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VARIANT - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CV32041 and autosomal dominant nonsyndromic deafness 3A 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 autosomal dominant nonsyndromic deafness 3A  (DOID:0110564)
  • 1 papers in RGD have been used to annotate CV32041
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal dominant 3a
  • Original References(s): PMID:10508996 PMID:11698809 PMID:11968091 PMID:12176179 PMID:12746422 PMID:12791041 PMID:12833397 PMID:14985372 PMID:15070423 PMID:15113126 PMID:15146474 PMID:15479191 PMID:15617550 PMID:15855033 PMID:15967879 PMID:16088916 PMID:16125251 PMID:16379542 PMID:16380907 PMID:17146393 PMID:18294064 PMID:18414213 PMID:18570691 PMID:18776652 PMID:18941476 PMID:18983339 PMID:19157576 PMID:19371219 PMID:19465004 PMID:19715472 PMID:19814620 PMID:19929407 PMID:19929408 PMID:20086291 PMID:20563649 PMID:22613756 PMID:22695344 PMID:22975760 PMID:23504403 PMID:23668481 PMID:24033266 PMID:24123366 PMID:24529908 PMID:24840842 PMID:25636251 PMID:25741868 PMID:26059209 PMID:26188157 PMID:26467025 PMID:28492532 PMID:29921236 PMID:3 PMID:30094485 PMID:30303587 PMID:30311386 PMID:30872814 PMID:30989077 PMID:31827275 PMID:33614373 PMID:9139825


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