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Specification:

US Minimal Common Oncology Data Elements (mCODE) (FHIR)
Raised in Version:

1.16.0 [deprecated]
Work Group:

Clinical Interoperability Council
Related URL:
http://hl7.org/fhir/us/mcode/2021May/StructureDefinition-mcode-cancer-genetic-variant.html
Related Artifact(s):

Cancer Genetic Variant [deprecated]
Grouping:
- Block-Vote-6
- Genetic
Resolution Description:

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

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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

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