Gene entry
SLC16A9
solute carrier family 16 member 9
- Chromosome
- 10
- Cytoband
- 10q21.2
- Variants (rsID)
- 19
SLC16A9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q21.2). Its official name is “solute carrier family 16 member 9”. The reference table lists 19 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs12356193Not classifiedintron_variantHepatitis a|Hepatitis B|Hepatitis|Gout|Lipoprotein Quantitative Trait Locus|Dementia|Arteries, Anomalies of|Hyperuricemia
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.