U.S. flag

An official website of the United States government

rs9924150 has not been reported to ClinVar. Refer to dbSNP record rs9924150 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

rs9924150

  • Clinical significance: not reported in ClinVar
  • Reference allele: A
  • Variation alleles: C, G, T
  • Variation type: single nucleotide variation
  • Organism: Homo sapiens
  • GRCh38.p14: NC_000016.10: 20,480,677
  • GRCh37.p13: NC_000016.9: 20,491,999
Genome Data Viewer
  • The following term was not found in ClinVar: rs9924150.
  • No items found.