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  1. FHIR Specification Feedback
  2. FHIR-32886

mCODE CancerGeneticVariant missing allelic frequency

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    Details

    • Type: Change Request
    • Status: Resolved - change required (View Workflow)
    • Priority: Medium
    • Resolution: Persuasive with Modification
    • Specification:
      US Minimal Common Oncology Data Elements (mCODE) (FHIR)
    • Raised in Version:
      1.16.0
    • Work Group:
      Clinical Interoperability Council
    • Related Artifact(s):
      Cancer Genetic Variant
    • Grouping:
    • Resolution Description:
      Hide

      We recognize the need for allelic frequency and also propose to add allelic state, which further qualifies whether the allele was heterozygous, homozygous, etc.

      Show
      We recognize the need for allelic frequency and also propose to add allelic state, which further qualifies whether the allele was heterozygous, homozygous, etc.
    • Resolution Vote:
      Saul Kravitz/Sherita Alai:4-0-0
    • Change Category:
      Correction
    • Change Impact:
      Non-compatible
    • Pre Applied:
      Yes

      Description

      Proposed: add a component to CancerGeneticVariant which aligns with allelic frequency in the CG Reporting IG: http://build.fhir.org/ig/HL7/genomics-reporting/StructureDefinition-variant-definitions.html#Observation.component:sample-allelic-frequency

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            Assignee:
            Unassigned Unassigned
            Reporter:
            may_terry May Terry
            Watchers:
            1 Start watching this issue

              Dates

              Created:
              Updated:
              Resolved:
              Vote Date: