ZNF79
zinc finger protein 79
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 Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7035039 | 9:130,187,473 | G/C | regulatory region variant | — |
| rs2539247743 | 9:130,191,122 | C/T | — | uncertain significance |
| rs1833808247 | 9:130,191,134 | C/G | — | uncertain significance |
| rs2539247766 | 9:130,191,137 | C/T | — | uncertain significance |
| rs200385658 | 9:130,191,197 | C/T | — | uncertain significance |
| rs546035895 | 9:130,197,394 | C/T | — | uncertain significance |
| rs143331329 | 9:130,197,400 | C/G | — | uncertain significance |
| rs2131952403 | 9:130,197,466 | C/G | — | uncertain significance |
| rs368686424 | 9:130,198,240 | G/T | — | uncertain significance |
| rs766356170 | 9:130,198,252 | G/A | — | uncertain significance |
| rs757843744 | 9:130,198,258 | G/A | — | uncertain significance |
| rs2539257896 | 9:130,198,259 | A/C | — | uncertain significance |
| rs371819507 | 9:130,198,268 | G/A | — | uncertain significance |
| rs1374807410 | 9:130,198,274 | C/T | — | uncertain significance |
| rs751759138 | 9:130,206,412 | A/G | — | uncertain significance |
| rs2539270158 | 9:130,206,433 | A/T | — | uncertain significance |
| rs147631403 | 9:130,206,442 | C/A | — | uncertain significance |
| rs1397308410 | 9:130,206,452 | C/G | — | uncertain significance |
| rs2539270506 | 9:130,206,494 | G/A | — | uncertain significance |
| rs201997776 | 9:130,206,524 | C/T | — | uncertain significance |
| rs1008526735 | 9:130,206,608 | A/T | — | uncertain significance |
| rs2539271045 | 9:130,206,649 | A/G | — | uncertain significance |
| rs900876013 | 9:130,206,722 | C/A | — | uncertain significance |
| rs371466147 | 9:130,206,794 | C/G | — | uncertain significance |
| rs142401803 | 9:130,206,820 | G/A | — | uncertain significance |
| rs765908223 | 9:130,206,829 | A/G | — | uncertain significance |
| rs765083551 | 9:130,206,850 | G/A | — | uncertain significance |
| rs1255354609 | 9:130,206,911 | G/A | — | uncertain significance |
| rs754073409 | 9:130,207,021 | T/A | — | uncertain significance |
| rs767530478 | 9:130,207,090 | A/T | — | uncertain significance |
| rs2539273113 | 9:130,207,120 | A/G | — | uncertain significance |
| rs375046752 | 9:130,207,156 | G/A | — | uncertain significance |
| rs2539273284 | 9:130,207,169 | C/G | — | uncertain significance |
| rs759721493 | 9:130,207,204 | A/G | — | uncertain significance |
| rs148709335 | 9:130,207,216 | G/A | — | uncertain significance |
| rs1336784539 | 9:130,207,225 | C/T | — | uncertain significance |
| rs770892949 | 9:130,207,279 | C/T | — | uncertain significance |
| rs777509271 | 9:130,207,376 | T/C | — | uncertain significance |
| rs781045400 | 9:130,207,387 | G/A | — | uncertain significance |
| rs370158712 | 9:130,207,427 | G/A | — | uncertain significance |
| rs151262945 | 9:130,207,454 | A/C | — | uncertain significance |
| rs755235307 | 9:130,207,465 | G/A | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.