ZNF799
zinc finger protein 799
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 Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs774905334 | 19:12,501,374 | T/C | — | uncertain significance |
| rs372914627 | 19:12,501,383 | T/C | — | uncertain significance |
| rs1220630414 | 19:12,501,443 | C/T | — | uncertain significance |
| rs369686614 | 19:12,501,447 | C/T | — | uncertain significance |
| rs1296625993 | 19:12,501,557 | C/A | — | uncertain significance |
| rs766588997 | 19:12,501,648 | G/C | — | uncertain significance |
| rs201843472 | 19:12,501,695 | C/A | — | uncertain significance |
| rs1368926163 | 19:12,501,887 | G/A | — | uncertain significance |
| rs1452008481 | 19:12,501,920 | C/T | — | uncertain significance |
| rs1969807337 | 19:12,501,962 | G/T | — | uncertain significance |
| rs200836165 | 19:12,501,982 | C/G | — | uncertain significance |
| rs2512617111 | 19:12,502,052 | T/G | — | uncertain significance |
| rs770678785 | 19:12,502,056 | T/C | — | uncertain significance |
| rs749239966 | 19:12,502,101 | C/T | — | uncertain significance |
| rs1969811808 | 19:12,502,139 | G/A | — | uncertain significance |
| rs761404500 | 19:12,502,195 | A/C | — | uncertain significance |
| rs2512617923 | 19:12,502,284 | C/A | — | uncertain significance |
| rs370285412 | 19:12,502,298 | T/G | — | uncertain significance |
| rs747580228 | 19:12,502,313 | T/C | — | uncertain significance |
| rs766322782 | 19:12,502,376 | T/C | — | uncertain significance |
| rs1454750354 | 19:12,502,388 | T/G | — | uncertain significance |
| rs200335804 | 19:12,502,395 | T/C | — | uncertain significance |
| rs752438094 | 19:12,502,452 | C/G | — | uncertain significance |
| rs2512618814 | 19:12,502,520 | G/C | — | uncertain significance |
| rs374091845 | 19:12,502,559 | G/A | — | uncertain significance |
| rs2512619044 | 19:12,502,580 | A/G | — | uncertain significance |
| rs186790203 | 19:12,502,581 | A/C | — | uncertain significance |
| rs373313750 | 19:12,502,616 | C/A | — | uncertain significance |
| rs749905471 | 19:12,502,689 | C/T | — | uncertain significance |
| rs372938658 | 19:12,502,740 | T/C | — | uncertain significance |
| rs2902320 | 19:12,502,746 | G/A | — | likely benign |
| rs199689877 | 19:12,502,775 | C/T | — | uncertain significance |
| rs370871446 | 19:12,502,783 | A/C | — | uncertain significance |
| rs143425729 | 19:12,502,893 | T/C | — | uncertain significance |
| rs183358373 | 19:12,502,932 | T/C | — | uncertain significance |
| rs1002442925 | 19:12,502,956 | G/C | — | uncertain significance |
| rs771718759 | 19:12,503,018 | C/A | — | uncertain significance |
| rs1480697615 | 19:12,503,445 | G/C | — | uncertain significance |
| rs1218018316 | 19:12,504,222 | C/G | — | uncertain significance |
| rs2910993 | 19:12,504,515 | T/C | — | — |
| rs4804675 | 19:12,527,280 | A/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.