ZNF585B
zinc finger protein 585B
Summary
Predicted to enable zinc ion binding activity. 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 Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200913496 | 19:37,676,134 | C/T | — | likely benign |
| rs199915911 | 19:37,676,153 | A/G | — | likely benign |
| rs772866995 | 19:37,676,173 | C/T | — | uncertain significance |
| rs545305580 | 19:37,676,284 | C/T | — | uncertain significance |
| rs1972324516 | 19:37,676,521 | C/T | — | uncertain significance |
| rs367647027 | 19:37,676,673 | C/T | — | uncertain significance |
| rs144514709 | 19:37,676,674 | G/A | — | uncertain significance |
| rs372920515 | 19:37,676,698 | T/G | — | uncertain significance |
| rs773453403 | 19:37,676,921 | C/A | — | uncertain significance |
| rs1398254813 | 19:37,676,956 | T/C | — | uncertain significance |
| rs368951761 | 19:37,677,007 | G/A | — | uncertain significance |
| rs141344261 | 19:37,677,042 | T/A | — | uncertain significance |
| rs1568505965 | 19:37,677,123 | T/G | — | uncertain significance |
| rs781363236 | 19:37,677,160 | T/C | — | likely benign |
| rs1158824676 | 19:37,677,266 | G/C | — | uncertain significance |
| rs2145430545 | 19:37,677,439 | C/A | — | uncertain significance |
| rs766818076 | 19:37,677,460 | T/C | — | uncertain significance |
| rs777460694 | 19:37,677,486 | C/T | — | uncertain significance |
| rs769198757 | 19:37,677,533 | G/C | — | uncertain significance |
| rs201140202 | 19:37,677,553 | T/C | — | uncertain significance |
| rs376430580 | 19:37,677,573 | C/T | — | uncertain significance |
| rs1449398364 | 19:37,677,665 | C/G | — | uncertain significance |
| rs139742522 | 19:37,677,691 | C/T | — | uncertain significance |
| rs45626541 | 19:37,677,748 | T/C | missense variant | — |
| rs761957504 | 19:37,677,790 | T/G | — | uncertain significance |
| rs756796425 | 19:37,677,892 | C/G | — | uncertain significance |
| rs144981550 | 19:37,677,913 | G/A | — | uncertain significance |
| rs2514130385 | 19:37,677,930 | T/C | — | uncertain significance |
| rs769573323 | 19:37,677,970 | G/A | — | uncertain significance |
| rs139032859 | 19:37,677,984 | G/T | — | likely benign |
| rs755457640 | 19:37,678,034 | A/C | — | uncertain significance |
| rs753269697 | 19:37,678,048 | C/T | — | uncertain significance |
| rs2145431164 | 19:37,678,068 | T/A | — | uncertain significance |
| rs763295313 | 19:37,680,578 | G/A | — | uncertain significance |
| rs2514133639 | 19:37,680,605 | G/A | — | uncertain significance |
| rs754051015 | 19:37,680,638 | G/C | — | uncertain significance |
| rs200393606 | 19:37,680,996 | G/A | — | likely benign |
| rs2514134401 | 19:37,681,032 | A/C | — | uncertain significance |
| rs967626700 | 19:37,681,045 | A/G | — | uncertain significance |
| rs11673344 | 19:37,684,966 | A/G | intron variant | — |
| rs778414637 | 19:37,697,956 | C/T | — | uncertain significance |
| rs145040657 | 19:37,697,988 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.