ZNF45
zinc finger protein 45
Summary
Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2513525164 | 19:44,417,584 | G/C | — | uncertain significance |
| rs2513526024 | 19:44,417,612 | T/C | — | uncertain significance |
| rs199739895 | 19:44,417,657 | T/G | — | uncertain significance |
| rs1241929265 | 19:44,417,682 | C/T | — | uncertain significance |
| rs2513531345 | 19:44,417,733 | T/C | — | uncertain significance |
| rs778240515 | 19:44,417,834 | C/T | — | uncertain significance |
| rs763424589 | 19:44,417,865 | G/A | — | uncertain significance |
| rs759845090 | 19:44,417,888 | C/T | — | uncertain significance |
| rs2513537384 | 19:44,417,904 | C/T | — | uncertain significance |
| rs1332851028 | 19:44,418,034 | A/T | — | uncertain significance |
| rs201102768 | 19:44,418,249 | C/T | — | uncertain significance |
| rs755737348 | 19:44,418,251 | C/T | — | uncertain significance |
| rs747193523 | 19:44,418,309 | G/A | — | uncertain significance |
| rs766281718 | 19:44,418,347 | T/A | — | uncertain significance |
| rs768890190 | 19:44,418,393 | G/A | — | uncertain significance |
| rs149776092 | 19:44,418,507 | T/C | — | uncertain significance |
| rs761511592 | 19:44,418,603 | C/G | — | uncertain significance |
| rs367546860 | 19:44,418,707 | T/A | — | uncertain significance |
| rs747650093 | 19:44,418,750 | C/G | — | uncertain significance |
| rs137972782 | 19:44,418,762 | A/G | — | uncertain significance |
| rs199803032 | 19:44,418,764 | G/A | — | uncertain significance |
| rs753977457 | 19:44,418,816 | C/T | — | likely benign |
| rs1453765975 | 19:44,418,870 | T/C | — | uncertain significance |
| rs767364054 | 19:44,418,926 | G/C | — | uncertain significance |
| rs142251233 | 19:44,418,951 | C/T | — | uncertain significance |
| rs922385213 | 19:44,418,959 | T/A | — | uncertain significance |
| rs759300611 | 19:44,418,980 | C/T | — | uncertain significance |
| rs780360639 | 19:44,418,984 | G/A | — | uncertain significance |
| rs769132754 | 19:44,418,989 | G/A | — | uncertain significance |
| rs1047452 | 19:44,419,029 | C/T | — | uncertain significance |
| rs140969700 | 19:44,419,053 | G/A | — | uncertain significance |
| rs1394288979 | 19:44,419,086 | G/A | — | uncertain significance |
| rs748631776 | 19:44,419,097 | T/C | — | uncertain significance |
| rs149724360 | 19:44,419,100 | G/C | — | uncertain significance |
| rs148906238 | 19:44,419,110 | C/G | — | uncertain significance |
| rs2513589861 | 19:44,419,131 | G/C | — | uncertain significance |
| rs917733870 | 19:44,419,164 | C/A | — | uncertain significance |
| rs2513595244 | 19:44,419,274 | G/A | — | uncertain significance |
| rs533527352 | 19:44,419,938 | G/A | — | — |
| rs446674 | 19:44,421,007 | G/A | intron variant | — |
| rs368691981 | 19:44,423,032 | A/C | — | uncertain significance |
| rs141989682 | 19:44,423,100 | G/T | — | uncertain significance |
| rs375066 | 19:44,423,570 | T/G | — | — |
| rs775164589 | 19:44,423,766 | C/T | — | uncertain significance |
| rs762329165 | 19:44,423,778 | C/T | — | uncertain significance |
| rs756350135 | 19:44,426,333 | G/A | — | uncertain significance |
| rs118145918 | 19:44,437,765 | G/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.