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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking RRAS2 and Noonan syndrome 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:8561053 (Homo sapiens)
  • 71 RGD objects have been annotated to Noonan syndrome  (DOID:3490)
  • 3 papers in RGD have been used to annotate RRAS2
  • Curation Notes: ClinVar Annotator: match by term: Noonan syndrome
  • Original References(s): PMID:25741868 PMID:31130282 PMID:31130285 PMID:8052619


    • An association has been curated linking RRAS2 and Noonan syndrome 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:15014878 (Homo sapiens)
  • 71 RGD objects have been annotated to Noonan syndrome  (DOID:3490)
  • 3 papers in RGD have been used to annotate RRAS2
  • Curation Notes: ClinVar Annotator: match by term: Noonan syndrome
  • Original References(s): PMID:25741868 PMID:31130282


    • An association has been curated linking RRAS2 and Noonan syndrome 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:15014879 (Homo sapiens)
  • 71 RGD objects have been annotated to Noonan syndrome  (DOID:3490)
  • 3 papers in RGD have been used to annotate RRAS2
  • Curation Notes: ClinVar Annotator: match by term: Noonan syndrome
  • Original References(s): PMID:25741868 PMID:28492532 PMID:31130282 PMID:31130285


    • An association has been curated linking RRAS2 and Noonan syndrome 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:15014876|RGD:15014877|RGD:151662853 (Homo sapiens) & RGD:15014876|RGD:15014877|RGD:151662853 (Homo sapiens) & RGD:15014876|RGD:15014877|RGD:151662853 (Homo sapiens)
  • 71 RGD objects have been annotated to Noonan syndrome  (DOID:3490)
  • 3 papers in RGD have been used to annotate RRAS2
  • Curation Notes: ClinVar Annotator: match by term: Noonan syndrome
  • Original References(s): PMID:25741868


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