Genetics University — Research, Education, Medical Genetics
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Gene entry

GM2A

ganglioside GM2 activator

Chromosome
5
Cytoband
5q33.1
Variants (rsID)
7

GM2A is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5q33.1). Its official name is “ganglioside GM2 activator”. The reference table lists 7 variants (rsID) for this gene.

Clinically classified variants

3 reference-table entries with clinical significance.

  • rs10076053Benignsingle nucleotide variantTay-Sachs disease, variant AB
  • rs1048719Benignsingle nucleotide variantTay-Sachs disease, variant AB
  • rs9324686Benignsingle nucleotide variantTay-Sachs disease, variant AB

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.