ZBTB41
zinc finger and BTB domain containing 41
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. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs781074124 | 1:197,127,301 | C/T | — | — |
| rs140474865 | 1:197,128,534 | G/A | — | likely benign |
| rs767850712 | 1:197,128,646 | T/C | — | uncertain significance |
| rs373986585 | 1:197,128,743 | G/A | — | uncertain significance |
| rs149802327 | 1:197,128,756 | C/T | — | likely benign |
| rs763695908 | 1:197,128,955 | G/C | — | uncertain significance |
| rs1395547905 | 1:197,128,972 | T/C | — | uncertain significance |
| rs1244671257 | 1:197,129,016 | G/A | — | uncertain significance |
| rs1427992728 | 1:197,144,152 | T/C | — | uncertain significance |
| rs145034971 | 1:197,146,188 | A/G | regulatory region variant | — |
| rs2527486840 | 1:197,147,559 | C/A | — | uncertain significance |
| rs149738372 | 1:197,149,834 | C/A | intron variant | — |
| rs1298336060 | 1:197,150,184 | A/C | — | uncertain significance |
| rs2527496165 | 1:197,150,185 | T/C | — | uncertain significance |
| rs375380482 | 1:197,150,220 | C/T | — | uncertain significance |
| rs185673641 | 1:197,152,484 | A/T | intron variant | — |
| rs10922177 | 1:197,153,767 | T/G | — | — |
| rs7410943 | 1:197,155,021 | A/T | — | — |
| rs1659935827 | 1:197,157,479 | C/T | — | uncertain significance |
| rs10922178 | 1:197,158,599 | C/T | intron variant | — |
| rs10922179 | 1:197,159,347 | G/T | — | — |
| rs41314027 | 1:197,159,791 | A/G | intron variant | — |
| rs10754217 | 1:197,160,338 | C/A | — | — |
| rs571071399 | 1:197,160,574 | G/A | — | — |
| rs760574157 | 1:197,160,843 | G/T | — | uncertain significance |
| rs756494262 | 1:197,160,961 | G/A | — | uncertain significance |
| rs2527528955 | 1:197,160,976 | C/T | — | uncertain significance |
| rs539565562 | 1:197,166,938 | G/A | — | — |
| rs761613772 | 1:197,168,577 | T/G | — | uncertain significance |
| rs749155408 | 1:197,168,748 | C/G | — | uncertain significance |
| rs746733285 | 1:197,168,771 | T/G | — | uncertain significance |
| rs201185833 | 1:197,168,897 | C/T | — | uncertain significance |
| rs760840833 | 1:197,168,967 | T/C | — | uncertain significance |
| rs200742919 | 1:197,168,987 | T/C | — | uncertain significance |
| rs187109878 | 1:197,169,011 | T/C | — | uncertain significance |
| rs965039907 | 1:197,169,044 | G/A | — | uncertain significance |
| rs374480968 | 1:197,169,045 | T/G | — | uncertain significance |
| rs755381458 | 1:197,169,213 | C/T | — | uncertain significance |
| rs141835493 | 1:197,169,248 | T/C | — | uncertain significance |
| rs199720512 | 1:197,169,445 | T/A | — | uncertain significance |
| rs1660281592 | 1:197,169,449 | T/G | — | uncertain significance |
| rs778235195 | 1:197,169,480 | T/C | — | uncertain significance |
| rs2527556992 | 1:197,169,549 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.