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VARIANT - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CV39001 and sudden infant death syndrome 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
  • 42 RGD objects have been annotated to sudden infant death syndrome  (DOID:9007)
  • 1 papers in RGD have been used to annotate CV39001
  • Curation Notes: ClinVar Annotator: match by term: Sudden Infant Death
  • Original References(s): PMID:18378609 PMID:19808477 PMID:22581653 PMID:25650408 PMID:25741868 PMID:28086167 PMID:28150151 PMID:28492532 PMID:29709244 PMID:30086531 PMID:30193851 PMID:32826072 PMID:32893267


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