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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.