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Gene entry

RYR3

ryanodine receptor 3

Chromosome
15
Cytoband
15q13.3-q14
Variants (rsID)
204

RYR3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q13.3-q14). Its official name is “ryanodine receptor 3”. The reference table lists 204 variants (rsID) for this gene.

Clinically classified variants

14 reference-table entries with clinical significance.

  • rs114825824Benignsingle nucleotide variantEpileptic encephalopathy
  • rs181264765Benignsingle nucleotide variantEpileptic encephalopathy
  • rs182257230Benignsingle nucleotide variantEpileptic encephalopathy
  • rs2229119Benignsingle nucleotide variantEpileptic encephalopathy
  • rs75782410Benignsingle nucleotide variantEpileptic encephalopathy
  • rs182972491Conflicting interpretationssingle nucleotide variantEpileptic encephalopathy|Inborn genetic diseases
  • rs201830013Conflicting interpretationssingle nucleotide variantEpileptic encephalopathy
  • rs114681942Likely benignsingle nucleotide variantEpileptic encephalopathy
  • rs41279214Likely benignsingle nucleotide variantEpileptic encephalopathy
  • rs138636427Uncertain significancesingle nucleotide variantEpileptic encephalopathy
  • rs139023249Uncertain significancesingle nucleotide variantEpileptic encephalopathy
  • rs41279210Uncertain significancesingle nucleotide variantEpileptic encephalopathy
  • rs4780144Not classifiedmissense_variant
  • rs674155Not classifiedsplice_region_variant&synonymous_variant

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.