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Gene entry

LAMC2

laminin subunit gamma 2

Chromosome
1
Cytoband
1q25.3
Variants (rsID)
35

LAMC2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q25.3). Its official name is “laminin subunit gamma 2”. The reference table lists 35 variants (rsID) for this gene.

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Clinically classified variants

10 reference-table entries with clinical significance.

  • rs113467864Benignsingle nucleotide variantJunctional epidermolysis bullosa
  • rs139043074Benignsingle nucleotide variantJunctional epidermolysis bullosa
  • rs144572936Benignsingle nucleotide variantJunctional epidermolysis bullosa|Junctional epidermolysis bullosa gravis of Herlitz
  • rs17481405Benignsingle nucleotide variantJunctional epidermolysis bullosa
  • rs2276543Benignsingle nucleotide variantJunctional epidermolysis bullosa
  • rs2296306Benignsingle nucleotide variantJunctional epidermolysis bullosa
  • rs3768593Benignsingle nucleotide variantJunctional epidermolysis bullosa|Junctional epidermolysis bullosa gravis of Herlitz
  • rs142335339Likely benignsingle nucleotide variantJunctional epidermolysis bullosa
  • rs118203899Pathogenicsingle nucleotide variantJunctional epidermolysis bullosa gravis of Herlitz|Epidermolysis bullosa, junctional 3B, severe
  • rs80356683Pathogenicsingle nucleotide variantJunctional epidermolysis bullosa gravis of Herlitz|Epidermolysis bullosa, junctional 3B, severe

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.