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Gene entry

SLC33A1

solute carrier family 33 member 1

Chromosome
3
Cytoband
3q25.31
Variants (rsID)
8

SLC33A1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q25.31). Its official name is “solute carrier family 33 member 1”. The reference table lists 8 variants (rsID) for this gene.

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Clinically classified variants

3 reference-table entries with clinical significance.

  • rs3804769Benignsingle nucleotide variantSpastic paraplegia|Congenital cataract-hearing loss-severe developmental delay syndrome|Hereditary spastic paraplegia 42
  • rs76440173Conflicting interpretationssingle nucleotide variantSpastic paraplegia|Hereditary spastic paraplegia 42|Hereditary spastic paraplegia
  • rs141818342Uncertain significancesingle nucleotide variantSpastic paraplegia|Hereditary spastic paraplegia

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.