Gene entry
EIF2B3
eukaryotic translation initiation factor 2B subunit gamma
- Chromosome
- 1
- Cytoband
- 1p34.1
- Variants (rsID)
- 12
EIF2B3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p34.1). Its official name is “eukaryotic translation initiation factor 2B subunit gamma”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs77068026Benignsingle nucleotide variantVanishing white matter disease
- rs113994022Conflicting interpretationssingle nucleotide variantVanishing white matter disease
- rs144054571Likely benignsingle nucleotide variantVanishing white matter disease
- rs113994024Pathogenicsingle nucleotide variantVanishing white matter disease
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.