Gene entry
LMNB1
lamin B1
- Chromosome
- 5
- Cytoband
- 5q23.2
- Variants (rsID)
- 12
LMNB1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5q23.2). Its official name is “lamin B1”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs36105360Benignsingle nucleotide variantAdult-onset autosomal dominant demyelinating leukodystrophy
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.