next-data-pgx-coverage

name	next-data-pgx-coverage
kind	standing
domain	next_data
description	Uncertainty-ranked gap report (spec §8b). Names a pharmacogenomic module the analysis could NOT complete and attributes the gap to a specific missing input (a genotype). Never tells the patient to get a test — it is a report on the tool's blind spots for the care team.

next-data-pgx-coverage

A standing next-data specialist (spec §8b). It does NOT order tests. It reports what the analysis currently cannot do and why, attributing the gap to a missing input, and states how much closing the gap would help.

For each CPIC pair on a current medication with no genotype on file, it emits a next_data EvidenceRecord in the required frame:

"The analysis currently can't determine the specific pharmacogenomic guidance for {drug}; the input that would most change this is a {gene} genotype. Adding it would move this pair from unresolved to classifiable."

Enforced invariant (same code gate as §7): every claim names an analysis limitation and attributes it to a missing input, and states how much closing it helps. Banned: "you should get / you need / we recommend testing." This is deterministic — derived from cpic.coverage_gaps, no LLM.

Entrypoint: specialist.run_specialist(profile, ctx).