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VARIANT - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CV49152 and Noonan syndrome 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • 2 RGD objects have been annotated to Noonan syndrome 4  (DOID:0060582)
  • 1 papers in RGD have been used to annotate CV49152
  • Curation Notes: ClinVar Annotator: match by term: Noonan syndrome 4
  • Original References(s): PMID:17143282 PMID:17586837 PMID:18854871 PMID:19352411 PMID:20133692 PMID:21340158 PMID:21387466 PMID:22190897 PMID:22465605 PMID:23487764 PMID:24033266 PMID:24803665 PMID:25741868 PMID:26607044 PMID:28492532 PMID:29493581 PMID:33128510 PMID:33771761


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