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GENE - TERM ANNOTATION REPORT

150 Annotations Found.

An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14705230 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10396220 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10401572 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:26795593 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10401569 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10397698 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13468352 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:22013194 PMID:24904429 PMID:27466704 PMID:27602407 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13530172 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13525797 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:23934111 PMID:25741868 PMID:27479843 PMID:31105003


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26900140 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13517339 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532 PMID:31780880


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12843850 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659819 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:18414213 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8601403 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:20437616 PMID:25262651 PMID:25741868 PMID:27864847 PMID:28133863 PMID:28492532 PMID:28973083 PMID:29186148 PMID:35104249


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10396228 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532 PMID:35104249


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13620547 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691762 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:25959266 PMID:26467025 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8601396 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:11690625 PMID:14534157 PMID:14985406 PMID:20119593 PMID:23360469 PMID:23692823 PMID:25741868 PMID:25982755 PMID:27779742 PMID:28492532 PMID:3360469


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10050224 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28399683 PMID:28492532 PMID:29056246 PMID:31199083 PMID:35104249


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151236103 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8597511 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:14534157 PMID:18483067 PMID:19453707 PMID:24375629 PMID:24586341 PMID:25959266 PMID:26138355 PMID:26704558 PMID:27535030 PMID:28492532 PMID:28717674 PMID:29263209 PMID:31152295 PMID:35104249 PMID:9425895 PMID:9872318


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8597514 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:11572947 PMID:17872363 PMID:22169383 PMID:22455920 PMID:24375629 PMID:25741868 PMID:25959266 PMID:28492532 PMID:35104249


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10396224 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:12754513 PMID:22275249 PMID:24318194 PMID:25741868 PMID:25880994 PMID:28492532 PMID:29760947 PMID:31152295 PMID:31832524 PMID:32139178 PMID:32573669 PMID:32581362 PMID:32917465 PMID:34711204 PMID:35104249


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10396227 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532 PMID:35104249


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10397655 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:10684873 PMID:11572947 PMID:12742592 PMID:14534157 PMID:17872363 PMID:25741868 PMID:27602407 PMID:29655203 PMID:35104249 PMID:9836639


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151732253 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:329352254 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12913531 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11631859 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8591062 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:22275249 PMID:22926866 PMID:23621294 PMID:23692823 PMID:25741868 PMID:25959266 PMID:27535030 PMID:27602407 PMID:27779742 PMID:28492532 PMID:30185235 PMID:32362866 PMID:34354098 PMID:34395220


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155697463 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12843033 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12894801 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:14534157 PMID:23692823 PMID:25741868 PMID:27779742 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155720534 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13821607 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13830513 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691752 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15187441 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691759 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15130093 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151876302 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12846584 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13828301 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659821 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:18414213 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21068174 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9693008 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12894346 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11634216 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25959266 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659816 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13830746 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10396203 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155691224 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691750 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127281161 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691768 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38497906 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127312840 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10396199 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532 PMID:29358611


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659824 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:18414213 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155705758 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11640169 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12880804 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15128863 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10397662 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532 PMID:29655203


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8601428 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:18353052 PMID:22275249 PMID:23440208 PMID:25741868 PMID:25959266 PMID:25982755 PMID:27779742 PMID:28492532 PMID:28717674 PMID:29056246 PMID:30440138 PMID:31440733 PMID:31512412


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10396204 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10050467 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12843291 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10396215 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38597966 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15120983 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155743456 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13532822 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691751 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10406446 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:26795593


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155742584 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691767 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10397642 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691765 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13830772 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:17475800 PMID:23360469 PMID:23708187 PMID:24107868 PMID:25740509 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10406921 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8604351 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:18353052 PMID:18414213 PMID:22275249 PMID:22455920 PMID:23440208 PMID:24318194 PMID:25741868 PMID:25982755 PMID:26993267 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10396194 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11614068 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127272694 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38477369 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691774 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10396202 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15122613 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691766 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691769 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10397684 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:23621294 PMID:24107868 PMID:25741868 PMID:25959266 PMID:26007637 PMID:27334371 PMID:28492532 PMID:29383681


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691764 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659815 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:18414213 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126767568 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659823 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9693007 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14710302 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12842557 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10396239 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10050119 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151729925 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25959266


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659820 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659811 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13830447 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10396193 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13830616 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10396200 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13620655 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13828943 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10396205 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659817 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:18414213 PMID:25741868 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13805497 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691770 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10052600 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155669217 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659809 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:18414213 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13539048 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691760 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8691753 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156358913 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155721896 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13464649 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659813 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:18414213 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13807457 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13822521 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13822669 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532 PMID:31199083


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38481546 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38463192 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155748172 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8601435 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:14534157 PMID:23692823 PMID:27779742 PMID:27888506 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155739832 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156089439 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10396208 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:12742592 PMID:25741868 PMID:25959266 PMID:26070303 PMID:28492532 PMID:29314763 PMID:30552426 PMID:31418850 PMID:32770121 PMID:33333793


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155985490 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11634218 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25959266 PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10397651 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:18515377 PMID:24318194 PMID:25741868 PMID:27861786 PMID:28492532 PMID:29390993 PMID:35104249


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13479670 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:23934111 PMID:25740509 PMID:25741868 PMID:28492532 PMID:28628100 PMID:28867141 PMID:33754465 PMID:35104249


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11634246 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25959266 PMID:35104249


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10396201 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532 PMID:35104249


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8601398 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:19380078 PMID:25741868 PMID:28492532 PMID:35104249


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10396237 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532 PMID:35104249


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659812 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:18414213 PMID:21685056 PMID:26467025 PMID:28492532 PMID:35104249


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12838377 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532 PMID:35104249


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8601412 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:18414213 PMID:20437616 PMID:25741868 PMID:26467025 PMID:28492532 PMID:35104249


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14703901 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155933980 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150332919 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13830388 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151733109 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532 PMID:31069529


  • An association has been curated linking KCNQ2 and genetic disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:153349825 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 5 papers in RGD have been used to annotate KCNQ2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


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