FGD5
FYVE, RhoGEF and PH domain containing 5
Summary
Predicted to enable guanyl-nucleotide exchange factor activity and small GTPase binding activity. Predicted to be involved in actin cytoskeleton organization; filopodium assembly; and regulation of cell shape. Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants131 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs535835096 | 3:14,860,586 | G/C | — | uncertain significance |
| rs1442963819 | 3:14,860,588 | G/T | — | uncertain significance |
| rs759256192 | 3:14,860,592 | C/T | — | uncertain significance |
| rs2470474866 | 3:14,860,627 | G/A | — | likely benign |
| rs777243314 | 3:14,860,735 | A/G | — | likely benign |
| rs1477801496 | 3:14,860,777 | G/A | — | uncertain significance |
| rs561368486 | 3:14,860,793 | C/T | — | likely benign |
| rs2470475519 | 3:14,860,805 | A/T | — | uncertain significance |
| rs934462434 | 3:14,860,818 | C/A | — | uncertain significance |
| rs775239574 | 3:14,860,835 | A/G | — | uncertain significance |
| rs931597932 | 3:14,860,855 | G/A | — | uncertain significance |
| rs868832283 | 3:14,860,880 | A/G | — | uncertain significance |
| rs1353175398 | 3:14,860,883 | G/A | — | likely benign |
| rs200549806 | 3:14,860,955 | C/T | — | uncertain significance |
| rs2470476406 | 3:14,861,006 | T/G | — | uncertain significance |
| rs1432089802 | 3:14,861,029 | G/A | — | uncertain significance |
| rs1400730892 | 3:14,861,056 | G/C | — | uncertain significance |
| rs144016950 | 3:14,861,103 | G/T | — | uncertain significance |
| rs1294232710 | 3:14,861,156 | A/G | — | uncertain significance |
| rs746189207 | 3:14,861,197 | C/T | — | uncertain significance |
| rs199756592 | 3:14,861,200 | G/A | — | uncertain significance |
| rs2036442346 | 3:14,861,216 | C/T | — | likely benign |
| rs1282833872 | 3:14,861,226 | T/G | — | uncertain significance |
| rs1044156733 | 3:14,861,246 | G/C | — | uncertain significance |
| rs368016397 | 3:14,861,294 | C/T | — | uncertain significance |
| rs759267412 | 3:14,861,344 | A/G | — | uncertain significance |
| rs376698279 | 3:14,861,359 | G/A | — | uncertain significance |
| rs758731769 | 3:14,861,395 | G/A | — | uncertain significance |
| rs1252809380 | 3:14,861,428 | G/A | — | uncertain significance |
| rs760484848 | 3:14,861,470 | G/C | — | uncertain significance |
| rs1448630696 | 3:14,861,510 | C/T | — | uncertain significance |
| rs200107291 | 3:14,861,538 | C/T | — | likely benign |
| rs546389054 | 3:14,861,539 | G/C | — | uncertain significance |
| rs767984289 | 3:14,861,542 | G/A | — | uncertain significance |
| rs2470478949 | 3:14,861,558 | T/C | — | uncertain significance |
| rs762092474 | 3:14,861,581 | A/G | — | likely benign |
| rs748006378 | 3:14,861,782 | G/A | — | uncertain significance |
| rs7636593 | 3:14,861,785 | G/A | — | benign |
| rs149850629 | 3:14,861,802 | C/T | — | benign |
| rs568677261 | 3:14,861,803 | G/A | — | uncertain significance |
| rs772985473 | 3:14,861,813 | A/T | — | uncertain significance |
| rs1375310421 | 3:14,861,867 | A/G | — | uncertain significance |
| rs2470480059 | 3:14,861,873 | T/C | — | uncertain significance |
| rs747328399 | 3:14,861,912 | G/C | — | uncertain significance |
| rs779159878 | 3:14,861,932 | G/A | — | likely benign |
| rs373582365 | 3:14,861,968 | T/C | — | uncertain significance |
