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rs398122328 has not been reported to ClinVar. Refer to dbSNP record rs398122328 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

rs398122328

  • Clinical significance: not reported in ClinVar
  • Reference allele: AA
  • Variation allele: AAA
  • Variation type: insertion/deletion
  • Organism: Homo sapiens
  • GRCh38.p14: NC_000001.11: 17,027,882
  • GRCh37.p13: NC_000001.10: 17,354,377
Genome Data Viewer
  • The following term was not found in ClinVar: rs398122328.
  • No items found.