The identifier pins the policy semantics adapted from Centre for Population
Genomics ClinVarbitration 2.2.11 (upstream commit
658b9f241eb2d43aa11214b153b19c1e18a16337) and records that decisions are
grouped per disease rather than only per variation. The identifier has no
package-local suffix: the view names, rather than a speculative v1, state
whether the output is disease-scoped or allele-scoped.