ZNF76
zinc finger protein 76
Summary
Enables DNA-binding transcription activator activity, RNA polymerase II-specific and sequence-specific double-stranded DNA binding activity. Involved in positive 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 |
|---|---|---|---|---|
| rs4713844 | 6:35,227,832 | T/G | — | — |
| rs4713845 | 6:35,228,387 | C/T | — | — |
| rs2006184 | 6:35,236,915 | G/T | — | — |
| rs4713847 | 6:35,239,470 | A/G | — | — |
| rs62403577 | 6:35,245,667 | C/T | — | — |
| rs2267663 | 6:35,250,682 | C/A | — | — |
| rs762342604 | 6:35,253,940 | G/A | — | uncertain significance |
| rs2534083511 | 6:35,253,952 | A/G | — | uncertain significance |
| rs2534085305 | 6:35,254,144 | G/A | — | uncertain significance |
| rs778936523 | 6:35,254,158 | A/G | — | uncertain significance |
| rs773965220 | 6:35,255,452 | G/A | — | uncertain significance |
| rs1789768972 | 6:35,255,468 | G/A | — | uncertain significance |
| rs760393947 | 6:35,255,477 | C/T | — | uncertain significance |
| rs752810193 | 6:35,255,486 | A/T | — | uncertain significance |
| rs760624974 | 6:35,255,582 | G/A | — | uncertain significance |
| rs141811881 | 6:35,255,590 | G/T | — | uncertain significance |
| rs765788420 | 6:35,258,106 | C/T | — | uncertain significance |
| rs960589056 | 6:35,258,118 | A/G | — | uncertain significance |
| rs764649836 | 6:35,258,131 | G/A | — | uncertain significance |
| rs148002061 | 6:35,258,455 | G/A | — | uncertain significance |
| rs765023943 | 6:35,258,481 | G/C | — | uncertain significance |
| rs756317384 | 6:35,259,075 | G/A | — | uncertain significance |
| rs754976796 | 6:35,259,079 | G/A | — | uncertain significance |
| rs759006880 | 6:35,259,091 | G/T | — | uncertain significance |
| rs1894650 | 6:35,259,261 | C/A | — | — |
| rs2534124498 | 6:35,259,356 | C/T | — | uncertain significance |
| rs375918169 | 6:35,259,373 | C/T | — | uncertain significance |
| rs2534124998 | 6:35,259,396 | C/G | — | uncertain significance |
| rs144626183 | 6:35,259,478 | G/A | — | uncertain significance |
| rs757460472 | 6:35,259,511 | A/G | — | uncertain significance |
| rs770887538 | 6:35,260,372 | C/T | — | uncertain significance |
| rs774825701 | 6:35,260,481 | C/T | — | uncertain significance |
| rs1557568 | 6:35,260,530 | C/G | missense variant | — |
| rs2534144802 | 6:35,261,546 | G/C | — | uncertain significance |
| rs139911434 | 6:35,261,643 | G/T | — | uncertain significance |
| rs762018098 | 6:35,261,672 | G/A | — | uncertain significance |
| rs45617037 | 6:35,262,191 | G/A | regulatory region variant | — |
| rs140919708 | 6:35,262,282 | C/T | — | uncertain significance |
| rs146688406 | 6:35,262,327 | G/A | — | uncertain significance |
| rs906444356 | 6:35,262,982 | G/A | — | uncertain significance |
| rs8205 | 6:35,263,677 | T/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.