ZBTB10
zinc finger and BTB domain containing 10
Summary
Enables telomeric DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II. Located in chromosome, telomeric region and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1815477686 | 8:81,399,122 | C/T | — | uncertain significance |
| rs2537315572 | 8:81,399,124 | A/G | — | uncertain significance |
| rs2537315574 | 8:81,399,125 | C/T | — | uncertain significance |
| rs1031094591 | 8:81,399,131 | A/G | — | uncertain significance |
| rs1221938119 | 8:81,399,135 | C/A | — | uncertain significance |
| rs150539196 | 8:81,399,180 | A/G | synonymous variant | — |
| rs573842562 | 8:81,399,185 | C/A | — | uncertain significance |
| rs1815481520 | 8:81,399,190 | C/T | — | uncertain significance |
| rs2537315843 | 8:81,399,194 | C/T | — | uncertain significance |
| rs968371125 | 8:81,399,227 | G/T | — | uncertain significance |
| rs759467188 | 8:81,399,257 | G/A | — | uncertain significance |
| rs1213629464 | 8:81,399,262 | G/A | — | uncertain significance |
| rs2537316143 | 8:81,399,278 | A/T | — | uncertain significance |
| rs749169552 | 8:81,399,281 | C/T | — | uncertain significance |
| rs772027446 | 8:81,399,284 | C/T | — | uncertain significance |
| rs1815490694 | 8:81,399,367 | G/A | — | uncertain significance |
| rs757441360 | 8:81,399,391 | G/C | — | uncertain significance |
| rs3802146 | 8:81,399,430 | G/A | — | uncertain significance |
| rs774717272 | 8:81,399,490 | C/A | — | uncertain significance |
| rs549797718 | 8:81,399,506 | A/G | — | uncertain significance |
| rs2131466699 | 8:81,399,511 | C/T | — | uncertain significance |
| rs1257648450 | 8:81,399,518 | C/A | — | uncertain significance |
| rs919227682 | 8:81,399,523 | A/G | — | likely benign |
| rs2537316921 | 8:81,399,531 | T/G | — | likely benign |
| rs2537316934 | 8:81,399,542 | A/T | — | uncertain significance |
| rs2537317065 | 8:81,399,569 | A/C | — | uncertain significance |
| rs1428651014 | 8:81,399,635 | G/A | — | uncertain significance |
| rs764512748 | 8:81,399,749 | C/T | — | uncertain significance |
| rs2537317712 | 8:81,399,802 | T/G | — | uncertain significance |
| rs767164986 | 8:81,399,904 | C/T | — | uncertain significance |
| rs1043388069 | 8:81,399,910 | C/T | — | uncertain significance |
| rs770972973 | 8:81,399,959 | C/T | — | uncertain significance |
| rs199498627 | 8:81,400,006 | G/A | — | uncertain significance |
| rs6473232 | 8:81,404,297 | C/G | intron variant | — |
| rs3932815 | 8:81,405,915 | C/A | — | — |
| rs55942834 | 8:81,411,215 | A/T | — | — |
| rs1477856134 | 8:81,411,776 | G/C | — | uncertain significance |
| rs775003308 | 8:81,412,147 | A/G | — | uncertain significance |
| rs1486129663 | 8:81,412,322 | T/G | — | uncertain significance |
| rs200512854 | 8:81,412,399 | A/G | — | uncertain significance |
| rs201224143 | 8:81,412,471 | G/T | — | uncertain significance |
| rs272617 | 8:81,417,591 | T/G | — | — |
| rs182120 | 8:81,418,642 | A/C | intron variant | — |
| rs272607 | 8:81,424,801 | T/G | intron variant | — |
| rs780240936 | 8:81,426,151 | A/G | — | uncertain significance |
| rs768949767 | 8:81,426,159 | C/G | — | uncertain significance |
| rs2537354896 | 8:81,426,169 | G/A | — | uncertain significance |
| rs1816262335 | 8:81,426,178 | G/A | — | uncertain significance |
| rs28588720 | 8:81,429,864 | T/C | intron variant | — |
| rs985024060 | 8:81,430,731 | A/C | — | uncertain significance |
| rs771647707 | 8:81,431,703 | T/A | — | uncertain significance |
| rs1451755936 | 8:81,431,755 | G/C | — | uncertain significance |
| rs1051920 | 8:81,438,420 | C/T | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.