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Gene entry

CRX

cone-rod homeobox

Chromosome
19
Cytoband
19q13.33
Variants (rsID)
13

CRX is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.33). Its official name is “cone-rod homeobox”. The reference table lists 13 variants (rsID) for this gene.

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Clinically classified variants

5 reference-table entries with clinical significance.

  • rs12974951Benignsingle nucleotide variantCone-rod dystrophy 2|Leber congenital amaurosis 7|Retinitis pigmentosa
  • rs7248427Benignsingle nucleotide variantLeber congenital amaurosis 7|Cone-rod dystrophy 2|Retinitis pigmentosa
  • rs73038753Benignsingle nucleotide variantLeber congenital amaurosis 7|Cone-rod dystrophy 2|Retinitis pigmentosa
  • rs145805694Conflicting interpretationssingle nucleotide variantRetinitis pigmentosa|Leber congenital amaurosis 7|Cone-rod dystrophy 2|Leber congenital amaurosis 7|Cone-rod dystrophy 2
  • rs61748442Conflicting interpretationssingle nucleotide variantRetinitis pigmentosa|Leber congenital amaurosis 1|Leber congenital amaurosis 7|Cone-rod dystrophy 2|Leber congenital amaurosis 7|Cone-rod dystrophy 2|Autosomal dominant retinitis pigmentosa

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.