ARFGAP2
ARF GTPase activating protein 2
Summary
Predicted to enable GTPase activator activity. Predicted to be involved in COPI coating of Golgi vesicle. Located in Golgi apparatus; cytosol; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs138370539 | 11:47,187,029 | C/T | — | benign |
| rs142683966 | 11:47,187,044 | C/T | — | likely benign |
| rs749706851 | 11:47,187,919 | T/A | — | uncertain significance |
| rs576771926 | 11:47,188,328 | G/A | — | uncertain significance |
| rs139591977 | 11:47,188,381 | G/A | — | uncertain significance |
| rs1413666492 | 11:47,188,394 | C/T | — | uncertain significance |
| rs763086182 | 11:47,188,409 | G/A | — | uncertain significance |
| rs200794218 | 11:47,188,426 | C/T | — | uncertain significance |
| rs35950498 | 11:47,188,427 | G/A | — | benign |
| rs755766412 | 11:47,188,430 | T/G | — | uncertain significance |
| rs756994670 | 11:47,189,475 | C/T | — | uncertain significance |
| rs2540281892 | 11:47,189,497 | C/G | — | uncertain significance |
| rs143546578 | 11:47,189,506 | T/C | — | uncertain significance |
| rs1759460176 | 11:47,189,563 | T/C | — | uncertain significance |
| rs754289541 | 11:47,189,568 | C/T | — | uncertain significance |
| rs373373969 | 11:47,189,698 | C/T | — | uncertain significance |
| rs34662994 | 11:47,189,728 | C/A | — | likely benign |
| rs780219540 | 11:47,189,735 | A/C | — | uncertain significance |
| rs2540297819 | 11:47,193,052 | T/C | — | uncertain significance |
| rs141420803 | 11:47,193,061 | T/A | — | uncertain significance |
| rs1193629451 | 11:47,193,064 | C/A | — | uncertain significance |
| rs2540298265 | 11:47,193,098 | T/C | — | uncertain significance |
| rs114371790 | 11:47,193,209 | A/G | — | benign |
| rs34580829 | 11:47,193,226 | C/T | — | benign |
| rs201018164 | 11:47,193,227 | G/A | — | uncertain significance |
| rs780788328 | 11:47,193,249 | C/T | — | uncertain significance |
| rs367812497 | 11:47,193,260 | C/T | — | uncertain significance |
| rs138040761 | 11:47,193,261 | G/A | — | benign |
| rs575856978 | 11:47,193,350 | A/G | — | benign |
| rs372871965 | 11:47,195,030 | G/A | — | uncertain significance |
| rs762487628 | 11:47,195,334 | A/G | — | likely benign |
| rs757406658 | 11:47,195,361 | G/T | — | uncertain significance |
| rs756613740 | 11:47,196,634 | T/C | — | uncertain significance |
| rs201392297 | 11:47,196,726 | C/T | — | likely benign |
| rs150524180 | 11:47,196,774 | G/A | — | uncertain significance |
| rs117324352 | 11:47,196,821 | T/C | — | likely benign |
| rs116818981 | 11:47,196,874 | A/G | — | likely benign |
| rs777699645 | 11:47,197,434 | T/A | — | uncertain significance |
| rs1426540768 | 11:47,197,454 | T/C | — | uncertain significance |
| rs568596407 | 11:47,198,061 | G/A | — | likely benign |
| rs772490982 | 11:47,198,382 | G/C | — | uncertain significance |
| rs751176662 | 11:47,198,413 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.