ZNF512B
zinc finger protein 512B
Summary
Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in negative regulation of miRNA transcription. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants82 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs762842894 | 20:62,591,232 | G/A | — | likely benign |
| rs1379005495 | 20:62,591,270 | C/T | — | uncertain significance |
| rs376871471 | 20:62,591,329 | C/T | — | likely benign |
| rs369036543 | 20:62,591,330 | G/A | — | uncertain significance |
| rs199516973 | 20:62,591,335 | G/A | — | likely benign |
| rs199552229 | 20:62,591,369 | G/A | — | uncertain significance |
| rs376212498 | 20:62,591,446 | T/C | — | uncertain significance |
| rs45570933 | 20:62,591,460 | A/G | — | benign |
| rs763691830 | 20:62,591,483 | G/C | — | uncertain significance |
| rs149002469 | 20:62,592,736 | G/A | — | likely benign |
| rs2058849431 | 20:62,592,756 | G/A | — | uncertain significance |
| rs143832625 | 20:62,592,757 | C/A | — | likely benign |
| rs754690373 | 20:62,593,699 | G/A | — | uncertain significance |
| rs817322 | 20:62,593,704 | G/A | — | benign |
| rs768856923 | 20:62,593,942 | G/A | — | uncertain significance |
| rs576813533 | 20:62,593,952 | G/A | — | likely benign |
| rs751259463 | 20:62,593,977 | C/T | — | uncertain significance |
| rs139546165 | 20:62,593,991 | G/A | — | likely benign |
| rs11905742 | 20:62,594,048 | C/T | — | likely benign |
| rs2275294 | 20:62,594,247 | G/A | intron variant | benign |
| rs147556068 | 20:62,594,454 | C/T | — | likely benign |
| rs375172742 | 20:62,594,480 | C/T | — | uncertain significance |
| rs748346953 | 20:62,594,503 | G/C | — | uncertain significance |
| rs747374274 | 20:62,594,554 | G/A | — | uncertain significance |
| rs2517563817 | 20:62,594,586 | G/A | — | likely benign |
| rs147461845 | 20:62,594,713 | C/A | — | benign |
| rs1269738355 | 20:62,594,750 | C/T | — | uncertain significance |
| rs1311979342 | 20:62,594,780 | T/G | — | uncertain significance |
| rs2058886993 | 20:62,595,167 | T/C | — | uncertain significance |
| rs817325 | 20:62,595,169 | G/A | — | benign |
| rs746049582 | 20:62,595,177 | C/T | — | uncertain significance |
| rs138981780 | 20:62,595,207 | T/C | — | uncertain significance |
| rs2517565972 | 20:62,595,215 | A/C | — | uncertain significance |
| rs759201145 | 20:62,595,458 | C/A | — | uncertain significance |
| rs375990139 | 20:62,595,499 | C/T | — | uncertain significance |
| rs6062599 | 20:62,595,547 | C/T | — | benign |
| rs912843826 | 20:62,595,855 | G/A | — | uncertain significance |
| rs116458703 | 20:62,595,882 | C/T | — | benign |
| rs925673130 | 20:62,595,885 | G/A | — | uncertain significance |
| rs773482008 | 20:62,595,902 | G/A | — | uncertain significance |
| rs766835635 | 20:62,595,912 | C/T | — | uncertain significance |
| rs1300861097 | 20:62,595,926 | C/T | — | uncertain significance |
| rs817326 | 20:62,595,990 | T/C | — | benign |
| rs1093455 | 20:62,596,205 | A/G | intron variant | — |
| rs545655258 | 20:62,597,344 | G/A | — | — |
| rs139142804 | 20:62,597,571 | C/T | — | benign |
| rs1414142381 | 20:62,597,614 | G/A | — | uncertain significance |
| rs754970855 | 20:62,597,662 | G/A | — | uncertain significance |
| rs45486695 | 20:62,597,666 | T/C | — | benign |
| rs373877494 | 20:62,597,674 | G/A | — | uncertain significance |
| rs775506701 | 20:62,597,687 | G/A | — | uncertain significance |
| rs546032250 | 20:62,597,690 | T/G | — | uncertain significance |
| rs817329 | 20:62,597,694 | G/T | — | benign |
| rs752813035 | 20:62,597,722 | G/A | — | uncertain significance |
| rs201493940 | 20:62,597,853 | G/A | — | likely benign |
| rs893792043 | 20:62,597,914 | C/T | — | uncertain significance |
| rs866740192 | 20:62,597,920 | G/T | — | uncertain significance |
| rs372152054 | 20:62,597,942 | T/C | — | uncertain significance |
| rs754486292 | 20:62,597,951 | C/T | — | uncertain significance |
| rs143583869 | 20:62,597,952 | G/T | — | likely benign |
| rs150966051 | 20:62,597,996 | T/C | — | likely benign |
| rs758705335 | 20:62,598,031 | C/T | — | uncertain significance |
| rs369481423 | 20:62,598,042 | G/T | — | uncertain significance |
| rs372709409 | 20:62,598,052 | C/T | — | uncertain significance |
| rs201037243 | 20:62,598,093 | G/A | — | likely benign |
| rs2517574048 | 20:62,598,106 | G/C | — | uncertain significance |
| rs1215329444 | 20:62,598,118 | C/T | — | uncertain significance |
| rs2517574449 | 20:62,598,274 | G/C | — | uncertain significance |
| rs369168842 | 20:62,598,293 | G/A | — | uncertain significance |
| rs143997740 | 20:62,598,343 | G/A | — | likely benign |
| rs568989469 | 20:62,598,756 | T/G | — | uncertain significance |
| rs2517575922 | 20:62,598,775 | C/G | — | uncertain significance |
| rs2058939438 | 20:62,598,776 | C/A | — | uncertain significance |
| rs2058939495 | 20:62,598,781 | T/G | — | uncertain significance |
| rs817330 | 20:62,598,815 | T/C | — | benign |
| rs199991276 | 20:62,598,816 | G/A | — | uncertain significance |
| rs367567220 | 20:62,598,861 | C/T | — | uncertain significance |
| rs2058943431 | 20:62,599,192 | G/A | — | uncertain significance |
| rs749657253 | 20:62,599,272 | C/A | — | uncertain significance |
| rs566593771 | 20:62,601,386 | C/G | — | — |
| rs79903344 | 20:62,602,062 | T/A | — | — |
| rs141385312 | 20:62,602,868 | T/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.