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<StructureDefinition xmlns="http://hl7.org/fhir">
  <id value="logicalmodel-Genomicvariantresult-R4" />
  <url value="http://linkehr.com/fhir/logicalmodel-genomicvariantresult-R4" />
  <identifier>
    <system value="openEHR-CKM" />
    <value value="openEHR-EHR-CLUSTER.genomic_variant_result.v1" />
  </identifier>
  <version value="0" />
  <name value="Genomicvariantresult" />
  <title value="Genomic variant result" />
  <status value="draft" />
  <date value="2024-06-18" />
  <publisher value="openEHR" />
  <contact>
    <telecom>
      <system value="url" />
      <value value="http://www.veratech.es" />
    </telecom>
  </contact>
  <description value="Findings and annotations related to one variant found in a human individual by a sequencing test." />
  <purpose value="To report findings and annotations related to one variant found in the genome by a sequencing test." />
  <fhirVersion value="4.0.0" />
  <mapping>
    <identity value="openEHR" />
    <uri value="http://openehr.org" />
    <name value="openEHR Mapping" />
  </mapping>
  <mapping>
    <identity value="openEHR-natural" />
    <uri value="http://openehr.org" />
    <name value="openEHR natural path" />
  </mapping>
  <kind value="logical" />
  <abstract value="false" />
  <type value="StructureDefinition" />
  <baseDefinition value="http://hl7.org/fhir/StructureDefinition/Element" />
  <snapshot>
    <element id="Genomic_variant_result">
      <path value="Genomic_variant_result" />
      <short value="Genomic variant result" />
      <definition value="Findings and annotations related to one variant found in a human individual by a sequencing test." />
      <min value="1" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result" />
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        <max value="1" />
      </base>
      <type>
        <code value="BackboneElement" />
      </type>
      <mustSupport value="true" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Bioinformatic_analysis_workflow">
      <path value="Genomic_variant_result.Bioinformatic_analysis_workflow" />
      <short value="Bioinformatic analysis workflow" />
      <definition value="Structured details about the bioinformatic analysis workflow or the protocol that is used." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Bioinformatic_analysis_workflow" />
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      <type>
        <code value="BackboneElement" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Reference_genome">
      <path value="Genomic_variant_result.Reference_genome" />
      <short value="Reference genome" />
      <definition value="Structured details about the specific version of the human sequence assembly used for annotation." />
      <min value="1" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Reference_genome" />
        <min value="1" />
        <max value="1" />
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      <type>
        <code value="BackboneElement" />
      </type>
      <mustSupport value="true" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Variant_identification">
      <path value="Genomic_variant_result.Variant_identification" />
      <short value="Variant identification" />
      <definition value="A reference to a specific variation recorded into an external biological variation database." />
      <min value="0" />
      <max value="*" />
      <base>
        <path value="Genomic_variant_result.Variant_identification" />
        <min value="0" />
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      <type>
        <code value="BackboneElement" />
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      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Variant">
      <path value="Genomic_variant_result.Variant" />
      <short value="Variant" />
      <definition value="Description of the variation at the genomic level following the HGVS nomenclature." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Variant" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.Variant.value">
      <path value="Genomic_variant_result.Variant.value" />
      <short value="Variant" />
      <definition value="Description of the variation at the genomic level following the HGVS nomenclature." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Variant.value" />
        <min value="0" />
        <max value="1" />
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      <type>
        <code value="BackboneElement" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Structured_variant">
      <path value="Genomic_variant_result.Structured_variant" />
      <short value="Structured variant" />
      <definition value="Structured description of the genomic variant." />
      <min value="0" />
      <max value="*" />
      <base>
        <path value="Genomic_variant_result.Structured_variant" />
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        <max value="*" />
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      <type>
        <code value="BackboneElement" />
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      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Transcript">
      <path value="Genomic_variant_result.Transcript" />
      <short value="Transcript" />
      <definition value="Structured details about the transcript which is potentially affected by the variant." />
      <min value="0" />
      <max value="*" />
      <base>
        <path value="Genomic_variant_result.Transcript" />
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        <max value="*" />
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        <code value="BackboneElement" />
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      <mustSupport value="false" />
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    </element>
    <element id="Genomic_variant_result.Transcript.Transcript_reference_sequence">
      <path value="Genomic_variant_result.Transcript.Transcript_reference_sequence" />
