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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking SDF2L1 and chromosome 22q11.2 deletion syndrome, distal 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
  • The annotation has been inferred by association of genotype and phenotype with RGD:38466430 (Homo sapiens)
  • 199 RGD objects have been annotated to chromosome 22q11.2 deletion syndrome, distal  (DOID:0060413)
  • 3 papers in RGD have been used to annotate SDF2L1
  • Curation Notes: ClinVar Annotator: match by term: Chromosome 22q11.2 deletion syndrome, distal
  • Original References(s): PMID:31690835


    • An association has been curated linking SDF2L1 and chromosome 22q11.2 deletion syndrome, distal 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
  • The annotation has been inferred by association of genotype and phenotype with RGD:14696123 (Homo sapiens)
  • 199 RGD objects have been annotated to chromosome 22q11.2 deletion syndrome, distal  (DOID:0060413)
  • 3 papers in RGD have been used to annotate SDF2L1
  • Curation Notes: ClinVar Annotator: match by term: Chromosome 22q11.2 deletion syndrome, distal
  • Original References(s): PMID:21681106


    • An association has been curated linking SDF2L1 and chromosome 22q11.2 deletion syndrome, distal 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
  • The annotation has been inferred by association of genotype and phenotype with RGD:38471637 (Homo sapiens)
  • 199 RGD objects have been annotated to chromosome 22q11.2 deletion syndrome, distal  (DOID:0060413)
  • 3 papers in RGD have been used to annotate SDF2L1
  • Curation Notes: ClinVar Annotator: match by term: Chromosome 22q11.2 deletion syndrome, distal
  • Original References(s): PMID:25741868


    • An association has been curated linking SDF2L1 and chromosome 22q11.2 deletion syndrome, distal 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
  • The annotation has been inferred by association of genotype and phenotype with RGD:405261827 (Homo sapiens)
  • 199 RGD objects have been annotated to chromosome 22q11.2 deletion syndrome, distal  (DOID:0060413)
  • 3 papers in RGD have been used to annotate SDF2L1
  • Curation Notes: ClinVar Annotator: match by term: Chromosome 22q11.2 deletion syndrome, distal
  • Original References(s): PMID:25741868 PMID:38177409


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