AGAP4
ArfGAP with GTPase domain, ankyrin repeat and PH domain 4
Summary
Predicted to enable GTPase activator activity and GTPase activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants72 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1169771928 | 10:46,321,374 | T/C | — | uncertain significance |
| rs2495569274 | 10:46,321,383 | A/C | — | uncertain significance |
| rs782077911 | 10:46,321,388 | T/G | — | uncertain significance |
| rs201101765 | 10:46,321,406 | A/G | — | uncertain significance |
| rs1290106805 | 10:46,321,466 | C/A | — | uncertain significance |
| rs1368321606 | 10:46,321,544 | G/A | — | uncertain significance |
| rs2058641797 | 10:46,321,560 | C/T | — | uncertain significance |
| rs1266177464 | 10:46,321,580 | A/T | — | uncertain significance |
| rs2058642549 | 10:46,321,590 | G/A | — | uncertain significance |
| rs2495571510 | 10:46,321,625 | A/G | — | uncertain significance |
| rs2495571519 | 10:46,321,628 | T/C | — | uncertain significance |
| rs1183546174 | 10:46,321,646 | C/T | — | uncertain significance |
| rs2058643960 | 10:46,321,655 | T/C | — | uncertain significance |
| rs1554896179 | 10:46,321,667 | G/A | — | uncertain significance |
| rs1229220870 | 10:46,321,686 | G/C | — | uncertain significance |
| rs1428646434 | 10:46,321,703 | T/A | — | uncertain significance |
| rs879956570 | 10:46,321,707 | C/T | — | uncertain significance |
| rs1482221451 | 10:46,321,722 | G/A | — | uncertain significance |
| rs1311210030 | 10:46,321,733 | T/A | — | uncertain significance |
| rs76023144 | 10:46,321,748 | G/A | — | uncertain significance |
| rs1294908497 | 10:46,321,753 | C/G | — | uncertain significance |
| rs200353759 | 10:46,321,757 | T/A | — | uncertain significance |
| rs879953237 | 10:46,321,758 | C/T | — | uncertain significance |
| rs373299289 | 10:46,321,772 | T/C | — | uncertain significance |
| rs202219577 | 10:46,321,810 | G/C | — | uncertain significance |
| rs201261369 | 10:46,321,875 | G/C | — | uncertain significance |
| rs1173273101 | 10:46,321,881 | G/A | — | uncertain significance |
| rs1170654608 | 10:46,321,890 | G/A | — | uncertain significance |
| rs781969562 | 10:46,321,899 | G/C | — | uncertain significance |
| rs1590010740 | 10:46,321,901 | C/T | — | uncertain significance |
| rs1187042801 | 10:46,321,902 | T/C | — | uncertain significance |
| rs782598354 | 10:46,322,028 | C/A | — | uncertain significance |
| rs2495575472 | 10:46,322,081 | G/A | — | uncertain significance |
| rs782791788 | 10:46,322,100 | T/G | — | uncertain significance |
| rs1290265434 | 10:46,322,132 | C/A | — | uncertain significance |
| rs1332671749 | 10:46,322,133 | G/A | — | uncertain significance |
| rs782486158 | 10:46,322,134 | C/T | — | likely benign |
| rs1438821705 | 10:46,322,147 | G/A | — | uncertain significance |
| rs1457313396 | 10:46,322,165 | G/A | — | uncertain significance |
| rs1316440233 | 10:46,322,210 | T/C | — | uncertain significance |
| rs1282313249 | 10:46,322,231 | T/C | — | uncertain significance |
| rs74803687 | 10:46,322,252 | G/A | — | uncertain significance |
| rs200665580 | 10:46,322,267 | C/A | — | likely benign |
| rs782666549 | 10:46,322,268 | T/C | — | uncertain significance |
| rs2495576969 | 10:46,322,273 | G/A | — | uncertain significance |
| rs1443014550 | 10:46,322,284 | A/C | — | uncertain significance |
| rs1590011415 | 10:46,322,285 | C/G | — | uncertain significance |
| rs781976923 | 10:46,322,316 | C/T | — | uncertain significance |
| rs140034862 | 10:46,322,330 | T/C | — | uncertain significance |
| rs4043112 | 10:46,322,354 | G/C | — | likely benign |
| rs2058659143 | 10:46,322,442 | T/C | — | uncertain significance |
| rs1295110141 | 10:46,322,487 | G/C | — | uncertain significance |
| rs1288429752 | 10:46,322,595 | C/T | — | uncertain significance |
| rs1327009720 | 10:46,322,679 | G/A | — | uncertain significance |
| rs782252245 | 10:46,322,682 | T/C | — | uncertain significance |
| rs1313743301 | 10:46,322,687 | C/T | — | uncertain significance |
| rs1373025033 | 10:46,322,699 | G/T | — | uncertain significance |
| rs1459932271 | 10:46,322,777 | G/C | — | uncertain significance |
| rs1183850151 | 10:46,322,816 | T/C | — | uncertain significance |
| rs75899554 | 10:46,322,819 | A/G | — | likely benign |
| rs1440872040 | 10:46,329,485 | T/C | — | uncertain significance |
| rs200116047 | 10:46,329,521 | G/A | — | uncertain significance |
| rs1452733813 | 10:46,329,551 | C/A | — | uncertain significance |
| rs1488819610 | 10:46,339,806 | C/T | — | uncertain significance |
| rs1372297990 | 10:46,342,588 | G/A | — | uncertain significance |
| rs201098582 | 10:46,342,598 | G/C | — | uncertain significance |
| rs2495744444 | 10:46,342,651 | C/T | — | uncertain significance |
| rs1211370902 | 10:46,342,677 | A/G | — | uncertain significance |
| rs1371059894 | 10:46,342,687 | C/T | — | uncertain significance |
| rs2495745367 | 10:46,342,708 | C/G | — | uncertain significance |
| rs1361206615 | 10:46,342,743 | T/A | — | uncertain significance |
| rs1248251534 | 10:46,342,762 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.