Gene entry
LMNB2
lamin B2
- Chromosome
- 19
- Cytoband
- 19p13.3
- Variants (rsID)
- 6
LMNB2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19p13.3). Its official name is “lamin B2”. The reference table lists 6 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs11084940Benignsingle nucleotide variantLipodystrophy, partial, acquired, susceptibility to|Progressive myoclonic epilepsy type 9
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.