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rs761246236 has not been reported to ClinVar. Refer to dbSNP record rs761246236 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

rs761246236

  • Clinical significance: not reported in ClinVar
  • Reference allele: CCAGAAGCCCCGAGACCTCC
  • Variation alleles: CC, CCAGAAGCCCCGAGACCTCCAGAAGCCCCGAGACCTCC
  • Variation type: insertion/deletion
  • Organism: Homo sapiens
  • GRCh38.p14: NC_000020.11: 1,393,201
  • GRCh37.p13: NC_000020.10: 1,373,845
Genome Data Viewer
  • The following term was not found in ClinVar: rs761246236.
  • No items found.