Gene entry
LBR
lamin B receptor
- Chromosome
- 1
- Cytoband
- 1q42.12
- Variants (rsID)
- 13
LBR is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q42.12). Its official name is “lamin B receptor”. The reference table lists 13 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs16844841Benignsingle nucleotide variantGreenberg dysplasia
- rs2230419Benignsingle nucleotide variantGreenberg dysplasia|Reynolds syndrome|Pelger-Huët anomaly
- rs148541545Conflicting interpretationssingle nucleotide variantGreenberg dysplasia
- rs200180113Conflicting interpretationssingle nucleotide variantReynolds syndrome|Greenberg dysplasia
- rs80299691Conflicting interpretationssingle nucleotide variantGreenberg dysplasia|Connective tissue disorder
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.