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rs4794799 has not been reported to ClinVar. Refer to dbSNP record rs4794799 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

rs4794799

  • Clinical significance: not reported in ClinVar
  • Reference allele: T
  • Variation alleles: A, C
  • Variation type: single nucleotide variation
  • Organism: Homo sapiens
  • GRCh38.p14: NC_000017.11: 39,056,998
  • GRCh37.p13: NC_000017.10: 37,213,251
Genome Data Viewer
  • The following term was not found in ClinVar: rs4794799.
  • No items found.