S I D E B A R

rs111033796 has not been reported to ClinVar. Refer to dbSNP record rs111033796 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

rs111033796

  • Clinical significance: not reported in ClinVar
  • Reference allele: T
  • Variation alleles: C, G
  • Variation type: single nucleotide variation
  • Organism: Homo sapiens
  • Gene(s): GALT
  • GRCh38.p12: chr9:34649472
  • GRCh37.p13: chr9:34649469
Genome Browser
  • The following term was not found in ClinVar: rs111033796.
  • No items found.
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