      <short value="Transcript reference sequence" />
      <definition value="Structured details about the transcribed reference sequence." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Transcript_reference_sequence" />
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        <code value="BackboneElement" />
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      <mustSupport value="false" />
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    </element>
    <element id="Genomic_variant_result.Transcript.DNA_region_name">
      <path value="Genomic_variant_result.Transcript.DNA_region_name" />
      <short value="DNA region name" />
      <definition value="The human readable name for the region of interest." />
      <min value="0" />
      <max value="*" />
      <base>
        <path value="Genomic_variant_result.Transcript.DNA_region_name" />
        <min value="0" />
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    </element>
    <element id="Genomic_variant_result.Transcript.DNA_region_name.value">
      <path value="Genomic_variant_result.Transcript.DNA_region_name.value" />
      <short value="DNA region name" />
      <definition value="The human readable name for the region of interest." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.DNA_region_name.value" />
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      <type>
        <code value="CodeableConcept" />
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      <mustSupport value="false" />
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    </element>
    <element id="Genomic_variant_result.Transcript.Distance_from_splicing_site">
      <path value="Genomic_variant_result.Transcript.Distance_from_splicing_site" />
      <short value="Distance from splicing site" />
      <definition value="Distance in nucleotides between mutation and exon–intron junction." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Distance_from_splicing_site" />
        <min value="0" />
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      </base>
    </element>
    <element id="Genomic_variant_result.Transcript.Distance_from_splicing_site.value">
      <path value="Genomic_variant_result.Transcript.Distance_from_splicing_site.value" />
      <short value="Distance from splicing site" />
      <definition value="Distance in nucleotides between mutation and exon–intron junction." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Distance_from_splicing_site.value" />
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      <type>
        <code value="Quantity" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Transcript.DNA_change">
      <path value="Genomic_variant_result.Transcript.DNA_change" />
      <short value="DNA change" />
      <definition value="Description of the variation at the DNA level following the HGVS nomenclature." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.DNA_change" />
        <min value="0" />
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    </element>
    <element id="Genomic_variant_result.Transcript.DNA_change.value">
      <path value="Genomic_variant_result.Transcript.DNA_change.value" />
      <short value="DNA change" />
      <definition value="Description of the variation at the DNA level following the HGVS nomenclature." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.DNA_change.value" />
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      <type>
        <code value="BackboneElement" />
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      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Transcript.Amino_acid_change">
      <path value="Genomic_variant_result.Transcript.Amino_acid_change" />
      <short value="Amino acid change" />
      <definition value="Description of the variation at the protein level following the HGVS nomenclature." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Amino_acid_change" />
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      </base>
    </element>
    <element id="Genomic_variant_result.Transcript.Amino_acid_change.value">
      <path value="Genomic_variant_result.Transcript.Amino_acid_change.value" />
      <short value="Amino acid change" />
      <definition value="Description of the variation at the protein level following the HGVS nomenclature." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Amino_acid_change.value" />
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        <code value="BackboneElement" />
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      <mustSupport value="false" />
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    </element>
    <element id="Genomic_variant_result.Transcript.Amino_acid_change_type">
      <path value="Genomic_variant_result.Transcript.Amino_acid_change_type" />
      <short value="Amino acid change type" />
      <definition value="Codified type for associated amino acid marker." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Amino_acid_change_type" />
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    </element>
    <element id="Genomic_variant_result.Transcript.Amino_acid_change_type.value_DV_CODED_TEXT">
      <path value="Genomic_variant_result.Transcript.Amino_acid_change_type.value_DV_CODED_TEXT" />
      <short value="Amino acid change type" />
      <definition value="Codified type for associated amino acid marker." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Amino_acid_change_type.value_DV_CODED_TEXT" />
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      <type>
        <code value="CodeableConcept" />
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    <element id="Genomic_variant_result.Transcript.Amino_acid_change_type.value_DV_TEXT">
      <path value="Genomic_variant_result.Transcript.Amino_acid_change_type.value_DV_TEXT" />
      <short value="Amino acid change type" />
      <definition value="Codified type for associated amino acid marker." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Amino_acid_change_type.value_DV_TEXT" />
