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GENE - TERM ANNOTATION REPORT

129 Annotations Found.

An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:151734674 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:13467885 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:126918580 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:38458288 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:21068127 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:127311082 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:127306385 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:127288532 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:13625246 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:151728801 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:13625247 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:38482755 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:38488124 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:15149649 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:15146465 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:15192508 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:15148017 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:151799214 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:26886369 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:127335815 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:151800156 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:26922131 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:127313584 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:127327449 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156371271 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:38497567 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:127238654 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:13828281 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:13625245 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:127241056 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:38489182 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:127237128 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:13811974 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:13804483 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:14742355 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:21073183 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:14743429 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:14734130 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152079500 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152170728 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152143257 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152140579 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152101115 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152175889 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152160286 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152036755 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152073712 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152062782 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152025986 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152145807 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152077700 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152129837 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152129378 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152146961 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152136403 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152064360 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152173974 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152073071 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152085087 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152074731 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152056138 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152123325 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152031164 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152117525 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152068680 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152056141 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152049923 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152144727 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152044506 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:152982537 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:155997654 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156419212 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:38485427 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:151667476 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:40888103 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: MYASTHENIC SYNDROME, CONGENITAL, 18, WITH INTELLECTUAL DISABILITY AND ATAXIA
  • Original References(s): PMID:25741868 PMID:33147442 PMID:33299146


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:11531301 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:25381298 PMID:25741868 PMID:33299146


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:127244003 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:25741868 PMID:33299146


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:127243278 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:25741868 PMID:28492532 PMID:33299146


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:25317241 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:25741868 PMID:33299146


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:150509304 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:25741868


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:126769437 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:126774019 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:126725571 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156114841 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:151761365 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:151865844 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:151745677 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:151825445 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:151857535 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:151790789 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:150453058 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:25741868 PMID:28492532 PMID:33299146


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:151727423 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:151848060 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:151867269 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:151884206 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:151804105 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:155645276 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:155702658 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156136200 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:13816782 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:151756551 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:155931747 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:155940710 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156406274 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156026957 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:155914704 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156163329 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:155939875 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156067051 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156092834 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156012792 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156136983 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156352967 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:155996964 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156244293 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156387977 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:150453069 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: MYASTHENIC SYNDROME, CONGENITAL, 18, WITH INTELLECTUAL DISABILITY AND ATAXIA
  • Original References(s): PMID:25741868 PMID:28492532 PMID:33299146


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156225626 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156058619 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156176773 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156082502 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:156212650 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:151749786 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: MYASTHENIC SYNDROME, CONGENITAL, 18, WITH INTELLECTUAL DISABILITY AND ATAXIA
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:404982602 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:28492532


  • An association has been curated linking SNAP25 and congenital myasthenic syndrome 18 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:155980827 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 18  (DOID:0110683)
  • 5 papers in RGD have been used to annotate SNAP25
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 18
  • Original References(s): PMID:25741868 PMID:28492532


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