Gene entry
SEPTIN12
septin 12
- Chromosome
- 16
- Cytoband
- 16p13.3
- Variants (rsID)
- 11
SEPTIN12 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16p13.3). Its official name is “septin 12”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs199696526Risk factorsingle nucleotide variantSpermatogenic failure 10
- rs371195126Risk factorsingle nucleotide variantSpermatogenic failure 10
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.