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      <type>
        <code value="CodeableConcept" />
      </type>
      <mustSupport value="false" />
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      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Transcript.RNA_change">
      <path value="Genomic_variant_result.Transcript.RNA_change" />
      <short value="RNA change" />
      <definition value="Description of the variation at the RNA level following the HGVS nomenclature." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.RNA_change" />
        <min value="0" />
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    </element>
    <element id="Genomic_variant_result.Transcript.RNA_change.value">
      <path value="Genomic_variant_result.Transcript.RNA_change.value" />
      <short value="RNA change" />
      <definition value="Description of the variation at the RNA level following the HGVS nomenclature." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.RNA_change.value" />
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        <code value="BackboneElement" />
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    <element id="Genomic_variant_result.Transcript.Predicted_impact">
      <path value="Genomic_variant_result.Transcript.Predicted_impact" />
      <short value="Predicted impact" />
      <definition value="Estimate of the effects that the variant may have on the transcript." />
      <min value="0" />
      <max value="*" />
      <base>
        <path value="Genomic_variant_result.Transcript.Predicted_impact" />
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    </element>
    <element id="Genomic_variant_result.Transcript.Predicted_impact.Predicted_impact_knowledge_base">
      <path value="Genomic_variant_result.Transcript.Predicted_impact.Predicted_impact_knowledge_base" />
      <short value="Predicted impact knowledge base" />
      <definition value="Structured details about the reference used to calculate the predicted impact." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Predicted_impact.Predicted_impact_knowledge_base" />
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    </element>
    <element id="Genomic_variant_result.Transcript.Predicted_impact.Score">
      <path value="Genomic_variant_result.Transcript.Predicted_impact.Score" />
      <short value="Score" />
      <definition value="The calculated value." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Predicted_impact.Score" />
        <min value="0" />
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    </element>
    <element id="Genomic_variant_result.Transcript.Predicted_impact.Score.value">
      <path value="Genomic_variant_result.Transcript.Predicted_impact.Score.value" />
      <short value="Score" />
      <definition value="The calculated value." />
      <min value="1" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Predicted_impact.Score.value" />
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      <type>
        <code value="Quantity" />
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      <mustSupport value="true" />
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    </element>
    <element id="Genomic_variant_result.Transcript.Predicted_impact.Qualitative_prediction">
      <path value="Genomic_variant_result.Transcript.Predicted_impact.Qualitative_prediction" />
      <short value="Qualitative prediction" />
      <definition value="Human readable version of the predicted impact." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Predicted_impact.Qualitative_prediction" />
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    <element id="Genomic_variant_result.Transcript.Predicted_impact.Qualitative_prediction.value">
      <path value="Genomic_variant_result.Transcript.Predicted_impact.Qualitative_prediction.value" />
      <short value="Qualitative prediction" />
      <definition value="Human readable version of the predicted impact." />
      <min value="0" />
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      <base>
        <path value="Genomic_variant_result.Transcript.Predicted_impact.Qualitative_prediction.value" />
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      <type>
        <code value="CodeableConcept" />
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      <mustSupport value="false" />
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    </element>
    <element id="Genomic_variant_result.Transcript.Functional_impact">
      <path value="Genomic_variant_result.Transcript.Functional_impact" />
      <short value="Functional impact" />
      <definition value="Interpretation of the variation linked to a specific paper." />
      <min value="0" />
      <max value="*" />
      <base>
        <path value="Genomic_variant_result.Transcript.Functional_impact" />
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        <code value="BackboneElement" />
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      <mustSupport value="false" />
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    </element>
    <element id="Genomic_variant_result.Transcript.Functional_impact.Impact">
      <path value="Genomic_variant_result.Transcript.Functional_impact.Impact" />
      <short value="Impact" />
      <definition value="Single word or phrase describing the reported impact of the specific variant." />
      <min value="1" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Functional_impact.Impact" />
        <min value="1" />
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    </element>
    <element id="Genomic_variant_result.Transcript.Functional_impact.Impact.value">
      <path value="Genomic_variant_result.Transcript.Functional_impact.Impact.value" />
      <short value="Impact" />
      <definition value="Single word or phrase describing the reported impact of the specific variant." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Functional_impact.Impact.value" />
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      <type>
