U.S. flag

An official website of the United States government

rs56335545 has not been reported to ClinVar. Refer to dbSNP record rs56335545 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

rs56335545

  • Clinical significance: not reported in ClinVar
  • Reference allele: T
  • Variation allele: C
  • Variation type: single nucleotide variation
  • Organism: Homo sapiens
  • GRCh38.p14: NC_000019.10: 1,789,721
  • GRCh37.p13: NC_000019.9: 1,789,720
Genome Data Viewer
  • The following term was not found in ClinVar: rs56335545.
  • No items found.