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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking LOC126863275 and FG Syndrome 1 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:26922746 (Homo sapiens)
  • 14 RGD objects have been annotated to FG Syndrome 1  (DOID:9007898)
  • 0 papers in RGD have been used to annotate LOC126863275
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 1
  • Original References(s): PMID:28492532


    • An association has been curated linking LOC126863275 and FG Syndrome 1 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:14392927 (Homo sapiens)
  • 14 RGD objects have been annotated to FG Syndrome 1  (DOID:9007898)
  • 0 papers in RGD have been used to annotate LOC126863275
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 1
  • Original References(s): PMID:25741868 PMID:28492532 PMID:34079076 PMID:36271811


    • An association has been curated linking LOC126863275 and FG Syndrome 1 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:13476889 (Homo sapiens)
  • 14 RGD objects have been annotated to FG Syndrome 1  (DOID:9007898)
  • 0 papers in RGD have been used to annotate LOC126863275
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 1
  • Original References(s): PMID:20301719 PMID:28492532 PMID:33057194 PMID:34079076 PMID:35982159 PMID:39825153


    • An association has been curated linking LOC126863275 and FG Syndrome 1 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:40815455 (Homo sapiens)
  • 14 RGD objects have been annotated to FG Syndrome 1  (DOID:9007898)
  • 0 papers in RGD have been used to annotate LOC126863275
  • Curation Notes: ClinVar Annotator: match by term: FG syndrome 1
  • Original References(s): PMID:25741868


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