        <code value="CodeableConcept" />
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      <mustSupport value="false" />
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    </element>
    <element id="Genomic_variant_result.Transcript.Functional_impact.Source">
      <path value="Genomic_variant_result.Transcript.Functional_impact.Source" />
      <short value="Source" />
      <definition value="The reference to the specific research paper." />
      <min value="0" />
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      <base>
        <path value="Genomic_variant_result.Transcript.Functional_impact.Source" />
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        <code value="BackboneElement" />
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    </element>
    <element id="Genomic_variant_result.Transcript.Gene">
      <path value="Genomic_variant_result.Transcript.Gene" />
      <short value="Gene" />
      <definition value="Structured details about the gene carrying the variant." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Gene" />
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      <type>
        <code value="BackboneElement" />
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      <mustSupport value="false" />
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    </element>
    <element id="Genomic_variant_result.Transcript.Gene.Gene_symbol">
      <path value="Genomic_variant_result.Transcript.Gene.Gene_symbol" />
      <short value="Gene symbol" />
      <definition value="The official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name." />
      <min value="1" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Gene.Gene_symbol" />
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    </element>
    <element id="Genomic_variant_result.Transcript.Gene.Gene_symbol.value">
      <path value="Genomic_variant_result.Transcript.Gene.Gene_symbol.value" />
      <short value="Gene symbol" />
      <definition value="The official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Gene.Gene_symbol.value" />
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    <element id="Genomic_variant_result.Transcript.Gene.Gene_name">
      <path value="Genomic_variant_result.Transcript.Gene.Gene_name" />
      <short value="Gene name" />
      <definition value="The full gene name approved by the HGNC that conveys the character or function of the gene." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Gene.Gene_name" />
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    </element>
    <element id="Genomic_variant_result.Transcript.Gene.Gene_name.value">
      <path value="Genomic_variant_result.Transcript.Gene.Gene_name.value" />
      <short value="Gene name" />
      <definition value="The full gene name approved by the HGNC that conveys the character or function of the gene." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Gene.Gene_name.value" />
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      <type>
        <code value="CodeableConcept" />
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      <mustSupport value="false" />
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    <element id="Genomic_variant_result.Transcript.Gene.Copy_number_overlap">
      <path value="Genomic_variant_result.Transcript.Gene.Copy_number_overlap" />
      <short value="Copy number overlap" />
      <definition value="The fraction of gene region covered by copy number." />
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      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Gene.Copy_number_overlap" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.Transcript.Gene.Copy_number_overlap.value">
      <path value="Genomic_variant_result.Transcript.Gene.Copy_number_overlap.value" />
      <short value="Copy number overlap" />
      <definition value="The fraction of gene region covered by copy number." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Gene.Copy_number_overlap.value" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="Ratio" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Transcript.Gene.Part_of_fusion">
      <path value="Genomic_variant_result.Transcript.Gene.Part_of_fusion" />
      <short value="Part of fusion" />
      <definition value="States if the gene is part of a fusion gene and if it is the first or second part of the fusion gene." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Gene.Part_of_fusion" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.Transcript.Gene.Part_of_fusion.value">
      <path value="Genomic_variant_result.Transcript.Gene.Part_of_fusion.value" />
      <short value="Part of fusion" />
      <definition value="States if the gene is part of a fusion gene and if it is the first or second part of the fusion gene." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Gene.Part_of_fusion.value" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="CodeableConcept" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Transcript.ACMG_classification">
      <path value="Genomic_variant_result.Transcript.ACMG_classification" />
      <short value="ACMG classification" />
      <definition value="The clinical significance according to the ACMG recommendations." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.ACMG_classification" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.Transcript.ACMG_classification.value">
      <path value="Genomic_variant_result.Transcript.ACMG_classification.value" />
      <short value="ACMG classification" />
      <definition value="The clinical significance according to the ACMG recommendations." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.ACMG_classification.value" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="CodeableConcept" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Transcript.Fusion_exon">
      <path value="Genomic_variant_result.Transcript.Fusion_exon" />
      <short value="Fusion exon" />
