ZNF765
zinc finger protein 765
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-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 Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2513976913 | 19:53,905,405 | G/C | — | uncertain significance |
| rs757121645 | 19:53,905,408 | G/T | — | uncertain significance |
| rs781686692 | 19:53,910,972 | T/C | — | uncertain significance |
| rs200009507 | 19:53,911,017 | A/G | — | uncertain significance |
| rs746730483 | 19:53,911,091 | C/A | — | uncertain significance |
| rs2513982847 | 19:53,911,098 | T/C | — | uncertain significance |
| rs767863058 | 19:53,911,131 | G/T | — | uncertain significance |
| rs199957795 | 19:53,911,182 | G/A | — | uncertain significance |
| rs2513983053 | 19:53,911,205 | A/T | — | uncertain significance |
| rs766839591 | 19:53,911,226 | C/G | — | uncertain significance |
| rs745979129 | 19:53,911,383 | A/G | — | uncertain significance |
| rs970019293 | 19:53,911,386 | G/T | — | uncertain significance |
| rs1435039393 | 19:53,911,397 | C/G | — | uncertain significance |
| rs749988925 | 19:53,911,502 | A/G | — | uncertain significance |
| rs191059800 | 19:53,911,553 | G/C | — | uncertain significance |
| rs201592752 | 19:53,911,580 | G/A | — | uncertain significance |
| rs199648986 | 19:53,911,676 | C/T | — | uncertain significance |
| rs371510706 | 19:53,911,677 | G/A | — | uncertain significance |
| rs201842363 | 19:53,911,723 | C/G | — | uncertain significance |
| rs1159023692 | 19:53,911,742 | T/C | — | uncertain significance |
| rs1439009993 | 19:53,911,758 | A/G | — | uncertain significance |
| rs780707311 | 19:53,911,767 | T/C | — | uncertain significance |
| rs150918190 | 19:53,911,845 | G/A | — | uncertain significance |
| rs149992982 | 19:53,911,934 | G/C | — | likely benign |
| rs376567196 | 19:53,912,012 | C/T | — | uncertain significance |
| rs1249280149 | 19:53,912,018 | C/T | — | uncertain significance |
| rs1248743358 | 19:53,912,021 | C/A | — | uncertain significance |
| rs377494165 | 19:53,912,045 | T/G | — | uncertain significance |
| rs763756956 | 19:53,912,229 | C/A | — | uncertain significance |
| rs367681789 | 19:53,912,299 | A/C | — | uncertain significance |
| rs2513985506 | 19:53,912,306 | G/A | — | uncertain significance |
| rs748249996 | 19:53,912,375 | G/A | — | uncertain significance |
| rs62117298 | 19:53,918,063 | T/C | downstream gene variant | — |
| rs537876632 | 19:53,925,693 | C/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.