ZNF652
zinc finger protein 652
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific. 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 Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs75904857 | 17:47,370,449 | T/A | — | — |
| rs2286015 | 17:47,371,065 | A/G | downstream gene variant | — |
| rs753274884 | 17:47,375,884 | G/A | — | uncertain significance |
| rs574166134 | 17:47,376,077 | G/A | — | uncertain significance |
| rs1331705141 | 17:47,376,116 | C/A | — | uncertain significance |
| rs2960172 | 17:47,379,581 | G/A | intron variant | — |
| rs140302625 | 17:47,379,867 | G/T | intron variant | — |
| rs2072153 | 17:47,390,014 | G/A | intron variant | — |
| rs2509150418 | 17:47,390,062 | A/C | — | uncertain significance |
| rs1483781833 | 17:47,390,063 | C/T | — | uncertain significance |
| rs201894922 | 17:47,390,147 | C/T | — | uncertain significance |
| rs576692626 | 17:47,394,195 | T/C | — | uncertain significance |
| rs2069811492 | 17:47,394,205 | A/G | — | uncertain significance |
| rs746820107 | 17:47,394,318 | C/T | — | uncertain significance |
| rs1056101745 | 17:47,394,346 | C/T | — | uncertain significance |
| rs753174346 | 17:47,394,415 | G/A | — | uncertain significance |
| rs368716483 | 17:47,394,516 | C/T | — | uncertain significance |
| rs147911323 | 17:47,394,529 | C/T | — | uncertain significance |
| rs1319668324 | 17:47,394,544 | C/T | — | uncertain significance |
| rs772394365 | 17:47,394,652 | C/G | — | uncertain significance |
| rs372646517 | 17:47,394,672 | G/A | — | uncertain significance |
| rs748592286 | 17:47,394,807 | T/G | — | uncertain significance |
| rs775150398 | 17:47,394,820 | C/T | — | uncertain significance |
| rs781689888 | 17:47,394,865 | T/C | — | uncertain significance |
| rs2509179066 | 17:47,394,870 | T/C | — | uncertain significance |
| rs2509179236 | 17:47,394,900 | A/G | — | uncertain significance |
| rs2069826745 | 17:47,394,930 | C/G | — | uncertain significance |
| rs201462279 | 17:47,394,942 | T/C | — | uncertain significance |
| rs751757876 | 17:47,394,965 | G/C | — | uncertain significance |
| rs573046820 | 17:47,395,002 | C/T | — | uncertain significance |
| rs146651680 | 17:47,395,003 | G/A | — | uncertain significance |
| rs1288503075 | 17:47,395,027 | C/G | — | uncertain significance |
| rs9907478 | 17:47,395,729 | C/T | intron variant | — |
| rs9889262 | 17:47,398,070 | T/A | intron variant | — |
| rs369322961 | 17:47,398,246 | G/A | — | — |
| rs12940887 | 17:47,402,807 | C/T | downstream gene variant | — |
| rs62076439 | 17:47,404,628 | G/T | upstream gene variant | — |
| rs73324308 | 17:47,405,338 | T/G | upstream gene variant | — |
| rs6504606 | 17:47,405,349 | A/T | — | — |
| rs77247327 | 17:47,411,493 | T/C | regulatory region variant | — |
| rs35587648 | 17:47,418,178 | G/A | intron variant | — |
| rs906741775 | 17:47,422,625 | C/A | — | — |
| rs7207729 | 17:47,423,740 | C/T | intron variant | — |
| rs6504608 | 17:47,424,681 | C/A | intron variant | — |
| rs7213090 | 17:47,432,577 | T/A | — | — |
| rs7210100 | 17:47,436,749 | G/A | upstream gene variant | — |
| rs112502960 | 17:47,439,302 | G/A | regulatory region variant | — |
| rs16948048 | 17:47,440,466 | A/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.