      <definition value="The number of the exon which is part of the fusion." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Fusion_exon" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.Transcript.Fusion_exon.value">
      <path value="Genomic_variant_result.Transcript.Fusion_exon.value" />
      <short value="Fusion exon" />
      <definition value="The number of the exon which is part of the fusion." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Transcript.Fusion_exon.value" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="Quantity" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Best_transcript_candidate">
      <path value="Genomic_variant_result.Best_transcript_candidate" />
      <short value="Best transcript candidate" />
      <definition value="The ID of the transcript with the highest predicted impact." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Best_transcript_candidate" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.Best_transcript_candidate.value">
      <path value="Genomic_variant_result.Best_transcript_candidate.value" />
      <short value="Best transcript candidate" />
      <definition value="The ID of the transcript with the highest predicted impact." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Best_transcript_candidate.value" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="CodeableConcept" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Conservation">
      <path value="Genomic_variant_result.Conservation" />
      <short value="Conservation" />
      <definition value="Structured details about the evolutionary conservation." />
      <min value="0" />
      <max value="*" />
      <base>
        <path value="Genomic_variant_result.Conservation" />
        <min value="0" />
        <max value="*" />
      </base>
      <type>
        <code value="BackboneElement" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Conservation.Conservation_score_knowledge_base">
      <path value="Genomic_variant_result.Conservation.Conservation_score_knowledge_base" />
      <short value="Conservation score knowledge base" />
      <definition value="Structured details about the reference used to calculate the conservation score." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Conservation.Conservation_score_knowledge_base" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="BackboneElement" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Conservation.Score">
      <path value="Genomic_variant_result.Conservation.Score" />
      <short value="Score" />
      <definition value="The conservation score." />
      <min value="1" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Conservation.Score" />
        <min value="1" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.Conservation.Score.value">
      <path value="Genomic_variant_result.Conservation.Score.value" />
      <short value="Score" />
      <definition value="The conservation score." />
      <min value="1" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Conservation.Score.value" />
        <min value="1" />
        <max value="1" />
      </base>
      <type>
        <code value="Quantity" />
      </type>
      <mustSupport value="true" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Read_depth">
      <path value="Genomic_variant_result.Read_depth" />
      <short value="Read depth" />
      <definition value="The total number of reads mapped at this specific location." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Read_depth" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.Read_depth.value">
      <path value="Genomic_variant_result.Read_depth.value" />
      <short value="Read depth" />
      <definition value="The total number of reads mapped at this specific location." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Read_depth.value" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="Quantity" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Allele_depth">
      <path value="Genomic_variant_result.Allele_depth" />
      <short value="Allele depth" />
      <definition value="The number of reads that support the reported variant." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Allele_depth" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.Allele_depth.value">
      <path value="Genomic_variant_result.Allele_depth.value" />
      <short value="Allele depth" />
      <definition value="The number of reads that support the reported variant." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Allele_depth.value" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="Quantity" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Allele_frequency">
      <path value="Genomic_variant_result.Allele_frequency" />
      <short value="Allele frequency" />
      <definition value="The relative frequency of an allele at a particular locus." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Allele_frequency" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.Allele_frequency.value">
      <path value="Genomic_variant_result.Allele_frequency.value" />
      <short value="Allele frequency" />
      <definition value="The relative frequency of an allele at a particular locus." />
      <min value="1" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Allele_frequency.value" />
        <min value="1" />
        <max value="1" />
      </base>
      <type>
        <code value="Quantity" />
      </type>
      <mustSupport value="true" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Population_allele_frequency_details">
      <path value="Genomic_variant_result.Population_allele_frequency_details" />
      <short value="Population allele frequency details" />
      <definition value="The relative frequency of a particular allele in the population." />
      <min value="0" />
      <max value="*" />
      <base>
        <path value="Genomic_variant_result.Population_allele_frequency_details" />
        <min value="0" />
        <max value="*" />
      </base>
      <type>
