Gene entry
KIF1C
kinesin family member 1C
- Chromosome
- 17
- Cytoband
- 17p13.2
- Variants (rsID)
- 15
KIF1C is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17p13.2). Its official name is “kinesin family member 1C”. The reference table lists 15 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs17707385Benignsingle nucleotide variantSpastic ataxia 2
- rs148934699Conflicting interpretationssingle nucleotide variantSpastic ataxia 2|Hereditary spastic paraplegia
- rs201800868Conflicting interpretationssingle nucleotide variantSpastic ataxia 2
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.