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Gene entry

RP1L1

RP1 like 1

Chromosome
8
Cytoband
8p23.1
Variants (rsID)
31

RP1L1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 8 (region 8p23.1). Its official name is “RP1 like 1”. The reference table lists 31 variants (rsID) for this gene.

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Clinically classified variants

9 reference-table entries with clinical significance.

  • rs117007660Benignsingle nucleotide variantOccult macular dystrophy
  • rs150752593Benignsingle nucleotide variantOccult macular dystrophy
  • rs150931842Benignsingle nucleotide variantOccult macular dystrophy
  • rs185749010Benignsingle nucleotide variantOccult macular dystrophy
  • rs4388421Benignsingle nucleotide variantOccult macular dystrophy|Retinitis pigmentosa 88
  • rs4840502Benignsingle nucleotide variantOccult macular dystrophy|Retinitis pigmentosa 88
  • rs79019225Benignsingle nucleotide variantOccult macular dystrophy
  • rs200996822Conflicting interpretationssingle nucleotide variant
  • rs77679870Conflicting interpretationssingle nucleotide variantOccult macular dystrophy

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.