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As we allow any field to be missing, it would be useful to have a concept of a "complete evidence string" and then track percentage of clinical annotations that generate at least one complete evidence string - analogous to ClinVar submission metrics. This lets us keep track of where we want to improve coverage (e.g. haplotype IDs).
Now that we are performing regular submissions, we should review the counts being gathered and the metrics spreadsheet, and add ones as needed.
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