ZNF618
zinc finger protein 618
Summary
Enables identical protein binding activity and transcription coregulator binding activity. Predicted to be involved in regulation of DNA-templated transcription. Located in pericentric heterochromatin. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1024304147 | 9:116,638,671 | C/T | — | uncertain significance |
| rs10817542 | 9:116,725,481 | G/A | regulatory region variant | — |
| rs754153795 | 9:116,731,402 | C/T | — | likely benign |
| rs756986676 | 9:116,731,403 | G/A | — | uncertain significance |
| rs143368881 | 9:116,731,434 | C/A | — | uncertain significance |
| rs776729997 | 9:116,750,606 | G/A | — | uncertain significance |
| rs780396604 | 9:116,750,669 | C/T | — | uncertain significance |
| rs773294604 | 9:116,750,689 | A/G | — | uncertain significance |
| rs377125895 | 9:116,750,722 | C/T | — | uncertain significance |
| rs200878518 | 9:116,750,780 | C/T | — | conflicting classifications of pathogenicity |
| rs1000560258 | 9:116,750,787 | C/G | — | uncertain significance |
| rs775436175 | 9:116,750,803 | G/A | — | uncertain significance |
| rs201855820 | 9:116,750,806 | G/A | — | uncertain significance |
| rs376782708 | 9:116,750,836 | G/A | — | uncertain significance |
| rs762284790 | 9:116,764,345 | C/T | — | uncertain significance |
| rs751004877 | 9:116,764,351 | G/A | — | uncertain significance |
| rs1841938295 | 9:116,770,624 | T/G | — | uncertain significance |
| rs755481458 | 9:116,770,653 | C/T | — | uncertain significance |
| rs748250242 | 9:116,770,654 | G/A | — | uncertain significance |
| rs376109951 | 9:116,770,656 | G/C | — | uncertain significance |
| rs372130052 | 9:116,770,784 | C/T | — | uncertain significance |
| rs10817555 | 9:116,773,749 | C/A | intron variant | — |
| rs10817556 | 9:116,775,859 | C/A | — | — |
| rs376012969 | 9:116,794,942 | C/T | — | uncertain significance |
| rs74355737 | 9:116,802,172 | A/C | intron variant | — |
| rs375567656 | 9:116,810,202 | C/G | — | uncertain significance |
| rs780005482 | 9:116,810,227 | T/C | — | uncertain significance |
| rs576360723 | 9:116,810,245 | C/T | — | uncertain significance |
| rs373820121 | 9:116,810,961 | T/C | — | uncertain significance |
| rs752559976 | 9:116,811,020 | G/A | — | uncertain significance |
| rs373735776 | 9:116,811,099 | A/G | — | uncertain significance |
| rs764817476 | 9:116,811,147 | C/T | — | uncertain significance |
| rs780831621 | 9:116,811,440 | C/T | — | uncertain significance |
| rs375985037 | 9:116,811,454 | C/T | — | benign |
| rs780059536 | 9:116,811,478 | C/G | — | uncertain significance |
| rs369712698 | 9:116,811,534 | G/A | — | uncertain significance |
| rs1408638590 | 9:116,811,648 | C/G | — | uncertain significance |
| rs374734468 | 9:116,811,692 | G/C | — | uncertain significance |
| rs1024739416 | 9:116,811,724 | C/G | — | uncertain significance |
| rs994809287 | 9:116,811,731 | C/T | — | uncertain significance |
| rs527742445 | 9:116,811,806 | G/T | — | uncertain significance |
| rs769482373 | 9:116,811,836 | G/A | — | uncertain significance |
| rs200838003 | 9:116,811,914 | G/A | — | uncertain significance |
| rs919315114 | 9:116,811,923 | G/A | — | uncertain significance |
| rs780544870 | 9:116,812,083 | A/G | — | uncertain significance |
| rs781696078 | 9:116,812,140 | C/T | — | uncertain significance |
| rs367991659 | 9:116,812,143 | G/T | — | uncertain significance |
| rs1846013374 | 9:116,812,337 | A/G | — | uncertain significance |
| rs368750835 | 9:116,812,382 | C/T | — | uncertain significance |
| rs1197332070 | 9:116,812,397 | A/G | — | uncertain significance |
| rs2498728637 | 9:116,812,404 | A/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.