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VARIANT - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CV315669 and Nonsyndromic Sensorineural Hearing Loss 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
  • 29 RGD objects have been annotated to Nonsyndromic Sensorineural Hearing Loss  (DOID:9007966)
  • 0 papers in RGD have been used to annotate CV315669
  • Curation Notes: ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Dominant

  • This annotation was curated on 2020-01-07 07:03:19.0 by RGD . For more information contact us

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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.