SERPINB11
serpin family B member 11
Summary
Predicted to enable serine-type endopeptidase inhibitor activity. Predicted to be located in cytoplasm. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1490122468 | 18:61,377,453 | T/C | — | uncertain significance |
| rs1160837972 | 18:61,377,482 | C/G | — | uncertain significance |
| rs964077675 | 18:61,377,489 | G/A | — | uncertain significance |
| rs1914484155 | 18:61,377,507 | A/T | — | uncertain significance |
| rs1377947239 | 18:61,377,515 | T/G | — | uncertain significance |
| rs201552669 | 18:61,377,548 | A/G | — | uncertain significance |
| rs566045959 | 18:61,377,588 | T/G | — | uncertain significance |
| rs746574229 | 18:61,378,569 | G/C | — | uncertain significance |
| rs779594525 | 18:61,379,847 | C/G | — | uncertain significance |
| rs193224810 | 18:61,379,911 | C/T | — | likely benign |
| rs574415754 | 18:61,379,916 | G/T | — | uncertain significance |
| rs749417694 | 18:61,383,278 | A/G | — | uncertain significance |
| rs374002477 | 18:61,383,345 | C/G | — | uncertain significance |
| rs537202592 | 18:61,383,353 | A/C | — | uncertain significance |
| rs775121004 | 18:61,387,294 | G/C | — | uncertain significance |
| rs1352031864 | 18:61,387,316 | T/C | — | uncertain significance |
| rs777795907 | 18:61,387,355 | G/A | — | uncertain significance |
| rs2511697474 | 18:61,387,385 | G/A | — | uncertain significance |
| rs542549713 | 18:61,388,080 | G/A | — | uncertain significance |
| rs572331029 | 18:61,388,132 | C/T | — | uncertain significance |
| rs2511698276 | 18:61,388,153 | T/C | — | uncertain significance |
| rs919545337 | 18:61,388,177 | G/A | — | uncertain significance |
| rs1254435404 | 18:61,388,197 | G/A | — | uncertain significance |
| rs189563348 | 18:61,389,026 | A/C | intron variant | — |
| rs751122140 | 18:61,390,248 | C/T | — | uncertain significance |
| rs891810696 | 18:61,390,259 | C/A | — | uncertain significance |
| rs373082225 | 18:61,390,287 | T/C | — | uncertain significance |
| rs1171036655 | 18:61,390,293 | G/C | — | uncertain significance |
| rs1914859198 | 18:61,390,314 | C/A | — | uncertain significance |
| rs575490613 | 18:61,390,376 | G/T | — | uncertain significance |
| rs554734554 | 18:61,390,424 | A/G | — | uncertain significance |
| rs368688268 | 18:61,390,482 | G/T | — | uncertain significance |
| rs369085630 | 18:61,390,539 | G/T | — | uncertain significance |
| rs1428809944 | 18:61,390,542 | C/T | — | uncertain significance |
| rs1914875648 | 18:61,390,587 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.