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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking CPSF1 and Myopia 27 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:25321968 (Homo sapiens)
  • 2 RGD objects have been annotated to Myopia 27  (DOID:9000382)
  • 6 papers in RGD have been used to annotate CPSF1
  • Curation Notes: ClinVar Annotator: match by term: Myopia 27
  • Original References(s): PMID:28492532 PMID:30689892


    • An association has been curated linking CPSF1 and Myopia 27 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 Myopia 27  (DOID:9000382)
  • 6 papers in RGD have been used to annotate CPSF1


    • An association has been curated linking CPSF1 and Myopia 27 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:404998494 (Homo sapiens)
  • 2 RGD objects have been annotated to Myopia 27  (DOID:9000382)
  • 6 papers in RGD have been used to annotate CPSF1
  • Curation Notes: ClinVar Annotator: match by term: Myopia 27
  • Original References(s): PMID:25741868


    • An association has been curated linking CPSF1 and Myopia 27 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:25321957|RGD:25321960|RGD:25321964 (Homo sapiens) & RGD:25321957|RGD:25321960|RGD:25321964 (Homo sapiens) & RGD:25321957|RGD:25321960|RGD:25321964 (Homo sapiens)
  • 2 RGD objects have been annotated to Myopia 27  (DOID:9000382)
  • 6 papers in RGD have been used to annotate CPSF1
  • Curation Notes: ClinVar Annotator: match by term: Myopia 27
  • Original References(s): PMID:30689892


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