SERPINA9
serpin family A member 9
Summary
Enables serine-type endopeptidase inhibitor activity. Predicted to be located in cytoplasm; extracellular region; and membrane. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants49 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201966528 | 14:94,929,380 | T/C | regulatory region variant | — |
| rs374213651 | 14:94,929,434 | G/A | — | likely benign |
| rs779518053 | 14:94,929,480 | T/C | — | uncertain significance |
| rs370040760 | 14:94,929,551 | G/A | — | uncertain significance |
| rs199738408 | 14:94,929,554 | C/T | — | uncertain significance |
| rs1385309859 | 14:94,929,569 | G/A | — | uncertain significance |
| rs149732440 | 14:94,929,676 | C/G | regulatory region variant | — |
| rs145631876 | 14:94,929,677 | T/A | regulatory region variant | — |
| rs202070363 | 14:94,931,042 | A/G | splice region variant | — |
| rs200842178 | 14:94,931,045 | T/G | — | uncertain significance |
| rs77274019 | 14:94,931,052 | C/A | — | uncertain significance |
| rs11628722 | 14:94,931,105 | A/G | missense variant | — |
| rs769429068 | 14:94,931,144 | T/C | — | uncertain significance |
| rs768085902 | 14:94,931,162 | G/A | — | uncertain significance |
| rs141014960 | 14:94,933,188 | T/C | downstream gene variant | — |
| rs752814721 | 14:94,933,464 | C/G | — | uncertain significance |
| rs1421119943 | 14:94,933,503 | A/C | — | uncertain significance |
| rs771427322 | 14:94,933,511 | C/G | — | uncertain significance |
| rs1358181806 | 14:94,933,567 | T/C | — | uncertain significance |
| rs753626112 | 14:94,933,569 | T/G | — | uncertain significance |
| rs1362775364 | 14:94,933,597 | C/T | — | uncertain significance |
| rs2503474386 | 14:94,933,599 | A/G | — | uncertain significance |
| rs1167935139 | 14:94,933,628 | C/T | — | uncertain significance |
| rs780251195 | 14:94,933,686 | G/C | — | uncertain significance |
| rs189300483 | 14:94,933,712 | C/G | — | uncertain significance |
| rs190975457 | 14:94,934,808 | A/C | downstream gene variant | — |
| rs575429531 | 14:94,935,585 | G/A | — | uncertain significance |
| rs371514591 | 14:94,935,630 | G/A | — | uncertain significance |
| rs751760583 | 14:94,935,647 | G/C | — | uncertain significance |
| rs373122783 | 14:94,935,660 | G/T | — | uncertain significance |
| rs776328898 | 14:94,935,792 | G/C | — | uncertain significance |
| rs35347445 | 14:94,935,807 | A/G | — | benign |
| rs374230953 | 14:94,935,888 | C/T | — | uncertain significance |
| rs755752926 | 14:94,935,949 | T/A | — | uncertain significance |
| rs748977210 | 14:94,935,955 | C/T | — | likely benign |
| rs771270945 | 14:94,935,984 | C/T | — | uncertain significance |
| rs1899205931 | 14:94,935,988 | G/C | — | uncertain significance |
| rs199573923 | 14:94,936,008 | C/T | — | uncertain significance |
| rs755841892 | 14:94,936,009 | G/A | — | uncertain significance |
| rs1899209757 | 14:94,936,033 | T/G | — | uncertain significance |
| rs1899210184 | 14:94,936,036 | T/G | — | uncertain significance |
| rs4905204 | 14:94,936,107 | G/A | missense variant | — |
| rs368995727 | 14:94,936,122 | T/C | — | uncertain significance |
| rs570822602 | 14:94,936,131 | G/T | — | uncertain significance |
| rs750901930 | 14:94,936,185 | C/T | — | uncertain significance |
| rs186926075 | 14:94,938,797 | G/A | intron variant | — |
| rs149294373 | 14:94,939,543 | T/C | intron variant | — |
| rs117009764 | 14:94,941,567 | G/A | intron variant | — |
| rs148065423 | 14:94,942,794 | G/A | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.