AGAP5
ArfGAP with GTPase domain, ankyrin repeat and PH domain 5
Summary
Predicted to enable GTPase activator activity and GTPase activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1307527810 | 10:75,434,397 | T/G | — | uncertain significance |
| rs1229929531 | 10:75,434,415 | G/A | — | uncertain significance |
| rs528329950 | 10:75,434,424 | C/T | — | uncertain significance |
| rs533481377 | 10:75,434,428 | C/T | — | uncertain significance |
| rs551514358 | 10:75,434,433 | G/T | — | uncertain significance |
| rs3901391 | 10:75,434,439 | G/C | — | uncertain significance |
| rs571472152 | 10:75,434,549 | G/C | — | uncertain significance |
| rs1335706138 | 10:75,434,632 | C/T | — | uncertain significance |
| rs753851533 | 10:75,434,715 | C/T | — | uncertain significance |
| rs757545488 | 10:75,434,716 | G/A | — | uncertain significance |
| rs113207551 | 10:75,434,725 | G/A | — | uncertain significance |
| rs3998273 | 10:75,434,766 | T/C | — | uncertain significance |
| rs1423232186 | 10:75,434,793 | C/G | — | uncertain significance |
| rs930400422 | 10:75,434,893 | G/C | — | uncertain significance |
| rs1330255388 | 10:75,434,895 | C/G | — | uncertain significance |
| rs2132437114 | 10:75,435,073 | A/G | — | uncertain significance |
| rs1220466224 | 10:75,435,081 | A/G | — | uncertain significance |
| rs1215715847 | 10:75,435,216 | T/G | — | uncertain significance |
| rs200899801 | 10:75,435,220 | T/G | — | uncertain significance |
| rs2081970984 | 10:75,435,286 | T/A | — | uncertain significance |
| rs1183289791 | 10:75,435,301 | C/T | — | uncertain significance |
| rs1287362918 | 10:75,435,396 | G/C | — | uncertain significance |
| rs112243735 | 10:75,435,417 | C/T | — | uncertain significance |
| rs1490343127 | 10:75,435,484 | C/T | — | uncertain significance |
| rs1254498982 | 10:75,435,489 | T/C | — | uncertain significance |
| rs774468046 | 10:75,435,589 | C/T | — | uncertain significance |
| rs200986858 | 10:75,435,673 | G/A | — | uncertain significance |
| rs1325195204 | 10:75,435,682 | G/A | — | uncertain significance |
| rs3878010 | 10:75,435,813 | G/A | — | uncertain significance |
| rs1324822282 | 10:75,435,823 | C/T | — | uncertain significance |
| rs765758599 | 10:75,436,509 | T/C | — | uncertain significance |
| rs1451940878 | 10:75,442,459 | T/C | — | uncertain significance |
| rs200112765 | 10:75,442,477 | G/C | — | uncertain significance |
| rs1385955220 | 10:75,442,520 | G/C | — | uncertain significance |
| rs76443711 | 10:75,449,789 | G/T | — | — |
| rs765878659 | 10:75,451,793 | T/C | — | likely benign |
| rs201189488 | 10:75,454,549 | G/T | — | uncertain significance |
| rs537981618 | 10:75,457,312 | G/A | — | uncertain significance |
| rs776630165 | 10:75,457,386 | G/A | — | uncertain significance |
| rs750852434 | 10:75,457,396 | T/A | — | uncertain significance |
| rs773341191 | 10:75,457,477 | C/T | — | uncertain significance |
| rs752304824 | 10:75,457,503 | A/G | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.