ZNF841
zinc finger protein 841
Summary
Predicted to enable DNA binding activity and zinc ion 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 Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1398122361 | 19:52,568,379 | G/A | — | uncertain significance |
| rs377124307 | 19:52,568,437 | C/T | — | likely benign |
| rs772636691 | 19:52,568,470 | G/A | — | uncertain significance |
| rs979189873 | 19:52,568,557 | G/A | — | uncertain significance |
| rs776919537 | 19:52,568,577 | T/C | — | uncertain significance |
| rs372204022 | 19:52,568,685 | C/A | — | uncertain significance |
| rs539659092 | 19:52,568,696 | C/T | — | uncertain significance |
| rs755610830 | 19:52,568,701 | G/C | — | uncertain significance |
| rs374436504 | 19:52,568,716 | T/C | — | uncertain significance |
| rs367789106 | 19:52,568,721 | C/T | — | uncertain significance |
| rs749554827 | 19:52,568,722 | G/A | — | uncertain significance |
| rs757941269 | 19:52,568,797 | G/A | — | uncertain significance |
| rs748140613 | 19:52,569,142 | G/A | — | uncertain significance |
| rs551604829 | 19:52,569,237 | A/G | — | uncertain significance |
| rs373036711 | 19:52,569,274 | C/T | — | uncertain significance |
| rs773615110 | 19:52,569,285 | C/T | — | uncertain significance |
| rs376585269 | 19:52,569,315 | A/G | — | uncertain significance |
| rs757207447 | 19:52,569,415 | A/G | — | uncertain significance |
| rs1568534930 | 19:52,569,574 | C/T | — | uncertain significance |
| rs376724302 | 19:52,569,607 | C/T | — | uncertain significance |
| rs2123211287 | 19:52,569,614 | A/C | — | uncertain significance |
| rs566077651 | 19:52,569,618 | A/G | — | uncertain significance |
| rs780165261 | 19:52,569,708 | C/T | — | likely benign |
| rs192036158 | 19:52,569,709 | G/A | — | uncertain significance |
| rs773350296 | 19:52,569,741 | A/G | — | likely benign |
| rs753338966 | 19:52,569,792 | T/C | — | uncertain significance |
| rs375970898 | 19:52,569,796 | G/A | — | uncertain significance |
| rs755277266 | 19:52,569,801 | A/C | — | uncertain significance |
| rs528358581 | 19:52,569,810 | G/A | — | uncertain significance |
| rs371538802 | 19:52,569,925 | T/C | — | uncertain significance |
| rs776445579 | 19:52,569,967 | T/C | — | uncertain significance |
| rs2513900795 | 19:52,570,114 | C/T | — | uncertain significance |
| rs200268840 | 19:52,570,239 | T/C | — | uncertain significance |
| rs1568536107 | 19:52,570,255 | A/G | — | uncertain significance |
| rs1407977330 | 19:52,570,284 | G/A | — | uncertain significance |
| rs554445138 | 19:52,570,308 | A/G | — | uncertain significance |
| rs781315508 | 19:52,570,339 | A/T | — | uncertain significance |
| rs572846890 | 19:52,570,371 | T/C | — | uncertain significance |
| rs538950785 | 19:52,570,398 | G/A | — | uncertain significance |
| rs2123221593 | 19:52,570,596 | A/G | — | uncertain significance |
| rs778822347 | 19:52,570,612 | C/T | — | uncertain significance |
| rs2513904934 | 19:52,570,623 | C/G | — | uncertain significance |
| rs1568536800 | 19:52,570,742 | G/C | — | uncertain significance |
| rs550291522 | 19:52,570,767 | C/T | — | uncertain significance |
| rs372086918 | 19:52,579,362 | A/G | — | uncertain significance |
| rs760286931 | 19:52,580,220 | C/T | — | uncertain significance |
| rs12460587 | 19:52,586,919 | T/G | intron variant | — |
| rs1196559564 | 19:52,588,048 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.