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Gene entry

LAMB2

laminin subunit beta 2

Chromosome
3
Cytoband
3p21.31
Variants (rsID)
27

LAMB2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p21.31). Its official name is “laminin subunit beta 2”. The reference table lists 27 variants (rsID) for this gene.

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Clinically classified variants

16 reference-table entries with clinical significance.

  • rs35713889Benignsingle nucleotide variantPierson syndrome|LAMB2-related infantile-onset nephrotic syndrome|Pierson syndrome|LAMB2-related infantile-onset nephrotic syndrome
  • rs61729152Benignsingle nucleotide variantPierson syndrome|LAMB2-related infantile-onset nephrotic syndrome|LAMB2-related infantile-onset nephrotic syndrome|Pierson syndrome
  • rs61729458Benignsingle nucleotide variantPierson syndrome|LAMB2-related infantile-onset nephrotic syndrome|Pierson syndrome|LAMB2-related infantile-onset nephrotic syndrome
  • rs74951356Benignsingle nucleotide variantLAMB2-related infantile-onset nephrotic syndrome|Pierson syndrome|Pierson syndrome|LAMB2-related infantile-onset nephrotic syndrome
  • rs75073433Benignsingle nucleotide variantLAMB2-related infantile-onset nephrotic syndrome|Pierson syndrome|Pierson syndrome|LAMB2-related infantile-onset nephrotic syndrome
  • rs79677861Benignsingle nucleotide variantLAMB2-related infantile-onset nephrotic syndrome|Pierson syndrome|Pierson syndrome|LAMB2-related infantile-onset nephrotic syndrome
  • rs148648480Conflicting interpretationssingle nucleotide variantPierson syndrome|LAMB2-related infantile-onset nephrotic syndrome|Pierson syndrome|LAMB2-related infantile-onset nephrotic syndrome
  • rs200738080Conflicting interpretationssingle nucleotide variantPierson syndrome|LAMB2-related infantile-onset nephrotic syndrome
  • rs201999373Conflicting interpretationssingle nucleotide variantPierson syndrome|LAMB2-related infantile-onset nephrotic syndrome|Pierson syndrome|LAMB2-related infantile-onset nephrotic syndrome
  • rs148246465Likely benignsingle nucleotide variantLAMB2-related infantile-onset nephrotic syndrome|Pierson syndrome|LAMB2-related infantile-onset nephrotic syndrome|Pierson syndrome
  • rs121912488Likely pathogenicsingle nucleotide variantPierson syndrome|LAMB2-related infantile-onset nephrotic syndrome|Nephrotic syndrome
  • rs151134957Uncertain significancesingle nucleotide variantPierson syndrome|LAMB2-related infantile-onset nephrotic syndrome
  • rs200658738Uncertain significancesingle nucleotide variantPierson syndrome|LAMB2-related infantile-onset nephrotic syndrome
  • rs200761921Uncertain significancesingle nucleotide variantPierson syndrome|LAMB2-related infantile-onset nephrotic syndrome
  • rs201458234Uncertain significancesingle nucleotide variantPierson syndrome|LAMB2-related infantile-onset nephrotic syndrome
  • rs267607207Uncertain significancesingle nucleotide variantPierson syndrome|LAMB2-related infantile-onset nephrotic syndrome|LAMB2-related infantile-onset nephrotic syndrome|Pierson syndrome

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.