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rs118152996 has not been reported to ClinVar. Refer to dbSNP record rs118152996 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

rs118152996

  • Clinical significance: not reported in ClinVar
  • Reference allele: C
  • Variation allele: T
  • Variation type: single nucleotide variation
  • Organism: Homo sapiens
  • GRCh38.p14: NC_000010.11: 113,854,811
  • GRCh37.p13: NC_000010.10: 115,614,570
Genome Data Viewer
  • The following term was not found in ClinVar: rs118152996.
  • No items found.