Gene entry
GABRG2
gamma-aminobutyric acid type A receptor subunit gamma2
- Chromosome
- 5
- Cytoband
- 5q34
- Variants (rsID)
- 17
GABRG2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5q34). Its official name is “gamma-aminobutyric acid type A receptor subunit gamma2”. The reference table lists 17 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs211037Benignsingle nucleotide variantEpilepsy, childhood absence 2|Febrile seizures, familial, 8|Seizure|Epilepsy, childhood absence 2|Febrile seizures, familial, 8
- rs143295869Conflicting interpretationssingle nucleotide variantEpilepsy, childhood absence 2|Epilepsy, childhood absence 2|Febrile seizures, familial, 8
- rs375294947Conflicting interpretationssingle nucleotide variantEpilepsy, childhood absence 2|Epilepsy, childhood absence 2|Febrile seizures, familial, 8
- rs868452487Conflicting interpretationssingle nucleotide variantFebrile seizures, familial, 8|Epilepsy, childhood absence 2
- rs121909673Pathogenicsingle nucleotide variantEpilepsy, childhood absence 2|Febrile seizures, familial, 8|Febrile seizures, familial, 8|Epilepsy, childhood absence 2
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.