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VARIANT - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CV21993 and autosomal recessive nonsyndromic deafness 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • 6 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 3  (DOID:0110488)
  • 1 papers in RGD have been used to annotate CV21993
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive nonsyndromic hearing loss 3
  • Original References(s): PMID:11735029 PMID:16199547 PMID:17546645 PMID:26763877 PMID:28492532


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