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VARIANT - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CV26129 and hereditary spastic paraplegia 2 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
  • 8 RGD objects have been annotated to hereditary spastic paraplegia 2  (DOID:0110773)
  • 1 papers in RGD have been used to annotate CV26129
  • Curation Notes: ClinVar Annotator: match by term: Spastic paraplegia 2
  • Original References(s): PMID:28492532 PMID:9056547


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