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Gene entry

LRRK2

leucine rich repeat kinase 2

Chromosome
12
Cytoband
12q12
Variants (rsID)
69

LRRK2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12q12). Its official name is “leucine rich repeat kinase 2”. The reference table lists 69 variants (rsID) for this gene.

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Clinically classified variants

36 reference-table entries with clinical significance.

  • rs10878245Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs10878307Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs10878371Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs10878405Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs11175964Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs11176013Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs11564148Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs1427263Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs150050676Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs33958906Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs33962975Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs33995883Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs34410987Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs35303786Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs41286466Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs4640000Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs7133914Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs72546327Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs7308720Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs78365431Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs7966550Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs79909111Benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs33995463Conflicting interpretationssingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs34778348Conflicting interpretationssingle nucleotide variantAutosomal dominant Parkinson disease 8|Parkinson disease
  • rs58559150Conflicting interpretationssingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs72546338Conflicting interpretationssingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs78501232Conflicting interpretationssingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs17466213Likely benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs74681492Likely benignsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs34637584Pathogenicsingle nucleotide variantAutosomal dominant Parkinson disease 8|Inborn genetic diseases|Young-onset Parkinson disease|Parkinson disease, late-onset
  • rs183902574Uncertain significancesingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs111341148Not classifiedsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs113589830Not classifiedsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs17519916Not classifiedsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs34015634Not classifiedsingle nucleotide variantAutosomal dominant Parkinson disease 8
  • rs75148313Not classifiedsingle nucleotide variantAutosomal dominant Parkinson disease 8

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.