RABGAP1
RAB GTPase activating protein 1
Summary
Enables GTPase activator activity and small GTPase binding activity. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1868590 | 9:125,694,610 | C/A | regulatory region variant | — |
| rs9409265 | 9:125,696,237 | G/C | — | — |
| rs369508364 | 9:125,696,599 | C/T | — | — |
| rs10985827 | 9:125,701,608 | T/C | coding sequence variant | — |
| rs192792836 | 9:125,719,427 | G/A | — | uncertain significance |
| rs775007107 | 9:125,719,442 | C/T | — | uncertain significance |
| rs2538469374 | 9:125,719,483 | C/T | — | uncertain significance |
| rs10818769 | 9:125,719,923 | C/T | — | — |
| rs9695700 | 9:125,723,227 | T/G | — | — |
| rs375853497 | 9:125,746,782 | G/C | — | uncertain significance |
| rs139609845 | 9:125,746,830 | A/G | — | uncertain significance |
| rs757241963 | 9:125,746,831 | T/A | — | uncertain significance |
| rs1360812458 | 9:125,746,843 | C/G | — | uncertain significance |
| rs552313132 | 9:125,746,977 | C/T | — | uncertain significance |
| rs1355164752 | 9:125,748,676 | A/T | — | uncertain significance |
| rs146784057 | 9:125,751,650 | A/G | — | uncertain significance |
| rs199950459 | 9:125,752,407 | G/A | — | uncertain significance |
| rs12335837 | 9:125,753,886 | T/C | regulatory region variant | — |
| rs10818775 | 9:125,755,571 | C/T | intron variant | — |
| rs749802603 | 9:125,758,837 | A/G | — | uncertain significance |
| rs2538682115 | 9:125,759,560 | A/C | — | uncertain significance |
| rs758703178 | 9:125,759,608 | A/T | — | uncertain significance |
| rs587364 | 9:125,760,863 | T/A | — | — |
| rs375554014 | 9:125,760,965 | G/A | — | uncertain significance |
| rs2030692055 | 9:125,772,642 | A/T | — | uncertain significance |
| rs1039966177 | 9:125,772,715 | G/C | — | uncertain significance |
| rs653441 | 9:125,778,647 | G/A | intron variant | — |
| rs554265256 | 9:125,782,330 | T/C | — | — |
| rs201053287 | 9:125,782,705 | C/G | — | uncertain significance |
| rs2430398 | 9:125,818,456 | G/C | intron variant | — |
| rs2488466 | 9:125,818,809 | T/G | regulatory region variant | — |
| rs2538950117 | 9:125,827,717 | G/C | — | uncertain significance |
| rs2538968794 | 9:125,835,888 | A/G | — | uncertain significance |
| rs2538974763 | 9:125,838,536 | A/T | — | uncertain significance |
| rs60371393 | 9:125,839,449 | T/A | — | — |
| rs117178690 | 9:125,852,118 | G/A | — | uncertain significance |
| rs368348244 | 9:125,852,653 | G/A | — | uncertain significance |
| rs773784771 | 9:125,860,063 | C/G | — | uncertain significance |
| rs142594031 | 9:125,861,010 | G/A | — | uncertain significance |
| rs7854147 | 9:125,863,350 | A/G | intron variant | — |
| rs763827537 | 9:125,863,867 | G/A | — | uncertain significance |
| rs754506974 | 9:125,863,899 | G/A | — | likely benign |
| rs1485048912 | 9:125,863,984 | T/G | — | uncertain significance |
| rs757193105 | 9:125,864,029 | A/C | — | uncertain significance |
| rs9032 | 9:125,866,772 | C/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.