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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking SNAP25 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13499313 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:26467025 PMID:28492532


    • An association has been curated linking SNAP25 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13500957|RGD:13625245|RGD:13625246 (Homo sapiens) & RGD:13500957|RGD:13625245|RGD:13625246 (Homo sapiens) & RGD:13500957|RGD:13625245|RGD:13625246 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking SNAP25 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126747131|RGD:126774019|RGD:127288532|RGD:13828281|RGD:15148017|RGD:15149649|RGD:38497567 (Homo sapiens) & RGD:126747131|RGD:126774019|RGD:127288532|RGD:13828281|RGD:15148017|RGD:15149649|RGD:38497567 (Homo sapiens) & RGD:126747131|RGD:126774019|RGD:127288532|RGD:13828281|RGD:15148017|RGD:15149649|RGD:38497567 (Homo sapiens) & RGD:126747131|RGD:126774019|RGD:127288532|RGD:13828281|RGD:15148017|RGD:15149649|RGD:38497567 (Homo sapiens) & RGD:126747131|RGD:126774019|RGD:127288532|RGD:13828281|RGD:15148017|RGD:15149649|RGD:38497567 (Homo sapiens) & RGD:126747131|RGD:126774019|RGD:127288532|RGD:13828281|RGD:15148017|RGD:15149649|RGD:38497567 (Homo sapiens) & RGD:126747131|RGD:126774019|RGD:127288532|RGD:13828281|RGD:15148017|RGD:15149649|RGD:38497567 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


    • An association has been curated linking SNAP25 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13828697|RGD:155714137|RGD:155738003 (Homo sapiens) & RGD:13828697|RGD:155714137|RGD:155738003 (Homo sapiens) & RGD:13828697|RGD:155714137|RGD:155738003 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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