SERGEF
secretion regulating guanine nucleotide exchange factor
Summary
Predicted to enable guanyl-nucleotide exchange factor activity. Involved in negative regulation of protein secretion. Located in cytosol and nucleoplasm. Biomarker of atherosclerosis. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs780954703 | 11:17,809,718 | T/C | — | uncertain significance |
| rs138152821 | 11:17,809,742 | C/T | — | uncertain significance |
| rs764337118 | 11:17,809,824 | G/T | — | uncertain significance |
| rs2497832511 | 11:17,809,840 | C/T | — | uncertain significance |
| rs777458585 | 11:17,809,874 | G/C | — | uncertain significance |
| rs147331551 | 11:17,809,879 | G/A | — | uncertain significance |
| rs138466972 | 11:17,809,895 | C/T | — | likely benign |
| rs142343672 | 11:17,871,273 | G/A | intron variant | — |
| rs528938287 | 11:17,897,398 | C/T | — | — |
| rs1191772689 | 11:17,899,761 | T/C | — | likely benign |
| rs59881258 | 11:17,934,885 | G/A | intron variant | — |
| rs4393297 | 11:17,943,664 | C/G | regulatory region variant | — |
| rs61884490 | 11:17,960,577 | G/T | intron variant | — |
| rs511604 | 11:17,967,419 | C/T | — | — |
| rs777339753 | 11:17,981,055 | T/A | — | uncertain significance |
| rs2670765 | 11:17,985,273 | T/C | intron variant | — |
| rs211098 | 11:17,991,892 | G/A | intron variant | — |
| rs371469105 | 11:18,010,152 | G/A | — | uncertain significance |
| rs768014018 | 11:18,010,156 | C/G | — | uncertain significance |
| rs570727205 | 11:18,010,175 | C/G | — | uncertain significance |
| rs1268594303 | 11:18,010,222 | T/C | — | uncertain significance |
| rs760627194 | 11:18,010,230 | A/C | — | uncertain significance |
| rs1456835762 | 11:18,017,351 | C/G | — | uncertain significance |
| rs748866471 | 11:18,017,353 | G/C | — | uncertain significance |
| rs369372033 | 11:18,017,405 | C/A | — | uncertain significance |
| rs199581346 | 11:18,017,406 | G/A | — | uncertain significance |
| rs2679116 | 11:18,019,673 | T/C | downstream gene variant | — |
| rs571272304 | 11:18,022,104 | G/A | — | uncertain significance |
| rs1398439820 | 11:18,026,053 | T/A | — | uncertain significance |
| rs768986141 | 11:18,028,173 | A/G | — | uncertain significance |
| rs2493967620 | 11:18,029,598 | C/A | — | uncertain significance |
| rs1289781467 | 11:18,029,622 | C/A | — | uncertain significance |
| rs2237908 | 11:18,032,538 | A/G | intron variant | — |
| rs2493976383 | 11:18,034,502 | G/A | — | uncertain significance |
| rs377166311 | 11:18,034,505 | A/C | — | uncertain significance |
| rs1271435861 | 11:18,034,527 | C/T | — | uncertain significance |
| rs921807829 | 11:18,034,548 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.