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Gene entry

KCNV2

potassium voltage-gated channel modifier subfamily V member 2

Chromosome
9
Cytoband
9p24.2
Variants (rsID)
15

KCNV2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9p24.2). Its official name is “potassium voltage-gated channel modifier subfamily V member 2”. The reference table lists 15 variants (rsID) for this gene.

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Clinically classified variants

7 reference-table entries with clinical significance.

  • rs142744007Benignsingle nucleotide variantCone dystrophy with supernormal rod response
  • rs150685794Benignsingle nucleotide variantCone dystrophy with supernormal rod response
  • rs17656693Benignsingle nucleotide variantCone dystrophy with supernormal rod response
  • rs201327014Benignsingle nucleotide variantCone dystrophy with supernormal rod response
  • rs7859993Benignsingle nucleotide variantCone dystrophy with supernormal rod response
  • rs145731729Conflicting interpretationssingle nucleotide variantCone dystrophy with supernormal rod response|Cone dystrophy 3
  • rs104894114Pathogenicsingle nucleotide variantCone dystrophy with supernormal rod response

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.