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rs71266894 has not been reported to ClinVar. Refer to dbSNP record rs71266894 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

rs71266894

  • Clinical significance: not reported in ClinVar
  • Reference allele: C
  • Variation alleles: A, G, T
  • Variation type: single nucleotide variation
  • Organism: Homo sapiens
  • GRCh38.p14: NC_000019.10: 54,222,997
  • GRCh37.p13: NC_000019.9: 54,726,869
Genome Data Viewer
  • The following term was not found in ClinVar: rs71266894.
  • No items found.