S I D E B A R

NM_002113.2:c.19delG has not been reported to ClinVar. Refer to dbSNP record rs769938205 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

rs769938205

  • Clinical significance: not reported in ClinVar
  • Reference allele: G
  • Variation allele: -
  • Variation type: deletion
  • Organism: Homo sapiens
  • Gene(s): CFHR1
  • GRCh38.p12: chr1:196819863
  • GRCh37.p13: chr1:196788993
Genome Browser
  • The following term was not found in ClinVar: NM_002113.2:c.19delG.
  • No items found.
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