ZNF385D
zinc finger protein 385D
Summary
Enables sequence-specific double-stranded DNA binding activity. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants49 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs150123252 | 3:21,462,732 | T/C | — | uncertain significance |
| rs767555449 | 3:21,462,768 | G/T | — | uncertain significance |
| rs368365503 | 3:21,462,830 | A/C | — | uncertain significance |
| rs774913590 | 3:21,462,848 | A/G | — | uncertain significance |
| rs1700730939 | 3:21,462,864 | C/T | — | uncertain significance |
| rs1159850406 | 3:21,465,487 | T/C | — | uncertain significance |
| rs2470455391 | 3:21,465,555 | T/G | — | uncertain significance |
| rs1285924539 | 3:21,467,072 | A/G | — | uncertain significance |
| rs149202584 | 3:21,467,150 | T/G | — | uncertain significance |
| rs147799404 | 3:21,478,476 | T/G | — | uncertain significance |
| rs778859200 | 3:21,478,546 | C/T | — | uncertain significance |
| rs766300939 | 3:21,478,584 | G/A | — | uncertain significance |
| rs1487764900 | 3:21,478,629 | A/G | — | uncertain significance |
| rs1352931272 | 3:21,478,638 | C/G | — | uncertain significance |
| rs149309820 | 3:21,478,645 | G/A | — | uncertain significance |
| rs1707151496 | 3:21,552,364 | G/A | — | uncertain significance |
| rs142788751 | 3:21,552,392 | T/C | — | uncertain significance |
| rs139940495 | 3:21,552,412 | G/A | — | uncertain significance |
| rs1023701507 | 3:21,552,413 | C/A | — | uncertain significance |
| rs202160349 | 3:21,552,487 | G/A | — | uncertain significance |
| rs758875450 | 3:21,552,505 | G/A | — | uncertain significance |
| rs201635507 | 3:21,606,093 | G/T | — | uncertain significance |
| rs2471528469 | 3:21,606,107 | T/A | — | uncertain significance |
| rs147921825 | 3:21,606,111 | C/T | — | benign |
| rs141254644 | 3:21,606,118 | C/T | — | uncertain significance |
| rs760045214 | 3:21,606,134 | C/A | — | uncertain significance |
| rs3821396 | 3:21,706,369 | G/A | intron variant | — |
| rs375357785 | 3:21,706,382 | T/C | — | uncertain significance |
| rs762043069 | 3:21,706,413 | C/T | — | uncertain significance |
| rs752571574 | 3:21,706,454 | G/A | — | uncertain significance |
| rs895861255 | 3:21,706,476 | G/A | — | uncertain significance |
| rs571099747 | 3:21,706,481 | C/T | — | uncertain significance |
| rs181361410 | 3:21,706,497 | G/A | — | uncertain significance |
| rs9816269 | 3:21,718,841 | T/C | intron variant | — |
| rs1490157 | 3:21,719,246 | C/T | intron variant | — |
| rs9310653 | 3:21,723,547 | C/T | — | — |
| rs7615960 | 3:21,730,246 | A/G | — | — |
| rs7650118 | 3:21,806,293 | C/G | — | — |
| rs531525204 | 3:21,819,985 | A/G | — | — |
| rs9808993 | 3:21,856,683 | G/C | — | — |
| rs259542 | 3:21,954,382 | T/C | — | — |
| rs541594711 | 3:21,954,839 | C/A | — | — |
| rs11719664 | 3:21,955,198 | C/G | — | — |
| rs7628630 | 3:21,977,337 | G/A | intron variant | — |
| rs774056131 | 3:22,081,231 | T/C | — | — |
| rs2593321 | 3:22,122,396 | C/T | intron variant | — |
| rs927458589 | 3:22,146,463 | T/G | — | — |
| rs6797769 | 3:22,171,297 | A/T | intron variant | — |
| rs1388551 | 3:22,292,571 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.