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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking VAMP1 and Congenital Myasthenic Syndrome 25 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 2 RGD objects have been annotated to Congenital Myasthenic Syndrome 25  (DOID:9004718)
  • 5 papers in RGD have been used to annotate VAMP1


    • An association has been curated linking VAMP1 and Congenital Myasthenic Syndrome 25 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:41407209 (Homo sapiens)
  • 2 RGD objects have been annotated to Congenital Myasthenic Syndrome 25  (DOID:9004718)
  • 5 papers in RGD have been used to annotate VAMP1
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 25, presynaptic
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking VAMP1 and Congenital Myasthenic Syndrome 25 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:14393082 (Homo sapiens)
  • 2 RGD objects have been annotated to Congenital Myasthenic Syndrome 25  (DOID:9004718)
  • 5 papers in RGD have been used to annotate VAMP1
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 25, presynaptic
  • Original References(s): PMID:25741868 PMID:28168212 PMID:28492532


    • An association has been curated linking VAMP1 and Congenital Myasthenic Syndrome 25 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:15143190 (Homo sapiens)
  • 2 RGD objects have been annotated to Congenital Myasthenic Syndrome 25  (DOID:9004718)
  • 5 papers in RGD have been used to annotate VAMP1
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 25, presynaptic
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking VAMP1 and Congenital Myasthenic Syndrome 25 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:401830156 (Homo sapiens)
  • 2 RGD objects have been annotated to Congenital Myasthenic Syndrome 25  (DOID:9004718)
  • 5 papers in RGD have been used to annotate VAMP1
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 25, presynaptic
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


    • An association has been curated linking VAMP1 and Congenital Myasthenic Syndrome 25 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:14393084|RGD:14393085 (Homo sapiens) & RGD:14393084|RGD:14393085 (Homo sapiens)
  • 2 RGD objects have been annotated to Congenital Myasthenic Syndrome 25  (DOID:9004718)
  • 5 papers in RGD have been used to annotate VAMP1
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 25, presynaptic
  • Original References(s): PMID:28600779


    • An association has been curated linking VAMP1 and Congenital Myasthenic Syndrome 25 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:13705828|RGD:14393083 (Homo sapiens) & RGD:13705828|RGD:14393083 (Homo sapiens)
  • 2 RGD objects have been annotated to Congenital Myasthenic Syndrome 25  (DOID:9004718)
  • 5 papers in RGD have been used to annotate VAMP1
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 25, presynaptic
  • Original References(s): PMID:28253535


    • An association has been curated linking VAMP1 and Congenital Myasthenic Syndrome 25 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:150470908|RGD:150504604 (Homo sapiens) & RGD:150470908|RGD:150504604 (Homo sapiens)
  • 2 RGD objects have been annotated to Congenital Myasthenic Syndrome 25  (DOID:9004718)
  • 5 papers in RGD have been used to annotate VAMP1
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 25, presynaptic
  • Original References(s): PMID:25741868


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