DENND6B
DENN domain containing 6B
Summary
Enables guanyl-nucleotide exchange factor activity. Predicted to be located in cytosol. Predicted to be active in recycling endosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs768971479 | 22:50,750,588 | C/G | — | uncertain significance |
| rs376393455 | 22:50,750,636 | G/T | — | uncertain significance |
| rs779572674 | 22:50,750,639 | C/T | — | uncertain significance |
| rs773433892 | 22:50,750,651 | T/C | — | uncertain significance |
| rs537118220 | 22:50,750,686 | C/G | — | uncertain significance |
| rs772899786 | 22:50,750,782 | C/T | — | uncertain significance |
| rs267606289 | 22:50,750,783 | G/A | — | uncertain significance |
| rs375517464 | 22:50,750,996 | C/T | — | uncertain significance |
| rs781252238 | 22:50,751,017 | G/A | — | uncertain significance |
| rs757154750 | 22:50,751,470 | T/C | — | uncertain significance |
| rs200103246 | 22:50,751,528 | G/T | — | uncertain significance |
| rs201791970 | 22:50,752,107 | C/A | — | uncertain significance |
| rs529694145 | 22:50,752,108 | G/A | — | uncertain significance |
| rs755492151 | 22:50,752,265 | G/A | — | uncertain significance |
| rs372222188 | 22:50,752,274 | C/T | — | uncertain significance |
| rs374647332 | 22:50,752,289 | G/A | — | uncertain significance |
| rs377719391 | 22:50,752,296 | C/T | — | uncertain significance |
| rs369498737 | 22:50,752,662 | C/T | — | uncertain significance |
| rs1007719572 | 22:50,752,916 | C/T | — | uncertain significance |
| rs370513147 | 22:50,753,043 | G/A | — | uncertain significance |
| rs371364338 | 22:50,753,082 | G/C | — | uncertain significance |
| rs763710719 | 22:50,753,229 | T/C | — | uncertain significance |
| rs2520078953 | 22:50,753,240 | A/G | — | uncertain significance |
| rs367892900 | 22:50,753,252 | G/A | — | uncertain significance |
| rs766471515 | 22:50,754,473 | G/A | — | uncertain significance |
| rs201688604 | 22:50,754,477 | G/A | — | uncertain significance |
| rs369068682 | 22:50,754,486 | C/T | — | uncertain significance |
| rs200196394 | 22:50,754,507 | G/A | — | uncertain significance |
| rs1485241907 | 22:50,754,614 | C/T | — | uncertain significance |
| rs1182678308 | 22:50,754,626 | G/A | — | uncertain significance |
| rs2520092189 | 22:50,754,647 | G/A | — | uncertain significance |
| rs201514629 | 22:50,754,649 | G/A | — | likely benign |
| rs772077237 | 22:50,754,668 | C/G | — | uncertain significance |
| rs779301016 | 22:50,754,824 | G/C | — | uncertain significance |
| rs1601816595 | 22:50,754,837 | G/T | — | uncertain significance |
| rs755057088 | 22:50,754,898 | C/T | — | uncertain significance |
| rs370248758 | 22:50,755,781 | C/T | — | uncertain significance |
| rs376619358 | 22:50,756,378 | C/T | — | uncertain significance |
| rs1054756736 | 22:50,757,410 | C/T | — | uncertain significance |
| rs2520165534 | 22:50,765,257 | A/T | — | uncertain significance |
| rs2520166570 | 22:50,765,345 | C/G | — | uncertain significance |
| rs2520166663 | 22:50,765,356 | G/A | — | uncertain significance |
| rs1356291683 | 22:50,765,363 | C/G | — | uncertain significance |
| rs1438568280 | 22:50,765,386 | C/T | — | uncertain significance |
| rs1187112324 | 22:50,765,404 | A/G | — | uncertain significance |
| rs572675392 | 22:50,765,594 | G/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.