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Type:
Change Request
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Resolution: Persuasive
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Priority:
Medium
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FHIR Core (FHIR)
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STU3
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Clinical Genomics
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MolecularSequence (was Sequence)
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10.6
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Bob D / Jamie: 16-1-0
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Enhancement
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Non-substantive
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STU3
Add Sequence.structureVariant.variantType: Currently no way to indicate the type os structural variant. We might use, for instance, LOINC 48019-4 DNA Change Type, to indicate the type of structural variant.
- is voted on by
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BALLOT-5439 Affirmative - Bob Dolin : 2018-May-FHIR IG CG R1
- Closed