Gene entry
BIN1
bridging integrator 1
- Chromosome
- 2
- Cytoband
- 2q14.3
- Variants (rsID)
- 25
BIN1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q14.3). Its official name is “bridging integrator 1”. The reference table lists 25 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs1060743Benignsingle nucleotide variantMyopathy, centronuclear, 2
- rs2228955Benignsingle nucleotide variantMyopathy, centronuclear, 2
- rs3754617Benignsingle nucleotide variant
- rs79527490Benignsingle nucleotide variant
- rs114833236Conflicting interpretationssingle nucleotide variantMyopathy, centronuclear, 2
- rs35535012Conflicting interpretationssingle nucleotide variantMyopathy, centronuclear, 2
- rs78967885Conflicting interpretationssingle nucleotide variantMyopathy, centronuclear, 2
- rs143820618Uncertain significancesingle nucleotide variantMyopathy, centronuclear, 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.