Gene entry
LMOD3
leiomodin 3
- Chromosome
- 3
- Cytoband
- 3p14.1
- Variants (rsID)
- 19
LMOD3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p14.1). Its official name is “leiomodin 3”. The reference table lists 19 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs111797345Benignsingle nucleotide variantNemaline myopathy 10
- rs116257053Benignsingle nucleotide variantNemaline myopathy 10
- rs145387235Benignsingle nucleotide variantNemaline myopathy 10
- rs35740823Benignsingle nucleotide variantNemaline myopathy 10
- rs74350755Benignsingle nucleotide variantNemaline myopathy 10
- rs75713718Benignsingle nucleotide variantNemaline myopathy 10
- rs80113271Benignsingle nucleotide variantNemaline myopathy 10
- rs9835034Conflicting interpretationssingle nucleotide variantNemaline myopathy 10
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.