ZNF284
zinc finger protein 284
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 DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs745994663 | 19:44,580,555 | A/G | — | uncertain significance |
| rs183397212 | 19:44,583,290 | G/A | intron variant | — |
| rs747066379 | 19:44,585,175 | T/G | — | uncertain significance |
| rs751666210 | 19:44,585,270 | A/G | — | uncertain significance |
| rs1395344502 | 19:44,586,230 | G/C | — | uncertain significance |
| rs1377992333 | 19:44,589,899 | C/A | — | uncertain significance |
| rs200347089 | 19:44,589,909 | G/A | — | uncertain significance |
| rs749034533 | 19:44,589,912 | C/G | — | uncertain significance |
| rs764131983 | 19:44,589,935 | C/A | — | uncertain significance |
| rs765538171 | 19:44,589,974 | C/G | — | uncertain significance |
| rs201954718 | 19:44,590,086 | G/A | — | uncertain significance |
| rs1225126466 | 19:44,590,112 | A/G | — | uncertain significance |
| rs199726468 | 19:44,590,136 | C/T | — | uncertain significance |
| rs749924228 | 19:44,590,235 | C/T | — | uncertain significance |
| rs909868910 | 19:44,590,254 | G/A | — | uncertain significance |
| rs751102538 | 19:44,590,335 | A/G | — | uncertain significance |
| rs1475880472 | 19:44,590,371 | A/G | — | uncertain significance |
| rs1159490166 | 19:44,590,389 | A/C | — | uncertain significance |
| rs373145363 | 19:44,590,634 | A/G | — | uncertain significance |
| rs2514364450 | 19:44,590,636 | G/A | — | uncertain significance |
| rs187624893 | 19:44,590,656 | T/A | — | uncertain significance |
| rs766500887 | 19:44,590,721 | G/C | — | uncertain significance |
| rs1416880191 | 19:44,590,725 | A/G | — | uncertain significance |
| rs770256401 | 19:44,590,800 | A/C | — | uncertain significance |
| rs1270213649 | 19:44,590,803 | G/A | — | uncertain significance |
| rs549267532 | 19:44,590,835 | G/A | — | uncertain significance |
| rs1444916745 | 19:44,590,875 | A/G | — | uncertain significance |
| rs372655473 | 19:44,590,889 | G/T | — | uncertain significance |
| rs767693823 | 19:44,590,919 | C/G | — | likely benign |
| rs760995733 | 19:44,590,922 | A/G | — | uncertain significance |
| rs1156563117 | 19:44,591,003 | A/G | — | likely benign |
| rs776834810 | 19:44,591,126 | C/T | — | uncertain significance |
| rs2514365827 | 19:44,591,151 | G/T | — | uncertain significance |
| rs753314705 | 19:44,591,159 | C/T | — | uncertain significance |
| rs202220702 | 19:44,591,355 | G/A | — | uncertain significance |
| rs201190255 | 19:44,591,366 | C/T | — | uncertain significance |
| rs776482669 | 19:44,591,378 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.