Gene entry
LAMC3
laminin subunit gamma 3
- Chromosome
- 9
- Cytoband
- 9q34.12
- Variants (rsID)
- 37
LAMC3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q34.12). Its official name is “laminin subunit gamma 3”. The reference table lists 37 variants (rsID) for this gene.
Clinically classified variants
12 reference-table entries with clinical significance.
- rs10901333Benignsingle nucleotide variantOccipital pachygyria and polymicrogyria
- rs10901344Benignsingle nucleotide variantOccipital pachygyria and polymicrogyria
- rs113259170Benignsingle nucleotide variant
- rs117361076Benignsingle nucleotide variant
- rs2275137Benignsingle nucleotide variantOccipital pachygyria and polymicrogyria
- rs34652877Benignsingle nucleotide variant
- rs45628035Benignsingle nucleotide variantOccipital pachygyria and polymicrogyria
- rs7024108Benignsingle nucleotide variantOccipital pachygyria and polymicrogyria
- rs140955110Conflicting interpretationssingle nucleotide variantOccipital pachygyria and polymicrogyria
- rs141724499Conflicting interpretationssingle nucleotide variant
- rs199535979Conflicting interpretationssingle nucleotide variant
- rs140066207Uncertain significancesingle nucleotide variant
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.