S I D E B A R

rs121912466 has not been reported to ClinVar. Refer to dbSNP record rs121912466 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

rs121912466

  • Clinical significance: not reported in ClinVar
  • Reference allele: G
  • Variation allele: A
  • Variation type: single nucleotide variation
  • Organism: Homo sapiens
  • Gene(s): ITGB4
  • GRCh38.p12: chr17:75742591
  • GRCh37.p13: chr17:73738672
Genome Browser
  • The following term was not found in ClinVar: rs121912466.
  • No items found.
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