Gene entry
SIX1
SIX homeobox 1
- Chromosome
- 14
- Cytoband
- 14q23.1
- Variants (rsID)
- 3
SIX1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q23.1). Its official name is “SIX homeobox 1”. The reference table lists 3 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs574976629Likely benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 23|Branchiootic syndrome 3
- rs104894478Pathogenicsingle nucleotide variantBranchiootic syndrome 3|Branchiootorenal syndrome 1|Autosomal dominant nonsyndromic hearing loss 23|Autosomal dominant nonsyndromic hearing loss 23|Branchiootic syndrome 3|Branchiootorenal syndrome 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.