Gene entry
PROS1
protein S
- Chromosome
- 3
- Cytoband
- 3q11.1
- Variants (rsID)
- 11
PROS1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q11.1). Its official name is “protein S”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs138925964Conflicting interpretationssingle nucleotide variantThrombophilia due to protein S deficiency, autosomal dominant|Thrombophilia due to protein S deficiency, autosomal recessive|Protein S deficiency disease
- rs201928951Conflicting interpretationssingle nucleotide variantThrombophilia due to protein S deficiency, autosomal recessive|Thrombophilia due to protein S deficiency, autosomal dominant|Protein S deficiency disease
- rs7614835Conflicting interpretationssingle nucleotide variantThrombophilia due to protein S deficiency, autosomal dominant|Thrombophilia due to protein S deficiency, autosomal recessive|Protein S deficiency disease
- rs121918474Pathogenicsingle nucleotide variantThrombophilia due to protein S deficiency, autosomal dominant|Thrombophilia due to protein S deficiency, autosomal recessive
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.