ZNF804B
zinc finger protein 804B
Summary
Predicted to enable zinc ion binding activity. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants93 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs145065922 | 7:88,389,408 | G/A | — | benign |
| rs73705514 | 7:88,406,552 | A/C | intron variant | — |
| rs17574755 | 7:88,472,733 | C/T | intron variant | — |
| rs10248351 | 7:88,481,442 | T/C | intron variant | — |
| rs1406503 | 7:88,560,878 | G/C | intron variant | — |
| rs12535041 | 7:88,573,471 | A/C | intron variant | — |
| rs6959888 | 7:88,596,385 | A/G | intron variant | — |
| rs3899697 | 7:88,599,785 | T/A | intron variant | — |
| rs28390077 | 7:88,682,301 | C/G | intron variant | — |
| rs10236237 | 7:88,695,070 | A/C | — | — |
| rs192018607 | 7:88,780,524 | T/C | intron variant | — |
| rs7777286 | 7:88,830,993 | C/G | intron variant | — |
| rs373862067 | 7:88,847,487 | T/C | — | uncertain significance |
| rs113588702 | 7:88,847,591 | T/C | — | benign |
| rs1232524831 | 7:88,956,669 | A/C | — | uncertain significance |
| rs755645043 | 7:88,956,723 | G/T | — | uncertain significance |
| rs747219977 | 7:88,962,713 | G/C | — | uncertain significance |
| rs1172168545 | 7:88,962,805 | G/C | — | uncertain significance |
| rs372995954 | 7:88,962,829 | C/A | — | uncertain significance |
| rs781202005 | 7:88,962,840 | C/T | — | uncertain significance |
| rs540004551 | 7:88,962,932 | T/G | — | uncertain significance |
| rs201970697 | 7:88,962,940 | A/G | — | uncertain significance |
| rs376211299 | 7:88,962,951 | G/A | — | uncertain significance |
| rs1379731584 | 7:88,963,032 | C/T | — | uncertain significance |
| rs1240013447 | 7:88,963,051 | C/T | — | uncertain significance |
| rs776309098 | 7:88,963,062 | A/G | — | uncertain significance |
| rs2484356116 | 7:88,963,077 | G/A | — | uncertain significance |
| rs151146081 | 7:88,963,117 | A/G | — | uncertain significance |
| rs140043558 | 7:88,963,123 | C/T | — | uncertain significance |
| rs761587371 | 7:88,963,141 | A/T | — | uncertain significance |
| rs1392060706 | 7:88,963,149 | C/T | — | uncertain significance |
| rs1474451742 | 7:88,963,209 | G/C | — | uncertain significance |
| rs761967142 | 7:88,963,249 | T/C | — | uncertain significance |
| rs142989053 | 7:88,963,299 | G/T | — | uncertain significance |
| rs889590737 | 7:88,963,383 | G/A | — | uncertain significance |
| rs751651281 | 7:88,963,400 | C/G | — | uncertain significance |
| rs141118086 | 7:88,963,401 | C/T | — | benign |
| rs143468643 | 7:88,963,464 | C/A | — | benign |
| rs148373338 | 7:88,963,475 | T/G | — | benign |
| rs116778830 | 7:88,963,521 | A/G | — | benign |
| rs2484357281 | 7:88,963,542 | A/G | — | likely benign |
| rs774701977 | 7:88,963,573 | G/T | — | uncertain significance |
| rs754365288 | 7:88,963,746 | C/T | — | uncertain significance |
| rs1562743675 | 7:88,963,776 | C/A | — | uncertain significance |
| rs184466523 | 7:88,963,855 | C/A | — | uncertain significance |
| rs781274730 | 7:88,963,892 | A/C | — | uncertain significance |
| rs114868448 | 7:88,963,925 | G/A | — | benign |
| rs377601222 | 7:88,964,019 | A/G | — | uncertain significance |
| rs140900637 | 7:88,964,031 | A/G | — | likely benign |
| rs201648055 | 7:88,964,209 | A/C | — | uncertain significance |
| rs764277813 | 7:88,964,281 | C/T | — | uncertain significance |
| rs202004727 | 7:88,964,323 | T/A | — | uncertain significance |
| rs2484359126 | 7:88,964,329 | A/G | — | uncertain significance |
| rs1276289854 | 7:88,964,497 | A/G | — | uncertain significance |
| rs1470703459 | 7:88,964,507 | T/A | — | likely benign |
| rs115159731 | 7:88,964,538 | C/T | — | benign |
| rs143293437 | 7:88,964,545 | T/C | — | uncertain significance |
| rs762611157 | 7:88,964,692 | G/A | — | likely benign |
| rs564078763 | 7:88,964,764 | C/T | — | uncertain significance |
| rs148180334 | 7:88,964,791 | C/T | — | uncertain significance |
| rs1791063079 | 7:88,964,797 | T/C | — | uncertain significance |
| rs79734979 | 7:88,964,815 | G/A | — | benign |
| rs754310291 | 7:88,964,826 | C/G | — | uncertain significance |
| rs774156300 | 7:88,964,871 | A/G | — | uncertain significance |
| rs140102475 | 7:88,964,888 | C/T | — | benign |
| rs138375583 | 7:88,964,957 | G/T | — | uncertain significance |
| rs59859857 | 7:88,965,036 | A/C | — | benign |
| rs144693443 | 7:88,965,048 | G/A | — | uncertain significance |
| rs752788019 | 7:88,965,121 | G/C | — | likely benign |
| rs73210814 | 7:88,965,159 | T/G | — | uncertain significance |
| rs78267196 | 7:88,965,186 | A/G | — | benign |
| rs148474033 | 7:88,965,189 | A/G | — | benign |
| rs560537958 | 7:88,965,208 | G/A | — | uncertain significance |
| rs2484361481 | 7:88,965,260 | G/T | — | uncertain significance |
| rs1194453666 | 7:88,965,265 | G/T | — | uncertain significance |
| rs78512598 | 7:88,965,293 | G/T | — | benign |
| rs141887526 | 7:88,965,325 | A/G | — | uncertain significance |
| rs150208448 | 7:88,965,367 | A/G | — | uncertain significance |
| rs142706585 | 7:88,965,497 | C/T | — | benign |
| rs892117573 | 7:88,965,529 | C/T | — | uncertain significance |
| rs200227988 | 7:88,965,614 | T/G | — | uncertain significance |
| rs753175516 | 7:88,965,711 | A/C | — | likely benign |
| rs182369154 | 7:88,965,720 | C/G | — | uncertain significance |
| rs11977547 | 7:88,965,721 | C/T | — | uncertain significance |
| rs111540405 | 7:88,965,743 | A/G | — | likely benign |
| rs758441039 | 7:88,965,826 | A/G | — | uncertain significance |
| rs1018302647 | 7:88,966,092 | C/T | — | uncertain significance |
| rs2484363459 | 7:88,966,116 | A/T | — | uncertain significance |
| rs771373207 | 7:88,966,230 | C/A | — | uncertain significance |
| rs775540062 | 7:88,966,258 | A/G | — | uncertain significance |
| rs776794544 | 7:88,966,269 | C/T | — | uncertain significance |
| rs1791105360 | 7:88,966,282 | C/G | — | uncertain significance |
| rs759232459 | 7:88,966,305 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.