ZNF696
zinc finger protein 696
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription 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 Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2272633 | 8:144,372,652 | G/T | coding sequence variant | — |
| rs375161994 | 8:144,375,212 | G/A | — | uncertain significance |
| rs11136280 | 8:144,375,859 | T/A | — | — |
| rs777128472 | 8:144,377,939 | C/T | — | uncertain significance |
| rs746739401 | 8:144,378,005 | G/A | — | uncertain significance |
| rs751008195 | 8:144,378,134 | G/A | — | uncertain significance |
| rs745462873 | 8:144,378,152 | G/C | — | uncertain significance |
| rs561321739 | 8:144,378,227 | G/A | — | likely benign |
| rs531866086 | 8:144,378,250 | G/C | — | uncertain significance |
| rs199744108 | 8:144,378,313 | C/A | — | uncertain significance |
| rs887307137 | 8:144,378,324 | A/G | — | uncertain significance |
| rs746139536 | 8:144,378,377 | G/A | — | uncertain significance |
| rs146124944 | 8:144,378,403 | C/T | — | likely benign |
| rs1328193412 | 8:144,378,404 | G/A | — | uncertain significance |
| rs781179297 | 8:144,378,434 | C/T | — | uncertain significance |
| rs1416993954 | 8:144,378,459 | G/A | — | uncertain significance |
| rs200159338 | 8:144,378,495 | C/T | — | uncertain significance |
| rs766621028 | 8:144,378,585 | T/C | — | uncertain significance |
| rs547770903 | 8:144,378,732 | A/G | — | uncertain significance |
| rs1002330844 | 8:144,378,743 | C/T | — | uncertain significance |
| rs566213035 | 8:144,378,764 | T/C | — | uncertain significance |
| rs1456923967 | 8:144,378,804 | C/G | — | uncertain significance |
| rs2537279584 | 8:144,378,834 | T/C | — | uncertain significance |
| rs759505200 | 8:144,378,836 | C/G | — | uncertain significance |
| rs748415620 | 8:144,378,891 | T/G | — | uncertain significance |
| rs1815725497 | 8:144,378,893 | C/T | — | uncertain significance |
| rs762941636 | 8:144,378,908 | G/A | — | uncertain significance |
| rs2129742668 | 8:144,378,947 | C/G | — | uncertain significance |
| rs182458703 | 8:144,382,206 | T/C | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.