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Gene entry

LRP4

LDL receptor related protein 4

Chromosome
11
Cytoband
11p11.2
Variants (rsID)
11

LRP4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11p11.2). Its official name is “LDL receptor related protein 4”. The reference table lists 11 variants (rsID) for this gene.

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Clinically classified variants

4 reference-table entries with clinical significance.

  • rs111426027Benignsingle nucleotide variantCenani-Lenz syndactyly syndrome|Congenital myasthenic syndrome 17|Sclerosteosis 2|Cenani-Lenz syndactyly syndrome
  • rs118009068Benignsingle nucleotide variantCenani-Lenz syndactyly syndrome|Cenani-Lenz syndactyly syndrome|Sclerosteosis 2|Congenital myasthenic syndrome 17
  • rs150253578Benignsingle nucleotide variantCenani-Lenz syndactyly syndrome|Congenital myasthenic syndrome 17|Sclerosteosis 2
  • rs72897663Benignsingle nucleotide variantCenani-Lenz syndactyly syndrome|Cenani-Lenz syndactyly syndrome|Sclerosteosis 2|Congenital myasthenic syndrome 17

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.