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Gene entry

LGI1

leucine rich glioma inactivated 1

Chromosome
10
Cytoband
10q23.33
Variants (rsID)
23

LGI1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q23.33). Its official name is “leucine rich glioma inactivated 1”. The reference table lists 23 variants (rsID) for this gene.

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Clinically classified variants

4 reference-table entries with clinical significance.

  • rs151104648Conflicting interpretationssingle nucleotide variantEpilepsy, familial temporal lobe, 1|Seizure|Autosomal dominant epilepsy with auditory features
  • rs202148793Conflicting interpretationssingle nucleotide variantEpilepsy, familial temporal lobe, 1|Autosomal dominant epilepsy with auditory features
  • rs202204627Conflicting interpretationssingle nucleotide variantEpilepsy, familial temporal lobe, 1|Autosomal dominant epilepsy with auditory features
  • rs119488099Pathogenicsingle nucleotide variantEpilepsy, familial temporal lobe, 1|Autosomal dominant epilepsy with auditory features

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.