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rs10687775 has not been reported to ClinVar. Refer to dbSNP record rs10687775 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

rs10687775

  • Clinical significance: not reported in ClinVar
  • Reference allele: AT
  • Variation allele: ATAAT
  • Variation type: insertion/deletion
  • Organism: Homo sapiens
  • GRCh38.p14: NC_000019.10: 57,874,501
  • GRCh37.p13: NC_000019.9: 58,385,869
Genome Data Viewer
  • The following term was not found in ClinVar: rs10687775.
  • No items found.