Gene entry
GAN
gigaxonin
- Chromosome
- 16
- Cytoband
- 16q23.2
- Variants (rsID)
- 29
GAN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q23.2). Its official name is “gigaxonin”. The reference table lists 29 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs2290948Benignsingle nucleotide variantGiant axonal neuropathy 1
- rs2290949Benignsingle nucleotide variantGiant axonal neuropathy 1
- rs144486241Conflicting interpretationssingle nucleotide variantGiant axonal neuropathy 1
- rs150344737Conflicting interpretationssingle nucleotide variantGiant axonal neuropathy 1
- rs369700456Conflicting interpretationssingle nucleotide variantGiant axonal neuropathy 1
- rs73589395Conflicting interpretationssingle nucleotide variantGiant axonal neuropathy 1
- rs119485092Pathogenicsingle nucleotide variantGiant axonal neuropathy 1
- rs747291494Pathogenicsingle nucleotide variantGiant axonal neuropathy 1
- rs143187097Uncertain significancesingle nucleotide variantGiant axonal neuropathy 1
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.