ZC3H7A
zinc finger CCCH-type containing 7A
Summary
Enables miRNA binding activity. Involved in miRNA processing. Acts upstream of with a positive effect on post-transcriptional regulation of gene expression. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants49 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2548397239 | 16:11,845,236 | G/C | — | uncertain significance |
| rs772025198 | 16:11,845,322 | A/G | — | uncertain significance |
| rs751022229 | 16:11,846,621 | G/A | — | uncertain significance |
| rs2548402579 | 16:11,850,115 | G/A | — | uncertain significance |
| rs913723732 | 16:11,850,134 | C/T | — | uncertain significance |
| rs1270562678 | 16:11,850,146 | T/C | — | uncertain significance |
| rs1221087968 | 16:11,850,217 | A/G | — | uncertain significance |
| rs763258711 | 16:11,855,323 | C/T | — | uncertain significance |
| rs2548408674 | 16:11,855,339 | C/T | — | uncertain significance |
| rs150872757 | 16:11,855,357 | C/G | — | uncertain significance |
| rs1229498448 | 16:11,855,862 | A/G | — | uncertain significance |
| rs1213940712 | 16:11,855,881 | T/C | — | uncertain significance |
| rs2052832207 | 16:11,858,966 | T/G | — | uncertain significance |
| rs756271883 | 16:11,859,386 | G/A | — | uncertain significance |
| rs201615324 | 16:11,859,419 | C/T | — | uncertain significance |
| rs771328297 | 16:11,859,536 | C/T | — | uncertain significance |
| rs2548416870 | 16:11,861,317 | C/T | — | likely benign |
| rs753275314 | 16:11,861,366 | C/T | — | uncertain significance |
| rs145528953 | 16:11,861,374 | A/G | — | uncertain significance |
| rs2548417086 | 16:11,861,405 | C/G | — | uncertain significance |
| rs201365387 | 16:11,862,255 | G/A | — | uncertain significance |
| rs2548418548 | 16:11,862,315 | C/T | — | uncertain significance |
| rs368634676 | 16:11,862,948 | A/G | — | uncertain significance |
| rs749811753 | 16:11,864,776 | G/A | — | uncertain significance |
| rs12445820 | 16:11,866,703 | C/G | intron variant | — |
| rs2053041288 | 16:11,868,118 | C/G | — | uncertain significance |
| rs2053042742 | 16:11,868,168 | T/C | — | uncertain significance |
| rs1567385281 | 16:11,868,222 | G/A | — | uncertain significance |
| rs976269305 | 16:11,868,228 | G/A | — | uncertain significance |
| rs764923536 | 16:11,868,229 | G/A | — | uncertain significance |
| rs750797587 | 16:11,868,235 | C/T | — | likely benign |
| rs749133352 | 16:11,868,249 | T/G | — | uncertain significance |
| rs146528075 | 16:11,868,267 | G/C | — | uncertain significance |
| rs775205398 | 16:11,868,274 | G/T | — | uncertain significance |
| rs760606858 | 16:11,868,276 | A/G | — | uncertain significance |
| rs774187742 | 16:11,868,306 | A/G | — | uncertain significance |
| rs755598571 | 16:11,868,337 | A/G | — | uncertain significance |
| rs2053046699 | 16:11,868,346 | G/A | — | uncertain significance |
| rs2548426105 | 16:11,868,363 | G/A | — | uncertain significance |
| rs142087765 | 16:11,868,869 | C/A | — | uncertain significance |
| rs762913160 | 16:11,870,383 | C/G | — | uncertain significance |
| rs539360046 | 16:11,870,636 | C/T | — | uncertain significance |
| rs2548429091 | 16:11,870,638 | G/T | — | uncertain significance |
| rs749760059 | 16:11,870,658 | T/A | — | uncertain significance |
| rs2053133225 | 16:11,873,019 | C/T | — | uncertain significance |
| rs966088989 | 16:11,873,149 | T/C | — | uncertain significance |
| rs2053135140 | 16:11,873,161 | T/C | — | uncertain significance |
| rs541990578 | 16:11,878,266 | A/G | — | — |
| rs28495625 | 16:11,891,361 | C/A | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.