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Gene entry

SLC25A22

solute carrier family 25 member 22

Chromosome
11
Cytoband
11p15.5
Variants (rsID)
20

SLC25A22 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11p15.5). Its official name is “solute carrier family 25 member 22”. The reference table lists 20 variants (rsID) for this gene.

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Clinically classified variants

19 reference-table entries with clinical significance.

  • rs142861804Benignsingle nucleotide variantEarly myoclonic encephalopathy|Early infantile epileptic encephalopathy with suppression bursts|Seizure
  • rs79919483Benignsingle nucleotide variantEarly myoclonic encephalopathy
  • rs116134953Conflicting interpretationssingle nucleotide variantEarly myoclonic encephalopathy|Early infantile epileptic encephalopathy with suppression bursts|Seizure
  • rs141430143Conflicting interpretationssingle nucleotide variantEarly infantile epileptic encephalopathy with suppression bursts
  • rs141975755Conflicting interpretationssingle nucleotide variantSeizure|Early infantile epileptic encephalopathy with suppression bursts
  • rs146300431Conflicting interpretationssingle nucleotide variantEarly myoclonic encephalopathy|Seizure|Early infantile epileptic encephalopathy with suppression bursts
  • rs146402942Conflicting interpretationssingle nucleotide variantEarly myoclonic encephalopathy|Seizure|Early infantile epileptic encephalopathy with suppression bursts
  • rs147840220Conflicting interpretationssingle nucleotide variantEarly myoclonic encephalopathy|Early infantile epileptic encephalopathy with suppression bursts
  • rs200072903Conflicting interpretationssingle nucleotide variantEarly myoclonic encephalopathy|Early infantile epileptic encephalopathy with suppression bursts
  • rs200603610Conflicting interpretationssingle nucleotide variantEarly infantile epileptic encephalopathy with suppression bursts|Macrocephaly|Developmental delay|Seizure
  • rs201574228Conflicting interpretationssingle nucleotide variantEarly myoclonic encephalopathy|Seizure|Early infantile epileptic encephalopathy with suppression bursts
  • rs370309722Conflicting interpretationssingle nucleotide variantEarly myoclonic encephalopathy|Early infantile epileptic encephalopathy with suppression bursts
  • rs376015598Conflicting interpretationssingle nucleotide variantEarly myoclonic encephalopathy|Early infantile epileptic encephalopathy with suppression bursts
  • rs587781167Conflicting interpretationssingle nucleotide variantEarly myoclonic encephalopathy
  • rs587781169Conflicting interpretationssingle nucleotide variantEarly myoclonic encephalopathy|Early infantile epileptic encephalopathy with suppression bursts
  • rs764930724Conflicting interpretationssingle nucleotide variantEarly infantile epileptic encephalopathy with suppression bursts
  • rs768604742Conflicting interpretationssingle nucleotide variantEarly myoclonic encephalopathy|Early infantile epileptic encephalopathy with suppression bursts
  • rs771026197Conflicting interpretationssingle nucleotide variantEarly myoclonic encephalopathy
  • rs121918334Pathogenicsingle nucleotide variantEarly myoclonic encephalopathy|Early infantile epileptic encephalopathy with suppression bursts

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.