Gene entry
BSND
barttin CLCNK type accessory subunit beta
- Chromosome
- 1
- Cytoband
- 1p32.3
- Variants (rsID)
- 14
BSND is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p32.3). Its official name is “barttin CLCNK type accessory subunit beta”. The reference table lists 14 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs141611486Benignsingle nucleotide variantBartter disease type 4a|Bartter syndrome
- rs144505461Benignsingle nucleotide variantBartter disease type 4a|Bartter syndrome
- rs6682884Benignsingle nucleotide variantBartter disease type 4a
- rs141403253Conflicting interpretationssingle nucleotide variantBartter disease type 4a|Bartter syndrome
- rs180858237Conflicting interpretationssingle nucleotide variantBartter disease type 4a|Bartter syndrome
- rs200246335Conflicting interpretationssingle nucleotide variantBartter disease type 4a|Bartter syndrome
- rs74315287Likely pathogenicsingle nucleotide variantBartter disease type 4a|Bartter syndrome
- rs74315289Pathogenicsingle nucleotide variantBartter disease type 4a|Bartter syndrome
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.