ZC3H18
zinc finger CCCH-type containing 18
Summary
Enables mRNA cap binding complex binding activity and protein-macromolecule adaptor activity. Involved in RNA destabilization. Located in nuclear speck. Part of ribonucleoprotein complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants82 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs530518382 | 16:88,638,872 | T/C | — | — |
| rs773948519 | 16:88,643,574 | G/A | — | uncertain significance |
| rs764534973 | 16:88,643,601 | T/C | — | uncertain significance |
| rs1914806905 | 16:88,643,607 | G/A | — | uncertain significance |
| rs368840643 | 16:88,643,620 | G/C | — | uncertain significance |
| rs34829088 | 16:88,643,633 | T/C | — | benign |
| rs202104890 | 16:88,643,634 | G/A | — | uncertain significance |
| rs1914810157 | 16:88,643,636 | T/G | — | likely benign |
| rs114157005 | 16:88,643,695 | C/T | — | uncertain significance |
| rs200921944 | 16:88,643,704 | C/T | — | likely benign |
| rs59918399 | 16:88,643,727 | C/T | — | likely benign |
| rs369582517 | 16:88,643,736 | G/A | — | uncertain significance |
| rs144227799 | 16:88,643,745 | C/G | — | uncertain significance |
| rs115806265 | 16:88,643,800 | G/A | — | uncertain significance |
| rs771206232 | 16:88,643,832 | G/A | — | uncertain significance |
| rs767226389 | 16:88,643,862 | G/A | — | uncertain significance |
| rs1914842529 | 16:88,643,993 | T/G | — | uncertain significance |
| rs776625358 | 16:88,644,025 | A/T | — | uncertain significance |
| rs1256093995 | 16:88,644,102 | G/A | — | uncertain significance |
| rs72809426 | 16:88,648,375 | G/A | intron variant | — |
| rs201965675 | 16:88,664,723 | G/A | — | uncertain significance |
| rs746214348 | 16:88,665,064 | C/G | — | uncertain significance |
| rs928864889 | 16:88,665,077 | C/T | — | uncertain significance |
| rs371225285 | 16:88,666,282 | A/C | — | uncertain significance |
| rs1048595680 | 16:88,666,332 | T/C | — | uncertain significance |
| rs2508097781 | 16:88,666,349 | G/A | — | uncertain significance |
| rs578175519 | 16:88,667,282 | G/T | — | — |
| rs568414801 | 16:88,675,343 | C/T | — | uncertain significance |
| rs776556506 | 16:88,677,714 | C/T | — | likely benign |
| rs1905265774 | 16:88,677,785 | A/C | — | uncertain significance |
| rs2508205012 | 16:88,677,818 | A/C | — | uncertain significance |
| rs982356121 | 16:88,677,833 | G/A | — | uncertain significance |
| rs1417683763 | 16:88,677,850 | G/A | — | uncertain significance |
| rs932749455 | 16:88,677,883 | C/T | — | uncertain significance |
| rs1469904989 | 16:88,677,919 | A/C | — | uncertain significance |
| rs1905274696 | 16:88,677,920 | A/G | — | uncertain significance |
| rs370061345 | 16:88,688,606 | C/T | — | uncertain significance |
| rs1248803463 | 16:88,688,630 | G/A | — | uncertain significance |
| rs775885714 | 16:88,688,724 | C/T | — | uncertain significance |
| rs2508300200 | 16:88,688,727 | T/C | — | uncertain significance |
| rs367748720 | 16:88,688,733 | C/T | — | uncertain significance |
| rs146052717 | 16:88,688,739 | G/A | — | uncertain significance |
| rs183567261 | 16:88,688,751 | G/A | — | uncertain significance |
| rs773596932 | 16:88,689,635 | C/T | — | uncertain significance |
| rs1906083689 | 16:88,689,647 | C/G | — | uncertain significance |
| rs778547212 | 16:88,689,682 | C/G | — | uncertain significance |
| rs772268865 | 16:88,690,383 | C/T | — | uncertain significance |
| rs374902859 | 16:88,690,395 | C/T | — | uncertain significance |
| rs759377088 | 16:88,690,396 | G/A | — | likely benign |
| rs747117189 | 16:88,690,446 | C/T | — | uncertain significance |
| rs763859632 | 16:88,690,455 | C/T | — | uncertain significance |
| rs778920136 | 16:88,691,020 | G/C | — | likely benign |
| rs770411740 | 16:88,691,035 | C/G | — | uncertain significance |
| rs776103058 | 16:88,691,036 | C/T | — | likely benign |
| rs939287165 | 16:88,691,068 | A/G | — | uncertain significance |
| rs201210182 | 16:88,691,096 | C/T | — | uncertain significance |
| rs116598906 | 16:88,691,146 | C/T | — | uncertain significance |
| rs139603213 | 16:88,691,616 | G/A | — | likely benign |
| rs749529346 | 16:88,694,040 | G/A | — | uncertain significance |
| rs146097985 | 16:88,694,088 | G/A | — | uncertain significance |
| rs2507471758 | 16:88,694,134 | C/A | — | uncertain significance |
| rs2507471956 | 16:88,694,160 | C/A | — | uncertain significance |
| rs142295038 | 16:88,694,161 | C/T | — | uncertain significance |
| rs151009473 | 16:88,694,179 | G/T | — | uncertain significance |
| rs2507473154 | 16:88,694,332 | A/T | — | uncertain significance |
| rs372155009 | 16:88,694,367 | G/A | — | uncertain significance |
| rs144394099 | 16:88,694,418 | G/T | — | uncertain significance |
| rs376734925 | 16:88,694,427 | C/T | — | uncertain significance |
| rs919892962 | 16:88,694,445 | C/T | — | uncertain significance |
| rs931314527 | 16:88,694,450 | C/G | — | uncertain significance |
| rs781375230 | 16:88,694,465 | G/A | — | uncertain significance |
| rs763334263 | 16:88,694,508 | A/G | — | uncertain significance |
| rs769221067 | 16:88,695,207 | C/A | — | uncertain significance |
| rs376093096 | 16:88,695,214 | A/T | — | uncertain significance |
| rs1441524934 | 16:88,695,241 | C/T | — | uncertain significance |
| rs1906483849 | 16:88,695,248 | C/G | — | uncertain significance |
| rs757651964 | 16:88,696,898 | C/T | — | uncertain significance |
| rs770054264 | 16:88,696,905 | G/A | — | uncertain significance |
| rs1218820465 | 16:88,696,932 | C/T | — | uncertain significance |
| rs200061680 | 16:88,696,944 | G/A | — | uncertain significance |
| rs374844312 | 16:88,696,953 | G/A | — | uncertain significance |
| rs368266096 | 16:88,697,588 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.