| rs777253442 | 3:14,862,049 | G/A | — | uncertain significance |
| rs532000328 | 3:14,862,143 | C/T | — | uncertain significance |
| rs1382589526 | 3:14,862,175 | G/T | — | uncertain significance |
| rs754634002 | 3:14,862,189 | G/T | — | uncertain significance |
| rs1360249841 | 3:14,862,191 | C/T | — | uncertain significance |
| rs182441976 | 3:14,862,262 | G/A | — | uncertain significance |
| rs778673810 | 3:14,862,274 | C/G | — | uncertain significance |
| rs200123013 | 3:14,862,275 | C/T | — | uncertain significance |
| rs772051616 | 3:14,862,338 | G/A | — | uncertain significance |
| rs762005263 | 3:14,862,350 | C/T | — | uncertain significance |
| rs144177006 | 3:14,862,376 | C/T | — | benign |
| rs201649366 | 3:14,862,401 | C/T | — | uncertain significance |
| rs2470481886 | 3:14,862,406 | T/C | — | uncertain significance |
| rs370742215 | 3:14,862,412 | A/G | — | likely benign |
| rs2470482099 | 3:14,862,475 | T/C | — | uncertain significance |
| rs756017066 | 3:14,862,495 | G/C | — | uncertain significance |
| rs370762215 | 3:14,862,506 | C/T | — | uncertain significance |
| rs151190469 | 3:14,862,636 | T/C | — | likely benign |
| rs780469962 | 3:14,862,683 | A/G | — | uncertain significance |
| rs997720229 | 3:14,862,761 | G/C | — | uncertain significance |
| rs555378624 | 3:14,862,770 | A/T | — | uncertain significance |
| rs2470483059 | 3:14,862,835 | T/C | — | uncertain significance |
| rs778185362 | 3:14,862,884 | C/T | — | uncertain significance |
| rs769563385 | 3:14,862,918 | G/T | — | uncertain significance |
| rs773067439 | 3:14,862,919 | A/G | — | uncertain significance |
| rs368010628 | 3:14,862,934 | A/G | — | uncertain significance |
| rs1266604563 | 3:14,862,970 | G/A | — | uncertain significance |
| rs140419004 | 3:14,863,038 | C/T | — | benign |
| rs17038795 | 3:14,863,060 | G/A | — | benign |
| rs141963627 | 3:14,863,096 | G/A | — | benign |
| rs76976054 | 3:14,864,586 | G/A | intron variant | — |
| rs60573957 | 3:14,884,409 | C/T | intron variant | — |
| rs1687295 | 3:14,889,756 | T/G | — | — |
| rs12108073 | 3:14,891,755 | G/A | intron variant | — |
| rs534805229 | 3:14,895,033 | G/A | — | — |
| rs294636 | 3:14,899,778 | G/C | — | — |
| rs13079221 | 3:14,901,525 | C/T | — | — |
| rs763733628 | 3:14,905,665 | C/T | — | likely benign |
| rs267599640 | 3:14,905,722 | G/A | — | likely benign |
| rs201768331 | 3:14,922,252 | C/T | — | likely benign |
| rs201501524 | 3:14,922,265 | C/G | — | uncertain significance |
| rs1898040 | 3:14,937,400 | G/A | — | — |
| rs6762862 | 3:14,938,024 | G/C | intron variant | — |
| rs182966141 | 3:14,939,186 | C/G | — | benign |
| rs58244401 | 3:14,939,337 | G/A | intron variant | — |
| rs60413292 | 3:14,939,506 | C/T | — | benign |
| rs766058296 | 3:14,939,561 | C/T | — | uncertain significance |
| rs754570338 | 3:14,939,566 | C/G | — | uncertain significance |
| rs1455650625 | 3:14,940,261 | G/A | — | uncertain significance |
| rs757177669 | 3:14,940,270 | A/G | — | uncertain significance |
| rs369369417 | 3:14,940,282 | C/T | — | uncertain significance |
| rs1213553807 | 3:14,940,292 | G/A | — | uncertain significance |
| rs368736589 | 3:14,942,537 | C/T | — | uncertain significance |
| rs375051384 | 3:14,942,543 | G/T | — | uncertain significance |
Showing 100 of 131 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.