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rs112611553 has not been reported to ClinVar. Refer to dbSNP record rs112611553 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

rs112611553

  • Clinical significance: not reported in ClinVar
  • Reference allele: AACATTAAC warning
  • Variation alleles: AAC, AACATTAACATTAAC
  • Variation type: insertion/deletion
  • Organism: Homo sapiens
  • GRCh38.p14: NC_000008.11: 85,214,592
  • GRCh37.p13: NC_000008.10: 86,126,827
Genome Data Viewer
  • The following term was not found in ClinVar: rs112611553.
  • No items found.