Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

252 Annotations Found.

An association has been curated linking CNGB3 and achromatopsia 3 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:13211262 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:17576681 PMID:27479814 PMID:28492532 PMID:28795510 PMID:35672425 PMID:9536098


  • An association has been curated linking CNGB3 and achromatopsia 3 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:8558555 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:10888875 PMID:10958649 PMID:12815043 PMID:15223812 PMID:15657609 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211244 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:12739741 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:8596733 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Total colorblindness with myopia
  • Original References(s): PMID:10888875 PMID:10958649 PMID:12815043 PMID:1347967 PMID:14757870 PMID:15161866 PMID:15657609 PMID:15712225 PMID:16379026 PMID:17265047 PMID:19592100 PMID:23805033 PMID:24033266 PMID:25741868 PMID:25770143 PMID:28041643 PMID:28492532 PMID:28795510 PMID:30718709 PMID:32860008 PMID:33546218 PMID:36909829


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211190 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211187 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13784255 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:22264887 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211226 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211199 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211100 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11549655 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13784077 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15712225 PMID:26106334 PMID:28005958 PMID:28224992 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:127286294 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868


  • An association has been curated linking CNGB3 and achromatopsia 3 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:9688338 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:10041428 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15459792 PMID:15657609 PMID:17576681 PMID:19592100 PMID:20079539 PMID:20574029 PMID:28492532 PMID:28795510 PMID:9536098


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11552417 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211209 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:10041435 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15657609 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:10041538 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:10958649 PMID:12187429 PMID:15657609 PMID:16199547 PMID:24148654 PMID:25741868 PMID:28492532 PMID:28795510 PMID:33546218


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211256 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211218 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13435025 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28041643 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211171 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11607583 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211179 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211186 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28868486 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211126 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211228 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211204 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:12740102 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211165 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:12740072 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:12739256 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211247 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211229 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15657609 PMID:27479814 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211193 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211276 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211215 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211197 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:12739986 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211164 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211181 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211265 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211196 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11608090 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211110 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:12739215 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211120 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211266 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211105 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211264 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211258 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211116 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211158 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:8642841 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211139 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211117 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:16319819 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211221 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211142 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:8646947 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211125 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211180 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211249 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11547114 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13506611 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11547664 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:10041628 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15657609 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11545415 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211097 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:16199547 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11543811 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:9688624 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11604504 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211107 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211135 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:16199547 PMID:28492532 PMID:28795510 PMID:30337596


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11606868 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211211 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211154 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15657609 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211188 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15657609 PMID:28492532 PMID:28795510 PMID:30718709


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211150 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13519831 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15712225 PMID:1572225 PMID:25741868 PMID:26106334


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13787136 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:23776498 PMID:26992781


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13784278 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13792290 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13786712 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211206 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28909691 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:8558559 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15712225 PMID:25474149 PMID:26106334 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28868149 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:12899665 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11545138 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11604194 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:21404203 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28867850 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11604744 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:9692819 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:23776498 PMID:25741868 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11600811 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11604838 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28873002 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28907614 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211198 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15657609 PMID:25205868 PMID:25616768 PMID:26106334 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11603168 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11635937 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28909400 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28906955 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:10041508 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:10958649 PMID:15657609 PMID:16319819 PMID:24148654 PMID:25741868 PMID:27479814 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11606762 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11650755 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11602782 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11601215 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11600100 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11645382 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11601847 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11645894 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28907130 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11598966 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11604635 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11607225 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11599838 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11604500 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11603570 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11599704 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:15164429 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11600827 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11605693 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11604063 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11608576 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28867854 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11600890 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11599012 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11605712 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28906951 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11643914 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11604089 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11648283 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11651117 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:150408981 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11638731 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:14397319 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:15015337 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868


  • An association has been curated linking CNGB3 and achromatopsia 3 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:150408978 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11606245 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11598700 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11548660 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868


  • An association has been curated linking CNGB3 and achromatopsia 3 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:40904315 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11606164 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28867975 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11607902 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13832708 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Total colorblindness with myopia
  • Original References(s): PMID:15223812 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28906769 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28871633 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:15194224 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11606176 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:15129351 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11577705 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11650562 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:15128096 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:15177431 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11658743 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28909226 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11543357 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15712225 PMID:25741868 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28872085 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11602403 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:15163053 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:15174269 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15712225 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:26889057 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:40904316 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:38499993 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28909228 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28907610 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28909027 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28909030 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28907132 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28867848 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28872573 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28909554 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28867689 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28909977 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28906957 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28867979 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28871874 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28907269 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28867973 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:42723022 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211195 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:16199547 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211236 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:17576681 PMID:28041643 PMID:28492532 PMID:28795510 PMID:9536098


