ZNF676
zinc finger protein 676
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 DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1301937233 | 19:22,362,778 | T/C | — | uncertain significance |
| rs532104019 | 19:22,362,793 | C/T | — | likely benign |
| rs774878650 | 19:22,362,817 | T/C | — | uncertain significance |
| rs2023708668 | 19:22,362,859 | T/A | — | uncertain significance |
| rs956826116 | 19:22,362,892 | T/G | — | uncertain significance |
| rs202153135 | 19:22,363,008 | C/G | — | likely benign |
| rs1372993570 | 19:22,363,023 | T/C | — | uncertain significance |
| rs200330533 | 19:22,363,048 | T/C | — | uncertain significance |
| rs372702194 | 19:22,363,056 | G/A | — | uncertain significance |
| rs763929340 | 19:22,363,074 | C/T | — | uncertain significance |
| rs200365534 | 19:22,363,114 | T/C | — | uncertain significance |
| rs752044501 | 19:22,363,199 | C/G | — | uncertain significance |
| rs201835667 | 19:22,363,234 | C/A | — | uncertain significance |
| rs201257480 | 19:22,363,274 | A/G | — | likely benign |
| rs1473342497 | 19:22,363,295 | G/A | — | likely benign |
| rs369300351 | 19:22,363,323 | C/T | — | uncertain significance |
| rs199601535 | 19:22,363,344 | G/A | — | uncertain significance |
| rs746950296 | 19:22,363,366 | C/T | — | uncertain significance |
| rs200273136 | 19:22,363,395 | C/T | — | uncertain significance |
| rs761280683 | 19:22,363,404 | T/C | — | uncertain significance |
| rs369672319 | 19:22,363,537 | T/C | — | uncertain significance |
| rs767350295 | 19:22,363,606 | C/G | — | uncertain significance |
| rs765193548 | 19:22,363,611 | T/C | — | uncertain significance |
| rs1291774986 | 19:22,363,731 | C/G | — | uncertain significance |
| rs559970266 | 19:22,363,736 | T/G | — | likely benign |
| rs200737633 | 19:22,363,749 | T/C | — | uncertain significance |
| rs545560102 | 19:22,363,784 | T/A | — | likely benign |
| rs770921118 | 19:22,363,797 | G/C | — | likely benign |
| rs755511645 | 19:22,363,829 | A/G | — | likely benign |
| rs1156963536 | 19:22,363,857 | C/A | — | uncertain significance |
| rs2023741036 | 19:22,363,933 | G/T | — | uncertain significance |
| rs765582913 | 19:22,363,937 | C/G | — | uncertain significance |
| rs1215098315 | 19:22,363,947 | T/C | — | uncertain significance |
| rs371456888 | 19:22,363,959 | T/C | — | uncertain significance |
| rs192725054 | 19:22,364,089 | T/C | — | uncertain significance |
| rs2023746006 | 19:22,364,113 | T/C | — | uncertain significance |
| rs772808312 | 19:22,364,129 | T/A | — | uncertain significance |
| rs376158454 | 19:22,364,158 | C/T | — | uncertain significance |
| rs2513070970 | 19:22,364,163 | G/T | — | uncertain significance |
| rs938116360 | 19:22,364,176 | A/G | — | uncertain significance |
| rs184119584 | 19:22,364,242 | C/T | — | uncertain significance |
| rs756136777 | 19:22,364,290 | C/G | — | uncertain significance |
| rs2023751338 | 19:22,364,293 | G/A | — | uncertain significance |
| rs2023751571 | 19:22,364,308 | A/G | — | uncertain significance |
| rs549335423 | 19:22,364,336 | A/C | — | uncertain significance |
| rs367723653 | 19:22,364,343 | A/G | — | uncertain significance |
| rs189442130 | 19:22,364,347 | C/T | — | uncertain significance |
| rs199670498 | 19:22,364,355 | G/A | — | uncertain significance |
| rs2513129001 | 19:22,375,861 | C/G | — | uncertain significance |
| rs281202 | 19:22,406,331 | A/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.