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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking LOC107988032 and FG Syndrome 2 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:156056653 (Homo sapiens)
  • 2 RGD objects have been annotated to FG Syndrome 2  (DOID:9002387)
  • 0 papers in RGD have been used to annotate LOC107988032
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking LOC107988032 and FG Syndrome 2 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:14702988 (Homo sapiens)
  • 2 RGD objects have been annotated to FG Syndrome 2  (DOID:9002387)
  • 0 papers in RGD have been used to annotate LOC107988032
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking LOC107988032 and FG Syndrome 2 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:12843222 (Homo sapiens)
  • 2 RGD objects have been annotated to FG Syndrome 2  (DOID:9002387)
  • 0 papers in RGD have been used to annotate LOC107988032
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532 PMID:35000503


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