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Gene entry

LITAF

lipopolysaccharide induced TNF factor

Chromosome
16
Cytoband
16p13.13
Variants (rsID)
33

LITAF is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16p13.13). Its official name is “lipopolysaccharide induced TNF factor”. The reference table lists 33 variants (rsID) for this gene.

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Clinically classified variants

6 reference-table entries with clinical significance.

  • rs1198Benignsingle nucleotide variantCharcot-Marie-Tooth disease type 1C
  • rs192516633Benignsingle nucleotide variantCharcot-Marie-Tooth disease type 1C
  • rs3743582Benignintron_variantCharcot-Marie-Tooth Disease, Demyelinating, Type 1c
  • rs9282774Benignsingle nucleotide variantCharcot-Marie-Tooth disease type 1C|Charcot-Marie-Tooth disease
  • rs141862602Conflicting interpretationssingle nucleotide variantCharcot-Marie-Tooth disease type 1C|Charcot-Marie-Tooth disease
  • rs104894519Pathogenicsingle nucleotide variantCharcot-Marie-Tooth disease type 1C|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.