ZBTB46
zinc finger and BTB domain containing 46
Summary
Predicted to enable DNA-binding transcription repressor activity, RNA polymerase II-specific and transcription cis-regulatory region binding activity. Involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants65 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs757028105 | 20:62,378,291 | G/A | — | uncertain significance |
| rs536518455 | 20:62,378,320 | G/A | — | uncertain significance |
| rs200624508 | 20:62,378,335 | C/T | — | uncertain significance |
| rs746631749 | 20:62,378,428 | C/T | — | uncertain significance |
| rs1290756472 | 20:62,378,435 | C/A | — | uncertain significance |
| rs1238455797 | 20:62,378,458 | C/T | — | uncertain significance |
| rs759004681 | 20:62,378,492 | C/T | — | uncertain significance |
| rs139827825 | 20:62,378,495 | C/T | — | uncertain significance |
| rs202051760 | 20:62,378,504 | C/T | — | uncertain significance |
| rs560993615 | 20:62,378,522 | C/T | — | uncertain significance |
| rs376393528 | 20:62,378,531 | C/T | — | uncertain significance |
| rs1362717741 | 20:62,378,533 | C/T | — | uncertain significance |
| rs781576028 | 20:62,378,546 | C/T | — | uncertain significance |
| rs2516039636 | 20:62,378,566 | C/T | — | uncertain significance |
| rs1404697448 | 20:62,378,614 | C/G | — | uncertain significance |
| rs1601379733 | 20:62,378,632 | T/C | — | uncertain significance |
| rs2315646 | 20:62,379,750 | T/G | regulatory region variant | — |
| rs4809333 | 20:62,383,923 | T/G | — | — |
| rs2516084265 | 20:62,384,203 | T/C | — | uncertain significance |
| rs73916646 | 20:62,404,985 | C/A | — | — |
| rs2516235155 | 20:62,407,153 | A/C | — | uncertain significance |
| rs773852418 | 20:62,407,157 | C/A | — | uncertain significance |
| rs755282623 | 20:62,407,193 | T/G | — | uncertain significance |
| rs563024650 | 20:62,407,217 | C/T | — | uncertain significance |
| rs779392769 | 20:62,407,238 | C/T | — | uncertain significance |
| rs532051172 | 20:62,407,256 | G/A | — | uncertain significance |
| rs146382366 | 20:62,407,259 | C/T | — | uncertain significance |
| rs750171292 | 20:62,407,280 | C/G | — | uncertain significance |
| rs778039092 | 20:62,407,292 | C/A | — | uncertain significance |
| rs370264129 | 20:62,407,312 | G/A | — | uncertain significance |
| rs13043476 | 20:62,408,781 | C/T | intron variant | — |
| rs6062314 | 20:62,409,713 | C/T | regulatory region variant | — |
| rs6089993 | 20:62,410,593 | A/T | — | — |
| rs12480840 | 20:62,410,897 | T/C | intron variant | — |
| rs532356829 | 20:62,416,196 | A/G | — | — |
| rs2315656 | 20:62,418,337 | G/A | intron variant | — |
| rs67047102 | 20:62,419,213 | C/T | intron variant | — |
| rs780850554 | 20:62,421,203 | G/A | — | uncertain significance |
| rs770925142 | 20:62,421,227 | G/A | — | uncertain significance |
| rs776879246 | 20:62,421,240 | G/A | — | uncertain significance |
| rs376320552 | 20:62,421,260 | T/C | — | uncertain significance |
| rs2516330793 | 20:62,421,308 | C/A | — | uncertain significance |
| rs146183314 | 20:62,421,485 | T/C | — | uncertain significance |
| rs2516334695 | 20:62,421,534 | C/T | — | uncertain significance |
| rs750696863 | 20:62,421,567 | C/T | — | uncertain significance |
| rs755017 | 20:62,421,622 | A/G | synonymous variant | association |
| rs1378671308 | 20:62,421,638 | A/G | — | uncertain significance |
| rs2092553050 | 20:62,421,907 | C/G | — | likely benign |
| rs2516339400 | 20:62,421,915 | T/G | — | uncertain significance |
| rs535280544 | 20:62,422,026 | C/T | — | uncertain significance |
| rs67415541 | 20:62,426,149 | A/C | intron variant | — |
| rs139136281 | 20:62,427,114 | C/T | regulatory region variant | — |
| rs6062533 | 20:62,429,101 | G/A | intron variant | — |
| rs8115058 | 20:62,432,709 | A/T | — | — |
| rs73323366 | 20:62,433,922 | G/A | intron variant | — |
| rs4809346 | 20:62,434,142 | T/C | intron variant | — |
| rs11697082 | 20:62,435,465 | G/A | regulatory region variant | — |
| rs73624724 | 20:62,436,398 | T/C | upstream gene variant | — |
| rs142880905 | 20:62,439,807 | C/G | intron variant | — |
| rs150947563 | 20:62,441,171 | C/T | intron variant | — |
| rs6062324 | 20:62,446,351 | G/A | coding sequence variant | — |
| rs28637955 | 20:62,447,327 | A/T | — | — |
| rs6011155 | 20:62,450,664 | T/C | downstream gene variant | — |
| rs6011159 | 20:62,452,309 | G/C | — | — |
| rs6062546 | 20:62,459,171 | C/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.