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Gene entry

GSDME

gasdermin E

Chromosome
7
Cytoband
7p15.3
Variants (rsID)
25

GSDME is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7p15.3). Its official name is “gasdermin E”. The reference table lists 25 variants (rsID) for this gene.

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Clinically classified variants

5 reference-table entries with clinical significance.

  • rs12540919Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 5
  • rs61731036Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 5
  • rs71535705Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 5
  • rs876305Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 5
  • rs138980048Conflicting interpretationssingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 5

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.