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rs112040677 has not been reported to ClinVar. Refer to dbSNP record rs112040677 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

rs112040677

  • Clinical significance: not reported in ClinVar
  • Reference allele: GACGGGGACGGGGACGGGGACGGGG
  • Variation alleles: GACGGGG, GACGGGGACGGGG, GACGGGGACGGGGACGGGG
  • Variation type: insertion/deletion
  • Organism: Homo sapiens
  • GRCh38.p14: NC_000002.12: 130,372,355
  • GRCh37.p13: NC_000002.11: 131,129,928
Genome Data Viewer
  • The following term was not found in ClinVar: rs112040677.
  • No items found.