Gene entry
SLC2A2
solute carrier family 2 member 2
- Chromosome
- 3
- Cytoband
- 3q26.2
- Variants (rsID)
- 18
SLC2A2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q26.2). Its official name is “solute carrier family 2 member 2”. The reference table lists 18 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs1800572Benignsingle nucleotide variantFanconi-Bickel syndrome|Monogenic diabetes
- rs5400Benignsingle nucleotide variantFanconi-Bickel syndrome
- rs5404Benignsingle nucleotide variantFanconi-Bickel syndrome|Type 2 diabetes mellitus
- rs79424762Benignsingle nucleotide variantFanconi-Bickel syndrome
- rs150851401Conflicting interpretationssingle nucleotide variantFanconi-Bickel syndrome
- rs76362149Conflicting interpretationssingle nucleotide variantFanconi-Bickel syndrome
- rs121909741Uncertain significancesingle nucleotide variantDiabetes mellitus type 2, susceptibility to|Monogenic diabetes
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.