SERPINA4
serpin family A member 4
Summary
Predicted to enable serine-type endopeptidase inhibitor activity. Located in extracellular exosome. Biomarker of diabetic retinopathy. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs882732 | 14:95,027,722 | G/A | regulatory region variant | — |
| rs148837645 | 14:95,028,931 | C/A | intron variant | — |
| rs769068863 | 14:95,029,889 | G/A | — | uncertain significance |
| rs372314134 | 14:95,030,018 | G/A | — | uncertain significance |
| rs2503649266 | 14:95,030,054 | C/T | — | uncertain significance |
| rs140377924 | 14:95,030,090 | C/A | — | uncertain significance |
| rs201138033 | 14:95,030,112 | G/A | — | uncertain significance |
| rs2503649904 | 14:95,030,159 | G/C | — | uncertain significance |
| rs1463278007 | 14:95,030,162 | T/A | — | uncertain significance |
| rs764474650 | 14:95,030,178 | G/A | — | uncertain significance |
| rs368977287 | 14:95,030,205 | A/G | — | likely benign |
| rs145028164 | 14:95,030,229 | C/A | — | uncertain significance |
| rs140563422 | 14:95,030,231 | C/T | — | benign |
| rs539993882 | 14:95,030,234 | G/A | — | likely benign |
| rs1902119849 | 14:95,030,270 | T/C | — | likely benign |
| rs2503650641 | 14:95,030,289 | A/G | — | uncertain significance |
| rs372759493 | 14:95,030,290 | T/A | — | uncertain significance |
| rs1450634979 | 14:95,030,294 | A/G | — | uncertain significance |
| rs369378451 | 14:95,030,301 | C/A | — | uncertain significance |
| rs766351953 | 14:95,030,316 | A/G | — | uncertain significance |
| rs550133117 | 14:95,030,339 | G/A | — | uncertain significance |
| rs748736850 | 14:95,030,357 | C/G | — | uncertain significance |
| rs2093266 | 14:95,032,787 | G/T | — | — |
| rs746077233 | 14:95,033,368 | G/C | — | uncertain significance |
| rs369263026 | 14:95,033,456 | C/T | — | uncertain significance |
| rs191488393 | 14:95,033,457 | G/A | — | uncertain significance |
| rs2503658395 | 14:95,033,571 | T/G | — | uncertain significance |
| rs5511 | 14:95,033,595 | A/T | intron variant | — |
| rs1258852245 | 14:95,034,519 | C/T | — | uncertain significance |
| rs929227047 | 14:95,034,541 | G/C | — | uncertain significance |
| rs763312128 | 14:95,034,558 | C/A | — | uncertain significance |
| rs547679516 | 14:95,035,756 | G/A | — | uncertain significance |
| rs145967569 | 14:95,035,764 | G/A | — | benign |
| rs568753504 | 14:95,035,823 | C/T | — | uncertain significance |
| rs756954859 | 14:95,035,829 | G/T | — | uncertain significance |
| rs753287491 | 14:95,035,850 | G/A | — | uncertain significance |
| rs376945073 | 14:95,035,877 | C/T | — | uncertain significance |
| rs143372998 | 14:95,035,883 | C/A | — | uncertain significance |
| rs1281981206 | 14:95,035,889 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.