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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking F9 and X-linked warfarin sensitivity 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 X-linked warfarin sensitivity  (DOID:0080839)
  • 21 papers in RGD have been used to annotate F9


    • An association has been curated linking F9 and X-linked warfarin sensitivity in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627912 (Homo sapiens)
  • 1 RGD objects have been annotated to X-linked warfarin sensitivity  (DOID:0080839)
  • 21 papers in RGD have been used to annotate F9
  • Curation Notes: ClinVar Annotator: match by term: COUMARIN SENSITIVITY, X-LINKED
  • Original References(s): PMID:10094553 PMID:10698280 PMID:25741868 PMID:2773937 PMID:28492532 PMID:8320491


    • An association has been curated linking F9 and X-linked warfarin sensitivity in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8561801 (Homo sapiens)
  • 1 RGD objects have been annotated to X-linked warfarin sensitivity  (DOID:0080839)
  • 21 papers in RGD have been used to annotate F9
  • Curation Notes: ClinVar Annotator: match by term: Warfarin sensitivity, X-linked
  • Original References(s): PMID:9233593


    • An association has been curated linking F9 and X-linked warfarin sensitivity in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21073817 (Homo sapiens)
  • 1 RGD objects have been annotated to X-linked warfarin sensitivity  (DOID:0080839)
  • 21 papers in RGD have been used to annotate F9
  • Curation Notes: ClinVar Annotator: match by term: Warfarin sensitivity, X-linked
  • Original References(s): PMID:28492532 PMID:29450643 PMID:29923114 PMID:30576981 PMID:8833911


    • An association has been curated linking F9 and X-linked warfarin sensitivity in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598584 (Homo sapiens)
  • 1 RGD objects have been annotated to X-linked warfarin sensitivity  (DOID:0080839)
  • 21 papers in RGD have been used to annotate F9
  • Curation Notes: ClinVar Annotator: match by term: COUMARIN SENSITIVITY, X-LINKED
  • Original References(s): PMID:2370049 PMID:25741868 PMID:28492532 PMID:7937052


    • An association has been curated linking F9 and X-linked warfarin sensitivity in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598540 (Homo sapiens)
  • 1 RGD objects have been annotated to X-linked warfarin sensitivity  (DOID:0080839)
  • 21 papers in RGD have been used to annotate F9
  • Curation Notes: ClinVar Annotator: match by term: COUMARIN SENSITIVITY, X-LINKED
  • Original References(s): PMID:19699296 PMID:22639855 PMID:2472424 PMID:25741868 PMID:2762170 PMID:28492532 PMID:2929599 PMID:3262389 PMID:35842956 PMID:3651597 PMID:9525872


    • An association has been curated linking F9 and X-linked warfarin sensitivity in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627300|RGD:15121553|RGD:15121719 (Homo sapiens) & RGD:11627300|RGD:15121553|RGD:15121719 (Homo sapiens) & RGD:11627300|RGD:15121553|RGD:15121719 (Homo sapiens)
  • 1 RGD objects have been annotated to X-linked warfarin sensitivity  (DOID:0080839)
  • 21 papers in RGD have been used to annotate F9
  • Curation Notes: ClinVar Annotator: match by term: COUMARIN SENSITIVITY, X-LINKED
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking F9 and X-linked warfarin sensitivity in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598535 (Homo sapiens)
  • 1 RGD objects have been annotated to X-linked warfarin sensitivity  (DOID:0080839)
  • 21 papers in RGD have been used to annotate F9
  • Curation Notes: ClinVar Annotator: match by term: COUMARIN SENSITIVITY, X-LINKED
  • Original References(s): PMID:19699296 PMID:2066105 PMID:22639855 PMID:24375831 PMID:25741868 PMID:2773937 PMID:28492532 PMID:28722788 PMID:31064749


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