Gene entry
SLITRK6
SLIT and NTRK like family member 6
- Chromosome
- 13
- Cytoband
- 13q31.1
- Variants (rsID)
- 3
SLITRK6 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 13 (region 13q31.1). Its official name is “SLIT and NTRK like family member 6”. The reference table lists 3 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs3825413Benignsingle nucleotide variantHigh myopia-sensorineural deafness syndrome
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.
