ZBTB40
zinc finger and BTB domain containing 40
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific. Involved in DNA damage response. Located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants70 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs767808568 | 1:22,816,535 | A/G | — | uncertain significance |
| rs528063989 | 1:22,816,635 | T/C | — | uncertain significance |
| rs551375407 | 1:22,816,674 | T/G | — | uncertain significance |
| rs115103344 | 1:22,816,687 | A/G | — | benign |
| rs745947519 | 1:22,816,833 | C/T | — | likely benign |
| rs776931634 | 1:22,816,871 | C/G | — | uncertain significance |
| rs369096143 | 1:22,816,893 | C/A | — | uncertain significance |
| rs755063136 | 1:22,817,090 | C/G | — | uncertain significance |
| rs1638602598 | 1:22,817,103 | C/T | — | uncertain significance |
| rs36115661 | 1:22,817,996 | G/A | — | benign |
| rs200179557 | 1:22,827,991 | G/A | — | likely benign |
| rs2522925766 | 1:22,827,998 | G/A | — | uncertain significance |
| rs577900930 | 1:22,828,002 | C/T | — | likely benign |
| rs209752 | 1:22,828,044 | T/C | — | benign |
| rs890585529 | 1:22,828,069 | G/A | — | uncertain significance |
| rs2522926314 | 1:22,828,078 | G/T | — | uncertain significance |
| rs2522926785 | 1:22,828,163 | C/T | — | uncertain significance |
| rs147907060 | 1:22,828,819 | C/A | — | uncertain significance |
| rs552328197 | 1:22,828,870 | T/C | — | uncertain significance |
| rs199935646 | 1:22,828,911 | T/C | — | uncertain significance |
| rs767371951 | 1:22,828,929 | A/C | — | uncertain significance |
| rs574053241 | 1:22,830,999 | C/G | — | — |
| rs773149332 | 1:22,832,603 | G/A | — | uncertain significance |
| rs750554698 | 1:22,832,621 | C/T | — | uncertain significance |
| rs371758282 | 1:22,832,622 | G/A | — | likely benign |
| rs748397949 | 1:22,832,665 | A/G | — | uncertain significance |
| rs770580272 | 1:22,832,666 | C/T | — | likely benign |
| rs371373012 | 1:22,832,708 | A/C | — | uncertain significance |
| rs1274896013 | 1:22,834,518 | G/A | — | uncertain significance |
| rs779514773 | 1:22,834,542 | A/G | — | uncertain significance |
| rs1244690882 | 1:22,834,617 | C/T | — | uncertain significance |
| rs757202869 | 1:22,835,111 | C/T | — | uncertain significance |
| rs943920964 | 1:22,835,173 | C/G | — | uncertain significance |
| rs755809587 | 1:22,835,185 | A/G | — | uncertain significance |
| rs759924811 | 1:22,835,635 | A/G | — | uncertain significance |
| rs209729 | 1:22,835,677 | G/A | — | benign |
| rs150068799 | 1:22,835,697 | G/A | — | uncertain significance |
| rs2522968324 | 1:22,837,759 | A/G | — | uncertain significance |
| rs201909816 | 1:22,838,238 | A/G | — | uncertain significance |
| rs758055914 | 1:22,838,300 | G/A | — | uncertain significance |
| rs34216459 | 1:22,838,308 | T/C | — | likely benign |
| rs1225836028 | 1:22,838,421 | A/G | — | uncertain significance |
| rs138771748 | 1:22,838,442 | G/A | — | uncertain significance |
| rs1422299493 | 1:22,838,460 | A/G | — | uncertain significance |
| rs1639251451 | 1:22,838,477 | T/C | — | uncertain significance |
| rs1392044603 | 1:22,838,490 | A/G | — | uncertain significance |
| rs781524065 | 1:22,838,493 | A/G | — | uncertain significance |
| rs182939277 | 1:22,838,519 | C/G | — | likely benign |
| rs201823800 | 1:22,838,556 | C/T | — | likely benign |
| rs2124460728 | 1:22,839,428 | C/T | — | uncertain significance |
| rs2522977451 | 1:22,839,431 | A/C | — | uncertain significance |
| rs768590722 | 1:22,843,852 | C/T | — | uncertain significance |
| rs2523006882 | 1:22,846,646 | G/A | — | uncertain significance |
| rs137897116 | 1:22,846,655 | C/T | — | uncertain significance |
| rs772602948 | 1:22,848,056 | G/C | — | uncertain significance |
| rs1320055304 | 1:22,848,101 | C/T | — | uncertain significance |
| rs142695294 | 1:22,848,867 | C/T | — | likely benign |
| rs527250370 | 1:22,848,937 | T/A | — | uncertain significance |
| rs2523017858 | 1:22,848,939 | T/A | — | uncertain significance |
| rs2523017897 | 1:22,848,942 | A/C | — | uncertain significance |
| rs374282664 | 1:22,850,701 | T/A | — | likely benign |
| rs374357053 | 1:22,850,708 | C/T | — | likely benign |
| rs1296331869 | 1:22,850,893 | G/T | — | uncertain significance |
| rs370617744 | 1:22,850,903 | C/T | — | uncertain significance |
| rs776709448 | 1:22,850,933 | C/T | — | likely benign |
| rs881646 | 1:22,852,715 | G/C | — | benign |
| rs2523034759 | 1:22,852,729 | A/G | — | uncertain significance |
| rs748303609 | 1:22,852,731 | C/G | — | uncertain significance |
| rs199799681 | 1:22,852,757 | G/C | — | uncertain significance |
| rs377364120 | 1:22,852,864 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.