U.S. flag

An official website of the United States government

rs6971387 has not been reported to ClinVar. Refer to dbSNP record rs6971387 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

rs6971387

  • Clinical significance: not reported in ClinVar
  • Reference allele: C
  • Variation alleles: A, G, T
  • Variation type: single nucleotide variation
  • Organism: Homo sapiens
  • GRCh38.p14: NC_000007.14: 1,495,995
  • GRCh37.p13: NC_000007.13: 1,535,631
Genome Data Viewer
  • The following term was not found in ClinVar: rs6971387.
  • No items found.