Gene entry
LINS1
lines homolog 1
- Chromosome
- 15
- Cytoband
- 15q26.3
- Variants (rsID)
- 13
LINS1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q26.3). Its official name is “lines homolog 1”. The reference table lists 13 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs12460Benignsingle nucleotide variantHistory of neurodevelopmental disorder
- rs12915007Benignsingle nucleotide variantHistory of neurodevelopmental disorder
- rs141855950Benignsingle nucleotide variant
- rs1047320Likely benignsingle nucleotide variantHistory 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.