ZBTB7C
zinc finger and BTB domain containing 7C
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of cell population proliferation. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants58 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1268205606 | 18:45,555,692 | G/A | — | uncertain significance |
| rs1157117346 | 18:45,555,699 | C/T | — | uncertain significance |
| rs2511457701 | 18:45,555,701 | G/A | — | uncertain significance |
| rs186779400 | 18:45,555,748 | G/A | — | likely benign |
| rs780606151 | 18:45,555,756 | C/T | — | uncertain significance |
| rs755323250 | 18:45,555,776 | C/T | — | uncertain significance |
| rs202024343 | 18:45,555,783 | C/G | — | uncertain significance |
| rs1182743921 | 18:45,555,784 | G/T | — | uncertain significance |
| rs200312432 | 18:45,555,806 | G/A | — | benign |
| rs775360190 | 18:45,555,810 | G/A | — | uncertain significance |
| rs7231151 | 18:45,555,829 | T/C | — | benign |
| rs2511459492 | 18:45,555,906 | T/C | — | uncertain significance |
| rs2511459650 | 18:45,555,924 | C/T | — | uncertain significance |
| rs543484162 | 18:45,555,960 | G/C | — | uncertain significance |
| rs563665130 | 18:45,555,981 | C/T | — | uncertain significance |
| rs748884752 | 18:45,556,010 | C/T | — | uncertain significance |
| rs775753682 | 18:45,556,037 | G/C | — | uncertain significance |
| rs772261302 | 18:45,556,140 | C/T | — | uncertain significance |
| rs761075831 | 18:45,556,158 | C/T | — | uncertain significance |
| rs1039249028 | 18:45,566,287 | C/T | — | uncertain significance |
| rs551388997 | 18:45,566,296 | T/G | — | uncertain significance |
| rs776594058 | 18:45,566,319 | G/C | — | uncertain significance |
| rs370122291 | 18:45,566,406 | A/G | — | uncertain significance |
| rs138978875 | 18:45,566,485 | C/T | — | uncertain significance |
| rs73953657 | 18:45,566,486 | G/A | — | benign |
| rs146193127 | 18:45,566,499 | G/A | — | uncertain significance |
| rs2036157187 | 18:45,566,535 | G/A | — | uncertain significance |
| rs773365727 | 18:45,566,590 | G/C | — | uncertain significance |
| rs2511492775 | 18:45,566,671 | G/T | — | uncertain significance |
| rs761479424 | 18:45,566,686 | C/T | — | uncertain significance |
| rs1467155310 | 18:45,566,758 | T/C | — | uncertain significance |
| rs886675482 | 18:45,566,763 | G/C | — | uncertain significance |
| rs1173673016 | 18:45,566,857 | G/A | — | uncertain significance |
| rs868558985 | 18:45,566,926 | A/T | — | uncertain significance |
| rs760300824 | 18:45,566,940 | G/A | — | uncertain significance |
| rs377491621 | 18:45,566,964 | G/C | — | uncertain significance |
| rs551094237 | 18:45,566,986 | C/T | — | uncertain significance |
| rs201261592 | 18:45,566,996 | C/A | — | uncertain significance |
| rs769797708 | 18:45,566,998 | C/T | — | uncertain significance |
| rs776468030 | 18:45,567,036 | T/A | — | uncertain significance |
| rs148618880 | 18:45,567,049 | C/T | — | uncertain significance |
| rs187400646 | 18:45,567,067 | C/G | — | uncertain significance |
| rs200362895 | 18:45,567,082 | C/T | — | uncertain significance |
| rs115080210 | 18:45,567,085 | C/A | — | uncertain significance |
| rs758879850 | 18:45,567,088 | C/G | — | uncertain significance |
| rs781681316 | 18:45,567,115 | C/T | — | uncertain significance |
| rs372893289 | 18:45,567,153 | T/C | — | uncertain significance |
| rs751782036 | 18:45,567,259 | C/T | — | uncertain significance |
| rs67466227 | 18:45,578,299 | C/G | intron variant | — |
| rs144488974 | 18:45,599,649 | C/G | regulatory region variant | — |
| rs11662183 | 18:45,651,464 | C/T | regulatory region variant | — |
| rs79272944 | 18:45,657,853 | G/T | intron variant | — |
| rs12605964 | 18:45,663,787 | C/G | — | — |
| rs12965052 | 18:45,665,900 | G/A | regulatory region variant | — |
| rs4258692 | 18:45,673,443 | A/C | intron variant | — |
| rs373095162 | 18:45,727,280 | G/A | — | — |
| rs1944582 | 18:45,815,417 | A/G | intron variant | — |
| rs11082671 | 18:45,865,597 | A/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.