Details
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Change Request
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Resolution: Persuasive with Modification
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Medium
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Genomics Reporting (FHIR)
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Clinical Genomics
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Variant
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Bret H / Jamie J : 12 - 0 - 1
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Enhancement
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Compatible, substantive
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current
Description
For our clinical genetic tests, we validate SNVs using Sanger and CNVs using MLPA. Would the Described or Complex Variant be the appropriate resource to include validation info? If so, what would be an appropriate field to house this info?
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