Gene entry
SMC3
structural maintenance of chromosomes 3
- Chromosome
- 10
- Cytoband
- 10q25.2
- Variants (rsID)
- 12
SMC3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q25.2). Its official name is “structural maintenance of chromosomes 3”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs117538515Benignsingle nucleotide variantCornelia de Lange syndrome 3
- rs142524280Conflicting interpretationssingle nucleotide variantCornelia de Lange syndrome 3|History of neurodevelopmental disorder
- rs3818903Conflicting interpretationssingle nucleotide variantCornelia de Lange syndrome 3
- rs76625999Conflicting interpretationssingle nucleotide variantCornelia de Lange syndrome 3|History of neurodevelopmental 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.