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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking LOC126861231 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:155685921|RGD:155686055|RGD:156215230|RGD:156231973 (Homo sapiens) & RGD:155685921|RGD:155686055|RGD:156215230|RGD:156231973 (Homo sapiens) & RGD:155685921|RGD:155686055|RGD:156215230|RGD:156231973 (Homo sapiens) & RGD:155685921|RGD:155686055|RGD:156215230|RGD:156231973 (Homo sapiens)
  • 23840 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate LOC126861231
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


    • An association has been curated linking LOC126861231 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:126757163|RGD:151716030|RGD:151861243|RGD:155703011|RGD:156171632|RGD:26913817 (Homo sapiens) & RGD:126757163|RGD:151716030|RGD:151861243|RGD:155703011|RGD:156171632|RGD:26913817 (Homo sapiens) & RGD:126757163|RGD:151716030|RGD:151861243|RGD:155703011|RGD:156171632|RGD:26913817 (Homo sapiens) & RGD:126757163|RGD:151716030|RGD:151861243|RGD:155703011|RGD:156171632|RGD:26913817 (Homo sapiens) & RGD:126757163|RGD:151716030|RGD:151861243|RGD:155703011|RGD:156171632|RGD:26913817 (Homo sapiens) & RGD:126757163|RGD:151716030|RGD:151861243|RGD:155703011|RGD:156171632|RGD:26913817 (Homo sapiens)
  • 23840 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate LOC126861231
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


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