shift regime: environments differ primarily in the mean of spurious features while the causal mechanism and causal marginals remain stable, as in multi-site clinical data or multi-batch genomics. Within this regime, causal features induce constant model sensitivity across environments while spurious features track shift. NSR formalises this as the squared coefficient of variation of per-environment sensitivity. Under a linear structural causal model (SCM) with
K≥3 non-degenerate environments, NSR achieves exact identification (Theorem~1). We fully characterise failure: weak shifts (
O(ε4) collapse), degenerate geometry, and proxy attenuation (
O((1−α)4)), giving practitioners quantitative criteria for assessing whether the regime holds. Finite-sample rates are
Op(n−1) under the null and
Op(n−1/2) under the alternative. Experiments confirm all theoretical predictions on synthetic data (area under the ROC curve [AUROC]
=1.000 under conditions satisfying the regime), show consistent rankings across five model families (Kendall
τ≥0.529), and recover six of eight causal features on bike-sharing data (Precision@7
=0.75) without modifying any trained model.