SERPINB2
serpin family B member 2
Summary
Predicted to enable serine-type endopeptidase inhibitor activity. Predicted to be involved in fibrinolysis and negative regulation of apoptotic process. Predicted to be located in extracellular region and plasma membrane. Predicted to be active in cornified envelope and extracellular space. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs79676280 | 18:61,553,077 | T/G | upstream gene variant | — |
| rs2049926552 | 18:61,558,802 | G/A | — | uncertain significance |
| rs200884637 | 18:61,562,554 | C/A | — | uncertain significance |
| rs138183373 | 18:61,562,568 | G/A | — | benign |
| rs200387636 | 18:61,562,580 | A/C | — | uncertain significance |
| rs149564761 | 18:61,562,581 | G/C | — | uncertain significance |
| rs6096 | 18:61,562,608 | G/A | — | benign |
| rs774883619 | 18:61,564,358 | C/T | — | uncertain significance |
| rs140108044 | 18:61,564,441 | G/A | — | benign |
| rs751668373 | 18:61,564,985 | T/C | — | uncertain significance |
| rs6099 | 18:61,568,970 | G/A | — | benign |
| rs2049992171 | 18:61,568,983 | C/T | — | likely benign |
| rs184826316 | 18:61,569,106 | G/A | — | uncertain significance |
| rs6100 | 18:61,569,645 | G/A | — | likely benign |
| rs149423477 | 18:61,569,663 | T/A | — | uncertain significance |
| rs2511666885 | 18:61,569,666 | A/G | — | uncertain significance |
| rs758753971 | 18:61,569,671 | C/T | — | uncertain significance |
| rs922692149 | 18:61,569,672 | G/A | — | likely benign |
| rs1425545942 | 18:61,569,687 | T/C | — | uncertain significance |
| rs147118804 | 18:61,569,695 | A/G | — | uncertain significance |
| rs148240038 | 18:61,569,760 | G/A | — | benign |
| rs147312209 | 18:61,569,778 | C/T | — | likely benign |
| rs376370601 | 18:61,570,178 | G/A | — | uncertain significance |
| rs373076588 | 18:61,570,301 | G/A | — | likely benign |
| rs763115247 | 18:61,570,337 | T/C | — | uncertain significance |
| rs139893427 | 18:61,570,402 | G/A | — | likely benign |
| rs34066931 | 18:61,570,412 | G/C | — | benign |
| rs764303590 | 18:61,570,417 | G/A | — | likely benign |
| rs753865643 | 18:61,570,444 | G/C | — | uncertain significance |
| rs761899611 | 18:61,570,495 | A/G | — | uncertain significance |
| rs6103 | 18:61,570,503 | C/G | missense variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.