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211103 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28341476 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:12740390 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:12357335 PMID:25741868 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:9480340 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Total colorblindness with myopia
  • Original References(s): PMID:15161866 PMID:16379026 PMID:22975760 PMID:22995991 PMID:24504161 PMID:25741868 PMID:28418496 PMID:28492532 PMID:28795510 PMID:30418171 PMID:32869108


  • An association has been curated linking CNGB3 and achromatopsia 3 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:14745045 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25616768 PMID:25741868 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:243063451 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868


  • An association has been curated linking CNGB3 and achromatopsia 3 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:11655600 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:8558556 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:10958649 PMID:15657609 PMID:25205868 PMID:25525159 PMID:25741868 PMID:27874104 PMID:28492532 PMID:28795510 PMID:29186038


  • An association has been curated linking CNGB3 and achromatopsia 3 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:126753442 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:33546218


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211146 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15657609 PMID:25741868 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211155 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:12740220 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211243 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211119 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15657609 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211115 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:151728563 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868


  • An association has been curated linking CNGB3 and achromatopsia 3 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:12739360 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211140 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211183 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:16199547 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211241 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:12739008 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:10888875 PMID:10958649 PMID:15657609 PMID:15712225 PMID:17652762 PMID:20079539 PMID:25558176 PMID:25741868 PMID:28041643 PMID:28492532 PMID:28795510 PMID:29769798


  • An association has been curated linking CNGB3 and achromatopsia 3 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:151752263 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:38467085 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:155737131 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:155736887 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:155736339 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:155728765 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:155736210 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:127242870 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:155726063 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:155736794 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:155737328 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:155736013 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:155724112 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:155799710 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15223812 PMID:25741868


  • An association has been curated linking CNGB3 and achromatopsia 3 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:155729470 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3


  • An association has been curated linking CNGB3 and achromatopsia 3 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:10041403 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15657609 PMID:16199547 PMID:25616768 PMID:25741868 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:14731645 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:16199547 PMID:25741868 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211170 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:16379026 PMID:23805033 PMID:25741868 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211156 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:16199547 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:10041429 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15657609 PMID:16319819 PMID:25741868 PMID:28492532 PMID:28795510 PMID:30418171


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211259 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:16199547 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:21068624 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:16199547 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:12740476 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:16199547 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13784985 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:12739877 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25558076 PMID:25558176 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:12739519 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:16199547 PMID:25558176 PMID:25741868 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28907134 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Total colorblindness with myopia
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211132 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211138 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:26922114 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:14757870 PMID:16379026 PMID:23805033 PMID:24148654 PMID:25741868 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:12739503 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:12740547 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:16199547 PMID:25741868 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211231 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28041643 PMID:28492532 PMID:28795510 PMID:29053603


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211104 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:28795510 PMID:9536098


  • An association has been curated linking CNGB3 and achromatopsia 3 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:28868490 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Total colorblindness with myopia
  • Original References(s): PMID:28492532


  • An association has been curated linking CNGB3 and achromatopsia 3 in Homo sapiens.        

  • The association was inferred from sequence or structural similarity (ISS)
  •  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Cngb3 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: OMIM:262300


  • An association has been curated linking CNGB3 and achromatopsia 3 in Homo sapiens.        

  • The association was inferred from experiment (EXP)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking CNGB3 and achromatopsia 3 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:40906458 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:26992781 PMID:28492532 PMID:32913385


  • An association has been curated linking CNGB3 and achromatopsia 3 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:10041426 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15459792 PMID:15657609 PMID:15712225 PMID:25741868 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211274 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:15657609 PMID:16199547 PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13211242 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:25741868 PMID:28492532 PMID:28795510 PMID:35119454


  • An association has been curated linking CNGB3 and achromatopsia 3 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:15015336 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:10888875 PMID:25741868 PMID:28492532 PMID:31544997 PMID:34703197


  • An association has been curated linking CNGB3 and achromatopsia 3 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:13787042 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532 PMID:28795510


  • An association has been curated linking CNGB3 and achromatopsia 3 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:12740309 (Homo sapiens)
  • 1 RGD objects have been annotated to achromatopsia 3  (DOID:0110008)
  • 10 papers in RGD have been used to annotate CNGB3
  • Curation Notes: ClinVar Annotator: match by term: Achromatopsia 3
  • Original References(s): PMID:28492532 PMID:28795510 PMID:32581362


  • Go Back to source page   Continue to Ontology report