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Gene entry

KIF1B

kinesin family member 1B

Chromosome
1
Cytoband
1p36.22
Variants (rsID)
33

KIF1B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p36.22). Its official name is “kinesin family member 1B”. The reference table lists 33 variants (rsID) for this gene.

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Clinically classified variants

9 reference-table entries with clinical significance.

  • rs117525287Benignsingle nucleotide variantCharcot-Marie-Tooth disease type 2|Neuroblastoma|Charcot-Marie-Tooth disease
  • rs141224290Benignsingle nucleotide variantCharcot-Marie-Tooth disease type 2|Hereditary cancer-predisposing syndrome|Charcot-Marie-Tooth disease
  • rs147066476Benignsingle nucleotide variantCharcot-Marie-Tooth disease type 2|Neuroblastoma|Charcot-Marie-Tooth disease
  • rs2297881Benignsingle nucleotide variantNeuroblastoma|Charcot-Marie-Tooth disease type 2|Charcot-Marie-Tooth disease|Charcot-Marie-Tooth disease type 2A1
  • rs41274458Benignsingle nucleotide variant
  • rs146436697Conflicting interpretationssingle nucleotide variantNeuroblastoma|Charcot-Marie-Tooth disease type 2
  • rs140015591Likely benignsingle nucleotide variantCharcot-Marie-Tooth disease type 2|Neuroblastoma
  • rs145846362Likely benignsingle nucleotide variantCharcot-Marie-Tooth disease type 2|Neuroblastoma|Charcot-Marie-Tooth disease
  • rs201500946Uncertain significancesingle nucleotide variantCharcot-Marie-Tooth disease type 2|Charcot-Marie-Tooth disease

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.