SNOMED has released PGx concepts like the following:

http://browser.ihtsdotools.org/?perspective=full&conceptId1=738535003&edition=us-edition&release=v20180301&server=https://prod-browser-exten.ihtsdotools.org/api/snomed&langRefset=900000000000509007

They take the form of "[GENE] [STATUS]"

Should we allow for these to be delivered? We have our own profiles that describe sending the STATUS (as a LOINC answer list), and it can reference a Genotype/Haplotype/Variant, which from "Computable Genetic Findings" allows for GENE. However, I am not sure how we support delivering the SNOMED codes I reference above?

Also consider: Should these SNOMED codes be delivered as report-level Interpretations rather than Genetic Impacts?