AGAP6
ArfGAP with GTPase domain, ankyrin repeat and PH domain 6
Summary
Predicted to enable GTPase activator activity and GTPase activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants60 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs782327008 | 10:51,748,512 | G/A | — | uncertain significance |
| rs1337991786 | 10:51,748,578 | G/A | — | uncertain significance |
| rs371327390 | 10:51,748,622 | A/G | — | likely benign |
| rs782310286 | 10:51,748,695 | G/C | — | uncertain significance |
| rs782153811 | 10:51,751,456 | G/A | — | uncertain significance |
| rs782285569 | 10:51,761,769 | G/A | — | likely benign |
| rs532966615 | 10:51,761,790 | T/C | — | likely benign |
| rs1842006468 | 10:51,768,531 | T/A | — | uncertain significance |
| rs1227565433 | 10:51,768,534 | T/C | — | uncertain significance |
| rs1842007540 | 10:51,768,562 | A/G | — | uncertain significance |
| rs782372580 | 10:51,768,591 | A/G | — | uncertain significance |
| rs781971646 | 10:51,768,607 | C/T | — | uncertain significance |
| rs781880638 | 10:51,768,622 | G/A | — | uncertain significance |
| rs1589108190 | 10:51,768,674 | C/A | — | uncertain significance |
| rs782716959 | 10:51,768,714 | G/A | — | uncertain significance |
| rs782485980 | 10:51,768,723 | A/G | — | uncertain significance |
| rs781941358 | 10:51,768,760 | G/A | — | uncertain significance |
| rs781821173 | 10:51,768,783 | T/A | — | uncertain significance |
| rs782699081 | 10:51,768,798 | G/C | — | uncertain significance |
| rs556692912 | 10:51,768,855 | A/G | — | uncertain significance |
| rs1554864785 | 10:51,768,883 | T/A | — | uncertain significance |
| rs2539920393 | 10:51,768,888 | A/G | — | uncertain significance |
| rs199932582 | 10:51,768,922 | C/T | — | uncertain significance |
| rs1344414577 | 10:51,768,945 | C/T | — | uncertain significance |
| rs782654601 | 10:51,769,006 | C/A | — | uncertain significance |
| rs1842024213 | 10:51,769,042 | G/T | — | uncertain significance |
| rs1206027049 | 10:51,769,165 | C/T | — | uncertain significance |
| rs782422992 | 10:51,769,183 | C/T | — | uncertain significance |
| rs2539921134 | 10:51,769,203 | A/T | — | uncertain significance |
| rs1554865019 | 10:51,769,215 | G/C | — | uncertain significance |
| rs570782198 | 10:51,769,288 | A/C | — | uncertain significance |
| rs1398777709 | 10:51,769,303 | T/C | — | uncertain significance |
| rs199841016 | 10:51,769,405 | G/A | — | uncertain significance |
| rs1280373476 | 10:51,769,407 | A/G | — | uncertain significance |
| rs200482356 | 10:51,769,408 | G/A | — | uncertain significance |
| rs781826206 | 10:51,769,435 | G/A | — | uncertain significance |
| rs1445124371 | 10:51,769,481 | G/A | — | uncertain significance |
| rs531472394 | 10:51,769,492 | T/G | — | uncertain significance |
| rs781979794 | 10:51,769,506 | A/G | — | uncertain significance |
| rs1418661628 | 10:51,769,551 | G/A | — | uncertain significance |
| rs1358264792 | 10:51,769,552 | A/T | — | uncertain significance |
| rs527558369 | 10:51,769,578 | C/T | — | uncertain significance |
| rs782697526 | 10:51,769,587 | C/T | — | uncertain significance |
| rs533152789 | 10:51,769,588 | G/A | — | uncertain significance |
| rs1842044994 | 10:51,769,599 | G/A | — | uncertain significance |
| rs569772586 | 10:51,769,656 | C/G | — | uncertain significance |
| rs782115209 | 10:51,769,668 | A/G | — | uncertain significance |
| rs782071621 | 10:51,769,690 | C/T | — | uncertain significance |
| rs782671554 | 10:51,769,734 | G/A | — | uncertain significance |
| rs781925022 | 10:51,769,755 | G/A | — | uncertain significance |
| rs781883461 | 10:51,769,782 | C/T | — | uncertain significance |
| rs1253848273 | 10:51,769,793 | T/A | — | uncertain significance |
| rs1217564685 | 10:51,769,794 | G/A | — | uncertain significance |
| rs576162483 | 10:51,769,804 | C/A | — | uncertain significance |
| rs1164738106 | 10:51,769,833 | G/A | — | uncertain significance |
| rs201492638 | 10:51,769,873 | A/G | — | uncertain significance |
| rs1219024064 | 10:51,769,875 | G/A | — | uncertain significance |
| rs1340105020 | 10:51,769,876 | C/A | — | uncertain significance |
| rs1391600696 | 10:51,769,878 | C/T | — | uncertain significance |
| rs1554865654 | 10:51,769,930 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.