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rs13281184 has not been reported to ClinVar. Refer to dbSNP record rs13281184 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

rs13281184

  • Clinical significance: not reported in ClinVar
  • Reference allele: C
  • Variation alleles: G, T
  • Variation type: single nucleotide variation
  • Organism: Homo sapiens
  • GRCh38.p14: NC_000008.11: 132,578,471
  • GRCh37.p13: NC_000008.10: 133,590,718
Genome Data Viewer
  • The following term was not found in ClinVar: rs13281184.
  • No items found.