ZNF283
zinc finger protein 283
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs535195863 | 19:44,337,084 | G/T | — | — |
| rs7255083 | 19:44,337,803 | T/C | intron variant | — |
| rs778828376 | 19:44,341,235 | G/A | — | uncertain significance |
| rs2514037246 | 19:44,341,240 | C/A | — | uncertain significance |
| rs367553149 | 19:44,341,251 | A/C | — | uncertain significance |
| rs770377766 | 19:44,341,289 | G/A | — | uncertain significance |
| rs201943823 | 19:44,341,305 | A/T | — | uncertain significance |
| rs1329482809 | 19:44,351,106 | C/T | — | uncertain significance |
| rs760941945 | 19:44,351,165 | T/G | — | uncertain significance |
| rs769569044 | 19:44,351,178 | A/C | — | uncertain significance |
| rs200882734 | 19:44,351,276 | T/G | — | uncertain significance |
| rs201560248 | 19:44,351,298 | A/G | — | uncertain significance |
| rs1446356539 | 19:44,351,343 | A/G | — | uncertain significance |
| rs776872047 | 19:44,351,373 | A/G | — | uncertain significance |
| rs1971438312 | 19:44,351,385 | A/C | — | uncertain significance |
| rs200156604 | 19:44,351,432 | A/G | — | uncertain significance |
| rs755039644 | 19:44,351,657 | C/T | — | uncertain significance |
| rs368697755 | 19:44,351,658 | G/A | — | uncertain significance |
| rs2514064154 | 19:44,351,673 | C/A | — | uncertain significance |
| rs772783546 | 19:44,351,726 | G/A | — | uncertain significance |
| rs368199070 | 19:44,351,742 | G/T | — | uncertain significance |
| rs767923566 | 19:44,351,752 | C/G | — | uncertain significance |
| rs778024301 | 19:44,351,768 | A/G | — | uncertain significance |
| rs61745999 | 19:44,351,815 | G/T | — | uncertain significance |
| rs770576480 | 19:44,351,817 | C/A | — | uncertain significance |
| rs2514065185 | 19:44,351,824 | T/G | — | uncertain significance |
| rs1281571909 | 19:44,351,826 | G/A | — | uncertain significance |
| rs2514066186 | 19:44,351,958 | C/A | — | uncertain significance |
| rs115541142 | 19:44,351,995 | C/T | — | benign |
| rs200352356 | 19:44,351,996 | G/A | — | uncertain significance |
| rs750726707 | 19:44,351,997 | G/C | — | uncertain significance |
| rs2514067568 | 19:44,352,132 | A/C | — | uncertain significance |
| rs191317922 | 19:44,352,264 | G/A | — | uncertain significance |
| rs182901111 | 19:44,352,333 | G/T | — | uncertain significance |
| rs377306727 | 19:44,352,414 | G/A | — | uncertain significance |
| rs2514070813 | 19:44,352,565 | T/G | — | uncertain significance |
| rs367872625 | 19:44,352,598 | T/A | — | uncertain significance |
| rs2514071239 | 19:44,352,620 | G/C | — | uncertain significance |
| rs200500734 | 19:44,352,680 | G/T | — | uncertain significance |
| rs1244593529 | 19:44,352,696 | A/G | — | uncertain significance |
| rs554030657 | 19:44,352,716 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.