Gene entry
SLC16A1
solute carrier family 16 member 1
- Chromosome
- 1
- Cytoband
- 1p13.2
- Variants (rsID)
- 18
SLC16A1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p13.2). Its official name is “solute carrier family 16 member 1”. The reference table lists 18 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs9429505Benignsingle nucleotide variantExercise-induced hyperinsulinism
- rs72552271Conflicting interpretationssingle nucleotide variantMetabolic myopathy due to lactate transporter defect
- rs11585690Likely benignsingle nucleotide variantExercise-induced hyperinsulinism
- rs77373295Uncertain significancesingle nucleotide variantExercise-induced hyperinsulinism
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.