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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking FANCF and genetic disease 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:126761074|RGD:151822822|RGD:151861464|RGD:156065486|RGD:156234151|RGD:156283561|RGD:401747904 (Homo sapiens) & RGD:126761074|RGD:151822822|RGD:151861464|RGD:156065486|RGD:156234151|RGD:156283561|RGD:401747904 (Homo sapiens) & RGD:126761074|RGD:151822822|RGD:151861464|RGD:156065486|RGD:156234151|RGD:156283561|RGD:401747904 (Homo sapiens) & RGD:126761074|RGD:151822822|RGD:151861464|RGD:156065486|RGD:156234151|RGD:156283561|RGD:401747904 (Homo sapiens) & RGD:126761074|RGD:151822822|RGD:151861464|RGD:156065486|RGD:156234151|RGD:156283561|RGD:401747904 (Homo sapiens) & RGD:126761074|RGD:151822822|RGD:151861464|RGD:156065486|RGD:156234151|RGD:156283561|RGD:401747904 (Homo sapiens) & RGD:126761074|RGD:151822822|RGD:151861464|RGD:156065486|RGD:156234151|RGD:156283561|RGD:401747904 (Homo sapiens)
  • 28217 RGD objects have been annotated to genetic disease  (DOID:630)
  • 13 papers in RGD have been used to annotate FANCF
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


    • An association has been curated linking FANCF and genetic disease 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:126730348|RGD:126736487|RGD:126918887|RGD:126922910|RGD:13492513|RGD:151853791|RGD:38456601 (Homo sapiens) & RGD:126730348|RGD:126736487|RGD:126918887|RGD:126922910|RGD:13492513|RGD:151853791|RGD:38456601 (Homo sapiens) & RGD:126730348|RGD:126736487|RGD:126918887|RGD:126922910|RGD:13492513|RGD:151853791|RGD:38456601 (Homo sapiens) & RGD:126730348|RGD:126736487|RGD:126918887|RGD:126922910|RGD:13492513|RGD:151853791|RGD:38456601 (Homo sapiens) & RGD:126730348|RGD:126736487|RGD:126918887|RGD:126922910|RGD:13492513|RGD:151853791|RGD:38456601 (Homo sapiens) & RGD:126730348|RGD:126736487|RGD:126918887|RGD:126922910|RGD:13492513|RGD:151853791|RGD:38456601 (Homo sapiens) & RGD:126730348|RGD:126736487|RGD:126918887|RGD:126922910|RGD:13492513|RGD:151853791|RGD:38456601 (Homo sapiens)
  • 28217 RGD objects have been annotated to genetic disease  (DOID:630)
  • 13 papers in RGD have been used to annotate FANCF
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FANCF and genetic disease 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:155924100|RGD:156156889|RGD:156292930|RGD:401745799|RGD:405762381|RGD:405762394|RGD:405762401|RGD:405762408|RGD:407492440|RGD:407492443 (Homo sapiens) & RGD:155924100|RGD:156156889|RGD:156292930|RGD:401745799|RGD:405762381|RGD:405762394|RGD:405762401|RGD:405762408|RGD:407492440|RGD:407492443 (Homo sapiens) & RGD:155924100|RGD:156156889|RGD:156292930|RGD:401745799|RGD:405762381|RGD:405762394|RGD:405762401|RGD:405762408|RGD:407492440|RGD:407492443 (Homo sapiens) & RGD:155924100|RGD:156156889|RGD:156292930|RGD:401745799|RGD:405762381|RGD:405762394|RGD:405762401|RGD:405762408|RGD:407492440|RGD:407492443 (Homo sapiens) & RGD:155924100|RGD:156156889|RGD:156292930|RGD:401745799|RGD:405762381|RGD:405762394|RGD:405762401|RGD:405762408|RGD:407492440|RGD:407492443 (Homo sapiens) & RGD:155924100|RGD:156156889|RGD:156292930|RGD:401745799|RGD:405762381|RGD:405762394|RGD:405762401|RGD:405762408|RGD:407492440|RGD:407492443 (Homo sapiens) & RGD:155924100|RGD:156156889|RGD:156292930|RGD:401745799|RGD:405762381|RGD:405762394|RGD:405762401|RGD:405762408|RGD:407492440|RGD:407492443 (Homo sapiens) & RGD:155924100|RGD:156156889|RGD:156292930|RGD:401745799|RGD:405762381|RGD:405762394|RGD:405762401|RGD:405762408|RGD:407492440|RGD:407492443 (Homo sapiens) & RGD:155924100|RGD:156156889|RGD:156292930|RGD:401745799|RGD:405762381|RGD:405762394|RGD:405762401|RGD:405762408|RGD:407492440|RGD:407492443 (Homo sapiens) & RGD:155924100|RGD:156156889|RGD:156292930|RGD:401745799|RGD:405762381|RGD:405762394|RGD:405762401|RGD:405762408|RGD:407492440|RGD:407492443 (Homo sapiens)
  • 28217 RGD objects have been annotated to genetic disease  (DOID:630)
  • 13 papers in RGD have been used to annotate FANCF
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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