-
Type:
Change Request
-
Resolution: Retracted
-
Priority:
Medium
-
Genomics Reporting (FHIR)
-
STU3
-
Clinical Genomics
-
(profiles) [deprecated]
-
1.1.1
-
-
Correction
Existing Wording: The technique used to detect the variation, alignment with the borders of major features of the underlying sequence (e.g. variants), the presumed cause of the difference (insertion of extra copies, inversion of a portion of the sequence, common patterns in the population (a common set of variations typically appear together), a known effect(a particular collection of changes may result in a known physical manifestation or disease - aka. a phenotype)
Proposed Wording: remove or shrink
Comment:
Not sure this is relevant or necessary.
Summary:
Remove or shrink text
- is voted on by
-
BALLOT-5473 Negative - Clement McDonald : 2018-May-FHIR IG CG R1
- Retracted