U.S. flag

An official website of the United States government

rs79233702 has not been reported to ClinVar. Refer to dbSNP record rs79233702 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

rs79233702

  • Clinical significance: not reported in ClinVar
  • Reference allele: G
  • Variation alleles: A, C
  • Variation type: single nucleotide variation
  • Organism: Homo sapiens
  • GRCh38.p14: NC_000024.10: 11,332,565
  • GRCh37.p13: NC_000024.9: 13,488,241
Genome Data Viewer
  • The following term was not found in ClinVar: rs79233702.
  • No items found.