Gene entry
THBD
thrombomodulin
- Chromosome
- 20
- Cytoband
- 20p11.21
- Variants (rsID)
- 5
THBD is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 20 (region 20p11.21). Its official name is “thrombomodulin”. The reference table lists 5 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs1042580Benignsingle nucleotide variantAtypical hemolytic-uremic syndrome with thrombomodulin anomaly
- rs3176123Benignsingle nucleotide variantAtypical hemolytic-uremic syndrome with thrombomodulin anomaly
- rs3176126Benignsingle nucleotide variantAtypical hemolytic-uremic syndrome with thrombomodulin anomaly
- rs41348347Benignsingle nucleotide variantThrombomodulin-related bleeding disorder|Atypical hemolytic-uremic syndrome with thrombomodulin anomaly
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.