        <code value="BackboneElement" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Population_allele_frequency_details.Population_allele_frequency_knowledge_base">
      <path value="Genomic_variant_result.Population_allele_frequency_details.Population_allele_frequency_knowledge_base" />
      <short value="Population allele frequency knowledge base" />
      <definition value="Structured details about the database used to calculate the allele frequency." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Population_allele_frequency_details.Population_allele_frequency_knowledge_base" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="BackboneElement" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Population_allele_frequency_details.Population_allele_frequency">
      <path value="Genomic_variant_result.Population_allele_frequency_details.Population_allele_frequency" />
      <short value="Population allele frequency" />
      <definition value="The population allele frequency." />
      <min value="1" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Population_allele_frequency_details.Population_allele_frequency" />
        <min value="1" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.Population_allele_frequency_details.Population_allele_frequency.value">
      <path value="Genomic_variant_result.Population_allele_frequency_details.Population_allele_frequency.value" />
      <short value="Population allele frequency" />
      <definition value="The population allele frequency." />
      <min value="1" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Population_allele_frequency_details.Population_allele_frequency.value" />
        <min value="1" />
        <max value="1" />
      </base>
      <type>
        <code value="Quantity" />
      </type>
      <mustSupport value="true" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.VCF_quality_filter">
      <path value="Genomic_variant_result.VCF_quality_filter" />
      <short value="VCF quality filter" />
      <definition value="Structured details about the quality filters that have been applied to the data." />
      <min value="0" />
      <max value="*" />
      <base>
        <path value="Genomic_variant_result.VCF_quality_filter" />
        <min value="0" />
        <max value="*" />
      </base>
      <type>
        <code value="BackboneElement" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.VCF_quality_filter.Filter_name">
      <path value="Genomic_variant_result.VCF_quality_filter.Filter_name" />
      <short value="Filter name" />
      <definition value="Name of the quality filter." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.VCF_quality_filter.Filter_name" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.VCF_quality_filter.Filter_name.value">
      <path value="Genomic_variant_result.VCF_quality_filter.Filter_name.value" />
      <short value="Filter name" />
      <definition value="Name of the quality filter." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.VCF_quality_filter.Filter_name.value" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="CodeableConcept" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.VCF_quality_filter.Description">
      <path value="Genomic_variant_result.VCF_quality_filter.Description" />
      <short value="Description" />
      <definition value="Quality filter extended description." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.VCF_quality_filter.Description" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.VCF_quality_filter.Description.value">
      <path value="Genomic_variant_result.VCF_quality_filter.Description.value" />
      <short value="Description" />
      <definition value="Quality filter extended description." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.VCF_quality_filter.Description.value" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="CodeableConcept" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.VCF_quality_filter.Filter_passed">
      <path value="Genomic_variant_result.VCF_quality_filter.Filter_passed" />
      <short value="Filter passed" />
      <definition value="Did the variant pass the quality filter?" />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.VCF_quality_filter.Filter_passed" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.VCF_quality_filter.Filter_passed.value">
      <path value="Genomic_variant_result.VCF_quality_filter.Filter_passed.value" />
      <short value="Filter passed" />
      <definition value="Did the variant pass the quality filter?" />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.VCF_quality_filter.Filter_passed.value" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="boolean" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Strand_bias_ratio">
      <path value="Genomic_variant_result.Strand_bias_ratio" />
      <short value="Strand bias ratio" />
      <definition value="The ratio of the strand bias." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Strand_bias_ratio" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.Strand_bias_ratio.value">
      <path value="Genomic_variant_result.Strand_bias_ratio.value" />
      <short value="Strand bias ratio" />
      <definition value="The ratio of the strand bias." />
      <min value="1" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Strand_bias_ratio.value" />
        <min value="1" />
        <max value="1" />
      </base>
      <type>
        <code value="Quantity" />
      </type>
      <mustSupport value="true" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Strand_bias_p_value">
      <path value="Genomic_variant_result.Strand_bias_p_value" />
      <short value="Strand bias p-value" />
      <definition value="The Phred-scaled p-value of the strand bias." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Strand_bias_p_value" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.Strand_bias_p_value.value">
      <path value="Genomic_variant_result.Strand_bias_p_value.value" />
      <short value="Strand bias p-value" />
      <definition value="The Phred-scaled p-value of the strand bias." />
