ZCCHC7
zinc finger CCHC-type containing 7
Summary
Enables RNA binding activity. Predicted to be involved in nuclear RNA surveillance. Located in cytosol and nucleolus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10973223 | 9:37,121,837 | T/C | regulatory region variant | — |
| rs139862637 | 9:37,126,436 | A/G | — | uncertain significance |
| rs558625927 | 9:37,126,523 | C/T | — | uncertain significance |
| rs149802071 | 9:37,126,555 | G/A | — | likely benign |
| rs140677565 | 9:37,126,657 | G/C | — | uncertain significance |
| rs1842553617 | 9:37,126,738 | A/G | — | uncertain significance |
| rs2489265730 | 9:37,126,841 | A/G | — | uncertain significance |
| rs187325042 | 9:37,126,850 | A/G | — | uncertain significance |
| rs190969738 | 9:37,126,928 | C/T | — | uncertain significance |
| rs144837215 | 9:37,130,575 | C/T | intron variant | — |
| rs10814514 | 9:37,175,765 | T/C | intron variant | — |
| rs71487717 | 9:37,199,699 | T/G | — | — |
| rs6476617 | 9:37,200,103 | G/A | intron variant | — |
| rs4526442 | 9:37,207,269 | T/C | upstream gene variant | — |
| rs495304 | 9:37,242,704 | T/C | — | — |
| rs13289199 | 9:37,278,064 | A/T | intron variant | — |
| rs1977756 | 9:37,279,161 | A/C | — | — |
| rs1407389823 | 9:37,304,195 | C/G | — | likely benign |
| rs2491063888 | 9:37,304,233 | T/C | — | uncertain significance |
| rs138176259 | 9:37,304,236 | T/G | — | likely benign |
| rs200010088 | 9:37,305,570 | G/T | — | uncertain significance |
| rs2491080479 | 9:37,305,590 | C/T | — | uncertain significance |
| rs308523 | 9:37,338,785 | C/T | intron variant | — |
| rs374266133 | 9:37,349,379 | C/T | — | uncertain significance |
| rs779726986 | 9:37,349,418 | A/G | — | uncertain significance |
| rs151266778 | 9:37,349,426 | G/A | — | uncertain significance |
| rs1196560167 | 9:37,349,436 | G/A | — | uncertain significance |
| rs894559842 | 9:37,349,440 | T/G | — | uncertain significance |
| rs1479894516 | 9:37,349,448 | A/C | — | uncertain significance |
| rs146954982 | 9:37,356,913 | T/C | — | uncertain significance |
| rs750124617 | 9:37,356,973 | A/C | — | uncertain significance |
| rs2491531553 | 9:37,356,983 | G/A | — | uncertain significance |
| rs773685265 | 9:37,357,032 | C/T | — | uncertain significance |
| rs763621620 | 9:37,357,081 | C/T | — | uncertain significance |
| rs754392778 | 9:37,357,099 | A/G | — | uncertain significance |
| rs1294203668 | 9:37,357,104 | C/T | — | uncertain significance |
| rs137970405 | 9:37,357,156 | A/G | — | uncertain significance |
| rs1182951489 | 9:37,357,218 | G/A | — | uncertain significance |
| rs143527847 | 9:37,357,222 | A/G | — | uncertain significance |
| rs1404426615 | 9:37,357,233 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.