Gene entry
SLC12A1
solute carrier family 12 member 1
- Chromosome
- 15
- Cytoband
- 15q21.1
- Variants (rsID)
- 22
SLC12A1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q21.1). Its official name is “solute carrier family 12 member 1”. The reference table lists 22 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs12902028Benignsingle nucleotide variantBartter disease type 1
- rs8025278Benignsingle nucleotide variantBartter disease type 1
- rs137853157Conflicting interpretationssingle nucleotide variantBartter disease type 1|Bartter syndrome|Familial hypokalemia-hypomagnesemia
- rs34819316Conflicting interpretationssingle nucleotide variantBartter disease type 1
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.