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rs4913681 has not been reported to ClinVar. Refer to dbSNP record rs4913681 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

rs4913681

  • Clinical significance: not reported in ClinVar
  • Reference allele: A warning
  • Variation alleles: G, T
  • Variation type: single nucleotide variation
  • Organism: Homo sapiens
  • GRCh38.p14: NC_000021.9: 10,592,389
  • GRCh37.p13: NC_000021.8: 10,920,066
Genome Data Viewer
  • The following term was not found in ClinVar: rs4913681.
  • No items found.