      <min value="1" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Strand_bias_p_value.value" />
        <min value="1" />
        <max value="1" />
      </base>
      <type>
        <code value="Quantity" />
      </type>
      <mustSupport value="true" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Genotype">
      <path value="Genomic_variant_result.Genotype" />
      <short value="Genotype" />
      <definition value="Genotype encoded as allele values." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Genotype" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.Genotype.value">
      <path value="Genomic_variant_result.Genotype.value" />
      <short value="Genotype" />
      <definition value="Genotype encoded as allele values." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Genotype.value" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="CodeableConcept" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Allelic_state">
      <path value="Genomic_variant_result.Allelic_state" />
      <short value="Allelic state" />
      <definition value="The level of occurrence of a single DNA marker within a set of chromosomes." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Allelic_state" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.Allelic_state.value_DV_CODED_TEXT">
      <path value="Genomic_variant_result.Allelic_state.value_DV_CODED_TEXT" />
      <short value="Allelic state" />
      <definition value="The level of occurrence of a single DNA marker within a set of chromosomes." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Allelic_state.value_DV_CODED_TEXT" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="CodeableConcept" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Allelic_state.value_DV_TEXT">
      <path value="Genomic_variant_result.Allelic_state.value_DV_TEXT" />
      <short value="Allelic state" />
      <definition value="The level of occurrence of a single DNA marker within a set of chromosomes." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Allelic_state.value_DV_TEXT" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="CodeableConcept" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Genotype_quality">
      <path value="Genomic_variant_result.Genotype_quality" />
      <short value="Genotype quality" />
      <definition value="Conditional genotype quality, encoded as a Phred quality." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Genotype_quality" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.Genotype_quality.value">
      <path value="Genomic_variant_result.Genotype_quality.value" />
      <short value="Genotype quality" />
      <definition value="Conditional genotype quality, encoded as a Phred quality." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Genotype_quality.value" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="Quantity" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Genotype_probability">
      <path value="Genomic_variant_result.Genotype_probability" />
      <short value="Genotype probability" />
      <definition value="A comma separated list of the log10-scaled genotype likelihoods for all possible genotypes, given the reference and the alternate alleles." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Genotype_probability" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.Genotype_probability.value">
      <path value="Genomic_variant_result.Genotype_probability.value" />
      <short value="Genotype probability" />
      <definition value="A comma separated list of the log10-scaled genotype likelihoods for all possible genotypes, given the reference and the alternate alleles." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Genotype_probability.value" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="CodeableConcept" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Specimen_identifier">
      <path value="Genomic_variant_result.Specimen_identifier" />
      <short value="Specimen identifier" />
      <definition value="Identification of the specimen used for the genomic result." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Specimen_identifier" />
        <min value="0" />
        <max value="1" />
      </base>
    </element>
    <element id="Genomic_variant_result.Specimen_identifier.value_DV_IDENTIFIER">
      <path value="Genomic_variant_result.Specimen_identifier.value_DV_IDENTIFIER" />
      <short value="Specimen identifier" />
      <definition value="Identification of the specimen used for the genomic result." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Specimen_identifier.value_DV_IDENTIFIER" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="BackboneElement" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Specimen_identifier.value_DV_URI">
      <path value="Genomic_variant_result.Specimen_identifier.value_DV_URI" />
      <short value="Specimen identifier" />
      <definition value="Identification of the specimen used for the genomic result." />
      <min value="0" />
      <max value="1" />
      <base>
        <path value="Genomic_variant_result.Specimen_identifier.value_DV_URI" />
        <min value="0" />
        <max value="1" />
      </base>
      <type>
        <code value="string" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
    <element id="Genomic_variant_result.Additional_details">
      <path value="Genomic_variant_result.Additional_details" />
      <short value="Additional details" />
      <definition value="Additional details to be captured." />
      <min value="0" />
      <max value="*" />
      <base>
        <path value="Genomic_variant_result.Additional_details" />
        <min value="0" />
        <max value="*" />
      </base>
      <type>
        <code value="BackboneElement" />
      </type>
      <mustSupport value="false" />
      <isModifier value="false" />
      <isSummary value="true" />
    </element>
  </snapshot>
</StructureDefinition>

name : Genomicvariantresult

{

}

<name value="Genomicvariantresult" />