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GENE - TERM ANNOTATION REPORT

57 Annotations Found.

An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11613841 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11631598 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11665420 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11629236 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11630129 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11630834 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627298 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11613975 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11666810 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11632051 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11629817 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11625665 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11628699 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11665913 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11631783 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11630694 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11628047 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11665358 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11630891 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11666194 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11666494 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11665332 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11629574 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11665384 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11629746 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11632052 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11629607 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11630578 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11631842 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11628377 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11631053 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b
  • Original References(s): PMID:28492532


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11631261 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b
  • Original References(s): PMID:28492532


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627217 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b
  • Original References(s): PMID:28492532


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28877046 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28878817 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28878640 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28878637 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28887121 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28877049 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28876875 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28878642 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15169904 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b
  • Original References(s): PMID:28492532


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28886902 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28887113 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598610 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b
  • Original References(s): PMID:15459172 PMID:16773570 PMID:21940798 PMID:25676666 PMID:25741868 PMID:28492532


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15182662 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b
  • Original References(s): PMID:28492532


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28887116 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28876868 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15145603 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b
  • Original References(s): PMID:28492532


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28876870 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11629686 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b
  • Original References(s): PMID:15459172


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11617605 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b
  • Original References(s): PMID:25741868


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11631087 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2b
  • Original References(s): PMID:25741868


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627434 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2B
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B 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
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking POF1B and primary ovarian insufficiency 2B in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14693382 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 2B  (DOID:0080859)
  • 4 papers in RGD have been used to annotate POF1B
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 2B
  • Original References(s): PMID:25741868


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