OGFOD3
2-oxoglutarate and iron dependent oxygenase domain containing 3
Summary
Predicted to enable several functions, including L-ascorbic acid binding activity; dioxygenase activity; and iron ion binding activity. Located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11546697 | 17:80,348,938 | A/G | downstream gene variant | — |
| rs62079522 | 17:80,352,234 | G/T | — | — |
| rs2509897803 | 17:80,352,276 | G/T | — | uncertain significance |
| rs62079523 | 17:80,352,303 | G/A | missense variant | — |
| rs750509197 | 17:80,352,311 | T/C | — | uncertain significance |
| rs145765136 | 17:80,352,320 | G/A | — | uncertain significance |
| rs575435237 | 17:80,352,347 | C/G | — | uncertain significance |
| rs542860141 | 17:80,352,348 | C/G | — | uncertain significance |
| rs2509897941 | 17:80,352,359 | C/A | — | uncertain significance |
| rs141341501 | 17:80,352,368 | G/A | — | uncertain significance |
| rs199562010 | 17:80,352,392 | C/T | — | uncertain significance |
| rs1450664980 | 17:80,352,395 | G/T | — | uncertain significance |
| rs145184893 | 17:80,352,400 | C/T | — | uncertain significance |
| rs373893804 | 17:80,352,404 | C/T | — | uncertain significance |
| rs2509898011 | 17:80,352,406 | G/T | — | uncertain significance |
| rs560916517 | 17:80,356,089 | G/A | — | uncertain significance |
| rs766110253 | 17:80,356,122 | C/T | — | uncertain significance |
| rs749128771 | 17:80,356,126 | C/A | — | uncertain significance |
| rs369169788 | 17:80,356,182 | G/T | — | uncertain significance |
| rs1399820894 | 17:80,356,191 | G/C | — | uncertain significance |
| rs778685999 | 17:80,361,826 | G/A | — | uncertain significance |
| rs765926113 | 17:80,361,868 | T/C | — | uncertain significance |
| rs368120240 | 17:80,361,874 | C/A | — | uncertain significance |
| rs527568467 | 17:80,363,201 | G/A | — | uncertain significance |
| rs1477475373 | 17:80,363,249 | C/T | — | uncertain significance |
| rs191470730 | 17:80,364,319 | C/G | — | uncertain significance |
| rs148998477 | 17:80,367,285 | C/T | — | likely benign |
| rs150938774 | 17:80,369,330 | C/T | splice region variant | — |
| rs761548449 | 17:80,369,338 | T/A | — | uncertain significance |
| rs767488958 | 17:80,369,340 | C/T | — | likely benign |
| rs2509921985 | 17:80,369,382 | C/T | — | uncertain significance |
| rs886182130 | 17:80,369,386 | C/T | — | uncertain significance |
| rs780739143 | 17:80,373,351 | C/T | — | likely benign |
| rs34028107 | 17:80,373,431 | C/T | — | benign |
| rs527862857 | 17:80,373,480 | C/T | — | uncertain significance |
| rs767640082 | 17:80,373,483 | G/A | — | uncertain significance |
| rs750689701 | 17:80,373,489 | C/T | — | uncertain significance |
| rs761016972 | 17:80,376,355 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.