Gene entry
SERPINH1
serpin family H member 1
- Chromosome
- 11
- Cytoband
- 11q13.5
- Variants (rsID)
- 12
SERPINH1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q13.5). Its official name is “serpin family H member 1”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs584961Benignsingle nucleotide variantOsteogenesis imperfecta type 10
- rs6704Benignsingle nucleotide variantOsteogenesis imperfecta type 10
- rs138193444Conflicting interpretationssingle nucleotide variantOsteogenesis imperfecta type 10|Osteogenesis imperfecta
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.