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Gene entry

TRPV3

transient receptor potential cation channel subfamily V member 3

Chromosome
17
Cytoband
17p13.2
Variants (rsID)
25

TRPV3 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 “transient receptor potential cation channel subfamily V member 3”. The reference table lists 25 variants (rsID) for this gene.

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Clinically classified variants

6 reference-table entries with clinical significance.

  • rs116535534Benignsingle nucleotide variantIsolated focal non-epidermolytic palmoplantar keratoderma
  • rs118043532Benignsingle nucleotide variantIsolated focal non-epidermolytic palmoplantar keratoderma
  • rs322937Benignsingle nucleotide variantIsolated focal non-epidermolytic palmoplantar keratoderma|Olmsted syndrome 1
  • rs395357Benignsingle nucleotide variantIsolated focal non-epidermolytic palmoplantar keratoderma|Olmsted syndrome 1
  • rs7208811Benignsingle nucleotide variantIsolated focal non-epidermolytic palmoplantar keratoderma
  • rs9912448Benignsingle nucleotide variantIsolated focal non-epidermolytic palmoplantar keratoderma

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.