ZNF668
zinc finger protein 668
Summary
Predicted to enable DNA-binding transcription repressor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and zinc ion binding activity. Involved in DNA repair. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs74720434 | 16:31,072,390 | C/T | — | benign |
| rs749151871 | 16:31,072,486 | C/T | — | uncertain significance |
| rs770664888 | 16:31,072,487 | G/A | — | uncertain significance |
| rs777728754 | 16:31,072,583 | G/A | — | uncertain significance |
| rs2544016796 | 16:31,072,615 | G/C | — | uncertain significance |
| rs1312240431 | 16:31,072,624 | C/T | — | uncertain significance |
| rs150560360 | 16:31,072,643 | G/C | — | uncertain significance |
| rs140466221 | 16:31,072,659 | C/G | — | likely benign |
| rs2544017047 | 16:31,072,700 | C/G | — | uncertain significance |
| rs750390728 | 16:31,072,784 | C/T | — | uncertain significance |
| rs2544018100 | 16:31,072,961 | C/A | — | uncertain significance |
| rs2544018123 | 16:31,072,973 | G/A | — | uncertain significance |
| rs2056927190 | 16:31,073,029 | A/C | — | uncertain significance |
| rs559052919 | 16:31,073,100 | G/C | — | uncertain significance |
| rs938491012 | 16:31,073,137 | C/T | — | uncertain significance |
| rs1178162893 | 16:31,073,138 | G/A | — | pathogenic |
| rs1177612829 | 16:31,073,147 | C/G | — | uncertain significance |
| rs2288003 | 16:31,073,208 | C/T | — | likely benign |
| rs1555498115 | 16:31,073,240 | T/C | — | uncertain significance |
| rs2143756208 | 16:31,073,294 | G/A | — | pathogenic |
| rs2544019478 | 16:31,073,381 | A/C | — | uncertain significance |
| rs138468406 | 16:31,073,458 | A/T | — | uncertain significance |
| rs2544019853 | 16:31,073,528 | A/T | — | uncertain significance |
| rs773506838 | 16:31,073,585 | G/A | — | uncertain significance |
| rs550440138 | 16:31,075,147 | G/A | — | uncertain significance |
| rs2056956998 | 16:31,075,164 | G/A | — | uncertain significance |
| rs2303223 | 16:31,075,175 | G/A | — | benign |
| rs746198994 | 16:31,075,222 | G/A | — | uncertain significance |
| rs780078099 | 16:31,075,231 | G/A | — | uncertain significance |
| rs138850929 | 16:31,075,235 | C/T | — | benign |
| rs2056958808 | 16:31,075,288 | C/T | — | uncertain significance |
| rs759082830 | 16:31,075,399 | G/A | — | uncertain significance |
| rs2544024249 | 16:31,075,483 | G/A | — | uncertain significance |
| rs1205256532 | 16:31,075,508 | C/T | — | likely benign |
| rs776177900 | 16:31,075,570 | C/T | — | uncertain significance |
| rs1017107130 | 16:31,075,625 | C/G | — | uncertain significance |
| rs768592728 | 16:31,075,633 | A/C | — | likely benign |
| rs1308476599 | 16:31,075,639 | C/T | — | uncertain significance |
| rs371432389 | 16:31,075,704 | G/T | — | uncertain significance |
| rs368506913 | 16:31,075,735 | T/C | — | uncertain significance |
| rs962933118 | 16:31,075,908 | T/A | — | uncertain significance |
| rs61750978 | 16:31,075,909 | C/T | — | likely benign |
| rs140985528 | 16:31,078,310 | G/A | upstream gene variant | — |
| rs8047803 | 16:31,079,834 | C/A | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.