ZNF169
zinc finger protein 169
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 Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs12347577 | 9:97,031,548 | G/A | — | — |
| rs3118754 | 9:97,050,947 | T/A | — | — |
| rs752179025 | 9:97,054,639 | G/A | — | uncertain significance |
| rs543204952 | 9:97,055,285 | G/A | — | uncertain significance |
| rs12378270 | 9:97,059,186 | G/A | intron variant | — |
| rs757852729 | 9:97,062,097 | A/G | — | uncertain significance |
| rs912931295 | 9:97,062,139 | C/T | — | uncertain significance |
| rs746982143 | 9:97,062,147 | A/C | — | uncertain significance |
| rs2538603063 | 9:97,062,171 | G/C | — | uncertain significance |
| rs748087303 | 9:97,062,385 | G/A | — | uncertain significance |
| rs775032176 | 9:97,062,424 | G/T | — | uncertain significance |
| rs777767548 | 9:97,062,441 | T/G | — | uncertain significance |
| rs566392862 | 9:97,062,478 | T/C | — | uncertain significance |
| rs752987255 | 9:97,062,558 | G/A | — | uncertain significance |
| rs1045085498 | 9:97,062,594 | C/T | — | uncertain significance |
| rs774688771 | 9:97,062,612 | G/A | — | uncertain significance |
| rs117481724 | 9:97,062,622 | C/T | — | uncertain significance |
| rs373178095 | 9:97,062,642 | G/T | — | uncertain significance |
| rs779140159 | 9:97,062,646 | G/A | — | uncertain significance |
| rs773919139 | 9:97,062,663 | G/T | — | likely benign |
| rs1486036861 | 9:97,062,759 | A/G | — | uncertain significance |
| rs145852094 | 9:97,062,780 | G/A | — | uncertain significance |
| rs999903650 | 9:97,062,784 | A/G | — | uncertain significance |
| rs1408153003 | 9:97,062,837 | C/T | — | uncertain significance |
| rs756784177 | 9:97,062,958 | C/A | — | uncertain significance |
| rs1282936752 | 9:97,063,020 | G/T | — | uncertain significance |
| rs772170085 | 9:97,063,029 | T/C | — | uncertain significance |
| rs781612317 | 9:97,063,074 | C/T | — | uncertain significance |
| rs748371549 | 9:97,063,075 | G/A | — | uncertain significance |
| rs769024042 | 9:97,063,116 | G/C | — | uncertain significance |
| rs2538608259 | 9:97,063,254 | A/G | — | uncertain significance |
| rs2538608389 | 9:97,063,282 | C/T | — | uncertain significance |
| rs754154707 | 9:97,063,318 | G/A | — | uncertain significance |
| rs773811687 | 9:97,063,383 | G/T | — | uncertain significance |
| rs777157079 | 9:97,063,422 | C/T | — | uncertain significance |
| rs540378819 | 9:97,063,495 | G/A | — | uncertain significance |
| rs748657947 | 9:97,063,549 | A/T | — | uncertain significance |
| rs2538609675 | 9:97,063,563 | T/C | — | uncertain significance |
| rs146409048 | 9:97,063,597 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.