Gene entry
SLC22A14
solute carrier family 22 member 14
- Chromosome
- 3
- Cytoband
- 3p22.2
- Variants (rsID)
- 28
SLC22A14 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p22.2). Its official name is “solute carrier family 22 member 14”. The reference table lists 28 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs818817Not classifiedmissense_variantBrugada Syndrome 1|Long Qt Syndrome 3|Brugada Syndrome|Ventricular Fibrillation, Paroxysmal Familial, 1|Progressive Familial Heart Block, Type Ia|Long Qt Syndrome|Sick Sinus Syndrome 1|Long Qt Syndrome 1|Cardiomyopathy, Dilated, 1e|Familial Long Qt Syndrome
- rs818819Not classifiedsynonymous_variantSystemic Lupus Erythematosus|Lupus Erythematosus
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.